High performance flow battery

Patent metadata

Field	Value
Publication number	US-10008729-B2
Application number	US-201414470779-A
Country	US
Kind code	B2
Filing date	Aug 27, 2014
Priority date	Mar 30, 2010
Publication date	Jun 26, 2018
Grant date	Jun 26, 2018

Abstract

High performance flow batteries, based on alkaline zinc/ferro-ferricyanide rechargeable (“ZnFe”) and similar flow batteries, may include one or more of the following improvements. First, the battery design has a cell stack comprising a low resistance positive electrode in at least one positive half cell and a low resistance negative electrode in at least one negative half cell, where the positive electrode and negative electrode resistances are selected for uniform high current density across a region of the cell stack. Second, a flow of electrolyte, such as zinc species in the ZnFe battery, with a high level of mixing through at least one negative half cell in a Zn deposition region proximate a deposition surface where the electrolyte close to the deposition surface has sufficiently high zinc concentration for deposition rates on the deposition surface that sustain the uniform high current density.

First claim

What is claimed is:

1. A method of charging a flow battery, comprising:
circulating a super-saturated electrolyte over a negative electrode plating zone on a surface of a negative electrode of a negative half cell in the flow battery;
wherein the super-saturated electrolyte is prepared by combining zinc oxide with sodium hydroxide (NaOH) pellets in a silicate-free and phosphate-free solution;
wherein the super-saturated electrolyte has a zinc ion concentration greater than the equilibrium saturation concentration of the zinc ion in the super-saturated electrolyte and a hydroxide concentration of between 2 normal (N) and 5 normal (N); and
wherein a mass transfer coefficient of the super-saturated electrolyte is sufficient to maintain a super-saturated electrolyte concentration of zinc ions in the negative electrode plating zone for a substantially uniform deposition of zinc on the surface at a uniform high current density.

2. The method of claim 1 , wherein the super-saturated electrolyte has a zinc solubility of greater than about 0.7M in 4N NaOH.

3. The method of claim 1 , wherein the super-saturated electrolyte has a zinc solubility of about 0.73M in 4N NaOH.

4. The method of claim 1 , wherein the super-saturated electrolyte is prepared by combining the zinc oxide and the sodium hydroxide pellets in water to form a first solution that comprises a zinc ion concentration greater than 0.7 normal (N) and a hydroxide concentration of greater than 4 normal (N) and mixing the first solution with a second solution to form the super-saturated electrolyte that has a zinc ion concentration of about 0.7 normal (N).

5. The method of claim 1 , wherein the super-saturated electrolyte is prepared by combining the zinc oxide and the sodium hydroxide pellets in water to form a first solution that comprises a zinc ion concentration greater than 0.7 normal (N) and a hydroxide concentration of greater than 4 normal (N) and mixing the first solution with a second solution to form the super-saturated electrolyte that has a zinc ion concentration of between 0.4 N about 0.7 N and a hydroxide concentration of between about 2N and about 4N.

6. The method of claim 1 , wherein circulating the super-saturated electrolyte over the negative plating zone further comprises delivering the super-saturated electrolyte through a porous structure that has a porosity of between 60% and 98% and has a surface that comprises nickel.

7. The method of claim 1 , wherein the uniform high current density is greater than 70 mA/cm 2 .

8. The method of claim 1 , wherein a mass transfer coefficient of the super-saturated electrolyte has a value in the approximate range of 5.3×10 −4 m/s to 12.4×10 −3 m/s.

9. The method of claim 1 , wherein the flow battery is a flow battery selected from the group consisting of: a ZnFe flow battery, a ZnHBr flow battery, a ZnBr flow battery, a CeZn flow battery; and a ZnCl flow battery.

10. The method of claim 1 , further comprising delivering the super-saturated electrolyte through a flow channel that is configured to provide a high rate of mixing within the negative electrode plating zone.

11. A method of charging a flow battery, comprising:
providing a uniform high current density across a positive electrode and a negative electrode, the uniform high current density passing through a negative electrode plating zone on a surface of the negative electrode of the flow battery;
circulating a super-saturated electrolyte through a flow channel of the negative electrode, wherein the flow channel is configured to provide mixing of the super-saturated electrolyte in the negative electrode plating zone on the surface of the negative electrode;
wherein the super-saturated electrolyte is prepared by combining zinc oxide with sodium hydroxide (NaOH) pellets in a silicate-free and phosphate-free solution;
wherein the super-saturated electrolyte has a zinc ion concentration greater than the equilibrium saturation concentration of the zinc ion in the super-saturated electrolyte and a hydroxide concentration of between 2 normal (N) and 5 normal (N); and
wherein a mass transfer coefficient of the super-saturated electrolyte is sufficient to maintain a super-saturated electrolyte concentration of zinc ions in the negative electrode plating zone for a substantially uniform deposition of zinc on the surface at the uniform high current density.

12. The method of claim 11 , wherein the super-saturated electrolyte has a zinc solubility of greater than about 0.7M in 4N NaOH.

13. The method of claim 11 , wherein the super-saturated electrolyte has a zinc solubility of about 0.73M in 4N NaOH.

14. The method of claim 11 , wherein the super-saturated electrolyte is prepared by combining the zinc oxide and the sodium hydroxide pellets in water to form a first solution that comprises a zinc ion concentration greater than 0.7 normal (N) and a hydroxide concentration of greater than 4 normal (N) and mixing the first solution with a second solution to form the super-saturated electrolyte that has a zinc ion concentration of about 0.7 normal (N).

15. The method of claim 11 , wherein the super-saturated electrolyte is prepared by combining the zinc oxide and the sodium hydroxide pellets in water to form a first solution that comprises a zinc ion concentration greater than 0.7 normal (N) and a hydroxide concentration of greater than 4 normal (N) and mixing the first solution with a second solution to form the super-saturated electrolyte that has a zinc ion concentration of between 0.4 N about 0.7 N and a hydroxide concentration of between about 2N and about 4N.

16. The method of claim 11 , wherein circulating the super-saturated electrolyte over the negative plating zone further comprises delivering the super-saturated electrolyte through a porous structure that has a porosity of between 60% and 98% and has a surface that comprises nickel.

17. The method of claim 11 , wherein the uniform high current density is greater than 70 mA/cm 2 .

18. The method of claim 11 , wherein a mass transfer coefficient of the super-saturated electrolyte has a value in the approximate range of 5.3×10 −4 m/s to 12.4×10 −3 m/s.

19. The method of claim 11 , wherein the flow battery is a flow battery selected from the group consisting of: a ZnFe flow battery, a ZnHBr flow battery, a ZnBr flow battery, a CeZn flow battery; and a ZnCl flow battery.

20. The method of claim 11 , wherein the flow channel is configured to provide a high rate of mixing of the super-saturated electrolyte in the negative electrode plating zone proximate the surface of the negative electrode.

Assignees

• Applied Materials Inc

Inventors

• Gordon Ii Joseph Grover
• Gotcher Alan J
• Sikha Godfrey
• Wilson Gregory J

Classifications

• H01M8/188

  by recharging of redox couples containing fluids; Redox flow type batteries · CPC title

• H01M8/20

  Indirect fuel cells, e.g. fuel cells with redox couple being irreversible (H01M8/18 takes precedence) · CPC title

• H01M8/04186 Primary

  of liquid-charged or electrolyte-charged reactants · CPC title

• H01M2/38

  Electricity · mapped topic

• H01M50/70 Primary

  Arrangements for stirring or circulating the electrolyte · CPC title