Synthesis of Li-excess layered cathode material with enhanced reversible capacity for Lithium ion batteries through the optimization of precursor synthesis method

被引:7
|
作者
Zhao, Wenwen [1 ]
Yamamoto, Shinji [2 ]
Tanaka, Akinobu [1 ]
Noguchi, Hideyuki [1 ]
机构
[1] Saga Univ, Grad Sch Sci & Engn, Dept Adv Technol Fus, Saga 8408520, Japan
[2] Nissan Motor Co Ltd, Nissan Res Ctr, Yokosuka, Kanagawa 2378523, Japan
关键词
Lithium ion battery; Li excess cathode; Synthesis method; Improved cycleability; Rate performance; POSITIVE-ELECTRODE; CO ELECTRODES; INTERCALATION; MN; FE; NI;
D O I
10.1016/j.electacta.2014.08.006
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
LixNi1/3Mn2/3O2 cathode materials have been synthesized through a facile reduction-ion exchange of P3-Na2/3Ni1/3Mn2/3O2 precursors prepared by solid state (SS), spray dry (SD) and co-precipitation (CP) methods. The influence of precursor synthesis method on the structure, morphology and electrochemical performances of LixNi1/3Mn2/3O2 has been investigated. X-ray diffraction (XRD) results of LixNi1/3Mn2/3O2 demonstrate that all the samples exhibit similar XRD patterns as those of Lithium-excess layered cathode materials. Scanning Electron Microscope (SEM) images and Brunauer-Emment-Teller (BET) results present that the particle size, particle aggregation and surface area changed greatly with the precursor synthesis method. Galvanostatic charge-discharge results show that Li1.41Ni0.32Mn0.66O2+delta, cathode prepared from co-precipitation precursor exhibited high first discharge capacity of ca. 270 mAhg(-1) with an initial cycle efficiency as high as 98%. The discharge capacity of Li1.41Ni0.32Mn0.66O2+delta cathode after 30 cycles is over 250 mAhg(-1) and it can deliver a discharge capacity roughly 210 mAhg(-1) at a current density of 500 mAg(-1) (2C rate). Also, it was found that Li1.41Ni0.32,Mn0.66O2+delta cathode shows enhanced electrochemical performance over the Li2/3Ni1/3Mn2/3O2 cathode with respect to reversible capacity and rate capability. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:347 / 356
页数:10
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