Method for determining the state of charge of a vanadium redox flow battery
US-2016372777-A1 · Dec 22, 2016 · US
US10833340B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10833340-B2 |
| Application number | US-201415033607-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 31, 2014 |
| Priority date | Nov 1, 2013 |
| Publication date | Nov 10, 2020 |
| Grant date | Nov 10, 2020 |
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The present invention relates to methods and apparatuses for determining the ratio of oxidized and reduced forms of a redox couple in solution, each method comprising: (a) contacting a first stationary working electrode and a first counter electrode to the solution; (b) applying a first potential at the first working electrode and measuring a first constant current; (c) applying a second potential at the first working electrode and measuring a second constant current; wherein the sign of the first and second currents are not the same; and wherein the ratio of the absolute values of the first and second currents reflects the ratio of the oxidized and reduced forms of the redox couple in solution. When used in the context of monitoring/controlling electrochemical cells, additional embodiments include those further comprising (d) oxidizing or reducing the solution, so as to alter the balance of the oxidized and reduced forms of the redox couple in solution, to a degree dependent on the ratio of the absolute values of the first and second currents. These embodiments may be used in the context of maintaining an electrochemical cell, stack, or system.
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What is claimed: 1. A method of determining a ratio of oxidized and reduced forms of a redox couple in solution, said method comprising: (a) contacting a first stationary working electrode and a first counter electrode to the solution; (b) applying a first potential at the first stationary working electrode relative to the first counter electrode and measuring a first constant current; (c) applying a second potential at the first stationary working electrode relative to the first counter electrode and measuring a second constant current; and (d) determining the ratio of oxidized and reduced forms of the redox couple in solution based on the ratio of the absolute values of the first and second constant currents; wherein the first and second constant currents have opposite signs, and wherein the first stationary working electrode and first counter electrode each has a surface area contacting the solution, and the surface area of the first stationary working electrode contacting the solution is less than 20% of that of the surface area of the first counter electrode contacting the solution. 2. The method of claim 1 , wherein the first potential is more positive than an equilibrium potential of the redox couple, and the second potential is more negative than the equilibrium potential of the redox couple. 3. The method of claim 2 , wherein a magnitude of a difference between the first potential and an equilibrium potential and a magnitude of a difference between the equilibrium potential and the second potential are substantially the same. 4. The method of claim 1 , wherein the first and second potentials are of substantially the same magnitude but opposite in sign. 5. The method of claim 1 , wherein the ratio of the oxidized and reduced forms of the redox couple are in a range of from about 5:95 to 95:5. 6. The method of claim 1 , wherein the ratio of the oxidized and reduced forms of the redox couple are in a range of from about 20:80 to 80:20. 7. The method of claim 1 , wherein the redox couple comprises a metal or metalloid of Groups 2-16, including the lanthanide and actinide elements, or a coordination compound thereof. 8. The method of claim 1 , wherein the redox couple is a reversible redox couple. 9. The method of claim 1 , wherein the solution is an aqueous solution. 10. The method of claim 1 , wherein the solution is a non-aqueous solution. 11. The method of claim 1 , wherein the solution is moving. 12. The method of claim 1 , wherein at least one of the first stationary working electrode or the first counter electrode comprises an allotrope of carbon. 13. The method of claim 1 , wherein a constancy of at least one of the first or second constant currents is characterized by a change of less than 0.1% over one second or less than 1% over ten seconds. 14. The method of claim 1 , wherein the solution is contained within a half-cell fluidic loop of an operating flow battery cell or other operating electrochemical cell, said operating electrochemical cell generating or storing electrical energy. 15. The method of claim 1 , wherein the ratio of oxidized and reduced forms of the redox couple in solution based on the ratio of the absolute values of the first and second constant currents is determined by applying an experimentally derived correction factor. 16. The method of claim 1 , wherein the redox couple is a reversible redox couple. 17. The method of claim 1 , wherein the redox couple is a quasi-reversible redox couple. 18. A method of maintaining an electrochemical cell, the cell having at least one half-cell comprising oxidized and reduced forms of a redox couple in solution, the method comprising: determining the ratio of the oxidized and reduced forms of the redox couple in solution according to the method of claim 1 ; and oxidizing or reducing the solution, so as to alter a balance of the oxidized and reduced forms of the redox couple in solution, to a degree dependent on the ratio of the absolute values of the first and second constant currents. 19. The method of claim 18 , wherein the first potential is more positive than an equilibrium potential of the redox couple and the second potential is more negative than the equilibrium potential of the redox couple. 20. The method of claim 19 , wherein the magnitude of the difference between the first potential and the equilibrium potential and the magnitude of the difference between the equilibrium potential and the second potential are substantially the same. 21. The method of claim 20 , wherein the first and second potentials are of substantially the same magnitude but opposite in sign. 22. The method of claim 18 , wherein the ratio of the oxidized and reduced forms of the redox couple are in a range of from about 5:95 to 95:5. 23. The method of claim 18 , wherein the ratio of the oxidized and reduced forms of the redox couple are in a range of from about 20:80 to 80:20. 24. The method of claim 18 , wherein the redox couple comprises a metal or metalloid of Groups 2-16, including the lanthanide and actinide elements, or a coordination compound thereof. 25. The method of claim 18 , wherein the redox couple is a reversible redox couple. 26. The method of claim 18 , wherein the solution is an aqueous solution. 27. The method of claim 18 , wherein the solution is a non-aqueous solution. 28. The method of claim 18 , wherein the solution is moving. 29. The method of claim 18 , wherein at least one of the first stationary working electrode or the first counter electrode comprises an allotrope of carbon. 30. The method of claim 18 , wherein a constancy of at least one of the first or second constant currents is characterized by a change of less than 0.1% over one second or less than 1% over ten seconds. 31. The method of claim 18 , wherein the solution is contained within a half-cell fluidic loop of an operating flow battery cell or other operating electrochemical cell, said operating electrochemical cell generating or storing electrical energy. 32. The method of claim 18 , wherein oxidizing or reducing the solution is performed electrochemically. 33. The method of claim 32 , wherein oxidizing or reducing the solution takes place in a rebalancing sub-system within a half-cell fluidic loop of an electrochemical cell. 34. A device comprising: at least one pair of electrodes independently in fluidic contact with an electrolyte solution, each pair of electrodes consisting of a first stationary working electrode and a first counter electrode; a control system, including a power source and sensors, associated with each pair of electrodes, said control system configured to be capable of applying first and second electric potentials at each of the first working electrodes relative to the first counter electrodes, and measuring first and second currents associated with said first and second electric potentials; and software capable of calculating the ratio of the absolute values of the first and second currents between each electrode pair, which reflects the ratio of the oxidized and reduced forms of a redox couple in solution; and the device used in the implementation of the method of claim 1 .
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