Room-Temperature Activation of Methane and Dry Re-forming with CO2 on Ni-CeO2(111) Surfaces: Effect of Ce3+ Sites and Metal-Support Interactions on C-H Bond Cleavage
; Ramírez, Pedro J. ; Liu, Zongyuan ; Gutiérrez, Ramón A. ; Grinter, David G. ; Carrasco, Javier ; Senanayake, Sanjaya D. ; Rodriguez, José A. ; Ganduglia Pirovano, Maria Veronica Otros responsables
Fecha
12/2016
Editorial
American Chemical Society
Revista
ACS Catalysis
Título del libro
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Institución organizadora
ISSN
2155-5435
eISSN
ISBN
Idioma
Inglés
Tipo del evento
Clasificación temática
Palabras clave
Ceria , Dft , Dry Re-Forming , Methane Activation , Nickel , Support Effect , Supported Catalysts , Xps
Resumen
The results of core-level photoemission indicate that Ni-CeO2(111) surfaces with small or medium coverages of nickel are able to activate methane at 300 K, producing adsorbed CHx and COx (x = 2, 3) groups. Calculations based on density functional theory predict a relatively low activation energy of 0.6-0.7 eV for the cleavage of the first C-H bond in the adsorbed methane molecule. Ni and O centers of ceria work in a cooperative way in the dissociation of the C-H bond at room temperature, where a low Ni loading is crucial for the catalyst activity and stability. The strong electronic perturbations in the Ni nanoparticles produced by the ceria supports of varying natures, such as stoichiometric and reduced, result in a drastic change in their chemical properties toward methane adsorption and dissociation as well as the dry reforming of methane reaction. The coverage of Ni has a drastic effect on the ability of the system to dissociate methane and catalyze the dry re-forming process.
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