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Yang, Changduk
Advanced Tech-Optoelectronic Materials Synthesis Lab.
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dc.citation.number 4 -
dc.citation.startPage e202102563 -
dc.citation.title CHEMSUSCHEM -
dc.citation.volume 15 -
dc.contributor.author Liu, Zuoji -
dc.contributor.author Mao, Qilong -
dc.contributor.author Wang, Jing -
dc.contributor.author Wu, Feiyan -
dc.contributor.author Zhou, Dan -
dc.contributor.author Cheng, Yujun -
dc.contributor.author Huang, Shaorong -
dc.contributor.author Huang, Bin -
dc.contributor.author Yang, Changduk -
dc.contributor.author Chen, Lie -
dc.date.accessioned 2023-12-21T14:38:38Z -
dc.date.available 2023-12-21T14:38:38Z -
dc.date.created 2022-02-11 -
dc.date.issued 2022-02 -
dc.description.abstract Unfused-ring acceptors (UFAs) show bright application prospects in organic solar cells (OSCs) thanks to their easy synthesis, low cost, and good device performance. The selection of central-core building block and suitable side chain are the key factors to achieve high-performance UFAs. Current tremendous endeavors for the development of UFAs mainly concentrate on obtaining higher short-circuit current density (J(sc)), albeit accompanied by low open-circuit voltage (V-oc) and modest fill factor (FF). Herein, two novel A-D-A '-D-A type UFAs (BTCD-IC and BTCD-2FIC), which have the same new electron-withdrawing central-core dithieno[3 ',2 ':3,4;2 '',3 '':5,6]-benzo[1,2-c][1,2,5]thiadia-zole (DTBT) and cyclopentadithiophene unit (CPDT, substituted by 2-butyl-1-octyl alkyl chain) coupling with different terminals, were designed and synthesized. Two UFAs showed strong and broad light absorption in the wavelength range of 300-850 nm owing to the strong intramolecular charge transfer effect favorable by DTBT core. Compared with BTCD-IC, BTCD-2FIC with F-containing terminal group exhibited higher molar extinction coefficient, lower energy level, higher charge mobility, stronger crystallinity, more ordered molecular stacking, and better film morphology. As a result, when blended with donor polymer PBDB-T (poly[(2,6-(4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)benzo[1,2-b:4,5-b ']dithiophene)-co-(1,3-di(5-thiophene-2-yl)-5,7-bis(2-ethylhexyl)benzo[1,2-c:4,5-c ']-dithiophene-4,8-dione)]), the BTCD-2FIC-based OSC achieved a superior power conversion efficiency (PCE) of 11.32 %, with a high V-oc of 0.85 V, a J(sc) of 18.24 mA cm(-2), and a FF of 73 %, than BTCD-IC-based OSC (PCE=8.96 %). Impressively, the simultaneously enhanced V-oc and FF values of the PBDB-T:BTCD-2FIC device were the highest values of the A-D-A '-D-A-type UFAs. The results demonstrate the application of electron-withdrawing DTBT central-core unit in efficient UFAs provides meaningful molecular design guidance for high-performance OSCs. -
dc.identifier.bibliographicCitation CHEMSUSCHEM, v.15, no.4, pp.e202102563 -
dc.identifier.doi 10.1002/cssc.202102563 -
dc.identifier.issn 1864-5631 -
dc.identifier.scopusid 2-s2.0-85123725656 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/57267 -
dc.identifier.url https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/cssc.202102563 -
dc.identifier.wosid 000747300100001 -
dc.language 영어 -
dc.publisher WILEY-V C H VERLAG GMBH -
dc.title Exploiting Novel Unfused-Ring Acceptor for Efficient Organic Solar Cells with Record Open-Circuit Voltage and Fill Factor -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Chemistry, Multidisciplinary; Green & Sustainable Science & Technology -
dc.relation.journalResearchArea Chemistry; Science & Technology - Other Topics -
dc.type.docType Article; Early Access -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor central-core -
dc.subject.keywordAuthor organic solar cells -
dc.subject.keywordAuthor photovoltaics -
dc.subject.keywordAuthor power conversion efficiency -
dc.subject.keywordAuthor unfused-ring acceptors -
dc.subject.keywordPlus ELECTRON-ACCEPTOR -
dc.subject.keywordPlus POLYMER -
dc.subject.keywordPlus STABILITY -
dc.subject.keywordPlus DONOR -

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