Nitrogen-doped porous carbon sphere/S composite material, preparation method thereof and application of nitrogen-doped porous carbon sphere/S composite material in lithium-sulfur battery
A nitrogen-doped porous carbon and composite material technology, which is applied in lithium batteries, carbon preparation/purification, battery electrodes, etc., can solve the problems of poor conductivity of active materials, achieve excellent conductivity, strong chemical and physical adsorption capacity, The effect of high electrical contact area
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Embodiment 1
[0047] Step 1: Preparation of nitrogen-doped porous carbon spheres for lithium-sulfur battery cathode sulfur carrier
[0048] (1) take by weighing an appropriate amount of zinc nitrate hexahydrate and add it to deionized water, configure the zinc nitrate aqueous solution of 0.012 mol / L to obtain A solution;
[0049] (2) Weigh an appropriate amount of 2-methylimidazole and add it to deionized water, configure 0.12 mol / L of 2-methylimidazole aqueous solution to obtain B solution;
[0050] (3) Mix the A solution with the B solution, control the temperature of the reaction solution to be 10°C, and stir the reaction for 3h;
[0051] (4) transferring the reaction solution obtained in step (3) into a centrifuge tube, using a centrifuge at 7000 rpm / min to separate the solid-phase product, washing with deionized water, and freeze-drying to obtain a white powder;
[0052] (5) The white powder of step (4) is placed in a quartz boat, and carbonized at 900° C. under a nitrogen atmosphere ...
Embodiment 2
[0062] Step 1: Preparation of nitrogen-doped porous carbon spheres for lithium-sulfur battery cathode sulfur carrier
[0063] (1) take by weighing an appropriate amount of zinc nitrate hexahydrate and add it to deionized water, configure the zinc nitrate aqueous solution of 0.012 mol / L to obtain A solution;
[0064] (2) Weigh an appropriate amount of 2-methylimidazole and add it to deionized water, configure 0.12 mol / L of 2-methylimidazole aqueous solution to obtain B solution;
[0065] (3) Mix the A solution with the B solution, control the temperature of the reaction solution to be 20°C, and stir the reaction for 3h;
[0066] (4) transferring the reaction solution obtained in step (3) into a centrifuge tube, using a centrifuge at 7000 rpm / min to separate the solid-phase product, washing with deionized water, and freeze-drying to obtain a white powder;
[0067] (5) The white powder of step (4) is placed in a quartz boat, and carbonized at 900° C. under a nitrogen atmosphere ...
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