Positive-Electrode Active Material and Power Storage Device
US-2015123050-A1 · May 7, 2015 · US
US12272822B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12272822-B2 |
| Application number | US-201816624319-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 14, 2018 |
| Priority date | Jun 26, 2017 |
| Publication date | Apr 8, 2025 |
| Grant date | Apr 8, 2025 |
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 positive electrode active material has a small difference in a crystal structure between the charged state and the discharged state. For example, the crystal structure and volume of the positive electrode active material, which has a layered rock-salt crystal structure in the discharged state and a pseudo-spinel crystal structure in the charged state at a high voltage of approximately 4.6 V, are less likely to be changed by charging and discharging as compared with those of a known positive electrode active material. In order to form the positive electrode active material having the pseudo-spinel crystal structure in the charged state, it is preferable that a halogen source such as a fluorine and a magnesium source be mixed with particles of a composite oxide containing lithium, a transition metal, and oxygen, which is synthesized in advance, and then the mixture be heated at an appropriate temperature for an appropriate time.
Opening claim text (preview).
The invention claimed is: 1. A method for manufacturing a positive electrode active material for a lithium-ion battery, the method comprising steps of: forming a first mixture by mixing lithium fluoride (LiF) and magnesium fluoride (MgF 2 ); pulverizing the first mixture to reduce a particle size of the first mixture, thereby yielding a pulverized first mixture; forming a second mixture by mixing a composite oxide containing lithium, a transition metal, and oxygen with the pulverized first mixture; and heating the second mixture at higher than or equal to 600° C. and lower than or equal to 950° C. and for longer than or equal to 3 hours, wherein a molar ratio of the lithium fluoride (LiF) and the magnesium fluoride (MgF 2 ) in the first mixture is LiF:MgF 2 =x:1 (0.1≤x≤0.5), wherein in the composite oxide, concentrations of elements other than the lithium, the transition metal, and the oxygen are less than or equal to 5,000 ppm wt when analysis is performed by a glow discharge mass spectroscopy, and wherein an atomic ratio of the transition metal (TM) in the composite oxide included in the second mixture to magnesium (Mg Mix1 ) included in the first mixture is TM:Mg Mix1 =1:y (0.0005≤y≤0.03). 2. The method for manufacturing a positive electrode active material for a lithium-ion battery according to claim 1 , wherein forming the first mixture and pulverizing the first mixture are performed as wet methods. 3. The method for manufacturing a positive electrode active material for a lithium-ion battery according to claim 2 , wherein, in the wet methods, acetone is used as a solvent. 4. The method for manufacturing a positive electrode active material for a lithium-ion battery according to claim 1 , wherein particles of the pulverized first mixture have an average diameter greater than or equal to 600 nm and less than or equal to 20 μm. 5. A method for manufacturing a positive electrode active material for a lithium-ion battery, the method comprising steps of: forming a first mixture by mixing lithium fluoride (LiF) and magnesium fluoride (MgF 2 ); pulverizing the first mixture to reduce a particle size of the first mixture, thereby yielding a pulverized first mixture; forming a second mixture by mixing a composite oxide containing lithium, a transition metal, and oxygen with the pulverized first mixture; and heating the second mixture at higher than or equal to 900° C. and for longer than or equal to 2 hours, wherein a molar ratio of the lithium fluoride (LiF) and the magnesium fluoride (MgF 2 ) in the first mixture is LiF:MgF 2 =x:1 (0.1≤x≤0.5), wherein in the composite oxide, concentrations of elements other than the lithium, the transition metal, and the oxygen are less than or equal to 5,000 ppm wt when analysis is performed by a glow discharge mass spectroscopy, and wherein an atomic ratio of the transition metal (TM) in the composite oxide included in the second mixture to magnesium (Mg Mix1 ) included in the first mixture is TM:Mg Mix1 =1:y (0.0005≤y≤0.03). 6. The method for manufacturing a positive electrode active material for a lithium-ion battery according to claim 5 , wherein forming the first mixture and pulverizing the first mixture are performed as wet methods. 7. The method for manufacturing a positive electrode active material for a lithium-ion battery according to claim 6 , wherein, in the wet methods, acetone is used as a solvent. 8. The method for manufacturing a positive electrode active material for a lithium-ion battery according to claim 5 , wherein particles of the pulverized first mixture have an average diameter greater than or equal to 600 nm and less than or equal to 20 μm. 9. A method for manufacturing a positive electrode active material for a lithium-ion battery, the method comprising steps of: forming a first mixture by mixing lithium fluoride (LiF) and magnesium fluoride (MgF 2 ); pulverizing the first mixture to reduce a particle size of the first mixture, thereby yielding a pulverized first mixture; forming a second mixture by mixing a composite oxide containing lithium, cobalt, nickel, manganese, aluminum, and oxygen with the pulverized first mixture; and heating the second mixture, wherein the heating is performed at any one of a first condition and a second condition, wherein the first condition is higher than or equal to 600° C. and lower than or equal to 950° C. and for longer than or equal to 3 hours, wherein the second condition is higher than or equal to 900° C. and for longer than or equal to 2 hours, wherein a molar ratio of the lithium fluoride (LiF) and the magnesium fluoride (MgF 2 ) in the first mixture is LiF:MgF 2 =x:1 (0.1≤x≤0.5), wherein in the composite oxide, concentrations of elements other than the lithium, the cobalt, the nickel, the manganese, the aluminum, and the oxygen are less than or equal to 5,000 ppm wt when analysis is performed by a glow discharge mass spectroscopy, and wherein an atomic ratio of a transition metal (TM) in the composite oxide included in the second mixture to magnesium (Mg Mix1 ) included in the first mixture is TM:Mg Mix1 =1:y (0.0005≤y≤0.03). 10. The method for manufacturing a positive electrode active material for a lithium-ion battery according to claim 9 , wherein forming the first mixture and pulverizing the first mixture are performed as wet methods. 11. The method for manufacturing a positive electrode active material for a lithium-ion battery according to claim 10 , wherein, in the wet methods, acetone is used as a solvent. 12. The method for manufacturing a positive electrode active material for a lithium-ion battery according to claim 9 , wherein particles of the pulverized first mixture have an average diameter greater than or equal to 600 nm and less than or equal to 20 μm.
containing halogen atoms, e.g. LiCoOxFy · CPC title
containing alkali metals · CPC title
containing manganese · CPC title
containing alkali metals, e.g. LiCoO2 · CPC title
containing halogen atoms, e.g. LiCoOxFy · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.