Probing the interaction of Au, Rh and bimetallic Au-Rh clusters with the TiO2 nanowire and nanotube support

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Abstract

Gold, rhodium and their coadsorbed layers were prepared on titanate nanowires and nanotubes and characterized by X-ray photoelectron spectroscopy (XPS), low energy ion scattering spectroscopy (LEIS), Fourier transform infrared spectroscopy (FTIR) and scanning electron microscope (SEM). On titanate nanowire and tube supports the gold 4f7/2 XP emission appeared after reduction at 83.7 eV and 85.6 eV indicating two different sizes or chemical environments of gold nanoclusters. The titanate nanostructures stabilize the nearly atomically dispersed state of gold (85.6 eV peaks in XPS). Small clusters also developed in rhodium containing samples besides the pure metallic state. Upon CO adsorption on Rh/titanate nanostructures the IR stretching frequencies characteristic of twin form were dominant, whereas bimetallic nanosystems featured a pronounced linear stretching vibration. By performing careful XPS, LEIS and SEM experiments, it was found that, for appropriate Au and Rh coverage, the Au almost completely covers the Rh nanoparticles. CO adsorbed on this surface may induce the surface reconstruction.

Original languageEnglish
Pages (from-to)1048-1055
Number of pages8
JournalSurface Science
Volume605
Issue number11-12
DOIs
Publication statusPublished - Jun 2011

Fingerprint

Gold
Nanotubes
Nanowires
nanotubes
nanowires
gold
Rhodium
X ray photoelectron spectroscopy
photoelectron spectroscopy
ion scattering
Carbon Monoxide
rhodium
Stretching
Nanostructures
Electron microscopes
electron microscopes
interactions
Spectroscopy
Scattering
Ions

Keywords

  • Bimetallic
  • CO adsorption
  • Core-shell structure
  • Gold
  • LEIS
  • Rhodium
  • Titania nanotube
  • Titania nanowire

ASJC Scopus subject areas

  • Surfaces and Interfaces
  • Condensed Matter Physics
  • Materials Chemistry
  • Surfaces, Coatings and Films

Cite this

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title = "Probing the interaction of Au, Rh and bimetallic Au-Rh clusters with the TiO2 nanowire and nanotube support",
abstract = "Gold, rhodium and their coadsorbed layers were prepared on titanate nanowires and nanotubes and characterized by X-ray photoelectron spectroscopy (XPS), low energy ion scattering spectroscopy (LEIS), Fourier transform infrared spectroscopy (FTIR) and scanning electron microscope (SEM). On titanate nanowire and tube supports the gold 4f7/2 XP emission appeared after reduction at 83.7 eV and 85.6 eV indicating two different sizes or chemical environments of gold nanoclusters. The titanate nanostructures stabilize the nearly atomically dispersed state of gold (85.6 eV peaks in XPS). Small clusters also developed in rhodium containing samples besides the pure metallic state. Upon CO adsorption on Rh/titanate nanostructures the IR stretching frequencies characteristic of twin form were dominant, whereas bimetallic nanosystems featured a pronounced linear stretching vibration. By performing careful XPS, LEIS and SEM experiments, it was found that, for appropriate Au and Rh coverage, the Au almost completely covers the Rh nanoparticles. CO adsorbed on this surface may induce the surface reconstruction.",
keywords = "Bimetallic, CO adsorption, Core-shell structure, Gold, LEIS, Rhodium, Titania nanotube, Titania nanowire",
author = "{\'A}. Kukovecz and G. P{\'o}t{\'a}ri and A. Oszk{\'o} and Z. K{\'o}nya and A. Erd{\'o}helyi and J. Kiss",
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T1 - Probing the interaction of Au, Rh and bimetallic Au-Rh clusters with the TiO2 nanowire and nanotube support

AU - Kukovecz, Á.

AU - Pótári, G.

AU - Oszkó, A.

AU - Kónya, Z.

AU - Erdóhelyi, A.

AU - Kiss, J.

PY - 2011/6

Y1 - 2011/6

N2 - Gold, rhodium and their coadsorbed layers were prepared on titanate nanowires and nanotubes and characterized by X-ray photoelectron spectroscopy (XPS), low energy ion scattering spectroscopy (LEIS), Fourier transform infrared spectroscopy (FTIR) and scanning electron microscope (SEM). On titanate nanowire and tube supports the gold 4f7/2 XP emission appeared after reduction at 83.7 eV and 85.6 eV indicating two different sizes or chemical environments of gold nanoclusters. The titanate nanostructures stabilize the nearly atomically dispersed state of gold (85.6 eV peaks in XPS). Small clusters also developed in rhodium containing samples besides the pure metallic state. Upon CO adsorption on Rh/titanate nanostructures the IR stretching frequencies characteristic of twin form were dominant, whereas bimetallic nanosystems featured a pronounced linear stretching vibration. By performing careful XPS, LEIS and SEM experiments, it was found that, for appropriate Au and Rh coverage, the Au almost completely covers the Rh nanoparticles. CO adsorbed on this surface may induce the surface reconstruction.

AB - Gold, rhodium and their coadsorbed layers were prepared on titanate nanowires and nanotubes and characterized by X-ray photoelectron spectroscopy (XPS), low energy ion scattering spectroscopy (LEIS), Fourier transform infrared spectroscopy (FTIR) and scanning electron microscope (SEM). On titanate nanowire and tube supports the gold 4f7/2 XP emission appeared after reduction at 83.7 eV and 85.6 eV indicating two different sizes or chemical environments of gold nanoclusters. The titanate nanostructures stabilize the nearly atomically dispersed state of gold (85.6 eV peaks in XPS). Small clusters also developed in rhodium containing samples besides the pure metallic state. Upon CO adsorption on Rh/titanate nanostructures the IR stretching frequencies characteristic of twin form were dominant, whereas bimetallic nanosystems featured a pronounced linear stretching vibration. By performing careful XPS, LEIS and SEM experiments, it was found that, for appropriate Au and Rh coverage, the Au almost completely covers the Rh nanoparticles. CO adsorbed on this surface may induce the surface reconstruction.

KW - Bimetallic

KW - CO adsorption

KW - Core-shell structure

KW - Gold

KW - LEIS

KW - Rhodium

KW - Titania nanotube

KW - Titania nanowire

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