Provided is an energy storage apparatus capable of appropriately controlling use of a silicon material in normal times and achieving long life, and a method of using the energy storage apparatus. One aspect of the present invention is an energy storage apparatus that includes an energy storage device and a measuring section for measuring an internal pressure change rate of the energy storage device, the energy storage device having a negative electrode that contains a carbon material and a silicon material. Another aspect of the present invention is a method of using the energy storage apparatus that includes performing discharge while the internal pressure change rate of the energy storage device is measured.

Provided is an energy storage apparatus capable of appropriately controlling use of a silicon material in normal times and achieving long life, and a method of using the energy storage apparatus. One aspect of the present invention is an energy storage apparatus that includes an energy storage device and a measuring section for measuring an internal pressure change rate of the energy storage device, the energy storage device having a negative electrode that contains a carbon material and a silicon material. Another aspect of the present invention is a method of using the energy storage apparatus that includes performing discharge while the internal pressure change rate of the energy storage device is measured.

The present invention discloses a method for lead carbon compression moulding comprising a first stacking step and a first compressing step so that a lead-carbon electrode is obtained through compressing a lead-carbon sandwich stacked of a lead material and a carbon material. Pressurization of the working environment or heating both the lead material and the carbon material is not required during the procedure. A massive production of lead-carbon electrode at room temperature can be anticipated. The lead-carbon electrode produced thereby enhance tolerance of the battery against instable electric current or voltage, and performance remains steady after multiple times of charge-discharge cycles. The lead-carbon electrode produced thereby demonstrates high potentials for application with low cost, low loss and high capacity.

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.

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.

Hybrid lithium-ion electrochemical cells include a first electrode having a first polarity and a first electroactive material that reversibly cycles lithium ions having a first maximum operational voltage and a second electrode having the first polarity with a second electroactive material having a second maximum operational voltage. A difference between the second and first maximum operational voltages defines a predetermined voltage difference. Also included are at least one third electrode including a third electroactive material that reversibly cycles lithium ions having a second polarity opposite to the first polarity, a separator, and electrolyte. A voltage modification component (e.g., diode) is in electrical communication with the first and the second electrodes. In a first operational state corresponding to charging, the at least one voltage modification component is configured to induce a voltage drop corresponding to the predetermined voltage difference providing high power density and high energy density hybrid lithium-ion electrochemical cells.

Hybrid lithium-ion electrochemical cells include a first electrode having a first polarity and a first electroactive material that reversibly cycles lithium ions having a first maximum operational voltage and a second electrode having the first polarity with a second electroactive material having a second maximum operational voltage. A difference between the second and first maximum operational voltages defines a predetermined voltage difference. Also included are at least one third electrode including a third electroactive material that reversibly cycles lithium ions having a second polarity opposite to the first polarity, a separator, and electrolyte. A voltage modification component (e.g., diode) is in electrical communication with the first and the second electrodes. In a first operational state corresponding to charging, the at least one voltage modification component is configured to induce a voltage drop corresponding to the predetermined voltage difference providing high power density and high energy density hybrid lithium-ion electrochemical cells.

A current collector of an electrochemical actuator is proposed, the current collector being coated with an interfacing layer, the interfacing layer being formed by coating on the current collector with a composition, the composition being formed by particles, at least 50% of the particles having a mean diameter by volume of less than or equal to 10 micrometers.

A current collector of an electrochemical actuator is proposed, the current collector being coated with an interfacing layer, the interfacing layer being formed by coating on the current collector with a composition, the composition being formed by particles, at least 50% of the particles having a mean diameter by volume of less than or equal to 10 micrometers.

An objective is to provide a novel aqueous electrolytic solution constituting an aqueous power storage device that stably operates even at a high voltage.

An electrolytic solution for a power storage device contains water as a solvent and has a composition in which an amount of the solvent is not greater than 4 mol with respect to 1 mol of an alkali metal salt.