Micron-scale spheroidal ferric fluoride positive electrode material and preparation method thereof
A positive electrode material, ferric fluoride technology, applied in the direction of ferric halide, battery electrodes, electrical components, etc., can solve the problems of complex and harsh preparation process conditions, high energy consumption, poor electrochemical performance, etc., and achieve simple preparation process and low energy consumption Low, time-consuming effect
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Embodiment 1
[0026]Prepare 40 mL of 0.5 mol / L ferric nitrate (Fe(NO 3 ) 3 9H 2 O) water / ethanol mixed solution (the volume ratio of water and ethanol is 1:1), and 0.02mol oleic acid is added thereto; It is 1mol / L ammonium fluoride aqueous solution that prepares 20 mL concentration by molar ratio 1:3, then The two solutions were added to 150 mL of ethanol solution with a concentration of 0.0055 mol / L polyethylene glycol (molecular weight: 20,000), and the two solutions were sonicated for 30 minutes, and then the two solutions were mixed, and stirred at a constant speed under normal temperature and pressure for 2 h. . The supernatant was discarded by centrifugation, and the precipitate was repeatedly washed with ethanol several times, and dried at 60°C for 8 hours to obtain the pure phase product FeF 3 (H 2 O) 0.33 .
Embodiment 2
[0028] Prepare 40 mL of 0.6 mol / L ferric chloride (FeCl 3 ·6H 2 0) water / ethanol solution (the volume ratio of water and ethanol is 1:1), and 0.025mol oleic acid is added thereto; It is 1mol / L ammonium bifluoride aqueous solution that prepares 24mL concentration by molar ratio 1:3, then two kinds The solutions were added to 150 mL of 0.0055 mol / L polyethylene glycol (molecular weight: 20,000) ethanol solution, and the two solutions were sonicated for 30 min, and then the two solutions were mixed and stirred at a constant speed for 4 h at normal temperature and pressure. The supernatant was discarded by centrifugation, and the precipitate was repeatedly washed with ethanol, and dried at 60°C for 12 hours to obtain the pure phase product FeF 3 (H 2 O) 0.33 .
Embodiment 3
[0030] Prepare 40 mL of 0.5 mol / L ferric nitrate (Fe(NO 3 ) 3 9H 2 O) water / ethylene glycol mixed solution (the volume ratio of water and ethylene glycol is 1:1), and 0.02mol octadecylamine is added thereto; 20 mL of concentration is prepared as 1mol / L fluorine at a molar ratio of 1:3 Ammonium chloride aqueous solution, and then the two solutions were added to 150mL ethanol solution with a concentration of 0.0055 mol / L polyethylene glycol (molecular weight: 20,000), and the two solutions were sonicated for 10 minutes, and then the two solutions were mixed. Stir at a constant speed for 2 h. The supernatant was discarded by centrifugation, and the precipitate was repeatedly washed with ethanol several times, and dried at 60°C for 8 hours to obtain the pure phase product FeF 3 (H 2 O) 0.33 .
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