Compound ammonium fluoroborate, nonlinear optical crystal of ammonium fluoroborate, and preparation method and use thereof

Abstract

A compound ammonium fluoroborate, a nonlinear optical crystal of ammonium fluoroborate, and a preparation method and use thereof; the compound has the chemical formula of NH.sub.4B.sub.4O.sub.6F with a molecular weight of 176.28, and is prepared by a solid phase reaction process; the crystal has the chemical formula of NH.sub.4B.sub.4O.sub.6F with a molecular weight of 176.28, belongs to the orthorhombic system, and has a space group of Pna2.sub.1 and the following unit cell parameters: a=7.615(3) , b=11.207(4) , c=6.604(3) , Z=4, V=563.6 .sup.3. The nonlinear optical crystal can be obtained by the method of the present invention. The present invention provides uses of the nonlinear optical crystal in producing harmonic light and a deep-ultraviolet frequency-multiplied light below 200 nm; and in making a frequency multiplication generator, a frequency up or down converter or an optical parametric oscillator.

Claims

1. A compound ammonium fluoroborate, wherein a chemical formula of the compound ammonium fluoroborate is NH.sub.4B.sub.4O.sub.6F and a molecular weight of the compound ammonium fluoroborate is 176.28.

2. A method for preparing a compound ammonium fluoroborate, wherein a chemical formula of the compound ammonium fluoroborate is NH.sub.4B.sub.4O.sub.6F and a molecular weight of the compound ammonium fluoroborate is 176.28; the method adopts a solid phase reaction process and comprises the steps of: mixing an NH.sub.4-containing compound, a Boron-containing compound, and a Fluorine-containing compound evenly at a molar ratio of NH.sub.4:B:F=(0.5-2):(3-5):(0.5-2) to obtain a mixture, sealing the mixture in a hydrothermal reactor or a quartz tube, placing the hydrothermal reactor or the quartz tube into a muffle furnace or a drying oven, raising a temperature to 150-580 C. at a rate of 20-40 C./h and keeping the temperature for 10-48 h, then reducing the temperature to 30 C. at a rate of 1-10 C./h, and opening the hydrothermal reactor or the quartz tube to obtain the compound ammonium fluoroborate; a chemical formula of the NH.sub.4-containing compound is NH.sub.4F, a chemical formula of the Boron-containing compound is H.sub.3BO.sub.3 or B.sub.2O.sub.3, and a chemical formula of the Fluorine-containing compound is NH.sub.4F or HF.

3. A nonlinear optical crystal of ammonium fluoroborate, wherein a chemical formula of the nonlinear optical crystal is NH.sub.4B.sub.4O.sub.6F and a molecular weight of the nonlinear optical crystal is 176.28; the nonlinear optical crystal is an orthorhombic crystal, a space group of the nonlinear optical crystal is Pna2.sub.1, and the nonlinear optical crystal has the following cell parameters: a=7.615(3) , b=11.207(4) , c=6.604(3) , Z=4, V=563.6 .sup.3.

4. A method for preparing a nonlinear optical crystal of ammonium fluoroborate, wherein a chemical formula of the nonlinear optical crystal is NH.sub.4B.sub.4O.sub.6F and a molecular weight of the nonlinear optical crystal is 176.28; the nonlinear optical crystal is an orthorhombic crystal, a space group of the nonlinear optical crystal is Pna2.sub.1, and the nonlinear optical crystal has the following cell parameters: a=7.615(3) , b=11.207(4) , c=6.604(3) , Z=4, V=563.6 .sup.3; the nonlinear optical crystal grown by a flux method, a Bridgman-Stockbarger method, a room temperature solution method or a solvothermal method; the room temperature solution method for growing the nonlinear optical crystal of ammonium fluoroborate comprises the following steps: a. mixing an NH.sub.4-containing compound, a Boron-containing compound, and a Flurine-containing compound evenly at a molar ratio of NH.sub.4:B:F=(0.5-2):(3-5):(0.5-2) to obtain a mixture, sealing the mixture in a hydrothermal reactor or a quartz tube, placing the hydrothermal reactor or the quartz tube into a muffle furnace or a drying oven, raising a first temperature to 150-580 C. at a rate of 20-40 C./h and keeping the first temperature for 10-48 h, then reducing the first temperature to 30 C. at a rate of 1-10 C./h, and opening the hydrothermal reactor or the quartz tube and removing the mixture to obtain a compound NH.sub.4B.sub.4O.sub.6F; a chemical formula of the NH.sub.4-containing compound is NH.sub.4F, a chemical formula of the Boron-containing compound is H.sub.3BO.sub.3 or B.sub.2O.sub.3, and a chemical formula of the Fluorine-containing compound is NH.sub.4F or HF; b. sealing the compound NH.sub.4B.sub.4O.sub.6F obtained in step a in the hydrothermal reactor or the quartz tube, placing the hydrothermal reactor or the quartz tube into the muffle furnace or the drying oven, raising a second temperature to 200-600 C. at a rate of 20-40 C./h and keeping the second temperature for 10-48 h, then reducing the second temperature to 30 C. at a rate of 1-5 C./h, and opening the hydrothermal reactor or the quartz tube to obtain a seed crystal of the NH.sub.4B.sub.4O.sub.6F; c. placing the seed crystal obtained in step b at a bottom of a container, and then placing the compound NH.sub.4B.sub.4O.sub.6F obtained in step a into the container; d. sealing the container in step c or sealing the container in step c after an addition of 10-100 mL of a solvent, placing the container into the muffle furnace or the drying oven, raising a third temperature to 150-600 C. at a rate of 20-40 C./h and keeping the third temperature for 10-48 h, then reducing the third temperature to 50 C. at a rate of 1-3 C./day, and then reducing the third temperature to 30 C. at a rate of 1-10 C./h, and opening the container to obtain the nonlinear optical crystal of ammonium fluoroborate, a size of the nonlinear optical crystal is 1-20 mm; the solvent is deionized water, anhydrous ethanol, N,N-dimethylformamide, N,N-dimethylacetamide or hydrofluoric acid; the flux method for growing the nonlinear optical crystal of ammonium fluoroborate comprises the following steps: a. mixing an NH.sub.4-containing compound, a Boron-containing compound, and a Fluorine-containing compound evenly at a molar ratio of NH.sub.4:B:F=(0.5-2):(3-5):(0.5-2) to obtain a mixture, sealing the mixture in a hydrothermal reactor or a first quartz tube, placing the hydrothermal reactor or the first quartz tube into a muffle furnace or a drying oven, raising a first temperature to 150-580 C. at a rate of 20-40 C./h and keeping the first temperature for 10-48 h, then reducing the first temperature to 30 C. at a rate of 1-10 C./h, and opening the hydrothermal reactor or the first quartz tube to obtain a compound NH.sub.4B.sub.4O.sub.6F; a chemical formula of the NH.sub.4-containing compound is NH.sub.4F, a chemical formula of the Boron-containing compound is H.sub.3BO.sub.3 or B.sub.2O.sub.3, and a chemical formula of the Fluorine-containing compound is NH.sub.4F or HF; b. sealing the compound NH.sub.4B.sub.4O.sub.6F obtained in step a in the hydrothermal reactor or the first quartz tube, placing the hydrothermal reactor or the first quartz tube into the muffle furnace or the drying oven, raising a second temperature to 200-600 C. at a rate of 20-40 C./h and keeping the second temperature for 10-48 h, then reducing the second temperature to 30 C. at a rate of 1-5 C./h, and opening the hydrothermal reactor or the first quartz tube to obtain a seed crystal of the NH.sub.4B.sub.4O.sub.6F; c. placing the seed crystal of the NH.sub.4B.sub.4O.sub.6F obtained in step b at a bottom of a second quartz tube, then mixing the compound NH.sub.4B.sub.4O.sub.6F obtained in step a with a flux at a molar ratio of 1:(1-10) to obtain a mix and placing the mix into the second quartz tube, and the second quartz tube was lame-sealed under 10.sup.3 Pa with a flame gun; a chemical formula of the flux is NH.sub.4F, NH.sub.4F:H.sub.3BO.sub.3, NH.sub.4F:B.sub.2O.sub.3, H.sub.3BO.sub.3 or B.sub.2O.sub.3; d. sealing the second quartz tube in step c or sealing the second quartz tube in step c after an addition of 10-100 mL of a solvent, placing the second quartz tube into the muffle furnace or the drying oven, raising a third temperature to 150-600 C. at a rate of 20-40 C./h and keeping the third temperature for 10-48 h, then reducing the third temperature to 50 C. at a rate of 1-3 C./day, and then reducing the third temperature to 30 C. at a rate of 1-10 C./h, and opening the second quartz tube and removing a product to obtain the nonlinear optical crystal of ammonium fluoroborate, a size of the nonlinear optical crystal is 1-20 mm; the solvent is deionized water, anhydrous ethanol, N,N-dimethylformamide, N,N-dimethylacetamide or hydrofluoric acid; the Bridgman-Stockbarger method for growing the nonlinear optical crystal of ammonium fluoroborate comprises the following steps: a. mixing an NH.sub.4-containing compound, a Boron-containing compound, and a Flurine-containing compound evenly at a molar ratio of NH.sub.4:B:F=(0.5-2):(3-5):(0.5-2) to obtain a mixture, sealing the mixture in a hydrothermal reactor or a quartz tube, placing the hydrothermal reactor or the quartz tube into a muffle furnace or a drying oven, raising a first temperature to 150-580 C. at a rate of 20-40 C./h and keeping the first temperature for 10-48 h, then reducing the first temperature to 30 C. at a rate of 1-10 C./h, and opening the hydrothermal reactor or the quartz tube and removing the mixture to obtain a compound NH.sub.4B.sub.4O.sub.6F; a chemical formula of the NH.sub.4-containing compound is NH.sub.4F, a chemical formula of the Boron-containing compound is H.sub.3BO.sub.3 or B.sub.2O.sub.3, and a chemical formula of the Fluorine-containing compound is NH.sub.4F or HF; b. sealing the compound NH.sub.4B.sub.4O.sub.6F obtained in step a in the hydrothermal reactor or the quartz tube, placing the hydrothermal reactor or the quartz tube into the muffle furnace or the drying oven, raising a second temperature to 200-600 C. at a rate of 20-40 C./h and keeping the second temperature for 10-48 h, then reducing the second temperature to 30 C. at a rate of 1-5 C./h, and opening the hydrothermal reactor or the quartz tube to obtain a seed crystal of the NH.sub.4B.sub.4O.sub.6F; c. placing the seed crystal obtained in step b at a bottom of a container, and then placing the compound NH.sub.4B.sub.4O.sub.6F obtained in step a into the container; d. sealing the container in step c and placing the container into a Bridgman-Stockbarger furnace, raising a third temperature to 300-600 C. and keeping the third temperature for 10-20 h, adjusting a position of the container to allow the compound NH.sub.4B.sub.4O.sub.6F to spontaneously nucleate or inoculate at 350-600 C., then lowering the container at a rate of 0.05-2 mm/h slowly while keeping a growth temperature constant or reducing the growth temperature slowly at a rate of 0-3 C./h, then reducing the third temperature of the Bridgman-Stockbarger furnace to 30 C. after a growth of the nonlinear optical crystal is completed, and removing the container to obtain the nonlinear optical crystal of ammonium fluoroborate, a size of the nonlinear optical crystal is 1-20 mm; the solvothermal method for growing the nonlinear optical crystal of ammonium fluoroborate comprises the following steps: a. mixing an NH.sub.4-containing compound, a Boron-containing compound, and an Fluorine-containing compound evenly at a molar ratio of NH.sub.4:B:F=(0.5-2):(3-5):(0.5-2) to obtain a first mixture, sealing the first mixture in a hydrothermal reactor or a quartz tube, placing the hydrothermal reactor or the quartz tube into a muffle furnace or a drying oven, raising a first temperature to 150-580 C. at a rate of 20-40 C./h and keeping the first temperature for 10-48 h, then reducing the first temperature to 30 C. at a rate of 1-10 C./h, and opening the hydrothermal reactor or the quartz tube to obtain a compound NH.sub.4B.sub.4O.sub.6F; a chemical formula of the NH.sub.4-containing compound is NH.sub.4F, a chemical formula of the Boron-containing compound is H.sub.3BO.sub.3 or B.sub.2O.sub.3, and a chemical formula of the Fluorine-containing compound is NH.sub.4F or HF; b. sealing the compound NH.sub.4B.sub.4O.sub.6F obtained in step a in the hydrothermal reactor or the quartz tube, placing the hydrothermal reactor or the quartz tube into the muffle furnace or the drying oven, raising a second temperature to 200-600 C. at a rate of 20-40 C./h and keeping the second temperature for 10-48 h, then reducing the second temperature to 30 C. at a rate of 1-5 C./h, and opening the hydrothermal reactor or the quartz tube to obtain a seed crystal of the NH.sub.4B.sub.4O.sub.6F; c. placing the seed crystal obtained in step b at a bottom of a container, and then placing the compound NH.sub.4B.sub.4O.sub.6F obtained in step a into the container; d. adding 10-100 mL of a solvent to the container in step c to obtain a second mixture, then subjecting the second mixture to ultrasonication to make the second mixture mix and dissolve thoroughly, adjusting a pH value of the second mixture to pH=1-11, performing a filtration with a qualitative filter paper, then sealing the container with a polyvinyl chloride film, a plurality of small holes are arranged in the polyvinyl chloride film and punched to adjust a volatilization rate of the solvent in the second mixture, and placing the container into a static environment without shaking, pollution and air convection, and leaving the second mixture to stand at room temperature to allow the nonlinear optical crystal to grow, so as to obtain the nonlinear optical crystal of ammonium fluoroborate, a size of the nonlinear optical crystal is 1-20 mm at an end of a crystal growth; the solvent is deionized water, anhydrous ethanol, N,N-dimethylformamide, N,N-dimethylacetamide or hydrofluoric acid.

5. The method for preparing the nonlinear optical crystal of ammonium fluoroborate of claim 4, wherein in step c of the steps of the flux method, a molar ratio of NH.sub.4F to H.sub.3BO.sub.3 in a flux system of NH.sub.4FH.sub.3BO.sub.3 is (1-3):(1-5); and a molar ratio of NH.sub.4F to B.sub.2O.sub.3 in a NH.sub.4FB.sub.2O.sub.3 system is (1-2):(1-4).

6. A method of producing a harmonic light, wherein the method comprises: using a nonlinear optical crystal of ammonium fluoroborate, wherein a chemical formula of the nonlinear optical crystal is NH.sub.4B.sub.4O.sub.6F and a molecular weight of the nonlinear optical crystal is 176.28; the nonlinear optical crystal is an orthorhombic system, a space group of the nonlinear optical crystal is Pna2.sub.1, and the nonlinear optical crystal has the following cell parameters: a=7.615(3) , b=11.207(4) , c=6.604(3) , Z=4, V=563.6 .sup.3; the harmonic light is a frequency-doubled, a frequency-tripled, a frequency-quadrupled, a frequency-quintupled or a frequency-sextupled harmonic light from a 1064 nm fundamental frequency light output from a Nd:YAG laser.

7. The method of claim 6, wherein the method comprises using the nonlinear optical crystal of ammonium fluoroborate in a production of a deep-ultraviolet frequency-multiplied light below 200 nm.

8. A method of making a frequency multiplication generator, a frequency up or down converter or an optical parametric oscillator, wherein the method comprises using a nonlinear optical crystal of ammonium fluoroborate, a chemical formula of the nonlinear optical crystal is NH.sub.4B.sub.4O.sub.6F and a molecular weight of the nonlinear optical crystal is 176.28; the nonlinear optical crystal is an orthorhombic system, a space group of the nonlinear optical crystal is Pna2.sub.1, and the nonlinear optical crystal has the following cell parameters: a=7.615(3) , b=11.207(4) , c=6.604(3) , Z=4, V=563.6 .sup.3.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 shows the powder XRD spectrum of the compound NH.sub.4B.sub.4O.sub.6F of the present invention, which is consistent with the theoretical XRDspectrum, demonstrating the presence of the compound NH.sub.4B.sub.4O.sub.6F;

(2) FIG. 2 shows the EDS spectrum of the compound NH.sub.4B.sub.4O.sub.6F of the present invention, which shows that the experimental and theoretical atomic ratios are basically the same, demonstrating the accuracy of the chemical formula NH.sub.4B.sub.4O.sub.6F of the compound;

(3) FIG. 3 shows the Raman spectrum of the compound NH.sub.4B.sub.4O.sub.6F of the present invention, in which the peak at 3139 cm.sup.1 demonstrates the presence of NH.sup.4+;

(4) FIG. 4 shows the structure of the NH.sub.4B.sub.4O.sub.6F crystal of the present invention;

(5) FIG. 5 illustrating the operating principle of the nonlinear optical device made of the NH.sub.4B.sub.4O.sub.6F crystal of the present invention, wherein 1 is a laser, 2 is convex lens, 3 is an NH.sub.4B.sub.4O.sub.6F crystal, 4 is convex lens, and 5 is a high relective lens.

DETAILED DESCRIPTION OF THE INVENTION

(6) The present invention will be further described in combination with the following examples. It should be noted that, the following examples are not intended to limit the protection scope of the present invention, and any alternations made based on the present invention do not against the spirit of the present invention. The raw materials or equipment used in the present invention are commercially available unless otherwise stated.

Example 1: Compound Preparation

(7) The compound NH.sub.4B.sub.4O.sub.6F was synthesized by the solid phase reaction process based on the reaction equation NH.sub.4F+2B.sub.2O.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F.

(8) NH.sub.4F and B.sub.2O.sub.3 were mixed uniformly at a molar ratio of 1:1.5 and placed into a 10 mm quartz tube. The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun, and then placed into a muffle furnace. The temperature was raised to 400 C. at a rate of 30 C./h and kept for 24 h and then reduced to 30 C. at a rate of 6 C./h, and the quartz tube was opened to obtain the compound NH.sub.4B.sub.4O.sub.6F.

Example 2: Compound Preparation

(9) The compound NH.sub.4B.sub.4O.sub.6F was synthesized by the solid phase reaction process based on the reaction equation NH.sub.4F+4H.sub.3BO.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F+6H.sub.2.

(10) NH.sub.4F and H.sub.3BO.sub.3 were mixed uniformly at a molar ratio of 1:3.5 and placed into a hydrothermal reactor having a volume of 23 mL and lined with polytetrafluoroethylene. The hydrothermal reactor was screwed tightly to be sealed and then was placed into a drying oven. The temperature was raised to 220 C. at a rate of 35 C./h and kept for 24 h and then reduced to 30 C. at a rate of 6 C./h, and the hydrothermal reactor was opened to obtain the compound NH.sub.4B.sub.4O.sub.6F.

Example 3: Synthesis of the Nonlinear Optical Crystal of NH.SUB.4.B.SUB.4.O.SUB.6.F by the Room Temperature Solution Method

(11) The compound NH.sub.4B.sub.4O.sub.6F was synthesized according to the specific operation steps in Example 1 based on the reaction equation NH.sub.4F+2B.sub.2O.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F.

(12) The resultant compound NH.sub.4B.sub.4O.sub.6F was sealed in a hydrothermal reactor and then the hydrothermal reactor was placed into a drying oven. The temperature was raised to 200 C. at a rate of 20 C./h and kept for 10 h and then reduced to 30 C. at a rate of 1 C./h, and the hydrothermal reactor was opened to obtain a seed crystal of NH.sub.4B.sub.4O.sub.6F.

(13) The resultant seed crystal was placed at the bottom of a clean beaker and then the resultant compound NH.sub.4B.sub.4O.sub.6F were placed into the beaker.

(14) 10 mL of hydrofluoric acid was added to the beaker as a solvent. The mixture was mixed and dissolved thoroughly by ultrasonication, adjusted to pH=5-6, and filtered with a qualitative filter paper. The beaker was sealed with a polyvinyl chloride film in which several small holes were punched to adjust the volatilization rate of the solvent in the solution, and was placed into a static environment without shaking, pollution and air convection. The mixture was left to stand at room temperature to obtain the NH.sub.4B.sub.4O.sub.6F crystal with a size of 5 mm6 mm8 mm at the end of the crystal growth.

Example 4: Synthesis of the Nonlinear Optical Crystal of NH.SUB.4.B.SUB.4.O.SUB.6.F by the Room Temperature Solution Method

(15) The compound NH.sub.4B.sub.4O.sub.6F was synthesized according to the specific operation steps in Example 1 based on the reaction equation NH.sub.4F+2B.sub.2O.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F.

(16) The resultant compound NH.sub.4B.sub.4O.sub.6F was placed into a 10 mm quartz tube. The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun, and then placed into a muffle furnace. The temperature was raised to 600 C. at a rate of 40 C./h and kept for 48 h and then reduced to 30 C. at a rate of 5 C./h, and the quartz tube was opened to obtain a seed crystal of NH.sub.4B.sub.4O.sub.6F.

(17) The resultant seed crystal was placed at the bottom of a conical flask and then the resultant compound NH.sub.4B.sub.4O.sub.6F were placed into the conical flask.

(18) 100 mL of anhydrous ethanol was added to the conical flask. The mixture was mixed and dissolved thoroughly by ultrasonication, and then filtered with a qualitative filter paper. The conical flask was sealed with a polyvinyl chloride film in which several small holes were punched to adjust the volatilization rate of the solvent in the solution, and was placed into a static environment without shaking, pollution and air convection. The mixture was left to stand at room temperature to obtain the NH.sub.4B.sub.4O.sub.6F crystal with a size of 7 mm6 mm4 mm at the end of the crystal growth.

Example 5: Growth of the NH.SUB.4.B.SUB.4.O.SUB.6.F Crystal by the Room Temperature Solution Method

(19) The compound NH.sub.4B.sub.4O.sub.6F was synthesized according to the specific operation steps in Example 2 based on the reaction equation NH.sub.4F+4H.sub.3BO.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F+6H.sub.2.

(20) The resultant compound NH.sub.4B.sub.4O.sub.6F was sealed in a hydrothermal reactor. Then the hydrothermal reactor was placed into a drying oven. The temperature was raised to 300 C. at a rate of 30 C./h and kept for 20 h and then reduced to 30 C. at a rate of 2 C./h, and the hydrothermal reactor was opened to obtain a seed crystal of NH.sub.4B.sub.4O.sub.6F.

(21) The resultant seed crystal was placed at the bottom of a beaker and then the compound NH.sub.4B.sub.4O.sub.6F obtained in step a was placed into the beaker.

(22) N,N-dimethylacetamide was added to the beaker. The mixture was mixed and dissolved thoroughly by ultrasonication, and then filtered with a qualitative filter paper. The beaker was sealed with a polyvinyl chloride film in which several small holes were punched to adjust the volatilization rate of the solvent in the solution, and was placed into a static environment without shaking, pollution and air convection. The mixture was left to stand at room temperature to obtain the NH.sub.4B.sub.4O.sub.6F crystal with a size of 13 mm8 mm5 mm at the end of the crystal growth.

Example 6: Growth of the NH.SUB.4.B.SUB.4.O.SUB.6.F Crystal by the Flux Method

(23) The compound NH.sub.4B.sub.4O.sub.6F was synthesized according to the specific operation steps in Example 2 based on the reaction equation NH.sub.4F+4H.sub.3BO.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F+6H.sub.2O.

(24) The resultant compound NH.sub.4B.sub.4O.sub.6F was placed into a 10 mm quartz tube. The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun and then placed into a muffle furnace. The temperature was raised to 400 C. at a rate of 30 C./h and kept for 30 h and then reduced to 30 C. at a rate of 2 C./h, and the quartz tube was opened to obtain a seed crystal of NH.sub.4B.sub.4O.sub.6F.

(25) The resultant seed crystal of NH.sub.4B.sub.4O.sub.6F was placed at the bottom of a quartz tube. Then the resultant compound NH.sub.4B.sub.4O.sub.6F and the flux NH.sub.4F were mixed at a molar ratio of 1:2, and placed into the quartz tube. The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun.

(26) Then the quartz tube was placed into a muffle furnace. The temperature was raised to 500 C. at a rate of 30 C./h and kept for 24 h, then reduced to 450 C. at a rate of 1.5 C./day, and then reduced to 30 C. at a rate of 2 C./h, and the quartz tube was cut to obtain the NH.sub.4B.sub.4O.sub.6F crystal with a size of 5 mm7 mm9 mm.

Example 7: Growth of the NH.SUB.4.B.SUB.4.O.SUB.6.F Crystal by the Flux Method

(27) The compound NH.sub.4B.sub.4O.sub.6F was synthesized according to the specific operation steps in Example 1 based on the reaction equation NH.sub.4F+2B.sub.2O.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F.

(28) The resultant compound NH.sub.4B.sub.4O.sub.6F was placed into a 10 mm quartz tube. The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun and then placed into a muffle furnace. The temperature was raised to 300 C. at a rate of 20 C./h and kept for 10 h and then reduced to 30 C. at a rate of 1 C./h, and the quartz tube was opened to obtain a seed crystal of NH.sub.4B.sub.4O.sub.6F.

(29) The seed crystal of NH.sub.4B.sub.4O.sub.6F was placed at the bottom of a 10 mm quartz tube. Then the compound NH.sub.4B.sub.4O.sub.6F and the flux NH.sub.4FH.sub.3BO.sub.3 (wherein the molar ratio of NH.sub.4F to H.sub.3BO.sub.3 is 1:1) were mixed at a molar ratio of 1:1, and placed into the quartz tube. The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun.

(30) Then the quartz tube was placed into a muffle furnace. The temperature was raised to 450 C. at a rate of 30 C./h and kept for 24 h, then reduced to 400 C. at a rate of 1.5 C./day, and then reduced to 30 C. at a rate of 2 C./h, and the quartz tube was cut to obtain the NH.sub.4B.sub.4O.sub.6F crystal with a size of 10 mm7 mm6 mm.

Example 8: Growth of the NH.SUB.4.B.SUB.4.O.SUB.6.F Crystal by the Flux Method

(31) The compound NH.sub.4B.sub.4O.sub.6F was synthesized according to the specific operation steps in Example 2 based on the reaction equation NH.sub.4F+4H.sub.3BO.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F+6H.sub.2O.

(32) The resultant compound NH.sub.4B.sub.4O.sub.6F was placed into a 10 mm quartz tube. The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun and then placed into a muffle furnace. The temperature was raised to 500 C. at a rate of 40 C./h and kept for 40 h and then reduced to 30 C. at a rate of 4 C./h, and the quartz tube was opened to obtain a seed crystal of NH.sub.4B.sub.4O.sub.6F.

(33) The resultant seed crystal of NH.sub.4B.sub.4O.sub.6F was placed at the bottom of a quartz tube. Then the resultant compound NH.sub.4B.sub.4O.sub.6F and the flux NH.sub.4FB.sub.2O.sub.3 (the molar ratio of NH.sub.4F to B.sub.2O.sub.3 is 1:4) were mixed at a molar ratio of 1:5, and placed into the quartz tube. The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun.

(34) Then the quartz tube was placed into a muffle furnace. The temperature was raised to 450 C. at a rate of 40 C./h and kept for 20 h, then reduced to 400 C. at a rate of 2 C./day, and then reduced to 30 C. at a rate of 3 C./h, and the quartz tube was cut to obtain the NH.sub.4B.sub.4O.sub.6F crystal with a size of 5 mm7 mm8 mm.

Example 9: Growth of the NH.SUB.4.B.SUB.4.O.SUB.6.F Crystal by the Flux Method

(35) The compound NH.sub.4B.sub.4O.sub.6F was synthesized according to the specific operation steps in Example 1 based on the reaction equation NH.sub.4F+2B.sub.2O.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F.

(36) The resultant compound NH.sub.4B.sub.4O.sub.6F was placed into a 10 mm quartz tube. The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun and then placed into a muffle furnace. The temperature was raised to 300 C. at a rate of 25 C./h and kept for 30 h and then reduced to 30 C. at a rate of 3 C./h, and the quartz tube was opened to obtain a seed crystal of NH.sub.4B.sub.4O.sub.6F.

(37) The seed crystal of NH.sub.4B.sub.4O.sub.6F was placed at the bottom of a 10 mm quartz tube. Then the compound NH.sub.4B.sub.4O.sub.6F and the flux H.sub.3BO.sub.3 were mixed at a molar ratio of 1:5, and placed into the quartz tube. The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun.

(38) Then the quartz tube was placed into a muffle furnace. The temperature was raised to 600 C. at a rate of 40 C./h and kept for 48 h, then reduced to 550 C. at a rate of 3 C./day, and then reduced to 30 C. at a rate of 10 C./h, and the quartz tube was cut to obtain the NH.sub.4B.sub.4O.sub.6F crystal with a size of 8 mm7 mm6 mm.

Example 10: Growth of the NH.SUB.4.B.SUB.4.O.SUB.6.F Crystal by the Flux Method

(39) The compound NH.sub.4B.sub.4O.sub.6F was synthesized according to the specific operation steps in Example 1 based on the reaction equation NH.sub.4F+2B.sub.2O.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F.

(40) The resultant compound NH.sub.4B.sub.4O.sub.6F was sealed in a hydrothermal reactor and the hydrothermal reactor was placed into a drying oven. The temperature was raised to 200 C. at a rate of 25 C./h and kept for 15 h and then reduced to 30 C. at a rate of 3 C./h, and the hydrothermal reactor was opened to obtain a seed crystal of NH.sub.4B.sub.4O.sub.6F.

(41) The seed crystal of NH.sub.4B.sub.4O.sub.6F was placed at the bottom of a 10 mm quartz tube. Then the compound NH.sub.4B.sub.4O.sub.6F and the flux NH.sub.4FH.sub.3BO.sub.3 (the molar ratio of NH.sub.4F to H.sub.3BO.sub.3 is 2:3) were mixed at a molar ratio of 1:10, and placed into the quartz tube. The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun.

(42) Then the quartz tube was placed into a muffle furnace. The temperature was raised to 450 C. at a rate of 30 C./h and kept for 24 h, then reduced to 400 C. at a rate of 1.5 C./day, and then reduced to 30 C. at a rate of 2 C./h, and the quartz tube was cut to obtain the NH.sub.4B.sub.4O.sub.6F crystal with a size of 8 mm6 mm4 mm.

Example 11: Growth of the NH.SUB.4.B.SUB.4.O.SUB.6.F Crystal by the Flux Method

(43) The compound NH.sub.4B.sub.4O.sub.6F was synthesized according to the specific operation steps in Example 2 based on the reaction equation NH.sub.4F+4H.sub.3BO.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F+6H.sub.2O.

(44) The resultant compound NH.sub.4B.sub.4O.sub.6F was placed into a 10 mm quartz tube. The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun and then placed into a muffle furnace. The temperature was raised to 500 C. at a rate of 40 C./h and kept for 40 h and then reduced to 30 C. at a rate of 4 C./h, and the quartz tube was opened to obtain a seed crystal of NH.sub.4B.sub.4O.sub.6F.

(45) The resultant seed crystal of NH.sub.4B.sub.4O.sub.6F was placed at the bottom of a quartz tube. Then the resultant compound NH.sub.4B.sub.4O.sub.6F and the flux NH.sub.4FB.sub.2O.sub.3 (the molar ratio of NH.sub.4F to B.sub.2O.sub.3 is 1:4) were mixed at a molar ratio of 1:5, and placed into the quartz tube. The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun.

(46) Then the quartz tube was placed into a muffle furnace. The temperature was raised to 400 C. at a rate of 40 C./h and kept for 20 h, then reduced to 350 C. at a rate of 2 C./day, and then reduced to 30 C. at a rate of 3 C./h, and the quartz tube was cut to obtain the NH.sub.4B.sub.4O.sub.6F crystal with a size of 5 mm7 mm7 mm.

Example 12: Growth of the NH.SUB.4.B.SUB.4.O.SUB.6.F Crystal by the Flux Method

(47) The compound NH.sub.4B.sub.4O.sub.6F was synthesized according to the specific operation steps in Example 1 based on the reaction equation NH.sub.4F+2B.sub.2O.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F.

(48) The resultant compound NH.sub.4B.sub.4O.sub.6F was sealed in a hydrothermal reactor and the hydrothermal reactor was placed into a drying oven. The temperature was raised to 200 C. at a rate of 25 C./h and kept for 30 h and then reduced to 30 C. at a rate of 3 C./h, and the hydrothermal reactor was opened to obtain a seed crystal of NH.sub.4B.sub.4O.sub.6F.

(49) The seed crystal of NH.sub.4B.sub.4O.sub.6F was placed at the bottom of a 10 mm quartz tube. Then the compound NH.sub.4B.sub.4O.sub.6F and the flux H.sub.3BO.sub.3 were mixed at a molar ratio of 1:5, and placed into the quartz tube. The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun.

(50) Then the quartz tube was placed into a muffle furnace. The temperature was raised to 600 C. at a rate of 40 C./h and kept for 48 h, then reduced to 550 C. at a rate of 3 C./day, and then reduced to 30 C. at a rate of 10 C./h, and the quartz tube was cut to obtain the NH.sub.4B.sub.4O.sub.6F crystal with a size of 8 mm6 mm4 mm.

Example 13: Growth of the NH.SUB.4.B.SUB.4.O.SUB.6.F Crystal by the Flux Method

(51) The compound NH.sub.4B.sub.4O.sub.6F was synthesized according to the specific operation steps in Example 2 based on the reaction equation NH.sub.4F+4H.sub.3BO.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F+6H.sub.2O.

(52) The resultant compound NH.sub.4B.sub.4O.sub.6F was placed into a 10 mm quartz tube. The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun and then placed into a muffle furnace. The temperature was raised to 550 C. at a rate of 35 C./h and kept for 40 h and then reduced to 30 C. at a rate of 5 C./h, and the quartz tube was opened to obtain a seed crystal of NH.sub.4B.sub.4O.sub.6F.

(53) The resultant seed crystal of NH.sub.4B.sub.4O.sub.6F was placed at the bottom of a quartz tube. Then the resultant compound NH.sub.4B.sub.4O.sub.6F and the flux NH.sub.4FB.sub.2O.sub.3 (the molar ratio of NH.sub.4F to B.sub.2O.sub.3 is 2:4) were mixed at a molar ratio of 1:5, and placed into the quartz tube. The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun.

(54) Then the quartz tube was placed into a muffle furnace. The temperature was raised to 450 C. at a rate of 35 C./h and kept for 36 h, then reduced to 400 C. at a rate of 4 C./day, and then reduced to 30 C. at a rate of 10 C./h, and the quartz tube was cut to obtain the NH.sub.4B.sub.4O.sub.6F crystal with a size of 5 mm7 mm9 mm.

Example 14: Growth of the NH.SUB.4.B.SUB.4.O.SUB.6.F Crystal by the Flux Method

(55) The compound NH.sub.4B.sub.4O.sub.6F was synthesized according to the specific operation steps in Example 1 based on the reaction equation NH.sub.4F+2B.sub.2O.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F.

(56) The resultant compound NH.sub.4B.sub.4O.sub.6F was placed into a 10 mm quartz tube. The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun and then placed into a muffle furnace. The temperature was raised to 550 C. at a rate of 40 C./h and kept for 25 h and then reduced to 30 C. at a rate of 4 C./h, and the quartz tube was cut to obtain a seed crystal of NH.sub.4B.sub.4O.sub.6F.

(57) The seed crystal of NH.sub.4B.sub.4O.sub.6F was placed at the bottom of a 10 mm quartz tube. Then the compound NH.sub.4B.sub.4O.sub.6F and the flux NH.sub.4FH.sub.3BO.sub.3 (the molar ratio of NH.sub.4F to H.sub.3BO.sub.3 is 3:5) were mixed at a molar ratio of 1:10, and placed into the quartz tube. The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun.

(58) Then the quartz tube was placed into a muffle furnace. The temperature was raised to 550 C. at a rate of 40 C./h and kept for 40 h, then reduced to 500 C. at a rate of 3 C./day, and then reduced to 30 C. at a rate of 8 C./h, and the quartz tube was cut to obtain the NH.sub.4B.sub.4O.sub.6F crystal with a size of 9 mm7 mm6 mm.

Example 15: Growth of the NH.SUB.4.B.SUB.4.O.SUB.6.F Crystal by the Flux Method

(59) The compound NH.sub.4B.sub.4O.sub.6F was synthesized according to the specific operation steps in Example 1 based on the reaction equation NH.sub.4F+2B.sub.2O.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F.

(60) The resultant compound NH.sub.4B.sub.4O.sub.6F was placed into a 10 mm quartz tube. The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun and then placed into a muffle furnace. The temperature was raised to 500 C. at a rate of 30 C./h and kept for 15 h and then reduced to 30 C. at a rate of 5 C./h, and the hydrothermal reactor or the quartz tube was opened to obtain a seed crystal of NH.sub.4B.sub.4O.sub.6F.

(61) The seed crystal of NH.sub.4B.sub.4O.sub.6F was placed at the bottom of a 10 mm quartz tube. Then the compound NH.sub.4B.sub.4O.sub.6F and the flux B.sub.2O.sub.3 were mixed at a molar ratio of 1:10, and placed into the quartz tube. The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun.

(62) Then the quartz tube was placed into a muffle furnace. The temperature was raised to 500 C. at a rate of 40 C./h and kept for 45 h, then reduced to 450 C. at a rate of 3 C./day, and then reduced to 30 C. at a rate of 6 C./h, and the quartz tube was cut to obtain the NH.sub.4B.sub.4O.sub.6F crystal with a size of 7 mm6 mm4 mm.

Example 16: Growth of the NH.SUB.4.B.SUB.4.O.SUB.6.F Crystal by the Bridgman-Stockbarger Method

(63) The compound NH.sub.4B.sub.4O.sub.6F was synthesized according to the specific operation steps in Example 1 based on the reaction equation NH.sub.4F+2B.sub.2O.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F.

(64) The resultant compound NH.sub.4B.sub.4O.sub.6F was placed into a 10 mm quartz tube. The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun and then placed into a muffle furnace. The temperature was raised to 600 C. at a rate of 40 C./h and kept for 48 h and then reduced to 30 C. at a rate of 5 C./h, and the hydrothermal reactor or the quartz tube was opened to obtain a seed crystal of NH.sub.4B.sub.4O.sub.6F.

(65) The resultant seed crystal was placed at the bottom of a platinum crucible and then the resultant compound NH.sub.4B.sub.4O.sub.6F were placed into the platinum crucible.

(66) The platinum crucible was sealed and placed into a Bridgman-Stockbarger furnace. The temperature was raised to 300 C. and kept for 10 h. The position of the platinum crucible was adjusted to allow the compound NH.sub.4B.sub.4O.sub.6F to nucleate spontaneously. Then the platinum crucible was lowered at a rate of 0.05 mm/h slowly while the growth temperature was kept constant. The temperature of the furnace was reduced to 30 C. after the growth of the crystal is completed, and the platinum crucible was removed to obtain the NH.sub.4B.sub.4O.sub.6F crystal with a size of 6 mm8 mm12 mm.

Example 17: Growth of the NH.SUB.4.B.SUB.4.O.SUB.6.F Crystal by the Bridgman-Stockbarger Method

(67) The compound NH.sub.4B.sub.4O.sub.6F was synthesized according to the specific operation steps in Example 1 based on the reaction equation NH.sub.4F+4H.sub.3BO.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F+6H.sub.2O.

(68) The resultant compound NH.sub.4B.sub.4O.sub.6F was sealed in a hydrothermal reactor, and the hydrothermal reactor was placed into a drying oven. The temperature was raised to 200 C. at a rate of 20 C./h and kept for 10 h and then reduced to 30 C. at a rate of 1 C./h, and the hydrothermal reactor was opened to obtain a seed crystal of NH.sub.4B.sub.4O.sub.6F.

(69) The resultant seed crystal was placed at the bottom of an iridium crucible and then the resultant compound NH.sub.4B.sub.4O.sub.6F were placed into the iridium crucible.

(70) The iridium crucible was sealed and placed into a Bridgman-Stockbarger furnace. The temperature was raised to 600 C. and kept for 20 h. The position of the iridium crucible was adjusted to allow the compound NH.sub.4B.sub.4O.sub.6F to inoculate at 350 C. Then the iridium crucible was lowered at a rate of 2 mm/h slowly while the temperature was reduced slowly at a rate of 3 C./h. The temperature of the furnace was reduced to 30 C. after the growth of the crystal is completed, and the iridium crucible was removed to obtain the NH.sub.4B.sub.4O.sub.6F crystal with a size of 7 mm6 mm5 mm.

Example 18: Growth of the NH.SUB.4.B.SUB.4.O.SUB.6.F Crystal by the Bridgman-Stockbarger Method

(71) The compound NH.sub.4B.sub.4O.sub.6F was synthesized according to the specific operation steps in Example 1 based on the reaction equation NH.sub.4F+2B.sub.2O.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F.

(72) The resultant compound NH.sub.4B.sub.4O.sub.6F was placed into a 10 mm quartz tube. The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun and then placed into a muffle furnace. The temperature was raised to 400 C. at a rate of 30 C./h and kept for 36 h and then reduced to 30 C. at a rate of 3 C./h, and the quartz tube was cut to obtain a seed crystal of NH.sub.4B.sub.4O.sub.6F.

(73) The resultant seed crystal was placed at the bottom of a ceramic crucible and then the resultant compound NH.sub.4B.sub.4O.sub.6F were placed into the ceramic crucible.

(74) The ceramic crucible was sealed and placed into a Bridgman-Stockbarger furnace. The temperature was raised to 400 C. and kept for 15 h. The position of the ceramic crucible was adjusted to allow the compound NH.sub.4B.sub.4O.sub.6F to inoculate at 500 C. Then the ceramic crucible was lowered at a rate of 0.5 mm/h slowly while the growth temperature was kept constant. The temperature of the furnace was reduced to 30 C. after the growth of the crystal is completed, and the ceramic crucible was removed to obtain the NH.sub.4B.sub.4O.sub.6F crystal with a size of 6 mm8 mm12 mm.

Example 19: Growth of the NH.SUB.4.B.SUB.4.O.SUB.6.F Crystal by the Bridgman-Stockbarger Method

(75) The compound NH.sub.4B.sub.4O.sub.6F was synthesized according to the specific operation steps in Example 1 based on the reaction equation NH.sub.4F+4H.sub.3BO.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F+6H.sub.2O.

(76) The resultant compound NH.sub.4B.sub.4O.sub.6F was sealed in a hydrothermal reactor and the hydrothermal reactor was placed into a drying oven. The temperature was raised to 200 C. at a rate of 20 C./h and kept for 10 h and then reduced to 30 C. at a rate of 1 C./h, and the hydrothermal reactor was opened to obtain a seed crystal of NH.sub.4B.sub.4O.sub.6F.

(77) The resultant seed crystal was placed at the bottom of a quartz tube and then the resultant compound NH.sub.4B.sub.4O.sub.6F were placed into the quartz tube.

(78) The quartz tube was vacuumized to reach a vacuum degree of 110.sup.3 Pa and sealed with a flame gun. Then the quartz tube was placed into a Bridgman-Stockbarger furnace. The temperature was raised to 600 C. and kept for 20 h. The position of the quartz tube was adjusted to allow the compound NH.sub.4B.sub.4O.sub.6F to inoculate at 600 C. Then the quartz tube was lowered at a rate of 1 mm/h slowly while the temperature was reduced slowly at a rate of 2 C./h. The temperature of the furnace was reduced to 30 C. after the growth of the crystal is completed, and the quartz tube was removed to obtain the NH.sub.4B.sub.4O.sub.6F crystal with a size of 7 mm 6 mm5 mm.

Example 20 Growth of the NH.SUB.4.B.SUB.4.O.SUB.6.F Crystal by the Solvothermal Method

(79) The compound NH.sub.4B.sub.4O.sub.6F was synthesized according to the specific operation steps in Example 2 based on the reaction equation NH.sub.4F+4H.sub.3BO.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F+6H.sub.2O.

(80) The resultant compound NH.sub.4B.sub.4O.sub.6F was sealed in a hydrothermal reactor and the hydrothermal reactor was placed into a drying oven. The temperature was raised to 200 C. at a rate of 20 C./h and kept for 10 h and then reduced to 30 C. at a rate of 1 C./h, and the hydrothermal reactor was opened to obtain a seed crystal of NH.sub.4B.sub.4O.sub.6F.

(81) The resultant seed crystal was placed at the bottom of the polytetrafluoroethylene lining of a hydrothermal reactor having a volume of 23 mL, and then the resultant compound NH.sub.4B.sub.4O.sub.6F was placed into the polytetrafluoroethylene lining.

(82) The solvent of deionized water was added to the polytetrafluoroethylene lining. The hydrothermal reactor was screwed tightly to be sealed and then was placed into a drying oven. The temperature was raised to 150 C. at a rate of 20 C./h and kept for 24 h, then reduced to 100 C. at a rate of 2 C./day and then reduced to 30 C. at a rate of 2 C./h, and the hydrothermal reactor was opened to obtain the NH.sub.4B.sub.4O.sub.6F crystal with a size of 5 mm6 mm8 mm.

Example 21 Growth of the NH.SUB.4.B.SUB.4.O.SUB.6.F Crystal by the Solvothermal Method

(83) The compound NH.sub.4B.sub.4O.sub.6F was synthesized according to the specific operation steps in Example 2 based on the reaction equation NH.sub.4F+4H.sub.3BO.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F+6H.sub.2O.

(84) The resultant compound NH.sub.4B.sub.4O.sub.6F was placed at the bottom of the polytetrafluoroethylene lining of a hydrothermal reactor having a volume of 23 mL, and the hydrothermal reactor was placed into a drying oven. The temperature was raised to 200 C. at a rate of 20 C./h and kept for 10 h and then reduced to 30 C. at a rate of 1 C./h, and the hydrothermal reactor was opened to obtain a seed crystal of NH.sub.4B.sub.4O.sub.6F.

(85) The resultant seed crystal was placed at the bottom of the polytetrafluoroethylene lining of a hydrothermal reactor, and then the resultant compound NH.sub.4B.sub.4O.sub.6F was placed into the polytetrafluoroethylene lining of the hydrothermal reactor.

(86) The solvent of 10 mL N,N-dimethylformamide was added to the polytetrafluoroethylene lining of the hydrothermal reactor. The hydrothermal reactor was screwed tightly to be sealed and then was placed into a drying oven. The temperature was raised to 150 C. at a rate of 20 C./h and kept for 24 h, then reduced to 100 C. at a rate of 2 C./day and then reduced to 30 C. at a rate of 2 C./h, and the hydrothermal reactor was opened to obtain the NH.sub.4B.sub.4O.sub.6F crystal with a size of 5 mm6 mm8 mm.

Example 22 Growth of the NH.SUB.4.B.SUB.4.O.SUB.6.F Crystal by the Solvothermal Method

(87) The compound NH.sub.4B.sub.4O.sub.6F was synthesized according to the specific operation steps in Example 2 based on the reaction equation NH.sub.4F+2B.sub.2O.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F.

(88) The resultant compound NH.sub.4B.sub.4O.sub.6F was placed at the bottom of a hydrothermal reactor having a volume of 100 mL and lined with stainless steel with a platinum sleeve, and the hydrothermal reactor was placed into a muffle furnace. The temperature was raised to 300 C. at a rate of 30 C./h and kept for 15 h and then reduced to 30 C. at a rate of 2 C./h, and the hydrothermal reactor was opened to obtain a seed crystal of NH.sub.4B.sub.4O.sub.6F.

(89) The resultant seed crystal was placed at the bottom of a hydrothermal reactor lined with stainless steel with a platinum sleeve, and then the resultant compound NH.sub.4B.sub.4O.sub.6F were placed into the hydrothermal reactor lined with stainless steel with the platinum sleeve.

(90) The solvent of 50 mL deionized water was added to the hydrothermal reactor lined with stainless steel with the platinum sleeve. The hydrothermal reactor was screwed tightly to be sealed and then was placed into a muffle furnace. The temperature was raised to 250 C. at a rate of 30 C./h and kept for 24 h, then reduced to 200 C. at a rate of 2 C./day and then reduced to 30 C. at a rate of 5 C./h, and the hydrothermal reactor was opened to obtain the NH.sub.4B.sub.4O.sub.6F crystal with a size of 5 mm6 mm8 mm.

Example 23 Growth of the NH.SUB.4.B.SUB.4.O.SUB.6.F Crystal by the Solvothermal Method

(91) The compound NH.sub.4B.sub.4O.sub.6F was synthesized according to the specific operation steps in Example 2 based on the reaction equation NH.sub.4F+4H.sub.3BO.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F+6H.sub.2O.

(92) The resultant compound NH.sub.4B.sub.4O.sub.6F was placed at the bottom of a hydrothermal reactor having a volume of 150 mL and lined with stainless steel with a platinum sleeve, and the hydrothermal reactor was placed into a muffle furnace. The temperature was raised to 500 C. at a rate of 35 C./h and kept for 48 h and then reduced to 30 C. at a rate of 4 C./h, and the hydrothermal reactor was opened to obtain a seed crystal of NH.sub.4B.sub.4O.sub.6F.

(93) The resultant seed crystal was placed at the bottom of a hydrothermal reactor lined with stainless steel with a platinum sleeve, and then the resultant compound NH.sub.4B.sub.4O.sub.6F were placed into the hydrothermal reactor lined with stainless steel with the platinum sleeve.

(94) The solvent of 80 mL hydrofluoric acid was added to the hydrothermal reactor lined with stainless steel with the platinum sleeve. The hydrothermal reactor was screwed tightly to be sealed and then was placed into a muffle furnace. The temperature was raised to 600 C. at a rate of 40 C./h and kept for 48 h, then reduced to 550 C. at a rate of 3 C./day and then reduced to 30 C. at a rate of 10 C./h, and the hydrothermal reactor was opened to obtain the NH.sub.4B.sub.4O.sub.6F crystal with a size of 5 mm6 mm8 mm.

Example 24 Growth of the NH.SUB.4.B.SUB.4.O.SUB.6.F Crystal by the Solvothermal Method

(95) The compound NH.sub.4B.sub.4O.sub.6F was synthesized according to the specific operation steps in Example 2 based on the reaction equation NH.sub.4F+4H.sub.3BO.sub.3.fwdarw.NH.sub.4B.sub.4O.sub.6F+6H.sub.2O.

(96) The resultant compound NH.sub.4B.sub.4O.sub.6F was placed at the bottom of the polytetrafluoroethylene lining of a hydrothermal reactor having a volume of 23 mL, and the hydrothermal reactor was placed into a drying oven. The temperature was raised to 220 C. at a rate of 40 C./h and kept for 48 h and then reduced to 30 C. at a rate of 5 C./h, and the hydrothermal reactor was opened to obtain a seed crystal of NH.sub.4B.sub.4O.sub.6F.

(97) The resultant seed crystal was placed at the bottom of the polytetrafluoroethylene lining of a hydrothermal reactor, and then the resultant compound NH.sub.4B.sub.4O.sub.6F was placed into the polytetrafluoroethylene lining of the hydrothermal reactor.

(98) The solvent of 10 mL N,N-dimethylacetamide was added to the polytetrafluoroethylene lining of the hydrothermal reactor. The hydrothermal reactor was screwed tightly to be sealed and then was placed into a drying oven. The temperature was raised to 210 C. at a rate of 40 C./h and kept for 35 h, then reduced to 160 C. at a rate of 3 C./day and then reduced to 30 C. at a rate of 4 C./h, and the hydrothermal reactor was opened to obtain the NH.sub.4B.sub.4O.sub.6F crystal with a size of 5 mm6 mm8 mm.

Example 25

(99) The NH.sub.4B.sub.4O.sub.6F crystal obtained in any one of Examples 1-24 was processed in the direction of phase matching, and placed in position 3 as shown in FIG. 5. A Q-switched Nd:YAG laser is used as a light source at room temperature, and the incident wavelength is 1064 nm. The Q-switched Nd:YAG laser 1 emits an infrared beam 2 with a wavelength of 1064 nm, which is then transmitted to an NH.sub.4B.sub.4O.sub.6F crystal 3, thus generating a green frequency-multiplied light with a wavelength of 532 nm, and the intensity of the output beam is about 3 times of that from KDP in the same condition.

Example 26

(100) The NH.sub.4B.sub.4O.sub.6F crystal obtained in any one of Examples 1-24 was processed in the direction of phase matching, and placed in position 3 as shown in FIG. 5. A Q-switched Nd:YAG laser is used as a light source at room temperature, and the incident wavelength is 532 nm. The Q-switched Nd:YAG laser 1 emits an infrared beam 2 with a wavelength of 532 nm, which is then transmitted to an NH.sub.4B.sub.4O.sub.6F crystal 3, thus generating a frequency-multiplied light with a wavelength of 266 nm, and the intensity of the output beam is about 1.5 times of that from BBO in the same condition.

Example 27

(101) The NH.sub.4B.sub.4O.sub.6F crystal obtained in any one of Examples 1-24 was processed in the direction of phase matching, and placed in position 3 as shown in FIG. 5. A Q-switched Nd:YAG laser is used as a light source at room temperature, and the incident wavelength is 355 nm. The Q-switched Nd:YAG laser 1 emits an infrared beam 2 with a wavelength of 355 nm, which is then transmitted to an NH.sub.4B.sub.4O.sub.6F crystal 3, and the outputting of a deep-ultraviolet frequency-multiplied light with a wavelength of 177.3 nm can be observed.