An efficient ni-s-b hydrogen evolution electrode and its preparation method and application
A hydrogen evolution electrode, ni-s-b technology, applied in the field of electrocatalytic hydrogen evolution, can solve the problems of easy generation of impurities, low coating strength, high equipment requirements, etc., and achieve excellent stability, low hydrogen evolution overpotential, and high hydrogen evolution catalytic activity.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0029] The present invention also provides a kind of preparation method of efficient Ni-S-B hydrogen evolution electrode, comprises the following steps:
[0030] (1) provide electroplating aqueous solution, described electroplating aqueous solution comprises the component of following concentration: nickel source 80~160g / L, thiourea 80~130g / L, boron source 10~45g / L, complexing agent 60~100g / L , conductive agent 20-60g / L, saccharin 0.5-5.0g / L, sulfosalicylic acid 5-30g / L;
[0031] (2) Using the nickel substrate as the cathode and the anode, the distance between the cathode and the anode being 0.5-3.0 cm, performing electroplating with the electroplating aqueous solution obtained in the step (1) to obtain a Ni-S-B hydrogen evolution electrode.
[0032] Preferably, during the electroplating process in the step (2), the temperature of the electroplating aqueous solution is 25-65° C., and the electroplating time is 40-100 min.
[0033] Preferably, the current density of electropla...
Embodiment 1
[0053] (1) Pretreatment of Ni matrix
[0054] First, the Ni sheet is mechanically polished to remove the oxide on the surface to make it metallic luster, and then cleaned with deionized water; then ultrasonically oscillated in lye and absolute ethanol for 20 minutes for chemical degreasing, wherein the lye is 15g / LNaOH, 60g / L Na 3 PO 4 12H 2 O, 25g / L Na 2 CO 3 and 15g / L Na 2 SiO 3 Then rinse with deionized water, boil and etch in 20% hydrochloric acid for 5 minutes, rinse with deionized water, dry naturally, and immerse in absolute ethanol solution for later use.
[0055] (2) Preparation of Ni-S-B hydrogen evolution electrode by electrodeposition
[0056] A double-anode and single-cathode system is adopted, and the Ni substrate treated in step (1) is used as the cathode and the anode. Composition of Ni-S-B plating solution: 140g / L NiSO 4 ·6H 2 O, 100g / L Thiourea, 40g / L Borax, 70g / L Na 3 C 6 h 5 o 7 2H 2 O, 20g / L NaCl, 1.5g / L saccharin, 5g / L sulfosalicylic acid,...
Embodiment 2
[0060] Step (1) is the same as step (1) in Example 1.
[0061] (2) Preparation of Ni-S-B hydrogen evolution electrode by electrodeposition
[0062] A dual-anode and single-cathode system is adopted, and the nickel sheet treated in step (1) is used as the cathode and the anode. Composition of Ni-S-B plating solution: 120g / L NiSO 4 ·6H 2 O, 80g / L thiourea, 30g / L borax, 80g / L Na 3 C 6 h 5 o 7 2H 2 O, 20g / L NaCl, 1.5g / L saccharin, 5g / L sulfosalicylic acid, the pH value of the plating solution is 3, the temperature of the plating solution is 50°C; the current density is 2A / dm 2 , The electrodeposition time is 70min. Rinse with deionized water after electroplating to remove residual plating solution, and dry naturally to prepare Ni-S-B hydrogen evolution electrode. The electrode composition was tested by an energy spectrometer, and the electrode composition was Ni: 70wt.%; S: 25wt.%; B: 5wt.%. The thickness of the electrodes was 20 μm. Step (3) is the same as step (3) in ...
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