MoO2-NiSx/CC hydrogen evolution electrocatalyst and preparation method thereof
An electrocatalyst, moo2-nisx technology, applied in the field of electrocatalytic hydrogen evolution, can solve the problems of low hydrogen production efficiency, limited large-scale commercial application, poor current density stability, etc., and achieves simple preparation method and excellent electrocatalytic hydrogen evolution performance. , the effect of long service life
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0027] One, embodiment 1: prepare MoO according to the following steps 2 -NiS x / CC Composite,
[0028] (1) Treatment of carbon cloth: Cut the carbon cloth into a size of 1×1.5 cm, then ultrasonically wash it in 0.5 mol / L sulfuric acid solution, deionized water and ethanol for 5 minutes, cycle wash three times, and dry it naturally for later use.
[0029] (2) Preparation of nickel nitrate solution: Weigh 1.16 g of nickel nitrate hexahydrate and dissolve it in 40 mL of deionized water, sonicate for 10 minutes, and prepare a 0.1 mol / L nickel nitrate solution for later use.
[0030] (3) Electrodeposition of nickel: The electrodeposition equipment is the French Bio-Logic VMP3 multi-channel electrochemical workstation, with carbon cloth as the working electrode, platinum sheet as the counter electrode, and a saturated calomel electrode as the reference electrode. Among them, using the configured nickel nitrate solution as the electroplating solution, at -10 mA / cm 2 Electrodeposi...
Embodiment 2
[0043] (1) Treatment of carbon cloth: Cut the carbon cloth into a size of 1×1.5 cm, then ultrasonically wash it in 0.5 mol / L sulfuric acid solution, deionized water and ethanol for 5 minutes, cycle wash three times, and dry it naturally for later use.
[0044] (2) Preparation of nickel nitrate solution: Weigh 1.16 g of nickel nitrate hexahydrate and dissolve it in 40 mL of deionized water, sonicate for 10 minutes, and prepare a 0.1 mol / L nickel nitrate solution for later use.
[0045] (3) Electrodeposition of nickel: the equipment for electrodeposition is the French Bio-Logic VMP3 multi-channel electrochemical workstation. A carbon cloth was used as the working electrode, a platinum sheet was used as the counter electrode, and a saturated calomel electrode was used as the reference electrode. Among them, with the configured nickel nitrate solution as the electroplating solution, at -10 mA / cm 2 Electrodeposition was carried out for 1 hour under the electric current. After the...
Embodiment 3
[0051] (1) Treatment of carbon cloth: Cut the carbon cloth into a size of 1×1.5 cm. Then ultrasonically wash in 0.5 mol / L sulfuric acid solution, deionized water, and ethanol for 5 minutes, and cycle wash three times. Let it dry naturally.
[0052] (2) Preparation of nickel nitrate solution: Weigh 1.16 g of nickel nitrate hexahydrate and dissolve it in 40 mL of deionized water, sonicate for 10 minutes, and prepare a 0.1 mol / L nickel nitrate solution for later use.
[0053] (3) Electrodeposition of nickel: the equipment for electrodeposition is the French Bio-Logic VMP3 multi-channel electrochemical workstation. A carbon cloth was used as the working electrode, a platinum sheet was used as the counter electrode, and a saturated calomel electrode was used as the reference electrode. With the prepared nickel nitrate solution as the electroplating solution, at -10 mA / cm 2 Electrodeposition was carried out for 1 hour under the electric current. After the electrodeposition, the ...
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