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We present an in-depth investigation of Au nanoparticles self-assembled on a zigzag-like TiO(x)/Pt(111) ultrathin polar film, whose structure is known in great detail. The peculiar pattern of defects (picoholes) templates a linear array of size-selected (ca. 1 nm) Au nanoparticles without disruption of the titania layer, as observed by scanning tunneling microscopy. Their structure and electronic properties have been investigated by several large-area spectroscopic tools, i.e. high-resolution core and valence level photoemission and angle-scanned and energy-scanned photoelectron diffraction. The comparison between experimental data and density functional theoretical calculations indicates that the Au atoms landing on the oxide film are rather mobile, and that the picoholes can act as effective trapping and nucleation centers for the growth of the Au nanoparticles. All the experimental results are in concord in indicating that the Au NPs are flat islands with a maximum thickness of 2-3 layers exposing the (111) surface.
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http://dx.doi.org/10.1039/b819791a | DOI Listing |
Phys Chem Chem Phys
July 2015
Department of Chemical Sciences, University of Padova, via Marzolo 1, I-35131 Padova, Italy.
The structure and thermal evolution of Fe nanoparticles deposited on a wetting TiOx ultrathin film epitaxially grown on Pt(111) has been characterized by various surface science techniques. Combining the results obtained it is shown that, at room temperature, metallic Fe nucleates randomly and oxidizes at the interface. A thermal treatment causes Fe migration through the TiOx layer, forming a mixed oxide and a new hexagonal ultrathin film phase.
View Article and Find Full Text PDFJ Phys Condens Matter
January 2013
Institute of Physical and Theoretical Chemistry, University of Bonn, Wegelerstrasse 12, D-53115 Bonn, Germany.
We have investigated the growth of ultrathin titanium oxide (TiO(x)) films on a Pt(3)Ti(111) single crystal surface as a function of oxidation temperature (300-1000 K) and oxygen exposure (up to 4500 l) by means of Auger electron spectroscopy, low-energy electron diffraction, ultraviolet photoelectron spectroscopy and high-resolution electron energy loss spectroscopy (HREELS). Both the surface composition and the surface structure of the resulting TiO(x) films exhibit a strong dependence on the preparation conditions. Loss of the chemical order and Ti segregation are observed at the Pt(3)Ti(111) surface upon oxygen exposures of more than 135 l at 1000 K.
View Article and Find Full Text PDFJ Phys Chem B
August 2006
Dipartimento di Scienze Chimiche and Unità di Ricerca INFM-CNR and INSTM, Università di Padova, Via Marzolo, I-35131 Padova, Italy.
Ultrathin ordered titanium oxide films on a Pt(111) surface have been prepared by reactive deposition and characterized by low-energy electron diffraction and scanning tunneling microscopy (STM). According to the postdeposition annealing condition, three different phases have been prepared which show a wagon-wheel-like (hereafter ww) morphological pattern. Two of them can be prepared as single phases (w- and w'-TiO(x)) and one (w(int)-TiO(x)) as a mixed phase which always coexists with at least one of the other two phases.
View Article and Find Full Text PDFJ Phys Chem B
December 2005
Dipartimento di Scienze Chimiche and Unità di Ricerca INFM-CNR, Università di Padova, Via Marzolo, I-35131 Padova, Italy.
Ultrathin ordered titanium oxide films on Pt(111) surface are prepared by reactive evaporation of Ti in oxygen. By varying the Ti dose and the annealing conditions (i.e.
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