Method of producing positive electrode active material for nonaqueous electrolyte secondary battery
US-10700353-B2 · Jun 30, 2020 · US
US2022102716A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2022102716-A1 |
| Application number | US-202117547783-A |
| Country | US |
| Kind code | A1 |
| Filing date | Dec 10, 2021 |
| Priority date | Mar 31, 2016 |
| Publication date | Mar 31, 2022 |
| Grant date | — |
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A method of producing a positive electrode active material for a nonaqueous electrolyte secondary battery, the method includes preparing nickel-containing composite oxide particles having a ratio 1 D 90 / 1 D 10 of a 90% particle size 1 D 90 to a 10% particle size 1 D 10 in volume-based cumulative particle size distribution is 3 or less; mixing the composite oxide particles and a lithium compound to obtain a first mixture; subjecting the first mixture to a first heat treatment at a first temperature and a second heat treatment at a second temperature higher than the first temperature to obtain a first heat-treated product; and subjecting the first heat-treated material to a dispersion treatment.
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1 . A method of producing a positive electrode active material for a nonaqueous electrolyte secondary battery, comprising: providing nickel-containing composite oxide particles; subjecting a first mixture containing the nickel-containing composite oxide particles and a lithium compound to a first heat treatment at a first temperature and a second heat treatment at a second temperature higher than the first temperature to obtain a first heat-treated material; and dissociating from the first heat-treated material the positive electrode active material, wherein the positive electrode active material comprises lithium-transition metal composite oxide particles having a ratio 2 D 50 / 2 D SEM of a 50% particle size 2 D 50 in volume-based cumulative particle size distribution to an average particle size 2 D SEM based on electron microscopic observation in a range of 1 to 4, wherein the lithium-transition metal composite oxide particles have a ratio 2 D 90 / 2 D 10 of a 90% particle size 2 D 90 to a 10% particle size 2 D 10 in volume-based cumulative particle size distribution is 4 or less, and wherein a molar ratio of nickel in a composition of the lithium-transition metal composite oxide to a total molar number of metals other than lithium is 0.3 to 0.6. 2 . The method according to claim 1 , wherein the lithium-transition metal composite oxide further contains cobalt and a molar ratio of cobalt in the composition to a total molar number of metals other than lithium is 0.4 or less. 3 . The method according to claim 1 , wherein the lithium-transition metal composite oxide further contains at least one of Mn or Al and a molar ratio of total molar number of Mn and Al in the composition to a total molar number of metals other than lithium is 0.5 or less. 4 . The method according to claim 1 , wherein a molar ratio of lithium in the composition to a total molar number of metals other than lithium is 1.0 to 1.3. 5 . The method according to claim 1 , wherein a molar ratio of oxygen in the composition to a total molar number of metals other than lithium is 1.9 to 2.1. 6 . The method according to claim 1 , wherein the first temperature is in a range of 850° C. to 950° C., and the second temperature is in a range of 980° C. to 1,100° C. 7 . The method according to claim 6 , further comprising: mixing the positive electrode active material dissociated from the first heat-treated material and a lithium compound to obtain a second mixture; and subjecting the second mixture to a heat treatment to obtain a second heat-treated material. 8 . The method according to claim 7 , wherein the composite oxide particles have a 50% particle size 1 D 50 in volume-based cumulative particle size distribution is in a range of 1 μm to 4 μm, and the lithium-transition metal composite oxide particles are configured such that the 50% particle size 2 D 50 in volume-based cumulative particle size distribution is in a range of 1 μm to 3 μm. 9 . The method according to claim 6 , wherein the composite oxide particles have a 50% particle size 1 D 50 in volume-based cumulative particle size distribution is in a range of 1 μm to 4 μm, and the lithium-transition metal composite oxide particles are configured such that the 50% particle size 2 D 50 in volume-based cumulative particle size distribution is in a range of 1 μm to 3 μm. 10 . The method according to claim 1 , further comprising: mixing the positive electrode active material dissociated from the first heat-treated material and a lithium compound to obtain a second mixture; and subjecting the second mixture to a heat treatment to obtain a second heat-treated material. 11 . The method according to claim 10 , wherein the composite oxide particles have a 50% particle size 1 D 50 in volume-based cumulative particle size distribution is in a range 1 μm to 4 μm, and the lithium-transition metal composite oxide particles are configured such that the 50% particle size 2 D 50 in volume-based cumulative particle size distribution is in a range of 1 μm to 3 μm. 12 . The method according to claim 1 , wherein the composite oxide particles have a 50% particle size 1 D 50 in volume-based cumulative particle size distribution is in a range of 1 μm to 4 μm, and the lithium-transition metal composite oxide particles are configured such that the 50% particle size 2 D 50 in volume-based cumulative particle size distribution is in a range of 1 μm to 3 μm. 13 . The method according to claim 1 , wherein the ratio 2 D 50 / 2 D SEM of the 2 D 50 to the 2 D SEM is in a range of 1 to 3. 14 . The method according to claim 1 , wherein the composite oxide particles have a ratio 1 D 90 / 1 D 10 of a 90% particle size 1 D 90 to a 10% particle size 1 D 10 in volume-based cumulative particle size distribution of 3 or less.
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