Silicon-carbon anode material for lithium ion batteries and preparation method thereof
A lithium-ion battery and negative electrode material technology, applied in battery electrodes, nanotechnology for materials and surface science, secondary batteries, etc., can solve the problems that are difficult to meet the needs of society and life, poor conductivity, low energy density, etc. problems, to achieve the effect of improving the first efficiency, improving conductivity, and the steps are simple and easy
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Embodiment 1
[0021] Step 1, wet ball milling: Weigh 30nm nano-silicon, spherical graphite and citric acid with a mass ratio of 1:7:5, disperse the nano-silicon in a certain amount of deionized water, and add 1% volume ratio of anhydrous Ethanol, ultrasonic 0.5h disperse, dissolve the coated carbon source in a small amount of water, mix the solution, pour it into a ball mill jar together with spherical graphite, and ball mill at 350r / min for 3h;
[0022] Step 2, spray drying: take out the dispersion liquid after ball milling, start spray drying, the air inlet temperature is 200°C, the outlet air temperature is 85°C, and the feed rate is 20ml / min for spray drying;
[0023] Step 3, sintering and carbonization: in the atmosphere furnace, under the protection of nitrogen atmosphere, keep the temperature at 850° C. for 3 hours, and finally obtain the desired silicon-carbon negative electrode material.
Embodiment 2
[0025] The difference from Embodiment 1 is that this embodiment includes the following steps
[0026] Step 1, wet ball milling: Weigh 30nm nano-silicon, spherical graphite and PVP with a mass ratio of 1:7:5, disperse the nano-silicon in a certain amount of deionized water, and add 1% volume ratio of absolute ethanol , disperse by ultrasonication for 0.5h, dissolve the coated carbon source in a small amount of water, mix the solution, pour it into a ball mill jar together with spherical graphite, and mill at 350r / min for 3h;
[0027] Step 3, sintering and carbonization: in an atmosphere furnace under the protection of a nitrogen atmosphere, keep the temperature at 650° C. for 3 hours, and finally obtain the required silicon-carbon negative electrode material.
[0028] Others are the same as in Example 1 and will not be repeated here.
Embodiment 3
[0030] Step 1, wet ball milling: Weigh 30nm particle size nano-silicon, spherical graphite and citric acid, the mass ratio is 1:5:5, disperse the nano-silicon in a certain amount of deionized water, add 1% volume ratio of anhydrous Ethanol, ultrasonic 0.5h disperse, dissolve the coated carbon source in a small amount of water, mix the solution, pour it into a ball mill jar together with spherical graphite, and ball mill at 350r / min for 3h;
[0031] Others are identical with embodiment 1 and are not repeated here.
[0032] Battery assembly: Mix and stir the silicon-carbon negative electrode material prepared in Examples 1-3 with conductive agent (superP), binder (CMC, SBR), and solvent to obtain electrode slurry, and then coat it on the current collector A negative electrode is obtained; the negative electrode is assembled with a counter electrode lithium sheet, a separator, and foamed nickel to obtain a half-cell to be tested.
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