锂(药物)
硫化物
硫黄
离聚物
锂硫电池
多硫化物
无机化学
材料科学
化学
化学工程
冶金
有机化学
电化学
电解质
电极
工程类
物理化学
内分泌学
共聚物
聚合物
医学
作者
Hyunseok Moon,Myeong‐Hwa Ryou,Anseong Park,Bo‐Quan Li,H. Kim,Namjun Park,Eun Byoul Lee,Kyung Yoon Chung,Jia‐Qi Huang,Taeeun Yim,Won Bo Lee,Sang‐Young Lee
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2025-03-13
卷期号:10 (4): 1654-1663
被引量:10
标识
DOI:10.1021/acsenergylett.4c03522
摘要
Electrode passivation limits the reversibility of lithium–sulfur (Li–S) batteries. Pivoting from the prevailing approaches that focus on electrode active materials and electrolytes, herein, we introduce a class of S electrode binders based on soft acidic–hard basic (SAHB) ionomers. The SAHB binder contains a soft cation (tetraallyl ammonium ion, TA+) paired with a hard counteranion (nitrate, NO3–), allowing matched interactions with Li polysulfides (LiPS) via soft acid–soft base (TA+–Sx2–) and hard base–hard acid (NO3––Li+) pairings. This intermolecular coupling retards LiPS diffusion, promoting three-dimensional granular Li sulfide (Li2S) growth, guided by a high Damköhler number (Da). Consequently, the SAHB binder enables a Li–S cell to achieve a high specific capacity of 1545 mAh gsulfur–1 (corresponding to 92.3% S utilization) and stable capacity retention (71.5% after 300 cycles at a current density of 1 C), outperforming previously reported S electrode binders.
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