RESUMO
A chromatographic approach for separating exfoliated graphene from natural flake graphite is presented. Graphene is an extremely strong, electrically and thermally conductive two-dimensional hexagonal array of carbon atoms with the potential to transform applications such as supercapacitors, composites, biosensors, ultra-thin touchscreens, and solar cells. However, many of these applications require the use of exfoliated graphene, and the current cost of this material can be prohibitive. The most cost-effective source of graphene is exfoliated graphite, and numerous approaches have been proposed for exfoliating graphite to graphene. Solution approaches are the most common, with graphite often exfoliated by extended sonication treatment followed by separation of graphene from graphite using centrifugation. This time-consuming approach results in low concentrations of small lateral dimension graphene, often in high-boiling-point organic solvents or containing stabilizers. In this study, a chromatographic approach is used in combination with a solvent interface trapping method of graphite exfoliation to isolate graphene. The interface trapping exfoliation approach uses a hydrophobic/hydrophilic solvent interface to spontaneously exfoliate graphite and form a graphene-stabilized water-in-oil emulsion. This emulsion contains both graphene and graphite, and when added to water-wet glass beads, graphene adsorbs onto the glass surface, leaving graphite in the hydrophobic mobile phase, where it is removed by washing with an additional oil phase. The efficiency of this scalable approach to separation is demonstrated by Raman spectroscopy, scanning electron microscopy, transmission electron microscopy, and Tyndall effect scattering.
RESUMO
Ion partitioning behavior in electrolyte solutions plays an important role in drug delivery and therapeutics, protein folding, materials science, filtration, and energy applications such as supercapacitors. Here, we show that the segregation of ions in solutions also plays an important role in the exfoliation of natural flake graphite to pristine graphene. Polarizable anions such as iodide and acetate segregate to the interfacial region of the aqueous phase during solvent interfacial trapping exfoliation of graphene. Ordered water layers and accumulated charges near the graphene surface aid in separating graphene sheets from bulk graphite, and, more importantly, reduce the reversibility of the exfoliation event. The observed phenomenon results not only in the improved stability of graphene-stabilized emulsions but also in a low-cost and environmentally friendly way of enhancing the production of graphene.