材料科学
卤化物
表面光电压
开尔文探针力显微镜
光伏
工作职能
X射线光电子能谱
紫外光电子能谱
带材弯曲
价(化学)
表面状态
紫外线
钙钛矿(结构)
反向光电发射光谱
光电发射光谱学
纳米技术
曲面(拓扑)
电子结构
光电子学
化学物理
凝聚态物理
无机化学
光伏系统
化学工程
光谱学
结晶学
原子力显微镜
图层(电子)
生物
生态学
有机化学
工程类
量子力学
数学
几何学
物理
化学
作者
Fengshuo Zu,Christian M. Wolff,Maryline Ralaiarisoa,Patrick Amsalem,Dieter Neher,Norbert Koch
标识
DOI:10.1021/acsami.9b05293
摘要
The tremendous success of metal-halide perovskites, especially in the field of photovoltaics, has triggered a substantial number of studies in understanding their optoelectronic properties. However, consensus regarding the electronic properties of these perovskites is lacking due to a huge scatter in the reported key parameters, such as work function (Φ) and valence band maximum (VBM) values. Here, we demonstrate that the surface photovoltage (SPV) is a key phenomenon occurring at the perovskite surfaces that feature a non-negligible density of surface states, which is more the rule than an exception for most materials under study. With ultraviolet photoelectron spectroscopy (UPS) and Kelvin probe, we evidence that even minute UV photon fluxes (500 times lower than that used in typical UPS experiments) are sufficient to induce SPV and shift the perovskite Φ and VBM by several 100 meV compared to dark. By combining UV and visible light, we establish flat band conditions (i.e., compensate the surface-state-induced surface band bending) at the surface of four important perovskites, and find that all are p-type in the bulk, despite a pronounced n-type surface character in the dark. The present findings highlight that SPV effects must be considered in all surface studies to fully understand perovskites' photophysical properties.
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