The hierarchical cobalt oxide-porous carbons composites and their high performance as an anode for lithium ion batteries enhanced by the excellent synergistic effect

被引:5
|
作者
Zhao, Shuping [1 ]
Liu, Wei [1 ]
Liu, Shuang [1 ]
Zhang, Yuan [1 ]
Wang, Huanlei [1 ]
Chen, Shougang [1 ]
机构
[1] Ocean Univ China, Inst Mat Sci & Engn, Qingdao 266100, Peoples R China
基金
中国国家自然科学基金;
关键词
Kapok fibers; Cobalt oxide; Anode; Lithium ion battery; STORAGE CAPACITY; ELECTROCHEMICAL PERFORMANCE; REVERSIBLE CAPACITY; ELECTRODE MATERIALS; ACTIVATED GRAPHENE; NANOSHEETS; NANOPARTICLES; SUPERCAPACITORS; NANOCOMPOSITES; NANOTUBES;
D O I
10.1016/j.electacta.2017.02.110
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The designed metal oxide-carbon composites are always considered as a potential candidate for high-performance electrode materials. In this work, we fabricated the CoO rods-porous carbon composites with a unique hierarchical architecture by utilizing porous biocarbons derived from kapok fibers (KFs). As the composites of CoO nanocrystals with the mean size of 10 nm and graphene-like carbon sheets, the CoO rods are homogeneously anchored on or inside the porous carbons, thus achieving a 3D hierarchical porous structure. When tested as anode materials for lithium-ion batteries, the as-obtained composites exhibit the high lithium storage of 1057 mAh g (1). More importantly, the CoO rods/porousbiocarbons composites display a superior long-term stable reversible capacity of about 550 mAh g (1) at the high current density of 5 A g (1) after 600 cycles. The superior electrochemical performance of the obtained composites has been attributed to the synergistic effect between CoO nanoparticles and porous biocarbons, which makes the composites favorable for fast electronic and ionic transfer, and superior stable structure. Therefore, we believe that the designed preparation of metal oxide architectures in low-cost and renewable porous biocarbons will be a valuable direction for exploring advanced electrode materials. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:511 / 520
页数:10
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