Holmium doped oxygen yttrium silicate up-conversion luminescent material, preparation method, and organic light emitting diode
A technology of yttrium oxysilicate and luminescent materials, which is applied in the fields of luminescent materials, chemical instruments and methods, semiconductor/solid-state device manufacturing, etc., to achieve the effects of complete crystallization, mild conditions, and low synthesis temperature
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[0028] The preparation method of the above-mentioned holmium-doped yttrium oxysilicate up-conversion luminescent material comprises the following steps;
[0029] Step S101, according to Me 2 Y 8 (SiO 4 ) 6 o 2 :xHo 3+ The stoichiometric ratio of each element is weighed as MeO, Y 2 o 3 , SiO and Ho 2 o 3 Powder, wherein, x is 0.01-0.06, and R is one of magnesium element, calcium element, strontium element and barium element.
[0030] Preferably, x is 0.03.
[0031] It can be understood that in this step, MeO, Y can also be weighed according to the molar ratio of 2:4:6: (0.01-0.08) 2 o 3 , SiO and Ho 2 o 3 Powder, wherein MeO is one of magnesium oxide, calcium oxide, strontium oxide and barium oxide.
[0032] Preferably, in this step, MeO, Y can also be weighed according to the molar ratio of 2:4:6:0.03 2 o 3 , SiO and Ho 2 o 3 Powder.
[0033] Step S102 , dissolving the weighed powder in nitric acid to prepare a solution with a metal cation concentration of 0...
Embodiment 1
[0052] Weigh MgO, Y 2 o 3 , SiO and Ho 2 o 3 The molar numbers of the powders are 2mmol, 4mmol, 6mmol and 0.03mmol respectively, which are dissolved in nitric acid to prepare a 1.5mol / L solution, and 0.01mol / L polyethylene glycol additive is added. Then put the solution into the atomization device, and then feed 5 L / min of argon gas into the atomization device. The solution precursor enters a quartz tube with a temperature of 180°C along with the argon carrier gas to generate the precursor, wherein the diameter of the quartz tube is 95mm and the length is 1.4m. Then the phosphor enters the condenser along with the airflow, and is finally collected by the microporous acid-resistant filter funnel. Collect the precursor of the phosphor powder, place it in a temperature-programmed furnace and calcinate for 3 hours at a calcining temperature of 1100°C to obtain Mg 2 Y 8 (SiO 4 ) 6 o 2 : 0.03Ho 3+ Up-converting phosphors.
[0053] The sequentially stacked substrate 1 uses...
Embodiment 2
[0058] Weigh MgO, Y 2 o 3 , SiO and Ho 2 o 3 The molar numbers of the powders are 2mmol, 4mmol, 6mmol and 0.01mmol respectively, which are dissolved in nitric acid to prepare a 3mol / L solution, and 0.05mol / L polyethylene glycol additive is added. Then put the solution into the atomization device, and then pass 1 L / min of argon gas into the atomization device. The solution precursor enters a quartz tube with a temperature of 220°C along with the argon carrier gas to generate the precursor, wherein the diameter of the quartz tube is 150mm and the length is 3m. Then the phosphor enters the condenser along with the airflow, and is finally collected by the microporous acid-resistant filter funnel. Collect the precursor of the phosphor, place it in a temperature-programmed furnace and calcinate it for 5 hours at a calcining temperature of 1300°C to obtain Mg 2 Y 8 (SiO 4 ) 6 o 2 : 0.01Ho 3+ Up-converting phosphors.
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