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Mesoporous core-shell phosphor and liquid phase preparation method

A fluorescent powder, core-shell technology, applied in the field of mesoporous core-shell materials and preparation, to achieve uniform particle size, high luminous intensity, and good dispersion

Active Publication Date: 2017-08-04
HARBIN ENG UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] In summary, there is no report on the scheme or route of yttrium oxyfluoride with general significance and applicable liquid phase method to prepare high-performance multifunctional structure.

Method used

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  • Mesoporous core-shell phosphor and liquid phase preparation method
  • Mesoporous core-shell phosphor and liquid phase preparation method
  • Mesoporous core-shell phosphor and liquid phase preparation method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0030] (1) Co-precipitation method to generate YOHCO 3 F: Yb / Er precursor. First, 1mol / L of Ln(NO 3 ) 3 The solution is Ln 2 o 3 (99.99%) placed in HNO 3 Dissolve in , heat to remove excess HNO 3 and diluted with deionized water. 1mL of Ln(NO 3 ) 3 (Ln=89%Y / 10%Yb / 1%Er) was added to 50ml of deionized water, then 3g of urea, and then 0.1g of KF. After fully stirring until the solution is uniform, the packaged beaker is placed in a water bath at 90°C for 3 hours without stirring. After the reaction was completed, the obtained product was centrifuged.

[0031] (2) Formation of YOF:Yb / Er@mSiO by sol-gel method 2 . First, the YOHCO 3 F: The Yb / Er precursor was calcined in air at 500°C for 3 hours to generate YOF:Yb / Er. SiO 2 The coating preparation method uses a typical method generation. The synthesized YOF:Yb / E sample was dissolved in 50mL of deionized water and 70mL of ethanol, and after ultrasonication until uniform, 0.3g of CTAB, 0.3mL of TEOS, and 1mL of conc...

Embodiment 2

[0033] (1) Co-precipitation method to generate YOHCO 3 F: Yb / Ho precursor. First, 1mol / L of Ln(NO 3 ) 3 The solution is Ln 2 o 3 (99.99%) placed in HNO 3 Dissolve in , heat to remove excess HNO 3 and diluted with deionized water. 1mL of Ln(NO 3 ) 3 (Ln=89%Y / 10%Yb / 1%Ho) was added to 50ml of deionized water, then 3g of urea, and then 0.1g of KF. After fully stirring until the solution is uniform, the packaged beaker is placed in a water bath at 90°C for 3 hours without stirring. After the reaction was completed, the obtained product was centrifuged.

[0034] (2) Generate YOF:Yb / Ho@mSiO by sol-gel method 2 . First, the YOHCO 3 F: The Yb / Ho precursor was calcined in air at 500 °C for 3 hours to generate YOF:Ln. SiO 2 The coating preparation method uses a typical method generation. The synthesized YOF:Yb / Ho sample was dissolved in 50mL of deionized water and 70mL of ethanol, and after ultrasonication until uniform, 0.3g of CTAB, 0.3mL of TEOS, and 1mL of concentra...

Embodiment 3

[0036] (1) Co-precipitation method to generate YOHCO 3 F: Yb / Tm precursor. First, 1mol / L of Ln(NO 3 ) 3 The solution is Ln 2 o 3 (99.99%) placed in HNO 3 Dissolve in , heat to remove excess HNO 3 and diluted with deionized water. 1mL of Ln(NO 3 ) 3 (Ln=79.7%Y / 20%Yb / 0.3%Tm) was added to 50ml of deionized water, then 3g of urea, and then 0.1g of KF. After fully stirring until the solution is uniform, the packaged beaker is placed in a water bath at 90°C for 3 hours without stirring. After the reaction was completed, the obtained product was centrifuged.

[0037] (2) Formation of YOF:Yb / Tm@mSiO by sol-gel method 2 . First, the YOHCO 3 The F:Yb / Tm precursor was calcined in air at 500°C for 3 hours to generate YOF:Yb / Tm. SiO 2 The coating preparation method uses a typical method generation. The synthesized YOF:Yb / Tm sample was dissolved in 50mL of deionized water and 70mL of ethanol, and after ultrasonication until uniform, 0.3g of CTAB, 0.3mL of TEOS, and 1mL of ...

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Abstract

The invention provides a liquid-phase preparation method of mesoporous core-shell phosphor. (1) Co-precipitation method is used to generate nanocrystalline yttrium oxyfluoride precursor; (2) Yttrium oxyfluoride YOF:Ln is obtained after calcination in air, and mesoporous silica is coated on the surface of YOF:Ln by sol-gel method Formation of core-shell structure YOF:Ln@mSiO 2 . The invention adopts a simple and easy coprecipitation method with high output to generate a yttrium oxyfluoride nanocrystal with good up-conversion fluorescence performance. The mesoporous silica is coated on the surface of yttrium oxyfluoride by a sol-gel method to form a mesoporous structure capable of loading drugs.

Description

technical field [0001] The present invention relates to a mesoporous core-shell material and its preparation method, specifically a mesoporous core-shell YOF:Ln@mSiO 2 Nanocrystals and methods of preparation. Background technique [0002] Rare earth oxides have good chemical stability, high mechanical strength, and high laser damage threshold, but the phonon energy of oxides is too high, resulting in low luminous efficiency of oxides doped with rare earth ions; fluorides have low acoustic Sub-energy, no radiation, low transition probability, high doping concentration, it is a better matrix for rare earth ions. Furthermore, the ion-doped rare earth oxyfluoride combines the advantages of the two. Yttrium oxyfluoride is a new type of luminescent substrate, which has both the physical and chemical stability of oxides and the low phonon properties of fluorides. Energy and higher doping concentration, so it has potential broad application prospects in the field of luminescent ma...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C09K11/85C09K11/02
Inventor 杨飘萍吕锐婵徐加廷杨丹贺飞盖世丽
Owner HARBIN ENG UNIV