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.

Graphene-based conductive ink and a preparation thereof. The graphene-based conductive ink includes a modified graphene nanomaterial, a first solvent and an ink binder. The modified graphene nanomaterial is prepared by subjecting a mixture of sodium sulfanilate, a natural flake graphite and a second solvent to liquid phase exfoliation. The second solvent is a mixture of water and a second alcohol.

The present disclosure provides a method for repairing defect of graphene, including: firstly introducing a composite fluid containing a reactive compound and a supercritical fluid to a reactor where the graphene powder has been placed, and impregnating the graphene powder with the composite fluid to passivate and repair the defect of graphene, wherein the reactive compound includes carbon, hydrogen, nitrogen, silicon or oxygen element; and separating the composite fluid from the graphene powder, simultaneously using molecular sieves to absorb the graphene from the composite fluid. The present disclosure further provides the graphene powder prepared by the method above. With the method of the present disclosure, it effectively reduces the ratio of the defect of the graphene, increases the content of the graphene, and has less-layer graphene with high thermal conductivity and electrical conductivity.

A conductive fiber including a metal-nanobelt-carbon-nanomaterial composite. A manufacturing method thereof includes preparing a composite including a carbon nanomaterial and metal nanobelts and manufacturing a conductive fiber by mixing the composite with a polymer. A fibrous strain sensor and a manufacturing method thereof are also provided. Thereby, a conductive fiber including a metal-nanobelt-carbon-nanomaterial composite, which is able to increase conductivity of the conductive fiber through synthesis of metal nanobelts enabling area contact and to exhibit good contact between the carbon nanomaterial and the metal nanobelts due to formation of the metal nanobelts on the surface of the carbon nanomaterial and superior dispersion uniformity, and a fibrous strain sensor including the conductive fiber can be obtained. The conductive fiber can be effectively applied to a strain sensor based on a principle by which resistance drastically increases with an increase in a distance between metal nanobelts aligned in a fiber direction upon tensile strain of metal nanobelts enabling area contact.

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.

This disclosure provides a sensor for detecting an analyte. The sensor can include an antenna and sensing material both disposed on a substrate, where the sensing is electrically coupled to the antenna. The sensing material can include a carbon structure including a multi-modal distribution of pore sizes that define a surface area including bonding sites configured to interact with one or more additives and the analyte. The carbon structure is configured to generate a resonant signal indicative of one or more characteristics of the analyte in response to an electromagnetic signal. The carbon structure can include distinctly sized interconnected channels defined by the surface area and configured to be infiltrated by the analyte, and exposed surfaces configured to adsorb the analyte. Each of the interconnected channels can include microporous pathways and/or mesoporous pathways, which can increase a responsiveness of the sensing material proportionate to the analyte within the carbon structure.

A material that can be used in a wide temperature range is provided. A graphene compound includes graphene or graphene oxide and a substituted or unsubstituted chain group, the chain group includes two or more ether bonds, and the chain group is bonded to the above graphene or graphene oxide through a Si atom. Alternatively, a method for forming a graphene compound includes a first step and a second step after the first step. In the first step, graphene oxide and a base are stirred under a nitrogen stream. In the second step, the mixture is cooled to room temperature, a silylating agent that has a group having two or more ether bonds is introduced into the mixture, and the obtained mixture is stirred. The base is butylamine, pentylamine, hexylamine, diethylamine, dipropylamine, dibutylamine, triethylamine, tripropylamine, or pyridine.

A process for preparing a graphene nanomaterial product, the process comprising: cavitating a liquid medium comprising a diaromatic hydrocarbon component to synthesise from the diaromatic hydrocarbon component a dispersion of graphene nanomaterial in the liquid medium; and obtaining a graphene nanomaterial product from the dispersion.

Provided are a graphene and a preparation method therefor. The method for preparing a graphene comprises following steps: i) placing a mixture of a magnesium powder and a solid oxide powder in a carbon dioxide-containing environment; and ii) heating the mixture to enable the magnesium powder to react with carbon dioxide, thereby obtaining a graphene. The specific surface area of the grapheme is 350-750 m.sup.2/g, and the pore volume is 1-2 cm.sup.3/g. The method for preparing a graphene in the present invention is simple and easy to carry out, and has a low cost and a high yield; and the graphene product has few impurities, a high carbon-oxygen ratio, and excellent capacitance performance and electrochemical stability.

Provided is a process for producing a graphene-based supercapacitor electrode from a supply of coke or coal powder, comprising: (a) exposing this powder to a supercritical fluid for a period of time in a pressure vessel to enable penetration of the supercritical fluid into internal structure of the coke or coal; wherein the powder is selected from petroleum coke, coal-derived coke, meso-phase coke, synthetic coke, leonardite, anthracite, lignite coal, bituminous coal, or natural coal mineral powder, or a combination thereof; (b) rapidly depressurizing the supercritical fluid at a fluid release rate sufficient for effecting exfoliation and separation of the coke or coal powder to produce isolated graphene sheets, which are dispersed in a liquid medium to produce a graphene suspension; and (c) shaping and drying the graphene suspension to form the supercapacitor electrode having a specific surface area greater than 200 m.sup.2/g.