The invention relates to a battery electrode foil comprising an aluminium alloy, wherein the aluminium alloy has the following composition in weight percent: Si: 0.07-0.12% by weight, Fe: 0.18-0.24% by weight, Cu: 0.03-0.08% by weight, Mn: 0.015-0.025% by weight, Zn: ≤0.01% by weight, Ti: 0.015-0.025% by weight, Zn: ≤0.01% by weight, Ti: 0.015-0.025% by weight, Mn: 0.015-0.025% by weight, Zn: ≤0.01% by weight, Ti: 0.015-0.025% by weight, wherein the aluminium alloy can contain impurities up to a maximum of 0.01% in each case, up to a maximum of 0.03% in total, but the proportion of aluminium must be at least 99.5% by weight; wherein the battery electrode foil has intermetallic phases of a diameter length of 0.1 to 1.0 μm with a density of ≤9500 particles/mm.sup.2. The invention further relates to a process for the production of a battery electrode foil, its use for the production of accumulators, and accumulators containing the battery electrode foil.

Provided are a separator for a secondary battery and an electrochemical device using the same. More particularly, a composite separator which has a lower Gurley permeability after curing than that before curing when forming a heat-resistant coating layer having low resistance, does not have a Gurley permeability which is greatly increased as compared with the Gurley permeability of a porous substrate itself before forming a coating layer to have an overall low Gurley permeability, and has a high surface hardness to have penetration stability, is provided.

A method of making an anode for use in an energy storage device is provided. The method includes providing a current collector having an electrically conductive substrate and a surface layer overlaying a first side of the electrically conductive substrate. A second side of the electrically conductive substrate includes a filament growth catalyst, wherein the second side is opposite the first. The method further includes depositing a lithium storage layer onto the surface layer using a first CVD process forming a plurality of lithium storage filamentary structures on the second side of the electrically conductive substrate using second CVD process.

Electrode protection in electrochemical cells, and more specifically, electrode protection in both aqueous and non-aqueous electrochemical cells, including rechargeable lithium batteries, are presented. Advantageously, electrochemical cells described herein are not only compatible with environments that are typically unsuitable for lithium, but the cells may be also capable of displaying long cycle life, high lithium cycling efficiency, and high energy density.

A battery can include a separator, a first current collector, a protective layer, and a first electrode. The first current collector and the protective layer can be disposed on one side of the separator. The first electrode can be disposed on an opposite side of the separator as the first current collector and the protective layer. Subjecting the battery to an activation process can cause metal to be extracted from the first electrode and deposited between the first current collector and the protective layer. The metal can be deposited to at least form a second electrode between the first current collector and the protective layer.

A porous film, including a binder and inorganic particles. The porous film includes pores formed by the binder. The pores at least include a part of the inorganic particles. The inorganic particles have particle sizes that Dv10 is in a range of 0.015 μm to 3 μm, Dv50 is in a range of 0.2 μm to 5 μm, and Dv90 is in a range of 1 μm to 10 μm. Dv10 of the inorganic particles is less than Dv50 of the inorganic particles, and Dv50 of the inorganic particles is less than Dv90 of the inorganic particles, and the inorganic particles have particle sizes that the ratio of Dv90 to Dv10 is in a range of 2 to 100.

This application relates to a positive electrode plate and an electrochemical device. The positive electrode plate comprises a metal current collector, a positive electrode active material layer and a safety coating disposed between the metal current collector and the positive electrode active material layer; the safety coating comprises a polymer matrix, a conductive material and an inorganic filler; the positive electrode active material layer comprises Li.sub.1+xNi.sub.aCo.sub.bMe.sub.(1−a−b)O.sub.2, wherein −0.1≤x≤0.2, 0.6≤a<1, 0<b<1, 0<(1−a−b)<1, and Me is at least one of Mn, Al, Mg, Zn, Ga, Ba, Fe, Cr, Sn, V, Sc, Ti and Zr; and the metal current collector is a porous aluminum-containing current collector. The positive electrode plate can improve safety and electrical performances of an electrochemical device (such as a capacitor, a primary battery, or a secondary battery).

An electrode body in which a battery sheet is wound around a first end thereof as an axis. The battery sheet includes: a current collector which includes a first layer and first and second metal layers; a first active material layer laminated on the first metal layer; a second active material layer laminated on the second metal layer; and a separator which comes into contact with the first or the second active material layer. The first and second metal layers are not laminated in at least a portion on the first and second surfaces of the first layer at the first end of the current collector, or the first or second metal layer is not laminated on a surface of either of the first surface or the second surface of the first layer which is on an outward side of a roll at a second end of the current collector.

Anodic materials for lithium ions batteries include a current collector and a superlattice disposed on at least a portion of the current collector, the superlattice comprising: alternating layers of an anode active material and an anode inactive material; and a plurality of channels that extend from the current collector through the alternating layers of anode active material and anode inactive material.

A method for forming a current collector is provided. At least two carbon nanostructure reinforced copper composite substrates are provided. The at least two carbon nanostructure reinforced copper composite substrates are stacked to form a composite substrate. An active metal layer is disposed on a surface of the composite substrate to form a first a composite structure. The first composite structure is pressed to form a second composite structure. The second composite structure is annealed to form a third composite structure. The third composite structure is de-alloyed to form a porous copper composite.