A resin composite material includes: fine graphite particles including plate-like graphite particles, an aromatic vinyl copolymer which is adsorbed on the plate-like graphite particles, and which contains a vinyl aromatic monomer unit represented by the following formula (1):
—(CH.sub.2—CHX)—  (1) (in the formula (1), X represents a phenyl group, a naphthyl group, an anthracenyl group, or a pyrenyl group, provided that these groups may have each a substituent), and at least one hydrocarbon chain which is bonded to the aromatic vinyl copolymer, and which is selected from the group consisting of alkyl chains, oligoolefin chains, and polyolefin chains.

A composite cathode active material, a cathode including the composite cathode active material, and a lithium battery including the cathode are provided. The composite cathode active material includes a core including a lithium metal oxide and a coating layer on the core, wherein the lithium metal oxide includes two or more transition metals including nickel (Ni), an amount of Ni within one mole of the two or more transition metals included in the lithium metal oxide is about 0.65 mol or greater, the coating layer includes LiF, and a resistance of the composite cathode active material is lower than that of the core.

Provided is a graphite plate, consisting essentially of: graphite; and pores, wherein said graphite plate has a porosity from 1% to 30%. Further provided is a method for producing a graphite plate, including: applying welding pressure to at least one glass-like carbon material in a state in which said at least one glass-like carbon material is maintained in an inert atmosphere under heating conditions, to produce a graphite plate having a porosity from 1% to 30%.

Provided is a graphite plate, consisting essentially of: graphite; and pores, wherein said graphite plate has a porosity from 1% to 30%. Further provided is a method for producing a graphite plate, including: applying welding pressure to at least one glass-like carbon material in a state in which said at least one glass-like carbon material is maintained in an inert atmosphere under heating conditions, to produce a graphite plate having a porosity from 1% to 30%.

The present disclosure provides a method of preparing graphene quantum dots by intercalation of graphite nanoparticles and continuous exfoliation in an aqueous solution. The preparation method has a short process time and uses graphite nanoparticles of several nm as a reactant. Thus, graphene quantum dots prepared by the preparation method are uniform in size and shape with minimized defects and improved electrical properties.

Oleophilic-hydrophobic-magnetic (OHM) porous materials are provided. In embodiments, an OHM porous material comprises a porous substrate having a solid matrix defining a plurality of pores distributed through the solid matrix, the OHM porous material further comprising a coating of a nanocomposite on surfaces of the solid matrix. The nanocomposite comprises a multilayer stack of a plurality of layers of a two-dimensional, layered material having nucleation sites interleaved between a plurality of layers of magnetic nanoparticles, wherein individual layers of magnetic nanoparticles in the plurality of layers of magnetic nanoparticles are each directly anchored on a surface of a layer of the plurality of layers of the two-dimensional, layered material via the nucleation sites, and are each separated by multiple layers of the plurality of layers of the two-dimensional, layered material. Methods of making and using the OHM porous materials are also provided.

A graphene dispersion is provided. The graphene dispersion is formed by a graphene powder and a processing solvent, wherein the graphene in the graphene dispersion has an average diameter of 0.5 μm to 1 μm, 3 to 5 layers, a solid content of 5% to 50%, and a residue oxygen content less than 1 wt %, and after being left to stand for 12 hours, the graphene dispersion has a distribution concentration increasing from the top section to the bottom section of the storage container, a viscosity of 5000 cps to 8000 cps, and a graphene concentration of 20 wt %.

A graphene dispersion is provided. The graphene dispersion is formed by a graphene powder and a processing solvent, wherein the graphene in the graphene dispersion has an average diameter of 0.5 μm to 1 μm, 3 to 5 layers, a solid content of 5% to 50%, and a residue oxygen content less than 1 wt %, and after being left to stand for 12 hours, the graphene dispersion has a distribution concentration increasing from the top section to the bottom section of the storage container, a viscosity of 5000 cps to 8000 cps, and a graphene concentration of 20 wt %.

A method of preparing a soft carbon material for high-voltage supercapacitors includes: providing an initial soft carbon material characterized by: (A) a first carbon layer spacing greater than 0.345 nm but less than 0.360 nm; (B) a crystal plane (002) with a length (L.sub.c) less than 6 nm; (C) a crystal plane (101) with a length (L.sub.a) less than 6 nm; and (D) an intensity ratio (I.sub.(002)/I.sub.(101)) of the crystal plane (002) to the crystal plane (101) obtained by XRD analysis being less than 60; performing an alkaline activation on the initial soft carbon material with an alkaline activator to obtain a first processing carbon material; and performing an electrochemical activation on the first processing carbon material with an electrolyte to obtain the soft carbon material for the high-voltage supercapacitors.

The present invention provides a method for preparation of sulfur functionalized graphene which contains the following steps: a) providing a dispersion of fluorinated graphite; b) subjecting the dispersion of fluorinated graphite to sonication and/or mechanical treatment and/or thermal treatment; c) preparing a metal polysulfide, starting from a metal sulfide and sulfur; d) contacting the product from step b) with the product of step c) at a temperature within the range of 10-110° C.; e) separating the solid product formed in step d) from the solution. Further provided are sulfur functionalized graphene with high sulfur loading obtained by this method, and its use in electrical cells.