异质结
动力学
材料科学
硫黄
原位
锂(药物)
化学工程
无机化学
纳米技术
化学
光电子学
有机化学
冶金
医学
物理
量子力学
工程类
内分泌学
作者
Ao Zhang,Junzhi Li,Guangshe Li,Liping Li
出处
期刊:Small
[Wiley]
日期:2025-05-28
卷期号:21 (29): e2504580-e2504580
标识
DOI:10.1002/smll.202504580
摘要
Abstract The interaction between catalysts and polysulfides plays a crucial role in the redox kinetics of lithium‐sulfur batteries (LSBs). However, the role of nanoscale heterostructures formed by non‐metal atoms in regulating the electronic state of catalysts is often overlooked. In this work, these electronic states are modulated by in situ constructing a Mo─S heterostructure in a Mo 2 C nanosphere. The introduction of sulfur atoms forms the anion heterointerface, altering the coordination environment of interfacial Mo atoms and strengthening Mo─S interactions. This modification significantly enhances lithium polysulfide (LiPS) adsorption and conversion kinetics when using a Mo 2 C‐MoS 2 heterostructure‐modified separator (Mo 2 C‐MoS 2 /PP) in LSBs. Furthermore, Mo 2 C‐MoS 2 /PP effectively suppresses the LiPS shuttle effect and improves cycling stability, achieving a low capacity decay rate of 0.036% per cycle over 500 cycles at 1C. This study proposes a comprehensive approach to modulate metal electronic states by non‐metal atoms nanoheterostructure, aiming to enhance the catalytic reaction kinetics of LSBs.
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