Carboxylic acid-assisted solid-state synthesis of LiFePO4/C composites and their electrochemical properties as cathode materials for lithium-ion batteries

被引:36
作者
Fey, George Ting-Kuo [1 ]
Lu, Tung-Lin [1 ]
Wu, Feng-Yu [2 ]
Li, Wen-Hsien [2 ]
机构
[1] Natl Cent Univ, Dept Chem & Mat Engn, Chungli 32054, Taiwan
[2] Natl Cent Univ, Dept Phys, Chungli 32054, Taiwan
关键词
LiFePO4; carbon; cathode; composite; carboxylic acid;
D O I
10.1007/s10008-008-0516-4
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
To enhance the capability of LiFePO4 materials, we attempted to coat carbon by incorporating various organic carboxylic acids as carbon sources. The purity of LiFePO4 was confirmed by XRD analysis. Galvanostatic cycling, cyclic voltammetry, electric impedance spectroscopy, and conductivity measurements were used to evaluate the material's electrochemical performance. The best cell performance was delivered by the sample coated with 60 wt.% malonic acid. Its first-cycle discharge capacity was 149 mA h g(-1) stop at a 0.2 C rate or 155 mA h g(-1) stop at a 0.1 C rate. The presence of carbon in the composite was verified by total organic carbon and Raman spectral analysis. The actual carbon content of LiFePO4 was 1.90 wt.% with the addition of 60 wt.% malonic acid. The LiFePO4/C samples sintered with 60 wt.% various carboxylic acids were measured by Raman spectral analysis. The intense broad bands at 1,350 and 1,580 cm(-1) stop are assigned to the D and G bands of residual carbon in LiFePO4/C composites, respectively. The peak intensity (I-D/I-G) ratio of the synthesized powders is from 0.907 to 0.935. Carbon coatings of LiFePO4 with low I-D/I-G ratios can be produced by incorporating carboxylic acid additives before the final calcining process. The use of carboxylic acid as a carbon source increases the overall conductivity (similar to 10(-4) stop S cm(-1) stop) of the material.
引用
收藏
页码:825 / 833
页数:9
相关论文
共 33 条
[1]   Thermal stability of LiFePO4-based cathodes [J].
Andersson, AS ;
Thomas, JO ;
Kalska, B ;
Häggström, L .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2000, 3 (02) :66-68
[2]   The source of first-cycle capacity loss in LiFePO4 [J].
Andersson, AS ;
Thomas, JO .
JOURNAL OF POWER SOURCES, 2001, 97-8 :498-502
[3]   Lithium extraction/insertion in LiFePO4:: an X-ray diffraction and Mossbauer spectroscopy study [J].
Andersson, AS ;
Kalska, B ;
Häggström, L ;
Thomas, JO .
SOLID STATE IONICS, 2000, 130 (1-2) :41-52
[4]   Reducing carbon in LiFePO4/C composite electrodes to maximize specific energy, volumetric energy, and tap density [J].
Chen, ZH ;
Dahn, JR .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2002, 149 (09) :A1184-A1189
[5]  
CHUNG SY, 2002, NATURE, V732, P22
[6]   An electrochemical impedance spectroscopic study of the transport properties of LiNi0.75Co0.25O2 [J].
Croce, F ;
Nobili, F ;
Deptula, A ;
Lada, W ;
Tossici, R ;
D'Epifanio, A ;
Scrosati, B ;
Marassi, R .
ELECTROCHEMISTRY COMMUNICATIONS, 1999, 1 (12) :605-608
[7]   A novel concept for the synthesis of an improved LiFePO4 lithium battery cathode [J].
Croce, F ;
D'Epifanio, A ;
Hassoun, J ;
Deptula, A ;
Olczac, T ;
Scrosati, B .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2002, 5 (03) :A47-A50
[8]   Optimization of carbon coatings on LiFePO4 [J].
Doeff, Marca M. ;
Wilcox, James D. ;
Kostecki, Robert ;
Lau, Grace .
JOURNAL OF POWER SOURCES, 2006, 163 (01) :180-184
[9]   Effect of surface carbon structure on the electrochemical performance of LiFePO4 [J].
Doeff, MM ;
Hu, YQ ;
McLarnon, F ;
Kostecki, R .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2003, 6 (10) :A207-A209
[10]   Electrochemical deposition and modification of LiFePO4 for the preparation of cathode with enhanced battery performance [J].
Eftekhari, A .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2004, 151 (11) :A1816-A1819