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.6653943832-476372018-04-25T08:42:16Z 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 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. 2018-04-25T08:42:16Z 2018-04-25T08:42:16Z 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/6653943832/47637 |
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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. |
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Journal |
author |
Chanitpa Khantha Viruntachar Kruefu Robert C. Coffin David L. Carroll Sukon Phanichphant |
spellingShingle |
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 |
author_facet |
Chanitpa Khantha Viruntachar Kruefu Robert C. Coffin David L. Carroll Sukon Phanichphant |
author_sort |
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 |
publishDate |
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/6653943832/47637 |
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