Preparation method for monatomic silicon-graphene nanoribbon composite material
A technology of graphene nanobelts and composite materials, applied in the direction of nanotechnology, nanotechnology, nanotechnology for materials and surface science, etc., can solve the problem of cycle stability and service life, and the combination of graphene and simple silicon is not tight , Simple silicon is easy to pulverize and fall off, etc., to achieve the effect of improving electrochemical performance, excellent rate performance, and low production cost
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Embodiment 1
[0027] The concrete steps of a kind of preparation method of elemental silicon-graphene nanoribbon composite material are as follows:
[0028] 1) Preparation of elemental silicon suspension
[0029] Add the elemental silicon material into deionized water and stir for 3 hours to obtain a suspension of elemental silicon, the ratio of the mass (g) of elemental silicon: the volume of deionized water (mL) is 1:500, and then add glucose to the suspension After 90 minutes, a homogeneous elemental silicon suspension was prepared. The mass ratio of glucose to elemental silicon is 1:10.
[0030] 2) Preparation of graphene nanoribbons
[0031] 2.1) adding graphitized carbon nanotubes into concentrated sulfuric acid and stirring for 12 hours to prepare mixture I,
[0032] 2.2) Then, potassium permanganate was added to mixture I, stirred at room temperature for 1 hour, then transferred to a water bath, and then stirred at a constant temperature of 80° C. for 4 hours to obtain mixture II...
Embodiment 2
[0038] A kind of preparation method of elemental silicon-graphene nanoribbon composite material, with embodiment 1, wherein:
[0039] In the 1st step, the stirring time is 0.5h, the mass (g) of elemental silicon: the ratio of deionized water volume (mL) is 1: 100, and a binder is added for ultrasonication for 10min. The mass ratio is 1:0.1.
[0040]2) The transition metal oxidation aid is osmium tetroxide, and the concentrated sulfuric acid is a strong oxidizing acid. The graphitized carbon nanotubes are added to the strong oxidizing acid and the stirring time is 1h, and the stirring time is 0.1h at room temperature. The temperature is 50° C., and the stirring time in a water bath is 1 h; the mass (g) of the carbon nanotube: the mass (g) of the oxidizing agent: the volume (mL) of the oxidizing acid is 1:1:50. Add hydrogen peroxide and deionized water in the mixture II, the mixed reaction time is 0.5h; the volume of the hydrogen peroxide (mL): the volume of the deionized water...
Embodiment 3
[0043] A kind of preparation method of elemental silicon-graphene nanoribbon composite material, with embodiment 1, wherein:
[0044] In step 1), the stirring time is 12h, the mass (g) of elemental silicon: the ratio of deionized water volume (mL) is 1:1000, and the binder is added for ultrasonication for 300min. The mass of the binder and elemental silicon The ratio is 1:50.
[0045] 2) The transition metal oxidation aid is potassium ferrate, and perchloric acid is a strong oxidizing acid. The graphitized carbon nanotubes are added to the strong oxidizing acid and the stirring time is 24 hours. The stirring time is 5 hours at room temperature. The temperature is 90°C, and the stirring time in a water bath is 1-10 h; the mass (g) of the carbon nanotube: the mass (g) of the oxidizing agent: the volume (mL) of the oxidizing acid is 1:10:2000. Add hydrogen peroxide and deionized water to the mixture II, and the mixing reaction time is 3h; the volume of the hydrogen peroxide (mL)...
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