Preparation method of honeycomb structure silicon-cobalt tetraoxide composite
A technology of tricobalt tetroxide and honeycomb structure, which is applied in cobalt oxide/cobalt hydroxide, structural parts, electrochemical generators, etc., and can solve problems such as structural stability and poor electrical conductivity, capacity fading, different structures and shapes, etc.
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[0055] Please refer to figure 1 According to a non-limiting embodiment of the present invention, a method for preparing a honeycomb structure silicon-cobalt tetroxide composite is provided, and the method includes the following steps.
[0056] Prepare silicon with a particle diameter of about 30-50 nm and an aqueous solution of cobalt nitrate hexahydrate with a concentration of about 4 g / L.
[0057] Disperse the prepared silicon into the aqueous solution of cobalt nitrate hexahydrate at a mass ratio of about 1:5000, add urea as a precipitating agent, and add polyethylene glycol as a dispersant, wherein the mass of urea and cobalt nitrate hexahydrate aqueous solution The ratio is about 1:36, and the volume ratio of polyethylene glycol and cobalt nitrate hexahydrate aqueous solution is about 1:30; the prepared mixed solution is first ultrasonically treated in a cell pulverizer for about 30 minutes, and then subjected to constant temperature magnetic stirring , the stirring temper...
Embodiment 1
[0067] A kind of preparation method of honeycomb structure silicon-cobalt trioxide compound, such as figure 1 As shown, the following steps S1-S6 are included.
[0068] In step S1, silicon with a particle size of about 30-50 nanometers and an aqueous solution of cobalt nitrate hexahydrate are prepared, and the aqueous solution of cobalt nitrate hexahydrate is prepared by adding about 0.55 g of cobalt nitrate hexahydrate to about 150 ml of deionized water.
[0069] In step S2, about 0.03 grams of nano-silicon is dispersed in about 150 milliliters of cobalt nitrate hexahydrate aqueous solution with about 4 grams of urea as a precipitating agent, ultrasonicated in a cell pulverizer for 30 minutes, and then subjected to a constant temperature magnetic force at 40° C. Stirred for 10h to prepare a suspension.
[0070] In step S3, hydrolysis conversion and self-assembly are carried out, the suspension obtained in step S2 is transferred to a stainless steel high-pressure hydrothermal...
Embodiment 2
[0076] Except that the constant temperature magnetic stirring temperature in step S2 is 45° C., other conditions are the same as in Example 1.
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