Electrochemical Nucleation and Growth of Gold Nanoparticles on Single-Walled Carbon Nanotubes: New Mechanistic Insights

被引:79
作者
Dudin, Petr V. [1 ]
Unwin, Patrick R. [1 ]
Macpherson, Julie V. [1 ]
机构
[1] Univ Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, England
基金
英国工程与自然科学研究理事会;
关键词
CURRENT-TIME TRANSIENTS; ANODIC OXIDE-FILMS; METAL NANOPARTICLES; GLASSY-CARBON; PHASE-CHANGE; ELECTRODEPOSITION; KINETICS; RATES; SILVER; ELECTROCRYSTALLIZATION;
D O I
10.1021/jp1043706
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
The electrodeposition mechanism of gold nanoparticles (NPs) on pristine single walled carbon nanotubes (SWNTs) at high driving forces has been elucidated using the microcapillary electrochemical method. Here, a small capillary (internal diameter similar to 50-100 mu m) filled with a gold plating solution, and positioned so that the capillary meniscus makes contact with a two-dimensional SWNT random network, was used to record current-time transients Nucleation and growth transients were observed in which the current increased with time to a maximum value beyond which the current decreased (planar diffusion regime) With increased driving force, the current maximum shifted dramatically to increasingly shorter times. Atomic force microscopy (AFM) analysis indicated that this was not due to significant differences in NP growth rates, but rather to increased densities of NPs formed at more cathodic potentials Detailed microscopic analysis showed that the size of the NPs initially increased with deposition time and the particle surface coverage was constant. However, at the highest driving forces the NP density decreased with deposition time and AFM revealed the presence of both larger and smaller particles at long times This was attributed to electrochemically induced Ostwald ripening, whereby larger particles grow at the expense of smaller ones. As NP nucleation and growth on SWNT two dimensional network electrodes is highly directional and enforced in particular locations, it is inappropriate to analyze electrochemical data using conventional models. There is thus a need to complement chronoamperometric measurements with high resolution microscopy to fully interpret nucleation on complex electrode surfaces.
引用
收藏
页码:13241 / 13248
页数:8
相关论文
共 72 条
[1]   Extracting nucleation rates from current-time transients - Part I: the choice of growth models [J].
Abyaneh, MY .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2002, 530 (1-2) :82-88
[2]   Extracting nucleation rates from current-time transients - Part II: comparing the computer-fit and pre-pulse method [J].
Abyaneh, MY ;
Fleischmann, M .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2002, 530 (1-2) :89-95
[3]   Extracting nucleation rates from current-time transients - Part I: the choice of growth models [J].
Abyaneh, MY .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2002, 530 (1-2) :82-88
[4]   Nanotubes from carbon [J].
Ajayan, PM .
CHEMICAL REVIEWS, 1999, 99 (07) :1787-1799
[5]   INSITU GENERATION AND CHARACTERIZATION OF GOLD(I) COMPLEXES FROM K[AUCL4] IN AQUEOUS-SOLUTIONS [J].
ANDERSON, JE ;
SAWTELLE, SM .
INORGANICA CHIMICA ACTA, 1992, 194 (02) :171-177
[6]   Granulation, Phase Change, and Microstructure - Kinetics of Phase Change. III [J].
Avrami, M .
JOURNAL OF CHEMICAL PHYSICS, 1941, 9 (02) :177-184
[7]   Kinetics of phase change I - General theory [J].
Avrami, M .
JOURNAL OF CHEMICAL PHYSICS, 1939, 7 (12) :1103-1112
[8]  
Avrami M., 1940, J. Chem. Phys, V8, P212, DOI [10.1063/1.1750631, DOI 10.1063/1.1750631]
[9]   Trace level cyclic voltarnmetry facilitated by single-walled carbon nanotube network electrodes [J].
Bertoncello, Paolo ;
Edgeworth, Jonathan P. ;
Macpherson, Julie V. ;
Unwin, Patrick R. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (36) :10982-+
[10]  
Canac F., 1933, CR HEBD ACAD SCI, V196, P51