Enhanced electrochemical performance from cross-linked polymeric network as binder for Li-S battery cathodes

被引:28
|
作者
Zhu, Shaoyin [1 ]
Yu, Jiaojiao [1 ]
Yan, Xiao [1 ]
Zhao, Erqing [1 ]
Wang, Yanqing [1 ]
Sun, Deye [1 ]
Jin, Yongcheng [1 ]
Kanamura, Kiyoshi [2 ]
机构
[1] Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, CAS Key Lab Biobased Mat, Qingdao 266101, Peoples R China
[2] Tokyo Metropolitan Univ, Dept Appl Chem, Grad Sch Urban Environm Sci, 1-1 Minami Ohsawa, Hachioji, Tokyo 1920397, Japan
关键词
Alginate; Hydrogel binder; Three-dimensional polymeric network; Sulfur cathode; Li-S battery; LITHIUM-SULFUR BATTERIES; POROUS CARBON; COMPOSITE CATHODES; GRAPHENE; ALGINATE; CYCLABILITY; BLOCKING; ANODES;
D O I
10.1007/s10800-016-0957-x
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A sulfur cathode with enhanced electrochemical properties is prepared by a hydrogel binder owning three-dimensional polymeric network for Li-S batteries. The promising high-performance binder (Alg-Ca2+) is constructed by an in situ interconnection of alginate chains by additive divalent cation with a facile and self-assembly strategy. With the assistance of 3D network, the sulfur/activated carbon composite cathode exhibits a higher rate capability and cycling performance compared to poly(vinylidene fluoride) binder, and the capacity retention is up to 80.6 % after 200 cycles (0.5C, 1C = 1675 mA g(-1)). Additionally, the electrochemical impedance spectroscopy also reveals a lower electrode resistance and better kinetic characteristics with Alg-Ca2+ as a binder. The improved electrochemical behaviors are assigned to the ability of maintaining the electrode stability due to the excellent mechanical property and amorphous structure. [GRAPHICS] .
引用
收藏
页码:725 / 733
页数:9
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