LAUSR

In bulk-heterojunction-based organic photovoltaics, strong light-absorbing ability is one of the most important advantages of nonfullerene acceptors prior to fullerene derivatives. Herein, a series of electron-donating units was asymmetrically connected at the imide positions of perylene diimide (PDI), which is a classic-electron acceptor building block. The photoinduced electron-transfer behaviors were compared in different substitutions by steady/time-resolved spectroscopy and theoretical simulation. The electron-donating ability as well as the donor–acceptor distance has a significant impact on the photoinduced electron transition from electron-donating units to the PDI core. Because of the process of charge transfer at excited states, a fast nonradiative deactivation is observed for the PDIs with relatively strong electron substituent. These results would help us to understand the electron-transfer processes from donor to acceptor in the case of the excited electron-acceptor molecule.