The active state of supported ruthenium oxide nanoparticles during carbon dioxide methanation

Carenco, Sophie;Sassoye, Capucine;Faustini, Marco;Eloy, Pierre;Salmeron, Miquel;et.al.
(2016) The Journal of Physical Chemistry Part C: Nanomaterials and Interfaces — Vol. 120, p. 15354-15361 (2016)

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Authors
  • Carenco, SophieUPMC Université de Paris
    Author
  • Sassoye, CapucineUPMC Université de Paris
    Author
  • Faustini, MarcoUPMC Université de Paris
    Author
  • Eloy, PierreUCLouvain
    Author
  • Author
  • Salmeron, MiquelLawrence Berkeley National Laboratory, USA
    Author
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Abstract
Ruthenium catalysts supported on TiO2 have been shown to have competitive activity and selectivity for the methanation of CO2. In particular, a catalyst using preformed RuO2 nanoparticles deposited on a TiO2 support showed competitive performances in a previous study. In this work, ambient-pressure X-ray photoelectron spectroscopy was employed to determine the chemical state of this catalyst under reaction conditions. The active state of ruthenium was found to be the metallic one. Surface adsorbates were monitored in the steady state, and CHx species were found to be favored over adsorbed carbon monoxide at increasing temperatures.
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Citations

Carenco, S., Sassoye, C., Faustini, M., Eloy, P., Debecker, D., Bluhm, H., & Salmeron, M. (2016). The active state of supported ruthenium oxide nanoparticles during carbon dioxide methanation. The Journal of Physical Chemistry Part C: Nanomaterials and Interfaces, 120, 15354-15361. https://doi.org/10.1021/acs.jpcc.6b06313 (Original work published 2016)