Facile fabrication of hierarchical porous Co3O4 nanoarrays as a free-standing cathode for lithium-oxygen batteries

被引:7
|
作者
Ren, Yanbiao [1 ,2 ]
Zhao, Shuang [2 ]
Li, Honglei [2 ]
Zhang, Shichao [2 ]
Liu, Jian [1 ]
Xiao, Yao [1 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Mat Sci & Engn, Qingdao 266042, Shandong, Peoples R China
[2] Beihang Univ, Sch Mat Sci & Engn, Beijing 100191, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Cobalt oxide; Free-standing catalyst; Binder/carbon free nanoarrays; Over-potential; Cyclic life; LI-O-2; BATTERIES; NANOSHEETS; CATALYSTS; CARBON; MORPHOLOGY; FOAM;
D O I
10.1016/j.jechem.2018.03.012
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Two shapes of Co3O4 nanoarrays (i.e., nanosheets, nanowires) with different densities of exposed catalytic active sites were synthesized through a facile hydrothermal method on Ni foam substrates and tested as the binder/carbon free and free-standing cathodes for Li-O-2 batteries. Particularly, the single crystalline feature of Co3O4 nanosheets with a predominant high reactivity {112} exposed crystal plane and hierarchical porous nanostructure displayed better catalytic performance for both oxygen reduction reaction (during discharge process) and oxygen evolution reaction (during charge process). Li-O-2 battery with Co3O4 nanosheets cathode exhibited a higher discharge specific capacity (965 mAh g(-1)), lower discharge/charge over-potential and better cycling performance over 63 cycles at 100 mA g(-1) with the specific capacity limited at 300 mAh g(-1). The superior catalytic performance of Co3O4 nanosheets cathode is ascribed to the enlarging specific area and increasing the exposed Co(3+)catalytic active sites within predominant {112} crystal plane which plays the key role in determining the adsorption energy for the reactants, enabling high round-trip efficiency and cyclic life. (C) 2018 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights reserved.
引用
收藏
页码:63 / 70
页数:8
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