Nickel phosphides electrocatalysts for hydrogen evolution and oxidation reactions
US-2016355936-A1 · Dec 8, 2016 · US
US9802821B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9802821-B2 |
| Application number | US-201615209618-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 13, 2016 |
| Priority date | Jul 13, 2015 |
| Publication date | Oct 31, 2017 |
| Grant date | Oct 31, 2017 |
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There is provided a method of preparing transition metal phosphide comprising the step of mixing a solution of a transition metal precursor and a phosphorous precursor under conditions to form the transition metal phosphide. There is also provided a transition metal phosphide particle made according to the method as defined herein. There is additionally provided a method of preparing a transition metal phosphide-based electrode used for producing hydrogen in the electrolysis of water.
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What is claimed is: 1. A method of preparing a transition metal phosphide comprising: heating a solution of a transition metal precursor and a phosphorous precursor at a temperature in the range of 90° C. to 130° C.; and mixing said solution to form said transition metal phosphide. 2. The method of claim 1 , wherein the transition metal precursor contains transition metal that is cobalt (Co), iron (Fe), nickel (Ni), manganese (Mn), or combinations thereof. 3. The method of claim 1 , further comprising the operation of adding an additive to said solution mixture to promote ionization and solubilization of said transition metal precursor. 4. The method of claim 3 , wherein said additive is oleylamine (OAM). 5. The method claim 1 , further comprising the operation of degassing the mixture. 6. The method of claim 5 , wherein said degassing of the mixture is undertaken in a vacuum and in an inert gas atmosphere. 7. The method of claim 5 , wherein said degassing operation is undertaken for a period of time in the range of 10 minutes to 30 minutes. 8. The method of claim 1 , further comprising the operation of heating the mixture at a predetermined temperature. 9. The method of claim 8 , wherein said predetermined temperature is in the range of 270 to 350° C. 10. The method of claim 8 , wherein the solution mixture is kept at said predetermined temperature for 90 minutes to 150 minutes. 11. The method of claim 1 , wherein said transition metal precursor is selected from the group consisting of transition metal acetylacetonate, transition metal carbonate, transition metal benzoylacetonate, transition metal bromide, transition metal chloride, transition metal fluoride, transition metal iodide, transition metal nitrate, transition metal oxalate, transition metal phosphate, transition metal sulphate, transition metal acetate, transition metal thiocyanate and mixtures thereof. 12. The method of claim 1 , wherein said phosphorous precursor is selected from the group consisting of trioctyl phosphine (TOP), tributyl phosphine, trinonyl phosphine oxide, trioctyl phosphine oxide (TOPO), trihexyl phosphine oxide, butyl diphenyl oxide and tert-butyl diphenyl oxide. 13. A transition metal phosphide particle made according to a method of preparing transition metal phosphide comprising heating a solution of a transition metal precursor and a phosphorous precursor at a temperature in the range of 90° C. to 130° C. and mixing said solution to form said transition metal phosphide. 14. The transition metal phosphide particle of claim 13 , wherein said transition metal phosphide particle is in the form of a wire, a rod, a sphere or a sheet. 15. The transition metal phosphide particle of claim 13 , wherein said transition metal phosphide is amorphous or semi-crystalline. 16. A method of preparing a transition metal phosphide-based electrode used for producing hydrogen in the electrolysis of water, comprising: a. mixing a solution of a transition metal precursor and a phosphorous precursor under conditions to form a transition metal phosphide solution; b. casting said transition metal phosphide solution onto a substrate; and c. annealing of the substrate coated with the transition metal phosphide solution. 17. The method of claim 16 , wherein said transition metal phosphide is dicobalt phosphide. 18. The method of claim 16 , wherein said annealing operation is undertaken at a temperature in the range of 200° C. to 350° C.
Electrodes formed of electrocatalysts on a substrate or carrier · CPC title
by electrolysis of water · CPC title
characterised by the material · CPC title
Other phosphides · CPC title
Cross-Sectional Technologies · mapped topic
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