Effect of Anion on Behaviour of Li-S Battery Electrolyte Solutions Based on N-Methyl-N-Butyl-Pyrrolidinium Ionic Liquids

被引:36
作者
Barghamadi, Marzieh [1 ,3 ]
Best, Adam S. [2 ]
Bhatt, Anand I. [1 ]
Hollenkamp, Anthony F. [1 ]
Mahon, Peter J. [3 ]
Musameh, Mustafa [2 ]
Ruether, Thomas [1 ]
机构
[1] CSIRO Energy Flagship, Clayton, Vic 3169, Australia
[2] CSIRO Mfg Flagship, Clayton, Vic 3169, Australia
[3] Swinburne Univ Technol, Dept Chem & Biotechnol, Sch Sci, Fac Sci Technol & Engn, Hawthorn, Vic 3122, Australia
关键词
Lithium-sulfur battery; Ionic liquid electrolytes; Polysulfide solubility; C(4)mpyr cation; THERMOPHYSICAL PROPERTIES; LITHIUM/SULFUR CELL; SULFUR CATHODE; GRAPHENE OXIDE; PERFORMANCE; REVERSIBILITY; INTERFACE; AIR;
D O I
10.1016/j.electacta.2015.08.132
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The electrochemical behaviour and electrical performance are investigated for a series of lithium-sulfur (Li-S) cells in which the electrolyte solutions are organic solvent-ionic liquid mixtures that are based on the 1-butyl-1-methylpyrrolidinium (C(4)mpyr) cation with a range of anions. In each case, performance is compared with cells that are based on a standard mixed-ether organic electrolyte. The capacity of cells assembled with electrolytes containing 1-butyl-1-methylpyrrolidinium tris (pentafluoroethyl) trifluorophosphate (C(4)mpyr-FAP), 1-butyl-1-methylpyrrolidinium trifluoromethanesulfonate (C(4)mpyr-OTf), or 1-butyl-1-methylpyrrolidinium tricyanomethanide (C(4)mpyr-TCM) decline rapidly due to low conductivity, high polysulfide solubility and side reaction of electrolyte with electrodes, respectively. Our results confirm that polysulfide solubility is strongly controlled by the anion of the ionic liquid and verify that not all ionic liquids decrease polysulfide solubility. In agreement with previous reports, 1-butyl-1-methylpyrrolidinium bis(trifluoromethanesulfonyl) imide (C(4)mpyr-TFSI) shows the best compatibility in Li-S batteries and has a higher coulombic efficiency of greater than 99% over 100 cycles. Furthermore, impedance spectroscopy confirms that electrolyte composition influences the SEI layer formed on the lithium anode and its subsequent impedance. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:636 / 644
页数:9
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