Metal‐N Coordination in Lithium‐Sulfur Batteries: Inhibiting Catalyst Passivation

Abstract Lithium‐sulfur (Li−S) batteries exhibit great potential as the next‐generation energy storage techniques. Application of catalyst is widely adopted to accelerate the redox kinetics of polysulfide conversion reactions and improve battery performance. Although significant attention has been devoted to seeking new catalysts, the problem of catalyst passivation remains underexplored. Herein, we find that metal‐N coordination has a previously overlooked role in preventing the catalyst passivation. In the case of nickel, the Ni catalyst reacts with S 8 to produce NiS x compounds on the surface, leading to catalyst passivation and slow the kinetics of LiPSs conversion. In contrast, when Ni is coordinated with N (typically Ni−N 4 ), S 8 remains stable on the surface. The Ni−N 4 exhibits excellent resistance to passivation and rapid kinetics of LiPSs conversion. Consequently, the sulfur cathode with Ni−N 4 exhibits a high rate capability of 604.11 mAh g −1 at 3 C and maintains a low capacity decay rate of 0.046 % per cycle over 1000 cycles at 2 C. Furthermore, preventing S passivation in M−N coordination applies not only to Ni−N 4 but also to various coordination numbers and transition metals. This study reveals a new aspect of metal‐N coordination in inhibiting catalyst passivation, improving our understanding of catalysts in Li−S batteries.