Resumen
A surfactant-assisted preparation method was successfully used to synthesize the Ce 0.8 Zr 0.2 O 2 nanophases that had homogeneous chemical composition, enhanced thermal stability and improved catalytic activity. Structural refinement by the Rietveld method confirmed that many cationic lattice defects were formed in the ceria-zirconia crystals due to incorporation of the cationic surfactant in the network of the solid. Zirconium dissolving into cubic structure of ceria improved its thermal stability but led to structure distortion. FT-IR in situ characterization showed that CO chemisorption on the palladium loaded ceria-zirconia catalyst formed linear and multibonded CO-metal complexes. It was also evidenced that CO 2 was produced in the CO chemisorption procedure from the pathways of CO disproportionation and CO reacting with lattice oxygen of the catalyst. Owing to high dispersion of the loaded metal palladium and defective structure of the ceria-zirconia support, the Pd/Ce 0.8 Zr 0.2 O 2 catalyst calcined at a temperature range between 873 and 1173K not only exhibited a more stable catalytic activity for CO oxidation but also performed a lower light-off temperature at cool start below 373K in comparison with Pd/CeO 2 .
Idioma original | Inglés |
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Páginas (desde-hasta) | 34-43 |
Número de páginas | 10 |
Publicación | Applied Surface Science |
Volumen | 230 |
N.º | 1-4 |
DOI | |
Estado | Publicada - 31 may. 2004 |
Publicado de forma externa | Sí |