Thiol-Ene Click Reaction for Fine Polarity Tuning of Polymeric Binders in Solution-Processed All-Solid-State Batteries

被引:98
作者
Lee, Kyulin [1 ,2 ]
Lee, Jieun [1 ,2 ]
Choi, Sunghun [1 ,2 ]
Char, Kookheon [1 ]
Choi, Jang Wook [1 ]
机构
[1] Seoul Natl Univ, Sch Chem & Biol Engn, 1 Gwanak Ro, Seoul 08826, South Korea
[2] Seoul Natl Univ, Inst Chem Proc, 1 Gwanak Ro, Seoul 08826, South Korea
基金
新加坡国家研究基金会;
关键词
PHOTO-CROSS-LINKING; ELECTROCHEMICAL PERFORMANCE; FUNCTIONALIZED RUBBERS; ARGYRODITE LI6PS5CL; ION CONDUCTORS; ELECTROLYTE; INTERFACE; STABILITY; LI10GEP2S12; MECHANISMS;
D O I
10.1021/acsenergylett.8b01726
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Recent studies of all-solid-state batteries (ASSBs) have identified sulfide-based electrolytes with comparable ionic conductivities as those of liquid counterparts. Nevertheless, solution-based manufacturing is unestablished, since it is challenging to find adhesive polymeric binders that can be dispersed in common solvents with sulfide electrolytes. Currently available binders exhibit insufficient electrode adhesion due to their low polarity and are compromised by the chemical stability of a slurry. Here, we report a thiol-ene click reaction used to graft styrene-butadiene-block-copolymer with carboxylic acid at an optimal concentration. With polarity tuning, the click binder results in a uniform electrode slurry without ruining the structure of the sulfide electrolytes, while enabling electrode adhesion 1.4 times as high as that of commercial lithium-ion battery electrodes. The click binder also allows ASSBs to deliver decent electrochemical performance, implying that fine polarity tuning of functional binders can constitute an important step forward in advancing ASSBs to a real scalable technology.
引用
收藏
页码:94 / +
页数:15
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