The present invention relates to a carbonaceous material which is derived from a plant, having a specific surface area of 1800 to 3000 m.sup.2/g as measured by a BET method, a hydrogen element content of 0.42% by mass or less and an oxygen element content of 1.5% by mass or less.

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.

The present disclosure relates to solid-state electrolytes and methods of making the same. The method includes admixing a sulfate precursor including one or more of Li.sub.2SO.sub.4 and Li.sub.2SO.sub.4.H.sub.2O with one or more carbonaceous capacitor materials. The first admixture is calcined to form an electrolyte precursor that is admixed with one or more additional components to form the solid-state electrolyte. When a ratio of the sulfate precursor to the one or more carbonaceous capacitor materials in the first admixture is about 1:2, the electrolyte precursor consists essentially of Li.sub.2S. When a ratio of the sulfate precursor to the one or more carbonaceous capacitor materials in the first admixture is less than about 1:2, the electrolyte precursor is a composite precursor including a solid-state capacitor cluster including the one or more carbonaceous capacitor materials and a sulfide coating including Li.sub.2S disposed on one or more exposed surfaces of the solid-state capacitor cluster.

The present application is directed to methods for solvent-free preparation of polymers and their subsequent processing into activated carbon materials. These methods unexpectedly demonstrate ability to tune pore structure in the polymer gel and carbon produced there from, while also providing distinct advantages over the current art.

The present application is directed to methods for solvent-free preparation of polymers and their subsequent processing into activated carbon materials. These methods unexpectedly demonstrate ability to tune pore structure in the polymer gel and carbon produced there from, while also providing distinct advantages over the current art.

A nitrogen-doped porous carbon material and a preparation method and an application thereof; wherein the nitrogen-doped porous carbon material has a specific surface area of 1600-3500 m.sup.2.Math.g.sup.−1, mesopores with a pore size of 2-50 nm account for 20-40% of all pores, an average pore size is 2-20 nm, and a mass fraction of nitrogen atoms in the porous carbon material is 13.6-19.3 wt %. When being used as a supercapacitor material, the porous carbon material has a larger specific capacitance and a better capacitance retention rate. At a current density of 0.1 A.Math.g.sup.−1, the porous carbon material has a specific capacitance of about 847 F.Math.g.sup.−1. After 5000 cycles of charging and discharging, the capacitance retention rate is about 99.7%. Moreover, the porous carbon material features an excellent pore structure distribution, thus providing good CO.sub.2 adsorption performance.

A nitrogen-doped porous carbon material and a preparation method and an application thereof; wherein the nitrogen-doped porous carbon material has a specific surface area of 1600-3500 m.sup.2.Math.g.sup.−1, mesopores with a pore size of 2-50 nm account for 20-40% of all pores, an average pore size is 2-20 nm, and a mass fraction of nitrogen atoms in the porous carbon material is 13.6-19.3 wt %. When being used as a supercapacitor material, the porous carbon material has a larger specific capacitance and a better capacitance retention rate. At a current density of 0.1 A.Math.g.sup.−1, the porous carbon material has a specific capacitance of about 847 F.Math.g.sup.−1. After 5000 cycles of charging and discharging, the capacitance retention rate is about 99.7%. Moreover, the porous carbon material features an excellent pore structure distribution, thus providing good CO.sub.2 adsorption performance.

A capacitive coupler provides high coupling capacitance through the use of an electrical double layer formed on opposite plates of the coupler. The coupler can be independent or provide a hydrodynamic or hydrostatic bearing as well as capacitive coupling and the circulated dielectric can provide for cooling of associated machinery.

A method for hydrolyzing cellulose into sugar to produce spherical capacitive carbon for the deep utilization of biomass and carbon materials. The present disclosure includes the following steps of: (1) crude cellulose pretreatment; (2) alkaline hydrolysis of cellulose; (3) separation of the cellulose from a hydrolyzed sugar liquor; (4) drying of an alkali-containing hydrolyzed sugar; (5) sintering of spherical capacitive carbon; (6) capacitive carbon post-processing; and (7) alkali recycling. In the method, biomass is used as a raw material, high-purity cellulose and hydrolyzed sugar are obtained through deep hydrolysis, the spherical capacitive carbon is sintered with the hydrolyzed sugar instead of sucrose and starch, and alkali is recycled. Pollution and waste are not generated, and more than 80% of the alkali can be recycled.