Co/CoO@N-C nanocomposites as high-performance anodes for lithium-ion batteries

被引:26
|
作者
Sun, Ming [1 ]
Zhang, Hui [1 ]
Wang, Yi-Fan [1 ]
Liu, Wei-Liang [1 ]
Ren, Man-Man [1 ]
Kong, Fan-Gong [2 ]
Wang, Shou-Juan [2 ]
Wang, Xin-Qiang [3 ]
Duan, Xiu-Lan [3 ]
Ge, Shou-Zhe [1 ]
机构
[1] Qilu Univ Technol, Sch Mat Sci & Engn, Key Lab Proc & Testing Technol Glass Funct Ceram, Shandong Acad Sci,Key Lab Amorphous & Polycrystal, Jinan 250353, Shandong, Peoples R China
[2] Qilu Univ Technol, Key Lab Pulp & Paper Sci & Technol, Minist Educ, Shandong Acad Sci, Jinan 250353, Shandong, Peoples R China
[3] Shandong Univ, State Key Lab Crystal Mat, Jinan 250100, Shandong, Peoples R China
关键词
Metal oxides; Nanocomposites; Nitrogen-doped carbon; Lithium-ion batteries; OXYGEN REDUCTION REACTION; DOPED CARBON; GRAPHENE OXIDE; STORAGE; CAPACITY; NANOPARTICLES; MICROSPHERES; COMPOSITES; ELECTRODES; NANOTUBES;
D O I
10.1016/j.jallcom.2018.08.312
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
Heterogeneous element doping carbon-coated transition metal oxides has been reported as an effective way to increase conductivity and accommodate volume changes during the charge/discharge of lithium-ion batteries thereby improving structural stability and cycle performance. Herein, we have successfully synthesized Co/CoO@N-C nanocomposites using polydopamine as a source of carbon and nitrogen via a simple one-step method. Owing to its desirable structural features, the as-synthesized Co/CoO@N-C nanocomposite anode manifests a greatly improved initial capacity of 1541mAh g(-1) and retains a high reversible value of 1115 mAh g(-1) at a current density of 200 mA g(-1) after 125 cycles. The morphology and physicochemical properties of the Co/CoO@N-C nanocomposites were characterized to provide insights into the promotional roles of nitrogen-doped carbon matrix and CoO loaded nanoparticles. The results demonstrate the potential of the Co/CoO@N-C nanocomposite as a promising anode material for lithium-ion batteries. (c) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:290 / 296
页数:7
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