Oxygen Vacancy Formation and Water Adsorption on Reduced AnO2 {111}, {110} and {100} Surfaces (An = U, Pu); A Computational Study

Wellington, Joseph P. W. and Tegner, Bengt and Collard, Jonathan and Kerridge, Andrew and Kaltsoyannis, Nikolas (2018) Oxygen Vacancy Formation and Water Adsorption on Reduced AnO2 {111}, {110} and {100} Surfaces (An = U, Pu); A Computational Study. The Journal of Physical Chemistry C, 122 (13). pp. 7149-7165. ISSN 1932-7447

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Abstract

The substoichiometric {111}, {110} and {100} surfaces of UO2 and PuO2 are studied computationally using two distinct yet related approaches based on density functional theory; the periodic electrostatic embedded cluster method (PEECM) and Hubbard-corrected periodic boundary condition DFT. First and second layer oxygen vacancy formation energies and geometries are presented and discussed; the energies are found to be substantially larger for UO2 vs PuO2, a result traced to the substantially more positive An(IV)/An(III) reduction potential for Pu, and hence relative ease of Pu(III) formation. For {110} and {100}, the significantly more stable dissociative water adsorption seen previously for stoichiometric surfaces [J. Nucl. Mater. 2016, 482, 124–134; J. Phys. Chem. C 2017, 121, 1675-1682] is also found for the defect surfaces. By contrast, vacancy creation substantially changes the most stable mode of water adsorption on the {111} surface, such that the almost degenerate molecular and dissociative adsorptions on the pristine surface are replaced by a strong preference for dissociative adsorption on the substoichiometric surface. The implications of this result for the formation of H2 are discussed. The generally very good agreement between the data from the embedded cluster and periodic DFT approaches provides additional confidence in the reliability of the results and conclusions.

Item Type:
Journal Article
Journal or Publication Title:
The Journal of Physical Chemistry C
Additional Information:
This document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of Physical Chemistry C, copyright ©2018 American Chemical Society after peer review and technical editing by the publisher.To access the final edited and published work see https://pubs.acs.org/doi/10.1021/acs.jpcc.7b11512
Uncontrolled Keywords:
/dk/atira/pure/subjectarea/asjc/2500/2504
Subjects:
ID Code:
124127
Deposited By:
Deposited On:
20 Mar 2018 14:30
Refereed?:
Yes
Published?:
Published
Last Modified:
23 Oct 2020 04:49