Inhibiting laser oxidation of UO2 via Th substitution

Abstract

Abstract UO2, a major component of nuclear fuels, undergoes volume-changing oxidation reactions that make its long-term storage challenging. The impact of substituting Th, which has a stable oxidation state of 4\xa0+\xa0as opposed to the stable 6+, 5+, or 4\xa0+\xa0states of U, into UO2 on the oxidation potential of the resulting isostructural solid solution is investigated. Hydrothermally grown single crystals of UxTh1-xO2, with x\u202f=\u202f0.1, 0.5, 0.75, 0.9, or 1.0 are subjected to a damaging 532\u202fnm laser whose power is tuned at ≥ 3.04\u202fmW to be simultaneously used as a driving force for oxidation and as an excitation source for μ-Raman spectroscopy. In so doing, the oxidation of UxTh1-xO2 to UxTh1-xO2+δ when x\u202f=\u202f0.9 or 0.75 can be tracked by the evolution of a peak near 630\u202fcm−1, which is indicative of the formation of oxygen interstitials. Higher Th contents disable this oxidation reaction and engender increased laser damage resistance. The oxidation of UO2 to U3O8 is found to be completely inhibited by all Th contents studied.