Structural and surface modifications of LiFePO4 olivine particles and their electrochemical properties

被引:150
作者
Nakamura, T [1 ]
Miwa, Y
Tabuchi, M
Yamada, Y
机构
[1] Univ Hyogo, Grad Sch Engn, Dept Elect Engn & Comp Sci, Kakogawa, Hyogo 6712201, Japan
[2] Natl Inst Adv Ind Sci & Technol, Osaka 5638577, Japan
关键词
D O I
10.1149/1.2192732
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
LiFePO4-based olivine compounds were prepared by the usual ceramic method, where some modifications were carried out in order to improve the electrical conductivity of the cathode compound. Considering that the cathode is made up of electrochemical active particles and a nonactive polymer binder, two different methods were applied. The first one is related to the improvement of the interparticle conduction, and the other is the enhancement of the conductivity in the active particle itself. The former was attained with thermal decomposition of an organic additive (pyrene) during the sample preparation process, and the precipitated carbon was investigated with Raman spectroscopy. The bulk conductivity of the olivine was improved with a partial substitution of Fe2+ with Mn2+, where the holes were incorporated into the valence band. These modifications significantly altered the electrochemical properties of the olivine cathode: large specific capacity (>140 mAh/g) and small capacity fading. Although the importance of carbon deposition was confirmed as reported elsewhere, the structural modification effect was also more important than the surface one. The result will contribute to reduce carbon content of LiFePO4-based positive electrodes, which is important for their practical use. (C) 2006 The Electrochemical Society.
引用
收藏
页码:A1108 / A1114
页数:7
相关论文
共 44 条
  • [1] The source of first-cycle capacity loss in LiFePO4
    Andersson, AS
    Thomas, JO
    [J]. JOURNAL OF POWER SOURCES, 2001, 97-8 : 498 - 502
  • [2] Lithium extraction/insertion in LiFePO4:: an X-ray diffraction and Mossbauer spectroscopy study
    Andersson, AS
    Kalska, B
    Häggström, L
    Thomas, JO
    [J]. SOLID STATE IONICS, 2000, 130 (1-2) : 41 - 52
  • [3] Fine-particle lithium iron phosphate LiFePO4 synthesized by a new low-cost aqueous precipitation technique
    Arnold, G
    Garche, J
    Hemmer, R
    Ströbele, S
    Vogler, C
    Wohlfahrt-Mehrens, A
    [J]. JOURNAL OF POWER SOURCES, 2003, 119 : 247 - 251
  • [4] 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
  • [5] BURA CM, 2004, J ELECTROCHEM SOC, V151, pA1032
  • [6] Synthesis of olivine-type LiFePO4 by emulsion-drying method
    Cho, TH
    Chung, HT
    [J]. JOURNAL OF POWER SOURCES, 2004, 133 (02) : 272 - 276
  • [7] Microscale measurements of the electrical conductivity of doped LiFePO4
    Chung, SY
    Chiang, YM
    [J]. ELECTROCHEMICAL AND SOLID STATE LETTERS, 2003, 6 (12) : A278 - A281
  • [8] Electronically conductive phospho-olivines as lithium storage electrodes
    Chung, SY
    Bloking, JT
    Chiang, YM
    [J]. NATURE MATERIALS, 2002, 1 (02) : 123 - 128
  • [9] A novel concept for the synthesis of an improved LiFePO4 lithium battery cathode
    Croce, F
    D'Epifanio, A
    Hassoun, J
    Deptula, A
    Olczac, T
    Scrosati, B
    [J]. ELECTROCHEMICAL AND SOLID STATE LETTERS, 2002, 5 (03) : A47 - A50
  • [10] Effect of surface carbon structure on the electrochemical performance of LiFePO4
    Doeff, MM
    Hu, YQ
    McLarnon, F
    Kostecki, R
    [J]. ELECTROCHEMICAL AND SOLID STATE LETTERS, 2003, 6 (10) : A207 - A209