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Identifying the nature of the active sites in methanol synthesis over Cu/ZnO/Al2O3 catalysts

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Laudenschleger,  Daniel
Research Department Schlögl, Max Planck Institute for Chemical Energy Conversion, Max Planck Society;

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Ruland,  Holger
Research Department Schlögl, Max Planck Institute for Chemical Energy Conversion, Max Planck Society;

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Muhler,  Martin
Research Department Schlögl, Max Planck Institute for Chemical Energy Conversion, Max Planck Society;
Laboratory of Industrial Chemistry, Ruhr Universität Bochum;

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Citation

Laudenschleger, D., Ruland, H., & Muhler, M. (2020). Identifying the nature of the active sites in methanol synthesis over Cu/ZnO/Al2O3 catalysts. Nature Communications, 11(1): 3898. doi:10.1038/s41467-020-17631-5.


Cite as: https://hdl.handle.net/21.11116/0000-0007-B447-E
Abstract
The heterogeneously catalysed reaction of hydrogen with carbon monoxide and carbon dioxide (syngas) to methanol is nearly 100 years old, and the standard methanol catalyst Cu/ZnO/Al2O3 has been applied for more than 50 years. Still, the nature of the Zn species on the metallic Cu-0 particles (interface sites) is heavily debated. Here, we show that these Zn species are not metallic, but have a positively charged nature under industrial methanol synthesis conditions. Our kinetic results are based on a self-built high-pressure pulse unit, which allows us to inject selective reversible poisons into the syngas feed passing through a fixed-bed reactor containing an industrial Cu/ZnO/Al2O3 catalyst under high-pressure conditions. This method allows us to perform surface-sensitive operando investigations as a function of the reaction conditions, demonstrating that the rate of methanol formation is only decreased in CO2-containing syngas mixtures when pulsing NH3 or methylamines as basic probe molecules. Methanol synthesis has a high potential for global CO2 reduction. Here, the authors identify the oxidation state of the zinc sites on the metallic copper particles as partially positive for an industrial Cu/ZnO/Al2O3 catalyst under high-pressure reaction conditions.