High Rate Charge and Discharge Characteristics of Graphite/SiOx Composite Electrodes

被引:9
作者
Yoshida, Shuhei [1 ,2 ]
Okubo, Takashi [2 ]
Masuo, Yuta [2 ]
Oba, Yasuyuki [1 ]
Shibata, Daisuke [1 ]
Haruta, Masakazu [2 ]
Doi, Takayuki [2 ]
Inaba, Minoru [2 ]
机构
[1] DENSO CORP, 1-1 Showa, Kariya, Aichi 4488661, Japan
[2] Doshisha Univ, Dept Mol Chsmitry & Biochem, 1-3 Tatara Miyakodani, Kyoto 6100321, Japan
关键词
Graphite/SiOx Composite Electrode; High Rate Charge and Discharge; Crack Formation; Ac Impedance Spectroscopy; LITHIUM-ION BATTERIES; NEGATIVE ELECTRODE; SILICON MONOXIDE; SIO; ANODES; EXTRACTION; INSERTION;
D O I
10.5796/electrochemistry.85.403
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Charge and discharge properties of a graphite/SiOx composite electrode were studied over a wide range of charge/ discharge rates (1/20 to 5C) for use in automotive applications. The graphite/SiOx (90/10 by weight) composite electrode gave a high reversible capacity (453 mAh.g(-1)), and showed a good capacity retention at a low rate of 1/ 20 C. However, the capacity decreased significantly on cycling at a high rate of 2 C. From the analysis of the charging and discharging processes, it was found that the charging reaction occurs predominantly at SiOx particles initially at higher potentials and then proceeds at graphite particles at lower potentials to be fully charged. This tendency was also supported by a dependence of the activation energy of the charge transfer reaction on the state of charge (SOC) estimated by ac impedance analysis. Because the composite electrode contains only 10% SiOx the current was excessively concentrated to the SiOx particles at the initial state when charged at high rates. This caused crack formation in SiOx particles, and the resulting contact loss between particles was considered as the reason for the observed poor cycleability at 2 C. (c) The Electrochemical Society of Japan, All rights reserved.
引用
收藏
页码:403 / 408
页数:6
相关论文
共 17 条
[1]   Solvated Li-ion transfer at interface between graphite and electrolyte [J].
Abe, T ;
Fukuda, H ;
Iriyama, Y ;
Ogumi, Z .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2004, 151 (08) :A1120-A1123
[2]   ALL-SOLID LITHIUM ELECTRODES WITH MIXED-CONDUCTOR MATRIX [J].
BOUKAMP, BA ;
LESH, GC ;
HUGGINS, RA .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1981, 128 (04) :725-729
[3]  
Guerfi A., 2011, J POWER SOURCES, V196, P5667
[4]  
Hahn J. R., 1991, PHYS REV B, V44, P9170
[5]  
Huijun H., 2016, INT J ELECTROCHEM SC, V11, P8697
[6]   High capacity Si/C nanocomposite anodes for Li-ion batteries [J].
Kim, IS ;
Kumta, PN .
JOURNAL OF POWER SOURCES, 2004, 136 (01) :145-149
[7]   Solid-state NMR and electrochemical dilatometry study on Li+ uptake/extraction mechanism in SiO electrode [J].
Kim, Taeahn ;
Park, Sangjin ;
Oh, Seung M. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2007, 154 (12) :A1112-A1117
[8]   Improvement of cycling stability of Si anode by mechanochemcial reduction and carbon coating [J].
Liu, Y. ;
Wen, Z. Y. ;
Wang, X. Y. ;
Yang, X. L. ;
Hirano, A. ;
Imanishi, N. ;
Takeda, Y. .
JOURNAL OF POWER SOURCES, 2009, 189 (01) :480-484
[9]   Preparation of fine silicon particles from amorphous silicon monoxide by the disproportionation reaction [J].
Mamiya, M ;
Takei, H ;
Kikuchi, M ;
Uyeda, C .
JOURNAL OF CRYSTAL GROWTH, 2001, 229 (01) :457-461
[10]   Analysis of SiO anodes for lithium-ion batteries [J].
Miyachi, M ;
Yamamoto, H ;
Kawai, H ;
Ohta, T ;
Shirakata, M .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2005, 152 (10) :A2089-A2091