Capacity fade of Li1+xMn2-xO4-based lithium-ion cells

被引:52
作者
Chen, ZH [1 ]
Amine, K [1 ]
机构
[1] Argonne Natl Lab, Argonne, IL 60439 USA
关键词
D O I
10.1149/1.2147073
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Mesocarbon microbeads (MCMB), soft carbon coated nature graphite (GDR), and soft carbon were investigated as the negative electrodes for spinel/carbon cells with the aim to understand the capacity loss mechanism of carbon/spinel cells at elevated temperatures. The high-temperature cycling performance of MCMB/spinel cell and GDR/spinel cell was improved by formatting the cells at 55 degrees C. In this case, a stable solid electrolyte interphase (SEI) was believed to form at 55 degrees C and hence protected the carbon electrodes from attack by the solvents and Mn2+. Particularly, the cycling performance of the cells was dramatically improved by limiting the upper cutoff voltage of the cells to 4.1 V. The poor performance of the cells cycled to 4.3 V was believed to be related to the extra electrochemical reactions of lithium removal from the lithium-rich manganese oxide spinel that occurs at about 4.5 V vs Li. The relationship between the accelerated capacity fade and extra electrochemical reaction of lithium-rich spinel is also discussed in this manuscript. (c) 2005 The Electrochemical Society. [DOI: 10.1149/1.2147073] All rights reserved.
引用
收藏
页码:A316 / A320
页数:5
相关论文
共 23 条
[1]   Failure mechanism and improvement of the elevated temperature cycling of LiMn2O4 compounds through the use of the LiAlxMn2-xO4-zFz solid solution [J].
Amatucci, GG ;
Pereira, N ;
Zheng, T ;
Tarascon, JM .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2001, 148 (02) :A171-A182
[2]   Improved lithium manganese oxide spinel/graphite Li-ion cells for high-power applications [J].
Amine, K ;
Liu, J ;
Kang, S ;
Belharouak, I ;
Hyung, Y ;
Vissers, D ;
Henriksen, G .
JOURNAL OF POWER SOURCES, 2004, 129 (01) :14-19
[3]  
AMINE K, IN PRESS J POWER SOU
[4]   Factors affecting the stabilization of Mn spinel capacity upon storing and cycling at high temperatures [J].
Antonini, A ;
Bellitto, C ;
Pasquali, M ;
Pistoia, G .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1998, 145 (08) :2726-2732
[5]   Self-discharge of LiMn2O4/C Li-ion cells in their discharged state -: Understanding by means of three-electrode measurements [J].
Blyr, A ;
Sigala, C ;
Amatucci, G ;
Guyomard, D ;
Chabre, Y ;
Tarascon, JM .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1998, 145 (01) :194-209
[6]   Oxygen lattice instability as a capacity fading mechanism for 5 V cathode materials [J].
Caballero, A ;
Hernán, L ;
Melero, M ;
Morales, J ;
Angulo, M .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2005, 152 (01) :A6-A12
[7]  
CHEN ZG, UNPUB
[8]   The cathode-electrolyte interface in the Li-ion battery [J].
Edström, K ;
Gustafsson, T ;
Thomas, JO .
ELECTROCHIMICA ACTA, 2004, 50 (2-3) :397-403
[9]   Influence of temperature on the interface chemistry of LixMn2O4 electrodes [J].
Eriksson, T ;
Andersson, AM ;
Gejke, C ;
Gustafsson, T ;
Thomas, JO .
LANGMUIR, 2002, 18 (09) :3609-3619
[10]   Synthesis and characterization of Li1+xMn2-xO4 for Li-ion battery applications [J].
Gao, Y ;
Dahn, JR .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1996, 143 (01) :100-114