Positive electrode active material for secondary battery, and method of preparing the same
US-2018261832-A1 · Sep 13, 2018 · US
US12288866B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12288866-B2 |
| Application number | US-201816614233-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 23, 2018 |
| Priority date | Nov 24, 2017 |
| Publication date | Apr 29, 2025 |
| Grant date | Apr 29, 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 method for preparing a positive electrode active material includes: a step for adding a reaction mixture containing a lithium-raw material and a nickel-manganese-cobalt precursor into a first crucible and performing a first heat treatment at a temperature of 500-800° C. to form a pre-sintered mixture; a step for extracting the pre-sintered mixture from the first crucible and pulverizing or classifying the same; and a step for adding the pulverized or classified pre-sintered mixture into a second crucible and performing a second heat treatment at a temperature of 700-1000° C. under an atmosphere in which an oxygen partial pressure is 20% or less to form a lithium nickel-manganese-cobalt-based positive electrode active material, wherein a volume of the pre-sintered mixture formed after the first heat treatment is reduced to a volume that is 20-50% of a volume of the reaction mixture added into the first crucible.
Opening claim text (preview).
The invention claimed is: 1. A method for preparing a positive electrode active material comprising: adding a reaction mixture containing a lithium-raw material and a nickel-manganese-cobalt precursor into a first crucible and performing a first heat treatment at a temperature of 500-800° C. under an oxygen atmosphere to form a pre-sintered mixture; extracting the pre-sintered mixture from the first crucible and pulverizing or classifying the pre-sintered mixture; and directly after the pulverizing or classifying of the pre-sintered mixture, adding the pulverized or classified pre-sintered mixture into a second crucible and performing a second heat treatment at a temperature of 700-1000° C. under an atmosphere in which an oxygen partial pressure is 20% or less to form a lithium nickel-manganese-cobalt-based positive electrode active material, wherein during the first heat treatment a volume of the pre-sintered mixture is reduced to a volume that is 20-50% of a volume of the reaction mixture added into the first crucible, wherein the oxygen partial pressure of the second heat treatment is lower than that of the first heat treatment, and wherein the lithium nickel-manganese-cobalt-based positive electrode active material is represented by Formula 1 below: Li 1+x [Ni a Mn b CO c M 1 1-a-b-c ] 1-x O 2 [Formula 1] wherein, 0.2≤x≤0.2, 0.6≤a≤0.98, 0.01≤b≤0.39 and 0.01≤c≤0.39, and M 1 is at least one selected from the group consisting of Cu, Fe, V, Cr, Ti, Zr, Zn, Al, In, Ta, Y, In, La, Sr, Ga, Sc, Gd, Sm, Ca, Ce, Nb, Mg, B, and Mo. 2. The method of claim 1 , wherein the second heat treatment is performed under a nitrogen atmosphere, a vacuum atmosphere, or a non-fluid atmosphere. 3. The method of claim 1 , wherein the lithium-raw material is at least one selected from the group consisting of lithium hydroxide and lithium carbonate. 4. The method of claim 1 , wherein the nickel-manganese-cobalt precursor is at least one selected from the group consisting of nickel-manganese-cobalt hydroxide, nickel-manganese-cobalt oxyhydroxide, nickel-manganese-cobalt carbonate, and a nickel-manganese-cobalt organic complex. 5. The method of claim 1 , wherein the reaction mixture further comprises a doping raw material. 6. The method of claim 5 , wherein the doping raw material is oxide, hydroxide, sulfide, oxyhydroxide, halide, or a mixture thereof comprising Cu, Fe, V, Cr, Ti, Zr, Zn, Al, In, Ta, Y, In, La, Sr, Ga, Sc, Gd, Sm, Ca, Ce, Nb, Mg, B, Mo or combination thereof. 7. The method of claim 1 , wherein the first crucible is a crucible formed of stainless steel, a crucible formed of nickel, or an alloy crucible. 8. The method of claim 1 , wherein the first heat treatment is performed for 1 hour to 12 hours. 9. The method of claim 1 , wherein a content of the sintered mixture added into the second crucible is 2-10 times a content of the sintered mixture formed from the first crucible. 10. The method of claim 1 , wherein the second crucible is a crucible formed of aluminum. 11. The method of claim 1 , further comprising adding a doping raw material to the second crucible before the second heat treatment. 12. The method of claim 1 , wherein the second heat treatment is performed for 2 hours to 20 hours.
Positive electrodes · CPC title
of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy · CPC title
of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy · CPC title
Electric properties · CPC title
Li-accumulators · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.