Hydrotalcite quantum dot electrocatalyst, preparation method thereof, application of hydrotalcite quantum dot electrocatalyst in electrocatalytic decomposition of water to produce oxygen
A technology of electrocatalysts and quantum dots, applied in chemical instruments and methods, physical/chemical process catalysts, metal/metal oxide/metal hydroxide catalysts, etc., to achieve low cost, simple process, and superior catalytic performance
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0049] 1. Preparation of NiCo-LDHs hydrotalcite quantum dot electrocatalyst:
[0050] Preparation of microemulsion: Add 5ml of isopropanol, 8ml of oleylamine, and 4ml of deionized water into the flask, stir until the solution is uniform, and obtain a microemulsion environment; add 0.0048mol of Ni(NO 3 ) 2 ·6H 2 O and 0.0024mol of Co(NO 3 ) 3 9H 2 O was added to the microemulsion prepared above, and after the salt was dissolved, the crystallization water was heated at 100°C for 27 hours.
[0051] After the reaction was completed, the product was filtered with suction, washed three times with a mixed solution of deionized water and ethanol with a volume ratio of 1:1, washed once with absolute ethanol, centrifuged, and dried at 60°C for 14 hours to obtain NiCo-LDHs Quantum dot precursor products.
[0052] The above precursor products were dispersed into formamide, sonicated by a high-power ultrasonic instrument for 4 hours, centrifuged at low speed to remove the bottom sedi...
Embodiment 2
[0059] Preparation of NiFe-LDH hydrotalcite quantum dot electrocatalyst:
[0060] Preparation of microemulsion: Add 3ml of isopropanol, 6ml of oleylamine dioctylamine, and 5ml of deionized water into the flask, and stir until the solution is uniform; add 0.004mol of Ni(NO 3 ) 2 ·6H 2 O and 0.002mol Fe(NO 3 ) 3 9H 2 O was added to the microemulsion prepared above, and after the salt was dissolved, the crystallization water was heated at 80°C for 20 hours.
[0061] After the reaction was completed, the product was filtered with suction, washed three times with a mixed solution of deionized water and ethanol with a volume ratio of 1:1, washed once with absolute ethanol, centrifuged, and dried at 90°C for 6 hours to obtain NiFe-LDHs Quantum dot precursor products.
[0062] Disperse the above precursor product into N,N-dimethylformamide, use a high-power ultrasonic instrument to sonicate for 6 hours, and centrifuge at low speed to remove the bottom sediment, and then perform ...
Embodiment 3
[0067] Preparation of NiTi-LDH hydrotalcite quantum dot electrocatalyst:
[0068] Preparation of microemulsion: Add 3ml of isopropanol, 5ml of oleylamine N,N-dimethyltetradecylamine, and 7ml of deionized water into the flask, stir until the solution is uniform; add 0.006mol of Ni(NO 3 ) 2 ·6H 2 O and 0.003 mil of TiCl4 were added to the microemulsion prepared above, and after the salt was dissolved, the crystallization water was heated at 120° C. for 15 hours.
[0069] After the reaction was completed, the product was suction-filtered, washed twice with a mixed solution of deionized water and ethanol with a volume ratio of 1:1, washed once with absolute ethanol, centrifuged, and dried at 70°C for 10 h to obtain NiTi-LDHs Quantum dot precursor products.
[0070] Disperse the above precursor products into N, N-dimethylformamide, use a high-power ultrasonic instrument to sonicate for 5 hours, and centrifuge at low speed to remove the bottom sediment, and then perform high-spee...
PUM
Property | Measurement | Unit |
---|---|---|
thickness | aaaaa | aaaaa |
particle diameter | 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