Abstract
The infrared absorption spectra of NO adsorbed on Ru(001) and on O(2 × 1)/Ru(001) have been re-examined to clarify several open questions in these systems, including an old puzzle regarding the insensitivity of IRAS to detect NO/Ru(001) on threefold bridge sites despite its clear presence in (specular) HREELS spectra. We find no indication for such an inconsistency in vibrational spectra as we observe both, the multiply coordinated v1-NO and the linear v2-NO species; we are able to detect their internal stretching modes with signal-to-noise ratios up to 1000:1. We attribute this to better instrumentation as well as to improved crystal perfection and layer homogeneity. These improvements reflect themselves in unparalleled 3 cm-1 linewidths of the vibrational bands and very narrow peaks in thermal desorption spectroscopy. As in the case of CO/O(2 × 1)/Ru(001), a (2 × 2) honeycomb structure must form for NO/O(2 × 1)/Ru(001) after annealing to 400 K. A consistent new picture of the processes occurring upon coadsorption and annealing can be obtained.
Original language | English |
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Pages (from-to) | L185-L192 |
Journal | Surface Science |
Volume | 370 |
Issue number | 1 |
DOIs | |
State | Published - 1 Jan 1997 |
Keywords
- Infrared absorption spectroscopy
- Low index single crystal surface
- Nitrogen oxides
- Oxygen
- Ruthenium
- Surface structure, morphology, roughness, and topography
- Thermal desorption spectroscopy
- Vibrations of adsorbed molecules