Method of preparing positive electrode active material for secondary battery and positive electrode active material for secondary battery prepared thereby
US-2019036119-A1 · Jan 31, 2019 · US
US11581535B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11581535-B2 |
| Application number | US-201916701621-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 3, 2019 |
| Priority date | Dec 10, 2018 |
| Publication date | Feb 14, 2023 |
| Grant date | Feb 14, 2023 |
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A method for producing a positive electrode active material, a positive electrode active material produced thereby, and a positive electrode and a lithium secondary battery including the same are provided. The method includes preparing a nickel-manganese-aluminum precursor having an atomic fraction of nickel of 90 atm % or greater in all transition metals, and mixing the nickel-manganese-aluminum precursor, a cobalt raw material, and a lithium raw material and heat treating the mixture.
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The invention claimed is: 1. A method for producing a positive electrode active material, comprising: preparing a nickel-manganese-aluminum precursor having an atomic fraction of nickel of 90 atm % or greater in all transition metals of the nickel-manganese-aluminum precursor; and mixing the nickel-manganese-aluminum precursor, a cobalt raw material, and a lithium raw material to obtain a mixture; and heat treating the mixture. 2. The method of claim 1 , wherein the nickel-manganese-aluminum precursor does not contain cobalt. 3. The method of claim 1 , wherein the nickel-manganese-aluminum precursor is represented by either Formula 1 below or Formula 2 below: Ni a1 Mn b1 Al c1 M d1 O⋅OH [Formula 1] in Formula 1, M is one or more selected from the group consisting of W, Cu, Fe, Ba, V, Cr, Ti, Zr, Zn, In, Ta, Y, In, La, Sr, Ga, Sc, Gd, Sm, Ca, Ce, Nb, Mg, B, and Mo, and 0.90≤a1≤0.98, 0.01≤b1<0.1, 0.01≤c1<0.1, and 0≤d1≤0.02, Ni a2 Mn b2 Al c2 M d2 (OH) 2 [Formula 2] in Formula 2, M is one or more selected from the group consisting of W, Cu, Fe, Ba, V, Cr, Ti, Zr, Zn, In, Ta, Y, In, La, Sr, Ga, Sc, Gd, Sm, Ca, Ce, Nb, Mg, B, and Mo, and 0.90≤a2≤0.98, 0.01≤b2<0.1, 0.01≤c2<0.1, and 0≤d2≤0.02. 4. The method of claim 1 , wherein the cobalt raw material is mixed in an amount, wherein a content of cobalt in the positive electrode active material is 4000-7000 ppm. 5. The method of claim 1 , wherein the heat treatment is performed at 730° C. to 780° C. for 6 to 18 hours. 6. The method of claim 3 , wherein in Formulas 1 and 2, the M is a doping element.
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