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dc.contributor.authorShunichi Fukuzumi*
dc.date.accessioned2018-11-21T16:30:52Z-
dc.date.available2018-11-21T16:30:52Z-
dc.date.issued2018*
dc.identifier.issn2193-5807*
dc.identifier.otherOAK-21958*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/246892-
dc.description.abstractA new naphthalenediimide (NDI) derivative linked to triphenylamine (TPA) and fullerene (TPA–NDI–C60 triad; S3) was designed, synthesized and characterized. Femtosecond laser transient absorption spectral measurements revealed that fast electron transfer from TPA to the singlet-excited state of NDI occurred to form a charge-separated state (TPA.+–NDI.−–C60) with a rate constant of approximately 1012 s−1, followed by the charge-shift reaction from NDI.− to C60 to produce the charge-separated state (TPA.+–NDI–C60 .−) that decayed by back electron transfer with a rate constant of 4.4×109 s−1 (with a corresponding lifetime of 230 ps). Organic bulk heterojunction solar cells were fabricated using the triad S3 as an n-type semiconductor along with the conventional donor polymer poly(3-hexylthiophene). The power conversion efficiency reached 3.03 % before annealing and 4.85 % after annealing in the optimized devices. To rationalize the performance of these organic photovoltaic devices, atomic force microscopy was used to study the morphology of poly(3-hexylthiophene):S3 blend surfaces, which were found to be well interlaced and free from projections, lumps, or indentations. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim*
dc.description.sponsorshipScience and Engineering Research Board*
dc.languageEnglish*
dc.publisherWiley-VCH Verlag*
dc.subjectbulk heterojunctions*
dc.subjectfullerenes*
dc.subjectnaphthalenediimide*
dc.subjectphotoinduced charge separation*
dc.subjecttriphenylamine*
dc.titleA Triphenylamine–Naphthalenediimide–Fullerene Triad: Synthesis, Photoinduced Charge Separation and Solution-Processable Bulk Heterojunction Solar Cells*
dc.typeArticle*
dc.relation.issue1*
dc.relation.volume7*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage220*
dc.relation.lastpage226*
dc.relation.journaltitleAsian Journal of Organic Chemistry*
dc.identifier.doi10.1002/ajoc.201700557*
dc.identifier.wosidWOS:000419962000028*
dc.identifier.scopusid2-s2.0-85037667609*
dc.author.googleSrivani D.*
dc.author.googleGupta A.*
dc.author.googleBhosale S.V.*
dc.author.googleOhkubo K.*
dc.author.googleBhosale R.S.*
dc.author.googleFukuzumi S.*
dc.author.googleBilic A.*
dc.author.googleJones L.A.*
dc.contributor.scopusidShunichi Fukuzumi(35430038100;58409757400)*
dc.date.modifydate20240401081001*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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