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The first connection of carbonyl-bridged triarylamine and diketopyrrolopyrrole functionalities to generate a three-dimensional, non-fullerene electron acceptor
We report for the first time the use of a carbonyl-bridged triarylamine core with diketopyrrolopyrrole terminal units to generate a three-dimensional, non-planar non-fullerene electron acceptor with favourable properties for use in organic photovoltaic devices. The carbonyl-bridged triarylamine-func...
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Published in: | Materials chemistry frontiers 2020-07, Vol.4 (7), p.2176-2183 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | We report for the first time the use of a carbonyl-bridged triarylamine core with diketopyrrolopyrrole terminal units to generate a three-dimensional, non-planar non-fullerene electron acceptor with favourable properties for use in organic photovoltaic devices. The carbonyl-bridged triarylamine-functionalized, small molecule non-fullerene electron acceptor, 2,6,10-tris(5-(2,5-bis(2-ethylhexyl)-3,6-dioxo-4-(thiophen-2-yl)-2,3,5,6-tetrahydropyrrolo[3,4-
c
]pyrrol-1-yl)thiophen-2-yl)-4
H
-benzo[9,1]quinolizino[3,4,5,6,7-
defg
]acridine-4,8,12-trione (coded as
R1
), was synthesized
via
the industrially viable, Suzuki cross-coupling reaction using commercially and cheaply available substrates. Using PTB7 as a donor, a power conversion efficiency of 9.33% was achieved in simple, solution-processable bulk-heterojunction devices, a result that is amongst the best in the literature for three-dimensional non-fullerene acceptors.
Carbonyl-bridged triarylamine-based, three-dimensional non-fullerene acceptor (
R1
); device: ITO/PEDOT:PSS/PTB7:
R1
(1: 1.2)/Ca/Al; PCE = 9.33% |
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ISSN: | 2052-1537 2052-1537 |
DOI: | 10.1039/d0qm00041h |