CN1588607A - Method for preparing cerium-doped lutetium pyrosilicate submicron imaging screen - Google Patents
Method for preparing cerium-doped lutetium pyrosilicate submicron imaging screen Download PDFInfo
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- CN1588607A CN1588607A CN 200410053440 CN200410053440A CN1588607A CN 1588607 A CN1588607 A CN 1588607A CN 200410053440 CN200410053440 CN 200410053440 CN 200410053440 A CN200410053440 A CN 200410053440A CN 1588607 A CN1588607 A CN 1588607A
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- 238000003384 imaging method Methods 0.000 title claims abstract description 28
- 238000000034 method Methods 0.000 title claims abstract description 16
- OHSVLFRHMCKCQY-UHFFFAOYSA-N lutetium atom Chemical compound [Lu] OHSVLFRHMCKCQY-UHFFFAOYSA-N 0.000 title claims abstract description 10
- 229910052765 Lutetium Inorganic materials 0.000 title claims abstract description 8
- 239000000758 substrate Substances 0.000 claims abstract description 25
- 239000013078 crystal Substances 0.000 claims abstract description 16
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims abstract description 12
- 238000002360 preparation method Methods 0.000 claims description 23
- 239000002243 precursor Substances 0.000 claims description 17
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 13
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 12
- LHXYFSDEWOLMCQ-UHFFFAOYSA-N cerium lutetium trihydroxy(trihydroxysilyloxy)silane Chemical compound [Lu].[Si](O)(O)(O)O[Si](O)(O)O.[Ce] LHXYFSDEWOLMCQ-UHFFFAOYSA-N 0.000 claims description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 10
- 230000032683 aging Effects 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 7
- 239000000126 substance Substances 0.000 claims description 7
- 229910052684 Cerium Inorganic materials 0.000 claims description 5
- 229910002651 NO3 Inorganic materials 0.000 claims description 5
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 5
- 239000008367 deionised water Substances 0.000 claims description 5
- 229910021641 deionized water Inorganic materials 0.000 claims description 5
- 230000007062 hydrolysis Effects 0.000 claims description 5
- 238000006460 hydrolysis reaction Methods 0.000 claims description 5
- 238000003760 magnetic stirring Methods 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- 239000002994 raw material Substances 0.000 claims description 5
- 238000007789 sealing Methods 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 claims description 3
- 229910052761 rare earth metal Inorganic materials 0.000 claims description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 238000005303 weighing Methods 0.000 claims description 2
- 230000003287 optical effect Effects 0.000 abstract description 3
- 238000010521 absorption reaction Methods 0.000 abstract description 2
- 238000003980 solgel method Methods 0.000 abstract 1
- 239000010408 film Substances 0.000 description 21
- 230000004397 blinking Effects 0.000 description 11
- 239000010409 thin film Substances 0.000 description 7
- HSJPMRKMPBAUAU-UHFFFAOYSA-N cerium(3+);trinitrate Chemical compound [Ce+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O HSJPMRKMPBAUAU-UHFFFAOYSA-N 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 230000007547 defect Effects 0.000 description 3
- KDJOAYSYCXTQGG-UHFFFAOYSA-N disilicic acid Chemical compound O[Si](O)(O)O[Si](O)(O)O KDJOAYSYCXTQGG-UHFFFAOYSA-N 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000003292 glue Substances 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000000693 micelle Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229910019655 synthetic inorganic crystalline material Inorganic materials 0.000 description 2
- NGDQQLAVJWUYSF-UHFFFAOYSA-N 4-methyl-2-phenyl-1,3-thiazole-5-sulfonyl chloride Chemical compound S1C(S(Cl)(=O)=O)=C(C)N=C1C1=CC=CC=C1 NGDQQLAVJWUYSF-UHFFFAOYSA-N 0.000 description 1
- 229910052688 Gadolinium Inorganic materials 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- -1 cerium ion Chemical class 0.000 description 1
- 229910019990 cerium-doped yttrium aluminum garnet Inorganic materials 0.000 description 1
- 238000005229 chemical vapour deposition Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- MWFSXYMZCVAQCC-UHFFFAOYSA-N gadolinium(iii) nitrate Chemical compound [Gd+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O MWFSXYMZCVAQCC-UHFFFAOYSA-N 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
- 238000010603 microCT Methods 0.000 description 1
- 238000001451 molecular beam epitaxy Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000004549 pulsed laser deposition Methods 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 229910052706 scandium Inorganic materials 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
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- Luminescent Compositions (AREA)
Abstract
A method for preparing a cerium-doped lutetium pyrosilicate submicron imaging screen is characterized in that the structural expression of the imaging screen is as follows: xReyLu1－x－y) 2Si2O7/(Lu1－yRey) 2Si2O7It is (Lu) having (010), (100) or (001) in the plane direction1－yRey) 2Si2O7Growing a layer (Ce) on the substrate by sol-gel methodxReyLu1－x－y) 2Si2O7The transparent fluorescent screen is composed of the scintillation film, wherein x is more than or equal to 0.001 and less than or equal to 0.01, and y is more than or equal to 0 and less than or equal to 0.3. Compared with the fluorescent screen in the prior art, the fluorescent screen has higher X-ray absorption coefficient and higher resolution; the substrate and the scintillation single crystal film have no mismatch problem, the single crystal film has high quality, and the optical quality of the fluorescent screen is good. Therefore, the scintillating phosphor screen adopting the invention can be widely usedThe method is widely applied to various application fields of microscopic X-ray imaging.
Description
Technical field
The present invention relates to sub-micrometer imaging, particularly a kind of fluoroscopic preparation method of cerium disilicic acid lutetium sub-micrometer imaging that mixes is specifically related to utilize sol-gel (Sol-Gel) method at unadulterated disilicic acid lutetium monocrystalline (Lu
1-yRe
y)
2Si
2O
7It is the doping trivalent cerium ion (Ce of 0.3-10 micron that substrate slice (thickness is about the 3-30 micron) is gone up growth one layer thickness
3+) disilicic acid lutetium monocrystal thin films (Ce
xRe
yLu
1-x-y)
2Si
2O
7, (0.001≤x≤0.01,0≤y≤0.3, wherein Re represents other rare earth element except that Lu, as: one of Y, Gd, Sc, In etc. or multiple mixing), thus prepare the phosphor screen (Ce that can be used for the X ray sub-micrometer imaging
xRe
yLu
1-x-y)
2Si
2O
7/ (Lu
1-yRe
y)
2Si
2O
7, (0.001≤x≤0.01,0≤y≤0.3).
Background technology
Micro-imaging technique has submicron resolution, detection efficient height, digitized degree height, can be implemented in advantage such as line detection in real time, has important effect in microscopic X-ray imaging fields such as phase contrast imaging, holographic imaging and microtomographies.Blinking screen is one of the key factor of the room and time resolution of decision x-ray imaging system.Reach the spatial resolution of submicron order, must have transparent, unscattered a, thickness to visible light several microns, have a phosphor screen of high light output.The shortcoming that the powder phosphor screen exists, the fluoroscopic light output of scintillating ceramic is lower, can not satisfy the demand.Therefore the phosphor screen that adopts the scintillation single crystal film to make becomes the focus that people study.At present, the monocrystal thin films phosphor screen in the imaging system mainly adopts SCF phosphor screens such as CsI (Tl), Ce:YAG/YAG and Ce:LuAG/YAG.Referring to: IEEE Trans.Nucl.Sci.1998, the 45th the 3rd phase of volume, the 492nd page; Referring to: J.Opt.Sco.Am.A,, the 15th the 7th phase of volume, the 1940th page in 1998; Referring to: Nucl.Instr.Meth.in Phys.Res.A.2002, the 486th volume, 309-314 page or leaf.
Recently, it is found that cerium ion-doped disilicic acid lutetium crystal (Ce:Lu
2-xM
xSi
2O
7, be called for short Ce:LPS) and be a kind of inorganic scintillation crystal preferably, this crystal belongs to monoclinic system, and lattice parameter is respectively: a=6.765 , b=8.839 , c=4.715 , β=101.96 °, density and effective atomic number are respectively 6.23g/cm3 and Z
Eff=4.The Ce:LPS scintillation crystal has higher light output, is about 13000-22000Ph/MeV, and optical attenuation is about 30ns faster, and does not have twilight sunset.Referring to: U.S.Pat.No:6,437,336.
At present, the method for preparing film is a lot, such as: liquid phase epitaxial method, sputtering method, vacuum evaporation and molecular beam epitaxy, sol-gal process, pulsed laser deposition, chemical vapour deposition technique and ultrasonic pyrolysis etc.Sol-gal process and above-mentioned other preparation film process have following advantage: can realize low temperature (500-1300 ℃) growth, have that process equipment is simple, low cost, easily obtain advantages such as large-area film.Because colloidal sol is obtained by solution, chemical composition is just the same in the micelle and between micelle, can effectively control stoichiometric proportion, realize trace doped, easily prepare the multicomponent homogeneous film, uniformity coefficient can reach the molecular level level, and can make some and be difficult to obtain with conventional method or unavailable at all product.
Summary of the invention
The purpose of this invention is to provide a kind of fluoroscopic preparation method of cerium disilicic acid lutetium sub-micrometer imaging that mixes, utilize our thin films to have even zero defect, large-area, high efficiency, high-resolution sub-micrometer imaging scintillation single crystal phosphor screen (Ce
xRe
yLu
1-x-y)
2Si
2O
7/ (Lu
1-yRe
y)
2Si
2O
7, wherein 0.001≤x≤0.01,0≤y≤0.3 can be controlled multicomponent chemical metering ratio effectively, realizes that micro-cerium mixes.
Technical solution of the present invention is as follows:
A kind of fluoroscopic preparation method of cerium disilicic acid lutetium sub-micrometer imaging that mixes is characterized in that the structure expression of this imaging fluorescent screen is: (Ce
xRe
yLu
1-x-y)
2Si
2O
7/ (Lu
1-yRe
y)
2Si
2O
7, 0.001≤x≤0.01,0≤y≤0.3 wherein, it is (010), (100) or (001) (Lu in crystal plane direction
1-yRe
y)
2Si
2O
7On (0≤y≤0.3) substrate by sol-gal process growth one deck (Ce
xRe
yLu
1-x-y)
2Si
2O
7The transparent cathode-ray screen that the flicker film constitutes.
The thickness of described substrate is the 3-30 micron.
The thickness of described flicker film is the 0.3-10 micron.
Described concrete steps of mixing the fluoroscopic preparation method of cerium disilicic acid lutetium sub-micrometer imaging are as follows:
1. at room temperature, press tetraethoxysilane: ethanol: deionized water=1: (1-6): volume ratio preparation mixed liquor (1-10);
2. selected x, y are according to chemical formula (Ce
xRe
yLu
1-x-y)
2Si
2O
7In stoichiometric proportion, weighing purity is raw material greater than 99.99% lutetium, cerium and other nitrate of rare earth element or acetate, be dissolved into by the＜1 go on foot in the liquid mixture prepared, make the Ce in the solution: Re: Lu: Si=x: y: (1-x-y): 1, and add the character of suitable assistant such as watery hydrochloric acid regulator solution;
3. solution fully stirred 18-24 hour with magnetic stirring apparatus, made it mix, and fully hydrolysis, and the sealing and standing ageing obtained transparent, uniform precursor sol more than three days then;
4. will clean (the Lu of dry crystal plane direction for (010), (100) or (001)
1-yRe
y)
2Si
2O
7, (0≤y≤0.3) single crystalline substrate substrate immerses in the precursor sol after the above-mentioned ageing, lifts out the solution face with the speed of 5-25cm/min and forms precursor film;
5. the substrate that this is had precursor film toasts 20-30min in 70 ℃ of-100 ℃ of baking ovens, to remove unnecessary solvent;
4. and 5. 6. repeating step repeats to lift repeatedly, till reaching required film thickness;
7. then film is placed on nitrogen N with substrate
2In the atmosphere furnace, be heated to 900-1200 ℃, be incubated 2-5 hour, cool to room temperature with the furnace, promptly obtain the present invention and mix cerium disilicic acid lutetium sub-micrometer imaging phosphor screen with the heating rate of 7-10 ℃/min.
The present invention utilizes the large tracts of land (Ce of sol-gal process (Sol-Gel) preparation
xRe
yLu
1-x-y)
2Si
2O
7/ (Lu
1-yRe
y)
2Si
2O
7, (0.001≤x≤0.01,0≤y≤0.3) monocrystalline blinking screen shows after testing: even zero defect has heavy density (along with the density that reduces of y is increased to 6.2g/cm from 6.0
3, high effective atomic number (Z
Eff=56-63.8), high light output (being about 70-75%NaI (Tl)), fast decay (30-50ns), energy efficiency Δ E/E is about 9% under 662keV, no twilight sunset, its emission wavelength can with advantages such as existing C CD and the more effective coupling of Si array.
Phosphor screen of the present invention is compared with phosphor screen in the technology formerly, has higher X-ray absorption coefficient and higher resolution; On the other hand, substrate adopts with the scintillation single crystal film forms identical monocrystalline composition, does not have mismatch problems, monocrystal thin films quality height, and fluoroscopic optical property is good.Therefore, adopt blinking screen of the present invention can be widely used in the various microscopic X-ray imaging fields.
Embodiment
Now further specify the fluoroscopic preparation method of the present invention in conjunction with following specific embodiment.
Embodiment 1:(Ce
0.005Lu
0.995)
2Si
2O
7/ Lu
2Si
2O
7The blinking screen
According to above-mentioned step of preparation process＜1〉at room temperature, the preparation mixed liquor, by tetraethoxysilane (TEOS): ethanol: deionized water is 1: 4: 8 (volume ratio); By processing step＜2〉be raw material with purity greater than 99.99% lutecium nitrate and cerous nitrate, according to chemical formula (Ce
0.005Lu
0.995)
2Si
2O
7In stoichiometric proportion calculated prescription, be dissolved in the mixed liquor of tetraethoxysilane (TEOS), second alcohol and water, and add the character of suitable HCl regulator solution.Ce in the solution that obtains: Lu: Si=0.005: 0.995: 2; By above-mentioned steps＜3〉solution fully stirred 24 hours with magnetic stirring apparatus, made it mix, and fully hydrolysis, and the sealing and standing ageing promptly obtained being suitable for transparent, the uniform precursor sol of even glue more than three days then; Set by step＜4〉will be of a size of φ 30 * 0.03mm, the cleaning drying, crystal plane direction is the Lu of (010)
2Si
2O
7The single crystalline substrate substrate immerses in the sol precursor after the above-mentioned ageing, lifts out the solution face with the speed of friction speed 20cm/min; By above-mentioned processing step＜5〉precursor film roasts 30min in 100 ℃ of baking ovens, to remove unnecessary solvent; By above-mentioned processing step＜6〉repeating step＜4〉and＜5, repeat to lift 10 times, till reaching 4 microns of required film thicknesses; By above-mentioned processing step＜7〉film is placed on nitrogen N with substrate base
2In the atmosphere furnace, be heated to 1200 ℃ with the speed of 7 ℃/min.Be incubated 5 hours, cool to room temperature with the furnace.Obtain the large tracts of land monocrystal thin films (Ce of transparent and homogeneous
0.005Lu
0.995)
2Si
2O
7, i.e. (Ce
0.005Lu
0.995)
2Si
2O
7/ Lu
2Si
2O
7The preparation of blinking screen finishes.
This blinking screen function admirable has higher resolution, is with a wide range of applications aspect microscopic X-ray imaging.
Embodiment 2:(Ce
0.005Gd
0.3Lu
0.695)
2Si
2O
7/ (Gd
0.3Lu
0.7)
2Si
2O
7The blinking screen
According to step of preparation process＜1 in the foregoing description 1〉at room temperature, the preparation mixed liquor, by tetraethoxysilane: ethanol: deionized water is 1: 5: 10 (volume ratio); By processing step＜2〉be raw material with purity greater than 99.99% lutecium nitrate, gadolinium nitrate and cerous nitrate, according to chemical formula (Ce
0.005Gd
0.3Lu
0.695)
2Si
2O
7In stoichiometric proportion calculated prescription, be dissolved in the mixed liquor of tetraethoxysilane (TEOS), second alcohol and water, and add the character of suitable HCl regulator solution.Ce in the solution that obtains: Gd: Lu: Si=0.005: 0.3: 0.695: 2; By above-mentioned steps＜3〉solution fully stirred 20 hours with magnetic stirring apparatus, made it mix, and fully hydrolysis, and the sealing and standing ageing is 4 days then, promptly obtains being suitable for transparent, the uniform precursor sol of even glue; Set by step＜4〉will be of a size of φ 30 * 0.03mm, the cleaning drying, crystal plane direction is the (Gd of (100)
0.3Lu
0.7)
2Si
2O
7The single crystalline substrate substrate immerses in the precursor sol after the above-mentioned ageing, lifts out the solution face with the speed of 15cm/min; By above-mentioned processing step＜5〉precursor film roasts 20min in 100 ℃ of baking ovens, to remove unnecessary solvent; By above-mentioned processing step＜6〉repeating step＜4〉and＜5, repeat to lift repeatedly, reach till 3 microns of the required film thicknesses; By above-mentioned processing step＜7〉film is placed on nitrogen N with substrate base
2In the atmosphere furnace, be heated to 1100 ℃ with the programming rate of 10 ℃/min.Be incubated 4 hours, cool to room temperature with the furnace.Obtain the large tracts of land monocrystal thin films (Ce of transparent and homogeneous
0.005Gd
0.3Lu
0.695)
2Si
2O
7I.e. (Ce
0.005Gd
0.3Lu
0.695)
2Si
2O
7/ (Gd
0.3Lu
0.7)
2Si
2O
7The preparation of blinking screen finishes.
Embodiment 3:(Ce
0.01Y
0.1Lu
0.89)
2Si
2O
7/ (Y
0.1Lu
0.9)
2Si
2O
7The blinking screen
According to step＜1 in the foregoing description 2〉at room temperature, the preparation mixed liquor, by tetraethoxysilane: ethanol: deionized water is 1: 3: 7 (volume ratio); By processing step＜2〉be raw material with purity greater than 99.99% lutecium nitrate, yttrium nitrate and cerous nitrate, according to chemical formula (Ce
0.01Y
0.1Lu
0.89)
2Si
2O
7In stoichiometric proportion calculated prescription, be dissolved in the mixed liquor of tetraethoxysilane (TEOS), second alcohol and water, and add the character of suitable HCl regulator solution.Ce in the solution that obtains: Y: Lu: Si=0.01: 0.1: 0.89: 2; By above-mentioned steps＜3〉solution fully stirred 24 hours with magnetic stirring apparatus, made it mix, and fully hydrolysis, and the sealing and standing ageing is 3 days then, promptly obtains being suitable for transparent, the uniform precursor sol of even glue; Set by step＜4〉will be of a size of φ 30 * 0.03mm, the cleaning drying, crystal plane direction is the (Y of (001)
0.1Lu
0.9)
2Si
2O
7The single crystalline substrate substrate immerses in the sol precursor after the above-mentioned ageing, lifts out the solution face with the speed of 25cm/min; By above-mentioned processing step＜5〉precursor film roasts 30min in 100 ℃ of baking ovens, to remove unnecessary solvent; By above-mentioned processing step＜6〉repeating step＜4〉and＜5, repeat to lift 10 times, till reaching 6 microns of required film thicknesses; By above-mentioned processing step＜7〉film is placed on nitrogen N with substrate base
2In the atmosphere furnace, be heated to 1050 ℃ with the speed of 8 ℃/min.Be incubated 5 hours, cool to room temperature with the furnace.Promptly obtain the large tracts of land monocrystal thin films (Ce of transparent and homogeneous
0.01Y
0.1Lu
0.89)
2Si
2O
7So far obtain the high complete monocrystalline blinking screen of high-quality (Ce
0.01Y
0.1Lu
0.89)
2Si
2O
7/ (Y
0.1Lu
0.9)
2Si
2O
7Preparation.
To the foregoing description, utilize the large tracts of land (Ce of sol-gal process (Sol-Gel) preparation
xRe
yLu
1-x-y)
2Si
2O
7/ (Lu
1-yRe
y)
2Si
2O
7, (0.001≤x≤0.01,0≤y≤0.3) monocrystalline blinking screen detects, and shows after testing: even zero defect has heavy density (along with the density that reduces of y is increased to 6.2g/cm from 6.0
3, high effective atomic number (Z
Eff=56-63.8), high light output (being about 70-75%NaI (Tl)), fast decay (30-50ns), energy efficiency Δ E/E is about 9% under 662keV, no twilight sunset, its emission wavelength can with advantages such as existing C CD and the more effective coupling of Si array.
Claims (4)
1, a kind of fluoroscopic preparation method of cerium disilicic acid lutetium sub-micrometer imaging that mixes is characterized in that the structure expression of this imaging fluorescent screen is: (Ce
xRe
yLu
1-x-y)
2Si
2O
7/ (Lu
1-yRe
y)
2Si
2O
7, it is (010), (100) or (001) (Lu in crystal plane direction
1-yRe
y)
2Si
2O
7On the substrate by sol-gal process growth one deck (Ce
xRe
yLu
1-x-y)
2Si
2O
7The transparent cathode-ray screen that the flicker film constitutes, wherein 0.001≤x≤0.01,0≤y≤0.3.
2, the fluoroscopic preparation method of cerium disilicic acid lutetium sub-micrometer imaging that mixes according to claim 1, the thickness that it is characterized in that described substrate is the 3-30 micron.
3, the fluoroscopic preparation method of cerium disilicic acid lutetium sub-micrometer imaging that mixes according to claim 1, the thickness that it is characterized in that described flicker film is the 0.3-10 micron.
4, the fluoroscopic preparation method of cerium disilicic acid lutetium sub-micrometer imaging that mixes according to claim 1 is characterized in that the step of this method is as follows:
1. at room temperature, press tetraethoxysilane: ethanol: deionized water=1: (1-6): volume ratio preparation mixed liquor (1-10);
2. selected x, y are according to chemical formula (Ce
xRe
yLu
1-x-y)
2Si
2O
7In stoichiometric proportion, weighing purity is raw material greater than 99.99% lutetium, cerium and other nitrate of rare earth element or acetate, be dissolved into by the＜1 go on foot in the liquid mixture prepared, make the Ce in the solution: Re: Lu: Si=x: y: (1-x-y): 1, and add the character of suitable assistant such as watery hydrochloric acid regulator solution;
3. solution fully stirred 18-24 hour with magnetic stirring apparatus, made it mix, and fully hydrolysis, and the sealing and standing ageing obtained transparent, uniform precursor sol more than three days then;
4. will clean (the Lu of dry crystal plane direction for (010), (100) or (001)
1-yRe
y)
2Si
2O
7, (0≤y≤0.3) single crystalline substrate substrate immerses in the precursor sol after the above-mentioned ageing, lifts out the solution face with the speed of 5-25cm/min and forms precursor film;
5. the substrate that this is had precursor film toasts 20-30min in 70 ℃ of-100 ℃ of baking ovens, to remove unnecessary solvent;
4. and 5. 6. repeating step repeats to lift repeatedly, till reaching required film thickness;
7. then film is placed on nitrogen N with substrate
2In the atmosphere furnace, be heated to 900-1200 ℃, be incubated 2-5 hour, cool to room temperature with the furnace, promptly obtain the present invention and mix cerium disilicic acid lutetium sub-micrometer imaging phosphor screen with the heating rate of 7-10 ℃/min.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB200410053440XA CN100358076C (en) | 2004-08-04 | 2004-08-04 | Method for preparing cerium-doped lutetium pyrosilicate submicron imaging screen |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB200410053440XA CN100358076C (en) | 2004-08-04 | 2004-08-04 | Method for preparing cerium-doped lutetium pyrosilicate submicron imaging screen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1588607A true CN1588607A (en) | 2005-03-02 |
| CN100358076C CN100358076C (en) | 2007-12-26 |
Family
ID=34602856
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|---|---|---|---|
| CNB200410053440XA Expired - Fee Related CN100358076C (en) | 2004-08-04 | 2004-08-04 | Method for preparing cerium-doped lutetium pyrosilicate submicron imaging screen |
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| Country | Link |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN102910637A (en) * | 2011-08-05 | 2013-02-06 | 中国科学院上海硅酸盐研究所 | Preparation method for rare earth silicate nano-powder |
| CN103243318A (en) * | 2013-05-15 | 2013-08-14 | 湖南省科学技术研究开发院 | Preparation method of broadband gradient LED (Light-emitting Diode) fluorescent film |
| CN104046984A (en) * | 2013-03-14 | 2014-09-17 | 中国科学院上海硅酸盐研究所 | Preparation method for cerium doped lutetium pyrosilicate scintillating film |
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| CN1142238C (en) * | 2001-11-26 | 2004-03-17 | 袁曦明 | Process for preparing nano yttrium aluminate as fluorescent powder |
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Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102910637A (en) * | 2011-08-05 | 2013-02-06 | 中国科学院上海硅酸盐研究所 | Preparation method for rare earth silicate nano-powder |
| CN102910637B (en) * | 2011-08-05 | 2014-11-05 | 中国科学院上海硅酸盐研究所 | Preparation method for rare earth silicate nano-powder |
| CN104046984A (en) * | 2013-03-14 | 2014-09-17 | 中国科学院上海硅酸盐研究所 | Preparation method for cerium doped lutetium pyrosilicate scintillating film |
| CN104046984B (en) * | 2013-03-14 | 2016-03-23 | 中国科学院上海硅酸盐研究所 | A kind of method preparing the lutetium pyrosilicate flicker film mixing cerium |
| CN103243318A (en) * | 2013-05-15 | 2013-08-14 | 湖南省科学技术研究开发院 | Preparation method of broadband gradient LED (Light-emitting Diode) fluorescent film |
| CN103243318B (en) * | 2013-05-15 | 2015-01-07 | 湖南省科学技术研究开发院 | Preparation method of broadband gradient LED (Light-emitting Diode) fluorescent film |
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