Stimulating the electrostatic interactions in composite cathodes using a slurry-fabricable polar binder for practical all-solid-state batteries

被引:1
|
作者
Jeong, Woo-Hyun [1 ,2 ]
Kim, Hyerim [2 ]
Kansara, Shivam [2 ]
Lee, Seungwon [2 ]
Agostini, Marco [3 ]
Kim, Kyungsu [1 ]
Hwang, Jang-Yeon [2 ,4 ]
Jung, Yun-Chae [1 ]
机构
[1] Korea Elect Technol Inst, Batteries Res Ctr, Seongnam 13509, Gyeonggi, South Korea
[2] Hanyang Univ, Dept Energy Engn, Seoul 04763, South Korea
[3] Sapienza Univ Rome, Dept Chem & Drug Technol, Ple Aldo Moro 5, I-00185 Rome, Italy
[4] Hanyang Univ, Dept Battery Engn, Seoul 04763, South Korea
基金
新加坡国家研究基金会;
关键词
All-solid-state battery; Polymer binder; Composite electrode; Pouch-Type Cell; Anodeless; ELECTROLYTES; ELECTRODES; PROGRESS;
D O I
10.1016/j.ensm.2024.103855
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
In this work, poly vinylidene fluoride-chlorotrifluoroethylene (PVdF-CTFE) is introduced as a slurry-fabricable polymer binder to fabricate a stable composite cathode using the complex materials of a Li[Ni0.7Co0.1Mn0.2] O2 cathode, Li6PS5Cl electrolyte, and super C carbon, for sulfide-based all-solid-state batteries (ASSBs). The high electronegativity of fluorine in the poly(vinylidene fluoride-chlorotrifluoroethylene (PVdF-CTFE) binder creates a polarized electronic environment in the composite cathode, promoting electrostatic interactions with Li ions. Compared with that of butadiene rubber (BR), the PVdF-CTFE binder has a stronger binding energy to the complex materials in the composite cathode, which enhances the mechanical rigidity of the composite cathode with highly uniform adhesion. In addition, uniform and close contact between the complex materials in the composite cathode reduces the resistance at the interfaces, lowering the energy barrier for Li+ diffusion, and eventually creates a fast Li+ diffusion pathway in the composite cathode. Thus, the pouch-type ASSBs cell, which comprises the composite cathode with the PVdF-CTFE binder, Li6PS5Cl electrolyte sheet, and silver-carbon (Ag/ C) anodeless electrode delivers a high reversible capacity of 198.5 mAh g-1 at 0.1 C and long-term cycling stability over 300 cycles with a capacity retention of 74.5 % at 0.5 C at 60 degrees C.
引用
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页数:10
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