多硫化物
插层(化学)
材料科学
电化学
硫黄
阴极
锂(药物)
氧化还原
相(物质)
化学工程
离子
电导率
离子电导率
无机化学
电极
纳米技术
化学
物理化学
有机化学
医学
工程类
电解质
冶金
内分泌学
作者
Jili Xu,Heng Wang,Ting He,Yan Xiao,Jia Yu,Jingkun Bi,Daixin Ye,Wenli Yao,Ya Tang,Hongbin Zhao,Jiujun Zhang
出处
期刊:Small
[Wiley]
日期:2023-04-12
卷期号:19 (29)
被引量:10
标识
DOI:10.1002/smll.202300042
摘要
Abstract Modifying sulfur cathodes with lithium polysulfides (LiPSs) adsorptive and electrocatalytic host materials is regarded as one of the most effective approaches to address the challenging problems in lithium‐sulfur (Li‐S) batteries. However, because of the high operating voltage window of Li–S batteries from 1.7 to 2.8 V, most of the host materials cannot participate in the sulfur redox reactions within the same potential region, which exhibit fixed or single functional property, hardly fulfilling the requirement of the complex and multiphase process. Herein, Chevrel phase Mo 6 S 8 nanosheets with high electronic conductivity, fast ion transport capability, and strong polysulfide affinity are introduced to sulfur cathode. Unlike most previous inactive hosts with a fixed affinity or catalytic ability toward LiPSs, the reaction involving Mo 6 S 8 is intercalative and the adsorbability for LiPSs as well as the ionic conductivity can be dynamically enhanced via reversible electrochemical lithiation of Mo 6 S 8 to Li‐ion intercalated Li x Mo 6 S 8 , thereby suppressing the shuttling effect and accelerating the conversion kinetics. Consequently, the Mo 6 S 8 nanosheets act as an effective dynamic‐phase promoter in Li–S batteries and exhibit superior cycling stability, high‐rate capability, and low‐temperature performance. This study opens a new avenue for the development of advanced hosts with dynamic regulation activity for high performance Li‐S batteries.
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