Towards the Synthesis of Graphene Azide from Graphene Oxide

Molecules. 2015 Nov 26;20(12):21050-7. doi: 10.3390/molecules201219747.

Abstract

In the last decades, organic azides haven proven to be very useful precursors in organic chemistry, for example in 1,3-dipolar cycloaddition reactions (click-chemistry). Likewise, azides can be introduced into graphene oxide with an almost intact carbon framework, namely oxo-functionalized graphene (oxo-G₁), which is a highly oxidized graphene derivative and a powerful precursor for graphene that is suitable for electronic devices. The synthesis of a graphene derivative with exclusively azide groups (graphene azide) is however still a challenge. In comparison also hydrogenated graphene, called graphene or halogenated graphene remain challenging to synthesize. A route to graphene azide would be the desoxygenation of azide functionalized oxo-G₁. Here we show how treatment of azide functionalized oxo-G₁ with HCl enlarges the π-system and removes strongly adsorbed water and some oxo-functional groups. This development reflects one step towards graphene azide.

Keywords: Raman; TGA-MS; graphene azide; graphene oxide.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adsorption
  • Azides / chemical synthesis*
  • Azides / chemistry*
  • Click Chemistry / methods
  • Cycloaddition Reaction / methods
  • Graphite / chemical synthesis*
  • Graphite / chemistry*
  • Hydrochloric Acid / chemistry
  • Oxides / chemistry
  • Water / chemistry

Substances

  • Azides
  • Oxides
  • Water
  • Graphite
  • Hydrochloric Acid