Room-temperature synthesis of Co(OH)2 hexagonal sheets and their topotactic transformation into Co3O4 (111) porous structure with enhanced lithium-storage properties

被引:37
作者
Li, Xue [1 ]
Xu, Gui-Liang [1 ]
Fu, Fang [1 ]
Lin, Zhou [1 ]
Wang, Qi [1 ]
Huang, Ling [1 ]
Li, Jun-Tao [1 ]
Sun, Shi-Gang [1 ]
机构
[1] Xiamen Univ, Dept Chem, Coll Chem & Chem Engn, State Key Lab Phys Chem Solid Surfaces, Xiamen 361005, Peoples R China
关键词
Co(OH)(2) material; Room-temperature; Co3O4 (111); Lithium batteries; ONE-POT SYNTHESIS; LI-ION BATTERIES; ELECTRODE MATERIALS; COBALT HYDROXIDE; SPINEL CO3O4; NANOPLATELETS; NANOPARTICLES; PERFORMANCE; FACILE; NICKEL;
D O I
10.1016/j.electacta.2013.01.043
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The beta-Co(OH)(2) sheets with uniform hexagonal shape were prepared using NaBH4 as the structure directing agent at room temperature. After thermal annealing in air at 450 degrees C for 2 h, the as-prepared beta-Co(OH)(2) sheets were converted into porous Co3O4 with the hexagonal sheet-like morphology (H-Co3O4). The textural properties of the as-prepared samples were characterized by field-emission scanning electron microscopy, transmission electron microscopy and powder X-ray diffraction. The results of lithium storage capability indicate that the H-Co3O4 electrode exhibits excellent cycleability and rate capacity. At a charge/discharge current density of 50 mA g(-1), a reversible capacity of 914 mAh g(-1) can be maintained after 40 cycles. When the current density is increased to 1600 mAh g(-1), a reversible capacity of 800 mAh g(-1) can be still obtained. The superior electrochemical performance is attributed to the porous 2D structures with a finite lateral size and enhanced open-edges, which facilitate Li-ion and electron diffusion through active materials. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:134 / 140
页数:7
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