Electrocatalytic Oxygen Evolution at Surface-Oxidized Multiwall Carbon Nanotubes

被引:521
作者
Lu, Xunyu [1 ]
Yim, Wai-Leung [2 ]
Suryanto, Bryan H. R. [1 ]
Zhao, Chuan [1 ]
机构
[1] Univ New S Wales, Sch Chem, Sydney, NSW 2052, Australia
[2] Agcy Sci Technol & Res, Inst High Performance Comp, Singapore 138632, Singapore
基金
澳大利亚研究理事会;
关键词
IN-SITU FORMATION; WATER OXIDATION; METALLIC IMPURITIES; EVOLVING CATALYST; OXIDE CATALYSTS; DOPED GRAPHENE; REDUCTION; NITROGEN; FILM; NANOPARTICLES;
D O I
10.1021/ja509879r
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Large-scale storage of renewable energy in the form of hydrogen (H-2) fuel via electrolytic water splitting requires the development of water oxidation catalysts that are efficient and abundant. Carbon-based nanomaterials such as carbon nanotubes have attracted significant applications for use as substrates for anchoring metal-based nanoparticles. We show that, upon mild surface oxidation, hydrothermal annealing and electrochemical activation, multiwall carbon nanotubes (MWCNTs) themselves are effective water oxidation catalysts, which can initiate the oxygen evolution reaction (OER) at overpotentials of 0.3 V in alkaline media. Oxygen-containing functional groups such as ketonic C=O generated on the outer wall of MWCNTs are found to play crucial roles in catalyzing OER by altering the electronic structures of the adjacent carbon atoms and facilitates the adsorption of OER intermediates. The well-preserved microscopic structures and highly conductive inner walls of MWCNTs enable efficient transport of the electrons generated during OER.
引用
收藏
页码:2901 / 2907
页数:7
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