Silicon-based negative electrode material for lithium ion battery and preparation thereof, negative electrode sheet and secondary battery
A silicon-based negative electrode material, lithium-ion battery technology, applied in secondary batteries, battery electrodes, negative electrodes, etc., can solve the problems of uneven distribution of composite silicon, no research on negative electrode materials for lithium-ion batteries, and high carbonization temperature. , to achieve the effects of favorable cost control, commercialization and popularization, excellent cycle stability and rate performance, and simple reaction method.
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Embodiment 1
[0038] 1 g of glucose was dissolved in 20 mL of deionized water to form a solution, and then 0.4 g of tin acetate (C 4 h 6 o 4 Sn), followed by the addition of 0.6 g of diatomaceous earth (80–100 nm), glucose was used as a carbon precursor in this experiment. After that, the solution was put into a centrifuge and stirred for 10 h. After the centrifugal stirring, the solution was put into a freeze dryer to freeze for 2 h, and then dried for 8 h. The freeze-dried product was carbonized at a high temperature of 500 °C for 4 h, and after naturally falling to room temperature, the target product C-SiO was finally obtained. x -Sn. Mix the prepared tin-coated silicon oxide active material, conductive carbon black, and binder polyvinylidene fluoride uniformly in a mass ratio of 8:1:1, and use 1-methyl-2-pyrrolidone as a solvent to prepare negative electrode slurry material, which was coated on a copper foil to make a negative electrode sheet, and dried overnight at 50 °C. The ele...
Embodiment 2
[0040] 1 g of glucose was dissolved in 20 mL of deionized water to form a solution, and then 0.3 g of tin acetate (C 4 h 6 o 4 Sn), followed by the addition of 0.7 g of diatomaceous earth (80–100 nm), glucose was used as a carbon precursor in this experiment. After that, the solution was put into a centrifuge and stirred for 10 h. After the centrifugal stirring, the solution was put into a freeze dryer to freeze for 2 h, and then dried for 8 h. The freeze-dried product was carbonized at a high temperature of 500 °C for 4 h, and after naturally falling to room temperature, the target product C-SiO was finally obtained. x -Sn. Mix the prepared tin-coated silicon oxide active material, conductive carbon black, and binder polyvinylidene fluoride uniformly in a mass ratio of 8:1:1, and use 1-methyl-2-pyrrolidone as a solvent to prepare negative electrode slurry material, which was coated on a copper foil to make a negative electrode sheet, and dried overnight at 50 °C. The ele...
Embodiment 3
[0043] 1 g of glucose was dissolved in 20 mL of deionized water to form a solution, and then 0.2 g of tin acetate (C 4 h 6 o 4 Sn), followed by the addition of 0.8 g of diatomaceous earth (80–100 nm), glucose was used as a carbon precursor in this experiment. After that, the solution was put into a centrifuge and stirred for 10 h. After the centrifugal stirring, the solution was put into a freeze dryer to freeze for 2 h, and then dried for 8 h. The freeze-dried product was carbonized at a high temperature of 500 °C for 4 h, and after naturally falling to room temperature, the target product C-SiO was finally obtained. x -Sn. Mix the prepared tin-coated silicon oxide active material, conductive carbon black, and binder polyvinylidene fluoride uniformly in a mass ratio of 8:1:1, and use 1-methyl-2-pyrrolidone as a solvent to prepare negative electrode slurry material, which was coated on a copper foil to make a negative electrode sheet, and dried overnight at 50 °C. The ele...
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