Guanine adsorption on the Cu(110) surface

The adsorption of guanine on Cu(110) has been studied by soft X-ray photoelectron spectroscopy (XPS) and near edge X-ray absorption fine structure (NEXAFS) spectroscopy. The valence band spectra, carbon and nitrogen 1s XPS and N K-edge absorption spectra were measured for a thin film, sub-monolayer...

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Bibliographic Details
Published inSurface science Vol. 605; no. 3; pp. 361 - 365
Main Authors Feyer, V., Plekan, O., Šutara, F., Cháb, V., Matolín, V., Prince, K.C.
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier B.V 01.02.2011
Elsevier
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Summary:The adsorption of guanine on Cu(110) has been studied by soft X-ray photoelectron spectroscopy (XPS) and near edge X-ray absorption fine structure (NEXAFS) spectroscopy. The valence band spectra, carbon and nitrogen 1s XPS and N K-edge absorption spectra were measured for a thin film, sub-monolayer and saturation coverage. We show that hydrogen bonding causes a significant core level shift in the thin film. At saturation coverage, guanine is tilted at 70° with respect to the surface, and bonds through the N1 nitrogen atom. On reducing the coverage, the orientation changes and the tilt angle of the molecular plane is reduced. For both coverages, guanine is singly deprotonated at the N1 site, and annealing to a higher temperature (500 K) is probably accompanied by further deprotonation of the amino groups. ► The electronic structure and adsorption geometry of guanine on Cu(110) have been investigated. ► In the multilayer the molecules interact via hydrogen bonding, it causes a significant core level shift. ► At low coverage guanine chemisorbs on Cu(110) via oxygen and nitrogen atoms, and dehydrogenation of nitrogen may occur.► The orientation of the molecule changes with coverage.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0039-6028
1879-2758
DOI:10.1016/j.susc.2010.11.002