Oxidative Passivation of Metal Halide Perovskites

被引:99
作者
Godding, Julian S. W. [1 ]
Ramadan, Alexandra J. [1 ]
Lin, Yen-Hung [1 ]
Schutt, Kelly [1 ]
Snaith, Henry J. [1 ]
Wenger, Bernard [1 ]
机构
[1] Univ Oxford, Clarendon Lab, Parks Rd, Oxford OX1 3PU, England
基金
英国工程与自然科学研究理事会; 欧盟地平线“2020”;
关键词
SOLAR-CELLS; AB-INITIO; OXYGEN; DEGRADATION; DETERMINES; STABILITY; IODIDE; FILM;
D O I
10.1016/j.joule.2019.08.006
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
Metal halide perovskites have demonstrated extraordinary potential as materials for next-generation optoelectronics including photovoltaics and light-emitting diodes. Nevertheless, our understanding of this material is still far from complete. One remaining puzzle is the phenomenon of perovskite "photo-brightening". the increase in photoluminescence during exposure to light in an ambient atmosphere Here, we propose a comprehensive mechanism for the reactivity of the archetypal perovskite, MAPbI(3), in ambient conditions. We establish the formation of lead-oxygen bonds by hydrogen peroxide as the key factor leading to perovskite photo-brightening. We demonstrate that hydrogen peroxide can be applied directly as an effective "post-treatment" to emulate the process and substantially improve photoluminescence quantum efficiencies. Finally, we show that the treatment can be incorporated into photovoltaic devices to give a 50 mV increase in open-circuit voltage, delivering high 19.2% steady-state power conversion efficiencies for inverted perovskite solar cells of the mixed halide, mixed cation perovskite FA(0.83)Cs(0.17)Pb(I-0.Br-9(0.1))(3).
引用
收藏
页码:2716 / 2731
页数:16
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