材料科学
异质结
光电子学
电致发光
钙钛矿(结构)
光伏
卤化物
半导体
离子键合
薄膜
氧化物
离子
图层(电子)
纳米技术
光伏系统
无机化学
化学工程
化学
工程类
生物
有机化学
冶金
生态学
作者
Sang-Hyun Chin,Lorenzo Mardegan,Francisco Palazón,Michele Sessolo,Henk J. Bolink
出处
期刊:ACS Photonics
[American Chemical Society]
日期:2022-07-07
卷期号:9 (7): 2483-2488
被引量:1
标识
DOI:10.1021/acsphotonics.2c00604
摘要
Metal halide perovskites have emerged as a promising group of materials for optoelectronic applications such as photovoltaics, light emission, and photodetectors. So-far, in particular, the stability of light-emitting devices is limited, which is in part attributed to the intrinsic ionic conductivity of these materials. High-performance devices inevitably contain heterojunctions similar to other optoelectronic devices based on oxide perovskites, II–VI, or III–V group semiconductors. To enable efficient heterojunctions, ion exchange at the interface between different layers should be controlled. Herein, we report a method that enables to control and monitor the extent of anion intermixing between solution-processed lead bromide and vacuum-deposited lead chloride perovskite films. Taking advantage of the ability to fine tune the layer thicknesses of the vacuum-deposited films, we systematically study the effect of film thickness on anionic intermixing. Using these multiple layers, we prepare proof of principle light-emitting devices exhibiting green and blue electroluminescence.
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