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Keywords
(9)
Charge Transfer
Coulomb Blockade
Crystal Structure
Double Layer
High Resolution
Mie Scattering
Surface Plasmon Resonance
Transmission Electron Microscope
Transition Metal
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Dithiocarbamate-protected ruthenium nanoparticles: Synthesis, spectroscopy, electrochemistry and STM studies
Dithiocarbamate-protected ruthenium nanoparticles: Synthesis, spectroscopy, electrochemistry and STM studies,10.1016/j.electacta.2007.01.082,Electroch
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Dithiocarbamate-protected ruthenium nanoparticles: Synthesis, spectroscopy, electrochemistry and STM studies
(
Citations: 7
)
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Wei Chen
,
Debraj Ghosh
,
Jia Sun
,
Moony C. Tong
,
Fengjun Deng
,
Shaowei Chen
Stable ruthenium nanoparticles were synthesized in a biphasic system with a protecting monolayer of dithiocarbamate derivatives. The core size of the resulting Ru particles was found to vary with the initial ligand–metal feed ratio. UV–vis spectroscopic measurements showed a
Mie scattering
profile, with no obvious surface-plasmon resonance. The size and crystal structures of the particles were characterized by transmission electron microscopic (TEM) measurements. A significant fraction of the nanoparticles was found within the size range of 2–4nm in diameter and of spherical shape from the TEM measurements. Clear lattice fringes could be observed in high-resolution TEM images with the fringe spacing consistent with the Ru(101) lattice planes. Electrochemical studies of Ru particles with different core size exhibited the solution-phase quantized charging of the particle double layers, analogous to those reported for gold and other transition-metal particles. The potential spacing between adjacent quantized charging peaks was found to vary with the particle core size, corresponding to the variation of the particle molecular capacitance. These charge-transfer properties were very consistent with the STM measurements of isolated nanoparticles which exhibit clear
Coulomb blockade
and staircase features.
Journal:
Electrochimica Acta - ELECTROCHIM ACTA
, vol. 53, no. 3, pp. 1150-1156, 2007
DOI:
10.1016/j.electacta.2007.01.082
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Citation Context
(2)
...In previous studies, size-controlled synthesis of silver and ruthenium nanoparticles has been achieved by controlling the initial dithiocarbamate ligand–metal feed ratios [
22
,
23
]...
Wentao Wei
,
et al.
Size-dependent catalytic activity of copper nanoclusters for oxygen el...
...Nonetheless, the absence of other contribution in the UV‐Vis spectrum (expected as bands for the precursors RuCl3 and Pd(CH3COO)2, around 400 nm, (
Chen et al. 2007;
Dhas and Gedanken 1998) are consistent with the hypothesis of a complete reduction in the zero oxidation state...
I. Concina
,
et al.
Stabilisation of monometallic nanoparticles by polyamide 6
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Citations
(7)
Size-dependent catalytic activity of copper nanoclusters for oxygen electroreduction in alkaline solution
Wentao Wei
,
Wei Chen
Journal:
International Journal of Smart and Nano Materials
, vol. ahead-of-p, no. ahead-of-p, pp. 1-10, 2012
Stabilisation of monometallic nanoparticles by polyamide 6
I. Concina
,
M. Zecca
Journal:
Journal of Nanoparticle Research - J NANOPART RES
, vol. 13, no. 3, pp. 1289-1300, 2011
The use of nanoparticles in electroanalysis: an updated review
(
Citations: 4
)
Fallyn W. Campbell
,
Richard G. Compton
Journal:
Analytical and Bioanalytical Chemistry - ANAL BIOANAL CHEM
, vol. 396, no. 1, pp. 241-259, 2010
Carbon-supported Pt–Ru nanoparticles prepared in glyoxylate-reduction system promoting precursor–support interaction
Ki Chul Park
,
In Young Jang
,
Winadda Wongwiriyapan
,
Shingo Morimoto
,
Yong Jung Kim
,
Yong Chae Jung
,
Tomohiro Toya
,
Morinobu Endo
Journal:
Journal of Materials Chemistry - J MATER CHEM
, vol. 20, no. 25, 2010
Water-soluble poly(4-styrenesulfonic acid- co-maleic acid) stabilized ruthenium(0) and palladium(0) nanoclusters as highly active catalysts in hydrogen generation from the hydrolysis of ammonia–borane
(
Citations: 6
)
Önder Metin
,
Şule Şahin
,
Saim Özkar
Journal:
International Journal of Hydrogen Energy - INT J HYDROGEN ENERG
, vol. 34, no. 15, pp. 6304-6313, 2009