Method for preparing rare-earth ytterbium-erbium-doped pyrochlore-phase nanofiber and application of nanofiber
A nanofiber, double-doping technology is applied in pharmaceutical formulations, medical preparations containing active ingredients, and inorganic raw material rayon, etc., to achieve the effects of good repeatability, meeting the requirements of mass production, and a simple and easy preparation method.
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[0037] A method for preparing rare earth ytterbium-erbium double-doped pyrochlore phase nanofibers of the present invention comprises the following steps:
[0038] S1, DMF and acetic acid are mixed and stirred according to the mass ratio of 1:(0.4~0.7), to obtain solution A;
[0039] S2. During continuous stirring, add tetrabutyl titanate with a mass ratio of 1:(3.8-4.5) to solution A to obtain solution B;
[0040] S3, mass ratio is 1:(4~20) ytterbium nitrate and erbium nitrate join in solution B and can obtain solution C in the constant stirring process, and the mass ratio of ytterbium nitrate and erbium nitrate and solution B is 1:(4~20) 4.7);
[0041] S4, adding bismuth nitrate with a mass ratio of 1: (15 to 34) to solution C during continuous stirring to obtain solution D;
[0042] S5. Add PVP with a mass fraction of 5-10% to the solution D and stir to form an electrospinning precursor solution;
[0043] S6. In the case of applying a 15-25 kV high-voltage power supply, ...
Embodiment 1
[0051] DMF and acetic acid are mixed according to the mass ratio of 0.4:1, form transparent solution by magnetic stirring; Then add the tetrabutyl titanate of 0.84ml and make it fully dissolve by stirring; Add the erbium nitrate of 0.031g and 0.106g of ytterbium nitrate; after it is fully dissolved, add 1.018g of bismuth nitrate and fully stir to dissolve it, and finally add PVP with a mass fraction of 5%, and obtain an electrospinning precursor solution after magnetic stirring.
[0052] Under the conditions of a control voltage of 15KV and a flow rate of 5 μl / m, a large amount of nanomaterials appeared on the collector. After the electrospinning was completed, the nanomaterials on the collector were transferred to the muffle furnace and heated at 2°C / min. Raise the rate to 700°C for 1 hour to obtain pyrochlore phase Bi with high crystallinity 2 Ti 2 o 7 : Yb 3+ , Er 3+ nanomaterials.
[0053] figure 1 Given the obtained Bi 2 Ti 2 o 7 : Yb 3+ ,Er 3+ Scanning electro...
Embodiment 2
[0055] DMF and acetic acid are mixed according to the mass ratio of 0.4:1, form transparent solution by magnetic stirring; Then add the tetrabutyl titanate of 0.85ml and make it fully dissolved by stirring; Add 0.015g of erbium nitrate and 0.182g of ytterbium nitrate; after it is fully dissolved, add 1.018g of bismuth nitrate and fully stir to dissolve it, and finally add PVP with a mass fraction of 6%, and obtain an electrospinning precursor solution after magnetic stirring.
[0056] Under the conditions of a control voltage of 17KV and a flow rate of 8μl / m, a large amount of nanomaterials appeared on the collector. After the electrospinning was completed, the nanomaterials on the collector were transferred to the muffle furnace and heated at 6°C / min. Raise the rate to 700°C for 1.5 hours to obtain pyrochlore phase Bi with high crystallinity 2 Ti 2 o 7 : Yb 3+ ,Er 3+ nanomaterials.
[0057] figure 2 The photothermal effect performance diagram obtained when the near-inf...
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