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Synthesis and characterization of diketopyrrolopyrrole-based conjugated polymer with biphenyl for organic photovoltaic cells

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dc.contributor.authorAyuningtias, Landep-
dc.contributor.authorMa, Jae Yeol-
dc.contributor.authorKim, Yu-Jin-
dc.contributor.authorKim, Yun-Hi-
dc.date.accessioned2025-07-16T00:30:12Z-
dc.date.available2025-07-16T00:30:12Z-
dc.date.issued2025-07-
dc.identifier.issn0253-2964-
dc.identifier.issn1229-5949-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/79440-
dc.description.abstractDesigning a moderate band gap is sometimes intentionally chosen. When the donor polymer has a deeper HOMO level, a higher Voc can be gained which boosts total PCE in organic photovoltaics (OPVs) (Liao et al., Joule 2020, 4(1), 189-206; Mamba et al., J. Phys. Chem. A 2021, 125(50), 10593-10603; Choi and Jo, Org. Electron. 2013, 14(6), 1621-1628; Jo et al., Org. Electron. 2012, 13(10), 2185-2191). This is crucial in DPP-based copolymer frameworks, which frequently have short band gaps and may experience poor Voc. Since DPP is a low bandgap due to strong-acceptor, thus, modifying it with weak donor units can raise the bandgap and lower the HOMO to make it suitable for multi-junctions or higher Voc. We report the synthesis, properties, and photovoltaic applications of a donor-acceptor (D-A) conjugated copolymer based on diketopyrrolopyrrole (DPP) and biphenyl, namely PDDPPhenyl. This polymer exhibits broad absorption ranging from 400 to 900 nm with a band gap of 1.59 eV. As expected, a low HOMO level of -5.29 was gained by introducing biphenyl as a weaker donor. The optimized weight ratio goes to 1:4 for PDPPPhenyl:PC71BM with 3.8% PCE.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisher대한화학회-
dc.titleSynthesis and characterization of diketopyrrolopyrrole-based conjugated polymer with biphenyl for organic photovoltaic cells-
dc.title.alternativeSynthesis and characterization of diketopyrrolopyrrole-based conjugated polymer with biphenyl for organic photovoltaic cells-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.1002/bkcs.70042-
dc.identifier.scopusid2-s2.0-105009853672-
dc.identifier.wosid001521797800001-
dc.identifier.bibliographicCitationBulletin of the Korean Chemical Society, v.46, no.7, pp 754 - 760-
dc.citation.titleBulletin of the Korean Chemical Society-
dc.citation.volume46-
dc.citation.number7-
dc.citation.startPage754-
dc.citation.endPage760-
dc.type.docTypeArticle-
dc.identifier.kciidART003227063-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusBAND-GAP DIKETOPYRROLOPYRROLE-
dc.subject.keywordPlusSOLAR-CELLS-
dc.subject.keywordPlusSEMICONDUCTOR-MATERIALS-
dc.subject.keywordPlusCOPOLYMERS-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusMORPHOLOGY-
dc.subject.keywordPlusTRANSISTORS-
dc.subject.keywordPlusTRANSPORT-
dc.subject.keywordAuthorbiphenyl-
dc.subject.keywordAuthorDPP-based copolymer-
dc.subject.keywordAuthorlow-lying HOMO-
dc.subject.keywordAuthororganic photovoltaics-
dc.subject.keywordAuthorweak donor-
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