dc.contributor.author | Wagalgave, S.M. | |
dc.contributor.author | Bhosale, S.V. | |
dc.contributor.author | Bhosale, R.S. | |
dc.contributor.author | Puyad, A.L. | |
dc.contributor.author | Chen, J. | |
dc.contributor.author | Li, J. | |
dc.contributor.author | Evans, R.A. | |
dc.contributor.author | Gupta, A. | |
dc.contributor.author | Bhosale, Sidhanath V. | |
dc.date.accessioned | 2019-06-03T09:47:26Z | |
dc.date.available | 2019-06-03T09:47:26Z | |
dc.date.issued | 2019 | |
dc.identifier.citation | Materials Chemistry Frontiers. 3(6); 2019; 1231-1237. | en_US |
dc.identifier.uri | https://doi.org/10.1039/C9QM00129H | |
dc.identifier.uri | http://irgu.unigoa.ac.in/drs/handle/unigoa/5684 | |
dc.description.abstract | A tetraphenylethylene-functionalized, three-dimensional non-fullerene electron acceptor, 9,9',9'',9'''-(ethene-1,1,2,2-tetrayltetrakis(benzene-4,1-diyl))tetrakis(4-(4-methylpiperidin-1-yl)-2,7-dioctylbenzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetraone) (coded as W8), which used naphthalene diimide units as terminal functionalities, was designed, synthesized and characterized. It was highly soluble (i.e. greater than 20 mg mL-1 in o-dichlorobenzene), thermally stable, and exhibited energy levels complementing those of the commonly used donor polymers, P3HT and PTB7. Not only is W8 the first reported example in the literature that comprises tetraphenylethylene and naphthalene diimide building blocks, but the device performances [D: A 1: 1.2 = 5.26 percent (P3HT); 8.58 percent (PTB7)] outlined herein are among the best in the investigated class of three-dimensional acceptors. | en_US |
dc.publisher | Royal Society of Chemistry | en_US |
dc.subject | Chemistry | en_US |
dc.title | An efficient, three-dimensional non-fullerene electron acceptor: Functionalizing tetraphenylethylene with naphthalene diimides | en_US |
dc.type | Journal article | en_US |
dc.identifier.impf | cs |