A manufacturing method of a porous carbon composite material includes the following steps. A polymer template is provided, the polymer template includes a polymer compound, and the polymer template has a plurality of pores. A coating step is performed, wherein a metal compound is coated on the polymer template to form a transition intermediate. A heating step is performed, wherein the transition intermediate is heated to transform the polymer template to a carbon template and transform the metal compound to a coating layer, and a porous carbon composite material is obtained.

A manufacturing method of a porous carbon composite material includes the following steps. A polymer template is provided, the polymer template includes a polymer compound, and the polymer template has a plurality of pores. A coating step is performed, wherein a metal compound is coated on the polymer template to form a transition intermediate. A heating step is performed, wherein the transition intermediate is heated to transform the polymer template to a carbon template and transform the metal compound to a coating layer, and a porous carbon composite material is obtained.

A method of producing graphite may include beneficiating an amount of coal to form a coal char, grinding the coal char to produce a crushed char and placing the crushed char in a porous container. Then, the method includes immersing the porous container in a molten salt bath. The molten salt bath includes a graphite anode. The method further includes applying an electrical potential across the porous container and the graphite anode such that a graphite deposit forms on the graphite anode. The graphite anode is removed from the molten salt bath and the graphite deposit is separated from the graphite anode to produce graphite fragments.

A method of producing graphite may include beneficiating an amount of coal to form a coal char, grinding the coal char to produce a crushed char and placing the crushed char in a porous container. Then, the method includes immersing the porous container in a molten salt bath. The molten salt bath includes a graphite anode. The method further includes applying an electrical potential across the porous container and the graphite anode such that a graphite deposit forms on the graphite anode. The graphite anode is removed from the molten salt bath and the graphite deposit is separated from the graphite anode to produce graphite fragments.

Provided is a laminated graphitic layer as an elastic heat spreader, the layer comprising: (A) a plurality of graphitic or graphene films prepared from (i) graphitization of a polymer film or pitch film, (ii) aggregation or bonding of graphene sheets, or (iii) a combination of (i) and (ii), wherein the graphitic or graphene film has a thermal conductivity of at least 200 W/mK, an electrical conductivity no less than 3,000 S/cm, and a physical density from 1.5 to 2.25 g/cm.sup.3; and (B) a conducting polymer network adhesive that bonds together the graphitic or graphene films to form the laminated graphitic layer; wherein the conductive polymer network adhesive is in an amount from 0.001% to 30% by weight and wherein the laminated graphitic layer preferably has a fully recoverable tensile elastic strain from 1% to 50% and an in-plane thermal conductivity from 100 W/mK to 1,750 W/mK.

A graphite composition is provided. A graphite composition according to one embodiment of the present invention comprises: a graphite composite in which nanoparticles having a catecholamine layer on the surface thereof are fixed on graphite; and graphite of at least one of graphite flakes, spherical graphite, and expanded graphite. According to this, since the graphite composition has a high dispersibility in a substrate of a different material, a composite material thus realized exhibits a uniform heat dissipation performance and can prevent mechanical strength from deteriorating at a specific position. In addition, since the compatibility with the substrate of a different material is excellent and thus the interface property with the substrate is excellent, the realized composite material can exhibit a further improved heat dissipation performance and mechanical strength. Furthermore, it is very easy to form shapes during injection/extrusion molding in combination with a substrate, and molding into complicated shapes is also possible.

A graphite composition is provided. A graphite composition according to one embodiment of the present invention comprises: a graphite composite in which nanoparticles having a catecholamine layer on the surface thereof are fixed on graphite; and graphite of at least one of graphite flakes, spherical graphite, and expanded graphite. According to this, since the graphite composition has a high dispersibility in a substrate of a different material, a composite material thus realized exhibits a uniform heat dissipation performance and can prevent mechanical strength from deteriorating at a specific position. In addition, since the compatibility with the substrate of a different material is excellent and thus the interface property with the substrate is excellent, the realized composite material can exhibit a further improved heat dissipation performance and mechanical strength. Furthermore, it is very easy to form shapes during injection/extrusion molding in combination with a substrate, and molding into complicated shapes is also possible.

A negative electrode material for a lithium-ion secondary cell, comprising carbon particles having an oxygen content of 0.15% by mass or less.

A negative electrode material for a lithium-ion secondary cell, comprising carbon particles having an oxygen content of 0.15% by mass or less.

Provided is a carbon material for a negative electrode of a lithium ion secondary battery, which has a small particle diameter, high initial charge-discharge efficiency, and a high 2C discharge rate, and achieves both input-output characteristics and durability. Disclosed is a carbon material for a negative electrode of a lithium ion secondary battery, in which a 50% by volume particle diameter in a cumulative frequency distribution is 1.0 μm or more and less than 5.0 μm, a specific surface area by a BET method is 6.5 m.sup.2/g or less, a tap density (D.sub.TAP) is 0.70 g/cm.sup.3 or more, and a Raman R value obtained by Raman spectroscopy is more than 0.100 and less than 0.300, and the carbon material has a carbonaceous film on a surface of graphitized material particles of a mesophase microbead.