First-Principles Study of the Hydrogen Resistance Mechanism of PuO 2 .

The in-depth investigation of hydrogen behaviors in Pu-oxide overlayers (mainly PuO and α-PuO) is critical for modeling the complex induction period of Pu hydriding. Within density functional theory (DFT) + + D3 schemes, our systematic first-principles calculations and ab initio thermodynamic evaluations reveal that the hydrogen incorporation, dissolution behaviors, and diffusion mechanism in PuO are quite different from those in α-PuO, among which the highly endothermic incorporation and dissolution of hydrogen are the primary hydrogen resistance mechanism of PuO. Since its difficult recombination, atomic H is the preferred existence state in PuO, but H will recombine spontaneously in α-PuO. In PuO, H diffusion is always clinging to O anions, whereas in α-PuO, H prefers to migrate along O vacancies with higher barriers. H dissolution in intact PuO is very difficult, which can only be driven by extremely high pressure P and temperature. Based on a series of theoretical studies, we conclude that the main interactions between hydrogen and Pu-oxide overlayers are not involved with chemical reactions, and intact PuO can effectively inhibit hydrogen permeation.