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
相关论文
共 49 条
  • [1] LATTICE-DYNAMICAL MODEL FOR ALKALI-METAL GRAPHITE-INTERCALATION COMPOUNDS
    ALJISHI, R
    DRESSELHAUS, G
    [J]. PHYSICAL REVIEW B, 1982, 26 (08): : 4523 - 4538
  • [2] [Anonymous], 2001, ELECTROCHEMICAL METH
  • [3] Covalent surface chemistry of single-walled carbon nanotubes
    Banerjee, S
    Hemraj-Benny, T
    Wong, SS
    [J]. ADVANCED MATERIALS, 2005, 17 (01) : 17 - 29
  • [4] Bard AJ, 1985, BIOELECTROCHEMISTRY, P319
  • [5] Bauer CM, 2012, THESIS TU MUNCHEN
  • [6] ON STRUCTURE OF CHARGED INTERFACES
    BOCKRIS, JO
    DEVANATHAN, MAV
    MULLER, K
    [J]. PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES A-MATHEMATICAL AND PHYSICAL SCIENCES, 1963, 274 (1356) : 55 - +
  • [7] ELECTRON-TRANSFER KINETICS AT MODIFIED CARBON ELECTRODE SURFACES - THE ROLE OF SPECIFIC SURFACE SITES
    CHEN, PH
    FRYLING, MA
    MCCREERY, RL
    [J]. ANALYTICAL CHEMISTRY, 1995, 67 (18) : 3115 - 3122
  • [8] Redox flow cells for energy conversion
    de Leon, C. Ponce
    Frias-Ferrer, A.
    Gonzalez-Garcia, J.
    Szanto, D. A.
    Walsh, F. C.
    [J]. JOURNAL OF POWER SOURCES, 2006, 160 (01) : 716 - 732
  • [9] Modification of the surface chemistry of activated carbons
    Figueiredo, JL
    Pereira, MFR
    Freitas, MMA
    Orfao, JJM
    [J]. CARBON, 1999, 37 (09) : 1379 - 1389
  • [10] Active nano-CuPt3 electrocatalyst supported on graphene for enhancing reactions at the cathode in all-vanadium redox flow batteries
    Flox, Cristina
    Rubio-Garcia, Javier
    Nafria, Raquel
    Zamani, Reza
    Skoumal, Marcel
    Andreu, Teresa
    Arbiol, Jordi
    Cabot, Andreu
    Ramon Morante, Joan
    [J]. CARBON, 2012, 50 (06) : 2372 - 2374