Electron microscopy study of CeOx–Pd/α-Al2O3 catalysts for methane dry reforming

We have investigated the interaction between Pd and Ce in a 0.47 wt % CeOx–Pd 1 wt %/ -Al2O3 catalyst that is used in the reforming reaction of CH4 with CO2. The freshly reduced catalyst was characterized by various electron microscopy techniques, such as elemental mapping, Z-contrast imaging, and e...

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Detalles Bibliográficos
Autores: Moreno, M. S., Wang, Feiya, Malac, M., Kasama, T., Gigola, Carlos Eugenio, Costilla, Ignacio Oscar, Sánchez, M. D.
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2009
País:Argentina
Institución:Consejo Nacional de Investigaciones Científicas y Técnicas
Repositorio:CONICET Digital (CONICET)
Idioma:inglés
OAI Identifier:oai:ri.conicet.gov.ar:11336/42795
Acceso en línea:http://hdl.handle.net/11336/42795
Access Level:acceso abierto
Palabra clave:reforming
Pd
Ce
methane
https://purl.org/becyt/ford/1.3
https://purl.org/becyt/ford/1
Descripción
Sumario:We have investigated the interaction between Pd and Ce in a 0.47 wt % CeOx–Pd 1 wt %/ -Al2O3 catalyst that is used in the reforming reaction of CH4 with CO2. The freshly reduced catalyst was characterized by various electron microscopy techniques, such as elemental mapping, Z-contrast imaging, and electron energy-loss spectroscopy to understand the role of Ce on a microscopic scale. The high spatial resolution elemental mapping indicates that CeOx is located in close proximity of the palladium nanoparticles. High-resolution lattice images and energy-loss spectra obtained in the vicinity of the Pd particles show an anisotropic distribution of CeOx crystallites limited to the interface region between Pd and the substrate but not covering the surface of the Pd nanoparticles. Energy-loss near edge fine structure of Pd M edges reveals that the Pd nanoparticles are not oxidized.