Fast Charge/Discharge of Li Metal Batteries Using an Ionic Liquid Electrolyte

被引:213
作者
Yoon, H. [1 ,2 ]
Howlett, P. C. [3 ]
Best, A. S. [2 ]
Forsyth, M. [3 ]
MacFarlane, D. R. [1 ]
机构
[1] Monash Univ, Sch Chem, Clayton, Vic 3800, Australia
[2] CSIRO, Div Energy Technol, Clayton, Vic 3169, Australia
[3] Deakin Univ, ARC Ctr Excellence Electromat Sci ACES, IFM, Burwood, Vic 3125, Australia
基金
澳大利亚研究理事会;
关键词
ELECTROCHEMICAL PROPERTIES; POLYMER ELECTROLYTES; TRANSFERENCE NUMBERS; LITHIUM; TEMPERATURE; IMIDE; BIS(FLUOROSULFONYL)IMIDE; BIS(TRIFLUOROMETHANESULFONYL)IMIDE; COMPATIBILITY; AIR;
D O I
10.1149/2.022310jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Because of their potentially superior safety characteristics, room temperature ionic liquids (RTILs or ILs) have been vigorously researched as a potential replacement for current commercial lithium battery electrolytes, which are based on volatile and flammable organic carbonates. However, relatively poor battery performance, which is a consequence of the higher viscosity and lower conductivity of these materials, has prevented them becoming mainstream electrolytes for commercial lithium batteries. Amongst various RTILs, those containing the bis(fluorosulfonyl)imide (FSI) anion exhibit high conductivities and diffusivities, making them interesting potential electrolytes for lithium metal batteries. Here, we evaluate the electrochemical stability, lithium electrochemistry, and Li+ transference numbers of FSI-based ionic liquid electrolytes intended for use in rechargeable Li metal batteries. We show that ILs containing high concentrations of lithium, up to 3.2 mol.kg(-1) in C(3)mpyr zgSI, have excellent rate capability (higher than that of standard battery electrolytes) with both the lithium metal electrode and LiCoO2 cathode, in spite of their significantly higher viscosities and lower conductivities. This unusual behavior is ascribed to the concomitant increase in transference number with increasing Li-salt concentration. (C) 2013 The Electrochemical Society. All rights reserved.
引用
收藏
页码:A1629 / A1637
页数:9
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