钝化
卤化物
金属
材料科学
钙钛矿(结构)
氧化磷酸化
冶金
无机化学
化学
纳米技术
结晶学
图层(电子)
生物化学
作者
Julian S.W. Godding,Alexandra J. Ramadan,Yen‐Hung Lin,Kelly Schutt,Henry J. Snaith,Bernard Wenger
出处
期刊:Joule
[Elsevier BV]
日期:2019-09-17
卷期号:3 (11): 2716-2731
被引量:105
标识
DOI:10.1016/j.joule.2019.08.006
摘要
Summary 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, MAPbI3, 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 FA0.83Cs0.17Pb(I0.9Br0.1)3.
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