Synthetic method for high-activity N-F co-doped bismuth vanadate visible light photocatalytic material
The technology of a photocatalytic material and a synthesis method is applied in the field of preparing N-F co-doped bismuth vanadate photocatalytic material, which can solve the problems of low visible light catalytic efficiency and the like, and achieve the effects of cheap and easy-to-obtain raw materials, good dispersibility and good degradation effect.
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Embodiment 1
[0027] The preparation method of the bismuth vanadate of the present embodiment may further comprise the steps:
[0028] 1) With a mass percentage of 97% Bi(NO 3 ) 3 ·5H 2 O, 98.5% NH 4 VO 3 As the source material, citric acid with a mass percentage of 99.5% was used as a chelating agent, and 4.8580 g (0.01 mol) of Bi(NO 3 ) 3 ·5H 2 O and 4.2028 g (0.02 mol) of citric acid monohydrate (C 6 h 8 o 7 ·H 2 O), add citric acid monohydrate to 50mL Bi(NO 3 ) 3 ·5H 2 O solution, A solution was obtained. Weigh 0.01 mol, 1.1698 g of NH at a molar ratio of 1:2 4 VO 3 and 0.02 mol, 4.2028 g of citric acid monohydrate (C 6 h 8 o 7 ·H 2 O), solution B dissolved in 50 mL of boiling distilled water. Mix liquid A and liquid B according to the molar ratio of Bi:V=1:1, adjust the pH value to 6-7 with ammonia water, keep stirring at 80 °C, evaporate, and finally obtain the dark blue bismuth vanadate precursor sol.
[0029] 2) The dried bismuth vanadate precursor sol was put i...
Embodiment 2
[0033] 1) With a mass percentage of 97% Bi(NO 3 ) 3 ·5H 2 O, 98.5% NH 4 VO 3 As the source material, citric acid with a mass percentage of 99.5% was used as a chelating agent, and 4.8580 g (0.01 mol) of Bi(NO 3 ) 3 ·5H 2 O and 4.2028 g (0.02 mol) of citric acid monohydrate (C 6 h 8 o 7 ·H 2 O), add citric acid monohydrate to 50mL Bi(NO 3 ) 3 ·5H 2 O solution to obtain A solution; weigh 0.01 mol, 1.1698 g of NH with a molar ratio of 1:2 4 VO 3 and 0.02 mol, 4.2028 g of citric acid monohydrate (C 6 h 8 o 7 ·H 2 O), dissolved in 50mL boiling distilled water to obtain liquid B; mix liquid A and liquid B according to the molar ratio of Bi:V=1:1, and 4 The molar ratio of F to Bi is 2% and NH is added 4 F in the mixed solution, and then adjust the pH value to 6-7 with ammonia water, continue to stir at 80 ° C, evaporate, and finally obtain the dark blue bismuth vanadate precursor sol.
[0034] 2) The dried bismuth vanadate precursor sol was put into a muffle furna...
Embodiment 3
[0038] According to the preparation method of the present invention of embodiment 2, different conditions are: NH 4 The molar ratio of F and Bi is changed to 4%, and the bismuth vanadate photocatalytic material of 4% N-F is prepared, and the UV-vis spectrum of the obtained product is shown in figure 1 (c), BiVO synthesized in this example 4 The optical absorption threshold of 556nm, the forbidden band width is 2.23 eV. figure 2 (c) is the XRD pattern of the product, the BiVO synthesized in this example 4 at 18.7 o , 28.8 o , 30.5 o , 34.5 o , 35.1 o , 37.8 o , 39.8 o , 42.4 o , 47.2 o , 53.2 o , 59.8 o , 63.6 o , 69.3 o The diffraction peak at the position is the characteristic peak of monoclinic bismuth vanadate, but the characteristic peak is obviously shifted to a small angle, and the unit cell volume is 310.33 nm 3 .
[0039] The photocatalytic performance of the synthesized bismuth vanadate was detected according to the method described in Example 1, an...
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