Conductive agent for negative electrode of lithium ion battery and preparation method for battery containing conductive agent
A conductive technology for lithium-ion batteries and negative electrodes, which is applied in battery electrodes, secondary batteries, and secondary battery repair/maintenance, etc. It can solve the problem of decreased rate performance and cycle performance, increased resistance to lithium ion diffusion, and increased coating volume, etc. problem, to achieve the effect of improving cycle performance, increasing rate performance, and improving rate performance
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Embodiment 1
[0040]1) Disperse 1g of polyacrylonitrile, 3ml of N-trimethylsilimidazole, and 0.6g of citric acid into 12mL of dimethylformamide solvent, and stir the mixed solution for 4 hours to disperse;
[0041] 2) Inject the uniformly dispersed precursor solution into a plastic syringe connected with a stainless steel needle, the diameter of which is 0.9mm;
[0042] 3) Adjust the injection rate of the syringe to 0.2mL / min through the precision propeller, and place an aluminum collector at about 15cm in the direction of the stainless steel needle to collect the prepared SiQDs / CNFs precursor;
[0043] 4) The prepared SiQDs / CNFs precursor was pre-oxidized in air for 1.5d, and then dried in a vacuum oven at 100°C for 10h;
[0044] 5) Place the dried precursor in a tube furnace with a protective atmosphere (argon:hydrogen = 95:5) for high-temperature carbonization. The high-temperature carbonization temperature is set to 700°C, the heating rate is 10°C / min, and the carbonization time is 8h,...
Embodiment 2
[0049] 1) Disperse 1g of polyimide, 2ml of N-trimethylsilimidazole, and 0.4g of citric acid into 12mL of dimethylformamide solvent, and stir the mixed solution for 3 hours to disperse;
[0050] 2) Inject the uniformly dispersed precursor solution into a plastic syringe connected with a stainless steel needle, the diameter of which is 0.9 mm;
[0051] 3) Adjust the injection rate of the syringe to 0.25mL / min through the precision propeller, and place an aluminum collector at about 15cm in the direction of the stainless steel needle to collect the prepared SiQDs / CNFs precursor;
[0052] 4) The prepared SiQDs / CNFs precursor was pre-oxidized in air for 2 days, and then dried in a vacuum oven at 100 °C for 10 hours;
[0053] 5) Place the dried precursor in a tube furnace with a protective atmosphere (argon:hydrogen = 95:5) for high-temperature carbonization. The high-temperature carbonization temperature is set to 700°C, the heating rate is 10°C / min, and the carbonization time is ...
Embodiment 3
[0058] 1) Disperse 1g of polyacrylonitrile, 2ml of aminopropyltrimethoxysilane, and 0.3g of ascorbic acid into 10mL of dimethylformamide solvent, and stir the mixed solution for 3 hours to disperse;
[0059] 2) Inject the uniformly dispersed precursor solution into a plastic syringe connected with a stainless steel needle, the diameter of which is 0.9 mm;
[0060] 3) Adjust the injection rate of the syringe to 0.2mL / min through the precision propeller, and place an aluminum collector at about 15cm in the direction of the stainless steel needle to collect the prepared SiQDs / CNFs precursor;
[0061] 4) The prepared SiQDs / CNFs precursor was pre-oxidized in air for 1.5d, and then dried in a vacuum oven at 95°C for 10h;
[0062] 5) Place the dried precursor in a tube furnace with a protective atmosphere (argon: hydrogen = 95:5) for high-temperature carbonization. The high-temperature carbonization temperature is set to 800°C, the heating rate is 10°C / min, and the carbonization time...
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