Nickel phosphide compound with multi-level pore structure and preparation method and application thereof
A technology of nickel phosphide and composites, which is applied in the field of electrocatalytic materials, can solve the problems of high cost and scarcity of platinum-based precious metals, and achieve the effects of high repeatability, cheap and easy raw materials, and suitable for mass production
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Embodiment 1
[0050] This embodiment provides a nickel phosphide composite with a multi-level hole structure. Its preparation process is as follows.
[0051] Nickel foam (with an average pore size of 250 microns) was ultrasonically cleaned with 1 mol / L hydrochloric acid, deionized water, and ethanol for 10 minutes respectively. Then prepare 30mL of a mixed solution of 0.1mol / L nickel chloride and 2mol / L ammonium chloride as the electrolyte, the nickel sheet as the counter electrode and reference electrode, the cleaned nickel foam as the working electrode, and submerge the nickel foam into the electrolyte 1cm 2 , in two-electrode mode with -1A cm -2 The constant current program was used for 500 seconds, and the resulting nickel foam was washed with deionized water and dried in a vacuum oven. Then soak the above 4 pieces of dried nickel foam in 30mL of an aqueous solution prepared by dissolving 1mmol nickel nitrate hexahydrate and 6mmol hexamethylenetetramine in deionized water, and transf...
Embodiment 2
[0053] Nickel foam (with an average pore size of 250 microns) was ultrasonically cleaned with 1 mol / L hydrochloric acid, deionized water, and ethanol for 10 minutes respectively. Then prepare 30mL of a mixed solution of 0.1mol / L nickel chloride and 2mol / L ammonium chloride as the electrolyte, the nickel sheet as the counter electrode and reference electrode, the cleaned nickel foam as the working electrode, and submerge the nickel foam into the electrolyte 1cm 2 , in two-electrode mode with -1A cm -2 The constant current program was used for 500 seconds, and the resulting nickel foam was washed with deionized water and dried in a vacuum oven. Then soak the above 4 pieces of dried nickel foam in 30mL of an aqueous solution prepared by dissolving 1mmol nickel nitrate hexahydrate and 6mmol hexamethylenetetramine in deionized water, and transfer it to the liner containing polytetrafluoroethylene Packaged in a hydrothermal kettle, hydrothermally reacted at 100°C for 10 hours, coo...
Embodiment 3
[0055] Nickel foam (with an average pore size of 250 microns) was ultrasonically cleaned with 1 mol / L hydrochloric acid, deionized water, and ethanol for 10 minutes respectively. Then prepare 30mL of a mixed solution of 0.1mol / L nickel chloride and 2mol / L ammonium chloride as the electrolyte, the nickel sheet as the counter electrode and reference electrode, the cleaned nickel foam as the working electrode, and submerge the nickel foam into the electrolyte 1cm 2 , in two-electrode mode with -1A cm -2 The constant current program was used for 500 seconds, and the resulting nickel foam was washed with deionized water and dried in a vacuum oven. Then soak the above 4 pieces of dried nickel foam in 30mL of an aqueous solution prepared by dissolving 1mmol nickel nitrate hexahydrate and 6mmol hexamethylenetetramine in deionized water, and transfer it to the liner containing polytetrafluoroethylene Packaged in a hydrothermal kettle, hydrothermally reacted at 120°C for 6 hours, cool...
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