High-specific-capacitance SnO2/C porous microsphere and production method thereof
A technology of porous microspheres and high specific capacitance, which is applied in the manufacture of hybrid/electric double layer capacitors, electrodes of hybrid capacitors, circuits, etc. the application prospect and the effect of enriching the pore structure
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Embodiment 1
[0035] S1. Weigh 2.0 g of triphenyl tin acetate and place it in a reaction vessel, and then add 50 ml of absolute ethanol to it, disperse after ultrasonic dispersion, stir and dissolve, and place the above solution in a closed high-temperature reactor at 5 ℃ min -1 The heating rate is increased to 500 ℃, and then kept at the corresponding temperature for 12 hours to obtain a black product;
[0036] S2. Filter and wash the cooled black product with deionized water and ethanol, and dry at 50°C for 8 hours to obtain a precursor;
[0037] S3. Put the precursor body into the tube furnace and set it at 2 m under nitrogen protection 3 / h The water vapor flow rate is heated and activated at 600 ℃ for 2 hours to prepare SnO 2 / C Porous microspheres.
Embodiment 2
[0039] S1. Weigh 3.0 g of triphenyl tin acetate and place it in a reaction vessel, then add 50 ml of absolute ethanol to it, disperse by ultrasonic and stir to dissolve, place the above solution in a closed high-temperature reactor, and heat it at 10 ℃ min -1 The heating rate is increased to 700 ℃, and then kept at the corresponding temperature for 12 hours to obtain a black product;
[0040] S2. Filter and wash the cooled black product with deionized water and ethanol, and dry at 80°C for 6 hours to obtain a precursor;
[0041] S3. Put the precursor body into the tube furnace and place it at 3 m under nitrogen protection 3 / h The water vapor flow rate is heated and activated at 700℃ for 2 hours to prepare SnO 2 / C Porous microspheres.
Embodiment 3
[0043] S1. Weigh 4.0 g of triphenyltin acetate and place it in a reaction vessel, then add 50 ml of absolute ethanol to it, disperse after ultrasonic dispersion, stir and dissolve, and place the above solution in a closed high-temperature reactor at 15℃ min -1 The heating rate is increased to 600 ℃, and then kept at the corresponding temperature for 12 hours to obtain a black product;
[0044] S2. Filter and wash the cooled black product with deionized water and ethanol, and dry at 80°C for 8 hours to obtain a precursor;
[0045] S3. Put the precursor body into the tube furnace and set it to 4 m 3 / h The water vapor flow rate is heated and activated at 600℃ for 2 hours to produce SnO 2 / C Porous microspheres.
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