An electrode for a battery includes an iron-containing substrate and a cobalt ferrite layer disposed over the iron-containing substrate. Advantageously, the cobalt ferrite layer inhibits corrosion of the iron-containing substrate. A nickel hydroxide layer is disposed over the cobalt ferrite layer. A battery incorporating the electrode is also provided.

The present disclosure relates to a negative electrode for a secondary battery that is improved in the peeling resistance and adhesiveness of the active material layer and thus can improve the life characteristics of the negative electrode and the lithium secondary battery, a method of manufacturing the same and a lithium secondary battery including same. The negative electrode for a secondary battery includes a metal current collector; and an active material layer formed on the metal current collector and containing a negative electrode active material, a binder, and a conductive material, wherein the active material layer has an average value of shear strength of 1.6 MPa or more as measured at a predetermined depth.

An electrochemical cell includes solid-state, printable anode layer, cathode layer and non-aqueous gel electrolyte layer coupled to the anode layer and cathode layer. The electrolyte layer provides physical separation between the anode layer and the cathode layer, and comprises a composition configured to provide ionic communication between the anode layer and cathode layer by facilitating transmission of multivalent ions between the anode layer and the cathode layer.

An all-solid-state secondary battery, wherein: an anode current collector that contains copper or copper alloy; a cathode current collector comprising aluminum, aluminum alloy or stainless steel, provided opposite to the anode current collector; an anode active material layer formed there between from the anode current collector side on the surface of the anode current collector; a solid electrolyte layer comprising a sulfide solid electrolyte that contains a monovalent or divalent metal and sulfur; and a cathode active material layer formed on the surface of the cathode current collector are layered successively, is used. A sulfidation resistant layer is formed on the surface of the anode current collector on which the anode active material layer is formed. Or, the surface of the anode current collector on which the anode active material layer is formed has a compressive strength of 1250 to 3000 MPa.

To provide a power storage device whose charge and discharge characteristics are unlikely to be degraded by heat treatment. To provide a power storage device that is highly safe against heat treatment. The power storage device includes a positive electrode, a negative electrode, a separator, an electrolytic solution, and an exterior body. The separator is located between the positive electrode and the negative electrode. The separator contains polyphenylene sulfide or solvent-spun regenerated cellulosic fiber. The electrolytic solution contains a solute and two or more kinds of solvents. The solute contains LiBETA. One of the solvents is propylene carbonate.

Embodiments of secondary batteries having electrode assemblies are provided. A secondary battery can comprise an electrode assembly having a stacked series of layers, the stacked series of layers having an offset between electrode and counter-electrode layers in a unit cell member of the stacked series. A set of constraints can be provided with a primary constraint system with first and second primary growth constraints separated from each other in a longitudinal direction, and connected by at least one primary connecting member, and a secondary constraint system comprises first and second secondary growth constraints separated in a second direction and connected by members of the stacked series of layers. The primary constraint system may at least partially restrain growth of the electrode assembly in the longitudinal direction, and the secondary constraint system may at least partially restrain growth in the second direction that is orthogonal to the longitudinal direction.

A metal support for an electrochemical element has a plate shape as a whole, and is provided with a plurality of penetration spaces that pass through the metal support from a front face to a back face. The front face is a face to be provided with an electrode layer. Each of front-side openings that are openings of the penetration spaces formed in the front face has an area of 3.0×10.sup.−4 mm.sup.2 or more and 3.0×10.sup.−3 mm.sup.2 or less.

This foil for a secondary battery negative electrode collector (negative electrode-collecting foil 5b) includes a first Cu layer (51) made of Cu or a Cu-based alloy, a stainless steel layer (52), and a second Cu layer (53) made of Cu or a Cu-based alloy, which are disposed in this order, a total thickness is 200 μm or less, and 0.01% proof stress is 500 MPa or more.

An electrochemical cell includes solid-state, printable anode layer, cathode layer and non-aqueous gel electrolyte layer coupled to the anode layer and cathode layer. The electrolyte layer provides physical separation between the anode layer and the cathode layer, and comprises a composition configured to provide ionic communication between the anode layer and cathode layer by facilitating transmission of multivalent ions between the anode layer and the cathode layer.

A clad material for a battery current collector includes a pinhole due to falling off of an intermetallic compound containing Al and Ni or an intermetallic compound containing Al and Fe from an outer surface of a first layer. A clad material for a battery current collector includes a clad material obtained by bonding a first layer made of Al or an Al alloy and a second layer made of any one of Ni, a Ni alloy, Fe, and a Fe alloy by rolling. The clad material has a thickness of 50 μm or less. In the clad material, an intermetallic compound layer constituted by an intermetallic compound containing Al and Ni or an intermetallic compound containing Al and Fe, the intermetallic compound layer having a thickness of 0.1 μm or more and 1 μm or less, is formed between the first layer and the second layer.