多硫化物
材料科学
阴极
锂(药物)
膜
电化学
化学工程
多孔性
离子
扩散
分离器(采油)
纳米技术
电解质
硫黄
电极
化学
复合材料
有机化学
物理化学
内分泌学
工程类
冶金
物理
热力学
医学
生物化学
作者
Dongbin Xiong,Shaozhuan Huang,Daliang Fang,Dong Yan,Guojing Li,Yaping Yan,Song Chen,Yilin Liu,Xueliang Li,Yew Von Lim,Ye Wang,Bingbing Tian,Yumeng Shi,Hui Ying Yang
出处
期刊:Small
[Wiley]
日期:2021-07-18
卷期号:17 (34)
被引量:75
标识
DOI:10.1002/smll.202007442
摘要
Abstract Detrimental lithium polysulfide (LiPS) shuttle effects and sluggish electrochemical conversion kinetics in lithium‐sulfur (Li‐S) batteries severely hinder their practical application. Separator modification has been extensively investigated as an effective strategy to address above issues. Nevertheless, in the case of functional separators, how to effectively block the LiPSs from diffusion while enabling the rapid Li ion transport remains a challenge. Herein, by using an “oxidation‐etching” method, MXene membranes are presented with controllable in‐plane pores as interlayer to regulate Li ion transportation and LiPS immobilization. Porous MXene membranes with optimized pore density and size can simultaneously anchor LiPS and ensure fast Li ion diffusion. Consequently, even with pure sulfur cathode, the improved Li–S batteries deliver excellent rate performance up to 2 C with a reversible capacity of 677.6 mAh g −1 and long‐term cyclability over 500 cycles at 1 C with a low capacity decay of 0.07% per cycle. This work sheds new insights into the design of high‐performance interlayers with manipulated nanochannels and tailored surface chemistry to regulate LiPSs trapping and Li ion diffusion in Li–S batteries.
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