Flexible ferrous phosphide/carbon nanofiber membrane, and preparation method and application thereof
A technology of carbon nanofibers and iron phosphide, applied in the fields of fiber chemical characteristics, rayon manufacturing, electrochemical generators, etc., can solve problems such as shedding, unstable electrode capacity effects, etc., to enhance electrical conductivity and maintain structural integrity , the effect of simple production method
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Embodiment 1
[0036] Preparation of iron phytate nanoparticles. The preparation of ferric phytate nanoparticles includes two steps of synthesis and purification.
[0037] Dissolve 1.0 g of phytic acid in 10 mL of water, adjust the pH to 6 with concentrated ammonia water as solution A. Weigh 0.944g FeCl 3, 1 g of urea and 0.2 g of surfactant cetyltrimethylammonium bromide (CTAB) were dissolved in 5 mL of deionized water as solution B. Slowly add solution B to solution A drop by drop, resulting in white precipitates, which are centrifuged with deionized water and collected. White Fe-based precursor powder (iron phytate) obtained after drying. like figure 1 As shown, the size of iron phytate nanoparticles is about 200-500nm.
Embodiment 2
[0039] Preparation of iron phytate nanoparticles. The preparation of ferric phytate nanoparticles includes two steps of synthesis and purification.
[0040] Dissolve 10.0 g of phytic acid in 10 mL of water, adjust the pH to 5 with concentrated ammonia water as A solution. Weigh 1g FeCl 3 , 1 g of ammonia water and 0.2 g of surfactant polyvinylpyrrolidone were dissolved in 5 mL of deionized water as solution B. Slowly add solution B to solution A drop by drop, resulting in white precipitates, which are centrifuged with deionized water and collected. White Fe-based precursor powder (iron phytate) obtained after drying. like figure 2 As shown in a, the size of iron phytate nanoparticles is about 500-1000 nm.
Embodiment 3
[0042] Preparation of iron phytate nanoparticles. The preparation of ferric phytate nanoparticles includes two steps of synthesis and purification.
[0043] Dissolve 5.0 g of phytic acid in 10 mL of water, adjust the pH to 4 with concentrated ammonia water as solution A. Weigh 1g FeCl 3 , 1 g of urea and 0.2 g of surfactant sodium dodecylbenzene sulfonate were dissolved in 5 mL of deionized water as solution B. Slowly add solution B to solution A drop by drop, resulting in white precipitates, which are centrifuged with deionized water and collected. White Fe-based precursor powder (iron phytate) obtained after drying. like figure 2 As shown in b, the size of iron phytate nanoparticles is about 500-1000nm.
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