CN105314877A - Rare earth ion doped KY2Cl7 glass-ceramic and preparation method thereof - Google Patents
Rare earth ion doped KY2Cl7 glass-ceramic and preparation method thereof Download PDFInfo
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- CN105314877A CN105314877A CN201510859959.5A CN201510859959A CN105314877A CN 105314877 A CN105314877 A CN 105314877A CN 201510859959 A CN201510859959 A CN 201510859959A CN 105314877 A CN105314877 A CN 105314877A
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- devitrified glass
- acetic acid
- rare earth
- earth ion
- ion doped
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Abstract
The invention discloses rare earth ion doped KY2Cl7 glass-ceramic which comprises the following components in percentage by mole: 87.5-92 percent of SiO2, 7.4-10 percent of KY2Cl7 and 0.6-3 percent of LnCl3, wherein LnCl3 refers to at least one of YbCl3, ErCl3, TmCl3 and HoCl3. The rare earth ion doped KY2Cl7 glass-ceramic disclosed by the invention is transparent, deliquesce-resistant, good in mechanical property and high in blue-violet transmittance and has the performances of low phonon energy and high up-conversion efficiency, so that the efficiency of an up-conversion laser is greatly improved. Moreover, the glass-ceramic is simple in preparation method and relatively low in production cost.
Description
Technical field
The present invention relates to a kind of rare earth ion doped devitrified glass, especially relate to a kind of rare earth ion doped KY being used as up-conversion luminescent material
2cl
7devitrified glass and preparation method thereof.
Background technology
When the up-conversion luminescence of rare earth ion refers to the sample when the excitation light irradiation doping with rare-earth ions adopting wavelength longer, launch the phenomenon that wavelength is less than the light of excitation wavelength.Utilize the upper conversion characteristic of rare earth ion, can obtain cheap, that can at room temperature work and export purplish blue green-light fiber laser continuously.The green up-conversion lasing of purplish blue can be applicable to the every field such as color monitor, data storing, information technology, laser printing and medical treatment.The efficiency improving up-conversion luminescence need reduce the phonon energy of substrate material, this is mainly because lower phonon energy can reduce the generation of non-radiative relaxation probability, improve the fluorescence lifetime of metastable level in the middle of rare earth ion, effectively can improve the efficiency of up-conversion luminescence.KY
2cl
7the lattice phonon energy Ratios fluorochemical of crystal is lower, is more suitable for as rear-earth-doped up-conversion luminescence matrix, rare earth ion doped KY
2cl
7crystal has the upper efficiency of conversion higher than rare earth ion doped crystal of fluoride, but KY
2cl
7the easy moisture absorption of crystal, need special processing and storage, be difficult to preparation, chemical stability and its practical application of the disadvantages affect such as physical strength is poor.
Transparent glass-ceramics is a kind of photoelectron material having crystal and glass advantage concurrently.Chloride current transparent glass-ceramics is mainly used as flashing and up-conversion luminescent material, and if publication number is CN103382089, name is called " containing Cs
3laCl
6nanocrystalline transparent sulfur-halogen glass pottery and preparation thereof " application for a patent for invention disclose doping Nd
3+or Er
3+ion, with Cs
3laCl
6for crystallite phase, glassy phase are the devitrified glass of sulfide, but the physical and chemical performance of sulfide is poorer than oxide compound, and not saturating in visible ray shortwave strong point, have impact on up-conversion luminescence efficiency; As publication number be CN103951231, name is called " rare earth ion doped Sr
2yCl
7devitrified glass and preparation method thereof " application for a patent for invention also disclose a kind of crystallite mutually for Sr
2yCl
7, glassy phase is P
2o
5with GeO
2be main devitrified glass, the rare earth ion of doping is Ce
3+, Eu
3+and Tb
3+in one, adopt melt supercooled method and subsequent heat treatment preparation, there is good scintillation properties, as flash luminous material.But also there is no trivalent rare earth ions Yb at present
3+, Er
3+, Tm
3+and Ho
3+the KY of doping
2cl
7devitrified glass is used for the open report of up-conversion luminescent material.
Summary of the invention
The rare earth ion doped KY that technical problem to be solved by this invention is to provide that a kind of phonon energy is low, little, the upper conversion quantum yield of radiationless transition probability is high, Deliquescence-resistant, good mechanical property, up-conversion luminescence are very strong
2cl
7devitrified glass and preparation method thereof.
The present invention solves the problems of the technologies described above adopted technical scheme: a kind of rare earth ion doped KY
2cl
7devitrified glass, its molar percentage is composed as follows: SiO
287.5 ~ 92mol%, KY
2cl
77.4 ~ 10mol%, LnCl
30.6 ~ 3mol%, wherein LnCl
3for YbCl
3, ErCl
3, TmCl
3and HoCl
3in at least one.
This devitrified glass molar percentage consists of: SiO
289mol%, KY
2cl
78mol%, ErCl
30.5mol%, YbCl
32.5mol%.
This devitrified glass molar percentage consists of: SiO
287.5mol%, KY
2cl
710mol%, TmCl
30.5mol%, YbCl
32mol%.
This devitrified glass molar percentage consists of: SiO
288mol%, KY
2cl
79mol%, ErCl
30.1mol%, TmCl
30.1mol%, YbCl
3: 2.8mol%.
Described rare earth ion doped KY
2cl
7the preparation method of devitrified glass, comprises the following steps:
(1) by mole% composition SiO
287.5 ~ 92mol%, KY
2cl
77.4 ~ 10mol%, LnCl
30.6 ~ 3mol%, wherein LnCl
3for YbCl
3, ErCl
3, TmCl
3and HoCl
3in at least one; Take at least one in acetic acid yttrium, Potassium ethanoate and acetic acid ytterbium, acetic acid erbium, acetic acid thulium and acetic acid holmium, wherein the deal of acetic acid yttrium, Potassium ethanoate is respectively by mole% KY in composition
2cl
7molar content take, the deal of acetic acid ytterbium, acetic acid erbium, acetic acid thulium and at least one in acetic acid holmium is respectively by LnCl in above-mentioned identical molar percentage composition
3molar content take, and above-mentioned acetate is dissolved in deionized water forms Acetate Solution, in Acetate Solution, add trichoroacetic acid(TCA) obtain transparent mixing solutions, wherein in trichoroacetic acid(TCA) and Acetate Solution, the mol ratio of metal ion summation is 3: 1;
(2) SiO in forming by the molar percentage identical with step (1)
2molar content take tetraethoxy and be dissolved in ethanol, obtain teos solution, then stir 1 hour after being mixed with teos solution by mixing solutions obtained for step (1), then regulate its pH value to 5 with dust technology, obtain precursor liquid;
(3) the precursor liquid room temperature ageing that step (2) obtains is placed on baking oven in 3 weeks, is warming up to 140 DEG C of dryings 9 days, obtains transparent xerogel;
(4) xerogel that step (3) obtains is placed in nitrogen fine annealing stove, thermal treatment 10 hours at the temperature of 570 ~ 600 DEG C, and then be cooled to 50 DEG C with the speed of 10 DEG C/h, close fine annealing stove power supply, automatically be cooled to room temperature, obtain transparent rare earth ion doped KY
2cl
7devitrified glass.
Compared with prior art, the invention has the advantages that: this devitrified glass has KY
2cl
7the feature that in the excellence of crystalline host material, the physical strength of conversion performance and silica glass, stability and being easy to is processed; The experiment proved that: by the rare earth ion doped KY obtained by preparation method of the present invention
2cl
7devitrified glass is transparent, Deliquescence-resistant, good mechanical property, royal purple light transmission rate are higher, has the performances such as low, the upper efficiency of conversion of phonon energy is high, upconversion laser efficiency can be made greatly to improve; In addition, the preparation method of this devitrified glass is simple and have good repeatability, and production cost is lower.
Accompanying drawing explanation
Fig. 1 is X-ray diffraction (XRD) figure of the devitrified glass that embodiment 1 obtains;
Fig. 2 is the Er that embodiment 1 obtains
3+, Yb
3+the KY of doping
2cl
7the 970nm laser apparatus of devitrified glass excites up-conversion luminescence spectrum;
Fig. 3 is the Er that comparative example 1 obtains
3+, Yb
3+the KY of doping
2f
7the 970nm laser apparatus of devitrified glass excites up-conversion luminescence spectrum.
Embodiment
Below in conjunction with accompanying drawing embodiment, the present invention is described in further detail.
Embodiment 1
Er
3+, Yb
3+doping KY
2cl
7the molar percentage of devitrified glass consists of: SiO
289mol%, KY
2cl
78mol%, ErCl
30.5mol%, YbCl
32.5mol%, the technique preparing devitrified glass of above composition is as follows:
(1) take acetic acid yttrium, Potassium ethanoate, acetic acid ytterbium and acetic acid erbium, wherein the deal of acetic acid yttrium, Potassium ethanoate is respectively by mole% KY in composition
2cl
7molar content take, the deal of acetic acid ytterbium and acetic acid erbium is respectively by YbCl in above-mentioned identical molar percentage composition
3, ErCl
3molar content take, be dissolved in deionized water by above-mentioned acetate and form Acetate Solution, add trichoroacetic acid(TCA) and obtain transparent mixing solutions in Acetate Solution, wherein in trichoroacetic acid(TCA) and Acetate Solution, the mol ratio of metal ion summation is 3: 1;
(2) SiO in forming by the molar percentage identical with step (1)
2molar content take tetraethoxy and be dissolved in ethanol, obtain teos solution, then stir 1 hour after being mixed with teos solution by mixing solutions obtained for step (1), then regulate its pH value to 5 with dust technology, obtain precursor liquid;
(3) the precursor liquid room temperature ageing that step (2) obtains is placed on baking oven in 3 weeks, is warming up to 140 DEG C of dryings 9 days, obtains transparent xerogel;
(4) xerogel that step (3) obtains is placed in nitrogen fine annealing stove, 570 ~ 600 DEG C of thermal treatments 10 hours, and then be cooled to 50 DEG C with the speed of 10 DEG C/h, close fine annealing stove power supply, automatically be cooled to room temperature, obtain transparent rare earth ion Er
3+, Yb
3+the KY of doping
2cl
7devitrified glass.
To obtained KY
2cl
7devitrified glass carries out X-ray diffraction test, obtains the XRD figure of this devitrified glass as shown in Figure 1, and its result is as follows: the XRD diffraction peak of the sample obtained through Overheating Treatment and KY
2cl
7the main diffraction peak of the standard x RD figure of crystalline phase all conforms to, and the material therefore obtained is KY
2cl
7the devitrified glass of crystallization phase.Measure by TRIAX550 fluorescence spectrophotometer, under 970nm laser apparatus shooting conditions, the up-conversion luminescence spectrum of this devitrified glass recorded as shown in Figure 2, the integration luminous intensity of green glow (533nm), green glow (546nm) and ruddiness (653nm) respectively about 5.47 × 10
5, 7.26 × 10
5, 4.92 × 10
5, green and red up-conversion luminescence is very strong.
Embodiment 2
Tm
3+, Yb
3+doping KY
2cl
7the molar percentage of devitrified glass consists of: SiO
287.5mol%, KY
2cl
710mol%, TmCl
30.5mol%, YbCl
32mol%, after the preparation identical with embodiment 1 and heat treatment process, obtains transparent rare earth ion Tm
3+, Yb
3+the KY of doping
2cl
7devitrified glass.This devitrified glass TRIAX550 fluorescence spectrophotometer is measured, under 970nm laser apparatus shooting conditions, observes strong blue up-conversion luminous.
Embodiment 3
Er
3+, Tm
3+, Yb
3+doping KY
2cl
7the molar percentage of devitrified glass consists of: SiO
288mol%, KY
2cl
79mol%, ErCl
30.1mol%, TmCl
30.1mol%, YbCl
32.8mol%, after the preparation identical with embodiment 1 and heat treatment process, obtains transparent rare earth ion Er
3+, Tm
3+, Yb
3+doping KY
2cl
7devitrified glass.This devitrified glass TRIAX550 fluorescence spectrophotometer is measured, under 970nm laser apparatus shooting conditions, observes strong blueness, green and red up-conversion luminescence.
Embodiment 4
Ho
3+doping KY
2cl
7the molar percentage of devitrified glass consists of: SiO
292mol%, KY
2cl
77.4mol%, HoCl
30.6mol%, after the preparation identical with embodiment 1 and heat treatment process, obtains transparent rare earth ion Ho
3+doping KY
2cl
7devitrified glass.This devitrified glass TRIAX550 fluorescence spectrophotometer is measured, and under 970nm laser apparatus shooting conditions, observes strong green and red up-conversion luminescence.
Comparative example 1
Er
3+, Yb
3+the KY of doping
2f
7the molar percentage of devitrified glass consists of: SiO
289mol%, KY
2f
78mol%, ErF
30.5mol%, YbF
32.5mol%, after the preparation identical with embodiment 1 and heat treatment process, obtains transparent rare earth ion Er
3+, Yb
3+the KY of doping
2f
7devitrified glass.Measure by TRIAX550 fluorescence spectrophotometer, under 970nm laser apparatus shooting conditions, the up-conversion luminescence spectrum of this devitrified glass recorded as shown in Figure 3, the integration luminous intensity of green glow (533nm), green glow (546nm) and ruddiness (653nm) respectively about 4.04 × 10
4, 5.57 × 10
4, 3.94 × 10
4, compare with embodiment 1, green and red Up-conversion Intensity is low, and the Er that embodiment 1 obtains is described
3+, Yb
3+the KY of doping
2cl
7the Er that the up-conversion luminescence performance test ratio 1 of devitrified glass obtains
3+, Yb
3+the KY of doping
2f
7devitrified glass is better.
Claims (5)
1. a rare earth ion doped KY
2cl
7devitrified glass, its molar percentage consists of: SiO
287.5 ~ 92mol%, KY
2cl
77.4 ~ 10mol%, LnCl
30.6 ~ 3mol%, wherein LnCl
3for YbCl
3, ErCl
3, TmCl
3and HoCl
3in at least one.
2. KY rare earth ion doped as claimed in claim 1
2cl
7devitrified glass, is characterized in that this devitrified glass molar percentage consists of: SiO
289mol%, KY
2cl
78mol%, ErCl
30.5mol%, YbCl
32.5mol%.
3. KY rare earth ion doped as claimed in claim 1
2cl
7devitrified glass, is characterized in that this devitrified glass molar percentage consists of: SiO
287.5mol%, KY
2cl
710mol%, TmCl
30.5mol%, YbCl
32mol%.
4. KY rare earth ion doped as claimed in claim 1
2cl
7devitrified glass, is characterized in that this devitrified glass molar percentage consists of: SiO
288mol%, KY
2cl
79mol%, ErCl
30.1mol%, TmCl
30.1mol%, YbCl
3: 2.8mol%.
5. KY rare earth ion doped as claimed in claim 1
2cl
7the preparation method of devitrified glass, is characterized in that comprising the following steps:
(1) by mole% composition SiO
287.5 ~ 92mol%, KY
2cl
77.4 ~ 10mol%, LnCl
30.6 ~ 3mol%, wherein LnCl
3for YbCl
3, ErCl
3, TmCl
3and HoCl
3in at least one; Take at least one in acetic acid yttrium, Potassium ethanoate and acetic acid ytterbium, acetic acid erbium, acetic acid thulium and acetic acid holmium, wherein the deal of acetic acid yttrium, Potassium ethanoate is respectively by mole% KY in composition
2cl
7molar content take, the deal of acetic acid ytterbium, acetic acid erbium, acetic acid thulium and at least one in acetic acid holmium is respectively by LnCl in above-mentioned identical molar percentage composition
3molar content take, and above-mentioned acetate is dissolved in deionized water forms Acetate Solution, in Acetate Solution, add trichoroacetic acid(TCA) obtain transparent mixing solutions, wherein in trichoroacetic acid(TCA) and Acetate Solution, the mol ratio of metal ion summation is 3: 1;
(2) SiO in forming by the molar percentage identical with step (1)
2molar content take tetraethoxy and be dissolved in ethanol, obtain teos solution, then stir 1 hour after being mixed with teos solution by mixing solutions obtained for step (1), then regulate its pH value to 5 with dust technology, obtain precursor liquid;
(3) the precursor liquid room temperature ageing that step (2) obtains is placed on baking oven in 3 weeks, is warming up to 140 DEG C of dryings 9 days, obtains transparent xerogel;
(4) xerogel that step (3) obtains is placed in nitrogen fine annealing stove, thermal treatment 10 hours at the temperature of 570 ~ 600 DEG C, and then be cooled to 50 DEG C with the speed of 10 DEG C/h, close fine annealing stove power supply, automatically be cooled to room temperature, obtain transparent rare earth ion doped KY
2cl
7devitrified glass.
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Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101024553A (en) * | 2006-02-24 | 2007-08-29 | 中国科学院福建物质结构研究所 | Alkaline-earth contained fluoride nano crystal transparent glass ceramic and its sol-gel preparing method |
JP5087450B2 (en) * | 2008-03-28 | 2012-12-05 | 三井造船株式会社 | Rotary distributor |
CN103951233A (en) * | 2014-05-08 | 2014-07-30 | 宁波大学 | Rare-earth-ion-doped LiYCl4 microcrystalline glass and preparation method thereof |
-
2015
- 2015-11-27 CN CN201510859959.5A patent/CN105314877A/en not_active Withdrawn
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101024553A (en) * | 2006-02-24 | 2007-08-29 | 中国科学院福建物质结构研究所 | Alkaline-earth contained fluoride nano crystal transparent glass ceramic and its sol-gel preparing method |
JP5087450B2 (en) * | 2008-03-28 | 2012-12-05 | 三井造船株式会社 | Rotary distributor |
CN103951233A (en) * | 2014-05-08 | 2014-07-30 | 宁波大学 | Rare-earth-ion-doped LiYCl4 microcrystalline glass and preparation method thereof |
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