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Composition-Tolerant Terpolymers for Efficient, Nonhalogenated Solvent-Processed Polymer Solar Cells

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dc.contributor.authorLim, C.-
dc.contributor.authorLee, S.-
dc.contributor.authorHan, D.-
dc.contributor.authorLee, Changyeon-
dc.contributor.authorKim, B.J.-
dc.date.accessioned2023-03-08T04:49:14Z-
dc.date.available2023-03-08T04:49:14Z-
dc.date.issued2022-11-
dc.identifier.issn0024-9297-
dc.identifier.issn1520-5835-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/61135-
dc.description.abstractThe design of terpolymers is a compelling strategy to improve the polymer solar cell (PSC) performance. However, the terpolymer composition at which the power conversion efficiency (PCE) of associated PSCs is typically optimized generally falls within a very narrow range, complicating the reproducible fabrication of optimal PSCs. In this study, a series of D-A1-D-A2 type random terpolymers (DTTz-X, where X = 10-60) is designed with structurally similar A1 and A2 accepting units. The sulfur atom of the benzothiadiazole subunit in the A1 (DTBT) unit is replaced by a nitrogen atom in the A2 (DTTz) unit, enabling the introduction of an alkyl solubilizing group while maintaining the overall structural properties of the terpolymer system. Consequently, the DTTz-X PDs maintain good optoelectronic properties at various A1/A2 ratios, while their processability in nonhalogenated solvents is significantly enhanced. Accordingly, the PSC performance of the terpolymer system shows good composition tolerance; i.e., the terpolymer system affords PSCs with PCEs exceeding 15% (up to 16.4%) over a broad range of DTTz compositions (10-40 mol %). This study establishes a useful design strategy for the development of efficient terpolymer donors for reproducible and eco-friendly fabrication of high-performance PSCs. © 2022 American Chemical Society.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherAmerican Chemical Society-
dc.titleComposition-Tolerant Terpolymers for Efficient, Nonhalogenated Solvent-Processed Polymer Solar Cells-
dc.typeArticle-
dc.identifier.doi10.1021/acs.macromol.2c01974-
dc.identifier.bibliographicCitationMacromolecules, v.55, no.23, pp 10395 - 10404-
dc.description.isOpenAccessN-
dc.identifier.wosid000891128200001-
dc.identifier.scopusid2-s2.0-85143064594-
dc.citation.endPage10404-
dc.citation.number23-
dc.citation.startPage10395-
dc.citation.titleMacromolecules-
dc.citation.volume55-
dc.type.docTypeArticle; Early Access-
dc.publisher.location미국-
dc.subject.keywordPlusADDITIVE-FREE-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusAGGREGATION-
dc.subject.keywordPlusACCEPTORS-
dc.subject.keywordPlusSCATTERING-
dc.subject.keywordPlusDESIGN-
dc.subject.keywordPlusDONORS-
dc.relation.journalResearchAreaPolymer Science-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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