Growth, electronic properties and reactivity of vanadium deposited onto a thin alumina film

被引:42
作者
Bäumer, M
Biener, J
Madix, RJ
机构
[1] Max Planck Gesell, Fritz Haber Inst, D-14195 Berlin, Germany
[2] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
aluminium oxide; clusters; growth; near edge X-ray absorption fine structure; scanning tunneling microscopy; surface structure; morphology; roughness and topography; synchrotron radiation; vanadium;
D O I
10.1016/S0039-6028(99)00400-8
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 interaction of metals with oxide surfaces plays an important role in the manner of growth of the metal/oxide interface and eventually for the electronic properties and chemical reactivity of the resultant surface. We have investigated such effects for vanadium on alumina. By using a thin alumina film grown on a NiAl(110) as a model substrate, we were able to apply scanning tunneling microscopy (STM) as well as electron spectroscopic techniques without charging problems. According to our STM results, vanadium deposition at 300 K results in the formation of small thin particles/islands partly incorporated into the film at low coverages. With increasing coverage three-dimensional growth is found. The thermal stability and the growth behaviour of these nuclei at elevated deposition temperatures (greater than or equal to 600 K) are in agreement with a strong metal substrate interaction. In the coverage regime below 0.1 ML, X-ray photoelectron and X-ray absorption spectroscopy data provide evidence that the deposits are oxidized to Vx+, 1<x<2. Furthermore, we have studied the interaction at 720 K and in an ambient atmosphere of oxygen in order to check how vanadium reacts with the alumina film under more severe conditions. In fact, a thickening of the alumina film has been observed, which we ascribe to a catalytic effect of vanadia on the alumina film growth. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:189 / 198
页数:10
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