Novel Insights into Enhanced Stability of Li-Rich Layered and High-Voltage Olivine Phosphate Cathodes for Advanced Batteries through Surface Modification and Electron Structure Design

Abstract

The design of cathode/electrolyte interfaces in high-energy density Li-ion batteries is critical to protect the surface against undesirable oxygen release from the cathodes when batteries are charged to high voltage. However, the involvement of the engineered interface in the cationic and anionic redox reactions associated with (de-)lithiation is often ignored, mostly due to the difficulty to separate these processes from chemical/catalytic reactions at the cathode/electrolyte interface. Here, a new electron energy band diagrams concept is developed that includes the examination of the electrochemical- and ionization- potentials evolution upon batteries cycling. The approach enables to forecast the intrinsic stability of the cathodes and discriminate the reaction pathways associated with interfacial electronic charge-transfer mechanisms. Specifically, light is shed on the evolution of cationic and anionic redox in high-energy density lithium-rich 0.33Li₂MnO₃·0.67LiNi_0.4Co_0.2Mn_0.4O₂ (HE-NCM) cathodes, particularly those that undergo surface modification through SO₂ and NH₃ double-gas treatment to suppress the structural degradation. The chemical composition and energy distribution of the occupied and unoccupied electronic states at the different charging/discharging states are quantitatively estimated by using advanced spectroscopy techniques, including operando Raman spectroscopy. The concept is successfully demonstrated in designing artificial interfaces for high-voltage olivine structure cathodes enabling stable battery operation up to 5.1 V versus Li⁺/Li.

Keywords: LCP; Lithium‐rich NCM; XANES and RPES and XPS and Raman; cathode/electrolyte interface; cationic and anionic redox; electrochemical potential and electronic structure; in‐situ and operando.