Provided is a fabrication method of an electrode for a secondary battery including coating an electrode slurry containing an electrode active material and a binder on a current collector; drying the current collector on which the electrode slurry is coated to form an electrode active material layer; and surface-treating the electrode active material layer formed on the current collector to remove a binder layer on a surface of the electrode active material layer.

An improved method of forming a transition metal layered oxide material for alkali-ion battery cathodes include combining an alkali-containing precursor and at least one transition metal precursor or other metal precursor at a low temperature of less than 100° C. to form a liquid eutectic alloy mixture. The mixture is then heated at a temperature between 300° C. to 500° C. to pre-calcinate the mixture, and subsequently the pre-calcinated mixture is subjected to a final calcination at a temperature of 500° C. to 1000° C. to obtain a crystalline oxide material. A P2-type or O3-type cathode may be formed with the layered oxide material, and a sodium-ion battery cell may include the so-formed P2-type or O3-type cathode.

To provide graphene oxide that has high dispersibility and is easily reduced. To provide graphene with high electron conductivity. To provide a storage battery electrode including an active material layer with high electric conductivity and a manufacturing method thereof. To provide a storage battery with increased discharge capacity. A method for manufacturing a storage battery electrode that is to be provided includes a step of dispersing graphene oxide into a solution containing alcohol or acid, a step of heating the graphene oxide dispersed into the solution, and a step or reducing the graphene oxide.

An electrode manufacturing system includes: a doping unit; a cleaning unit: and a conveyor unit. The doping unit performs a process of doping an active material in a strip-shaped electrode with an alkali metal, the strip-shaped electrode including an active material layer formed portion in which an active material layer including the active material is formed, and an active material layer unformed portion in which the active material layer is not formed. The cleaning unit cleans the active material layer unformed portion that is adjacent to the active material layer formed portion. The conveyor unit conveys the electrode from the doping unit to the cleaning unit.

A method of manufacturing a carbon-metal organic framework composite includes: preparing a mixed solution comprising a metal ion precursor and an organic ligand precursor; forming a Metal-Organic Framework (MOF) on a surface of a carbon support using the mixed solution; and carbonizing the MOF formed on the surface of the carbon support to form a Carbonized Metal-Organic Framework (C-MOF).

An electrode improved for achieving a storage battery having both a high electrode strength and favorable electrode conductivity is provided. The electrode includes graphene and a modified polymer in an active material layer or includes a layer substantially formed of carbon particles and an active material layer including a modified polymer over a current collector. The modified polymer has a poly(vinylidene fluoride) structure and partly has a polyene structure or an aromatic ring structure. The polyene structure or the aromatic ring structure is sandwiched between poly(vinylidene fluoride) structures.

Among other things, the present disclosure relates to re-purposing used lithium-ion batteries. The present disclosure includes treating an electrode using a solvent prior to electrochemically relithiating the electrode. In some embodiments, the relithiation may be done using a roll-to-roll device, wherein the electrode may be secured on a first pin and a second pin, then it may be unwound and submerged in an electrolyte solution. Lithium ions may be inserted into the electrode using a voltage. The layer of lithium may provide lithium ions to the electrode.

A device for supplementing an electrode sheet with lithium and a method for supplementing electrode sheet with the lithium. The device includes two first rolling wheels, a second rolling wheel, a lithium ribbon providing mechanism, a first transfer film conveying mechanism, a second transfer film conveying mechanism and an electrode sheet providing mechanism; the two first rolling wheels are opposite each other, and the second rolling wheel is adjacent to the first rolling wheel; the lithium ribbon providing mechanism is used for feeding a lithium ribbon between the second rolling wheel and the first rolling wheel; the first transfer film conveying mechanism is used for conveying a first transfer film carrying a first release agent and transferring the first release agent to the lithium ribbon; the electrode sheet providing mechanism is used for providing the electrode sheet.

Provided is a method for producing a composite alloy for use in an electrode for an alkaline storage battery, including a powder preparation step of preparing a hydrogen storage alloy powder containing Ti and Cr and having a BCC structure, an etching step of applying an acid to the hydrogen storage alloy powder prepared in the powder preparation step, a Pd film forming step of coating the surface of the hydrogen storage alloy powder subjected to the etching step with Pd using a substitution plating method, and a heat treatment step of heating the hydrogen storage alloy powder having a Pd film formed, at said heating being a temperature of 500° C. or less, wherein in the Pd coating forming step, the hydrogen storage alloy powder is coated with Pd under the condition that the Pd element weight ratio of the composite alloy to be produced is 0.47% or more.

A non-aqueous electrolyte secondary battery comprises a positive electrode, a negative electrode, a separator, and an electrolyte solution. At least part of the separator is interposed between the positive electrode and the negative electrode. The negative electrode includes a negative electrode substrate and a negative electrode active material layer. The negative electrode active material layer is placed on a surface of the negative electrode substrate. Voids are formed in the negative electrode active material layer. In a cross section parallel to a thickness direction of the negative electrode active material layer, the voids have an average equivalent circle diameter from 9.6 μm to 35.8 μm, an average circularity of 0.26 or more, and an area percentage from 3.1% to 30.9%.