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Adsorption sites in...
Adsorption sites in coadsorption systems determined by photoemission spectroscopy : K and CO coadsorbed on Rh(111)
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- Strisland, F. (author)
- Norwegian University of Science and Technology
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- Beutler, A. (author)
- Lund University,Lunds universitet,Synkrotronljusfysik,Fysiska institutionen,Institutioner vid LTH,Lunds Tekniska Högskola,Synchrotron Radiation Research,Department of Physics,Departments at LTH,Faculty of Engineering, LTH
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- Jaworowski, A. J. (author)
- Lund University,Lunds universitet,Synkrotronljusfysik,Fysiska institutionen,Institutioner vid LTH,Lunds Tekniska Högskola,Synchrotron Radiation Research,Department of Physics,Departments at LTH,Faculty of Engineering, LTH
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- Nyholm, R. (author)
- Lund University,Lunds universitet,Synkrotronljusfysik,Fysiska institutionen,Institutioner vid LTH,Lunds Tekniska Högskola,Synchrotron Radiation Research,Department of Physics,Departments at LTH,Faculty of Engineering, LTH
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- Setlik, B. (author)
- University of Rhode Island
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- Heskett, D. (author)
- University of Rhode Island
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- Andersen, J. N. (author)
- Lund University,Lunds universitet,Synkrotronljusfysik,Fysiska institutionen,Institutioner vid LTH,Lunds Tekniska Högskola,Synchrotron Radiation Research,Department of Physics,Departments at LTH,Faculty of Engineering, LTH
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(creator_code:org_t)
- 1998
- 1998
- English 14 s.
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In: Surface Science. - 0039-6028. ; 410:2-3, s. 330-343
- Related links:
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Abstract
Subject headings
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- The adsorption sites of coadsorbed K and CO on the Rh(111) surface have been determined using high-resolution core-level spectroscopy, low-energy electron diffraction and site-resolved photoelectron diffraction. For both a (2 × 2)-2CO-1K and a (2√3 × 2√3)-6CO-1K structure, we find that the CO molecules occupy threefold hollow sites and the K atoms on-top sites, contrary to the adsorption sites of K (threefold hollow site) and CO (on-top site below 0.5 monolayers) if adsorbed alone on Rh(111). Deposition of K onto a CO precovered surface is found to induce large shifts towards lower binding energy of the C and O 1s core levels (∼0.7 eV for C 1s and ∼1.5 eV for O 1s). The major part of these shifts is shown to arise from the K-induced site change of the CO molecules. This finding may be of importance in the interpretation of XPS data of related co-adsorption systems. Finally, it is suggested that the C and O 1s binding energies provide useful fingerprints of the CO adsorption site also for co-adsorption systems.
Keyword
- Co-adsorption
- High-resolution core-level photoemission
- Photoelectron diffraction
Publication and Content Type
- art (subject category)
- ref (subject category)
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