Relationship between Carbon Nanotube Structure and Electrochemical Behavior: Heterogeneous Electron Transfer at Electrochemically Activated Carbon Nanotubes

被引:96
作者
Pumera, Martin [1 ,2 ]
Sasaki, Toshio [3 ]
Iwai, Hideo [4 ]
机构
[1] Natl Inst Mat Sci, Ctr Biomat, Biomat Syst Grp, Tsukuba, Ibaraki, Japan
[2] Natl Inst Mat Sci, Int Ctr Mat Nanoarchitecton, Tsukuba, Ibaraki, Japan
[3] Nagoya Univ, Ecotopia Sci Inst, High Voltage Electron Microscope Lab, Chikusa Ku, Nagoya, Aichi 4640814, Japan
[4] Natl Inst Mat Sci, Ctr Mat Anal, Tsukuba, Ibaraki, Japan
关键词
carbon nanotubes; electrochemistry; electron transfer; nanostructures; photoelectron spectroscopy;
D O I
10.1002/asia.200800218
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The electrochemical activation of multiwalled carbon nanotubes (MWCNTs) (at potentials of 1.5-2.0 V vs Ag/AgCl for 60-360 s) results in significantly increased rate constants (k(obs)(0)) for heterogeneous electron-transfer with [Fe(CN)(6)](3-14-) (from 8.34 x 10(-5)cms(-1) for as-received MWCNTs to 3.67 x 10(-3) cm s(-1) for MWCNTs that were electrochemically activated at 2.0 V for 180s). The increase in the value of k(obs)(0), arises from the introduction of wall defects exposing edge planes of the MWCNTs, as observed by high-resolution TEM. The density of the edge plane defects increases from almost zero (for as-received MWCNTs) to 3.7%, (for MWCNTs electrochemically activated at 2.0 V for 180s). High-resolution X-ray photoelectron spectroscopy (HR-XPS), Raman spectroscopy, and electrochemical impedance spectroscopy were used to gain a better understanding of the phenomena. HR-XPS revealed that the increase in electrochemical activation potential increases the number of oxygen-containing groups on the surface of carbon nanotubes.
引用
收藏
页码:2046 / 2055
页数:10
相关论文
共 48 条
[1]   New electrodes for old: from carbon nanotubes to edge plane pyrolytic graphite [J].
Banks, CE ;
Compton, RG .
ANALYST, 2006, 131 (01) :15-21
[2]   Electrocatalysis at graphite and carbon nanotube modified electrodes: edge-plane sites and tube ends are the reactive sites [J].
Banks, CE ;
Davies, TJ ;
Wildgoose, GG ;
Compton, RG .
CHEMICAL COMMUNICATIONS, 2005, (07) :829-841
[3]   Investigation of modified basal plane pyrolytic graphite electrodes: definitive evidence for the electrocatalytic properties of the ends of carbon nanotubes [J].
Banks, CE ;
Moore, RR ;
Davies, TJ ;
Compton, RG .
CHEMICAL COMMUNICATIONS, 2004, (16) :1804-1805
[4]   Understanding the electrochemical reactivity of bamboo multiwalled carbon nanotubes: the presence of oxygenated species at tube ends may not increase electron transfer kinetics [J].
Banks, Craig E. ;
Ji, Xiaobo ;
Crossley, Alison ;
Compton, Richard G. .
ELECTROANALYSIS, 2006, 18 (21) :2137-2140
[5]   COBALT-CATALYZED GROWTH OF CARBON NANOTUBES WITH SINGLE-ATOMIC-LAYERWALLS [J].
BETHUNE, DS ;
KIANG, CH ;
DEVRIES, MS ;
GORMAN, G ;
SAVOY, R ;
VAZQUEZ, J ;
BEYERS, R .
NATURE, 1993, 363 (6430) :605-607
[6]   ACTIVATION OF HIGHLY ORDERED PYROLYTIC-GRAPHITE FOR HETEROGENEOUS ELECTRON-TRANSFER - RELATIONSHIP BETWEEN ELECTROCHEMICAL PERFORMANCE AND CARBON MICROSTRUCTURE [J].
BOWLING, RJ ;
PACKARD, RT ;
MCCREERY, RL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (04) :1217-1223
[7]   Adsorption of gases in multimolecular layers [J].
Brunauer, S ;
Emmett, PH ;
Teller, E .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1938, 60 :309-319
[8]   Demonstration of the importance of oxygenated species at the ends of carbon nanotubes for their favourable electrochemical properties [J].
Chou, A ;
Böcking, T ;
Singh, NK ;
Gooding, JJ .
CHEMICAL COMMUNICATIONS, 2005, (07) :842-844
[9]  
Davies T.J., 2005, ANGEW CHEM, V117, P5251
[10]   Nanotrench arrays reveal insight into graphite electrochemistry [J].
Davies, TJ ;
Hyde, ME ;
Compton, RG .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (32) :5121-5126