4.6 Article

Synergistic effect of benzoselenadiazole core and alkoxy side chain substitution on the photovoltaic performance of non-fullerene acceptors

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 11, Issue 42, Pages 22769-22774

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d3ta04364a

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In this study, a novel Y-series small molecule acceptor was developed by adopting benzoselenadiazole as the central core and introducing alkoxy side chains on the beta-position of thiophene moieties. The introduction of alkoxy side chains led to upshifted energy levels and optimized morphology, leading to improved power conversion efficiency.
Y-series small-molecule acceptors (SMAs) have attracted extensive research interest as they boost the power conversion efficiencies of organic solar cells (OSCs) and research communities have begun to concentrate on the structure-property relationship and further structural optimization of this A-DA ' D-A type SMA. In this study, we developed a novel Y-series SMA, called Y6-Se-O, by adopting benzoselenadiazole as the central core and alkoxy side chains on the beta-position of thiophene moieties. The alkoxy substitution yields obvious effects on frontier orbitals of molecules and thus open-circuit voltage (VOC) of the corresponding devices. The lowest unoccupied molecular orbital (LUMO) level of Y6-Se-O is up-shifted compared to that of Y6-Se, therefore, a higher VOC of 0.94 V was attained. Additionally, when mixed with the donor polymer PM6, the Y6-Se-O-based blend films can maintain optimal morphology with stronger crystallinity and reasonable phase segregation, which leads to efficient charge dissociation, suppressed recombination, and balanced charge transportation. As a result, the PM6:Y6-Se-O-based devices reached a better efficiency of 17.5%. Our study demonstrated that the introduction of alkoxy side chains is an effective approach to tuning the optoelectrical properties of SMAs and facilitates both VOC and efficiencies. We developed a novel Y-series small molecule acceptor by adopting benzoselenadiazole central core and alkoxy side chains on the beta-position of thiophene moieties, inducing a boost in performance due to upshifted energy levels and optimized morphology.

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