Iodine Vacancy Redistribution in Organic–Inorganic Halide Perovskite Films and Resistive Switching Effects

Organic–inorganic halide perovskite (OHP) materials, for example, CH₃NH₃PbI₃ (MAPbI₃), have attracted significant interest for applications such as solar cells, photodectors, light-emitting diodes, and lasers. Previous studies have shown that charged defects can migrate in perovskites under an electric field and/or light illumination, potentially preventing these devices from practical applications. Understanding and control of the defect generation and movement will not only lead to more stable devices but also new device concepts. Here, it is shown that the formation/annihilation of iodine vacancies (V_I's) in MAPbI₃ films, driven by electric fields and light illumination, can induce pronounced resistive switching effects. Due to a low diffusion energy barrier (≈0.17 eV), the V_I's can readily drift under an electric field, and spontaneously diffuse with a concentration gradient. It is shown that the V_I diffusion process can be suppressed by controlling the affinity of the contact electrode material to I⁻ ions, or by light illumination. An electrical-write and optical-erase memory element is further demonstrated by coupling ion migration with electric fields and light illumination. These results provide guidance toward improved stability and performance of perovskite-based optoelectronic systems, and can lead to the development of solid-state devices that couple ionics, electronics, and optics.

Electric field and light illumination controlled iodine vacancy (V_I) redistribution and resistive switching effects are demonstrated in organic–inorganic halide perovskite films. The diffusion energy barrier of V_I is ≈0.17 eV. The V_I diffusion dynamics can be modulated through engineering the anode material and controlling illumination conditions. An electrical-write and optical-erase memory element is demonstrated.

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