材料科学
锂(药物)
异质结
电解质
枝晶(数学)
化学工程
介孔材料
纳米技术
电化学
图层(电子)
硫黄
电极
催化作用
光电子学
化学
有机化学
物理化学
内分泌学
工程类
冶金
医学
数学
几何学
作者
Yifan Gao,Yuwei Deng,Shenxin Xia,Xiangyun Xi,Zhebin Zhang,Yajun Wang,Dong Yang,Tongtao Li,Angang Dong
出处
期刊:Small
[Wiley]
日期:2024-04-22
卷期号:20 (35): e2402412-e2402412
被引量:15
标识
DOI:10.1002/smll.202402412
摘要
Abstract The industrialization of lithium–sulfur (Li–S) batteries faces challenges due to the shuttling effect of lithium polysulfides (LiPSs) and the growth of lithium dendrites. To address these issues, a simple and scalable method is proposed to synthesize 2D membranes comprising a single layer of cubic graphitic cages encased with few‐layer, curved MoS 2 . The distinctive 2D architecture is achieved by confining the epitaxial growth of MoS 2 within the open cages of a 2D‐ordered mesoporous graphitic framework (MGF), resulting in MoS 2 @MGF heterostructures with abundant sulfur vacancies. The experimental and theoretical studies establish that these MoS 2 @MGF membranes can act as a multifunctional interlayer in Li–S batteries to boost their comprehensive performance. The inclusion of the MoS 2 @MGF interlayer facilitates the trapping and conversion kinetics of LiPSs, preventing their shuttling effect, while simultaneously promoting uniform lithium deposition to inhibit dendrite growth. As a result, Li–S batteries with the MoS 2 @MGF interlayer exhibit high electrochemical performance even under high sulfur loading and lean electrolyte conditions. This work highlights the potential of designing advanced MoS 2 ‐encased heterostructures as interlayers, offering a viable solution to the current limitations plaguing Li–S batteries.
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