Alkali metal secondary battery negative electrode active material and preparation method thereof
A negative electrode active material and secondary battery technology, applied in the field of electrochemical power supply, can solve problems such as poor material rate performance, achieve the effects of low price, maintain structural stability, and accelerate electron transfer
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[0049] The sample preparation process is as follows: take the sample powder, add absolute ethanol, and obtain a sample suspension after ultrasonic dispersion, use a dropper to take the suspension and drop it on the copper grid or carbon film, vacuumize and dry it, and then send it to the sample room for observation. The instrument model is HRTEM, TecnaiG2 F20 S-TWIN, 200KV.
[0050] (2) Transmission electron microscope (TEM) test of the negative electrode active material:
[0051] The sample preparation process is as follows: take the sample powder, add absolute ethanol, and obtain a sample suspension after ultrasonic dispersion, use a dropper to take the suspension and drop it on the copper grid or carbon film, vacuumize and dry it, and then send it to the sample room for observation. The instrument model is HRTEM, TecnaiG2 F20 S-TWIN, 200KV.
[0052] (3) X-ray diffraction (XRD) test of negative electrode active material:
[0053] The crystal structure of the material was c...
Embodiment 1
[0063] This embodiment is used to illustrate the preparation of the negative electrode active material of the present invention and its application in sodium-ion secondary batteries and lithium-ion secondary batteries. The specific steps are:
[0064] (1) Weigh 30mg of surfactant PVP-K30 and dissolve it in 60ml of ethylene glycol solvent, and magnetically stir for 360min to dissolve it; under magnetic stirring, add 30mg of Fe(NO 3 ) 3 9H 2 O, continue to stir for 2h, obtain mixed solution 1;
[0065] (2) Transfer the mixed solution 1 to a three-necked flask and put it in an oil bath, add condensed water to reflux, control the stirring speed to 600r / min, and reflux at 90°C for 90min. After the reaction is completed, transfer it to the reactor and seal it. , react at 180°C for 12h, centrifuge, wash the precipitate with ethanol, and dry at 60°C to obtain precursor particles.
[0066] (3) Weigh 100 mg of titanium isopropoxide and dissolve it in 30 ml of ethanol to obtain mixed ...
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