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The role of carbon species in heterogeneous catalytic processes: an in situ soft x-ray photoelectron spectroscopy study

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Vass,  Elaine M.
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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Teschner,  Detre
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., Hävecker, M., Zafeiratos, S., Teschner, D., Knop-Gericke, A., & Schlögl, R. (2008). The role of carbon species in heterogeneous catalytic processes: an in situ soft x-ray photoelectron spectroscopy study. Journal of Physics: Condensed Matter, 20(18): 184016. doi:10.1088/0953-8984/20/18/184016.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0010-FEC7-5
Abstract
High pressure X-ray photoelectron spectroscopy (XPS) is used to characterize heterogeneous catalytic processes. The success of the new technique based on the possibility to correlate the catalytic activity and the electronic structure of an active surface. The dynamic character of a catalyst surface can be demonstrated impressively by this technique. In this contribution the basics of high pressure XPS will be discussed. Three examples of heterogeneous catalytic reactions are presented in this contribution. The selective hydrogenation of 1-pentyne over Pd based catalysts and the dehydrogenation of n-butane and the oxidation of ethylene over V based catalysts.
It is shown, that the formation of subsurface carbons plays an important role in all the examples. The incorporated carbon changes the electronic structure of the surface and so controls the selectivity of the reaction. A change of the educts in the reaction atmosphere induces modifications of the electronic surface structure of the operation catalysts.