材料科学
钙钛矿(结构)
化学稳定性
兴奋剂
二价
化学工程
能量转换效率
扩散
无机化学
纳米技术
光电子学
化学
热力学
物理
工程类
冶金
作者
Jue Gong,Mengjin Yang,Dominic Rebollar,Jordan Rucinski,Zachary Liveris,Kai Zhu,Tao Xu
标识
DOI:10.1002/adma.201800973
摘要
The chemical stabilities of hybrid perovskite materials demand further improvement toward long-term and large-scale photovoltaic applications. Herein, the enhanced chemical stability of CH3NH3PbI3 is reported by doping the divalent anion Se2− in the form of PbSe in precursor solutions to enhance the hydrogen-bonding-like interactions between the organic cations and the inorganic framework. As a result, in 100% humidity at 40 °C, the 10% w/w PbSe-doped CH3NH3PbI3 films exhibited >140-fold stability improvement over pristine CH3NH3PbI3 films. As the PbSe-doped CH3NH3PbI3 films maintained the perovskite structure, a top efficiency of 10.4% with 70% retention after 700 h aging in ambient air is achieved with an unencapsulated 10% w/w PbSe:MAPbI3-based cell. As a bonus, the incorporated Se2− also effectively suppresses iodine diffusion, leading to enhanced chemical stability of the silver electrodes.
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