钙钛矿(结构)
卤化物
碘化物
铅(地质)
降级(电信)
碘
材料科学
挥发
化学工程
分解
无机化学
化学
纳米技术
冶金
地质学
有机化学
电气工程
工程类
地貌学
作者
Shenghao Wang,Yan Jiang,Emilio J. Juárez‐Pérez,Luis K. Ono,Yabing Qi
出处
期刊:Nature Energy
[Springer Nature]
日期:2016-12-22
卷期号:2 (1)
被引量:542
标识
DOI:10.1038/nenergy.2016.195
摘要
Efficiencies of organic–inorganic lead halide perovskite solar cells (PSCs) have significantly increased in recent years, but instability issues impede their further development and application. Previous studies reported that volatile species (for example, iodine, I2) were generated when perovskites were subjected to moisture, oxygen, light illumination, applied electric field, and thermal stress (all of which are relevant to the operation of PSCs in practical applications). Here we show that I2 vapour causes severe degradation of MAPbI3 (MA: CH3NH3+) perovskite, due to chemical chain reactions. Furthermore, I2 vapour could also induce degradation of other iodide-based perovskites, such as FAPbI3 (FA: HC(NH2)2+) and FA0.8Cs0.2PbI3. The results reveal a universal degradation factor for iodide-based perovskite by I2. As the release of I2 is nearly inevitable during practical applications, this work suggests that MAPbI3 may not be suitable for long-term stable solar cells and it is imperative to develop other types of perovskite material to achieve stable PSCs. Extensive efforts are under way to tackle the degradation issue—one of the biggest challenges for the practical application of perovskite-based solar cells. Here the authors show that CH3NH3PbI3 and several other iodine-containing perovskites are inherently unstable due to decomposition caused by self-generated I2.
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