A kind of preparation method of electrode material for hydrogen production by electrolysis of water
An electrode material and electrolyzed water technology, applied in the environmental field, can solve the problems of limited application and few electrocatalysts, and achieve the effects of reduced production cost, good crystallinity, and excellent hydrogen evolution ability of electrolyzed water
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0024] First weigh 0.1mmol of cobalt perchlorate, 0.1mmol of 1,4-naphthalene diacid (H2ndc), 0.1mmol of 1,4-bis(imidazol-1-yl)butane and 2mL of 0.1M sodium hydroxide solution in a beaker , add 2mL of deionized water and 4mL of absolute ethanol to it and stir for 30 minutes to disperse evenly. The above mixed solution was transferred to a polytetrafluoroethylene reactor and placed in a 140°C oven for 72 hours to react, and then the temperature was slowly lowered to 30°C over 5 hours to obtain a purple blocky crystal product. After ultrasonic cleaning with deionized water and drying at 60 °C, Co(ndc)(bidp)(H 2 O), take 40mg Co-MOFs and 10mg of acetylene black composite to prepare the electrocatalyst.
Embodiment 2
[0026] First weigh 0.1mmol of cobalt perchlorate, 0.2mmol of 1,4-naphthalene diacid (H2ndc), 0.1mmol of 1,4-bis(imidazol-1-yl)butane and 2mL of 0.1M sodium hydroxide solution in a beaker , add 2mL of deionized water and 4mL of absolute ethanol to it and stir for 30 minutes to disperse evenly. The above mixed solution was transferred to a polytetrafluoroethylene reactor and placed in a 160°C oven to react for 72 hours, and then slowly cooled down to 30°C over 5 hours to obtain a purple blocky crystal product. After ultrasonic cleaning with deionized water and drying at 60 °C, Co(ndc)(bidp)(H 2 O), take 40mg Co-MOFs and 10mg of acetylene black composite to prepare the electrocatalyst.
Embodiment 3
[0028] First weigh 0.1mmol of cobalt perchlorate, 0.2mmol of 1,4-naphthalene diacid (H2ndc), 0.2mmol of 1,4-bis(imidazol-1-yl)butane and 2mL of 0.1M sodium hydroxide solution in a beaker , add 2mL of deionized water and 4mL of absolute ethanol to it and stir for 30 minutes to disperse evenly. The above mixed solution was transferred to a polytetrafluoroethylene reactor and placed in a 180°C oven for 72 hours to react, and then the temperature was slowly lowered to 30°C over 5 hours to obtain a purple blocky crystal product. After ultrasonic cleaning with deionized water and drying at 60 °C, Co(ndc)(bidp)(H 2 O), take 40mg Co-MOFs and 10mg of acetylene black composite to prepare the electrocatalyst.
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


