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  Highly dispersed Ni0/NixMg1-xO catalysts derived from solid solutions: How metal and support control the CO2 hydrogenation

Millet, M.-M., Tarasov, A., Girgsdies, F., Algara-Siller, G., Schlögl, R., & Frei, E. (2019). Highly dispersed Ni0/NixMg1-xO catalysts derived from solid solutions: How metal and support control the CO2 hydrogenation. ACS Catalysis, 9(9), 8534-8546. doi:10.1021/acscatal.9b02332.

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 Creators:
Millet, Marie-Mathilde1, Author              
Tarasov, Andrey1, Author              
Girgsdies, Frank1, Author              
Algara-Siller, Gerardo1, Author              
Schlögl, Robert1, 2, Author              
Frei, Elias1, Author              
Affiliations:
1Inorganic Chemistry, Fritz Haber Institute, Max Planck Society, ou_24023              
2Research Department Schlögl, Max Planck Institute for Chemical Energy Conversion, Max Planck Society, ou_3023874              

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 Abstract: Among the Ni-based catalysts studied for CO2 activation reactions, NixMg1-xO solid solutions present advantageous characteristics, mainly linked with the homogeneous distribution of the Ni species inside the MgO structure, leading to highly dispersed Ni0 supported catalysts. In this work, we report on the preparation and characterization of NixMg1-xO pre-catalysts calcined at different temperatures. The resulting Ni0/NixMg1-xO catalysts were tested for the methanation of CO2. Following the structural, morphological and chemical changes during both the calcination and the reduction, we were able to observe clear correlations between the reactivity of the catalysts and their physical properties, leading to a better understanding of the reaction mechanism and the respective contributions of the metal and the support. While no change was observed in the formation of CH4 over the range of temperature tested, the CO formation as by-product clearly changed with the increasing temperatures. Our results are consistent with the hypothesis that two different CO formation mechanisms are occurring, but depending on the temperature, one dominates over the other. This study illustrates the importance of the complex interplay of metal particles and oxidic support (likely at the interface), both actively participating in the CO2 characterization of hydrogenation mechanism.

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Language(s): eng - English
 Dates: 2019-06-042019-09-06
 Publication Status: Published online
 Pages: 13
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1021/acscatal.9b02332
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Title: ACS Catalysis
  Abbreviation : ACS Catal.
Source Genre: Journal
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Publ. Info: Washington, DC : ACS
Pages: 13 Volume / Issue: 9 (9) Sequence Number: - Start / End Page: 8534 - 8546 Identifier: ISSN: 2155-5435
CoNE: https://pure.mpg.de/cone/journals/resource/2155-5435