Ferrochrome co-doped nickel-based hydroxide self-supporting electrode for fully hydrolyzing water and preparation method thereof
A self-supporting electrode and hydroxide technology, applied in the direction of electrodes, electrolysis process, electrolysis components, etc., can solve the problems of restricting the wide application of catalysts, high price, low reserves, etc., to achieve multiple reaction active sites, low cost, high temperature low effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0026] The preparation method of the chromium-iron co-doped nickel-based hydroxide self-supporting electrode for total water splitting of the present invention, the specific steps include:
[0027] Step 1: Pretreat the nickel foam. Cut the nickel foam into 1cm×5cm blocks, ultrasonically clean it in acetone solution for 10min, then pour it into the prepared 3mol / L hydrochloric acid solution for ultrasonic cleaning for 5min, and finally rinse it alternately with absolute ethanol and ultrapure water 3 times, and then vacuum-dried at 25°C for 12 hours before use;
[0028] Step 2: Mix 170mg of nickel nitrate hexahydrate, 55mg of chromium nitrate nonahydrate, 45mg of ferric chloride hexahydrate, 125mg of urea, and 1.5mL of dimethylformamide, and add 20ml of ultrapure water, magnetic Stir for 20min, stir evenly to obtain solution A;
[0029] Step 3: Soak the spare nickel foam obtained in step 1 in the solution A obtained in step 2, transfer it to the hydrothermal reaction kettle of...
Embodiment 2
[0037] The preparation method of the chromium-iron co-doped nickel-based hydroxide self-supporting electrode for total water splitting of the present invention, the specific steps include:
[0038] Step 1: Pretreat the nickel foam. Cut the nickel foam into 1cm×5cm blocks, ultrasonically clean it in acetone solution for 15min, then pour it into the prepared 1mol / L hydrochloric acid solution for ultrasonic cleaning for 10min, and finally rinse it alternately with absolute ethanol and ultrapure water 2 times, and then vacuum-dried at 35°C for 10 hours before use;
[0039] Step 2: Mix 180mg of nickel nitrate hexahydrate, 65mg of chromium nitrate nonahydrate, 35mg of ferric chloride hexahydrate, 115mg of urea, and 1.6mL of dimethylformamide, and add 21ml of ultrapure water, magnetically Stir for 21min, stir evenly to obtain solution A;
[0040] Step 3: Soak the spare nickel foam obtained in step 1 in the solution A obtained in step 2, transfer it to the hydrothermal reaction kettle...
Embodiment 3
[0043] The preparation method of the chromium-iron co-doped nickel-based hydroxide self-supporting electrode for total water splitting of the present invention, the specific steps include:
[0044] Step 1: Pretreat the nickel foam. Cut the nickel foam into 1cm×5cm blocks, ultrasonically clean it in acetone solution for 11min, then pour it into the prepared 2mol / L hydrochloric acid solution for ultrasonic cleaning for 8min, and finally rinse it alternately with absolute ethanol and ultrapure water 3 times, and then vacuum-dried at 30°C for 11 hours before use;
[0045] Step 2: Mix 175mg of nickel nitrate hexahydrate, 60mg of chromium nitrate nonahydrate, 40mg of ferric chloride hexahydrate, 120mg of urea, and 1.7mL of dimethylformamide, and add 22ml of ultrapure water. Stir for 22 minutes, stir evenly to obtain solution A;
[0046] Step 3: Soak the spare nickel foam obtained in step 1 in the solution A obtained in step 2, transfer it to the hydrothermal reaction kettle of p-p...
PUM
Property | Measurement | Unit |
---|---|---|
Current density | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com