Reduction of High Surface Area CeO₂−ZrO₂ Mixed Oxides

The objective of this study was to examine the mechanism of the reduction by hydrogen of ceria−zirconia (CZ) mixed oxides having a high BET surface area (100 m 2 g -1 ). Three methods were used in parallel to assess the Ce 3+ content, the surface and bulk oxygen vacancy concentrations, and the resulting oxygen storage capacity (OSC): temperature programmed reduction, Fourier transform infrared (FT-IR) measurements of methanol adsorbed on the reduced surfaces, and a Faraday microbalance to determine the magnetic susceptibility of the reduced oxides. The three methods conclude that the introduction of zirconium into the ceria lattice has a positive influence on the OSC. Compared to pure ceria, the CZ mixed oxides exhibit better redox properties, with a lower temperature of initial reduction and a higher reduction percentage for all compositions. The reducibility increases with the zirconium content, however the OSC per gram of solid is practically the same for Zr contents between 20% and 50%. The reduction process very rapidly involves the bulk, but a treatment at room temperature under oxygen of the reduced samples oxidizes them almost completely. However, the FT-IR results underline the differing behavior of ceria for the distinct surface and bulk reduction processes.