Issue 27, 2012

Facile synthesis of MWCNT–ZnFe2O4 nanocomposites as anode materials for lithium ion batteries

Abstract

Monodisperse ZnFe2O4 nanoparticles with sizes less than 10 nm have been successfully assembled on multi-walled carbon nanotubes (MWCNTs) by in situ high-temperature decomposition of the precursor iron(III) acetylacetonate, zinc acetate and MWCNTs in polyol solution. A possible formation mechanism was proposed, which suggests that the ZnFe2O4 nanoparticles are formed on the surface of MWCNTs through an aggregation thermochemical reaction process between ZnO and γ-Fe2O3 subparticles. It was found that the coverage density on the MWCNTs could be easily controlled by changing the concentration of the precursor. As anode materials for Li-ion batteries, the MWCNT–ZnFe2O4 nanocomposites showed high rate capability and superior cycling stability with a specific capacity of 1152 mA h g−1, which was much higher than that of ZnFe2O4 nanoparticles. The MWCNTs served as good electron conductors and volume buffers in improving the lithium performance of MWCNT–ZnFe2O4 nanocomposites during the discharge–charge process. Magnetic measurements showed that the MWCNT–ZnFe2O4 nanocomposites are superparamagnetic at room temperature and the magnetization of the samples can be controlled by the reaction conditions. The as-synthesized MWCNT–ZnFe2O4 nanocomposites are water dispersible and can be manipulated by an external magnetic field. Therefore, the nanocomposites have significant potential for application in the fields of energy storage, composites, wastewater treatment and biomaterials.

Graphical abstract: Facile synthesis of MWCNT–ZnFe2O4 nanocomposites as anode materials for lithium ion batteries

Supplementary files

Article information

Article type
Paper
Submitted
27 Mar 2012
Accepted
16 May 2012
First published
18 May 2012

J. Mater. Chem., 2012,22, 13674-13681

Facile synthesis of MWCNT–ZnFe2O4 nanocomposites as anode materials for lithium ion batteries

J. Sui, C. Zhang, D. Hong, J. Li, Q. Cheng, Z. Li and W. Cai, J. Mater. Chem., 2012, 22, 13674 DOI: 10.1039/C2JM31905E

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