Multivalent Li-Site Doping of Mn Oxides for Li-Ion Batteries

Doping is the most common strategy to suppress the intrinsic structural instability of several families of cathode materials, thus improving their electrochemical performance. During the electrode synthesis, the dopants have a low probability to occupy cationic Li sites, but it is well-known that, during the normal operation of the battery, such probability increases via inter- or intralayer diffusion. In this work, we investigate the effect of 10 Li-site cationic dopants (Mg, Ti, V, Nb, Fe, Ru, Co, Ni, Cu, Al) on the electrochemical properties of Li 2 MnO 3 and LiMnO 2 cathode materials using density functional theory. Our results show that, although Mn sites are thermodynamically favorable over Li-site doping, the small thermodynamic barriers between both configurations can be easily overcome during the material synthesis and/or the extraction/insertion of Li during the cycling process of the battery. Also, due to charge balance and diffusion channel opening, some of the Li-site dopants were found to act as activation centers, facilitating the diffusion of the neighboring Li ions. Additionally, they constitute a new activation mechanism for the electrochemically inactive Li 2 MnO 3 . These findings explain some of the unusual observed effects of Li-site doping, as compared to the more common transition-metal site doping, and therefore provide a new direction toward the optimization of the electrochemical performance of layered oxide cathode materials.