a ti 3 c 2 t x / Preparation method of sulfur-carbon composite material
A technology of sulfur-carbon composite materials and carbon materials, which is applied to structural parts, electrical components, battery electrodes, etc., can solve the problems of reducing the utilization rate of sulfur active substances, slow migration speed, and slow electrochemical reaction kinetics, etc., to achieve Prevent the movement of polysulfides, increase the lifespan, and reduce the effect of the shuttle effect
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Embodiment 1
[0020] (1) Add 1g of octaphenyloctasilsesquioxane to 50mL of 1,2-dichloroethane, mechanically stir at 50°C to dissolve, then add 0.05g of Ti 3 AlC 2 Ceramic powder, stirred to form a suspension;
[0021] (2) Add 0.05g of anhydrous aluminum chloride catalyst and 10g of carbon tetrachloride crosslinking agent to the suspension, stir for 5 hours for crosslinking reaction, after the reaction, add ethanol / water solution, ethanol / dilute hydrochloric acid solution for washing, Washing with water and drying in vacuum to obtain the precursor;
[0022] (3) Place the precursor in a muffle furnace protected by a nitrogen atmosphere, calcinate at 800 °C for 5 h, and heat up at a rate of 1 °C / min;
[0023] (4) The carbonized product was etched in 20% hydrofluoric acid for 24 hours. After the corrosion, the solution was added to deionized water for centrifugation, and then the precipitate was dried to obtain Ti 3 C 2 T x / Spherical porous carbon material;
[0024] (5) Add 0.1g Ti 3 C...
Embodiment 2
[0026] (1) Add 1g of octaphenyloctasilsesquioxane to 100mL of 1,2-dichloroethane, mechanically stir at 70°C to dissolve, then add 0.5gTi 3 AlC 2 Ceramic powder, stirred to form a suspension;
[0027] (2) Add 0.1g of anhydrous aluminum chloride catalyst and 40g of carbon tetrachloride cross-linking agent to the suspension, stir and cross-link for 10 hours, after the reaction, add ethanol / water solution, ethanol / dilute hydrochloric acid solution for washing, Washing with water and drying in vacuum to obtain the precursor;
[0028] (3) The precursor was placed in a muffle furnace protected by a nitrogen atmosphere, and calcined at 1200 °C for 1 h, with a heating rate of 5 °C / min;
[0029] (4) The carbonized product was etched in 50% hydrofluoric acid for 4 hours, the solution was added to deionized water for centrifugation after corrosion, and then the precipitate was dried to obtain Ti 3 C 2 T x / Spherical porous carbon material;
[0030] (5) Add 0.3g Ti 3 C 2 T x / Sph...
Embodiment 3
[0032] (1) Add 1g of octaphenyloctasilsesquioxane to 70mL of 1,2-dichloroethane, mechanically stir at 60°C to dissolve, then add 0.1g of Ti 3AlC 2 Ceramic powder, stirred to form a suspension;
[0033] (2) Add 0.08g of anhydrous aluminum chloride catalyst and 20g of carbon tetrachloride crosslinking agent to the suspension, stir for 8 hours for crosslinking reaction, after the reaction, add ethanol / water solution, ethanol / dilute hydrochloric acid solution for washing, Washing with water and drying in vacuum to obtain the precursor;
[0034] (3) The precursor was placed in a muffle furnace protected by a nitrogen atmosphere, and calcined at 1000 °C for 3 h, with a heating rate of 3 °C / min;
[0035] (4) The carbonized product was etched in 30% hydrofluoric acid for 16 hours, and the solution was added to deionized water for centrifugation after corrosion, and then the precipitate was dried to obtain Ti 3 C 2 T x / Spherical porous carbon material;
[0036] (5) Add 0.2g Ti ...
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