The Effect of Microstructure on the Galvanostatic Discharge of Graphite Anode Electrodes in LiCoO2-Based Rocking-Chair Rechargeable Batteries

被引:75
作者
Smith, Madeleine [1 ]
Garcia, R. Edwin [1 ]
Horn, Quinn C. [2 ]
机构
[1] Purdue Univ, Sch Mat Engn, W Lafayette, IN 47906 USA
[2] Exponent Failure Anal Associates, Natick, MA 01760 USA
基金
美国国家科学基金会;
关键词
LITHIUM-ION BATTERIES; INTERCALATION-INDUCED STRESS; POROUS INSERTION ELECTRODES; COMPUTER-SIMULATIONS; HEAT-GENERATION; SYSTEMS; CELLS; ARCHITECTURES; PARTICLES; CAPACITY;
D O I
10.1149/1.3216000
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
By starting from experimentally determined cross sections of rechargeable lithium-ion batteries, the effect of microstructure on the galvanostatic discharge of a LiCoO2 vertical bar LiC6 cell was numerically modeled. Results demonstrate that when small graphite particles are part of a population with large particle sizes, diminished macroscopic power densities develop and limit the response of the entirety of the cell. Small particle-size populations electrochemically interact with large particle-size populations and lead to a macroscopic capacity loss, compared to cells with uniform particle size. Such capacity loss is a result of the lithium exchange between small and large anode particle-size populations, instead of the lithium exchange between electrode particles of opposite polarity. The analysis suggests that graphite particles of size smaller than the average value dominate the macroscopic electrical response of the device, for the induced localized lithium depletion leads to an increase in the polarization losses of the anode. Lithium depletion in the anode starts in the small particles, is followed by particles of complex morphology and rough surfaces, and continues with the depletion of large particles embedded in a fast diffusion environment. (C) 2009 The Electrochemical Society. [DOI: 10.1149/1.3216000] All rights reserved.
引用
收藏
页码:A896 / A904
页数:9
相关论文
共 50 条
[1]   Comparison between computer simulations and experimental data for high-rate discharges of plastic lithium-ion batteries [J].
Arora, P ;
Doyle, M ;
Gozdz, AS ;
White, RE ;
Newman, J .
JOURNAL OF POWER SOURCES, 2000, 88 (02) :219-231
[2]   Mathematical modeling of the lithium deposition overcharge reaction in lithium-ion batteries using carbon-based negative electrodes [J].
Arora, P ;
Doyle, M ;
White, RE .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1999, 146 (10) :3543-3553
[3]   DYNAMIC ASPECTS OF SOLID-SOLUTION CATHODES FOR ELECTROCHEMICAL POWER SOURCES [J].
ATLUNG, S ;
WEST, K ;
JACOBSEN, T .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1979, 126 (08) :1311-1321
[4]  
ATLUNG S, 1984, J ELECTROCHEM SOC, V131, P1200, DOI 10.1149/1.2115778
[5]   Mathematical modeling of secondary lithium batteries [J].
Botte, GG ;
Subramanian, VR ;
White, RE .
ELECTROCHIMICA ACTA, 2000, 45 (15-16) :2595-2609
[6]  
CHIANG YM, 2001, EL SOC M SAN FRANC C
[7]   Electronically conductive phospho-olivines as lithium storage electrodes [J].
Chung, SY ;
Bloking, JT ;
Chiang, YM .
NATURE MATERIALS, 2002, 1 (02) :123-128
[8]   Effect of electrolyte composition on lithium dendrite growth [J].
Crowther, Owen ;
West, Alan C. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2008, 155 (11) :A806-A811
[9]   Modeling side reactions in composite LiyMn2O4 electrodes [J].
Darling, R ;
Newman, J .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1998, 145 (03) :990-998
[10]   Batteries - fifty years of materials development [J].
Dell, RM .
SOLID STATE IONICS, 2000, 134 (1-2) :139-158