IP Library › Granted Patent US 9,944,537
Granted Patent B2
US 9,944,537 · App. 14/526,577 · Granted Apr 17, 2018

Positive electrode composition for non-aqueous electrolyte secondary battery and method of manufacturing thereof

Inventors: Kosuke Shimokita (Itano-gun, JP); Makoto Shimahara (Tokushima, JP); Kiyofumi Inouchi (Anan, JP)
Assignee: NICHIA CORPORATION
C01G53/50H01M4/505H01M4/525H01M10/0525C01P2002/50C01P2006/40H01M2004/028H01M2220/20H01M2220/30Y02E60/122
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 9,944,537
App. No.
14/526,577
Granted
Apr 17, 2018
Kind
B2
Abstract

The present invention provides a positive electrode composition for a non-aqueous electrolyte secondary battery, wherein the composition includes a lithium-transition metal composite oxide represented by the following compositional formula: Li a Ni 1-x-y Co x M 1 y M 2 z Mo α Nb β O 2 wherein 1.00≤a≤1.50, 0.00≤x≤0.50, 0.00≤y≤0.50, 0.000≤z≤0.020, 0.002≤α≤0.020, 0.002≤β≤0.020, and 0.00≤x+y≤0.70, M 1 represents at least one element selected from the group consisting of Mn and Al, and M 2 represents at least one element selected from the group consisting of Zr, Ti, Mg, Ta, and V, and a boron compound including at least boron and oxygen.

Claims (21)

1. A positive electrode composition for a non-aqueous electrolyte secondary battery, the composition comprising a lithium-transition metal composite oxide represented by the following formula:

Li a Ni 1-x-y Co x M 1 y M 2 z Mo α Nb β O 2

wherein 1.00≤a≤1.50, 0.00≤x≤0.50, 0.00≤y≤0.50, 0.000≤z≤0.020, 0.002≤α≤0.020, 0.002≤β≤0.020, and 0.00≤x+y≤0.70, M 2 represents at least one element selected from the group consisting of Zr, Ti, Mg, Ta, and V, and a boron compound comprising a calcined product of orthoboric acid or a salt thereof.

2. The positive electrode composition according to claim 1 , wherein an amount of the boron compound is 2.0 mol % or less in terms of boron, based on the mole of the lithium-transition metal composite oxide.

3. The positive electrode composition according to claim 2 , wherein a raw material compound for the boron compound is orthoboric acid.

4. The positive electrode composition according to claim 2 , wherein a calcination temperature employed for obtaining the calcined product is 450° C. or lower.

5. The positive electrode composition according to claim 1 , wherein a raw material compound for the boron compound is orthoboric acid.

6. The positive electrode composition according to claim 1 , wherein a calcination temperature employed for obtaining the calcined product is 450° C. or lower.

7. A positive electrode for use in a non-aqueous electrolyte secondary battery, the positive electrode comprising the positive electrode composition for a non-aqueous electrolyte secondary battery according to claim 1 .

8. A non-aqueous electrolyte secondary battery comprising the positive electrode according to claim 7 , a negative electrode, and a non-aqueous electrolyte.

9. The positive electrode composition according to claim 1 , wherein 0.3≤y≤0.50.

10. The positive electrode composition according to claim 1 , wherein α=0.01 and β=0.005.

11. A method for producing a positive electrode composition for a non-aqueous electrolyte secondary battery, the method comprising:

providing a lithium-transition metal composite oxide represented by the following compositional formula:

Li a Ni 1-x-y Co x M 1 y M 2 z Mo α Nb β O 2

wherein 1.00≤a≤1.50, 0.00≤x≤0.50, 0.00≤y≤0.50, 0.000≤z≤0.020, 0.002≤α≤0.020, 0.002≤β≤0.020, and 0.00≤x+y≤0.70, M 2 represents at least one element selected from the group consisting of Zr, Ti, Mg, Ta, and V;

mixing the provided lithium-transition metal composite oxide with orthoboric acid to obtain a raw material mixture; and

calcining the obtained raw material mixture at a calcination temperature from 200° C. to 400° C.

12. The method according to claim 11 , wherein the calcination for the raw material mixture is conducted at a calcination temperature between 200° C. and 250° C.

13. The method according to claim 11 , wherein 0.3≤y≤0.50.

14. The method according to claim 11 , wherein α=0.01 and β=0.005.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2015
From: SHIMOKITA, KOSUKE; SHIMAHARA, MAKOTO; INOUCHI, KIYOFUMI
To: NICHIA CORPORATION
Reel/Frame 034672/0148 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2015
From: SHIMOKITA, KOSUKE; SHIMAHARA, MAKOTO; INOUCHI, KIYOFUMI
To: NICHIA CORPORATION
Reel/Frame 034672/0365 →
Priority Claims (2)
JP 2013-223784 · Oct 29, 2013 · national
JP 2014-219323 · Oct 28, 2014 · national
Continuity (1)
Related Publication 20150118564A1 · Apr 30, 2015