Long-Term Thermal Stability of Nonfullerene Organic Solar Cells via Facile Self-Assembled Interface Passivation

Although the morphological instability of the bulk-heterojunction (BHJ) organic solar cells (OSCs) based on a small-molecule nonfullerene acceptor (SM-NFA) is regarded as an important issue for understanding thermal stability, interfacial deterioration between the chemically vulnerable SM-NFAs and an interfacial layer containing reactive species is also crucial. Herein, we identified that chemical degradation of SM-NFA on a zinc oxide (ZnO) interfacial layer under thermal stress is more critical by systematically examining three SM-NFAs that have different thermal transition temperature ( T g ) values; as T g decreased, the interfacial degradation of SM-NFAs increased. However, the introduction of a highly polar and volatile molecule, 5-methyl-1 H -benzotriazole (M-BT), into the BHJ effectively passivates the defects of the ZnO surface by forming a self-assembled layer. The optimized target device exhibited excellent long-term thermal stability that retains above 85% of the initial efficiency after 1000 h (= T 85 ) at 85 °C under a N 2 atmosphere, while a short T 85 within 20 h was obtained in the control device.