Electrochemistry at chemically assembled single-wall carbon nanotube arrays

被引:76
作者
Diao, P
Liu, ZF [1 ]
机构
[1] Peking Univ, Coll Chem & Mol Engn, Ctr Nanoscale Sci & Technol, Beijing 100871, Peoples R China
[2] Beijing Univ Aeronaut & Astronaut, Sch Mat Sci & Engn, Beijing 100083, Peoples R China
关键词
D O I
10.1021/jp052666r
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
Single-wall carbon nanotubes (SWNTs) chemically assembled on gold substrates were employed as electrodes to investigate the charge transfer process between SWNTs and the underlying substrates. Cyclic voltammetry (CV) indicates that the assembled SWNTs allow electron communication between a gold electrode and the redox couple in solution, though the SWNTs are linked directly onto the insulating monolayer of 11-amino-n-undecanethiol (AUT) on the Au substrate. An electron transfer (ET) mechanism, which contains an electron tunneling process across the AUT monolayer, is proposed to explain the CV behavior of Au/AUT/SWNT electrodes. Electrochemical measurements show that the apparent electron tunneling resistance, which depends on the surface density of assembled SWNTs, has apparent effects similar to those of solution resistance on CV behavior. The theory of solution resistance is used to describe the apparent tunneling resistance. The experimental results of the dependence of ET parameter psi on the potential scan rate v are in good agreement with the theoretical predictions. Kinetic studies of the chemical assembly of SWNTs by atomic force microscopic (AFM), electrochemical, and Raman spectroscopic methods reveal that two distinct assembly kinetics exist: a relatively fast step that is dominated by the surface reaction, and a successive slow step that is governed by bundle formation.
引用
收藏
页码:20906 / 20913
页数:8
相关论文
共 52 条
[1]   CHARGE-TRANSFER AT PARTIALLY BLOCKED SURFACES - A MODEL FOR THE CASE OF MICROSCOPIC ACTIVE AND INACTIVE SITES [J].
AMATORE, C ;
SAVEANT, JM ;
TESSIER, D .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1983, 147 (1-2) :39-51
[2]   Subband population in a single-wall carbon nanotube diode [J].
Antonov, RD ;
Johnson, AT .
PHYSICAL REVIEW LETTERS, 1999, 83 (16) :3274-3276
[3]   Contacting carbon nanotubes selectively with low-ohmic contacts for four-probe electric measurements [J].
Bachtold, A ;
Henny, M ;
Terrier, C ;
Strunk, C ;
Schonenberger, C ;
Salvetat, JP ;
Bonard, JM ;
Forro, L .
APPLIED PHYSICS LETTERS, 1998, 73 (02) :274-276
[4]   FORMATION OF MONOLAYER FILMS BY THE SPONTANEOUS ASSEMBLY OF ORGANIC THIOLS FROM SOLUTION ONTO GOLD [J].
BAIN, CD ;
TROUGHTON, EB ;
TAO, YT ;
EVALL, J ;
WHITESIDES, GM ;
NUZZO, RG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (01) :321-335
[5]  
BARD AJ, 1980, ELECTROCHEMICAL METH, P129
[6]   Carbon nanotube actuators [J].
Baughman, RH ;
Cui, CX ;
Zakhidov, AA ;
Iqbal, Z ;
Barisci, JN ;
Spinks, GM ;
Wallace, GG ;
Mazzoldi, A ;
De Rossi, D ;
Rinzler, AG ;
Jaschinski, O ;
Roth, S ;
Kertesz, M .
SCIENCE, 1999, 284 (5418) :1340-1344
[7]   Contact resistance in metal-molecule-metal junctions based on aliphatic SAMs: Effects of surface linker and metal work function [J].
Beebe, JM ;
Engelkes, VB ;
Miller, LL ;
Frisbie, CD .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (38) :11268-11269
[8]   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
[9]   Novel electrochemical interfaces with a tunable kinetic barrier by self-assembling organically modified silica gel and gold nanoparticles [J].
Bharathi, S ;
Nogami, M ;
Ikeda, S .
LANGMUIR, 2001, 17 (01) :1-4
[10]   Single-electron transport in ropes of carbon nanotubes [J].
Bockrath, M ;
Cobden, DH ;
McEuen, PL ;
Chopra, NG ;
Zettl, A ;
Thess, A ;
Smalley, RE .
SCIENCE, 1997, 275 (5308) :1922-1925