The influence of SiO 2 , TiO 2 , and ZrO 2 on the structural and redox properties of CeO 2 were systematically investigated by various techniques namely, X-ray diffraction (XRD), Raman spectroscopy (RS), UV-Vis diffuse reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), high-resolution transmission electron microscopy (HREM), BET surface area, and thermogravimetry methods. The effect of supporting oxides on the crystal modification of ceria was also mainly focused. The investigated oxides were obtained by soft chemical routes with ultrahigh dilute solutions and were subjected to thermal treatments from 773 to 1073 K. The XRD results suggest that the CeO 2 -SiO 2 sample primarily consists of nanocrystalline CeO 2 on the amorphous SiO 2 surface. Both crystalline CeO 2 and TiO 2 -anatase phases were noted in the case of CeO 2 -TiO 2 sample. Formation of cubic Ce 0.75 Zr 0.25 O 2 and Ce 0.6 Zr 0.4 O 2 (at 1073 K) were observed in the case of CeO 2 -ZrO 2 sample. The cell 'a' parameter estimations revealed an expansion of the ceria lattice in the case of CeO 2 -TiO 2 , while a contraction is noted in the case of CeO 2 -ZrO 2 . The DRS studies suggest that the supporting oxides significantly influence the band gap energy of CeO 2 . Raman measurements disclose the presence of oxygen vacancies, lattice defects, and displacement of oxide ions from their normal lattice positions in the case of CeO 2 -TiO 2 and CeO 2 -ZrO 2 samples. The XPS studies revealed the presence of silica, titania, and zirconia in their highest oxidation states, Si(IV), Ti(IV), and Zr(IV) at the surface of the materials. Cerium is present in both Ce 4+ and Ce 3+ oxidation states. The HREM results reveal well-dispersed CeO 2 nanocrystals over the amorphous SiO 2 matrix in the case of CeO 2 -SiO 2 , isolated CeO 2 and TiO 2 (A) nanocrystals and some overlapping regions in the case of CeO 2 -TiO 2 , and nanosized CeO 2 and Ce-Zr oxides in the case of CeO 2 -ZrO 2 sample. The exact structural features of these crystals as determined by digital diffraction analysis of HREM experimental images reveal that the CeO 2 is mainly in cubic fluorite geometry. The oxygen storage capacity (OSC) as determined by thermogravimetry reveals that the OSC of mixed oxides is more than that of pure CeO 2 and the CeO 2 -ZrO 2 exhibits highest OSC.