Carbon dioxide electroreduction cathode and preparation method thereof
A carbon dioxide, cathode technology, applied in the direction of electrodes, electrolysis components, electrolysis process, etc., can solve problems such as inapplicability, achieve the effect of improving selectivity and activity, reducing mass transfer resistance, and increasing specific surface area
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0054] Nitrogen-doped nano-carbon materials were prepared using nano-calcium carbonate as a template. Accurately weigh 5g of sucrose, add 2g of ethylenediamine into 10ml of water and stir until completely dispersed, then add 5g of calcium carbonate, heat and mechanically stir in a water bath at 80°C to make it completely dispersed, and put it in a vacuum at 80°C after the water is completely evaporated Dry for 24h. Then put the dried product into high temperature tube furnace for carbonization, N 2 Treat at 850℃ for 3h, change CO 2 Purge at 850°C for 1 hour to obtain nanoparticle / carbon composites, then remove calcium carbonate with an appropriate amount of 2M dilute hydrochloric acid, filter and then vacuum dry at 80°C for 24 hours to obtain the macroporous nitrogen-doped nanocarbon material.
[0055] Dissolve 6.16 resorcinol in 7 mL of deionized water to form solution A; then dropwise add 8.4 ml of formaldehyde solution with a mass concentration of 37% to form a transpare...
Embodiment 2
[0060] Nitrogen-doped nano-carbon materials were prepared using nano-calcium carbonate as a template. Accurately weigh 5g of sucrose, add 2g of ethylenediamine into 10ml of water and stir until completely dispersed, then add 5g of calcium carbonate, heat and mechanically stir in a water bath at 80°C to make it completely dispersed, and put it in a vacuum at 80°C after the water is completely evaporated Dry for 24h. Then put the dried product into high temperature tube furnace for carbonization, N 2 Treat at 850℃ for 3h, change CO 2 Purge at 850°C for 1 hour to obtain nanoparticle / carbon composites, then remove calcium carbonate with an appropriate amount of 2M dilute hydrochloric acid, filter and then vacuum dry at 80°C for 24 hours to obtain the macroporous nitrogen-doped nanocarbon material.
[0061] Dissolve 7.06g of melamine in 10mL of deionized water to form solution A; add dropwise 12.3ml of formaldehyde solution with a mass concentration of 37% to the stirring soluti...
Embodiment 3
[0064] P-doped nano-carbon materials were prepared using nano-alumina as a template. Accurately weigh 3.15g of melamine, 5.0ml of formaldehyde solution, 10ml of water, stir at 85°C for 20min until completely dissolved and become transparent, then add 4g of alumina after 0.2g of triphenylphosphine, heat in a water bath at 80°C and Stir mechanically to make it completely dispersed, and put it into vacuum drying at 60°C for 24 hours after the water is completely evaporated. Then put the dried product into a high-temperature tube furnace for carbonization, the atmosphere is nitrogen, and the gas flow is controlled at 20ml / min. Take out by carbonization at 900°C for 2h to obtain the nanoparticle / carbon composite, then remove nano-alumina with an appropriate amount of 2M dilute hydrochloric acid, and vacuum dry at 80°C for 24h after filtration to obtain the P-doped macroporous carbon material (phosphorus content 0.9%).
[0065] Dissolve 7.06g of melamine in 10mL of deionized water...
PUM
Property | Measurement | Unit |
---|---|---|
thickness | aaaaa | aaaaa |
thickness | aaaaa | aaaaa |
thickness | 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