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김봉수

Kim, BongSoo
Polymer & Organic Semiconductor Lab.
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dc.citation.number 1 -
dc.citation.startPage e12421 -
dc.citation.title ECOMAT -
dc.citation.volume 6 -
dc.contributor.author Jung, Hyeonwoo -
dc.contributor.author Kim, Jongyoun -
dc.contributor.author Park, Jaehyoung -
dc.contributor.author Jahankhan, Muhammad -
dc.contributor.author Hwang, Youngjun -
dc.contributor.author Kang, Byeongjae -
dc.contributor.author Kim, Hyerin -
dc.contributor.author Park, Ho-Yeol -
dc.contributor.author Ahn, Pyeongkang -
dc.contributor.author Um, Duhyeon -
dc.contributor.author Jee, Je-Sung -
dc.contributor.author Shin, Won Suk -
dc.contributor.author Kim, Bongsoo -
dc.contributor.author Jin, Sung-Ho -
dc.contributor.author Song, Chang Eun -
dc.contributor.author Lee, Youngu -
dc.date.accessioned 2023-12-27T10:05:12Z -
dc.date.available 2023-12-27T10:05:12Z -
dc.date.created 2023-11-19 -
dc.date.issued 2024-01 -
dc.description.abstract The transition of polymer solar cells (PSCs) from laboratory-scale unit cells to industrial-scale modules requires the development of new p-type polymers for high-performance large-area PSC modules based on environmentally friendly processes. Herein, a series of 1D/2A terpolymers (PBTPttBD) composed of benzo[1,2-b:4,5-b']dithiophene (BDT-F), thieno[3,4-c]pyrrole-4,6(5H)-dione (TPD-TT), and benzo-[1,2-c:4,5-c']dithiophene-4,8-dione (BDD) is synthesized for nonhalogenated solvent processed PSC submodules. The optical, electrochemical, charge-transport, and nano-morphological properties of the PBTPttBD terpolymers are modulated by adjusting the molar ratio of the TPD-TT and BDD components. PBTPttBD-75:BTP-eC11-based PSC submodules, processed with o-xylene, achieve a notable PCE of 11.57% over a 55 cm(2 ) active area. This PCE value is among the highest reported using a nonhalogenated solvent over a 55 cm(2 )active area module. The optimized PSC submodule exhibits minimal cell-to-module loss, which can be attributed to the optimized crystallinity of the PBTPttBD-75:BTP-eC11 photoactive layer system and favorable film formation kinetics.image -
dc.identifier.bibliographicCitation ECOMAT, v.6, no.1, pp.e12421 -
dc.identifier.doi 10.1002/eom2.12421 -
dc.identifier.issn 2567-3173 -
dc.identifier.scopusid 2-s2.0-85174543718 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/67126 -
dc.identifier.wosid 001093576600001 -
dc.language 영어 -
dc.publisher WILEY -
dc.title Achieving an excellent efficiency of 11.57% in a polymer solar cell submodule with a 55 cm2 active area using 1D/2A terpolymers and environmentally friendly nonhalogenated solvents -
dc.type Article -
dc.description.isOpenAccess TRUE -
dc.relation.journalWebOfScienceCategory Chemistry, Physical; Green & Sustainable Science & Technology; Materials Science, Multidisciplinary -
dc.relation.journalResearchArea Chemistry; Science & Technology - Other Topics; Materials Science -
dc.type.docType Article; Early Access -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor cell-to-module loss -
dc.subject.keywordAuthor nonhalogenated solvents -
dc.subject.keywordAuthor polymer solar cells -
dc.subject.keywordAuthor submodules -
dc.subject.keywordAuthor terpolymers -
dc.subject.keywordPlus ORGANIC PHOTOVOLTAICS -
dc.subject.keywordPlus BENZODITHIOPHENE -

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