All-small-molecule organic solar cells based on cyclometalated tris-Ir(III) complexes as donor materials

Abstract

Cyclometalated tris-Ir(III) complexes with six-coordinated octahedral configuration are beneficial to reduce aggregation for improved film morphology in organic solar cells (OSCs). Herein, two homoleptic tris-Ir complexes of eBz3Ir and eTBz3Ir showing majority absorption from UV to light-blue range are designed as electron donor materials. Owing to the extended π-conjugation by an extra thiophene ring in each ligand, eTBz3Ir exhibits red-shifted and stronger absorption as well as better charge transport property than eBz3Ir. Therefore, when employing the fused-ring non-fullerene acceptor Y6 or L8-BO to fabricate all-small-molecule OSCs (ASMOSCs), eTBz3Ir blended devices demonstrate higher efficiency than eBz3Ir, with maximum power conversion efficiency (PCE) achieving at 9.48/7.55% for Y6 and 10.48/6.46% for L8-BO devices, respectively. To our knowledge, over 10% PCE is among the highest values for binary ASMOSCs based on organometallic Ir complexes as photovoltaic materials. Such uncompetitive solar-light absorption but relatively high PCE indicates homoleptic Ir complexes with octahedral configurations are expected as promising photoactive materials for high-efficiency ASMOSCs.