X-ray Absorption Spectroscopy Illustrates the Participation of Oxygen in the Electrochemical Cycling of Li4Mn2O5

A combination of oxygen redox and Mn-based oxides would be the best option for high-energy-density Li-ion batteries crucial for a sustainable society. The disordered rock-salt Li4Mn2O5 was recently reported to display a very large capacity of 460 mAh/g with moderate reversibility. Previous studies proposed the involvement of lattice oxygen redox in such intriguing electrochemical performance, whereas no direct evidence was presented. To clarify the charge compensation mechanism, we systematically investigated the evolution of the electronic structure of both Mn and O upon cycling via Mn/OK-edge X-ray absorption spectroscopy (XAS). Mn K-edge XAS unequivocally demonstrates the participation of Mn redox upon the initial stages of charging, yet changes are arrested at the high potentials, while O continues to evolve according to O K-edge XAS. Upon discharging, both Mn and O are simultaneously reduced, but to states different from pristine. The results highlight the significance of a disordered structure in maintaining the reversible redox chemistry of both transition metals and oxygen to design cathode materials with high energy density.

Automated summary

A combination of oxygen redox and Mn-based oxides is considered the best option for high-energy-density Li-ion batteries, and the disordered rock-salt Li4Mn2O5 has shown promising capacity and reversibility. In this study, the charge compensation mechanism was investigated through Mn/OK-edge X-ray absorption spectroscopy (XAS). The results provide direct evidence of Mn redox participation during charging and highlight the role of a disordered structure in maintaining reversible redox chemistry for high-energy density cathode materials.