Lanthanum titanate red fluorescent material taking Sm<3+> as luminescence center, and preparation method thereof
A technology of red fluorescence and lanthanum titanate, applied in luminescent materials, chemical instruments and methods, etc., can solve problems such as poor color purity, low conversion efficiency, and poor color rendering of mixed light
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Embodiment 1
[0034] a Sm 3+ The preparation method of the lanthanum titanate red fluorescent material which is the luminescence center comprises the following steps: weighing 1.98mmol lanthanum acetate (La(CH 3 COO) 3 , A.R.), 0.02mmol samarium acetate (Sm(CH 3 COO) 3 , A.R.) was dissolved in an appropriate amount of distilled water, and 1 mmol of tetrabutyl titanate (C 16 h 36 o 4 Ti, A.R.), dissolved in 30ml methanol, dropwise added 10mmol nitric acid (HNO 3 , A.R.), magnetically stirred for 1 h, put into an oil bath at 80° C. for about 8 h, and a colloidal precipitate, the precursor sol C, was obtained.
[0035] The precursor sol C was taken out and placed in a corundum crucible, and calcined in a muffle furnace at 1100° C. for 4 hours to obtain the required lanthanum titanate red phosphor.
Embodiment 2
[0037] a Sm 3+ The preparation method of the lanthanum titanate red fluorescent material which is the luminescence center comprises the following steps: weighing 1.94mmol lanthanum acetate (La(CH 3 COO) 3 , A.R.), 0.06mmol samarium acetate (Sm(CH 3 COO) 3 , A.R.) was dissolved in an appropriate amount of distilled water, and 1 mmol of tetrabutyl titanate (C 16 h36 o 4 Ti, A.R.), dissolved in 50ml ethanol, dropwise added 10mmol nitric acid (HNO 3 , A.R.), stirred mechanically for 1.5 h, put it in a water bath at 60° C. for about 10 h, and obtained a colloidal precipitate, the precursor sol C. The precursor sol C was taken out and placed in a corundum crucible, and calcined in a muffle furnace at 1100° C. for 4 hours to obtain the desired phosphor.
Embodiment 3
[0039] A Sm 3+ The preparation method of the lanthanum titanate red fluorescent material as the luminescent center: comprises the following steps: weigh 1.9mmol lanthanum nitrate (La(CH 3 COO) 3 , A.R.), 0.1mmol samarium nitrate (Sm(CH 3 COO) 3 , A.R.) was dissolved in an appropriate amount of distilled water, and 1 mmol of tetrabutyl titanate (C 16 h 36 o 4 Ti, A.R.), dissolved in 50ml butanol, dropwise added 10mmol nitric acid (HNO 3 , A.R.), magnetically stirred for 1.5 h, put into a water bath at 60°C for about 10 h, and a colloidal precipitate, the precursor sol C, was obtained. The precursor sol C was taken out and placed in a corundum crucible, and calcined in a muffle furnace at 1200° C. for 3 hours to obtain the desired phosphor.
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