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Direct connection of an amine to oligothiophene to generate push-pull chromophores for organic photovoltaic applications

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dc.contributor.author Agarwal, A.
dc.contributor.author Hundal, A.
dc.contributor.author Chen, J-Y.
dc.contributor.author Bilic, A.
dc.contributor.author Xiang, W.
dc.contributor.author Bhosale, S.V.
dc.contributor.author Li, J-L.
dc.contributor.author Evans, R.A.
dc.contributor.author Gupta, A.
dc.date.accessioned 2019-01-31T03:47:02Z
dc.date.available 2019-01-31T03:47:02Z
dc.date.issued 2019
dc.identifier.citation Dyes and Pigments. 162; 2019; 315-323. en_US
dc.identifier.uri https://doi.org/10.1016/j.dyepig.2018.10.048
dc.identifier.uri http://irgu.unigoa.ac.in/drs/handle/unigoa/5570
dc.description.abstract Through the direct connection of the donor nitrogen atom to oligothiophenes, herein we report three novel, donor materials for evaluation in bulk-heterojunction solar cells. The direct substitution enhances the charge transfer transition, thus improving the light-harvesting ability of the target chromophores. The influence of various terminal acceptor functionalities on the optoelectronic and photovoltaic properties was systematically studied. The target chromophore, T3, bearing oxoindenemalononitrile acceptor unit afforded a power conversion efficiency of 6.12% when paired with the conventional acceptor, PC sub(61) BM, a result that is the highest in the current literature for push-pull chromophores. en_US
dc.publisher Elsevier en_US
dc.subject Chemistry en_US
dc.title Direct connection of an amine to oligothiophene to generate push-pull chromophores for organic photovoltaic applications en_US
dc.type Journal article en_US
dc.identifier.impf y


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