Abstract
Silica-supported CeO 2 and CeO 2–ZrO 2 nanocomposite oxides were synthesized by a novel deposition–precipitation method and subjected to thermal treatments at 773–1073 K to study their sintering behavior and oxygen storage/release capacity (OSC). The prepared catalysts were characterized using thermogravimetry, BET surface area, X-ray diffraction, Raman spectroscopy, X-ray photoelectron spectroscopy, high-resolution transmission electron microscopy and other techniques. BET measurements indicate that CeO 2–ZrO 2/SiO 2 (CZS) samples possess more specific surface area and substantial resistance towards thermal sintering relative to CeO 2/SiO 2 (CS) samples. XRD profiles reveal only the broad diffraction lines due to CeO 2 in the case of CS while CZS discloses Ce 0.75Zr 0.25O 2, Ce 0.6Zr 0.4O 2 and Ce 0.5Zr 0.5O 2 phases depending on the treatment temperature. Raman measurements of both series of samples indicate the presence of oxygen vacancies, lattice defects and displacement of oxygen ions from their ideal lattice positions. XPS studies indicate the presence of cerium at the surface in both 4+ and 3+ oxidation states. The HREM results reveal well dispersed CeO 2 (∼3–4 nm) and Ce–Zr oxide particles (∼5 nm) over the amorphous SiO 2 matrix in the case of CS and CZS samples, respectively. There was no significant increase in the size of the dispersed nano-oxides even after calcination at 1073 K. Both the samples exhibit reasonably high OSC values.
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