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
医学
共聚物
内分泌学
聚合物
作者
Hyun-Seok 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
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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