Nano-silicon material and application thereof
A nano-silicon and nano-technology, which is applied in the application field of nano-silicon materials and lithium-ion battery negative electrode materials, can solve the problems of increasing synthesis cost, synthesis difficulty, and difficulty in meeting large-scale production, and achieves low cost, high yield, Easy to amplify composite effects
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[0043] Example 1
[0044] The first step: Pass the untreated attapulgite through 200 mesh molecular sieves, add 10 g of it to 300 mL of 2M HCl solution, and react at 70°C for 30 hours. Filter, wash with water to neutrality, dry in an oven at 80°C, heat treatment in a muffle furnace at 600°C for 4h to obtain nano-SiO with rod-like structure 2 . The scanning electron microscope photos such as figure 1 As shown, the length is 300-800nm and the width is 20-40nm.
[0045] Step 2: Combine Mg and SiO 2 Powder massager ratio 2:1 evenly ground (2g SiO 2 ), placed in a porcelain boat, and reacted in a tube furnace at 680°C under Ar atmosphere for 4 hours. The product was stirred and reacted in 1M HCl and 6% HF at room temperature for 5 hours and 10 minutes, respectively, to obtain a uniform particle size distribution of less than 100nm Elemental silicon material (0.8g), the scanning electron microscope photos are as follows figure 2 Shown. According to its transmission electron microsco...
Example Embodiment
[0049] Example 2:
[0050] The first, third and fourth steps are shown in Example 1. In the second step, the Mg powder and SiO 2 The molar ratio is set to 3:1 (2g SiO 2 ), where the magnesium powder is laid flat on the lower layer of the porcelain boat, SiO 2 Coat evenly on the upper porous stainless steel net and react at 850°C for 5 hours. The charge and discharge performance and discharge capacity of the prepared battery are the same as those of Example 1.
Example Embodiment
[0051] Example 3:
[0052] The first, second, and fourth steps are shown in Example 1. In the third step, the C source for coating Si comes from glucose. The obtained elemental silicon material was ultrasonically dispersed in an ethanol solution with a certain amount of glucose dissolved at 200°C. Hydrothermal treatment for 5h. The filtered, washed, and dried sample was heat-treated in a tube furnace at 700°C for 3h under an Ar atmosphere. The charge and discharge performance and discharge capacity of the prepared battery are the same as those of Example 1.
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