Silicon-oxygen negative electrode material and preparation method thereof, negative electrode plate and secondary battery
A technology of negative electrode material and negative electrode sheet, applied in the field of negative electrode sheet and secondary battery, silicon-oxygen negative electrode material and its preparation, can solve the problems of low initial efficiency, unstable SEI and short cycle life of lithium battery, and improve the transmission power. The effect of improving the dynamic performance and improving the cycle life
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[0023] The first aspect of the present invention is to provide a method for preparing a silicon-oxygen negative electrode material, comprising the following steps:
[0024] S1. Add the silicone material to an alkaline solution with a pH value of 8 to 9 to disperse, add dopamine hydrochloride to continue the dispersion, wash and centrifuge, and dry to obtain silicone dopamine nanoparticles; sinter the silicone dopamine nanoparticles to obtain Silicon Oxygen Carbon Nanoparticles;
[0025] S2. Mix and stir the silicon oxygen carbon nanoparticles and the titanium source, heat to 70-90°C and maintain for 0.1-1h, cool, wash and centrifuge, and dry at 70-90°C for 6-12h to obtain titanium silicon oxygen carbon nanoparticles ;
[0026] S3. Dissolve the titanium silicon oxygen carbon nanoparticles in water, ultrasonically disperse them, then add dopamine hydrochloride to continue dissolving and dispersing, then add a strong alkaline substance to stir, wash and centrifuge, and dry at 70...
Embodiment 1
[0048] A method for preparing a silicon-oxygen negative electrode material, comprising the following steps:
[0049] S1. Add 0.6 g of tris hydroxymethyl aminomethane into 490 mL of deionized water and disperse it completely. After being uniformly dispersed, slowly add a hydrochloric acid solution with a concentration of 0.1 M and mix evenly. Adjust the pH value to 8.5 to obtain a Tris-HCl solution; 0.2g of SiO with D50 of 3~6μm x (0x @Carbon Nanoparticles;
[0050] S2, 0.5g of the SiO x @Carbon nanoparticles and 0.5g tetrabutyl titanate are fully stirred, heated to 80°C and maintained for 0.5h, naturally cooled to room temperature, washed with deionized water and centrifuged, dried at 80°C for 8h to obtain SiO x @C@TiO 2 ;
[0051] S3, 10g SiO x @C@TiO 2 Dissolve in 200mL deionized water, ultrasonically disperse for 30~60min, then add 0.4g dopamine hydrochloride to continue dissolving and dispersing, then add 0.25g trishydroxymethylaminomethane and stir for 5~30min, wash...
Embodiment 2
[0053] The difference from Example 1 is that in the preparation of step S1, 0.4 g of dopamine hydrochloride was added, that is, the mass ratio of silicon-oxygen material to dopamine hydrochloride was 0.5:1.
[0054] The rest are the same as in Embodiment 1, and will not be repeated here.
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