The Potential of X-ray Photoelectron Spectroscopy for Determining Interface Dipoles of Self-Assembled Monolayers
In the current manuscript we assess to what extent X-ray photoelectron spectroscopy (XPS) is a suitable tool for probing the dipoles formed at interfaces between self-assembled monolayers and metal substrates. To that aim, we perform dispersion-corrected, slab-type band-structure calculations on a n...
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doaj-ff7d6fad8372457980bdfe4b84ca99dc2020-11-25T03:46:25ZengMDPI AGApplied Sciences2076-34172020-08-01105735573510.3390/app10175735The Potential of X-ray Photoelectron Spectroscopy for Determining Interface Dipoles of Self-Assembled MonolayersThomas C. Taucher0Egbert Zojer1Institute of Solid State Physics, Graz University of Technology, NAWI Graz, Petersgasse 16, 8010 Graz, AustriaInstitute of Solid State Physics, Graz University of Technology, NAWI Graz, Petersgasse 16, 8010 Graz, AustriaIn the current manuscript we assess to what extent X-ray photoelectron spectroscopy (XPS) is a suitable tool for probing the dipoles formed at interfaces between self-assembled monolayers and metal substrates. To that aim, we perform dispersion-corrected, slab-type band-structure calculations on a number of biphenyl-based systems bonded to an Au(111) surface via different docking groups. In addition to changing the docking chemistry (and the associated interface dipoles), the impacts of polar tail group substituents and varying dipole densities are also investigated. We find that for densely packed monolayers the shifts of the peak positions of the simulated XP spectra are a direct measure for the interface dipoles. In the absence of polar tail group substituents they also directly correlate with adsorption-induced work function changes. At reduced dipole densities this correlation deteriorates, as work function measurements probe the difference between the Fermi level of the substrate and the electrostatic energy far above the interface, while core level shifts are determined by the local electrostatic energy in the region of the atom from which the photoelectron is excited.https://www.mdpi.com/2076-3417/10/17/5735X-ray photoelectron spectroscopyXPSself-assembled monolayerSAMcollective electrostaticsband-structure calculation |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Thomas C. Taucher Egbert Zojer |
spellingShingle |
Thomas C. Taucher Egbert Zojer The Potential of X-ray Photoelectron Spectroscopy for Determining Interface Dipoles of Self-Assembled Monolayers Applied Sciences X-ray photoelectron spectroscopy XPS self-assembled monolayer SAM collective electrostatics band-structure calculation |
author_facet |
Thomas C. Taucher Egbert Zojer |
author_sort |
Thomas C. Taucher |
title |
The Potential of X-ray Photoelectron Spectroscopy for Determining Interface Dipoles of Self-Assembled Monolayers |
title_short |
The Potential of X-ray Photoelectron Spectroscopy for Determining Interface Dipoles of Self-Assembled Monolayers |
title_full |
The Potential of X-ray Photoelectron Spectroscopy for Determining Interface Dipoles of Self-Assembled Monolayers |
title_fullStr |
The Potential of X-ray Photoelectron Spectroscopy for Determining Interface Dipoles of Self-Assembled Monolayers |
title_full_unstemmed |
The Potential of X-ray Photoelectron Spectroscopy for Determining Interface Dipoles of Self-Assembled Monolayers |
title_sort |
potential of x-ray photoelectron spectroscopy for determining interface dipoles of self-assembled monolayers |
publisher |
MDPI AG |
series |
Applied Sciences |
issn |
2076-3417 |
publishDate |
2020-08-01 |
description |
In the current manuscript we assess to what extent X-ray photoelectron spectroscopy (XPS) is a suitable tool for probing the dipoles formed at interfaces between self-assembled monolayers and metal substrates. To that aim, we perform dispersion-corrected, slab-type band-structure calculations on a number of biphenyl-based systems bonded to an Au(111) surface via different docking groups. In addition to changing the docking chemistry (and the associated interface dipoles), the impacts of polar tail group substituents and varying dipole densities are also investigated. We find that for densely packed monolayers the shifts of the peak positions of the simulated XP spectra are a direct measure for the interface dipoles. In the absence of polar tail group substituents they also directly correlate with adsorption-induced work function changes. At reduced dipole densities this correlation deteriorates, as work function measurements probe the difference between the Fermi level of the substrate and the electrostatic energy far above the interface, while core level shifts are determined by the local electrostatic energy in the region of the atom from which the photoelectron is excited. |
topic |
X-ray photoelectron spectroscopy XPS self-assembled monolayer SAM collective electrostatics band-structure calculation |
url |
https://www.mdpi.com/2076-3417/10/17/5735 |
work_keys_str_mv |
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