Ultrathin Polyimide Coating for a Spinel LiNi0.5Mn1.5O4 Cathode and Its Superior Lithium Storage Properties under Elevated Temperature Conditions

被引:41
作者
Kim, M. C. [1 ]
Kim, S. H. [1 ]
Aravindan, V. [2 ]
Kim, W. S. [3 ]
Lee, S. Y. [4 ]
Lee, Y. S. [1 ]
机构
[1] Chonnam Natl Univ, Fac Appl Chem Engn, Kwangju 500757, South Korea
[2] Nanyang Technol Univ, Energy Res Inst NTU ERI N, Singapore 637553, Singapore
[3] Daejung EM Co Ltd, Inchon 405820, South Korea
[4] Ulsan Natl Inst Sci & Technol, Interdisciplinary Sch Green Energy, Ulsan 689798, South Korea
关键词
NANOSTRUCTURED ELECTRODE MATERIALS; ELECTROCHEMICAL ENERGY-STORAGE; LICOPO4; CATHODES; ION; PERFORMANCE; LI2COPO4F; BATTERIES; LIPF6;
D O I
10.1149/2.013308jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
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 degrees 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. (C) 2013 The Electrochemical Society. All rights reserved.
引用
收藏
页码:A1003 / A1008
页数:6
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