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A series of V-shaped small molecule non-fullerene electron acceptors for efficient bulk-heterojunction devices

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dc.contributor.author Rao, P.S.
dc.contributor.author More, V.G.
dc.contributor.author Jangale, A.D.
dc.contributor.author Bhosale, S.V.
dc.contributor.author Bhosale, R.S.
dc.contributor.author Puyad, A.L.
dc.contributor.author Chen, J-Y.
dc.contributor.author Li, J-L
dc.contributor.author Bhosale, Sidhanath V.
dc.contributor.author Gupta, A.
dc.contributor.author Sharma, G.D.
dc.date.accessioned 2020-06-17T09:03:32Z
dc.date.available 2020-06-17T09:03:32Z
dc.date.issued 2019
dc.identifier.citation Dyes and Pigments. 171; 2019; ArticleID_107677. en_US
dc.identifier.uri https://doi.org/10.1016/j.dyepig.2019.107677
dc.identifier.uri http://irgu.unigoa.ac.in/drs/handle/unigoa/6086
dc.description.abstract Two simple semiconducting acceptor-acceptor sub(1)-donor-acceptor (A-A sub(1)-D-A) modular, small molecule non-fullerene electron acceptors, 2-(4-(7-hexadecyl-1,3,6,8-tetraoxo-3,6,7,8-tetrahydrobenzo[lmn][3,8]phenanthrolin-2(1H)-yl)phenyl)-3-(6-((4-(7-hexadecyl-1,3,6,8-tetraoxo-3,6,7,8-tetrahydrobenzo[lmn][3,8]phenanthrolin-2(1H)-yl)phenyl)ethynyl)-9-octyl-9H-carbazol-3-yl)buta-1,3-diene-1,1,4,4-tetracarbonitrile (NDICz-5) and 2-(4-(3,3-dicyano-2-(4-(7-hexadecyl-1,3,6,8-tetraoxo-3,6,7,8-tetrahydrobenzo[lmn][3,8]phenanthrolin-2(1H)-yl)phenyl)-1-(6-((4-(7-hexadecyl-1,3,6,8-tetraoxo-3,6,7,8-tetrahydrobenzo[lmn][3,8]phenanthrolin-2(1H)-yl)phenyl)ethynyl)-9-octyl-9H-carbazol-3-yl)allylidene)cyclohexa-2,5-dien-1-ylidene)malononitrile (NDICz-6), were designed, synthesized and characterized for application in solution-processable bulk-heterojunction solar cells. The optoelectronic and photovoltaic properties of NDICz-5 and NDICz-6 were directly compared with those of a structural analogue, 7,7'-(((9-octyl-9H-carbazole-3,6-diyl)bis(ethyne-2,1-diyl))bis(4,1-phenylene))bis(2-hexadecylbenzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetraone) (NDICz-4), which was designed based on an A-D-A format. All of these new materials were designed to be V-shaped and comprised an electron rich carbazole donor core (D) together with electron deficient naphthalene diimide terminal core (A). In the simple A-D-A system, naphthalene diimide was the terminal functionality, whereas in the A-A sub(1)-D-A system, tetracyanoethylene (TCNE) and tetracyanoquinodimethane (TCNQ) derived functionalities were incorporated as A sub(1) units by keeping D/A units constant. The inclusion of A sub(1) was mainly done to induce cross-conjugation within the molecular backbone and hence to improve light-harvesting. The physical and optoelectronic properties were characterized by ultraviolet-visible, thermogravimetric analysis, photo-electron spectroscopy in air and cyclic voltammetry. These new materials exhibited energy levels complementing those of the conventional donor polymer poly(3-hexyl thiophene) (P3HT). Solution-processable bulk-heterojunction devices were fabricated with NDICz-4, NDICz-5 and NDICz-6 as non-fullerene electron acceptors. Studies on the photovoltaic properties revealed that the best P3HT: NDI-Cz6-based device showed an impressive enhanced power conversion efficiency of 7.58 percent, an increase of around two-fold with respect to as-cast blend, after solvent vapor annealing using carbon disulfide. Not only are the results among the best in the current literature using the conventional donor polymer P3HT, but clearly demonstrate that A-A sub(1)-D-A type, V-shaped small molecules are promising non-fullerene acceptors in the research field of organic solar cells. en_US
dc.publisher Elsevier en_US
dc.subject Chemistry en_US
dc.title A series of V-shaped small molecule non-fullerene electron acceptors for efficient bulk-heterojunction devices en_US
dc.type Journal article en_US
dc.identifier.impf y


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