Synthesis and Electrochemical Properties of Li[Ni1/3Co1/3Mn1/3]O2 for Lithium Ion Batteries

被引:1
|
作者
Li, Lin [1 ,2 ,3 ]
Feng, Chuanqi [1 ,2 ]
Zheng, Hao [1 ,2 ]
Wang, Jun [4 ]
Wang, Jiazhao [4 ]
He, Peixin [1 ,3 ]
机构
[1] Hubei Univ, Hubei Collaborat Innovat Ctr Adv Organ Chem Mat, Wuhan 430062, Peoples R China
[2] Anshun Univ, Coll Chem & Chem Engn, Anshun 561000, Peoples R China
[3] Hubei Univ, Fac Mat Sci & Engn, Wuhan 430062, Peoples R China
[4] Univ Wollongong, Inst Superconducting & Elect Mat, Wollongong, NSW 2522, Australia
关键词
Co-Precipitation Reaction; Lithium-Ion Batteries; Cathode Materials; Electrochemical Properties; CATHODE MATERIAL; HIGH-POWER; PERFORMANCE; LI(NI1/3CO1/3MN1/3)O-2; LINI1/3CO1/3MN1/3O2; ELECTROLYTE; BEHAVIOR; LIMN2O4;
D O I
10.1166/sam.2017.2298
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The layered compound Li[Ni1/3Co1/3Mn1/3]O-2 was synthesized using a combination of the co-precipitation and the solid phase reaction method. The samples were characterized by X-ray diffraction, scanning electron microscopy, cyclic voltammetry and galvanostatic charge/discharge profile measurements. The results showed that the layer-structured compound Li[Ni1/3Co1/3Mn1/3]O-2 was successfully formed. The morphology of the powder featured a hierarchical micron-scale spherical shape which was composed of agglomerated nanoparticles. The temperature of the synthesis affected the electrochemical properties of the resulting compound. The samples synthesized at 850 degrees C showed a higher initial specific capacity (176 mAh/g), and a higher reversible discharge capacity (157 mAh/g), as well as better cycling stability at the current density of 20 mA/g, compared to the samples synthesized at other temperatures. When the current densities for charge/discharge were increased, the sample synthesized at 850 degrees C still showed the best electrochemical performance among all the samples. The Li[Ni1/3Co1/3Mn1/3]O-2 synthesized at 850 degrees C is a promising cathode material for lithium ion battery application.
引用
收藏
页码:331 / 335
页数:5
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