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 PDF

Info

Publication number
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
Authority
CN
China
Prior art keywords
devitrified glass
acetic acid
rare earth
earth ion
ion doped
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
CN201510859959.5A
Other languages
Chinese (zh)
Inventor
张为欢
夏海平
欧阳绍业
张志雄
王倩
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ningbo University
Original Assignee
Ningbo University
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ningbo University filed Critical Ningbo University
Priority to CN201510859959.5A priority Critical patent/CN105314877A/en
Publication of CN105314877A publication Critical patent/CN105314877A/en
Withdrawn legal-status Critical Current

Links

Landscapes

  • Glass Compositions (AREA)

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

A kind of rare earth ion doped KY 2cl 7devitrified glass and preparation method thereof
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.
CN201510859959.5A 2015-11-27 2015-11-27 Rare earth ion doped KY2Cl7 glass-ceramic and preparation method thereof Withdrawn CN105314877A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510859959.5A CN105314877A (en) 2015-11-27 2015-11-27 Rare earth ion doped KY2Cl7 glass-ceramic and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510859959.5A CN105314877A (en) 2015-11-27 2015-11-27 Rare earth ion doped KY2Cl7 glass-ceramic and preparation method thereof

Publications (1)

Publication Number Publication Date
CN105314877A true CN105314877A (en) 2016-02-10

Family

ID=55243296

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510859959.5A Withdrawn CN105314877A (en) 2015-11-27 2015-11-27 Rare earth ion doped KY2Cl7 glass-ceramic and preparation method thereof

Country Status (1)

Country Link
CN (1) CN105314877A (en)

Citations (3)

* Cited by examiner, † Cited by third party
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

Patent Citations (3)

* Cited by examiner, † Cited by third party
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

Similar Documents

Publication Publication Date Title
CN105254184A (en) Li3YCl6 glass ceramics doped with rare earth ions and preparation method of Li3YCl6 glass ceramics
CN105314860A (en) Rare earth ion doped LaCl3 glass ceramics and preparation method thereof
CN105293921A (en) Rare earth ion doped K3LuCl6 glass ceramic and preparation method thereof
CN105330164A (en) Rare earth ion doped PbCl2 microcrystalline glass and preparation method thereof
CN105314871A (en) Rare earth ion doped YCl3 microcrystalline glass and preparation method thereof
CN105314863A (en) Rare earth ion doped BaCl2 glass ceramics and preparation method thereof
CN105314876A (en) Rare-earth ion doping Cs2YCl5 glass ceramics and preparation method thereof
CN105314873A (en) Rare earth ion-doped CeBr3 microcrystalline glass and preparation method thereof
CN105330163A (en) Rare earth ion doped SrI2 microcrystalline glass and preparation method thereof
CN105293926A (en) Rear earth ion-doped K2GdBr5 microcrystalline glass and preparation method thereof
CN105314877A (en) Rare earth ion doped KY2Cl7 glass-ceramic and preparation method thereof
CN105293923A (en) Rare earth ion doped K3GdCl6 glass ceramic and preparation method thereof
CN105271775A (en) Rare earth ion doped KGd2Cl7 microcrystal glass and preparation method thereof
CN105314869A (en) Rare earth ion doped CdCl2 glass ceramic and preparation method thereof
CN105271774A (en) Rare-earth ion doped NaLuCl4 microcrystalline glass and preparation method thereof
CN105314865A (en) Rare earth ion doped SrCl2 microcrystalline glass and preparation method thereof
CN105314867A (en) Rare earth ion doped CaCl2 glass-ceramic and preparation method thereof
CN105271771A (en) Rare earth ion doped Rb3LaC16 microcrystal glass and preparation method thereof
CN105271773A (en) Rare earth ion doped Cs3CeC16 glass ceramic and preparation method thereof
CN105271776A (en) Rare-earth-ion-doped Cs2LuCl5 microcrystalline glass and preparation method thereof
CN105271768A (en) Rare earth ion doped K2CeCl5 glass ceramic and preparation method thereof
CN105293927A (en) Rear earth ion-doped NaGdCl4microcrystalline glass and preparation method thereof
CN105314857A (en) Rare earth ion doped LuCl3 glass ceramics and preparation method thereof
CN105293924A (en) Rare earth ion doped Cs2NaYBr6 glass ceramic and preparation method thereof
CN105271772A (en) Rare earth ion doped Cs2NaCeBr6 glass ceramic and preparation method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
WW01 Invention patent application withdrawn after publication

Application publication date: 20160210

WW01 Invention patent application withdrawn after publication