Abstract

New synthesis routes to tailor graphene properties by controlling the concentration and chemical configuration of dopants show great promise. Herein we report the direct reproducible synthesis of 2-3% nitrogen-doped ‘few-layer’ graphene from a solid state nitrogen carbide a-C:N source synthesized by femtosecond pulsed laser ablation. Analytical investigations, including synchrotron facilities, made it possible to identify the configuration and chemistry of the nitrogen-doped graphene films. Auger mapping successfully quantified the 2D distribution of the number of graphene layers over the surface, and hence offers a new original way to probe the architecture of graphene sheets. The films mainly consist in a Bernal ABA stacking three-layer architecture, with a layer number distribution ranging from 2 to 6. Nitrogen doping affects the charge carrier distribution but has no significant effects on the number of lattice defects or disorders, compared to undoped graphene synthetized in similar conditions. Pyridinic, quaternary and pyrrolic nitrogen are the dominant chemical configurations, pyridinic N being preponderant at the scale of the film architecture. This work opens highly promising perspectives for the development of self-organized nitrogen-doped graphene materials, as synthetized from solid carbon nitride, with various functionalities, and for the characterization of 2D materials using a significant new methodology.

Details

Title
Nano-Architecture of nitrogen-doped graphene films synthesized from a solid CN source
Author
Maddi, Chiranjeevi 1 ; Bourquard, Florent 1 ; Barnier, Vincent 2 ; Avila, José 3 ; Maria-Carmen Asensio 3 ; Tite, Teddy 1 ; Donnet, Christophe 1 ; Garrelie, Florence 1 

 Univ Lyon, Université Jean Monnet, Laboratoire Hubert Curien UMR 5516, Saint-Étienne, France 
 Laboratoire Georges Friedel, Ecole Nationale Supérieure des Mines, Saint-Etienne, France 
 Synchrotron SOLEIL & Université Paris-Saclay, Saint Aubin, Gif sur Yvette, France 
Pages
1-13
Publication year
2018
Publication date
Feb 2018
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2004118101
Copyright
© 2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.