Abstract

AbstractThe inverted perovskite solar cell has made great progress in recent years and the quality of the heterojunction has played a key role. Here, a series of halide‐substituted benzoic acid molecules are investigated as the bridge between nickel oxide and the perovskite, constructing a stable and efficient buried heterojunction via halogen bonding. The designed molecules are anchored at the surface of NiO by the coordination between the carboxyl and hydroxyl groups. On the opposite site of the molecules, strong halogen bonding is formed by binding the undercoordinated I− at the buried surface of the perovskite, which inhibits the generation of I2 under continuous light soaking and thereby suppresses the formation of voids. Moreover, the highly directional halogen bonding is beneficial for the oriented growth of perovskite crystals, which accelerate the carrier transport. As a result, the champion device yields a power conversion efficiency (PCE) of 22.02% and the encapsulated device maintains 91.86% of the initial PCE under continuous 1‐sun illumination at 55 °C for 1000 h.

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