New functionalized ionic liquids based on pyrrolidinium and piperidinium cations with two ether groups as electrolytes for lithium battery

被引:103
作者
Fang, Shaohua [1 ,2 ]
Zhang, Zhengxi [1 ]
Jin, Yide [1 ]
Yang, Li [1 ,2 ]
Hirano, Shin-ichi [2 ]
Tachibana, Kazuhiro [3 ]
Katayama, Shingo [4 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Chem & Chem Technol, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Hirano Inst Mat Innovation, Shanghai 200240, Peoples R China
[3] Yamagata Univ, Fac Engn, Dept Chem & Chem Engn, Yamagata 9928510, Japan
[4] Shoei Chem Inc, Tokyo 1980025, Japan
基金
国家高技术研究发展计划(863计划);
关键词
Lithium battery; Ionic liquid; Electrolyte; Functionalized cation; ELECTROCHEMICAL PROPERTIES; LOW-VISCOSITY; LI/LICOO2; CELL; MOLTEN-SALTS; CATHODE; CARBONATE;
D O I
10.1016/j.jpowsour.2011.02.047
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
Four new functionalized ILs based on piperidinium and pyrrolidinium cations with two ether groups and TFSI- anion are synthesized and characterized. Physical and electrochemical properties of these ILs, including melting point, thermal stability, viscosity, conductivity and electrochemical stability, are investigated. All the ILs are liquids at room temperature, and the viscosities of P(2o1)(2)-TFSI and P(2o1)(2o2)-TFSI are 55 and 53 mPas at 25 degrees C, respectively. Behavior of lithium redox, chemical stability against lithium metal and charge-discharge characteristics of lithium batteries, are also investigated for these IL electrolytes with 0.6 mol kg(-1) LiTFSI. Though the cathodic limiting potentials of these ILs are 0.4 V versus Li/Li+, the lithium plating and striping on Ni electrode can be observed for these IL electrolytes, and these IL electrolytes show good chemical stability against lithium metal. Li/LiFePO4 cells using these IL electrolytes without additives have good capacity and cycle property at the current rate of 0.1 C, and the cell using the P(2o1)(2o2)-TFSI electrolyte owns good rate property. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:5637 / 5644
页数:8
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