Composite photocatalyst and preparation method thereof
A catalyst and composite light technology, applied in chemical instruments and methods, physical/chemical process catalysts, chemical/physical processes, etc., can solve the problems of low hydrogen production catalyst activity, low hydrogen production rate, etc., and achieve simple installation and low price. , the effect of high catalytic activity
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specific Embodiment approach 1
[0016] Specific implementation mode one: the composite photocatalyst of this implementation mode is made of Zn(Ac) 2 2H 2 O, Cd(Ac) 2 2H 2 O, made from the third main group compound and thioacetamide; Zn(Ac) 2 2H 2 O and Cd(Ac) 2 2H 2 The molar ratio of O is 1:1~5, Zn(Ac) 2 2H 2 The molar ratio of O to the third main group compound is 1:0.01~0.10, Zn(Ac) 2 2H 2 The molar ratio of O to thioacetamide is 1:4.03~12.30; the third main group compound is InCl 3 4H 2 O or GaCl 3 .
specific Embodiment approach 2
[0017] Specific embodiment two: the preparation method of composite photocatalyst of this embodiment realizes according to the following steps: one, weigh Zn (Ac) 2 2H 2 O, Cd(Ac) 2 2H 2 O, the third main group compound and thioacetamide, Zn(Ac) 2 2H 2 O and Cd(Ac) 2 2H 2 The molar ratio of O is 1:1~5, Zn(Ac) 2 2H 2 The molar ratio of O to the third main group compound is 1:0.01~0.1, Zn(Ac) 2 2H 2 The molar ratio of O to thioacetamide is 1:4.03~12.30, and then they are added to 5~20mL of acetone or ethanol solution to form a mixture; 2. Seal the mixture obtained in step 1 and put it into an ultrasonic reactor , react at 40-80°C for 0.5-18h; 3. Cool the product obtained in step 2 to room temperature, wash it with absolute ethanol for 2-5 times, and then dry it in an oven at 50°C for 0.5-5h to obtain Composite photocatalyst; wherein the third main group compound in step 1 is InCl 3 4H 2 O or GaCl 3 .
specific Embodiment approach 3
[0018] Specific embodiment three: the difference between this embodiment and specific embodiment two is that in step one, Zn(Ac) 2 2H 2 O, Cd(Ac) 2 2H 2 O, add the third main group compound and thioacetamide to 7-10mL of acetone or ethanol solution. Others are the same as in the second embodiment.
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