Search

Lithium‐excess cation‐disordered rocksalt materials are a promising class of transition metal‐based cathodes that exhibit high specific capacity and energy density. The exceptional performance is achieved through participation of anionic redox in addition to cationic redox reactions in the electrochemistry. However, anionic redox reactions accompanied by oxygen evolution, accelerated electrolyte breakdown, and structural evolution lead to voltage hysteresis and low initial Coulombic efficiency. Herein, an Al2O3 layer with varying thickness has been coated onto a high‐entropy disordered rocksalt oxyfluoride cathode through atomic layer deposition to enhance battery performance. The results indicate that the utilization of a uniform Al2O3 coating improves the capacity retention and rate capability of the cathode, with the performance being strongly dependent on the layer thickness. Further investigation into cathode–electrolyte interfacial reactions reveals that the thin protecting Al2O3 coating can reduce the decomposition of electrolyte on the cathode surface but cannot prevent bulk phase degradation during prolonged cycling. These findings highlight the need for optimized coating design on the disordered rocksalt cathode to improve battery performance.

We present a methodology for accessing the cation short-range ordering (SRO) in disordered rocksalt (DRX) materials by decomposing their pair distribution function (PDF) pattern in terms of a set of basis PDFs, pre-determined via Metropolis non-negative matrix factorisation analysis. These basis PDFs, underpinned by structure modelling, point to specific SRO types that subsequently enable identification and quantification of their presence in the DRX structure. Rapid identification of the evolution of SRO addresses a key bottleneck in the analysis and understanding of high energy density characteristics of DRX materials.