Ionomers for improving the durability of membrane electrochemical devices and electrodes derived therefrom
US-2024120456-A1 · Apr 11, 2024 · US
US10367217B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10367217-B2 |
| Application number | US-201514616968-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 9, 2015 |
| Priority date | Feb 9, 2015 |
| Publication date | Jul 30, 2019 |
| Grant date | Jul 30, 2019 |
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A method of making a component of a membrane electrode assembly comprising the steps of forming an electrode on an air-permeable backer comprising ePTFE, depositing a mixture comprising ionomer and a water-insoluble alcohol onto said electrode, drying said mixture to form a protective ionomer layer, and depositing an ePTFE-reinforced ionomer layer onto said protective ionomer layer.
Opening claim text (preview).
What is claimed is: 1. A method of making a component for a membrane electrode assembly comprising the steps of: (a) providing an air-permeable backer; (b) depositing an electrode onto said backer; (c) depositing an aqueous wet layer comprising a fluoroionomer mixture comprising a water-insoluble alcohol and an ionomer onto said electrode; (d) substantially drying said wet layer to form a protective ionomer layer; and (e) depositing, after substantially drying said wet layer, a proton conducting composite wet layer onto said protective ionomer layer, wherein the proton conducting composite wet layer has an occlusive interior volume. 2. A method as defined in claim 1 wherein the air-permeable backer comprises an expanded polymer having release characteristics. 3. A method as defined in claim 2 wherein the expanded polymer is ePTFE. 4. A method as defined in claim 3 wherein said expanded polymer has a mass per area of less than about 16 g/m 2 of ePTFE. 5. A method as defined in claim 3 wherein said expanded polymer has a bubble point of greater than about 70 psi. 6. A method as defined in claim 3 wherein said air-permeable backer has a Z-strength sufficient to prevent cohesive failure of said ePTFE when said electrode is peeled off of said air-permeable backer. 7. A method as defined in claim 1 wherein the air-permeable backer is a gas diffusion layer. 8. A method as defined in claim 1 further comprising coupling a fabric to said backer. 9. A method as defined in claim 8 wherein said air-permeable backer is dimensionally stable within +/−4% throughout the manufacturing process. 10. A method as defined in claim 8 wherein said fabric comprises polyester. 11. A method as defined in claim 8 wherein said fabric has a thickness of less than about 0.006 inches. 12. A method as defined in claim 8 wherein said fabric has a mass/area of less than about 64 g/yd 2 . 13. A method as defined in claim 8 further comprising the step of bonding said fabric to said backer with an adhesive in a discontinuous pattern. 14. A method as defined in claim 13 wherein said fabric is dot-laminated to said backer with a urethane adhesive. 15. A method as defined in claim 13 wherein said adhesive is a solvent-resistant adhesive. 16. A method as defined in claim 1 wherein said ionomer is perfluorosulfonic acid (PFSA) ionomer. 17. A method as defined in claim 1 wherein said wet layer is aqueous and comprises greater than about 60 wt % water. 18. A method as defined in claim 1 wherein said wet layer is aqueous and comprises greater than about 90 wt % water. 19. A method as defined in claim 1 wherein said wet layer is aqueous and comprises less than about 3 wt % of said water-insoluble alcohol. 20. A method as defined in claim 1 wherein said wet layer is aqueous and comprises less than about 5 wt % of said water-insoluble alcohol. 21. A method as defined in claim 1 wherein said water-insoluble alcohol comprises hexanol. 22. A method as defined in claim 1 wherein said wet layer further comprises a water-soluble alcohol. 23. A method as defined in claim 22 wherein said wet layer comprises less than about 10 wt % of said water-soluble alcohol. 24. A method as defined in claim 22 wherein said water-soluble alcohol comprises glycol ether present in an amount of less than about 5 wt %. 25. A method as defined in claim 1 wherein said proton conducting composite wet layer comprises an ionomer. 26. A method as defined in claim 1 wherein said proton conducting composite wet layer comprises a reinforcement. 27. A method as defined in claim 26 wherein said reinforcement comprises an ePTFE membrane. 28. A method as defined in claim 1 further comprising the step of depositing an ionomer layer onto said proton conducting composite wet layer. 29. A method as defined in claim 28 further comprising the step of depositing another electrode onto said ionomer layer. 30. A method as defined in claim 1 further comprising the step of depositing another electrode onto said proton conducting layer. 31. A method as defined in claim 1 wherein said protective ionomer layer has a thickness of about 0.1 to about 25 microns. 32. A method as defined in claim 1 wherein said protective ionomer layer has a thickness of about 0.1 to about 10 microns. 33. A method as defined in claim 1 wherein said protective ionomer layer has a thickness of about 0.1 to about 3 microns.
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