钙钛矿(结构)
光催化
二氧化钛
光化学
材料科学
紫外线
卤化物
辐照
化学工程
化学
无机化学
光电子学
催化作用
复合材料
有机化学
核物理学
工程类
物理
作者
Pengjie Hang,Jiangsheng Xie,Ge Li,Ying Wang,Desheng Fang,Yuxin Yao,Danyan Xie,Can Cui,Keyou Yan,Jianbin Xu,Deren Yang,Xuegong Yu
出处
期刊:iScience
[Cell Press]
日期:2019-10-12
卷期号:21: 217-227
被引量:61
标识
DOI:10.1016/j.isci.2019.10.021
摘要
The inorganic metal oxides (IMOs), including titanium dioxide (TiO2) and tin dioxide (SnO2), inevitably induce decomposition of perovskite under UV illumination owing to their photocatalytic activity, and the use of a UV filter will add extra cost and reduce the effective power output. Here, we first reveal that the weak Pb-I bond in I-based perovskite is prone to breakage under UV photocatalysis, leading to serious degradation of the SnO2/perovskite interface. We introduced a chlorine-rich mixed-halide perovskite interlayer (ClMPI), which possesses an excellent tolerance to photocatalysis owing to the strong Pb-Cl bond, between the SnO2 and I-based perovskite. The ClMPI-based device achieves an enhanced efficiency of up to 21.01% (certified 20.17%). Most importantly, the resultant devices can maintain >94% of their initial performance after 180 h under outdoor solar irradiation, >80% after 500 h under UV irradiation, and 500 h under continuous full spectrum illumination at their maximum power points.
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