A preparation method for in-situ growth of mesoporous compound semiconductor material with high stability
A compound semiconductor and stable technology, which is applied in the direction of nanotechnology, chemical instruments and methods, nanotechnology, etc. for materials and surface science, can solve the problem of low catalytic activity, and achieve simple and easy preparation process, optimized design, The novel effect of the method
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[0024] The invention provides a preparation method for in-situ growth of a mesoporous compound semiconductor material with high catalytic stability.
[0025] The preparation method of the present invention comprises: (1) select one kind to have six-membered ring structure, melting point is lower and can be combined with graphitic carbon nitride (g-C 3 N 4 ) Organic substances that undergo polycondensation reactions, such as barbituric acid, 2,5-dibromopyridine, 2,4-dibromoquinoline, 2,5-dibromopyrimidine, etc., and g-C 3 N 4 The precursors (urea, cyanamide, dicyandiamide) are mixed according to a certain ratio and ground, and the grinding time at room temperature is 10 to 60 minutes;
[0026] (2) The mixture after grinding is heated up to the reaction temperature according to a certain heating rate, such as 4K / min, and calcined to obtain modified graphite-like carbon nitride (mg-C 3 N 4 ) materials, collected for later use;
[0027] (3) Weigh the mg-C obtained by calcinat...
Embodiment 1
[0045] Weigh 3g of cyanamide, add 10mg of 2,5-dibromopyridine, grind at room temperature for 30 minutes, collect it in a mortar, raise the temperature to 650°C at a heating rate of 10K / min, and keep it for 3h. Obtain the modified graphite-like carbon nitride material mg-C 3 N 4 . The amount of ammonium molybdate and thiourea is controlled as 1:1, weigh 20mg ammonium molybdate and corresponding thiourea; weigh mg-C 3 N 4 Material 0.15g, dispersed in 50mL of water, ultrasonic treatment for 10min. The solution was transferred to a hydrothermal kettle and reacted for 12 hours at 120°C. The product was centrifuged, washed with water, and freeze-dried to obtain the final product.
[0046] Figure 1a and Figure 1b For the MoS obtained in Example 1 2 、MoS 2 / mg-C 3 N 4 Scanning electron microscope (SEM) photograph of the compound semiconductor material. It can be seen from the photo that the prepared MoS 2 The material is a nano-flower material.
[0047] Figure 2a and ...
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