Morphological solution for enhancement of electrochemical kinetic performance of LiFePO4

被引:62
|
作者
Li, Lianxing [1 ]
Tang, Xincun [1 ,2 ]
Liu, Hongtao [1 ]
Qu, Yi [1 ]
Lu, Zhouguang [1 ]
机构
[1] Cent S Univ, Coll Chem & Chem Engn, Changsha 410083, Peoples R China
[2] Cent S Univ, State Key Lab Powder Met, Changsha 410083, Peoples R China
基金
中国国家自然科学基金;
关键词
Cathode material; Lithium-ion cell; Solvothermal; Nanosheet; Electrochemical kinetics; ELECTRODE PERFORMANCE; PHOSPHO-OLIVINES; LITHIUM; NANOPARTICLES; DIFFUSION; LIXFEPO4;
D O I
10.1016/j.electacta.2010.09.048
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
LiFePO4/Cnanosheet composite has been prepared via a low-temperature solvothermal reaction followed by high-temperature treatment. The as-prepared sample is characterized by XRD, FDR, Raman, SEM, and TEM. It is confirmed that the nanosheets are composed of ca. 50 nm thickness of crystalline LiFePO4-core coated with ca. 10 nm thickness of carbon-shell. The charge-discharge tests show that the as-fabricated LiFePO4/C nanosheet cathode in lithium-ion cell demonstrates high reversible capacity (164 mAh g(-1) at 0.1 C) and good cycle stability (columbic efficiency 100% during 100 cycles). The cyclic voltammetric analysis indicates Li+ diffusion determines the whole electrode reaction kinetics, and the diffusion coefficient estimated by EIS is comparable to the reported data. The enhanced kinetic behavior of the as-fabricated cathode is actually originated from the nano-dimensional sheet-like morphology, which facilitates Li+ migration due to the shortened diffusion distance, and simultaneously increased exchangeable Li+ amount considering more accessible active surface. In addition, the uniformly coated thin conductive carbons contribute a lot for this enhancement because of considerably improved electronic conductivity. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:995 / 999
页数:5
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