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Stabilization of the Active Ruthenium Oxycarbonate Phase for Low-Temperature CO 2 Methanation.

Carmen Tébar-SolerVlad Martin DiaconescuLaura SimonelliAlexander MissyulVirginia Perez-DiesteIgnacio Villar-GarcíaDaviel GómezJean-Blaise BrubachPascale RoyAvelino CormaPatricia Concepcion
Published in: ACS catalysis (2024)
Interstitial carbon-doped RuO 2 catalyst with the newly reported ruthenium oxycarbonate phase is a key component for low-temperature CO 2 methanation. However, a crucial factor is the stability of interstitial carbon atoms, which can cause catalyst deactivation when removed during the reaction. In this work, the stabilization mechanism of the ruthenium oxycarbonate active phase under reaction conditions is studied by combining advanced operando spectroscopic tools with catalytic studies. Three sequential processes: carbon diffusion, metal oxide reduction, and decomposition of the oxycarbonate phase and their influence by the reaction conditions, are discussed. We present how the reaction variables and catalyst composition can promote carbon diffusion, stabilizing the oxycarbonate catalytically active phase under steady-state reaction conditions and maintaining catalyst activity and stability over long operation times. In addition, insights into the reaction mechanism and a detailed analysis of the catalyst composition that identifies an adequate balance between the two phases, i.e., ruthenium oxycarbonate and ruthenium metal, are provided to ensure an optimum catalytic behavior.
Keyphrases
  • highly efficient
  • room temperature
  • ionic liquid
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  • reduced graphene oxide
  • visible light
  • carbon dioxide
  • electron transfer
  • gold nanoparticles
  • molecular dynamics simulations