催化作用
插层(化学)
多硫化物
硫化物
材料科学
化学吸附
锂(药物)
电化学
无机化学
化学工程
硫黄
化学
电极
物理化学
电解质
有机化学
冶金
医学
工程类
内分泌学
作者
Jin Wang,Shaohua Yang,Zijia Xu,Guo Ai,Ting Zhang,Wenfeng Mao
标识
DOI:10.1002/admi.202101699
摘要
Abstract Various catalysts are adopted to boost the conversion chemistry of Lithium sulfur (Li‐S) batteries, but most of them are electrochemical‐active in a working Li‐S cell, and the changes of their chemical state and the induced influence toward the Li‐S catalytic mechanism are unclear. Herein, a dynamic catalytic mechanism is proposed by the selection of Li + ‐interaction‐reversible VS 2 catalyst as a representative species to address this issue. The VS 2 catalyst with ultrastable Li + intercalation/deintercalation characteristics, fast charge transport capability, and active capacity contribution can provide a strong and dynamic chemisorption toward polysulfide (LiPS). The resulting Li‐S batteries exhibit excellent cyclability at 3 C with capacity attenuation of 81.23% over 250 cycles and good rate capability up to 8 C. Moreover, a new insight toward the dynamic catalytic changes induced by the prominent Li + intercalation process of metal sulfide is proposed, which can provide more opportunities for the evolutional design for Li‐S catalysts.
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