First-principles study of iron oxyfluorides and lithiation of FeOF

First-principles studies of iron oxyfluorides in the FeF2 rutile framework (FeOxF2-x, 0 <= x <= 1) are performed using density functional theory (DFT) in the general gradient approximation (GGA) with a Hubbard U correction. Studies of O/F orderings reveal FeOF to be particularly stable compared to other FeOxF2-x (x not equal 1) structures, where FeF2-FeOF mixing is not energetically favored. The band gap of FeF2 is found to decrease as oxygen is substituted into its structure. The GGA + U electronic structure evolves from that of a Mott-Hubbard insulator (x = 0) to a charge transfer semiconductor (x = 1). Lithiation studies reveal that lithiation sites offering mixed O/F environments are the most stable. An insertion voltage plateau up to Li0.5FeOF on lithiation is found, in agreement with recent Li-ion battery experiments. The energetics of further lithiation with respect to conversion scenarios are discussed. DOI: 10.1103/PhysRevB.87.094118