IP Library Granted Patent US 10,396,396
Granted Patent B2
US 10,396,396 · App. 15/994,276 · Granted Aug 27, 2019

Lithium-ion conductive garnet and method of making membranes thereof

Inventors: Michael Edward Badding (Campbell, NY); Curtis Robert Fekety (Corning, NY); Tricia Anne Harnas (Elmira, NY); Yanxia Ann Lu (Painted Post, NY); Ying Shi (Painted Post, NY); Zhen Song (Painted Post, NY)
Assignee: Corning Incorporated
H01M10/0562C01G25/006C04B35/48C04B35/50H01B1/08H01M10/0525C01P2002/54C01P2002/72C01P2002/77C01P2002/88C01P2004/03C01P2006/32C01P2006/40H01M2300/0071
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Quick Facts
Patent No.
US 10,396,396
App. No.
15/994,276
Granted
Aug 27, 2019
Kind
B2
Abstract

A gallium doped garnet composition of the formula: Li 7−3y La 3 Zr 2 Ga y O 12 where y is from 0.4 to 2.0, and as defined herein. Also disclosed is a method for making a dense Li-ion conductive cubic garnet membrane, comprising one of two alternative lower temperature routes, as defined herein.

Claims (39)

1. A method of making a Li-ion conductive cubic garnet, comprising:

forming a nitrate source aqueous solution comprising a first nitrate source and a nitrate dopant source;

contacting the nitrate source aqueous solution and a carbohydrate source and heating in a first heating step to form a nano-particle ash;

a second heating step of the nano-particle ash to produce a garnet nanoprecursor;

pelletizing the garnet nanoprecursor to form a Li-ion conductive cubic garnet pellet; and

a third heating step of the garnet pellet to form a dense Li-ion conductive cubic garnet membrane.

2. The method of claim 1 , wherein:

the first nitrate source comprises a mixture of LiNO 3 , La(NO 3 ) 3 , and ZrN 2 O 7 ;

the nitrate dopant source is at least one element from Groups IIA to VIIA, and IIIB to IVB;

the carbohydrate source has from 5 to 10 carbon atoms; and

the nano-particle ash has a size in a range of 10 nm to 50 nm.

3. The method of claim 1 , wherein the dense Li-ion conductive cubic garnet membrane has a Li-ion conductivity in a range of 0.2×10 −3 S/cm to 2.0×10 −3 S/cm.

4. The method of claim 1 , wherein the third heating step is conducted in a closed platinum vessel, and wherein the garnet pellet is a pellet surrounded in a garnet burying powder comprising at least one micrometer sized Li-oxide garnet.

5. The method of claim 1 , wherein the nitrate dopant source is at least one of a metal nitrate, or a mixture of at least two different metal nitrates.

6. The method of claim 1 , further comprising: adding from 1 wt. % to 20 wt. % excess of a nitrate source containing Li to compensate for Li losses during the third heating step.

7. The method of claim 1 , wherein a mole ratio of the nitrate source aqueous solution to the carbohydrate source in the contacting step is in a range of 1:1 to 1:4.

8. The method of claim 7 , wherein the first heating step is conducted at a temperature in a range of 200° C. to 550° C.

9. The method of claim 1 , wherein the second heating step is conducted at a temperature in a range of 650° C. to 700° C. to form nano-sized garnet nanoprecursor particles having a size in a range of 10 nm to 100 nm.

10. The method of claim 1 , wherein the third heating step is conducted at a temperature in a range of 950° C. to 1200° C. for a time in a range of 0.5 hr to 30 hrs.

11. The method of claim 10 , wherein the third heating step is held at 800° C. for a time in a range of 2 hrs to 6 hrs to form and stabilize a pure cubic garnet phase.

12. A method of making a Li-ion conductive cubic garnet, comprising:

forming a nitrate source aqueous solution comprising of a first nitrate source and a nitrate dopant source;

contacting the nitrate source aqueous solution and a carbohydrate source and heating in a first heating step to form a nano-particle ash;

a second heating step of the nano-particle ash to produce a Li-ion conductive pure cubic garnet powder;

milling the cubic garnet powder to produce a sub-micron powder;

pelletizing the sub-micron powder to form a garnet pellet; and

a third heating step of the garnet pellet to form a dense Li-ion conductive cubic garnet membrane.

13. The method of claim 12 wherein:

the first nitrate source comprises a mixture of LiNO 3 , La(NO 3 ) 3 , and ZrN 2 O 7 ;

the nitrate dopant source is at least one element from Groups IIA to VIIA, and IIIB to IVB;

the carbohydrate source has from 5 to 10 carbon atoms;

the cubic garnet powder comprises irregularly-shaped, porous particles before milling;

the sub-micron powder comprises sub-micron-sized particles having a size in a range of 100 nm to 1000 nm after milling.

14. The method of claim 12 , further comprising: adding from 1 wt. % to 20 wt. % excess of a nitrate source containing Li to compensate for Li losses during the third heating step.

15. The method of claim 12 , wherein the dense Li-ion conductive cubic garnet membrane has a Li-ion conductivity in a range of 0.2×10 −3 S/cm to 2.0×10 −3 S/cm.

16. The method of claim 12 , wherein a mole ratio of the nitrate source aqueous solution to the carbohydrate source in the contacting step is in a range of 1:1 to 1:4.

17. The method of claim 16 , wherein the first heating step is conducted at a temperature in a range of 200° C. to 550° C.

18. The method of claim 12 , wherein the second heating step is conducted at a temperature in a range of 775° C. to 1000° C. to form Li-ion conductive pure cubic garnet powder having irregularly-shaped micron-sized particles.

19. The method of claim 12 , wherein the third heating step is conducted at a temperature in a range of 950° C. to 1200° C.

Continuity (3)
Division 14879346 · Oct 9, 2015
Provisional Application 62064605 · Oct 16, 2014
Related Publication 20180277893A1 · Sep 27, 2018
Cited By (6)
US 12,237,475 US 12,240,143 US 12,378,164 US 12,469,876 US 12,479,771 US 12,533,869