Published November 20, 2014 | Version v1
Journal article

Synthesis of LiNi0.5Mn1.5O4 cathode with excellent fast charge-discharge performance for lithium-ion battery

  • 1. Key Laboratory of Functional Inorganic Material Chemistry, Ministry of Education, School of Chemistry and Materials Science, Heilongjiang University, Harbin 150080 (China)
  • 2. School of Chemistry and Chemical Engineering, Anhui University of Technology, Maanshan, Anhui 243002 (China)

Description

Well-defined LiNi0.5Mn1.5O4 powder has been synthesized by ethylene glycol (EG)-assisted oxalic acid co-precipitation method. The structure and physicochemical properties of this as-prepared powder were investigated by powder X-ray diffraction (XRD), Raman spectra (RS), scanning electron microscopy (SEM), cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and galvanostatic charge–discharge test in detail. XRD shows impurity phase of LiyNi1-yO due to the oxygen loss reaction at high temperatures. SEM indicates that LiNi0.5Mn1.5O4 synthesized by EG-assisted method has a uniform and narrow size distribution under 1 μm. RS confirms that both samples have Fd-3 m space group. EIS and CV test exhibit that LiNi0.5Mn1.5O4 electrode synthesized by EG-assisted method has lower potential polarization, smaller charge transfer resistance, higher reversibility and larger lithium ion diffusion coefficient than the one obtained by ammonium hydroxide co-precipitation method. Galvanostatic charge–discharge test reveals that LiNi0.5Mn1.5O4 synthesized by EG-assisted method shows higher discharge capacity than that the one synthesized by ammonium hydroxide co-precipitation method at each rate

Availability note (English)

Available from http://dx.doi.org/10.1016/j.electacta.2014.09.119

Additional details

Identifiers

DOI
10.1016/j.electacta.2014.09.119;
PII
S0013-4686(14)01963-X;

Publishing Information

Journal Title
Electrochimica Acta
Journal Volume
147
Journal Page Range
p. 250-256
ISSN
0013-4686
CODEN
ELCAAV

Optional Information

Copyright
Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.