Phase evolution in the UO2-CeO2 system under oxidizing and reducing conditions: X-ray diffraction and spectroscopic studies

The solid-solution formation mechanism and defect dynamics in U1-xCexO2 +/-delta solid solutions have been inves-tigated by means of X-ray diffraction (XRD) analysis, Raman spectroscopy, and X-ray absorption near-edge structure (XANES) spectroscopy. Diffraction studies have revealed the formation of single-phase solid solu-tions with a fluorite-type structure at x <= 0.2 and a single-phase fluorite-type structure with broadened diffraction peaks, attributed to inhomogeneity in the O/M ratio, at 0.3 <= x <= 0.8 under reducing conditions. Oxidizing conditions result in the formation of single-phase solid solutions with fluorite-type structure at x >= 0.4. Upon the formation of Ce3+ in solid solutions at x <= 0.2 under reducing conditions, charge neutrality is achieved through oxygen vacancy creation and formation of higher oxidation states of uranium through a charge compensation mechanism. Lattice parameter-composition relationships for fluorite-type phases synthesized under oxidizing conditions show a decrease in lattice parameters as compared to their stoichiometric counter-parts due to the oxidation of U4+ to U5+/U6+. XANES studies provide direct experimental evidence of the presence of Ce3+ in solid solutions, despite synthesis under oxidizing conditions.

Automated summary

The formation mechanism and defect dynamics in U1-xCexO2 +/-delta solid solutions were studied using X-ray diffraction (XRD) analysis, Raman spectroscopy, and X-ray absorption near-edge structure (XANES) spectroscopy. XRD studies showed the formation of single-phase solid solutions with a fluorite-type structure at x <= 0.2 and a single-phase fluorite-type structure with broadened diffraction peaks at 0.3 <= x <= 0.8 under reducing conditions. Under oxidizing conditions, single-phase solid solutions with a fluorite-type structure were formed at x >= 0.4. The presence of Ce3+ in solid solutions was confirmed through XANES studies, despite synthesis under oxidizing conditions.