Bismuth ion-doped wavelength-adjustable color-changing luminescent material and preparation method thereof
A technology of luminescent materials and color-changing materials, applied in the field of luminescent materials, can solve the problems of complex process, easy copying of information, high cost, etc., and achieve the effect of stable chemical and physical properties
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Embodiment 1
[0031] Synthesis:
[0032] 1) Weigh 0.2764g potassium carbonate (K 2 CO 3 ), 0.7894g barium carbonate (BaCO3 ), 0.4806g silicon dioxide (SiO 2 ), 0.4471g yttrium oxide (Y 2 O 3 ), 0.0093g bismuth oxide (Bi 2 O 3 ) into the agate mortar, add 5ml absolute ethanol (C 2 H 6 O) After grinding for 20min to dryness.
[0033] 2) Transfer the mixed powder obtained in step 1) into a corundum crucible and put it in a tube furnace, heat it up to 1100 ° C for calcination for 4 hours, and cool with the furnace to obtain a white solid product, namely KBaY 0.99 Si 2 O 7 :0.01Bi 3+ Luminescent material.
[0034] figure 1 is the KBaY obtained in Example 1 of the present invention 0.99 Si 2 O 7 :0.01Bi 3+ XRD pattern of figure 1 It can be seen that the KBaY obtained in Example 1 0.99 Si 2 O 7 :0.01Bi 3+ The XRD results are consistent with the standard diffraction peaks, and the intensity of the diffraction peaks is high.
[0035] figure 2 is the KBaY obtained in Example ...
Embodiment 2
[0038] Synthesis:
[0039] 1) Weigh 0.2764g potassium carbonate (K 2 CO 3 ), 0.7894g barium carbonate (BaCO 3 ), 0.4806g silicon dioxide (SiO 2 ), 0.4381g yttrium oxide (Y 2 O 3 ), 0.028g bismuth oxide (Bi 2 O 3 ) into the agate mortar, add 4 ml of absolute ethanol (C 2 H 6 O) After grinding for 30min to dryness.
[0040] 2) Transfer the mixed powder obtained in step 1) into a corundum crucible and put it in a tube furnace, heat it up to 1200 ° C for calcination for 3 hours, and cool with the furnace to obtain a white solid product, namely KBaY 0.97 Si 2 O 7 :0.03Bi 3+ Luminescent material.
[0041] Figure 4 is the KBaY obtained in Example 2 of the present invention 0.97 Si 2 O 7 :0.03Bi 3+ XRD pattern of Figure 4 It can be seen that the KBaY obtained in Example 2 0.97 Si 2 O 7 :0.03Bi 3+ XRD results with KBaYSi 2 O 7 Standard cards have good matching and good crystallinity.
[0042] Figure 5 is the KBaY obtained in Example 2 of the present invent...
Embodiment 3
[0045] Synthesis:
[0046] 1) Weigh 0.2764g potassium carbonate (K 2 CO 3 ), 0.7894g barium carbonate (BaCO 3 ), 0.4806g silicon dioxide (SiO 2 ), 0.4246g yttrium oxide (Y 2 O 3 ), 0.056g bismuth oxide (Bi 2 O 3 ) into the agate mortar, add 2ml absolute ethanol (C 2 H 6 O) After grinding for 40min to dryness.
[0047] 2) Transfer the mixed powder obtained in step 1) into a corundum crucible and put it in a tube furnace, heat it up to 1300 ° C for calcination for 1 hour, and cool with the furnace to obtain a white solid product, namely KBaY 0.94 Si 2 O 7 :0.06Bi 3+ Luminescent material.
[0048] Figure 7 is the KBaY obtained in Example 3 of the present invention 0.94 Si 2 O 7 :0.06Bi 3+ XRD pattern of Figure 7 It can be seen that the KBaY obtained in Example 3 0.94 Si 2 O 7 :0.06Bi 3+ The XRD results are consistent with the standard diffraction peaks, and the purity is high.
[0049] Figure 8 is the KBaY obtained in Example 3 of the present invention...
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