Trap States in Lead Iodide Perovskites

钙钛矿(结构) 碘化物 化学 氯化铅 带隙 太阳能电池 放松(心理学) 化学物理 电子 彭宁离子阱 氯化物 光电子学 结晶学 无机化学 材料科学 离子 物理 有机化学 社会心理学 量子力学 心理学
作者
Xiaoxi Wu,M. Tuan Trinh,Daniel Niesner,Haiming Zhu,Zachariah M. Norman,Jonathan S. Owen,Omer Yaffe,Bryan Kudisch,Xiaoyang Zhu
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:137 (5): 2089-2096 被引量:945
标识
DOI:10.1021/ja512833n
摘要

Recent discoveries of highly efficient solar cells based on lead iodide perovskites have led to a surge in research activity on understanding photo carrier generation in these materials, but little is known about trap states that may be detrimental to solar cell performance. Here we provide direct evidence for hole traps on the surfaces of three-dimensional (3D) CH3NH3PbI3 perovskite thin films and excitonic traps below the optical gaps in these materials. The excitonic traps possess weak optical transition strengths, can be populated from the relaxation of above gap excitations, and become more significant as dimensionality decreases from 3D CH3NH3PbI3 to two-dimensional (2D) (C4H9NH3I)2(CH3NH3I)(n-1)(PbI2)(n) (n = 1, 2, 3) perovskites and, within the 2D family, as n decreases from 3 to 1. We also show that the density of excitonic traps in CH3NH3PbI3 perovskite thin films grown in the presence of chloride is at least one-order of magnitude lower than that grown in the absence of chloride, thus explaining a widely known mystery on the much better solar cell performance of the former. The trap states are likely caused by electron-phonon coupling and are enhanced at surfaces/interfaces where the perovskite crystal structure is most susceptible to deformation.
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