Extended Conjugation and End-Group Modification of Silicon-Bridged Carbazole-Based Non-Fullerene Acceptors in Indoor Organic Photovoltaics
In this work, the strategies of extended conjugation and end-group modification are used to design four non-fullerene acceptors, DTTSiC-2F, DTTSiC-2Cl, DTTSiC-4F, and DTTSiC-4Cl. To investigate the influence of extended conjugation and end-group modification, grazing-incidence wide-angle X-ray scatt...
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Published in | ACS applied energy materials Vol. 5; no. 11; pp. 13851 - 13860 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
American Chemical Society
28.11.2022
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Subjects | |
Online Access | Get full text |
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Summary: | In this work, the strategies of extended conjugation and end-group modification are used to design four non-fullerene acceptors, DTTSiC-2F, DTTSiC-2Cl, DTTSiC-4F, and DTTSiC-4Cl. To investigate the influence of extended conjugation and end-group modification, grazing-incidence wide-angle X-ray scattering is used to analyze the packing alignment of the molecules. Photovoltaic performances under both AM 1.5G and indoor conditions are examined. Owing to the push-pull effect, DTTSiC-2F and DTTSiC-2Cl manifest a much higher lowest unoccupied molecular orbital, resulting in higher V OC. DTTSiC-4F and DTTSiC-4Cl manifest higher J SC due to the red-shifted and stronger absorption. Under indoor conditions, devices based on PM6:DTTSiC-4Cl exhibit a power conversion efficiency of 19.18% with a V OC of 0.79 V, a J SC of 92.15 μA/cm2, and an FF of 73.21%, proving that extended conjugation and end-group modification are particularly promising strategies for developing indoor organic photovoltaics. |
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ISSN: | 2574-0962 2574-0962 |
DOI: | 10.1021/acsaem.2c02472 |