Synthesis of bimetallic structures for use as catalysts
US-11766660-B1 · Sep 26, 2023 · US
US12080895B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12080895-B2 |
| Application number | US-202217883912-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 9, 2022 |
| Priority date | Aug 9, 2022 |
| Publication date | Sep 3, 2024 |
| Grant date | Sep 3, 2024 |
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A method for making a branched metal nanocatalyst including providing a first metal precursor solution having a first metal precursor, wherein providing the first metal precursor solution includes combining a first metal ion source and a first alkylamine, and providing a second metal precursor solution, wherein providing the second metal precursor solution includes combining a second metal ion source and a second alkylamine, heating the second metal precursor solution, combining the first metal precursor solution with the second metal precursor solution to provide a reaction solution, and holding the reaction solution at an elevated temperature for a reaction time to provide a branched metal nanocatalyst. Also described are nanocatalysts prepared according to the method.
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What is claimed is: 1. A method for making a branched metal nanocatalyst, comprising: providing a first metal precursor solution comprising a first metal precursor, wherein providing the first metal precursor solution comprises combining a first metal ion source and a first alkylamine, and providing a second metal precursor solution, wherein providing the second metal precursor solution comprises combining a second metal ion source and a second alkylamine, heating the second metal precursor solution; combining the first metal precursor solution with the second metal precursor solution to provide a reaction solution; and holding the reaction solution at an elevated temperature for a reaction time to provide a branched metal nanocatalyst. 2. The method of claim 1 , wherein the first metal ion source is selected from a group consisting of sodium hexachloroplatinate hexahydrate, chloroplatinic acid hexahydrate, platinum chloride, platinum acetylacetonate, hydrates thereof, and combinations thereof. 3. The method according to claim 1 , wherein the first alkylamine is selected from a group consisting of oleylamine, hexadectylamine, dodecylamine, octadecylamine, tetradecylamine, and combinations thereof. 4. The method of claim 1 , wherein the first metal precursor is selected from a group consisting of Pt-OLA, Pt-HDA, Pt-DD, Pt-ODA, and Pt-TDA. 5. The method of claim 1 , wherein the second metal ion source is selected from a group consisting of sodium hexachloroplatinate hexahydrate, chloroplatinic acid hexahydrate, platinum chloride, platinum acetylacetonate, hydrates thereof, and combinations thereof. 6. The method according to claim 1 , wherein the second alkylamine is selected from a group consisting of oleylamine, hexadectylamine, dodecylamine, octadecylamine, tetradecylamine, and combinations thereof. 7. The method of claim 1 , wherein the elevated temperature is between about 100 and 300° C. 8. The method of claim 1 , wherein the elevated temperature is between about 100 and 200° C. 9. The method of claim 1 , wherein the branched metal nanocatalyst comprises platinum. 10. The method of claim 9 , wherein branched metal nanocatalyst is enclosed by high-index facets. 11. The method according to claim 9 , wherein the branched metal nanocatalyst has a mass activity of at least 0.44 A/mg Pt at 0.9 V with <40% loss in initial activity after 100,000 cycles in a proton exchange membrane fuel cell. 12. The method of claim 1 , wherein a concentration of the first metal precursor provided to the reaction solution is between about 1 and 200 mg/mL. 13. The method of claim 1 , wherein an atomic molar ratio of the first metal ion source to the first alkylamine combined to provide the first metal precursor solution is from about 1:1 to 1:200. 14. The method of claim 13 , wherein the atomic molar ratio of the first metal ion source to the first alkylamine combined to provide the first metal precursor solution is from about 1:10 to 1:160. 15. The method of claim 1 , wherein an atomic molar ratio of the second metal ion source to the second alkylamine combined to provide the first metal precursor solution is from about 1:1 to 1:500. 16. The method of claim 15 , wherein the atomic molar ratio of the second metal ion source to the second alkylamine combined to provide the first metal precursor solution is from about 1:10 to 1:360. 17. A branched metal nanocatalyst prepared by the method according to claim 1 , wherein the branched metal nanocatalyst comprises platinum, and wherein branched metal nanocatalyst is enclosed by high-index facets.
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