Abstract

Reduced graphene oxide/Fe3C hybrids were prepared through Fe-based intercalation of graphite oxide (GtO). Altering pH (acidic to basic) of aqueous GtO dispersion, the immobilization of Fe-based intercalant bearing amino benzoate groups (IFe) was strongly affected following either the nucleophilic substitution (sample: IGO) or ion exchange path (sample: IGO/b). Subsequent pyrolysis of the intercalated materials provided magnetic hybrid materials (samples: r-IGO and r-IGO/b), differing in terms of BET surface area (87 and 163m2/g), magnetization (70 and 43J/T/kg), resistance (3 and 3.7Ohm) and capacitance (5 and 17F/g) correspondingly, displaying both magnetic and supercapacitor behavior. IFe triggered after thermal treatment in vacuum the formation of Fe3C nanoparticles encapsulated in a graphite shell whose incorporation into the multi-layer reduced graphene oxide (GO) matrix provided multi-functional materials. In these materials, aggregation is prevented in two directions: (a) between adjacent Fe3C nanoparticles, since the graphitic shell offers isolation, and (b) between bundles of neighboring multi-layer graphenes, due to Fe3C nanoparticle interference. The graphitic shell assists cohesion of encapsulated Fe3C nanoparticles with the graphene matrix as well as chemical stability, affording thus materials appropriate for a variety of applications.

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