Substrate-termination and H2O-coverage dependent dissociation of H2O on Fe3O4(111)

被引:37
作者
Cutting, R. S. [3 ]
Muryn, C. A. [4 ]
Vaughan, D. J. [3 ]
Thornton, G. [1 ,2 ]
机构
[1] UCL, London Ctr Nanotechnol, London WC1H 0AJ, England
[2] UCL, Dept Chem, London WC1H 0AJ, England
[3] Univ Manchester, Williamson Res Ctr Mol Environm Sci, Sch Earth Atmospher & Environm Sci, Manchester M13 9PL, Lancs, England
[4] Univ Manchester, Sch Chem, Manchester M13 9PL, Lancs, England
基金
英国工程与自然科学研究理事会; 英国自然环境研究理事会;
关键词
X-ray photoclectron spectroscopy; ultraviolet photoelectron spectroscopy; scanning tunneling microscopy; iron oxide; water;
D O I
10.1016/j.susc.2008.01.012
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The reaction of Fe3O4(111) with water vapour has been studied with scanning tunnelling microscopy (STM) and with X-ray and UV-photoemission as a function of water partial pressure and temperature. The photoemission results point to dissociation to form surface hydroxyls at a partial pressure of 10(-6) mbar H2O and a Substrate temperature of about 200 K. At 298 K it is known that dissociation occurs at around 10(-3) mbar [Kendelewicz et al., Surf. Sci. 453 (2000) 32]. This difference suggests that an intermolecular mechanism of dissociation is involved. It also suggests that the pressure dependence arises from a coverage term rather than differences in the Gibbs Free Energies of the oxide and hydroxide, as previously proposed. The STM results indicate that dissociation takes place on a termination of Fe3O4(111) thought to contain a 1/4 monolayer (ML) of Fe3+ ions on top of a close-packed oxygen monolayer. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1155 / 1165
页数:11
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