Mathematical modeling of the lithium deposition overcharge reaction in lithium-ion batteries using carbon-based negative electrodes

被引:443
作者
Arora, P [1 ]
Doyle, M
White, RE
机构
[1] Univ S Carolina, Dept Chem Engn, Ctr Electrochem Engn, Columbia, SC 29208 USA
[2] DuPont Co Inc, Cent Res & Dev, Expt Stn, Wilmington, DE 19880 USA
关键词
D O I
10.1149/1.1392512
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The processes that lead to capacity fading affect severely the cycle life and rate behavior of lithium-ion cells. One such process is the overcharge of the negative electrode causing lithium deposition, which can lead to capacity losses including a loss of active lithium and electrolyte and represents a potential safety hazard. A mathematical model is presented to predict lithium deposition on the negative electrode under a variety of operating conditions. The Li(x)C6\1 M LiPF6, 2:1 ethylene carbonate/dimethyl carbonate, poly(vinylidene fluoride-hexalfuoropropylene) \LiMn2O4 cell is simulated to investigate the influence of lithium deposition on the charging behavior of intercalation electrodes. The model is used to study the effect of key design parameters (particle size, electrode thickness, and mass ratio) on the lithium deposition overcharge reaction. The model predictions are compared for coke and gaphite-based negative electrodes. The cycling behavior of these cells is simulated before and after overcharge to understand the effect of overcharge on extended cycling. These results can be used to establish operational and design limits within which safety hazards and capacity fade problems, inherent in these cells, can be minimized. (C) 1999 The Electrochemical Society. S0013-4651(99)01-088-5. All rights reserved.
引用
收藏
页码:3543 / 3553
页数:11
相关论文
共 16 条
[1]  
Arora P, 1998, ELEC SOC S, V98, P29
[2]   Capacity fade mechanisms and side reactions in lithium-ion batteries [J].
Arora, P ;
White, RE ;
Doyle, M .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1998, 145 (10) :3647-3667
[3]   Modeling side reactions in composite LiyMn2O4 electrodes [J].
Darling, R ;
Newman, J .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1998, 145 (03) :990-998
[4]   ELECTROCHEMICAL DECOMPOSITION OF PROPYLENE CARBONATE ON GRAPHITE [J].
DEY, AN ;
SULLIVAN, BP .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1970, 117 (02) :222-&
[5]   Comparison of modeling predictions with experimental data from plastic lithium ion cells [J].
Doyle, M ;
Newman, J ;
Gozdz, AS ;
Schmutz, CN ;
Tarascon, JM .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1996, 143 (06) :1890-1903
[6]   MODELING OF GALVANOSTATIC CHARGE AND DISCHARGE OF THE LITHIUM POLYMER INSERTION CELL [J].
DOYLE, M ;
FULLER, TF ;
NEWMAN, J .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1993, 140 (06) :1526-1533
[7]   STUDIES OF LITHIUM INTERCALATION INTO CARBONS USING NONAQUEOUS ELECTROCHEMICAL-CELLS [J].
FONG, R ;
VONSACKEN, U ;
DAHN, JR .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1990, 137 (07) :2009-2013
[8]   SIMULATION AND OPTIMIZATION OF THE DUAL LITHIUM ION INSERTION CELL [J].
FULLER, TF ;
DOYLE, M ;
NEWMAN, J .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1994, 141 (01) :1-10
[9]  
GERONOV Y, 1980, ELECTROCHEMICAL S PV, V807, P115
[10]  
Hsu DD, CHEM PERIODIC TABLE