Method for producing a solid nanocomposite material based on hexa- and octa-cyanometallates of alkali metals
US-2017260083-A1 · Sep 14, 2017 · US
US11951464B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11951464-B2 |
| Application number | US-201917270662-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 21, 2019 |
| Priority date | Aug 23, 2018 |
| Publication date | Apr 9, 2024 |
| Grant date | Apr 9, 2024 |
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The present invention relates in part to a method of fabricating multimetallic nanoparticles, the method comprising the steps of providing a substrate; activating the substrate surface; adsorbing a cationic transition metal complex onto the substrate surface to form a substrate-supported cationic transition metal complex; adsorbing an anionic transition metal complex onto the substrate-supported cationic transition metal complex to form a substrate-supported multimetallic complex salt; and reducing the substrate-supported multimetallic complex salt to provide a plurality of multimetallic nanoparticles. The invention also relates in part to a composition of multimetallic nanoparticles comprising at least two metals Ma and Mb; wherein the ratio of Ma to Mb is between about 2:1 and about 1:2.
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We claim: 1. A method of fabricating multimetallic nanoparticles, the method comprising: providing a substrate; activating the substrate surface; adsorbing a cationic transition metal complex onto the substrate surface to form a substrate-supported cationic transition metal complex; adsorbing an anionic transition metal complex onto the substrate-supported cationic transition metal complex to form a substrate-supported multimetallic complex salt; and reducing the substrate-supported multimetallic complex salt to provide a plurality of multimetallic nanoparticles. 2. The method of claim 1 , wherein the step of activating the substrate surface comprises the step of treating the substrate surface with a base. 3. The method of claim 1 , wherein the substrate has a specific surface area above about 500 m 2 /g. 4. The method of claim 1 , wherein the charge of the cationic transition metal complex is an integer value between +2 and +4. 5. The method of claim 1 , wherein the cationic transition metal complex is a polyammine complex. 6. The method of claim 1 , wherein the step of adsorbing a cationic transition metal complex onto the substrate surface comprises the step adding an aqueous solution comprising the cationic transition metal complex to an aqueous suspension comprising the substrate. 7. The method of claim 1 , wherein the anionic transition metal complex is selected from the group consisting of Na 2 PtCl 4 , K 2 PtCl 4 , Na 2 IrCl 6 , K 2 IrCl 6 , NaAuCl 4 , and KAuCl 4 . 8. The method of claim 1 , wherein the molar ratio of cationic transition metal complex to anionic transition metal complex is about 1:1. 9. The method of claim 1 , wherein the step of adsorbing an anionic transition metal complex onto the substrate-supported cationic transition metal complex further comprises the steps of: preparing an aqueous solution of the anionic transition metal complex; adding a phase transfer agent to the aqueous solution; adding an aprotic solvent to the aqueous solution to form a biphasic mixture; separating the aprotic solvent from the biphasic mixture; and adding the aprotic solvent to a suspension of the substrate-supported cationic transition metal complex in an aprotic solvent. 10. The method of claim 9 , wherein the aprotic solvent is selected from the group consisting of a chlorinated solvent, an aromatic solvent, and an aliphatic solvent. 11. The method of claim 9 , wherein the phase transfer agent is a quaternary ammonium salt or a crown ether. 12. The method of claim 1 , wherein the step of adsorbing an anionic transition metal complex onto the substrate-supported cationic transition metal complex to form a substrate-supported multimetallic complex salt further comprises the step of: adsorbing a second cationic transition metal complex onto the anionic transition metal complex. 13. The method of claim 12 , wherein the step of adsorbing a second cationic transition metal complex onto the anionic transition metal complex further comprises the steps of: exchanging at least one counterion of the second cationic transition metal complex with a non-coordinative anion; and adding the second cationic transition metal complex to a suspension of the substrate in an aprotic solvent. 14. The method of claim 1 , wherein the step of reducing the substrate-supported multimetallic complex salt comprises the step of treating the substrate-supported multimetallic complex salt with an atmosphere comprising hydrogen gas at a temperature of about 400° C.
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