Bulletin of the American Physical Society
APS March Meeting 2020
Volume 65, Number 1
Monday–Friday, March 2–6, 2020; Denver, Colorado
Session X21: Surfaces, Interfaces, Solids
11:15 AM–1:27 PM,
Friday, March 6, 2020
Room: 302
Sponsoring
Unit:
DCP
Chair: George Thurston, Rochester Institute of Technology
Abstract: X21.00009 : On-surface synthesis of graphene nanostructures on non-metallic substrates*
Presenter:
Marek Kolmer
(Oak Ridge National Laboratory)
Authors:
Marek Kolmer
(Oak Ridge National Laboratory)
Ann-Kristin Steiner
(Friedrich Alexander University Erlangen-Nuremberg)
Rafal Zuzak
(Jagiellonian University in Krakow)
Lukasz Zajac
(Jagiellonian University in Krakow)
Mads Engelund
(Espeem S.A.R.L)
Szymon Godlewski
(Jagiellonian University in Krakow)
Wonhee Ko
(Oak Ridge National Laboratory)
Miguel Angel Fuentes-Cabrera
(Oak Ridge National Laboratory)
Jingsong Huang
(Oak Ridge National Laboratory)
An-Ping Li
(Oak Ridge National Laboratory)
Marek Szymonski
(Jagiellonian University in Krakow)
Konstantin Amsharov
(Friedrich Alexander University Erlangen-Nuremberg)
Here, we will present a method to tackle this long-standing challenge of on-surface synthesis of predesigned carbon nanostructures directly on non-metallic substrates [1]. We will show that thermally triggered intra-molecular C-C coupling is effectively realized on a model transition metal oxide substrate via selective activation of C-F bonds and corresponding cyclodehydrofluorination reactions. Our low temperature STM, XPS and mass spectroscopy experiments prove that flexible oligophenylene chains can be transformed into predesigned nanographene molecules. Finally, we will discuss a strategy to combine C-F bond activation with previous reports on the inter-molecular C-C bond formation [2,3].
[1] M. Kolmer et al., Science, 363, 57-60 (2019);
[2] M. Kolmer et al., Angew. Chem. Int. Ed., 52, 10300 (2013);
[3] M. Kolmer et al., Chem. Comm., 51, 1127 (2015).
*Part of work was conducted at the Center for Nanophase Materials Sciences (CNMS), which is a DOE Office of Science User Facility.
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