Abstract
Recently, sulfide solid-state electrolytes with excellent ionic conductivity and facile electrode integration have gained prominence in the field of all-solid-state batteries (ASSBs). However, owing to their inherently high reactivity, sulfide electrolytes interact with the cathode, forming interfacial layers that adversely affect the electrochemical performance of all-solid-state cells. Unlike conventional cathode-coating methods that involve the formation of surface coatings from high-cost source materials, the proposed strategy involves the doping of precursors with low-cost oxides (Nb(2)O(5), Ta(2)O(5), and La(2)O(3)) prior to cathode fabrication. This novel approach aims to improve the stability of the cathode-sulfide electrolyte interface. Notably, doping significantly improved the discharge capacity, rate capability, and cyclic performance of cathodes while reducing their impedance resistance. Scanning electron microscopy, transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS) indicated a gradient dopant-concentration profile (with a high level of dopant at the surface) in the doped cathodes. Cathode doping, particularly with Nb and Ta, caused a reduction in cation mixing owing to crystal-structure adjustments and ionic-conductivity enhancements. XPS and high-resolution TEM confirmed that gradient doping effectively minimized cathodic side reactions, possibly due to the formation of a coating-like protective layer in the cathode-electrolyte interface coupled with structural stabilization attributed to the doping process. The protective ability of the interfacial layer generated by gradient doping was confirmed to be comparable to that of conventional surface coatings. Therefore, this study could guide the future development of low-cost, high-performance ASSBs, opening new frontiers in sustainable energy storage.