Niobium Phosphide‐Induced Sulfur Cathode Interface with Fast Lithium‐Ion Flux Enables Highly Stable Lithium–Sulfur Catalytic Conversion

Research on the Li-S catalytic chemistry primarily focus on the development of high-performance catalysts and the exploration of their reaction mechanisms, with limited attention given to the impact on the interface at the cathode. Moreover, regulating the Li⁺ flux at the cathode interface can enhance Li₂S conversion kinetics without compromising the intrinsic catalytic activity of catalyst. This work presents a paradigm that employs interface regulation to enhance Li-S battery (LSB) cycling stability. A novel phosphorus doped carbon supported niobium phosphide nanocrystals (NbP/PC) catalyst is developed and demonstrates exceptional intrinsic activity for lithium polysulfide conversion while it facilitates lithium salt dissociation through intermolecular hybridization. The NbP-induced functional interface layer with abundant LiF and Li₃N provides efficient Li⁺ transport channel for Li₂S decomposition, which further mitigates the passivation of active sites. In consequence, the assembled LSB exhibits a capacity retention rate of 0.04 % per cycle after 1100 cycles at a 1 C. Furthermore, the pouch battery with an energy density of 451 Wh kg^-1 maintains stable performance over 20 cycles. This strategy addresses the limitations of traditional catalytic material design in the chemical regulation of the cathodic interface for promising future of LSBs.