Effects of inorganic salts on the morphological, structural, and electrochemical properties of prepared nickel-rich Li[Ni0.6Co0.2Mn0.2]O2

被引:75
作者
Kim, Ki Jae [1 ]
Jo, Yong Nam [1 ]
Lee, Won Jong [1 ]
Subburaj, T. [1 ]
Prasanna, K. [1 ]
Lee, Chang Woo [1 ]
机构
[1] Kyung Hee Univ, Coll Engn, Dept Chem Engn, Yongin 446701, Gyeonggi, South Korea
关键词
Lithium ion battery; Inorganic salts; Nickel-rich; Void channel; High power density; LITHIUM-ION BATTERIES; CORE-SHELL STRUCTURE; CATHODE MATERIAL; NANOPARTICLES; PERFORMANCE; LINI1/3CO1/3MN1/3O2; COPRECIPITATION; KINETICS; OXIDE;
D O I
10.1016/j.jpowsour.2014.06.057
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 cathode active materials Li[Ni0.6Co0.2Mn0.2]O-2 are synthesized using different inorganic salts, sulfate [NiSO4 center dot 6H(2)O, CoSO4 center dot 7H(2)O, MnSO4 center dot H2O], nitrate [M(NO3)(2)center dot 6H(2)O (M = Ni, Co, Mn)] and acetate [M(CH3COO)(2)center dot 4H(2)O (M = Ni, Co, Mn)]. The X-ray diffraction (XRD) patterns indicate that sulfate and nitrate starting materials formed a well-ordered hexagonal alpha-NaFeO2 layered structure (space group: 166, R (3) over barm). However, acetate starting material is led to a poorly layered structure compared to the other materials. Field emission scanning electron microscope (FE-SEM) images show that sulfate and acetate starting materials formed nano-sized primary particles with a size of about 200-500 nm and 300 nm, and void channels. However, the primary particles with a size of 300 nm from nitrate starting material agglomerate together to form micro-sized secondary particles. The initial discharge capacities of the sulfate, nitrate, and acetate starting materials are 138.3, 142.4, and 135.9 mAh g(-1) at 1 C-rate in the voltage range 3.0-4.3 V vs. Li/Li+, respectively. The discharge capacity retentions of sulfate, nitrate, and acetate starting materials are 92.5%, 63.9%, and 78.1% at 1 C-rate after 50 cycles, and 83.2%, 48.0%, and 71.7% at 6 C-rate after 100 cycles, respectively. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:349 / 355
页数:7
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