Bolat, Rustem ; Guevara, Jose M. ; Leinen, Philipp ; Knol, Marvin ; Arefi, Hadi H. ; Maiworm, Michael ; Findeisen, Rolf ; Temirov, Ruslan ; Hofmann, Oliver T. ; Maurer, Reinhard J. ; Tautz, F. Stefan ; Wagner, Christian (2024)
Electrostatic potentials of atomic nanostructures at metal surfaces quantified by scanning quantum dot microscopy.
In: nature communications, 15
doi: 10.1038/s41467-024-46423-4
Article, Bibliographie
Abstract
The discrete and charge-separated nature of matter — electrons and nuclei — results in local electrostatic fields that are ubiquitous in nanoscale structures and relevant in catalysis, nanoelectronics and quantum nanoscience. Surface-averaging techniques provide only limited experimental access to these potentials, which are determined by the shape, material, and environment of the nanostructure. Here, we image the potential over adatoms, chains, and clusters of Ag and Au atoms assembled on Ag(111) and quantify their surface dipole moments. By focusing on the total charge density, these data establish a benchmark for theory. Our density functional theory calculations show a very good agreement with experiment and allow a deeper analysis of the dipole formation mechanisms, their dependence on fundamental atomic properties and on the shape of the nanostructures. We formulate an intuitive picture of the basic mechanisms behind dipole formation, allowing better design choices for future nanoscale systems such as single-atom catalysts.
Item Type: | Article |
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Erschienen: | 2024 |
Creators: | Bolat, Rustem ; Guevara, Jose M. ; Leinen, Philipp ; Knol, Marvin ; Arefi, Hadi H. ; Maiworm, Michael ; Findeisen, Rolf ; Temirov, Ruslan ; Hofmann, Oliver T. ; Maurer, Reinhard J. ; Tautz, F. Stefan ; Wagner, Christian |
Type of entry: | Bibliographie |
Title: | Electrostatic potentials of atomic nanostructures at metal surfaces quantified by scanning quantum dot microscopy |
Language: | English |
Date: | 13 March 2024 |
Publisher: | Springer |
Journal or Publication Title: | nature communications |
Volume of the journal: | 15 |
DOI: | 10.1038/s41467-024-46423-4 |
Abstract: | The discrete and charge-separated nature of matter — electrons and nuclei — results in local electrostatic fields that are ubiquitous in nanoscale structures and relevant in catalysis, nanoelectronics and quantum nanoscience. Surface-averaging techniques provide only limited experimental access to these potentials, which are determined by the shape, material, and environment of the nanostructure. Here, we image the potential over adatoms, chains, and clusters of Ag and Au atoms assembled on Ag(111) and quantify their surface dipole moments. By focusing on the total charge density, these data establish a benchmark for theory. Our density functional theory calculations show a very good agreement with experiment and allow a deeper analysis of the dipole formation mechanisms, their dependence on fundamental atomic properties and on the shape of the nanostructures. We formulate an intuitive picture of the basic mechanisms behind dipole formation, allowing better design choices for future nanoscale systems such as single-atom catalysts. |
Additional Information: | Art.No.: 2259 |
Divisions: | 18 Department of Electrical Engineering and Information Technology 18 Department of Electrical Engineering and Information Technology > Institut für Automatisierungstechnik und Mechatronik 18 Department of Electrical Engineering and Information Technology > Institut für Automatisierungstechnik und Mechatronik > Control and Cyber-Physical Systems (CCPS) |
Date Deposited: | 04 Apr 2024 11:47 |
Last Modified: | 30 Apr 2024 13:13 |
PPN: | 517680025 |
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