CN102660773A - Non-linear optical crystal boric acid cadmium yttrium oxide - Google Patents

Non-linear optical crystal boric acid cadmium yttrium oxide Download PDF

Info

Publication number
CN102660773A
CN102660773A CN2012101253060A CN201210125306A CN102660773A CN 102660773 A CN102660773 A CN 102660773A CN 2012101253060 A CN2012101253060 A CN 2012101253060A CN 201210125306 A CN201210125306 A CN 201210125306A CN 102660773 A CN102660773 A CN 102660773A
Authority
CN
China
Prior art keywords
boric acid
yttrium
cadmium
crystal
acid oxygen
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.)
Pending
Application number
CN2012101253060A
Other languages
Chinese (zh)
Inventor
叶宁
邹国红
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.)
Fujian Institute of Research on the Structure of Matter of CAS
Original Assignee
Fujian Institute of Research on the Structure of Matter of CAS
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 Fujian Institute of Research on the Structure of Matter of CAS filed Critical Fujian Institute of Research on the Structure of Matter of CAS
Priority to CN2012101253060A priority Critical patent/CN102660773A/en
Publication of CN102660773A publication Critical patent/CN102660773A/en
Pending legal-status Critical Current

Links

Images

Abstract

The present invention relates to Non-linear optical crystal boric acid cadmium yttrium oxide, chemical formula Cd4YO (BO3) 3 belongs to monoclinic system, space group Cm, and cell parameter is
Figure DDA0000157383110000011
Figure DDA0000157383110000012
Figure DDA0000157383110000013
α=γ=90 °, β=100.088 °, z=2, unit-cell volume are
Figure DDA0000157383110000014
Its Clock Multiplier Factor is 5.2 times of KH2PO4 (KDP). It is 340-6250nm through wave band. It is sintered at high temperature using solid phase synthesis process and obtains Cd4YO (BO3) 3 compound. Using molten-salt growth method, monocrystal can be gone out with successful growth by making fluxing agent with B2O3. Cd4YO (BO3) 3 has nonlinear optical effect, and does not deliquesce, and physico-chemical property is stablized, and can be used widely in various non-linear optical fields.

Description

Nonlinear optical crystal boric acid oxygen cadmium yttrium
Technical field
The present invention relates to a kind of new type light electronic functional material and growth method and purposes, particularly relate to a kind of non-linear optical crystal material, i.e. boric acid oxygen cadmium yttrium, its chemical formula is Cd 4YO (BO 3) 3
Technical background
The crystalline non-linear optical effect is meant a kind of like this effect: when a branch of laser with certain polarization direction passes through a non-linear optic crystal (like Cd by certain incident direction 4YO (BO 3) 3The time, the frequency of this light beam will change.
Crystal with non-linearity optical effect is called non-linear optic crystal.Utilize non-linear optic crystal to carry out the laser frequency conversion, widen the scope of optical maser wavelength, make the application of laser more extensive.Especially crystal such as borate family non-linear optic crystal such as BBO, LBO, KBBF, SBBO, TBO, KABO, BABO receive much attention with its excellent optical property.
Applicable non-linear optic crystal mainly is LBO (LiB in the ultraviolet region at present 3O 5) and BBO (BaB 2O 4) two kinds, their growing technology and growth technique are very ripe, can grow high quality, large-sized monocrystalline.Bbo crystal is one of ultraviolet non-linear optic crystal that can produce up to now effective five frequencys multiplication, can also obtain the output of effective 193nm simultaneously through the method with frequency.This crystal has bigger specific refractory power, can realize the direct frequency multiplication from 202.8nm to the 2600nm scope, therefore is widely used in optical parametric oscillation and the various harmonic generator.LBO has wide transparency range, and optical homogeneity is good, and Clock Multiplier Factor is moderate, and acceptance angle can be realized 90 ° of noncritical phase matchings than broad.Because the degree of birefringence of LBO is too little, thereby limited its phase matched scope in the ultraviolet region.Because the anisotropy of the thermal expansivity of lbo crystal; Cause when the high temperature plated film, causing easily the damage of quartz crystal device; And bbo crystal has faint deliquescence, in the device fabrication process, causes damage easily, remedies this defective so we must seek novel ultraviolet nonlinear crystal.
The novel non-linearity crystal should have and very wide sees through wave band and big non-linear effectiveness, and good physical and chemical performance.Introduce asymmetric unitary CdO nGet into the RE borate system and can effectively increase non-linear effect, also can obtain good physical and chemical performance.Through solid phase synthesis, crystal growth, single crystal structure determination, we have obtained Cd 4YO (BO 3) 3, confirmed that this imagination is possible.
Summary of the invention
The object of the present invention is to provide a kind of boric acid oxygen cadmium yttrium compound, its chemical formula is Cd 4YO (BO 3) 3
Another object of the present invention is to provide a kind of boric acid oxygen cadmium yttrium compound preparation method.
Another object of the present invention is to provide a kind of boric acid oxygen cadmium yttrium non-linear optic crystal, its chemical formula is Cd 4YO (BO 3) 3
A purpose more of the present invention is to provide a kind of growth method of boric acid oxygen cadmium yttrium non-linear optic crystal.
A further object of the invention is to provide the purposes of boric acid oxygen cadmium yttrium non-linear optic crystal.
Technical scheme of the present invention is following:
Boric acid oxygen cadmium yttrium compound provided by the invention, its chemical formula is Cd 4YO (B0 3) 3
The preparation method of boric acid oxygen cadmium yttrium compound provided by the invention; Its step is following: the raw materials of compound that will contain Cd, Y and B is Cd: Y: B=4 in its mol ratio: after 1: 3 ratio uniform mixing grinds; Pack in the platinum alloy crucible, slowly heat up after 300~400 ℃ pre-burning 1~5 hour; Be cooled to room temperature, take out and grind; 800~900 ℃ of following sintering 12~20 hours, be cooled to room temperature then, take out and grind, obtain Powdered boric acid oxygen cadmium yttrium compound of the present invention, it is carried out XRD detect that (Fig. 3 a), its molecular formula is Cd 4YO (BO 3) 3The described Cd of containing raw materials of compound is oxide compound or the carbonate that contains cadmium, and the described Y of containing raw materials of compound is oxide compound or the carbonate that contains yttrium, and the described B of containing raw materials of compound is B 2O 3Or H 3BO 3.
Boric acid oxygen cadmium yttrium non-linear optic crystal provided by the invention, its chemical formula is Cd 4YO (BO 3) 3, belonging to oblique system, spacer is Cm, unit cell parameters does
Figure BDA0000157383090000031
Figure BDA0000157383090000033
α=γ=90 °, β=100.088 °, z=2, unit-cell volume does
Figure BDA0000157383090000034
Crystalline structure such as Fig. 2.
The growth method of boric acid oxygen cadmium yttrium non-linear optic crystal provided by the invention, its step is following: with B 2O 3Be fluxing agent growth; Solute and solvent mol ratio are 1/2~1/1 when being benchmark with B, and raw material is mixed according to the above ratio, heat up 1150~1200 ℃ to melt fully to raw material; Behind the constant temperature 1~20 hour; Be cooled to above 5~10 ℃ of temperature of saturation rapidly, then by every day 1~5 ℃ speed be cooled to 800 ℃, close stove; After treating that sample is cooled to room temperature, water flush away fusing assistant promptly obtains 0.5 * 0.4 * 0.4mm boric acid oxygen cadmium yttrium non-linear optic crystal that is of a size of of the present invention.
The raw materials of compound that adopts is oxide compound or the carbonate that contains cadmium, contains the oxide compound or the carbonate of yttrium, and B 2O 3Or H 3BO 3, the lenticular boric acid oxygen cadmium yttrium that obtains, grind into powder carries out XRD to it and detects result such as Fig. 3 b again.
The growth method of boric acid oxygen cadmium yttrium non-linear optic crystal provided by the invention, its step is following: adopt B 2O 3The fusing assistant system; Solute and solvent mol ratio are 1/2~1/1 when being benchmark with B; Raw material is mixed according to the above ratio, heat up 1150~1200 ℃ and melt fully to raw material, constant temperature is after 1~20 hour; Be cooled to above 5~10 ℃ of temperature of saturation rapidly, the lower end that seed crystal is fixed on seed rod contacts the beginning crystal growth with melt liquid level; The speed of rotation of seed rod is 10~20 rev/mins, is cooled to temperature of saturation, slowly lowers the temperature by 1~5 ℃/day speed then; Cooling is lifted from liquid level with crystal after finishing, and reduces to room temperature with 10~30 ℃/hour speed, obtains 12 * 10 * 10mm boric acid oxygen cadmium yttrium non-linear optic crystal that is of a size of of the present invention.Be of a size of 12 * 10 * 10mm, grind into powder carries out XRD to it and detects result such as Fig. 3 b again.
The purposes of boric acid oxygen cadmium yttrium non-linear optic crystal provided by the invention, this nonlinear optical crystal boric acid oxygen cadmium yttrium are used for the frequency transformation of laser apparatus laser output.
It is that the laser beam of 1.064 μ m produces 2 frequencys multiplication that the purposes of boric acid oxygen cadmium yttrium non-linear optic crystal provided by the invention, this crystal are used for wavelength, the humorous glistening light of waves output of 3 frequencys multiplication.
The purposes of boric acid oxygen cadmium yttrium non-linear optic crystal provided by the invention, described non-linear optic crystal is the harmonic generator that is used for the ultraviolet region, optical parameter and amplifying device and fiber waveguide device.
The purposes of boric acid oxygen cadmium yttrium non-linear optic crystal provided by the invention, described non-linear optic crystal are optical parameter and the amplifying device from infrared to the ultraviolet region.
It is Cd that effect of the present invention is to provide a kind of chemical formula 4YO (BO 3) 3Compound, the non-linear optic crystal of this compound.Use powder frequency multiplication testing method to measure Cd 4YO (BO 3) 3The phase matched ability, its powder frequency-doubled effect is KH for its Clock Multiplier Factor 2PO 4(KDP) 5.2 times.Cd 4YO (BO 3) 3Crystal can be realized 2 frequencys multiplication of Nd:YAG (λ=1.064 μ m), and, can predict Cd 4YO (BO 3) 3Can be used in the harmonic generator of 3 frequencys multiplication of Nd:YAG.In addition, Cd 4YO (BO 3) 3The monocrystalline water white transparency is congruent melting compound, about 1100 ℃ of fusing point, and chemicalstability is good.So can predict Cd 4YO (BO 3) 3To in various non-linear optical fields, obtain widespread use.
Description of drawings
Fig. 1 is Cd 4YO (BO 3) 3Crystal is as the canonical schema of frequency-doubling crystal application non-linear hour optical effect, and wherein 1 is laser apparatus, and the 2nd, incoming laser beam, the 3rd, through the Cd of crystal aftertreatment and optics processing 4YO (BO 3) 3Single crystal, the 4th, the outgoing laser beam that is produced, the 5th, filter plate.
Fig. 2 is Cd 4YO (BO 3) 3The crystal unit cell structural representation.
Fig. 3 is Cd 4YO (BO 3) 3X XRD X collection of illustrative plates, wherein 3a is solid phase synthesis Cd 4YO (BO 3) 3The diffractogram of powdered sample, 3b are Cd 4YO (BO 3) 3The monocrystalline last diffractogram of pulverizing.Powder x ray diffraction data uses the MiniFlex diffractometer to collect at normal temperatures.
Embodiment
Embodiment 1
Adopt high temperature solid state reaction synthetic compound Cd 4YO (BO 3) 3
Raw materials used: CdCO 32.7587 gram (0.016mol)
Y 2O 30.4516 gram (0.002mol)
H 3BO 30.7432 gram (0.012mol)
Its chemical equation is:
8CdCO 3+Y 2O 3+6H 3BO 3=2Cd 4YO(BO 3) 3
The concrete operations step is following: after in operation box, above-mentioned raw materials being weighed up by above-mentioned dosage, put into that mortar mixes and carefully grind, in the platinum alloy crucible of the Φ 30 * 30mm that packs into then; With spoon it is compressed and to add a cover, put into retort furnace (retort furnace places stink cupboard, and the fume hood exhaust mouth is through the water tank exhaust); Slowly be warming up to 400 ℃ and constant temperature pre-burning 3 hours; The beginning temperature rise rate must be slow, prevents and treats the variation that causes proportioning because of decomposition, and solid state reaction is fully carried out.Crucible is taken out in the cooling back, and this moment, sample was more loose.Then take out sample and in operation box, grind again evenly, place crucible to compress again and add a cover, in 900 ℃ of following sintering 20 hours, took out the cooling back in retort furnace, and at this moment sample is formed one, sample is put into mortar smash grinding to pieces and promptly get product.This product is carried out X-ray analysis, and (Fig. 3 a) and Cd for the gained spectrogram 4YO (BO 3) 3The monocrystalline last X ray picture (Fig. 3 b) of pulverizing is consistent.
Embodiment 2
Adopt high temperature solid state reaction synthetic compound Cd 4YO (BO 3) 3
Raw materials used: CdO 2.0546 grams (0.016mol)
Y 2O 30.4516 gram (0.002mol)
H 3BO 30.7432 gram (0.012mol)
Its chemical equation is:
8CdO+Y 2O 3+6H 3BO 3=2Cd 4YO(BO 3) 3
The concrete operations step is following: after in operation box, above-mentioned raw materials being weighed up by above-mentioned dosage, put into that mortar mixes and carefully grind, in the platinum alloy crucible of the Φ 30 * 30mm that packs into then; With spoon it is compressed and to add a cover, put into retort furnace (retort furnace places stink cupboard, and the fume hood exhaust mouth is through the water tank exhaust); Slowly be warming up to 400 ℃ and constant temperature pre-burning 3 hours; The beginning temperature rise rate must be slow, prevents and treats the variation that causes proportioning because of decomposition, and solid state reaction is fully carried out.Crucible is taken out in the cooling back, and this moment, sample was more loose.Then take out sample and in operation box, grind again evenly, place crucible to compress again and add a cover, in 900 ℃ of following sintering 20 hours, took out the cooling back in retort furnace, and at this moment sample is formed one, sample is put into mortar smash grinding to pieces and promptly get product.This product is carried out X-ray analysis, and (Fig. 3 a) and Cd for the gained spectrogram 4YO (BO 3) 3The monocrystalline last X ray picture (Fig. 3 b) of pulverizing is consistent.
Embodiment 3
Adopt molten-salt growth crystal Cd 4YO (BO 3) 3
Crystal growing apparatus is homemade wire spiral process furnace, and temperature controlling instruments is a 908PHK20 type automatic temperature control instrument able to programme.Select B for use 2O 3Make fusing assistant, sporadic nucleation obtains crystal.
Raw materials used:
Figure BDA0000157383090000061
The concrete operations step is following: after above-mentioned raw materials is weighed up by above-mentioned dosage, mix, in the platinum alloy crucible of the Φ 60 * 60mm that packs into then; Place in the self-control reactors; Heat up 1200 ℃ and melt fully to raw material, constant temperature was cooled to above 5~10 ℃ of temperature of saturation rapidly after 10 hours; Then by every day 3 ℃ speed be cooled to 600 ℃, close stove.After treating the sample cooling, water flush away fusing assistant promptly obtains transparent Cd 4YO (BO 3) 3Monocrystalline, it is of a size of 0.5 * 0.4 * 0.4mm.
Embodiment 4
Adopt molten-salt growth crystal Cd 4YO (BO 3) 3
Crystal growing apparatus is homemade wire spiral process furnace, and temperature controlling instruments is a 908PHK20 type automatic temperature control instrument able to programme.Select B for use 2O 3Make fusing assistant, the crystal that instance 3 is obtained carries out orientation and cuts into the seed crystal that is designed.
Raw materials used:
Figure BDA0000157383090000071
The concrete operations step is following: after above-mentioned raw materials is weighed up by above-mentioned dosage, mix, in the platinum alloy crucible of the Φ 60 * 60mm that packs into then; Place in the self-control reactors, heat up 1200 ℃ and melt fully to raw material, constant temperature is after 10 hours; Be cooled to above 5~10 ℃ of temperature of saturation rapidly; Seed crystal is fixed on the lower end of seed rod, imports crucible, seed crystal is contacted with melt liquid level begin crystal growth from the aperture of furnace roof portion.The speed of rotation of seed rod is 15 rev/mins, is cooled to temperature of saturation, slowly lowers the temperature by 1 ℃/day speed then.Cooling is lifted from liquid level with crystal after finishing, and reduces to room temperature with 20 ℃/hour speed, promptly obtains the Cd of large-size 4YO (BO 3) 3Monocrystalline, it is of a size of 12 * 10 * 10mm.
Embodiment 5
With the crystal that instance 4 obtains, processing cutting, orientation; Polishing is placed on the position of 3 in the device shown in Figure 1; At room temperature, with transferring Q Nd:YAG laser to do the input light source, incident wavelength is 1064nm; Observe tangible 532nm frequency multiplication green glow output, output intensity is about 5.2 times of equal conditions KDP.

Claims (9)

1. compound boric acid oxygen cadmium yttrium is characterized in that: its chemical formula Cd 4YO (BO 3) 3, belonging to oblique system, spacer is Cm, unit cell parameters does
Figure FDA0000157383080000011
Figure FDA0000157383080000012
Figure FDA0000157383080000013
α=γ=90 °, β=100.088 °, z=2, unit-cell volume does
Figure FDA0000157383080000014
2. the preparation method of the boric acid oxygen cadmium yttrium compound of a claim 1 is characterized in that: after the raw materials of compound that will contain Cd, Y and B grinds by the suitable proportion uniform mixing, slowly heat up after 300~400 ℃ pre-burning 1~5 hour; Be cooled to room temperature, take out and grind; 800~900 ℃ of following sintering 12~20 hours, be cooled to room temperature and can obtain boric acid oxygen cadmium yttrium compound then.
3. the non-linear optic crystal of the compound boric acid oxygen cadmium yttrium of claim 1.
4. the growth method of the described boric acid oxygen of claim 3 a cadmium yttrium non-linear optic crystal adopts molten-salt growth, it is characterized in that: with B 2O 3Be fluxing agent growth; Solute and solvent mol ratio are 1/2~1/1 when being benchmark with B, and raw material is mixed according to the above ratio, heat up 1150~1200 ℃ to melt fully to raw material; Behind the constant temperature 1~20 hour; Be cooled to above 5~10 ℃ of temperature of saturation rapidly, then by every day 1~5 ℃ speed be cooled to 800 ℃, close stove; After treating that sample is cooled to room temperature, water flush away fusing assistant promptly obtains described boric acid oxygen cadmium yttrium non-linear optic crystal.
5. the growth method of the described boric acid oxygen of claim 3 a cadmium yttrium non-linear optic crystal adopts molten-salt growth, it is characterized in that: adopt B 2O 3The fusing assistant system; Solute and solvent mol ratio are 1/2~1/1 when being benchmark with B; Raw material is mixed according to the above ratio, heat up 1150~1200 ℃ and melt fully to raw material, constant temperature is after 1~20 hour; Be cooled to above 5~10 ℃ of temperature of saturation rapidly, the lower end that seed crystal is fixed on seed rod contacts the beginning crystal growth with melt liquid level; The speed of rotation of seed rod is 10~20 rev/mins, is cooled to temperature of saturation, slowly lowers the temperature by 1~5 ℃/day speed then; Cooling is lifted from liquid level with crystal after finishing, and reduces to room temperature with 10~30 ℃/hour speed, obtains described boric acid oxygen cadmium yttrium non-linear optic crystal.
6. the purposes of the described boric acid oxygen of claim 3 a cadmium yttrium non-linear optic crystal is characterized in that: this non-linear optic crystal is used for the frequency transformation of laser apparatus laser output.
7. the purposes of the described boric acid oxygen of claim 6 a cadmium yttrium non-linear optic crystal is characterized in that: it is that the laser beam of 1.064 μ m produces 2 frequencys multiplication or the humorous glistening light of waves output of 3 frequencys multiplication that this crystal is used for wavelength.
8. the purposes of the described boric acid oxygen of claim 6 a cadmium yttrium non-linear optic crystal, it is characterized in that: described non-linear optic crystal is used to prepare the harmonic generator of ultraviolet region, optical parameter and amplifying device and fiber waveguide device.
9. the purposes of the described boric acid oxygen of claim 6 a cadmium yttrium non-linear optic crystal, it is characterized in that: described non-linear optic crystal is used to prepare optical parameter and the amplifying device from infrared to the ultraviolet region.
CN2012101253060A 2012-04-25 2012-04-25 Non-linear optical crystal boric acid cadmium yttrium oxide Pending CN102660773A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2012101253060A CN102660773A (en) 2012-04-25 2012-04-25 Non-linear optical crystal boric acid cadmium yttrium oxide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2012101253060A CN102660773A (en) 2012-04-25 2012-04-25 Non-linear optical crystal boric acid cadmium yttrium oxide

Publications (1)

Publication Number Publication Date
CN102660773A true CN102660773A (en) 2012-09-12

Family

ID=46770346

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2012101253060A Pending CN102660773A (en) 2012-04-25 2012-04-25 Non-linear optical crystal boric acid cadmium yttrium oxide

Country Status (1)

Country Link
CN (1) CN102660773A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103451730A (en) * 2012-06-05 2013-12-18 中国科学院理化技术研究所 Cd4RO(BO3)3 compound, Cd4RO(BO3)3 optical crystal, and preparation method and application thereof

Citations (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04155318A (en) * 1990-10-18 1992-05-28 Sharp Corp Light wave-length converting device
CN1194292A (en) * 1997-03-26 1998-09-30 肖志国 Long persistence luminescent silicate material and its producing method
CN1201082A (en) * 1998-04-02 1998-12-09 山东大学 Sulfocyanic-acid-matches type crystal material, preparation method and use thereof
CN1215767A (en) * 1997-10-28 1999-05-05 中国科学院福建物质结构研究所 Non-linear optic crystal aluminium-oxygen-barium borate
CN1485960A (en) * 2002-09-29 2004-03-31 中国科学院福建物质结构研究所 Tunable green-blue-purple laser
CN1492548A (en) * 2002-10-22 2004-04-28 中国科学院福建物质结构研究所 Solid tunable laser
CN1691442A (en) * 2004-04-20 2005-11-02 中国科学院福建物质结构研究所 Frequency multiplication ultraviolet solid laser applying non-linear laser crystal
CN101019241A (en) * 2004-08-04 2007-08-15 英特曼帝克司公司 Novel phosphor system for a white light emitting diode
CN101545138A (en) * 2008-03-25 2009-09-30 中国科学院福建物质结构研究所 Non-linear optical crystal-sodium beryllate borate, growth method and application thereof
CN101775655A (en) * 2010-01-13 2010-07-14 福州高意通讯有限公司 Laser crystal and preparation method thereof
CN102031562A (en) * 2009-09-28 2011-04-27 中国科学院福建物质结构研究所 Non-linear optical crystal bismuth cadmium borate
CN102260913A (en) * 2010-05-12 2011-11-30 中国科学院福建物质结构研究所 Novel nonlinear optical crystal rubidium beryllium borate
WO2012009945A1 (en) * 2010-07-20 2012-01-26 中国科学院新疆理化技术研究所 Barium fluoroborate, nonlinear optical crystal of barium fluoroborate, the production methods and uses thereof

Patent Citations (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04155318A (en) * 1990-10-18 1992-05-28 Sharp Corp Light wave-length converting device
CN1194292A (en) * 1997-03-26 1998-09-30 肖志国 Long persistence luminescent silicate material and its producing method
CN1215767A (en) * 1997-10-28 1999-05-05 中国科学院福建物质结构研究所 Non-linear optic crystal aluminium-oxygen-barium borate
CN1201082A (en) * 1998-04-02 1998-12-09 山东大学 Sulfocyanic-acid-matches type crystal material, preparation method and use thereof
CN1485960A (en) * 2002-09-29 2004-03-31 中国科学院福建物质结构研究所 Tunable green-blue-purple laser
CN1492548A (en) * 2002-10-22 2004-04-28 中国科学院福建物质结构研究所 Solid tunable laser
CN1691442A (en) * 2004-04-20 2005-11-02 中国科学院福建物质结构研究所 Frequency multiplication ultraviolet solid laser applying non-linear laser crystal
CN101019241A (en) * 2004-08-04 2007-08-15 英特曼帝克司公司 Novel phosphor system for a white light emitting diode
CN101545138A (en) * 2008-03-25 2009-09-30 中国科学院福建物质结构研究所 Non-linear optical crystal-sodium beryllate borate, growth method and application thereof
CN102031562A (en) * 2009-09-28 2011-04-27 中国科学院福建物质结构研究所 Non-linear optical crystal bismuth cadmium borate
CN101775655A (en) * 2010-01-13 2010-07-14 福州高意通讯有限公司 Laser crystal and preparation method thereof
CN102260913A (en) * 2010-05-12 2011-11-30 中国科学院福建物质结构研究所 Novel nonlinear optical crystal rubidium beryllium borate
WO2012009945A1 (en) * 2010-07-20 2012-01-26 中国科学院新疆理化技术研究所 Barium fluoroborate, nonlinear optical crystal of barium fluoroborate, the production methods and uses thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103451730A (en) * 2012-06-05 2013-12-18 中国科学院理化技术研究所 Cd4RO(BO3)3 compound, Cd4RO(BO3)3 optical crystal, and preparation method and application thereof
CN103451730B (en) * 2012-06-05 2016-11-23 中国科学院理化技术研究所 Cd4rO (BO3)3compound, Cd4rO (BO3)3optical crystal and preparation method and purposes

Similar Documents

Publication Publication Date Title
CN101545138B (en) Non-linear optical crystal-sodium beryllate borate, growth method and application thereof
CN101498040B (en) K3B6O10 Br nonlinear optical crystal, preparation and use
CN101435108B (en) Large size nonlinear optical crystal lead bromoborate preparation method
CN101545141A (en) Sulfurized gallium and barium monocrystal as well as growing method and infrared nonlinear optical device thereof
CN102838093B (en) LiGaGe2Se6 compound, LiGaGe2Se6 nonlinear optical crystals, and preparation method and application thereof
CN103950912B (en) RbBa 2(PO 3) 5compound, RbBa 2(PO 3) 5non-linear optic crystal and method for making thereof and purposes
CN105668577A (en) K3Ba3Li2Al4B6O20F compound, K3Ba3Li2Al4B6O20F nonlinear optical crystal, preparation method and application thereof
CN103288058B (en) Li2In2GeSe6 compound and Li2In2GeSe6 nonlinear optical crystal as well as preparation methods and applications thereof
CN102976287A (en) BaGa2GeSe6 compound, BaGa2GeSe6 non-linear optical crystal and their preparation methods and use
CN102021640B (en) Aluminum-barium fluoborate (BaAlBo3F2) non-linear optical crystal, and growth method and application thereof
CN101984151B (en) Di lithium tetra borate rubidium nonlinear optic crystal, preparation method and application thereof
CN101295119A (en) Novel nonlinear optical crystal boric acid aluminum gallium bismuth
CN102352533B (en) Nonlinear optical crystal boric acid beryllium sodium caesium
CN101984149B (en) Method for preparing large chlorine barium borate nonlinear optic crystal and application thereof
CN102650075B (en) Non-linear optical crystal cadmium fluoroborate
CN101974783B (en) Compound cesium lithium borate (CLBO) nonlinear optical crystal, preparation method and application thereof
CN102660771A (en) Boric acid oxygen cadmium gadolinium as nonlinear optical crystal
CN1321228C (en) Boron aluminate, non-linear optic crystal of boron aluminate, growth method and usage
CN105502329A (en) RbNaMgP2O7 compound, RbNaMgP2O7 nonlinear optical crystal and preparing method and usage thereof
CN102260912A (en) Novel nonlinear optical crystal low-temperature phase kalium beryllium borate
CN102260911A (en) Novel nonlinear optical crystal medium temperature-phase potassium beryllium borate
CN103290479B (en) Li 2in 2siSe 6compound, Li 2in 2siSe 6non-linear optic crystal and method for making and purposes
CN103031602A (en) Nonlinear optical crystal potassium calcium carbonate fluoride
CN102660773A (en) Non-linear optical crystal boric acid cadmium yttrium oxide
CN102660772A (en) Nonlinear optics crystal boric acid of oxygen, cadmium and lutetium

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20120912