Critical Role of the End-group Acceptor in Enhancing the Efficiency of Indacenodithiophene-Benzothiadiazole-Linked Nonfullerene Organic Solar Cells through Morphology Optimization

Abstract

Solution-processed organic solar cells (OSCs) have great promise for next-generation solar energy conversion technologies. Innovative acceptors are constantly being designed to improve device efficiency. In this work, we designed and synthesized a series of A–π–D–π–A type non-fullerene acceptor (NFA) molecules, named IB-TOT, IB-TOM, IB-IOO, and IB-IOM for their applications in OSCs. All molecules showed high thermal stability, broad photoabsorption, and relatively lower highest occupied molecular orbital (HOMO) energy levels from −5.48eV to −5.58eV. The optimized OSCs based on these NFAs and PTB7-Th donor deliver power conversion efficiencies (PCEs) of 8.19%, 5.50%, 2.42%, and 3.10% for IB-TOT, IB-TOM, IB-IOO, and IB-IOM molecules, respectively. The higher PCE of IB-TOT-based OSCs is attributed to their excellent miscibility and superior interpenetrating network morphology compared to the other three compounds. These results demonstrate that using the 3-ethylrhodanine acceptor unit to construct the NFA molecule is a successful approach for outstanding achievement in OSCs.