Aromatic ring and cyano group co-doped carbon nitride nanosheet as well as preparation method and application thereof
A technology of carbon nitride and co-doping, applied in nanotechnology, chemical instruments and methods, nanotechnology, etc. for materials and surface science, can solve the problem of unseen thermal preparation methods and narrow carbon nitride light absorption range To achieve the effects of improving photocatalytic performance, widening the response range of visible light, good controllability and universality
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Embodiment 1
[0029] Weigh 5g of urea, finely grind and evenly disperse it in 30mL of dimethyl sulfoxide, add 2mg of p-aminobenzaldehyde and stir well, put it in a reaction kettle to heat and react, the constant temperature is 200°C, the constant temperature time is 12h, and the product is obtained by alcohol washing and drying UCN-PABA-0.002.
[0030] from figure 1 It can be seen from the scanning electron microscope that the sample UCN-PABA-0.002 is a porous sheet structure with a slightly curled edge and a uniform surface. At 2θ=12.9° and 27.2°, they correspond to the (100) and (002) planes of GCN, respectively. ( figure 2 ), and absorbs in visible light ( image 3 ), under visible light irradiation (a 300W xenon lamp is equipped with a filter of λ≥420nm) for photocatalytic reaction, and the hydrogen production rate is 18.66 μmol / h.
Embodiment 2
[0032] The photocatalyst was prepared according to the method of Example 1, except that the doping amount of PABA was 4 mg, and other conditions remained unchanged, and it was named UCN-PABA-0.004.
[0033] Under the same photocatalytic reaction conditions as in Example 1, the hydrogen production rate was 26.26 μmol / h.
Embodiment 3
[0035] The photocatalyst was prepared according to the method of Example 1, except that the doping amount of PABA was 6 mg, and other conditions remained unchanged, and it was named UCN-PABA-0.006.
[0036] Under the same photocatalytic reaction conditions as in Example 1, the hydrogen production rate was 30.67 μmol / h.
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