Novel Mn<4+> activated high color purity fluoride red light emitting material preparation method
A technology of red light-emitting and light-emitting materials, applied in the fields of light-emitting materials, chemical instruments and methods, etc., can solve the problems of high color temperature, lack of spectrum in the red light region, poor color rendering index, etc.
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Embodiment 1
[0015] Weigh 0.062g of potassium hexafluoromanganate and dissolve it in 5 mL of hydrofluoric acid (40 wt %), stir at room temperature until completely dissolved, add 0.760 mL of hexafluorozirconic acid (45 wt %) aqueous solution to this solution, stir for 10 min; Then add 1.305g KF solid and continue to stir for 30 min. The resulting precipitate was washed 3 times with anhydrous acetic acid and anhydrous methanol, and finally dried in a vacuum oven for 24 hours. The orange-red powder obtained was the final product K 3 ZrF 7 :Mn 4+ .
[0016] The XRD diffraction pattern of this fluorescent powder is attached figure 1 shown, with standard card JCPDS 10-0372 (K 3 ZrF 7 ) in contrast, the two are completely consistent, and no diffraction peaks of any heterogeneous phases are observed, which indicates that the samples we synthesized have a single crystal phase.
[0017] attached figure 2 Shown are the room temperature excitation spectrum (monitored at 627 nm) and emission s...
Embodiment 2
[0020] Weigh 0.031g of potassium hexafluoromanganate and dissolve it in 5 mL of hydrofluoric acid (40 wt %), stir at room temperature until completely dissolved, add 0.760 mL of hexafluorozirconic acid (45 wt %) aqueous solution to this solution, stir for 10 min; then add 1.740g of potassium fluoride solid and continue stirring for 60 min. The resulting precipitate was washed 3 times with anhydrous acetic acid and anhydrous methanol, and finally dried in a vacuum oven for 24 hours. The orange-red powder obtained was the final product K 3 ZrF 7 :Mn 4+ .
Embodiment 3
[0022] Weigh 0.093g of potassium hexafluoromanganate and dissolve it in 10 mL of hydrofluoric acid (40 wt %), stir at room temperature until completely dissolved, add 0.760 mL of hexafluorozirconic acid (45 wt %) aqueous solution to this solution, stir for 10 min; then add 1.305g of potassium fluoride solid and continue stirring for 30 min. The resulting precipitate was washed 3 times with anhydrous acetic acid and anhydrous methanol, and finally dried in a vacuum oven for 24 hours. The orange-red powder obtained was the final product K 3 ZrF 7 :Mn 4+ .
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