CN113737282A - Compound zinc rubidium germanate nonlinear optical crystal and preparation method and use thereof - Google Patents
Compound zinc rubidium germanate nonlinear optical crystal and preparation method and use thereof Download PDFInfo
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- CN113737282A CN113737282A CN202111036792.4A CN202111036792A CN113737282A CN 113737282 A CN113737282 A CN 113737282A CN 202111036792 A CN202111036792 A CN 202111036792A CN 113737282 A CN113737282 A CN 113737282A
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- rubidium
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- 239000013078 crystal Substances 0.000 title claims abstract description 146
- 150000001875 compounds Chemical class 0.000 title claims abstract description 82
- FCVNIFURPQDSDK-UHFFFAOYSA-N [Zn].[Rb] Chemical compound [Zn].[Rb] FCVNIFURPQDSDK-UHFFFAOYSA-N 0.000 title claims abstract description 39
- 230000003287 optical effect Effects 0.000 title claims abstract description 35
- 238000002360 preparation method Methods 0.000 title abstract description 8
- 239000002994 raw material Substances 0.000 claims abstract description 23
- 238000000034 method Methods 0.000 claims abstract description 18
- 239000000126 substance Substances 0.000 claims abstract description 9
- 230000004907 flux Effects 0.000 claims abstract 4
- 239000011259 mixed solution Substances 0.000 claims abstract 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 60
- YBMRDBCBODYGJE-UHFFFAOYSA-N germanium oxide Inorganic materials O=[Ge]=O YBMRDBCBODYGJE-UHFFFAOYSA-N 0.000 claims description 44
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 44
- 238000001816 cooling Methods 0.000 claims description 38
- 229910003069 TeO2 Inorganic materials 0.000 claims description 36
- 239000011701 zinc Substances 0.000 claims description 36
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 claims description 35
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 34
- 229910052701 rubidium Inorganic materials 0.000 claims description 34
- 229910052725 zinc Inorganic materials 0.000 claims description 34
- 239000011787 zinc oxide Substances 0.000 claims description 31
- 239000007788 liquid Substances 0.000 claims description 26
- FGDZQCVHDSGLHJ-UHFFFAOYSA-M rubidium chloride Chemical compound [Cl-].[Rb+] FGDZQCVHDSGLHJ-UHFFFAOYSA-M 0.000 claims description 24
- CPRMKOQKXYSDML-UHFFFAOYSA-M rubidium hydroxide Chemical compound [OH-].[Rb+] CPRMKOQKXYSDML-UHFFFAOYSA-M 0.000 claims description 24
- ONDPHDOFVYQSGI-UHFFFAOYSA-N zinc nitrate Chemical compound [Zn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ONDPHDOFVYQSGI-UHFFFAOYSA-N 0.000 claims description 23
- 238000002156 mixing Methods 0.000 claims description 22
- 229910000026 rubidium carbonate Inorganic materials 0.000 claims description 21
- 239000003795 chemical substances by application Substances 0.000 claims description 19
- JAAGVIUFBAHDMA-UHFFFAOYSA-M rubidium bromide Chemical compound [Br-].[Rb+] JAAGVIUFBAHDMA-UHFFFAOYSA-M 0.000 claims description 18
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 claims description 18
- 150000003839 salts Chemical class 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 15
- 150000002290 germanium Chemical class 0.000 claims description 14
- 229910052732 germanium Inorganic materials 0.000 claims description 14
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims description 14
- WPFGFHJALYCVMO-UHFFFAOYSA-L rubidium carbonate Chemical compound [Rb+].[Rb+].[O-]C([O-])=O WPFGFHJALYCVMO-UHFFFAOYSA-L 0.000 claims description 14
- 238000010438 heat treatment Methods 0.000 claims description 13
- 229910001953 rubidium(I) oxide Inorganic materials 0.000 claims description 12
- 238000001354 calcination Methods 0.000 claims description 10
- PVADDRMAFCOOPC-UHFFFAOYSA-N oxogermanium Chemical compound [Ge]=O PVADDRMAFCOOPC-UHFFFAOYSA-N 0.000 claims description 10
- 239000000843 powder Substances 0.000 claims description 10
- 229910001952 rubidium oxide Inorganic materials 0.000 claims description 10
- CWBWCLMMHLCMAM-UHFFFAOYSA-M rubidium(1+);hydroxide Chemical compound [OH-].[Rb+].[Rb+] CWBWCLMMHLCMAM-UHFFFAOYSA-M 0.000 claims description 10
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 claims description 10
- 229910000368 zinc sulfate Inorganic materials 0.000 claims description 10
- KEDRKJFXBSLXSI-UHFFFAOYSA-M hydron;rubidium(1+);carbonate Chemical compound [Rb+].OC([O-])=O KEDRKJFXBSLXSI-UHFFFAOYSA-M 0.000 claims description 9
- 239000012535 impurity Substances 0.000 claims description 9
- 239000012071 phase Substances 0.000 claims description 9
- RTHYXYOJKHGZJT-UHFFFAOYSA-N rubidium nitrate Inorganic materials [Rb+].[O-][N+]([O-])=O RTHYXYOJKHGZJT-UHFFFAOYSA-N 0.000 claims description 9
- 229910000344 rubidium sulfate Inorganic materials 0.000 claims description 9
- GANPIEKBSASAOC-UHFFFAOYSA-L rubidium(1+);sulfate Chemical compound [Rb+].[Rb+].[O-]S([O-])(=O)=O GANPIEKBSASAOC-UHFFFAOYSA-L 0.000 claims description 9
- 239000011592 zinc chloride Substances 0.000 claims description 9
- 235000005074 zinc chloride Nutrition 0.000 claims description 9
- 229960001763 zinc sulfate Drugs 0.000 claims description 9
- 238000000227 grinding Methods 0.000 claims description 8
- 229940102127 rubidium chloride Drugs 0.000 claims description 8
- KHAUBYTYGDOYRU-IRXASZMISA-N trospectomycin Chemical compound CN[C@H]([C@H]1O2)[C@@H](O)[C@@H](NC)[C@H](O)[C@H]1O[C@H]1[C@]2(O)C(=O)C[C@@H](CCCC)O1 KHAUBYTYGDOYRU-IRXASZMISA-N 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 6
- 239000002131 composite material Substances 0.000 claims description 5
- 238000003746 solid phase reaction Methods 0.000 claims description 5
- 150000003297 rubidium Chemical class 0.000 claims description 4
- 150000003751 zinc Chemical class 0.000 claims description 4
- 230000008569 process Effects 0.000 claims description 3
- NZZJOHSPSIMUFV-UHFFFAOYSA-L C([O-])([O-])=O.[Ge+2] Chemical compound C([O-])([O-])=O.[Ge+2] NZZJOHSPSIMUFV-UHFFFAOYSA-L 0.000 claims description 2
- VXXCTRXMBKNRII-UHFFFAOYSA-L S(=O)(=O)([O-])[O-].[Ge+2] Chemical compound S(=O)(=O)([O-])[O-].[Ge+2] VXXCTRXMBKNRII-UHFFFAOYSA-L 0.000 claims description 2
- GGBJMFNBQAJSMV-UHFFFAOYSA-L [Ge+2].C([O-])(O)=O.C([O-])(O)=O Chemical compound [Ge+2].C([O-])(O)=O.C([O-])(O)=O GGBJMFNBQAJSMV-UHFFFAOYSA-L 0.000 claims description 2
- WNPMJIKMURUYFG-UHFFFAOYSA-N [N+](=O)([O-])[O-].[Ge+2].[N+](=O)([O-])[O-] Chemical compound [N+](=O)([O-])[O-].[Ge+2].[N+](=O)([O-])[O-] WNPMJIKMURUYFG-UHFFFAOYSA-N 0.000 claims description 2
- 230000007547 defect Effects 0.000 claims description 2
- VJHDVMPJLLGYBL-UHFFFAOYSA-N tetrabromogermane Chemical compound Br[Ge](Br)(Br)Br VJHDVMPJLLGYBL-UHFFFAOYSA-N 0.000 claims description 2
- IEXRMSFAVATTJX-UHFFFAOYSA-N tetrachlorogermane Chemical compound Cl[Ge](Cl)(Cl)Cl IEXRMSFAVATTJX-UHFFFAOYSA-N 0.000 claims description 2
- GGQZVHANTCDJCX-UHFFFAOYSA-N germanium;tetrahydrate Chemical compound O.O.O.O.[Ge] GGQZVHANTCDJCX-UHFFFAOYSA-N 0.000 claims 1
- 229910000464 lead oxide Inorganic materials 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 238000002844 melting Methods 0.000 claims 1
- 230000008018 melting Effects 0.000 claims 1
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 claims 1
- PCHQDTOLHOFHHK-UHFFFAOYSA-L zinc;hydrogen carbonate Chemical compound [Zn+2].OC([O-])=O.OC([O-])=O PCHQDTOLHOFHHK-UHFFFAOYSA-L 0.000 claims 1
- 230000005540 biological transmission Effects 0.000 abstract description 3
- 230000000694 effects Effects 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 16
- 238000002425 crystallisation Methods 0.000 description 14
- 230000008025 crystallization Effects 0.000 description 14
- 239000000155 melt Substances 0.000 description 14
- 230000002269 spontaneous effect Effects 0.000 description 14
- AHLATJUETSFVIM-UHFFFAOYSA-M rubidium fluoride Inorganic materials [F-].[Rb+] AHLATJUETSFVIM-UHFFFAOYSA-M 0.000 description 8
- ZPEJZWGMHAKWNL-UHFFFAOYSA-L zinc;oxalate Chemical compound [Zn+2].[O-]C(=O)C([O-])=O ZPEJZWGMHAKWNL-UHFFFAOYSA-L 0.000 description 8
- DUXDETQJUQZYEX-UHFFFAOYSA-L oxalate;rubidium(1+) Chemical compound [Rb+].[Rb+].[O-]C(=O)C([O-])=O DUXDETQJUQZYEX-UHFFFAOYSA-L 0.000 description 7
- 238000005303 weighing Methods 0.000 description 7
- 229910052697 platinum Inorganic materials 0.000 description 6
- 239000012856 weighed raw material Substances 0.000 description 6
- -1 alkali metal cation Chemical class 0.000 description 3
- 229910052593 corundum Inorganic materials 0.000 description 3
- 239000010431 corundum Substances 0.000 description 3
- 238000002441 X-ray diffraction Methods 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- JHAFEVXNMDQGTR-UHFFFAOYSA-L C(C(=O)[O-])(=O)[O-].[Ge+2] Chemical compound C(C(=O)[O-])(=O)[O-].[Ge+2] JHAFEVXNMDQGTR-UHFFFAOYSA-L 0.000 description 1
- 229910005833 GeO4 Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000002050 diffraction method Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 238000000634 powder X-ray diffraction Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000000985 reflectance spectrum Methods 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000004088 simulation Methods 0.000 description 1
- 238000010532 solid phase synthesis reaction Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 239000011686 zinc sulphate Substances 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B29/00—Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
- C30B29/10—Inorganic compounds or compositions
- C30B29/16—Oxides
- C30B29/22—Complex oxides
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B17/00—Single-crystal growth onto a seed which remains in the melt during growth, e.g. Nacken-Kyropoulos method
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B28/00—Production of homogeneous polycrystalline material with defined structure
- C30B28/02—Production of homogeneous polycrystalline material with defined structure directly from the solid state
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- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B9/00—Single-crystal growth from melt solutions using molten solvents
- C30B9/04—Single-crystal growth from melt solutions using molten solvents by cooling of the solution
- C30B9/08—Single-crystal growth from melt solutions using molten solvents by cooling of the solution using other solvents
- C30B9/12—Salt solvents, e.g. flux growth
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/35—Non-linear optics
- G02F1/355—Non-linear optics characterised by the materials used
- G02F1/3551—Crystals
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Abstract
本发明公开了一种化合物锗酸锌铷非线性光学晶体及其制备方法和用途，该化合物的化学式为Rb2ZnGe2O6，其制备方法是，将含铷化合物、含锌化合物、含锗化合物原料均匀混合并充分研磨，置于马弗炉中，先低温下预烧除去原料中的水分和气体，再升温锻烧，期间多次取出研磨并继续锻烧，制得化合物锗酸锌铷。进一步的将化合物与助熔剂混合升温得到混合溶液，在晶体生长炉中，制备出锗酸锌铷非线性光学晶体。本发明的技术效果是：所获晶体具有优良的热稳定性，较宽的透光范围，硬度适中，物化性能稳定等优点，采用本发明所述方法获得的化合物锗酸锌铷可用于制备倍频器件。
The invention discloses a compound zinc rubidium germanate non-linear optical crystal and its preparation method and application. The chemical formula of the compound is Rb 2 ZnGe 2 O 6 . The preparation method is as follows: The compound raw materials are uniformly mixed and fully ground, placed in a muffle furnace, pre-fired at a low temperature to remove the moisture and gas in the raw materials, and then heated up and calcined. . Further, the compound and the flux are mixed and heated to obtain a mixed solution, and a zinc rubidium germanate nonlinear optical crystal is prepared in a crystal growth furnace. The technical effect of the invention is that the obtained crystal has the advantages of excellent thermal stability, wider light transmission range, moderate hardness, stable physical and chemical properties, etc. The compound zinc rubidium germanate obtained by the method of the invention can be used to prepare frequency device.
Description
Technical Field
The invention relates to compounds of the formula Rb2ZnGe2O6Compound (2) zinc rubidium germanate anda zinc-rubidium germanate nonlinear optical crystal, a preparation method of the crystal and a nonlinear optical device manufactured by using the crystal.
Background
The nonlinear optical crystal (NLO) can realize the conversion of laser wavelength, and is a key material for preparing optical devices, because of good stability and high laser damage threshold, inorganic nonlinear optical crystal has gained important application in military affairs, medical treatment, precision processing and communication field2O4) Crystal, LBO (LiB)3O5) Crystal, KBe2BO3F2(KBBF) crystal, KDP (KH)2PO4) Crystal, LN (LiNbO)3) Crystals, and the like. Although these materials have great application value, some defects exist, such as phase change problem of BBO crystal in the growth process, deliquescence problem of CLBO and KDP crystal, lamellar growth habit and extremely toxic raw material problem of KBBF crystal, low laser damage threshold of LN crystal and the like. With the continuous progress and development of science and technology, high and new technologies put forward higher requirements on nonlinear optical crystals, and the development of novel inorganic nonlinear optical crystal materials with excellent performance is particularly urgent.
The germanate crystal has excellent properties such as good stability, wide light-transmitting wave band, high damage threshold and the like, and is an excellent candidate material for a nonlinear optical crystal material. Will d10Zn of electronic structure2+Cation and electron transition alkali metal cation (Rb) having no d-d in ultraviolet region+) With GeO4The combination of groups aims to increase the transmission range and the frequency doubling response of the germanate. Therefore, the design and synthesis of the alkali metal zinc-containing germanate nonlinear optical crystal with excellent comprehensive performance are of great significance.
Disclosure of Invention
The invention aims to provide a compound rubidium zinc germanate nonlinear optical crystal with a chemical formula of Rb2ZnGe2O6；
The second purpose of the invention is to provide a preparation method for synthesizing a compound rubidium zinc germanate by adopting a solid phase reaction method and growing a rubidium zinc germanate nonlinear optical crystal by adopting a high-temperature melt method;
the third purpose of the invention is to provide the application of the rubidium zinc germanate nonlinear optical device.
The technical scheme for realizing the purpose is as follows:
the chemical formula of the compound zinc-rubidium germanate provided by the invention is Rb2ZnGe2O6(ii) a Uniformly mixing and fully grinding raw materials of a rubidium-containing compound, a zinc-containing compound and a germanium-containing compound, placing the raw materials in a muffle furnace, pre-burning at low temperature to remove moisture and gas in the raw materials, heating and calcining, taking out and grinding for multiple times during the heating and calcining, and continuously calcining to obtain a compound, namely, zinc-rubidium germanate;
the rubidium-containing compound comprises at least one of rubidium oxide, rubidium carbonate, rubidium bicarbonate, rubidium sulfate, rubidium hydroxide or rubidium salt;
the zinc-containing compound is at least one of zinc oxide or zinc salt; the zinc salt comprises at least one of zinc chloride, zinc nitrate, zinc oxalate and zinc sulfate;
the germanium-containing compound is at least one of germanium oxide or germanium salt; the germanium salt comprises at least one of germanium chloride, germanium bromide, germanium nitrate, germanium oxalate, germanium carbonate, germanium bicarbonate, and germanium sulfate.
The zinc-rubidium germanate compound can be prepared according to the following chemical reaction formula by adopting a solid-phase reaction method:
1)Rb2CO3+ZnO+2GeO2→Rb2ZnGe2O6+CO2↑
2)2RbHCO3+ZnO+2GeO2→Rb2ZnGe2O6+H2O↑+2CO2↑
3)2RbNO3+ZnO+2GeO2→Rb2ZnGe2O6+2NO2↑+0.5O2↑
4)2Rb(OH)+ZnO+2GeO2→Rb2ZnGe2O6+H2O↑+
5)2Rb2(SO4)+2ZnO+4GeO2→2Rb2ZnGe2O6+2SO2↑+O2↑
6)Rb2O+ZnO+2GeCl4+2O2→Rb2ZnGe2O6+4Cl2↑
7)2RbF+ZnO+2GeO2+0.5O2→Rb2ZnGe2O6+F2↑
8)2RbCl+ZnO+2GeO2+0.5O2→Rb2ZnGe2O6+Cl2↑
9)2RbBr+ZnO+2GeO2+0.5O2→Rb2ZnGe2O6+Br2↑
10)Rb2O+ZnO+2GeO2→Rb2ZnGe2O6
11)2Rb2(C2O4)+2ZnO+4GeO2→2Rb2ZnGe2O6+4CO↑+O2↑
12)Rb2CO3+Zn(NO3)2+2GeO2→Rb2ZnGe2O6+CO2↑+2NO2↑+0.5O2↑
13)Rb2O+Zn(NO3)2+2GeO2→Rb2ZnGe2O6+2NO2↑+0.5O2↑
14)2RbNO3+Zn(NO3)2+2GeO2→Rb2ZnGe2O6+4NO2↑+O2↑
15)2Rb(OH)+Zn(NO3)2+2GeO2→Rb2ZnGe2O6+2NO2↑+H2O↑+O2↑
16)2RbHCO3+Zn(NO3)2+2GeO2→Rb2ZnGe2O6+H2O↑+2CO2↑+2NO2↑+0.5O2↑
17)Rb2CO3+Zn(Cl)2+0.5O2+2GeO2→Rb2ZnGe2O6+CO2↑+Cl2↑
18)Rb2CO3+ZnSO4+2GeO2→Rb2ZnGe2O6+CO2↑+SO2↑+0.5O2↑
the invention provides a zinc-rubidium germanate nonlinear optical crystal, the chemical formula of the compound is Rb2ZnGe2O6Molecular weight 238.74, not containing a center of symmetry, belonging to the orthorhombic system, space group C2221Cell parameter of
The ultraviolet cut-off edge is 315nm, and the product has stable property and is not deliquescent.
The invention provides a preparation method of rubidium zinc germanate nonlinear optical crystal, which adopts a molten salt growth method to grow the rubidium zinc germanate nonlinear optical crystal, and the specific growth scheme is as follows:
a. uniformly mixing the compound zinc-rubidium germanate single-phase polycrystalline powder with a fluxing agent, heating the mixture to the temperature of 850-;
or directly heating a mixture of the rubidium-containing compound, the zinc-containing compound and the germanium-containing compound or a mixture of the rubidium-containing compound, the zinc-containing compound, the germanium-containing compound and a fluxing agent to 1150 ℃ at a temperature rise rate of 1-100 ℃/h, keeping the temperature for not less than 24 hours to obtain a mixed melt, and then cooling to 1000 ℃ at a temperature of 600 ℃, wherein the molar ratio of the rubidium-containing compound, the zinc-containing compound and the germanium-containing compound to the fluxing agent is 1:1:2: 0-20;
the fluxing agent is primarily a self fluxing agent, such as Rb2CO3、Rb2O、RbOH、RbF、RbCl、GeO2Rubidium salt, germanium salt or composite adjuvantFluxes, e.g. Rb2CO3-GeO2、Rb2O-GeO2、RbF-GeO2、RbCl-GeO2、Rb2CO3-TeO2、Rb2O-TeO2、RbF-TeO2、RbCl-TeO2、GeO2-TeO2、GeO2-TeO2-Rb2O、GeO2-TeO2-Rb2CO3One or more of (a).
The compound zinc-rubidium germanate single-phase polycrystalline powder is prepared by adopting a solid-phase synthesis method, and comprises the following steps of mixing a rubidium-containing compound, a zinc-containing compound and a germanium-containing compound, preparing zinc-rubidium germanate by adopting a solid-phase reaction method, uniformly mixing raw materials of the rubidium-containing compound, the zinc-containing compound and the germanium-containing compound, grinding, placing the mixture into a Pt crucible and placing the Pt crucible into a muffle furnace, pre-burning to remove moisture and gas in the raw materials, heating to the temperature of 500-850 ℃, taking out the mixture for grinding for many times and continuing to calcine, wherein the calcining time is not less than 72 hours, and cooling to the room temperature to obtain the compound zinc-rubidium germanate single-phase polycrystalline powder.
b. B, preparing zinc germanate rubidium seed crystals, namely slowly cooling the mixed melt obtained in the step a to room temperature at the speed of 0.5-10 ℃/h, and spontaneously crystallizing to obtain the zinc germanate rubidium seed crystals;
c. placing the Pt crucible containing the mixed melt prepared in the step a into a crystal growth furnace, fixing the seed crystal obtained in the step b on a seed crystal rod, putting the seed crystal above the liquid level from top to bottom, preheating the seed crystal for 10-30 minutes, putting the seed crystal on the liquid level of the melt when the temperature is 5-10 ℃ higher than the saturation point, keeping the temperature for 5-10 minutes to remove impurities on the surface of the seed crystal, and then reducing the temperature to the saturation point at the cooling rate of 1-10 ℃/min;
d. and slowly cooling at the speed of 1-5 ℃/day, growing at the rotating speed of 5-50rpm of the seed rod, after the crystal grows to the required size, lifting the crystal to be 1cm above the liquid level, cooling to the room temperature at the speed of 10-100 ℃/h, and finally opening a hearth to take out the crystal to obtain the rubidium zinc germanate nonlinear optical crystal.
The fluxing agent Rb2CO3-GeO2In the system of Rb2CO3With GeO2The molar ratio of (A) to (B) is 1-4: 2-6; rb2O-GeO2In the system of Rb2O and GeO2The molar ratio of (A) to (B) is 1-4: 2-6; RbF-GeO2RbF and GeO in the system2The molar ratio of (A) to (B) is 1-6: 2-4; RbCl-GeO2RbCl and GeO in the system2The molar ratio of (A) to (B) is 1-6: 2-4; rb2CO3-TeO2In the system of Rb2CO3And TeO2The molar ratio of (A) to (B) is 1-3: 2-6; rb2O-TeO2In the system of Rb2O and TeO2The molar ratio of (A) to (B) is 1-3: 2-6; RbF-TeO2RbF and TeO in the system2The molar ratio of (1-8) to (2-4); RbCl-TeO2RbCl and TeO in the system2The molar ratio of (1-8) to (2-4); GeO2-TeO2GeO in the system2And TeO2The molar ratio of (A) to (B) is 1-3: 2-6; GeO2-TeO2-Rb2CO3GeO in the system2And TeO2And Rb2CO3The molar ratio of (1-3: 2-4: 2-6); GeO2-TeO2-Rb2GeO in O system2And TeO2And Rb2The molar ratio of O is 1-3:2-4: 2-6;
the chemical formula of the zinc rubidium germanate nonlinear optical crystal prepared by the invention is Rb2ZnGe2O6Molecular weight 238.74, not containing a center of symmetry, belonging to the orthorhombic system, space group C2221Cell parameter of
The ultraviolet cut-off edge is 315nm, and the thermal stability is excellent.
Because Rb is used in the process of growing the rubidium zinc germanate nonlinear optical crystal2CO3、Rb2O、RbOH、RbF、RbCl、GeO2Rubidium or germanium salts, self-fluxing agents or composite fluxing agents, e.g. Rb2CO3-GeO2、Rb2O-GeO2、RbF-GeO2、RbCl-GeO2、Rb2CO3-TeO2、Rb2O-TeO2、RbF-TeO2、RbCl-TeO2、GeO2-TeO2，GeO2-TeO2-Rb2O、GeO2-TeO2-Rb2CO3And the like, target crystals with larger sizes are easily obtained; the obtained crystal has the advantages of excellent thermal stability, wider light transmission range, moderate hardness, stable physical and chemical properties and the like. The compound rubidium zinc germanate obtained by the method can be used for preparing a frequency doubling device, and at room temperature, a Nd-YAG Q-switched laser light source is adopted, infrared light with the incident wavelength of 1064nm is incident, and green laser with the wavelength of 532nm can be output.
Drawings
FIG. 1 is Rb of the present invention2ZnGe2O6The X-ray diffraction pattern of the powder is similar to the X-ray diffraction pattern based on the simulation of the crystal structure.
FIG. 2 shows Rb of the present invention2ZnGe2O6The structure diagram of the unit cell.
FIG. 3 shows Rb according to the present invention2ZnGe2O6Ultraviolet and visible diffuse reflectance spectrum.
FIG. 4 shows Rb of the present invention2ZnGe2O6The working principle of the nonlinear optical device made of crystal is shown schematically, wherein 1 is a laser, 2 is an incident laser beam, and 3 is Rb2ZnGe2O6Crystal, 4 the laser beam generated and 5 a filter.
Detailed Description
The invention is described in detail below with reference to the following figures and examples:
example 1:
according to the reaction formula: rb2CO3+ZnO+2GeO2→Rb2ZnGe2O6+CO2↓ [ O ] synthetic compound Rb2ZnGe2O6；
Will Rb2CO3ZnO and GeO2Weighing according to the molar ratio of 1:1:2, putting into a mortar, uniformly mixing and grinding, and then putting into an opening with the diameter of 60mm multiplied by 60mmPlacing the corundum crucible in a muffle furnace, slowly heating to 350 ℃ for calcination, keeping the temperature for 24 hours to remove moisture and gas, heating to 750 ℃ for calcination for 24 hours, taking out the corundum crucible, grinding, placing the corundum crucible in the muffle furnace, heating to 800 ℃ for calcination for not less than 48 hours to prepare compound zinc rubidium germanate single-phase polycrystalline powder, and analyzing by using powder X-ray diffraction test, wherein the X-ray spectrogram of the obtained sample powder and zinc rubidium Rb germanate2ZnGe2O6The theoretical X-ray spectrograms obtained from the single crystal structure are consistent, and refer to the attached figure 1;
the prepared compound of zinc germanate, rubidium and Rb2ZnGe2O6Single-phase polycrystalline powder and fluxing agent RbF-GeO2With a molar ratio Rb2ZnGe2O6:RbF-GeO21:3, wherein RbF and GeO2The molar ratio of the Pt filaments to the Pt filaments is 4:1, uniformly mixing, pressing, putting into a Pt crucible with the diameter of 60mm multiplied by 60mm, heating the mixed raw materials to 850 ℃ at the heating rate of 10-100 ℃/h, keeping the temperature for not less than 24 hours to uniformly mix the melt, putting the Pt filaments into the liquid level, and then cooling to induce spontaneous crystallization; the crystal has the chemical formula of Rb2ZnGe2O6Molecular weight 238.74, not containing a center of symmetry, belonging to the orthorhombic system, space group C2221Cell parameter of
The ultraviolet cut-off edge is 315nm, and the product has stable property and is not deliquescent, see figure 2 and figure 3.
Slowly cooling the melt at the speed of 1-5 ℃/h to obtain zinc germanate rubidium seed crystals;
growing crystals in a compound melt: subjecting Rb obtained by spontaneous crystallization to2ZnGe2O6Fixing seed crystal on seed crystal rod by platinum wire, preheating seed crystal 1-2cm above liquid surface, immersing seed crystal below liquid surface at 5-10 deg.C above saturation point, maintaining for 5-10 min to remove surface impurities, and rapidly cooling to saturation point；
Cooling at a rate of 1-3 deg.C/day with seed rod rotation speed of 5-50rpm, cooling to room temperature at a rate of 10-50 deg.C/hr for crystal extraction liquid level 1cm above, and taking out crystal to obtain Rb2ZnGe2O6And (4) crystals.
The rubidium carbonate used as the raw material in the reaction formula may be replaced by other rubidium-containing salts such as rubidium oxide, rubidium chloride, rubidium bromide, rubidium nitrate, rubidium oxalate, rubidium hydroxide, rubidium bicarbonate or rubidium sulfate, etc., the zinc oxide may be replaced by other zinc-containing salts such as zinc chloride, zinc nitrate, zinc oxalate or zinc sulfate, etc., and the germanium oxide may be replaced by other germanium salts.
Example 2:
according to the reaction formula: 2RbNO3+ZnO+2GeO2→Rb2ZnGe2O6+2NO2↑+0.5O2↓ [ O ] synthetic compound Rb2ZnGe2O6；
Converting RbNO3ZnO and GeO2Directly weighing raw materials according to the mol ratio of 2:1:2, and mixing the weighed raw materials with a fluxing agent Rb2O-GeO2Mixing according to a molar ratio of 1:3, wherein Rb is2O and GeO2The molar ratio of the Pt filament to the Pt filament is 4:1, the mixture is put into a platinum crucible with the diameter of 60mm multiplied by 60mm, the temperature is raised to 950 ℃, the constant temperature is kept for not less than 24 hours, the melt is uniformly mixed, the Pt filament is added, and then the temperature is reduced to induce spontaneous crystallization;
slowly cooling at the cooling rate of 1-5 ℃/h, and spontaneously crystallizing to obtain zinc germanate rubidium seed crystals;
growing crystals in a compound melt: subjecting Rb obtained by spontaneous crystallization to2ZnGe2O6Using small crystal grains as seed crystals, fixing the seed crystals on a seed crystal rod by using a platinum wire, firstly placing the seed crystals above the liquid level for preheating treatment at a position of 1-2cm, then immersing the seed crystals below the liquid level when the temperature is 5-10 ℃ higher than the saturation point, keeping for 5-10 minutes to remove surface impurities, and then quickly cooling to the saturation point temperature;
cooling at a rate of 1-3 deg.C/day with seed rod rotation speed of 5-50rpm, removing liquid surface of the crystal after crystal growth, and cooling to room temperature at a rate of 10-50 deg.C/hTaking out the crystal from the furnace to obtain Rb2ZnGe2O6And (4) crystals.
The rubidium nitrate used as the raw material in the reaction formula may be replaced by other rubidium-containing salts such as rubidium oxide, rubidium chloride, rubidium bromide, rubidium carbonate, rubidium oxalate, rubidium hydroxide, rubidium bicarbonate or rubidium sulfate, etc., the zinc oxide may be replaced by other zinc-containing salts such as zinc chloride, zinc nitrate, zinc oxalate or zinc sulfate, etc., and the germanium oxide may be replaced by other germanium salts.
Example 3:
according to the reaction formula: 2Rb (OH) + ZnO +2GeO2→Rb2ZnGe2O6+H2O ↓syntheticcompound Rb2ZnGe2O6；
Rb (OH), ZnO and GeO2Directly weighing raw materials according to the mol ratio of 2:1:2, and mixing the weighed raw materials with a fluxing agent RbF-TeO2Mixing according to the mol ratio of 1:3, wherein RbF and TeO2The molar ratio of the Pt filament to the Pt filament is 3:1, the mixture is put into a platinum crucible with the diameter of 60mm multiplied by 60mm, the temperature is raised to 900 ℃, the constant temperature is kept for not less than 24 hours, the melt is uniformly mixed, the Pt filament is added, and then the temperature is reduced to induce spontaneous crystallization;
slowly cooling the melt at the speed of 1-5 ℃/h to obtain zinc germanate rubidium seed crystals;
growing crystals in a compound melt: subjecting Rb obtained by spontaneous crystallization to2ZnGe2O6Using small crystal grains as seed crystals, fixing the seed crystals on a seed crystal rod by using a platinum wire, firstly placing the seed crystals above the liquid level for preheating treatment at a position of 1-2cm, then immersing the seed crystals below the liquid level when the temperature is 5-10 ℃ higher than the saturation point, keeping for 5-10 minutes to remove surface impurities, and then quickly cooling to the saturation point temperature;
cooling at a rate of 1-3 deg.C/day, rotating the seed rod at 5-50rpm, removing the crystal liquid surface after crystal growth, cooling to room temperature at a rate of 10-50 deg.C/hr, and taking out the crystal from the furnace to obtain Rb2ZnGe2O6And (4) crystals.
The rubidium hydroxide as the raw material in the reaction formula may be replaced by other rubidium-containing salts such as rubidium oxide, rubidium chloride, rubidium bromide, rubidium carbonate, rubidium nitrate, rubidium oxalate, rubidium bicarbonate, and rubidium sulfate, the zinc oxide may be replaced by other zinc-containing salts such as zinc chloride, zinc nitrate, zinc oxalate, and zinc sulfate, and the germanium oxide may be replaced by other germanium salts.
Example 4:
according to the reaction formula: 2Rb2SO4+2ZnO+4GeO2→2Rb2ZnGe2O6+2SO2↑+O2↓ [ O ] synthetic compound Rb2ZnGe2O6；
Will Rb2(SO4)，ZnO，GeO2Directly weighing raw materials according to the mol ratio of 1:1:2, and mixing the weighed raw materials with a fluxing agent GeO2-TeO2Mixing according to a molar ratio of 1:3, wherein GeO is2And TeO2The molar ratio of the Pt filament to the Pt filament is 1:4, the mixture is put into a platinum crucible with the diameter of 60mm multiplied by 60mm, the temperature is raised to 900 ℃, the constant temperature is kept for not less than 24 hours, the melt is uniformly mixed, the Pt filament is added, and then the temperature is reduced to induce spontaneous crystallization;
slowly cooling the melt at the speed of 1-5 ℃/h to obtain zinc germanate rubidium seed crystals;
growing crystals in a compound melt: subjecting Rb obtained by spontaneous crystallization to2ZnGe2O6Using small crystal grains as seed crystals, fixing the seed crystals on a seed crystal rod by using a platinum wire, firstly placing the seed crystals above the liquid level for preheating treatment at a position of 1-2cm, then immersing the seed crystals below the liquid level at a temperature of 5 ℃ higher than the saturation point, keeping for 10 minutes to remove surface impurities, and then rapidly cooling to the saturation temperature of 850 ℃;
cooling at a rate of 1-3 deg.C/day, rotating the seed rod at 5-50rpm, removing the crystal liquid surface after crystal growth, cooling to room temperature at a rate of 10-50 deg.C/hr, and taking out the crystal from the furnace to obtain Rb2ZnGe2O6And (4) crystals.
The raw material rubidium sulfate in the reaction formula can be replaced by other rubidium-containing salts such as rubidium oxide, rubidium chloride, rubidium bromide, rubidium carbonate, rubidium nitrate, rubidium oxalate, rubidium bicarbonate or rubidium hydroxide, etc., zinc oxide can be replaced by other zinc-containing salts such as zinc chloride, zinc nitrate, zinc oxalate or zinc sulfate, etc., and germanium oxide can be replaced by other germanium salts.
Example 5:
according to the reaction formula: 2RbCl + ZnO +2GeO2+0.5O2→Rb2ZnGe2O6+Cl2↓ [ O ] synthetic compound Rb2ZnGe2O6；
Mixing RbCl, ZnO and GeO2Directly weighing raw materials according to the mol ratio of 2:1:2, and mixing the weighed raw materials with a fluxing agent RbF-TeO2Uniformly mixing according to the molar ratio of 1:2, wherein RbF and TeO are2The molar ratio of the Pt filament to the Pt filament is 3:1, the mixture is put into a platinum crucible with the diameter of 60mm multiplied by 60mm, the temperature is raised to 850 ℃, the constant temperature is kept for not less than 24 hours, the melt is uniformly mixed, and the Pt filament is put into the crucible at the same time, and then the temperature is reduced to induce spontaneous crystallization;
slowly cooling the melt at the speed of 1-5 ℃/h to obtain zinc germanate rubidium seed crystals;
growing crystals in a compound melt: subjecting Rb obtained by spontaneous crystallization to2ZnGe2O6Using small crystal grains as seed crystals, fixing the seed crystals on a seed crystal rod by using a platinum wire, firstly placing the seed crystals above the liquid level for preheating treatment at a position of 1-2cm, then immersing the seed crystals below the liquid level when the temperature is 5-10 ℃ higher than the saturation point, keeping for 5-10 minutes to remove surface impurities, and then quickly cooling to the saturation point temperature;
cooling at a rate of 1-3 deg.C/day, rotating the seed rod at 5-50rpm, removing the crystal liquid surface after crystal growth, cooling to room temperature at a rate of 10-50 deg.C/hr, and taking out the crystal from the furnace to obtain Rb2ZnGe2O6And (4) crystals.
The rubidium chloride used as raw material in the reaction formula may be replaced by other rubidium-containing salts such as rubidium oxide, rubidium bromide, rubidium carbonate, rubidium nitrate, rubidium oxalate, rubidium bicarbonate, rubidium hydroxide, and rubidium sulfate, the zinc oxide may be replaced by other zinc-containing salts such as zinc chloride, zinc nitrate, zinc oxalate, and zinc sulfate, and the germanium oxide may be replaced by other germanium salts.
Example 6:
according to the reaction formula: 2RbBr + ZnO +2GeO2+0.5O2→Rb2ZnGe2O6+Br2↓ [ O ] synthetic compound Rb2ZnGe2O6；
Mixing RbBr, ZnO and GeO2Directly weighing raw materials according to the mol ratio of 2:1:2, and mixing the weighed raw materials with a fluxing agent RbF-TeO2Uniformly mixing according to the molar ratio of 1:2, wherein RbF and TeO are2The molar ratio of the Pt filament to the Pt filament is 3:1, the mixture is put into a platinum crucible with the diameter of 60mm multiplied by 60mm, the temperature is raised to 850 ℃, the constant temperature is kept for not less than 24 hours, the melt is uniformly mixed, the Pt filament is added, and then the temperature is reduced to induce spontaneous crystallization;
slowly cooling the melt at the speed of 1-5 ℃/h to obtain zinc germanate rubidium seed crystals;
growing crystals in a compound melt: subjecting Rb obtained by spontaneous crystallization to2ZnGe2O6Using small crystal grains as seed crystals, fixing the seed crystals on a seed crystal rod by using a platinum wire, firstly placing the seed crystals above the liquid level for preheating treatment at a position of 1-2cm, then immersing the seed crystals below the liquid level when the temperature is 5-10 ℃ higher than the saturation point, keeping for 5-10 minutes to remove surface impurities, and then quickly cooling to the saturation point temperature;
cooling at a rate of 1-3 deg.C/day, rotating the seed rod at 5-50rpm, removing the crystal liquid surface after crystal growth, cooling to room temperature at a rate of 10-50 deg.C/hr, and taking out the crystal from the furnace to obtain Rb2ZnGe2O6And (4) crystals.
The rubidium bromide used as the raw material in the reaction formula may be replaced by other rubidium-containing salts such as rubidium oxide, rubidium chloride, rubidium carbonate, rubidium nitrate, rubidium oxalate, rubidium bicarbonate, rubidium hydroxide, and rubidium sulfate, the zinc oxide may be replaced by other zinc-containing salts such as zinc chloride, zinc nitrate, zinc oxalate, and zinc sulfate, and the germanium oxide may be replaced by other germanium salts.
Example 7:
according to the reaction formula: rb2O+ZnO+2GeO2→Rb2ZnGe2O6Synthesis of Compound Rb2ZnGe2O6；
Will Rb2O, ZnO and GeO2Directly weighing raw materials according to the mol ratio of 1:1:2, and mixing the weighed raw materials with a fluxing agent GeO2-TeO2-Rb2Mixing O at a molar ratio of 1:1, wherein GeO2And TeO2And Rb2The molar ratio of O is 1:2:2, the mixture is put into a platinum crucible with the diameter of 60mm multiplied by 60mm, the temperature is raised to 950 ℃, the melt is uniformly mixed, meanwhile, Pt filaments are put in, and then the temperature is reduced to induce spontaneous crystallization;
slowly cooling the melt at the speed of 1-5 ℃/h to obtain zinc germanate rubidium seed crystals;
growing crystals in a compound melt: subjecting Rb obtained by spontaneous crystallization to2ZnGe2O6Using small crystal grains as seed crystals, fixing the seed crystals on a seed crystal rod by using a platinum wire, firstly placing the seed crystals above the liquid level for preheating treatment at a position of 1-2cm, then immersing the seed crystals below the liquid level when the temperature is 5-10 ℃ higher than the saturation point, keeping for 5-10 minutes to remove surface impurities, and then quickly cooling to the saturation point temperature;
cooling at a rate of 1-3 deg.C/day, rotating the seed rod at 5-50rpm, removing the crystal liquid surface after crystal growth, cooling to room temperature at a rate of 10-50 deg.C/hr, and taking out the crystal from the furnace to obtain Rb2ZnGe2O6And (4) crystals.
The rubidium oxide as the raw material in the reaction formula may be replaced by other rubidium-containing salts such as rubidium chloride, rubidium bromide, rubidium carbonate, rubidium nitrate, rubidium oxalate, rubidium bicarbonate, rubidium hydroxide, and rubidium sulfate, the zinc oxide may be replaced by other zinc-containing salts such as zinc chloride, zinc nitrate, zinc oxalate, and zinc sulfate, and the germanium oxide may be replaced by other germanium salts.
Example 8:
with Rb2ZnGe2O6Crystal preparation of nonlinear optics:
rb obtained in examples 1 to 72ZnGe2O6The nonlinear optical crystal is processed according to the crystallography data and the required size, angle and thickness, and the light-passing surface is polished, so that the nonlinear optical crystal can be used as a nonlinear optical device.
Fixing the obtained crystal at position 3 as shown in FIG. 4, and using a Q-switched Nd-YAG laser as light source at room temperature to emit infrared light with wavelength of 1064nm and infrared light beam 2 with wavelength of 1064nm to emit Rb2ZnGe2O6After crystallizationGreen frequency doubling light with the wavelength of 532nm is generated, the emergent light beam 4 contains infrared light with the wavelength of 1064nm and green light with the wavelength of 532nm, and green laser with the wavelength of 532nm is obtained after passing through the filter 5.
Claims (5)
1. The compound rubidium zinc germanate nonlinear optical crystal is characterized in that the chemical formula of the compound is Rb2ZnGe2O6Molecular weight 238.74, not containing a center of symmetry, belonging to the orthorhombic system, space group C2221Cell parameter of
The ultraviolet cut-off edge of the compound is 315 nm.
2. The method for preparing the compound rubidium zinc germanate nonlinear optical crystal according to claim 1, wherein the rubidium zinc germanate nonlinear optical crystal is prepared by a molten salt growth method, and the method comprises the following steps:
a. mixing rubidium-containing compound, zinc-containing compound and germanium-containing compound to prepare zinc germanate, rubidium germanate and Rb through a solid-phase reaction method2ZnGe2O6Wherein the molar ratio of the element rubidium in the rubidium-containing compound to the element zinc in the zinc-containing compound to the element germanium in the germanium-containing compound is 2:1: 2;
b. the compound zinc-rubidium germanate is prepared by a solid-phase reaction method, and the specific process comprises the following steps: fully and uniformly mixing rubidium-containing compound, zinc-containing compound and germanium-containing compound raw materials, grinding, placing in a muffle furnace, calcining at low temperature to remove moisture and gas in the mixed materials, heating and continuing calcining, taking out and grinding for multiple times during the calcining, and cooling to room temperature to obtain a compound zinc germanate rubidium;
the rubidium-containing compound comprises at least one of rubidium oxide, rubidium hydroxide, or a rubidium salt; the rubidium salt comprises at least one of rubidium chloride, rubidium bromide, rubidium nitrate, rubidium carbonate, rubidium bicarbonate and rubidium sulfate;
the zinc-containing compound is at least one of zinc oxide or zinc salt; the zinc salt comprises at least one of zinc chloride, zinc nitrate, zinc bicarbonate and zinc sulfate;
the germanium-containing compound is at least one of germanium oxide or germanium salt; the germanium salt comprises at least one of germanium chloride, germanium bromide, germanium nitrate, germanium carbonate, germanium bicarbonate, and germanium sulfate;
heating any one of the obtained compound zinc-rubidium germanate single-phase polycrystalline powder or a mixture of any one of the obtained compound zinc-rubidium germanate single-phase polycrystalline powder and a fluxing agent to obtain a uniform mixed melt;
or directly heating and melting a mixture of the rubidium-containing compound, the zinc-containing compound and the germanium-containing compound or a mixture of the rubidium-containing compound, the zinc-containing compound, the germanium-containing compound and a fluxing agent to obtain uniform mixed melt;
c. and c, placing the Pt crucible containing the mixed solution prepared in the step b into a crystal growth furnace, fixing one end of the seed crystal by using a platinum wire, putting the other end of the seed crystal into the liquid surface to melt off surface impurities or defects when the temperature is 5-10 ℃ higher than the saturation point, and then quickly cooling to below the saturation temperature or growing at constant temperature to prepare the rubidium zinc germanate nonlinear optical crystal.
3. The method for preparing the rubidium zinc germanate nonlinear optical crystal according to claim 2, wherein the molar ratio of the compound rubidium zinc germanate single-phase polycrystalline powder to the fluxing agent is 1: 0-20; the flux comprises rubidium hydroxide, germanium hydroxide, rubidium oxide, germanium oxide, rubidium salt, germanium salt, lead oxide or composite flux, wherein the composite flux comprises Rb2O-GeO2、RbF-GeO2、RbF-TeO2,、Rb2O-TeO2,、GeO2-TeO2Or GeO2-TeO2-Rb2And O is one of the compounds.
4. The method for preparing the rubidium zinc germanate nonlinear optical crystal according to claim 3, wherein a composite fluxing agent Rb is used2O-GeO2In the system of Rb2O and GeO2The molar ratio of (A) to (B) is 1-4: 2-6; RbF-GeO2RbF and GeO in the system2The molar ratio of (A) to (B) is 1-6: 2-4; rb2O-TeO2In the system of Rb2O and TeO2Is prepared from (A) and (B)The molar ratio is 1-3: 2-6; RbF-TeO2RbF and TeO in the system2The molar ratio of (1-8) to (2-4); GeO2-TeO2GeO in the system2And TeO2The molar ratio of (A) to (B) is 1-3: 2-6; GeO2-TeO2-Rb2GeO in O system2And TeO2And Rb2The molar ratio of O is 1-3:2-4: 2-6.
5. Use of the rubidium zinc germanate nonlinear optical crystal of claim 1, wherein the rubidium zinc germanate nonlinear optical crystal is used for manufacturing a frequency doubling generator, an upper frequency converter, a lower frequency converter and an optical parametric oscillator.
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| CN115506022B (en) * | 2022-08-23 | 2024-04-05 | 天津理工大学 | Compound niobium germanate cesium birefringent crystal and preparation method and use thereof |
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