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
[11]   Nano-network electronic conduction in iron and nickel olivine phosphates [J].
Herle, PS ;
Ellis, B ;
Coombs, N ;
Nazar, LF .
NATURE MATERIALS, 2004, 3 (03) :147-152
[12]   Approaching theoretical capacity of LiFePO4 at room temperature at high rates [J].
Huang, H ;
Yin, SC ;
Nazar, LF .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2001, 4 (10) :A170-A172
[13]   More on the performance of LiFePO4 electrodes -: The effect of synthesis route, solution composition, aging, and temperature [J].
Koltypin, M. ;
Aurbach, D. ;
Nazar, L. ;
Ellis, B. .
JOURNAL OF POWER SOURCES, 2007, 174 (02) :1241-1250
[14]   Raman and FTIR Spectroscopy Investigations of Carbon-Coated LixFePO4 Materials [J].
Maccario, M. ;
Croguennec, L. ;
Desbat, B. ;
Couzi, M. ;
Le Cras, F. ;
Servant, L. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2008, 155 (12) :A879-A886
[15]   Electrochemical performances in temperature for a C-containing LiFePO4 composite synthesized at high temperature [J].
Maccario, M. ;
Croguennec, L. ;
Le Cras, F. ;
Delmas, C. .
JOURNAL OF POWER SOURCES, 2008, 183 (01) :411-417
[16]   Electrochemically Induced Phase Transformation in Nanoscale Olivines Li1-xMPO4 (M = Fe, Mn) [J].
Meethong, Nonglak ;
Kao, Yu-Hua ;
Tang, Ming ;
Huang, Hsiao-Ying ;
Carter, W. Craig ;
Chiang, Yet-Ming .
CHEMISTRY OF MATERIALS, 2008, 20 (19) :6189-6198
[17]   Polymeric gel electrolyte containing alkyl phosphate for lithium-ion batteries [J].
Morita, M ;
Niida, Y ;
Yoshimoto, N ;
Adachi, K .
JOURNAL OF POWER SOURCES, 2005, 146 (1-2) :427-430
[18]   One-Pot Microwave-Hydrothermal Synthesis and Characterization of Carbon-Coated LiMPO4 (M=Mn, Fe, and Co) Cathodes [J].
Murugan, A. Vadivel ;
Muraliganth, T. ;
Manthiram, A. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2009, 156 (02) :A79-A83
[19]   Effect of structure on the Fe3+/Fe2+ redox couple in iron phosphates [J].
Padhi, AK ;
Nanjundaswamy, KS ;
Masquelier, C ;
Okada, S ;
Goodenough, JB .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1997, 144 (05) :1609-1613
[20]   Phospho-olivines as positive-electrode materials for rechargeable lithium batteries [J].
Padhi, AK ;
Nanjundaswamy, KS ;
Goodenough, JB .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1997, 144 (04) :1188-1194