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Phenanthro[110,9,8-cdefg]carbazole-Thiophene, Donor-Donor Copolymer for Narrow Band Green-Selective Organic Photodiode

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dc.contributor.authorSung, Min Jae-
dc.contributor.authorKim, Kyounghwan-
dc.contributor.authorKwon, Soon-Ki-
dc.contributor.authorKim, Yun-Hi-
dc.contributor.authorChung, Dae Sung-
dc.date.accessioned2022-12-26T18:34:46Z-
dc.date.available2022-12-26T18:34:46Z-
dc.date.issued2017-07-
dc.identifier.issn1932-7447-
dc.identifier.issn1932-7455-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/13590-
dc.description.abstractA new donor donor copolymer consisting of phenanthro[1,10,9,8-cdefg]carbazole and thiophene unit (PP-Th) was synthesized for narrow band green-selective organic photodiode application. Thanks to well-defined intramolecular conjugation and inhibited intermolecular interaction of PP-Th compared to its donor- acceptor type analogues, PP-Th revealed narrow band green-selective absorption peak at 510 nm with low full width at half-maximum value of 98 nm. In addition, deep ionization energy of PP-Th, as confirmed by photophysical analyses, made it less susceptible to oxidational degradation. Green-selective organic photodiodes (OPDs) were fabricated utilizing PP-Th as a green absorbing donor material and ZnO as a nonabsorbing acceptor material. The optimized OPD rendered a very low dark current of 2 nA cm(-2) and a high detectivity of 1.42 x 10(12) Jones with narrow band green-selectivity. Moreover, PP-Th enabled OPD with a high 3-dB bandwidth of 3.1 kHz and a high linear dynamic range of 84.9 dB. Furthermore, the responsivity of the OPD could be maintained for more than 30 days under atmospheric condition, revealing excellent stability of PP-Th.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherAmerican Chemical Society-
dc.titlePhenanthro[110,9,8-cdefg]carbazole-Thiophene, Donor-Donor Copolymer for Narrow Band Green-Selective Organic Photodiode-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1021/acs.jpcc.7b04793-
dc.identifier.scopusid2-s2.0-85026633274-
dc.identifier.wosid000406726200048-
dc.identifier.bibliographicCitationThe Journal of Physical Chemistry C, v.121, no.29, pp 15931 - 15936-
dc.citation.titleThe Journal of Physical Chemistry C-
dc.citation.volume121-
dc.citation.number29-
dc.citation.startPage15931-
dc.citation.endPage15936-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.subject.keywordPlusPOLYMER SOLAR-CELLS-
dc.subject.keywordPlusFLUORESCENCE DETECTION-
dc.subject.keywordPlusCONJUGATED POLYMERS-
dc.subject.keywordPlusHIGH-RESPONSIVITY-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusPHOTODETECTOR-
dc.subject.keywordPlusEFFICIENCY-
dc.subject.keywordPlusDEVICES-
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