Effect of metal ion concentration in precursor solution on structure and electrochemical performance of LiNi0.6Co0.2Mn0.2O2

被引:24
|
作者
Ma, Yitian [1 ]
Li, Li [1 ,2 ]
Wang, Lecai [1 ]
Luo, Rui [1 ]
Xu, Siwenyu [1 ]
Wu, Feng [1 ,2 ]
Chen, Renjie [1 ,2 ]
机构
[1] Beijing Inst Technol, Sch Mat Sci & Engn, Beijing Key Lab Environm Sci & Engn, Beijing 100081, Peoples R China
[2] Collaborat Innovat Ctr Elect Vehicles Beijing, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
LiNi0.6Mn0.2Co0.2O2; Carbonate co-precipitation; Metal ion concentration; Lithium-ion battery; LINI1/3CO1/3MN1/3O2 CATHODE MATERIAL; HIERARCHICAL LINI1/3CO1/3MN1/3O2; DESIGNED SYNTHESIS; LITHIUM; COPRECIPITATION; ENERGY; NANOSCALE; BATTERIES; DIFFUSION; DENSITY;
D O I
10.1016/j.jallcom.2018.11.189
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
LiNi0.6Mn0.2Co0.2O2 (622NCM) cathode materials are synthesized by a carbonate co-precipitation process. We decomposed Co and Mn carbonates to form porous CoMnO3 precursors, which were impregnated with Ni and Li salts to form final materials. To provide better hosts for the Ni and Li salts, we design the co-precipitation solutions with different total metal ion concentrations to achieve precursors with stable structures and appropriate porosity. We obtained 622NCM with hierarchical and porous properties, which shortened the lithium ion transmission distance and improved the electrolyte infiltration rate and rate capability. Furthermore, our 622NCM cathode materials showed no loss of thermodynamic or electrochemical stability during cycling. The most suitable concentration was determined to be 0.03 mol L-1 and the as-prepared 622NCM (0.03-622NCM) cathode material exhibited good cycle reversibility, a high capacity, and good rate capability, delivering a discharge capacity of 152 mA h g(-1) at 0.2 C. A capacity of more than 100 mA h g(-1) was achieved at a high rate of 5 C. This study provides guidance for preparing nickel-rich ternary cathode materials for high-performance lithium-ion batteries. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:643 / 651
页数:9
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