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Synthesis of Poly(benzothiadiazole-co-dithienobenzodithiophenes) and Effect of Thiophene Insertion for High-Performance Polymer Solar Cells

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dc.contributor.authorYun, Hui-Jun-
dc.contributor.authorLee, Yun-Ji-
dc.contributor.authorYoo, Seung-Jin-
dc.contributor.authorChung, Dae Sung-
dc.contributor.authorKim, Yun-Hi-
dc.contributor.authorKwon, Soon-Ki-
dc.date.accessioned2022-12-27T00:21:16Z-
dc.date.available2022-12-27T00:21:16Z-
dc.date.issued2013-09-
dc.identifier.issn0947-6539-
dc.identifier.issn1521-3765-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/20471-
dc.description.abstractWe describe herein the synthesis of novel donor-acceptor conjugated polymers with dithienobenzodithiophenes (DTBDT) as the electron donor and 2,1,3-benzothiadiazole as the electron acceptor for high-performance organic photovoltaics (OPVs). We studied the effects of strategically inserting thiophene into the DTBDT as a substituent on the skeletal structure on the opto-electronic performances of fabricated devices. From UV/Vis absorption, electrochemical, and field-effect transistor analyses, we found that the thiophene-containing DTBDT derivative can substantially increase the orbital overlap area between adjacent conjugated chains and thus dramatically enhance charge-carrier mobility up to 0.55cm(2)V(-1)s(-1). The outstanding charge-transport characteristics of this polymer allowed the realization of high-performance organic solar cells with a power conversion efficiency (PCE) of 5.1%. Detailed studies on the morphological factors that enable the maximum PCE of the polymer solar cells are discussed along with a hole/electron mobility analysis based on the space-charge-limited current model.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherJohn Wiley & Sons Ltd.-
dc.titleSynthesis of Poly(benzothiadiazole-co-dithienobenzodithiophenes) and Effect of Thiophene Insertion for High-Performance Polymer Solar Cells-
dc.typeArticle-
dc.publisher.location독일-
dc.identifier.doi10.1002/chem.201300445-
dc.identifier.scopusid2-s2.0-84884535156-
dc.identifier.wosid000324579600045-
dc.identifier.bibliographicCitationChemistry - A European Journal, v.19, no.39, pp 13242 - 13248-
dc.citation.titleChemistry - A European Journal-
dc.citation.volume19-
dc.citation.number39-
dc.citation.startPage13242-
dc.citation.endPage13248-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusENERGY-CONVERSION EFFICIENCY-
dc.subject.keywordPlusCONJUGATED POLYMER-
dc.subject.keywordPlusELECTRONIC-PROPERTIES-
dc.subject.keywordPlusPHOTOVOLTAIC CELLS-
dc.subject.keywordPlusDESIGN RULES-
dc.subject.keywordPlusPOLY(3-HEXYLTHIOPHENE)-
dc.subject.keywordPlusMORPHOLOGY-
dc.subject.keywordPlusACCEPTOR-
dc.subject.keywordPlusDONORS-
dc.subject.keywordAuthorcopolymerization-
dc.subject.keywordAuthordonor-acceptor systems-
dc.subject.keywordAuthorphotovoltaic systems-
dc.subject.keywordAuthorthin films-
dc.subject.keywordAuthorsemiconductors-
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