The conundrum of relaxation volumes in first-principles calculations of charged defects in UO2

Goyal, A. and Mathew, K. and Hennig, R.G. and Chernatynskiy, A. and Stanek, C.R. and Murphy, S.T. and Andersson, D.A. and Phillpot, S.R. and Uberuaga, B.P. (2019) The conundrum of relaxation volumes in first-principles calculations of charged defects in UO2. Applied Sciences, 9 (24). ISSN 2076-3417

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The defect relaxation volumes obtained from density-functional theory (DFT) calculations of charged vacancies and interstitials are much larger than their neutral counterparts, seemingly unphysically large. We focus on UO 2 as our primary material of interest, but also consider Si and GaAs to reveal the generality of our results. In this work, we investigate the possible reasons for this and revisit the methods that address the calculation of charged defects in periodic DFT. We probe the dependence of the proposed energy corrections to charged defect formation energies on relaxation volumes and find that corrections such as potential alignment remain ambiguous with regards to its contribution to the charged defect relaxation volume. We also investigate the volume for the net neutral defect reactions comprising individual charged defects, and find that the aggregate formation volumes have reasonable magnitudes. This work highlights the issue that, as is well-known for defect formation energies, the defect formation volumes depend on the choice of reservoir. We show that considering the change in volume of the electron reservoir in the formation reaction of the charged defects, analogous to how volumes of atoms are accounted for in defect formation volumes, can renormalize the formation volumes of charged defects such that they are comparable to neutral defects. This approach enables the description of the elastic properties of isolated charged defects within an overall neutral material.

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Journal Article
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Applied Sciences
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22 Jan 2020 10:35
Last Modified:
16 Sep 2023 02:06