Co3O4/Co nanoparticles enclosed graphitic carbon as anode material for high performance Li-ion batteries

被引:168
|
作者
Yan, Zhiliang [1 ]
Hu, Qiyang [1 ]
Yan, Guochun [1 ]
Li, Hangkong [2 ]
Shih, Kaimin [2 ]
Yang, Zhewei [1 ]
Li, Xinhai [1 ]
Wang, Zhixing [1 ]
Wang, Jiexi [1 ,2 ]
机构
[1] Cent S Univ, Sch Met & Environm, 932 South Lushan Rd, Changsha 410083, Hunan, Peoples R China
[2] Univ Hong Kong, Dept Civil Engn, Hong Kong, Hong Kong, Peoples R China
关键词
Lithium ion battery; Catalytic graphitization; Anode; Conversion reaction; Thermal oxidation; LITHIUM STORAGE; CATHODE MATERIAL; CATALYTIC GRAPHITIZATION; OXIDE NANOSHEETS; ARRAYS; NANOCOMPOSITE; ELECTRODES; NANOTUBES; COMPOSITE; GRAPHENE;
D O I
10.1016/j.cej.2017.03.146
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The composite of Co3O4, Co and graphitized carbon is synthesized by carbonization and cobalt-catalyzed graphitization of carboxymethyl chitosan, followed by low-temperature thermal oxidation. At the high temperature, the Co(+2) is reduced to metallic Co and the produced Co acts as a catalyst for the graphitization of the pyrolytic carbon. The low-temperature oxidation is conducted to selectively oxidize Co to Co3O4 while the carbon remains unreacted. The structure analysis indicates that three crystal phases (graphite, metallic Co, Co3O4) accompanied with amorphous carbon are co-existed in the composite. Morphological results demonstrate that a lot of graphite grains around the Co element are distributed in the carbon. The electrochemical testing results indicate that the composite shows good electrochemical performance. It delivers a reversible capacity of 843 mAh g(-1) at low current density, and remains 88.9% after 60 cycles at 200 mA g(-1). Even performed at 1 A g(-1), it also exhibits 493 mAh g(-1). The performance improvement is mainly due to the high capacity of Co3O4, high conductivity of graphitic carbon and metallic cobalt, the porous structure offering enough ion transport pathways and relieving the strain during cycling. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:495 / 501
页数:7
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