A kind of synthesis method and application of p, s, n co-doped mesoporous carbon material with high s content
A synthesis method and co-doping technology, applied in the preparation/purification of carbon, hybrid capacitor electrodes, electrical components, etc., to achieve high specific capacity, good long-distance cycle ability, and increase the possibility of effect
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Embodiment 1
[0046] The preparation of embodiment 1 mesoporous carbon material SNPPC-800
[0047] Weigh 2-aminothiazole (0.1282g), sodium dihydrogen phosphate (0.1536g), and mix evenly by hand, then put 2-aminothiazole on two layers of ZnCl2 (0.1736g each) in the middle of the material, in a sandwich shape, placed in a quartz boat, placed in a tube furnace, heated at 5°C / min to each temperature section for 2h under N2 (speed 30ml / min) atmosphere, Obtain black powder, wash off residual ZnCl with 35% hydrochloric acid 2 , washed three times with deionized water and ethanol, dried in a vacuum oven at 80°C for 3 h, and finally in a tube furnace for N 2 (speed 30ml / min) atmosphere, 200 ℃ for 2h, obtained high S content P, S, N co-doped mesoporous carbon material SNPPC-800, S content up to 12.58%, specific surface area up to 1122.46m 2 / g.
[0048] The S, N, P co-doped mesoporous carbon material obtained by the present invention is used as an oxygen reduction catalyst for a fuel cell, and its ...
Embodiment 2
[0055] The preparation of embodiment 2 mesoporous carbon material SNPPC-700
[0056] Weigh ZnCl 2 (0.8815g), 2-aminothiazole (0.1282g), ZnCl 2 (0.8815g), the ZnCl 2 2-aminothiazole placed on two layers of ZnCl 2 In the middle of the material, in a sandwich shape, placed in a quartz boat and placed in a tube furnaceN 2 (30ml / min) under the atmosphere, the temperature was raised to 700°C at 5°C / min, and kept for 8h to obtain a black powder, which was washed with 35% hydrochloric acid to remove the residual ZnCl 2 , washed five times with deionized water and ethanol, dried in a vacuum oven at 80°C for 3 h, and finally in a tube furnace with N 2 (30ml / min) atmosphere, keep at 200°C for 2h to obtain the final product S, N, P co-doped mesoporous carbon material SNPPC-700.
[0057] The test conditions for catalytic oxygen reduction reaction performance are the same as those in Example 1.
Embodiment 3
[0058] The preparation of embodiment 3 mesoporous carbon material SNPPC-600
[0059] Weigh ZnCl 2 (0.8815g), 2-aminothiazole (0.1282g), ZnCl 2 (0.8815g), the ZnCl 2 2-aminothiazole placed on two layers of ZnCl 2 In the middle of the material, in a sandwich shape, placed in a quartz boat and placed in a tube furnaceN 2 (30ml / min) under the atmosphere, the temperature was raised to 600°C at 5°C / min, and kept for 8h to obtain a black powder, which was washed with 35% hydrochloric acid to remove the residual ZnCl 2 , washed several times with deionized water and ethanol, dried in a vacuum oven at 80 °C for 3 h, and finally in a tube furnace for N 2 (30ml / min) atmosphere, keep at 200°C for 2h to obtain the final product S, N, P co-doped mesoporous carbon material SNPPC-600.
[0060] The test conditions for catalytic oxygen reduction reaction performance are the same as those in Example 1.
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