Electron transfer kinetics of the VO2+/VO2+ - Reaction on multi-walled carbon nanotubes

被引:110
作者
Friedl, Jochen [1 ,2 ]
Bauer, Christoph M. [1 ,2 ]
Rinaldi, Ali [1 ]
Stimming, Ulrich [1 ,2 ,3 ]
机构
[1] TUM CREATE, Singapore 138602, Singapore
[2] Tech Univ Munich, Dept Phys E19, D-85748 Garching, Germany
[3] Tech Univ Munich, IAS, D-85748 Garching, Germany
基金
新加坡国家研究基金会;
关键词
SURFACE-CHEMISTRY; OXIDATION; ABSORPTION; ADSORPTION; GRAPHENE;
D O I
10.1016/j.carbon.2013.06.076
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
Multi-walled carbon nanotubes (MWCNTs) are suitable electrode materials for the all-vanadium redox flow battery. In addition to their high specific surface area, catalytic properties for the VO2+/VO2+ redox reaction have been reported in literature. Electrochemical impedance spectroscopy was employed to study the VO2+/VO2+ and the Fe2+/Fe3+-reaction on MWCNTs with varying amounts of surface functional groups. Our analysis method is based on taking the large electrochemical interface area of the MWCNTs into account to obtain a truly comparable value for the exchange current density When evaluating the results for Fe2+/Fe3+ it was found that the exchange current density on MWCNTs decorated with a large amount of functional groups is more than 10 times larger than for thermally defunctionalized MWCNTs. For the VO2+/VO2+ reaction, however, a decrease in activity for an increase in amount of functional groups was observed. A possible reaction mechanism and the influence of defects on MWCNTs are discussed. This work distinguishes itself from previous publications, by showing the absence of a catalytic effect of functional groups for the VO2+/VO2+ reaction. Therefore, a new discourse in understanding the catalytic effect of MWCNTs and specifically of the surface functional groups of carbon materials in electrochemical reactions is necessary.
引用
收藏
页码:228 / 239
页数:12
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