Disclosed herein is a composite material that is formed from a polymer, acetylated collagen and graphene, which can be used as a super-capacitor material. Also disclosed herein are methods of making said composite material and its intermediates, as well as a supercapacitor made using said material.

Materials and methods for preparing electrode film mixtures and electrode films including reduced damage bulk active materials are provided. In a first aspect, a method for preparing an electrode film mixture for an energy storage device is provided, comprising providing an initial binder mixture comprising a first binder and a first active material, processing the initial binder mixture under high shear to form a secondary binder mixture, and nondestructively mixing the secondary binder mixture with a second portion of active materials to form an electrode film mixture.

Materials and methods for preparing electrode film mixtures and electrode films including reduced damage bulk active materials are provided. In a first aspect, a method for preparing an electrode film mixture for an energy storage device is provided, comprising providing an initial binder mixture comprising a first binder and a first active material, processing the initial binder mixture under high shear to form a secondary binder mixture, and nondestructively mixing the secondary binder mixture with a second portion of active materials to form an electrode film mixture.

An electricity storage device includes a negative electrode having a layered structure that includes an organic backbone layer containing an aromatic compound having an aromatic ring structure, the aromatic compound being in the form of dicarboxylate anions, and an alkali metal element layer containing an alkali metal element coordinated with oxygen in the dicarboxylate anions to form a backbone, a positive electrode that provides electric double-layer capacity, and a nonaqueous electrolyte solution provided between the negative electrode and the positive electrode, the nonaqueous electrolyte solution containing an alkali metal salt. The layered structure may be provided in layers by a π-electron interaction of the aromatic compound and may have a monoclinic crystal structure belonging to the space group P2.sub.1/c. The positive electrode may contain activated carbon having a specific surface area of 1,000 m.sup.2/g or more.

An object of the present invention is to provide a carbonaceous material used for an electric double layer capacitor having a high electrostatic capacity and capable of maintaining the high electrostatic capacity and energy density over a long period and a method for producing the same. The present invention relates to a carbonaceous material having a specific surface area of 1,200 m.sup.2/g to 1,800 m.sup.2/g according to a BET method, an R-value of 1.2 or more and a G-band half-value width of 70 cm.sup.−1 or more according to a Raman spectrum.

An object of the present invention is to provide a carbonaceous material used for an electric double layer capacitor having a high electrostatic capacity and capable of maintaining the high electrostatic capacity and energy density over a long period and a method for producing the same. The present invention relates to a carbonaceous material having a specific surface area of 1,200 m.sup.2/g to 1,800 m.sup.2/g according to a BET method, an R-value of 1.2 or more and a G-band half-value width of 70 cm.sup.−1 or more according to a Raman spectrum.

Disclosed herein is a composition comprising a shell that is substantially carbon encapsulating a volume that contains a nanoform of silicon and a void space. Disclosed herein too is a method of fabricating a composition comprising combining a nanoform of silicon with a carbon precursor and sintering the combination with a laser.

A system and method are provided to create porous surface coatings. In use, a material layer includes synthesized carbon-containing composite materials, wherein the synthesized carbon-containing composite materials comprise a porosity characteristic, and at least one of: heat transfer characteristics, resistance to corrosion characteristics, or non-ablative erosion characteristics. Additionally, a bonding layer comprising at least some of the synthesized carbon-containing composite materials is bonded by at least one of, a carbon-to-carbon bond, or a metal-to-carbon bond to a substrate. Further, a surface interfacial layer comprising at least some of the synthesized carbon-containing composite materials is hydraulically smooth.

The process comprises treating 90-190 g titanium (IV) chloride in 10-100 ml de-ionized water for preparing Titanium cation (Ti.sup.4+); treating 130-275 ml potassium persulfate in 10-100 ml double-distilled water and keeping at constant temperature to obtain sulphate/oxide; dipping substrates into titanium (IV) chloride solution and re-dipping in de-ionized water to remove loosely bonded ions, if could be any; dipping substrates into potassium persulfate solution and re-dipping in de-ionized water to remove loosely bonded ions, if could be any, and keeping at 50-90° C. for complete one cycle; treating obtained Titanium cation (Ti.sup.4+) with sulphate/oxide and obtaining whitish layer on the substrate surface by necked eyes after about 10-15 cycles, suggesting initiation of film formation, wherein the deposition thickness of TiO.sub.2 layer is increased from 0.3-2.0-micron on determined 5-50 deposition cycles; and rinsing deposited films with de-ionized water and air annealed at 400-600° C. temperature to obtain anatase TiO.sub.2.

The process comprises treating 90-190 g titanium (IV) chloride in 10-100 ml de-ionized water for preparing Titanium cation (Ti.sup.4+); treating 130-275 ml potassium persulfate in 10-100 ml double-distilled water and keeping at constant temperature to obtain sulphate/oxide; dipping substrates into titanium (IV) chloride solution and re-dipping in de-ionized water to remove loosely bonded ions, if could be any; dipping substrates into potassium persulfate solution and re-dipping in de-ionized water to remove loosely bonded ions, if could be any, and keeping at 50-90° C. for complete one cycle; treating obtained Titanium cation (Ti.sup.4+) with sulphate/oxide and obtaining whitish layer on the substrate surface by necked eyes after about 10-15 cycles, suggesting initiation of film formation, wherein the deposition thickness of TiO.sub.2 layer is increased from 0.3-2.0-micron on determined 5-50 deposition cycles; and rinsing deposited films with de-ionized water and air annealed at 400-600° C. temperature to obtain anatase TiO.sub.2.