Provided is a secondary battery electrode having a sufficient peel strength between a base material and a material mixture layer without the need for increasing a binder addition amount. A secondary battery electrode includes a base material and a material mixture layer made of an electrode material mixture containing an active material and a binder. The material mixture layer has a multilayer structure of at least two or more layers stacked on the base material. In the multilayer structure of the material mixture layer, a first material mixture layer stacked on a surface of the base material has a higher contained binder concentration than those of other material mixture layers. The thickness of the first material mixture layer is preferably equal to or less than the total thickness of the other material mixture layers.

An electrolyte for a lithium metal battery and a lithium metal battery including the same, more specifically an electrolyte for a lithium metal battery including a lithium salt, an organic solvent and an additive, wherein the additive includes a functional group that binds to lithium metal at one end thereof and a fluorinated hydrocarbon group at the other end. The electrolyte for the lithium metal battery includes an additive including particular functional groups to improve the stability of the lithium metal and suppress the side reaction at the surface, thereby enabling the lithium metal battery to have high capacity, high stability, and long life.

An object is to provide an electrode active material having a novel structure, said electrode active material enabling Li.sub.2S to be used as an electrode. The problem is solved by a solid solution with an antifluorite crystal structure comprising Li, Cu, and S as main constituents.

Provided are methods of effecting cation exchange in MXene materials so as to stabilize the materials. Also provided are compositions, comprising layered MXene materials that comprise an organic cation between layers. Also provided are MXene compositions comprising a chalcogen disposed thereon, the MXene composition further optionally comprising a quaternary ammonium halide disposed thereon.

A method for producing a graphene oxide-based compound for an air electrode of a metal-air battery. A nitrogen and sulfur-based organic compound is added to an aqueous suspension of a graphene oxide. The water of the suspension is evaporated in order to obtain a powder. This powder is heated under an inert atmosphere in order to sublime the organic compound and stimulate the incorporation of nitrogen from the organic compound into the graphitic sites of the graphene oxide. The nitrogen and sulfur-doped graphene oxide is added to a second aqueous suspension comprising a cobalt nitrate-based compound. This second suspension is heated in order to form nanoparticles of cobalt oxide at the surface of at least one nitrogen and sulfur-doped graphene oxide sheet.

Provided is a sulfur-carbon material composite body which, when used for an electrode of a secondary battery, is unlikely to degrade cycle characteristics at the time of charging and discharging of the secondary battery. Disclosed is a sulfur-carbon material composite body including a first carbon material having a graphene layered structure; a spacer at least partially disposed between graphene layers of the first carbon material or at an end of the first carbon material; and sulfur or a sulfur-containing compound at least partially disposed between the graphene layers of the first carbon material or at the end of the first carbon material.

A rechargeable battery includes an iron electrode comprising carbonyl iron composition dispersed over a fibrous electrically conductive substrate. The carbonyl iron composition includes carbonyl iron and at least one additive. A counter-electrode is spaced from the iron electrode. An electrolyte is in contact with the iron electrode and the counter-electrode such that during discharge. Iron in the iron electrode is oxidized with reduction occurring at the counter-electrode such that an electric potential develops. During charging, iron oxides and hydroxides in the iron electrode are reduced with oxidation occurring at the counter-electrode (i.e., a nickel electrode or an air electrode).

Methods of applying as-prepared alkaline source materials for a secondary battery. The cathode includes an alkaline source material with or without coating including an alkali metal oxide, an alkali metal sulfide, an alkali metal salt, or a combination of any two or more thereof. An as-prepared spread coating layer for a secondary battery, the coating layer includes an alkaline source material, including an alkali metal oxide, an alkali metal sulfide, and an alkali metal salt, with or without coating, a conductive carbon, a catalyst, or a combination of any two or more thereof. An as-prepared electrolyte for a secondary battery, the electrolyte includes an alkaline source material including an alkali metal oxide, an alkali metal sulfide, an alkali metal salt, or a combination of any two or more thereof.

Provided are sulfide solid electrolyte particles which have sufficient ion conductivity and which are configured to suppress hydrogen sulfide generation, and an all-solid-state battery comprising the sulfide solid electrolyte particles. Disclosed are sulfide solid electrolyte particles comprising Li, P, S and a halogen as constituent elements and having a Li/P molar ratio of more than 3, wherein an oxygen/sulfur element ratio of a particle surface measured by XPS is 0.29 or more and 0.81 and less, and an oxygen/sulfur element ratio at a depth of 30 nm (in terms of a SiO.sub.2 sputter rate) from the particle surface measured by XPS, is 0.29 or less.

A method for manufacturing an electrochemical device, implementing a process for manufacturing a porous electrode having a porous layer deposited on a substrate, the porous layer having a porosity of between 20% and 60% by volume and pores with an average diameter of less than 50 nm. The method includes providing a substrate and a colloidal suspension including aggregates or agglomerates of monodisperse primary nanoparticles of an active electrode material, having an average primary diameter of between 2 and 60 nm, the aggregates or agglomerates having an average diameter of between 50 nm and 300 nm, then depositing a layer from the colloidal suspension on the substrate, then drying and consolidating the layer to obtain a mesoporous layer, and then depositing a coating of an electronically conductive material on and inside the pores of the layer.