A sol-assisted solvothermal method for preparing lithium vanadium phosphate/carbon composite cathode material with particle-rod mixed morphology and its preparation method
An auxiliary solvent, lithium vanadium phosphate technology, applied in the field of electrochemical power supply, can solve the problems of large particle size, high synthesis temperature, unfavorable production, etc., and achieve the effects of improving conductivity, increasing specific surface area, and improving conductivity
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Embodiment 1
[0018] 1.1420 g Li 2 CO 3 , 2.3632 g NH 4 VO 3 and 3.5212 g NH 4 h 2 PO 4 Ball mill with absolute ethanol (50ml) for 10 hours to obtain a milky white or light yellow slurry; quickly transfer the above slurry to a beaker, stir thoroughly for 30 minutes, and slowly add 3.8202 grams of oxalic acid to obtain a yellow suspension; Heat the yellow suspension in an oil bath at 80°C and keep stirring for 5 hours to volatilize the absolute ethanol to obtain a blue suspension; continue stirring the above blue suspension until it cools to room temperature and transfer to the reaction and ultrasonically for 40 minutes to obtain a uniform suspension; transfer the above reaction kettle to a constant temperature oven, keep it warm at 180°C for 24 hours, and cool it to room temperature naturally to obtain a concentrated precursor and transfer it to a beaker for drying to obtain Concentrate the precursor; Grind the concentrated precursor into powder and add Li 2 CO 3 , NH 4 VO 3 , NH ...
Embodiment 2
[0020] 1.1420 g Li 2 CO 3 , 2.3632 g NH 4 VO 3 and 3.5212 g NH 4 h 2 PO 4 Ball mill with absolute ethanol (50ml) for 10 hours to obtain a milky white or light yellow slurry; quickly transfer the above slurry to a beaker, stir thoroughly for 30 minutes, and slowly add 3.8202 grams of oxalic acid to obtain a yellow suspension; Heat the yellow suspension in an oil bath at 80°C and keep stirring for 5 hours to volatilize the absolute ethanol to obtain a blue suspension; continue stirring the above blue suspension until it cools to room temperature and transfer to the reaction and ultrasonically for 40 minutes to obtain a uniform suspension; transfer the above reaction kettle to a constant temperature oven, keep it warm at 180°C for 24 hours, and cool it to room temperature naturally to obtain a concentrated precursor and transfer it to a beaker for drying to obtain Concentrate the precursor; Grind the concentrated precursor into powder and add Li 2 CO 3 , NH 4 VO 3 , NH ...
Embodiment 3
[0022] 1.1420 g Li 2 CO 3 , 2.3632 g NH 4 VO 3 and 3.5212 g NH 4 h 2 PO 4 Ball mill with absolute ethanol (50ml) for 10 hours to obtain a milky white or light yellow slurry; quickly transfer the above slurry to a beaker, stir thoroughly for 30 minutes, and slowly add 3.8202 grams of oxalic acid to obtain a yellow suspension; Heat the yellow suspension in an oil bath at 80°C and keep stirring for 5 hours to volatilize absolute ethanol to obtain a blue suspension; continue stirring the above blue suspension until it cools to room temperature, and transfer to the reaction and ultrasonically for 40 minutes to obtain a uniform suspension; transfer the above reaction kettle to a constant temperature oven, keep it warm at 180°C for 24 hours, and cool it to room temperature naturally to obtain a concentrated precursor and transfer it to a beaker for drying to obtain Concentrate the precursor; Grind the concentrated precursor into powder and add Li 2 CO 3 , NH 4 VO 3 , NH 4 ...
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