“…Nevertheless, the long-term stability of PSCs remains a major barrier to their commercialization. The degradation of PSCs is mainly attributed to the hybrid ionic nature of perovskite materials, which is intrinsically unstable in the presence of moisture, oxygen, heat and light. − In addition, inhomogeneity of polycrystalline perovskite films due to imperfect stoichiometric ratios, nonequilibrium reactions, and partial evaporation of the organic components also deteriorates the long-term stability of PSCs . For instance, state-of-the-art PSCs have typically utilized excess lead iodide (PbI 2 ) (5–10 mol %) in the precursor solution to prepare polycrystalline perovskite films. , This is due to the fact that a slight excess of PbI 2 at the perovskite grain boundaries (GBs) and surfaces has some benefits for high efficiency PSCs, including defect passivation, reduction of halide vacancy concentration, and enhancement of carrier lifetime. − However, excess PbI 2 can be a double-edged sword for PSCs. , Numerous publications have reported that excess PbI 2 readily decomposes to gaseous I 2 and metallic Pb 0 under light and thermal stress, acting as catalytic sites to trigger perovskite decomposition. − It is therefore necessary to manage the unstable PbI 2 in perovskite films to achieve an efficient and stable PSC.…”