<i>Ab Initio</i>Atomistic Thermodynamics Study of the (001) Surface of LiCoO₂in a Water Environment and Implications for Reactivity under Ambient Conditions

Abstract

We use GGA + U methodology to model the bulk and surface structure of varying stoichiometries of the (001) surface of LiCoO 2 . The DFT energies obtained for these surface-slab models are used for two thermodynamic analyses to assess the relative stabilities of different surface configurations, including hydroxylation. In the first approach, surface free energies are calculated within a thermodynamic framework, and the second approach is a surface-solvent ion exchange model. We find that, for both models, the −CoO–H 1/2 surface is the most stable structure near the O-rich limit, which corresponds to ambient conditions. We find that surfaces terminated with Li are higher in energy, and we go on to show that H and Li behave differently on the (001) LiCoO 2 surface. The optimized geometries show that terminal Li and H occupy nonequivalent surface sites. In terms of electronic structure, Li and H terminations exhibit distinct bandgap characters, and there is also a distinctive distribution of charge at the surface. We go on to probe how the variable Li and H terminations affect reactivity, as probed through phosphate adsorption studies.