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  3. Tailoring electronic states of nanographenes through heteroatom substitution and substrate interactions

Tailoring electronic states of nanographenes through heteroatom substitution and substrate interactions

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BORIS DOI
10.48620/96012
Abstract
Technology advances demand new materials for faster and more efficient electronics. Carbon-based nanostructures, particularly planar nanographenes, offer tunable electronic properties through atomic-scale design. This thesis explores different strategies to control these properties in nanographenes synthesized via on-surface synthesis (a bottom-up arrpoach in UHV) and characterized by scanning probe techniques. Three approaches are investigated: geometry and edge structure, heteroatom substitution, and substrate choice. Seventeen-atom-wide graphene nanoribbons are grown and integrated into devices, demonstrating favorable transport behavior. Nitrogen substitution, shown to be compatible with on-surface synthesis, enables doping of the nanographenes but leads to charge transfer to Au(111). To mitigate this effect, TbAu₂ is introduced as a substrate, enabling reduced charging and magnetic coupling. These findings highlight pathways to engineer nanographene electronic properties.
Year of graduation
2025
Theses Type
dissertation
Subject(s)
500 Science > 540 Chemistry
600 Technology > 660 Chemical engineering
Keyword(s)
Nanographene
•
On-surface synthesis
•
Scanning Tunneling Spectrosocpy
•
Heteroatom substitution
•
Spin
•
Ferromagentism
Language(s)
en
Author(s)
Bassi, Nicolò  
Faculty/Graduate School
Faculty of Science  
Institute
EMPA
Related Publications(s)
Preferential graphitic-nitrogen formation in pyridine-extended graphene nanoribbons.  
Optimized Synthesis and Device Integration of Long 17-Atom-Wide Armchair Graphene Nanoribbons.  
Proximity-Driven Magnetic Coupling between an Open-Shell Nanographene and a Rare-Earth Surface Alloy.  
Access(Rights)
embargo
Primary OA Publication
true
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