Ionic liquids doped with a lithium salt are alternative electrolytes for lithium-ion batteries that offer some advantages compared to organic carbonates based liquid electrolytes. Ionic liquids display a low vapor pressure which leads to nonflammability. The main drawback of ionic liquid-based electrolytes is the low lithium-ion conductivity due to relatively high viscosity of ionic liquids. A lot of research has been devoted to developing ionic liquids with low viscosity. However, so far, these ionic liquids could be obtained only at the expense of lower thermal and/or electrochemical stability. In recent years, mixtures of organic carbonates-based electrolytes and ionic liquids have been proposed as a solution to overcome the lithium-ion transport limitations of ionic liquid-based electrolytes while improving safety due to a lower flammability than that of organic carbonates electrolytes [1, 2].
Herein, we report the results of physical-chemical and electrochemical investigations performed on mixed electrolytes based on an ionic liquid, 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide (BMP-TFSI), and organic electrolytes (LiTFSI in EC/DMC) with nanostructured silicon-anode for lithium-ion batteries. The ionic conductivity, lithium-ion transference number, viscosity and electrochemical stability windows of all different ionic liquid content mixtures were investigated and compared with carbonates-based electrolyte. The specific capacity and cycling stability of the nanostructured silicon-anode were investigated at different C-rates at room temperature. A reversible capacity of 3480 mAh g-1 (of Si) at C/10 and 1600 mAh g-1 at 5C is obtained with cells having electrolyte mixture with a composition of 1:1. This study indicates that safety and electrochemical performance of the Si-anode for Li-ion battery can be improved by using mixed ionic liquid and carbonates-based electrolytes.
[1] A. Guerfi, M. Dontigny, P. Charest, M. Petitclerc, M. Lagacé, A. Vijh, K. Zaghib, J. Power Sources 195 (2010) 845-852.
[2] R.-S. Kühnel and A. Balducci, J. Phys. Chem. C 118 (2014) 5742-5748.
