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New D-A-D-A-D push-pull organic semiconductors with different benzo[1,2-b:4, 5-b '] dithiophene cores for solution processed bulk heterojunction solar cells

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dc.contributor.authorDo, Kwangseok-
dc.contributor.authorCho, Nara-
dc.contributor.authorSiddiqui, S. A.-
dc.contributor.authorSingh, Surya Prakash-
dc.contributor.authorSharma, Ganesh D.-
dc.contributor.authorKo, Jaejung-
dc.date.accessioned2021-09-04T13:02:41Z-
dc.date.available2021-09-04T13:02:41Z-
dc.date.created2021-06-18-
dc.date.issued2015-09-
dc.identifier.issn0143-7208-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/92594-
dc.description.abstractThe synthesis and characterization of two D-A-D-A-D push-pull organic semiconductors based on either his- (2-ethylhexyloxy) benzo [1,2-b:4,5-b'] dithiophene or bis- (triisopropylsilylethynyl) benzodithiophene electron rich core are described. The optical and electrochemical properties of these compounds indicate that these materials can absorb sunlight over a wide spectral range from 350 to 700 nm and exhibit suitable energy levels for efficient exciton dissociation. These small molecules were used as donor coupled with phenyl-C-71-butyric acid methyl ester acceptor for the fabrication of solution processed small molecule bulk heterojunction solar cells. The rigid and -conjugation of the silylacetylene substituted analog pi-extended compared to the hexyloxy substituted analog facilitates intermolecular packing interactions of small pi-pi charge transfer and intermolecular molecule which induce a deep HOMO level, producing a high open circuit voltage of similar to 0.98 V. The achieved PCE was 5.69% when the active layer hexyloxy analog: phenyl-C-71-butyric acid methyl ester was processed with optimized 1-chloronaphathalene additive. (C) 2015 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER SCI LTD-
dc.subjectOPEN-CIRCUIT VOLTAGE-
dc.subjectSMALL MOLECULES-
dc.subjectPHOTOVOLTAIC APPLICATIONS-
dc.subjectELECTRONIC-PROPERTIES-
dc.subjectCONJUGATED POLYMERS-
dc.subjectPHASE-SEPARATION-
dc.subjectPERFORMANCE-
dc.subjectEFFICIENCY-
dc.subjectMORPHOLOGY-
dc.subjectRECOMBINATION-
dc.titleNew D-A-D-A-D push-pull organic semiconductors with different benzo[1,2-b:4, 5-b '] dithiophene cores for solution processed bulk heterojunction solar cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorKo, Jaejung-
dc.identifier.doi10.1016/j.dyepig.2015.04.012-
dc.identifier.scopusid2-s2.0-84928620808-
dc.identifier.wosid000356747300017-
dc.identifier.bibliographicCitationDYES AND PIGMENTS, v.120, pp.126 - 135-
dc.relation.isPartOfDYES AND PIGMENTS-
dc.citation.titleDYES AND PIGMENTS-
dc.citation.volume120-
dc.citation.startPage126-
dc.citation.endPage135-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryChemistry, Applied-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Textiles-
dc.subject.keywordPlusOPEN-CIRCUIT VOLTAGE-
dc.subject.keywordPlusSMALL MOLECULES-
dc.subject.keywordPlusPHOTOVOLTAIC APPLICATIONS-
dc.subject.keywordPlusELECTRONIC-PROPERTIES-
dc.subject.keywordPlusCONJUGATED POLYMERS-
dc.subject.keywordPlusPHASE-SEPARATION-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusEFFICIENCY-
dc.subject.keywordPlusMORPHOLOGY-
dc.subject.keywordPlusRECOMBINATION-
dc.subject.keywordAuthorPush-pull organic semiconductors-
dc.subject.keywordAuthorBulk heterojunction organic solar cells-
dc.subject.keywordAuthorPower conversion efficiency-
dc.subject.keywordAuthorSolvent additives-
dc.subject.keywordAuthorSmall molecules-
dc.subject.keywordAuthorSolution process-
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