X-ray photoelectron and Raman spectroscopy of nanostructured ceria in soot oxidation under operando conditions

Ceria nanoshapes exhibiting different amounts of {100}, {110} and {111} facets (cubes, rods, octahedra and polyhedra) were prepared, characterized, tested in the carbon soot oxidation reaction, and studied by operando near ambient pressure X-ray photoelectron spectroscopy (NAP-XPS) and operando Rama...

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Detalles Bibliográficos
Autores: García de Andrés, Xènia|||0000-0003-0795-4168, Soler Turu, Lluís|||0000-0003-1591-3366, Casanovas Grau, Albert, Escudero, Carlos, Llorca Piqué, Jordi|||0000-0002-7447-9582
Tipo de recurso: artículo
Fecha de publicación:2021
País:España
Institución:Universitat Politècnica de Catalunya (UPC)
Repositorio:UPCommons. Portal del coneixement obert de la UPC
Idioma:inglés
OAI Identifier:oai:upcommons.upc.edu:2117/361755
Acceso en línea:https://hdl.handle.net/2117/361755
https://dx.doi.org/10.1016/j.carbon.2021.03.009
Access Level:acceso abierto
Palabra clave:Atomic absortion spectroscopy
Spectrum analysis
Raman spectroscopy
Ceria
Nanoshapes
Soot oxidation
NAP-X
PSAP-XPS
Operando characterization
Espectroscòpia d'absorció atòmica
Anàlisi espectral
Espectroscòpia Raman
Àrees temàtiques de la UPC::Energies
Descripción
Sumario:Ceria nanoshapes exhibiting different amounts of {100}, {110} and {111} facets (cubes, rods, octahedra and polyhedra) were prepared, characterized, tested in the carbon soot oxidation reaction, and studied by operando near ambient pressure X-ray photoelectron spectroscopy (NAP-XPS) and operando Raman spectroscopy up to 550 °C. The specific soot oxidation reaction rate (mgC·m-2·min-1) clearly indicated that the {110} and {100} crystallographic planes of ceria were more active than the {111} ones for the oxidation of carbon soot. As deduced from the Ce 3d and O 1s signals recorded using different photon energies, all ceria nanoshapes experienced progressive reduction upon increasing the temperature under Ar, which was accompanied by the formation of oxygen vacancies. Raman studies revealed that, at this stage, isolated graphene layers in carbon soot reacted with ceria lattice oxygen atoms following a Mars-Van Krevelen mechanism. After exposure to O2 at 550 °C, a broad signal in the O 1s region at 531.2–532.5 eV was ascribed to surface active oxygen species, such as peroxide (O22-) and superoxide (O2-) species, generated from the interaction of molecular O2 with oxygen vacancies, which proved to be highly reactive to oxidize the graphitic structures of carbon soot.