SiNPs@CA@GO composite material as well as preparation method and application thereof
A composite material, citric acid technology, applied in nanotechnology, electrical components, electrochemical generators, etc. for materials and surface science, can solve the problems of poor shape retention, high price, complex synthesis process, etc., and achieve stable cycle The effect of improved performance, easy industrial production, and simple production process
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Embodiment 1
[0035] Example 1: Comparison of SiNPs@CA and SiNPs@PVDF composite electrodes
[0036] (1) Disperse 10 mg, 20 mg, 40 mg, and 80 mg of SiNPs in 100 mL of deionized water, respectively, add 10 mg of citric acid monohydrate (CA), and stir for 2 h. Freeze dried. SiNPs@CA with SiNPs:CA ratios of 1:1, 2:1, 4:1, and 8:1 were obtained.
[0037] (2) Disperse 10 mg, 20 mg, 40 mg, and 80 mg of SiNPs in 100 mL of deionized water, respectively, add 10 mg of polyvinylidene fluoride (PVDF), and stir for 2 h. Freeze dried. SiNPs@PVDF with SiNPs:PVDF ratios of 1:1, 2:1, 4:1, and 8:1 were obtained.
[0038] The above materials were prepared as working electrodes, and their specific capacity and cycle stability were tested. The results are as follows: figure 2 shown. from figure 2 It can be seen from the figure that the capacities of the four groups of Si@PVDF composite electrodes show a downward trend. Compared with Si@PVDF, the capacity cycle trend of the four groups of Si@CA is stable,...
Embodiment 2
[0039] Example 2: Preparation of SiNPs@CA@GO Composite Anode Material
[0040] (1) Disperse 40mg, 50mg, 60mg, and 70mg of SiNPs in 50mL of deionized water, respectively, add 60mg, 50mg, 40mg, and 30mg of citric acid (CA), and stir for 2h. SiNPs@CA of 40% SiNPs, 50% SiNPs, 60% SiNPs, and 70% SiNPs were obtained.
[0041] (2) Disperse 4 parts of 25mg graphene oxide (GO) in 30mL deionized water respectively, and ultrasonically for 30min.
[0042] (3) Add the graphene oxide (GO) treated in step (2) to SiNPs@CA of step (1) 40% SiNPs, 50% SiNPs, 60% SiNPs, and 70% SiNPs respectively. Get SiNPs@CA@GO. Ultrasonic for 2h, freeze-dried. Denote as sample 1, sample 2, sample 3, sample 4.
Embodiment 3
[0043] Embodiment 3: the preparation of working electrode
[0044]According to the active material: conductive carbon black = 9:1 mixing, at the same time add an appropriate amount of N-methylpyrrolidine copper (NMP) to make slurry (stir for 12h), apply the mixed slurry evenly on the copper foil with a film applicator, set Dry in a vacuum oven at 120°C (12h); after taking it out, use a punching machine to punch out After weighing the electrode sheet, place it again in a vacuum oven at 60°C for 2 hours; assemble it into a battery in a glove box with Ar atmosphere, water and air content below 0.1ppm.
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