异质结
材料科学
氧化还原
锂(药物)
动力学
催化作用
化学工程
背景(考古学)
纳米技术
化学
光电子学
内分泌学
古生物学
工程类
物理
生物
冶金
医学
量子力学
生物化学
作者
Pengqian Guo,Weixin Chen,Yifan Zhou,Fangyan Xie,Guoyu Qian,Pengfeng Jiang,Deyan He,Xia Lu
出处
期刊:Small
[Wiley]
日期:2022-10-30
卷期号:18 (50)
被引量:32
标识
DOI:10.1002/smll.202205158
摘要
Although lithium-sulfur batteries (LSBs) promise high theoretical energy density and potential cost effectiveness, their applications are severely impeded by the shuttling and sluggish redox kinetics of lithium polysulfides (LiPSs). In this context, a Co9 S8 @MoS2 heterostructure is sophisticatedly designed as an efficient catalytic host to boost the sulfur reduction reaction/evolution reaction (SRR/SER) kinetics and suppresses the LiPSs shuttling in LSBs. The results indicate that the electronic structure is manipulated in the Co9 S8 @MoS2 heterostructure, where the built-in electric fields (BIEFs) within the heterointerfaces enable the sufficient adsorption sites to accelerate the ionic diffusion/charge transfer kinetics for LiPSs redox, thus enhancing the sulfur conversion. By tuning the electronic structure, the metal d-band of Co9 S8 @MoS2 heterostructure plays an important role in adsorbing and catalyzing the conversion of LiPSs, thus promoting the reaction kinetics of the corresponding LSBs. This work unlocks the potential of heterostructures as promising catalysts to the design of high-energy and stabilized LSBs.
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