Electrochemical behavior of LiFePO4/C cathode material for rechargeable lithium batteries

被引:88
作者
Liao, XZ [1 ]
Ma, ZF
He, YS
Zhang, XM
Wang, L
Jiang, Y
机构
[1] Shanghai Jiao Tong Univ, Dept Chem Engn, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Instrumental Anal Ctr, Shanghai 200230, Peoples R China
关键词
D O I
10.1149/1.2008988
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Electrochemical behavior of LiFePO4/C cathode material synthesized by ballmilling technique from a mixture of Fe powder, FePO4 center dot 4H2O, Li3PO4 center dot 1/2H(2)O, and sucrose was studied in half-cells using lithium metal as anode. The prepared LiFePO4/C cathode material exhibits excellent rate capability with initial discharge capacities of 141 mAh/g (1 C ), 127 mAh/g (2 C), 119 mAh/g (3 C), and 109 mAh/g (5 C), respectively. Good cycling performance under 2 C charge-discharge rate could be obtained at room temperature with a discharge capacity of 125-131 mAh/g for 300 cycles. Impedance spectroscopy was applied to investigate the material behavior during the 2 C rate charge-discharge cycling. It is found that the Nyquist plots of the cycled lithium cell at discharged state are comprised of one or two semicircles in high-to-medium frequency range followed by an inclined line in low-frequency range. The first semicircle at higher frequency shows close relationship with the cycling performance of the lithium cell. Thus, it may be used to predict the cycle life of the LiFePO4/C cathode. Through a combined X-ray diffraction (XRD) analysis and scanning electron microscope observation on the LiFePO4/C cathode upon the 2 C rate cycling, we correlated the observed capacity fading after 300 cycles at 2 C charge-discharge rate with the LiFePO4 particle cracking and the increase of particle contact resistance. No significant phase change of LiFePO4/C was observed even after 800 cycles according to the XRD patterns. (c) 2005 The Electrochemical Society.
引用
收藏
页码:A1969 / A1973
页数:5
相关论文
共 24 条
  • [1] Lithium iron(II) phospho-olivines prepared by a novel carbothermal reduction method
    Barker, J
    Saidi, MY
    Swoyer, JL
    [J]. ELECTROCHEMICAL AND SOLID STATE LETTERS, 2003, 6 (03) : A53 - A55
  • [2] Recent developments on lithium ion batteries at SAFT
    Broussely, M
    [J]. JOURNAL OF POWER SOURCES, 1999, 81 : 140 - 143
  • [3] BUSTAM A, 2002, ELECTROCHIM ACTA, V48, P165
  • [4] Electronically conductive phospho-olivines as lithium storage electrodes
    Chung, SY
    Bloking, JT
    Chiang, YM
    [J]. NATURE MATERIALS, 2002, 1 (02) : 123 - 128
  • [5] Ethylmethylcarbonate, a promising solvent for Li-ion rechargeable batteries
    EinEli, Y
    Thomas, SR
    Koch, V
    Aurbach, D
    Markovsky, B
    Schechter, A
    [J]. JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1996, 143 (12) : L273 - L277
  • [6] Comparison between different LiFePO4 synthesis routes and their influence on its physico-chemical properties
    Franger, S
    Le Cras, F
    Bourbon, C
    Rouault, H
    [J]. JOURNAL OF POWER SOURCES, 2003, 119 : 252 - 257
  • [7] LiFePO4 synthesis routes for enhanced electrochemical performance
    Franger, S
    Le Cras, F
    Bourbon, C
    Rouault, H
    [J]. ELECTROCHEMICAL AND SOLID STATE LETTERS, 2002, 5 (10) : A231 - A233
  • [8] Approaching theoretical capacity of LiFePO4 at room temperature at high rates
    Huang, H
    Yin, SC
    Nazar, LF
    [J]. ELECTROCHEMICAL AND SOLID STATE LETTERS, 2001, 4 (10) : A170 - A172
  • [9] Novel synthesis route for LiFePO4/C cathode materials for lithium-ion batteries
    Liao, XZ
    Ma, ZF
    Wang, L
    Zhang, XM
    Jiang, Y
    He, YS
    [J]. ELECTROCHEMICAL AND SOLID STATE LETTERS, 2004, 7 (12) : A522 - A525
  • [10] Structural and electrochemical characterization of carbonaceous mesophase spherule anode material for rechargeable lithium batteries
    Ma, ZF
    Yuan, XZ
    Li, D
    Liao, XZ
    Hu, HP
    Ma, JQ
    Wang, JF
    [J]. ELECTROCHEMISTRY COMMUNICATIONS, 2002, 4 (02) : 188 - 192