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Understanding heterogeneous catalysis on an atomic scale: A combined surface science and reactivity investigation for the dehydrogenation of ethylbenzene over iron oxide catalysts

MPS-Authors
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Kuhrs,  Christian
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Arita,  Yoshinobu
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Weiss,  Werner
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Ranke,  Wolfgang
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

Kuhrs, C., Arita, Y., Weiss, W., Ranke, W., & Schlögl, R. (2000). Understanding heterogeneous catalysis on an atomic scale: A combined surface science and reactivity investigation for the dehydrogenation of ethylbenzene over iron oxide catalysts. Topics in Catalysis, 14(1-4), 111-123. doi:10.1023/A:1009067302464.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0011-1993-0
Abstract
In order to study the dehydrogenation of ethylbenzene to styrene, epitaxial iron oxide model catalyst
films with Fe3O4(111), a-Fe2O3(0001) and KFexOy(111) stoichiometry were prepared in single crystal
quality on Pt(111). They were investigated using surface science techniques before and after
atmospheric pressure reaction experiments in a newly designed single crystal flow reactor. As
expected from low pressure measurements, Fe3O4(111) is catalytically inactive. The catalytic activity
of a-Fe2O3(0001) starts after an activation period of about 45 minutes. After that, the surface is
essentially clean but shows a high concentration of defects. On the potassium promoted films, however,
the activation period is much longer, the activity then is higher and the surface gets covered completely
with carbon and oxygen during reaction. This indicates a different reaction pathway on the promoted
films with a carbon-oxygen species as catalytically active species