甲脒
材料科学
钙钛矿(结构)
钝化
卤化物
化学工程
电致发光
热稳定性
能量转换效率
光伏系统
相(物质)
降级(电信)
二极管
碘化物
阳极
兴奋剂
纳米技术
无机化学
光伏
光致发光
发光二极管
光电子学
作者
Yong Luo,Z. Ouyang,Mingxuan Qiu,Feilong Fang,Zhiyu Wang,Chuanxi Zhao,Zhijuan Zhao,Jian Qing,Wenjie Mai
标识
DOI:10.1002/adfm.202515799
摘要
Abstract 3D organic–inorganic metal halide perovskite solar cells (PSCs) have demonstrated remarkable power conversion efficiencies (PCEs) exceeding 27%, yet their susceptibility to degradation under environmental stressors like moisture, heat, and light hinders their commercial viability. Quasi‐2D perovskites offer enhanced stability but suffer from inferior photovoltaic performance due to the insulating nature of organic cations and random phase distribution. This study first introduces a new multifunctional sulfonate additive, formamidinium 4‐methylbenzenesulfonate (FATsO), to address these challenges. FATsO simultaneously passivates iodide anions and lead ions through hydrogen bonding and Lewis acid‐base interactions, promoting a uniform phase distribution and efficient energy transfer. The ─NH 2 + group in FATsO stabilizes the [PbI 6 ] 4 − framework, while the ─SO 3 − group passivates uncoordinated Pb 2+ defects. Additionally, hydrogen bonding between PEA+ and ─SO 3 − restricts PEA+ diffusion, enhancing phase uniformity. As a result, FATsO‐modified PSCs achieve a PCE of 18.28%, which is a champion PCE in the reported values of MA‐based quasi‐2D PSCs with n ≤ 4 up to now. Meanwhile, when the PSC worked as a light‐emitting diode (LED) under forward bias, the electroluminescence external quantum efficiency (EQEEL) reached 2.24%. In addition, the optimized devices exhibit enhanced stability under thermal and humidity environments.
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