Issue 30, 2014

Sputtering graphite coating to improve the elevated-temperature cycling ability of the LiMn2O4 electrode

Abstract

To improve the cycle performance of LiMn2O4 at elevated temperature, a graphite layer is introduced to directly cover the surface of a commercial LiMn2O4-based electrode via room-temperature DC magnetron sputtering. The as-modified cathodes display improved capacity retention as compared to the bare LiMn2O4 cathode (BLMO) at 55 °C. When sputtering graphite for 30 min, the sample shows the best cycling performance at 55 °C, maintaining 96.2% capacity retention after 200 cycles. Reasons with respect to the graphite layer for improving the elevated-temperature performance of LiMn2O4 are systematically investigated via the methods of cyclic voltammetry, electrochemical impedance spectroscopy, X-ray photoelectron spectrometry, scanning and transmission electron microscopy, X-ray diffraction and inductively coupled plasma-atomic emission spectrometry. The results demonstrate that the graphite coated LiMn2O4 cathode has much less increased electrode polarization and electrochemical impedance than BLMO during the elevated-temperature cycling process. Furthermore, the graphite layer is able to alleviate the severe dissolution of manganese ions into the electrolyte and mitigate the morphological and structural degradation of LiMn2O4 during cycling. A model for the electrochemical kinetics process is also suggested for explaining the roles of the graphite layer in suppressing the Mn dissolution.

Graphical abstract: Sputtering graphite coating to improve the elevated-temperature cycling ability of the LiMn2O4 electrode

Supplementary files

Article information

Article type
Paper
Submitted
12 Mar 2014
Accepted
30 May 2014
First published
30 May 2014

Phys. Chem. Chem. Phys., 2014,16, 16021-16029

Author version available

Sputtering graphite coating to improve the elevated-temperature cycling ability of the LiMn2O4 electrode

J. Wang, Q. Zhang, X. Li, Z. Wang, H. Guo, D. Xu and K. Zhang, Phys. Chem. Chem. Phys., 2014, 16, 16021 DOI: 10.1039/C4CP01069H

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