A negative electrode for a lithium secondary battery, a method for preparing a negative electrode for a lithium secondary battery, and a lithium secondary battery including the negative electrode. The negative electrode for a lithium secondary battery includes a negative electrode current collector layer, a first negative electrode active material layer on one surface or both surfaces of the negative electrode current collector layer, and a second negative electrode active material layer on a surface opposite to a surface of the first negative electrode

Systems and methods for batteries comprising a cathode, an electrolyte, and an anode, where prelithiation reagents are utilized to treat one or more of the anode and cathode. In one embodiment, the prelithiation reagent is a Li-organic complex solution comprising naphthalene and metallic lithium dissolved in an inhibitor-free THF.

A composite nanoarchitecture unit is disclosed. The unit comprises a columnar film grown on top of another layer where the columns touch each other at the top forming arches having optimized characteristics. This nanoarchitecture unit, called nano-vault, achieves high mechanical stability for films under strong and variable stress action.

In fields related to battery cathode material technologies, a nano-silicon composite material and a preparation method thereof, an electrode material, and a battery are provided to resolve large volume expansion of a cathode material of a battery and a serious side reaction with an electrolyte. The nano-silicon composite material includes a core, a first coating layer, and a second coating layer. The core includes a nano-silicon crystal. The first coating layer covers a surface of the core. The first coating layer is of a porous structure. A material of the first coating layer includes bisilicate and silicon oxide in a deoxidized state. The second coating layer covers a surface of the first coating layer. A material of the second coating layer includes silicon dioxide in a deoxidized state.

In an anode for a secondary battery, a method for preparing the anode, a secondary battery including the anode, and an apparatus for applying a magnetic field, the anode for a secondary battery includes an anode mixture layer on at least one surface of an anode current collector, in which a z-tensor value of a pore in the anode mixture layer is 0.25 or more. The method includes applying an anode mixture slurry including an anode active material to at least one surface of an anode current collector; and drying the anode mixture slurry to form an anode mixture layer. During at least one of the applying and the drying, a magnetic field in which a direction of a line of magnetic force and magnetic force strength change is applied from both upper and lower surfaces of the anode current collector to orient the anode active material and the pore.

A lithium secondary battery includes a positive electrode, and a negative electrode in which deposition and dissolution reactions of lithium metal occur. The negative electrode includes a negative electrode layer. The negative electrode layer contains, as a negative electrode active material, an alloy of the lithium metal and dissimilar metal. An element percentage of lithium element in the alloy is 40.00 atomic % or more and 99.97 atomic % or less when the lithium secondary battery is fully charged.

A negative electrode for a rechargeable lithium battery and a rechargeable lithium battery including the same are disclosed. The negative electrode may include a silicon-based negative active material and a binder, where the binder is an acryl-based copolymer, the acryl-based copolymer including an acrylic acid first monomer, an acrylonitrile second monomer, and a (meth)acrylate third monomer. The acrylic acid first monomer may include acrylic acid substituted with lithium ions. The (meth)acrylate third monomer may include an ethylene glycol group, and a weight-average molecular weight (Mw) of the (meth)acrylate third monomer is less than about 900 g/mol.

A method of manufacturing a negative electrode includes styrene butadiene rubber on at least one surface of a negative electrode current collector, applying a second slurry including a negative electrode active material and a polyacrylic acid-based binder onto the first slurry, and drying and rolling the negative electrode current collector to which the first slurry and the second slurry are applied. The negative electrode active material includes a silicon-based negative electrode active material. According to the present disclosure, expansion and contraction of a silicon-based negative electrode active material during charging and discharging may be alleviated, and electrode flexibility may be improved, resulting in a significant improvement in lifespan properties of a secondary battery.

A unit stack-cell structure and an all-solid-state secondary battery including the same, the unit stack-cell structure includes a plurality of stacked unit cells, each unit cell of the plurality of stacked unit cells including a laminate in which a cathode layer; a solid electrolyte layer; an anode layer; and an elastic layer are sequentially arranged, wherein the elastic layer has a compressive strength of greater than or equal to about 0.28 MPa and less than about 0.6 MPa in a compressibility interval in a range of about 40% to about 70%.

A secondary battery includes a negative electrode plate including a negative electrode current collector, a first negative electrode material layer including a first negative electrode active material, and a second negative electrode material layer including a second negative electrode active material. The first negative electrode material layer is located between the negative electrode current collector and the second negative electrode material layer. The first negative electrode active material includes a first artificial graphite and a second artificial graphite. The first artificial graphite includes secondary particles. An amorphous carbon coating layer is provided on a surface of the first artificial graphite. The second artificial graphite includes primary particles. No amorphous carbon coating layer is provided on a surface of the second artificial graphite.