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Effects of side chains on physical and photovoltaic properties of methyl thiophene-3-carboxylate containing dithienopyrrole-based copolymers

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dc.contributor.authorCho, Min Ju-
dc.contributor.authorSeo, Jangwon-
dc.contributor.authorYoon, Seung Hee-
dc.contributor.authorChoi, Dong Hoon-
dc.contributor.authorPrasad, Paras N.-
dc.date.accessioned2021-09-05T20:23:49Z-
dc.date.available2021-09-05T20:23:49Z-
dc.date.created2021-06-15-
dc.date.issued2013-10-01-
dc.identifier.issn0379-6779-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/101919-
dc.description.abstractTo enhance the open circuit voltage (V-oc,) of bulk heterojunction (BHJ) polymer solar cells (PSCs) fabricated using dithieno[3,2-b:2 ',3 '-d]pyrrole (DTP)-based copolymers, methyl thiophene-3-carboxylate was introduced as a weak acceptor into the polymer backbone. Two types of copolymers showed different optical and electrochemical properties even though both had an identical polymer backbone, with one of them having alkyl side chains tethered to the DTP unit. The energy level of the highest occupied molecular orbital (HOMO) of PDTPMT-C11 with a Y-branched alkyl chain was -5.22 eV, which was lower by 0.53 eV than that of PDTPMT-C12 with linear alkyl chains. The PSC, fabricated using PDTPMT-C11 and [6,6]-phenyl-C71-butyric acid methyl ester (PC71 BM), showed a power conversion efficiency (PCE) of 1.8% with a V-oc of 0.73 V. while the PSC comprising PDTPMT-C12:PC71 BM BHJ-PSC had PCE of 0.23%, which was limited by a relatively lower V-oc, (0.26 V) corresponding to the HOMO level (-4.69 eV) of PDTPMT-C12. (C) 2013 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE SA-
dc.subjectPOLYMER SOLAR-CELLS-
dc.subjectOPEN-CIRCUIT VOLTAGE-
dc.subjectSEMICONDUCTING POLYMERS-
dc.subjectPERFORMANCE-
dc.subjectDIKETOPYRROLOPYRROLE-
dc.subjectPOLYTHIOPHENES-
dc.subjectALKYL-
dc.titleEffects of side chains on physical and photovoltaic properties of methyl thiophene-3-carboxylate containing dithienopyrrole-based copolymers-
dc.typeArticle-
dc.contributor.affiliatedAuthorChoi, Dong Hoon-
dc.identifier.doi10.1016/j.synthmet.2013.08.023-
dc.identifier.scopusid2-s2.0-84884828988-
dc.identifier.wosid000326996700004-
dc.identifier.bibliographicCitationSYNTHETIC METALS, v.182, pp.22 - 27-
dc.relation.isPartOfSYNTHETIC METALS-
dc.citation.titleSYNTHETIC METALS-
dc.citation.volume182-
dc.citation.startPage22-
dc.citation.endPage27-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaPhysics-
dc.relation.journalResearchAreaPolymer Science-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPhysics, Condensed Matter-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.subject.keywordPlusPOLYMER SOLAR-CELLS-
dc.subject.keywordPlusOPEN-CIRCUIT VOLTAGE-
dc.subject.keywordPlusSEMICONDUCTING POLYMERS-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusDIKETOPYRROLOPYRROLE-
dc.subject.keywordPlusPOLYTHIOPHENES-
dc.subject.keywordPlusALKYL-
dc.subject.keywordAuthorOrganic semiconductor-
dc.subject.keywordAuthorConjugated polymer-
dc.subject.keywordAuthorPolymer solar cells-
dc.subject.keywordAuthorThiophene-3-carboxylate-
dc.subject.keywordAuthorDithienopyrrole-
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