Preparation method of nitrogen-doped lithium vanadate/lithium iron phosphate composite material
A lithium iron phosphate and composite material technology, applied in electrical components, electrochemical generators, battery electrodes, etc., can solve the problems of unstable structure, low gram capacity, poor stability, etc., and achieve improved stability, high gram capacity, The effect of increasing capacity
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Embodiment 1
[0021] (1) Dissolve 1 g of oxalic acid in 40 mL of deionized water, stir magnetically at room temperature to form a transparent aqueous oxalic acid solution, then dissolve 0.351 g of ammonium metavanadate and 0.024 g of lithium hydroxide in the aqueous solution of oxalic acid, and dissolve the obtained mixed solution Magnetically stirred at ambient temperature for 30 minutes to obtain an orange-yellow transparent solution;
[0022] (2) Transfer the orange-yellow transparent solution obtained above to an autoclave, seal the autoclave, place it at 150° C. for 12 hours, and then wait for the temperature of the autoclave to drop to ambient temperature, and take out the reaction product;
[0023] (3) After washing the reaction product obtained above three times with deionized water and absolute ethanol, place it at 80° C. for 12 hours, and then calcinate it at 450° C. for 4 hours to obtain lithium vanadate powder material;
[0024] (4) Dissolve 1 g of oxalic acid in 40 mL of deioni...
Embodiment 2
[0030] (1) Dissolve 1.6g oxalic acid in 40mL deionized water, stir magnetically at room temperature to form a transparent oxalic acid aqueous solution, then dissolve 0.702g ammonium metavanadate and 0.048g lithium hydroxide in this oxalic acid aqueous solution, and mix the obtained The solution was magnetically stirred for 30 min at ambient temperature to obtain an orange-yellow transparent solution;
[0031] (2) Transfer the orange-yellow transparent solution obtained above to an autoclave, seal the autoclave, and place it at 160° C. for 8 hours, then wait for the temperature of the autoclave to drop to ambient temperature, and take out the reaction product;
[0032] (3) Washing the reaction product obtained above three times with deionized water and absolute ethanol, drying at 80°C for 12h, and then calcining at 500°C for 5h to obtain lithium vanadate powder material;
[0033] (4) Dissolve 1.6g oxalic acid in 40mL deionized water, stir at room temperature to form a transpare...
Embodiment 3
[0039] (1) Dissolve 1.2g oxalic acid in 40mL deionized water, stir magnetically at room temperature to form a transparent oxalic acid aqueous solution, then dissolve 0.351g ammonium metavanadate and 0.024g lithium hydroxide in this oxalic acid aqueous solution, and mix the obtained The solution was magnetically stirred for 30 min at ambient temperature to obtain an orange-yellow transparent solution;
[0040] (2) Transfer the orange-yellow transparent solution obtained above to an autoclave, seal the autoclave, and place it at 140° C. for 12 hours, then wait for the temperature of the autoclave to drop to ambient temperature, and take out the reaction product;
[0041] (3) Washing the above-mentioned reaction product with deionized water and absolute ethanol three times, drying at 80°C for 12 hours, and then calcining at 400°C for 6 hours to obtain lithium vanadate powder material;
[0042] (4) Dissolve 1.2g oxalic acid in 40mL deionized water, stir at room temperature to form...
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