Electrode active substance and method for producing same
A technology of electrode active material and manufacturing method, applied in battery electrodes, chemical instruments and methods, circuits, etc., can solve the problems of insufficient electronic conductivity, reduced capacity, and reduced battery density of phosphate-based electrode active materials
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Embodiment 1
[0104] A solution in which lithium acetate, iron (III) citrate, and phosphoric acid are dissolved in water at a mass ratio of 1:1:1 is mixed with an aqueous polyvinyl alcohol solution to obtain a uniform solution.
[0105] The concentration of the solution is LiFePO 4 It is 5 mass% in conversion, and 8 mass% in polyvinyl alcohol conversion.
[0106] Then, add 100g of the above LiMnPO to 100g of this solution 4 , And then use a ball mill for dispersion treatment to obtain LiMnPO 4 Of slurry.
[0107] LiMnPO 4 After drying the slurry with a heating dryer, heat treatment was performed at 600° C. for 1 hour in a nitrogen atmosphere to obtain the electrode active material A1 of Example 1.
Embodiment 2
[0109] The electrode active material A2 of Example 2 was obtained in accordance with Example 1, except that lithium acetate was replaced with lithium nitrate, iron (III) citrate was replaced with iron (III) nitrate, and polyvinyl alcohol was replaced with glucose.
Embodiment 3
[0111] Obtain LiMnPO containing LiMnPO according to Example 1 4 Of slurry.
[0112] Then, the LiMnPO-containing 4 The slurry was sprayed and dried in a 150°C atmosphere with a spray dryer.
[0113] Then, the dried product was heat-treated at 600° C. for 1 hour in a nitrogen atmosphere to obtain an electrode active material A3 of Example 3.
[0114] Observation of the particle shape of the electrode active material A3 with a scanning electron microscope (SEM) revealed that it is a spherical secondary particle with an average particle diameter of 10 μm.
[0115] figure 1 The scanning electron microscope (SEM) image of the electrode active material A3 of Example 3 is shown.
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