Patent classifications
H01M4/1397
Systems and methods for potassium enhancing silicon-containing anodes for improved cyclability
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 material. The methods may also include displacing the sodium ions with potassium ions to form a compression 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.
PREPARATION METHOD OF CATHODE MATERIAL FOR SECONDARY BATTERY
A preparation method of a cathode material for a secondary battery is provided. First, a lithium metal phosphate material and a first conductive carbon are provided. The lithium metal phosphate material is made of a plurality of secondary particles. Each of the secondary particles is formed by the aggregation of a plurality of primary particles. An interparticle space is formed between the plurality of primary particles. Next, the lithium metal phosphate material and the first conductive carbon are mixed by a mechanical method, and a composite material is prepared. The first conductive carbon is uniformly arranged in the interparticle space. After that, a second conductive carbon, a binder and a solvent are provided. Finally, the composite material, the second conductive carbon, the binder and the solvent are mixed, and a cathode material for preparing a positive plate is prepared.
PREPARATION METHOD OF CATHODE MATERIAL FOR SECONDARY BATTERY
A preparation method of a cathode material for a secondary battery is provided. First, a lithium metal phosphate material and a first conductive carbon are provided. The lithium metal phosphate material is made of a plurality of secondary particles. Each of the secondary particles is formed by the aggregation of a plurality of primary particles. An interparticle space is formed between the plurality of primary particles. Next, the lithium metal phosphate material and the first conductive carbon are mixed by a mechanical method, and a composite material is prepared. The first conductive carbon is uniformly arranged in the interparticle space. After that, a second conductive carbon, a binder and a solvent are provided. Finally, the composite material, the second conductive carbon, the binder and the solvent are mixed, and a cathode material for preparing a positive plate is prepared.
Negative electrode active material for lithium secondary battery and method for preparing the same
A negative electrode active material including a core, an intermediate layer on a surface of the core, and a shell layer on a surface of the intermediate layer, wherein the core includes a silicon oxide of SiO.sub.x (0<x<2); the intermediate layer includes a lithium silicate, the shell layer includes lithium fluoride (LiF) and the intermediate layer is present in an amount of 5 wt %-15 wt % based on a total weight of the negative electrode active material. Also, a method for preparing the negative electrode active material, and a negative electrode and lithium secondary battery including the same. The negative electrode active material provides excellent initial efficiency and life characteristics.
Negative electrode active material for lithium secondary battery and method for preparing the same
A negative electrode active material including a core, an intermediate layer on a surface of the core, and a shell layer on a surface of the intermediate layer, wherein the core includes a silicon oxide of SiO.sub.x (0<x<2); the intermediate layer includes a lithium silicate, the shell layer includes lithium fluoride (LiF) and the intermediate layer is present in an amount of 5 wt %-15 wt % based on a total weight of the negative electrode active material. Also, a method for preparing the negative electrode active material, and a negative electrode and lithium secondary battery including the same. The negative electrode active material provides excellent initial efficiency and life characteristics.
Positive electrode for lithium ion battery, lithium ion battery and method of producing positive electrode for lithium ion battery
A positive electrode (21) includes a positive electrode current collector (21A), and a positive electrode mixture layer (21B) which is formed on the positive electrode current collector (21A) and contains a positive electrode active material. The positive electrode mixture layer (21B) includes a first positive electrode active material (21B-1) composed of LiVPO.sub.4F and a second positive electrode active material (21B-2) composed of LiVP.sub.2O.sub.7. In addition, a mixing ratio of the first positive electrode active material (21B-1) and the second positive electrode active material (21B-2) contained in the positive electrode mixture layer (21B) is represented by (1−x)LiVPO.sub.4F+xLiVP.sub.2O.sub.7 (x is a mass ratio, 0<x≤0.21).
Positive electrode for lithium ion battery, lithium ion battery and method of producing positive electrode for lithium ion battery
A positive electrode (21) includes a positive electrode current collector (21A), and a positive electrode mixture layer (21B) which is formed on the positive electrode current collector (21A) and contains a positive electrode active material. The positive electrode mixture layer (21B) includes a first positive electrode active material (21B-1) composed of LiVPO.sub.4F and a second positive electrode active material (21B-2) composed of LiVP.sub.2O.sub.7. In addition, a mixing ratio of the first positive electrode active material (21B-1) and the second positive electrode active material (21B-2) contained in the positive electrode mixture layer (21B) is represented by (1−x)LiVPO.sub.4F+xLiVP.sub.2O.sub.7 (x is a mass ratio, 0<x≤0.21).
Metal sulfide composite materials for batteries
Lithium-ion batteries are provided that variously comprise anode and cathode electrodes, an electrolyte, a separator, and, in some designs, a protective layer. In some designs, at least one of the electrodes may comprise a composite of (i) Li2S and (ii) conductive carbon that is embedded in the core of the composite. In some designs, the protective layer may be disposed on at least one of the electrodes via electrolyte decomposition. Various methods of fabrication for lithium-ion battery electrodes and particles are also provided.
Metal sulfide composite materials for batteries
Lithium-ion batteries are provided that variously comprise anode and cathode electrodes, an electrolyte, a separator, and, in some designs, a protective layer. In some designs, at least one of the electrodes may comprise a composite of (i) Li2S and (ii) conductive carbon that is embedded in the core of the composite. In some designs, the protective layer may be disposed on at least one of the electrodes via electrolyte decomposition. Various methods of fabrication for lithium-ion battery electrodes and particles are also provided.
LITHIUM IRON PHOSPHATE POSITIVE ELECTRODE SHEET, PREPARATION METHOD THEREFOR, AND LITHIUM IRON PHOSPHATE LITHIUM-ION BATTERY
A lithium iron phosphate cathode sheet, a preparation method thereof, and a lithium iron phosphate lithium-ion battery are disclosed, wherein the lithium iron phosphate cathode sheet includes lithium iron phosphate particles, and in the lithium iron phosphate particles, in terms of particle number, a percentage of lithium iron phosphate particles with a particle size in the range of 50 nm-500 nm is 70-90%, a percentage of lithium iron phosphate particles with a particle size greater than 500 nm and less than 1000 nm is 5-20%, and a percentage of lithium iron phosphate particles with a particle size in the range of 1 μm-10 μm is 2-10%.