4.6 Article

Safe ionic liquid-sulfolane/LiDFOB electrolytes for high voltage Li-1.15(Ni0.36Mn0.64)(0.85)O-2 lithium ion battery at elevated temperatures

Journal

ELECTROCHIMICA ACTA
Volume 270, Issue -, Pages 426-433

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2018.03.108

Keywords

High temperature lithium ion batteries; Safety; High voltage; Ionic liquids electrolytes; Cathode-electrolyte interface

Funding

  1. National Natural Science Foundation [51574166]
  2. Scientific and Technological Research and Development Foundation of Shenzhen City [JCYJ20160301145911673]

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In this study, 1-methyl-1-butylpiperidinium bis(trifluoromethanesulfonyl)-imide (PP14TFSI)-sulfolane/lithium difluoro(oxalato) borate (LiDFOB) based electrolytes with inherent thermal stability and low flammability are investigated as promising alternatives of conventional LiPF6/carbonate electrolyte in high voltage Li/Li-1.15(Ni0.36Mn0.64)(0.85)O-2 cells at elevated temperatures. The safe and stable electrolyte candidates are selected by optimizing relative composition and represent high oxidative stability (higher than 5.2 V vs Li/Li+) above 55 degrees C. The Li/Li-1.15(Ni0.36Mn0.64)(0.85)O-2 cells with E60 electrolyte achieved 172.5 and 238.8 mAh g(-1) after 50 cycles between 2.0 and 4.6 V at 0.5C at 55 and 70 degrees C. Moreover, the Li/Li-1.15(Ni0.36Mn0.64)(0.85)O-2 cell with E60 electrolyte obtains a superior discharge capacity of 97.9 mAh g(-1) at high rate of 3C at 70 degrees C. At extremely high temperature of 85 degrees C, the cell with E60 electrolyte delivers 218.7 mAh g(-1) after 50 cycles at 1C. The excellent cycling performance in high voltage Li/Li-1.15(Ni0.36Mn0.64)(0.85)O-2 cells at elevated temperatures is attributed to the intrinsic oxidative stability and the compact and stable cathode-electrolyte interface (CEI) film derived from E60 electrolyte. We believe it a promising candidate that can be safely used for high voltage Li-rich cells at elevated temperature. (c) 2018 Elsevier Ltd. All rights reserved.

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