Preparation of LiFePO4/Carbon/PANI-CSA Composite and Its Properties as High-Capacity Cathodes for Lithium Ion Batteries

被引:17
|
作者
Su, Chang [1 ]
Lu, Guoqiang [1 ]
Xu, Lihuang [1 ]
Zhang, Cheng [1 ]
机构
[1] Zhejiang Univ Technol, Coll Chem Engn & Mat Sci, State Key Lab Breeding Base Green Chem Synth Tech, Hangzhou 310014, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
IONOTHERMAL SYNTHESIS; ELECTROCHEMICAL REACTIVITY; SOLVOTHERMAL SYNTHESIS; ELECTRODE MATERIALS; HYDROTHERMAL METHOD; PHOSPHO-OLIVINES; LIFEPO4; POLYANILINE; POLYMERS; PERFORMANCE;
D O I
10.1149/2.082203jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In this work, the spindle-shaped LiFePO4 coating with carbon layer (C-LFP) was successfully synthesized in glycerol solvent assisted by a mild heat-treatment at 600 degrees C for 2 h. Then camphorsulfonic acid doped polyaniline (PANI-CSA) as the conductive polymer was compound with C-LFP to prepare C-LFP/PANI-CSA composite. The morphology, crystal structure and charge-discharge performance of the prepared samples were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and galvanostatic charge-discharge testing. The results showed that the reactant concentration seriously affected the microstructure and electrochemical properties of the resulting LiFePO4 cathodes in lithium ion batteries. And a spindle-shaped LiFePO4 with suitable size has been successfully synthesized at the moderate reactant concentration of 0.5 M. After modified with PANI-CSA, the resulted C-LFP2/PANI-CSA composite cathodes displayed a significantly improved specific capacity and rate capability. And specially, that the C-LFP/10% PANI-CSA composite exhibited the best performance with an initial discharge capacity of 165.3 mAh . g(-1) at a constant current of 0.1 C. Electrochemical impedance measurements also demonstrated that the coating of polyaniline significantly decreased the charge-transfer resistance of C-LiFePO4 electrodes. (C) 2012 The Electrochemical Society. [DOI: 10.1149/2.082203jes] All rights reserved.
引用
收藏
页码:A305 / A309
页数:5
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