Organic-inorganic hybrid lead iodide visible light catalytic material and preparation method thereof
A catalytic material and visible light technology, applied in organic compound/hydride/coordination complex catalysts, chemical instruments and methods, physical/chemical process catalysts, etc., can solve the problem of poor photochemical stability and low photocatalytic efficiency of lead iodide, etc. problem, to achieve the effect of small band gap and stable visible light catalytic performance
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Embodiment 1
[0026] The preparation method of the organic-inorganic hybrid lead iodide visible light catalytic material of the present invention comprises the following steps:
[0027] i) Weigh the raw material Fe(SO 4 )·7H 2 O, 2,2-bipyridine, PbI 2 and KI, add 0.5mLHI, 4mLN.N-dimethylformamide and 1mLH according to the molar ratio of 2:6:8:2 2 O in the mixed solution, then put the mixture into the reaction kettle and seal;
[0028] ii) Put the sealed hydrothermal kettle into an electric blast drying oven with programmed temperature control, heat it to 140°C for 5 hours, then react at a constant temperature of 140°C for 6 days, drop to room temperature, and the synthesis reaction ends;
[0029] iii) Open the reaction kettle, carry out suction filtration to the solid-liquid mixture, and dry the material obtained by suction filtration to obtain a black-red block crystal material, which is the target compound [Fe(2.2-bipy) 3 ] 2 Pb 8 I21 . After washing with distilled water and ethano...
Embodiment 2
[0031] The preparation method of the organic-inorganic hybrid lead iodide visible light catalytic material of the present invention comprises the following steps:
[0032] i) Weigh the raw material Fe(SO 4 )·7H 2 O, 2,2-bipyridine, PbI 2 and KI, add 0.5mLHI, 4mLN.N-dimethylformamide and 1mLH according to the molar ratio of 2.5:6.5:8.5:2.5 2 O in the mixed solution, then put the mixture into the reaction kettle and seal;
[0033] ii) Put the sealed hydrothermal kettle into an electric blast drying oven with programmed temperature control, heat it up to 140°C for 5 hours, then react at a constant temperature of 160°C for 8 days, drop to room temperature, and the synthesis reaction ends;
[0034] iii) Open the reaction kettle, carry out suction filtration to the solid-liquid mixture, and dry the material obtained by suction filtration to obtain a black-red block crystal material, which is the target compound [Fe(2.2-bipy) 3 ] 2 Pb 8 I 21 . After washing with distilled wat...
Embodiment 3
[0039] Figure 4 Shown is the compound [Fe(2.2-bipy) 3 ] 2 Pb 8 I 21 Absorbance curve of RhB under catalysis. 30mg [Fe(2.2-bipy) 3 ] 2 Pb 8 I 21 The sample is dispersed in a 30ml container with a concentration of 1×10 -5 In the quartz reactor of mol / L Rhodamine B (RhB) solution, after dispersing in the ultrasonic cleaner for 30 minutes, put it into the dark room, and stir for 10 hours under the condition of no light, to ensure that RhB and the prepared photocatalytic material powder reach Adsorption-desorption equilibrium. After the adsorption-desorption equilibrium was reached, the photodegradation ability of the photocatalytic material on RhB was measured using a 500W xenon lamp as a visible light source. Take out 4mL test solution every 10min for analysis, stop after 60min of reaction. The concentration change of RhB was obtained by measuring the absorbance of the solution with an ultraviolet-visible spectrophotometer. Compound [Fe(2.2-bipy) 3 ] 2 Pb 8 I 21 ...
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