Gas Diffusion Electrodes and Methods for Fabricating and Testing Same
US-2015376803-A1 · Dec 31, 2015 · US
US9548501B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9548501-B2 |
| Application number | US-200913498665-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 17, 2009 |
| Priority date | Dec 17, 2009 |
| Publication date | Jan 17, 2017 |
| Grant date | Jan 17, 2017 |
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A supported catalyst is prepared by a process that includes establishing shell-removal conditions for a supported catalyst intermediate that includes capped nanoparticles of a catalyst material dispersed on a carbon support. The capped nanoparticles each include a platinum alloy core capped in an organic shell. The shell-removal conditions include an elevated temperature and an inert gas atmosphere that is substantially free of oxygen. The organic shell is removed from the platinum alloy core under the shell-removal conditions to limit thermal decomposition of the carbon support and thereby limit agglomeration of the catalyst material such that the supported catalyst includes an electrochemical surface area of at least 30 m 2 /g Pt .
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What is claimed is: 1. A method, comprising: forming a supported catalyst having an electrochemical surface area of at least 30 m 2 /g Pt , the forming including: establishing shell-removal conditions for a supported catalyst intermediate, the supported catalyst intermediate including nanoparticles of a catalyst material dispersed on a carbon support, the nanoparticles each including a platinum alloy core having an organic shell that fully surrounds the platinum alloy core, the establishing including providing an elevated temperature and an inert gas atmosphere, the inert gas atmosphere being substantially free of oxygen, wherein a concentration of oxygen in the inert gas atmosphere is less than one part per million; and removing the organic shell that fully surrounds the platinum alloy core in the shell-removal conditions. 2. The method of claim 1 , wherein the electrochemical surface area is 30-150 m 2 /g Pt . 3. The method of claim 1 , wherein the electrochemical surface area is 40-120 m 2 /g Pt . 4. The method of claim 1 , wherein the electrochemical surface area is 40-60 m 2 /g Pt . 5. The method of claim 1 , wherein the catalyst material comprises platinum, cobalt, and nickel in a composition Pt x Co y Ni z , where the variables x, y, and z are atomic percentages that sum to 100, and x is 20%-60%, y is 20%-60%, and z=100−x−y, and the catalyst material has an oxygen reduction reaction mass activity of greater than 2.5 relative to an unalloyed platinum catalyst. 6. The method of claim 1 , wherein the catalyst material comprises platinum, cobalt, and nickel in a composition Pt x Co y Ni z , where the variables x, y, and z are atomic percentages that sum to 100, and x is 20%-60%, y is 20%-60%, and z=100−x−y, and the catalyst material has an oxygen reduction reaction mass activity of 2.5-6 relative to an unalloyed platinum catalyst. 7. The method of claim 1 , wherein the elevated temperature of the shell-removal conditions is 220° C.-600° C. 8. The method of claim 1 , wherein the inert gas atmosphere is selected from a group consisting of nitrogen, argon, and combinations thereof. 9. The method of claim 1 , wherein the catalyst material comprises platinum and at least one alloy metal selected from a group consisting of iron, nickel, cobalt, iridium, chromium, molybdenum, palladium, rhodium, gold, copper and vanadium. 10. The method of claim 1 , wherein the catalyst material comprises platinum, cobalt, and at least one alloy metal M selected from a group consisting of iron, nickel, iridium, chromium, molybdenum, palladium, rhodium, gold, copper and vanadium and having a composition Pt x Co y M z , where the variables x, y, and z are atomic percentages that sum to 100, and x is 20%-60%, y is 20%-60%, and z=100−x−y. 11. The method of claim 1 , wherein the catalyst material comprises platinum, cobalt, and nickel in a composition Pt x Co y Ni z , where the variables x, y, and z are atomic percentages that sum to 100, and x is 20%-60%, y is 20%-60%, and z=100−x−y. 12. The method of claim 1 , wherein the nanoparticles have an average particle size of 1-10 nanometers. 13. The method of claim 1 , wherein the nanoparticles have an average particle size of 3-6 nanometers. 14. A method, comprising: forming a supported catalyst having an electrochemical surface area of at least 30 m 2 /g Pt , establishing shell-removal conditions for a supported catalyst intermediate, the supported catalyst intermediate including nanoparticles of a catalyst material dispersed on a carbon support, the nanoparticles each including a platinum alloy core having an organic shell that fully surrounds the platinum alloy core, the establishing including providing an elevated temperature and a reducing gas atmosphere, wherein a concentration of oxygen in the reducing gas atmosphere is less than one part per million, the reducing gas atmosphere including a reducing agent to react with oxygen in the reducing gas atmosphere such that the oxygen is consumed before reacting with the carbon support; and completely removing the organic shell from the platinum alloy core in the shell-removal conditions. 15. The method of claim 14 , further comprising: annealing the supported catalyst intermediate after removing the organic shell. 16. The method of claim 14 wherein the reducing agent includes hydrogen. 17. A method, comprising: forming a supported catalyst, the forming including: treating a supported catalyst intermediate in a heat chamber, the supported catalyst intermediate including nanoparticles of a catalyst material dispersed on a carbon support, the nanoparticles each including a platinum alloy core having an organic shell that fully surrounds the platinum alloy core, the treating including: elevating a temperature of the heat chamber; providing an inert gas atmosphere in the heat chamber, the inert gas atmosphere being substantially free of oxygen, wherein a concentration of oxygen in the inert gas atmosphere is less than one part per million; and removing the organic shell that fully surrounds the platinum alloy core, wherein the removing exposes an electrochemical surface area of the platinum alloy core, the electrochemical surface area of the platinum alloy core being at least 30 m 2 /g Pt . 18. The method of claim 17 wherein the treating includes regulating a concentration of the inert gas atmosphere in the heat chamber during removing of the organic shell from the platinum alloy core. 19. The method of claim 17 wherein the electrochemical surface area is 40-120 m 2 /g Pt .
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