摘要

Perylene diimide (PDI), which features intense absorption, a low-lying energy level, and high electron mobility, is a promising building block for electron acceptors in organic solar cells (OSCs). However, this planar molecule has a strong tendency to form large aggregates during film formation which strongly limits its OSC performance. Herein, we report a new and simple PDI derivative, B(PDI)(3), in which a central benzene unit is employed to connect three PDI arms. This compact arrangement of sterically bulky PDI moieties leads to a twisted molecular geometry of the resultant structure. This suppresses the strong crystallization tendency of PDI chromophores, owing to the broken molecular coplanarity and symmetry. Therefore, B(PDI) 3 is applied as a non-fullerene acceptor in OSCs, providing a good power conversion efficiency of 5.65% when blended with the PTB7-Th donor.