Room-temperature single-phase Li insertion/extraction in nanoscale LixFePO4

被引:634
作者
Gibot, Pierre [1 ]
Casas-Cabanas, Montse [1 ]
Laffont, Lydia [1 ]
Levasseur, Stephane [2 ]
Carlach, Philippe [2 ]
Hamelet, Stephane [1 ]
Tarascon, Jean-Marie [1 ]
Masquelier, Christian [1 ]
机构
[1] Univ Picardie Jules Verne, CNRS, UMR 6007, Lab React & Chim Solides, F-80039 Amiens 9, France
[2] UMICORE Res & Dev, B-2250 Olen, Belgium
关键词
D O I
10.1038/nmat2245
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
Classical electrodes for Li-ion technology operate by either single-phase or two-phase Li insertion/de-insertion processes, with single-phase mechanisms presenting some intrinsic advantages with respect to various storage applications. We report the feasibility to drive the well-established two-phase room-temperature insertion process in LiFePO4 electrodes into a single-phase one by modifying the material's particle size and ion ordering. Electrodes made of LiFePO4 nanoparticles (40 nm) formed by a low-temperature precipitation process exhibit sloping voltage charge/discharge curves, characteristic of a single-phase behaviour. The presence of defects and cation vacancies, as deduced by chemical/physical analytical techniques, is crucial in accounting for our results. Whereas the interdependency of particle size, composition and structure complicate the theorists' attempts to model phase stability in nanoscale materials, it provides new opportunities for chemists and electrochemists because numerous electrode materials could exhibit a similar behaviour at the nanoscale once their syntheses have been correctly worked out.
引用
收藏
页码:741 / 747
页数:7
相关论文
共 29 条
  • [1] Armand M., 2002, World Patent, Patent No. 0227823
  • [2] Hydrothermal synthesis of lithium iron phosphate
    Chen, Jiajun
    Whittingham, M. Stanley
    [J]. ELECTROCHEMISTRY COMMUNICATIONS, 2006, 8 (05) : 855 - 858
  • [3] Size effects on carbon-free LiFePO4 powders
    Delacourt, C.
    Poizot, P.
    Levasseur, S.
    Masquelier, C.
    [J]. ELECTROCHEMICAL AND SOLID STATE LETTERS, 2006, 9 (07) : A352 - A355
  • [4] Crystal chemistry of the olivine-type LixFePO4 system (0 ≤ x ≤ 1) between 25 and 370°C
    Delacourt, C
    Rodríguez-Carvajal, J
    Schmitt, B
    Tarascon, JM
    Masquelier, C
    [J]. SOLID STATE SCIENCES, 2005, 7 (12) : 1506 - 1516
  • [5] The existence of a temperature-driven solid solution in LixFePO4 for 0 ≤ x ≤ 1
    Delacourt, C
    Poizot, P
    Tarascon, JM
    Masquelier, C
    [J]. NATURE MATERIALS, 2005, 4 (03) : 254 - 260
  • [6] DELACOURT C, 2007, Patent No. 20070051
  • [7] Surface structures and crystal morphologies of LiFePO4:: relevance to electrochemical behaviour
    Fisher, Craig A. J.
    Islam, M. Saiful
    [J]. JOURNAL OF MATERIALS CHEMISTRY, 2008, 18 (11) : 1209 - 1215
  • [8] Is small particle size more important than carbon coating?: An example study on LiFePO4 cathodes
    Gaberscek, Miran
    Dominko, Robert
    Jamnik, Janez
    [J]. ELECTROCHEMISTRY COMMUNICATIONS, 2007, 9 (12) : 2778 - 2783
  • [9] GONZALEZPLATAS J, 2002, J GRAPHIC FOURIER PR
  • [10] Atomic-scale investigation of defects, dopants, and lithium transport in the LiFePO4 olivine-type battery material
    Islam, MS
    Driscoll, DJ
    Fisher, CAJ
    Slater, PR
    [J]. CHEMISTRY OF MATERIALS, 2005, 17 (20) : 5085 - 5092