Polymer semiconductor carbon nitride nanorod catalyst and preparation method thereof
A semiconductor and nanorod technology, which is applied in the polymer semiconductor carbon nitride nanorod catalyst and its preparation, and in the field of polymer synthesis, can solve the problems of serious recombination of photogenerated carriers, poor mass transfer, large particle size, etc., and achieve Optimized shape, increased surface area, and easy recycling
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Embodiment 1
[0038] Step 1: Mix 0.875g KCl and 0.275g triblock copolymer surfactant polyoxyethylene-polyoxypropylene-polyoxyethylene EO 20 -PO 70 -EO 20 (P123) was dissolved in 120mL of 2M hydrochloric acid solution, stirred rapidly to form a uniform and transparent solution, added 3.15mmol organosilane precursor 1,4-bis(triethoxysilyl)benzene and continued to stir vigorously, reducing the stirring rate Stirring was continued at 30°C for 24h. Add the milky white turbid liquid obtained above into a 100mL polytetrafluoroethylene liner, place it in a thermostat at 70°C, and let it stand for 30h. Organic silicon nanotubes are obtained after extraction, filtration and drying. Synthesis process see figure 1 .
[0039] Step 2: Combine 1g B-SNT and 1g CH 2 N 2 Dissolve in 10mL ethanol solution, sonicate for 30min and then stir slowly for 12h, evaporate the ethanol solvent, and obtain B-SNT / CH after drying 2 N 2 Complex.
[0040] Step 3: Put the composite prepared in step 2 into a muffle ...
Embodiment 2
[0044] Step 1: 1.75g KCl and 0.55g triblock copolymer surfactant polyoxyethylene-polyoxypropylene-polyoxyethylene EO 20 -PO 70 -EO 20 (P123) was dissolved in 120mL of 1.8M hydrochloric acid solution, stirred rapidly to form a uniform transparent solution, added 2.8mmol organosilane precursor 1,4-bis(triethoxysilyl)benzene and continued to stir vigorously, reduce the stirring Stirring was continued at 35 °C for 18 h. Add the milky white turbid liquid obtained above into a 100mL polytetrafluoroethylene liner, place it in a thermostat at 90°C, and let it stand for 25 hours. Organic silicon nanotubes are obtained after extraction, filtration and drying. Synthesis process see figure 1 .
[0045] Step 2: Combine 1g B-SNT and 5g CH 2 N 2 Dissolve in 60mL ethanol solution, sonicate for 120min and then stir slowly for 24h, evaporate the ethanol solvent, and obtain B-SNT / CH after drying 2 N 2 Complex.
[0046] Step 3: Put the composite prepared in step 2 into a muffle furnac...
Embodiment 3
[0050] Step 1: Mix 3.5g KCl and 1.1g triblock copolymer surfactant polyoxyethylene-polyoxypropylene-polyoxyethylene EO 20 -PO 70 -EO 20 (P123) was dissolved in 120mL 2.2M hydrochloric acid solution, stirred rapidly to form a uniform transparent solution, added 2.45mmol organosilane precursor 1,4-bis(triethoxysilyl)benzene and continued to stir vigorously, reduce the stirring Stirring was continued at 40 °C for 12 h. Add the milky white turbid liquid obtained above into a 100mL polytetrafluoroethylene liner, place it in a thermostat at 110°C, and let it stand for 20 hours. Organic silicon nanotubes are obtained after extraction, filtration and drying. Synthesis process see figure 1 .
[0051] Step 2: Combine 1g B-SNT and 3g CH 2 N 2 Dissolved in 35mL ethanol solution, stirred slowly for 18h after ultrasonication for 75min, evaporated the ethanol solvent, and obtained B-SNT / CH after drying 2 N 2 Complex.
[0052] Step 3: Put the composite prepared in step 2 in a muffle...
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