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Low-oxidation-state Ru sites stabilized in carbon-doped RuO2 with low-temperature CO2 activation to yield methane

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URI: http://hdl.handle.net/10498/30776

DOI: 10.1038/S41563-023-01540-1

ISSN: 1476-4660

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Author/s
Tébar Soler, Carmen; Martin Diaconescu, Vlad; Simonelli, Laura; Missyul, Alexander; Pérez-Dieste, Virginia; Villar-García, Ignacio; Brubach, Jean-Blaise; Roy, Pascale; López Haro, MiguelAuthority UCA; Calvino Gámez, José JuanAuthority UCA; Concepción, Patricia; Corma, Avelino
Date
2023
Department
Ciencia de los Materiales e Ingeniería Metalúrgica y Química Inorgánica
Source
Nature Materials 22: 762-768 (2023)
Abstract
The generation of methane fuel using surplus renewable energy with CO as the carbon source enables both the decarbonization and substitution of fossil fuel feedstocks. However, high temperatures are usually required for the efficient activation of CO. Here we present a solid catalyst synthesized using a mild, green hydrothermal synthesis that involves interstitial carbon doped into ruthenium oxide, which enables the stabilization of Ru cations in a low oxidation state and a ruthenium oxycarbonate phase to form. The catalyst shows an activity and selectivity for the conversion of CO into methane at lower temperatures than those of conventional catalysts, with an excellent long-term stability. Furthermore, this catalyst is able to operate under intermittent power supply conditions, which couples very well with electricity production systems based on renewable energies. The structure of the catalyst and the nature of the ruthenium species were acutely characterized by combining advanced imaging and spectroscopic tools at the macro and atomic scales, which highlighted the low-oxidation-state Ru sites (Ru, 0 < n < 4) as responsible for the high catalytic activity. This catalyst suggests alternative perspectives for materials design using interstitial dopants.
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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
This work is under a Creative Commons License Attribution-NonCommercial-NoDerivatives 4.0 Internacional

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