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20536 results about "Graphite oxide" patented technology

Graphite oxide, formerly called graphitic oxide or graphitic acid, is a compound of carbon, oxygen, and hydrogen in variable ratios, obtained by treating graphite with strong oxidizers. The maximally oxidized bulk product is a yellow solid with C:O ratio between 2.1 and 2.9, that retains the layer structure of graphite but with a much larger and irregular spacing.

Method for preparing graphene or graphene oxide by using high-efficiency and low-cost mechanical stripping

The invention provides a method for preparing graphene or graphene oxide by using high-efficiency and low-cost mechanical stripping and relates to a preparation method of the graphene or the graphene oxide, solving the problems that the traditional micro-mechanical stripping method has low efficiency and can not be used for large-batch production. The method comprises the following step of separating carbon materials by utilizing solid particles and a liquid working medium (or gas working medium) and adopting mechanical stripping to obtain the graphene or the graphene oxide, wherein the carbon materials comprise graphite powder, expanded graphite, expandable graphite or graphite powder oxide. By using automatic machinery and using a great deal of solid particles for assisting stripping processes, the invention greatly increases the contact areas and the stripping times of the stripping processes, the carbon materials are subject to a great amount of stripping processes in a short time through the shearing and impacting functions of the solid particles on the carbon materials, and thereby the method obviously improves the stripping efficiency, has low cost and is suitable for the industrial and large-batch production of the graphene or the graphene oxide.
Owner:HARBIN INST OF TECH

Method of producing nano-scaled graphene and inorganic platelets and their nanocomposites

Disclosed is a method of exfoliating a layered material (e.g., graphite and graphite oxide) to produce nano-scaled platelets having a thickness smaller than 100 nm, typically smaller than 10 nm, and often between 0.34 nm and 1.02 nm. The method comprises: (a) subjecting the layered material in a powder form to a halogen vapor at a first temperature above the melting point or sublimation point of the halogen at a sufficient vapor pressure and for a duration of time sufficient to cause the halogen molecules to penetrate an interlayer space of the layered material, forming a stable halogen-intercalated compound; and (b) heating the halogen-intercalated compound at a second temperature above the boiling point of the halogen, allowing halogen atoms or molecules residing in the interlayer space to exfoliate the layered material to produce the platelets. Alternatively, rather than heating, step (a) is followed by a step of dispersing the halogen-intercalated compound in a liquid medium which is subjected to ultrasonication for exfoliating the halogen-intercalated compound to produce the platelets, which are dispersed in the liquid medium. The halogen can be readily captured and re-used, thereby significantly reducing the impact of halogen to the environment. The method can further include a step of dispersing the platelets in a polymer or monomer solution or suspension as a precursor step to nanocomposite fabrication.
Owner:GLOBAL GRAPHENE GRP INC

Silicon graphene composite anode material of lithium ion battery and preparation method of silicon graphene composite anode material

The invention discloses a silicon graphene composite anode material of a lithium ion battery and a preparation method of the silicon graphene composite anode material. The material consists of the following components in percentage by weight: 10 to 99 percent of silicon powder with the particle size of between 20 nanometers and 5 micrometers, 1 to 90 percent of graphene and 0 to 40 percent of amorphous carbon, wherein the graphene forms a three-dimensional conducting network with an internal cavity, and wraps the silicon powder in the internal cavity to form spherical or sphere-like composite particles with the particle size of between 500 nanometers and 15 micrometers. The preparation method of the material comprises the following steps of: uniformly dispersing the silicon powder and graphene oxide in a solvent; and performing spray drying, reducing, and cladding by using the amorphous carbon. Compared with the prior art, the invention has the advantages that: the material has high capacity and high cycle performance and is subjected to a constant-current charge-discharge test at the current density of 200mA/g, the reversible capacity of the material after 30-times circulation is still 1502mA/g, and the capacity retention rate of the material is up to 98 percent; and the preparation method is simple and practicable, high in yield and suitable for mass industrial production.
Owner:浙江钠创新能源有限公司

Preparation method of silicon and carbon-coated graphene composite cathode material

ActiveCN103050666ARealize in situ restorationThe preparation process is simple, convenient and practicalMaterial nanotechnologyCell electrodesCarbon coatedStructural stability
The invention discloses a preparation method of a silicon and carbon-coated graphene composite cathode material. The technical problem to be solved is to enhance the electronic conductivity of the silicon-based cathode material, buffer the volume effect produced in the process of deintercalation of the lithium in the silicon-based cathode material and enhance the structure stability in the circulation process of the material at the same time. The material is prepared by using a spray drying-thermally decomposing treatment process in the invention. The preparation method comprises the following steps of: evenly dispersing nano silicon and graphite micro powder in a dispersion solution of oxidized graphene, carrying out thermal treatment under an inert protection atmosphere after spray drying, subsequently cooling along a furnace to obtain the silicon and carbon-coated graphene composite cathode material. The extra binder does not need to add in the process of manufacturing balls in the invention and the outer oxidized graphene is thermally reduced in situ to graphene in the thermal treatment process of the composite precursor, so that the process is simple and easy to operate; and the practical degree is high. The prepared composite material has the advantages of great reversible capacity, designable capacity, good cycling performance and high-current discharging performance, high tap density and the like.
Owner:CENT SOUTH UNIV
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