A kind of preparation method of lithium titanate coated with hydroxyapatite
A technology of hydroxyapatite and lithium titanate coating, which is applied in the direction of active material electrodes, electrical components, battery electrodes, etc., can solve the problem of insufficient energy release speed, potential safety hazards of lithium dendrite precipitation, and low charging and discharging platform, etc. problems, achieve excellent electrochemical performance, low price, and inhibit growth
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Embodiment 1
[0021] A preparation method for hydroxyapatite-coated lithium titanate, comprising the following steps:
[0022] (1) Using isopropanol as a solvent, prepare a concentration of 0.1mol / L lithium hydroxide solution and a concentration of 0.1mol / L tetrabutyl titanate solution respectively;
[0023] (2) Ultrasonically disperse 0.0735g of hydroxyapatite with a mass fraction of 1% in isopropanol, add 0.0735g of ethylenediaminetetraacetic acid with a mass fraction of 1%, and slowly add 40mL of 0.1 mol / L lithium hydroxide solution, 50mL 0.1mol / L tetrabutyl titanate solution, in which the molar ratio of lithium ions to titanium ions is 4:5; stir in a water bath at 40°C for 1 hour to obtain a gel, and place the gel in Vacuum drying at 60°C, grinding and crushing to obtain the precursor;
[0024] (3) The precursor was placed in a muffle furnace, and calcined at 650° C. for 5 hours in an air atmosphere to obtain a hydroxyapatite-coated lithium titanate negative electrode material.
Embodiment 2
[0027] A preparation method for hydroxyapatite-coated lithium titanate, comprising the following steps:
[0028] (1) Using absolute ethanol as a solvent, prepare a concentration of 0.5mol / L lithium acetate solution respectively, and a concentration of 0.6mol / L tetraethyl titanate;
[0029] (2) Ultrasonic disperse 1.1020g of hydroxyapatite with a mass fraction of 3% in absolute ethanol, add 1.1020g of oxalic acid with a mass fraction of 3%, and slowly add 60mL of 0.5mol / L lithium acetate under constant magnetic stirring Solution, 62.5mL0.6mol / L tetraethyl titanate, in which the molar ratio of lithium ions to titanium ions is 4:5; stir in a water bath at 50°C for 3h to obtain a gel, and dry the gel in vacuum at 70°C , grinding and pulverizing to obtain the precursor;
[0030] (3) The precursor was placed in a muffle furnace and calcined at 750° C. for 6 hours in an air atmosphere to obtain a lithium titanate negative electrode material coated with hydroxyapatite.
[0031] The ...
Embodiment 3
[0033] A preparation method for hydroxyapatite-coated lithium titanate, comprising the following steps:
[0034] (1) taking diethanolamine as solvent, preparing concentration respectively is 1mol / L lithium nitrate solution, and concentration is 1.1mol / L tetraisopropyl titanate solution;
[0035] (2) Ultrasonic disperse 1.8366g of hydroxyapatite with a mass fraction of 5% in diethanolamine, add 3.6732g of citric acid with a mass fraction of 10%, and slowly add 40mL of 1mol / L lithium nitrate solution under constant magnetic stirring , 45.5mL1.1mol / L tetraisopropyl titanate solution, wherein the molar ratio of lithium ions to titanium ions is 4:5; stir in a water bath at 60°C for 5h to obtain a gel, and dry the gel under vacuum at 70°C dry, grind and pulverize to obtain the precursor.
[0036] (3) The precursor was placed in a muffle furnace and calcined at 800° C. for 8 hours in an air atmosphere to obtain a hydroxyapatite-coated lithium titanate negative electrode material.
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