Praseodymium-ytterbium co-doped yttrium vanadate up-conversion luminescent material and preparation method and application thereof
A technology of luminescent materials and co-doping, which is applied in the fields of luminescent materials, chemical instruments and methods, semiconductor/solid-state device manufacturing, etc.
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[0027] The preparation method of the above-mentioned praseodymium-ytterbium co-doped yttrium vanadate up-conversion luminescent material comprises the following steps:
[0028] Step S 11. According to Y 1-x-y VO 4 :xPr 3+ ,yYb 3+ The stoichiometric ratio of each element is weighed as Y 2 o 3 , V 2 o 5 , Pr 2 o 3 and Yb 2 o 3 Powder, wherein, x is 0.01-0.08, and y is 0-0.1.
[0029] In this step, preferably, x is 0.05 and y is 0.06.
[0030] Step S13, mixing and dissolving the powder weighed in step S11 evenly in an acidic solvent for crystallization treatment to obtain crystals, dissolving the crystals in the solvent, and then adding ammonia water to adjust the pH value to 1-6 to obtain a mixed solution.
[0031] In this step, preferably, the acidic solvent includes nitric acid with a concentration of 30% by mass or sulfuric acid with a concentration of 30% by mass.
[0032] In this step, preferably, the solvent is distilled water or a mixed solution of distilled ...
Embodiment 1
[0042] Choose Y 2 o 3 , V 2 o 5 , Pr 2 o 3 and Yb 2 o 3 The powder is mixed according to the molar number of each component being 0.89mmol, 1mmol, 0.05mmol and 0.06mmol. After mixing, dissolve in a nitric acid solvent with a concentration of 30% for crystallization treatment to obtain crystals, then dissolve the crystals in distilled water and add ammonia water to the solution to adjust the pH value to 5. Then the mixed solution was transferred to a stainless steel reaction kettle lined with polytetrafluoroethylene, and kept at 300°C for 3 hours to obtain a precipitate. Then the obtained precipitate was repeatedly washed with ethanol and distilled water, and evaporated to dryness at 100°C to obtain the general chemical formula Y 0.89 VO 4 :0.05Pr 3+ , 0.06Yb 3+ up-converting phosphors.
[0043] Preparation of organic light-emitting diodes The substrate 1 stacked in sequence uses soda-lime glass, the cathode 2 uses a metal Ag layer, and the organic light-emitting la...
Embodiment 2
[0048] Choose Y 2 o 3 , V 2 o 5 , Pr 2 o 3 and Yb 2 o 3 The powder is mixed according to the molar number of each component being 0.91mmol, 1mmol, 0.08mmol and 0.1mmol. After mixing, it is dissolved in a sulfuric acid solvent with a concentration of 30% for crystallization treatment to obtain crystals, and then the crystals are dissolved in distilled water and ammonia water is added to the solution to adjust the pH value to 5. Then the mixed solution was transferred to a stainless steel reaction kettle lined with polytetrafluoroethylene, and kept at 300°C for 3 hours to obtain a precipitate. Then the obtained precipitate was repeatedly washed with ethanol and distilled water, and evaporated to dryness at 100°C to obtain the general chemical formula Y 0.82 VO 4 :0.08Pr 3+ , 0.1yb 3+ up-converting phosphors.
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