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Cu-Zn Alloy Formation as Unfavored State for Efficient Methanol Catalysts

MPG-Autoren
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Frei,  Elias
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Zwiener,  Leon
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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

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Girgsdies,  Frank
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Lunkenbein,  Thomas
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Schlögl,  Robert
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;
Department of Heterogeneous Reactions Max-Planck-Institute for Chemical Energy Conversion;

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cctc.202000777.pdf
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Zitation

Frei, E., Gaur, A., Lichternberg, H., Zwiener, L., Scherzer, M., Girgsdies, F., et al. (2020). Cu-Zn Alloy Formation as Unfavored State for Efficient Methanol Catalysts. ChemCatChem, 12(16), 4029-4033. doi:10.1002/cctc.202000777.


Zitierlink: https://hdl.handle.net/21.11116/0000-0006-A746-F
Zusammenfassung
The active sites of Cu/ZnO‐based catalysts, commercially applied for the hydrogenation of CO2 or CO2‐rich synthesis gas, are still subject of current debates. Generally, the discussion is focused on the nature of the interfacial contact between Cu and ZnO, particularly whether it is rather of oxidic (Cu−ZnO) or alloying (Cu−Zn) character. We report on kinetic investigations on a Cu/ZnO : Al high performance catalyst activated at different temperatures. Incrementally increasing temperature under reductive conditions leads also to increased CuZn‐alloy formation, analyzed by in‐situ X‐ray diffraction, in‐situ X‐ray absorption spectroscopy and high resolution transmission electron microscopy. The combination of the catalytic data and the complementary characterization techniques provide valuable insights on the relevant reaction sites for CH3OH formation. Our results highlight the complexity of the interfacial contact with evidence for Cu−ZnO reaction sites and clarify the negative impact of CuZn alloy formation on the nature of the active site.