Provided is a surface-treated copper foil in which in order to avoid failures of electronic parts by corrosion, a high bond strength between an electrolytic copper foil and a resin base material can be maintained even when the surface-treated copper foil is exposed to corrosive gases and microparticles, and a method for manufacturing the same. The surface-treated copper foil of the present invention comprises an electrolytic copper foil, a roughened layer covering at least one surface side of the electrolytic copper foil, and a rust preventive layer further covering the roughened layer, wherein the rust preventive layer is at least one surface of the surface-treated copper foil; the rust preventive layer comprises at least a nickel layer; and the thickness of the nickel layer is 0.8 to 4.4 g/m.sup.2 in terms of mass per unit area of nickel; and the noncontact roughness Spd of the rust preventive layer is 1.4 to 2.6 peaks/μm.sup.2 and the surface roughness RzJIS of the rust preventive layer is 1.0 to 2.5 μm. The method for manufacturing the surface-treated copper foil forms the roughened layer having higher roughnesses than the noncontact roughness Spd and surface roughness RzJIS on one surface of the electrolytic copper foil, and thereafter forming the rust preventive layer meeting the predetermined condition.

A first electrode current collector is joined to a multilayer of a positive electrode core in a part including no positive electrode active material layer of the first electrode core, by ultrasonic welding in a joint area. The joint area, at which the multilayers of the first electrode core where the first electrode cores are stacked is joined to the first electrode current collector by ultrasonic welding, includes a plurality of core recesses. A core projection is formed between each adjacent pair of the plurality of core recesses of the multilayer of the first electrode core with the first electrode core flexed in a convex shape. A gap in an arc shape is formed between the adjacent pair of the layers of the first electrode core forming the core projection. The gap has a length decreasing from an apex to a bottom of the core projection.

According to the present disclosure, it is possible to inhibit the electrically conductive foreign substance from falling off and being peeled off from the electrode plate that has been already manufactured, so as to contribute in improving the safety property of the secondary battery. The manufacturing method of the electrode plate herein disclosed includes a precursor preparing step for preparing an electrode precursor 20A including an active material provided area A1 in which an electrode active material layer 24 is provided on a surface of the electrode core 22 and including a core exposed area A2 in which the electrode active material layer 24 is not provided and the electrode core 22 is exposed, and an active material provided area cutting step for cutting the active material provided area A1 by a pulse laser, and a core exposed area cutting step for cutting the core exposed area A2 by the pulse laser. Then, in the case where the pulse width (ns) of the pulse laser is represented by X and the lap rate (%) is represented by Y for the core exposed area cutting step, a condition represented by Y≥−3log X+106 is satisfied. According to the manufacturing method of the electrode plate as described above, it is possible to inhibit the electrically conductive foreign substance from falling off and being peeled off from the electrode plate that has been already manufactured, and thus it is possible to contribute in improving the safety property of the secondary battery.

The invention provides process for producing a stable Si or Ge electrode structure comprising cycling a Si or Ge nanowire electrode until a structure of the Si nanowires form a continuous porous network of Si or Ge ligaments.

A method for the preparation of an electrode comprising a substrate made of an aluminium based material, vertically aligned carbon nanotubes and an electrically conductive polymer matrix, the method comprising the following successive steps: (a) synthesising, on a substrate made of an aluminium based material, a carpet of vertically aligned carbon nanotubes according to the technique of CVD (Chemical Vapour Deposition) at a temperature less than or equal to 650° C.; (b) electrochemically depositing the polymer matrix on the carbon nanotubes from an electrolyte solution including at least one precursor monomer of the matrix, at least one ionic liquid and at least one protic or aprotic solvent. Further disclosed is the prepared electrode and a device for storing and returning electricity such as a supercapacitor comprising the electrode.

An energy storage device according to an aspect of the present invention includes: a negative electrode including a negative substrate made of pure aluminum or an aluminum alloy, a conductive layer directly or indirectly layered on the negative substrate and containing a conductive agent, and a negative active material layer containing a negative active material capable of occluding lithium ions at a potential of 0.05 V vs. Li/Li.sup.+ or lower; and a positive electrode opposed to the negative electrode and including a positive substrate and a positive active material layer directly or indirectly layered on the positive substrate, and the negative active material layer is layered on the negative substrate and the conductive layer so as to include a region in contact with the negative substrate and a region in contact with the conductive layer.

A positive electrode current collector and a positive electrode plate, a battery, a battery module, a battery pack, and an apparatus including the positive electrode current collector are provided. In some embodiments, a positive electrode current collector is provided, including an organic support layer and an aluminum-based conductive layer disposed on at least one surface of the organic support layer, where the aluminum-based conductive layer contains Al and at least one modifying element selected from O, N, F, B, S, and P, an XPS spectrogram of the aluminum-based conductive layer with a surface passivation layer removed through etching has at least a first peak falling in a range of 70 eV to 73.5 eV and a second peak falling in a range of 73.5 eV to 78 eV, and a ratio x of peak intensity of the second peak to that of the first peak satisfies 0<x≤3.0.

The present disclosure relates to a secondary battery module including a nonaqueous electrolyte secondary battery and an elastic body. The elastic body has a compressive elastic modulus of 5 MPa to 120 MPa. The positive electrode includes a positive electrode collector with a thermal conductive rate of 65 W/(m.Math.K) to 150 W/(m.Math.K). The negative electrode includes a negative electrode active material layer including a first layer and a second layer sequentially formed from a side with the negative electrode collector. The first layer contains first carbon-based active material particles with a 10% proof stress of 3 MPa or less. The second layer contains second carbon-based active material particles with a 10% proof stress of 5 MPa or greater.

Systems and methods for water soluble weak acidic resins as carbon precursors for silicon-dominant anodes may include an electrode coating layer on a current collector, where the electrode coating layer is formed from silicon and pyrolyzed water-soluble acidic polyamide imide as a primary resin carbon precursor. The electrode coating layer may include a pyrolyzed water-based acidic polymer solution additive. The polymer solution additive may include one or more of: polyacrylic acid (PAA) solution, poly (maleic acid, methyl methacrylate/methacrylic acid, butadiene/maleic acid) solutions, and water soluble polyacrylic acid. The electrode coating layer may include conductive additives. The current collector may include a metal foil, where the metal current collector includes one or more of a copper, tungsten, stainless steel, and nickel foil in electrical contact with the electrode coating layer. The electrode coating layer may be more than 70% silicon.

An engineered particle for an energy storage device, the engineered particle includes an active material particle, capable of storing alkali ions, comprising an outer surface, a conductive coating disposed on the outer surface of the active material particle, the conductive coating comprising a M.sub.xAl.sub.ySi.sub.zO.sub.w film; and at least one carbon particle disposed within the conductive coating. For the M.sub.xAl.sub.ySi.sub.zO.sub.w film, M is an alkali selected from the group consisting of Na and Li, and 1≤x≤4, 0≤y≤1, 1≤z≤2, and 3≤w≤6.