Design and synthesis of star-shaped non-fullerene acceptors based on triarylamine core for organic photovoltaic applications

Abstract Non-fullerene acceptors were synthesized with triphenylamine (TPA) and 9-phenylcarbazole core functionalized with oxindole moiety, as well as electron accepting groups such as cyano and trifluoromethyl groups, leading to precisely tuned molecular electronic structures and intermolecular arrangements. This approach maintained high thermal stability and excellent electron mobility while optimizing optoelectronic properties, providing a novel strategy for developing organic photovoltaic materials. LUMO levels of three receptors were comparable to PC61BM. The decomposition temperatures of all three acceptors exceeded 380 °C under N2 flow, indicating the exceptional thermal stability. Notably, the acceptor consisting of TPA core with three oxindole moieties exhibited the red-shifted and intense UV-vis absorption spectrum and the narrowest optical bandgap (Egopt = 2.14 eV). Furthermore, the higher electron mobility was observed in this compound compared to analogues with 9-phenylcarbozle unit. The power conversion efficiency of the device based on TPA core acceptor and regio-regular poly(3-hexylthiophene) surpassed those of the devices based on the other two acceptors.

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Publication Details

Journal
Chemistry Letters
Published
2024-11-25
DOI
https://doi.org/10.1093/chemle/upae217
Primary Topic
Fullerene Chemistry and Applications
Type
article
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Design and synthesis of star-shaped non-fullerene acceptors based on triarylamine core for organic photovoltaic applications

Kenji Ogino, Hongyu Fu
Chemistry Letters
Fullerene Chemistry and Applications
article

Design and synthesis of star-shaped non-fullerene acceptors based on triarylamine core for organic photovoltaic applications

Kenji Ogino, Hongyu Fu
article en

Abstract

Abstract Non-fullerene acceptors were synthesized with triphenylamine (TPA) and 9-phenylcarbazole core functionalized with oxindole moiety, as well as electron accepting groups such as cyano and trifluoromethyl groups, leading to precisely tuned molecular electronic structures and intermolecular arrangements. This approach maintained high thermal stability and excellent electron mobility while optimizing optoelectronic properties, providing a novel strategy for developing organic photovoltaic materials. LUMO levels of three receptors were comparable to PC61BM. The decomposition temperatures of all three acceptors exceeded 380 °C under N2 flow, indicating the exceptional thermal stability. Notably, the acceptor consisting of TPA core with three oxindole moieties exhibited the red-shifted and intense UV-vis absorption spectrum and the narrowest optical bandgap (Egopt = 2.14 eV). Furthermore, the higher electron mobility was observed in this compound compared to analogues with 9-phenylcarbozle unit. The power conversion efficiency of the device based on TPA core acceptor and regio-regular poly(3-hexylthiophene) surpassed those of the devices based on the other two acceptors.

Chemistry LettersVol. 53(12)
Tokyo University of Agriculture and Technology (JP)
Openalex Percentile: Top 84%
Fullerene Chemistry and Applications
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Design and synthesis of star-shaped non-fullerene acceptors based on triarylamine core for organic photovoltaic applications — Kenji Ogino, Hongyu Fu · Chemistry Letters (2024) | TGRS Research Map | TGRS