A new approach to improve the electrochemical performance of Li-rich cathode material by precursor pretreatment

被引:30
作者
Wang, Meng [1 ]
Luo, Min [1 ,4 ]
Chen, Yunbo [1 ]
Chen, Lin [1 ]
Yan, Shuo [2 ]
Ren, Yongzhi [3 ]
Chu, Mo [4 ]
机构
[1] China Acad Machinery Sci & Technol, Adv Manufacture Technol Ctr, Beijing 100083, Peoples R China
[2] Guizhou Zoomwe Zhengyuan Adv Mat Co Ltd, Guiyang 554300, Guizhou, Peoples R China
[3] Guizhou Fuyuan Adv Mat Co Ltd, Guiyang 554300, Guizhou, Peoples R China
[4] China Univ Min & Technol, Beijing 100083, Peoples R China
基金
中国国家自然科学基金;
关键词
Lithium-ion battery; Li-rich material; Carbonate precursor; Pretreatment time; LITHIUM BATTERIES M; HIGH-CAPACITY; OXYGEN LOSS; HIGH-POWER; X-RAY; ION; ELECTRODES; MN; STABILITY; NI;
D O I
10.1016/j.jallcom.2016.12.054
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The layered Li-rich 0.5Li(2)MnO(3)center dot 0.5LiNi(1/3)Mn(1/3)Co(1/3)O(2) cathode material was synthesized via a coprecipitation method. The carbonate precursor was pretreated in the mother liquor for various time and the effects on the electrochemical performance were studied. Field emission scanning electron microscope (FESEM) and X-ray diffraction (XRD) were used to characterize the micromorphology and structure of the material. Meanwhile, charge-discharge test and electrochemical impedance spectroscopy (EIS) were employed to study its electrochemical performance. It was found that an extended precursor pretreatment time can result in relatively excellent hexagonal ordering structure and low degree of cation mixing. The material synthesized by the precursor aged in mother liquid for 12 h possessed excellent electrochemical performance. The initial discharge capacity was 262.7 mAh g(-1) with the coulombic efficiency of 82.1% at 0.1 C. And the capacity retention after 50 cycles at 1.0 C was 76.9%. EIS test showed that the material had the lowest charge transfer resistance (32.02 Omega) and highest diffusion coefficientsD(Li+)(3.45 x 10(-14) cm(2) s(-1)). (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:891 / 899
页数:9
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