钙钛矿(结构)
材料科学
钝化
带隙
卤化物
能量转换效率
光电子学
开路电压
光致发光
X射线光电子能谱
溴化物
无机化学
化学工程
纳米技术
电压
化学
图层(电子)
工程类
物理
量子力学
作者
Yong Li,Weidong Xu,Nursultan Mussakhanuly,Yongyoon Cho,Jueming Bing,Jianghui Zheng,Shi Tang,Yang Liu,Guozheng Shi,Zeke Liu,Qing Zhang,James R. Durrant,Wanli Ma,Anita Ho‐Baillie,Shujuan Huang
标识
DOI:10.1002/adma.202106280
摘要
The power conversion efficiency (PCE) of solution-processed organic-inorganic mixed halide perovskite solar cells has achieved rapid improvement. However, it is imperative to minimize the voltage deficit (Woc = Eg /q - Voc ) for their PCE to approach the theoretical limit. Herein, the strategy of depositing homologous bromide salts on the perovskite surface to achieve a surface and bulk passivation for the fabrication of solar cells with high open-circuit voltage is reported. Distinct from the conclusions given by previous works, that homologous bromides such as FABr only react with PbI2 to form a large-bandgap perovskite layer on top of the original perovskite, this work shows that the bromide also penetrates the perovskite film and passivates the perovskite in the bulk. This is confirmed by the small-bandgap enlargement observed by absorbance and photoluminescence, and the bromide element ratio increasing in the bulk by time-of-flight secondary-ion mass spectrometry and depth-resolved X-ray photoelectron spectroscopy. Furthermore, a clear suppression of non-radiative recombination is confirmed by a variety of characterization methods. This work provides a simple and universal way to reduce the Woc of single-junction perovskite solar cells and it will also shed light on developing other high-performance optoelectronic devices, including perovskite-based tandems and light-emitting diodes.
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