Electrochemical behavior of biphenyl as polymerizable additive for overcharge protection of lithium ion batteries

被引:143
作者
Xiao, LF [1 ]
Ai, XP [1 ]
Cao, YL [1 ]
Yang, HX [1 ]
机构
[1] Wuhan Univ, Dept Chem, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金;
关键词
lithium ion battery; overcharge protection; electro-polymerization; electrolyte additive; biphenyl;
D O I
10.1016/j.electacta.2004.04.013
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Electrochemical properties and working mechanism of biphenyl as a polymerizable electrolyte additive for overcharge protection of lithium ion batteries are studied by microelectrode voltarnmetry, charge-discharge measurements and SEM characterization of the overcharged cell's components. The experimental results reveal that biphenyl can electrochemically polymerize at the overcharge potential of 4.5-4.75 V (versus Li/Li+) to form a layer of conductive film on the cathode surface and the polymer deposits may develop to penetrate the separator to reach the anode surface, resulting an internal short-circuit to prevent from the cell voltage runaway. On the other hand, the electro-oxidative polymerization of biphenyl produces excessive gas and heat, which help to enhance the sensitivities of electric disconnecting devices. In addition, it is also found that the use of biphenyl as an electrolyte additive does not significantly influence the normal performances of the lithium ion batteries. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4189 / 4196
页数:8
相关论文
共 19 条
[1]   Aromatic compounds as redox shuttle additives for 4 V class secondary lithium batteries [J].
Adachi, M ;
Tanaka, K ;
Sekai, K .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1999, 146 (04) :1256-1261
[2]   On safety of lithium-ion cells [J].
Biensan, P ;
Simon, B ;
Pérès, JP ;
de Guibert, A ;
Broussely, M ;
Bodet, JM ;
Perton, F .
JOURNAL OF POWER SOURCES, 1999, 81 :906-912
[3]   POWDER MICROELECTRODES [J].
CHA, CS ;
LI, CM ;
YANG, HX ;
LIU, PF .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1994, 368 (1-2) :47-54
[4]   THERMAL-STABILITY OF LIXCOO2, LIXNIO2 AND LAMBDA-MNO2 AND CONSEQUENCES FOR THE SAFETY OF LI-ION CELLS [J].
DAHN, JR ;
FULLER, EW ;
OBROVAC, M ;
VONSACKEN, U .
SOLID STATE IONICS, 1994, 69 (3-4) :265-270
[5]   RECHARGEABLE LI1+XMN2O4/CARBON CELLS WITH A NEW ELECTROLYTE-COMPOSITION - POTENTIOSTATIC STUDIES AND APPLICATION TO PRACTICAL CELLS [J].
GUYOMARD, D ;
TARASCON, JM .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1993, 140 (11) :3071-3081
[6]   A study of LiMn2O4 synthesized from Li2CO3 and MnCO3 [J].
Hu, XH ;
Ai, XP ;
Yang, HX ;
Li, SX .
JOURNAL OF POWER SOURCES, 1998, 74 (02) :240-243
[7]   Gas generation mechanism due to electrolyte decomposition in commercial lithium-ion cell [J].
Kumai, K ;
Miyashiro, H ;
Kobayashi, Y ;
Takei, K ;
Ishikawa, R .
JOURNAL OF POWER SOURCES, 1999, 81 :715-719
[8]   The reactions of Li0.5CoO2 with nonaqueous solvents at elevated temperatures [J].
MacNeil, DD ;
Dahn, JR .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2002, 149 (07) :A912-A919
[9]  
MAO H, 2000, Patent No. 6074776
[10]  
Mao H., 1998, U. S. Pat, Patent No. 5776627