钝化
催化作用
多硫化物
材料科学
硫黄
镍
金属
无机化学
锂(药物)
过渡金属
动力学
化学工程
化学
纳米技术
冶金
电极
物理化学
有机化学
电解质
医学
图层(电子)
内分泌学
物理
量子力学
工程类
作者
Xin Ao,Yang Kong,Shangquan Zhao,Zhongxin Chen,Yong Li,Xingyu Liao,Bingbing Tian
标识
DOI:10.1002/anie.202415036
摘要
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 S8 to produce NiSx 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‐N4), S8 remains stable on the surface. The Ni‐N4 exhibits excellent resistance to passivation and rapid kinetics of LiPSs conversion. Consequently, the sulfur cathode with Ni‐N4 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‐N4 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.
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