A kind of preparation method and application of nano tio2(b)/carbon composite fiber for negative electrode of lithium ion battery
A lithium-ion battery, carbon composite technology, applied in the fields of electrochemistry and material chemistry, to achieve the effects of low production cost, guaranteed purity, and controllable component structure
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Embodiment 1
[0018] Embodiment 1 prepares TiO 2 (B) / C composite fiber Ⅰ
[0019] Under the condition of magnetic stirring, 0.8g of tetrabutyl titanate and 0.4g of PVP were dissolved in a mixed solution of 6mL of ethanol, 2mL of acetic acid and 1mL of N,N-dimethylformamide, mixed and stirred evenly. Take 10mL of the solution with a syringe, the front of the spinneret is a copper mesh collection device, the voltage is 10kV, and the flow rate is 1.0mL / h. After spinning, the TBT / PVP precursor fiber was obtained, the fiber membrane was carefully removed, and vacuum dried at 60°C. Then, under the protection of nitrogen, the temperature was raised to 300° C. for calcination at a rate of 2° C. / min, and the temperature was kept for 120 minutes.
[0020] Dissolve 0.35 g of the calcined sample in 10M NaOH solution to obtain a suspension. React in a closed 50mL hydrothermal kettle at 200°C for 24 hours. After stopping the reaction, wash the precipitated product with 0.1M hydrochloric acid and deion...
Embodiment 2
[0022] Embodiment 2 prepares TiO 2 (B) / C composite fiber Ⅱ
[0023] Under magnetic stirring conditions, 0.8 g of tetrabutyl titanate and 0.4 g of PVP were dissolved in a mixed solution of 5 mL of ethanol, 2 mL of acetic acid and 1 mL of N,N-dimethylformamide. Mix and stir well. Take 10mL of the solution with a syringe, the front of the spinneret is a copper mesh collection device, the voltage is 11kV, and the flow rate is 1.0mL / h. After spinning, the TBT / PVP precursor fiber was obtained, the fiber membrane was carefully removed, and vacuum dried at 60°C. Then, under the protection of nitrogen, the temperature was raised to 500° C. for calcination at a rate of 2° C. / min, and the temperature was kept for 120 minutes.
[0024] Dissolve 0.4 g of the calcined sample in 10M NaOH solution to obtain a suspension, react in a closed 50mL hydrothermal kettle at 180°C for 24 hours, stop the reaction, and wash the precipitated product with 0.1M hydrochloric acid and deionized water Was...
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