Narrow-band deep ultraviolet luminescent material and preparation method thereof
A luminescent material, deep ultraviolet technology, applied in luminescent materials, chemical instruments and methods, etc., can solve the problems of polluted environment, high production cost, lamp mercury poisoning, etc., and achieve good luminescent performance, high product quality, simple and reliable process. Effect
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Embodiment 1
[0026] Embodiment 1: Sol-gel method prepares Y 2.99 al 5 o 12 :0.01Gd
[0027] At room temperature, 1.495mmolY 2 o 3 , 2.5mmol Al 2 o 3 and 0.005 mmol Gd 2 o 3 Dissolve in a container with 2ml of nitric acid and 2ml of deionized water. After cooling, add 30ml of a mixed solution of ethanol and water with a volume ratio of 3:1, add 1.68g of citric acid under stirring conditions, the molar ratio of citric acid and metal ions in the raw material is 2:1, and heat and stir in a water bath at 80°C After 2 hours, a uniform and transparent precursor sol can be obtained, and then the precursor sol is dried at 150° C. for 6 hours to obtain a xerogel. Grind the xerogel into powder, put the ground powder into a high-temperature box furnace to raise the temperature to 1200°C, and sinter at this temperature for 6h. Obtained UV-emitting phosphor Y 2.99 al 5 o 12 : 0.01Gd. The particle size distribution is uniform, and it emits ultraviolet light under the excitation of low-volta...
Embodiment 2
[0028] Embodiment 2: sol-gel method is prepared (Y 0.86 La 0.1 ) 3 al 5 o 12 :0.12Gd
[0029] At room temperature, 1.29mmol Y 2 o 3 , 0.15mmol La 2 o 3 , 2.5mmol Al 2 o 3 and 0.06 mmol Gd 2 o 3Dissolve in a container with 2ml of nitric acid and 2ml of deionized water. After cooling, add 30ml of a mixed solution of ethanol and water with a volume ratio of 2:1, add 1.68g of citric acid under stirring conditions, the molar ratio of citric acid and metal ions in the raw material is 2:1, and heat and stir in a water bath at 70°C After 6 hours, a uniform and transparent precursor sol can be obtained, and then the precursor sol is dried at 180° C. for 4 hours to obtain a xerogel. Grind the xerogel into powder, then put the ground powder into a high-temperature box furnace to raise the temperature to 1600°C, and sinter at this temperature for 4 hours to obtain an ultraviolet-emitting phosphor (Y 0.86 La 0.1 ) 3 al 5 o 12 : 0.12Gd. The particle size distribution is u...
Embodiment 3
[0030] Embodiment 3: sol-gel method is prepared (Y 0.86 Lu 0.04 ) 3 (Al 0.2 Ga 0.8 ) 5 o 12 :0.3Gd
[0031] At room temperature, 1.29mmol Y 2 o 3 , 0.06mmol Lu 2 o 3 , 0.5mmol Al 2 o 3 , 2.0mmolGa 2 o 3 and 0.15 mmol Gd 2 o 3 Dissolve in a container with 2ml of nitric acid and 2ml of deionized water. After cooling, add 30ml of a mixed solution of ethanol and water with a volume ratio of 6:1, add 2.52g of citric acid under stirring conditions, the molar ratio of citric acid and metal ions in the raw material is 3:1, and heat and stir in a water bath at 85°C After 5 hours, a uniform and transparent precursor sol can be obtained, and then the precursor sol is dried at 140° C. for 8 hours to obtain a xerogel. Grind the xerogel into powder, then put the ground powder into a high-temperature box furnace to raise the temperature to 1500°C, and sinter at this temperature for 8 hours to obtain an ultraviolet-emitting phosphor (Y 0.86 Lu 0.04 ) 3 (Al 0.2 Ga 0.8 ) ...
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