Method for preparing composite carbon cathode material for super-capacitor battery
A technology for supercapacitor batteries and anode materials, applied in the field of electrochemistry, can solve the problems affecting the high rate of supercapacitor batteries, large capacity and high energy density performance, inability to maximize supercapacitor batteries, poor conductivity of lithium titanium oxide, etc. problems, to achieve good lithium-ion intercalation/de-cycling performance, excellent capacitor energy storage performance, and good high-rate charge-discharge performance
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Embodiment 1
[0038] 1. Mixing the surface nano-sized natural graphite and resin in a ratio of 1:1 by weight, and at the same time,
[0039] Add NaOH template agent whose particle size distribution is 1-2nm, medium particle 5-50nm, large particle 60-100nm, ethanol and mix thoroughly, then evaporate to dryness at a low temperature of 50-60°C to obtain the precursor;
[0040] 2. Put the prepared precursor under the protective atmosphere of ammonia gas, first according to the heating system of 5-10°C / min,
[0041] Heating to 200°C, constant temperature for 2 hours, then heating to 600°C at a heating rate of 1-5°C / min, constant temperature for 2 hours; then cooling with the furnace; the core-shell material of the three-dimensional hierarchical hole shell coated with micropores is obtained The pore size distribution of the micropores is as follows: the pore size of the macropore is 50-120nm, the pore size of the medium pore is 3-50nm, and the pore size of the small pore is less than 2nm.
[004...
Embodiment 2
[0056] 1. Mix the surface nano-sized natural graphite and coal tar in a ratio of 3:1 by weight, and at the same time, add SiO with a particle size distribution of 1-2nm for particles, 5-50nm for medium particles, and 60-100nm for large particles 2 After the template agent and acetone are fully mixed, evaporate to dryness at a low temperature of 70-80°C to obtain the precursor;
[0057] 2. Under the protective atmosphere of nitrogen and hydrogen (nitrogen:hydrogen = 1:1), heat the prepared precursor to 300°C at a heating rate of 5-10°C / min, keep the temperature for 3 hours, and then press 1-5 ℃ / min heating system to 700 ℃, constant temperature for 6h; then cool with the furnace; obtain core-shell material with three-dimensional hierarchical hole shell covered with micropores; the pore size distribution of the micropores is: the pore size of the macropores is 50-120nm, medium pore diameter is 3-50nm, and small pore diameter is less than 2nm.
[0058] 3. Removal of template agen...
Embodiment 3
[0071] 1. Mix the surface nano-sized natural graphite and asphalt in a ratio of 10:1 by weight. At the same time, add Ni(OH) with a particle size distribution of 1-2nm for particles, 5-50nm for medium particles, and 60-100nm for large particles. 2 After fully mixing the template agent and methanol, evaporate to dryness at a low temperature of 90-100°C to obtain the precursor;
[0072] 2. Under the protective atmosphere of argon, heat the prepared precursor to 400°C at a heating rate of 5-10°C / min, keep the temperature for 5 hours, and then heat it to 800°C at a heating rate of 1-5°C / min , constant temperature for 10h; then cool with the furnace; obtain the core-shell material of the three-dimensional layered hole shell coated with micropores on the core material; the micropore diameter distribution is: the macropore diameter is 50-120nm, the mesopore diameter is 3- 50nm, the small hole diameter is less than 2nm.
[0073] 3. Removal of template agent: use dilute nitric acid to...
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