Vibrational spectra of alumina- and silica-supported vanadia revisited:: An experimental and theoretical model catalyst study

被引:244
作者
Magg, N
Immaraporn, B
Giorgi, JB
Schroeder, T
Bäumer, M
Döbler, J
Wu, ZL
Kondratenko, E
Cherian, M
Baerns, M
Stair, PC
Sauer, J
Freund, HJ
机构
[1] Max Planck Gesell, Fritz Haber Inst, Chem Phys Abt, D-14195 Berlin, Germany
[2] Humboldt Univ, Inst Chem, D-10099 Berlin, Germany
[3] Northwestern Univ, Evanston, IL 60208 USA
[4] Inst Appl Chem ACA Berlin Adlershof, D-12474 Berlin, Germany
基金
英国工程与自然科学研究理事会; 加拿大自然科学与工程研究理事会;
关键词
vanadium oxide; alumina; silica; scanning tunneling microscopy (STM); x-ray photoelectron spectroscopy (XPS); infrared (IR) spectroscopy; carbon monoxide; DFT calculation; Raman spectra; catalysis;
D O I
10.1016/j.jcat.2004.04.021
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
Oxide-supported vanadia particles were prepared via evaporation of vanadium metal in an oxygen ambient. As support oxides, we have employed thin, well-ordered alumina and silica films grown on top of NiAl(110) and Mo(112) surfaces. According to our analysis, the vanadia particles exhibit very similar morphology on both supports but differ in the extent of particle-support interactions. It is shown that these differences in the vanadia-support interface region strongly affect the CO adsorption behavior of the particles. The measured vibrational spectra of the model systems are interpreted on the basis of DFT calculations for model compounds and surface models for both the vanadia/silica and the vanadia/alumina system. The combined information is then compared with Raman spectra of real catalytic materials such as vanadia supported over delta-Al2O3 and mesoporous SiO2 (MCM-41) taken at different laser wavelengths. A consistent interpretation is developed, which shows that the accepted interpretation of vibrational spectra from vanadia catalysts must be revised. (C)d 2004 Elsevier Inc. All rights reserved.
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页码:88 / 100
页数:13
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