摘要
Modulating hot carrier dynamics is crucial in tin halide perovskite photovoltaics, particularly under indoor illumination with limited photon flux. Herein, a fullerene derivative bearing four piperazine groups (denoted as TPPC) is synthesized to engineer the perovskite/C 60 interface. The TPPC molecule exhibits a dipole moment of 1.97 Debye, leading to enhanced adsorption energy on perovskite surface and robust interfacial interaction. The newly formed surface dipole optimizes the interfacial energy level alignment via a cascade gradient, enabling modulation of interfacial hot carrier dynamics. Consequently, TPPC-treated photovoltaic devices achieve a champion power conversion efficiency (PCE) of 22.49% and a maximum output power density ( P out ) of 64.1 μW cm -2 under white light-emitting diode illumination (3000 K, 1000 lux, 285 μW cm -2 ). Large-area (1.21 cm 2 ) devices attain a PCE of 17.94% (certified: 15.93%) and a maximum P out of 51.2 μW cm -2 under the same illumination conditions.
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