Glass ceramic for excitation of high-power semiconductor light source and preparation method and use thereof

Abstract

The present invention discloses a glass ceramic for excitation of high-power semiconductor light source. An expression of constitution of the glass ceramic is (1x)A: xB, wherein x as a weight percentage of B, is ranging from 1% to 30%; A as a precursor glass, has a composition of aSb.sub.2O.sub.3-bB.sub.2O.sub.3-cZnO-dM.sub.2O, a, b, c, d being molar percentages, a+b+c+d=100%, M among M.sub.2O represents an alkali metal, and M.sub.2O is an alkali metallic oxide or an alkali metallic carbonate; and B is a YAG:Ce.sup.3+ fluorescent powder. The precursor glass provided by the present invention has a relatively low remelting temperature, without devitrification during the process of preparing the final products or absorption of blue light. The product glass ceramic has a luminous efficiency of 300 lm/W to 400 lm/W. A white light semiconductor light source is prepared by the product glass ceramic in combination with the high-power blue light semiconductor light source. A preparation method provided by the present invention has advantages such as low cost, excellent performances, and being green, pollution-free and suitable for the large-scale industrial production. The present invention can be applied in the field of illumination light source and display light source, such as head-lights of vehicles, searchlights, projectors and laser cinemas.

Claims

1. A glass ceramic for excitation of a high-power semiconductor light source, comprising, an expression of constitution of the glass ceramic is (1x)A: xB, wherein x as a weight percentage of B, is ranging from 1% to 30%; A as a precursor glass, has a composition of aSb.sub.2O.sub.3-bB.sub.2O.sub.3-cZnO-dM.sub.2O, a, b, c and d being molar percentages, a+b+c+d=100%, M among M.sub.2O represents an alkali metal, and M.sub.2O is an alkali metallic oxide or an alkali metallic carbonate; and B is a YAG:Ce.sup.3+ fluorescent powder.

2. The glass ceramic for excitation of the high-power semiconductor light source according to claim 1, wherein a:b:c:d=(40-60):(15-20):(5-20):(15-20).

3. The glass ceramic for excitation of the high-power semiconductor light source according to claim 2, wherein a:b:c:d=(50-60):(17.5-20):(5-10):(17.5-20).

4. The glass ceramic for excitation of the high-power semiconductor light source according to claim 1, wherein M is selected from a group consisting of Li, Na and K.

5. A preparation method for the glass ceramic for excitation of the high-power semiconductor light source according to claim 1, the preparation method comprises steps as follow: S1. Mixing each constituent raw material of a precursor glass according to molar percentages, followed by high-temperature melting, cooling and grinding to obtain a precursor glass powder; S2. Mixing the precursor glass powder in S1 with a YAG:Ce.sup.3+ fluorescent powder according to a weight percentage, followed by a melt reaction, holding, annealing and polishing to obtain the glass ceramic for the excitation of the high-power semiconductor light source.

6. The preparation method according to claim 5, wherein in S1, a temperature of the high-temperature melting is ranging from 900 C. to 1100 C., and a time for the high-temperature melting is ranging from 5 minutes to 60 minutes.

7. The preparation method according to claim 5, wherein in S1, a time for the grinding is ranging from 6 hours to 24 hours.

8. The preparation method according to claim 5, wherein in S2, a temperature of the melt reaction is ranging from 600 C. to 750 C., a time for the holding is ranging from 10 minutes to 50 minutes; a temperature of the annealing is ranging from 200 C. to 400 C., and a time for the annealing is ranging from 3 hours to 5 hours.

9. Use of the glass ceramic for the excitation of the high-power semiconductor light source according to claim 1 in preparing a high-power white light illumination and display light source.

10. The use according to claim 9, wherein the glass ceramic for the excitation of the high-power semiconductor light source is combined with a blue light semiconductor light source to prepare the high-power white light illumination and display light source.

11. Use of the glass ceramic for the excitation of the high-power semiconductor light source according to claim 2 in preparing a high-power white light illumination and display light source.

12. Use of the glass ceramic for the excitation of the high-power semiconductor light source according to claim 3 in preparing a high-power white light illumination and display light source.

13. Use of the glass ceramic for the excitation of the high-power semiconductor light source according to claim 4 in preparing a high-power white light illumination and display light source.

14. The use according to claim 11, wherein the glass ceramic for the excitation of the high-power semiconductor light source is combined with a blue light semiconductor light source to prepare the high-power white light illumination and display light source.

15. The use according to claim 12, wherein the glass ceramic for the excitation of the high-power semiconductor light source is combined with a blue light semiconductor light source to prepare the high-power white light illumination and display light source.

16. The use according to claim 13, wherein the glass ceramic for the excitation of the high-power semiconductor light source is combined with a blue light semiconductor light source to prepare the high-power white light illumination and display light source.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 is XRD patterns of a precursor glass and a YAG:Ce.sup.3+-PiG sample prepared in Embodiment 1.

(2) FIG. 2 is SEM patterns of a YAG:Ce.sup.3+-PiG sample prepared in Embodiment 2.

(3) FIG. 3 is excitation and emission spectrums of the YAG:Ce.sup.3+-PiG prepared in Embodiment 4 (the excitation and emission spectrums of a YAG:Ce.sup.3+ fluorescent powder and a YAG:Ce.sup.3+-PiG glass ceramic respectively, wherein an excitation wavelength is 450 nm and a monitoring emission wavelength is 550 nm).

(4) FIG. 4 is electroluminescence spectrograms of a white light laser light source prepared by the YAG:Ce.sup.3+-PiG in combination with a high-power blue light semiconductor light source in Embodiment 5.

(5) FIG. 5 is a current variation curve of a lumen versus a laser drive current, for the white light laser light source prepared by the YAG:Ce.sup.3+-PiG in combination with the high-power blue light semiconductor light source in Embodiment 5.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

(6) The present invention is further described below in combination with specific embodiments and drawings. However, the embodiments are not intended to limit the present invention in any manner. Unless specified, agents, methods and devices used in the present invention are conventional in the technical field.

(7) Unless specified, agents and materials used in the present invention are commercially available.

Embodiment 1

(8) A synthesis process of a glass ceramic with B:A=23:77

(9) TABLE-US-00001 TABLE 1 Constitution of raw materials and the synthesis process of a precursor glass in Embodiment 1 Raw materials Sb.sub.2O.sub.3 H.sub.3BO.sub.3 ZnO K.sub.2CO.sub.3 Mass (g) 17.4911 2.1642 0.4070 2.4186

(10) A constitution of A was a:b:c:d=60:17.5:5:17.5, shown as the corresponding mass in Table 1. Analytically pure diantimony trioxide (Sb.sub.2O.sub.3), boric acid (H.sub.3BO.sub.3), zinc oxide (ZnO) and potassium carbonate (K.sub.2CO.sub.3) were precisely weighed according to Table 1. The raw materials precisely weighed were transferred into a crucible after being grinded for 1 to 2 hours in an agate mortar, and then were melted in a furnace for 30 minutes at 900 C. Molten glass was poured into a graphite mold for quenching. Glass cullet was taken out and grinded for 6 hours to obtain an A powder standby. The B powder and the A powder was weighed according to a mass ratio of 23:77, and then was poured into the crucible after being grinded sufficiently for 0.5 hour in the agate mortar, followed by being melted in the furnace for 30 minutes at 700 C. Then the molten glass was poured into a preheated graphite mold for molding, and at last was annealed in the furnace for 4 hours at 350 C., and thus a sample was obtained. The sample was cut into an appropriate thickness by a diamond wire cutting machine, and was polished to mirror plane on both sides, and thus a YAG:Ce.sup.3+-PiG glass ceramic for packaging complying with requirements was obtained. Particularly, FIG. 1 is XRD patterns of the synthesized YAG:Ce.sup.3+-PiG glass ceramic, wherein an XRD curve of a YAG:Ce.sup.3+ fluorescent powder is shown as Glass fit and the standard card PDF #33-0040 is shown as JPCDS (33-0040). It can be observed that there is no new crystal generated in a glass matrix during the synthesis, and crystal diffraction peaks of the YAG:Ce.sup.3+-PiG glass ceramic are in one-to-one correspondence with diffraction peaks of the YAG:Ce fluorescent powder and the standard card of the YAG, indicating that the synthesized YAG:Ce.sup.3+-PiG glass ceramic (a glass ceramic for excitation of a high-power semiconductor light source) comprises the YAG:Ce fluorescent powder.

Embodiment 2: A Synthesis Process of a Glass Ceramic with B:A=5:95

(11) TABLE-US-00002 TABLE 2 Constitution of the raw materials and the synthesis process of a precursor glass in Embodiment 2 Raw materials Sb.sub.2O.sub.3 H.sub.3BO.sub.3 ZnO K.sub.2CO.sub.3 Mass (g) 16.0335 2.4733 0.4070 2.7641

(12) The constitution of A was a:b:c:d=55:20:5:20, shown as the corresponding mass in Table 2. Analytically pure diantimony trioxide (Sb.sub.2O.sub.3), boric acid (H.sub.3BO.sub.3), zinc oxide (ZnO) and potassium carbonate (K.sub.2CO.sub.3) were precisely weighed according to table 2. The raw materials precisely weighed were transferred into the crucible after being grinded for 1 to 2 hours in the agate mortar, and then were melted in the furnace for 15 minutes at 950 C. Molten glass was poured into the graphite mold for quenching. Glass cullet was taken out and grinded for 6 hours to obtain an A powder standby. The B powder and the A powder was weighed according to a mass ratio of 5:95, and then was poured into the crucible after being grinded sufficiently for 0.5 hour in the agate mortar, followed by being melted in the furnace for 30 minutes at 650 C. Then the molten glass was poured into the preheated graphite mold for molding, and at last was annealed in the furnace for 3 hours at 350 C., and thus a sample was obtained. The sample was cut into an appropriate thickness by the diamond wire cutting machine and was polished to mirror plane on both sides, and thus the YAG:Ce.sup.3+-PiG glass ceramic for packaging complying with the requirements was obtained. FIG. 2 is SEM patterns of the sample. FIG. 2a is SEM graphs where particle-like parts in dark are the YAG:Ce.sup.3 fluorescent powder, while parts in light are the glass raw materials. FIG. 2b is the corresponding EDS energy spectrum data of Area 1 and Area 2 in FIG. 2a. Constituent elements of the Area 1 part are Y, Al, O, Ce, etc., representing Y.sub.3Al.sub.5O.sub.12:Ce.sup.3+, without a composition of glass. The constituent elements of the Area 2 part are Sb, K, Zn, O, etc., which are the constituent elements of glass, without Y.sub.3Al.sub.5O.sub.12:Ce.sup.3+. It's indicated that the YAG:Ce.sup.3+ fluorescent powder existed well in the glass without any erosion or destruction.

Embodiment 3: A Synthesis Process of a Glass Ceramic with B:A=5:95

(13) TABLE-US-00003 TABLE 3 Constitution of the raw materials and the synthesis process of a precursor glass in Embodiment 3 Raw materials Sb.sub.2O.sub.3 H.sub.3BO.sub.3 ZnO K.sub.2CO.sub.3 Mass (g) 13.1183 2.1642 1.6282 1.8548

(14) The constitution of A was a:b:c:d=60:17.5:5:17.5, shown as the corresponding mass in Table 3. Analytically pure diantimony trioxide (Sb.sub.2O.sub.3), boric acid (H.sub.3BO.sub.3), zinc oxide (ZnO) and sodium carbonate (Na.sub.2CO.sub.3) were precisely weighed according to Table 3. The raw materials precisely weighed were transferred into the crucible after being grinded for 1 to 2 hours in the agate mortar, and then were melted in the furnace for 30 minutes at 920 C. Molten glass was poured into the graphite mold for quenching. Glass cullet was taken out and grinded for 6 hours to obtain an A powder standby. The B powder and the A powder was weighed according to a mass ratio of 5:95, and then was poured into the crucible after being grinded sufficiently for 0.5 hour in the agate mortar, followed by being melted in the furnace for 30 minutes at 700 C. Then the molten glass was poured into the preheated graphite mold for molding, and at last was annealed in the furnace for 4 hours at 350 C., and thus a sample was obtained. The sample was cut into an appropriate thickness by the diamond wire cutting machine and was polished to mirror plane on both sides, and thus the YAG:Ce.sup.3+-PiG glass ceramic for packaging complying with the requirements was obtained.

Embodiment 4: A Synthesis Process of a Glass Ceramic with B:A=5:95

(15) TABLE-US-00004 TABLE 4 Constitution of the raw materials and the synthesis process of a precursor glass in Embodiment 4 Raw materials Sb.sub.2O.sub.3 H.sub.3BO.sub.3 ZnO K.sub.2CO.sub.3 Mass (g) 11.6607 2.4733 1.6282 2.7641

(16) The constitution of A was a:b:c:d=55:20:5:20, shown as the corresponding mass in Table 4. Analytically pure diantimony trioxide (Sb.sub.2O.sub.3), boric acid (H.sub.3BO.sub.3), zinc oxide (ZnO) and potassium carbonate (K.sub.2CO.sub.3) were precisely weighed according to Table 4. The raw materials precisely weighed were transferred into the crucible after being grinded for 1 to 2 hours in the agate mortar, and then were melted in the furnace for 15 minutes at 950 C. Molten glass was poured into a graphite mold for quenching. Glass cullet was taken out and grinded for 6 hours to obtain an A powder standby. The B powder and the A powder was weighed according to a mass ratio of 5:95, and then was poured into an aluminum oxide crucible after being grinded sufficiently for 0.5 hour in the agate mortar, followed by being melted in the furnace for 30 minutes at 700 C. The molten glass was poured into the preheated graphite mold for molding, and at last was annealed in the furnace for 4 hours at 350 C., and thus a sample was obtained. The sample was cut into an appropriate thickness by the diamond wire cutting machine and was polished to mirror plane on both sides, and thus the YAG:Ce.sup.3+-PiG glass ceramic for packaging complying with the requirements was obtained. FIG. 3 is excitation and emission spectrums of the YAG:Ce.sup.3+-PiG glass ceramic. The emission spectrum of the YAG:Ce.sup.3+-PiG glass ceramic is almost consistent with the emission spectrum of a YAG:Ce.sup.3+ fluorescent powder. The excitation spectrum of the YAG:Ce.sup.3+-PiG glass ceramic has a slight difference with the excitation spectrum of the YAG:Ce.sup.3+ fluorescent powder, since the glass matrix has an absorption of light of which a wavelength is less than 400 nm.

Embodiment 5: A Synthesis Process of a Glass Ceramic with B:A=23:77

(17) TABLE-US-00005 TABLE 5 Constitution of the raw materials and the synthesis process of a precursor glass in Embodiment 5 Raw materials Sb.sub.2O.sub.3 H.sub.3BO.sub.3 ZnO K.sub.2CO.sub.3 Mass (g) 14.5759 2.4733 0.8141 2.7641

(18) The constitution of A was a:b:c:d=50:20:10:20, shown as the corresponding mass in Table 5. Analytically pure diantimony trioxide (Sb.sub.2O.sub.3), boric acid (H.sub.3BO.sub.3), zinc oxide (ZnO) and potassium carbonate (K.sub.2CO.sub.3) were precisely weighed according to Table 5. The raw materials precisely weighed were transferred into the crucible after being grinded for 1 to 2 hours in the agate mortar, and then were melted in the furnace for 20 minutes at 930 C. Molten glass was poured into the graphite mold for quenching. Glass cullet was taken out and grinded for 6 hours to obtain an A powder standby. The B powder and the A powder was weighed according to a mass ratio of 23:77, and then was poured into the aluminum oxide crucible after being grinded sufficiently for 0.5 hour in the agate mortar, followed by being melted in the furnace for 30 minutes at 690 C. The molten glass was poured into the preheated graphite mold for molding, and at last was annealed in the furnace for 4 hours at 350 C., and thus a sample was obtained. The sample was cut into an appropriate thickness by the diamond wire cutting machine and was polished to mirror plane on both sides, and thus the YAG:Ce.sup.3+-PiG glass ceramic for packaging complying with the requirements was obtained. FIG. 4 and FIG. 5 are test data of the sample tested on a laser semiconductor light source, wherein the spectrograms in FIG. 4 is electroluminescence spectrograms at different drive currents, and FIG. 5 is lumen variation curves corresponding to different drive currents. Specific data is shown in Table 6.

(19) TABLE-US-00006 TABLE 6 Efficiency test of the sample under excitation of a blue light semiconductor light source Sample Embodiment 5 Laser internal efficiency 80.1% Luminous efficiency lm/W 366.93 Absorbance of blue light 93.6%

Embodiment 6: A Synthesis Process of a Glass Ceramic with B:A=23:77

(20) TABLE-US-00007 TABLE 7 Constitution of the raw materials and the synthesis process of precursor glass in Embodiment 6 Raw materials Sb.sub.2O.sub.3 H.sub.3BO.sub.3 ZnO Li.sub.2CO.sub.3 Mass (g) 14.5759 2.4733 0.8141 1.4778

(21) The constitution of A was a:b:c:d=50:20:10:20, shown as the corresponding mass in Table 7. Analytically pure diantimony trioxide (Sb.sub.2O.sub.3), boric acid (H.sub.3BO.sub.3), zinc oxide (ZnO) and lithium carbonate (Li.sub.2CO.sub.3) were precisely weighed according to Table 7. The raw materials precisely weighed were transferred into the crucible after being grinded for 1 to 2 hours in the agate mortar, and then were melted in the furnace for 20 minutes at 930 C. Molten glass was poured into the graphite mold for quenching. Glass cullet was taken out and grinded for 6 hours to obtain an A powder standby. The B powder and the A powder was weighed according to a mass ratio of 23:77, and then was poured into the aluminum oxide crucible after being grinded sufficiently for 0.5 hour in the agate mortar, followed by being melted in the furnace for 30 minutes at 690 C. The molten glass was poured into the preheated graphite mold for molding, and at last was annealed in the furnace for 4 hours at 350 C., and thus a sample was obtained. The sample was cut into an appropriate thickness by the diamond wire cutting machine and was polished to mirror plane on both sides, and thus the YAG:Ce.sup.3+-PiG glass ceramic for packaging complying with the requirements was obtained.