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The first connection of carbonyl-bridged triarylamine and diketopyrrolopyrrole functionalities to generate a three-dimensional, non-fullerene electron acceptor

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posted on 2024-11-02, 14:03 authored by Ratan Jadhav, Rahul Hangarge, Mahmood Aljabri, Kerba More, Jing-Yu Chen, Lathe JonesLathe Jones, Richard Evans, Jing-Liang Li, Sheshanath Bhosale, Akhil Gupta
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)-4H-benzo[9,1]quinolizino[3,4,5,6,7-defg]acridine-4,8,12-trione (coded asR1), was synthesizedviathe 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.

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Related Materials

  1. 1.
    DOI - Is published in 10.1039/d0qm00041h
  2. 2.
    ISSN - Is published in 20521537

Journal

Materials Chemistry Frontiers

Volume

4

Issue

7

Start page

2176

End page

2183

Total pages

8

Publisher

Royal Society of Chemistry

Place published

United Kingdom

Language

English

Copyright

This journal is © The Royal Society of Chemistry and the Chinese Chemical Society 2020

Former Identifier

2006103063

Esploro creation date

2023-05-02

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