IP Library › Granted Patent US 9,601,770
Granted Patent B2
US 9,601,770 · App. 14/504,526 · Granted Mar 21, 2017

Precursor for preparation of lithium composite transition metal oxide and method of preparing the same

Inventors: Byung Chun Park (Daejeon, KR); Sun Sik Shin (Daejeon, KR); Sang Min Park (Daejeon, KR); Ho Suk Shin (Daejeon, KR); Hye Lim Jeon (Gyeonggi-do, KR); Bo Ram Lee (Daejeon, KR)
Assignee: LG Chem, Ltd.
H01M4/505C01G45/00C01G45/02C01G53/006C01G53/44H01M4/131H01M4/362H01M4/525C01P2004/03
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 9,601,770
App. No.
14/504,526
Granted
Mar 21, 2017
Kind
B2
Abstract

Disclosed are a transition metal precursor for preparation of a lithium composite transition metal oxide, the transition metal precursor including a composite transition metal compound represented by Formula 1 below and a hydrocarbon compound, and a method of preparing the same: Mn a M b (OH 1-x ) 2   (1) wherein M is at least two selected from the group consisting of Ni, Co, Mn, Al, Cu, Fe, Mg, B, Cr, and second period transition metals; 0.4≦a≦1; 0≦b≦0.6; a+b≦1; and 0≦x≦0.5, in which the transition metal precursor includes a particular composite transition metal compound and a hydrocarbon compound, and thus, when a lithium composite transition metal oxide is prepared using the same, carbon may be present in lithium transition metal oxide particles and/or on surfaces thereof, whereby a secondary battery including the lithium composite transition metal oxide exhibits excellent rate characteristics and long lifespan.

Claims (33)

1. A transition metal precursor for preparation of a lithium composite transition metal oxide, the transition metal precursor comprising a composite transition metal compound represented by Formula 1 below and a hydrocarbon compound:

Mn a M b (OH 1-x ) 2   (1)

wherein M is at least two selected from the group consisting of Ni, Co, Mn, Al, Cu, Fe, Mg, B, Cr, Ti and Zr;

0.4≦a≦1;

0≦b≦0.6;

a+b≦1; and

0<x<0.5,

wherein an amount of the hydrocarbon compound is in a range of 0.1 to 10 wt % based on a total amount of the transition metal precursor, wherein the transition metal precursor has closed pores, and at least a portion of the hydrocarbon compound is contained in the closed pores.

2. The transition metal precursor according to claim 1 , wherein M is at least one transition metal selected from the group consisting of Ni and Co.

3. The transition metal precursor according to claim 1 , wherein 0.5≦a≦1.

4. The transition metal precursor according to claim 1 , wherein 0.1≦b≦0.5.

5. The transition metal precursor according to claim 1 , wherein the composite transition metal compound is a composite transition metal compound represented by Formula 2 below:

Mn a′ Ni c Co 1-(a′+c+d) M′ d (OH 1-x ) 2   (2)

wherein 0.6≦a′≦1;

0.1≦c≦0.5;

0≦d≦0.1;

a′+c+d≦1;

M′ is at least one selected from the group consisting of Al, Mg, Cr, Ti, Cu, Fe, and Zr; and

x is the same as defined in claim 1 .

6. The transition metal precursor according to claim 1 , wherein an amount of the composite transition metal compound is 30 wt % or greater based on a total amount of the transition metal precursor.

7. The transition metal precursor according to claim 1 , wherein the hydrocarbon compound is a saccharide-based material.

8. The transition metal precursor according to claim 7 , wherein the saccharide-based material is at least one selected from the group consisting of fructose, sucrose, glucose, galactose, lactose, maltose, starch, and dextrin.

9. The transition metal precursor according to claim 8 , wherein the saccharide-based material is sucrose.

10. The transition metal precursor according to claim 1 , wherein the hydrocarbon compound is present in the transition metal precursor and/or on a surface thereof.

11. A method of preparing the transition metal precursor according to claim 1 , the method comprising:

preparing an aqueous transition metal solution containing a transition metal salt for preparation of the transition metal precursor;

mixing a hydrocarbon compound into the aqueous transition metal solution in an amount of 0.01 to 10 mol % based on a total amount of the aqueous transition metal solution; and

performing co-precipitation by adding a strong base to the mixed solution.

12. The method according to claim 11 , wherein the transition metal salt is a sulfate, and the strong base is sodium hydroxide.

13. The method according to claim 12 , wherein the sulfate is at least one selected from the group consisting of nickel sulfate, cobalt sulfate, and manganese sulfate.

14. A cathode active material prepared by mixing the transition metal precursor according to claim 1 and a lithium precursor and sintering the mixture in an oxidizing atmosphere.

15. The cathode active material according to claim 14 , wherein the cathode active material comprises lithium transition metal oxide particles and carbon present in the particles and/or on surfaces of the particles.

16. A lithium secondary battery comprising the cathode active material according to claim 14 .

Assignments (2)
ASSIGNMENT CONVEYING 50% OF ALL RIGHT, TITLE AND INTEREST Recorded Nov 8, 2021
From: LG CHEM, LTD.
To: LG ENERGY SOLUTION, LTD.
Reel/Frame 058054/0651 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 7, 2016
From: PARK, BYUNG CHUN; SHIN, SUN SIK; PARK, SANG MIN; SHIN, HO SUK; JEON, HYE LIM; LEE, BO RAM
To: LG CHEM, LTD.
Reel/Frame 037430/0674 →
Priority Claims (1)
KR 10-2012-0047427 · May 4, 2012 · national
Continuity (2)
Continuation PCTKR2013003714 · Apr 30, 2013
Related Publication 20150034865A1 · Feb 5, 2015