Journal of Materials Chemistry · 2008 · 562 citations · 13 references
Natural SciencesMaterials EngineeringMaterials ScienceMaterials ChemistryNanomaterialsPhysical ChemistryCarbon NanomaterialsElectrochemical Energy StorageGraphene NanomaterialsRedox-active MaterialsSupercapacitor MaterialsSupercapacitorsGrapheneGraphene CharacterizationGraphene Energy Storage MaterialsGraphene MaterialsGraphene SynthesisGraphene-based MaterialsRedox PropertiesX-ray Diffraction Analysis
Graphene has been prepared by different methods: pyrolysis of camphor under reducing conditions (CG), exfoliation of graphitic oxide (EG), conversion of nanodiamond (DG) and arc evaporation of SiC (SG). The samples were examined by X-ray diffraction (XRD), transmission electron microscopy, atomic force microscopy, Raman spectroscopy and magnetic measurements. Raman spectroscopy shows EG and DG to exhibit smaller in-plane crystallite sizes, but in combination with XRD results EG comes out to be better. The CG, EG and DG samples prepared by us have BET surface areas of 46, 925 and 520 m2 g−1 respectively and exhibit significant hydrogen uptake up to 3 wt%. EG also exhibits a high CO2 uptake (34.7 wt%). Electrochemical redox properties of the graphene samples have been examined in addition to their use in electrochemical supercapacitors. Functionalization of EG and DG through amidation has been carried out with the purpose of solubilizing them in non-polar solvents. Water-soluble graphene has been produced by extensive acid treatment of EG or treatment with polyethylene glycol.
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