A method for pre-lithiation of a negative electrode and a negative electrode formed by the method, the method including forming a mixture of inorganic material powder and molten lithium, forming a lithium metal-inorganic material composite ribbon, rolling the ribbon into a film and bonding the lithium metal-inorganic material composite film on a surface of a negative electrode to form a lithium metal-inorganic material composite layer on the surface of the negative electrode. This method reduces the deterioration of lithium during application of a mixture slurry and a negative electrode for a secondary battery, manufactured by the method for pre-lithiation, has improved initial irreversibility, and a secondary battery manufactured using such a negative electrode has excellent charging and discharging efficiency.

Provided are anode for secondary battery, preparation method thereof and secondary battery. The anode comprises metal foil and a compact film of metal phosphates disposed on a surface of the metal foil, wherein the compact film of metal phosphates comprises one or more of aluminum phosphate, copper phosphate, iron phosphate, tin phosphate, zinc phosphate, nickel phosphate, manganese phosphate, lead phosphate, antimony phosphate, cadmium phosphate and bismuth phosphate. Disposed on the surface of the metal foil is a film of metal phosphates which insulates against electrons and is arranged such that metallic ions such as lithium ions can pass therethrough. The film of metal phosphates functions like a solid electrolyte interphase, improves the compatibility of the anode with the electrolyte solution, reduces the decomposition of the electrolyte solution, and improves charging and discharging efficiency, cyclability, high and low temperatures performance and safety performance of battery.

A electrochemical device negative electrode includes: a negative electrode core material; and a negative electrode material layer supported on the negative electrode core material. The negative electrode material layer contains a carbon material. And a surface layer portion of the negative electrode material layer has a lithium carbonate-containing region.

Disclosed are functionalized Group IVA particles, methods of preparing the Group IVA particles, and methods of using the Group IVA particles. The Group IVA particles may be passivated with at least one layer of material covering at least a portion of the particle. The layer of material may be a covalently bonded non-dielectric layer of material. The Group IVA particles may be used in various technologies, including lithium ion batteries and photovoltaic cells.

The present disclosure relates to a prelithiation solution and a method for preparing a prelithiated anode using the same. The prelithiation solution and the method for preparing a prelithiated anode using the same according to the present disclosure allow uniform intercalation of lithium ions throughout the anode chemically in a solution via a simple process of immersing the anode in a prelithiation solution having a sufficiently low redox potential as compared to an anode active material. A prelithiated anode prepared by this method has an ideal initial coulombic efficiency and a lithium secondary battery with a high energy density can be prepared based thereon. In addition, the prepared anode is advantageously applicable to large-scale production due to superior stability even in dry air.

The present disclosure relates to a sodium-ion storage material and an electrode material for a sodium-ion battery, an electrode material for a seawater battery, an electrode for a sodium-ion battery, an electrode for a seawater battery, a sodium-ion battery, and a seawater battery, which include the sodium-ion storage material. Specifically, the sodium-ion storage material may include one or more materials selected from the group consisting of Cu.sub.xS, FeS, FeS.sub.2, Ni.sub.3S, NbS.sub.2, SbO.sub.x, SbS.sub.x, SnS and SnS.sub.2, wherein 0<x≤2. When the sodium-ion storage material according to the present disclosure is used, it may exhibit high discharge capacity, and when the sodium-ion storage material is applied to a sodium-ion battery which is a secondary battery, it may exhibit excellent charge/discharge cycle characteristics.

Cathode active materials for lithium-ion batteries comprise a hybrid nanocomposite of graphene and copper fluoride. Such cathode active materials are used, together with a polymeric binder material and optionally a conductive additive to form a cathode for a lithium-ion battery. Methods of producing hybrid nanocomposites of graphene and copper fluoride include hydrothermally reacting functionalized graphene, such as graphene oxide, and precursors of copper fluoride, such as aqueous fluorosilicic acid. Such hydrothermal reactions include sequential heating and freeze drying steps to produce a CuF.sub.2-graphene nanocomposite.

Various methods and techniques for enhancing a silicon-containing anode for a battery cell are presented. The methods may include providing a silicon-containing anode having reversible electrochemical capabilities including a silicon-containing material and an anode material compatible with a lithium-ion battery chemistry having porous and conductive mechanical properties. The methods may also include enriching a surface layer of the silicon-containing anode with sodium ions to intersperse the sodium ions between silicon atoms of the silicon-containing matieral. The methods may also include displacing the sodium ions with potassium ions to form a comrpession layer in the silicon-containing anode. The potassium ions may place the silicon atoms of the silicon-containing material in a pre-compressive state to counteract internal stress exerted on the silicon-containing material.

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.

The present technology relates to a method of manufacturing a negative electrode, and the method includes: manufacturing a negative electrode having a negative electrode active material layer formed thereon by coating a negative electrode slurry including a negative electrode active material at least on one surface of a current collector; pre-lithiating the negative electrode; and forming an inorganic coating layer on a surface of the negative electrode active material layer by aging the pre-lithiated negative electrode under an CO.sub.2 atmosphere.