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Reactivity between molybdenum and TiO2 (110) surfaces:: evidence of a sub-monolayer mode and a multilayer mode
被引:12
作者:
Domenichini, B
Krüger, P
Brevet, A
Bourgeois, S
Li, Z
Moller, PJ
机构:
[1] Univ Bourgogne, CNRS, UMR 5613, LRRS, F-21078 Dijon, France
[2] Aarhus Univ, ISA, DK-8000 Aarhus, Denmark
[3] Univ Copenhagen, Dept Chem, DK-2100 Copenhagen, Denmark
关键词:
molybdenum;
TiO2;
surface;
photoemission;
synchrotron radiation;
VASP;
D O I:
10.1016/j.apsusc.2004.09.149
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:
Small amounts of molybdenum (from 0.03 to 1.3 eqML) were deposited on non-stoichiometric TiO2 (1 1 0) surface. The deposits were investigated by means of LEED and X-ray/UV photoemission using synchrotron radiation. For the smallest 41 coverage (< 0.2 eqML), deposition leads to oxidation of molybdenum into species close to Mo4+. In such a case, states appearing in TiO2, band gap are mainly due to reduced titanium. For higher coverages, metallic behaviour of molybdenum is observed. This phenomenon was explained, thanks to first principle calculations, as a decrease of the Mo-O interactions for the benefit of the Mo-Mo interactions as the surface molybdenum atom density increases. (c) 2004 Elsevier B.V. All rights reserved.
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页码:403 / 407
页数:5
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