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dc.contributor.author Jung, Hyeonwoo -
dc.contributor.author Kim, Honggi -
dc.contributor.author Kim, Jongyoun -
dc.contributor.author Jang, Soyeong -
dc.contributor.author Lee, Youngu -
dc.date.accessioned 2022-11-17T11:40:14Z -
dc.date.available 2022-11-17T11:40:14Z -
dc.date.created 2022-09-08 -
dc.date.issued 2022-10 -
dc.identifier.issn 0253-2964 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/17167 -
dc.description.abstract Conjugated polymers for bulk heterojunction polymer solar cells (BHJ PSCs) should be processed with nonhalogenated solvents because of environmental concerns. Here, we report novel regioregular copolymers for high-performance PSCs processed with nonhalogenated solvents. The regioregular copolymers (i.e., rr-PfBT2f4T-2OD and rr-PfBT2f4T-2DT) consist of 3 '',4 '-difluoro-2,2 ':5 ',2 '':5 '',2"'-quaterthiophene (2f4T) with different side chains (2-octadodecyl (OD) and 2-decyltetradecyl (DT)) and 5-fluorobenzo[c][1,2,5]thiadiazole (fBT). The regioregular copolymers with controlled fBT orientation show high solubility in nonhalogenated solvents. Both regioregular copolymers possess suitable energy levels, leading to sufficient energy offsets with a nonfullerene acceptor, BTP-eC11. An rr-PfBT2f4T-2DT:BTP-eC11-blended film exhibited predominant face-on orientation compared to the rr-PfBT2f4T-2OD:BTP-eC11-blended film. In addition, the rr-PfBT2f4T-2DT:BTP-eC11-blended film showed much more balanced hole/electron mobility (mu(h)/mu(e) similar to 4.73) than rr-PfBT2f4T-2OD:BTP-eC11-blended film (mu(h)/mu(e) similar to 45.86). Therefore, rr-PfBT2f4T-2DT:BTP-eC11-based PSCs, processed with 1,2,4-trimethylbenzene, showed a power conversion efficiency of 13.21% which is 60% higher than rr-PfBT2f4T-2OD:BTP-eC11-based PSCs. -
dc.language English -
dc.publisher 대한화학회 -
dc.title Side-chain engineering of regioregular copolymers for high-performance polymer solar cells processed with nonhalogenated solvents -
dc.type Article -
dc.identifier.doi 10.1002/bkcs.12606 -
dc.identifier.wosid 000842500900001 -
dc.identifier.scopusid 2-s2.0-85136788503 -
dc.identifier.bibliographicCitation Bulletin of the Korean Chemical Society, v.43, no.10, pp.1200 - 1206 -
dc.identifier.kciid ART002888563 -
dc.description.isOpenAccess FALSE -
dc.subject.keywordAuthor nonhalogenated solvent -
dc.subject.keywordAuthor polymer solar cell -
dc.subject.keywordAuthor regioregular copolymer -
dc.subject.keywordAuthor side-chain engineering -
dc.subject.keywordPlus POWER CONVERSION EFFICIENCY -
dc.subject.keywordPlus CONJUGATED POLYMERS -
dc.subject.keywordPlus RANDOM TERPOLYMERS -
dc.subject.keywordPlus DONOR POLYMERS -
dc.subject.keywordPlus FLUORINE ATOM -
dc.subject.keywordPlus BENZODITHIOPHENE -
dc.subject.keywordPlus SEGMENTS -
dc.subject.keywordPlus DESIGN -
dc.citation.endPage 1206 -
dc.citation.number 10 -
dc.citation.startPage 1200 -
dc.citation.title Bulletin of the Korean Chemical Society -
dc.citation.volume 43 -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.description.journalRegisteredClass kci -
dc.relation.journalResearchArea Chemistry -
dc.relation.journalWebOfScienceCategory Chemistry, Multidisciplinary -
dc.type.docType Article -
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Department of Energy Science and Engineering Organic & Printed Electronics Laboratory(OPEL) 1. Journal Articles

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