Mobile iodides capture for highly photolysis- and reverse-bias-stable perovskite solar cells.
Xiaoxue RenJifei WangYun LinYingwei WangHaipeng XieHan HuangBin YangYanfa YanYongli GaoJun HeJinsong HuangYongbo YuanPublished in: Nature materials (2024)
For halide perovskites that are susceptible to photolysis and ion migration, iodide-related defects, such as iodine (I 2 ) and iodine vacancies, are inevitable. Even a small number of these defects can trigger self-accelerating chemical reactions, posing serious challenges to the durability of perovskite solar cells. Fortunately, before I 2 can damage the perovskites under illumination, they generally diffuse over a long distance. Therefore, detrimental I 2 can be captured by interfacial materials with strong iodide/polyiodide (I x - ) affinities, such as fullerenes and perfluorodecyl iodide. However, fullerenes in direct contact with perovskites fail to confine I x - ions within the perovskite layer but cause detrimental iodine vacancies. Perfluorodecyl iodide, with its directional I x - affinity through halogen bonding, can both capture and confine I x - . Therefore, inverted perovskite solar cells with over 10 times improved ultraviolet irradiation and thermal-light stabilities (under 85 °C and 1 sun illumination), and 1,000 times improved reverse-bias stability (under ISOS-V ageing tests) have been developed.