| Literature DB >> 22605771 |
Lindsay R Merte1, Guowen Peng, Ralf Bechstein, Felix Rieboldt, Carrie A Farberow, Lars C Grabow, Wilhelmine Kudernatsch, Stefan Wendt, Erik Lægsgaard, Manos Mavrikakis, Flemming Besenbacher.
Abstract
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.Entities:
Year: 2012 PMID: 22605771 DOI: 10.1126/science.1219468
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728