Positive electrode active material and preparation method thereof, secondary battery, battery module, battery pack and electrical device
US-2024387819-A1 · Nov 21, 2024 · US
US2019148711A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2019148711-A1 |
| Application number | US-201816097049-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jan 26, 2018 |
| Priority date | Jan 31, 2017 |
| Publication date | May 16, 2019 |
| Grant date | — |
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The present invention relates to a positive electrode active material for a lithium secondary battery including a lithium cobalt oxide having a core-shell structure, wherein the lithium cobalt-doped oxide of the core and the lithium cobalt-doped oxide of the shell include each independently three kinds of dopants and satisfy specific conditions, a method for producing the same, and a positive electrode and a secondary battery containing the positive electrode active material.
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1 . A positive electrode active material for a lithium secondary battery comprising a lithium cobalt-doped oxide having a core-shell structure, wherein the lithium cobalt-doped oxide of the core and the lithium cobalt-doped oxide of the shell include each independently three kinds of dopants and satisfy the following (a) or (b): (a) the ratio between the average oxidation number of the dopants present in the core and the average oxidation number of the dopants present in the shell satisfies the following condition (1); 0.7≤ t (ratio)= OC/OS< 0.95 (1) wherein, OC is the average oxidation number of the dopants present in the core, and OS is the average oxidation number of the dopants present in the shell, or (b) the dopants of the core are a metal (M1) having an oxidation number of +2, a metal (M2) having an oxidation number of +3 and a metal (M3) having a oxidation number of +4, the contents of M1, M2 and M3 satisfy the following condition (2) based on the molar ratio; the dopants of the shell are a metal (M1′) having an oxidation number of +2, a metal (M2′) having an oxidation number of +3 and a metal (M3′) having a oxidation number of +4, and the contents of M1′, M2′ and M3′ satisfy the following condition (3) based on the molar ratio, 2≤ r (molar ratio)= CM 1/( CM 2+ CM 3)≤3 (2) 0.5≤ r ′(molar ratio)= CM 1′/( CM 2′+ CM 3′)<2 (3) wherein CM1 is the content of M1, CM2 is the content of M2, CM3 is the content of M3, CM1′ is the content of M1′, CM2′ is the content of M2′, and CM3′ is the content of M3′. 2 . The positive electrode active material according to claim 1 , wherein in the step (a), t (ratio) satisfies the condition of 0.8≤t<0.95. 3 . The positive electrode active material according to claim 1 , wherein in the step (b), r(molar ratio) satisfies the condition of 2≤r≤2.5, and r′ (molar ratio) satisfies the condition of 0.5≤r′≤1.5. 4 . The positive electrode active material according to claim 1 , wherein the lithium cobalt-doped oxide having a core-shell structure maintains the crystal structure without phase change in the range where the positive electrode potential during full charge is higher than 4.5 V on the basis of a Li potential. 5 . The positive electrode active material according to claim 1 , wherein the lithium cobalt-doped oxide of the core has a composition of the following Chemical Formula (1): Li a Co 1-x-y-z M1 x M2 y M3 z O 2 (1) wherein, M1, M2 and M3 are each independently one element selected from the group consisting of Ti, Mg, Al, Zr, Ba, Ca, Ta, Nb, Mo, Ni, Zn, Si, V and Mn; 0.95≤a≤1.05; 0<x≤0.04, 0<y≤0.04, and 0<z≤0.04. 6 . The positive electrode active material according to claim 1 , wherein the lithium cobalt-doped oxide of the shell has a composition of the following Chemical Formula (2): Li b Co 1-s-t-w M1′ s M2′ t M3′ w O 2 (2) wherein, M1′, M2′ and M3′ are each independently one element selected from the group consisting of Ti, Mg, Al, Zr, Ba, Ca, Ta, Nb, Mo, Ni, Zn, Si, V and Mn; 0.95≤b≤1.05; 0<s≤0.04, 0<t≤0.04, and 0<w≤0.04. 7 . The positive electrode active material according to claim 5 , wherein the M1 and M1′ are metals having an oxidation number of +2, the M2 and M2′ are metals having an oxidation number of +3, and the M3 and M3′ are metals having an oxidation number of +4. 8 . The positive electrode active material according to claim 7 , wherein the M1 and M1′ are each independently one element selected from the group consisting of Mg, Ca, Ni and Ba; the M2 and M2′ are each independently one element selected from the group consisting of Ti, Al, Ta and Nb; and the M3 and M3′ are each independently selected from the group consisting of Ti, Ta, Nb, Mn and Mo and are elements different from M2 and M2′. 9 . The positive electrode active material according to claim 1 , wherein the thickness of the shell is 50 to 2000 nm. 10 . The positive electrode active material according to claim 1 , wherein Al 2 O 3 having a thickness of 50 nm to 100 nm is coated onto the surface of the shell. 11 . A method for producing a lithium cobalt-doped oxide having a core-shell structure of the positive electrode active material according to claim 1 , the method comprising the steps of: (i) preparing a doped cobalt precursor containing three kinds of dopants by co-precipitation; (ii) mixing the doped cobalt precursor and a lithium precursor, and subjecting them to a primary calcination to prepare core particles; and (iii) mixing the core particles, the cobalt precursor, the lithium precursor, and the three kinds of dopant precursors, and subjecting them to a secondary calcination to form a shell on the core particle surface, thereby preparing a lithium cobalt-doped oxide having a core-shell structure. 12 . The method according to claim 11 , wherein in the step (i), dopant element-containing salts and cobalt salts are dissolved in water, and then the solution is converted to a basic atmosphere and subjected to a co-precipitation to prepare a doped cobalt oxide as the doped cobalt precursor. 13 . A method for producing a lithium cobalt-doped oxide having a core-shell structure of the positive electrode active material according to claim 1 , the method comprising the steps of: (i) mixing a cobalt precursor, a lithium precursor, and three kinds of dopant precursors and subjecting them to a primary calcination to prepare core particles; and (ii) mixing the core particles, the cobalt precursor, the lithium precursor, and the three kinds of dopant precursors independently of said step (i), and subjecting them to a secondary calcination to form a shell on the core particle surface, thereby preparing a lithium cobalt-doped oxide having a core-shell structure. 14 . The method according to claim 11 , wherein the dopants of the three kinds of dopant precursors have different oxidation numbers. 15 . The method according to claim 11 , wherein the lithium cobalt-doped oxide having a core-shell structure satisfies the following conditions (a) and (b): (a) the ratio between the average oxidation number of the dopants present in the core and the average oxidation number of the dopants present in the shell satisfies the following condition (1); 0.7≤ t (ratio)= OC/OS< 0.95 (1) wherein, OC is the average oxidation number of the dopants present in the core, and OS is the average oxidation number of the dopants present in the shell, or (b) the dopants of the core are a metal (M1) having an oxidation number of +2, a metal (M2) having an oxidation number of +3 and a metal (M3) having a oxidation number of +4, the contents of M1, M2, and M3 satisfy the following condition (2) based on the molar ratio; the dopants of the shell are a metal (M1′) having an oxidation number of +2, a metal (M2′) having an oxidation number of +3 and a metal (M3′) having a oxidation number of +4, and the contents of M1′, M2′ and M3′ satisfy the following condition (3) based on the molar ratio, 2≤ r (molar ratio)= CM 1/( CM 2+ CM 3)≤3 (2) 0.5≤ r ′(molar ratio)= CM 1′/( CM 2′+ CM 3′)<2 (3) wherein CM1 is the content of M1, CM2 is the content of M2, CM3 is the content of M3, CM1′ is the content of M1′, CM2′ is the content of M2′, and CM3′ is the content of M3′. 16 . The method according to claim 11 , wherein the primary calcination is performed at a temperature of 850° C. to 1100° C. for 8 to 12 hours, and the secondary calcination is performed at a temperature of 700° C. to 1100° C. for 5 to 12 hours. 17 . A positive electrode in which a positive electrode mixture containing the positive electrode active material ac
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