钙钛矿(结构)
卤化物
碘化物
分解
水分
材料科学
腐蚀
太阳能电池
散射
化学工程
金属
化学
化学物理
无机化学
光电子学
光学
复合材料
冶金
结晶学
有机化学
工程类
物理
作者
Kyle M. Fransishyn,Soumya Kundu,Timothy L. Kelly
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2018-08-14
卷期号:3 (9): 2127-2133
被引量:42
标识
DOI:10.1021/acsenergylett.8b01300
摘要
The main downfall of perovskite solar cells is that they degrade rapidly when exposed to heat, light, and moisture. Although previous work has elucidated the decomposition pathways of lead halide perovskites, there has been little direct insight into how perovskite decomposition affects device performance. Therefore, in order to better understand this correlation, we performed in situ grazing-incidence wide-angle X-ray scattering (GIWAXS) measurements on methylammonium lead iodide solar cells. We show that the formation of hydrate phases is not the most important device degradation pathway; rather, as water penetrates the cell, the mobility of iodide ions increases, leading to corrosion of the metallic top contact. Furthermore, the work reveals a temperature dependence to the perovskite decomposition pathway, with higher temperatures suppressing the formation of both intermediates and byproducts. The work suggests that the rigorous exclusion of moisture and the design of corrosion-resistant electrodes may help produce longer-lived perovskite solar cells.
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