PMMA-assisted synthesis of Li1-xNi0.5Mn1.5O4-δ for high-voltage lithium batteries with expanded rate capability at high cycling temperatures

被引:43
作者
Arrebola, J. C. [1 ]
Caballero, A. [1 ]
Hernan, L. [1 ]
Morales, J. [1 ]
机构
[1] Univ Cordoba, Dept Quim Inorgan & Ingn Quim, E-14071 Cordoba, Spain
关键词
PMMA; spinel; lithium batteries; high temperature;
D O I
10.1016/j.jpowsour.2008.02.076
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
In this work, poly(methyl methacrylate) (PMMA), a non-surfactant polymer was used to synthesize nonstoichiometric Li0.82Ni0.52Mn1.52O4-delta (0 <= delta <= 0.25) spinels. The presence of the polymer was found to be beneficial with a view to facilitating the use of the spinel in electrodes for lithium batteries. Thus, PMMA allowed spinel particles of a high crystallinity and uniform size and shape to be obtained, and particle size to be tailored by using an appropriate calcining temperature and time. By controlling these variables, spinels in nanometric, submicrometric and micrometric particle sizes were prepared and characterized by chemical analysis, X-ray diffraction, electron microscopy, thermogravimetry and nitrogen adsorptions measurements. The spinels were obtained as highly crystalline phases with lithium and oxygen deficiency and some cation disorder as revealed by chemical analysis, thermogravimetric and XRD data. Their electrochemical performance in two-electrode cells was tested at room temperature and 50 degrees C over a wide range of charge/discharge rates (from C/4 to 4C). Cell performance was found to depend on particle size rather than on structural properties. Thus, the spinel best performing at 50 degrees C was that consisting of submicrometric particles, which delivered a high capacity and exhibited the best capacity retention and rate capability. Particles of submicronic size share the advantages of nanometric particles (viz. the ability to withstand high charge/discharge rates) and micrometric particles (a high capacity and stability at low rates). (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:852 / 858
页数:7
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