A kind of bifunctional cobalt diselenide material and its preparation and application
A technology of cobalt diselenide and cobalt salt, which is applied in the direction of binary selenium/tellurium compounds, chemical instruments and methods, chemical/physical processes, etc., can solve the problems of catalytic activity, stability and electrocatalytic properties, and achieve the preparation The effect of simple method and high catalytic activity
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0033] The present invention provides a method for preparing cobalt diselenide, which includes the following steps:
[0034] (1) Put the mixed aqueous solution of soluble cobalt salt, soluble ammonium salt and carbon-containing precipitant together with the conductive substrate in a hydrothermal reaction vessel for hydrothermal reaction to obtain a cobalt precursor; wherein the mixed aqueous solution is soluble The molar ratio of cobalt salt, soluble ammonium salt and carbon-containing precipitant may be 1:(1-20):(10-50), and the concentration of the soluble ammonium salt in the mixed aqueous solution may be 0.01-0.3 mol / L;
[0035] The conductive substrate can be conductive glass or conductive metal substrate, such as foamed nickel, foamed copper, etc., preferably foamed nickel; foamed nickel can be of various sizes. The carbon-containing precipitant is preferably urea. Under the temperature of hydrothermal reaction, urea reacts with other raw materials to combine metal atoms af...
Embodiment 1
[0041] figure 1 The preparation process of the dual-functional catalyst cobalt diselenide provided in this example is shown, including the following steps:
[0042] (1) Precursor preparation: 2.5mmol of cobalt nitrate, 10mmol of ammonium fluoride, 25mmol of urea raw materials were dissolved in 40mL of deionized water and reacted hydrothermally at 120°C for 16 hours. The precursor is obtained by washing and drying.
[0043] (2) Stable cobalt diselenide nanotubes: Mix selenium powder and sodium hydroxide at a molar ratio of 3.75 millimoles to 7.5 millimoles with 0.14 milliliters of hydrazine hydrate (85% by mass) and 50 milliliters of dimethylamide. Put the cobalt basic carbonate precursor into the two-step hydrothermal selenization reaction, react at 180°C for 1 hour, and obtain the cobalt diselenide catalyst after the reaction is dried. figure 2 The scanning electron microscope image of the stable cobalt diselenide catalyst provided by the example of the present invention is shown...
Embodiment 2
[0046] (1) Precursor preparation: 2.5mmol of cobalt nitrate, 10mmol of ammonium fluoride, 25mmol of urea raw materials were dissolved in 40mL of deionized water and reacted hydrothermally at 120°C for 16 hours. The precursor is obtained by washing and drying.
[0047] (2) Stable cobalt diselenide nanotubes: Mix selenium powder and sodium hydroxide at a molar ratio of 3.75 millimoles to 7.5 millimoles with 1 ml of hydrazine hydrate (85% by mass) and 50 ml of dimethylamide. Put the cobalt basic carbonate precursor into the two-step hydrothermal selenization reaction, react at 180°C for 1 hour, and obtain the cobalt diselenide catalyst after the reaction is dried.
[0048] (3) Preparation of electrode: The cobalt diselenide catalyst was finally dried at 60° C. for 6 hours, and small pieces of 1 square centimeter were cut out to obtain electrodes. The electrochemical performance of the catalyst was carried out in a three-electrode test cell. Ag / AgCl was used as the reference electrode...
PUM
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