铅(地质)
碘化物
钙钛矿(结构)
氯化铅
材料科学
无机化学
化学
化学工程
冶金
地质学
有机化学
结晶学
地貌学
氯化物
工程类
作者
Zeeshan Ahmad,Rebecca A. Scheidt,Matthew P. Hautzinger,Kai Zhu,Matthew C. Beard,Giulia Galli
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2022-05-10
卷期号:7 (6): 1912-1919
被引量:12
标识
DOI:10.1021/acsenergylett.2c00850
摘要
The presence of unreacted lead iodide in organic–inorganic lead halide perovskite solar cells is widely correlated with an increase in power conversion efficiency. We investigate the mechanism for this increase by identifying the role of surfaces and interfaces present between methylammonium lead iodide perovskite films and excess lead iodide. We show how type I and II band alignments arising under different conditions result in either passivation of surface defects or hole injection. Through first-principles simulations of solid–solid interfaces, we find that lead iodide captures holes from methylammonium lead iodide and modulates the formation of defects in the perovskite, affecting recombination. Using surface-sensitive optical spectroscopy techniques, such as transient reflectance and time-resolved photoluminescence, we show how excess lead iodide affects the diffusion and surface recombination velocity of charge carriers in methylammonium lead iodide films. Our coupled experimental and theoretical results elucidate the role of excess lead iodide in perovskite solar cells.
科研通智能强力驱动
Strongly Powered by AbleSci AI