IP Library Granted Patent US 10,044,036
Granted Patent B2
US 10,044,036 · App. 15/100,479 · Granted Aug 7, 2018

Positive active material for lithium secondary battery, electrode for lithium secondary battery and lithium secondary battery

Inventors: Daisuke Yoshikawa (Kyoto, JP); Daisuke Endo (Kyoto, JP)
Assignee: GS Yuasa International Ltd.
H01M4/525C01G53/006C01G53/50H01B1/08H01M4/131H01M4/505H01M10/0525C01P2002/50C01P2002/52C01P2002/74C01P2004/32C01P2006/11C01P2006/14C01P2006/16H01M10/052H01M2004/028
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,044,036
App. No.
15/100,479
Granted
Aug 7, 2018
Kind
B2
Abstract

Provided is a positive active material for a lithium secondary battery containing a lithium transition metal composite oxide. The lithium transition metal composite oxide has an α-NaFeO 2 structure. A transition metal (Me) includes Co, Ni and Mn and a molar ratio Li/Me of lithium (Li) to the transition metal is larger than 1.2 and smaller than 1.6. The lithium transition metal composite oxide has a pore volume of 0.055 to 0.08 cc/g in a pore region in which a pore size, at which a differential pore volume determined by a BJH method from an adsorption isotherm using a nitrogen gas adsorption method exhibits a maximum value, is within a range up to 60 nm, and exhibits a single phase belonging to a space group R3-m at 1000° C.

Claims (13)

1. A positive active material for a lithium secondary battery containing a lithium transition metal composite oxide, wherein the lithium transition metal composite oxide has an α-NaFeO 2 structure, transition metals (Me) include Co, Ni and Mn and a molar ratio Li/Me of lithium (Li) to the transition metal is larger than 1.2 and smaller than 1.6, the lithium transition metal composite oxide has a pore volume of 0.055 to 0.08 cc/g in a pore region where a pore size, at which a differential pore volume determined by a BJH (Barrett-Joyner-Halenda) method from an adsorption isotherm using a nitrogen gas adsorption method exhibits a maximum value, is within a range up to 60 nm, and the lithium transition metal composite oxide exhibits a single phase belonging to a space group R3-m at 1000° C.

2. The positive active material for a lithium secondary battery according to claim 1 , wherein in the lithium transition metal composite oxide, a half width of the diffraction peak belonging to the (003) plane in X-ray diffraction measurement is within a range of 0.202° to 0.265°.

3. The positive active material for a lithium secondary battery according to claim 1 , wherein a molar ratio of Mn to the transition metal element Me (Mn/Me) is 0.5 or more.

4. The positive active material for a lithium secondary battery according to claim 1 , wherein a molar ratio of Mn to the transition metal element Me (Mn/Me) is 0.5 or more and 0.75 or less.

5. The positive active material for a lithium secondary battery according to claim 1 , wherein a molar ratio of Co to the transition metal element Me (Co/Me) is 0.05 or more and 0.40 or less.

6. The positive active material for a lithium secondary battery according to claim 1 , wherein a molar ratio of Co to the transition metal element Me (Co/Me) is 0.10 or more and 0.30 or less.

7. An electrode for a lithium secondary battery containing the positive active material for a lithium secondary battery according to claim 1 .

8. A lithium secondary battery comprising the electrode for a lithium secondary battery according to claim 7 .

9. A method for producing the positive active material for a lithium secondary battery according to claim 1 , wherein the lithium transition metal composite oxide is prepared by undergoing a precursor preparation step of preparing a precursor containing Co, Ni and Mn as transition metal elements; a calcination step of mixing the precursor and a Li salt and heat-treating the resulting mixture at a temperature of 800° C. or higher to prepare an oxide; and an acid treatment step of acid-treating the oxide.

10. The method for producing the positive active material for a lithium secondary battery according to claim 9 , wherein the precursor is a carbonate compound.

11. The method for producing the positive active material for a lithium secondary battery according to claim 10 , wherein in the calcination step, heat treatment is performed at a temperature of 800° C. or higher and 900° C. or lower.

12. The method for producing the positive active material for a lithium secondary battery according to claim 9 , wherein the precursor preparation step includes a step of coprecipitating a carbonate from an aqueous solution with a pH of 7.5 to 11 including Co, Ni and Mn.

13. The method for producing the positive active material for a lithium secondary battery according to claim 9 , wherein in the acid treatment step, sulfuric acid is used.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 31, 2016
From: YOSHIKAWA, DAISUKE; ENDO, DAISUKE
To: GS YUASA INTERNATIONAL LTD.
Reel/Frame 038752/0244 →
Priority Claims (1)
JP 2013-249361 · Dec 2, 2013 · national
Continuity (1)
Related Publication 20160301073A1 · Oct 13, 2016