Positive electrode active material and preparation method thereof, positive electrode plate, secondary battery, battery module, battery pack, and electric apparatus
US-2024429384-A1 · Dec 26, 2024 · US
US2025320131A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2025320131-A1 |
| Application number | US-202519251723-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jun 26, 2025 |
| Priority date | Feb 16, 2021 |
| Publication date | Oct 16, 2025 |
| Grant date | — |
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The present invention provides a cathode active material for a secondary battery, which includes a lithium metal oxide particle having a form of a secondary particle in which a plurality of primary particles are agglomerated, wherein the primary particles comprise a particle having a triangular shape which has a size of a minimum internal angle of 45° or more and a maximum height of 0.5 μm or more.
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What is claimed is: 1 . A method of manufacturing a cathode active material for a secondary battery comprising: performing a co-precipitation reaction in a reaction solution including a metal salt, a chelating agent and a co-precipitating agent; and obtaining a metal hydroxide particle formed by the co-precipitation reaction, wherein the step of performing the co-precipitation reaction comprises: a first co-precipitation reaction performed while maintaining a pH of the reaction solution and a concentration of the chelating agent in the reaction solution; a secondary co-precipitation reaction performed while decreasing the pH of the reaction solution and increasing the concentration of the chelating agent in the reaction solution; and a third co-precipitation reaction performed while maintaining the pH of the reaction solution and the concentration of the chelating agent in the reaction solution, wherein co-precipitation reaction to third co-precipitation reaction are sequentially performed. 2 . The method of manufacturing a cathode active material for a secondary battery according to claim 1 , wherein the reaction solution is prepared by mixing an aqueous solution containing the metal salt, and an aqueous solution containing the chelating agent and the co-precipitating agent. 3 . The method of manufacturing a cathode active material for a secondary battery according to claim 1 , wherein when a total reaction time of the co-precipitation reaction is 1 T, the reaction time of the secondary co-precipitation reaction is 0.001 T to 0.02 T. 4 . The method of manufacturing a cathode active material for a secondary battery according to claim 1 , wherein in the second co-precipitation reaction, the pH of the reaction solution is decreased by 0.7 to 2.5 from the pH in the first co-precipitation reaction, and the concentration of the chelating agent in the reaction solution is increased to a numerical value of 1.2 to 2.5 times based on the concentration thereof in the first co-precipitation reaction. 5 . The method of manufacturing a cathode active material for a secondary battery according to claim 1 , wherein the metal hydroxide particle has a form of a secondary particle in which a plurality of primary particles are aggregated, and the primary particles comprise a particle having a triangular shape. 6 . The method of manufacturing a cathode active material for a secondary battery according to claim 5 , wherein the particle having the triangular shape is formed before a time of 0.6 T elapses from the start of the co-precipitation reaction when a total reaction time of the co-precipitation reaction is 1 T. 7 . The method of manufacturing a cathode active material for a secondary battery according to claim 5 , wherein a maximum height of the triangular shape is 0.5 μm or more. 8 . The method of manufacturing a cathode active material for a secondary battery according to claim 1 , wherein the metal salt contains nickel. 9 . The method of manufacturing a cathode active material for a secondary battery according to claim 8 , wherein the metal salt further contains at least one of Co, Mg, Sr, Ba, B, Al, Si, Mn, Ti, Zr and W. 10 . The method of manufacturing a cathode active material for a secondary battery according to claim 9 , wherein a molar ratio of nickel among all metals contained in the metal salt is 0.8 or more. 11 . The method of manufacturing a cathode active material for a secondary battery according to claim 8 , wherein, in the step of performing the co-precipitation reaction, a concentration of Ni2+ in the reaction solution is maintained at 50 to 100 ppm. 12 . The method of manufacturing a cathode active material for a secondary battery according to claim 1 , wherein, during the third co-precipitation reaction, a solid content concentration in the reaction solution is controlled to 30 to 55% by weight. 13 . The method of manufacturing a cathode active material for a secondary battery according to claim 1 , further comprising: mixing the metal hydroxide particle and a lithium source; and calcining the mixture of the metal hydroxide particle and the lithium source to prepare a lithium metal oxide particle. 14 . The method of manufacturing a cathode active material for a secondary battery according to claim 13 , wherein the lithium metal oxide particle has a form of a secondary particle in which a plurality of primary particles are aggregated, wherein the primary particles comprise a particle having a triangular shape which has a size of a minimum internal angle of 45° or more and a maximum height of 0.5 μm or more. 15 . The method of manufacturing a cathode active material for a secondary battery according to claim 13 , wherein the calcination is performed in a temperature range of 670 to 785° C.
of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy · CPC title
Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries · CPC title
Micrometer sized, i.e. from 1-100 micrometer · CPC title
Agglomerated particles · CPC title
extending in three dimensions · CPC title
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