According to the invention there is provided an electrothermic composition comprising: a carbon component; a graphite component having a crystallinity of 99.9% and wherein the graphite is heat treated at a temperature of 2500° C. to 3000° C., and a binder, whereby the composition has a thermal coefficient of electrical resistance (TCR) of ±0.0001 to 0.0010 per ° C. over a temperature range of from about 20° C. to 60° C. in an airborne environment, wherein the ratio of the first conductive component and the second resistor component is selected between 10:1 to 1:10.

A negative electrode for a lithium ion secondary battery includes: a negative electrode current collector (11); and a negative electrode active material for a lithium ion secondary battery, which is disposed on the negative electrode current collector and contains a carbon material and an aqueous binder. The carbon material is a graphite particle having a covering layer containing amorphous carbon by 5 wt % or less relative to a total weight of the carbon material.

Provided is a negative electrode for a lithium ion secondary battery including: a negative electrode current collector; and a negative electrode active material for a lithium ion secondary battery which is disposed on the negative electrode current collector and contains a carbon material and an aqueous binder. The carbon material is a graphite particle having a covering layer containing amorphous carbon by 5 wt % or less relative to a total weight of the carbon material

Provided is a carbon material capable of obtaining a non-aqueous secondary battery, which has high capacity, initial efficiency, and low charging resistance and is excellent in productivity. As a result thereof, a high-performance non-aqueous secondary battery is stably provided with efficiency. A composite carbon material for a non-aqueous secondary battery is provided, which contains at least a bulk mesophase artificial graphite particle (A) and graphite particle (B) having an aspect ratio of 5 or greater, and which is capable of absorbing and releasing lithium ions. A graphite crystal layered structure of the graphite particle (B) is arranged in the same direction as a direction of an outer peripheral surface of the bulk mesophase artificial graphite particle (A) at a part of a surface of the bulk mesophase artificial graphite particle (A), and an average circularity of the composite carbon material is 0.9 or greater.

A non-flaky carbon material having specific optical structures, wherein the ratio between the peak intensity I110 of (110) plane and the peak intensity I004 of (004) plane of a graphite crystal determined by the powder XRD measurement, I110/I004, is 0.10 or more and 0.35 or less; an average circularity is 0.80 or more and 0.95 or less; d002 is 0.337 nm or less; and the total pore volume of pores having a diameter of 0.4 μm or less measured by the nitrogen gas adsorption method is 25.0 μl/g or more and 40.0 μl/g or less. Also disclosed is a method for producing the carbon material, a carbon material for a battery electrode, a paste for an electrode incorporating the carbon material for a battery electrode, an electrode for a lithium battery incorporating a formed body of the paste for an electrode, a lithium-ion secondary battery including the electrode and a method for producing the electrode.

Embodiments described herein relate generally to large scale synthesis of thinned graphite and in particular, few layers of graphene sheets and graphene-graphite composites. In some embodiments, a method for producing thinned crystalline graphite from precursor crystalline graphite using wet ball milling processes is disclosed herein. The method includes transferring crystalline graphite into a ball milling vessel that includes a grinding media. A first and a second solvent are transferred into the ball milling vessel and the ball milling vessel is rotated to cause the shearing of layers of the crystalline graphite to produce thinned crystalline graphite.

Embodiments described herein relate generally to large scale synthesis of thinned graphite and in particular, few layers of graphene sheets and graphene-graphite composites. In some embodiments, a method for producing thinned crystalline graphite from precursor crystalline graphite using wet ball milling processes is disclosed herein. The method includes transferring crystalline graphite into a ball milling vessel that includes a grinding media. A first and a second solvent are transferred into the ball milling vessel and the ball milling vessel is rotated to cause the shearing of layers of the crystalline graphite to produce thinned crystalline graphite.

Described are systems and methods of storing adsorbing diborane on carbon adsorption medium.

Described are systems and methods of storing adsorbing diborane on carbon adsorption medium.

An anode active material, and an electrochemical device and electronic device using such anode active material. Also, an anode active material, including graphite. Controlling a graphitization degree of particles of different particle sizes of the anode active material can achieve a balance between kinetic performance and first cycle efficiency of the electrochemical device.