Abstract

Obtaining a large open-circuit voltage (VOC ) and high short-circuit current density (JSC ) simultaneously is important in improving power conversion efficiency (PCE) of organic photovoltaics. The ternary strategy with using a higher lowest unoccupied molecular orbital (LUMO) level nonfullerene acceptor (NFA) guest can achieve increased VOC , yet JSC is decreased or maintained, so it's still a challenge to offer increased VOC and JSC values concurrently via the newly presented VOC -increased ternary strategy. To overcome this issue, a new narrow bandgap NFA TT-S-4F is reported by introducing 3,6-dimethoxylthieno[3,2-b]thiophene (TT) as π-spacers to connect electron-rich core with terminal groups, so as to upshift the LUMO level and extend π-system. When adding 10% TT-S-4F into binary system based on PTB7-Th:IEICO-4F, the higher-LUMO-level of TT-S-4F, the increased charge mobilities, the reduced trap-assisted combination loss, and a finer nanofiber structure and increased phase separation size are obtained, which simultaneously promotes JSC , VOC , and fill factor (FF), thus obtaining an optimal PCE (12.5%vs 11.5%). This work illustrates that an extending conjugated backbone with large π-spacers and inclusion of alkylthiophenyl side-chains is a concept to synthesize NFA guests for use on the VOC -increased ternary strategy that enables to realize simultaneously increased JSC , VOC , and FF.

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