NiCo2O4 nanosheets and nanocones as additive-free anodes for high-performance Li-ion batteries

被引:32
作者
Ren, Qing-Qing [1 ]
Wang, Zhen-Bo [1 ]
Ke, Ke [1 ,2 ]
Zhang, Si-Wen [1 ]
Yin, Bo-Si [1 ]
机构
[1] Harbin Inst Technol, Sch Chem & Chem Engn, MIIT Key Lab Crit Mat Technol New Energy Convers, 92 West Da Zhi St, Harbin 150001, Heilongjiang, Peoples R China
[2] Chilwee Power Co Ltd, Changxing 313100, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Lithium ion batteries; Electrochemical performance; NiCo2O4; Hydrothermal route; FACILE SYNTHESIS; ELECTRODE MATERIALS; NANOWIRE ARRAYS; NANOROD ARRAYS; METAL-OXIDES; COMPOSITE; MICROSPHERES; SUPERCAPACITOR; MECHANISM; CAPACITY;
D O I
10.1016/j.ceramint.2017.07.083
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Development of novel electrode materials with high energy and power densities for lithium-ion batteries (LIBs) is the key to meet the demands of electric vehicles. Transition metal oxides that can react with large amounts of Li+ for electrochemical energy storage are considered promising anode materials for LIBs. In this work, NiCo2O4 nanosheets and nanocones on Ni foam have been synthesized via general hydrothermal growth and low-temperature annealing treatment. They exhibit high rate capacities and good cyclic performance as LIB anodes owing to their architecture design, which reduces ion and electron transport distance, expands the electrode-electrolyte contact, increases the structural stability, and buffers volume change during cycles. Notably, NiCo2O4 nanosheets deliver an initial capacity of 2239 mAh g(-1) and a rate capacity of 964 mAh g(-1) at current densities of 100 and 5000 mA g(-1), respectively. The corresponding values of nanocones are 1912 and 714 mAh g(-1). Hence, the as-synthesized NiCo2O4 nanosheets and nanocones, which are carbon-free and binder free with higher energy densities and stronger connections between active materials and current collectors for better stability, are promising for use in advanced anodes for high-performance LIBs.
引用
收藏
页码:13710 / 13716
页数:7
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