Helical-ribbon carbon nanofibers produced on an industrial scale were successfully converted in highly functionalized graphene nanoplatelets by using a slight modification of the Hummers oxidation method.The duration of the oxidative process severely affected the interlayer spacing in the resulting nanoplatelets and, consequently, they showed very different exfoliation behavior. Therefore, it was possible to obtain a variety of graphene-related products through their ultrasonication or thermal treatments such as exfoliation-reduction by flash-pyrolysis in air at temperatures between 400 and 1000 C or standard activation with CO 2 at 800 C. Detailed comparison of the functionalized carbon nanoplatelets, graphene oxides, reduced graphene oxides and activated carbon nanoplatelets reveals the wide spectrum of their properties with specific surface areas in the range of 4-500 m 2 g À1 , oxygen content from 38 to 5 wt% and different structural ordering. This study also underlines the impact of the structural, textural and chemical changes experienced by the carbon nanofibers along the various processes on the performance as supercapacitor electrodes. This preliminary study, based on cyclic voltammetry in 2 M H 2 SO 4 aqueous electrolyte, is a summary of the strengths and weaknesses of the different graphene-related materials for this application. The helical-ribbon carbon nanofibers displayed only 10 F g À1 , the capacitance of the functionalized graphene nanoplatelets greatly rose to 104 F g À1 with clear contributions from pseudocapacitance. Values around 100-120 F g À1 were found for the graphene oxides and activated graphene nanoplatelets although a marked resistive character is detected.Flash-pyrolysis at 1000 C leads to lower capacitance (79 F g À1 ) but much quicker charge propagation.Among all these materials, the lower-cost functionalized graphene nanoplatelets displayed the better behavior for aqueous supercapacitors.