X射线光电子能谱
结合能
化学计量学
金红石
材料科学
星团(航天器)
表面能
电荷(物理)
分析化学(期刊)
表面状态
化学物理
结晶学
原子物理学
曲面(拓扑)
化学
物理化学
核磁共振
复合材料
物理
有机化学
量子力学
色谱法
计算机科学
程序设计语言
数学
几何学
作者
Zhiquan Jiang,Wenhua Zhang,Jin Li,Xin Yang,Faqiang Xu,Junfa Zhu,Weixin Huang
摘要
The electronic structures of Au clusters deposited on the stoichiometric and reduced rutile TiO2(110) surfaces were investigated by means of X-ray photoelectron spectroscopy. With the increasing Au thickness, the Au 4f binding energy shifts monotonically toward lower binding energy on the stoichiometric surface, essentially demonstrating a particle size effect. On the reduced surface, the Au 4f binding energy exhibits a monotonically downward shift with the increasing Au thickness below 1.5 Å, then unexpectedly shifts to higher binding energy when the Au thickness increases from 1.5 Å to 2 Å. The Au 4f binding energy shift observed on the reduced surface can be reasonably explained by a collective contribution from the particle size effect and the charge transfer from the reduced surface to Au clusters. Our results experimentally present direct XPS evidence for the charge transfer from the reduced TiO2(110) surface to Au clusters.
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