多硫化物
异质结
材料科学
化学工程
硫黄
分离器(采油)
成核
催化作用
兴奋剂
锂(药物)
化学
电极
光电子学
有机化学
电解质
物理
物理化学
工程类
冶金
热力学
医学
内分泌学
作者
Junpu Zhang,Wen Xi,Yu Feng,Youfang Zhang,Rui Wang,Yansheng Gong,Beibei He,Huanwen Wang,Jun Jin
标识
DOI:10.1016/j.cej.2023.146009
摘要
Lithium-sulfur (Li-S) batteries have been regarded as potential candidates for next-generation high-performance energy storage systems due to the rich sulfur reserves, nontoxicity, high theoretical capacity, and energy density. However, the Li-S batteries suffer from the slow reaction kinetics and lithium polysulfide (LiPSs) shuttling. To address these issues, a bimetallic sulfide MoS2-SnS heterostructure has been constructed by a salt-template method to modify the separator of Li-S batteries. The 3D porous MoS2-SnS heterostructure on N-doped carbon (MoS2-SnS/NC) can improve the LiPSs adsorption and accelerate the LiPSs conversion and Li2S uniform nucleation/deposition due to its pore structure, polar bond, and built-in electric field at the interface of MoS2 and SnS. Therefore, the prepared MoS2-SnS/NC-PP heterostructure exhibits a high initial capacity (1504.6 mAh g-1), superior rate performance (690.1 mAh g-1 at 4C), and good cycling stability (0.07 % capacity decay rate at 400 cycles at 4C). When the sulfur loading is 3.50 mg cm−2, the Li-S battery delivers a capacity of 635 mAh g-1.
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