Improved Charge Collection in Highly Efficient CsPbBrI2 Solar Cells with Light-Induced Dealloying

被引:108
|
作者
Niezgoda, J. Scott [1 ]
Foley, Benjamin J. [1 ]
Chen, Alexander Z. [1 ]
Choi, Joshua J. [1 ]
机构
[1] Univ Virginia, Dept Chem Engn, Charlottesville, VA 22904 USA
来源
ACS ENERGY LETTERS | 2017年 / 2卷 / 05期
关键词
METHYLAMMONIUM LEAD IODIDE; ORGANOMETAL TRIHALIDE PEROVSKITE; SINGLE-PHOTON EMISSION; HALIDE PEROVSKITES; PHOTOVOLTAIC EFFICIENCY; CH3NH3PBI3; PEROVSKITE; ION MIGRATION; STABILITY; NANOCRYSTALS; DIFFUSION;
D O I
10.1021/acsenergylett.7b00258
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Halide dealloying in CsPbBrI2 perovskite solar cells proves to be critical in achieving high performance. This dealloying occurs under steady illumination and is a reversible process, suggesting transitions between equilibrium states under dark and illuminated environments. Through decoupling charge collection in the electron- and hole-transporting layers, our photoluminescence, X-ray diffraction, and solar cell device characterization results suggest that the light-induced halide dealloying improves hole collection in solar cells, resulting in increased efficiency (9.2% +/- 0.64 on average with a champion power conversion efficiency of 10.3%). Our results provide deeper insights on the impact of dealloying on perovskite solar cell performance and highlight the growing potential of all -inorganic perovskite solar cells.
引用
收藏
页码:1043 / 1049
页数:7
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