Positive electrode active material for secondary battery, method of preparing the same, and secondary battery including the positive electrode active material

Patent metadata

Field	Value
Publication number	US-10854870-B2
Application number	US-201916251940-A
Country	US
Kind code	B2
Filing date	Jan 18, 2019
Priority date	Jun 17, 2015
Publication date	Dec 1, 2020
Grant date	Dec 1, 2020

Abstract

The present invention provides a method of preparing a positive electrode active material for a secondary battery including preparing a first transition metal-containing solution including a nickel raw material, a cobalt raw material, and a manganese raw material and a second transition metal-containing solution including a nickel raw material, a cobalt raw material, and a manganese raw material in a concentration different from that of the first transition metal-containing solution; preparing a reaction solution, in which nickel manganese cobalt-based composite metal hydroxide particles are formed, by adding an ammonium cation-containing complexing agent and a basic compound as well as the second transition metal-containing solution to the first transition metal-containing solution and performing a co-precipitation reaction in a pH range of 11 to 13.

First claim

The invention claimed is:

1. A method of preparing a positive electrode active material for a secondary battery comprising:
preparing a first transition metal-containing solution including a nickel raw material, a cobalt raw material, and a manganese raw material and a second transition metal-containing solution including a nickel raw material, a cobalt raw material, and a manganese raw material in a concentration different from that of the first transition metal-containing solution;
preparing a reaction solution, in which nickel manganese cobalt-based composite metal hydroxide particles are formed, by adding an ammonium cation-containing complexing agent and a basic compound as well as the second transition metal-containing solution to the first transition metal-containing solution to allow a mixing ratio of the first transition metal-containing solution to the second transition metal-containing solution to be gradually changed from 100 vol %:0 vol % to 0 vol %:100 vol % and performing a co-precipitation reaction in a pH range of 11 to 13;
growing the nickel manganese cobalt-based composite metal hydroxide particles by adding an ammonium cation-containing complexing agent and a basic compound to the reaction solution until a pH of the reaction solution reaches 8 or more to less than 11; and
mixing the grown nickel manganese cobalt-based composite metal hydroxide particles with a lithium-containing raw material and performing a heat treatment.

2. The method of claim 1 , wherein the preparing of the reaction solution, in which nickel manganese cobalt-based composite metal hydroxide particles are formed, is performed in a temperature range of 40° C. to 70° C.

3. The method of claim 1 , wherein the ammonium cation-containing complexing agent comprises one selected from the group consisting of NH 4 OH, (NH 4 ) 2 SO 4 , NH 4 NO 3 , NH 4 Cl, CH 3 COONH 4 , and NH 4 CO 3 , or a mixture of two or more thereof.

4. The method of claim 1 , wherein the basic compound comprises one selected from the group consisting of a hydrate of alkali metal, a hydroxide of alkali metal, a hydrate of alkaline earth metal, and a hydroxide of alkaline earth metal, or a mixture of two or more thereof.

5. The method of claim 1 , wherein the growing of the nickel manganese cobalt-based composite metal hydroxide particles is performed by changing a pH of a reactant at a rate of 1 per hour to 2.5 per hour.

6. The method of claim 1 , wherein the heat treatment is performed in a temperature range of 250° C. to 1,000° C.

7. The method of claim 1 , wherein the heat treatment is performed by a multi-stage heat-treatment method which comprises a first heat treatment at 250° C. to 450° C. for 5 hours to 15 hours, a second heat treatment at 450° C. to 600° C. for 5 hours to 15 hours, and a third heat treatment at 700° C. to 900° C. for 5 hours to 15 hours.

8. A method of preparing a precursor of a positive electrode active material for a secondary battery comprising:
preparing a first transition metal-containing solution including a nickel raw material, a cobalt raw material, and a manganese raw material and a second transition metal-containing solution including a nickel raw material, a cobalt raw material, and a manganese raw material in a concentration different from that of the first transition metal-containing solution;
preparing a reaction solution, in which nickel manganese cobalt-based composite metal hydroxide particles are formed, by adding an ammonium cation-containing complexing agent and a basic compound as well as the second transition metal-containing solution to the first transition metal-containing solution to allow a mixing ratio of the first transition metal-containing solution to the second transition metal-containing solution to be gradually changed from 100 vol %:0 vol % to 0 vol %:100 vol % and performing a co-precipitation reaction in a pH range of 11 to 13; and
growing the nickel manganese cobalt-based composite metal hydroxide particles by adding an ammonium cation-containing complexing agent and a basic compound to the reaction solution until a pH of the reaction solution reaches 8 or more to less than 11.

Assignees

• Lg Chemical Ltd

Inventors

• Lee Sang Wook
• Jung Wang Mo
• Kang Seong Hoon
• Park Byung Chun
• Shin Ju Kyung
• Park Sang Min

Classifications

• H01M2220/30

  Batteries in portable systems, e.g. mobile phone, laptop · CPC title

• H01M2004/028

  Positive electrodes · CPC title

• H01M4/1391

  of electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx · CPC title

• H01M4/0471

  involving thermal treatment, e.g. firing, sintering, backing particulate active material, thermal decomposition, pyrolysis · CPC title

• Y02T10/70

  Energy storage systems for electromobility, e.g. batteries · CPC title