Oxygen evolution reaction catalyst, preparation, application, electrolysis device and seawater cracking method
A technology for oxygen evolution reaction and catalyst, applied in the electrolysis process, electrolysis components, electrodes, etc., can solve the problem of inability to meet high current density and other problems, achieve excellent OER performance, high performance, and meet the effect of high current density
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0035] The application also provides a method for preparing an oxygen evolution reaction catalyst, comprising the following steps:
[0036] After the nickel foam is immersed in the ethanol solution of the metal precursor, it is taken out and dried; the ethanol solution of the metal precursor is an ethanol solution of ferric chloride and nickel chloride;
[0037] Ammonium bicarbonate is added into the ethanol solution of the metal precursor to dissolve, and the dried nickel foam is immersed in it, taken out and dried to obtain an oxygen evolution reaction catalyst.
[0038] Specifically, a metal precursor ethanol solution may be prepared first, and ferric chloride and nickel chloride are dissolved in ethanol to form a solution. Then immerse the nickel foam in the ethanol solution of the metal precursor for a certain period of time, such as 10 to 20 minutes, and then take it out. The nickel foam can be flattened and dried, such as drying at room temperature or by drying at a rel...
Embodiment 1
[0063] Preparation of catalysts for oxygen evolution reaction (amorphous / nanocrystalline and crystalline FeNiCH / NF)
[0064] Clean the NF three times ultrasonically with 3.0M hydrochloric acid, 95% ethanol and deionized water to remove impurities such as nickel oxide on the surface. A piece of NF (20×10×1.8mm) was immersed in 24.4mM FeCl 3 ·6H 2 O+2.71mM NiCl 2 ·6H 2 O in 60 mL of ethanol for 15 minutes, and then dried in air overnight. Then 0.71g NH 4 HCO 3 Add to the ethanol solution of the metal precursor mentioned above and stir vigorously. The above-mentioned NF was immersed in the above-mentioned solution for 6 hours at room temperature, so that the surface was covered with a layer of basic iron-nickel carbonate (FeNiCH). The obtained amorphous / nanocrystalline FeNiCH / NF was soaked in deionized water for 10-20 minutes to remove surface impurities, and then dried overnight in air to obtain amorphous / nanocrystalline and crystalline FeNiCH / NF.
Embodiment 2
[0066] This embodiment provides a kind of electrolysis device, and its electrolysis device comprises electrolytic cell, and the anode of electrolytic cell is the amorphous / nanocrystalline and crystalline FeNiCH / NF of embodiment 1, and the negative electrode of electrolytic cell is MoNi 4 / NF.
[0067] Mo Ni 4 The / NF catalyst can be synthesized using the following exemplary method.
[0068] Mo Ni 4 / NF catalyst synthesis. Clean the NF three times ultrasonically with 3.0M hydrochloric acid, 95% ethanol and deionized water to remove impurities such as nickel oxide on the surface. Prepare 15mL containing Ni(NO 3 ) 2 ·6H 2 O(0.04M) and (NH 4 ) 6 Mo 7 o 24 4H 2 O (0.01M) aqueous solution, transfer the aqueous solution and a piece of NF (20 × 10 × 1.8 mm) to a stainless steel autoclave with a capacity of 40 mL of polytetrafluoroethylene lining, keep it sealed at 150 ° C for 6 hours, and then naturally cool to room temperature. After washing with deionized water, NiMoO w...
PUM
Property | Measurement | Unit |
---|---|---|
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