材料科学
钙钛矿(结构)
偶极子
钙钛矿太阳能电池
光电子学
化学工程
离子键合
工作(物理)
能量转换效率
极地的
分子
化学物理
热力学
离子
有机化学
化学
物理
工程类
天文
作者
Tengteng Yang,Wangen Zhao,Xin Liu,Shengzhong Liu
标识
DOI:10.1002/aenm.202204192
摘要
Abstract The ionic nature of the organic‐inorganic hybrid perovskite material is prone to react with different functional groups. Here, a series of polar molecules with permanent dipole moments are designed to modify the perovskite surface termination. It is observed that proper interfacial design can significantly reduce trap state density for effective charge transfer. The energy level of the substrate can be adjusted by the magnitude and direction of the dipole moment. As a result, a high 24.54% photo‐electric conversion efficiency is reached by introducing pentafluoride benzene moieties with carboxylic functional groups. In addition, the humidity and heat stability of the perovskite device is obviously improved. This work demonstrates the importance of chemical interactions at perovskite termination and paves the way for further enhancing the performance of perovskite solar cells.
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