Enhancement of electrochemical behavior of nanostructured LiFePO4/Carbon cathode material with excess Li

被引:51
|
作者
Bazzi, K. [1 ]
Nazri, M. [1 ]
Naik, V. M. [2 ]
Garg, V. K. [3 ]
Oliveira, A. C. [3 ]
Vaishnava, P. P. [4 ]
Nazri, G. A. [1 ]
Naik, R. [1 ]
机构
[1] Wayne State Univ, Dept Phys & Astron, Detroit, MI 48201 USA
[2] Univ Michigan, Dept Nat Sci, Dearborn, MI 48128 USA
[3] Univ Brasilia, Inst Fis, BR-70919970 Brasilia, DF, Brazil
[4] Kettering Univ, Dept Phys, Flint, MI 48504 USA
关键词
Lithium battery; Lithium iron phosphate; Nanomaterial; LITHIUM-ION; HYDROTHERMAL SYNTHESIS; CARBON; PERFORMANCE; CONDUCTIVITY; FE; COMPOSITE; MOSSBAUER; NANOWIRE; DEFECTS;
D O I
10.1016/j.jpowsour.2015.11.086
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
We have synthesized carbon coated LiFePO4 (C-LiFePO4) and C-Li1.05FePO4 with 5 mol% excess Li via sol-gel method using oleic acid as a source of carbon for enhancing electronic conductivity and reducing the average particle size. Although the phase purity of the crystalline samples was confirmed by x-ray diffraction (XRD), the Fe-57 Mossbauer spectroscopy analyses show the presence of ferric impurity phases in both stoichiometric and non-stoichiometric C-LiFePO4 samples. Transmission electron microscopy measurements show nanosized C-LiFePO4 particles uniformly covered with carbon, with average particle size reduced from similar to 100 nm to similar to 50 nm when excess lithium is used. Electrochemical measurements indicate a lower charge transfer resistance and better electrochemical performance for C-Li1.05FePO4 compared to that of C-LiFePO4. The aim of this work is to systematically analyze the nature of impurities formed during synthesis of LiFePO4 cathode material, and their impact on electrochemical performance. The correlation between the morphology, charge transfer resistance, diffusion coefficient and electrochemical performance of C-LiFePO4 and C-Li1.05FePO4 cathode materials are discussed. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:17 / 23
页数:7
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