Journal
PHYSICAL REVIEW B
Volume 82, Issue 3, Pages -Publisher
AMER PHYSICAL SOC
DOI: 10.1103/PhysRevB.82.035114
Keywords
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Funding
- European Commission [211690]
- Matinex program
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Point-defect formation energies in uranium dioxide UO2 are still a matter of debate due to the significant discrepancies between the various studies published in the literature. These discrepancies stem from the density functional theory (DFT)+U approximation that creates multiple energy minima and complexifies the search for the ground state. We report here DFT+U values of the formation energies for the single oxygen interstitial and vacancy in UO2, both in the fluorite and the Jahn-Teller distorted structures, using a scheme developed on bulk UO2 [B. Dorado, B. Amadon, M. Freyss, and M. Bertolus, Phys. Rev. B 79, 235125 (2009)] and based on occupation matrix control. We first investigate the Jahn-Teller distortion in UO2 in the noncollinear antiferromagnetic order and we show that the distortion stabilizes the system by 50 meV/UO2 compared to the fluorite structure. Moreover, it is found that the oxygen atoms are displaced in the < 111 > directions, in agreement with experiments. For the bulk fluorite structure, we show that the use of the Dudarev approach of the DFT+U without occupation matrix control systematically yields the first metastable state, located 45 meV/UO2 above the ground state. As a result, all previously published point-defect formation energies are largely underestimated. We then use the occupation matrix control scheme to calculate the formation energies of the single oxygen interstitial and vacancy in UO2. We confirm that this scheme always allows one to reach the lowest energy states and therefore yields reliable formation energies. Finally, we compare our values with those obtained in previous studies and show that the discrepancies observed stem from the calculations of defective supercells which have reached different metastable states.
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