Hydrothermal synthesis of highly nitrogen-doped few-layer graphene via solid–gas reaction
[Display omitted] •A novel approach to synthesis of N-doped few-layer graphene has been developed.•The high doping levels of N in products are achieved.•XPS and XANES results reveal a thermal transformation of N bonding configurations.•The developed method is cost-effective and eco-friendly. Nitroge...
Gespeichert in:
Veröffentlicht in: | Materials research bulletin 2015-01, Vol.61, p.252-258 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | [Display omitted]
•A novel approach to synthesis of N-doped few-layer graphene has been developed.•The high doping levels of N in products are achieved.•XPS and XANES results reveal a thermal transformation of N bonding configurations.•The developed method is cost-effective and eco-friendly.
Nitrogen-doped (N-doped) graphene sheets with high doping concentration were facilely synthesized through solid–gas reaction of graphene oxide (GO) with ammonia vapor in a self-designed hydrothermal system. The morphology, surface chemistry and electronic structure of N-doped graphene sheets were investigated by TEM, AFM, XRD, XPS, XANES and Raman characterizations. Upon hydrothermal treatment, up to 13.22at% of nitrogen could be introduced into the crumpled few-layer graphene sheets. Both XPS and XANES analysis reveal that the reaction between oxygen functional groups in GO and ammonia vapor produces amide and amine species in hydrothermally treated GO (HTGO). Subsequent thermal annealing of the resultant HTGO introduces a gradual transformation of nitrogen bonding configurations in graphene sheets from amine N to pyridinic and graphitic N with the increase of annealing temperature. This study provides a simple but cost-effective and eco-friendly method to prepare N-doped graphene materials in large-scale for potential applications. |
---|---|
ISSN: | 0025-5408 1873-4227 |
DOI: | 10.1016/j.materresbull.2014.09.088 |