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|Title:||Ultrathin polyimide coating for a spinel LiNi0.5Mn1.5O4 cathode and its superior lithium storage properties under elevated temperature conditions||Authors:||Kim, M. C.
Kim, S. H.
Kim, W. S.
Lee, Y. S.
|Issue Date:||2013||Source:||Kim, M. C., Kim, S. H., Aravindan, V., Kim, W. S., Lee, S. Y., & Lee, Y. S. (2013). Ultrathin Polyimide Coating for a Spinel LiNi0.5Mn1.5O4 Cathode and Its Superior Lithium Storage Properties under Elevated Temperature Conditions. Journal of the Electrochemical Society, 160(8), A1003-A1008.||Series/Report no.:||Journal of the electrochemical society||Abstract:||In this study, we present the influence of polyimide (PI) coating concentration on the electrochemical properties of high voltage, spinel phase LiNi0.5Mn1.5O4 cathodes, particularly under elevated temperature conditions. First, the adipic acid-mediated sol-gel technique was employed to synthesize sub-micron sized LiNi0.5Mn1.5O4 particles, where Mn was in the 4+ state. Thermal polymerization was used to produce the PI coating from polyamic acid. The presence of the PI layer was confirmed by transmission electron microscopy and Fourier-transform infrared analyzes. All test cells delivered good cycleability under ambient temperature conditions, irrespective of the PI coating concentration, with a prominent plateau at 4.7 V vs. Li, whereas all test cells experienced the poorest electrochemical behavior under elevated temperature conditions except 0.3 wt.% PI. The 0.3 wt.% PI coated LiNi0.5Mn1.5O4 phase delivered excellent cycleability with capacity retention of > 90% at 55°C. Poor compatibility and severe reactivity toward the electrolyte solution resulted in the poorest performance which was clearly evidenced by the scanning electron microscopy analysis and supported well by impedance studies after galvanostatic cycling.||URI:||https://hdl.handle.net/10356/96345
|ISSN:||0013-4651||DOI:||http://dx.doi.org/10.1149/2.013308jes||Rights:||© 2013 The Electrochemical Society. This paper was published in Journal of The Electrochemical Society and is made available as an electronic reprint (preprint) with permission of The Electrochemical Society. The paper can be found at the following official DOI: [http://dx.doi.org/10.1149/2.013308jes]. One print or electronic copy may be made for personal use only. Systematic or multiple reproduction, distribution to multiple locations via electronic or other means, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper is prohibited and is subject to penalties under law.||Fulltext Permission:||open||Fulltext Availability:||With Fulltext|
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