Disclosed herein is a stabilised Na-ion oxide P3 phase of formula (I): P3-Na.sub.xM.sub.yO.sub.z Where, x>0.66, 0.8≤y≤1.0, z≤2; and M is selected from one or more of the group consisting of a 3d transition metal, a 4d transition metal, Al, Mg, B, Si, Sn, Sr and Ca. The stabilised Na-ion oxide P3 phase of formula (I) may be particularly useful as an active material in a Na-ion battery.

Disclosed is a method for improving the performance of a layered electrode material. An interlayer spacing of the layered electrode material is measured and donated as (b). A salt compound is selected and added into a solvent with a molecular diameter of (c) to prepare an electrolytic solution, where a diameter (a) of a cation in the salt compound is smaller than the interlayer spacing (b), and c>b−a. The electrolytic solution is used as the working electrolytic solution for the layered electrode material.

Disclosed is a method for improving the performance of a layered electrode material. An interlayer spacing of the layered electrode material is measured and donated as (b). A salt compound is selected and added into a solvent with a molecular diameter of (c) to prepare an electrolytic solution, where a diameter (a) of a cation in the salt compound is smaller than the interlayer spacing (b), and c>b−a. The electrolytic solution is used as the working electrolytic solution for the layered electrode material.

A method for producing a positive electrode active material, a positive electrode active material produced thereby, and a positive electrode and a lithium secondary battery including the same are provided. The method includes preparing a nickel-manganese-aluminum precursor having an atomic fraction of nickel of 90 atm % or greater in all transition metals, and mixing the nickel-manganese-aluminum precursor, a cobalt raw material, and a lithium raw material and heat treating the mixture.

A method for producing a positive electrode active material, a positive electrode active material produced thereby, and a positive electrode and a lithium secondary battery including the same are provided. The method includes preparing a nickel-manganese-aluminum precursor having an atomic fraction of nickel of 90 atm % or greater in all transition metals, and mixing the nickel-manganese-aluminum precursor, a cobalt raw material, and a lithium raw material and heat treating the mixture.

The present specification relates to a method for manufacturing an electrode, an electrode manufactured by the same, an electrode structure including the electrode, a fuel cell or a metal-air secondary battery including the electrode, a battery module including the fuel cell or the metal-air secondary battery, and a composition for manufacturing an electrode.

The present specification relates to a method for manufacturing an electrode, an electrode manufactured by the same, an electrode structure including the electrode, a fuel cell or a metal-air secondary battery including the electrode, a battery module including the fuel cell or the metal-air secondary battery, and a composition for manufacturing an electrode.

A single-electrode battery subassembly includes a separator comprising an electrolyte. The separator has a first surface and an opposing second surface. A single electrode is disposed over the first surface of the separator. A removable, electrically inert substrate disposed on the second surface of the separator.

A single-electrode battery subassembly includes a separator comprising an electrolyte. The separator has a first surface and an opposing second surface. A single electrode is disposed over the first surface of the separator. A removable, electrically inert substrate disposed on the second surface of the separator.

An alkaline battery has a positive electrode mixture containing manganese dioxide and a conductive material filling a tubular positive electrode can that is closed at one end. A negative electrode mixture containing a zinc powder filling on an inner peripheral side of a separator is disposed on an inside of the positive electrode mixture. The negative electrode mixture contains zinc particles with a granularity of 75 μm or less at 25 to 40 mass %. The positive electrode mixture has a plurality of tubular pellets stacked inside the positive electrode can coaxially with the positive electrode can. A sum s of lengths of gaps between the pellets is set at 1 to 14% with respect to a sum d of lengths of the pellets. Thus, a sufficient amount of the electrolyte is held in the gaps and between the pellets in the positive electrode.