Insights into the reactivity of Ni-La catalysts for CO2methanation

Efficient catalysts are essential for CO2 methanation reaction, a key process for sustainable energy applications. This study investigates the structural and chemical properties of Ni-La perovskite-based catalysts synthesized via one-pot and impregnation methods by microwave-assisted synthesis to im...

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Detalles Bibliográficos
Autores: Consentino, Luca, González-Castaño, Miriam, Garcia-Moncada, Nuría, Bobadilla, Luis F., Gruttadauria, Michelangelo, Liotta, Leonarda Francesca, Odriozola, José Antonio
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2025
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/393517
Acceso en línea:http://hdl.handle.net/10261/393517
https://api.elsevier.com/content/abstract/scopus_id/105004169894
Access Level:acceso abierto
Palabra clave:Catalyst structure
CO2methanation
In situ DRIFTS-MS
NAP-XPS
Ni-La perovskites
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Descripción
Sumario:Efficient catalysts are essential for CO2 methanation reaction, a key process for sustainable energy applications. This study investigates the structural and chemical properties of Ni-La perovskite-based catalysts synthesized via one-pot and impregnation methods by microwave-assisted synthesis to improve Ni dispersion and phase homogeneity. Reduction temperature emerges as a key factor influencing catalyst structure and performance. Catalysts reduced at lower temperatures retain perovskite structures, leading to enhanced metal-support interactions, which are crucial for CO2 activation and methane production. In contrast, higher reduction temperatures decompose the perovskite phase into metallic Ni and La2O3, which alters the catalytic behavior. The impregnation method enhances Ni dispersion, leading to higher metallic Ni availability and superior catalytic performance. Oxygen vacancies and carbonate species formed on the catalyst surface are identified as central to the reaction mechanism, facilitating CO2 adsorption and conversion. This research underscores the importance of structure-to-function relationships, focusing on how synthesis methods and reduction conditions shape surface species generation and CO2 methanation rates. These insights advance the design of highly efficient catalysts for CO2 conversion, addressing environmental challenges and fostering sustainable energy solutions.