电解质
迈克尔反应
聚合物
离子
高分子化学
聚合物电解质
化学
高分子科学
化学工程
材料科学
有机化学
离子电导率
物理化学
电极
工程类
催化作用
作者
Michelle Lehmann,Ji-young Ock,Catalin Gainaru,Alexei P. Sokolov,X. Chelsea Chen,Tomonori Saito
出处
期刊:Macromolecules
[American Chemical Society]
日期:2025-04-16
卷期号:58 (9): 4708-4714
被引量:5
标识
DOI:10.1021/acs.macromol.5c00422
摘要
Single-ion conducting polymer electrolytes present a possible route for achieving high energy density next-generation batteries due to their flexible nature and high cation transport number. The trifluoromethanesulfonimide (TFSI) functional group represents one of the most efficient tethered anions for Li-ion conductivity. However, the covalent attachment of TFSI groups into polymer electrolytes has been challenging and costly due to its synthetic difficulty and limited commercial availability of building blocks. Here, we present a new polymer electrolyte synthesized by the Michael addition reaction between poly(allylamine) (PAA) and a vinyl TFSI anion under mild reaction conditions. The resulting PAATFSI exhibits a lower glass transition temperature and several orders of magnitude higher Li-ion conductivity than similar TFSI-based single-ion conducting homopolymers in the dry state. Moreover, PAATFSI exhibits excellent Li-ion conductivity (2.7 × 10–4 S/cm at 30 °C) with the addition of a plasticizer (60 wt % of carbonate solvent), which enables stable lithium–metal battery performance. This study demonstrates a facile route for the synthesis of new single-ion conducting polymer electrolytes that opens a library of possibilities to enable the realization of polymer-based batteries.
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