LiPF6/methyl difluoroacetate electrolyte with vinylene carbonate additive for Li-ion batteries

被引:50
作者
Sato, Kazuya [2 ]
Zhao, Liwei [1 ]
Okada, Shigeto [1 ]
Yamaki, Jun-ichi [1 ]
机构
[1] Kyushu Univ, Inst Mat Chem & Engn, Fukuoka 8168580, Japan
[2] Kyushu Univ, Interdisciplinary Grad Sch Engn Sci, Fukuoka 8168580, Japan
关键词
Li-ion batteries; Electrolyte; Additive; Thermal stability; LITHIUM INTERCALATED GRAPHITE; ACCELERATING RATE CALORIMETRY; THERMAL-STABILITY; CELLS; ANODE; TEMPERATURE; BEHAVIOR; SOLVENT;
D O I
10.1016/j.jpowsour.2011.02.068
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A methyl difluoroacetate (MFA)-based LiPF6 solution was applied as an electrolyte to improve the thermal stability of Li-ion batteries. The addition of vinylene carbonate (VC) improved the electrochemical characteristics of the electrolyte significantly, and satisfactory reversible capacity and cycling performance were obtained with a graphite negative electrode. The thermal stability of the electrolytes was investigated with DSC. Regardless of whether or not VC was used, the electrolyte exothermically decomposed at a temperature higher than 450 degrees C. The thermal behavior of a mixture of lithiated graphite and VC-added electrolyte was also studied in detail. The ratio between the electrolyte and the electrode was a dominant factor in the heat generation of the mixture. A sharp exothermic peak at about 330 degrees C was observed when the electrode was superabundant, but the heat value was much smaller than that obtained with 1 mol dm(-3) LiPF6/EC-DMC electrolyte under the same conditions. When the electrolyte was superabundant, a mild exothermic decomposition of the electrolyte became the dominant reaction in the mixture. X-ray photoelectron spectroscopic analysis was carried out on delithiated graphite electrodes to study the effect of VC additive on solid electrolyte interphase (SEI) modification. VC-added MFA-based electrolyte was considered to be a good candidate for developing safer Li-ion batteries. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:5617 / 5622
页数:6
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