AlF3-coated Li(Li0.17Ni0.25Mn0.58)O2 as cathode material for Li-ion batteries

被引:186
|
作者
Li, G. R. [1 ]
Feng, X. [1 ]
Ding, Y. [1 ]
Ye, S. H. [1 ]
Gao, X. P. [1 ]
机构
[1] Nankai Univ, Inst New Energy Mat Chem, Tianjin Key Lab Met & Mol Based Mat Chem, Tianjin 300071, Peoples R China
关键词
Lithium-ion batteries; Cathode; Li-rich layered oxide; Surface coating; High-rate capability; SOLID-SOLUTION CATHODES; ELECTROCHEMICAL PERFORMANCE; SIGNIFICANT IMPROVEMENT; SURFACE MODIFICATION; LITHIUM; OXIDE; NANOCRYSTALLINE; DIFFRACTION; ELECTRODES; CELLS;
D O I
10.1016/j.electacta.2012.05.142
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Li-rich layered oxide is prepared and coated with an AlF3 layer by a chemical deposition method. The as-prepared and AlF3 -coated Li-rich materials are characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The as-prepared Li-rich oxide has a typical layered structure with the chemical formula of Li(Li0.17Ni0.Mn-25(0.58))O-2, and the AlF3 layer with a thickness of about 5-7 nm is coated on the surface of the Li(Li0.17Ni0.25Mn0.58)O-2 grains. Galvanostatic charge-discharge tests at various rates show that the AlF3-coated Li(Li0.17Ni0.25Mn0.58)O-2 has an obviously enhanced electrochemical performance compared with the as-prepared sample. At 0.2 C rate, the AlF3-coated sample provides a large capacity of more than 250 mAh g(-1). The coulombic efficiency in the initial cycle is improved to 89.5% from 76.4%. At 5 C rate, the reversible capacity of the AlF3-coated sample is stable at above 104 mAh g(-1) after 200 cycles, much higher than that of the as-prepared sample. According to the analysis from electrochemical impedance spectra (EIS), the improvements of the electrochemical performance are mainly attributed to the pre-activation of the Li-rich layered oxide induced by the AlF3 coating and the maintenance of more active sites for the lithium ion intercalation/extraction in the AlF3-coated sample. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:308 / 315
页数:8
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