CN1974888A - Zr dopped lithium niobate crystal - Google Patents
Zr dopped lithium niobate crystal Download PDFInfo
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- CN1974888A CN1974888A CN 200610129356 CN200610129356A CN1974888A CN 1974888 A CN1974888 A CN 1974888A CN 200610129356 CN200610129356 CN 200610129356 CN 200610129356 A CN200610129356 A CN 200610129356A CN 1974888 A CN1974888 A CN 1974888A
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- lithium niobate
- crystal
- niobate crystal
- dopped
- photorefraction
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- Crystals, And After-Treatments Of Crystals (AREA)
- Optical Modulation, Optical Deflection, Nonlinear Optics, Optical Demodulation, Optical Logic Elements (AREA)
Abstract
The present invention belongs to the field of non-linear optical crystal technology, and is especially Zr doped lithium niobate crystal with Zr4+ doping amount greater than 0.01 mol%. The new photorefraction resisting doped ion Zr4+ of the present invention has low doping threshold, capacity of growing high quality crystal and high capacity of resisting photorefraction, and the crystal with Zr4+ over the threshold has the photorefraction resisting capacity 6 magnitudes higher than that of lithium niobate crystal and 3 magnitudes higher than that of (4.6 mol %) Mg doped lithium niobate crystal. The Zr doped lithium niobate crystal may be used in replacing high Mg doped lithium niobate crystal and has wide application.
Description
[technical field]: the invention belongs to the non-linear optic crystal technical field.
[background technology]: lithium niobate crystals is a kind of multi-functional, multiduty photoelectric material.A key property of lithium niobate crystals is that light is sold off, and it has opened up the application of crystal at aspects such as Hologram Storage, light amplification on the one hand, but has simultaneously limited its application at aspects such as frequency inverted, Q-switch, parametric oscillation, optical waveguidess again.Mixing some foreign ion in lithium niobate crystals is effective means, for example a Mg who improves the anti-light folding of lithium niobate crystals ability
2+, Zn
2+, Sc
3+, In
3+, Hf
4+Deng, what wherein be most widely used is to mix Mg2+ in lithium niobate crystals.But magnesium-doped lithium niobate crystal exists significantly not enough, the threshold concentration height that promptly mixes, and effective segregation coefficient is not equal to 1, is difficult to grow the crystal of high optical quality.Therefore, it is crucial seeking new anti-photorefraction dopant ion.
[summary of the invention]: the objective of the invention is to solve existing lithium niobate crystals and have doping threshold concentration height, effective segregation coefficient is not equal to 1, is difficult to grow the crystalline problem of high optical quality, and a kind of Zr dopped lithium niobate crystal is provided.
Zr dopped lithium niobate crystal provided by the invention is to mix zirconium ion Zr in lithium niobate crystals
4+, zirconium ion Zr
4+Incorporation greater than 0.01mol%.
The preparation of Zr dopped lithium niobate crystal is to use Czochralski grown.
Advantage of the present invention and effect: it is low that Zr dopped lithium niobate crystal provided by the invention has the doping threshold value, and the anti-photorefraction ability is strong, advantages such as easy growth.The threshold concentration of Zr dopped lithium niobate crystal is below 2mol%, and threshold value is low, and the impurity that mix is few, is easy to the crystal of growing high quality.Zr dopped lithium niobate crystal is after doping content reaches 2mol%, and crystal is 20MW/cm in light intensity
2Strong illumination under do not have light injury to produce, than improved 6 magnitudes with the composition lithium niobate crystals, improved 3 magnitudes than congruent magnesium (4.6mol%) lithium niobate crystals of mixing.
Zr dopped lithium niobate crystal provided by the invention can replace the application of highly magnesium-doped lithium niobate crystals fully, has huge market outlook.
[embodiment]:
Embodiment 1:
Take by weighing the ZrO of 2mol%
2[Li
2CO
3]/[Nb
2O
5The material of]=0.94.With the powder oven dry, thorough mixing 24 hours on mixer then 850 ℃ of constant temperature 2 hours, made Li 150 ℃ of following constant temperature 2 hours
2CO
3Fully decompose, became the double doping lithium niobate powder in 2 hours 1100 ℃ of calcinings.(2) with this powder compacting, be put in the platinum crucible, heat with intermediate frequency furnace, the Czochralski crystal pulling method along the c direction of principal axis by drawing process growth double-doped lithium niobate crystals such as neck, shouldering, isometrical, ending, pulling rate 1mm, rotating speed 14rpm, 20 ℃ of gas-liquid temperature differences, 1.5 ℃/mm of thermograde in the melt, the warm ladder in melt top is 1.0 ℃/mm.(3) crystal after the growth through operations such as orientation, cutting, grinding and polishings, can be mixed the lithium niobate crystals that zirconium is 2mol% in 1200 ℃ of polings, annealing.Observing crystal by the hot spot distortion is 20MW/cm in light intensity
2Strong illumination under do not have light injury to produce.And obtaining crystal under the high power laser light irradiation by holographic recording, the variation of crystal refractive index only is 0.71 * 10
-6
Embodiment 2:
Take by weighing the ZrO of 3mol%
2[Li
2CO
3]/[Nb
2O
5The material of]=0.94.With the powder oven dry, thorough mixing 24 hours on mixer then 850 ℃ of constant temperature 2 hours, made Li 150 ℃ of following constant temperature 2 hours
2CO
3Fully decompose, became the double doping lithium niobate powder in 2 hours 1100 ℃ of calcinings.(2) with this powder compacting, be put in the platinum crucible, heat with intermediate frequency furnace, the Czochralski crystal pulling method along the c direction of principal axis by drawing process growth double-doped lithium niobate crystals such as neck, shouldering, isometrical, ending, pulling rate 1mm, rotating speed 14rpm, 20 ℃ of gas-liquid temperature differences, 1.5 ℃/mm of thermograde in the melt, the warm ladder in melt top is 1.0 ℃/mm.(3) crystal after the growth through operations such as orientation, cutting, grinding and polishings, can be mixed the lithium niobate crystals that zirconium is 3mol% in 1200 ℃ of polings, annealing.Observing crystal by the hot spot distortion is 20MW/cm in light intensity
2Strong illumination under do not have light injury to produce.And obtaining crystal under the high power laser light irradiation by holographic recording, the variation of crystal refractive index only is 0.71 * 10
-6
Embodiment 3:
Take by weighing the ZrO of 5mol%
2[Li
2CO
2]/[Nb
2O
5The material of]=0.94.With the powder oven dry, thorough mixing 24 hours on mixer then 850 ℃ of constant temperature 2 hours, made Lic 150 ℃ of following constant temperature 2 hours
2O
3Fully decompose, became the double doping lithium niobate powder in 2 hours 1100 ℃ of calcinings.(2) with this powder compacting, be put in the platinum crucible, heat with intermediate frequency furnace, the Czochralski crystal pulling method along the c direction of principal axis by drawing process growth double-doped lithium niobate crystals such as neck, shouldering, isometrical, ending, pulling rate 1mm, rotating speed 14rpm, 20 ℃ of gas-liquid temperature differences, 1.5 ℃/mm of thermograde in the melt, the warm ladder in melt top is 1.0 ℃/mm.(3) growth after crystal in 1200 ℃ of polings, annealing, through operations such as orientation, cutting, grinding and polishings, can mix zirconium is 5mol%, lithium niobate crystals.Observing crystal by the hot spot distortion is 20MW/cm in light intensity
2Strong illumination under do not have light injury to produce.And obtaining crystal under the high power laser light irradiation by holographic recording, the variation of crystal refractive index only is 0.61 * 10
-6
More than three real row proof Zr dopped lithium niobate crystals of the present invention are optical materials that a kind of threshold value of mixing is low, the anti-photorefraction ability is strong.
Claims (1)
1, a kind of Zr dopped lithium niobate crystal is characterized in that mixing zirconium ion Zr in lithium niobate crystals
4+, zirconium ion Zr
4+Incorporation greater than 0.01mol%.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006101293560A CN100497758C (en) | 2006-11-11 | 2006-11-11 | Zr dopped lithium niobate crystal |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006101293560A CN100497758C (en) | 2006-11-11 | 2006-11-11 | Zr dopped lithium niobate crystal |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1974888A true CN1974888A (en) | 2007-06-06 |
| CN100497758C CN100497758C (en) | 2009-06-10 |
Family
ID=38125228
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2006101293560A Expired - Fee Related CN100497758C (en) | 2006-11-11 | 2006-11-11 | Zr dopped lithium niobate crystal |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN100497758C (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102296365A (en) * | 2010-06-24 | 2011-12-28 | 南开大学 | vanadium-doped lithium niobate crystal |
| CN106929917A (en) * | 2017-04-25 | 2017-07-07 | 南开大学 | A kind of 90 ° of double-doped lithium niobate crystals of phase matched of room temperature |
| JP2021070605A (en) * | 2019-10-30 | 2021-05-06 | 住友金属鉱山株式会社 | Method for growing oxide single crystal |
-
2006
- 2006-11-11 CN CNB2006101293560A patent/CN100497758C/en not_active Expired - Fee Related
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102296365A (en) * | 2010-06-24 | 2011-12-28 | 南开大学 | vanadium-doped lithium niobate crystal |
| CN102296365B (en) * | 2010-06-24 | 2014-03-05 | 南开大学 | Vanadium-doped lithium niobate crystal |
| CN106929917A (en) * | 2017-04-25 | 2017-07-07 | 南开大学 | A kind of 90 ° of double-doped lithium niobate crystals of phase matched of room temperature |
| JP2021070605A (en) * | 2019-10-30 | 2021-05-06 | 住友金属鉱山株式会社 | Method for growing oxide single crystal |
| JP7294063B2 (en) | 2019-10-30 | 2023-06-20 | 住友金属鉱山株式会社 | Oxide single crystal growth method |
Also Published As
| Publication number | Publication date |
|---|---|
| CN100497758C (en) | 2009-06-10 |
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Granted publication date: 20090610 Termination date: 20121111 |