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dc.contributor.authorDinçalp, Haluk
dc.contributor.authorMurat, Gözde
dc.contributor.authorİçli, Sıddık
dc.date.accessioned2022-10-04T07:09:55Z
dc.date.available2022-10-04T07:09:55Z
dc.date.issued2014
dc.identifier.urihttp://hdl.handle.net/20.500.12481/12534
dc.description.abstractThree electron-deficient small molecules based on 2,1,3-benzothiadiazole (BTD) units namely, 4,7-bis (3-methoxyphenyl)-2,1,3-benzothiadiazole (BT1), (3-{7-[3-(dimethylamino)phenyl]-2,1,3-benzothiadi azole-4-yl}phenyl)dimethylamine (BT2) and 3,30 -(2,1,3-benzothiadiazole-4,7-dyl)dianiline (BT3) were synthesized and their photophysical properties were investigated systematically to understand their potential usage in ternary organic solar cells (OSCs) as additive material to enhance the cell efficiency. All these molecules show broad absorption bands in 350–750 nm on glass substrate and their optical band gaps were calculated to be around 2.50–2.80 eV. BTD fluorescence dynamics were measured in polymer:BT1:fullerene blends with varying emission wavelengths of active layer. Fluorescence emission and time resolved measurements indicated photoinduced energy shift from BT1 dye to fullerene and also from polymer to BT1 dye upon excitation of the active layer.tr_TR
dc.language.isoentr_TR
dc.publisherOptical Materialstr_TR
dc.rightsinfo:eu-repo/semantics/openAccesstr_TR
dc.subjectBenzothiadiazole, Organic photovoltaic,Time resolved,emission spectra, Solid state emission, Charge-separationtr_TR
dc.titleImprovement of intramolecular charge transfer within a donor–acceptor blend by doping novel synthesized benzothiadiazole small molecules in solid statetr_TR
dc.typeMakaletr_TR
dc.contributor.MCBUauthorDinçalp, Haluk
dc.contributor.MCBUauthorMurat, Gözde
dc.contributor.departmentEnstitüler > Fen Bilimleri Enstitüsü > Fen Bilimleri > Kimya ABDtr_TR
dc.identifier.ORC-ID0000-0002-9097-3716tr_TR
dc.identifier.categoryOfPublishedMaterialMakale - Uluslararası Hakemli Dergitr_TR
dc.identifier.nameOfPublishedMaterialOptical Materialstr_TR
dc.identifier.DOI-ID10.1016/j.optmat.2014.04.019tr_TR
dc.identifier.volume36tr_TR
dc.identifier.issue9tr_TR
dc.identifier.startpage1525tr_TR
dc.identifier.endpage1533tr_TR
dc.identifier.indicesWeb Of Science (WOS)tr_TR
dc.identifier.indicesScopus (DOI)tr_TR
dc.identifier.issn/e-issnISSN: 0925-3467


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