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This synthesis reveals new uranium host phases in carbon-rich mantle, suggesting significant implications for geochemical processes.
It is well established that a significant amount of heat produced in the Earth’s mantle is due to the decay of uranium. However, uranium cannot be incorporated in large amounts into the most common mantle minerals. Here, we suggest that carbonates could be host phases for uranium in carbon-rich mantle lithologies. Two anhydrous uranium carbonates, U 2 [CO 3 ] 3 and U[CO 3 ] 2 , were simultaneously synthesized by a reaction of UO 2 with CO 2 in a laser-heated diamond anvil cell at 20(1) GPa and 1800(200) K. Their crystal structures were obtained from synchrotron-based single crystal diffraction data and reproduced by density functional theory-based calculations. In U 2 [CO 3 ] 3 trivalent uranium cations are present, while uranium is four-valent in U[CO 3 ] 2 . The synthesis of U 2 [CO 3 ] 3 and U[CO 3 ] 2 is a significant extension of the chemistry of uranium compounds and we provide a straightforward synthesis route for a U III -containing compound.
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Spahr et al. (2026) studied this question.
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