Preparation of a carbon nanofiber/natural graphite composite and an evaluation of its electrochemical properties as an anode material for a Li-ion battery

被引:19
作者
Jang, Sang-Min [2 ]
Miyawaki, Jin [1 ]
Tsuji, Masaharu [1 ]
Mochida, Isao [1 ]
Yoon, Seong-Ho [1 ]
Kang, Fei-yu [3 ]
机构
[1] Kyushu Univ, IMCE, Fukuoka 8168580, Japan
[2] Kyushu Univ, Interdisciplinary Grad Sch Engn Sci, Fukuoka 8168580, Japan
[3] Tsinghua Univ, Dept Mat Sci & Engn, Beijing 100084, Peoples R China
关键词
Natural graphite; Li-ion battery; Carbon nanofiber; Rate capability; Volumetric stability; ATMOSPHERE ELECTRON-MICROSCOPY; NATURAL GRAPHITE; CATALYTIC INFLUENCE; LITHIUM; PERFORMANCE; GASIFICATION;
D O I
10.1016/S1872-5805(09)60018-4
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A carbon nanofiber (CNF)/natural graphite (NG) composite was prepared to improve the rate capability of as-received NG to be used as the anode material in a Li-ion battery. Optimum control over both the amount and shape of the CNFs to enable their growth on NG remarkably improved the cycle performance and rate capability of the as-received NG. The first-cycle discharge capacity of the CNF/NG composite was 95% of that of the as-received NG. The amount of crown CNFs was controlled to be less than 15% of the as-received NG. CNF growth on the surface edges of NG in an ivy leaf shape proved to be most effective in improving the rate capability by controlling the extent of volumetric expansion and shrinkage occurring in the charge and discharge processes. Schematic structural models of the as-received NG and CNF/NG composite were proposed to account for the volumetric stability of the electrode in repeated charge-discharge processes. The improved rate capability is ascribed to the thin solid electrolyte interphase and reduced volumetric chance of the anode in the charge/discharge processes, both of which are achieved by growing ivy-like CNFs over the graphite surface.
引用
收藏
页码:89 / 96
页数:8
相关论文
共 14 条
[1]   CONTROLLED ATMOSPHERE ELECTRON-MICROSCOPY STUDIES OF GRAPHITE GASIFICATION .3. CATALYTIC INFLUENCE OF MOLYBDENUM AND MOLYBDENUM TRIOXIDE [J].
BAKER, RTK ;
HARRIS, PS ;
KEMPER, DJ ;
WAITE, RJ .
CARBON, 1974, 12 (02) :179-187
[2]   CONTROLLED ATMOSPHERE ELECTRON-MICROSCOPY STUDIES OF GRAPHITE GASIFICATION .1. CATALYTIC INFLUENCE OF ZINC [J].
BAKER, RTK ;
HARRIS, PS .
CARBON, 1973, 11 (01) :25-&
[3]   Effect of graphite crystal structure on lithium electrochemical intercalation [J].
Guerin, K ;
Fevrier-Bouvier, A ;
Flandrois, S ;
Couzi, M ;
Simon, B ;
Biensan, P .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1999, 146 (10) :3660-3665
[4]   Poly (acrylonitrile) encapsulated graphite as anode materials for lithium ion batteries [J].
Guo, KK ;
Pan, QM ;
Fang, SB .
JOURNAL OF POWER SOURCES, 2002, 111 (02) :350-356
[5]   Modeling and simulation of the dynamic behavior of a polymer electrolyte membrane fuel cell [J].
Yerramalla, S ;
Davari, A ;
Feliachi, A ;
Biswas, T .
JOURNAL OF POWER SOURCES, 2003, 124 (01) :104-113
[6]  
JANG SM, 2006, INT C CARB JUL 16 21, P120
[7]   High-rate-capable lithium-ion battery based on surface-modified natural graphite anode and substituted spinel cathode for hybrid electric vehicles [J].
Kottegoda, IRM ;
Kadoma, Y ;
Ikuta, H ;
Uchimoto, Y ;
Wakihara, M .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2005, 152 (08) :A1595-A1599
[8]   Determination of the absolute and relative extents of basal plane surface area and "non-basal plane surface" area of graphites and their impact on anode performance in lithium ion batteries [J].
Olivier, JP ;
Winter, M .
JOURNAL OF POWER SOURCES, 2001, 97-8 :151-155
[9]   Cycling performance of low-cost lithium ion batteries with natural graphite and LiFePO4 [J].
Shim, J ;
Striebel, KA .
JOURNAL OF POWER SOURCES, 2003, 119 :955-958
[10]   Performance of large-scale secondary lithium batteries for electric vehicles and home-use load-leveling systems [J].
Takei, K ;
Ishihara, K ;
Kumai, K ;
Iwahori, T ;
Miyake, K ;
Nakatsu, T ;
Terada, N ;
Arai, N .
JOURNAL OF POWER SOURCES, 2003, 119 :887-892