Molecular adsorption on V2O3(0001)/Au(111) surfaces

被引:12
|
作者
Bandara, Athula
Abu-Haija, Mohammad
Hoebel, Frank
Kuhlenbeck, Helmut
Rupprechter, Guenther
Freund, Hans-Joachim
机构
[1] Fritz Haber Inst, Dept Phys Chem, D-14195 Berlin, Germany
[2] Vienna Univ Technol, Inst Mat Chem, A-1210 Vienna, Austria
关键词
vanadium oxide; carbon monoxide; propane; propene; temperature-programmed desorption; photoelectron spectroscopy; catalysis;
D O I
10.1007/s11244-007-0332-6
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The adsorption of carbon monoxide (CO), propane (C3H8) and propene (C3H6) on V2O3(0001) films grown on Au(111) was studied by Temperature Programmed Desorption (TPD) and X-ray Photoelectron Spectroscopy (XPS). The "oxidized" surface (i.e., as prepared exhibiting V=O termination), the "reduced" surface (i.e., V=O groups being removed by electron irradiation), as well as the oxygen pre-covered reduced surface were investigated. Both TPD and XPS indicate that the oxidized surface has little affinity for CO adsorption, while the reduced surface readily binds CO (CO amount approx. 10 times higher). Accordingly, CO can be used to titrate the presence or absence of vanadyl oxygen (via adsorption on the vanadium atoms) but also of defects like surface oxygen vacancies. For propane and propene, desorption of the parent molecules was the major process, i.e., surface reactions were absent under the applied conditions. When oxygen was pre-adsorbed on the reduced surface, the adsorption properties resembled that of the oxidized surface, i.e., the vanadyl groups were (partially) re-established. TPD and XPS provide a handle to differentiate the binding sites on the V2O3 surface.
引用
收藏
页码:223 / 230
页数:8
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