The innovation of high-performance fused-ring electron acceptors (FREAs) has carried the field of organic solar cells (OSCs) toward a new stage of development. However, due to high synthetic complexity and production costs, FREAs may not be the most promising candidates for future commercialization applications. To address these disadvantages of FREAs, a series of low-cost acceptors, named as noncovalently FREAs (NFREAs), is successfully constructed by employing the strategy of noncovalently conformational locks. Herein, a novel NFREA (BDTO-4F) based on 3,7-dialkyloxybenzo[1,2-b:4,5-b']dithiophene is synthesized and fully characterized. Benefiting from the complementary absorption of the donor and acceptor, balanced charge transport, and favorable film morphology, J52:BDTO-4F based OSCs afford a satisfied power conversion efficiency of 12.09%, much higher than PBDB-T:BDTO-4F-based devices (8.30%). It is worth mentioning that BDTO-4F possesses a higher figure-of-merit value of 55.65 in comparison with several representative FREAs based on a cost-efficiency evaluation. This work demonstrates the potential of the novel benzo[1,2-b:4,5-b″]dithiophene derivative for constructing low-cost and high-performance NFREAs, providing a valuable insight on the materials design.
Keywords: benzodithiophene; noncovalently conformational locks; noncovalently fused-ring electron acceptors; organic solar cells.
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