On-Surface Synthesis of Nanographenes and Graphene Nanoribbons on Titanium Dioxide
Loading...
Identifiers
Publication date
Advisors
Tutors
Editors
Journal Title
Journal ISSN
Volume Title
Publisher
ACS Publications
Abstract
The article describes the formation of two types of nanographenes from custom designed and synthesized molecular precursors, through thermally induced intramolecular cyclodehydrogenation reactions on the semiconducting TiO2(110)-(1×1) surface. The obtention of the nanographenes was confirmed by the combination of high-resolution scanning tunneling microscopy (STM) and spectroscopy (STS) measurements, and corroborated by theoretical modeling. The application of this protocol on differently shaped molecular precursors demonstrates the ability to induce a highly efficient planarization reaction both within strained pentahelicenes as well as between vicinal phenyl rings. Additionally, by the combination of successive Ullmann-type polymerization and cyclodehydrogenation reactions, the archetypic 7-armchair graphene nanoribbons (7-AGNRs) have also been fabricated on the titanium dioxide surface from the standard 10,10′-dibromo-9,9′-bianthryl (DBBA) molecular precursors. These examples of the effective cyclodehydrogenative planarization processes provide perspectives for the rational design and synthesis of molecular nanostructures on semiconductors
Description
Artículo científico revisado por pares publicado en ACS Nano. Se deposita la versión editorial en acceso abierto conforme a la política de la editorial.
Bibliographic citation
R. Zuzak, J. Castro-Esteban, M. Engelund, D. Pérez, D. Peña, S. Godlewski. On-Surface Synthesis of Nanographenes and Graphene Nanoribbons on Titanium Dioxide. ACS Nano 2023, 17, 3, 2580–2587 (DOI: 10.1021/acsnano.2c10416)
Relation
Has part
Has version
Is based on
Is part of
Is referenced by
Is version of
Requires
Publisher version
https://doi.org/10.1021/acsnano.2c10416Sponsors
Rights
Copyright © 2023 The Authors. Published by American Chemical Society. This publication is licensed under CC-BY 4.0.
Attribution 4.0 International
Attribution 4.0 International








