Impact of grain boundaries on efficiency and stability of organic-inorganic trihalide perovskites

被引:244
|
作者
Chu, Zhaodong [1 ]
Yang, Mengjin [2 ]
Schulz, Philip [2 ]
Wu, Di [1 ]
Ma, Xin [1 ]
Seifert, Edward [1 ]
Sun, Liuyang [1 ]
Li, Xiaoqin [1 ]
Zhu, Kai [2 ]
Lai, Keji [1 ]
机构
[1] Univ Texas Austin, Dept Phys, Austin, TX 78712 USA
[2] Natl Renewable Energy Lab, Golden, CO 80401 USA
基金
美国国家科学基金会;
关键词
SOLAR-CELLS; CH3NH3PBI3; PEROVSKITE; HALIDE PEROVSKITES; CARRIER LIFETIME; THIN-FILMS; PLANAR; DEGRADATION; RECOMBINATION; MOBILITIES; ROUTE;
D O I
10.1038/s41467-017-02331-4
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Organic-inorganic perovskite solar cells have attracted tremendous attention because of their remarkably high power conversion efficiencies. To further improve device performance, it is imperative to obtain fundamental understandings on the photo-response and long-term stability down to the microscopic level. Here, we report the quantitative nanoscale photo-conductivity imaging on two methylammonium lead triiodide thin films with different efficiencies by light-stimulated microwave impedance microscopy. The microwave signals are largely uniform across grains and grain boundaries, suggesting that microstructures do not lead to strong spatial variations of the intrinsic photo-response. In contrast, the measured photoconductivity and lifetime are strongly affected by bulk properties such as the sample crystallinity. As visualized by the spatial evolution of local photoconductivity, the degradation process begins with the disintegration of grains rather than nucleation and propagation from visible boundaries between grains. Our findings provide insights to improve the electro-optical properties of perovskite thin films towards large-scale commercialization.
引用
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页数:8
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