钙钛矿(结构)
材料科学
卤化物
纳米技术
结晶学
化学工程
化学
无机化学
工程类
作者
Siyu Yan,Jay B. Patel,Jae Eun Lee,Karim A. Elmestekawy,Sinclair R. Ratnasingham,Qimu Yuan,Laura M. Herz,Nakita K. Noel,Michael B. Johnston
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-09-01
卷期号:8 (10): 4008-4015
被引量:4
标识
DOI:10.1021/acsenergylett.3c01368
摘要
Metal halide perovskite semiconductors have shown significant potential for use in photovoltaic (PV) devices. While fabrication of perovskite thin films can be achieved through a variety of techniques, thermal vapor deposition is particularly promising, allowing for high-throughput fabrication. However, the ability to control the nucleation and growth of these materials, particularly at the charge-transport layer/perovskite interface, is critical to unlocking the full potential of vapor-deposited perovskite PV. In this study, we explore the use of a templating layer to control the growth of coevaporated perovskite films and find that such templating leads to highly oriented films with identical morphology, crystal structure, and optoelectronic properties independent of the underlying layers. Solar cells incorporating templated FA0.9Cs0.1PbI3–xClx show marked improvements with steady-state power conversion efficiency over 19.8%. Our findings provide a straightforward and reproducible method of controlling the charge-transport layer/coevaporated perovskite interface, further clearing the path toward large-scale fabrication of efficient PV devices.
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