Abstract

The co-doping of graphene with nitrogen and sulfur was investigated aiming at understanding their interactions with the presence of oxygen in graphene. The co-doped graphene (NS-G) was synthesized via a one-pot hydrothermal route using graphene oxide as starting material and L-cysteine, an amino acid containing both N and S, as the doping agent. The obtained NS-G with a three-dimensional hierarchical structure containing both macropores and mesopores exhibited excellent mechanical stabilities under both wet and dry conditions. As compared to N or S singly doped graphene, the co-doped sample contains significantly higher concentrations of N and S species especially pyrollic N groups. The co-doped sample considerably outperformed the singly doped samples when used as free-standing electrode in supercapacitors due to enhanced pseudocapacitance. The simultaneous incorporation of S and N species with the presence of oxygen significantly modified the surface chemistry of carbon leading to considerably higher doping levels, although directly bonding between N and S is neither likely nor detected. Hence, the synergetic effect between N and S occurred through carbon atoms in neighboring hexagonal rings in a graphene sheet.

Highlights

  • The co-doping of graphene with nitrogen and sulfur was investigated aiming at understanding their interactions with the presence of oxygen in graphene

  • The co-doped nitrogen and sulfur codoped graphene (NS-G), singly doped nitrogen doped graphene (N-G) and sulfur doped graphene (S-G) hydrogels were successfully synthesized via the one-pot hydrothermal method

  • By weighing the samples before and after drying it was found that the obtained NS-G, S-G and N-G hydrogels contained about 97.6 wt%, 98.7 wt% and 98.1 wt% of water, respectively

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Summary

Introduction

The co-doping of graphene with nitrogen and sulfur was investigated aiming at understanding their interactions with the presence of oxygen in graphene. The simultaneous incorporation of S and N species with the presence of oxygen significantly modified the surface chemistry of carbon leading to considerably higher doping levels, directly bonding between N and S is neither likely nor detected. The incorporation of heteroatoms in carbon materials can significantly modify their surface and bulk properties and considerably broaden their applications in various fields. Obtained graphene oxide (GO) or graphene inevitably contains oxygen, and the nitrogen doping can be realized by partially replacing oxygen with nitrogen through wet chemistry method or thermal treatment in the gas phase. Recent progress demonstrated that substitutional doping of graphene with heteroatoms could substantially modify the electrical conductivity, surface activity, chemical reactivity and mechanical properties of graphene, which are essential for energy storage applications[24,25,26]

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