IP Library Granted Patent US 8,785,080
Granted Patent B2
US 8,785,080 · App. 11/968,798 · Granted Jul 22, 2014

Passivated metallic bipolar plates and a method for producing the same

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Quick Facts
Patent No.
US 8,785,080
App. No.
11/968,798
Granted
Jul 22, 2014
Kind
B2
Abstract

A method including providing a substrate; treating the substrate to form a passive layer, wherein the passive layer has a thickness of at least 3 nm; and depositing an electrically conductive coating over the substrate, wherein the coating has a thickness of about 0.1 nm to about 50 nm.

Claims (57)

1. A method comprising:

providing a first fuel cell bipolar plate substrate having a reactant gas flow field defined in a surface;

treating the first substrate to form a passive oxide layer on the substrate with a thickness of at least 3 nm, wherein the treating comprises at least one of soaking the substrate in boiling de-ionized water, or applying to the substrate a heat treatment above 400° C.;

depositing an electrically conductive metal coating on the passive oxide layer on the substrate, wherein the coating has a thickness of about 0.1 nm to about 50 nm.

2. A method as set forth in claim 1 wherein the treating the first substrate further comprises removing residual iron from the first substrate.

3. A method as set forth in claim 1 wherein the depositing comprises at least one of magnetron sputtering, electron beam evaporation, or ion assisted deposition.

4. A method as set forth in claim 1 wherein the passive layer has a thickness such that the thickness will not increase subsequent to the treating of the first substrate to form the passive layer when used in a fuel cell.

5. A method as set forth in claim 1 wherein the electrically conductive metal coating comprises at least one of platinum, ruthenium, or iridium.

6. A method as set forth in claim 1 wherein the first substrate comprises at least one of stainless steel, titanium, aluminum, or nickel base alloy.

7. A method as set forth in claim 1 wherein the first substrate comprises a bipolar plate.

8. A method as set forth in claim 1 wherein the electrically conductive metal coating has a thickness of about 0.1 nm to about 2 nm.

9. A method as set forth in claim 1 further comprising:

providing a second fuel cell substrate, wherein the first fuel cell substrate comprises a first bipolar plate and wherein the second fuel cell substrate comprises a second bipolar plate;

providing a soft goods portion comprising a polymer electrolyte membrane comprising a first face and a second face, a cathode electrode overlying the first face of the polymer electrolyte membrane, a first gas diffusion media layer overlying the cathode electrode, an anode electrode underlying the second face of the polymer electrolyte membrane, and a second gas diffusion media layer underlying the anode electrode; and

wherein the first bipolar plate overlies the first gas diffusion media layer, and the second bipolar plate underlies the second gas diffusion media layer.

10. A method as set forth in claim 9 further comprising providing a first microporous layer between the first gas diffusion media layer and the cathode electrode.

11. A method as set forth in claim 9 further comprising providing a second microporous layer between the second gas diffusion media layer and the anode electrode.

12. A method as set forth in claim 1 wherein the electrically conductive metal coating consists essentially of platinum, ruthenium, or iridium.

13. A method as set forth in claim 1 wherein the electrically conductive metal coating is porous.

14. A method as set forth in claim 9 wherein one of the first gas diffusion media layer and the second gas diffusion media layer includes a woven carbon cloth treated with a hydrophobic material.

15. A method as set forth in claim 9 wherein one of the first gas diffusion media layer and the second gas diffusion media layer has an average pore size of between 5 and 40 micrometers.

16. A method as set forth in claim 9 wherein one of the first gas diffusion media layer and the second gas diffusion media layer has an thickness of between 100 and 500 micrometers.

17. A method as set forth in claim 10 wherein the first microporous layer comprises a plurality of particles and a binder, wherein the binder and the plurality of particles are in a liquid phase comprising a mixture of organic solvent and water.

18. A method as set forth in claim 17 wherein the first microporous layer is dried and results in the first microporous layer comprising 60-90 weight percent particles and 10-40 weight percent binder.

19. A product comprising:

a first fuel cell bipolar plate substrate having a reactant gas flow field defined in a surface comprising a passive oxide layer thereon, wherein the passive layer has a thickness of at least 3 nm; and

a porous electrically conductive metal coating with the proviso that the electrically conductive metal coating does not include gold or platinum or vanadium on the passive oxide layer on the substrate, wherein the coating has a thickness of about 0.1 nm to about 50 nm.

20. A product as set forth in claim 19 wherein the electrically conductive metal coating comprises at least one of ruthenium, or iridium.

21. A product as set forth in claim 19 wherein the substrate comprises at least one of stainless steel, titanium, aluminum, or nickel base alloy.

22. A product as set forth in claim 19 wherein the electrically conductive metal coating has a thickness of about 0.1 nm to about 2 nm.

23. A product as set forth in claim 19 wherein the first fuel cell substrate comprises a first bipolar plate.

24. A product as set forth in claim 19 further comprising:

a second fuel cell substrate, wherein the first fuel cell substrate comprises a first bipolar plate and the second fuel cell substrate comprises a second bipolar plate;

a soft goods portion comprising a polymer electrolyte membrane comprising a first face and a second face, a cathode electrode overlying the first face of the polymer electrolyte membrane, a first gas diffusion media layer overlying the cathode electrode, an anode electrode underlying the second face of the polymer electrolyte membrane, and a second gas diffusion media layer underlying the anode electrode;

wherein the first bipolar plate overlies the first gas diffusion media layer, and the second bipolar plate underlies the second gas diffusion media layer.

25. A product as set forth in claim 24 further comprising a first microporous layer between the first gas diffusion media layer and the cathode electrode.

26. A product as set forth in claim 24 further comprising a second microporous layer between the second gas diffusion media layer and the anode electrode.

27. A product as set forth in claim 19 wherein the electrically conductive metal coating comprises at least one of ruthenium or iridium; wherein the substrate comprises at least one of stainless steel, titanium, aluminum, or nickel base alloy; and wherein the electrically conductive coating has a thickness of about 0.1 nm to about 2 nm.

28. A product as set forth in claim 19 wherein the electrically conductive metal coating consists essentially of ruthenium, or iridium.

29. A product as set forth in claim 25 wherein the first microporous layer comprises a plurality of particles and a binder, wherein the binder and the plurality of particles are in a liquid phase comprising a mixture of organic solvent and water.

30. A product as set forth in claim 29 wherein the first microporous layer is dried and results in the first microporous layer comprising 60-90 weight percent particles and 10-40 weight percent binder.

31. A method comprising:

providing a first fuel cell bipolar plate substrate having a reactant gas flow field defined in a surface;

treating the substrate to form a passive oxide layer on the substrate with a thickness of at least 3 nm, wherein the treating comprises contacting the substrate with a nitric acid solution;

depositing an electrically conductive metal coating with the proviso that the electrically conductive metal coating does not include gold or platinum or vanadium on the passive oxide layer on the substrate, wherein the coating has a thickness of about 0.1 nm to about 50 nm.

32. A method comprising:

providing a first fuel cell bipolar plate substrate having a reactant gas flow field defined in a surface;

treating the substrate to form a passive oxide layer on the substrate with a thickness of at least 3 nm, wherein the treating comprises soaking the substrate in boiling de-ionized water;

depositing an electrically conductive metal coating on the passive oxide layer on the substrate, wherein the coating has a thickness of about 0.1 nm to about 50 nm.

33. A method comprising:

providing a first fuel cell bipolar plate substrate having a reactant gas flow field defined in a surface;

treating the first substrate to form a passive oxide layer on the substrate with a thickness of at least 3 nm, wherein the treating comprises applying to the substrate a heat treatment above 400° C.;

depositing an electrically conductive metal coating on the passive oxide layer on the substrate, wherein the coating has a thickness of about 0.1 nm to about 50 nm.

34. A method comprising:

providing a first fuel cell bipolar plate substrate having a reactant gas flow field defined in a surface;

treating the first substrate to form a passive oxide layer on the substrate with a thickness of at least 3 nm, wherein the treating comprises at least one of contacting the substrate with a nitric acid solution, soaking the substrate in boiling de-ionized water, or applying to the substrate a heat treatment above 400° C.;

depositing an electrically conductive metal coating with the proviso that the electrically conductive metal coating does not include gold or platinum or vanadium on the passive oxide layer on the substrate, wherein the coating has a thickness of about 0.1 nm to about 50 nm.

Assignments (12)
RELEASE OF SECURITY INTEREST Recorded Nov 7, 2014
From: WILMINGTON TRUST COMPANY
To: GM GLOBAL TECHNOLOGY OPERATIONS LLC
Reel/Frame 034185/0587 →
CHANGE OF NAME Recorded Feb 10, 2011
From: GM GLOBAL TECHNOLOGY OPERATIONS, INC.
To: GM GLOBAL TECHNOLOGY OPERATIONS LLC
Reel/Frame 025781/0035 →
SECURITY AGREEMENT Recorded Nov 8, 2010
From: GM GLOBAL TECHNOLOGY OPERATIONS, INC.
To: WILMINGTON TRUST COMPANY
Reel/Frame 025324/0475 →
RELEASE OF SECURITY INTEREST Recorded Nov 5, 2010
From: UAW RETIREE MEDICAL BENEFITS TRUST
To: GM GLOBAL TECHNOLOGY OPERATIONS, INC.
Reel/Frame 025315/0001 →
RELEASE OF SECURITY INTEREST Recorded Nov 4, 2010
From: UNITED STATES DEPARTMENT OF THE TREASURY
To: GM GLOBAL TECHNOLOGY OPERATIONS, INC.
Reel/Frame 025245/0780 →
SECURITY AGREEMENT Recorded Aug 28, 2009
From: GM GLOBAL TECHNOLOGY OPERATIONS, INC.
To: UAW RETIREE MEDICAL BENEFITS TRUST
Reel/Frame 023162/0187 →
SECURITY AGREEMENT Recorded Aug 27, 2009
From: GM GLOBAL TECHNOLOGY OPERATIONS, INC.
To: UNITED STATES DEPARTMENT OF THE TREASURY
Reel/Frame 023156/0215 →
RELEASE OF SECURITY INTEREST Recorded Aug 21, 2009
From: CITICORP USA, INC. AS AGENT FOR BANK PRIORITY SECURED PARTIES; CITICORP USA, INC. AS AGENT FOR HEDGE PRIORITY SECURED PARTIES
To: GM GLOBAL TECHNOLOGY OPERATIONS, INC.
Reel/Frame 023155/0880 →
RELEASE OF SECURITY INTEREST Recorded Aug 20, 2009
From: UNITED STATES DEPARTMENT OF THE TREASURY
To: GM GLOBAL TECHNOLOGY OPERATIONS, INC.
Reel/Frame 023124/0670 →
SECURITY AGREEMENT Recorded Apr 16, 2009
From: GM GLOBAL TECHNOLOGY OPERATIONS, INC.
To: CITICORP USA, INC. AS AGENT FOR BANK PRIORITY SECURED PARTIES; CITICORP USA, INC. AS AGENT FOR HEDGE PRIORITY SECURED PARTIES
Reel/Frame 022554/0479 →
SECURITY AGREEMENT Recorded Feb 4, 2009
From: GM GLOBAL TECHNOLOGY OPERATIONS, INC.
To: UNITED STATES DEPARTMENT OF THE TREASURY
Reel/Frame 022201/0448 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 4, 2008
From: ABD ELHAMID, MAHMOUD H.; DADHEECH, GAYATRI VYAS; MIKHAIL, YOUSSEF M.
To: GM GLOBAL TECHNOLOGY OPERATIONS, INC.
Reel/Frame 020316/0342 →