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Dehydrogenation and Oxidative Dehydrogenation of n-Butane using Vanadium Based Catalysts: an in situ XPS study

MPS-Authors
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Vass,  Elaine M.
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Teschner,  Detre
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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Zafeiratos,  Spiros
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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

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Citation

Vass, E. M., Teschner, D., Hävecker, M., Zafeiratos, S., Schnörch, P., Knop-Gericke, A., et al. (2007). Dehydrogenation and Oxidative Dehydrogenation of n-Butane using Vanadium Based Catalysts: an in situ XPS study. In K. Godehusen (Ed.), BESSY Annual Report 2006 (pp. 94-96). Berlin: Berliner Elektronenspeicherring-Gesellschaft für Synchrotronstrahlung m.b.H. (BESSY).


Cite as: https://hdl.handle.net/11858/00-001M-0000-0011-02D4-A
Abstract
The surface electronic structure of VxOy/alumina catalysts (1-8 wt% V) was investigated using high pressure in situ XPS and XAS. Link between the electronic structure of vanadium and catalytic activity was established.