碘化物
钙钛矿(结构)
卤化物
铅(地质)
钝化
光致发光
材料科学
化学
无机化学
光化学
化学工程
化学物理
纳米技术
光电子学
结晶学
地质学
图层(电子)
地貌学
工程类
作者
Zeeshan Ahmad,Rebecca A. Scheidt,Matthew P. Hautzinger,Kai Zhu,Matthew C. Beard,Giulia Galli
出处
期刊:Cornell University - arXiv
日期:2022-01-01
标识
DOI:10.48550/arxiv.2201.12473
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.
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