Inorganic SE materials have narrow intrinsic electrochemical windows, which provokes the need of the passivation of SEs for the reversible operation of all-solid-state batteries. In particular, the adoption of conventional LixMO2 (M = Ni, Co, Mn, Al) cathode materials to all-solid-state Li-ion or Li batteries (ASLBs) suffers from huge interfacial resistances. In-depth understanding on the evolution at the electrode−SE interfaces is required and imperative for the practical development of high performance ASLBs.
Ni-rich layered oxide cathode materials (LiMO2, M = Ni, Co, Mn, Al) were susceptible to severe disintergration of the secondary particles even at the
initial charge and discharge due to anisotropic volumetric strains, which led to poor electrochemical performance of low ICE and degradation of cycle
retention. In this regard, recently emerging research directions for advanced types of cathodes and SEs are highly pursued.
Our group develops solution processable SEs for surface coating of active materials in ASBs. The homogeneous SE solutions formed by solution process
could be used for direct SE coatings on active materials or the infiltration of slurry-cast porous electrodes used in conventional LIBs. Solution process
offers the intimate ionic contacts between active materials and SE, thereby enhanced electrochemical performance of ASBs. Furthermore, solution
process enables the scalable process of cell fabrication for ASBs.