Transition metal-containing catalysts and catalyst combinations including transition metal-containing catalysts and processes for their preparation and use as oxidation catalysts
US-8962513-B2 · Feb 24, 2015 · US
US9272334B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9272334-B2 |
| Application number | US-201213653688-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 17, 2012 |
| Priority date | Apr 12, 2011 |
| Publication date | Mar 1, 2016 |
| Grant date | Mar 1, 2016 |
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Methods of synthesizing platinum-nickel-alloy nanoparticles and supported catalysts comprising the nanoparticles are provided. The methods may comprise forming a reaction mixture in a reaction vessel; heating the reaction mixture sealed in the reaction vessel to a reaction temperature; maintaining the temperature of the reaction vessel for a period of time; cooling the reaction vessel; and removing platinum-alloy nanoparticles from the reaction vessel. The reaction mixture may comprise a platinum precursor, a nickel precursor, a formamide reducing solvent, and optionally a cobalt precursor. In some embodiments the reaction temperature is at or below the boiling point of the formamide reducing solvent, such as from about 120° C. to about 150° C., for example. The platinum-alloy nanoparticles provide favorable electrocatalytic activity when supported on a catalyst support material.
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What is claimed is: 1. A method of synthesizing platinum-nickel-alloy nanoparticles, the method comprising: forming a reaction mixture in a reaction vessel, wherein the reaction mixture does not include a capping agent, the reaction mixture comprising: (a) a platinum precursor; (b) a nickel precursor; and (c) a formamide reducing solvent; heating the reaction mixture in the reaction vessel to a reaction temperature of at least 120° C.; maintaining the temperature of the reaction vessel for at least 1 hour; cooling the reaction vessel; and removing platinum-nickel alloy nanoparticles from the reaction vessel. 2. The method of claim 1 , wherein the reaction temperature is from 120° C. to the boiling point of the formamide reducing solvent. 3. The method of claim 2 , wherein the molar ratio of platinum to nickel in the reaction mixture is from about 0.5:1 to about 3:1. 4. The method of claim 2 , wherein the molar ratio of platinum to nickel in the reaction mixture is about 1:1. 5. The method of claim 4 , wherein the reaction temperature is from about 130° C. to 150° C. 6. The method of claim 1 , further comprising stirring the reaction mixture in the reaction vessel while the reaction mixture is heated and while the reaction temperature is maintained. 7. The method of claim 1 , further comprising sealing the reaction vessel before heating the reaction mixture. 8. The method of claim 1 , wherein the reaction vessel is left unsealed during the heating of the reaction mixture and the maintaining of the temperature of the vessel. 9. The method of claim 1 , wherein the temperature is maintained for at least 6 hours. 10. The method of claim 1 , wherein the formamide reducing solvent is selected from alkyl-substituted formamides having the formula R 1 R 2 N—C(═O)H, where R 1 and R 2 are independently selected from hydrogen and a C 1 -C 6 hydrocarbyl. 11. The method of claim 1 , wherein the formamide reducing solvent is selected from the group consisting of formamide, N-methylformamide, N-ethylformamide, N,N-dimethylformamide and N,N-diethylformamide. 12. The method of claim 1 , wherein the formamide reducing solvent is N,N-dimethylformamide. 13. The method of claim 1 , wherein the platinum precursor is platinum(II) acetylacetonate and the nickel precursor is nickel(II) acetylacetonate. 14. The method of claim 1 , wherein the reaction mixture further comprises a cobalt precursor, and the molar ratio of platinum to the sum of nickel and cobalt in the reaction mixture is about 1:1. 15. The method of claim 14 , wherein the cobalt precursor is selected from the group consisting of cobalt(II) acetylacetonate, cobalt(III) acetylacetonate, and mixtures thereof. 16. A method of synthesizing platinum-nickel-alloy nanoparticles, the method comprising: forming a reaction mixture in a reaction vessel, wherein the reaction mixture does not include a capping agent, the reaction mixture comprising: (a) platinum(II) acetylacetonate; (b) nickel(II) acetylacetonate; and (c) N,N-dimethylformamide, wherein the molar ratio of platinum to nickel in the reaction mixture is about 1:1; heating the reaction mixture in the reaction vessel to a reaction temperature of from about 130° C. to about 145° C.; maintaining the temperature of the reaction vessel for from about 6 hours to about 24 hours; stirring the reaction vessel while maintaining the temperature; cooling the reaction vessel; and removing platinum-nickel-alloy nanoparticles from the reaction vessel. 17. The method of claim 16 , wherein the reaction vessel is a glass vial or a polytetrafluoroethylene vessel. 18. The method of claim 17 , further comprising sealing the reaction vessel before heating the reaction mixture. 19. The method of claim 16 , wherein the platinum-nickel alloy nanoparticles exhibit a platinum mass activity greater than 0.70 mA/μ Pt at 0.90 V. 20. A supported catalyst comprising: platinum-nickel-alloy nanoparticles prepared according to the method of claim 2 , wherein: the platinum-nickel-alloy nanoparticles comprise a molar ratio of platinum to nickel of about 3:1, the platinum-nickel-alloy nanoparticles comprise cuboctahedral nanoparticles, and the platinum-nickel-alloy nanoparticles have a mean particle size of from about 3 nm to about 15 nm; and a catalyst support having the platinum-nickel-alloy nanoparticles dispersed on outer surfaces of the catalyst support.
Nanosized particles · CPC title
Manufacture or treatment of nanostructures · CPC title
supported on carriers, e.g. powder carriers · CPC title
starting from liquid metal compounds, e.g. solutions · CPC title
Alloys or mixtures with metallic elements · CPC title
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