材料科学
二硫化钼
催化作用
硫黄
锂(药物)
氮化物
碳化
纳米技术
化学工程
化学吸附
钼
碳纤维
复合数
冶金
复合材料
化学
有机化学
图层(电子)
内分泌学
扫描电子显微镜
工程类
医学
作者
Mincai Zhao,Pengcheng Tan,Daoping Cai,Yangjie Liu,Chaoqi Zhang,Ban Fei,Baisheng Sa,Qidi Chen,Hongbing Zhan
标识
DOI:10.1002/adfm.202211505
摘要
Abstract Lithium–sulfur (Li–S) batteries hold great promise for the next‐generation energy storage system. However, their commercial applications are severely hindered by myriads of drawbacks such as poor electrical conductivity of sulfur, sluggish redox reaction kinetics of sulfur species, “shuttling effect” of soluble lithium polysulfides (LiPSs) and uncontrollable dendritic Li growth. Herein, it is conceptually demonstrated that sluggish conversion kinetics of LiPSs is markedly stimulated by exquisite heterointerface modulation at nanoscale level over transition metal carbides and nitrides. In this scenario, N‐doped carbon coupled with molybdenum nitride/carbide (Mo 2 N‐MoC/NC) hybrid nanocomposites are designed through a one‐step carbonization‐nitridation process, wherein component regulation induced dense heterointerfaces are in situ produced. Benefiting from high electrical conductivity, strong chemical adsorption, and superior catalytic activity afforded by dense heterointerfaces, the Mo 2 N‐MoC/NC modified separators significantly restrict the soluble LiPSs shuttling and simultaneously suppress the Li dendrite generation. The assembled Li–S batteries with Mo 2 N‐MoC/NC modified separators exhibit remarkable electrochemical performance. Integrated experimental and theoretical results substantiate the boosted chemisorption and catalytic conversion of LiPSs endowed by such dense heterointerfaces. The work will open a new vista for rationally constructing multifarious heterostructured materials for the communities of Li‐S batteries.
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