The effect of side-chain structure on copolymer-based bulk heterojunction solar cells
This paper describes the synthesis and photovoltaic studies of copolymer based on benzo[1,2-b:4,5-b-]dithiophene and 2,1,3-benzothiadiazole. Bulk-heterojunction solar cells were fabricated by using chlorobenzene, and 2% chloronapthalene as a solvent additive in chlorobenzene. The copolymers as the e...
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th-cmuir.6653943832-523742018-09-04T09:36:27Z The effect of side-chain structure on copolymer-based bulk heterojunction solar cells Chanitpa Khantha Viruntachar Kruefu Robert C. Coffin David L. Carroll Sukon Phanichphant Chemistry Materials Science Physics and Astronomy This paper describes the synthesis and photovoltaic studies of copolymer based on benzo[1,2-b:4,5-b-]dithiophene and 2,1,3-benzothiadiazole. Bulk-heterojunction solar cells were fabricated by using chlorobenzene, and 2% chloronapthalene as a solvent additive in chlorobenzene. The copolymers as the electron donor were blended with [6,6]-phenyl-C61-butyric acid methyl ester (PC61BM) as the electron acceptor. The effect of side-chain on BDT was compared between 4,8-bis(1-pentylhexyl)benzo[1,2-b: 4,5-b-]dithiophene (C11BDT) and 4,8-bis(1-butylhexyl)benzo[1,2-b:4,5-b-]dithioph ene (C9BDT). The power conversion efficiency (PCE) was improved with the shorter side-chain. The highest PCE was found in PC9BDTBT with 2.29%. Copyright © Taylor & Francis Group, LLC. 2018-09-04T09:24:15Z 2018-09-04T09:24:15Z 2013-09-27 Journal 15635287 15421406 2-s2.0-84884515693 10.1080/15421406.2013.804389 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84884515693&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/52374 |
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Chemistry Materials Science Physics and Astronomy Chanitpa Khantha Viruntachar Kruefu Robert C. Coffin David L. Carroll Sukon Phanichphant The effect of side-chain structure on copolymer-based bulk heterojunction solar cells |
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This paper describes the synthesis and photovoltaic studies of copolymer based on benzo[1,2-b:4,5-b-]dithiophene and 2,1,3-benzothiadiazole. Bulk-heterojunction solar cells were fabricated by using chlorobenzene, and 2% chloronapthalene as a solvent additive in chlorobenzene. The copolymers as the electron donor were blended with [6,6]-phenyl-C61-butyric acid methyl ester (PC61BM) as the electron acceptor. The effect of side-chain on BDT was compared between 4,8-bis(1-pentylhexyl)benzo[1,2-b: 4,5-b-]dithiophene (C11BDT) and 4,8-bis(1-butylhexyl)benzo[1,2-b:4,5-b-]dithioph ene (C9BDT). The power conversion efficiency (PCE) was improved with the shorter side-chain. The highest PCE was found in PC9BDTBT with 2.29%. Copyright © Taylor & Francis Group, LLC. |
format |
Journal |
author |
Chanitpa Khantha Viruntachar Kruefu Robert C. Coffin David L. Carroll Sukon Phanichphant |
author_facet |
Chanitpa Khantha Viruntachar Kruefu Robert C. Coffin David L. Carroll Sukon Phanichphant |
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Chanitpa Khantha |
title |
The effect of side-chain structure on copolymer-based bulk heterojunction solar cells |
title_short |
The effect of side-chain structure on copolymer-based bulk heterojunction solar cells |
title_full |
The effect of side-chain structure on copolymer-based bulk heterojunction solar cells |
title_fullStr |
The effect of side-chain structure on copolymer-based bulk heterojunction solar cells |
title_full_unstemmed |
The effect of side-chain structure on copolymer-based bulk heterojunction solar cells |
title_sort |
effect of side-chain structure on copolymer-based bulk heterojunction solar cells |
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2018 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84884515693&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/52374 |
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