Non-graphitizing carbons (NGCs) are an important class of solid carbons which cannot be converted into graphite by high-temperature heat treatment. They include commercially valuable materials such as activated carbon and glassy carbon. These carbons have been intensively studied for decades, but there is still no agreement about their detailed atomic structure, or the reasons for their resistance to graphitization. The first models for graphitizing and NGCs were proposed by Rosalind Franklin in the early 1950s, and while these are broadly correct, they are incomplete. Many alternative models of NGCs have been put forward since Franklin's time, but none has received universal acceptance. Diffraction and spectroscopic techniques can provide important insights into the nature of these carbons, but only direct microscopic imaging can reveal their true atomic structure. Here, we apply aberration-corrected transmission electron microscopy to an activated carbon prepared from waste biomass and present evidence for the presence of pentagonal and heptagonal carbon rings. This provides support for a model of the structure of NGC made up of curved fragments in which non-hexagonal rings are dispersed randomly throughout hexagonal networks.

The chemical exfoliation of graphite to produce graphene and its oxide is undoubtedly an economical method for scalable production. Carbon researchers have dedicated significant resources to developing new exfoliation methods leads to graphene oxides with high quality. However, only a few studies have been dedicated to the effect of the starting graphite material on the resulting GO. Herein, we have prepared two different GOs through chemical exfoliation of graphite materials having different textural and structural characteristics. All samples have been subjected to structural investigations and comprehensive characterizations using Raman, X-ray diffraction, scanning electron microscopy, TGA, N₂ physisorption, and FTIR spectroscopy. Our results provide direct evidence of how the crystallite size of the raw graphite affects the oxidation degree, surface functionality, and sheet size of the resulting GO. Building on these significant understandings, the optimized GO achieves a highly specific capacitance of 191 F·g⁻¹ at the specific current of 0.25 A·g⁻¹ in an aqueous electrolyte. This superior electrochemical performance was attributed to several factors, among which the specific surface area was accessible to the electrolyte ions and oxygenated functional groups on the surface, which can significantly modify the electronic structure of graphene and further enhance the surface energy.