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RAIRS Characterization of CO and O Coadsorption on Cu(111).

ABSTRACT: 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.

SUBMITTER: Zhang D

PROVIDER: S-EPMC9376953 | biostudies-literature | 2022 Aug

REPOSITORIES: biostudies-literature

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RAIRS Characterization of CO and O Coadsorption on Cu(111).

Zhang Diyu D Jansen Charlotte C Berg Otto T OT Bakker Joost M JM Meyer Jörg J Kleyn Aart W AW Juurlink Ludo B F LBF

The journal of physical chemistry. C, Nanomaterials and interfaces 20220728 31

In a study preliminary to investigating CO<sub>2</sub> 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<sup>-1</sup> for a surface temperature of ∼80 K. We accurately reproduce the previously determined redshift of the absorption band with increasing C ...[more]

PMID: 35983315

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Project description:Copper-based catalysts gain activity through the presence of poorly coordinated Cu atoms and incomplete oxidation at the surface. The catalytic mechanisms can in principle be observed by controlled dosing of reactants to single-crystal substrates. However, the interconnected influences of surface defects, partial oxidation, and adsorbate coverage present a large matrix of conditions that have not been fully explored in the literature. We recently characterized oxygen and carbon monoxide coadsorption on Cu(111), a nominally defect-free surface, and now extend our study to the stepped surface Cu(211). Temperature-programmed desorption of CO adsorbed to bare metal surfaces confirms that two sites dominate desorption from a saturated layer: atop terrace atoms of local (111) character and atop step edge atoms with CO bound more strongly to the latter. At low coverage, discrete CO resonances in reflection adsorption infrared spectra can be assigned to these sites: 2077 cm-1 for extended (111) terraces, 2093 cm-1 for step sites, and additional kink-adsorbed molecules at 2110 cm-1. With increasing coverage, in contrast to Cu(111), the infrared spectral features on Cu(211) evolve and shift as a consequence of dipole-dipole coupling between differentially occupied types of sites. Auger electron spectroscopy shows that exposure to background O2 oxidizes the (211) surface at a rate nearly 1 order of magnitude greater than (111); we argue that the resulting surface is stoichiometric Cu2O, as previously found for Cu(111). This oxide binds CO less strongly than the bare metal and the underlying crystal cut continues to influence the adsorption sites available to CO. On oxidized (111) terraces, broad absorption peaks at 2115-2120 cm-1; on oxidized Cu(211), CO adsorbed to step sites appears as a resolved secondary peak at 2144 cm-1. This suite of spectroscopic signatures, obtained under carefully controlled conditions, will help to determine the origin and fate of adsorbed species in future studies of reaction mechanisms on copper.

Dataset Information

RAIRS Characterization of CO and O Coadsorption on Cu(111).

Publications

RAIRS Characterization of CO and O Coadsorption on Cu(111).

Similar Datasets

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