A kind of oxide red luminous body without rare earth doping and lighting device
A technology for red light-emitting and lighting devices, applied in semiconductor devices, light-emitting materials, chemical instruments and methods, etc., can solve the problems of complex preparation methods, no commercialization, and high equipment requirements, and achieve improved luminous efficiency, improved color purity, The effect of reducing energy consumption
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Embodiment 1
[0041] This example is used to illustrate the rare earth-doped oxide red emitter and its preparation method of the present invention.
[0042] According to Ba in Table 1 Example 1 0.994 SO 4 : Bi 0.006 The stoichiometric ratio, weighed high-purity BaCO 3 (31.38 g), (NH 4 ) 2 SO 4 (25.37 g, 20% excess), Bi 2 o 3 (0.22 grams), and 0.4mol / L hydrochloric acid (500 milliliters). BaCO 3 , Bi 2 o 3 Dissolve in hydrochloric acid (the first aqueous solution), heat to 80°C on a water bath, and set aside. Will (NH 4 ) 2 SO 4 Dissolve in deionized water (the second aqueous solution), transfer the second aqueous solution to a separatory funnel, and slowly drop it into the first aqueous solution at 80°C, stirring continuously during the process. The prepared precipitate was aged at 80°C for 2 hours, filtered and washed 3 times with distilled water, and dried at 180°C for 2 hours. The dried precipitate was solid-phase sintered at 850°C for 2 hours, cooled naturally to room te...
Embodiment 2
[0046] This example is used to illustrate the rare earth-doped oxide red emitter and its preparation method of the present invention.
[0047] According to Ba in Table 1 Example 2 0.887 Sr 0.10 SO 4 : Bi 0.005 ,Pb 0.008 The stoichiometric ratio, weighed high-purity BaCO 3 (28.01 g), PbCO 3 (0.34 g), SrCO 3 (2.36 g), (NH 4 ) 2 SO 4 (27.49 g, 30% excess), Bi 2 o 3 (0.19 g), and 0.4 mol / L hydrochloric acid (500 ml). BaCO 3 , PbCO 3 , SrCO 3 , Bi 2 o 3 Dissolve in hydrochloric acid (first aqueous solution), heat to 90°C on a water bath, and set aside. Will (NH 4 ) 2 SO 4 Dissolve in deionized water (the second aqueous solution), transfer the second aqueous solution to a separatory funnel, and slowly drop it into the first aqueous solution at 90° C., stirring continuously during the process. The prepared precipitate was aged at 90°C for 1 hour, filtered and washed 3 times with distilled water, and dried at 180°C for 2 hours. The dried precipitate was solid-pha...
Embodiment 3
[0051] This example is used to illustrate the rare earth-doped oxide red emitter and its preparation method of the present invention.
[0052] According to Ba in Table 1 Example 3 0.976 Cd 0.02 SO 4 : Bi 0.004 The stoichiometric ratio, weighed high-purity BaCO 3 (30.82 g), CdCO 3 (0.11 g), (NH 4 ) 2 SO 4 (31.71 g, 50% excess), Bi 2 o 3 (0.15 g), and 0.4 mol / L hydrochloric acid (500 ml). BaCO 3 , CdCO 3 , Bi 2 o 3 Dissolve in hydrochloric acid (first aqueous solution), heat to 85°C on a water bath, and set aside. Will (NH 4 ) 2 SO 4 Dissolve in deionized water (the second aqueous solution), transfer the second aqueous solution to a separatory funnel, and slowly drop it into the first aqueous solution at 85°C, stirring continuously during the process. The prepared precipitate was aged at 85°C for 3 hours, filtered and washed three times with distilled water, and dried at 180°C for 1 hour. The dried precipitate was solid-phase sintered at 800°C for 4 hours, coo...
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