Hydrothermal preparation method of graphene-coated sulfur/porous carbon composite positive electrode material
A composite cathode material, graphene coating technology, applied in battery electrodes, electrical components, electrochemical generators, etc., can solve problems such as low electrochemical performance, and achieve the effect of inhibiting dissolution loss
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[0058] Specific embodiment 1: The hydrothermal preparation method of the graphene-coated sulfur / porous carbon composite cathode material of this embodiment is carried out in the following steps:
[0059] 1. Preparation of graphene slurry: the graphene slurry is composed of graphene and water, and graphene sheets are uniformly dispersed in the slurry; wherein the water content of the graphene slurry is 90%-99.99%;
[0060] 2. Preparation of sulfur / porous carbon composite material, where the porous carbon material is one or more of activated carbon, graphene, carbon black, carbon nanotubes, template porous carbon, carbon fiber, carbon aerogel, and carbide-derived carbon Composition, the mass ratio of sulfur to porous carbon in the sulfur / porous carbon composite material is 1:(0.02~20);
[0061] 3. According to the mass ratio of graphene in the graphene slurry to sulfur in the sulfur / porous carbon composite material as (0.02-20):1, add the sulfur / porous carbon composite material prepare...
Example Embodiment
[0063] Embodiment 2: The difference between this embodiment and Embodiment 1 is that the specific preparation method of the graphene slurry in step 1 is as follows:
[0064] (1) Weigh graphite and reducing agent; the mass ratio of graphite to reducing agent is 1:(0.1~1000); the reducing agent is one or a combination of ascorbic acid, KOH, NaOH, LiOH and ammonia;
[0065] (2) Oxidizing the graphite weighed in step (1) into graphite oxide;
[0066] (3) The concentration of graphite oxide is 0.01mg mL -1 ~50mg mL -1 , Adding the graphite oxide obtained in step (2) to water, peeling and dispersing for 0.5-10h under ultrasonic conditions with a frequency of 20-100KHz, to obtain an aqueous graphene oxide dispersion;
[0067] (4) Add a reducing agent to the graphene oxide aqueous dispersion obtained in step (3) at a temperature of 4℃~100℃, and reduce for 0.2h~24h under ultrasonic conditions with a frequency of 20~100KHz to obtain Graphene aqueous dispersion;
[0068] (5) The graphene aqueous ...
Example Embodiment
[0071] Specific embodiment three: This embodiment is different from specific embodiment one or two in that the method of oxidizing graphite to graphite oxide in step (2) is as follows: add 120 mL of H with a mass percentage of 98% in a dry beaker 2 SO 4 , Then put the beaker in an ice water bath, add 5g graphite and 2.5g NaNO 3 , Stirring at a speed of 50-500 rpm, while gradually adding 15g powdered KMnO 4 , Continue the reaction for 2h under ice-water bath and stirring conditions; move the beaker into a constant temperature oil bath at 35±1℃ and continue the reaction for 2h; slowly add 360mL of distilled water under stirring conditions at a speed of 50~500 rpm, and control the temperature to be constant Continue the constant temperature reaction at 75°C for 1h; add 1000mL of distilled water at 40°C, add 50mL of hydrogen peroxide with a mass percentage of 30%, and then vacuum filter; wash the filter cake with 5% mass percentage of hydrochloric acid until No SO in the filtrate 4 2...
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