Unraveling the Defect-Dominated Broadband Emission Mechanisms in (001)-Preferred Two-Dimensional Layered Antimony-Halide Perovskite Film

By adding molar-controlled SbCl₃ in a Cs₃Sb₂Cl₉ precursor, we employed a low-temperature solution-processed approach to prepare high-quality (001)-preferred Cs₃Sb₂Cl₉ thin film, which demonstrates a stable defect-dominated broadband emission at room temperature. Density functional theory calculations reveal that the defect emission originates from the donor–acceptor pair (DAP) recombination between chlorine vacancy (V_Cl) and cesium vacancy (V_Cs). Furthermore, V_Cl + V_Cs DAP is more stable on the (001) surface. The improved film quality and the more stable V_Cl + V_Cs DAP increase the activation energy related to defect states, resulting in an enhancement of the defect emission for the high-quality (001)-preferred film. This work provides deep insight into the key role of the (001) surface in defect emission and a feasible strategy to enhance the defect emission in 2D halide perovskites A₃B₂X₉ (A = CH₃NH₃, Cs, Rb; B = Bi, Sb; X = Cl, Br, I) by control of the thin film preferred orientation.