电化学
选择性
氧化还原
手性(物理)
材料科学
多硫化物
硫黄
分子
成核
密度泛函理论
电子传输链
化学工程
插层(化学)
锂(药物)
相(物质)
亚稳态
动力学
纳米技术
化学物理
扩散
电导率
组合化学
储能
催化作用
化学
无机化学
化学稳定性
电极
膜
电化学动力学
光化学
合理设计
纳米结构
离解(化学)
作者
Daye Lee,Hee Jo Song,Jeongyoub Lee,Kihyun Kim,Chang Hoon Lee,Jooho Moon,Dong-Wan Kim
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-03-04
标识
DOI:10.1021/acsnano.5c18764
摘要
Lithium-sulfur batteries (LSBs) promise high energy density but face critical challenges owing to sluggish sulfur redox kinetics and uncontrolled lithium polysulfide (LiPS) shuttling. Here, we demonstrate that chiral materials directly enhance LSB performance. By intercalating chiral methylbenzylamine (MBA) molecules into MoS2 layers, R-ChiMoS2 is synthesized, which stabilizes the metastable 1T phase and enables spin-selective electron transport through the chirality-induced spin selectivity (CISS) effect. The modified structure exhibits expanded interlayer spacing and coexisting 1T/2H domains, offering abundant active sites and stronger LiPS binding. As a result, R-ChiMoS2 accelerates sulfur reduction and oxidation reactions, lowers the Li2S nucleation barrier, and improves Li+ diffusion compared with bulk 2H or racemic counterparts. Incorporation of R-ChiMoS2@carbon nanotubes (CNTs) into separators further enhances conductivity and ensures durable LiPS blocking. Consequently, the resulting LSBs deliver high reversible capacity, outstanding rate capability up to 5.0 C, and long-term cycling stability under high sulfur-loading conditions. This study highlights chirality engineering as an effective design strategy for regulating spin-selective charge transport and advancing electrochemical energy storage performance.
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