开尔文探针力显微镜
卤化物
表面光电压
材料科学
反向光电发射光谱
钙钛矿(结构)
光电发射光谱学
工作职能
光谱学
价(化学)
紫外线
角分辨光电子能谱
价带
紫外光电子能谱
金属
X射线光电子能谱
电子结构
带隙
光电子学
纳米技术
凝聚态物理
化学
物理
无机化学
核磁共振
结晶学
有机化学
冶金
原子力显微镜
量子力学
作者
Fengyu Zhang,Scott H. Silver,Nakita K. Noel,Florian Ullrich,Barry P. Rand,Antoine Kahn
标识
DOI:10.1002/aenm.201903252
摘要
Abstract In this essay, a case study is presented on the electronic structure of several metal halide perovskites (MHP) using Kelvin probe (KP)‐based surface photovoltage (SPV) measurements and ultraviolet photoemission spectroscopy (UPS) to demonstrate the advantages, but also the pitfalls, of using these techniques to characterize the surfaces of these materials. The first part addresses the loss of halide species from perovskite surfaces upon supragap illumination in vacuum. This has the potential to cause both a long‐term alteration of the sample work function and a modification of the KP tip during SPV measurements. If undetected, this leads to a misinterpretation of the MHP surface potential. The second part illustrates the difficulties in determining the valence band maximum (VBM) of MHP surfaces with UPS and stresses the importance of taking into account the low density of states at the VBM edge. Given this circumstance, specific care must be taken to eliminate measurement artifacts in order to ascertain the presence or absence of low densities of electronic gap states above the VBM. This essay also highlights issues such as film degradation, nonequilibrium situations (e.g., SPV), and satellite emissions, which occur during photoemission spectroscopy.
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