Positive electrode active material and preparation method thereof, positive electrode plate, secondary battery, battery module, battery pack, and electric apparatus
US-2024429384-A1 · Dec 26, 2024 · US
US11545668B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11545668-B2 |
| Application number | US-201314437347-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 21, 2013 |
| Priority date | Oct 22, 2012 |
| Publication date | Jan 3, 2023 |
| Grant date | Jan 3, 2023 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
A method for producing an electrode material for a lithium-ion secondary battery. The method includes the following steps: (a) mixing components of a basic ingredient or active substance of electrode material and a conductive carbon material to obtain a conductive carbon material-composited material; (b) mixing the conductive carbon material-composited material and a surface layer-forming material; an (c) burning the mixture obtained at step (b) to obtain the electrode material. Also, a lithium-ion secondary battery including an electrode which comprises the material.
Opening claim text (preview).
The invention claimed is: 1. A method for producing an electrode material for a lithium-ion secondary battery, comprising: (a) mixing components of an active substance of electrode material and a conductive carbon material to obtain a solution, supplying the solution to a chamber, and carrying out a single hydrothermal reaction in the chamber to obtain a conductive carbon material-composited material, wherein the conductive carbon material comprises carbon black and at least one type of fibrous carbon material, wherein the hydrothermal reaction is performed for a period of less than 24 hours; (b) mixing the conductive carbon material-composited material and a surface layer-forming material to form a mixture, wherein the surface layer-forming material is adapted to form a surface layer on the conductive carbon material-composited material; and (c) burning the mixture obtained at step (b) to obtain the electrode material, wherein the surface layer-forming material forms a surface layer on the conductive carbon material-composited material. 2. The method according to claim 1 , wherein the hydrothermal reaction is performed at a temperature of about 100 to 350° C. 3. The method according to claim 1 , wherein a solid-phase reaction occurs during step (a). 4. The method according to claim 1 , wherein step (b) comprises immersing the conductive carbon material-composited material into a water solution including the surface layer-forming material, and removing the water by drying. 5. The method according to claim 1 , wherein step (c) is performed at a temperature that is higher than a temperature at which the surface layer-forming material forms activated covalent bonds with carbon atoms of the conductive carbon material, for a period of about 3 to 12 hours. 6. The method according to claim 1 , wherein step (c) is performed at a temperature of about 500 to 800° C. 7. The method according to claim 1 , wherein the components of the active substance of electrode material are a lithium-containing compound; a phosphorus-containing compound; and a transition metal-containing compound. 8. The method according to claim 1 , wherein the conductive carbon material comprises a mixture of two types of fibrous material, a first type having a length of about 1000 to 3000 nm and a diameter of about 5 to 15 nm; and a second type having a length of about 5000 to 10000 nm and a diameter of about 70 to 150 nm. 9. The method according to claim 1 , wherein a mass ratio of carbon black to fibrous carbon material is in the range of about 1:3 to about 8:1 . 10. The method according to claim 1 , wherein the surface layer-forming material is an organic substance. 11. The method according to claim 1 , wherein the electrode material is a cathode material, and a total content of carbon material in the cathode material is higher than about 2 mass %. 12. The method according to claim 1 , wherein the electrode material is an anode material, and a total content of carbon material in the anode material is higher than about 1 mass %. 13. The method according to claim 1 , wherein the electrode material is an anode material, and a thickness of the surface layer is about 1 to 10 nm. 14. The method according to claim 1 , wherein the electrode material is an anode material containing titanium. 15. The method of claim 7 , wherein the active substance is an olivine-type lithium-containing transition metal phosphate compound. 16. The method of claim 15 , wherein the olivine-type lithium-containing transition metal phosphate compound is LiFePO 4 , LiCoPO 4 , or LiMnPO 4 . 17. The method of claim 1 , wherein the conductive carbon material comprises at least two types of fibrous carbon material, wherein the types of fibrous carbon material are of different sizes. 18. The method of claim 10 , wherein the organic substance is a sugar. 19. The method of claim 18 , wherein the sugar is a polysaccharide or lactose. 20. The method of claim 1 , wherein the surface layer comprises at least one carbon phase selected from graphene phase and amorphous phase. 21. The method of claim 1 , wherein step (c) is performed under inert atmosphere, at a temperature that is lower than a temperature at which the conductive carbon material-composited material decomposes.
Carbon or graphite · CPC title
Manufacturing or production processes characterised by the final manufactured product · CPC title
containing plural metal, or metal and ammonium · CPC title
of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy (H01M4/505, H01M4/525 take precedence) · CPC title
Oxygenated metallic salts or polyanionic structures, e.g. borates, phosphates, silicates, olivines · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.