质子
扩散
氧化物
单层
扫描隧道显微镜
化学物理
催化作用
化学
过渡金属
密度泛函理论
氧气
表面扩散
材料科学
纳米技术
无机化学
分析化学(期刊)
物理化学
计算化学
吸附
热力学
有机化学
物理
量子力学
作者
Lindsay R. Merte,Guowen Peng,Ralf Bechstein,Felix Rieboldt,Carrie A. Farberow,Lars C. Grabow,Wilhelmine Kudernatsch,Stefan Wendt,Erik Lægsgaard,Manos Mavrikakis,Flemming Besenbacher
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2012-05-17
卷期号:336 (6083): 889-893
被引量:299
标识
DOI:10.1126/science.1219468
摘要
The diffusion of hydrogen atoms across solid oxide surfaces is often assumed to be accelerated by the presence of water molecules. Here we present a high-resolution, high-speed scanning tunneling microscopy (STM) study of the diffusion of H atoms on an FeO thin film. STM movies directly reveal a water-mediated hydrogen diffusion mechanism on the oxide surface at temperatures between 100 and 300 kelvin. Density functional theory calculations and isotope-exchange experiments confirm the STM observations, and a proton-transfer mechanism that proceeds via an H(3)O(+)-like transition state is revealed. This mechanism differs from that observed previously for rutile TiO(2)(110), where water dissociation is a key step in proton diffusion.
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