多硫化物
材料科学
化学工程
电解质
催化作用
碳纳米管
成核
锡
无机化学
溶解
电极
纳米技术
化学
物理化学
有机化学
工程类
冶金
作者
Gwan Hyeon Park,Sandya Rani Mangishetti,Won‐Gwang Lim,Junhyuk Ji,Yun Ho Jeong,Jeongbin Cho,Hansol Bae,Changshin Jo,Won Bae Kim
出处
期刊:Small
[Wiley]
日期:2025-06-27
卷期号:21 (45): e2503534-e2503534
被引量:4
标识
DOI:10.1002/smll.202503534
摘要
Abstract Lithium–sulfur batteries undergo solid–liquid–solid phase transitions based on a dissolution–deposition reaction mechanism. To effectively suppress the shuttling of soluble polysulfides, catalysts should be incorporated into the cathode to enhance both the adsorption and conversion processes. The formation of a triphasic interface among the catalyst, conductive material, and electrolyte plays a key role in facilitating these reactions. In this study, a composite catalyst (Sn@NBGNs‐CNTs), consisting of metallic tin microparticles anchored on nitrogen and boron co‐doped graphene nanosheets and partially exfoliated carbon nanotubes, is synthesized as a sulfur host via a simple method. This structure effectively anchors polysulfides at the interface and provided abundant active sites to accelerate redox reaction kinetihcs. As a result, it facilitated charge transfer and polysulfide transport at the interface, leading to an increase in the nucleation–growth rate constants of Li 2 S as determined using the critical deposition voltage from the potentiostatic intermittent titration technique. Consequently, the electrode exhibits excellent cycling stability, retaining 93% of its initial capacity after 350 cycles at 1 C with an extremely low‐capacity decay rate of 0.003% per cycle.
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