共 34 条
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
相关论文