Negative electrode active material, preparation method thereof, electrode, battery
A technology of negative electrode active material and negative electrode active material, applied in active material electrodes, negative electrodes, batteries, etc., can solve the problems of low ionic and electronic conductivity, low Coulomb efficiency, etc., and achieve high energy density, high energy density, and expansion. small effect
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[0066] [Preparation method of negative electrode active material]
[0067] figure 1 It is a flow chart of the preparation of the negative electrode active material of an exemplary embodiment of the present invention.
[0068] S101: Prepare silicon oxide particles.
[0069] The concrete process of preparation can adopt following steps to carry out:
[0070] First, in an inert gas atmosphere or under reduced pressure, the mixture of metal silicon powder and silicon dioxide powder is heated in the temperature range of 900 ° C to 1600 ° C to generate silicon oxide gas, and the mixture of metal silicon powder and silicon dioxide powder The molar ratio is set in the range of 0.5-1.5. The gas generated by the heating reaction of the raw materials will be deposited on the adsorption plate. When the temperature in the reaction furnace is lowered to below 100°C, the sediment is taken out, crushed and pulverized using equipment such as a ball mill, jet mill, etc., to obtain silicon o...
Embodiment 1-1
[0105] Weigh 1000 grams of silicon oxide particles with a median particle size of 6 μm (atomic ratio of silicon to oxygen is 1:1), and place them in a CVD furnace. Using acetylene as a carbon source, the coating reaction was carried out at 950 ° C to obtain silicon oxide particles coated with a relatively complete carbon film layer, in which the coverage rate of the carbon film layer reached 95%, and the thickness of the carbon film layer was 20nm.
[0106] Next, configure a hydrofluoric acid solution with a concentration of 2mol / L, add the above-mentioned silicon-oxygen particles coated with a carbon film layer, and continue to react for 24 hours at a stirring speed of 300r / min to obtain silicon-oxygen particles with a porous shell. Among them, the porous shell layer is mainly macropores with a pore diameter larger than 400nm, and the carbon film layer remains intact (as shown in Figure 3(a) and Figure 3(b)).
[0107] Next, the hot doping method is used for lithium metal dopi...
Embodiment 1-2
[0112] The silicon oxide compound particles were coated with a carbon film layer using a process similar to that of Example 1-1, wherein the carbon film layer had a coverage rate of 96% and a thickness of 40 nm.
[0113] Next, configure a hydrofluoric acid solution with a concentration of 12mol / L, add the above-mentioned silicon-oxygen particles coated with a carbon film layer, and continue to react for 1 hour at a stirring speed of 500r / min to obtain silicon-oxygen particles with a porous shell. The carbon film layer remains intact, and at the same time no macropores can be seen from the outer surface of the particle (such as Figure 4 shown). Then observe the cross-section of the porous shell of the particle, as Figure 5As shown, it can be seen that the material mainly contains mesopores of 10-30nm; through nitrogen adsorption and desorption test analysis, it is found that the material also contains a small amount of micropores.
[0114] Next, the above silicon oxide powd...
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Abstract
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