Cesium-lithium-borate crystal and its application to frequency conversion of laser light

The present invention provides a cesium-lithium-borate crystal, which can be used as a high-performance wavelength converting crystal, having a chemical composition expressed as CsLiB6O10, and substituted cesium-lithium-borate crystals expressed by the following formula:

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Description
FIELD OF THE INVENTION

[0001] The present invention relates to a cesium-lithium-borate crystal and crystals with substituted chemical compositions thereof. More particularly, the present invention relates to a cesium-lithium-borate crystal and crystals with substituted chemical compositions thereof which are used as frequency converting nonlinear optical crystals in laser oscillators and optical parametric oscillators used in blue and ultraviolet lithography, laser microprocessing, scientific and industrial measurement and laser nuclear fusion, a method for manufacturing same, and an optical apparatus using same.

PRIOR ART AND PROBLEMS

[0002] Laser oscillators used in ultraviolet lithography, laser microprocessing, scientific and industrial measurement and laser nuclear fusion must generate stable blue and ultraviolet rays efficiently. One of the methods to achieve the above object which is attracting the general attention to day is the method to efficiently obtain blue and ultra-violet rays by frequency conversion of a light source using nonlinear optical crystals.

[0003] A pulse YAG laser oscillator, a type of laser oscillators, for example, uses nonlinear optical crystals to convert frequency of a light source to generate the third (wavelength: 355 nm) or the fourth (wavelength: 266 nm) harmonics of the pulse YAG laser.

[0004] Many contrivances on the frequency converting non-linear optical crystals which are indispensable for generating ultraviolet rays have been announced. For example, beta barium methaborate (&bgr;-BaB2O4), lithium triborate (LiB3O5), cesium triborate (CsB3O5) and other borate crystals are known. These frequency converting nonlinear optical crystals for generating blue and ultraviolet rays will pass wavelengths of 200 nm and below, and have a large nonlinear optical coefficient.

[0005] It is very difficult, however, to grow crystals of &bgr;-BaB2O4, one of such frequency converting nonlinear optical crystals, because of the tendency of causing phase transition in the production process. Further, angular allowance is very tight, and thus this particular substance has a very low level of generality.

[0006] Furthermore, for LiB3O5 other frequency converting nonlinear optical crystal, the growth timeis very long as a result of flux growth in the production process, and this crystal is only good for phase matching for rays down to about 555 nm wavelengths for second harmonic generation. This crystal is used, for example, for generation of the third harmonic (wavelength: 355 nm) of Nd-YAG lasers, but cannot be used for generating the fourth harmonic (wavelength: 266 nm).

SUMMARY OF THE INVENTION

[0007] The present invention was developed to overcome the above-mentioned drawbacks of the prior art and has an object to provide a cesium-lithium-borate crystal and crystals with substituted chemical compositions which are high-performance frequency converting nonlinear optical crystals that pass shorter wavelengts, have a high conversion efficiency, and have a large temperature and angular allowance, a method for manufacturing such crystals, and a method for utilizing same.

[0008] As means to solve the above-mentioned problems, the present invention provides a cesium-lithium-borate crystal having a chemical composition expressed as CsLiB6O10.

[0009] The present invention provides also a substituted cesium-lithium-borate crystal having a chemical composition expressed by the following formula:

Cs1−xLi1−yMx+yB6O10

[0010] (where, M is at least one alkali metal element other than Cs and Li, and x and y satisfy the relationship of 0≦x≦1 and 0≦y≦1, and x and y never take simultaneously a value of 0 or 1), or the following formula:

Cs2(1−z)Li2LzB12O20

[0011] (where, L is at least one alkali earth metal element, and 0z<1).

[0012] Furthermore, the present invention provides also a method for manufacturing the above-mentioned crystals by heating and melting a raw material mixture of constituent elements, a method for manufacturing the above-mentioned crystals through growth by the melt methods comprising the crystal pulling method and top seeded kyropoulos method, and a method for manufacturing the above-mentioned crystals through growth by the flux method.

[0013] The present invention furthermore provides a frequency converter and an optical parametric oscillator provided with the above cesium-lithium-borate crystal or the crystal with a substituted chemical composition as optical means.

BRIEF DESCRIPTION OF THE DRAWINGS

[0014] FIG. 1 shows a structural view illustrating an example of structure of a five-zone furnace for growing a cesium-lithium-borate crystal which is an embodiment of the present invention.

[0015] FIG. 2 shows a three-dimensional structural diagram illustrating the structure of the cesium-lithium-borate crystal of the present invention.

[0016] FIG. 3 shows a graph illustrating transmission spectrum of the cesium-lithium-borate crystal of the present invention.

[0017] FIG. 4 shows a graph illustrating the refractive index dispersion curve for the cesium-lithium-borate crystal of the present invention.

[0018] FIG. 5 shows a relational diagram illustrating the relationship between the mixing ratio of boron oxide (B2O3) and temperature during manufacture of the cesium-lithium-borate crystal of the present invention.

[0019] FIG. 6 shows a graph illustrating the relationship between the phase matching angle &thgr; and the incident laser wavelength of a crystal capable of generating the second harmonic (SHG) in Nd:YAG laser with the cesium-lithium-borate crystal which is an embodiment of the present invention.

[0020] FIG. 7 shows a graph illustrating the relationship between the walk-off angle and the incident laser wavelength in Nd:YAG laser of a cesium-lithium-borate crystal which is an embodiment of the present invention.

[0021] FIG. 8 shows a graph illustrating the fourth harmonic generating characteristics of a cesium-lithium-borate crystal which is an embodiment of the present invention.

[0022] FIG. 9 shows a graph illustrating a theoretical curve of non-critical phase matching wavelength resulting from generation of a sum frequency, and wavelength of the resultant sum frequency for a cesium-lithium-borate crystal which is an embodiment of the present invention.

[0023] FIG. 10 is a photograph taking the place of a drawing of the fifth harmonic, and the second and fourth harmonics of Nd:YAG laser available by the generation of sum frequency for a cesium-lithium-borate crystal which is an embodiment of the present invention.

[0024] FIG. 11 shows a schematic representation of the beam pattern of the fifth harmonic, and the second and fourth harmonics of Nd:YAG laser available by the generation of sum frequency for a cesium-lithium-borate crystal which is an embodiment of the present invention.

[0025] FIG. 12 shows a graph illustrating the phase matching tuning curve of Type-I OPO using a cesium-lithium-borate crystal which is an embodiment of the present invention with wavelengths of the excited light of 213 nm, 266 nm, 355 nm and 532 nm.

[0026] FIG. 13 shows a A graph illustrating the phase matching tuning curve of Type-II OPO using a cesium-lithium-borate crystal which is an embodiment of-the present invention with a wavelength of the excited light of 532 nm; and

[0027] FIG. 14 shows a graph illustrating power X-ray diffraction data regarding Cs1−xLiRbxB6O10 crystal.

DETAILED DESCRIPTOIN OF THE INVENTION

[0028] The present inventor noticed the fact that the borate crystals such as beta-barium methaborate (&bgr;-BaB2O4), lithium triborate (LiB3O5), and cesium triborate (CsB3O5), which are conventionally used as frequency converting nonlinear optical crystals for generating blue and ultraviolet rays, were generally borate crystals containing independent metals, and found that high-performance borate crystals never seen before can be realized by adding a plurality of kinds of metal ions.

[0029] The present inventor produced several kinds of borate crystals containing ions of two or more kinds of metals such as an alkali metal and an alkali earth metal, and irradiated them with an Nd YAG laser (wavelength: 1,064 nm) to generate the second harmonic (wavelength: 532 nm) in order to find an optimum metal combination through a number of experimental verifications.

[0030] As a result, he has found that the borate crystals containing both Cs and Li, in particular, generate very strong second harmonic, and has developed totally new crystals including the cesium-lithium-borate crystal and crystals with substituted chemical compositions thereof of the present invention.

[0031] Prescribed crystals of the present invention are manufactured by heating and melting a mixture of raw materials such as cesium carbonate (Cs2CO3), lithium carbonate (Li2CO3) and boron oxide (B2O3). The reaction is expressed, for example, by the following formula:

Cs2CO3+Li2CO3+6B2O3−2CsLiB6O10+2CO2

or

Cs2CO3+Li2CO3+12H3BO3−2CsLiB6O10+2CO2→+18H2O→

[0032] As a cesium-lithium-borate crystal substituted by an alkali metal element or an alkali earth metal element (M) other than Cs and Li, there is conceivable a crystal using an arbitrary alkali metal element other than Cs and Li, as expressed by the following formula:

Cs1−xLi1−yMx+yB6O10

[0033] Examples of composition include a composition with 0<x≦0.01 when the alkali metal element (M) is Na (sodium), a composition with 0<x≦0.1 when M is K (potassium), and a composition with 0<x≦1 when M is Rb (rubidium) as being within a suitable range from the point of view of manufacture and physical properties. It is needless to mention that a plurality of alkali metal elements may be added.

[0034] By adding these alkali metal ions, it is possible to change the refractive index and phase matching angle, and to improve angular allowance and temperature allowance, and by simultaneously causing a structural change in crystal, a more stable crystal which is hard to crack and free from becoming white-muddy is available.

[0035] In the case of the following formula:

Cs2(1−z)Li2LzB12O20

[0036] Ions of alkali earth metals (L) such as Ba, Sr, Ca, Mg and Be are added. It is needless to mention that a plurality of alkaliearth metal elements may be added.

[0037] As in the case with alkali metals alone, addition of these alkali earth metal ions permits changing the refractive index and the phase matching angle, and improvement of angular allowance and temperature allowance. At the same time, it is possible to obtain a more stable crystal by changing crystal structure.

[0038] In the present invention, the above-mentioned crystals can be used in frequency wave conversion or optical parametric oscillation (OPO). In other words, the present invention permits achievement of an optical apparatus provided with the above-mentioned crystals.

[0039] Now, the present invention will be described in further detail by means of examples. It is needless to mention that the present invention is not limited to the following examples.

EXAMPLE 1

[0040] Raw materials used were Cs2CO3, Li2CO3, and B2O3. These materials were mixed in a mol ratio of 1:1:6, and heated and melted to synthesize crystals. The melting point of the crystal was 848° C.

[0041] There was obtained a transparent crystal measuring 30×25×25 mm after approximately two weeks' growth period using the top seed method and temperature decrease method to grow the crystal from the melt.

[0042] The chemical structural formula of the crystal obtained is CsLiB6O10 according to the result of compsitional analysis such as ICP emission spectral analysis and ICP mass spectroscopy. Measurement of the melting point through a differential thermal analysis revealed a melting point of 848° C. of this cesium-lithium-borate crystal. This crystal belongs to tetragonal system (space group 142d) according to the result of an X-ray structural analysis. Further, this cesium-lithium-borate crystal is transparent for the visible radiations, and it passes light of wavelengths down to 180 nm.

[0043] The effective second-order nonlinear optical constant was deff=4dKDP according to the result of analysis by the powder method.

[0044] Further, a part of this cesium-lithium-borate crystal measuring 30×25×25 mm was cut by the angle of phase matching, and polished. The polished crystal was then irradiated by 1.06 &mgr;m neodymium YAG laser light. Green rays of 0.53 &mgr;m wavelength (the second harmonic), was obtained efficiently.

[0045] A cesium-lithium-borate crystal measuring 10 diameter ×20 mm was grown by the revolving pull-up method (rate of revolution: 10 rpm; pull-up rate: 0.5 mm/h). This was confirmed to be the same as that described above.

EXAMPLE 2

[0046] A cesium-lithium-borate crystal (CsLiB6O10) comprising a stoichiometric chemical composition was manufactured by heating and melting a mixture of cesium carbonate (Cs2CO3), lithium carbonate (Li2CO3) and boron oxide (B2O3), and the resultant cesium-lithium-borate crystal was grown by the top seeded kyropoulos method in a five-zone furnace. FIG. 1 shows the structure of the five-layer controlled growing furnace used for growing the crystal. This five-layer controlled growing furnace has a structure in which a cylindrical platinum crucible is installed in an upright five-stage resistance heating furnace capable of keeping a uniform temperature in the furnace. The seed crystal of CsLiB6O10 was attached to a platinum rod. The growing crystal was rotated at a rate of 15 rpm with inverting the rotation direction in every three minutes. Temperature in the platinum crucible was kept at 848° C., the melting point of the crystal. This permitted growth of a transparent and high-quality cesium-lithium-borate crystal, measuring 2.9 cm×2.0 cm×2.2 cm, free from cracks in about four days. This represents a very short period of growth as compared with the conventional growth of a nonlinear optical borate crystal for frequency conversion. It is thus possible to easily grow a cesium-lithium-borate crystal in a very short period of time for growth by the application of the growing method of the cesium-lithium-borate crystal of the present invention.

[0047] According to the result of crystal structural analysis by means of a Rigaku AFC5R X-ray diffraction apparatus, the cesium-lithium-borate crystal was a tetragonal crystal belonging to the space group 142d symmetrical group, with a crystal lattice constant of a=10,494 and c=8,939 Å, and a calculated density of 2.461 g/cm. FIG. 2 shows the three-dimensional structure of this cesium-lithium-borate crystal, which suggests a structure in which a cesium atom is present in a channel of borate ring comprising boron and oxygen. It is clear that this crystal has a structure quite different from that of LiB3O5 or CsB3O5 (both are or the rhombic), nonlinear optical crystal so far commonly used.

[0048] This cesium-lithium-borate crystal was transparent relative to a light having a wavelength of from 180 nm to 2750 nm, according to the result of measurement of transmission spectra. FIG. 3 shows the transmission spectrum in the short wavelength region. As is clear from FIG. 3, the crystal had an absorption edge of 180 nm which was shorter by about 9 nm than that of the conventional &bgr;-BaB2O4 (189 nm).

[0049] The refractive index of this cesium-lithium-borate crystal was measured by the prism method within a wavelength range of from 240 nm to 1,064 nm. FIG. 4 shows a dispersion curve of the refractive index. In FIG. 4, “no” represents the refractive index for the normal light, and “ne” indicates that for an abnormal light.

[0050] The approximation formula of refractive index (Sellmeier's equation) as available from this refractive index dispersion curve is as follows: 1 n o 2 = 2.19974 + 1.18388 × 10 - 2 λ 2 - 8.77048 × 10 - 3 - 8.52469 × 10 - 5 ⁢ λ 2 n e 2 = 2.05386 + 9.4403 × 10 - 3 λ 2 - 8.62428 × 10 - 3 - 7.82600 × 10 - 5 ⁢ λ 2

EXAMPLE 3

[0051] The relationship between the mixing ratio of B2O3 and temperature upon manufacture of this cesium-lithium-borate crystal was determined. The mixing ratio of B2O3 was varied within a range of from 66.7% to 83.3% while keeping a constant mixing ratio of 1:1 between the initial raw materials Cs2CO3 and Li2CO3, and the melting point of the crystal was determined by placing a sintered powder of the resultant mixture into a differential thermal analyzer. FIG. 5 is a graph illustrating the relationship between the mixing ratio of B2O3 and temperature in this case. In FIG. 5, Cs2CO3 and Li2CO3 mixed at a ratio of 1:1 are represented by Cs2O Li2O. As is evident from FIG. 5, a CsLiB6O10 crystal was stably available with a mixing ratio of B2O3 within a range of from 66.7% to 81.8%. With a mixing ratio of B2O3 of under 66.7%, CBO precipitated along with CsLiB6O10 crystal, and with a mixing ratio within a range of from 81.8 to 83.8%, unknown crystals other than CsLiB6O10 crystal precipitated simultaneously, thus resulting in unstable manufacture of the crystal. In the manufacture of this cesium-lithium-borate crystal, therefore, the mixing ratio of B2O3, an initial raw material, should preferably be kept within a range of from 66.7% to 81.8%. The CsLiB6O10 crystal stably manufactured can melt congruently at 848° C.

[0052] Since this cesium-lithium-borate crystal is a congruently melting crystal, it is possible to grow a high-quality crystal with a constant composition easily within a short period of time through adoption of the Top-seeded kyropoulos method, crystal pulling method or the flux method, as compared with the conventional &bgr;-BaB2O4 tending to easily cause phase transition during growth from the melt and LiB3O5 requiring a long growth period for flux growth.

EXAMPLE 4

[0053] A cesium-lithium-borate crystal was manufactured by heating and melting 12 kg mixture of cesium carbonate (Cs2CO3), lithium carbonate (Li2CO3) and boron oxide (B2O3) mixed at a ratio of 1:1:5.5 (B2O3 accounting for 73.3%). The resultant cesium-lithium-borate crystal was largely grown by the flux method in a five-zone furnace. As large crystal growth requires a large temperature drops the flux method is suitable. For the purpose of growing a large crystal, a large platinum crucible having a diameter of 20 cm and a height of 20 cm was employed. In this Example, the growth saturation temperature was measured to be 845° C. The crystal was grown by reducing the growing temperature from 845° C. to 843.5° C. at a daily rate of about 0.1° C. A large transparent crystal measuring 13 cm×12 cm×10 cm and weighing about 1.6 kg could be grown in about 12 days. In this crystal growth, there was no unstable growth such as hopper growth observed in the conventional growth of LiB3O5 crystal, proving a very stable growth.

EXAMPLE 5

[0054] By using the cesium-lithium-borate crystal (CsLiB6O10) of the present invention as a frequency converting nonlinear optical crystal of an Nd:YAG laser, the second harmonic (SHG: wavelength: 532 nm) of the Nd:YAG laser (wavelength: 1,064 nm) was generated.

[0055] FIG. 6 illustrates the relationship between the phase matching angle &thgr; of the crystal permitting second harmonic generation (SHG) and the input laser wavelength. In FIG. 6, the dotted line represents the calculated values based on Sellmeier's equation for Type-I SHG, the solid line, the calculated values for Type-II SHG by Sellmeier's equation, and the black plots are observed values. The limit of SHG wavelength is 477 nm in Type-I, and 640 nm in Type-II. As is clear from FIG. 6, for example, the Type-I SHG of Nd:TAG laser beam having a wavelength of 1,064 nm shows an incident angle of 29.6° in calculation and about 30° in observation. The Type-I SHG of Nd:YAG laser beam having a wavelength of 532 nm gives an incident angle of 62.5° in calculation and 62° in observation. There is suggested a satisfactory agreement.

[0056] FIG. 7 is a graph illustrating the relationship between the walk-off angle and the wavelength for Type-I SHG obtained through calculation from Sellmeier's equation. In FIG. 7, the solid line represents CsLiB6O10 of the present invention, and the dotted line, the conventional &bgr;-BaB2O4.

[0057] Table 1 shows, for CsLiB6O10 of the present invention and the conventional &bgr;-BaB2O4 Type-I SHG, with an incident wavelengths of 1,0649 &mgr;m and 532 nm, calculated values of phase matching angle &thgr;, effective nonlinear optical coefficient deff, angular allowance &Dgr;&thgr;.L, spectral allowance &Dgr;&lgr;.L, temperature allowance &Dgr;T. L, walk-off angle, and laser damage threshold value. As to the refractive index for &bgr;-BaB2O4 necessary for calculating these values, those in literature released in “J. Appl. Phys. Vol. 62, D. Eimerl, L, Davis, S. Velsko, B. K. Graham and A. Zalkin (1987), p. 1968.”

[0058] The effective nonlinear optical constant deff was derived from comparison with SHG of KH2PO4 (KDP) crystal. CsLiB6O10 has a crystal structure identical with that of KDP.

[0059] The second-order nonlinear optical coefficient is expressed as d36, where d36(CLBO)=2.2×d36(KDP)=0.95 pm/r, and its relationship with deff is deff =−d36 sin &thgr; sin 2&phgr;. The value of deff was calculated by means of this formula. A value of 0.435 pm/V was used as the standard value of d36 of KDP.

[0060] The angular allowance &Dgr;&thgr;.L and the spectral allowance &Dgr;&lgr;. L were calculated in accordance with Sellmeier's equation.

[0061] The temperature allowance &Dgr;T. L, which could not be obtained from calculation, was actually measured within a range of from 20° C. to 150° C. 1 TABLE 1 Fundamental Phase- Walk-off Damage wavelength matching deff &Dgr;&thgr;l &Dgr;&lgr;l &Dgr;Tl angle threshold (nm) Crystal angle (&thgr;) (pm/V) (mrad · cm) (nm · cm) (° C. · cm) (deg) (GW/cm2) 1064 CLBO 29.6 0.47 1.02 7.03 1.78 26 BBO 21 2.06 0.51 2.11 3.20 13.5 532 CLBO 62.5 1.01 0.49 0.13 9.4 1.83 BBO 48 1.85 0.17 0.07 4.5 4.80 488 CLBO 77.9 1.16 0.84 0.09 0.98 BBO 1.88 0.16 0.05 4.66

[0062] As is clear from Table 1, the CsLiB6O10 of the present invention has a smaller effective nonlinear optical constant as compared with the conventional BBO. The CsLiB6O10 of the invention is however larger in angular allowance, wavelength allowance and temperature allowance and smaller in walk-off angle. The cesium-lithium-borate crystal of the present invention therefore permits more effective frequency conversion than that with the conventional nonlinear optical crystal.

EXAMPLE 6

[0063] The fourth harmonic (4HG; wavelength: 266 nm) of Nd:YAG laser (wavelength: 1,064 nm) was generated by using the cesium-lithium-borate crystal (CsLiB6O10) of the present invention in Nd:YAG laser. The second harmonic (SHG) of Q-switch laser having a pulse width of 8 nanoseconds was employed as the incident light with a beam diameter of 4 mm and repetition rate at 10 Hz. FIG. 8 is a graph illustrating the relationship between the energy output of the incident light SHG and the energy output of 4HG, i.e., generation characteristics of the fourth harmonic. In FIG. 8, the solid line represents the CsLiB6O10 of the present invention, and the dotted line indicates &bgr;-BaB2O4. The sample length was 9 mm for CsLiB6O10 and 7 mm for &bgr;-BaB2O4. As is evident from FIG. 8, according as the energy of the incident light SHG becomes larger, &bgr;-BaB2O4's 4HG energy shows a tendency toward saturation, whereas CsLiB6O10 of the invention is proportional to the square of the incident energy, and in the high incident energy region with a high energy of incident light, a 4HG output energy larger than that of &bgr;-BaB2O4 is available. The cesium-lithium-borate crystal of the present invention can therefore be used as a very excellent wavelength converting nonlinear optical crystal capable of generating ultraviolet rays of a high output energy.

EXAMPLE 7

[0064] The fifth harmonic (5HG; wavelength: 213 nm) of Nd:YAG laser (wavelength: 1,064 nm) was generated by using the cesium-lithium-borate crystal (CsLiB6O10) of the present invention in the Nd:YAG laser.

[0065] FIG. 9 is a graph illustrating the results of calculation of a frequency capable of generating a sum frequency (107 1+&ohgr;2=&ohgr;3) of two frequencies (&ohgr;1 and &ohgr;2) in CsLiB6O10 of the invention, as derived from Sellmeir's equation. The abscissa represents the light wavelength &lgr;1 corresponding to the frequency &ohgr;1, and the ordinate represents the light wavelength &lgr;2 corresponding to the frequency &ohgr;2 and the light wavelength &lgr;3 corresponding to the frequency &ohgr;3. In FIG. 9, the region shadowed with oblique lines above the solid line is the region in which a sum frequency can be generated. The dotted line represents the wavelength &lgr;3 available as a result of a sum frequency. For example, assuming that an Nd:YAG laser has a basic wave (wavelength: 1,064 nm) &ohgr;, then &ohgr;+4&ohgr;=5&ohgr; is possible. In other words, the fifth harmonic can be generated by the sum frequency of the basic wave and the fourth harmonic. Generation of the fifth harmonic by adding the second and third harmonics is however impossible.

[0066] In FIG. 9, the black plots represent the wavelength available from sum frequency of &ohgr;+4&ohgr; and that available from sum frequency of 2&ohgr;+3&ohgr;. Presence of only black plots representing &ohgr;+4&ohgr; in the slashed region reveals that the fifth harmonic can be generated only from the sum frequency of &ohgr;+4&ohgr;. As is evident from the dotted line (wavelength: &lgr;3) in FIG. 9, a wavelength of even under 200 nm can be generated from a sum frequency by properly selecting wavelengths &lgr;1 and &lgr;2.

[0067] FIG. 10 illustrates a photograph of the beam pattern of the fifth harmonic of Nd:YAG laser generated with CsLiB6O10 of the present invention. FIG. 11 is a schematic view of crystal arrangement upon generation of the second harmonic, the fourth harmonic and the fifth harmonic in this case. Table 2 shows energy values of the individual frequencies of CsLiB6O10(LLBO) of the invention and the conventional &bgr;-BaB2O4(BBO). As is clear from Table 2, while 5&ohgr; available from the conventional &bgr;-BaB2O4(BB0) is 20 mJ, what is available from CsLiB6O10 of the invention is a higher output of 35 mJ. The cesium-lithium-borate crystal of the present invention can therefore generate the fifth harmonic of a higher output than the conventional &bgr;-BaB2O4, and can be used as a nonlinear optical crystal for generating a very excellent fifth harmonic. The beam pattern obtained from FIG. 10 is closest to circle, suggesting that it is possible to generate second harmonics throughout the entire beam. This is attributable to a larger angular allowance &Dgr;&thgr;.L and temperature allowance &Dgr;T. L of CLBO than BBO. 2 TABLE 2 Harmonic 2&ohgr; 4&ohgr; 5&ohgr; Crystal Pouwer (mJ) 350 110 35 CLBO Power (mJ) 500  80 20 BBO

EXAMPLE 8

[0068] The output of wavelength of 488 nm of Ar laser was converted into a second harmonic by means of the cesium-lithium-borate crystal of the present invention. Table 1 presented above shows, for the CsLiB6O10 of the invention and the conventional &bgr;-BaB2O4 relative to Type-I SHG with an incident wavelength of 488 nm, calculated values of phase matching angle &thgr;, effective nonlinear optical coefficien deff, angular allowance. &Dgr;&thgr;.L, spectral allowance &Dgr;&lgr;. L, and walk-off angle. The same calculating methods as in the Example 5 were used for these calculations. As is clear from Table 1, CsLiB6O10 has a walk-off angle of 0.98° which is very close to the noncritical phasematching. This demonstrates that the cesium-lithium-borate crystal of the invention gives a very high conversion efficiency as compared with the conventional &bgr;-BaB2O4.

EXAMPLE 9

[0069] The cesium-lithium-borate crystal of the present invention was used for optical parametric oscillation (OPO).

[0070] Optical parametric oscillation (OPO) is a process of wavelength conversion comprising exciting a nonlinear polarization within a nonlinear optical crystal with a laser beam, thereby dividing the energy of the excited beam through nonlinear oscillation of polarized electrons into a signal light and an idler light. Because of the possibility to tune a wavelength region within a wide range, a wider application of OPO is expected. The cesium-lithium-borate crystal of the invention, having a relatively large effective nonlinear optical coefficient, can supply a longer crystal length, because of the lasiness of growing a large crystal. and further to a larger power density of the excited beam because of the high laser damage threshold value, thus providing excellent characteristics as an OPO crystal.

[0071] FIG. 12 is a phase matching tuning curve diagram illustrating the relationship between the wavelengths of the signal light produced in Type-I with excited light wavelengths of 213 nm, 266 nm, 355 nm and 532 nm, and the corresponding phase matching angles. FIG. 13 is a phase matching tuning curve diagram illustrating the relationship between the wavelength of the signal light produced in Type-II with a wavelength of the excited light of 532 nm and the corresponding phase matching angle. As is clear from FIGS. 12 and 13, the cesium-lithium-borate crystal of the present invention exhibits excellent properties also as an OPO crystal.

[0072] Particularly OPO based on excitation with the fourth harmonic (wavelength: 266 nm) of Nd:YAG laser gives a variable-wavelength laser beam near 300 nm. This has been impossible in the conventional &bgr;-BaB2O4 because of the small angular allowance &Dgr;&thgr;.L and the large walk-off.

EXAMPLE 10

[0073] An Rb (rubidium)-substituted cesium-lithium-borate crystal Cs1−xLiRbxB6O10 was manufactured in the same manner as in the Example 2.

[0074] According to the results of evaluation of the resultant crystal by the powder X-ray diffraction method, as shown in FIG. 14, particularly, the interval between reflection peak of (312) plane and reflection peak of (213) plane becomes gradually arrower by sequentially increasing the amount of added Rb from x=0.2, to 0.5 and then 0.7 to the X-ray diffraction pattern of the sample (Rb, x=O) not added with Rb. This shows that Cs and Rb enter into the crystal at an arbitrary ratio. The crystal added with Rb arbitrarily is the same tetragonal crystal as CLBO not added with Rb, and the lattice constant varies accordingly.

[0075] Since it is possible to add Rb ions in an arbitrary amount, it is possible to change the refractive index of the crystal, and this reveals the possibility to improve the phase matching angle, angular allowance and temperature allowance.

[0076] Similarly, crystals with amounts (x) of added Rb of under 0.1 were manufactured. It was confirmed as a result that the stability of crystal structure was more satisfactory.

EXAMPLE 11

[0077] Crystals were manufactured in the same manner as in the Example 10 except that K or Na was added in place of Rb. Availability of high-quality crystals was confirmed with a constituent ratio (x) of under 0.1 for &kgr; (potassium), and under 0.01 for Na (sodium).

[0078] Crystals in which K or Na was coexistent with Rb were also manufactured. In this case, in a composition:

Cs1−xLi1−yRbx(Na, K)yB6O10,

[0079] a more stable crystal was obtained with 0<x≦1 and 0<y <0.1.

EXAMPLE 12

[0080] Crystals were manufactured in the same manner as in the Example 10 except that an alkali earth metal element was added in place of an alkali metal.

[0081] For example, in the case of a composition Cs2(1-Z)Li2BaZB12O20, it was confirmed that a stable crystal is available with 0<z-≦0.1.

[0082] According to the present invention, as described above in detail, a novel cesium-lithium-borate crystal and substituted cesium-lithium-borate crystals are provided. These crystals permit conversion of frequency, has a high converting efficiency, and wide temperature allowance and angular allowance, and can be used as a high-performance frequency converting crystal. Furthermore, the CsLiB6O10 crystal has a low melting point of 848° C., and because of the congruency of CsLiB6O10 crystal, it is possible to easily grow a large high-quality crystal having a stable composition by the application of the melt methods based on the Top-seeded kilopoulos method, crystal pulling method or the flux method.

Claims

1. A cesium-lithium-borate crystal having a chemical composition expressed as CsLiB6O10.

2. A substituted cesium-lithium-borate crystal having a chemical composition expressed by the following formula:

Cs1−xLi1−yMx+yB6O10
(where, M is at least one alkali metal element other than Cs and Li, and x and y satisfy the relationship of 0≦×≦1 and 0≦y≦1, and x and y never take simultaneously a value of 0 or 1).

3. A substituted cesium-lithium-borate crystal having a chemical composition expressed by the following formula:

Cs2(1−z)Li2LzB12O20
(where, L is at least one alkali earth metal element, and 0<z<1).

4. A crystal as claimed in claim 1, at least one alkali metal ion other than Cs and Li is added for improving of optical and mechanical properties.

5. A crystal as claimed in 1, at least one alkali earth metal ion is added for improving of optical and mechanical properties.

6. A method for manufacturing a crystal as claimed in any one of claims 1 to 5, which comprises the step of heating and melting a raw material mixture of constituent elements, thereby manufacturing said crystal.

7. A method for manufacturing the crystal as claimed in any one of claims 1 to 5, which comprises the step of growing the crystal by the melt method.

8. A method for manufacturing the crystal as claimed in any one of claims 1 to 5, which comprises the step of growing the crystal by the flux method.

9. A frequency converting apparatus which is provided with any of the crystals as claimed in claims 1 to 5 as optical means.

10. An apparatus as claimed in claim 9 for generating the second, third, fourth or fifth harmonic of a laser.

11. An optical parametric oscillator which is provided with any of the crystals as claimed in claims 1 to 5 as optical means.

Patent History
Publication number: 20030030039
Type: Application
Filed: Aug 15, 2002
Publication Date: Feb 13, 2003
Inventors: Takatomo Sasaki (Osaka), Akio Hiraki (Hyogo), Yusuke Mori (Osaka), Sadao Nakai (Osaka)
Application Number: 10218655
Classifications
Current U.S. Class: Inorganic Crystalline Solid (252/584); Oxygen Containing (423/277)
International Classification: C01B035/10;