Performance improvement on LiFePO4/C composite cathode for lithium-ion batteries

被引:14
作者
Cech, Ondrej [1 ]
Thomas, Jorge E. [2 ]
Sedlarikova, Marie [1 ]
Fedorkova, Andrea [1 ,3 ]
Vondrak, Jiri [1 ]
Sergio Moreno, Mario [4 ]
Visintin, Arnaldo [2 ]
机构
[1] Brno Univ Technol, Fac Elect Engn & Commun, Dept Elect & Elect Technol, Brno 61600, Czech Republic
[2] UNLP, Inst Invest Fisicoquim Teor & Aplicadas INIFTA, Fac Ciencias Exactas, CCT La Plata CONICET, RA-1900 La Plata, Argentina
[3] Safarik Univ, Fac Sci, Inst Chem, SK-04154 Kosice, Slovakia
[4] Comis Nacl Energia Atom, Ctr Atom Bariloche, RA-8400 San Carlos De Bariloche, Argentina
关键词
Lithium-ion battery; Phosphate; Cathode; LiFePO4; Cobalt;
D O I
10.1016/j.solidstatesciences.2013.03.017
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Temperature glycine assisted solid-state synthesis was used to prepare LiFePO4/C composite samples with two types of material improvements. It will be shown how can addition of a high conductive support as well as doping with supervalent metal ions improve the electrochemical performance of Li-ion cathode. Three samples with different properties were prepared and investigated - pure LiFePO4/C with no material improvements, LiFePO4/C prepared with multi walled carbon nanotubes (MWCNT) conductive support and LiFePO4/C doped by 1% of cobalt. Glycine was used as inorganic carbon coating precursor during the synthesis of all samples. XRD measurements confirmed production of highly crystalline LiFePO4 cathode material with diameter varying between 40 nm and 200 nm. Electrochemical measurements confirmed increasing the intra-particle conductivity by MWCNT or Co doping. Galvanostatic battery testing shows that LiFePO4/MWCNT/C composite delivers highest capacity 130 mA h g(-1) at C/5. LiFePO4/MWCNT/C cathode material prepared by solid state synthesis exhibit excellent electrochemical performances, improved conductivity, and good rate capability compared to the LiFePO4/C composite material. (C) 2013 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:110 / 114
页数:5
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