{"id":16645,"date":"2024-12-04T12:56:37","date_gmt":"2024-12-04T04:56:37","guid":{"rendered":"https:\/\/dac.nycu.edu.tw\/?post_type=portfolio&#038;p=16645"},"modified":"2026-08-05T19:24:15","modified_gmt":"2026-08-05T11:24:15","slug":"%e8%a8%b1%e5%8d%83%e6%a8%b9-%e8%ac%9b%e5%ba%a7%e6%95%99%e6%8e%88","status":"publish","type":"portfolio","link":"https:\/\/dac.nycu.edu.tw\/en\/portfolio-item\/%e8%a8%b1%e5%8d%83%e6%a8%b9-%e8%ac%9b%e5%ba%a7%e6%95%99%e6%8e%88\/","title":{"rendered":"Chair Professor Chain-Shu Hsu"},"content":{"rendered":"\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-1pomh8x-883aceaf2c4e341de91bb418614871d0\">\n.avia-section.av-1pomh8x-883aceaf2c4e341de91bb418614871d0{\nmargin-top:-50px;\nmargin-bottom:0px;\n}\n.avia-section.av-1pomh8x-883aceaf2c4e341de91bb418614871d0 .av-parallax 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class=\"av-section-color-overlay-wrap\"><div class=\"av-section-color-overlay\"><\/div><div class='container av-section-cont-open' style='height:280px'><main  role=\"main\" itemprop=\"mainContentOfPage\"  class='template-page content  av-content-full alpha units'><div class='post-entry post-entry-type-page post-entry-16645'><div class='entry-content-wrapper clearfix'>\n<div  class='flex_column av-1onw8xt-ec09ac091bcd5d5e2a80b7b76dabdcaf av_one_full  avia-builder-el-1  avia-builder-el-no-sibling  first flex_column_div  '     ><p>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-5x3lpd-17ba7be20094bf36725c180a0f517c37\">\n#top .av-special-heading.av-5x3lpd-17ba7be20094bf36725c180a0f517c37{\npadding-bottom:10px;\ncolor:#ffffff;\n}\nbody .av-special-heading.av-5x3lpd-17ba7be20094bf36725c180a0f517c37 .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-5x3lpd-17ba7be20094bf36725c180a0f517c37 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\/>\n<\/p><\/div>\n<\/div><\/div><\/main><!-- close content main element --><\/div><\/div><\/div><div id='after_section_1'  class='main_color av_default_container_wrap container_wrap fullsize'  ><div class='container av-section-cont-open' ><div class='template-page content  av-content-full alpha units'><div class='post-entry post-entry-type-page post-entry-16645'><div class='entry-content-wrapper clearfix'>\n\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-1jhk00x-c993aeef8f7652346ca06bcf1b464c88\">\n#top .hr.hr-invisible.av-1jhk00x-c993aeef8f7652346ca06bcf1b464c88{\nheight:5px;\n}\n<\/style>\n<div  class='hr av-1jhk00x-c993aeef8f7652346ca06bcf1b464c88 hr-invisible  avia-builder-el-5  el_after_av_section  el_before_av_hr  avia-builder-el-first  av-small-hide av-mini-hide'><span class='hr-inner '><span class=\"hr-inner-style\"><\/span><\/span><\/div>\n\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" 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avia_image ' src=\"https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2025\/05\/\u8a31\u5343\u6a39Chain-Shu-Hsu.png\" alt='\u8a31\u5343\u6a39Chain-Shu Hsu' title='\u8a31\u5343\u6a39Chain-Shu Hsu'  height=\"510\" width=\"600\"  itemprop=\"thumbnailUrl\" srcset=\"https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2025\/05\/\u8a31\u5343\u6a39Chain-Shu-Hsu.png 600w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2025\/05\/\u8a31\u5343\u6a39Chain-Shu-Hsu-235x200.png 235w\" sizes=\"(max-width: 600px) 100vw, 600px\" \/><\/div><\/div><\/div><\/div>\n<div class='av-flex-placeholder'><\/div>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-1ebcwap-65eb1d5a5c4ce249f99daf5f1284bbf8\">\n.flex_column.av-1ebcwap-65eb1d5a5c4ce249f99daf5f1284bbf8{\nwidth:65.166666666667%;\nmargin-left:0;\n}\n#top .flex_column_table.av-equal-height-column-flextable.av-1ebcwap-65eb1d5a5c4ce249f99daf5f1284bbf8 .av-flex-placeholder{\nwidth:4.5%;\n}\n<\/style>\n<div  class='flex_column av-1ebcwap-65eb1d5a5c4ce249f99daf5f1284bbf8 av_two_third  avia-builder-el-9  el_after_av_one_third  el_before_av_hr  flex_column_table_cell av-equal-height-column av-align-middle  '     ><p>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-m49txynp-9bb3a2b37c1750a6c6342d4959446b58\">\n#top .av-special-heading.av-m49txynp-9bb3a2b37c1750a6c6342d4959446b58{\nmargin:0 0 0 0;\npadding-bottom:10px;\ncolor:#005daf;\n}\nbody .av-special-heading.av-m49txynp-9bb3a2b37c1750a6c6342d4959446b58 .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-m49txynp-9bb3a2b37c1750a6c6342d4959446b58 .special-heading-inner-border{\nborder-color:#005daf;\n}\n.av-special-heading.av-m49txynp-9bb3a2b37c1750a6c6342d4959446b58 .av-subheading{\nfont-size:15px;\n}\n\n@media only screen and (min-width: 480px) and (max-width: 767px){ \n#top .av-special-heading.av-m49txynp-9bb3a2b37c1750a6c6342d4959446b58{\nmargin:30px 0 0 0;\n}\n}\n\n@media only screen and (max-width: 479px){ \n#top .av-special-heading.av-m49txynp-9bb3a2b37c1750a6c6342d4959446b58{\nmargin:30px 0 0 0;\n}\n}\n<\/style>\n<div  class='av-special-heading av-m49txynp-9bb3a2b37c1750a6c6342d4959446b58 av-special-heading-h2 custom-color-heading blockquote modern-quote  avia-builder-el-10  el_before_av_heading  avia-builder-el-first '><h2 class='av-special-heading-tag '  itemprop=\"headline\"  >\u8a31\u5343\u6a39 Chain-Shu Hsu<\/h2><div class=\"special-heading-border\"><div class=\"special-heading-inner-border\"><\/div><\/div><\/div><br \/>\n\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-1cr9foh-4a49fef59b6645f2742547c923f5575b\">\n#top .av-special-heading.av-1cr9foh-4a49fef59b6645f2742547c923f5575b{\nmargin:0 0 0 0;\npadding-bottom:20px;\ncolor:#005daf;\n}\nbody .av-special-heading.av-1cr9foh-4a49fef59b6645f2742547c923f5575b .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-1cr9foh-4a49fef59b6645f2742547c923f5575b .special-heading-inner-border{\nborder-color:#005daf;\n}\n.av-special-heading.av-1cr9foh-4a49fef59b6645f2742547c923f5575b .av-subheading{\nfont-size:15px;\n}\n\n@media only screen and (min-width: 480px) and (max-width: 767px){ \n#top .av-special-heading.av-1cr9foh-4a49fef59b6645f2742547c923f5575b{\nmargin:0 0 0 0;\n}\n}\n\n@media only screen and (max-width: 479px){ \n#top .av-special-heading.av-1cr9foh-4a49fef59b6645f2742547c923f5575b{\nmargin:0 0 0 0;\n}\n}\n<\/style>\n<div  class='av-special-heading av-1cr9foh-4a49fef59b6645f2742547c923f5575b av-special-heading-h3 custom-color-heading blockquote modern-quote  avia-builder-el-11  el_after_av_heading  el_before_av_textblock  title-line'><h3 class='av-special-heading-tag '  itemprop=\"headline\"  >Chair Professor<\/h3><div class=\"special-heading-border\"><div class=\"special-heading-inner-border\"><\/div><\/div><\/div><br \/>\n<section  class='av_textblock_section av-m49tzmbs-ac4e0de261c21660b032f215786d291a '   itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/CreativeWork\" ><div class='avia_textblock link_text'  itemprop=\"text\" ><p>Tell | 03-5712121 #31523<\/p>\n<p>office | TKB R716A<\/p>\n<p>Email | cshsu@nycu.edu.tw<\/p>\n<p>Lab Tel |\u00a003-5712121 #56514<\/p>\n<\/div><\/section><br \/>\n\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-1bubqht-bd281dd9facf691d4d9236f2c5d24e67\">\n#top .hr.hr-invisible.av-1bubqht-bd281dd9facf691d4d9236f2c5d24e67{\nheight:15px;\n}\n<\/style>\n<div  class='hr av-1bubqht-bd281dd9facf691d4d9236f2c5d24e67 hr-invisible  avia-builder-el-13  el_after_av_textblock  el_before_av_buttonrow '><span class='hr-inner '><span class=\"hr-inner-style\"><\/span><\/span><\/div><br \/>\n<div  class='avia-buttonrow-wrap av-m49u1giy-175bc11cb2d5eb3cc8e5ca379263f9db avia-buttonrow-left  avia-builder-el-14  el_after_av_hr  avia-builder-el-last '>\n\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-m49u1fkq-864103f8dae6713b7b8fca91b6677b53\">\n#top #wrap_all .avia-button.av-m49u1fkq-864103f8dae6713b7b8fca91b6677b53{\nmargin-bottom:5px;\nmargin-right:5px;\n}\n#top #wrap_all .avia-button.av-m49u1fkq-864103f8dae6713b7b8fca91b6677b53:hover{\nopacity:1;\ntransition:all 0.4s ease-in-out;\n}\n<\/style>\n<a href='https:\/\/scholar.nycu.edu.tw\/zh\/persons\/chain-shu-hsu'  class='avia-button av-m49u1fkq-864103f8dae6713b7b8fca91b6677b53 avia-icon_select-yes-right-icon avia-size-medium av-icon-on-hover avia-color-theme-color'  target=\"_blank\"  rel=\"noopener noreferrer\"  aria-label=\"NYCU Academic Hub \/ \u7814\u767c\u512a\u52e2\u5e73\u53f0\"><span class='avia_iconbox_title' >NYCU Academic Hub \/ \u7814\u767c\u512a\u52e2\u5e73\u53f0<\/span><span class='avia_button_icon avia_button_icon_right avia-iconfont avia-font-entypo-fontello' data-av_icon='\ue881' data-av_iconfont='entypo-fontello' ><\/span><\/a>\n<\/div><\/p><\/div><\/div><!--close column table wrapper. Autoclose: 1 -->\n\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-1a0tesx-a2f3644a38fa9bb77149ce7d0d53f54d\">\n#top .hr.hr-invisible.av-1a0tesx-a2f3644a38fa9bb77149ce7d0d53f54d{\nheight:30px;\n}\n<\/style>\n<div  class='hr av-1a0tesx-a2f3644a38fa9bb77149ce7d0d53f54d hr-invisible  avia-builder-el-15  el_after_av_two_third  el_before_av_one_full  av-desktop-hide av-medium-hide'><span class='hr-inner '><span class=\"hr-inner-style\"><\/span><\/span><\/div>\n<div class='flex_column_table av-18da2b5-f7bc35d2967d418e28430bc19af47e6d sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-18da2b5-f7bc35d2967d418e28430bc19af47e6d\">\n.flex_column.av-18da2b5-f7bc35d2967d418e28430bc19af47e6d{\nwidth:100%;\nmargin-left:0;\nborder-radius:0 50px 0 0;\npadding:25px 30px 15px 30px;\nbackground-color:#ffeca0;\n}\n#top .flex_column_table.av-equal-height-column-flextable.av-18da2b5-f7bc35d2967d418e28430bc19af47e6d .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-18da2b5-f7bc35d2967d418e28430bc19af47e6d av_one_full  avia-builder-el-16  el_after_av_hr  el_before_av_one_full  double-line-wy titlebox-mob first flex_column_table_cell av-equal-height-column av-align-top  '     ><style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-15z9s9d-013f8bb338a8a2500c285e47377abc28\">\n#top .av-special-heading.av-15z9s9d-013f8bb338a8a2500c285e47377abc28{\npadding-bottom:10px;\n}\nbody .av-special-heading.av-15z9s9d-013f8bb338a8a2500c285e47377abc28 .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-15z9s9d-013f8bb338a8a2500c285e47377abc28 .av-subheading{\nfont-size:15px;\n}\n<\/style>\n<div  class='av-special-heading av-15z9s9d-013f8bb338a8a2500c285e47377abc28 av-special-heading-h3 blockquote modern-quote  avia-builder-el-17  avia-builder-el-no-sibling '><h3 class='av-special-heading-tag '  itemprop=\"headline\"  >Education<\/h3><div class=\"special-heading-border\"><div class=\"special-heading-inner-border\"><\/div><\/div><\/div><\/div><\/div><!--close column table wrapper. Autoclose: 1 -->\n<div class='flex_column_table av-14pd1sx-e197a2ea517031dc6e9c4e59d5aa93d6 sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-14pd1sx-e197a2ea517031dc6e9c4e59d5aa93d6\">\n#top .flex_column_table.av-equal-height-column-flextable.av-14pd1sx-e197a2ea517031dc6e9c4e59d5aa93d6{\nmargin-top:0px;\nmargin-bottom:0px;\n}\n.flex_column.av-14pd1sx-e197a2ea517031dc6e9c4e59d5aa93d6{\nwidth:100%;\nmargin-left:0;\nborder-width:2px;\nborder-color:#ffeca0;\nborder-style:solid;\npadding:30px 30px 30px 30px;\n}\n#top .flex_column_table.av-equal-height-column-flextable.av-14pd1sx-e197a2ea517031dc6e9c4e59d5aa93d6 .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-14pd1sx-e197a2ea517031dc6e9c4e59d5aa93d6 av_one_full  avia-builder-el-18  el_after_av_one_full  el_before_av_one_full  first flex_column_table_cell av-equal-height-column av-align-top  column-top-margin'     ><section  class='av_textblock_section av-132228h-0260b24b61d67e0265e765e196f26bca '   itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/CreativeWork\" ><div class='avia_textblock'  itemprop=\"text\" ><p>1975 B.S.\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0Department of Chemistry, National Taiwan Normal University, Taipei, Taiwan, R.O.C.<\/p>\n<p>1978 M.S..\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0Department of Chemistry, National Tsing Hua University, Hsinchu, Taiwan, R.O.C.<\/p>\n<p>1987 Ph.D.\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0Department of Macromolecular Science, Case Western Reserve University,Cleveland, OH, U.S.A.<\/p>\n<\/div><\/section><\/div><\/div><!--close column table wrapper. Autoclose: 1 -->\n<div class='flex_column_table av-11oz34h-af662ff6021154f1659c7e80cb99dc81 sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-11oz34h-af662ff6021154f1659c7e80cb99dc81\">\n.flex_column.av-11oz34h-af662ff6021154f1659c7e80cb99dc81{\nwidth:100%;\nmargin-left:0;\nborder-radius:0 50px 0 0;\npadding:25px 30px 15px 30px;\nbackground-color:#3a4586;\n}\n#top .flex_column_table.av-equal-height-column-flextable.av-11oz34h-af662ff6021154f1659c7e80cb99dc81 .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-11oz34h-af662ff6021154f1659c7e80cb99dc81 av_one_full  avia-builder-el-20  el_after_av_one_full  el_before_av_one_full  double-line-wy titlebox-mob first flex_column_table_cell av-equal-height-column av-align-top  column-top-margin'     ><style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-zcf3sh-a0ab52f4684df68f1286af63717c8307\">\n#top .av-special-heading.av-zcf3sh-a0ab52f4684df68f1286af63717c8307{\npadding-bottom:10px;\ncolor:#ffffff;\n}\nbody .av-special-heading.av-zcf3sh-a0ab52f4684df68f1286af63717c8307 .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-zcf3sh-a0ab52f4684df68f1286af63717c8307 .special-heading-inner-border{\nborder-color:#ffffff;\n}\n.av-special-heading.av-zcf3sh-a0ab52f4684df68f1286af63717c8307 .av-subheading{\nfont-size:15px;\n}\n<\/style>\n<div  class='av-special-heading av-zcf3sh-a0ab52f4684df68f1286af63717c8307 av-special-heading-h3 custom-color-heading blockquote modern-quote  avia-builder-el-21  avia-builder-el-no-sibling '><h3 class='av-special-heading-tag '  itemprop=\"headline\"  >Experiencse<\/h3><div class=\"special-heading-border\"><div class=\"special-heading-inner-border\"><\/div><\/div><\/div><\/div><\/div><!--close column table wrapper. Autoclose: 1 -->\n<div class='flex_column_table av-xxp6rl-0b3c7c4efb9c541907dae6f9471be9c5 sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-xxp6rl-0b3c7c4efb9c541907dae6f9471be9c5\">\n#top .flex_column_table.av-equal-height-column-flextable.av-xxp6rl-0b3c7c4efb9c541907dae6f9471be9c5{\nmargin-top:0px;\nmargin-bottom:0px;\n}\n.flex_column.av-xxp6rl-0b3c7c4efb9c541907dae6f9471be9c5{\nwidth:100%;\nmargin-left:0;\nborder-width:2px;\nborder-color:#3a4586;\nborder-style:solid;\npadding:30px 30px 30px 30px;\n}\n#top .flex_column_table.av-equal-height-column-flextable.av-xxp6rl-0b3c7c4efb9c541907dae6f9471be9c5 .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-xxp6rl-0b3c7c4efb9c541907dae6f9471be9c5 av_one_full  avia-builder-el-22  el_after_av_one_full  el_before_av_one_full  first flex_column_table_cell av-equal-height-column av-align-top  column-top-margin'     ><section  class='av_textblock_section av-mhebq876-4ea5a5a2082bc64c329b92d0d66a7267 '   itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/CreativeWork\" ><div class='avia_textblock'  itemprop=\"text\" ><p>2021- present Senior Chair Professor, NYCU<\/p>\n<p>2010- 2021\u00a0\u00a0\u00a0\u00a0\u00a0Senior Chair Professor, NCTU<\/p>\n<p>2016- 2017\u00a0\u00a0\u00a0President, The Chemical Society Located in Taipei<\/p>\n<p>2008-2010\uff1b\u00a0\u00a0\u00a0\u00a0\u00a0Vice President, NCTU<\/p>\n<p>2012-2015<\/p>\n<p>2011\/12-2013\/12\u00a0\u00a0\u00a0\u00a0\u00a0President, Pacific Polymer Federation<\/p>\n<p>2003-2007\uff1b2011\u00a0\u00a0\u00a0Vice Chancellor, University System of Taiwan<\/p>\n<p>2012-2013\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0President, The Polymer Society, Taipei<\/p>\n<p>2003-2011\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0President, Taiwan OLED \/ PLED Society<\/p>\n<p>2008-2009\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0President, ROC Taiwan Liquid Crystal Society<\/p>\n<p>2006-2007\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0Director, Office of Achieving Top University Project, NCTU<\/p>\n<p>1998\uff1b2005-2008\u00a0\u00a0\u00a0Associate of Dean, College of Science, NCTU<\/p>\n<p>1998-2002\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0Dean, Office of Research and Development, NCTU<\/p>\n<p>1994-1998\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0Chairman, Department of Applied Chemistry, NCTU<\/p>\n<\/div><\/section><\/div><\/div><!--close column table wrapper. Autoclose: 1 -->\n<div class='flex_column_table av-pfjvsh-b682ae6ddb42bf4f3451c3bc8a75b61e sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-pfjvsh-b682ae6ddb42bf4f3451c3bc8a75b61e\">\n.flex_column.av-pfjvsh-b682ae6ddb42bf4f3451c3bc8a75b61e{\nwidth:100%;\nmargin-left:0;\nborder-radius:0 50px 0 0;\npadding:25px 30px 15px 30px;\nbackground-color:#ffeca0;\n}\n#top .flex_column_table.av-equal-height-column-flextable.av-pfjvsh-b682ae6ddb42bf4f3451c3bc8a75b61e .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-pfjvsh-b682ae6ddb42bf4f3451c3bc8a75b61e av_one_full  avia-builder-el-24  el_after_av_one_full  el_before_av_one_full  double-line-wy titlebox-mob first flex_column_table_cell av-equal-height-column av-align-top  column-top-margin'     ><style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-nqiiup-3da51cf8410fb7a6d50c58dd7bf7cd39\">\n#top .av-special-heading.av-nqiiup-3da51cf8410fb7a6d50c58dd7bf7cd39{\npadding-bottom:10px;\n}\nbody .av-special-heading.av-nqiiup-3da51cf8410fb7a6d50c58dd7bf7cd39 .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-nqiiup-3da51cf8410fb7a6d50c58dd7bf7cd39 .av-subheading{\nfont-size:15px;\n}\n<\/style>\n<div  class='av-special-heading av-nqiiup-3da51cf8410fb7a6d50c58dd7bf7cd39 av-special-heading-h3 blockquote modern-quote  avia-builder-el-25  avia-builder-el-no-sibling '><h3 class='av-special-heading-tag '  itemprop=\"headline\"  >Honors<\/h3><div class=\"special-heading-border\"><div class=\"special-heading-inner-border\"><\/div><\/div><\/div><\/div><\/div><!--close column table wrapper. Autoclose: 1 -->\n<div class='flex_column_table av-mstlq9-6122e57253955992691098f92e67953b sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-mstlq9-6122e57253955992691098f92e67953b\">\n#top .flex_column_table.av-equal-height-column-flextable.av-mstlq9-6122e57253955992691098f92e67953b{\nmargin-top:0px;\nmargin-bottom:0px;\n}\n.flex_column.av-mstlq9-6122e57253955992691098f92e67953b{\nwidth:100%;\nmargin-left:0;\nborder-width:2px;\nborder-color:#ffeca0;\nborder-style:solid;\npadding:30px 30px 15px 30px;\n}\n#top .flex_column_table.av-equal-height-column-flextable.av-mstlq9-6122e57253955992691098f92e67953b .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-mstlq9-6122e57253955992691098f92e67953b av_one_full  avia-builder-el-26  el_after_av_one_full  el_before_av_one_full  first flex_column_table_cell av-equal-height-column av-align-top  column-top-margin'     ><section  class='av_textblock_section av-l29dhd-87347c808413d8dec8f866f332472da4 '   itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/CreativeWork\" ><div class='avia_textblock'  itemprop=\"text\" ><ul>\n<li>Excellent Research Awards, National Science Council (1994-1995, 1996-1997, 1998-1999)<\/li>\n<li>Research Fellow, National Science Council (2000-2003)<\/li>\n<li>Prize, France-Taiwan Scientific Foundation (2006)<\/li>\n<li>Outstanding Research Award, The Polymer Society, Taipei (2007)<\/li>\n<li>TECO Award, TECO Technology Foundation\uff082007\uff09<\/li>\n<li>Ho Chin Tui Award (2007)<\/li>\n<li>Fellow, The ASIA-Pacific Academy of Materials (APAM) (2008)<\/li>\n<li>Academic Award, Ministry of Education, ROC (2008)<\/li>\n<li>Nano-tech Award, Taiwan Nanotechnology Industry Development Association (2011)<\/li>\n<li>SPSJ International Award, The Society of Polymer Science, Japan (2014)<\/li>\n<li>Y. Z. Hsu Scientific Chair Professor (2016)<\/li>\n<li>Lifetime Achievement Award, The Polymer Society, Taipei (2016)<\/li>\n<li>Fellow, The Polymer Society, Taipei (2018)<\/li>\n<li>SID Slottow-Owaki Prize (2019)<\/li>\n<li>Academic Award, the Chemical Society Located in Taipei (2019)<\/li>\n<li>Annual National Professorship Awards, Ministry of Education (2020)<\/li>\n<li>National Innovation Award, Research Center for Biotechnology and Medicine Policy (2021)<\/li>\n<li>Outstanding Achievement Award, The Phi Tau Phi Scholastic Honor Society (2022)<\/li>\n<li>National Innovation Award, Research Center for Biotechnology and Medicine Policy (2022)<\/li>\n<\/ul>\n<\/div><\/section><\/div><\/div><!--close column table wrapper. Autoclose: 1 -->\n<div class='flex_column_table av-iy5bi9-46b5b0ae903807e536e9a46783264b6f sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-iy5bi9-46b5b0ae903807e536e9a46783264b6f\">\n.flex_column.av-iy5bi9-46b5b0ae903807e536e9a46783264b6f{\nwidth:100%;\nmargin-left:0;\nborder-radius:0 50px 0 0;\npadding:25px 30px 15px 30px;\nbackground-color:#3a4586;\n}\n#top .flex_column_table.av-equal-height-column-flextable.av-iy5bi9-46b5b0ae903807e536e9a46783264b6f .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-iy5bi9-46b5b0ae903807e536e9a46783264b6f av_one_full  avia-builder-el-28  el_after_av_one_full  el_before_av_one_full  double-line-wy titlebox-mob first flex_column_table_cell av-equal-height-column av-align-top  column-top-margin'     ><style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-gtltz5-ab56734ba458e659b0224de041fc0f8d\">\n#top .av-special-heading.av-gtltz5-ab56734ba458e659b0224de041fc0f8d{\npadding-bottom:10px;\ncolor:#ffffff;\n}\nbody .av-special-heading.av-gtltz5-ab56734ba458e659b0224de041fc0f8d .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-gtltz5-ab56734ba458e659b0224de041fc0f8d .special-heading-inner-border{\nborder-color:#ffffff;\n}\n.av-special-heading.av-gtltz5-ab56734ba458e659b0224de041fc0f8d .av-subheading{\nfont-size:15px;\n}\n<\/style>\n<div  class='av-special-heading av-gtltz5-ab56734ba458e659b0224de041fc0f8d av-special-heading-h3 custom-color-heading blockquote modern-quote  avia-builder-el-29  avia-builder-el-no-sibling '><h3 class='av-special-heading-tag '  itemprop=\"headline\"  >Publication<\/h3><div class=\"special-heading-border\"><div class=\"special-heading-inner-border\"><\/div><\/div><\/div><\/div><\/div><!--close column table wrapper. Autoclose: 1 -->\n<div class='flex_column_table av-gf7sa9-086a6e4104aa0f5ba9c5c238ce8e3f8e sc-av_one_full av-equal-height-column-flextable'>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-gf7sa9-086a6e4104aa0f5ba9c5c238ce8e3f8e\">\n#top .flex_column_table.av-equal-height-column-flextable.av-gf7sa9-086a6e4104aa0f5ba9c5c238ce8e3f8e{\nmargin-top:0px;\nmargin-bottom:0px;\n}\n.flex_column.av-gf7sa9-086a6e4104aa0f5ba9c5c238ce8e3f8e{\nwidth:100%;\nmargin-left:0;\nborder-width:2px;\nborder-color:#3a4586;\nborder-style:solid;\npadding:30px 30px 30px 30px;\n}\n#top .flex_column_table.av-equal-height-column-flextable.av-gf7sa9-086a6e4104aa0f5ba9c5c238ce8e3f8e .av-flex-placeholder{\nwidth:0%;\n}\n<\/style>\n<div  class='flex_column av-gf7sa9-086a6e4104aa0f5ba9c5c238ce8e3f8e av_one_full  avia-builder-el-30  el_after_av_one_full  el_before_av_one_full  first flex_column_table_cell av-equal-height-column av-align-top  column-top-margin'     ><style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-dqfrwh-e6760127aa9fa27a53638152e15b31b7\">\n#top .togglecontainer.av-dqfrwh-e6760127aa9fa27a53638152e15b31b7 p.toggler{\ncolor:#555555;\nbackground-color:#f8f8f8;\nborder-color:#ffffff;\n}\n#top .togglecontainer.av-dqfrwh-e6760127aa9fa27a53638152e15b31b7 p.toggler:not(.activeTitle):hover{\nbackground-color:#ffeca0;\n}\n#top .togglecontainer.av-dqfrwh-e6760127aa9fa27a53638152e15b31b7 p.toggler .toggle_icon{\ncolor:#005daf;\nborder-color:#005daf;\n}\n#top .togglecontainer.av-dqfrwh-e6760127aa9fa27a53638152e15b31b7 p.toggler .toggle_icon > span{\ncolor:#005daf;\nborder-color:#005daf;\n}\n#top .togglecontainer.av-dqfrwh-e6760127aa9fa27a53638152e15b31b7 .toggle_wrap .toggle_content{\ncolor:#555555;\nbackground-color:#f8f8f8;\nborder-color:#ffffff;\n}\n<\/style>\n<div  class='togglecontainer av-dqfrwh-e6760127aa9fa27a53638152e15b31b7 av-minimal-toggle  avia-builder-el-31  avia-builder-el-no-sibling ' >\n<section class='av_toggle_section av-d4j8k1-bcc6c9429da61d1c5ee4782f4760704e'  itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/CreativeWork\" ><div role=\"tablist\" class=\"single_toggle\" data-tags=\"{All} \"  ><p id='toggle-toggle-id-1' data-fake-id='#toggle-id-1' class='toggler  av-title-above av-inherit-border-color'  itemprop=\"headline\"  role='tab' tabindex='0' aria-controls='toggle-id-1' data-slide-speed=\"200\" data-title=\"Publications\" data-title-open=\"\" data-aria_collapsed=\"Click to expand: Publications\" data-aria_expanded=\"Click to collapse: Publications\">Publications<span class=\"toggle_icon\"><span class=\"vert_icon\"><\/span><span class=\"hor_icon\"><\/span><\/span><\/p><div id='toggle-id-1' aria-labelledby='toggle-toggle-id-1' role='region' class='toggle_wrap  av-title-above'  ><div class='toggle_content invers-color av-inherit-border-color'  itemprop=\"text\" ><p>1.\u00a0\u00a0\u00a0 C. C. Chang, N. K. Sung-Yu,<strong> C. S. Hsu<\/strong> and C. T. Chang, &#8220;A Novel Method for the Prepatation of Uranium Complexes via Electrolytic Amalgamation&#8221;, Inorg. Chem., 18, 855 (1979).<\/p>\n<p>2.\u00a0\u00a0\u00a0 <strong>C. S. Hsu<\/strong>, J. M. Rodriguez-Parada and V. Percec, &#8220;Liquid Crystalline Polymers Containing Heterocycloalkane Mesogens 1. Side-Chain Liquid Crystalline Polymethacrylates and Polyacrylates Containing 2,5-Disubstituted-1,3-dioxane Mesogens&#8221;, Makromol. Chem., 188, 1017 (1987).<\/p>\n<p>3.\u00a0\u00a0\u00a0 <strong>C. S. Hsu<\/strong>, J. M. Rodriguez-Parada and V. Percec, &#8220;Liquid Crystalline Polymers Containing Heterocycloalkane Mesogens 2. Side-Chain Liquid Crystalline Polysiloxanes Containing 2,5-Disubstituted-1,3- dioxane Meso gens&#8221;, J. Polym. Sci., Polym. Chem., 25, 2425 (1987).<\/p>\n<p>4.\u00a0\u00a0\u00a0<strong> C. S. Hsu<\/strong> and V. Percec, &#8220;Synthesis and Characterization of Liquid Crystalline Polysiloxanes Containing Benzyl Ether Mesogens&#8221;, J. Polym. Sci., Polym. Chem., 25, 2820 (1987).<\/p>\n<p>5.\u00a0\u00a0\u00a0 <strong>C. S. Hsu<\/strong> and V. Percec, &#8220;Liquid Crystalline Polymers Containing Heterocycloalkane Mesogens 3. Biphasic Side-Chain Liquid Crystal-line Polysiloxanes Containing trans-5-(n-Undecanyl)-2- (4-cyanophenyl)-1,3-dioxane Side Groups&#8221;, Makromol. Chem. Rapid Commun., 8, 331 (1987).<\/p>\n<p>6.\u00a0\u00a0\u00a0 <strong>C. S. Hsu<\/strong> and V. Percec, &#8220;Liquid Crystalline Polymers Containing Heterocycloalkane Mesogens 4. Biphasic Side-Chain Liquid Crystalline Polysiloxanes Containing trans-5-(n-Undecanyl)-2-(4- methoxyphenyl)-1,3-dioxane and trans-2-(n-Decanyl)-5-(4-methoxyphenyl)-1,3-dioxane Mesogens&#8221;, Polym. Bull., 17, 49 (1987).<\/p>\n<p>7.\u00a0\u00a0\u00a0<strong> C. S. Hsu<\/strong> and V. Percec, &#8220;Synthesis and Characterization of Biphasic Liquid Crystalline Polysiloxanes Containing 4-Undecanyloxy-4&#8242;-cyanobiphenyl Side Groups&#8221;, Polym. Bull., 18, 91 (1987).<\/p>\n<p>8.\u00a0\u00a0\u00a0<strong> C. S. Hsu<\/strong> and V. Percec, &#8220;Liquid Crystalline Polymers Containing Heterocylolkanedyl Groups as Mesogens 6. Liquid Crystalline Poly[trans-11-(4-(5-(4-methoxyphenyl)-1,3-dioxan-2-yl) -2,6- dimethyl-phenoxy) undecyl methacrylate] and Poly[trans-11-(4-(5-(4-methoxy-phenyl)-1,3-dioxan- 2-yl)-2,6-dimethylphenoxy)undecyl acrylate]&#8221;, Makromol. Chem., 189, 1141 (1988).<\/p>\n<p>9.\u00a0\u00a0\u00a0 V. Percec, <strong>C. S. Hsu<\/strong> and D. Tomazos, &#8221;Synthesis and Characterization of Liquid Crystalline Copolymethacrylates, Copolyacrylates and Copolysiloxanes Containing 4-Methoxy-4&#8242;-hydroxy- \u03b1 -methylstilbene and 4-Hydroxy-4&#8242;-methoxy-\u03b1-methylstilbene Constitutional Isomers as Side Groups&#8221;, J. Polym. Sci., Polym. Chem., 26, 2047 (1988).<\/p>\n<p>10. <strong>C. S. Hsu<\/strong> and V. Percec, &#8220;Synthesis and Characterization of Liquid Crystalline Polyacrylates and Polymethacrylates Containing Benzyl Ether and Diphenyl Ethane Based Mesogens&#8221;, J. Polym. Sci. Polym.Chem., 27, 453 (1989).<\/p>\n<p>11. <strong>C. S. Hsu<\/strong>, &#8220;Main-Chain Liquid Crystalline Polymers&#8221;, Chemistry (The Chinese Chem. Soc., Taiwan), 47, 223 (1989).<\/p>\n<p>12. <strong>C. S. Hsu<\/strong> and C. J. Hsieh, &#8220;Side-Chain Liquid Crystalline Polymers&#8221;, Chemistry (The Chinese Chem. Soc. Taiwan), 47, 228 (1989).<\/p>\n<p>13. C. J. Hsieh, <strong>C. S. Hsu<\/strong>, G. H. Hsiue and V. Percec, &#8220;Synthesis and Characterization of Side-Chain Liquid Crystalline Polysiloxannes Containing Oligooxyethylene Spacers and Benzyl Ethyl Based Mesogenic Side Groups&#8221;, J. Polym. Sci. Polym. Chem., 28, 425 (1990).<\/p>\n<p>14. J. S. Wen, G. H. Hsiue and <strong>C. S. Hsu<\/strong>, &#8220;Liquid Crystalline Polymers Containing Macrocyclic Polyethers 1. Side-Chain Liquid Crystalline Polysiloxanes Containing Benzo-15-crown-5 Based Mesogenic Side-Groups&#8221;, Makromol. Chem. Rapid Commun., 11, 151 (1990).<\/p>\n<p>15. V. Percec and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis and Mesomorphic Behavior of Poly(methylsiloxane)s and Poly(methylsiloxane-co-dimethylsiloxane)s Containing Oligeooxyethylene Spacers and Mesogenic Side Groups&#8221;, Polym. Bull., 23, 463 (1990).<\/p>\n<p>16. C. J. Hsieh, G. H. Hsiue and <strong>C. S. Hsu<\/strong>, &#8220;Ionic Conductivity and Morphology of Polymer Electrolytes Based on a Side-Chain Liquid Crystalline Polysiloxane Containing Oligooxyethylene Spacers and 6-Cyano-2-naphthyl Benzyl Ether Mesogens&#8221;, Makromol. Chem., 191, 2195 (1990).<\/p>\n<p>17. <strong>C. S. Hsu<\/strong> and Y. H. Lu, &#8220;Synthesis and Characterization of Side-Chain Liquid Crystalline Polysiloxanes Containing 4-Alkanyloxyphenyl trans-4- Alkylcyclohexanoate Side Groups&#8221;, J. Polym. Sci. Polym. Chem., 29, 977 (1991).<\/p>\n<p>18. <strong>C. S. Hsu<\/strong> and Y. H. Lu, &#8220;Synthesis and Mesomorphic Behavior of Poly ( methylsiloxane )s Containing trans-Cyclohexane Based Mesogenic Side Groups&#8221;, Polym. Bull., 25, 169 (1991).<\/p>\n<p>19. J. S. Wen, G. H. Hisue and <strong>C. S. Hsu<\/strong>, &#8220;Liquid Crystalline Polymers Containing Macrocyclic Polyethers, 2. Side-Chain Liquid Crystalline Copolysiloxanes Containing Mesogenic Units Based on 1,3-Dioxane-2,5-diyl Group and Benzo-15-crown-5&#8221;, Makromol. Chem., 192, 2243 (1991).<\/p>\n<p>20. D. S. Chen, G. H. Hsiue and <strong>C. S. Hsu<\/strong>, &#8220;Gas Permeation Through a Side-Chain Liquid Crystalline Polysiloxane Based Membrane&#8221;, Makromol. Chem., 192, 2021 (1991).<\/p>\n<p>21. D. S. Chen, G. H. Hsiue and <strong>C. S. Hsu<\/strong>, &#8220;Gas Permeation Through Two Side-Chain Liquid Crystalline Polymethacrylate-based Membranes Containing 4-Methoxyphenyl 4-hexanyloxy benzoate or 4-Cyanophenyl 4-hexanyloxybenzoate Mesogenic Side Groups&#8221;, Makromol. Chem., 193, 1469 (1992).<\/p>\n<p>22. T. M. Juang, C. F. Chang and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis of Side-Chain Liquid Crystalline Polymethacrylates, Polymethacrylates and Polysiloxanes Containing 4-Cyanobiphenyl 4-Alkanyloxbenzyl Ether Side Groups&#8221;, Polym. Bull. 28, 403 (1992).<\/p>\n<p>23. <strong>C. S. Hsu<\/strong>, J. H. Lin, L. R. Chou and G. H. Hsiue, &#8220;Synthesis and Characteriztion of Ferroelectric Liquid Crystalline Polysiloxanes and Polymethacrylates Containing ((S)-2-Methyl-1-butoxy)phenyl 4-Alkanyloxybiphenyl-4&#8242;-carboxylate Side Groups&#8221;, Macromolecules, 25, 7126 (1992).<\/p>\n<p>24. S. T. Wu, J. D. Margerum, H. B. Meng, L. R. Dalton, <strong>C. S. Hsu<\/strong> and S. H. Lung, &#8220;Room-Temperature Diphenyl-diacetylene Liquid Crystals&#8221;, Appl. Phys. Lett., 61, 630 (1992).<\/p>\n<p>25. S. T. Wu, <strong>C. S. Hsu<\/strong>, Y. N. Chen and S. R. Wang, &#8220;Fluorinated Diphenyl-diacetylene and Tolane Liquid Crystals with Low Threshold Voltage&#8221;, Appl. Phys. Lett., 61, 2275 (1992).<\/p>\n<p>26. <strong>C. S. Hsu<\/strong> and Y. H. Lu, &#8220;Synthesis and Characterization of Liquid Crystalline Monomers and Side-Chain Polymers Containing Diphenyl diacetylene Mesogens&#8221;, Mol. Cryst. Liq. Cryst., 225, 1 (1993).<\/p>\n<p>27. J. L. Lin and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis of High Temperature Mesomorphic Polysiloxanes and Their Use as Stationary Phase for High Resolution Gas Chromatography&#8221;, Polymer, 25, 153 (1993).<\/p>\n<p>28. <strong>C. S. Hsu<\/strong> and L. B. Chen, &#8220;Synthesis and Characterization of Block Copolymers of Polyether sulfone with Liquid Crystalline Polyesters&#8221;, Materials Chemistry and Physics, 34, 28 (1993).<\/p>\n<p>29. <strong>C. S. Hsu<\/strong>, L. J. Shih and G. H. Hsiue, &#8220;Synthesis of Ferroelectric Liquid Crystalline Polysiloxanes and Polymethacrylates with Broad Temperature Ranges of Chiral Smectic C Phase&#8221;, Macromolecules, 26, 3161 (1993).<\/p>\n<p>30. G. H. Hsiue, J. S. Wen and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis and Characterization of Liquid Crystalline Copolysiloxanes Containing Azobenzene Dyes and 1,3-Dioxane Based Mesogenic Side Groups&#8221;, Polym. Bull., 30, 141 (1993).<\/p>\n<p>31. <strong>C. S. Hsu<\/strong>, T. M. Juang and Y. J. Leu, &#8220;Synthesis and Characterization of Chiral Smectic Side-Chain Liquid Crystalline Polysiloxanes Containing 2,5-Disubstituted-1,3-dioxane Based Mesogenic Side Groups&#8221;, Mol. Cryst. Liq. Cryst., 237, 223 (1993).<\/p>\n<p>32. S. T. Wu, <strong>C. S. Hsu<\/strong>, Y. N. Chen, S. R. Wang and S. H. Lung, &#8220;Fluoro Diphenyldiacetylene and Tolane Liquid Crystals for Display Application&#8221;, Optical Engineering, 32, 1792 (1993).<\/p>\n<p>33. T. M. Juang, Y. N. Chen, S. H. Lung, Y. H. Lu, <strong>C. S. Hsu<\/strong> and S. T. Wu, &#8220;Synthesis and Characterization of Novel Fluorinated Diphenyldiacetylene Liquid Crystals&#8221;, Liq. Cryst., 15, 529 (1993).<\/p>\n<p>34. S. T. Wu and <strong>C. S. Hsu<\/strong>, &#8220;Physical Properties of Fluorinated Diphenyldiautylene and Tolane Liquid Crystals&#8221;, Proc. SPIE, 1911, 39 (1993).<\/p>\n<p>35. G. H. Hsiue, <strong>C. S. Hsu<\/strong>, J. T. Shy, and C. J. Hu, &#8220;Research on the Liquid Crystalline Polymeric Materials for the Electro-Optical Applications&#8221;, National Science Council Monthly, 21, 860 (1993).<\/p>\n<p>36. <strong>C. S. Hsu<\/strong>, T. M. Juang, J. H. Lin and M. C. Lin, &#8220;The Influence of Lateral Substituents on the Phase Behavior of Side-Chain Liquid Crystalline Polysiloxanes Containing trans-2,5- Disubstitated- 1,3-Dioxanebased Mesogenic Side Groups&#8221;, J. of Polym. Resear., 1, 7 (1994).<\/p>\n<p>37. S. T. Wu, J. D. Margerum, H. B. Meng, <strong>C. S. Hsu<\/strong> and L. R. Dalton, &#8220;Optential Liquid Crystal Mixtures for CO2 Laser Application&#8221;, Appl. Phys. Lett., 64, 1204 (1994).<\/p>\n<p>38. C. J. Hsieh, S. H. Wu, G. H. Hsiue and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis and Thermal Behavior of Side-Chain Liquid Crystalline Polymethacrylates Containing Tolane-Based Mesogenic Side Groups&#8221;, J. Polym. Sci., Polym. Chem., 32, 1077 (1994).<\/p>\n<p>39. Y. H. Lu, K. T. Tsay, <strong>C. S. Hsu<\/strong> and H. L. Chang, &#8220;Synthesis and Characterization of Side-Chain Liquid Crystalline Polymethcrylates Containing Fluorinated Diphenyldiacetylene Side Groups&#8221;, Mol. Cryst. and Liq. Cryst., 250, 85 (1994).<\/p>\n<p>40. Y. H. Lu, H. L. Chang and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis of Side-Chain Liquid Crystalline Polyoxetanes Containing 4-Dodecanyloxyphenyl\u00a0 trans-4-Alkylcyclohexanoate Side Groups&#8221;, Polymer Bulletin, 33, 151 (1994).<\/p>\n<p>41. G. H. Hsiue, P. J. Hsieh and <strong>C. S .Hsu<\/strong>, &#8220;Synthesis and X-ray diffraction of Ferroelectric Liquid Crystalline Polysiloxanes&#8221;, Polymer Bulletin, 33, 159 (1994).<\/p>\n<p>42. M. L. Liu, Y. H. Lu and <strong>C. S. Hsu<\/strong>, &#8221; Synthesis of Ferroelectric Liquid Crystalline Polysiloxanes Containing (s) &#8211; 2 \u2013 Methylbutyl Alkyloxybiphenyl &#8211; 4&#8242; &#8211; carboxylate and (23, 3 s) &#8211; 2 &#8211; Chloro &#8211; 3 -Methylpentyl 4 &#8211; Alkyloxybiphynyl &#8211; 4&#8242; &#8211; carboxylate &#8220;, J. of Polym. Resear. 1, 321 (1994).<\/p>\n<p>43. G. H. Hsiue, J. H. Chen, <strong>C. S. Hsu<\/strong>, &#8220;Broad Temperature Range of Chiral Smectic C Phase in Some Ferroelectric Side-Chain Liquid Crystalline Polysiloxanes Containing Oligooxyethylene Spacers&#8221;, Mat. Res. Soc., 328, 697 (1994).<\/p>\n<p>44. Y. H. Lu and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis of Side-Chain Liquid Crystalline Polyoxetanes Containing 4-Alkanyloxyphenyl trans-4-Alkylcyclohexanoate Side Groups&#8221;, Macromolecules, 28, 1673 (1995).<\/p>\n<p>45. <strong>C. S. Hsu<\/strong>, L. J. Shih and G. H. Hsiue, &#8220;Synthesis and Electro-optical Properties of Some Ferroelectric Liquid Crystalline Polymers&#8221;, Macromolecular Symposium, 98, 883 (1995).<\/p>\n<p>46. <strong>C. S. Hsu<\/strong>, S. M. Chen and K. T. Tsai, &#8220;High Birefringent Liquid Crystals&#8221;, Mol. Cryst. and Liq. Cryst., 261, 79 (1995).<\/p>\n<p>47. Y. H. Wu, Y. H. Lu and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis of Side-Chain Liquid Crystalline Polymethacrylates Containing Fluorinated Diarylacetylene-Based Mesogenic Side Groups&#8221;, J. of Macromol. Sci. Pure Appl. Chem., A32, 1471 (1995).<\/p>\n<p>48. <strong>C. S. Hsu<\/strong>, K. T. Tsay, A. C. Chang, S. R. Wang and S. T. Wu, &#8220;Synthesis of Fouorinated Naphthylphenylacetylenic and naphthylphenyldiacetylenic Liquid Crystals&#8221;, Liq. Cryst., 19, 409 (1995).<\/p>\n<p>49. <strong>C. S. Hsu<\/strong> and G. H. Hsiue, &#8220;Molecular Design of Ferroelectric Liquid Crystalline Polymers&#8221;, Pure &amp; Appl. Chem. 67, 2005 (1995).<\/p>\n<p>50. Y. M. Chang, <strong>C. S. Hsu<\/strong> and M. C. Liu, &#8220;Synthesis ofCharacterization of Segmented Copolymers of Aromatic Polyether Sulfone and Thermotropic Liquid Crystalline Poly (oxy-1,4- phenylenecarbonyl-co-oxy-2,6-naphthaloyl)&#8221;, Materials Chemistry and Physics, 43, 250 (1996).<\/p>\n<p>51. Y. H. Lu, <strong>C. S. Hsu<\/strong>, C. H. Chou and T. H. Chou, &#8220;Preparation of Poly(2,5-thienyleneethylene and poly(2,5-furyleneethylene) by Vapor Phase Pyrolysis of (5-Methyl-2-thienyl)methyl Benzoate and (5-Methyl-2-furyl)methyl Benzoate&#8221;, Macromolecules, 29, 5546 (1996).<\/p>\n<p>52. <strong>C. S. Hsu<\/strong> and L. J. Shih, &#8220;Synthensis of Side-chain Liquid Crystallien Polysiloxanes Containing 4-(S)-2-Methyl-1-buty1 (6-(4-alkanyloxy -phenyl)-4\u2018-carbonyloxy)naphenylene-2-carboxylate and 4(S)-2-Methyl-1-butyl 6-[4-alkanyloxybiphenylphenyl)-4\u2018-carbonyloxy]naphthylene-2-carboxylate Side Groups&#8221;, J. Polym. Resear. , 3 , 185 (1996).<\/p>\n<p>53. <strong>C. S. Hsu<\/strong> and B. S. Her, &#8220;Synthesis of Ferroeectric Liquid Crystalline Polymethanylates Containing Diphenyl Ethane Based Mesogens&#8221;, Macromol. Chem. and Phys. 197 , 4105 (1996).<\/p>\n<p>54. <strong>C. S. Hsu<\/strong> and C. J. Lee, &#8220;Synthesis of Ferrelectric Liquid Crystalline Polymers by Ring Opening Polymerization&#8221;, Mat. Res. Soc., 425, 101 (1996).<\/p>\n<p>55. S. T. Wu and <strong>C. S. Hsu<\/strong>, &#8220;Correlation of Molecular Structures and Properties on Diphenyldiacetylene Liquid Crystal&#8221;, Mat. Res. Soc., 425, 33 (1996).<\/p>\n<p>56. <strong>C. S. Hsu<\/strong> and C. H. Tsai, &#8220;Effect of Lateral Substituent on the Mesomorphic Properties of Ferroelectric Side-chain Liquid\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Crystalline Polysiloxanes&#8221;, Liquid Cryst., 22, 669 (1997).<\/p>\n<p>57. <strong>C. S. Hsu<\/strong> and Y. J. Leu, &#8220;Synthesis of Liquid Crystalline Polysiloxanes Containing Naphthalene-Based Mesogens and Chiral Side Chains&#8221;, Mol. Cryst. Liq. Cryst., 300, 83 (1997).<\/p>\n<p>58. <strong>C. S. Hsu<\/strong>, &#8220;The Application of Side-chain Liquid Crystalline Polymers&#8221;, Progress in Polymer Science, 22, 829 (1997).<\/p>\n<p>59. S. T. Wu, <strong>C. S. Hsu<\/strong> and J. M. Chen, &#8220;Room Temperature Difluoro-tolane and Diphenyl- diacetylene Liquid Crystals with Negative\u00a0\u00a0\u00a0\u00a0 Dielectric Anisotropy&#8221;, Mol. Cryst. Liq. Cryst., 304, 441 (1997).<\/p>\n<p>60. S. T. Wu, and <strong>C. S. Hsu<\/strong>, &#8220;Laterally Fluorinated Liquid Crystals for Display Application&#8221;, Proc. of. SPIE, 3015, 8 (1997).<\/p>\n<p>61. H. L. Chang, Y. M. Chang and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis and Characterization of Segmented Copolyesters of Aromatic\u00a0 Polyether Sulfone with Liquid Crystalline Polyesters Containing Flexible Spacers&#8221;, J. Polym. Resear., 4, 101 (1997).<\/p>\n<p>62. <strong>C. S. Hsu<\/strong>, P. H. Chu, H. L. Chang and T. H. Hsieh, &#8220;Effect of Lateral Substituents on the Mesomorphic Properties of Side-Chain Liquid Crystalline Polysiloxanes Containing 4-[(S)- 2-Methyl-1-butoxy]phenyl 4-(Alkenyloxy) benzoate Side Groups&#8221;, J. Polym. Sci. A, Polym. Chem., 35, 2793 (1997).<\/p>\n<p>63. H. L. Chang and <strong>C. S. Hsu<\/strong>, &#8220;Thermally Stimulated Current and DSC Studies of the Dual Glass Transitions in Side-Chain Liquid rystalline Copolysiloxanes Containing 4-[(S)-2- Methybutoxy]phenyl 3-Chloro-4-Alkenyloxybenzoate Side Groups&#8221;, Macromol. Chem. Phys., 198, 2985 (1997).<\/p>\n<p>64. <strong>C. S. Hsu<\/strong> and H. L. Chen, &#8220;Preparation of Anisotropic Films for Liquid Crystal Display Application&#8221;, Proc. of SPIE, 3421, 46 (1998).<\/p>\n<p>65. K. T. Tsay, <strong>C. S. Hsu<\/strong> and S. T. Wu, &#8220;Synthesis of Asymmetruc Tolane Liquid Crystals for Display Application&#8221;, Proc. of SPIE, 3421, 142 (1998).<\/p>\n<p>66. <strong>C. S. Hsu<\/strong> and T. L. Lin, &#8220;Synthesis of Conjugated Polymers by Vapor Deposition Poly Polymerization&#8221;, Mat. Res. Soc., 488, 347-357 (1998).<\/p>\n<p>67. <strong>C. S. Hsu<\/strong> and W. L. Liau, &#8220;Synthesis of Ferroelectric Liquid Crystalline Polyoxiranes and Polyoxitanes By Ring Opening Polymerization&#8221;, Mol. Cryst. Liq. Cryst., 318, 1 (1998).<\/p>\n<p>68. S. T. Wu, <strong>C. S. Hsu<\/strong> and K. F. Shyu, &#8220;High Birefrigence and Wide Nematic Range bis &#8211; tolane Liquid Crystals&#8221;, Appl. Phys. Lett., 74, 344 (1999).<\/p>\n<p>69. S. T. Wu, <strong>C. S. Hsu<\/strong> and Y. Y. Chuang, &#8220;Room Temperature Bis-tolane Liquid Crystals&#8221;, Jpn. J. Appl. Phys., 38, L286 (1999).<\/p>\n<p>70. S. T. Wu, <strong>C. S. Hsu<\/strong>, K. F. Shyu, Y. Y. Chuang, H. B. Cheng, Z. Chai, G. M. Day, L. Guo and L. R. Dalton, &#8220;High Birefringence Bistolane Liquid Crystals for Display Application&#8221;, SID Tech. Digest, 30, 706 (1999).<\/p>\n<p>71. S. T. Wu, R. N. Schwartz, Q. T. Zhang, S. Marder and <strong>C. S Hsu<\/strong>, &#8220;Colorless High Dielectric Compounds for Low Voltage Liquid Crystal Application&#8221;, Mat. Res. Soc.(1999).<\/p>\n<p>72. <strong>C. S. Hsu<\/strong>, G. Fan and Y. H. Lu, &#8220;Synthesis and characterization of Side-Chain Liquid Crystalline Polyoxetanes Containing 4-(Alkanyloxy) phenyl- 4-Pentyl- benzoate Side Groups&#8221;, J. Polym. Research, 6, 155 (1999).<\/p>\n<p>73.<strong> C. S. Hsu<\/strong> and H. L. Chen, &#8220;Preparation of Liquid Crystalline Thermosets\uff1aIn Situ Photopolymerization of Oriented Liquid Crystal Diacrylates&#8221;, J. Polym Sci. A. Polym. Chem., 37, 3929 (1999).<\/p>\n<p>74. <strong>C. S. Hsu<\/strong>, K. F. Shyu, Y. Y. Chuang and S. T. Wu, &#8220;Synthesis of Laterally Substituted Bistolane Liquid Crystals&#8221;, Liq. Cryst. 27, 283 (2000).<\/p>\n<p>75. Y. J. Liao,<strong> C. S. Hsu<\/strong> and S. T. Wu, &#8220;Dipping and Photo-Induced Liquid Crystal Alignments Using Silane Surfactant&#8221;, Jpn. J. Appl. Phys., 39, L90 (2000).<\/p>\n<p>76. S. T. Wu, <strong>C. S. Hsu<\/strong>, Y. Y. Chuang and H. B. Cheng, &#8220;Physical Properties of Polar Bistolane Liquid Crystals&#8221;, Jpn. J. Appl. Phys., 39, L38 (2000).<\/p>\n<p>77. L. H. Wu, Y. C. Wang and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis and Characterization of Thiophene &#8211; Containing Liquid Crystals&#8221;, Liquid Crystals, 27, 1503 (2000).<\/p>\n<p>78. L. H. Wu, C. S. Chu, N. Janarthanan and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis and Characterization of Ferroelectric Side Chain Liquid Crystal Polymer bearing Banana-Shaped Chiral Mesogens&#8221;, J. Polym. Resear., 7, 125 (2000).<\/p>\n<p>79. L. H. Wu, S. J. Luo, <strong>C. S. Hsu<\/strong> and S. T. Wu, &#8220;Obliquely Tilted Discotic Phase Compensation Films&#8221;, Jpn. J. Appl. Phys., 39, L869 (2000).<\/p>\n<p>80. L. H. Wu, W. C. Lee, <strong>C. S. Hsu<\/strong> and S. T. Wu, &#8220;Photo-Induced Liquid Crystal Alignment with Discotic Films&#8221;, Jpn. J. Appl. Phys., 39, 5899 (2000).<\/p>\n<p>81. A. K. Li, S. S. Yang , W. Y. Jean, <strong>C. S. Hsu<\/strong> and B. R. Hsieh, &#8220;Poly(2,3-diphenylene Vinylene) Derivatives having Liquid Crystalline Side Groups&#8221;, Chem. Mater., 12, 2741 (2000).<\/p>\n<p>82. A. K. Li, N. Janarthanan and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis of Substituted Poly (arylene vinylene) films by Vapor Deposition Polymerization&#8221;, Polymer Bulletin, 45, 129 (2000).<\/p>\n<p>83. C. H. Lin and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis of High Temperature cholesteric copolysiloxanes and their use as stationary phases for resolution gas chromatography&#8221;, Polymer Bulletin, 45, 53 (2000).<\/p>\n<p>84. C. H. Lin and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis and Characterization of Cholesteric Liquid Crystalline Copolysiloxanes Containing 4-biphenyl 4-allyloxybenzoate and [S]-1-(2-naphthyl)ethyl 6-[4-(10-undecen-1-yloxy) biphenyl-4\u2019-carbonloxy]-2-naphthoate Side Groups&#8221;, J. Polym. Resear., 7, 167 (2000).<\/p>\n<p>85. W. C. Lee, <strong>C. S. Hsu<\/strong> and S. T. Wu, &#8220;Liquid Crystal Alignment with a photo-crosslinkable and Solvent-soluble polyimide Film&#8221;, Jpn. J. Appl. Phys., 39, L471 (2000).<\/p>\n<p>86. L. H. Wu, N. Janarthanan and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis and Characterization of Naphthalene-Substituted Triphenylene Discotic Liquid Crystals&#8221;, Liquid Crystals, 28, 17 (2001).<\/p>\n<p>87. W. C. Lee, <strong>C. S. Hsu<\/strong> and S. T. Wu, &#8220;Sensitivity of the Photo-Crosslinkable Polyimide for Liquid Crystal Alignment&#8221;, Jpn. J. Appl. Phys., 40, 5942 (2001).<\/p>\n<p>88. C. H. Ting and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis and Photoluminescence Property of Polyacetylenes Containing Liquid Crystalline Side Groups&#8221;, J. Polym. Resear., 8, 159 (2001).<\/p>\n<p>89. C. H. Ting and <strong>C. S. Hsu<\/strong>, &#8220;Photoluminescence and Electroluminescence Characteristics of New Disubstituted Polyacetylenes&#8221;, Jpn. J. Appl. Phys., 40, 5342 (2001).<\/p>\n<p>90. W. C. Lee, J. T. Chen, <strong>C. S. Hsu<\/strong> and S. T. Wu, &#8220;Synthesis of alkyl-branched main chain copolyimides and their effect on the pretilt angles of liquid crystal alignment&#8221;, Liq. Cryst., 29, 907 (2002).<\/p>\n<p>91. C. H. Ting, J. T. Chen and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis and Thermal and Photoluminescence Properties of Liquid Crystalline Polyacetylenes Containing 4-Alkanyloxyphenyl trans-4-Alkylcyclohexanoate Side Groups&#8221;, Macromolecules, 35, 1180 (2002).<\/p>\n<p>92. S. W. Chang and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis and Electroluminescence of Side-chain Liquid Crystalline Polyacrylates and Polyoxiranes Containing Bistolane Side Groups&#8221;, J. Polym. Research, 9, 1 (2002).<\/p>\n<p>93. S. W. Chang, A. K. Li, C. W. Liao and <strong>C. S. Hsu<\/strong>, &#8220;Polarized Blue Emission Based on a Side Chain Liquid Crystalline Polyacrylate Containing Bis-tolane Side Groups&#8221;, Jpn. J. Appl. Phys., 41, 1374 (2002).<\/p>\n<p>94. A. Cady, Z. Q. Liu, X. F. Han, S. T. Wang, M. Veum, N. Janarthanan, <strong>C. S. Hsu<\/strong>, D. A. Olson and C. C. Huang, &#8220;Effect of Enantiomeric Excess on Surface Structures and Phase Sequences in Free-standing Liquid Crystal Films&#8221;, Phys. Rev. E., 66, 061704 (2002).<\/p>\n<p>95. W. Yan, <strong>C. S. Hsu<\/strong> and Y. Wei, &#8220;Synthesis and characterization of small band-gap conjugated polymers-Poly(pyrrolyl methines)&#8221;, Chinese Chemical Letters, 13, 988, (2002).<\/p>\n<p>96. W. Yan, Z. X. Wei, <strong>C. S. Hsu<\/strong> and M. X. Wan, &#8220;Synthesis of Microspheres of Poly(pyrrolyl methine) by Interfacial Polymerization&#8221;, Synth. Met. 135, 213 (2003).<\/p>\n<p>97. S. Gauza, F. Du, J. R. Wu, S. T. Wu, A. Spadlo, R. Dabrowski, N. Janarthanan and <strong>C. S. Hsu<\/strong>, &#8220;High Birefringence and Low Viscosity LC Mixtures&#8221;, SID 03 Digest, 2003.<\/p>\n<p>98. M. Veum, P. Messman, Z. Q. Liu, C. C. Huang, N. Janarthanan and <strong>C. S. Hsu<\/strong>, &#8220;Unique approach to measuring temperature variation of surface tension in smectic liquid crystals&#8221;, Review of Scientific Instruments, 74, 5151 (2003).<\/p>\n<p>99. K. L. Tzeng, H. F. Meng, M. F. Tzeng, Y. S. Chen, C. H. Liu, S. F. Horng, Y. Z. Yang, S. M. Chang, <strong>C. S. Hsu<\/strong> and C. C. Chi, &#8220;One-polymer active pixel&#8221;, Appl. Phys. Lett., 84, 619 (2004).<\/p>\n<p>100.\u00a0\u00a0\u00a0 C. C. Huang, H. F. Meng, G. K. Ho, C. H. Chen, <strong>C. S. Hsu<\/strong>, J. H. Huang, S. F. Horng, B. X. Chen and L. C. Chen, &#8220;Color-tunable multi-layer light-emitting diodes based on conjugated polymers&#8221;, Appl. Phys. Lett., 84, 1195 (2004).<\/p>\n<p>101.\u00a0\u00a0\u00a0 P. T. Lin, S. T. Wu, C. Y. Chang and <strong>C. S. Hsu<\/strong>, &#8220;UV STABILITY OF HIGH BIREFRINGENCE LIQUID CRYSTALS&#8221;, Mol. Cryst. Liq. Cryst., 411, 243 (2004).<\/p>\n<p>102.\u00a0\u00a0\u00a0 C. P. Chang, C. Y. Chao, J. H. Huang, A. K. Li, <strong>C. S. Hsu<\/strong>, M. S. Lin, B. R. Hsieh and A. C. Su, &#8220;Fluorescent Conjugated Polymer Films as TNT Chemosensors&#8221;, Syn. Metals, 144, 297 (2004).<\/p>\n<p>103.\u00a0\u00a0\u00a0 Z. L. Li, S. C. Yang, H. F. Meng, Y. S. Chen, Y. Z. Yang, C. H. Liu, S. F. Horng, <strong>C. S. Hsu<\/strong>, L. C. Chen, J. P. Hu, and R. H. Lee, &#8220;Patterning-Free Integration of Polymer Light-Emitting Diode and Polymer Transistor&#8221;,<a href=\"http:\/\/www.cc.nctu.edu.tw\/%7Epolymer\/Files\/Reserch\/PatternFreeProof.pdf\"> Appl. Phys. Lett., 84,<\/a> 3558 (2004).<\/p>\n<p>104.\u00a0\u00a0\u00a0 G. K. Ho,\u00a0H. F. Meng, <strong>C. S. Hsu<\/strong>, S. F. Horng, and L. C. Chen, &#8220;Efficient White Light Emission in Conjugated Polymer Homojunctions&#8221;, Appl. Phys. Lett., 85, 4576 (2004).<\/p>\n<p>105.\u00a0\u00a0\u00a0 Z. L. Li, H. F. Meng, S. F. Horng, <strong>C. S. Hsu<\/strong>, L. C. Chen and S. M. Chang, &#8220;Strong red emission in heterojunctions of conjugated polymer blends&#8221;, Appl. Phys. Lett., 84, 4944 (2004).<\/p>\n<p>106.\u00a0\u00a0\u00a0 S. Gauza, C. H. Wen, S. T. Wu, N. Janarthanan and <strong>C. S. Hsu<\/strong>, &#8220;Super High Birefringence Isothiocyanato Biphenyl-Bistolane Liquid Crystals&#8221;, Jpn. J. Appl. Phys., 43, 7634 (2004).<\/p>\n<p>107.\u00a0\u00a0\u00a0 F. I. Wu, R. Dodda, K. Jakka, J. H. Huang, <strong>C. S. Hsu<\/strong> and C. F. Shu, &#8220;Enhancing the thermal and spectral stabilities of polyfluorene-based blue light-emitting materials by incorporating pendent spiro-cycloakyl groups&#8221;, Polymer, 45, 4257(2004).<\/p>\n<p>108.\u00a0\u00a0\u00a0 S. H. Yang, J. T. Chen, A. K. Li, C. H. Huang, K. B. Chen, B. R. Hsieh and <strong>C. S. Hsu<\/strong>, &#8221; New Soluble Poly(2,3-diphenylphenylene vinylene) Derivatives for Light- Emitting Diodes&#8221;, Thin Solid Films, 477, 73 (2005).<\/p>\n<p>109.\u00a0\u00a0\u00a0 S. H. Yang, T. P. Nguyen, P. Le Rendu and <strong>C. S. Hsu<\/strong>, &#8220;Optical and electrical investigations of poly(p-phenylene vinylene)\/silicon oxide and poly(p-phenylene vinylene)\/titanium oxide nanocomposites&#8221;, Thin Solid Films, 471, 230 (2005).<\/p>\n<p>110.\u00a0\u00a0\u00a0 S. H. Yang, T. P. Nguyen, P. Le Rendu and <strong>C. S. Hsu<\/strong>, &#8220;Optical and electrical properties of PPV\/SiO<sub>2<\/sub> and PPV\/TiO<sub>2<\/sub> composite materials&#8221;, Composites Part A: Appl. Sci. Manufac., 36, 509 (2005).<\/p>\n<p>111.\u00a0\u00a0\u00a0 H. H. Liao, H. F. Meng, S. F. Horng, J. T. Shy, K. Chen, and <strong>C. S. Hsu<\/strong>, &#8220;Triplet exciton formation and decay in polyfluorene light emitting diode&#8221;, Physical Review B, 72, 113203 (2005).<\/p>\n<p>112.\u00a0\u00a0\u00a0 C. J. Bhongale, C. W. Chang, C. S. Lee, E. W. G. Diau and <strong>C. S. Hsu<\/strong>, &#8220;Relaxation Dynamics and Structural Characterization of Organic Nanoparticles with Enhanced Emission&#8221;, J. Phys. Chem. B, 109, 13472 (2005).<\/p>\n<p>113.\u00a0\u00a0\u00a0 K. B. Chen, H. C. Li, C. K. Chen, S. H Yang, B. R. Hsieh, and <strong>C. S. Hsu<\/strong>, &#8220;Novel Poly(2,3-diphenyl-1,4-phenylenevinylene) Derivatives Containing Long Branched Alkoxy and Fluorenyl Substituents: Synthesis, Characterization and Their Applications for Polymer Light-Emitting Diodes&#8221;, Macromolecules, 38, 8617 (2005).<\/p>\n<p>114.\u00a0\u00a0\u00a0 Y. H. Yao, L. R. Kung and <strong>C. S. Hsu<\/strong>, &#8220;Polarized White Emission from Fluorene-Based Polymer Blends&#8221;, Jpn. J. Appl. Phys., 44, p. 7648 (2005).<\/p>\n<p>115.\u00a0\u00a0\u00a0 C. J. Bhongale, C. W. Chang, E. W. G. Diau, <strong>C. S. Hsu<\/strong>, Y. Dong and B. Z. Tang, &#8220;Formation of nanostructures of hexaphenylsilole with enhanced color-tunable emissions&#8221;, Chem. Phys. Lett., 419, 444 (2006).<\/p>\n<p>116.\u00a0\u00a0\u00a0 C. H. Huang, S. H. Yang, K. B. Chen, and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis and Light Emitting Properties of Polyacetylenes Having Pendent Fluorene Groups&#8221;, J. Polym. Sci. A. Polym. Chem., 44, 519 (2006).<\/p>\n<p>117.\u00a0\u00a0\u00a0 C. H. Sung, L. R. Kung, <strong>C. S. Hsu<\/strong>, T. F. Lin and R. M Ho, &#8220;Induced Twisting in Self-assembly of Chiral Schiff-based Rod-Coil Amphiphiles&#8221;, Chem. Mater., 18, 352 (2006).<\/p>\n<p>118.\u00a0\u00a0\u00a0 C. J. Bhongale and <strong>C. S. Hsu<\/strong>, &#8220;Emission Enhancement by Formation of Aggregates in Hybrid Chromophoric Surfactant Amphiphile\/Silica Nanocomposites&#8221;, Angew. Chem.-Int. Edit., 45, 1404 (2006).<\/p>\n<p>119.\u00a0\u00a0\u00a0 Y. H. Yao, L. R. Kung, S. W. Chang and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis of UV-curable liquid crystalline diacrylates for the application of polarized electroluminescence&#8221;, Liq. Cryst., 33, 33 (2006).<\/p>\n<p>120.\u00a0\u00a0\u00a0 K. B. Chen, H. Y. Chen, S. H. Yang, and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis and Opto-electrical Properties of Stellar Polyfluorene Derivatives Containing Polyhedral Oligomeric Silsesquioxanes as the Center Core&#8221;, J. Polym. Res., 13, 237 (2006).<\/p>\n<p>121.\u00a0\u00a0\u00a0 S. R. Tseng, S. C. Lin, H. F. Meng, H. H. Liao, C. H. Yeh, H. C. Lai, S. F. Horng and <strong>C. S. Hsu<\/strong>, &#8220;General method to solution-process multilayer polymes light-emitting diodes&#8221; Appl. Phys. Lett., 88, 163501 (2006).<\/p>\n<p>122.\u00a0\u00a0\u00a0 C. J. Bhongale, C. H. Yang and <strong>C. S. Hsu<\/strong>, \u201cBergman cyclopolymerization within the channels of functional hybrid nanocomposites formed by co-assembly of silica and polymerizable surfactant monomer\u201d, Chem. Commun., 2274 (2006).<\/p>\n<p>123.\u00a0\u00a0\u00a0 Y. H. Yao, L. R. Kung and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis of Benzothiadiazo-Based Liquid Crystalline Polyacrylates for Polarized Light Emitting Diodes&#8221;, J. Polym. Res., 13, 277 (2006).<\/p>\n<p>124.\u00a0\u00a0\u00a0 K. B. Chen, Y. P. Chang, S. H. Yang and <strong>C. S. Hsu<\/strong>, &#8220;Novel dendritic light-emitting materials containing polyhedral oligomeric silsesquioxanes core&#8221;, Thin Solid Films, 514, 103 (2006).<\/p>\n<p>125.\u00a0\u00a0\u00a0 Y. Y. Lin, C. Cheng, H. H. Liao, S. F. Horng, H. F. Meng and <strong>C. S. Hsu<\/strong>, &#8220;Integration of polymer light-emitting diode and polymer waveguide on Si substrate&#8221;, Appl. Phys. Lett., 89, 063501 (2006).<\/p>\n<p>126.\u00a0\u00a0\u00a0 K. B. Chen, M. H. Chen, S. H. Yang, C. H. Hsieh, <strong>C. S. Hsu<\/strong>, C. C. Chen, and H. J. Chien, \u201cElectroluminescence from a Conjugated Polymer Grafted with CdSe\/ZnS: High Brightness and Improved Efficiency\u201d J. Polym. Sci. A. Polym. Chem., 44, 5378 (2006).<\/p>\n<p>127.\u00a0\u00a0\u00a0 W. L. Hsu, Y. C. Li, H. L. Chen, W. Liou, U. S. Jeng, H. K. Lin, W. L. Liu and <strong>C. S. Hsu<\/strong>, &#8220;Thermally-Induced Order-Order Transition of DNA-Cationic Surfactant Complexes&#8221; Langmuir, 22, 7521 (2006).<\/p>\n<p>128.\u00a0\u00a0\u00a0 S. H. Yang, H. C. Li, C. K. Chen, C. H. Hsieh and <strong>C. S. Hsu<\/strong>, &#8220;Highly Substituted\u00a0\u00a0\u00a0\u00a0\u00a0 Poly(2,3-diphenyl-1,4-phenylene vinylene) Derivatives Having Bulky Phenyl and Fluorenyl Pendant Groups: Synthesis, Charaterization, and Electro-optical Properties&#8221; J. Polym. Sci. A. Polym. Chem., 44, 6738 (2006).<\/p>\n<p>129.\u00a0\u00a0\u00a0 Y. H. Yao, S. H. Yang and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis of Laterally Attached Side-Chain Liquid Crystalline Poly(\u03c1-phenylene vinylene) and Polyfluorene Derivatives for the Application of Polarized Electroluminescence&#8221; Polymer, 47, 8297 (2006).<\/p>\n<p>130.\u00a0\u00a0\u00a0 Y. M. Liao, N. Janarthanan, <strong>C. S. Hsu<\/strong>, S. Gauza, and S. T. Wu, &#8220;Synthesis and Mesomorphic Properties of Fluoro and Isothiocyanato Biphenyl Tolane Liquid Crystals&#8221; Liq. Cryst., 33, 1199 (2006).<\/p>\n<p>131.\u00a0\u00a0\u00a0 T. F. Lin, R. M. Ho, C. H. Sung and <strong>C. S. Hsu<\/strong>, &#8220;Helical Morphologies of Thermotropic Liquid-Crystalline Chiral Schiff-Based Rod-Coil Amphiphiles&#8221;, Chem. Mater., 18, 5510 (2006).<\/p>\n<p>132.\u00a0\u00a0\u00a0 Y. C. Li, K. B. Chen, H. L. Chen, <strong>C. S. Hsu<\/strong>, C. S. Tsao and S. A. Chen, &#8220;Fractal Aggregates of Conjugated Polymer in Solution State&#8221; Langmuir, 22, 11009 (2006).<\/p>\n<p>133.\u00a0\u00a0\u00a0 H. F. Meng, C. C. Liu, C. J. Jiang, Y. L . Yeh, S. F. Horng and <strong>C. S. Hsu<\/strong>, &#8220;Effect of gate metal on polymer transistor with glass substrate&#8221; Appl. Phys. Lett., 89, 243503 (2006).<\/p>\n<p>134.\u00a0\u00a0\u00a0 H. H. Liao, H. F. Meng, S. F. Horng, W. S. Lee, J. M. Yang, C. C. Liu, J. T. Shy, F. C. Chen and <strong>C. S. Hsu<\/strong>, &#8220;Triplet exciton energy transfer in polyfluorene doped with heavy metal complexes studied using photoluminescence and photoinduced absorption&#8221; Phys. Review B, 74, 245211 (2006).<\/p>\n<p>135.\u00a0\u00a0\u00a0 C. H. Yang, C. J. Bhongale, C. H. Chou, S. H. Yang, C. N. Lo, T. M. Chen and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis and Light Emitting Properties of Sulfide-Containing Polyfluorenes and Their Nanocomposites with CdSe Nanocrystals : A Simple Process to Suppress Keto-defect&#8221; Polymer, 48, 116 (2007). (SCI)<\/p>\n<p>136.\u00a0\u00a0\u00a0 C. H. Yang, C. J. Bhongale, Y. M. Liao and <strong>C. S. Hsu<\/strong>, &#8220;Fabrication of the Hybrid Chromophoric Amphiphile\/Silica Nanocomposite-based Light Emitting Devices with Enhanced Performance&#8221; J. Mater. Chem., 17, 243 (2007).<\/p>\n<p>137.\u00a0\u00a0\u00a0 C. H. Huang, C. H. Huang, T. P. Nguyen and <strong>C. S. Hsu<\/strong>, &#8220;Self-assembly monolayer of anatase titanium oxide from solution process on indium tin oxide glass substrate for polymer photovoltaic cells&#8221; Thin Solid Films, 515, 6493 (2007).<\/p>\n<p>138.\u00a0\u00a0\u00a0 H. H. Liao, C. M. Yang, C. H. Wu, S. F. Horng, W. S. Lee, H. F. Meng, J. T. Shy and <strong>C. S. Hsu<\/strong>, &#8220;Large enhancement of intersystem crossing in polyfluorenes by iridium-complex doping&#8221; J. Appl. Phys., 90, 013504 (2007).<\/p>\n<p>139.\u00a0\u00a0\u00a0 S. R. Tseng, S. Y. Li, H. F. Meng, Y. H. Yu, C. M. Yang, H. H. Liao, S. F. Horng and <strong>C. S. Hsu<\/strong>, &#8221; High-efficiency blue multilayer polymer light-emitting diode based on poly(9,9-dioctylfluorene)&#8221; J. Appl. Phys., 101, 084510 (2007).<\/p>\n<p>140.\u00a0\u00a0\u00a0 C. J. Su, Y. C. Liu, H. L. Chen, Y. C. Li, H. K. Lin, W. L. Liu and <strong>C. S. Hsu<\/strong>, &#8220;Two-Dimensional Densely Packed DNA Nanostructure Derived from DNA Complexation with a Low-Generation Poly(amidoamine) Dendrimer&#8221; Langmuir, 23, 975 (2007).<\/p>\n<p>141.\u00a0\u00a0\u00a0 Y. M. Liao, H. L. Chen and <strong>C. S. Hsu<\/strong>, S. Gauza, and S. T. Wu, &#8220;Synthesis and Mesomorphic Properties of Super High Birefringence Isothiocyanato Bistolane Liquid Crystals&#8221; Liquid Crystals, 34, 507 (2007).<\/p>\n<p>142.\u00a0\u00a0\u00a0 C. H. Huang, C. W. Lee, <strong>C. S. Hsu<\/strong>, C. Renaud, and T. P. Nguyen, &#8220;Electro-optical Properties of Poly(1-(difluorophenyl)-2-(4-alkylcyclohexylphenyl)acetylene) Organic Light-Emitting Diodes&#8221; Thin Solid Films, 515, 7671 (2007).<\/p>\n<p>143.\u00a0\u00a0\u00a0 S. H. Yang, S. Y. Chen and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis and Opto-Electrical Properties of Dendron-Containing Poly(2,3-diphenyl-1,4-phenylenevinylene) Derivatives&#8221; J. Polym. Sci. A. Polym. Chem., 45, 3440 (2007).<\/p>\n<p>144.\u00a0\u00a0\u00a0 S. H. Yang, P. Le Rendu, T. P. Nguyen and <strong>C. S. Hsu<\/strong>, &#8220;Fabrication of MEH-PPV\/SIO<sub>2<\/sub> and MEH-PPV\/TIO<sub>2<\/sub> Nanocomposites with Enhanced Luminescent Stabilities&#8221; Rev. Adv. Mater. Sci., 15, 144 (2007).<\/p>\n<p>145.\u00a0\u00a0\u00a0 Z. Q. Liu, B. K. McCoy, S. T. Wang, R. Pindak, W. Caliebe, P. Barois, P. Fernandes, H. T. Nguyen, <strong>C. S. Hsu<\/strong>, S. Wang and C. C. Huang, &#8220;Unique Pitch Evolution in the Smectic-C<sup>*<\/sup><sub>\u03b1<\/sub>Phase&#8221; Phys. Rev. Lett., 99, 077802 (2007).<\/p>\n<p>146.\u00a0\u00a0\u00a0 C. H. Chou, C. H. Yang, <strong>C. S. Hsu<\/strong> and T. M. Chen, &#8220;Hybrid White-light Emitting-LED Based on Luminescent Polyfluorene Polymer and Quantum Dots&#8221;, J. Nanosci. Nanotecchnol., 7, 2785 (2007).<\/p>\n<p>147.\u00a0\u00a0\u00a0 S. Gauza, Y. Zhao, T. L. Cor, S. T. Wu, A. Ziolek, R. Dabrowski, O. Catanescu, L. C. Chien and <strong>C. S. Hsu<\/strong>, &#8220;High Figure-of-Merit Laterally Fluorinated Biphenyltolane-lsothiocyanates&#8221; Mol. Cryst. Liq. Cryst., 479, 169 (2007).<\/p>\n<p>148.\u00a0\u00a0\u00a0 C. W. Lee, C. H. Chou, J. H. Huang, <strong>C. S. Hsu<\/strong> and T. P. Nguyen, &#8220;Investigations of organic light emitting diodes with CdSe(ZnS) quantum dots&#8221; Mater. Sci. Eng. B., 147, 307 (2008).<\/p>\n<p>149.\u00a0\u00a0\u00a0 C. M. Yang, H. H. Liao, S. F. Horng, S. R. Tseng, H. F. Meng and <strong>C. S. Hsu<\/strong>, &#8220;Electron Mobility and Electroluminescence Efficiency of Blue Conjugated Polymers&#8221;, Synth. Met., 158, 25 (2008).<\/p>\n<p>150.\u00a0\u00a0\u00a0 C. Y. Chang, S. Y. Chien, <strong>C. S. Hsu<\/strong>, S. Gauza , S. T. Wu, &#8220;Synthesis of laterally substituted \u03b1-methylstilbene-tolane liquid crystals&#8221; Liq. Cryst., 35, 1 (2008).<\/p>\n<p>151.\u00a0\u00a0\u00a0 Y. C. Chao, M. H. Xie, M. Z. Dai, H. F. Meng, S. F. Horng and <strong>C. S. Hsu<\/strong>, &#8220;Polymer hot-carrier transistor with low bandgap emitter&#8221;, Appl. Phys. Lett. , 92, 093310 (2008).<\/p>\n<p>152.\u00a0\u00a0\u00a0 S. R. Tseng, S. Y. Li, H. F. Meng, Y. H. Yu, C. M. Yang, H. H. Liao, S. F. Horng and <strong>C. S. Hsu<\/strong>, &#8220;Deep blue light-emitting diode based on high molecular weight Poly(9,9-dioctylfluorene) with high efficiency and color stability&#8221;, Organic Electronics, 9, 279 (2008).<\/p>\n<p>153.\u00a0\u00a0\u00a0 S. R. Tseng, H. F. Meng C. H. Yeh, H. C. Lai, S. F. Horng, H. H. Liao, <strong>C. S. Hsu<\/strong> and L. C. Lin, &#8221; High-efficiency blue multilayer polymer light-emitting diode fabricated by a general liquid buffer method&#8221; Synthetic Metals, 158,130 (2008).<\/p>\n<p>154.\u00a0\u00a0\u00a0 Y. C. Chao, H. F. Meng, S. F. Horng and <strong>C. S. Hsu<\/strong>, &#8220;High-performance solution-processed polymer space-charge-limited transistor&#8221;, Organic Electronics, 9, 310 (2008).<\/p>\n<p>155.\u00a0\u00a0\u00a0 T. F. Lin, R. M. Ho, C. H. Sung and <strong>C. S. Hsu<\/strong>, &#8220;Variation of Helical Twisting Power in Self-Assembled Sugar-Appended Schiff Base Chiral Rod-Coil Amphiphiles&#8221;, Chem. Mater., 20, 1404 (2008).<\/p>\n<p>156.\u00a0\u00a0\u00a0 K. C. Tang, S. R. Tseng, W. S. Li, H. F. Meng, S. F. Horng and <strong>C. S. Hsu<\/strong>, &#8220;Broad band and white phosphorescent polymer light-emitting diodes in multilayer structure&#8221; Synth. Met., 158, 287 (2008).<\/p>\n<p>157.\u00a0\u00a0\u00a0 C. W. Lee, Y. Jpsse, <strong>C. S. Hsu<\/strong> and T. P. Nguyen, &#8220;Green emitting polyhedral oligometric silsesquioxanes\/ poly(phenylene vinylene) derivative materials for highly efficient organic light emitting diodes (OLEDs)&#8221; Eur. Phys. J. Appl. Phys., 42, 213 (2008).<\/p>\n<p>158.\u00a0\u00a0\u00a0 S. C. Lin, T. F. Lin, R. M. Ho, C. Y. Chang and <strong>C. S. Hsu<\/strong>, &#8220;Hierarchical Superstructures with Helical Sense in the Self-Assembled Achiral Banana-Shaped Liquid Crystalline Molecules&#8221; Adv. Funct. Mater., 18, 3386 (2008).<\/p>\n<p>159.\u00a0\u00a0\u00a0 T. P. Nguyen, C. Renaud, C. H. Huang, C. N. Lo, C. W. Lee and <strong>C. S. Hsu<\/strong>, &#8221; Effect of electrical operation on the defect states in organic semiconductors&#8221; J. Mater. Sci. Mater. Electron., 19, S92 (2008).<\/p>\n<p>160.\u00a0\u00a0\u00a0 P. D. Vellis, J. A. Mikroyannidis, C. N. Lo, and<strong> C. S. Hsu<\/strong>, &#8220;Synthesis of Terpridine Ligands and Their Complextion with Zn2+ and Ru2+ for Optoelectronic Applications&#8221; J. Polym. Sci. A Polym. Chem., 46, 7702 (2008).<\/p>\n<p>161.\u00a0\u00a0\u00a0 C. W. Lee, C. Renaud, <strong>C. S. Hsu<\/strong> and T. P. Nguyen, &#8220;Traps and performance of MEH-PPV\/CdSe(ZnS) nanocomposities based OLEDs&#8221; Nanotechnology, 19, 455202 (2008).<\/p>\n<p>162.\u00a0\u00a0\u00a0 S. Jaradat, P. Brimicombe, C. Southern, S. Siemianowski, E. DiMasi, M. Osipov, R. Pindak, H. F. Gleeson, Z. Q. Liu, B. K. McCoy, S. T. Wang, W. Caliebe, P. Barois, P. Fernandes, H. T. Nguyen, <strong>C. S. Hsu<\/strong> and C. C. Huang, &#8220;Investigating Orientational Order of Liquid Crystals&#8221;, Science Highlight, Brookhaven Bulletin (2008).<\/p>\n<p>163.\u00a0\u00a0\u00a0 C. W Lee, S. H. Yang, <strong>C. S. Hsu<\/strong> and H. F. Meng, &#8220;Improved Efficiency in Organic Light Emitting Diodes Made with CdSe\/ZnS Quantum Dots and a Semiconducting Polymer&#8221; J. Nanosci. Nanotechnol., 9, 2076 (2009).<\/p>\n<p>164.\u00a0\u00a0\u00a0 S. H. Yang, C. H. Huang, C. H. Chen and <strong>C. S. Hsu<\/strong>, \u201cSynthesis and electroluminescent properties of disubstituted polyacetylene derivatives containing multi-fluorophenyl and cyclohexylphenyl side groups\u201d Macromol. Chem. Phys.,210, 37 (2009).<\/p>\n<p>165.\u00a0\u00a0\u00a0 S. R. Tseng, Y. S. Chen, H. F. Meng, H. C. Lai,m C. H. Yeh, S. F. Horng, H. H. Liao and <strong>C. S. Hsu<\/strong>, &#8220;Electron transport and electroluminescent efficiency of conjugated polymers&#8221; Synth. Met., 159, 137 (2009).<\/p>\n<p>166.\u00a0\u00a0\u00a0 S. H. Yang and<strong> C. S. Hsu<\/strong>, &#8220;Liquid Crystalline Conjugated Polymers and Their Applications in Organic Electronics&#8221; J. Polym. Sci. A Polym. Chem., 47, 2713 (2009).<\/p>\n<p>167.\u00a0\u00a0\u00a0 Z. Xu, L. M. Chen, G. Wen Yang, C. H. Huang, J. Hou,Y. Wu, G. Li, <strong>C. S. Hsu<\/strong> and Yang Yang, \u201cVertical phase separation in poly(3-hexylthiophene):fullerence derivative blends and its advantage for inverted structure solar cells\u201d Adv. Funct. Mater., 19, 1227 (2009).<\/p>\n<p>168.\u00a0\u00a0\u00a0 C. Y. Chang, K. W. Ho, <strong>C. S. Hsu<\/strong>, C. H. Lin, S. Gauza and S. T. Wu, &#8220;Synthesis and mesomorphic properties of \u03b1-methylstilbene based liquid crystals&#8221; Liquid Crsytals, 36, 425 (2009).<\/p>\n<p>169.\u00a0\u00a0\u00a0 Y. C. Li, C. Y. Chen, Y. X. Chang, P. Y. Chuang, J. H. Chen, H. L. Chen, <strong>C. S. Hsu<\/strong>, V. Ivanov, P. Khalatur and S. A. Chen, &#8220;Scattering Study of the Conformational Structure and Aggregation Behavior of a Conjugated Polymer Solution&#8221; Langmuir, 25, 4668. (2009).<\/p>\n<p>170.\u00a0\u00a0\u00a0 M. S. Mehata,<strong> C. S. Hsu<\/strong>, Y. P. Lee and N. Ohta, &#8220;Electric field effects on photoluminescence of polyfluorene thin films: Dependence on excitation wavelength, field strength and temperature&#8221; J. Phys. Chem. C, 113, 11907 (2009).<\/p>\n<p>171.\u00a0\u00a0\u00a0 S. C. Liao, C. S. Lai, D. D. Yeh, M. H. Rahman, <strong>C. S. Hsu<\/strong>, H. L. Chen and S. A. Chen, &#8220;Supramolecular structures of an amphiphilic hairy-rod conjugated copolymer bearing poly(ethylene oxide) side chain&#8221; J. of Reactive and Functional Polymers , 69, 498 (2009).<\/p>\n<p>172.\u00a0\u00a0\u00a0 L. Pan, S. Wang, <strong>C. S. Hsu<\/strong> and C. C. Huang, &#8220;Surface-induced ordering effect in one antiferroelectric liquid crystal compound&#8221; Phy. Rev. E., 79, 031704 (2009).<\/p>\n<p>173.\u00a0\u00a0\u00a0 Y. H. Chang, S. R. Tseng, C. Y. Chen, H. F. Meng, E. C. Chen, S. F. Horng, <strong>C. S. Hsu<\/strong>, &#8220;Polymer solar cell by blade coating&#8221;, Organic Electronics, 10, 741 (2009).<\/p>\n<p>174.\u00a0\u00a0\u00a0 Y. J. Cheng, S. H. Yang and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis of Conjugated Polymers for Organic Solar Cell Application&#8221; Chemical Reviews, 109, 5868 (2009).<\/p>\n<p>175.\u00a0\u00a0\u00a0 M. S. Ho and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis and Hierarchial Superstructures of Side-chain Liquid Crystal Polyacetylenes Containing Galactopyranoside End-groups&#8221; J. Polym. Sci. A Polym. Chem., 47, 6596 (2009).<\/p>\n<p>176.\u00a0\u00a0\u00a0 C. H. Yang, S. H. Yang and <strong>C. S. Hsu<\/strong>, &#8220;Solution \u2013processable phosphorescent to organic light-emitting diodes based on chromophoric amphiphile\/silica nanocomposite&#8221; Nanolotechnology, 20, 315601 (2009).<\/p>\n<p>177.\u00a0\u00a0\u00a0 W. W. Tsai, Y. C. Chao, E. C. Chen, H. W. Zan, H. F. Meng and <strong>C. S. Hsu<\/strong>, &#8220;Increasing organic vertical carrier mobility for the application of high speed bilayered organic photodetector&#8221; Appl. Phys. Lett., 95, 213308 (2009).<\/p>\n<p>178.\u00a0\u00a0\u00a0 L. Pan, S. Wang, <strong>C. S. Hsu<\/strong> and C. C. Huang, &#8220;Thickness dependent phase behavior of antiferroelectric liquid crystal films&#8221; Phy. Rev. Lett., 103, 187802 (2009).<\/p>\n<p>179.\u00a0\u00a0\u00a0 P. H. Wang, M. S. Ho, S. H. Yang, K. B. Chen and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis of Thermal-stable and Photo-crosslinkable Polyfluorenes for the Applications of Polymer Light Emitting Diodes&#8221; J. Polym. Sci. A Polym. Chem., 48, 516 (2010).<\/p>\n<p>180.\u00a0\u00a0\u00a0 M. S. Ho and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis and self-assembled nanostructures of novel chiral amphiphilic liquid crystals containing \u03b2-d-galactopyranoside end-groups&#8221; Liquid Crystals, 37, 293 (2010).<\/p>\n<p>181.\u00a0\u00a0\u00a0 Q. Song, S. Gauza, H. Xianyu, S. T. Wu, Y. M. Liao, C. Y. Chang and <strong>C. S. Hsu<\/strong>, &#8220;High birefringence lateral difluoro phenyl tolane liquid crystals&#8221; Liquid Crystals,37, 139 (2010).<\/p>\n<p>182.\u00a0\u00a0\u00a0 C. H. Chen, C. H. Hsieh, M. Dubosc, Y. J. Cheng and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis and Characterization of Bridged Bithiophene-Based Conjugated 2 Polymers for Photovoltaic Applications: Acceptor Strength and 3 Ternary Blends&#8221; Macromolecules, 43, 697 (2010).<\/p>\n<p>183.\u00a0\u00a0\u00a0 E. C. Chen, C. Y. Chang, J. T. Shieh, S. R. Tseng, H. F. Meng, <strong>C. S. Hsu<\/strong> and S. F. Horng, &#8220;Polymer photodetector with voltage-adjustable photocurrent spectrum&#8221; Appl. Phys. Lett., 96, 043507 (2010).<\/p>\n<p>184.\u00a0\u00a0\u00a0 C. H. Hsieh, Y. J. Cheng, P. J. Li, C. H. Chen, M. Dubosc, R. M. Liang and <strong>C. S. Hsu<\/strong>, &#8220;High Efficient and Stable Inverted Polymer Solar Cells Integrated with a Cross-Linked Fullerene Material as an Interlayer&#8221; J. Am. Chem. Soc., 132, 4887 (2010).<\/p>\n<p>185.\u00a0\u00a0\u00a0 J. S. Wu, Y. J. Cheng, M. Dubosc, C. H. Hsieh, C. Y. Chang, <strong>C. S. Hsu<\/strong>, &#8220;Donor-Acceptor Polymers Based on Multi-fused Heptacyclic Structures: Synthesis, Characterization and Photovoltaic Applications&#8221; Chem. Commun, 46, 3259 (2010).<\/p>\n<p>186.\u00a0\u00a0\u00a0 M. S. Mehata, <strong>C. S. Hsu<\/strong>, Y. P. Lee and N. Ohta, &#8220;Electric-Field-Induced Enhancement\/ Quenching of Photoluminescence of \u03c0-Conjugated Polymer S3-PPV: Excitation Energy Dependence&#8221; J. Phys. Chem. B, 114, 6258 (2010).<\/p>\n<p>187.\u00a0\u00a0\u00a0 Y. C. Chao, S. D. Yeh, H. W. Zan, G. F. Chang, H. F. Meng, C. H. Hung, T. C. Meng, <strong>C. S. Hsu<\/strong> and S. F. Horng, &#8220;Real-time and indicator-free detection of aqueous nitric oxide with hydrogel film&#8221; Appl. Phys. Lett., 96, 223702 (2010).<\/p>\n<p>188.\u00a0\u00a0\u00a0 T. F. Lin, R. M. Ho, C. H. Sung, M. S. Ho and <strong>C. S. Hsu<\/strong>, &#8220;Twist Ferrocene Wires from Self-Assembly of Chiral Rod-Coil Organometallics&#8221; Chem.\u2013Eur. J. , 16,7385 (2010).<\/p>\n<p>189.\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 C. H. Chen, Y. J. Cheng, M. Dubosc, C. H. Hsieh, C. C. Chu and <strong>C. S. Hsu<\/strong>, &#8220;Alternating and Diblock Donor-Acceptor Conjugated Polymers Based on Diindeno[1,2-b:2\u2019,1\u2019-d]thiophene Structure: Synthesis, Characterization, and applications&#8221; Chem.-Asia J., 5, 2483 (2010).<\/p>\n<p>190.\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Y. J. Cheng, C. H. Hsieh, Y. He, <strong>C. S. Hsu<\/strong> and Y. F. Li., &#8220;Combination of Indene-C60 Bis-adduct and Cross-linked Fullerene Interlayer Leading to Highly Efficient Inverted Polymer Solar Cells&#8221; J. Am. Chem. Soc. 132, 17381(2010).<\/p>\n<p>191.\u00a0\u00a0\u00a0 Y. H. Lee, A. Yabushita, <strong>C. S. Hsu<\/strong>, S. H. Yang, I. Iwakura, C. W. Luo, K. H. Wu and T. Kobayashi, &#8220;Ultrafast relaxation dynamics of photoexcitations in poly(3-hexylthiophene) for the determination of the defect concentration&#8221; Chem. Phys. Lett., 498, 71 (2010).<\/p>\n<p>192.\u00a0\u00a0\u00a0 J. A. Mikroyannidis, P. D. Vellis, S. H. Yang and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis, electroluminescence, and photovoltaic cells of new vinylene-copolymers with 4-(anthracene-10-yl)-2, 6-diphenylpyridine segments&#8221; J. of Appl. Polym. Sci., 115, 731 (2010).<\/p>\n<p>193.\u00a0\u00a0\u00a0 P. Ding, C. C. Chu, B. Liu, B. Peng, Y. P. Zou, Y. He, K. Zhou and <strong>C. S. Hsu<\/strong>, &#8220;A High-Mobility Low-Bandgap Copolymer for Efficient Solar Cells&#8221; Macromol. Chem. Phys., 211, 2555 (2010).<\/p>\n<p>194.\u00a0\u00a0\u00a0 E. C. Chen, S. R. Tseng, Y. C. Chao, H. F. Meng, C. F. Wang, W. C. Chen, <strong>C. S. Hsu<\/strong> and S. F. Horng, &#8220;Polymer infrared photo-detector with high sensitivity up to 1100 nm&#8221; Synthetic Metals, 161, 1618 (2010).<\/p>\n<p>195.\u00a0\u00a0\u00a0 H. M. Shih, C. J. Lin, S. R. Tseng, C. H. Lin and <strong>C. S. Hsu<\/strong>,&#8221;Synthesis of New Blue Anthracene-based Conjugated Polymers and Their Applications in Polymer Light Emitting Diodes&#8221; Macromol. Chem. Phys., 212, 1100 (2011).<\/p>\n<p>196.\u00a0\u00a0\u00a0 J. L. Wu, F. C. Chen, Y. S. Hsiao, F. C. Chien, P. Chen, C. H. Kuo, Michael Huang and <strong>C. S. Hsu<\/strong>, &#8220;Surface Plasmonic Effects of Metallic Nanoparticles on the Performance of Polymer Bulk-Heterojunction Solar Cells&#8221; ACS Nano, 5, 959 (2011).<\/p>\n<p>197.\u00a0\u00a0\u00a0 Y. J. Cheng, C. H. Hsieh, P. J. Li and <strong>C. S. Hsu<\/strong>, &#8220;Morphological Stabilization by In Situ Polymerization of Fullerene Derivatives Leading to Efficient, Thermally Stable Organic Photovoltaics&#8221; Adv. Funct. Mater., 21, 1723 (2011).<\/p>\n<p>198.\u00a0\u00a0\u00a0 Y. F. Lin, C.H. Chen, W.J. Xie, S.H. Yang, <strong>C. S. Hsu<\/strong>, M.T. Lin and W.B. Jian, &#8220;Nano Approach Investigation of Conduction Mechanism in Polyaniline Nanofibers&#8221; ACS Nano, 5, 1541 (2011).<\/p>\n<p>199.\u00a0\u00a0\u00a0 Y. J. Cheng, L. C. Huang, F. Y. Cao, W. S. Kao, C. Y. Chang and <strong>C. S. Hsu<\/strong>, &#8220;Alternating \u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Copolymers Incorporating Cyclopenta[2,1-b:3,4-b0]dithiophene Unit and Organic Dyes for \u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Photovoltaic Applications&#8221; J. Polym. Sci. A Polym. Chem., 49, 1791 (2011).<\/p>\n<p>200.\u00a0\u00a0\u00a0 Y. J. Cheng, J. S. Wu, P. I. Shih, C. Y. Chang, P. C. Jwo, W. S. Kao and <strong>C. S. Hsu<\/strong>, \u00a0\u00a0\u00a0\u00a0\u00a0 &#8220;Carbazole-Based Ladder-Type Heptacylic Arene with Aliphatic Side Chains Leading to Enhanced \u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Efficiency of Organic Photovoltaics&#8221; Chem. Mater., 23, 2361 (2011).<\/p>\n<p>201.\u00a0\u00a0\u00a0 C. N. Lo and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis and Electroluminescence Properties of White-Light Single Polyfluorenes with High Molecular Weight by Click Reaction&#8221; J. Polym. Sci. A Polym. Chem, 49, 3355-3365 (2011).<\/p>\n<p>202.\u00a0\u00a0\u00a0 K. H. Lo, Y. M. Liao, F. Massuyeau, Z. Y. Chun, R. M. Ho, <strong>C. S. Hsu<\/strong>, J. L. Duvail, and S. Lefrant, &#8220;Induced Chain Alignment of Conjugated Polymers within Nanoporous Template&#8221; Adv. Funct. Mater., 21, 2729-2736 (2011).<\/p>\n<p>203.\u00a0\u00a0\u00a0 C. Y. Chang, C. E. Wu, S. Y. Chen, C. Chi, Y. J. Cheng, <strong>C. S. Hsu<\/strong>, Y. L. Wang and Y. Li, \u201cEnhanced Performance and Stability of a Polymer Solar Cell by Incorporation of Vertically Aligned, Cross-Linked Fullerene Nanorods\u201c, Angew. Chem.-Int. Edit., 50, 9386-9390 (2011).<\/p>\n<p>204.\u00a0\u00a0\u00a0 J. T. Chen and <strong>C. S. Hsu<\/strong>, &#8220;Conjugated polymer nanostructures for organic solar cell applications&#8221; Polymer Chemistry, 2, 2707-2722 (2011).<\/p>\n<p>205.\u00a0\u00a0\u00a0 Y. J. Cheng, C. H. Chen, Y. S. Lin, C. Y. Chang and <strong>C. S. Hsu<\/strong>, &#8220;Ladder-Type Nonacyclic Structure Consisting of Alternate Thiophene and Benzene Units for Efficient Conventional and Inverted Organic Photovoltaics&#8221; Chem. Mater., 23, 5068-5075 (2011).<\/p>\n<p>206.\u00a0\u00a0\u00a0 C. H. Chen, Y. J. Cheng, C. Y. Chang and <strong>C. S. Hsu<\/strong>, &#8220;Donor-Acceptor Random Copolymers Based on a Ladder-Type Nonacyclic Unit &#8211; Synthesis, Characterization, and Photovoltaic Applications&#8221; Macromolecules, 44, 8415-8424 (2011).<\/p>\n<p>207.\u00a0\u00a0\u00a0 Y. J. Cheng, C. H. Chen, Y. J. Ho, S. W. Chang, H. A. Witek and <strong>C. S. Hsu<\/strong>, &#8220;Thieno[3,2-b]pyrrolo donor fused with benzothiadiazolo, benzoselenadiazolo and quinoxalino acceptors:Synthesis, characterization, and molecular properties&#8221; Organic Letters, 13, 5484-5487 (2011).<\/p>\n<p>208.\u00a0\u00a0\u00a0 Y. J. Cheng, M. H. Liao, C. Y. Chang, W. S. Kao, C. E. Wu and <strong>C. S. Hsu<\/strong>,&#8221;Di(4-methylphenyl) methano-C60 Bis-Adduct for Efficient and Stable Organic Photovoltaics with Enhanced Open- Circuit Voltage&#8221; Chem. Mater., 23, 4056 (2011).<\/p>\n<p>209.\u00a0\u00a0\u00a0 Y. M. Liao, H. M. Shih, K. H. Hsu, <strong>C. S. Hsu<\/strong>, Y. C. Chao, S. C. Lin, C. Y. Chen and H. F. Meng, &#8220;High-performance poly(2,3-diphenyl-1,4-phenylene vinylene)-based polymer light-emitting diodes by blade coating method&#8221; Polymer, 52, 3717 (2011).<\/p>\n<p>210.\u00a0\u00a0\u00a0 P. Ding, C. C. Chu, Y. Zou, D. Xiao, C. Pan and <strong>C. S. Hsu<\/strong> &#8220;New low bandgap conjugated polymer derived from 2,7-carbazole and 5,6-bis(octyloxy)-4,7-di(thiophen-2-yl)benzothiadiazole: Synthesis and photovoltaic properties&#8221; J. of Appl. Polym. Sci., 123, 99-107 (2012).<\/p>\n<p>211.\u00a0\u00a0\u00a0 E. C. Chen, C. Y. Shih, M. Z. Dai, H. C. Yeh, Y. C. Chao, H. F. Meng, H. W. Zan, W. R. Liu, Y. C. Chiu, Y. T. Yeh, C. J. Sun, S. F. Horng and <strong>C. S. Hsu<\/strong>, &#8220;Polymer Infrared Proximity Sensor Array&#8221; IEEE Trans. Electron Devices, 58, 1215 (2011).<\/p>\n<p>212.\u00a0\u00a0\u00a0 Y. J. Cheng, M. H. Liao, H. M. Shih, P. I. Shih and <strong>C. S. Hsu<\/strong>, &#8220;Exciplex Electroluminescence Induced by Cross-linked Hole-Transporting Materials for White Light Polymer Light-Emitting Diodes&#8221; Macromolecules, 44, 5968 (2011).<\/p>\n<p>213.\u00a0\u00a0\u00a0 H. M. Shih, R. C. Wu, P. I. Shih, C. L. Wang and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis of Fluorene-based Hyperbranched Polymers for Solution-Processable Blue, Green, Red, and White Light-Emitting Devices&#8221; J. Polym. Sci. A Polym. Chem., 50, 696 (2012).<\/p>\n<p>214.\u00a0\u00a0\u00a0 C. Y. Chang, Y. J. Cheng, S. H. Hung, J. S. Wu, W. S. Kao, C. H. Lee and <strong>C. S. Hsu<\/strong>, &#8220;Combination of Molecular, Morphological and Interfacial Engineering to Achieve Highly Efficient and Stable Plastic Solar Cells&#8221; Adv. Mater. 24, 549 (2012).<\/p>\n<p>215.\u00a0\u00a0\u00a0 S. C. Chien, F. C. Chen, M. K. Chung and <strong>C. S. Hsu<\/strong>, &#8220;Self-Assembled Poly(ethylene glycol) Buffer Layers in Polymer Solar Cells: Toward Superior Stability and Efficiency&#8221; J. of Phys. Chem., 116, 1354 (2012).<\/p>\n<p>216.\u00a0\u00a0\u00a0 J. S. Wu, Y. J. Cheng, T. Y. Lin, C. Y. Chang, and <strong>C. S. Hsu<\/strong>, &#8220;Dithienocarbazole-Based Ladder-Type Heptacyclic Arenes with Silicon, Carbon, and Nitrogen Bridges: Synthesis, Molecular Properties, Field-Effect Transistors, and Photovoltaic Applications&#8221; Adv. Funct. Mater., 22, 1711 (2012).<\/p>\n<p>217.\u00a0\u00a0\u00a0 Y. C. Wu, X. Ren, E. Q. Chen, H. M. Lee, J. L. Duvail, C. L. Wang and <strong>C. S. Hsu<\/strong>, &#8220;Preservation of Photoluminescence Efficiency in the Ordered Phases of Poly(2,3-Diphenyl-1,4-Phenylene Vinylene) via Disturbing the Intermolecular \u03c0-\u03c0 Interactions with Dendritic Aliphatic Side Chains&#8221; Macromolecules, 45, 4540 (2012).<\/p>\n<p>218.\u00a0\u00a0\u00a0 Y. J. Cheng, Y. J. Ho, C. H. Chen, W. S. Kao, C. E. Wu, S. L. Hsu and <strong>C. S. Hsu<\/strong>., &#8220;Synthesis, Photophysical and Photovoltaic Properties of Conjugated Polymers Containing Fused Donor-Acceptor Dithienopyrrolobenzothiadiazole and Dithienopyrroloquinoxaline Arenes&#8221; Macromolecules, 45, 2690-2698 (2012).<\/p>\n<p>219.\u00a0\u00a0\u00a0 P. Ding, Y. Zou, C. C. Chu, D. Xiao and <strong>C. S. Hsu<\/strong>., &#8220;Effects of thiophene units on substituted benzothiadiazole and benzodithiophene copolymers for photovoltaic applications&#8221; J. Appl. Polym. Sci., 125, 3936 (2012).<\/p>\n<p>220.\u00a0\u00a0\u00a0 Y. J. Cheng, S. W. Cheng, C. Y. Chang, W. S. Kao, M. H. Liao and <strong>C. S. Hsu<\/strong>., &#8220;Diindenothieno[2,3-b]thiophene arene for efficient organic photovoltaics with an extra high open-circuit voltage of 1.14 eV&#8221; Chem. Commun., 48, 3203 (2012).<\/p>\n<p>221.\u00a0\u00a0\u00a0 Y. J. Cheng, C. H. Chen, T. Y. Lin and C. S. Hsu., &#8220;Dithienocyclopentathieno[3,2-b]thiophene Hexacyclic Arene for Solution-Processed Organic Field-Effect Transistors and Photovoltaic Applications&#8221; Chem.-Asian J., 7, 818-825 (2012).<\/p>\n<p>222.\u00a0\u00a0\u00a0 S. Y. Chen, Y. T. Yen, Y. Y. Chen, <strong>C. S. Hsu<\/strong>, Y. L. Chueh and L. J. Chen., &#8220;Large scale two-dimensional nanobowl array high efficiency polymer solar cell&#8221; RSC Adv., 2, 1314 (2012).<\/p>\n<p>223.\u00a0\u00a0\u00a0 C. L. Wang, W. B. Zhang, H. J. Sun, R. M. Van Horn, R. R. Kulkarni, C. C. Tsai, <strong>C. S. Hsu<\/strong>, B. Lotz, X. Gong and S. Z. D. Cheng, &#8220;A Supramolecular &#8220;Double-Cable&#8221; Structure with a 129(44) Helix in a Columnar Porphyrin-C-60 Dyad and its Application in Polymer Solar Cells&#8221; Adv. Energy Mater., 2, 1375 (2012).<\/p>\n<p>224.\u00a0\u00a0\u00a0 H. Y. Hung, C. W. Lu, C. Y. Lee, <strong>C. S. Hsu<\/strong> and Y. Z. Hsieh, &#8220;Analysis of metal ion impurities in liquid crystals using high resolution inductively coupled plasma mass spectrometry&#8221; Analytical Methods, 4, 3631 (2012).<\/p>\n<p>225.\u00a0\u00a0\u00a0 Y. L. Chen, C. Y. Chang, Y. J. Cheng and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis of a New Ladder-Type Benzodi(cyclopentadithiophene) Arene with Forced Planarization Leading to an Enhanced Efficiency of Organic Photovoltaics&#8221; Chem. Mater., 24, 3964 (2012).<\/p>\n<p>226.\u00a0\u00a0\u00a0 C. A. Tseng, J. S. Wu, T. Y. Lin, W. S. Kao, C. E. Wu, S. L. Hsu, Y. Y. Liao, <strong>C. S. Hsu<\/strong>, H. Y. Huang, Y. Z. Hsieh and Y. J. Cheng, &#8220;A Pentacyclic Nitrogen-Bridged Thienyl-Phenylene-Thienyl Arene for Donor-Acceptor Copolymers: Synthesis, Characterization, and Applications in Field-Effect Transistors and Polymer Solar Cells&#8221; Chem.-Asian J., 7, 2102 (2012).<\/p>\n<p>227.\u00a0\u00a0\u00a0 Y. F. Lin, S. C. Chiu, S. T. Wang, S. K. Fu, C. H. Chen, W. J. Xie, S. H. Yang, <strong>C. S. Hsu<\/strong>, J. F. Chen, X. Zhou, Z. Liu, J. Fang and W. B. Jian, &#8220;Dielectrophoretic placement of quasi-zero-, one-, and two-dimensional nanomaterials into nanogap for electrical characterizations&#8221; Electrophoresis, 33, 2475 (2012).<\/p>\n<p>228.\u00a0\u00a0\u00a0 M. S. Mehata, <strong>C. S. Hsu<\/strong>, Y. P. Lee and N. Ohta, &#8220;Electroabsorption and Electrophoto lumine-<\/p>\n<p>scence of Poly(2,3-diphenyl-5-hexyl-p-phenylene vinylene)&#8221; J. Phys. Chem. C., 116, 14789 (2012).<\/p>\n<p>229.\u00a0\u00a0\u00a0 C. W. Chang, C. J. Bhongale, C. S. Lee, W. K. Huang, <strong>C. S. Hsu<\/strong> and E. W. G. Diau, &#8220;Relaxation Dynamics and Structural Characterization of Organic Nanobelts with Aggregation-Induced&#8221; J. Phys. Chem. C., 116, 15146 (2012).<\/p>\n<p>230.\u00a0\u00a0\u00a0 W. C. Chen, S. C. Chien, F. C. Chen and <strong>C. S. Hsu<\/strong>, &#8220;Stacked Structures for Assembling Multiple Organic Photovoltaic Devices Source&#8221; Applied Physics Express, 5, 072301 (2012).<\/p>\n<p>231.\u00a0\u00a0\u00a0 \u00a0S. C. Lin, R. M Ho, C. Y. Chang and <strong>C. S. Hsu<\/strong>, &#8220;Hierarchical Superstructures with Control of Helicity from the Self-Assembly of Chiral Bent-Core Molecules&#8221; Chem. Eur. J., 18, 9091 (2012).<\/p>\n<p>232.\u00a0\u00a0\u00a0 J. S. Wu, C. T. Lin, C. L. Wang, Y. J. Cheng and <strong>C. S. Hsu<\/strong>, &#8220;New Angular-Shaped and Isomerically Pure Anthradithiophene with Lateral Aliphatic Side Chains for Conjugated Polymers: Synthesis, Characterization, and Implications for Solution-Prossessed Organic Field-Effect Transistors and Photovoltaics&#8221; Chem. Mater., 24, 2391 (2012).<\/p>\n<p>233.\u00a0\u00a0\u00a0 L. D. Pan, <strong>C. S. Hsu<\/strong> and C. C. Huang, &#8220;Surface-Surface Interaction in Smectic Liquid Crystal Films&#8221; Phys. Rev. Lett., 108, 027801 (2012).<\/p>\n<p>234.\u00a0\u00a0\u00a0 Y. C. Wu, Y. H. Chao, C. L. Wang, C. T. Wu, <strong>C. S. Hsu<\/strong>, Y. L. Zeng and C. Y. Lin, &#8220;Porphyrin-diindenothieno[2,3-b]thiophene alternating copolymer blue-light harvester in ternary-blend polymer solar cells&#8221; J. Polym. Sci. A Polym. Chem, 50, 5032 (2012).<\/p>\n<p>235.\u00a0\u00a0\u00a0 C. S. Kao, F. C. Chen, M. H. Huang and <strong>C. S. Hsu<\/strong>, &#8220;Plasmonic-enhanced Performance for Polymer Solar Cells Prepared with Inverted Structures&#8221; Appl. Phys. Lett., 101, 193902 (2012).<\/p>\n<p>236.\u00a0\u00a0\u00a0 H. H. Chang, C. E. Tsai, Y. Y. Lai, D. Y. Choiu, S. L. Hsu, <strong>C. S. Hsu<\/strong> and Y. J. Cheng, &#8220;Synthesis, Molecular and Photovoltaic Properties of Donor-Acceptor Conjugated Polymers Incorporating a New Heptacylic Indacenodithieno[3,2-b]thiophene Arene&#8221; Macromolecules, 45, 9282 (2012).<\/p>\n<p>237.\u00a0\u00a0\u00a0 Y. Y. Lai, Y.J. Cheng, C. H. Chen, S. W. Cheng, F. Y. Cao and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis, photophysical and photovoltaic properties of a new class of two-dimensional conjugated polymers containing donor-acceptor chromophores as pendant groups&#8221; Polym. Chem., 4, 3333 (2013).<\/p>\n<p>238.\u00a0\u00a0\u00a0 Y. L. Chen, W. S. Kao, C. E. Tsai, Y. Y. Lai, Y. J. Cheng and <strong>C. S. Hsu<\/strong>, &#8220;A new ladder-type benzodi(cyclopentadithiophene)-based donor-acceptor polymer and a modified hole-collecting PEDOT: PSS layer to achieve tandem solar cells with an open-circuit voltage of 1.62 V&#8221; Chem. Commun., 49, 7702 (2013).<\/p>\n<p>239.\u00a0\u00a0\u00a0 X. K. Ren, Y. C. Wu, S. J. Wang, S. D. Jiang, J. F. Zheng, S. Yang, E. Q. Chen, C. L. Wang and <strong>C. S. Hsu<\/strong>, &#8220;Crystal Structure and Molecular Packing Behavior of Poly(2,3-diphenyl-1,4-phenylenevinylene) Derivatives Containing Alkyl Side-Chains<sup>&#8221; <\/sup>Macromolecules, 46, 155 (2013).<\/p>\n<p>240.\u00a0 F. Massuyeau, Y. Zhao, A. A. Mel, A. Yaya, F. Geschier, E. Gautron, S. Lefrant, J. Y. Mevellec, C. Ewels and <strong>C. S. Hsu<\/strong>, &#8220;Improved photoconductive properties of composite nanofibers based on aligned conjugated polymer and singlewalled carbon nanotubes&#8221; Nano Res. 6, 149 (2013).<\/p>\n<p>241.\u00a0\u00a0\u00a0 K. H. Lo, M. C. Li, R. M. Ho, Y. C. Zhao, F. Massuyeau, W. T. Chuang, J. L. Duvail, S. Lefrant and <strong>C. S. Hsu<\/strong>, &#8220;Luminescence Enhancement of Pyrene\/Dispersant Nanoarrays Driven by the Nanoscale Spatial Effect on Mixing&#8221; Langmuir, 29, 1627 (2013).<\/p>\n<p>242.\u00a0\u00a0\u00a0 J. S. Wu, Y. Y. Lai, Y. J. Cheng, C. Y. Chang, C. L. Wang and <strong>C. S. Hsu<\/strong>, &#8220;A New sp2-sp2 Dialkylethylene-Bridged Heptacyclic Ladder-Type Arene for High Efficiency Polymer Solar Cells&#8221; Adv. Energy. Mater., 3, 457 (2013).<\/p>\n<p>243.\u00a0 C. L. Wang, W. B. Zhang, X. F. Yu, K. Yue, H. J. Sun, C. H. Hsu, <strong>C. S. Hsu<\/strong>, J. Joseph, D. A. Modarelli and S. Z. D. Cheng, &#8220;Facile Synthesis and Photophysical Properties of SphereSquare Shape Amphiphiles Based on Porphyrin[60]Fullerene Conjugates&#8221; Chem.-Asian J., 8, 947 (2013).<\/p>\n<p>244.\u00a0 J. F. Jheng, Y. Y. Lai, J. S. Wu, Y. H. Chao, C. L. Wang and <strong>C. S. Hsu<\/strong>, &#8220;Influences of the Non-Covalent Interaction Strength on Reaching High Solid-State Order and Device Performance of a Low Bandgap Polymer with Axisymmetrical Structural Units&#8221; Adv. Mater., 25, 2445 (2013).<\/p>\n<p>245.\u00a0 Y. Y. Lai, P. I. Shih, Y. P. Li, C. E. Tsai, J. S. Wu, Y. J. Cheng and <strong>C. S. Hsu<\/strong>, &#8220;Interface Engineering to Enhance the Efficiency of Conventional Polymer Solar Cells by Alcohol-\/Water-Soluble C-60 Materials Doped with Alkali Carbonates&#8221; ACS Appl. Mater. Inter., 5, 5122 (2013).<\/p>\n<p>246.\u00a0 W. W. Liang, C. Y. Chang, Y. Y. Lai, S. W. Cheng, H. H. Chang, Y. Y. Lai, Y. J. Cheng, C. L Wang and <strong>C. S. Hsu<\/strong>, &#8220;Formation of Nanostructured Fullerene Interlayer through Accelerated Self-Assembly and Cross-Linking of Trichlorosilane Moieties Leading to Enhanced Efficiency of Photovoltaic Cells&#8221; Macromolecules, 46, 4781 (2013).<\/p>\n<p>247.\u00a0 J. T. Chen and <strong>C. S. Hsu<\/strong>, &#8220;Poly(2,3-diphenyl-1,4-phenylenevinylene) (DP-PPV) derivatives: Synthesis, properties, and their applications in polymer light-emitting diodes&#8221; Polymer, 54, 4045 (2013).<\/p>\n<p>248.\u00a0 H. H. Chang, C. E. Tsai, Y. Y. Lai, W. W. Liang, S. L. Hsu, <strong>C. S. Hsu<\/strong> and Y. J. Cheng, &#8220;A New Pentacyclic Indacenodiselenophene Arene and Its Donor\u2013Acceptor Copolymers for Solution-Processable Polymer Solar Cells and Transistors: Synthesis, Characterization, and Investigation of Alkyl\/Alkoxy Side-Chain Effect&#8221; Macromolecules, 46, 7715 (2013).<\/p>\n<p>249.\u00a0 T. H. Lee, K. Y. Wu, T. Y. Lin, J. S. Wu, C. L. Wang and <strong>C. S. Hsu<\/strong>, &#8220;Role of the Comonomeric Units in Reaching Linear Backbone, High Solid-State Order and Charge Mobilities in Heptacyclic Arene-Based Alternating Copolymers&#8221; Macromolecules 46, 7687 (2013).<\/p>\n<p>250.\u00a0 C. Y. Chang, L. Zuo, H. L. Yip. Y. Li, C. Z. Li, <strong>C. S. Hsu<\/strong>, Y. J. Cheng, H. Chen and A. K.-Y. Jen, &#8220;A Versatile Fluoro-Containing Low-Bandgap Polymer for Efficient Semitransparent and Tandem Polymer Solar Cells&#8221; Adv. Funct. Mater. 23, 5084 (2013).<\/p>\n<p>251.\u00a0 Y. H. Chao, J. S. Wu, C. E. Wu, J. F. Jheng, C. L. Wang and <strong>C. S. Hsu<\/strong>, &#8220;Solution-processed (Graphene Oxide)-(d\u00a0<sup>0<\/sup>\u00a0Transition Metal Oxide) Composite Anodic Buffer Layers toward High-performance and Durable Inverted Polymer Solar Cells&#8221; Adv. Energy. Mater. 3, 1279 (2013).<\/p>\n<p>252.\u00a0 K. S. Tan, M. K, Chuang, F. C. Chen and <strong>C. S. Hsu<\/strong>, &#8220;Solution-Processed Nanocomposites Containing Molybdenum Oxide and Gold Nanoparticles as Anode Buffer Layers in Plasmonic-Enhanced Organic Photovoltaic Devices&#8221; ACS Appl. Mater. Inter. 5, 12419 (2013).<\/p>\n<p>253.\u00a0 M. H. Liao, C. E. Tsai, Y. Y. Lai, F. Y. Cao, J. S. Wu, C. L. Wang, <strong>C. S. Hsu<\/strong>, I. Liau and Y. J. Cheng, &#8220;Morphological Stabilization by Supramolecular Perfluorophenyl-C<sub>60 <\/sub>Interactions Leading to Efficient and Thermally Stable Organic Photovoltaics&#8221; Adv. Funct. Mater. 24, 1418 (2014).<\/p>\n<p>254.\u00a0 M. K. Chuang, S. W. Lin, F. C. Chen, C. W. Chu and <strong>C. S. Hsu<\/strong>, &#8220;Gold nanoparticle-decorated graphene oxides for plasmonic-enhanced polymer photovoltaic devices&#8221; Nanoscale 6, 1573 (2014).<\/p>\n<p>255.\u00a0 W. T. Lin, Y. T. Lin, C. H. Chou, F. C. Chen and <strong>C. S. Hsu<\/strong>, &#8220;Organic solar cells comprising multiple-device stacked structures exhibiting complementary absorption behavior&#8221; Sol. Energy Mater. Sol. Cells 120, 724 (2014).<\/p>\n<p>256.\u00a0 T. H. Lee and<strong> C. S. Hsu<\/strong>, &#8220;Synthesis of fluorinated terphenyl liquid crystals with 3-propylcyclopentane end group&#8221; Liquid Crystals 41, 1235 (2014).<\/p>\n<p>257.\u00a0 Y. Y. Lai, Y. J. Cheng and <strong>C. S. Hsu<\/strong>, &#8220;Applications of functional fullerene materials in polymer solar cells&#8221;, Energy Environ. Sci. <strong>7<\/strong>, 1866 (2014).<\/p>\n<p>258.\u00a0 Y. H. Chao, J. F. Jheng, J. S. Wu, K. Y. Wu, H. H. Peng, M. C. Tsai, C. L. Wang, Y. N. Hsiao, C. L. Wang, C. Y. Lin and <strong>C. S. Hsu<\/strong>, &#8220;Porphyrin-Incorporated 2D D\u2013A Polymers with Over 8.5% Polymer Solar Cell Efficiency&#8221; Adv. Mater. 26, 5205 (2014).<\/p>\n<p>259.\u00a0 Y. T. Lin, C. H. Chou, F. C. Chen, C. W. Chu and <strong>C. S. Hsu<\/strong>, &#8220;Reduced optical loss in mechanically stacked multi-junction organic solar cells exhibiting complementary absorptions&#8221; Optics Express 22, A481 (2014).<\/p>\n<p>260.\u00a0 C. Y. Chang, L. Zuo, H. L. Yip, C. Z. Li, Y. Li, <strong>C. S. Hsu<\/strong>, Y. J. Cheng, H. Z. Chen and A. K. Y. Jen, &#8220;Highly Efficient Polymer Tandem Cells and Semitransparent Cells for Solar Energy&#8221; Adv. Energy Mater. 4, 1301645 (2014).<\/p>\n<p>261.\u00a0 J. Y. Chen, M. H. Yu, C. Y. Chang, Y. H. Chao, K. W. Sun and <strong>C. S. Hsu<\/strong>, &#8220;Enhanced Performance of Organic Thin Film Solar Cells Using Electrodes with Nanoimprinted Light-Diffraction and Light-Diffusion Structures&#8221; ACS Appl. Mater. Interfaces 6, 6164 (2014).<\/p>\n<p>262.\u00a0 J. S. Wu, J. F. Jheng, J. Y. Chang, Y. Y. Lai, K. Y. Wu, C. L. Wang and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis and morphological studies of a poly(5,6-difluorobenzo-2,1,3-thiadiazole-4,7-diyl- altquater chalcogeno- phene) opolymer with 7.3% polymer solar cell efficiency&#8221; Polymer Chemistry, 5, 6472 (2014).<\/p>\n<p>263.\u00a0 P. C. Jwo, Y. Y. Lai, C. E. Tsai, Y. Y. Lai, W. W. Liang, <strong>C. S. Hsu<\/strong> and Y. J. Cheng, &#8220;A New Ladder-Type Germanium-Bridged Dithienocarbazole Arene and Its Donor-Acceptor Conjugated Copolymers: Synthesis, Molecular Properties, and photovoltaic Applications&#8221; Macromolecules, 47, 7386 (2014).<\/p>\n<p>264.\u00a0 Y. Y. Lai, M. H. Liao, Y. T. Chen, F. Y. Cao, <strong>C. S. Hsu<\/strong> and Y. J. Cheng &#8220;Compact bis-adduct fullerenes and additive-assisted morphological optimization for efficient organic photovoltaics&#8221; ACS Applied materials &amp; Interfaces, 6, 20102 (2014).<\/p>\n<p>265.\u00a0 M. K. Chuang, F. C. Chen and <strong>C. S. Hsu<\/strong> &#8220;Gold Nanoparticle-Graphene Oxide Nanocomposites That Enhance the Device Performance of Polymer Solar Cells&#8221; J. of Nanomaterials, 736879 (2014).<\/p>\n<p>266.\u00a0 H. Wei, Y. H. Chao, C. Kang, C. Li, H. Lu, X. Gong, H. Dong, W. Hu, <strong>C. S. Hsu<\/strong> and Z. Bo &#8220;High-Efficiency Large-Bandgap Material for Polymer Solar Cells&#8221; Macromol. Rapid Commun., 36, 84 (2015).<\/p>\n<p>267.\u00a0 K. Y. Wu, C. C. Chiu, W. T. Chuang, C. L. Wang and <strong>C. S. Hsu<\/strong> &#8220;The backbone rigidity and its influence on the morphology and charge mobility of FBT based conjugated polymers&#8221; Polymer Chemistry, 6, 1309 (2015).<\/p>\n<p>268.\u00a0 Y. C. Wu, P. \u00a0Leowanawat,\u00a0H. J. Sun, B. E. Partridge, M. Peterca, R. Graf, H. W. Spiess, X. B. Zeng, G. Ungar, <strong>C. S. Hsu<\/strong>, P. A. Heiney and V. Percec &#8220;Complex Columnar Hexagonal Polymorphism in Supramolecular Assemblies of a Semifluorinated Electron-Accepting Naphthalene Bisimide&#8221; J. Am. Chem. Soc., 137, 807 (2015).<\/p>\n<p>269.\u00a0 T. H. Lee, J. T. Chen and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis of cyclopentyloxy terphenyl liquid crystals with negative dielectric anisotropy&#8221; Liquid Crystals, 42, 104 (2015).<\/p>\n<p>270.\u00a0 J. S. Wu, S. W. Cheng, Y. J. Cheng and <strong>C. S. Hsu<\/strong> &#8220;Donor\u2013acceptor conjugated polymers based on multifused ladder-type arenes for organic solar cells&#8221; Chem. Soc. Rev., 44, 1113 (2015).<\/p>\n<p>271.\u00a0 K. Y. Wu, T. Y. Wu, S. T. Chang, <strong>C. S. Hsu<\/strong> and C. L. Wang\u00a0&#8220;A Facile PDMS-Assisted Crystallization for the Crystal-Engineering of C-60 Single-Crystal Organic Field-Effect Transistors &#8221; Adv. Mater., 27, 4371 (2015).<\/p>\n<p>272.\u00a0 J. Yuan, Y. Zou, R. Chi, Y. H. Chao, Z. Wang, M. Ma, Y. He, Y. Li, A. Rindgen, W. Ma, D. Xiao, Z. Bo, X. Xu, L. Li and <strong>C. S. Hsu<\/strong>, &#8220;Incorporation of Fluorine onto Different Positions of Phenyl Substituted Benzo[1,2-b:4,5-b &#8216;]dithiophene Unit: Influence on Photovoltaic Properties&#8221; Macromolecules, 48, 4347 (2015).<\/p>\n<p>273.\u00a0 R. Cui, Y. Zou, L. Xiao, <strong>C. S. Hsu<\/strong>, M. L. Keshtov, D. Godovsky and Y. Li, &#8220;Efficient solar cells based on a new polymer from fluorinated benzothiadiazole and alkylthienyl substituted thieno[2,3-f]benzofuran&#8221; Dyes and Pigments, 116, 139 (2015).<\/p>\n<p>274.\u00a0 S. W. Cheng, C. E. Tsai, W. W. Liang, Y. L. Chen, F. Y. Cao, <strong>C. S. Hsu<\/strong> and Y. J. Cheng, &#8221; Angular-Shaped 4,9-Dialkylnaphthodithiophene-Based Donor-Acceptor Copolymers for Efficient Polymer Solar Cells and High-Mobility Field-Effect Transistors&#8221; Macromolecules, 48, 2030 (2015).<\/p>\n<p>275.\u00a0 C. E. Tsai, M. H. Liao, Y. L . Chen, S. W. Cheng, Y. Y. Lai, Y. J. Cheng and <strong>C. S. Hsu<\/strong>,\u00a0 &#8220;Triarylamine-based crosslinked hole-transporting material with an ionic dopant for high-performance PEDOT:PSS-free polymer solar cells&#8221; J. Mater. Chem. C, 3, 6158 (2015).<\/p>\n<p>276.\u00a0 Y. T. Chen, T. W. Huang, C. L. Wang and <strong>C. S. Hsu<\/strong>, &#8220;Influences of the backbone randomness on the properties, morphology and performances of the fluorinated benzoselenadiazole-benzothiadiazole based random copolymers&#8221; Polymer Chemistry, 6, 3728 (2015).<\/p>\n<p>277.\u00a0 C. F. Hung, J. Y Chang, S. H. Huang, K. Y. Wu, J. F. Jheng, W. T. Chuang, <strong>C. S. Hsu<\/strong> and C. L. Wang, &#8220;Polymorphisms and morphological studies of a difluorobenzothiadiazole conjugated copolymer with 7.8% polymer solar cell efficiency&#8221; J. Mater. Chem. A, 7, 3968 (2015).<\/p>\n<p>278.\u00a0 Y. H. Chao, Y. Y. Huang, J. Y. Chang, S. H. Peng, W. Y. Tu, Y. J. Cheng, J. Hou and <strong>C. S. Hsu<\/strong>, &#8220;A crosslinked fullerene matrix doped with an ionic fullerene as a cathodic buffer layer toward highperformance and thermally stable polymer and organic metallohalide perovskite solar cells&#8221; J. Mater. Chem. A, 3, 20382 (2015).<\/p>\n<p>279.\u00a0 S. W. Cheng, D. Y. Chiou, C. E. Tsai,\u00a0W. W. Liang, Y. Y. Lai, J. Y. Hsu, <strong>C. S. Hsu<\/strong>, I. Osaka,\u00a0K. Takimiya and Y. J. Cheng, &#8220;Angular-Shaped 4,9-Dialkyl &#8211; and -Naphthodithiophene-Based Donor-Acceptor Copolymers: Investigation of Isomeric Structural Effects on Molecular Properties and Performance of Field-Effect Transistors and Photovoltaics&#8221; Adv. Funct. Mater. 25, 6131 (2015).<\/p>\n<p>280.\u00a0 J. Mai, T. K. Lau, J. Li, S. H. Peng, <strong>C. S. Hsu<\/strong>, U. S. Jeng, J. Zeng, N. Zhao, X. Xiao and X. Lu, &#8220;Understanding Morphology Compatibility for High-Performance Ternary Organic Solar Cells&#8221; Chem. Mater. 28, 6186 (2016).<\/p>\n<p>281.\u00a0 C. E. Tsai, R. H. Yu, F. J. Lin, Y. Y. Lai, J. Y. Hsu, S. W. Cheng, <strong>C. S. Hsu<\/strong> and Y. J. Cheng, &#8221; Synthesis of a 4,9-Didodecyl Angular-Shaped Naphthodiselenophene Building Block To Achieve High-Mobility Transistors&#8221; Chem. Mater. 28, 5121 (2016).<\/p>\n<p>282.\u00a0 Y. Y. Huang, G. Ganesh, Y. H. Chao and <strong>C. S. Hsu<\/strong>, &#8220;Rejuvenation of perovskite solar cells&#8221; J. of Mater. Chem. C, 4, 7595 (2016).<\/p>\n<p>283.\u00a0 Y. C. Pao, C. T. Yang, Y. Y. Lai, W. C. Huang, <strong>C. S. Hsu<\/strong> and Y. J. Cheng, &#8220;Synthesis and field-effect transistor properties of a diseleno[3,2-b:2 &#8216;,3 &#8216;-d]silole-based donor-acceptor copolymer: investigation of chalcogen effect&#8221; Polymer Chemistry, 7, 4654 (2016).<\/p>\n<p>284.\u00a0 W. L. Liau, T. H. Lee, J. T. Chen and <strong>C. S. Hsu<\/strong>, &#8220;The synthesis of anthradithiophene-based liquid crystals and their applications in organic thin film transistors&#8221; J. of Mater. Chem. C, 4, 2284 (2016).<\/p>\n<p>285.\u00a0 M. Li, Y. H. Chao, T. Kang, Z. K. Wang, Y. G. Yang, S. L. Feng, Y. Hu, X. Y. Gao, L. S. Liao and <strong>C. S. Hsu<\/strong>, &#8220;Enhanced crystallization and stability of perovskites by a cross-linkable fullerene for high-performance solar cells&#8221; J. of Mater. Chem. A, 4, 15088 (2016).<\/p>\n<p>286.\u00a0 C. F. Huang, S. H. Huang, C. T. Hsieh, Y. H. Chao, C. H. Li, S. L. Wu, Y. F. Huang, C. Y. Hong, <strong>C. S. Hsu<\/strong>, W. T. Chuang and C. L. Wang, &#8220;Stepwise Structural Evolution of a DTS-F2BT Oligomer and Influence of Structural of Structural Disorder on Organic Field Effect Transistors and Organic Photovoltaic Performance&#8221; Chem. Mater. 28, 8980 (2016).<\/p>\n<p>287.\u00a0 M. S. Ho, B. E. Partridge, H. J. Sun, D. Sahoo, P. Leowanawat, M. Peterca, R. Graf, H. W. Spiess, X. Zeng, G. Ungar, P. A. Heiney, <strong>C. S. Hsu<\/strong> and V. Percec, &#8220;Screening Libraries of Semifluorinated Arylene Bisimides to Discover and Predict and Predict Thermodynamically Controlled Helical Crystallization&#8221; ACS Comb. Sci. 18, 723 (2016).<\/p>\n<p>288.\u00a0 W. L. Liau, Y. J. Su, H. F. Tseng, J. T Chen and <strong>C. S. Hsu<\/strong> &#8220;Synthesis and Characterization of Liquid Crystal Molecules Based on Thieno [3,2-b] Thiophene and Their Application in Organic Field-Effect Transistors&#8221; Liquid Crystals, 44, 557 (2017).<\/p>\n<p>289.\u00a0 J. Zhang, C. Yang, R. Zhang, R. Chen, Z. Zhang, W. Zhang, S. H. Peng, X. Chen, G. Liu, <strong>C. S. Hsu<\/strong> and C. S. Lee, &#8220;Biocompatible D-A Semiconducting Polymer Nanoparticle with Light-Harvesting Unit for Highly Effective Photoacoustic Imaging Guided Photothermal Therapy&#8221; Adv. Funct. Mater., 27, 1605094 (2017).<\/p>\n<p>290.\u00a0\u00a0\u00a0 S. H. Peng, T. W. Huang, G. Gollavelli and <strong>C. S. Hsu<\/strong>, &#8220;Thiophene and diketopyrrolopyrrole based conjugated polymers as efficient alternatives for spiro-OMeTAD in perovskite solar cells as hole transporting layers&#8221; J. of Mater. Chem. C, 5, 5193 (2017).<\/p>\n<p>291.\u00a0\u00a0\u00a0 S. H. Peng, W. Y. Tu, G. Gollavelli and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis of diketopyrrolopyrrole based conjugated polymers containing thieno[3,2-b] thiophene flanking groups for high performance thin film transistors&#8221; Polym. Chem. , 8, 3431 (2017).<\/p>\n<p>292.\u00a0\u00a0\u00a0 J. Mai, H. Lu, T. K. Lau, S. H. Peng, <strong>C. S. Hsu<\/strong>, W. Hua, N. Zhao, X. Xiao and X. H. Lu, &#8220;High efficiency ternary organic solar cell with morphology-compatible polyemrs&#8221; J. of Mater. Chem. A, 5, 11739 (2017).<\/p>\n<p>293.\u00a0\u00a0\u00a0 F. J. Lin, W. T. Chuang, C. L. Wang, Q. Wang, H. Liu, <strong>C. S. Hsu<\/strong> and L. Jiang, &#8220;Directional Solution Coating by the Chinese Brush: A Facile Apporach to Improving Molecular Alignment for High-Performance Polymer TFTs&#8221; Adv. Mater., 29, 1606987 (2017).<\/p>\n<p>294.\u00a0\u00a0\u00a0 S. L. Chang, F. Y. Cao, W. C. Huang, P. K. Huang, <strong>C. S. Hsu<\/strong> and Y. J. Cheng, &#8220;Highly efficient Inverted D:A(1):A2) Ternary Blend Organic Photovoltaics Combining a Ladder-type Non-Fullerene Acceptor and a Fullerene Acceptor&#8221; ACS Appl. Mater. Interfaces, 9, 24797 (2017).<\/p>\n<p>295.\u00a0\u00a0\u00a0 T. Kang, C. M. Tsai, Y. H. Jiang, G. Gollavelli, N. Mohanta, E.W.G Diau and <strong>C. S. Hsu<\/strong>, &#8220;Interfacial Engineering with Cross-Linkable Fullerene Derivatives for High-Performance Perovskite Solar Cells&#8221; ACS Appl. Mater. Interfaces, 9, 38530 (2017).<\/p>\n<p>296.\u00a0\u00a0\u00a0 Y. T. Hsiao, C. H. Li, S. L. Chang, S. Heo, K. Tajima, Y. J. Cheng and <strong>C. S. Hsu<\/strong>, &#8221; Haptacyclic Carbazole-Based Ladder-Type Nonfullerene Acceptor with Side-Chain Optimization for Efficient Organic Photovoltaics&#8221; ACS Appl. Mater. Interfaces, 9, 42035 (2017).<\/p>\n<p>297.\u00a0\u00a0\u00a0 K. E. Hung, C. E. Tsai, S. L. Chang, Y. Y. Lai, U. S. Jeng, F. Y. Cao, <strong>C. S. Hsu<\/strong>, C. J. Su and Y. J. Cheng, &#8221; Bispentafluorophenyl-Containing Additive: Enhancing Efficiency and Morphological Stability of Polymer Solar Cells via Hand-Grabbing-Like Supramolecular Pentafluorophenyl\u2013Fullerene Interactions&#8221; ACS Appl. Mater. Interfaces, 9, 43861 (2017).<\/p>\n<p>298.\u00a0\u00a0\u00a0 M. Li, Z. K. Wang, T. Kang, Y. Yang, X. Gao, <strong>C. S. Hsu<\/strong>, Y. Li and L. S. Liao, &#8220;Graphdiyne-modified cross-linkable fullerene as an efficient electrontransporting layer in organometal halide perovskite solar cells&#8221; Nano Energy, 43, 47 (2018).<\/p>\n<p>299.\u00a0\u00a0\u00a0 F. J. Lin, S. D. Lin, C. H. Chin, W. T. Chuang and <strong>C. S. Hsu<\/strong>, &#8221; Novel conjugated polymers based on bis-dithieno[3,2-<em>b<\/em>;2\u2032,3\u2032-<em>d<\/em>]pyrrole vinylene donor and diketopyrrolopyrrole acceptor: side chain engineering in organic field effect transistors &#8221; Polym. Chem. , 9, 28 (2018).<\/p>\n<p>300.\u00a0\u00a0\u00a0 W. C. Wang, T. T. Yeh, W. L. Liau, J. T. Chen and <strong>C. S. Hsu<\/strong>, &#8221; Anthradithiophene-based liquid crystal molecules: High carrier mobilities enhanced by rubbed polyimides for the applicaiotn in organic field-effect transistors&#8221; Organic Electronics, 57, 82 (2018).<\/p>\n<p>301.\u00a0\u00a0\u00a0 S. L. Chang, F. Y. Cao, W. C. Huang, P. K. Huang, K. H. Huang,<strong> C. S. Hsu<\/strong> and Y. J. Cheng, &#8221; New Thieno[3,2-b]thiophene-Based Acceptor: Tuning Acceptor Strength of Ladder-Type N-Type Materials to Simultaneously Achieve Enhances V-OC and J(SC) of Nonfullerene Solar Cells&#8221; ACS Energy Letters, 3, 1722 (2018).<\/p>\n<p>302.\u00a0\u00a0\u00a0 C. C. Chang, J. H. Tao, C. E. Tsai, Y. J. Cheng and <strong>C. S. Hsu<\/strong>, &#8220;Cross-linked triarylamine-Based Hole-Transporting Layer for Solution-Processed PEDOT:PSS-Free Inverted Perovskite Solar Cells &#8221; ACS Appl. Mater. Interfaces, 10, 21466 (2018).<\/p>\n<p>303.\u00a0\u00a0\u00a0 F. J. Wang, K. Nakano, H. Yoshida, K. Hashimoto, H. Segawa, <strong>C. S. Hsu<\/strong> and K. Tajima, &#8221; Effects of end-on oriented polymer chains at the donor\/acceptor interface in organic solar cells&#8221; J. of Mater. Chem. A, 6, 22889 (2018).<\/p>\n<p>304.\u00a0\u00a0\u00a0 C. H. Li, C. C. Chang, Y. H. Hsiao, S. H. Peng, Y. J. Su, S. Heo, K. Tajima, M. C. Tsai, C. Y. Lin and <strong>C. S. Hsu<\/strong>, &#8220;Porphyrin Containing Polymer as a Superior Blue Light Absorbing Additive to Afford High Jsc Ternary Solar Cells&#8221; ACS Appl. Mater. Interfaces, 11, 1156 (2019).<\/p>\n<p>305.\u00a0\u00a0\u00a0 Y. M. Yeh, C. H. Huang, S. H. Peng, C. C. Chang and <strong>C. S. Hsu<\/strong>, &#8220;Synthesis of Novel Conjugated Polymers Based on Benzo[1,2-d:4,5-d\u2019]-bis(1,2,3)triazole) for Applications in Organic Field-Effect Transistors&#8221; Polymer Chemistry, 10, 1471 (2019).<\/p>\n<p>306.\u00a0\u00a0\u00a0 S. T. Wu, C. C. Weng, B. R. Li and <strong>C. S. Hsu<\/strong>, &#8220;Fabrication of magnetic liquid marbles using superhydrophobic atmospheric pressure plasma jet-formed fluorinated silica nanocomposites&#8221; J. Mater. Sci. , 54, 10179 (2019).<\/p>\n<p>307.\u00a0\u00a0\u00a0 M. Li, Y. G. Yang, Z. K. Wang, T. Kang, Q. Wang, SH. Turren-Cruz, X. Y. Gao, <strong>C. S. Hsu<\/strong>, L. S. Liao, A. Abate, &#8220;Perovskite Grains Embraced in a Soft Fullerene Network Make Highly Efficient Flexible Solar Cells with Superior Mechanical Stability&#8221; Adv. Mater. , 31, 1901519 (2019).<\/p>\n<p>308.\u00a0\u00a0\u00a0 T. W. Chen, Y. T. Hsiao, Y. W. Lin, C. C. Chang, W. T. Chuang, Y. Li and <strong>C. S. Hsu<\/strong>, &#8220;Fluorinated heptacyclic carrbazole-based laddertype acceptors with aliphatic side chains for efficient fullerene-free organic solar cells&#8221; Mater. Chem. Front., 3, 829 (2019).<\/p>\n<p>309.\u00a0\u00a0\u00a0 T. W. Chen, C. C. Chang, Y. T. Hsiao, C. Chan, L. Hong, L. Zhong, W. T. Chuang, J. Hou, Y. Li and <strong>C. S. Hsu<\/strong>, &#8220;Single-Junction Organic Solar Cell Containing Fluorinated Heptacyclic Carbazole-Based Ladder-Type Acceptor Affords over 13% Efficiency with Solution-processed Cross-linkable Fullernee as Interfacial Layer&#8221; ACS Appl. Mater. Interfaces, 11, 31069 (2019).<\/p>\n<p>310.\u00a0\u00a0\u00a0 S. L. Chang, K. E. Hung, F. Y. Cao, K. H. Huang, <strong>C. S. Hsu<\/strong>, C. Y. Liao, C. H. Lee and Y. J. Cheng, &#8220;Isomerically Pure Benzothiophene-Incorporated Acceptor: Achieving Improved\u00a0V<sub>oc<\/sub>\u00a0and\u00a0J<sub>sc<\/sub>\u00a0of Nonfullerene Organic Solar Cells via End Group Manipulation&#8221; ACS Appl. Mater. Interfaces, 11, 33179 (2019).<\/p>\n<p>311.\u00a0\u00a0\u00a0 S. T. Wu, C. Y. Huang, C. C. Weng, C. C. Chang, B. R. Li and <strong>C. S. Hsu<\/strong>, &#8220;Rapid Prototyping of an Open-Surface Microfluidic Platform Using Wettability-Patterned Surfaces Prepared by an Atmospheric-Pressure Plasma Jet&#8221; ACS Omega, 4, 16292 (2019).<\/p>\n<p>312.\u00a0\u00a0\u00a0 T. W. Chen, K. L. Peng, Y. W. Lin, Y. J. Su, K. J. Ma, L. Hong, C. C. Chang, J. Hou and <strong>C. S. Hsu<\/strong>, &#8220;A Chlorinated Nonacyclic Carbazole-Based Acceptor Affords over 15% Efficiency in Organic Solar Cells&#8221; J. of Mater. Chem. A, <strong>8<\/strong>, 1131 (2020).<\/p>\n<p>313.\u00a0\u00a0\u00a0 Y. M. Yeh, M. Ueda and <strong>C. S. Hsu<\/strong>, &#8220;Alkaline-developable positive-type photosensitive polyimide with high mechanical strength and high resolution based on chain extendable poly(amic acid), thermally degradable cross-linker and photoacid generator&#8221; J. Polym. Sci. A Polym. Chem., 58, 948 (2020).<\/p>\n<p>314.\u00a0\u00a0\u00a0 W. C. Wang, S. Y. Chen, Y. W. Yang, <strong>C. S. Hsu<\/strong> and K. Tajima, &#8220;Face-on reorientation of pi-conjugated polymers in thin films by surface-segregated monolayers&#8221; J. Mater. Chem. A, 8, 6268 (2020).<\/p>\n<p>315.\u00a0\u00a0\u00a0 S. L. Chang, F. Y. Cao, K. S. Huang, W. L. Lee, M. H. Lee, <strong>C. S. Hsu<\/strong> and Y. J. Cheng, &#8220;2-Dimensional cross-shaped tetrathienonaphthalene-based ladder-type acceptor for high-efficiency organic solar cells&#8221; J. of Mater. Chem. A, 8, 12141 (2020).<\/p>\n<p>316.\u00a0\u00a0\u00a0 T. W. Chen, J. Y. Yu, Y. W. Lin, S. H. Peng, S. H. Wu, Y. J. Su, V. K. Karapala, L. Hong, H. Yao, J. Hou and <strong>C. S. Hsu<\/strong>, &#8220;Chlorinated Carbon-Bridged and Silicon-Bridged Carbazole-Based Non-fullerene Acceptors Manifest Synergistic Enhancement in Ternary Organic Solar Cell with Efficiency over 15%&#8221; Solar RRL, 4, 2000357 (2020).<\/p>\n<p>317.\u00a0\u00a0\u00a0 W. C. Wang, Y. W. Lin, S. H. Peng, C. T. Chuang, C. C. Chang and <strong>C. S. Hsu<\/strong>, &#8221; A Strategy of Designing Near-Infrared Porphyrin-based Non-fullerene Acceptors for Panchromatic Organic Solar Cells&#8221; Organic Electronics, 86, 105899 (2020).<\/p>\n<p>318.\u00a0\u00a0\u00a0 Y. M. Yeh, V. K. Karapala, M. Ueda and <strong>C. S. Hsu<\/strong>, &#8220;Low -Temperature -Curable and Positive -Type Photosensitive Polyimide with High Mechanical Strength, High Resolution and Good Pot -Life Based on Chain Extendable Poly(Amic Acid), Thermal Degradable Crosslinker, Chain Extender, Thermal Base Generator and Photoacid Generator\u201d J. Photopolym. Sci. Technol., 6, 623 (2020).<\/p>\n<p>319.\u00a0\u00a0\u00a0 V. K. Karapala, T. W. Chen, K. J. Ma, P. L. Lu, Y. J. Su, W. D. Fu, H. M. Shih, S. J. Lu, T. Y. Lee, C. F. Chang, J. T. Chen and <strong>C. S. Hsu<\/strong>, &#8220;Exploring Ternary Organic Solar Cells for the Improved Efficiency of 16.5% with the Compatible Nonacyclic Carbazole-Based Nonfullerene Acceptors as the Third Componen&#8221; ACS Appl. Energy Maters, 4, 2847 (2021).<\/p>\n<p>320.\u00a0\u00a0\u00a0 T. W. Chen, V. K. Karapala, J. T. Chen and <strong>C. S. Hsu<\/strong>, &#8221; Recent advances of carbazole-based nonfullerene acceptors: Molecular design, optoelectronic properties, and photovoltaic performance in organic solar cells&#8221; J. Chin. Chem. Soc., <strong>68, <\/strong>1186 (2021).<\/p>\n<p>321.\u00a0\u00a0\u00a0 Y. M. Yeh, V. K. Karapala, M. Ueda and\u00a0<strong>C. S. Hsu<\/strong>,\u00a0&#8220;Low-temperature curable, alkaline-developable, and negative-type photosensitive polyimide with high resolution and mechanical properties based on chain extendable poly(amic acid) and photo-base generator&#8221; Polym. Adv. Technol., 32, 663 (2021).<\/p>\n<p>322.\u00a0\u00a0\u00a0 L. Hong, H. F. Yao, Y. Cui,\u00a0R. N. Yu, Y. W. Lin, T. W. Chen, Y. Xu, J. Z. Qin, <strong>C. S. Hsu<\/strong>, Z. Y. Ge and J. H. Hou, &#8220;Simultaneous Improvement of Efficiency and Stability of Organic Photovoltaic Cells by using a Cross-Linkable Fullerene Derivative&#8221;, Small, 17, 2101733 (2021).<\/p>\n<p>323.\u00a0\u00a0\u00a0 Y. J. Su, S. C. Huang, T.W. Chen, L. C. Chueh, Y. Chi, L. Hong, H. F. Yao, J. H. Hou, J. T. Chen and <strong>C. S. Hsu<\/strong>, &#8220;Elucidating End-Group Modifications of Carbazole-Based Nonfullerene Acceptors in Indoor Applications for Achieving a PCE of over 20%&#8221;, ACS Appl. Mater. Interfaces, 13, 26247 (2021).<\/p>\n<p>324.\u00a0\u00a0\u00a0 C. W. Chang, H. H. Hsu, <strong>C. S. Hsu<\/strong> and J. T. Chen, &#8220;Achieving area-selective atomic layer deposition with fluorinated self-assembled monolayers&#8221;, J. Mater.Chem. C, 41, 145898 (2021).<\/p>\n<p>325.\u00a0\u00a0\u00a0 Y. J. Su, H. Nie, S. C. Huang, Y. H. Huang, T. W. Chen, K. K. Hsu, T. Y. Lee, H. M. Shih, C. W. Ko and <strong>C. S. Hsu<\/strong>, &#8220;Green-Solvent-Processable Organic Photovoltaics with High Performances Enabled by Asymmetric Non-Fullerene Acceptors&#8221;, ACS Appl. Mater. Interfaces, 13, 59043 \u00a0(2021).<\/p>\n<p>326.\u00a0\u00a0\u00a0 HZ. Gao, XQ. Wei, RN Yu, F. Y. Cao, YS Gong, ZW Ma, Y. J. Cheng, <strong>C. S. Hsu<\/strong> and ZA Tan, &#8220;Coordination-Induced Defects Elimination of SnO2 Nanoparticles via a Small Electrolyte Molecule for High-Performance Inverted Organic Solar Cells&#8221;, Adv. Opt. Mater., 10, 2102031 (2022).<\/p>\n<p>327.\u00a0\u00a0\u00a0 ZW Ma, YM Dong, Y. J. Su, RN Yu, HZ Gao, YS Gong, ZY Lee, CH Yang, <strong>C. S. Hsu<\/strong> and ZA Tan, &#8220;Morphological Stabilization in Organic Solar Cells via a Fluorene-Based Crosslinker for Enhanced Efficiency and Thermal Stability&#8221;, ACS Appl. Mater. Interfaces, 14, 1187 (2022).<\/p>\n<p>328.\u00a0\u00a0\u00a0 YS Gong, RN Yu, HZ Gao, ZW Ma, YM Dong, Y. J. Su, T. W. Chen, <strong>C. S. Hsu<\/strong> and ZA Tan, &#8221; Improving charge transport and reducing non-radiative energy loss via a nonacyclic carbazole-based third component for over 18% efficiency polymer solar cells &#8220;, J of Mater. Chem. A, 10, 7090 (2022).<\/p>\n<p>329.\u00a0\u00a0\u00a0 K. E. Hung, Y. S. Lin, Y. J. Xue, H. R. Yang, Y. Y. Lai, J. W. Chang, C. J. Su, A. C. Su, <strong>C. S. Hsu<\/strong>, U. S. Jeng and Y. J. Cheng, &#8220;Non-Volatile Perfluorophenyl-Based Additive for Enhanced Efficiency and Thermal Stability of Nonfullerene Organic Solar Cells via Supramolecular Fluorinated Interactions&#8221;, Adv. Energy Mater., 12, 2103702 (2022).<\/p>\n<p>330.\u00a0\u00a0\u00a0 W. C. Wang, K. Nakano, D. Hashizume, <strong>C. S. Hsu<\/strong> and K. Tajima, &#8220;Tuning Molecular Conformations to Enhance Spontaneous Orientation Polarization in Organic Thin Films&#8221;, ACS Appl. Mater. Interfaces, 14, 18773-18781 (2022).<\/p>\n<p>331.\u00a0\u00a0\u00a0 MR Busireddy, T. W. Chen, S. C. Huang, H. B. Nie, Y. J. Su, C. T. Chuang, P. J. Kuo, J. T. Chen and <strong>C. S. Hsu<\/strong>, &#8220;Fine Tuning Alkyl Substituents on Dithienoquinoxaline-Based Wide-Bandgap Polymer Donors for Organic Photovoltaics&#8221;, ACS Appl. Mater. Interfaces, 14, 22353 (2022).<\/p>\n<p>332.\u00a0\u00a0\u00a0 HB Nie, S. C. Huang, C. Y. Lai, MR Busireddy, Y. J. Su, T. W. Chen, P. J. Kuo, J. T. Chen and<strong> C. S. Hsu<\/strong>, &#8220;Water\/Alcohol-Soluble Conjugated Polymers Based on Cyclopentadithiophene and Fluorene as Cathode Interlayers Elevate the Stability and Efficiency in Organic Solar Cells &#8220;, <em>ACS<\/em>\u00a0Appl. Energy Mater., 5, 9495 (2022).<\/p>\n<p>333.\u00a0\u00a0\u00a0 MR Busireddy, T. W. Chen, S. C. Huang, Y. J. Su, Y. M. Wang, W. T. Chuang, J. T. Chen and <strong>C. S. Hsu<\/strong>, &#8220;PBDB-T-Based Binary-OSCs Achieving over 15.83% Efficiency via End-Group Functionalization and Alkyl-Chain Engineering of Quinoxaline-Containing Non-Fullerene Acceptors&#8221;, <em>ACS<\/em>\u00a0Appl. Mater. Interfaces, 14, 41264 (2022).<\/p>\n<p>334.\u00a0\u00a0\u00a0 S. C. Huang, MR Busireddy, H. F. Chang, I. C. Pan, C. H. Ho, C. W. Ko, Y. W. Tsai, J. M. Lin, J. T. Chen and <strong>C. S. Hsu<\/strong>, &#8220;Achieving High-Performance Organic Photovoltaics by Morphology Optimization of Active Layers Using Fluorene-Based Solid Additives &#8220;, Solar RRL, 6, 2200805 (2022).<\/p>\n<p>335.\u00a0\u00a0\u00a0 Y. J. Su, S. H. Wu, S. C. Huang, HB Nie, T. W. Chen, J. T. Chen and <strong>C. S. Hsu<\/strong>, &#8220;Extended Conjugation and End-Group Modification of Silicon-Bridged Carbazole-Based Non-Fullerene Acceptors in Indoor Organic Photovoltaics&#8221;, ACS Appl. Energy Mater.,\u00a05, 13851 (2022).<\/p>\n<p>336.\u00a0\u00a0\u00a0 HB Nie, MR Busireddy, H. M. Shih, C. W. Ko, J. T. Chen, C. C. Chang and <strong>C. S. Hsu<\/strong>, &#8220;High-Performance Inverted Organic Solar Cells via the Incorporation of Thickness-Insensitive and Low-Temperature-Annealed Non-Conjugated Polymers as Electron Transport Materials&#8221;, <em>ACS<\/em>\u00a0Appl. Mater. Interfaces,\u00a015, 1718 (2023).<\/p>\n<p>337.\u00a0\u00a0\u00a0 W. C. Wang, K. Nakano, <strong>C. S. Hsu<\/strong> and K. Tajima, &#8220;Synthesis of 2,5,8-Tris(1-phenyl-1H-benzo[d]imidazol-2-yl)benzo[1,2-b:3,4-b?:5,6-b?] Trithiophenes and Their Spontaneous Orientation Polarization in Thin Films&#8221;, <em>ACS<\/em>\u00a0Appl. Mater. Interfaces,\u00a016, 20294 (2023).<\/p>\n<p>338.\u00a0\u00a0\u00a0 C. C. Wei, T. H. Wu, J. W. Huang, B. L. Young, W. B. Jian, Y. L. Lin, J. T. Chen, <strong>C. S. Hsu<\/strong>, Y. R. Ma and K. Tsukagoshi, &#8220;Nanoparticulate films of WO3 and MoO3 composites for enhancing UV light electrochromic transmittance variation and energy storage applications&#8221;, <em>Electrochimica Acta<\/em>,\u00a0442, 141897 (2023).<\/p>\n<p>339.\u00a0\u00a0\u00a0 C. W. Chang, Y. H. Tseng, <strong>C. S. Hsu<\/strong> and J. T. Chen, &#8220;Area-Selective Atomic Layer Deposition on Metal\/Dielectric Patterns: Amphiphobic Coating, Vaporizable Inhibitors, and Regenerative Processing&#8221;, <em>ACS<\/em>\u00a0Appl. Mater. Interfaces,\u00a015, 28817 (2023).<\/p>\n<p>340.\u00a0\u00a0\u00a0 MR Busireddy, S. C. Huang, Y. J. Su, Z. Y. Lee, C. H. Wang, J. T. Chen and<strong> C. S. Hsu<\/strong>, &#8220;Eco-Friendly Solvent-Processed Dithienosilicon-Bridged Carbazole-Based Small-Molecule Acceptors Achieved over 25.7% PCE in Ternary Devices under Indoor Conditions &#8220;, <em>ACS<\/em>\u00a0Appl. Mater. Interfaces, 15, 24658 (2023).<\/p>\n<p>341.\u00a0\u00a0\u00a0 K Gugujonovic, F. Mayr, B. Hailegnaw, S. Poellner, R. Zahrhuber, A. Planer, C. H. Wang, <strong>C. S. Hsu<\/strong>, and MC Scharber, &#8220;c-PCBSD, a cross-linked fullerene derivative, as a cathodic interlayer in wide-band gap perovskite solar cells &#8220;, <em>Monatshefte Fur Chemie<\/em>,\u00a0 (2023).<\/p>\n<p>342.\u00a0\u00a0\u00a0 W. C. Wang, K. Nakano , Y. Tanaka, K. Kurihara, H. Ishii, K. Adachi, D. Hashizume, <strong>C. S. Hsu<\/strong>, and K. Tajima, &#8220;Stable spontaneous orientation polarization by widening the optical band gap with 1,3,5,7-tetrakis(1-phenyl-1H-benzo[d]imidazol-2-yl)adamantane&#8221;, J of Mater. Chem. A, 11, 13039 (2023).<\/p>\n<p>343.\u00a0\u00a0\u00a0 Y. J. Xue, Z. Y. Lai, H. C. Lu, J. C. Hong,\u00a0C. L. Tsai ,C. L. Huang, K. H. Huang, C. F. Lu, Y. Y. Lai, <strong>C. S. Hsu<\/strong>, J. M. Lin, J. W. Chang, S. Y. Chien, G. H. Lee, U. S. Jeng, Y. J.\u00a0Cheng, &#8221; Unraveling the Structure-Property-Performance Relationships of Fused-Ring Nonfullerene Acceptors: Toward a C-Shaped\u00a0ortho-Benzodipyrrole-Based Acceptor for Highly Efficient Organic Photovoltaics&#8221;, J. Am. Chem. Soc., 146, 833 (2023).<\/p>\n<p>344.\u00a0\u00a0\u00a0 \u00a0C. H. Wang, MR Busireddy, S.C. Huang, HB Nie, Y.S. Liu, B.Y. Lai, L.H. Meng, W.T. Chuang, MC Scharber, J.T. Chen and <strong>C.S. Hsu<\/strong>, &#8221; Phenoxy Group-Containing Asymmetric Non-Fullerene Acceptors Achieved Higher\u00a0V<sub>OC<\/sub>\u00a0over 1.0 V through Alkoxy Side-Chain Engineering for Organic Solar Cells &#8220;, <em>ACS<\/em>\u00a0Appl. Mater. Interfaces, 15, 58683(2023).<\/p>\n<p>345.\u00a0\u00a0\u00a0 Y. H. Lee, J. W. Lin, Y. C. Huang, Y. J. Huang, MR Busireddy, J. T. Chen and<strong> C. S. Hsu<\/strong>, &#8221; High Thermally Stable Anthracene-Based Polyimides with Low Dielectric Constants and Dissipation Factors &#8220;, ACS Appl. Polym. Mater., 5, 10196, 2024.<\/p>\n<p>346.\u00a0\u00a0\u00a0 Y. J. Huang, J. W. Lin, Y. H. Lee, MR Busireddy, J. T. Chen and <strong>C. S. Hsu<\/strong>, &#8221; Monomer ratio-controlled polyimides with enhanced dielectric properties and thermal stabilities through crosslinking network &#8220;, J.\u00a0Polym.\u00a0Sci., 62, 1145(2024).<\/p>\n<p>347.\u00a0\u00a0\u00a0 W. C. Ke, J. W. Lin, MR Busireddy, Y. H. Lee, J. T. Chen and <strong>C. S. Hsu<\/strong>, &#8220;Enhancing the mechanical and dielectric properties of high thermally stable polyimides via a crosslinkable bicyclo[2.2.2] oct-7-ene-2,3,5,6-tetracarboxylic dianhydride monomer &#8220;, Polymer, 290, 126495, 2024.<\/p>\n<p>348.\u00a0\u00a0\u00a0 J. W. Lin, Y. J. Huang, MR Busireddy, J. T. Chen and <strong>C. S. Hsu<\/strong>, &#8221; Colorless Poly(amide-imide)s with Low Dielectric Constants and Enhanced Mechanical Properties through Tri-Armed Cross-Linkers &#8220;, ACS Appl. Polym. Mater., 6, 1294, 2024.<\/p>\n<p>349.\u00a0\u00a0\u00a0 JB Zhao, ZH Su, J. Pascual, HZ Wu, HB Wang, MH Aldamasy, ZJ Zhou, CY Wang, GX Li, Z Li, CY Wang, GX Li, Z Li, XY Gao, <strong>C. S. Hsu<\/strong> and M Li, &#8221; Suppressed Defects by Functional Thermally Cross-Linked Fullerene for High-Efficiency Tin-Lead Perovskite Solar Cells &#8220;, Adv. Mater., 36, 2406246, 2024.<\/p>\n<p>350.\u00a0\u00a0\u00a0 J. W. Lin, T. C. Chao, MR Busireddy, J. T. Chen and <strong>C. S. Hsu<\/strong>, &#8220;Green Approaches in Manufacturing Polyimides: From Eugenol-Based Monomers to Cross-Linked Polyimides with Low Dielectric Properties Utilizing \u03b3-Valerolactone as the Solvent&#8221;, \u00a0<em>ACS Sustainable Chem. Eng<\/em>., 12, 14009, 2024.<\/p>\n<p>351.\u00a0\u00a0\u00a0 Y. H. Lee, M. F. Hsu, G. Q. Wu, J. W. Lin, MR Busireddy, J. T. Chen and <strong>C. S. Hsu<\/strong>, &#8221; High Thermal and Low Dielectric Polyimides Based on Ether-Linked Xanthone-Based Diamines Having Bulky Trifluoromethyl Groups &#8220;, \u00a0ACS Appl. Polym. Mater., 6, 15082 (2024).<\/p>\n<p>352.\u00a0\u00a0\u00a0 K. H. Huang, C. C. Tseng, C. L. Tsai, Y. J. Xue, H. C. Lu, C. F. Lu, Y. Y. Chang, C. L. Huang, I. J. Hsu, Y. Y. Lai, Y. P. Zheng, B. H. Jiang, C. P. Chen, S. Y. Chien, U. S. Jeng, <strong>C. S. Hsu<\/strong> and Y. J. Cheng, &#8220;Highly Crystalline Selenium-Substituted C-Shaped Ortho-Benzodipyrrole-Based A-D-A-Type Nonfullerene Acceptor Enabling Solution-Processed Single-Crystal-Like Thin Films for Air-Stable, High-Mobility N-Type Transistors&#8221;, Adv. Funct. Mater., 35, 2419176 (2025).<\/p>\n<p>353.\u00a0\u00a0\u00a0 J. W. Lin, MR Busireddy, J. T. Chen, K. Tajima and <strong>C. S. Hsu<\/strong>, &#8220;Phenothiazine-Based Solid Additives for Optimizing Film Morphologies in High-Performance Organic Photovoltaics Source&#8221;, ACS Appl. Energy Mater., 8, 2506 (2025).<\/p>\n<p>354.\u00a0\u00a0\u00a0 MR Busireddy, L. H. Meng, J. W. Lin, W. C. Ke, J. T. Chen and <strong>C. S. Hsu<\/strong>, &#8220;Achieving Low Dissipation Factors and Low Dielectric Constants via Thermally Stable Naphthalene-Based Poly(ester-imide)s with Fluorine Groups&#8221;, <em>ACS<\/em>\u00a0Appl. Mater. Interfaces, 17, 18931 (2025).<\/p>\n<p>355.\u00a0\u00a0\u00a0 M. Srinivaas, Y. Y. Lee, MR Busireddy, <strong>C. S. Hsu<\/strong>, SB Devi, R. Boddula, GS Kamble, GP Chang-Chien, &#8220;Polyimides in next-generation energy devices: Applications in Li-ion batteries to solar cells &#8220;, J. Power Sources, 641, 236780 (2025).<\/p>\n<p>356.\u00a0\u00a0\u00a0 C. C. Tseng, L. L. Yeh, C. Y. Chang, C. L. Huang, C. L. Tsai, Y. J. Xue, F. C. Chen, <strong>C. S. Hsu<\/strong>, T. Y. Chu, J. P. Lu, U. S. Jeng and Y. J. Cheng, &#8220;A C<sub>6<\/sub>F<sub>5<\/sub>-functionalized benzimidazole acceptor enabling supramolecular fluorinated interactions for enhanced photovoltaic performance and thermal stability&#8221;, J. Mater. Chem. A, 13, 20519 (2025).<\/p>\n<p>357.\u00a0\u00a0\u00a0 C. L. Tsai, H. C. Lu, C. C. Tseng, Y. J. Xue, K. E. Hung, C. S. Wu, C. C. Chang, <strong>C. S. Hsu<\/strong>, K. Gugujonovic, MC. Scharber, F. Y. Cao and Y. J. Cheng, &#8220;Perfluorophenyl-Incorporated Ferrocene: A Non-Volatile Solid Additive for Boosting Efficiency and Stability in Organic Solar Cells &#8220;, <em>ACS<\/em>\u00a0Appl. Mater. Interfaces, 17, 32722 (2025).<\/p>\n<p>358.\u00a0\u00a0\u00a0 H. N. Yu, H. Y. Chen, GD\u00a0Sharma, Y. J. Cheng, <strong>C. S. Hsu<\/strong>, T. Y. Chu, JP Lu and F. C. Chen, &#8221; Computational Modeling of Indoor Organic Photovoltaics: Dataset Curation, Predictive Analysis, and Machine Learning Approaches&#8221;, Arch. Comput. Methods Eng., in press. (2025).<\/p>\n<\/div><\/div><\/div><\/section>\n<section class='av_toggle_section av-mhe9mlr2-61ecf8b81943fa097b8d5f1e360f6129'  itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/CreativeWork\" ><div role=\"tablist\" class=\"single_toggle\" data-tags=\"{All} \"  ><p id='toggle-toggle-id-2' data-fake-id='#toggle-id-2' class='toggler  av-title-above av-inherit-border-color'  itemprop=\"headline\"  role='tab' tabindex='0' aria-controls='toggle-id-2' data-slide-speed=\"200\" data-title=\"Patents\" data-title-open=\"\" data-aria_collapsed=\"Click to expand: Patents\" data-aria_expanded=\"Click to collapse: Patents\">Patents<span class=\"toggle_icon\"><span class=\"vert_icon\"><\/span><span class=\"hor_icon\"><\/span><\/span><\/p><div id='toggle-id-2' aria-labelledby='toggle-toggle-id-2' role='region' class='toggle_wrap  av-title-above'  ><div class='toggle_content invers-color av-inherit-border-color'  itemprop=\"text\" ><p>1.\u00a0\u00a0\u00a0\u00a0\u00a0 \u859b\u656c\u548c,\u8a31\u5343\u6a39,\u8b1d\u660c\u5fd7, \u201c\u96e2\u5b50\u578b\u5c0e\u96fb\u6027\u5074\u93c8\u6db2\u6676\u805a\u5408\u7269\u96fb\u89e3\u8cea\u201d, R.O.C. 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Patent 52050, Feb. 1992\/02-2007\/02<\/p>\n<p>3.\u00a0\u00a0\u00a0\u00a0\u00a0 \u859b\u656c\u548c,\u8a31\u5343\u6a39,\u8b1d\u660c\u5fd7,\u9673\u767b\u5c71, \u201cIonic Conducting Polymer Electrolytes Based on a Side-chain Crystalline Polymer\u201d, U.S. Patent US5091274, 1992\/02\/25-2007\/02.<\/p>\n<p>4.\u00a0\u00a0\u00a0\u00a0\u00a0 \u859b\u656c\u548c,\u8a31\u5343\u6a39,\u8b1d\u660c\u5fd7, \u201cIonic Conducting Polymer Electrolytes Based on a Side Chain Liquid Crystalline Polymer\u201d, Japan Patent JP0419903, 1992\/02-2007\/02.<\/p>\n<p>5.\u00a0\u00a0\u00a0\u00a0\u00a0 \u859b\u656c\u548c,\u8a31\u5343\u6a39,\u6eab\u4fca\u7965, \u201cSide-chain Liquid Crystalline Polymer Containing Crown Ether Based Mesogens\u201d, U.S. Patent US5241036, 1993\/08\/31-2008\/08.<\/p>\n<p>6.\u00a0\u00a0\u00a0\u00a0\u00a0 \u8a31\u5343\u6a39,\u65bd\u529b\u4ec1,\u5468\u4f36\u84c9,\u859b\u656c\u548c,\u201c\u4e00\u7a2e\u4ee5\u7532\u4ee3\u4e19\u70ef\u9178\u916f\u70ba\u4e3b\u5e79\u4e4b\u6db2\u6676\u805a\u5408\u7269\u201d, R.O.C. Patent 072437, 1995\/07\/01-2014\/05\/13.<\/p>\n<p>7.\u00a0\u00a0\u00a0\u00a0\u00a0 \u8a31\u5343\u6a39,\u5442\u5b9c\u5883,\u65bd\u529b\u4ec1,\u859b\u656c\u548c, \u201c\u4e00\u7a2e\u4ee5\u805a\u77fd\u6c27\u70f7\u70ba\u4e3b\u5e79\u4e4b\u6db2\u6676\u805a\u5408\u7269\u201d, R.O.C. Patent 072438, 1995\/07\/01-2014\/05\/31.<\/p>\n<p>8.\u00a0\u00a0\u00a0\u00a0\u00a0 \u8a31\u5343\u6a39,\u5442\u5b9c\u5883,\u65bd\u529b\u4ec1,\u859b\u656c\u548c, \u201cA Liquid Crystalline Polymers having a Polysiloxane Backbone\u201d, U.S. Patent US5495037, 1996\/02\/27-2016.<\/p>\n<p>9.\u00a0\u00a0\u00a0\u00a0\u00a0 \u8a31\u5343\u6a39,\u6797\u5fd7\u9d3b,\u65bd\u529b\u4ec1,\u859b\u656c\u548c, \u201c\u4e00\u7a2e\u4ee5\u65cb\u5149\u6027\u5c64\u5217\u6db2\u6676\u805a\u5408\u7269\u201d, R.O.C. Patent 073815, 1996-2017.<\/p>\n<p>10.\u00a0\u00a0 \u8a31\u5343\u6a39,\u6797\u5fd7\u9d3b,\u65bd\u529b\u4ec1,\u859b\u656c\u548c, \u201cChiral smectic liquid crystalline polymers\u201d, U.S. Patent US5563230, 1996\/10\/08-2016.<\/p>\n<p>11.\u00a0\u00a0 \u8a31\u5343\u6a39,\u5f35\u66f8\u6587,\u80e1\u6587\u4e2d,\u5f35\u6c38\u6607, \u201c\u5177\u53cd\u61c9\u6027\u7684\u4e09\u82ef\u57fa\u96d9\u4e59\u7094\u5316\u5408\u7269\u53ca\u542b\u8a72\u5316\u5408\u7269\u7684\u6db2\u6676\u805a\u5408\u7269\u201d, China Patent ZL01134217.X, 2001\/10\/26-2021\/10\/25.<\/p>\n<p>12.\u00a0\u00a0 \u8a31\u5343\u6a39,\u9673\u6167\u502b, \u201c\u6db2\u6676\u986f\u793a\u5668\u88dc\u511f\u819c\u53ca\u5176\u88fd\u9020\u65b9\u6cd5\u201d, R.O.C. Patent 159935, 2002\/07\/11-2017\/09\/14.<\/p>\n<p>13.\u00a0\u00a0 \u8a31\u5343\u6a39,\u9673\u6167\u502b, \u201cViewing Angle Compensator for Liquid Crystal Display and Method for Fabrication the same\u201d, U.S. Patent US6338902B1, 2002\/01\/15-2020\/10\/31.<\/p>\n<p>14.\u00a0\u00a0 \u5433\u9f8d\u6d77,\u8a31\u5343\u6a39,\u4e01\u6e05\u83ef, \u201c\u88fd\u9020\u6b63\u8ca0\u6df7\u5408\u578b\u5149\u5b78\u88dc\u511f\u819c\u4e4b\u65b9\u6cd5\u3001\u6b63\u8ca0\u6df7\u5408\u578b\u5149\u96fb\u88dc\u511f\u819c\u53ca\u4f7f\u7528\u5b83\u4e4b\u6db2\u6676\u5143\u4ef6\u6216\u6db2\u6676\u986f\u793a\u5668\u201d, R.O.C. Patent 192286, 2003\/12\/11-2022\/08\/01.<\/p>\n<p>15.\u00a0\u00a0 \u5f35\u654f\u5fe0,\u8a31\u5343\u6a39,\u5f90\u570b\u5cf0,\u838a\u96c5\u96f2, \u201cAcetylene derivatives having three 1, 4-phenylene rings, and liquid crystal composition and liquid crystal display device each comparising the same \u201d, Japan Patent JP3544162, 2004\/07\/16-2020\/01\/05.<\/p>\n<p>16.\u00a0\u00a0 \u8a31\u5343\u6a39,\u5f90\u570b\u5cf0,\u838a\u96c5\u96f2,\u5f35\u654f\u5fe0, \u201c\u4e09\u82ef\u57fa\u96d9\u4e59\u7094\u5316\u5408\u7269\u542b\u6709\u8a72\u5316\u5408\u7269\u4e4b\u6db2\u6676\u7d44\u5408\u7269\u53ca\u6db2\u6676\u986f\u793a\u88dd\u7f6e\u201d, R.O.C. Patent I229122, 2005\/03\/11-?.<\/p>\n<p>17.\u00a0\u00a0 \u8a31\u5343\u6a39,\u9ece\u5b89\u570b,\u8b1d\u70b3\u69ae,\u674e\u8208\u9293, \u201c\u6709\u6a5f\u96fb\u6fc0\u767c\u5149\u9ad8\u5206\u5b50\u5316\u5408\u7269\u201d, R.O.C. Patent 224481, 2004\/11\/21-2023\/12\/11.<\/p>\n<p>18.\u00a0\u00a0 \u8a31\u5343\u6a39, \u4e01\u6e05\u83ef, \u8b1d\u80b2\u6750, \u9673\u745e\u5802, \u201c\u5149\u5b78\u819c\u53ca\u5176\u88fd\u9020\u65b9\u6cd5\u201d, R.O.C. Patent I293375 (2008)<\/p>\n<p>19.\u00a0\u00a0 \u6797\u4e16\u660c, \u5ed6\u83ef\u8ce2, \u8a31\u5343\u6a39, \u5b5f\u5fc3\u98db, \u6d2a\u52dd\u5bcc, \u201c\u591a\u5c64\u6709\u6a5f\u5206\u5b50\u5149\u96fb\u5143\u4ef6\u4e4b\u88fd\u9020\u65b9\u6cd5\u201d, R.O.C. Patent I283083, 2007\/06\/21-2025\/11\/10.<\/p>\n<p>20.\u00a0\u00a0 \u6797\u4e16\u660c, \u5ed6\u83ef\u8ce2, \u8a31\u5343\u6a39, \u5b5f\u5fc3\u98db, \u6d2a\u52dd\u5bcc, \u201cManufacturing multilayer conjugate polymer optoelectronics device by using buffer layer\u201d, U.S. Patent US8017175B2, 2005\/12\/20-2029\/9\/29.<\/p>\n<p>21.\u00a0\u00a0 \u674e\u9053\u5f18, \u912d\u529f\u9f8d, \u66fe\u80b2\u5357, \u8a31\u5343\u6a39, \u5f35\u6649\u5f65, \u5433\u8a69\u8070, \u201c\u5177\u9ad8\u96d9\u6298\u5c04\u7387\u4e4b\u6db2\u6676\u6dfb\u52a0\u7269\u3001\u542b\u6709\u6b64\u6db2\u6676\u6dfb\u52a0\u7269\u4e4b\u6db2\u6676\u7d44\u6210\u7269\u53ca\u6db2\u6676\u986f\u793a\u5668\u201d, R.O.C. Patent I290166, 2007\/11\/21.<\/p>\n<p>22.\u00a0\u00a0 \u5b5f\u5fc3\u98db, \u6d2a\u52dd\u5bcc, \u8a31\u5343\u6a39, \u80e1\u7d00\u5e73, \u6797\u570b\u68df, \u9673\u5bb6\u52f3\u7b49, \u201c\u6709\u6a5f\u9ad8\u5206\u5b50\u767c\u5149\u4e8c\u6975\u9ad4\u88dd\u7f6e\u53ca\u61c9\u7528\u4e4b\u986f\u793a\u5668\u201d,R.O.C. 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Patent I422525, 2014\/01\/11-2030\/09\/09.<\/p>\n<p>26.\u00a0\u00a0 \u8a31\u5343\u6a39, \u912d\u5f65\u5982, \u8b1d\u671d\u7fd4, \u674e\u4f69\u84c9, \u201cPolymerizable fullerene derivative and their use in organic photovoltaic cells\u201d, U.S. Patent 9085543B2, 2015\/07\/21-2031\/03\/11.<\/p>\n<p>27.\u00a0\u00a0 \u8a31\u5343\u6a39, \u912d\u5f65\u5982, \u5433\u5fe0\u61b2, \u9673\u52c7\u9f8d, \u912d\u52dd\u6587, \u5f35\u6853\u7444, \u9673\u79cb\u7fd4, \u201c\u5316\u5408\u7269\u53ca\u5176\u5408\u6210\u65b9\u6cd5\u201d, R.O.C. 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Patent I499611, 2015\/09\/11-2033\/11\/13.<\/p>\n<p>32.\u00a0\u00a0 \u8a31\u5343\u6a39, \u5433\u5fe0\u61b2,\u8d99\u7fca\u7fd4, \u912d\u4fca\u4e30, \u6797\u656c\u582f,\u8521\u660e\u6a5f, \u738b\u9032\u7acb, \u738b\u5efa\u9686, \u201cConjugated polymer compound\u201d, U.S. Patent 9217063, 2015\/12\/22-2024\/09\/30.<\/p>\n<p>33.\u00a0\u00a0 \u8a31\u5343\u6a39, \u912d\u5f65\u5982, \u5ed6\u660e\u9d3b, \u8521\u54f2\u6069, \u66f9\u5cef\u6ea2, \u8cf4\u80b2\u82f1, \u8cf4\u6600\u4f51, \u201c\u4e00\u7a2e\u5149\u96fb\u6750\u6599\u53ca\u5176\u61c9\u7528\u201d, R.O.C. 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Patent I 780811, 2022\/10\/11-2041\/07\/08.<\/p>\n<p>38.\u00a0\u00a0 \u65bd\u5b8f\u65fb\u3001\u8def\u76db\u667a\u3001\u6f58\u5b9c\u5448\u3001\u5f90\u570b\u51f1\u3001\u674e\u6893\u6e90\u3001\u5f35\u7d14\u9cf3\u3001\u8a31\u5343\u6a39\u3001\u9673\u5b97\u5a01, \u201c\u4e5d\u5143\u7a20\u74b0\u5316\u5408\u7269\u8207\u6709\u6a5f\u5149\u4f0f\u96fb\u6c60\u201d\uff0cR.O.C. Patent I723909B\u3002<\/p>\n<p>39.\u00a0\u00a0 \u8a31\u5343\u6a39, \u8303\u6587\u660c, \u738b\u5609\u5f6c, \u201cStrechable conductive substrate\u201d, US Patent 11627657B2.<\/p>\n<p>40.\u00a0\u00a0 \u8a31\u5343\u6a39, \u8303\u6587\u660c, \u738b\u5609\u5f6c, \u201cStretchable display module\u201d, US Patent.<\/p>\n<\/div><\/div><\/div><\/section>\n<\/div><\/div><\/div><!--close column table wrapper. Autoclose: 1 -->\n\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-5edqg1-c93394da4cc6163607252465c4638c13\">\n.flex_column.av-5edqg1-c93394da4cc6163607252465c4638c13{\npadding:30px 30px 15px 30px;\nbackground-color:#e9f3ff;\n}\n<\/style>\n<div  class='flex_column av-5edqg1-c93394da4cc6163607252465c4638c13 av_one_full  avia-builder-el-32  el_after_av_one_full  el_before_av_one_full  first flex_column_div  column-top-margin'     ><p>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-3pcsxt-fe5c46f604f77cc5e179384fed3ce48e\">\n#top .av-special-heading.av-3pcsxt-fe5c46f604f77cc5e179384fed3ce48e{\npadding-bottom:10px;\n}\nbody .av-special-heading.av-3pcsxt-fe5c46f604f77cc5e179384fed3ce48e .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-3pcsxt-fe5c46f604f77cc5e179384fed3ce48e .av-subheading{\nfont-size:15px;\n}\n<\/style>\n<div  class='av-special-heading av-3pcsxt-fe5c46f604f77cc5e179384fed3ce48e av-special-heading-h3 blockquote modern-quote  avia-builder-el-33  el_before_av_textblock  avia-builder-el-first '><h3 class='av-special-heading-tag '  itemprop=\"headline\"  >Research Highlights<\/h3><div class=\"special-heading-border\"><div class=\"special-heading-inner-border\"><\/div><\/div><\/div><br \/>\n<section  class='av_textblock_section av-mhe9o5he-f3cbce77d411fad754c2dbb9e44436d7 '   itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/CreativeWork\" ><div class='avia_textblock'  itemprop=\"text\" ><p style=\"font-size: 18px;\">Eco-Friendly Solvent-Processed Dithienosilicon-Bridged Carbazole-Based Small-Molecule Acceptors Achieved over 25.7% PCE in Ternary Devices under Indoor Conditions<\/p>\n<\/div><\/section><br \/>\n<div id='av-masonry-1' class='av-masonry av-1uf1e9-9cf348f1d864e5534ca7864265cc7710 noHover av-fixed-size av-large-gap av-hover-overlay- av-masonry-animation- av-masonry-col-2 av-caption-always av-caption-style- av-masonry-gallery ' data-post_id=\"16645\"><div class=\"av-masonry-container isotope av-js-disabled\"><div class='av-masonry-entry isotope-item av-masonry-item-no-image '><\/div><a href=\"https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u8a31\u5343\u6a39\u57161-1-1030x334.jpg\" data-srcset=\"https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u8a31\u5343\u6a39\u57161-1-1030x334.jpg 1030w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u8a31\u5343\u6a39\u57161-1-300x97.jpg 300w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u8a31\u5343\u6a39\u57161-1-768x249.jpg 768w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u8a31\u5343\u6a39\u57161-1-1536x498.jpg 1536w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u8a31\u5343\u6a39\u57161-1-2048x664.jpg 2048w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u8a31\u5343\u6a39\u57161-1-1500x486.jpg 1500w, 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><\/div><\/div><\/figure><\/a><!--end av-masonry entry--><\/div><\/div><\/p><\/div>\n<div  class='flex_column av-av_one_full-7714eba142aeda1f8b5272a3c372b279 av_one_full  avia-builder-el-36  el_after_av_one_full  avia-builder-el-last  first flex_column_div  column-top-margin'     ><p>\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-msg00hmz-973938ff8c5a974a76557045e28cfe2f\">\n#top .av-special-heading.av-msg00hmz-973938ff8c5a974a76557045e28cfe2f{\npadding-bottom:0;\n}\nbody .av-special-heading.av-msg00hmz-973938ff8c5a974a76557045e28cfe2f .av-special-heading-tag .heading-char{\nfont-size:25px;\n}\n.av-special-heading.av-msg00hmz-973938ff8c5a974a76557045e28cfe2f .av-subheading{\nfont-size:15px;\n}\n<\/style>\n<div  class='av-special-heading av-msg00hmz-973938ff8c5a974a76557045e28cfe2f av-special-heading-h3 blockquote modern-quote  avia-builder-el-37  el_before_av_image  avia-builder-el-first '><h3 class='av-special-heading-tag '  itemprop=\"headline\"  ><\/p>\n<div class=\"title-style-1\">Research Highlights<\/div>\n<p><\/h3><div class=\"special-heading-border\"><div class=\"special-heading-inner-border\"><\/div><\/div><\/div><br \/>\n\n<style type=\"text\/css\" data-created_by=\"avia_inline_auto\" id=\"style-css-av-msg01hzd-2e93b9ea20cd33a95f5cb903bc56c038\">\n.avia-image-container.av-msg01hzd-2e93b9ea20cd33a95f5cb903bc56c038 img.avia_image{\nbox-shadow:none;\n}\n.avia-image-container.av-msg01hzd-2e93b9ea20cd33a95f5cb903bc56c038 .av-image-caption-overlay-center{\ncolor:#ffffff;\n}\n<\/style>\n<div  class='avia-image-container av-msg01hzd-2e93b9ea20cd33a95f5cb903bc56c038 av-styling-no-styling avia-align-center  avia-builder-el-38  el_after_av_heading  avia-builder-el-last '   itemprop=\"image\" itemscope=\"itemscope\" itemtype=\"https:\/\/schema.org\/ImageObject\" ><div class=\"avia-image-container-inner\"><div class=\"avia-image-overlay-wrap\"><img decoding=\"async\" fetchpriority=\"high\" class='wp-image-20223 avia-img-lazy-loading-not-20223 avia_image ' src=\"https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u8a31\u5343\u6a39-1030x713.png\" alt='\u8a31\u5343\u6a39 Chain-Shu Hsu' title='\u8a31\u5343\u6a39'  height=\"713\" width=\"1030\"  itemprop=\"thumbnailUrl\" srcset=\"https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u8a31\u5343\u6a39-1030x713.png 1030w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u8a31\u5343\u6a39-289x200.png 289w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u8a31\u5343\u6a39-768x532.png 768w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u8a31\u5343\u6a39-705x488.png 705w, https:\/\/dac.nycu.edu.tw\/wp-content\/uploads\/2024\/12\/\u8a31\u5343\u6a39.png 1040w\" sizes=\"(max-width: 1030px) 100vw, 1030px\" \/><\/div><\/div><\/div><\/p><\/div>\n","protected":false},"excerpt":{"rendered":"<p>Chain-Shu Hsu \u8a31\u5343\u6a39<br \/>\nConjugated Polymer, Polymer Light-emitting Diode, Organic TFT, Polymer Solar Cell<br \/>\nTel | 03-5712121 #31523<br \/>\nEmail | cshsu@nycu.edu.tw<br \/>\nOffice | TKB R716A<\/p>\n","protected":false},"author":20,"featured_media":16646,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"tags":[],"portfolio_entries":[198,196],"class_list":["post-16645","portfolio","type-portfolio","status-publish","has-post-thumbnail","hentry","portfolio_entries-01-en","portfolio_entries--en"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.6 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Chair Professor Chain-Shu Hsu - \u570b\u7acb\u967d\u660e\u4ea4\u901a\u5927\u5b78\u61c9\u7528\u5316\u5b78\u7cfb<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/dac.nycu.edu.tw\/en\/portfolio-item\/\u8a31\u5343\u6a39-\u8b1b\u5ea7\u6559\u6388\/\" \/>\n<meta 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