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

Authors :
Tébar-Soler C
Diaconescu VM
Simonelli L
Missyul A
Perez-Dieste V
Villar-García I
Gómez D
Brubach JB
Roy P
Corma A
Concepción P
Source :
ACS catalysis [ACS Catal] 2024 Mar 06; Vol. 14 (6), pp. 4290-4300. Date of Electronic Publication: 2024 Mar 06 (Print Publication: 2024).
Publication Year :
2024

Abstract

Interstitial carbon-doped RuO <subscript>2</subscript> catalyst with the newly reported ruthenium oxycarbonate phase is a key component for low-temperature CO <subscript>2</subscript> 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.<br />Competing Interests: The authors declare no competing financial interest.<br /> (© 2024 The Authors. Published by American Chemical Society.)

Details

Language :
English
ISSN :
2155-5435
Volume :
14
Issue :
6
Database :
MEDLINE
Journal :
ACS catalysis
Publication Type :
Academic Journal
Accession number :
38510664
Full Text :
https://doi.org/10.1021/acscatal.3c05679