Novel silicon-carbon composite negative electrode material and preparation method thereof
A silicon-carbon composite, negative electrode material technology, applied in the direction of negative electrode, battery electrode, active material electrode, etc., can solve the problems of not particularly obvious effect and battery capacity attenuation.
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[0022] The invention discloses a preparation method of a novel silicon-carbon composite negative electrode material, which includes the following steps:
[0023] (1) SiO 2 The microspheres are dispersed in a solution containing a dispersant. SiO used 2 The average particle size D50 of the microspheres is 0.01-20 microns, and the dispersant used is hydroxymethylcellulose (CMC), cetyltrimethylammonium bromide (CTAB), sodium pyrophosphate, sodium hexametaphosphate or One of sodium polyacrylate, the solvent used is one or more of water, methanol, ethanol, propanol, acetone, ether, N,N-2-methylformamide; the SiO used 2 The mass ratio of the solvent to the dispersant is 1:1-5, and the volume of the solvent used is 50-150mL.
[0024] (2) Add metal salts to the solution obtained in step (1) and mix well. The metal salt used to form MOF is Co(NO 3 ) 2 , Zn(NO 3 ) 2 , Bi(NO 3 ) 2 , Cu(NO 3 ) 2 , Fe(NO 3 ) 2 One or several in the solution, the metal salt used and SiO 2 The...
Embodiment 1
[0031] A method for preparing a novel silicon-carbon composite negative electrode material, comprising the following steps:
[0032] (1) 1g of SiO with a particle size of 0.01 micron 2 The microspheres were added to 100mL methanol solution, and 4g dispersant CTAB was added at the same time, and ultrasonically dispersed for 3h to make the dispersion uniform.
[0033] (2) Add 4g Zn(NO 3 ) 2 ·6H 2 O and 0.2g Co(NO 3 ) 2 ·6H 2 O, stirred for 2h.
[0034] (3) Dissolve 12.2g of the organic ligand 2-methylimidazole in 100mL of ethanol solution, slowly pour it into the solution of step (2) after the dissolution is complete, stir for 1 hour and then centrifuge and dry to obtain MOF-coated SiO 2 precursor material.
[0035] (4) SiO coated on 4g MOF 2 10g metal Mg powder was added to the precursor material, mixed evenly, then transferred to a tube furnace, and heated at 5°C / min to 700°C for 6h in a nitrogen atmosphere.
[0036](5) Wash the obtained powder through 1M HCl solutio...
Embodiment 2
[0044] A method for preparing a novel silicon-carbon composite negative electrode material, comprising the following steps:
[0045] (1) 0.5g of SiO with a particle size of 0.05 microns 2 The microspheres were added to 80mL of methanol solution, and 2g of dispersant sodium pyrophosphate was added at the same time, and ultrasonically dispersed for 3h to make the dispersion uniform.
[0046] (2) Add 2g Zn(NO 3 ) 2 ·6H 2 O, stirred for 2h.
[0047] (3) Dissolve 4g of 2-methylimidazole as an organic ligand in 80mL ethanol solution. After the dissolution is complete, slowly pour it into the solution in step (2), stir for 1 hour, and then centrifuge and dry to obtain MOF-coated SiO 2 precursor material.
[0048] (4) SiO coated on 3g MOF 2 6.2g metal Mg powder was added to the precursor material, mixed evenly, then transferred to a tube furnace, and heated at 1°C / min to 600°C for 3h in an argon atmosphere.
[0049] (5) The obtained powder is washed with 1M HF solution and deio...
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