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In situ surface analysis in selective oxidation catalysis: n-Butane conversion over VPP

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Bluhm,  Hendrik
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Hävecker,  Michael
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Kleimenov,  Evgueni
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Knop-Gericke,  Axel
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Liskowski,  Andrzej
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Schlögl,  Robert
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Su,  Dang Sheng
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Citation

Bluhm, H., Hävecker, M., Kleimenov, E., Knop-Gericke, A., Liskowski, A., Schlögl, R., et al. (2003). In situ surface analysis in selective oxidation catalysis: n-Butane conversion over VPP. Topics in Catalysis, 23, 99-107. doi:10.1023/A:1024824404582.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0011-11E6-9
Abstract
In-situ analysis of the surface of a working selective oxidation catalyst is an essential yet rarely conducted experiment in attempts to derive structure-function relationships. The case study of n-butane oxidation over vanadyl pyrophosphate (VPP) is used to develop a general working hypothesis and to illustrate that the molecular properties of the substrate set boundary conditions on the surface chemical properties of the catalyst. Experiments using in-situ X-ray photoelectron spectroscopy (XPS) and in-situ low energy X-ray absorption spectroscopy are used to derive compositional, electronic, and geometric structural information of the surface of the working VPP. These data allow the conclusion that a surface phase different from VPP must be present covering at least part of the active material. The recent data together with literature observations are used to derive a scenario explaining the function of VPP as a unique catalytic system.