Metal organic framework-based ternary composite material and preparation method thereof
A metal-organic framework and composite material technology, which is applied in the field of metal-organic framework-based ternary composite materials and their preparation, can solve the problem of insufficient catalytic performance, low visible light utilization rate and hydrogen production rate, and reduction of photocatalytic reaction active sites. and other problems, to achieve the effect of increasing the light absorption range, good photocatalytic cycle stability, and promoting the interfacial charge transfer efficiency.
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[0028] The preparation method of the metal-organic framework-based ternary composite material of the present invention specifically comprises the following steps:
[0029] Step S1, dissolving a certain amount of chloroplatinic acid hexahydrate and polyvinylpyrrolidone in water and methanol respectively, then mixing the two solutions, heating to boiling reflux, and then removing the solvent to obtain Pt nanoparticles;
[0030] Step S2, a certain amount of ZrCl 4 Dissolve 2-aminoterephthalic acid in DMF, then add a certain amount of acetic acid and the DMF solution of Pt nanoparticles, disperse evenly, transfer to a hydrothermal kettle, react for a period of time at 80 ° C ~ 120 ° C, and finally wash and dry getPt@MOF;
[0031] Step S3, dissolving Pt@MOF in ethanol, then adding cadmium acetate, heating up to 80°C-100°C after dissolving, then slowly adding an aqueous solution of thioacetamide, keeping it at 80°C-100°C for a period of time, then washing and drying , and finally ...
Embodiment 1
[0039] In this example, the preparation of metal-organic framework-based ternary composites is described in detail.
[0040] Step S1, preparation of PtNPs:
[0041] Dissolve 5~10mL of chloroplatinic acid (25mM) and 44.3~133.9mg of PVP in 90~95mL of deionized water and 60mL of methanol respectively, then mix them, heat up to boiling and reflux for 2~5h, and then remove the solvent by rotary evaporation. The modified PtNPs were washed by centrifugation and finally dispersed in DMF for later use.
[0042] Step S2, preparation of Pt@MOF:
[0043] Dissolve 46.6mg of ZrCl4 and 36.2mg of 2-aminoterephthalic acid in DMF, then add 2.0-5.0mL of glacial acetic acid and 0-280μL of PtNPs in DMF, ultrasonically disperse evenly and transfer to a hydrothermal kettle, 80-140 ℃ for 24 hours, and finally centrifuged, washed and dried to obtain Pt@MOF.
[0044] Step S3, preparation of Pt@NH2-UiO-66 / CdS:
[0045] Dissolve 20-60 mg of Pt@MOF in 10 mL of ethanol, add 24.3 mg of cadmium acetate d...
Embodiment 2
[0049] The difference between this embodiment and embodiment 1 is that the amount of PVP added in step S1 becomes 88.6 mg, and the rest are the same as in embodiment 1.
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