Preparation method of Y0.95F3:0.05Ce<3+> nano particle fluorophor

A technology of nanoparticles and phosphors, which is applied in the direction of chemical instruments and methods, luminescent materials, etc., can solve the problems of unsatisfactory luminous intensity of products, insufficient closeness of onlooker aggregation, and uneven dispersion, and achieve stable luminescence, low price, and dispersed uniform effect

Inactive Publication Date: 2018-11-06
CHONGQING UNIV OF ARTS & SCI
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] At present, it seems that the preparation method of rare earth doped luminescent nanoparticles will produce toxic and harmful substances such as HF during the preparation process, which is not good for people and the environment. At the same time, it also has complex operations, high production costs, low yi

Method used

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  • Preparation method of Y0.95F3:0.05Ce&lt;3+&gt; nano particle fluorophor
  • Preparation method of Y0.95F3:0.05Ce&lt;3+&gt; nano particle fluorophor
  • Preparation method of Y0.95F3:0.05Ce&lt;3+&gt; nano particle fluorophor

Examples

Experimental program
Comparison scheme
Effect test

Example Embodiment

[0025] Example 1: One Y 0.95 F 3 :0.05Ce 3+ Preparation of Nanoparticle Phosphor

[0026] Accurately weigh 47.8825gY(NO 3 ) 3 .6H 2 O is dissolved and diluted in a 500ml volumetric flask to make 0.25mol / L Y(NO 3 ) 3 The solution is reserved. Add 5.4265g Ce(NO 3 ) 3 .6H 2 O is dissolved and diluted in a 50ml volumetric flask to form 0.25mol / L Ce(NO 3 ) 3 The solution is reserved. Use a pipette to accurately pipette 19ml 0.25mol / L Y(NO 3 ) 3 , 1000μl 0.25mol / L Ce(NO 3 ) 3 , Plus 3.4848g (control RE 3+ :SDBS=1:2, where RE 3+ Is the trivalent rare earth ion Ce 3+ And Y 3+ Sum) Sodium dodecylbenzene sulfonate (SDBS) in a 100ml small glue beaker, then add a stir bar, temperature 23℃, magnetic stirrer, set stirring speed 100r / min, stir 52min, then add 2.800g (2314μl) 1-butyl-3-methylimidazole tetrafluoroborate, covered with plastic wrap (airtight), stirred for 4h at 100r / min. The mixture was transferred to a 100ml polytetrafluoroethylene reactor. The reaction kettle was place

Example Embodiment

[0028] Example 2: The product prepared in Example 1 was tested as follows

[0029] The product obtained in Example 1 was subjected to XRD test:

[0030] The radiation source is Cu Ba, the wavelength is 1.54060m, the scanning angle is 20°~80°, the voltage is 30kV, the current is 20mA, and the scanning speed is 2.4° / min. The XRD diffraction pattern of X-ray nanoparticles is as follows figure 1 Shown. It can be seen from the figure that the XRD diffraction angle 2θ is 24.208±0.2°, 25.610±0.2°, 27.532±0.2°, 30.701±0.2°, 35.688±0.2°, 40.675±0.2°, 43.584±0.2°, 45.143±0.2°, 46.649±0.2°, 47.221±0.2°, 48.675±0.2°, 50.909±0.2°, 51.844±0.2°, 52.987±0.2°, 54.649±0.2°, etc., there are engagement peaks.

[0031] The product prepared in Example 1 will be scanned by electron microscope, and the scanning results are shown in figure 2 .

[0032] by figure 2 It can be seen that Y 0.95 F 3 ,0.05Ce 3+ The product is a short-rod aggregated nanomaterial with a high degree of aggregation and uniform disper

Example Embodiment

[0035] Example 3: Stability experiment:

[0036] Take the Y prepared in Example 1 0.95 F 3 :0.05Ce 3 The finished nano-particle phosphor was placed in an ordinary sealed plastic bag for 3 months, and then taken out after 3 months for XRD testing. The experimental results showed that the XRD diffraction pattern did not change significantly, and the product components can be considered unchanged. The fluorescence intensity is compared with 0 days, the similarity is over 99%, and the luminous intensity is basically unchanged, so it can be considered that this product has good light stability.

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Abstract

The invention relates to a preparation method of a Y0.95F3:0.05Ce<3+> nano particle fluorophor. The method comprises the steps of taking Y(NO3)3.6H2O, Ce(NO3)3.6H2O, 1-butyl-3-methylimidazole tetrafluoroborate and a surfactant as raw materials, and performing solution preparation, prepared solution stirring, hydrothermal reaction, centrifugal washing, drying and the like. The preparation method ofthe Y0.95F3:0.05Ce<3+> nano particle fluorophor successfully achieves Ce doping; no toxic and harmful substances such as HF are generated in a preparation process; the method is environmentally friendly, and does not pollute an environment; a prepared product is high in luminous intensity and stable in luminescence; a finished product is in a short rod form, and is high in aggregation degree anduniform in dispersion; a luminous refracting surface is smooth; a luminous effect is good; the finished product is high in purity and yield; the yield is as high as 98.3%; the luminous stability is good; the luminous intensity after placement for 3 months almost has no change as compared with that on day 0; the preparation raw materials are simple, easy to obtain and low in price; and the method is worthy of market popularization and application.

Description

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Claims

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Application Information

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Owner CHONGQING UNIV OF ARTS & SCI
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