Development of isomer-free fullerene bisadducts for efficient polymer solar cells

Isomer-free fullerene bisadducts have been predicted to be high-performance acceptors for bulk-heterojunction (BHJ) solar cells. They can afford a higher open-circuit voltage compared with monoadducts because of the higher LUMO levels, and can also provide a higher short-circuit current and fill factor compared with the isomer mixture because of reduced energetic disorder. However, the application of isomer-free fullerene bisadducts in BHJ solar cells has met synthetic challenges. In this work, a new regioselective synthesis method, the so-called prebisaddition-confined bisfunctionalization (PCB), was developed for preparing isomer-free C-60 bisadducts. This synthesis was highly selective for obtaining homo-and hetero-bisadducts with an e configuration''. Isomer-free C-60 bisadducts, e-C-60[C((CO2Bu)-Bu-t)(2)](2), e-NC(60)BA and e-PPMF, were successfully synthesized via PCB. The gram-scale synthesis of e-C-60[C((CO2Bu)-Bu-t)(2)](2) was realized. Single crystals of e-PPMF and two intermediates were obtained. Electrochemical studies proved that a single isomer has reduced energetic disorder. e-PPMF featuring a compact methano group and a solubilizing side chain showed good performance in P3HT and low-bandgap polymer solar cells. A decent power conversion efficiency (PCE) of 8.11% was achieved in solar cells consisting of e-PPMF and the low-bandgap polymer PPDT2FBT. The outstanding photovoltaic performance of e-PPMF among the fullerene bisadducts results from its better packing and reduced energetic disorder.