Flexible N/SnOx@ rGO composite material based on biological material substrate, preparation method and application thereof
A technology of composite materials and biomaterials, applied in the field of flexible N/SnOx@rGO composite materials and its preparation, can solve the problems of poor electrode stability, large volume change, poor conductivity, etc., and achieve strong crystallinity, simple process, and small size Effect
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[0037] The invention provides a method for preparing a flexible N / SnOx@rGO composite material based on a biomaterial substrate, comprising the following steps:
[0038]S1, uncarbonized absorbent cotton substrate SnO x Preparation of nanostructures;
[0039] The absorbent cotton was pretreated, the medical absorbent cotton was peeled off and cut into 3cm×3cm×0.1cm cubes, washed alternately with deionized water and ethanol three times, and dried at 30°C to obtain absorbent cotton A; then, SnCl 4 ·5H 2 O and deionized water were mixed according to the ratio of (0.5-2.0) g: (50-100) mL, and after stirring for 1 hour, solution B was obtained; solution B was mixed with 6 mL of 25% ammonia water to obtain solution C; absorbent cotton A Put it into solution C for mixing and ultrasonic treatment for 1 to 3 hours to obtain absorbent cotton D, that is, non-carbonized absorbent cotton substrate SnO x Nano-structure;
[0040] S2, flexible carbon substrate N / SnO x Preparation of nanost...
Embodiment 1
[0053] S1, uncarbonized absorbent cotton substrate SnO x Preparation of nanostructures:
[0054] First, pretreat the absorbent cotton, peel off the medical absorbent cotton and cut it into a cube of 3cm×3cm×0.1cm, wash it alternately with deionized water and ethanol three times, and dry it at 30°C to obtain absorbent cotton A; then, 0.6g SnCl 4 ·5H 2 O and 60ml of deionized water were mixed, stirred for 1 hour to obtain solution B; solution B was mixed with 6ml of 25% ammonia water to obtain solution C; absorbent cotton A was put into solution C for mixing and then ultrasonically treated for 1 hour to obtain absorbent cotton d. That is, uncarbonized absorbent cotton substrate SnO x Nano-structure.
[0055] S2, flexible carbon substrate N / SnO x Preparation of nanostructures:
[0056] Absorbent cotton D was freeze-dried to obtain absorbent cotton E; finally, absorbent cotton E was carbonized in a tube furnace at 700°C for 5 hours, and 200 sccm of N 2 Obtain carbonized ab...
Embodiment 2
[0063] S1, uncarbonized absorbent cotton substrate SnO x Preparation of nanostructures:
[0064] First, pretreat the absorbent cotton, peel off the medical absorbent cotton and cut it into a cube of 3cm×3cm×0.1cm, wash it alternately with deionized water and ethanol three times, and dry it at 30°C to obtain absorbent cotton A; then, 0.8g SnCl 4 ·5H 2 O and 60mL deionized water were mixed, stirred for 1 hour to obtain solution B; solution B was mixed with 6mL 25% ammonia water to obtain solution C; absorbent cotton A was put into solution C for mixing and then ultrasonically treated for 1 hour to obtain absorbent cotton d. That is, uncarbonized absorbent cotton substrate SnO x Nano-structure.
[0065] S2, flexible carbon substrate N / SnO x Preparation of nanostructures:
[0066] Absorbent cotton D was freeze-dried to obtain absorbent cotton E; finally, absorbent cotton E was carbonized in a tube furnace at 700°C for 5 hours, and 200 sccm of N 2 Obtain carbonized absorben...
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