| Literature DB >> 29200262 |
Marco Di Giovannantonio1, Okan Deniz1, José I Urgel1, Roland Widmer1, Thomas Dienel1, Samuel Stolz1, Carlos Sánchez-Sánchez1, Matthias Muntwiler2, Tim Dumslaff3, Reinhard Berger4, Akimitsu Narita3, Xinliang Feng4, Klaus Müllen3, Pascal Ruffieux1, Roman Fasel1,5.
Abstract
On-surface synthesis is a powerful route toward the fabrication of specific graphene-like nanostructures confined in two dimensions. This strategy has been successfully applied to the growth of graphene nanoribbons of diverse width and edge morphology. Here, we investigate the mechanisms driving the growth of 9-atom wide armchair graphene nanoribbons by using scanning tunneling microscopy, fast X-ray photoelectron spectroscopy, and temperature-programmed desorption techniques. Particular attention is given to the role of halogen functionalization (Br or I) of the molecular precursors. We show that the use of iodine-containing monomers fosters the growth of longer graphene nanoribbons (average length of 45 nm) due to a larger separation of the polymerization and cyclodehydrogenation temperatures. Detailed insight into the growth process is obtained by analysis of kinetic curves extracted from the fast X-ray photoelectron spectroscopy data. Our study provides fundamental details of relevance to the production of future electronic devices and highlights the importance of not only the rational design of molecular precursors but also the most suitable reaction pathways to achieve the desired final structures.Entities:
Keywords: fast X-ray photoelectron spectroscopy; graphene nanoribbons; halogen substitution; on-surface synthesis; reaction kinetics; scanning tunneling microscopy
Year: 2017 PMID: 29200262 DOI: 10.1021/acsnano.7b07077
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881