Cycling degradation of an automotive LiFePO4 lithium-ion battery

被引:327
作者
Zhang, Yancheng [1 ]
Wang, Chao-Yang [1 ]
Tang, Xidong [2 ,3 ]
机构
[1] Penn State Univ, Dept Mech & Nucl Engn, University Pk, PA 16802 USA
[2] Gen Motors, GM R&D, Warren, MI 48090 USA
[3] Gen Motors, Planning, Warren, MI 48090 USA
关键词
LiFePO4; Lithium-ion battery; Cycling degradation; Electrochemical impedance spectroscopy; Electric-only range; LONG-TERM CYCLABILITY; HIGH-TEMPERATURE; HIGH-POWER; ELECTRODE MATERIALS; CARBON; CELLS; PERFORMANCE; CAPACITY; PHOSPHATES; LIXFEPO4;
D O I
10.1016/j.jpowsour.2010.08.070
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
Degradation of a high capacity prismatic LiFePO4 cell with deep cycling at elevated temperature of 50 degrees C is studied by electrochemical impedance spectroscopy as well as capacity and power fading characterization at different test temperatures (45, 25, 0 and -10 degrees C. The capacity and power fade evidently becomes more severe at lower temperature. In particular, the power fade at low temperatures (e.g., 0 and -10 degrees C) rather than capacity loss is a major limitation of the LiFePO4 cell. The primary mechanism for capacity fade is loss of cyclable lithium in the cell resulting from lithium-consuming solid electrolyte interphase (SEI) layer growth and side reactions. The increased interfacial resistance (R-W) due to the catalytic growth of SEI layer on the graphite anode and increased electrolyte resistance are the main sources for power fade. (C) Elsevier B.V. All rights reserved.
引用
收藏
页码:1513 / 1520
页数:8
相关论文
共 40 条
[1]   High-temperature storage and cycling of C-LiFePO4/graphite Li-ion cells [J].
Amine, K ;
Liu, J ;
Belharouak, I .
ELECTROCHEMISTRY COMMUNICATIONS, 2005, 7 (07) :669-673
[2]   Differential voltage analyses of high-power, lithium-ion cells 1. Technique and application [J].
Bloom, I ;
Jansen, AN ;
Abraham, DP ;
Knuth, J ;
Jones, SA ;
Battaglia, VS ;
Henriksen, GL .
JOURNAL OF POWER SOURCES, 2005, 139 (1-2) :295-303
[3]   Effect of cathode composition on capacity fade, impedance rise and power fade in high-power, lithium-ion cells [J].
Bloom, I ;
Jones, SA ;
Battaglia, VS ;
Henriksen, GL ;
Christophersen, JP ;
Wright, RB ;
Ho, CD ;
Belt, JR ;
Motloch, CG .
JOURNAL OF POWER SOURCES, 2003, 124 (02) :538-550
[4]   Enhanced high-temperature cycle performance of LiFePO4/carbon batteries by an ion-sieving metal coating on negative electrode [J].
Chang, Hao-Hsun ;
Wu, Hung-Chun ;
Wu, Nae-Lih .
ELECTROCHEMISTRY COMMUNICATIONS, 2008, 10 (12) :1823-1826
[5]   Reducing carbon in LiFePO4/C composite electrodes to maximize specific energy, volumetric energy, and tap density [J].
Chen, ZH ;
Dahn, JR .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2002, 149 (09) :A1184-A1189
[6]   Electronically conductive phospho-olivines as lithium storage electrodes [J].
Chung, SY ;
Bloking, JT ;
Chiang, YM .
NATURE MATERIALS, 2002, 1 (02) :123-128
[7]   The existence of a temperature-driven solid solution in LixFePO4 for 0 ≤ x ≤ 1 [J].
Delacourt, C ;
Poizot, P ;
Tarascon, JM ;
Masquelier, C .
NATURE MATERIALS, 2005, 4 (03) :254-260
[8]   Identify capacity fading mechanism in a commercial LiFePO4 cell [J].
Dubarry, Matthieu ;
Liaw, Bor Yann .
JOURNAL OF POWER SOURCES, 2009, 194 (01) :541-549
[9]   Electrochemical-thermal modeling of automotive Li-ion batteries and experimental validation using a three-electrode cell [J].
Fang, Weifeng ;
Kwon, Ou Jung ;
Wang, Chao-Yang .
INTERNATIONAL JOURNAL OF ENERGY RESEARCH, 2010, 34 (02) :107-115
[10]   Thermal modeling of a cylindrical LiFePO4/graphite lithium-ion battery [J].
Forgez, Christophe ;
Do, Dinh Vinh ;
Friedrich, Guy ;
Morcrette, Mathieu ;
Delacourt, Charles .
JOURNAL OF POWER SOURCES, 2010, 195 (09) :2961-2968