Photocatalytic material, preparation method thereof and application of photocatalytic material to visible light water splitting hydrogen production
A technology of photocatalytic materials and composite materials, which is applied in the application field of visible light decomposition of water to produce hydrogen, can solve the problems of photocorrosion and high recombination rate of photogenerated charge carriers, reduce energy consumption and cost, and the preparation method is simple and controllable. The effect of increasing the number
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[0047] The present invention also provides the above-mentioned composite material (Cd 1-x Zn x S / WO 3-y / CoO / NiO) preparation method, it comprises the steps:
[0048] 1) Preparation of Cd 1-x Zn x S solid solution nanocrystal, where 0≤x≤1;
[0049] 2) The Cd of step 1) 1-x Zn x S solid solution nanocrystal, WCl 4 Disperse in ethylene glycol solvent, carry out ion adsorption and hydrolysis oxidation reaction, and prepare Cd 1-x Zn x S / WO 3-y composite materials;
[0050] 3) the Cd of step 2) 1-x Zn x S / WO 3-y The composite material is dispersed in an aqueous solution of nickel acetate and cobalt acetate containing a sacrificial agent, and deposited in situ under light irradiation to prepare the composite material Cd 1-x Zn x S / WO 3-y / CoO / NiO, 0≤y≤0.3.
[0051] According to one embodiment of the present invention, in step 1), the Cd 1-x Zn x The preparation method of S solid solution nanocrystals is not particularly limited, and it can be prepared by conventi...
preparation example 1
[0084] (1) Synthesis of Cd 0.85 Zn 0.15 S nanorods.
[0085] Pour 35 ml of ethylenediamine into the cleaned and dried polytetrafluoroethylene liner (50 ml), then add 1.7 mmol of cadmium nitrate, 0.3 mmol of zinc nitrate, and 4.0 mmol of sublimated sulfur successively, stir and Sonicate for 5 minutes to dissolve, then stir the suspension for 30 minutes to mix well. Then, the reaction kettle was screwed tightly and sealed, and then put into an electric heating constant temperature blast drying oven, and reacted for 12 hours at 200 degrees Celsius. After the reaction was finished, it was naturally cooled to room temperature, and the product was taken out, centrifuged, and washed three times alternately with ethanol and deionized water. Finally, put the sample product into a vacuum drying oven and dry it at 80 degrees Celsius for 5 hours to obtain Cd 0.85 Zn 0.15 S nanorods.
[0086] figure 1 for the obtained Cd 0.85 Zn 0.15 SEM images of 1D nanocrystals. from figure 1 ...
preparation example 2
[0091] Step (1) is the same as the step (1) of Preparation Example 1;
[0092] (2) Synthesis of Cd 0.85 Zn 0.15 S / 0.08WO 3-y Composite nanorods; where, WCl 4 The concentration is 0.08M, so it is recorded as Cd 0.85 Zn 0.15 S / 0.08WO 3-y .
[0093] 0.6g of Cd from step 1) 1-x Zn x S solid solution nanocrystals were ultrasonically dispersed in ethylene glycol, and then WCl dissolved in ethylene glycol by ultrasonic was added 4 solution, after stirring the mixture evenly, continue to stir at room temperature for 0.5-1 hour, after the solid product in the solution is centrifuged, wash it once with ethanol and then wash it twice with deionized water, and dry it in vacuum at 80 degrees Celsius for 5 hours , synthesized to obtain Cd 1-x Zn x S / 0.08WO 3-y composite material.
[0094] Figure 4 is Cd 0.85 Zn 0.15 S / 0.08WO 3-y TEM and high-resolution TEM images of composite nanorods. From the transmission diagram, it can be found that the product retains the morphology ...
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