Abstract
Oxygen evolution energies were calculated for the {100}, {110}, {111}, and {112} type facets of the rock-salt-structured cation-disordered Li-excess, Mn-rich Li-ion (DRX) cathode Li(2)MnO(2)F at the fully lithiated, 25% delithiation, and 50% delithiation states. Our calculations showed that Li(2)MnO(2)F remains much more robust to O loss than its nonfluorinated counterparts, as has been shown in experimental work. In particular, the {110} and {112} facets are the most resilient against O loss. Focusing on the {100} type facet, which previous work has shown to be the most likely exposed facet of Li(2)MnO(2)F, it was found that higher proportions of Li in an O coordination shell lead to lower O evolution energy (Ẽ(O)) and facilitate O loss. It was also found that at higher states of delithiation, surface fluorine had a weaker effect in increasing Ẽ(O), meaning the protective effect of F against O loss is more effective at higher lithiation states. Electronic structure chemical bonding analysis revealed weaker bonding interactions between Li and O correlated with lower Ẽ(O) and hence a higher propensity for surface O loss..