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In-situ Investigations of Co@Al2O3 Ammonia Decomposition Catalysts: The Interaction between Support and Catalyst

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Weidenthaler,  Claudia
Research Group Weidenthaler, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Schmidt,  Wolfgang
Research Group Schmidt, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Leiting,  Sebastian
Research Group Weidenthaler, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Ternieden,  Jan
Research Group Weidenthaler, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Kostis,  Alexander
Service Department Lehmann (EMR), Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Ulucan,  Tolga Han
Research Group Weidenthaler, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Budiyanto,  Eko
Research Group Tüysüz, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Citation

Weidenthaler, C., Schmidt, W., Leiting, S., Ternieden, J., Kostis, A., Ulucan, T. H., et al. (2022). In-situ Investigations of Co@Al2O3 Ammonia Decomposition Catalysts: The Interaction between Support and Catalyst. ChemCatChem, 14(20): e202200688. doi:10.1002/cctc.202200688.


Cite as: https://hdl.handle.net/21.11116/0000-000B-3431-3
Abstract
Cracking of ammonia, a hydrogen carrier with high storage capacity, gains increasing attention for fuel cell systems for heavy load transportation. In this work, we studied the influence of metal loading and synthesis temperatures on the properties of Co@Al2O3 catalysts. The combination of in situ bulk characterization methods with in situ surface spectroscopy provides insights into the structure-property relation of the Co catalyst on the γ-Al2O3 support. At too high temperatures, the formation of CoAl2O4 during synthesis or during the catalytic reaction itself results in inactive mixed metal aluminium spinels which do not contribute to the catalytic reaction. The amount of ‘active’ Co catalyst thus varies significantly as well as its catalytic activity. The latter is correlated to the size of the reduced Co particles on the alumina support. The experiments also highlight that the state of the catalyst changes after reaction which strongly emphasizes the necessity of in situ studies.