Preparation method of Fe4[Fe(CN)6]3@Co3[Co(CN)6]2 composite material and application of Fe4[Fe(CN)6]3@Co3[Co(CN)6]2 composite material
A technology for composite materials and negative electrode materials, which is applied in the field of preparation of Fe4[Fe6]3Co3[Co6]2 composite materials, can solve the problem of not meeting the needs of high-power electronic equipment and continuous use, existing safety hazards, and poor rate performance and other issues, to achieve the effect of low preparation cost and broad commercial application prospects
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[0032] Prepare a hydrochloric acid solution with a concentration of 0.1mol / L, measure 50mL, add polyvinylpyrrolidone (K309mmol), mix well, then add potassium hexacyanocobaltate (Ⅲ) (0.3mmol) and hexacyanoferric (Ⅱ) Potassium acid (0.3mmol). Stir at room temperature for 15 min. After mixing evenly, transfer it to an 80mL reaction kettle, place the reaction kettle in an oven, raise the temperature from room temperature to 160℃ at a rate of 3-5℃ / min, keep it warm for 48h, cool to room temperature, and centrifuge the separated product with deionized water Alternately washed with ethanol for 6 times, and dried in a vacuum oven at 60°C to obtain Fe 4 [Fe(CN) 6 ] 3 co 3 [Co(CN) 6 ] 2 composite material.
[0033] The electrochemical performance of the composite electrode material was tested by a button simulated battery. The slurry used when assembling the battery is a mixed slurry composed of active material, carbon black and sodium carboxymethyl cellulose, and the mass ratio...
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