Carbon compound cathode material for ultracapacitor battery
A technology of supercapacitor battery and negative electrode material, applied in the field of electrochemistry, can solve the problem of high rate, large capacity and high energy density performance of supercapacitor battery, unable to maximize supercapacitor battery, poor conductivity of lithium titanium oxide, etc. The problem is to achieve good lithium ion intercalation/deintercalation cycle performance, good electric double layer energy storage and lithium ion de/intercalation energy storage characteristics, and good high-rate charge-discharge performance.
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Embodiment 1
[0028] 1. Add 100 grams of surface-nanoized natural graphite, 100 grams of resin, and 300 g of NaOH template agent with a particle size distribution of 1-2 nm, medium particle 5-50 nm, and large particle 60-100 nm, and add them to methanol for mechanical ball milling for 1 hour, then , and evaporated to dryness at a low temperature of 50-60°C to obtain a precursor;
[0029] 2. Heat the prepared precursor to 200°C at a heating rate of 5-10°C / min under an ammonia protective atmosphere, and then heat it to 600°C at a heating rate of 1-5°C / min. , cooled with the furnace after constant temperature for 2h; the core-shell material of the three-dimensional hierarchical hole shell coated with micropores was obtained on the core material; detected by the nitrogen adsorption-desorption isotherm method, the pore size distribution of the micropores was: the pore size of the macropores was 50-120nm, medium pore diameter is 3-50nm, and small pore diameter is less than 2nm.
[0030] 3. Remov...
Embodiment 2
[0038] 1. Add 100 grams of surface-nanometerized artificial graphite, 100 grams of resin, and 300 g of NaOH template agent with a particle size distribution of 1-2 nm, medium particle 5-50 nm, and large particle 60-100 nm, and add them to methanol for mechanical ball milling for 1 hour, then , and evaporated to dryness at a low temperature of 50-60°C to obtain a precursor;
[0039] 2. Heat the prepared precursor to 300°C at a heating rate of 5-10°C / min under an ammonia protection atmosphere, and then heat it to 700°C at a heating rate of 1-5°C / min. , cooled with the furnace after constant temperature for 5h; the core-shell material of the three-dimensional hierarchical pore shell coated with micropores was obtained on the core material; the nitrogen adsorption-desorption isotherm method was used to detect the distribution of the micropore diameter: the macropore diameter was at 50-120nm, medium pore diameter is 3-50nm, and small pore diameter is less than 2nm.
[0040] 3. Rem...
Embodiment 3
[0048] 1. Add 100 grams of mesophase carbon microspheres (CMS) with surface nanometerization, 100 grams of resin, and 300 g of NaOH template agent with a particle size distribution of 1-2nm, 5-50nm, and 60-100nm, into methanol Mechanical ball milling for 1 hour, and then evaporating to dryness at a low temperature of 50-60°C to obtain the precursor;
[0049] 2. Heat the prepared precursor to 400°C at a heating rate of 5-10°C / min under an ammonia protection atmosphere, and then heat it to 800°C at a heating rate of 1-5°C / min. , cooled with the furnace after constant temperature for 10h; the core-shell material of the three-dimensional layered hole shell coated with micropores was obtained on the core material; detected by the nitrogen adsorption-desorption isotherm method, the pore size distribution of the micropores was: macropore pore size 50-120nm, medium pore diameter 3-50nm, small pore diameter less than 2nm.
[0050] 3. Removing the template agent: use dilute nitric acid...
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