An example method includes providing coal and extracting the graphene from the coal. The graphene may be extracted using any suitable technique, such as the Hummers method, a modified Hummers method, or exfoliation of graphite. The graphene may include impurities or other electrical properties that depend at least partially on the composition of the coal. The method may further include forming a life science device from the graphene. The life science device may include, for example, a biosensor or a drug delivery system.

A voltage tunable solar-blind UV detector using a EG/SiC heterojunction based Schottky emitter bipolar phototransistor with EG grown on p-SiC epi-layer using a chemically accelerated selective etching process of Si using TFS precursor.

The present disclosure provides a dispersible graphene platelet and a method of making same. The structure of the graphene platelet 10 comprises a base layer 1 of graphene on which at least one discontinuous layer 2, 3, 4 of graphene is stacked, with each layer of graphene above the base layer having a smaller surface area than the layer it is stacked upon. The edges of the base layer and the discontinuous layers stacked upon it are all at least partially functionalised 5, providing a structure with graphene-like properties owing to the base layer and relatively high dispersibility owing to the increased amount of functionalised groups on each platelet. The platelets may be used for a number of applications, for example in the production of electrodes or composite materials.

Provided are methods of directly growing a carbon material. The method may include a first operation and a second operation. The first operation may include adsorbing carbons onto a substrate by supplying the carbons to the substrate. The second operation may include removing unreacted carbon residues from the substrate after suspending the supplying the carbons of the first operation. The two operations may be repeated until a desired graphene is formed on the substrate. The substrate may be maintained at a temperature less than 700° C. In another embodiment, the method may include forming a carbon layer on a substrate, removing carbons that are not directly adsorbed to the substrate on the carbon layer, and repeating the two operations until desired graphene is formed on the substrate. The forming of the carbon layer includes supplying individual carbons onto the substrate by preparing the individual carbons.

The invention relates to the production of carbon nanomaterials, for example graphene, and can be used to produce graphene for use in nanoelectronics. Graphene is produced by stratifying graphite particles, differing in that graphite particles undergo electrodynamic fluidization in a vacuum in which the energy of the graphite particles exceeds the work necessary for their cleavage along the cleavage planes on graphene layers during brittle fracture when striking against the electrodes. The method makes it possible to obtain graphene with high productivity, economy and purity of the product.

A graphene product obtained from Graphene Nanofibers (GNFs), having a modified crystal structure and a defined size distribution. The product is non-toxic and has useful biological properties such as wound healing and improving skin appearance. The product can be used in therapy.

A method for the manufacture of pristine graphite from Kish graphite including three different steps A, B and C; the pristine obtained with among others a high amount of carbon atoms, i.e. a pristine graphene having a high purity; and the use of this pristine graphene.

A method for the manufacture of reduced graphene oxide from Kish graphite including the pretreatment of kish graphite, the oxidation of pre-treated kish graphite into graphene oxide and the reduction of graphene oxide into reduced graphene oxide, the reduced graphene oxide and the use of the graphene oxide.

A method for the manufacture of graphene oxide from Kish graphite including the pretreatment of kish graphite and the oxidation of pre-treated kish graphite into graphene oxide, the graphene oxide obtained with at least 45% by weight of oxygen functional groups and the use of the graphene oxide.

Graphene is a single layer carbon-based material known for high strength, high flexibility, high electrical conductivity, high surface area, hydrophobicity and barrier property. Introduction of surface functional groups on graphene enhances most of these properties. A facile and economical process to prepare amine and fluoride functionalized graphenes is disclosed. The disclosed processes utilize direct functionalization of pristine graphene without pre-functionalization (GO). Successful functionalization of both aminated and fluorinated graphenes were confirmed by the analyses of FT-IR, thermal gravimetric analysis (TGA), Raman, UV-Vis, and dispersion study. Amine functional groups can react with epoxy resin and urethane resin to form a covalent bond, and fluorinated graphene can give high hydrophobicity and durability, therefore both can be applied as a material or a component in polymer and composite coatings for corrosion protection, moisture or gas barriers.