电解质
材料科学
锂(药物)
离子
硫黄
化学工程
热传导
高分子化学
无机化学
电极
化学
有机化学
复合材料
物理化学
冶金
内分泌学
工程类
医学
作者
Huimin Wang,Mengdi Geng,Jing Bai,Dezhong Zhou,Weibo Hua,Sheng Liu,Xueping Gao
出处
期刊:Materials horizons
[Royal Society of Chemistry]
日期:2024-10-15
卷期号:12 (1): 141-149
被引量:9
摘要
All-solid-state lithium-sulfur batteries (ASSLSBs) using poly(ethylene oxide) (PEO) electrolytes offer significant advantages in energy density and safety. However, their development is hampered by the slow Li+ conduction in solid polymer electrolytes and sluggish electrochemical conversion at the cathode-electrolyte interface. Herein, we fabricate a self-healing poly(β-amino ester) with a comb-like topological structure and multiple functional groups, synthesized through a Michael addition strategy. This material modifies the PEO-based solid-state electrolyte, creating fast Li+ transport channels and improving polysulfides conversion kinetics at the electrode surface. Consequently, both modified all-solid-state lithium symmetric cells and lithium-sulfur batteries exhibit improved electrochemical performance. This work demonstrates an expanded interpenetrating macromolecular engineering approach to develop highly ion-conductive solid polymer electrolytes for ASSLSBs.
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