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김봉수

Kim, BongSoo
Polymer & Organic Semiconductor Lab.
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dc.citation.endPage 3869 -
dc.citation.number 10 -
dc.citation.startPage 3861 -
dc.citation.title MACROMOLECULES -
dc.citation.volume 46 -
dc.contributor.author Kim, Seul-Ong -
dc.contributor.author Kim, Youn-Su -
dc.contributor.author Yun, Hui-Jun -
dc.contributor.author Kang, Il -
dc.contributor.author Yoon, Youngwoon -
dc.contributor.author Shin, Nara -
dc.contributor.author Son, Hae Jung -
dc.contributor.author Kim, Honggon -
dc.contributor.author Ko, Min Jae -
dc.contributor.author Kim, BongSoo -
dc.contributor.author Kim, Kyungkon -
dc.contributor.author Kim, Yun-Hi -
dc.contributor.author Kwon, Soon-Ki -
dc.date.accessioned 2023-12-22T04:06:23Z -
dc.date.available 2023-12-22T04:06:23Z -
dc.date.created 2018-09-10 -
dc.date.issued 2013-05 -
dc.description.abstract We report the synthesis, characterization, and solar cell 15 properties of new donor-acceptor-type low band gap polymers (POBDTPD and PEBDTPD) that incorporate dialkoxybenzodithiophene (BDT) as the g donor and N-octyl-2,7-dithia-5-azacyclopenta[a]pentalene-4,6-dione (DTPD) as the acceptor. The newly developed DTPD moiety was carefully designed to lower a band gap via strong interaction between donor acceptor moieties and keep polymer energy levels deep. Remarkably, the DTPD acceptor moiety effectively widens the light absorption range of the polymers up to similar to 900 nm while positioning their HOMO and LUMO levels in the optimal range, i.e., -5.3 3 and -4.0 eV, respectively, for high power conversion efficiencies (PCEs) as we intended. Solar cell devices were fabricated according to the structure ITO/PEDOT:PSS/photoactive (polymer:PC70BM)/TiO2/Al. The POBDTPD devices exhibited a PCE of 4.7% with a V-oc of 070 V, a J(sc) of 10.6 in mA/cm(2), and a FF of 0.64. The PEBDTPD devices yielded a higher PCE of 5.3% with a V-oc of 0.72 V, a J(sc) of 13.5 mA/cm(2), and a FF of 0.54. AFM, TEM, and PL quenching measurements revealed that the high J(sc)s are a result of the appropriate morphology and efficient charge separation. In comparing the performances of the two polymer devices, the higher J(sc) for the PEBDTPD device was attributed to its better nanoscale phase separation, smoother surface, and higher carrier mobility in the polymer:PC70BM blend films. The higher FF for the POBDTPD device was ascribed to a good balance between the hole and electron mobilities. Overall, we demonstrate that the DTPD unit is a promising electron accepting moiety to develop high performance low band gap polymers. -
dc.identifier.bibliographicCitation MACROMOLECULES, v.46, no.10, pp.3861 - 3869 -
dc.identifier.doi 10.1021/ma400257q -
dc.identifier.issn 0024-9297 -
dc.identifier.scopusid 2-s2.0-84878340266 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/24810 -
dc.identifier.url https://pubs.acs.org/doi/10.1021/ma400257q -
dc.identifier.wosid 000319795800016 -
dc.language 영어 -
dc.publisher AMER CHEMICAL SOC -
dc.title N-Octyl-2,7-dithia-5-azacyclopenta[a]pentalene-4,6-dione-Based Low Band Gap Polymers for Efficient Solar Cells -
dc.type Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus OPEN-CIRCUIT VOLTAGE -
dc.subject.keywordPlus CONJUGATED POLYMERS -
dc.subject.keywordPlus PHOTOVOLTAIC APPLICATIONS -
dc.subject.keywordPlus SEMICONDUCTING POLYMERS -
dc.subject.keywordPlus CONVERSION EFFICIENCY -
dc.subject.keywordPlus ORGANIC PHOTOVOLTAICS -
dc.subject.keywordPlus TANDEM POLYMER -
dc.subject.keywordPlus PERFORMANCE -
dc.subject.keywordPlus DONOR -
dc.subject.keywordPlus DIKETOPYRROLOPYRROLE -

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