Poly(benzodithiophene) Homopolymer for High-Performance Polymer Solar Cells with Open-Circuit Voltage of Near 1 V: A Superior Candidate To Substitute for Poly(3-hexylthiophene) as Wide Bandgap Polymer

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dc.contributor.authorKang, Tae Euiko
dc.contributor.authorKim, Taesuko
dc.contributor.authorWang, Chengko
dc.contributor.authorYoo, Seung-Hyupko
dc.contributor.authorKim, Bum-Joonko
dc.date.accessioned2015-06-03T06:20:31Z-
dc.date.available2015-06-03T06:20:31Z-
dc.date.created2015-05-26-
dc.date.created2015-05-26-
dc.date.issued2015-04-
dc.identifier.citationCHEMISTRY OF MATERIALS, v.27, no.7, pp.2653 - 2658-
dc.identifier.issn0897-4756-
dc.identifier.urihttp://hdl.handle.net/10203/198696-
dc.description.abstractConjugated homopolymers can be synthesized more simply and reproducibly at lower cost than widely developing donor-acceptor (DA) alternating copolymers. However, except for well-known poly(3-hexylthiophene) (P3HT), almost no successful homopolymer-based polymer solar cells (PSCs) have been reported because of their relatively wide band gap and unoptimized energy levels that limit the values of short circuit current (J(SC)) and open-circuit voltage (V-OC) in PSCs. Herein, we report the development of poly(4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b:4,5-b]dithiophene) (PBDTT) homopolymer that has high light absorption coefficients and nearly perfect energy alignment with that of [6,6]-phenyl-C71-butyric acid methyl ester (PC71BM). Therefore, we were able to produce high-performance PSCs with the power conversion efficiency (PCE) of 6.12%, benefiting from both high V-OC (0.93 V) and J(SC) (11.95 mA cm(-2)) values. To the best of our knowledge, this PCE value is one of the highest values reported for the homopolymer donor-based PSCs. Significantly, the optimized condition of the device was achieved without any solvent additive or thermal treatment. Therefore, PBDTT is a promising candidate to take over the role of P3HT in tandem solar cells and ternary blend solar cells.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.subjectPOWER CONVERSION EFFICIENCY-
dc.subjectDONOR-ACCEPTOR COPOLYMERS-
dc.subjectCONJUGATED POLYMER-
dc.subjectPHOTOVOLTAIC PERFORMANCE-
dc.subjectSOLVENT ADDITIVES-
dc.subjectSIDE-CHAINS-
dc.subjectMORPHOLOGY-
dc.subjectBENZODITHIOPHENE-
dc.subjectDESIGN-
dc.subjectENERGY-
dc.titlePoly(benzodithiophene) Homopolymer for High-Performance Polymer Solar Cells with Open-Circuit Voltage of Near 1 V: A Superior Candidate To Substitute for Poly(3-hexylthiophene) as Wide Bandgap Polymer-
dc.typeArticle-
dc.identifier.wosid000353176100048-
dc.identifier.scopusid2-s2.0-84927722411-
dc.type.rimsART-
dc.citation.volume27-
dc.citation.issue7-
dc.citation.beginningpage2653-
dc.citation.endingpage2658-
dc.citation.publicationnameCHEMISTRY OF MATERIALS-
dc.identifier.doi10.1021/acs.chemmater.5b00481-
dc.contributor.localauthorYoo, Seung-Hyup-
dc.contributor.localauthorKim, Bum-Joon-
dc.contributor.nonIdAuthorKim, Taesu-
dc.contributor.nonIdAuthorWang, Cheng-
dc.type.journalArticleArticle-
dc.subject.keywordPlusPOWER CONVERSION EFFICIENCY-
dc.subject.keywordPlusDONOR-ACCEPTOR COPOLYMERS-
dc.subject.keywordPlusCONJUGATED POLYMER-
dc.subject.keywordPlusPHOTOVOLTAIC PERFORMANCE-
dc.subject.keywordPlusSOLVENT ADDITIVES-
dc.subject.keywordPlusSIDE-CHAINS-
dc.subject.keywordPlusMORPHOLOGY-
dc.subject.keywordPlusBENZODITHIOPHENE-
dc.subject.keywordPlusDESIGN-
dc.subject.keywordPlusENERGY-
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