4.5 Article

Ionic liquid-based electrolyte with dual-functional LiDFOB additive toward high-performance LiMn2O4 batteries

Journal

IONICS
Volume 23, Issue 6, Pages 1399-1406

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s11581-016-1966-9

Keywords

Ionic liquid-based electrolyte; LiMn2O4 batteries; Dual-functional additive; Solid electrolyte interface

Funding

  1. National Program on the National High Technology Research and Development Program of China (863 program) [2013AA050905]
  2. Key Project of Natural Science Foundation of Shandong Province [ZR2015QZ01]
  3. 135 Projects Fund of CAS-QIBEBT Director Innovation Foundation
  4. Qingdao Institute of Bioenergy and Bioprocess Technology Director Technology Foundation

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Manganese oxide-based cathodes are one of the most promising lithium-ion battery (LIB) cathode materials due to their cost-effectiveness, high discharge voltage plateau (above 4.0 V vs. Li/Li+), superior rate capability, and environmental benignity. However, these batteries using conventional LiPF6-based electrolytes suffer from Mn dissolution and poor cyclic capability at elevated temperature. In this paper, the ionic liquid (IL)-based electrolytes, consisting of 1-butyl-1-methylpyrrolidinium bis(trifluoromethanesulfon)imidate (PYR1,4-TFSI), propylene carbonate (PC), lithium bis(trifluoromethanesulfon)imide (LiTFSI), and lithium oxalyldifluoroborate (LiDFOB) additive, were explored for improving the high temperature performance of the LiMn2O4 batteries. It was demonstrated that LiTFSI-ILs/PC electrolyte associated with LiDFOB addition possessed less Mn dissolution and Al corrosion at the elevated temperature in LiMn2O4/Li batteries. Cyclic voltammetry and electrochemical impedance spectroscopy implied that this kind of electrolyte also contributed to the formation of a highly stable solid electrolyte interface (SEI), which was in accordance with the polarization measurement and the Li deposition morphology of the symmetric lithium metal cell, thus beneficial for improving the cycling performance of the LiMn2O4 batteries at the elevated temperature. Cyclic voltammetry and electrochemical impedance spectroscopy implied that the cells using this kind of electrolyte exhibited better interfacial stability, which was further verified by the polarization measurement and the Li deposition morphology of the symmetric lithium metal cell, thus beneficial for improving the cycling performance of the LiMn2O4 batteries at the elevated temperature. These unique characteristics would endow this kind of electrolyte a very promising candidate for the manganese oxide-based batteries.

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