Evolving Defect Chemistry of (Pu,Am)O2± x

Neilson, W.D. and Steele, H. and Murphy, S.T. (2021) Evolving Defect Chemistry of (Pu,Am)O2± x. The Journal of Physical Chemistry C, 125 (28). pp. 15560-15568. ISSN 1932-7447

Full text not available from this repository.


The β decay of 241Pu to 241Am results in a significant ingrowth of Am during the interim storage of PuO2. Consequently, the safe storage of the large stockpiles of separated Pu requires an understanding of how this ingrowth affects the chemistry of PuO2. This work combines density functional theory (DFT) defect energies and empirical potential calculations of vibrational entropies to create a point defect model to predict how the defect chemistry of PuO2 evolves due to the incorporation of Am. The model predicts that Am occupies Pu sites in (Pu,Am)O2±x in either the +III or +IV oxidation state. High temperatures, low oxygen-to-metal (O/M) ratios, or low Am concentrations favor Am in the +III oxidation state. Am (+III) exists in (Pu,Am)O2±x as the negatively charged (AmPu1-) defect, requiring charge compensation from holes in the valence band, thereby increasing the conductivity of the material compared to Am-free PuO2. Oxygen vacancies take over as the charge compensation mechanism at low O/M ratios. In (Pu,Am)O2±x, hypo- and (negligible) hyperstoichiometry is found to be provided by the doubly charged oxygen vacancy (VO 2+) and singly charged oxygen interstitial (Oi 1-), respectively.

Item Type:
Journal Article
Journal or Publication Title:
The Journal of Physical Chemistry C
Uncontrolled Keywords:
?? density functional theoryoxygen vacanciescharge compensationcharge compensation mechanismcharged oxygen vacanciesempirical potentialshyperstoichiometrynegatively chargedpoint defect model (pdm)vibrational entropyplutonium compoundssurfaces, coatings and f ??
ID Code:
Deposited By:
Deposited On:
27 Aug 2021 12:20
Last Modified:
28 May 2024 11:45