Infrared reflection absorption spectroscopic (IRRAS) measurements were conducted for carbon monoxide (CO) adsorption on Pt(111) bimetallic surfaces with various thicknesses of deposited Ni, i.e., Nix/Pt(111) (x, Ni thickness in nanometer units), which were fabricated using molecular beam epitaxy at substrate temperatures of 343-473 K. The reflection high-energy electron diffraction (RHEED) patterns for the 343-K-deposited Ni 0:1nm-0:6nm /Pt(111) reveal Ni epitaxial growth on Pt(111). The CO exposure to the clean Pt(111) surface at 323 K engenders linearly bonded and bridge-bonded CO-Pt bands at 2093 and 1858 cm-1. The 343-K-deposited Ni0:1nm /Pt(111) gives rise to a new band at 2070 cm-1 in addition to the CO-Pt(111) bands. T he new band is most prominent for the Ni0:3nm /Pt(111), on which the bridge-bonded CO on the Ni admetal layer appears at 1874 cm-1. For the Ni0:6nm /Pt(111), the 2070 cm-1 band decreases in intensity and the bridge-bonded CO on the Ni admetal-layerdominates the spectrum, with accompanying weak absorption at 2035 cm-1 caused by linearly adsorbed CO on the Ni layer. The low-energy electron diffraction (LEED) pattern for the 343-K-deposited Ni 0:3nm /Pt(111) shows incommensurate higher-order extra spots surrounding integer spots. In contrast, the incommensurate pattern changes to its original six-fold symmetry for the 473-K-deposited Ni0:3nm /Pt(111). In contrast, the RHEED pattern for the 473-K-deposited Ni 0:3nm /Pt(111) revealed streaks having slightly wider separations than those for the clean Pt(111). The IRRAS spectrum for the 1.0-L-CO exposed 473-K-deposited Ni0:3nm /Pt(111) reveals single-absorption at 2074 cm-1. We discuss the CO adsorption behavior of Nix/Pt(111) . © 2009 The Surface Science Society of Japan.
CITATION STYLE
Wadayama, T., Yoshida, H., Todoroki, N., & Oda, S. (2009). Carbon monoxide adsorption on Ni/Pt(111) surfaces investigated by infrared reflection absorption spectroscopy. In e-Journal of Surface Science and Nanotechnology (Vol. 7, pp. 230–233). The Japan Society of Vacuum and Surface Science. https://doi.org/10.1380/ejssnt.2009.230
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