IP Library Granted Patent US 9,382,274
Granted Patent B2
US 9,382,274 · App. 14/164,839 · Granted Jul 5, 2016

Aqueous redox flow batteries featuring improved cell design characteristics

Inventors: Arthur J. Esswein (San Francisco, CA); Steven Y. Reece (Cambridge, MA); Evan R. King (Quincy, MA); John Goeltz (Cambridge, MA); Desiree D. Amadeo (Belmont, MA)
Assignee: Lockheed Martin Advanced Energy Storage, LLC
C07F7/28H01M4/9008H01M8/188H01M8/20Y02E60/528
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Quick Facts
Patent No.
US 9,382,274
App. No.
14/164,839
Granted
Jul 5, 2016
Kind
B2
Abstract

Provided are compositions having the formula M n Ti(L1)(L2)(L3) wherein L1 is a catecholate, and L2 and L3 are each independently selected from catecholates, ascorbate, citrate, glycolates, a polyol, gluconate, glycinate, hydroxyalkanoates, acetate, formate, benzoates, malate, maleate, phthalates, sarcosinate, salicylate, oxalate, a urea, polyamine, aminophenolates, acetylacetone or lactate; each M is independently Na, Li, or K; n is 0 or an integer from 1-6. Also provided are energy storage systems.

Claims (28)

1. A composition having the formula M n Ti(L1)(L2)(L3) wherein:

L1 is a catecholate, and L2 and L3 are each independently selected from catecholates, ascorbate, citrate, glycolates, a polyol, gluconate, glycinate, hydroxyalkanoates, acetate, formate, benzoates, malate, maleate, phthalates, sarcosinate, salicylate, oxalate, a urea, polyamine, aminophenolates, acetylacetone or lactate;

each M is independently Na, Li, or K;

n is 0 or an integer from 1-6; and provided that when both L1 and L2 are a catecholate, L3 is not oxalate, urea, catecholate or acetylacetone.

2. The composition of claim 1 , wherein said catecholate comprises 1,2-dihydroxybenzene, 1,2,3-trihydroxybenzene, 1,2,4-trihydroxybenzene or a mixture thereof.

3. A flow battery comprising the composition of claim 1 .

4. A composition having the formula M n Ti(catecholate) 2 (hydroxycatecholate);

wherein n is 0 or an integer from 1 to 6.

5. The composition of claim 4 , wherein said hydroxycatecholate comprises 1,2,3-trihydroxybenzene or 1,2,4-trihydroxybenzene.

6. An aqueous solution comprising one or more compositions having the formula M n Ti(L1)(L2)(L3) wherein:

L1, L2, and L3 are each independently selected from catecholates, ascorbate, citrate, glycolates, polyols, gluconate, glycinate, hydroxyalkanoates, acetate, formate, benzoates, malate, maleate, phthalates, sarcosinate, salicylate, oxalate, ureas, a polyamine, aminophenolates, acetylacetone or lactate, provided that at least one of L1, L2, and L3 is a catecholate;

each M is independently Na, Li, or K;

n is 0 or an integer from 1-6; and

wherein the composition is present in a concentration greater than 0.5 M.

7. The aqueous solution of claim 6 , wherein when L1 and L2 are a catecholate, L3 is not oxalate, urea, catecholate or acetylacetone.

8. The aqueous solution of claim 6 , wherein said catecholate comprises 1,2-dihydroxybenzene, 1,2,3-trihydroxybenzene, 1,2,4-trihydroxybenzene or a mixture thereof.

9. The aqueous solution of claim 6 , wherein the composition has the formula M n Ti(catecholate) 2 (hydroxycatecholate).

10. The aqueous solution of claim 9 , wherein said hydroxycatecholate comprises 1,2,3-trihydroxybenzene or 1,2,4-trihydroxybenzene.

11. The aqueous solution of claim 6 , wherein the composition is of the formula M n Ti(catecholate) 3 .

12. The aqueous solution of claim 6 , additionally comprising a buffer.

13. The aqueous solution of claim 12 , wherein said buffer is a salt of phosphate, borate, carbonate, silicate, tris(hydroxymethyl)aminomethane (tris), 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES), piperazine-N,N′-bis(ethanesulfonic acid) (PIPES), and combinations thereof.

14. The aqueous solution of claim 6 having a pH of 1-13.

15. The aqueous solution of claim 6 having a pH of 2-12.

16. The aqueous solution of claim 6 having a pH of 4-10.

17. The aqueous solution of claim 5 , wherein at least one of L1, L2, and L3 is a catecholate bearing a sulfonic acid or a salt thereof.

18. The aqueous solution of claim 17 , wherein at least one of L1, L2, and L3 is a catecholate bearing one sulfonic acid or a salt thereof.

19. The aqueous solution of claim 6 having a pH of about 7 to about 13.

20. The aqueous solution of claim 6 having a pH of about 9 to about 13.

Assignments (4)
CHANGE OF NAME Recorded Jul 12, 2018
From: LOCKHEED MARTIN ADVANCED ENERGY STORAGE, LLC
To: LOCKHEED MARTIN ENERGY, LLC
Reel/Frame 046570/0942 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 6, 2018
From: ESSWEIN, ARTHUR J.; GOELTZ, JOHN; KING, EVAN R.; REECE, STEVEN Y.; AMADEO, DESIREE D.
To: SUN CATALYTIX CORPORATION
Reel/Frame 046282/0771 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE ADDRESS PREVIOUSLY RECORDED AT REEL: 034795 FRAME: 0513. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Feb 25, 2015
From: SUN CATALYTIX CORPORATION
To: LOCKHEED MARTIN ADVANCED ENERGY STORAGE, LLC
Reel/Frame 035089/0681 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 23, 2015
From: SUN CATALYTIX CORPORATION
To: LOCKHEED MARTIN ADVANCED ENERGY STORAGE, LLC
Reel/Frame 034795/0513 →
Continuity (8)
Continuation In Part 13796004 · Mar 12, 2013
Continuation In Part 13795878 · Mar 12, 2013
Provisional Application 61739538 · Dec 19, 2012
Provisional Application 61739140 · Dec 19, 2012
Provisional Application 61738546 · Dec 18, 2012
Provisional Application 61683260 · Aug 15, 2012
Provisional Application 61676473 · Jul 27, 2012
Related Publication 20140138576A1 · May 22, 2014