X射线光电子能谱
结合能
薄膜
化学计量学
分析化学(期刊)
费米能级
氧气
材料科学
带隙
氢
化学
纳米技术
原子物理学
物理化学
核磁共振
物理
有机化学
光电子学
色谱法
量子力学
电子
作者
J. Szuber,G. Czempik,R. Larciprete,Dorota Koziej,B. Adamowicz
标识
DOI:10.1016/s0040-6090(01)00982-8
摘要
In this paper, the XPS study of SnO2 thin films deposited by the L-CVD technique are presented. The influence of exposition of the as-deposited samples to oxygen O2 and hydrogen H2 on their stoichiometry was determined. Moreover, on the basis of detailed shape analysis of the Sn3d5/2 and O1s XPS peaks, the chemical shift of binding energy corresponding to the change of sample stoichiometry was separated from a shift of the binding energy corresponding to the change of interface Fermi level position EF–Ev in the band gap, using a new procedure of deconvolution of the core level XPS peaks. The shift of the Sn3d5/2 peak by approximately 0.5 eV towards the lower binding energy after highest H2 exposure was interpreted as a true chemical shift due to an increase of Sn2+ component, whereas the shift of Sn3d5/2 peak and O1s peak after highest O2 exposure by approximately 0.5 eV towards the lower binding energy was interpreted as a result of the shift of the interface Fermi level position in the band gap towards the top of valence band at the surface, which corresponds to a deep accumulation layer typical for SnO2 thin films.
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