A n,s co-doped graphene/molybdenum selenide/cofe-ldh airgel and its preparation
A graphene and co-doping technology, which is applied in the direction of graphene, binary selenium/tellurium compounds, cobalt compounds, etc., can solve the problems of low utilization efficiency, restrictions on widespread use, and scarce resources, and achieve low cost and batch production. The effect of small difference and safe operation
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[0048] N, S co-doped graphene / MoSe of the preferred embodiment of the present invention 2 The preparation method of / CoFe-LDH comprises:
[0049] S1, ultrasonically disperse graphite oxide in deionized water to prepare a graphene oxide lamellar dispersion. Preferably, the concentration of the prepared graphene oxide sheet dispersion is 0.5-3mg mL -1 , more preferably 2mg mL -1 .
[0050] Specifically, the graphite oxide is prepared by the following method:
[0051] S11, under ice bath and vigorous stirring, NaNO 3 Add concentrated sulfuric acid until NaNO 3 completely dissolved.
[0052] For example: adding concentration to the three-necked reaction flask is 98% concentrated sulfuric acid (H 2 SO 4 ), and the reaction bottle was placed in an ice-water bath and stirred at 150rpm, adding NaNO 3 , and continue to stir in an ice-water bath to dissolve it. Wherein, the concentrated sulfuric acid and NaNO 3 The weight ratio is: 60:1~100:1.
[0053] S12, maintain ice bath,...
Embodiment 1
[0082] A kind of N,S co-doped graphene / MoSe 2 The preparation method of / CoFe-LDH airgel comprises:
[0083] (1) Preparation of graphene oxide (GO) lamellar dispersion: disperse 200 mg of the above-mentioned graphite oxide in 100 mL of deionized water, and ultrasonically disperse for 1 hour to obtain a tan GO lamellar dispersion with a GO concentration of 2 mg mL -1 .
[0084] (2) Preparation of ultra-thin MoSe by liquid phase exfoliation 2 Preparation of nanosheet dispersion: 20mg bulk MoSe 2 Add 4 mL of isopropanol (IPA) / water mixed solvent with a volume fraction of 60%, put it into an ultrasonic instrument and perform ultrasonic vibration treatment with a power of 200W and a frequency of 40kHz for 4 hours, and maintain the ultrasonic wave by adding circulating cooling water. The temperature was controlled at room temperature during the process. Subsequently, the sonicated solution was centrifuged at 4000 rpm for 20 min to remove the unexfoliated bulk MoSe at the bottom....
Embodiment 2
[0096] The reaction and operating conditions of this example are basically the same as those of Example 1, except that the reducing agent in Example 1 is ascorbic acid, and the crosslinking agent is polypyrrole.
[0097] According to the test, the composite airgel prepared by the present invention has excellent electrocatalytic water splitting performance as an electrocatalytic water splitting electrode, which is obtained by Figure 5-8 As shown, when the current density is 100mA / cm 2 , the overpotential of the hydrogen evolution reaction is -290mV, and the overpotential of the oxygen evolution reaction is 1.65V.
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