Application of three-dimensional sheet-shaped porous carbon material jointly doped with nitrogen and sulfur
A technology of nitrogen-sulfur co-doping and porous carbon materials, which is applied in the preparation/purification of carbon, electrical components, battery electrodes, etc., can solve the problems of potential safety hazards, limited application and industrial production, poor performance of acidic media, etc. Long, great application potential and industrial value, good stability
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Embodiment 1
[0044] S1: React 28mL of pyridine, 2mL of hexachlorobutadiene and 1g of thiocyanuric acid in a polytetrafluoroethylene-lined autoclave at 200°C and 2MPa for 4 hours, wherein pyridine, hexachlorobutadiene The mass ratio of alkene and thiocyanuric acid is 24:3:1.
[0045] S2: Release the pressure to normal pressure, remove excess solvent from the reaction, and obtain sample A.
[0046] S3: Mix 1 g of the obtained sample with 6 g of thiourea;
[0047] S4: Put the sample under inert gas N 2 Perform high temperature treatment at 1000°C for 2 hours under protection to obtain sample B;
[0048] S5: Ball milling the obtained sample B for 15 minutes to obtain the three-dimensional flake nitrogen-sulfur co-doped porous carbon material. Name it C1.
Embodiment 2-4
[0049] Embodiment 2-4: the investigation of reaction raw material in the step S1
[0050] Except that no thiocyanuric acid was added in step S1 and step S5 was not carried out, other operations were all unchanged, so that embodiment 2 was carried out sequentially and named as C2. Except that step S3 and step S5 were not carried out, other operations were unchanged, so that embodiment 3 was carried out sequentially, named as C3. Except that step S5 was not carried out, other operations were kept unchanged, so that embodiment 4 was carried out sequentially, named as C4.
Embodiment 5-8
[0051] Embodiment 5-8: the investigation of reaction raw material ratio in the step S1
[0052] Change the mass ratio of hexachlorobutadiene and thiocyanuric acid in the raw material of step S1 to 6:1, 3:1, 3:2, and 1:1 respectively, and the other operations are all unchanged to obtain embodiment C5- C8.
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