Preparation method of graphite-ferroferric oxide composite cathode material
A technology of ferroferric oxide and negative electrode materials, applied in battery electrodes, electrical components, circuits, etc., can solve the problems of poor electrical conductivity, difficulty in commercial application, and need to improve the first charge and discharge efficiency, and achieve fast charge and discharge speed , high capacity and long service life
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Embodiment 1
[0015] Prepare the ferrous chloride solution that concentration is 1.5mol / L with deionized water and ferrous chloride, prepare the potassium hydroxide solution that concentration is 2mol / L with deionized water and potassium hydroxide, heat ferrous chloride solution To 95°C, add the potassium hydroxide solution to the ferrous chloride solution by spraying, while bubbling oxygen into the solution, stop spraying the sodium hydroxide solution when no new precipitates appear, and then add chlorine Carbon black with a ferrous content of 2% is blown into oxygen for 20 minutes, and the precipitate is obtained by filtration, and the precipitate is washed with deionized water until there are no hydrochloride particles, and the precipitate is dried at 800°C for reduction , crush the reduced material to pass through a 30-mesh sieve to obtain the active material Fe 3 o 4 .
[0016] First, uniformly coat the carbon layer on the surface of the nano-silicon sphere powder by chemical vapor ...
Embodiment 2
[0019] With deionized water and ferrous chloride preparation concentration is the ferrous chloride solution of 2mol / L, with deionized water and potassium hydroxide preparation concentration is the potassium hydroxide solution of 3mol / L, ferrous chloride solution is heated to At 99°C, add the potassium hydroxide solution to the ferrous chloride solution by spraying, while bubbling oxygen into the solution, stop spraying the sodium hydroxide solution when no new precipitates appear, and then add the chloride solution. Carbon black with a ferrous content of 3% was blown with oxygen for 40 minutes, and the precipitate was obtained by filtration. The precipitate was washed with deionized water until no hydrochloride particles were present. After the precipitate was dried, it was reduced at 850°C. The reduced material is crushed to pass through a 30-mesh sieve to obtain the active material Fe 3 o 4 .
[0020] First, uniformly coat the carbon layer on the surface of the nano-silic...
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