碘化物
钙钛矿(结构)
吸附
光化学
氧化还原
无机化学
金属
材料科学
水溶液中的金属离子
卤化物
化学
化学工程
结晶学
有机化学
工程类
作者
Zihan Fang,Xijiao Mu,Guo‐Bin Xiao,Jing Cao
标识
DOI:10.1002/anie.202418834
摘要
Imperfections in metal halide perovskites, such as those induced by light exposure or thermal stress, compromise device performance and stability. A key challenge is immobilizing volatile iodine produced by iodide oxidation and regenerating impurities like elemental lead and iodine. Here, we address this by integrating a redox‐active supramolecular assembly of nickel octaethylporphyrin into perovskite film, functioning as both an immobilizer and redox shuttle. Decorated ethyl groups in porphyrin distorts the π ring, increasing the axial ligand adsorption capacity of central metal ion, while reducing intermolecular interactions and promoting iodine adsorption achieving a maximum uptake of 3.83 mg mg‐1 to iodine. Adsorbed iodine transfers more electrons to Ni ions, leading to a weakened interaction within I‐I bond and facilitating the production of iodide ions. Such a situation further enables selective oxidation of metallic lead defects to Pb2+. Porphyrin supramolecule facilitates hole transport across perovskite grain boundaries, leading to a champion device efficiency of 25.37% for a 0.10 cm2 active area, outperforms the value of control device being 23.96%. Modified devices without encapsulation exhibit significantly enhanced stability, maintaining over 90% of its initial performance after 1,000 hours of continuous 1‐sun illumination at maximum power point at 65 oC.
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