Patent Application
20160145769
The present invention belongs to the fields of materials science and optics in the inorganic chemistry field, particularly relates a deep ultraviolet non-linear optical crystal of barium borate hydrate having a chemical formula of Ba2B11O22H7, and a preparation method and use thereof.
Discovery of laser has brought great changes to human civilization. In 1960, Maiman succeeded in producing the first ruby laser in the world. Since the laser has characteristics such as high energy density, high directivity and coherence, it has a wide range of applications in many areas and has been combined with a number of disciplines to form several application technologies, such as photovoltaic technology, laser medical treatment and photobiology, laser processing, laser detection and measurement technology, laser holography, laser radar, laser guidance, laser isotope separation, laser controlled nuclear fusion, laser weapons, and so on. The laser obtained directly by using a laser crystal is limited in wave band, while using the frequency conversion crystals can convert a laser at a limited wavelength into a laser in a new band, which is a key means of obtaining new laser sources. However, the key issue of achieving high-efficiency conversion in laser wavelength is the availability of a high-quality and excellent-performance non-linear optical crystal.
In 1961, Franken et al. observed the frequency-doubled effect in the quartz crystal for the first time, which not only marked the naissance of the non-linear optical discipline, but also strongly promoted the development of non-linear optical material science. Non-linear optical crystal has frequency conversion effect, electro-optic effect, photorefractive effect etc., and can be used in the fields of laser frequency conversion, electro-optical modulation, signal processing and the like. It is an important basic material for the growing optoelectronics industry and an important mainstay for the development of solid-state laser technology, infrared technology, optical communication and information processing and other fields, and is playing a more and more important role in scientific research, industries, transportation, national defense, health care and the like. Over the past decade, although the non-linear optical crystals for blue/green light and ultraviolet (UV) and deep ultraviolet (DUV) have attracted broad attention, these crystals have their limitations and have been difficult to obtain a wider range of applications. For example, the β-BaB2O4 (BBO) crystal has photorefractive effect at its quadruplicated frequency, which hinders the application of quadniplicated frequency. Additionally, the β-BaB2O4 (BBO) crystal has a small receiving angle and a large walk-off angle, so in order to obtain high conversion efficiency, it is required that the pump laser beam has good beam quality (low divergence angle and good mode). The 1390 crystal would be deliquescent to some extent, causing some inconvenience while using. The LiB3O5 (LBO) crystal is deliquescent to some extent as well. Neither of these two crystals can generate a light below 200 nm by direct frequency doubling. The layers of the KBe2BO3F2 (KBBF) crystal are associated with each other via ionic bonds between K and F, i.e. the bonding force between the layers is weak, for this reason, it has a strong layer-by-layer growth habit and is difficult to grow thick, difficult to process and easy to dissociate, and thus difficult for practical use. Therefore, there is an urgent need to develop a practical new non-linear optical crystal having better performance and matching shorter wave band, and many countries around the world are actively looking for such a new non-linear optical crystal.
In recent years, when developing new non-linear optical crystals, it is not only focused on the optical and mechanical properties, but also more emphasizing on the preparation characteristics. It is hoped that the new crystal materials are easy to prepare so as to obtain low-price, high-quality and large-size non-linear optical crystals. Under the guide of the design concept of introducing alkaline earth metal cations into the boron-oxygen framework to improve the performance, the anions, taking boron-oxygen primitives as the foundation, have large band gaps, small probability of two-photon absorption and high laser damage threshold, and is helpful to obtain strong non-linear optical effects; the B—O bonds facilitate transmission of broad band light. The cations selecting from alkaline earth metal ions have no transition of d0 electrons in the ultraviolet region, which is conductive to ultraviolet transmission.
The objective of the present invention is to provide a transparent deep ultraviolet non-linear optical crystal of barium borate hydrate Ba2B11O22H7 in order to fill in the spectrum blank in wavelengths of the lasers emitted by various laser devices.
Another objective of the present invention is to provide a method for preparing the deep ultraviolet non-linear optical crystal of barium borate hydrate Ba2B11O22H7 in an easy and simple way of using a hydrothermal method.
Yet another objective of the present invention is to provide a use of the Ba2B11O22H7 non-linear optical device.
The technical schemes of the present invention are described as follows:
The deep ultraviolet non-linear optical crystal of barium borate hydrate provided in the present invention has a chemical formula of Ba2B11O22H7, belongs to the monoclinic system, has a space group of P21, with lattice parameters of a=6.7719(10) Å, b=21.1195(4) Å, c=6.8274(10) Å. β=119.3950(10)° and a molecular weight of 752.65.
The method for preparing said deep ultraviolet non-linear optical crystal of barium borate hydrate Ba2B11O22H7 uses the hydrothermal method to prepare the crystals, and is conducted specifically according to the following steps:
(a) BaCl2, Ba(CH3COO)2.H2O, BaSO4, Ba(ClO4)2, BaCO3 or Ba(NO3)2 is added into the polytetrafluoroethylene liner of a 23-125 ml, high-pressure reactor, H3BO3 or B2O3 is then added, and then 8-70 mL of deionized water is added, followed by mixing uniformly to obtain a mixture solution;
In Step (a), the molar ratio of Ba2+ to BO33− is 1:0.3-6; the molar ratio of Ba2+ to B2O3 is 1:0.15-3;
(b) Into the mixture solution of Step (a), a mineralizer lithium hydroxide, sodium hydroxide, potassium hydroxide, ammonia or ethylenediamine is added and mixed, wherein the volume ratio of mineralizer to mixture solution is 1:2-70;
(c) The lid of the polytetrafluoroethylene liner charged with the mixture solution of Step (b) is tightened, and then the polytetrafluoroethylene liner is loaded into the corresponding high-pressure reactor, followed by tightening the piston of the reactor;
(d) The high-pressure reactor of Step (c) is placed in a thermotank, heated to 120-210 ° C. at a rate of 20-60 ° C./h, held at this temperature for 3-25 days, and then cooled to room temperature by slow cooling at a rate of 1-50 ° C./h or natural cooling;
(e) The high-pressure reactor is opened and the solution containing the crystal is filtered to obtain a transparent non-linear optical crystal of barium borate hydrate Ba2B11O22H7 as analyzed and identified by X-Ray Single Crystal Diffactometor.
In Step (c), the solution is placed in a clean and contamination-free high-pressure reactor.
The deep ultraviolet non-linear optical crystal of barium borate hydrate Ba2B11O22H7 in the present invention is prepared by the hydrothermal method according to the following chemical reaction equations:
2BaCl2+11H3BO3→Ba2B11O22H7+4Cl−+11H2O+4H+ (1)
2Ba(CH3COO)2.H2O+11H3BO3→Ba2B11O22H7+4CH3COO−+13H2O+4H+ (2)
2BaSO4+11H3BO3→Ba2B11O22H7+2SO42−+11H2O+4H+ (3)
2Ba(ClO4)2+11H3BO3→Ba2B11O22H7+4ClO4−+11H2O+4H+ (4)
2BaCO3+11H3BO3→Ba2B11O22H7+2CO32−+11H2O+4H+ (5)
2Ba(NO3)2+11H3BO3→Ba2B11O22H7+4NO3−+11H2O+4H+ (6)
2BaCl2+11/2B2O3+11/2H2O→Ba2B11O22H7+4Cl−+4H+ (7)
2Ba(CH3COO)2+11/2B2O3+11/2H2O→Ba2B11O22H7+4CH3COO−+4H+ (8)
2BaSO4+11/2B2O3+11/2H2O→Ba2B11O22H7+2SO42−+4H+ (9)
2Ba(ClO4)2+11/2B2O3+11/2H2O→Ba2B11O22H7+4ClO4−+4H+ (10)
2BaCO3+11/2B2O3+11/2H2O→Ba2B11O22H7+2CO32−+4H+ (11)
2Ba(NO3)2+11/2B2O3+11/2H2O→Ba2B11O22H7+4NO3−+4H+ (12)
The present invention provides a use of the deep ultraviolet non-linear optical crystal of barium borate hydrate Ba2B11O22H7, wherein the non-linear optical crystal of barium borate hydrate Ba2B11O22H7 is used for preparing non-linear optical devices, including frequency doubling generator, upper frequency converter, lower frequency converter, optical parametric oscillator, that is allowing for transmission of at least one beam of fundamental wave of incident light to generate at least one beam of coherent light at a different frequency from the incident light.
The invention has the following advantages:
The deep ultraviolet non-linear optical crystal of barium borate hydrate Ba2B11O22H7 provided in the present invention has an ultraviolet cutoff edge of below 175 nm, a non-linear optical effect of about 2 times as much as that of KDP, a space group of P21. For the crystal, the preparation is simple, the growth cycle is short, and the starting material used has low toxicity and little poison to human. The method for preparing the crystal comprises mixing the starting materials at a certain ratio, using the hydrothermal method to allow for a high-temperature and high-pressure reaction in a sealed reactor at a certain temperature range and then obtain the transparent deep ultraviolet non-linear optical crystal of barium borate hydrate Ba2B11O22H7 in a way of programmed cooling or holding at constant temperature, wherein the process is simple and easy to operate. The resulting deep ultraviolet non-linear optical crystal of barium borate hydrate Ba2B11O22H7 has no special requirement for the precision of optical processing and can be used to prepare non-linear optical devices, including frequency doubling generator, upper frequency converter, lower frequency converter or optical parametric oscillator.
The present invention will be described in details hereinafter in combination of the accompanying drawings and the following examples:
The crystal was prepared according to
2BaCl2+11H3BO3→Ba2B11O22H7+4Cl−+11H2O+4H+
and the specific procedure as follows:
(a) According to a molar ratio of BaCl2:H3BO3=1:4, BaCl2 was added into the polytetrafluoroethylene liner of a 23 mL high-pressure reactor. H3BO3 was then added, and then 10 mL of deionized water was added, followed by mixing uniformly to obtain a mixture solution;
(b) Into the mixture solution of Step (a), a mineralizer 1 mL of 3 mol/L LiOH solution was added and mixed, wherein the volume ratio of the mineralizer to the mixture solution was 1:10;
(c) The lid of the polytetrafluoroethylene liner charged with the mixture solution of Step (b) was tightened, and then the polytetrafluoroethylene liner was loaded into the corresponding clean and contamination-free high-pressure reactor, followed by tightening the piston of the reactor;
(d) The high-pressure reactor of Step (c) was placed in a thermotank, heated to 180° C. at a rate of 20° C./h, held at this temperature for 3 days, followed by slowly cooling to room temperature at a rate of 2° C./h;
(e) The high-pressure reactor was opened and the solution containing the crystal was filtered repeatedly to obtain a relatively transparent Ba2B11O22H7 non-linear optical crystal as analyzed and identified by X-Ray Single Crystal Diffactometor.
The crystal was prepared according to
2Ba(CH3COO)2.H2O+11H3BO3→Ba2B11O22H7+4CH3COO−+13H2O+4H+
and the specific procedure as follows:
(a) According to a molar ratio of Ba(CH3COO)2.H2O:H3BO3=1:2, Ba(CH3COO)2.H2O was added into the polytetrafluoroethylene liner of a 80 mL high-pressure reactor, H3BO3 was then added, and then 35 mL of deionized water was added, followed by mixing uniformly to obtain a mixture solution;
(b) Into the mixture solution of Step (a), a mineralizer 0.5 mL of 3 mol/L NaOH solution was added and mixed, wherein the volume ratio of the mineralizer to the mixture solution was 1:70;
(c) The lid of the polytetrafluoroethylene liner charged with the mixture solution of Step (b) was tightened, and then the polytetrafluoroethylene liner was loaded into the corresponding clean and contamination-free high-pressure reactor, followed by tightening the piston of the reactor;
(d) The high-pressure reactor of Step (c) was placed in a thermotank, heated to 200° C. at a rate of 30° C./h, held at this temperature for 6 days, followed by naturally cooling to room temperature;
(e) The high-pressure reactor was opened and the solution containing the crystal was filtered repeatedly to obtain a relatively transparent Ba2B11O22H7 non-linear optical crystal as analyzed and identified by X-Ray Single Crystal Diffactometor.
The crystal was prepared according to
2BaSO4+11H3BO3→Ba2B11O22H7+2SO42−+11H2O+4H+
and the specific procedure as follows:
(a) According to a molar ratio of BaSO4:H3BO3=1:6, BaSO4 was added into the polytetrafluoroethylene liner of a 23 mL high-pressure reactor, H3BO3 was then added, and then 10 mL of deionized water was added, followed by mixing uniformly to obtain a mixture solution;
(b) Into the mixture solution of Step (a), a mineralizer 0.5 mL of 3 mol/L KOH solution was added and mixed, wherein the volume ratio of the mineralizer to the mixture solution was 1:20;
(c) The lid of the polytetrafluoroethylene liner charged with the mixture solution of Step (b) tightened, and then the polytetrafluoroethylene liner was loaded into the corresponding clean and contamination-free high-pressure reactor, followed by tightening the piston of the high-pressure reactor;
(d) The high-pressure reactor of Step (c) was placed in a thermotank, heated to 210° C. at a rate of 50° C./h, held at this temperature for 10 days, followed by slowly cooling to room temperature at a rate of 30° C./h;
(e) The high-pressure reactor was opened and the solution containing the crystal was filtered to obtain a transparent Ba2B11O22H7 non-linear optical crystal as analyzed and identified by X-Ray Single Crystal Diffactometor,
The crystal was prepared according to
2Ba(ClO4)2+11H3BO3→Ba2B11O22H7+4ClO4−+11H2O+4H+
and the specific procedure as follows:
(a) According to a molar ratio of Ba(ClO4)2:H3BO3=1:5, Ba(ClO4)2 was added into the polytetrafluoroethylene liner of a 125 mL high-pressure reactor, H3BO3 was then added, and then 70 mL of deionized water was added, followed by mixing uniformly to obtain a mixture solution;
(b) Into the mixture solution of Step (a), a mineralizer 5 mL of ethylenediamine was added and mixed, wherein the volume ratio of the mineralizer to the mixture solution was 1:14;
(c) The lid of the polytetrafluoroethylene liner charged with the mixture solution of Step (b) was tightened, and then the polytetrafluoroethylene liner was loaded into the corresponding clean and contamination-free high-pressure reactor, followed by tightening the piston of the reactor;
(d) The high-pressure reactor of Step (c) was placed in a thermotank, heated to 120° C. at a rate of 25° C./h, held at this temperature for 25 days, followed by naturally cooling to room temperature;
(e) The high-pressure reactor was opened and the solution containing the crystal was filtered to obtain a transparent Ba2B11O22H7 non-linear optical crystal as analyzed and identified by X-Ray Single Crystal Diffactometor.
The crystal was prepared according to
2BaCO3+11H3BO3→Ba2B11O22H7+2CO32−+11H2O+4H+
and the specific procedure as follows:
(a) According to a molar ratio of BaCO3:H3BO3=1:6, BaCO3 was added into the polytetrafluoroethylene liner of a 23 mL high-pressure reactor, H3BO3 was then added, and then 10 mL of deionized water was added, followed by mixing uniformly to obtain a mixture solution;
(b) Into the mixture solution of Step (a), a mineralizer 5 mL of ammonia was added and mixed, wherein the volume ratio of the mineralizer and the mixture solution was 1:2;
(c) The lid of the polytetrafluoroethylene liner charged with the mixture solution of Step (b) was tightened, and then the polytetrafluoroethylene liner was loaded into the corresponding clean and contamination-free high-pressure reactor, followed by tightening the piston of the reactor;
(d) The high-pressure reactor of Step (c) was placed in a thermotank, heated to 210° C. at a rate of 40° C./h, held at this temperature for 6 days, followed by slowly cooling to room temperature at a rate of 25° C./h;
(e) The high-pressure reactor was opened and t le solution containing the crystal was filtered to obtain a transparent Ba2B11O22H7 non-linear optical crystal as analyzed and identified by X-Ray Single Crystal Diffactometor.
The crystal was prepared according to
2Ba(NO3)2+11H3BO3→Ba2B11O22H7+4NO3−+11H2O+4H+
and the specific procedure as follows:
(a) According to a molar ratio of Ba(NO3)2:H3BO3=1:0.3, Ba(NO3)2 was added into the polytetrafluoroethylene liner of a 23 mL high-pressure reactor, H3BO3 was then added, and then 10 mL of deionized water was added, followed by mixing uniformly to obtain a mixture solution;
(b) Into the mixture solution of Step (a), a mineralizer 0.5 mL of KOH was added and mixed, wherein the volume ratio of the mineralizer to the mixture solution was 1:20;
(c) The lid of the polytetrafluoroethylene liner charged with the mixture solution of Step (b) was tightened, and then the polytetrafluoroethylene liner was loaded into the corresponding clean and contamination-free high-pressure reactor, followed by tightening the piston of the reactor;
(d) The high-pressure reactor of Step (c) was placed in a thermotank, heated to 210° C. at a rate of 40° C./h, held at this temperature for 6 days, followed by slowly cooling to room temperature at a rate of 25° C./h;
(e) The high-pressure reactor was opened and the solution containing the crystal was filtered to obtain a transparent Ba2B11O22H7 non-linear optical crystal as analyzed and identified by X-Ray Single Crystal Diffactometor.
The crystal was prepared according to
2BaCl2+11/2B2O3+11/2H2O→Ba2B11O22H7+4Cl−+4H+
and the specific procedure as follows:
(a) According to a molar ratio of BaCl2:B2O3=1:2, BaCl2 was added was added into the polytetrafluoroethylene liner of a 23 mL high-pressure reactor, B2O3 was then added, and then 10 mL of deionized water was added, followed by mixing uniformly to obtain a mixture solution;
(b) Into the mixture solution of Step (a), a mineralizer 1 mL of 3 mol/L LiOH solution was added and mixed, wherein the volume ratio of the mineralizer and the mixture solution was 1:10;
(c) The lid of the polytetrafluoroethylene liner charged with the mixture solution of step (b) was tightened, and then the polytetrafluoroethylene liner was loaded into the corresponding clean and contamination-free high-pressure reactor, followed by tightening the piston of the reactor;
(d) The high-pressure reactor of Step (c) was placed in a thermotank, heated to 180° C. at a rate of 20° C./h, increased, held at this temperature for 3 days, followed by slowly cooling to room temperature at a rate of 2° C./h;
(e) The high-pressure reactor was opened and the solution containing the crystal was filtered repeatedly to obtain a relatively transparent Ba2B11O22H7 non-linear optical crystal as analyzed and identified by X-Ray Single Crystal Diffactometor.
The crystal was prepared according to
2Ba(CH3COO)2.H2O+11/2B2O3+11/2H2O→Ba2B11O22H7+4CH3COO−+4H+
and the specific procedure as follows:
(a) According to a molar ratio of Ba(CH3COO)2.H2O:B2O3=1:1, Ba(CH3COO)2.H2O was added into the polytetrafluoroethylene liner of a 80 mL high-pressure reactor, B2O3 was then added, and then 35 mL of deionized water was added, followed by mixing uniformly to obtain a mixture solution;
(b) Into the mixture solution of Step (a), a mineralizer 0.5 mL of 3 mol/L NaOH solution was added and mixed, wherein the volume ratio of the mineralizer and the mixture solution was 1:70;
(c) The lid of the polytetrafluoroethylene liner charged with the mixture solution of Step (b) was tightened, and then the polytetrafluoroethylene liner was loaded into the corresponding clean and contamination-free high-pressure reactor, followed by tightening the piston of the reactor;
(d) The high-pressure reactor of Step (c) was placed in a thermotank, heated to 200° C. at a rate of 30° C./h, held at this temperature for 6 days, followed by naturally cooling to room temperature;
(e) The high-pressure reactor was opened and the solution containing the crystal was filtered repeatedly to obtain a relatively transparent Ba2B11O22H7 non-linear optical crystal as analyzed and identified by X-Ray Single Crystal Diffactometor.
The crystal was prepared according to
2BaSO4+11/2B2O3+11/2H2O→Ba2B11O22H7+2SO42−+4H+
and the specific procedure as follows:
(a) According to a molar ratio of BaSO4:B2O3=1.3. BaSO4 was added into the polytetrafluoroethylene liner of a 23 mL high-pressure reactor, B2O3 was then added, and then 10 mL of deionized water was added, followed by mixing uniformly to obtain a mixture solution;
(b) Into the mixture solution of Step (a), a mineralizer 0.5 mL of 3 mol/L KOH solution was added and mixed, wherein the volume ratio of the mineralizer and the mixture solution was 1:20;
(c) The lid of the polytetrafluoroethylene liner charged with the mixture solution of Step (b) was tightened, and then the polytetrafluoroethylene liner was loaded into the corresponding clean and contamination-free high-pressure reactor, followed by tightening the piston of the reactor;
(d) The high-pressure reactor of Step (c) was placed in a thermotank, heated to 210° C. at a rate of 50° C./h, held at this temperature for 10 days, followed by slowly cooling to room temperature at a rate of 30° C./h;
(e) The high-pressure reactor was opened and the solution containing the crystal was filtered to obtain a transparent Ba2B11O22H7 non-linear optical crystal as analyzed and identified by X-Ray Single Crystal Diffactometor.
The crystal was prepared according to
2Ba(ClO4)2+11/2B2O3+11/2H2O→Ba2B11O22H7+4ClO4−+4H+
and the specific procedure as follows:
(a) According to a molar ratio of Ba(ClO4)2:B2O3=1:2.5, Ba(ClO4)2 was added into the polytetrafluoroethylene liner of a 125 mL high-pressure reactor, B2O3 was then added, and then 70 mL of deionized water was added, followed by mixing uniformly to obtain a mixture solution;
(b) Into the mixture solution of Step (a), a mineralizer 5 mL of ethylenediamine was added and mixed, wherein the volume ratio of the mineralizer and the mixture solution was 1:14;
(c) The lid of the polytetrafluoroethylene liner charged with the mixture solution of Step (b) was tightened, and then the polytetrafluoroethylene liner was loaded into the corresponding clean and contamination-free high-pressure reactor, followed by tightening the piston of the reactor;
(d) The high-pressure reactor of Step (c) was placed in a thermotank, heated to 120° C. at a rate of 25° C./h, held at this temperature for 25 days, followed by naturally cooling to room temperature;
(e) The high-pressure reactor was opened and the solution containing the crystal was filtered to obtain a transparent Ba2B11O22H7 non-linear optical crystal as analyzed and identified by X-Ray Single Crystal Diffactometor.
The crystal was prepared according to
2BaCO3+11/2B2O3+11/2H2O→Ba2B11O22H7+2CO32−+4H+
and the specific procedure as follows:
(a) According to a molar ratio of BaCO3:B2O3=1:3, BaCO3 was added into the polytetrafluoroethylene liner of a 23 mL high-pressure reactor, B2O3 was then added, and then 10 mL of deionized water was added, followed by mixing uniformly to obtain a mixture solution;
(b) Into the mixture solution of Step (a), a mineralizer 5 mL of ammonia was added and mixed, wherein the volume ratio of the mineralizer and the mixture solution was 1:2;
(c) The lid of the polytetrafluoroethylene liner charged with the mixture solution of Step (b) was tightened, and then the polytetrafluoroethylene liner was loaded into the corresponding clean and contamination-free high-pressure reactor, followed by tightening the piston of the reactor;
(d) The high-pressure reactor of Step (c) was placed in a thermotank, heated to 210° C. at a rate of 40° C./h, increased, held at this temperature for 6 days, followed by slowly cooling to room temperature at a rate of 25° C./h;
(e) The high-pressure reactor was opened and the solution containing the crystal was filtered to obtain a transparent Ba2B11O22H7 non-linear optical crystal as analyzed and identified by X-Ray Single Crystal Diffactometor.
The crystal was prepared according to
2Ba(NO3)2+11/2B2O3+11/2H2O→Ba2B11O22H7+4NO3−+4H+
and the specific procedure as follows:
(a) According to a molar ratio of Ba(NO3)2:B2O3=1:0.15, Ba(NO3)2 was added into the polytetrafluoroethylene liner of a 23 mL high-pressure reactor, B2O3 was then added, and then 10 mL of deionized water was added, followed by mixing uniformly to obtain a mixture solution;
(b) Into the mixture solution of Step (a), a mineralizer 0.5 mL of KOH was added and mixed, wherein the volume ratio of the mineralizer and the mixture solution was 1:20;
(c) The lid of the polytetrafluoroethylene liner charged with the mixture solution of Step (b) was tightened, and then the polytetrafluoroethylene liner was loaded into the corresponding clean and contamination-free high-pressure reactor, followed by tightening the piston of the reactor;
(d) The high-pressure reactor of Step (c) was placed in a thermotank, heated to 210° C. at a rate of 40° C./h, held at this temperature for 6 days, followed by slowly cooling to room temperature at a rate of 25° C./h;
(e) The high-pressure reactor was opened and the solution containing the crystal was filtered to obtain a transparent Ba2B11O22H7 non-linear optical crystal as analyzed and identified by X-Ray Single Crystal Diffactometor.
Any one of the non-linear optical crystals obtained in Examples 1-12 was arranged at the position (3) as shown in
As shown in
| Number | Date | Country | Kind |
|---|---|---|---|
| 201310504643.5 | Oct 2013 | CN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2014/071241 | 1/23/2014 | WO | 00 |
