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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Main Authors: Thomas C. Taucher, Egbert Zojer
Format: Article
Language:English
Published: MDPI AG 2020-08-01
Series:Applied Sciences
Subjects:
XPS
SAM
Online Access:https://www.mdpi.com/2076-3417/10/17/5735
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spelling 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
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