IP Library Granted Patent US 7,018,607
Granted Patent B2
US 7,018,607 · App. 10/603,910 · Granted Mar 28, 2006

Cathode material for lithium battery

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Quick Facts
Patent No.
US 7,018,607
App. No.
10/603,910
Granted
Mar 28, 2006
Kind
B2
Abstract

A method is disclosed for synthesizing a crystalline metal oxide powder material containing two or more uniformly distributed metal elements. Crystalline, water containing, oxygen containing inorganic acid salts of the metals are heated to liquefy the salts. The apparent solution contains a uniform mixture of the metal elements. The water is removed from the liquid and the resulting powder calcined in air to decompose the acid salts to a mixed metal crystalline oxide. The method is particularly useful to make doped LiNiO 2 type crystals using hydrated nitrate or nitrite salts of Li, Ni and the dopant elements. Examples of useful salts are LiNO 3 .H 2 O, Ni(NO 3 ) 2 .6H 2 O, Co(NO 3 ) 2 .6H 2 O, Al(NO 3 ) 3 .9H 2 O, and Mg(NO 3 ) 2 .6H 2 O.

Claims (23)

1. A method of making a crystalline metal oxide powder material comprising two or more metal elements combined in uniform proportions with oxygen in the crystal structure, said method comprising:

combining water soluble, crystalline, water containing, oxygen containing inorganic acid salt compounds of at least two of said metals into a body of crystals that contains said two metals in separate compounds;

heating the body of crystals with microwave radiation to remove the water from the crystals and form a liquid mixture containing said water and a uniform distribution of said metal elements;

removing the water under reduced atmospheric pressure to form a dry mixture of metal acid salt compounds; and

heating the dry mixture to decompose said acid to leave a powder residue of said metal oxide powder material.

2. The method as recited in claim 1 in which at least two of said metals are initially contained in hydrated nitrate or hydrated nitrite compounds.

3. The method as recited in claim 2 in which said metal oxide powder comprises two or more metals selected from the group consisting of aluminum, cobalt, lithium, nickel, magnesium and manganese.

4. The method as recited in claim 3 in which said water containing, crystalline, oxygen containing inorganic acid salt compounds are selected from the group consisting of LiNO 3 .H 2 O, Ni(NO 3 ) 2 .6H 2 O, Co(NO 3 ) 2 .6H 2 O, Al(NO 3 ) 3 .9H 2 O, and Mg(NO 3 ) 2 .6H 2 O.

5. A method of synthesizing a crystalline material of Li(Ni x M 1-x )O 2 , where M is one or more dopant metals for said crystalline material and 0.5≦x≦0.7, said method comprising:

combining water soluble, crystalline, oxygen containing inorganic acid salt compounds of each of lithium, nickel and at least one of said dopant metals into a body of crystals where at least two of said salt compounds contain water;

heating the body of crystals to with microwave radiation remove the water from the crystals and form a liquid mixture containing said water and a uniform distribution of Li, Ni and said dopant metals;

removing the water under reduced atmospheric pressure to form a dry mixture of metal salt compounds; and

heating the dry mixture to decompose said acid to leave a powder residue of said Li(Ni x M 1-x )O 2 material.

6. The method as recited in claim 5 in which dopant metals are selected from the group consisting of aluminum, cobalt, magnesium and titanium, said titanium being used as titanium dioxide.

7. The method as recited in claim 5 in which each of said inorganic acid compounds is a nitrate or nitrite compound.

8. The method as recited in claim 6 in which each of said inorganic acid compounds is a nitrate or nitrite compound.

9. The method as recited in claim 7 in which said nitrate compounds are selected from the group consisting of LiNO 3 .H 2 O, Ni(NO 3 ) 2 .6H 2 O, Co(NO 3 ) 2 .6H 2 O, Al(NO 3 ) 3 .9H 2 O, and Mg(NO 3 ) 2 .6H 2 O.

10. A method of synthesizing a crystalline material of Li(Ni x M 1-x )O 2 , where M is one or more dopant metals for said crystalline material and 0.5≦x≦0.7, said method comprising:

combining water soluble, crystalline, nitrate or nitrite compounds of each of lithium, nickel and at least one of said dopant metals into a body of crystals where at least two of said nitrate or nitrite compounds contain water;

heating the body of crystals with microwave radiation to remove the water from the crystals and form a liquid mixture comprising a solution containing said water and a uniform distribution of Li, Ni and said dopant metals;

removing the water under reduced atmospheric pressure to form a dry mixture of metal salt compounds; and

heating the dry mixture to decompose said acid to leave a powder residue of said Li(Ni x M 1-x )O 2 material.

11. The method as recited in claim 10 in which said nitrate compounds are selected from the group consisting of LiNO 3 .H 2 O, Ni(NO 3 ) 2 .6H 2 O, Co(NO 3 ) 2 .6H 2 O, Al(NO 3 ) 3 .9H 2 O, and Mg(NO 3 ) 2 .6H 2 O.

Assignments (13)
RELEASE OF SECURITY INTEREST Recorded Nov 7, 2014
From: WILMINGTON TRUST COMPANY
To: GM GLOBAL TECHNOLOGY OPERATIONS LLC
Reel/Frame 034183/0680 →
CHANGE OF NAME Recorded Feb 10, 2011
From: GM GLOBAL TECHNOLOGY OPERATIONS, INC.
To: GM GLOBAL TECHNOLOGY OPERATIONS LLC
Reel/Frame 025780/0902 →
SECURITY AGREEMENT Recorded Nov 8, 2010
From: GM GLOBAL TECHNOLOGY OPERATIONS, INC.
To: WILMINGTON TRUST COMPANY
Reel/Frame 025327/0262 →
RELEASE OF SECURITY INTEREST Recorded Nov 4, 2010
From: UNITED STATES DEPARTMENT OF THE TREASURY
To: GM GLOBAL TECHNOLOGY OPERATIONS, INC.
Reel/Frame 025245/0347 →
RELEASE OF SECURITY INTEREST Recorded Nov 4, 2010
From: UAW RETIREE MEDICAL BENEFITS TRUST
To: GM GLOBAL TECHNOLOGY OPERATIONS, INC.
Reel/Frame 025311/0725 →
SECURITY AGREEMENT Recorded Aug 28, 2009
From: GM GLOBAL TECHNOLOGY OPERATIONS, INC.
To: UAW RETIREE MEDICAL BENEFITS TRUST
Reel/Frame 023161/0911 →
SECURITY AGREEMENT Recorded Aug 27, 2009
From: GM GLOBAL TECHNOLOGY OPERATIONS, INC.
To: UNITED STATES DEPARTMENT OF THE TREASURY
Reel/Frame 023156/0001 →
RELEASE OF SECURITY INTEREST Recorded Aug 21, 2009
From: CITICORP USA, INC. AS AGENT FOR BANK PRIORITY SECURED PARTIES; CITICORP USA, INC. AS AGENT FOR HEDGE PRIORITY SECURED PARTIES
To: GM GLOBAL TECHNOLOGY OPERATIONS, INC.
Reel/Frame 023127/0273 →
RELEASE OF SECURITY INTEREST Recorded Aug 20, 2009
From: UNITED STATES DEPARTMENT OF THE TREASURY
To: GM GLOBAL TECHNOLOGY OPERATIONS, INC.
Reel/Frame 023124/0470 →
SECURITY AGREEMENT Recorded Apr 16, 2009
From: GM GLOBAL TECHNOLOGY OPERATIONS, INC.
To: CITICORP USA, INC. AS AGENT FOR BANK PRIORITY SECURED PARTIES; CITICORP USA, INC. AS AGENT FOR HEDGE PRIORITY SECURED PARTIES
Reel/Frame 022553/0399 →
SECURITY AGREEMENT Recorded Feb 4, 2009
From: GM GLOBAL TECHNOLOGY OPERATIONS, INC.
To: UNITED STATES DEPARTMENT OF THE TREASURY
Reel/Frame 022201/0547 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2009
From: GENERAL MOTORS CORPORATION
To: GM GLOBAL TECHNOLOGY OPERATIONS, INC.
Reel/Frame 022117/0047 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 3, 2003
From: NAZRI, GHOLAM-ABBAS; GARABEDIAN, GREGORY CHARLES
To: GENERAL MOTORS CORPORATION
Reel/Frame 014553/0428 →