Cd<1-x>Zn<x>S-Ni/MoS<2> composite photocatalyst, and preparation method and application thereof
A cd1-xznxs-ni, composite light technology, applied in catalyst activation/preparation, physical/chemical process catalysts, chemical instruments and methods, etc., can solve the problem of difficulty in preparing nanospheres, and achieve excellent photocatalytic water splitting. The effect of efficiency, low cost and simple operation method
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0052] (1) Synthesis of CdS assembled nanospheres
[0053] Pour 100 ml of deionized water into a clean and dry beaker (250 ml), then add 7 ml of 0.1 mol / liter sodium citrate aqueous solution, 5 ml of 0.1 mol / liter cadmium chloride aqueous solution, and 10 ml 0.1 mol / L thiourea aqueous solution, and finally 2 ml of ammonia water was added dropwise, and stirred for 5 minutes to obtain a clear and transparent solution. Then put the beaker into an ultrasonic machine (ultrasonic power is 500 watts) after being sealed with a plastic wrap, and react at 50 degrees Celsius for 6 hours. After the reaction was finished, it was naturally cooled to room temperature, the product was separated by centrifugation, and washed three times alternately with ethanol and deionized water. Finally, the product was put into a vacuum drying oven and dried at 70 degrees Celsius for 6 hours to obtain CdS assembled nanospheres.
[0054] figure 1 is the X-ray diffraction pattern of the obtained CdS assem...
Embodiment 2
[0058] (1)MoS 2 Preparation of nanosheets
[0059] 1 mmol MoCl 5 and 10.1 mmoles of thioacetamide were sequentially added into 35 ml of N,N-dimethylformamide solvent for ultrasonic dissolution, and then stirred evenly to obtain a precursor solution. The precursor solution was transferred to a 50 ml polytetrafluoroethylene-lined autoclave, and placed in an oven at 200 degrees Celsius for 24 hours to react. After the reactor was cooled to room temperature, the solid product in the solution was centrifuged, washed alternately with water and ethanol for 3 times, and dried in a vacuum oven at 70 degrees Celsius for 6 hours to obtain MoS 2 Nanosheets.
[0060] figure 1 is the obtained MoS 2 The X-ray diffraction pattern of the nanosheet, it can be seen that the diffraction signal of the product is consistent with that of MoS 2 consistent with.
[0061] (2)MoS 2 Photolysis of water hydrogen production activity test of nanosheets
[0062] Take 20 mg of MoS synthesized in step...
Embodiment 3
[0064] Step (1) is with the step (1) of embodiment 1
[0065] Step (2) is the same as the step (1) of embodiment 2
[0066] (3) Synthesis of CdS / MoS 2 nanospheres. 0.02 g of MoS from step (2) 2 Nanosheets were added to 100 ml of N,N-dimethylformamide for ultrasonic exfoliation for 3 hours, then 0.2 g of CdS nanospheres prepared in step (1) were added, and after ultrasonic mixing for 1 hour, stirring was continued for 12 hours for electrostatic adsorption assembly process . After the reaction was completed, the solid product in the solution was centrifuged, washed three times alternately with water and ethanol, and dried in a vacuum oven at 70 degrees Celsius for 6 hours to obtain CdS / MoS 2 composite nanospheres.
[0067] (4)CdS / MoS 2 Photolysis of Water and Hydrogen Production Activity of Composite Nanospheres
[0068] First take 20 mg of CdS / MoS synthesized in step (3) 2 The composite nanospheres were ultrasonically dispersed in 100 ml of lactic acid aqueous solution co...
PUM
Property | Measurement | Unit |
---|---|---|
diameter | 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