Stefan R. Kachel
Chemisorption and Physisorption at the Metal/Organic Interface: Bond Energies of Naphthalene and Azulene on Coinage Metal Surfaces
Kachel, Stefan R.; Klein, Benedikt P.; Morbec, Juliana M.; Schöniger, Maik; Hutter, Mark; Schmid, Martin; Kratzer, Peter; Meyer, Bernd; Tonner, Ralf; Michael Gottfried, J.
Authors
Benedikt P. Klein
Dr Juliana Maria Abreu Da Silva Morbec j.morbec@keele.ac.uk
Maik Schöniger
Mark Hutter
Martin Schmid
Peter Kratzer
Bernd Meyer
Ralf Tonner
J. Michael Gottfried
Abstract
Organic/inorganic hybrid interfaces play a prominent role in organic (opto)electronics, heterogeneous catalysis, sensors, and other current fields of technology. The performance of the related devices and processes depends critically on the nature and strength of interfacial interaction. Here, we use the molecular isomers naphthalene (Nt) and azulene (Az) on the Ag(111) and Cu(111) surfaces as model systems that cover different bonding regimes from physisorption to chemisorption. Az also serves as a model for nonalternant molecular electronic materials and for topological 5–7 defects in graphene. The interaction energies are determined from the quantitative analysis of temperature-programmed desorption data. On both surfaces, Az binds more strongly than Nt, with zero-coverage desorption energies (in kJ/mol) of 120 for Az/Ag and 179 for Az/Cu, compared to 103 for Nt/Ag and 114 for Nt/Cu. The integrated experimental energies are compared with adsorption energies from density-functional theory (DFT) calculations, which include van der Waals contributions using four different correction schemes for the PBE functional: (1) the DFT-D3 scheme with Becke–Johnson damping, (2) the vdWsurf correction based on DFT-TS, (3) a many-body dispersion correction scheme, and (4) the D3surf scheme. Differences in the performance of these methods are discussed. Periodic energy decomposition analysis reveals details of the surface chemical bond and confirms that Az/Cu forms a chemisorptive bond, while the other systems are physisorbed. The variation of the adsorbate–substrate interaction with the topology of the p-electron system and the type of surface can be employed to modify the interface properties in graphene-based and organic electronic devices.
Citation
Kachel, S. R., Klein, B. P., Morbec, J. M., Schöniger, M., Hutter, M., Schmid, M., …Michael Gottfried, J. (2020). Chemisorption and Physisorption at the Metal/Organic Interface: Bond Energies of Naphthalene and Azulene on Coinage Metal Surfaces. Journal of Physical Chemistry C, 8257 - 8268. https://doi.org/10.1021/acs.jpcc.0c00915
Acceptance Date | Mar 31, 2020 |
---|---|
Publication Date | Apr 16, 2020 |
Journal | The Journal of Physical Chemistry C |
Print ISSN | 1932-7447 |
Publisher | American Chemical Society |
Pages | 8257 - 8268 |
DOI | https://doi.org/10.1021/acs.jpcc.0c00915 |
Keywords | organic (opto)electronics, heterogeneous catalysis, sensors |
Publisher URL | https://pubs.acs.org/doi/abs/10.1021/acs.jpcc.0c00915 |
Files
2020_02_25_Azulen_TPD_rev_final (1).docx
(3.1 Mb)
Document
Publisher Licence URL
https://creativecommons.org/licenses/by-nc/4.0/
You might also like
Interaction between pentacene molecules and monolayer transition metal dichalcogenides
(2023)
Journal Article
Defect induced room temperature ferromagnetism in high quality Co-doped ZnO bulk samples
(2021)
Journal Article
Downloadable Citations
About Keele Repository
Administrator e-mail: research.openaccess@keele.ac.uk
This application uses the following open-source libraries:
SheetJS Community Edition
Apache License Version 2.0 (http://www.apache.org/licenses/)
PDF.js
Apache License Version 2.0 (http://www.apache.org/licenses/)
Font Awesome
SIL OFL 1.1 (http://scripts.sil.org/OFL)
MIT License (http://opensource.org/licenses/mit-license.html)
CC BY 3.0 ( http://creativecommons.org/licenses/by/3.0/)
Powered by Worktribe © 2025
Advanced Search