posted on 2022-07-28, 13:12authored byDiyu Zhang, Charlotte Jansen, Otto T. Berg, Joost M. Bakker, Jörg Meyer, Aart W. Kleyn, Ludo B. F. Juurlink
In a study preliminary to investigating CO2 dissociation,
we report our results on oxygen and carbon monoxide coadsorption on
Cu(111). We use reflection adsorption infrared spectroscopy and Auger
electron spectroscopy to characterize and quantify adsorbed species.
On clean Cu(111), the CO internal stretch mode appears initially at
2077 cm–1 for a surface temperature of ∼80
K. We accurately reproduce the previously determined redshift of the
absorption band with increasing CO coverage. We subsequently oxidize
the surface by exposure to O2 at 300 K to ensure O2 dissociation. The band’s frequency and line shape
of subsequently adsorbed CO at ∼80 K are not affected. However,
the maximum absorbance and integrated peak intensities drop with increasing
O coverage. The data suggest that CO is not adsorbed near O, likely
as a consequence of the mechanism of Cu(111) surface oxidation by
O2 at 300 K. We discuss whether our RAIRS results may be
used to quantify CO2 dissociation in the zero-coverage
limit.