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A method for making catalysts of noble metal nanoparticles or alloy nanoparticles or both having shaped morphology, the method including the steps of: pretreating a support material; impregnating metal precursors onto the support material; and then reducing the impregnated metal precursors into shap

A method for making catalysts of noble metal nanoparticles or alloy nanoparticles or both having shaped morphology, the method including the steps of: pretreating a support material; impregnating metal precursors onto the support material; and then reducing the impregnated metal precursors into shaped metal nanoparticles or shaped alloy nanoparticles or both using a functional gas atmosphere.

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1. A method for making catalysts of noble metal nanoparticles or alloy nanoparticles or both having shaped morphology, the method comprising the steps of: pretreating a support material;impregnating metal precursors onto said support material; andreducing the impregnated metal precursors into shaped

1. A method for making catalysts of noble metal nanoparticles or alloy nanoparticles or both having shaped morphology, the method comprising the steps of: pretreating a support material;impregnating metal precursors onto said support material; andreducing the impregnated metal precursors into shaped metal nanoparticles or shaped alloy nanoparticles or both using a functional gas atmosphere wherein, after reduction, the functional gas atmosphere absorbs to either the (100) planes of the impregnated metal precursors to give the shaped metal nanoparticle or shaped alloy nanoparticles a cubic morphology or to the (111) planes of the impregnated metal precursors to give the shaped metal nanoparticle or shaped alloy nanoparticles either a tetrahedral or an octahedral morphology. 2. The method of claim 1 wherein the support material is selected from the group consisting of carbon, silica, silicon carbide, silicon nitride, carbon nitride, aluminum oxide, titanium oxide, cerium oxide, zirconium oxide, zeolite, aluminum silicate, magnesium aluminate, and polymers. 3. The method of claim 1 wherein the step of pretreating the support material comprises removing moisture from the support material. 4. The method of claim 1 wherein the step of pretreating the support material comprises modifying the support material with surface groups. 5. The method of claim 1 wherein the metal precursors are selected from the group consisting of inorganic salts or organic species. 6. The method of claim 5 wherein the metal precursors are selected from the group consisting of metal chlorides, metal sulfates, metal nitrates, metal cyanides, metal phosphates, metal acetylacetonates, metal stearates, metal acetates, metal carbonyls, metal propionates, metal fluoroacetylacetonates, metal fluoroacetates and mixtures thereof. 7. The method of claim 1 wherein the metal precursors are chosen such that the shaped metal nanoparticles or shaped alloy nanoparticles or both formed in said step of reducing are selected from platinum, palladium, rhodium, ruthenium, iridium, rhenium, tungsten, alloys of two or more of the forgoing, and alloys of one or more of the forgoing with one or more transition metals. 8. The method of claim 7 wherein the transition metals are selected from iron, copper, nickel, cobalt, silver, gold, molybdenum, titanium, vanadium, zinc, cadmium, mercury, gallium, indium, tin, lead, and bismuth. 9. The method of claim 1 wherein impregnating metal precursors onto said support material comprises: dissolving the metal precursors in a solvent to make a metal precursor solution;mixing said metal precursor solution with said support material to make a catalyst forming mixture; anddrying said catalyst forming mixture. 10. The method of claim 9 wherein the solvent is selected from the group consisting of water, ethanol, acetone, hexane, chloroform, toluene, methanol, propanol, dimethyl ether, tetrahydrofuran, and dimethyl sulfoxide. 11. The method of claim 9 wherein the metal precursor solution is mixed for a period of from 5 minutes or more to 180 minutes or less. 12. The method of claim 9 wherein the catalyst forming mixture is dried for a period of from 10 minutes or more to 240 minutes or less at a temperature of from room temperature or greater to 150° C. or less. 13. The method of claim 1 wherein the functional gas atmosphere are selected from the group consisting of carbon monoxide, nitric oxide, ammonia, acetylene and mixtures thereof. 14. The method of claim 13 wherein the functional gas atmosphere further includes a gas selected from hydrogen, inert gas and mixtures thereof. 15. The method of claim 13 wherein the functional gas atmosphere includes a mixture of carbon monoxide and hydrogen. 16. The method of claim 15 wherein the majority of the functional gas atmosphere is carbon monoxide and the minority of the functional gas atmosphere is hydrogen. 17. The method of claim 1 wherein the reduction of the impregnated metal precursors is conducted by heating the precursors on the support material to a temperature of greater than 50° C. and less than 300° C. and keeping the precursors on the support material at that temperature for a period of greater than 0 minutes and less than 180 minutes. 18. The method of claim 1 wherein, after said step of reducing, the method further comprises the step of removing the functional gas atmosphere.