IP Library Granted Patent US 10,964,966
Granted Patent B2
US 10,964,966 · App. 16/469,766 · Granted Mar 30, 2021

Flow batteries incorporating a nitroxide compound within an aqueous electrolyte solution

Inventors: Zachariah M. Norman (Belmont, MA); Matthew Millard (Belmont, MA); Emily Grace Nelson (Watertown, MA); Scott Thomas Humbarger (Somerville, MA)
Assignee: Lockheed Martin Energy, LLC
H01M8/188C07D209/04C07D209/46C07D221/00C07D279/12C07F1/005C07F3/003H01M4/368H01M4/60
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Quick Facts
Patent No.
US 10,964,966
App. No.
16/469,766
Granted
Mar 30, 2021
Kind
B2
Abstract

Flow batteries can include a first half-cell containing a first aqueous electrolyte solution, a second half-cell containing a second aqueous electrolyte solution, and a separator disposed between the first half-cell and the second half-cell. The first aqueous electrolyte solution contains a first redox-active material, and the second aqueous electrolyte solution contains a second redox-active material. At least one of the first redox-active material and the second redox-active material is a nitroxide compound or a salt thereof. Particular nitroxide compounds can include a doubly bonded oxygen contained in a ring bearing the nitroxide group, a doubly bonded oxygen appended to a ring bearing the nitroxide group, sulfate or phosphate groups appended to a ring bearing the nitroxide group, various heterocyclic rings bearing the nitroxide group, or acyclic nitroxide compounds.

Claims (39)

1. A flow battery comprising:

a first half-cell containing a first aqueous electrolyte solution;

a second half-cell containing a second aqueous electrolyte solution; and

a separator disposed between the first half-cell and the second half-cell;

wherein at least one of the first redox-active material and the second redox-active material comprises a nitroxide compound having a structure of:

or a salt form thereof;

wherein:

R 1 -R 4 are, independently, optionally substituted C 1 -C 10 straight chain or branched alkyl;

each R 5 is, independently, H; optionally substituted alkyl, alkenyl, alkynyl, aryl, aralkyl, heterocyclyl, or heteroaryl; C 1 -C 6 polyol; C(═O)R 6 ; C(═O)OR 6 ; C(═O)NR 6 R 6 ; OR 6 ; O(C═O)R 6 ; SR 6 ; S(═O)R 6 ; S(═O) 2 R 6 ; NR 6 R 6 ; NR 6 (C═O)R 6 ; NR 6 (C═O)NR 6 R 6 ; (CH 2 ) 1-10 CO 2 H; (CH 2 ) 1-10 (CHOH)CO 2 H; CH 2 (OCH 2 CH 2 ) x OCH 3 ; CH(OH)CH 2 OH; halogen; cyano; sulfonyl; or perfluoroalkyl;

each R 6 is, independently, H; optionally substituted alkyl, alkenyl, alkynyl, aryl, aralkyl, heterocyclyl, or heteroaryl; perfluoroalkyl; (CH 2 ) 1-10 CO 2 H; (CH 2 ) 1-10 (CHOH)CO 2 H; (CH 2 CH 2 O) x CH 3 ; CH 2 (OCH 2 CH 2 ) x OCH 3 ; CH(OH)CH 2 OH; or C 2 -C 6 polyol;

optional double bonds are present;

a and b are, independently, 1 or 2; and

x is an integer in a range between 0 and about 100;

A 2 is C(═O)R 8 , C(═O)OR 8 , C(═O)NR 9 R 9 , NR 9 C(═O)R 9 , S(═O)OH, S(═O)R 8 , S(═O) 2 R 8 , S(═O) 2 NR 9 R 9 , OS(═O) 2 OR 10 , NR 9 C(═O)NR 9 R 9 , NR 9 C(═S)NR 9 R 9 , NR 9 S(═O) 2 R 8 , P(═O)(OR 9 ) 2 , P(═O)R 8 OR 9 , P(═O)R 8 , OP(═O)OR 10 or PR 9 ;

R 8 is optionally substituted alkyl, alkenyl, alkynyl, aryl, aralkyl, heterocyclyl, or heteroaryl; perfluoroalkyl; (CH 2 ) 1-10 CO 2 H; (CH 2 ) 1-10 (CHOH)CO 2 H; (CH 2 CH 2 O) x CH 3 ; CH 2 (OCH 2 CH 2 ) x OCH 3 ; CH(OH)CH 2 OH; or C 1 -C 6 polyol;

R 9 is H; optionally substituted alkyl, alkenyl, alkynyl, aryl, aralkyl, heterocyclyl, or heteroaryl; perfluoroalkyl; (CH 2 ) 1-10 CO 2 H; (CH 2 ) 1-10 (CHOH)CO 2 H; (CH 2 CH 2 O) x CH 3 ; CH 2 (OCH 2 CH 2 ) x OCH 3 ; CH(OH)CH 2 OH; or C 2 -C 6 polyol; and

wherein R 10 is H; optionally substituted alkyl, alkenyl, alkynyl, aryl, aralkyl, heterocyclyl, or heteroaryl; perfluoroalkyl; (CH 2 ) 1-10 CO 2 H; (CH 2 ) 1-10 (CHOH)CO 2 H; (CH 2 CH 2 O) x CH 3 ; CH 2 (OCH 2 CH 2 ) x OCH 3 ; CH(OH)CH 2 OH; or C 2 -C 6 polyol.

2. The flow battery of claim 1 , wherein each R 5 is H, and R 1 -R 4 are each methyl.

3. The flow battery of claim 1 , wherein A 2 is S(═O)OH, S(═O)R 8 , S(═O) 2 R 8 , S(═O) 2 NR 9 R 9 , OS(═O)OR 10 , NR 9 C(═O)NR 9 R 9 , NR 9 C(═S)NR 9 R 9 , or NR 9 S(═O) 2 R 8 .

4. The flow battery of claim 3 , wherein A 2 is S(═O) 2 NR 9 R 9 or NR 9 C(═S)NR 9 R 9 , and at least one R 9 bound to N is H.

5. The flow battery of claim 3 , wherein A 2 is OS(═O)OR 10 .

6. The flow battery of claim 5 , wherein R 10 is H.

7. The flow battery of claim 1 , wherein the nitroxide compound is present in only the first aqueous electrolyte solution.

8. The flow battery of claim 7 , wherein the first aqueous electrolyte solution is a positive electrolyte solution and the first half-cell is a positive half-cell of the flow battery.

9. The flow battery of claim 8 , wherein the second half cell is a negative half-cell of the flow battery, and the second redox-active material is a coordination compound.

10. The flow battery of claim 9 , wherein the coordination compound comprises a titanium coordination compound.

11. The flow battery of claim 9 , wherein the coordination compound has a formula of:

D g M(L 1 )(L 2 )(L 3 )

wherein:

M is a transition metal or main group metal;

D is ammonium, tetraalkylammonium, an alkali metal ion, or any combination thereof;

g is an integer in a range between 0 and 6; and

L 1 , L 2 and L 3 are ligands.

12. The flow battery of claim 11 , wherein the transition metal is titanium.

13. The flow battery of claim 11 , wherein at least one of L 1 , L 2 and L 3 is a catecholate ligand or a substituted catecholate ligand.

14. The flow battery of claim 1 , wherein the salt form is an alkali metal salt form, a combination of alkali metal salt forms, an ammonium salt form, a tetraalkylammonium salt form, or any combination thereof.

15. The flow battery of claim 1 , wherein A 2 is —OS(═O) 2 OR 10 or a salt thereof.

16. The flow battery of claim 1 , wherein the nitroxide compound is [2,2,6,6,-tetramethyl-4-(sulfooxy)piperidin-1-yl]oxidanyl or a salt thereof.

17. The flow battery of claim 15 , wherein the nitroxide compound is an alkali metal, ammonium, or tetraalkylammonium salt of [2,2,6,6,-tetramethyl-4-(sulfooxy)piperidin-1-yl]oxidanyl.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 14, 2019
From: NORMAN, ZACHARIAH M.; MILLARD, MATTHEW; NELSON, EMILY GRACE; HUMBARGER, SCOTT THOMAS
To: LOCKHEED MARTIN ADVANCED ENERGY STORAGE, LLC
Reel/Frame 049468/0659 →
CHANGE OF NAME Recorded Jun 14, 2019
From: LOCKHEED MARTIN ADVANCED ENERGY STORAGE, LLC
To: LOCKHEED MARTIN ENERGY, LLC
Reel/Frame 049476/0544 →