A fluorene-functionalized covalent organic framework material and its preparation and thermoelectric applications
A technology of covalent organic framework and fluorene function, applied in the field of material chemistry, to achieve the effects of uniform pore size distribution, good thermoelectric performance, and good thermal stability
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Embodiment 1
[0019] The synthesis of embodiment 1.FL-COF-1 material
[0020] 2,7-diaminofluorene (DAFL, 31 mg) and benzene-1,3,5-tricarbaldedyde (TFB, 17.1 mg) were added to the ampoule, followed by o-dichlorobenzene (1.35 mL) and n-butanol (0.15 mL) and 3M acetic acid solution (0.25mL) was sonicated for 10min to make it evenly mixed, and then frozen in liquid nitrogen-vacuumized-thawed again, and the above operation was repeated three times. The flame was sealed under vacuum conditions, and the reaction was carried out at 120°C for 72 hours. After the reaction, the product was collected and washed three times with tetrahydrofuran and acetone respectively, and dried at 120°C under vacuum for 12 hours. Finally, a yellow powder was obtained, which was the product FL-COF-1, with a yield of 78% and a BET specific surface area of 980m 2 g -1 , the pore volume is 0.54m 3 g -1 . Information analysis results obtained by infrared spectroscopy: at 1624cm -1 The characteristic absorption peak ...
Embodiment 2-4
[0021] The synthesis of embodiment 2-4 FL-COF-1 material
[0022] Method as described in embodiment 1, its difference is following table:
[0023]
Embodiment 5I2
[0024] Embodiment 5.I 2 Synthesis of @FL-COF-1 materials
[0025] Weigh 60 mg of the sample obtained in Example 3 and place it in a small glass bottle (5 mL), then place it flat in a brown bottle (60 mL) containing 400 mg of iodine element, seal the brown bottle, and place it in an oven at 75 ° C to make it fully iodine. Doped for 24 hours. After cooling to room temperature, it was dried under vacuum (0.1-1Mpa) at 75°C for 6 hours to obtain the final product I 2 @FL-COF-1.
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