材料科学
钙钛矿(结构)
串联
能量转换效率
带隙
光电子学
卤化物
化学工程
纳米技术
无机化学
复合材料
工程类
化学
作者
Tianfei Xu,Wanchun Xiang,Junjie Yang,Dominik J. Kubicki,Wolfgang Tress,Tao Chen,Zhimin Fang,Yali Liu,Shengzhong Liu
标识
DOI:10.1002/adma.202303346
摘要
Abstract Due to their excellent thermal stability and ideal bandgap, metal halide inorganic perovskite based solar cells (PSCs) with inverted structure are considered as an excellent choice for perovskite/silicon tandem solar cells. However, the power conversion efficiency (PCE) of inverted inorganic perovskite solar cells (PSCs) still lags far behind that of conventional n–i–p PSCs due to interfacial energy level mismatch and high nonradiative charge recombination. Herein, the performance of inverted PSCs is significantly improved by interfacial engineering of CsPbI 3− x Br x films with 2‐mercapto‐1‐methylimidazole (MMI). It is found that the mercapto group can preferably react with the undercoordinated Pb 2+ from perovskite by forming Pb–S bonds, which appreciably reduces the surface trap density. Moreover, MMI modification results in a better energy level alignment with the electron‐transporting material, promoting carrier transfer and reducing voltage deficit. The above combination results in an open‐circuit voltage enhancement by 120 mV, yielding a champion PCE of 20.6% for 0.09 cm 2 area and 17.3% for 1 cm 2 area. Furthermore, the ambient, operational and heat stabilities of inorganic PSCs with MMI modification are also greatly improved. The work demonstrates a simple but effective approach for fabricating highly efficient and stable inverted inorganic PSCs.
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