Positive Electrode Active Material for Lithium Secondary Battery, Method for Manufacturing the Same, and Positive Electrode and Lithium Secondary Battery Comprising the Same

Patent metadata

Field	Value
Publication number	US-2024132375-A1
Application number	US-202218269155-A
Country	US
Kind code	A1
Filing date	Jan 14, 2022
Priority date	Jan 15, 2021
Publication date	Apr 25, 2024
Grant date	—

Abstract

A positive electrode active material for a lithium secondary battery has secondary micro particles having an average particle size (D50) of 1 to 10 μm formed by agglomeration of primary macro particles having an average particle size (D50) of 0.5 to 3 μm and a lithium-M oxide coating layer on all or part of a surface, wherein M is at least one selected from the group consisting of boron, cobalt, manganese and magnesium. The secondary macro particles have an average particle size (D50) of 5 to 20 μm formed by agglomeration of primary micro particles having a smaller average particle size (D50) than the primary macro particles. The primary macro particles and the primary micro particles are represented by Li a Ni 1−b−c−d Co b Mn c Q d O 2+δ , wherein 1.0≤a≤1.5, 0<b<0.2, 0<c<0.2, 0≤d≤0.1, 0<b+c+d≤0.2, −0.1≤δ≤1.0, and Q is at least one type of metal selected from the group consisting of Al, Mg, V, Ti and Zr.

First claim

1 . A positive electrode active material for a lithium secondary battery, comprising:
secondary micro particles having a lithium-M oxide coating layer on all or part of a surface, wherein M is at least one selected from the group consisting of boron, cobalt, manganese and magnesium, wherein an average particle size (D50) of the secondary micro particles is from 1 to 10 μm formed by agglomeration of primary macro particles having an average particle size (D50) of 0.5 to 3 μm; and secondary macro particles having an average particle size (D50) of 5 to 20 μm formed by agglomeration of primary micro particles having a smaller average particle size (D50) than the primary macro particles, wherein the primary macro particles and the primary micro particles are represented by Li a Ni 1−b−c−d Co b Mn c Q d O 2+δ , wherein 1.0≤a≤1.5, 0<b<0.2, 0<c<0.2, 0≤d≤0.1, 0<b+c+d≤0.2, −0.1≤δ≤1.0, and Q is at least one type of metal selected from the group consisting of Al, Mg, V, Ti and Zr.

2 . The positive electrode active material for a lithium secondary battery according to claim 1 , wherein a ratio of the average particle size (D50) of the secondary macro particles:the average particle size (D50) of the secondary micro particles is 5:1 to 2:1.

3 . The positive electrode active material for a lithium secondary battery according to claim 1 , wherein the secondary micro particles are present in an amount of 10 to 100 parts by weight based on 100 parts by weight of the secondary macro particles.

4 . The positive electrode active material for a lithium secondary battery according to claim 1 , wherein M in the lithium-M oxide coating layer is at least one selected from the group consisting of boron and cobalt.

5 . The positive electrode active material for a lithium secondary battery according to claim 1 , wherein M in the lithium-M oxide coating layer is present in an amount of 0.05 to 10 parts by weight based on 100 parts by weight of the secondary micro particles.

6 . The positive electrode active material for a lithium secondary battery according to claim 1 , wherein a bonding strength between the primary macro particles of the secondary micro particles is smaller than a bonding strength between the primary micro particles of the secondary macro particles.

7 . A method for manufacturing the positive electrode active material of claim 1 for a lithium secondary battery, comprising:
(S 1 ) mixing a transition metal containing solution comprising nickel, cobalt, manganese and Q (Q is at least one type of metal selected from the group consisting of Al, Mg, V, Ti and Zr) at a predetermined mole ratio, an ammonia aqueous solution and a basic aqueous solution to form a transition metal hydroxide precursor particle, followed by separation and drying, and grinding the transition metal hydroxide precursor particle to a predetermined average particle size (D50) to form the ground transition metal hydroxide precursor;
(S 2 ) mixing the ground transition metal hydroxide precursor particle with a lithium raw material and sintering in an oxygen atmosphere to prepare a core micro particle formed by agglomeration of primary macro particles having an average particle size (D50) of 0.5 to 3 μm, wherein the primary macro particles are represented by Li a Ni 1−b−c−d Co b Mn c Q d O 2+δ ,
wherein 1.0≤a≤1.5, 0<b<0.2, 0<c<0.2, 0≤d≤0.1, 0<b+c+d≤0.2, −0.1≤δ≤1.0, and Q is at least one type of metal selected from the group consisting of Al, Mg, V, Ti and Zr, wherein the primary macro particles;
(S 3 ) mixing a solution of precursor comprising at least one selected from the group consisting of boron, cobalt, manganese and magnesium with the core micro particle, spraying and drying using a spray dryer and sintering in an oxygen atmosphere to prepare secondary micro particles having an average particle size (D50) of 1 to 10 μm formed by agglomeration of primary macro particles having an average particle size (D50) of 0.5 to 3 μm and a lithium-M oxide coating layer, on all or part of a surface, wherein M is at least one selected from the group consisting of boron, cobalt, manganese and magnesium; and
(S 4 ) preparing secondary macro particles having an average particle size (D50) of 5 to 20 μm formed by agglomeration of primary micro particles having a smaller average particle size (D50) than the primary macro particles, wherein the primary micro particles are represented by Li a Ni 1−b−c−d Co b Mn c Q d O 2+δ , wherein 1.0≤a≤1.5, 0<b<0.2, 0<c<0.2, 0≤d≤0.1, 0<b+c+d≤0.2, −0.1≤δ≤1.0, and Q is at least one type of metal selected from the group consisting of Al, Mg, V, Ti and Zr), and mixing the secondary macro particles with the secondary micro particles.

8 . The method of claim 7 , wherein the average particle size (D50) of the secondary macro particles:the average particle size (D50) of the secondary micro particles is 5:1 to 2:1.

9 . The method f of claim 7 , wherein the secondary micro particles are present in an amount of 10 to 100 parts by weight based on 100 parts by weight of the secondary macro particles.

10 . The method of claim 7 , wherein M in the lithium-M oxide coating layer is at least one selected from the group consisting of boron and cobalt.

11 . The method of claim 7 , wherein M in the lithium-M oxide coating layer is present in an amount of 0.05 to 10 parts by weight based on 100 parts by weight of the secondary micro particles.

12 . A positive electrode for a lithium secondary battery comprising the positive electrode active material according to claim 1 .

13 . A lithium secondary battery comprising the positive electrode according to claim 12 .

Assignees

• Lg Energy Solution Ltd

Inventors

• Lho Eun-Sol
• Do Joong-Yeop
• Park Kang-Joon
• Han Gi-Beom
• Kwak Min
• Park Sang-Min
• Lee Dae-Jin
• Lee Sang-Wook
• Jung Wang-Mo

Classifications

• C01G53/82

  Compounds containing nickel, with or without oxygen or hydrogen, and containing two or more other elements · CPC title

• C01G53/50 Primary

  of the type (MnO2)n-, e.g. Li(NixMn1-x)O2 or Li(MyNixMn1-x-y)O2 · CPC title

• H01M10/052

  Li-accumulators · CPC title

• C01P2004/03

  obtained by SEM · CPC title

• C01P2004/61

  Micrometer sized, i.e. from 1-100 micrometer · CPC title