JP2021038346A - Ceramic composite - Google Patents

Abstract

To provide a ceramic composite capable of uniformly scattering primary light and wavelength-converted secondary light to improve wavelength conversion efficiency.SOLUTION: This ceramic composite has, as a lamellar structure, at least two oxide phases of a Y3Al5O12 phase and an Al2O3 phase, has an average value of lamellar spacing in the Y3Al5O12 phase of 0.5-20 μm, and contains 10-500 ppm of MgO. Furthermore, the Y3Al5O12 phase is activated by Ce, and the Ce content is 0.01-5.0 mol%.SELECTED DRAWING: Figure 9

Description

The present invention relates to a ceramic composite, and more particularly to a ceramic composite having two oxide phases, a _{Y 3} Al ₅ O ₁₂ phase and an Al ₂ O _{3 phase, as a lamellar structure.}

Currently, a light emitting diode (LED: Light Emitting Diode) or a semiconductor laser that emits blue light is used as a light source, and a part of the blue light is wavelength-converted to yellow light by a wavelength conversion member, and a mixture of blue light and yellow light is used. Lighting devices that irradiate white light are widespread. Such an illumination device, using a _{YAG (Y 3 Al 5 O 12} ) based phosphor material of the wavelength conversion member, which is containing a phosphor powder in a resin or glass is proposed.

Further, Patent Documents 1 _{and 2 propose a ceramic composite having a lamellar structure in which the Y 3} Al ₅ O ₁₂ phase and the Al 2 O ₃ phase are continuously three-dimensionally entangled with each other as eutectics. .. In such a ceramic composite described in Patent Documents 1 and _2, as well as wavelength conversion of blue light into yellow light in the Y ₃ Al _{5 O 12 phase,} of Y ₃ Al _{5 O 12} phase and the _Al 2 _{O 3} phase Blue light and yellow light are scattered at the interface, and white can be obtained by mixing colors.

Japanese Patent No. 4609319 Japanese Patent No. 5246376

However, in Patent Documents 1 and 2, are manufactured ceramic composites using a Bridgman method as unidirectional solidification method, since the moving speed of the crucible and 1 to 20 mm / _Time, Y ₃ Al _{5 O 12} phase and There was a limit to the miniaturization of the Al ₂ O _{3 phase.} Moreover, in the Bridgman method, a colony structure is formed due to the disorder of the solid-liquid interface. Therefore, in the ceramic composites described in Patent Documents 1 and 2, the emission of blue light, which is the primary light, and yellow light, which has been wavelength-converted, is uneven, and the colors may be sufficiently mixed to obtain uniform white light. It was difficult. In particular, when the ceramic composite is thin, the unevenness of Y ₃ Al ₅ O ₁₂ phase by colony structure, there is unevenness in the wavelength conversion, it is difficult to obtain a uniform white light.

Therefore, the present invention has been made in view of the above-mentioned conventional problems, and provides a ceramic composite capable of uniformly scattering primary light and wavelength-converted secondary light to improve wavelength conversion efficiency. The purpose is to do.

In order to solve the above problems, the ceramic composite of the present invention has at least _{two oxide phases of Y 3} Al ₅ O ₁₂ phase and Al ₂ O ₃ phase as a lamellar structure, and the Y ₃ Al ₅ O _{12 phase is described above.} The average value of the lamellar intervals in the phase is 0.5 μm or more and 20 μm or less, and MgO is contained in an amount of 10 ppm or more and 500 ppm or less.

In such a ceramic composite of the present invention, _{the average value of the lamella spacing in the Y 3} Al ₅ O ₁₂ phase is 0.5 μm or more and 20 μm or less, and MgO is contained in an amount of 10 ppm or more and 500 ppm or less. It is possible to uniformly scatter the secondary light and improve the wavelength conversion efficiency.

In one embodiment of the present invention, the _Y 3 _Al 5 _{O 12} phase is activated with Ce.

Further, in one aspect of the present invention, the content of Ce is 0.01 mol% or more and 5.0 mol% or less.

Further, in one aspect of the present invention, the thickness is 0.5 mm or more and 2.0 mm or less.

Further, in one aspect of the present invention, the shape of the ceramic composite in the plane direction is a square shape having a width of 0.5 mm or more and 300 mm or less and a length of 10 mm or more and 1000 mm or less, or a diameter of 0.5 mm or more and 2 mm or less. The shape.

INDUSTRIAL APPLICABILITY The present invention can provide a ceramic composite capable of uniformly scattering primary light and wavelength-converted secondary light to improve wavelength conversion efficiency.

It is a schematic block diagram which shows the manufacturing apparatus of the ceramic composite by the EFG method. (A) It is a top view which shows typically an example of the die which concerns on embodiment of this invention. (B) It is a front view of the figure (a). (C) It is a side view of the figure (a). (A) It is explanatory drawing which shows an example of the seed crystal which concerns on embodiment of this invention. (B) It is explanatory drawing which shows the other example of the seed crystal which concerns on embodiment of this invention. (C) It is explanatory drawing which shows still another example of the seed crystal which concerns on embodiment of this invention. It is a perspective view which shows typically the positional relationship between a seed crystal and a partition plate in embodiment of this invention. (A) It is a front view which shows typically the positional relationship between a seed crystal and a partition plate in embodiment of this invention. (B) It is a front view which shows the state of melting a part of a seed crystal in embodiment of this invention. (A) In the seed crystal according to the embodiment of the present invention, it is explanatory drawing which shows the seed crystal which the lower side has a comb tooth shape. (B) In the seed crystal according to the embodiment of the present invention, it is explanatory drawing which shows the seed crystal which the lower side has a saw-shaped shape. It is a perspective view which shows typically the spreading process of the ceramic composite which concerns on embodiment of this invention. FIG. 5 is a perspective view partially showing a plurality of ceramic composites according to an embodiment of the present invention obtained by the EFG method. It is a micrograph which shows the surface of the ceramic composite 2 obtained by the EFG method. It is a micrograph showing the lamellar structure when the pulling speed by the EFG method is changed, and shows the case of pulling at a small speed. It is a micrograph showing the lamellar structure when the pulling speed by the EFG method is changed, and shows the case of pulling at a medium speed. It is a micrograph showing the lamellar structure when the pulling speed by the EFG method is changed, and shows the case of pulling at a large speed. It is a perspective view which shows another form of the growth process of the ceramic composite by the EFG method.

Hereinafter, embodiments of the present invention will be described in detail with reference to the drawings. The same or equivalent components, members, and processes shown in the drawings shall be designated by the same reference numerals, and redundant description thereof will be omitted as appropriate. 1 to 8 are views for explaining a plurality of ceramic composites according to an embodiment of the present invention and a method for producing the same.

As shown in FIG. 1, the ceramic composite manufacturing apparatus 1 is composed of a growing container 3 for growing the ceramic composite 2 and a pulling container 4 for pulling up the grown ceramic composite 2, and is composed of an EFG (Edge-defined Film). -Fed. Growt) method is used to grow and grow the ceramic composite 2.

The growing container 3 includes a crucible 5, a crucible drive unit 6, a heater 7, an electrode 8, a die 9, and a heat insulating material 10. The crucible 5 is made of molybdenum or tungsten and melts the raw material. The crucible drive unit 6 rotates the crucible 5 about its vertical direction. The heater 7 heats the crucible 5. Further, the electrode 8 energizes the heater 7. The die 9 is installed in the crucible 5 and determines the liquid level shape of the raw material melt (hereinafter, simply referred to as “melt” if necessary) 21 when pulling up the ceramic composite 2. The heat insulating material 10 surrounds the crucible 5, the heater 7, and the die 9.

Further, the growing container 3 includes an atmospheric gas introduction port 11 and an exhaust port 12. The atmosphere gas introduction port 11 is an introduction port for introducing, for example, argon gas as an atmosphere gas into the growing container 3, and prevents oxidative consumption of the crucible 5, the heater 7, and the die 9. On the other hand, the exhaust port 12 is provided for exhausting the inside of the growing container 3.

The pull-up container 4 includes a shaft 13, a shaft drive unit 14, a gate valve 15, and a substrate entrance / exit 16, and pulls up a plurality of flat plate-shaped ceramic composites 2 grown and grown from the seed crystal 17. The shaft 13 holds the seed crystal 17. Further, the shaft drive unit 14 raises and lowers the shaft 13 toward the crucible 5, and rotates the shaft 13 about the raising and lowering direction. The gate valve 15 separates the growing container 3 and the pulling container 4. Further, the substrate entrance / exit 16 takes in and out the seed crystal 17.

The manufacturing apparatus 1 also has a control unit (not shown), which controls the rotation of the crucible drive unit 6 and the shaft drive unit 14.

Next, the die 9 will be described. The die 9 is made of molybdenum and has a large number of partition plates 18 as shown in FIG. FIG. 2 shows a case where 30 partition plates 18 are formed and 15 dies 9 are formed as an example of dies. The partition plates 18 have the same flat plate shape and are arranged in parallel with each other so as to form a minute gap (slit) 19 to form one die 9. The slit 19 is provided over substantially the entire width of the die 9. Further, since the plurality of dies 9 have the same shape and are arranged in parallel at predetermined intervals so that their longitudinal directions are parallel to each other, a plurality of slits 19 are provided. A slope 30 is formed on the upper portion of each partition plate 18, and an acute-angled opening 20 is formed by arranging the slopes 30 facing each other. Further, the slit 19 has a role of raising the melt 21 from the lower end of each die 9 to the opening 20 by a capillary phenomenon.

The raw material charged into the crucible 5 melts (raw material melt) based on the temperature rise of the crucible 5 to become the melt 21. A part of the melt 21 penetrates into the slit 19 of the die 9, rises in the slit 19 based on the capillary phenomenon as described above, is exposed from the opening 20, and the raw material melt pool 22 is exposed at the opening 20. Is formed (see FIG. 5 (a)). In the EFG method, the ceramic composite 2 grows according to the shape of the melt surface formed by the raw material melt pool (hereinafter, referred to as “melt pool” if necessary) 22. In the die 9 shown in FIG. 2, since the shape of the melt surface is an elongated rectangle, a flat plate-shaped ceramic composite 2 is manufactured.

Next, the seed crystal 17 will be described. As shown in FIGS. 1, 4, and 5, in the present embodiment, a flat plate-shaped ceramic composite substrate is used as the seed crystal 17. Further, the seed crystal 17 is arranged so that the plane direction of the seed crystal 17 and the longitudinal direction of the die 9 are orthogonal to each other at an angle of 90 °. Further, since the seed crystal 17 and the ceramic composite 2 are also orthogonal to each other at an angle of 90 °, the side surface of the ceramic composite 2 is shown in FIG.

If the contact area of the lower part of the shaft 13 with the substrate holder (not shown) is large, the seed crystal 17 is deformed due to stress due to the difference in the coefficient of thermal expansion, and is damaged in some cases. On the contrary, the seed crystal 17 may be loosened due to the difference in the coefficient of thermal expansion. Therefore, it is preferable that the contact area between the seed crystal 17 and the substrate holder is small. Further, the seed crystal 17 needs to have a substrate shape that can be securely fixed to the substrate holder.

FIG. 3 is a diagram showing an example of the substrate shape of the seed crystal 17. Of these, FIGS. (A) and (B) show a notch 23 provided in the upper part of the seed crystal 17. Using this notch 23, for example, a U-shaped substrate holder can be inserted from the lower side of two notches 23 to reliably hold the seed crystal 17 while reducing the contact area. Become.

Further, as shown in FIG. 3C, a notch hole 24 may be provided inside the seed crystal 17. Using the notch holes 24, for example, locking claws are inserted into two notch holes 24 to securely hold the seed crystal 17 while reducing the contact area between the substrate holder and the seed crystal 17. It becomes possible.

Next, a method of manufacturing the ceramic composite 2 using the manufacturing apparatus 1 will be described. First, granulated raw material powder (for example, aluminum oxide 64.71% by weight, yttrium oxide 35.02% by weight, magnesium oxide 0.003% by weight, cerium oxide 0. (Powder containing 27% by weight) is charged into the crucible 5 containing the die 9 in a predetermined amount and filled. The raw material powder may contain compounds and elements other than the above, depending on the purity or composition of the ceramic composite to be produced.

Subsequently, in order not to oxidatively consume the crucible 5, the heater 7, or the die 9, the inside of the growing container 3 is replaced with argon gas to bring the oxygen concentration to a predetermined value or less.

Next, the crucible 5 is heated to a predetermined temperature by heating with the heater 7, and the raw material powder is melted. Since the melting point of aluminum oxide is about 2050 ° C. to 2072 ° C., the heating temperature of the crucible 5 is set to a temperature equal to or higher than the melting point (for example, 2100 ° C.). After a while after heating, the raw material powder melts and the raw material melt 21 is prepared. Further, a part of the melt 21 rises through the slit 19 of the die 9 due to the capillary phenomenon and reaches the surface of the die 9, and a melt pool 22 is formed on the upper portion of the slit 19.

Next, as shown in FIGS. 4 and 5, the seed crystal 17 is lowered while being held at an angle perpendicular to the longitudinal direction of the melt pool 22 at the upper part of the slit 19, and the seed crystal 17 is melted in the melt pool 22. Contact the liquid surface. The seed crystal 17 is introduced into the pull-up container 4 from the substrate entrance / exit 16 in advance. In FIG. 4, in order to give priority to the visibility of the slit 19 and the opening 20, the melt 21 and the melt pool 22 are not shown.

FIG. 4 is a diagram showing the positional relationship between the seed crystal 17 and the partition plate 18. As described above, by making the plane direction of the seed crystal 17 orthogonal to the longitudinal direction of the partition plate 18, the contact area between the seed crystal 17 and the melt 21 can be reduced. Therefore, the contact portion of the seed crystal 17 becomes familiar with the melt 21, and crystal defects are less likely to occur in the ceramic composite 2 that is grown and grown.

When the seed crystal 17 is brought into contact with the melt surface, the lower part of the seed crystal 17 may be brought into contact with the upper part of the partition plate 18 to be melted. FIG. 5B is a diagram showing a state in which a part of the seed crystal 17 is melted. By melting a part of the seed crystal 17 in this way, the temperature difference between the seed crystal 17 and the melt 21 can be quickly eliminated, and the occurrence of crystal defects in the ceramic composite 2 can be further reduced. Is possible.

Subsequently, the substrate holder is pulled up at a predetermined ascending speed to start pulling up the seed crystal 17. Specifically, the shaft 13 raises the substrate holder at a predetermined speed.

In addition, in order to facilitate the alignment of the seed crystal with respect to the opening 20 of the die 9, the lower side of the seed crystal 17 may be provided with irregularities. FIG. 6 is a diagram illustrating the shape of the lower side of the seed crystal 17, in which FIG. 6A shows a case where the lower side has a comb tooth shape and FIG. 6B shows a case where the lower side has a sawtooth shape.

The distance between the irregularities is adjusted to the distance between the openings 20, and the convex portion is aligned with the center of the melt pool 22. By providing the convex portion, the convex portion can be used as the growth start point of the ceramic composite 2, and the ceramic composite 2 can be formed more easily. The shape of the unevenness is not limited to that shown in FIG. 6, and may be, for example, a corrugated uneven shape.

The substrate holder is raised at a predetermined speed, and the ceramic composite 2 is crystal-grown around the seed crystal 17 so as to widen in the longitudinal direction of the die 9 as shown in FIG. 7 (spreading). When the ceramic composite 2 is widened to the full width of the die 9 (the end of the partition plate 18) (full spread), a flat plate-shaped ceramic composite 2 having a wide area and having a width similar to the full width of the die 9 is grown. (Straight body process). FIG. 7 is a schematic view showing how the width of the ceramic composite 2 is expanded by the spreading step. By obtaining the wide ceramic composite 2, the yield of the ceramic composite product is improved.

After the ceramic composite 2 is grown to the full width of the die 9 by the spreading step, a flat plate-shaped straight body portion 26 having a constant width similar to the full width of the die 9 is formed at a predetermined speed as shown in FIG. To obtain a flat plate-shaped ceramic composite 2 by pulling it up to a predetermined length (straight body length).

After that, the obtained ceramic composite 2 is allowed to cool, the gate valve 15 is opened, the gate valve 15 is moved to the pulling container 4, and the ceramic composite 2 is taken out from the substrate entrance / exit 16. The appearance of the obtained flat plate-shaped ceramic composite 2 is shown in FIG. The length of the straight body is not particularly limited, but is preferably 2 inches or more (50.8 mm or more).

Further, as shown in FIG. 13, the total width of the die 9 and the width of the seed crystal 17 may be the same, and the ceramic composite 2 may be grown and grown with the same width as the total width of the seed crystal 17. In FIG. 13, the melt 21 and the melt pool 22 are not shown in order to give priority to the visibility of the slit 19.

By using the manufacturing apparatus 1, the seed crystal 17, and the die 9 as described above, a plurality of ceramic composites 2 can be simultaneously manufactured from the common seed crystal 17. Therefore, it is possible to reduce the manufacturing cost of the ceramic composite 2 per sheet.

Further, in the EFG method, a plurality of ceramic composites 2 are grown and grown. Therefore, by uniformly cooling and allowing the plurality of ceramic composites 2 to cool, a uniform lamellar structure without variation can be obtained.

Therefore, the die 9 including the seed crystal 17 and the partition plate 18 needs to be precisely positioned. Therefore, as shown in FIG. 1, the manufacturing apparatus 1 is provided with a crucible drive unit 6 for rotating the crucible 5 on which the die 9 is installed, and a control unit (not shown) for controlling the rotation thereof. Further, the shaft 13 is also provided with a shaft drive unit 14 that rotates the shaft 13 and a control unit (not shown) that controls the rotation thereof. That is, the positioning of the seed crystal 17 with respect to the die 9 is adjusted by rotating the shaft 13 or the crucible 5 by the control unit. Precise positioning of the seed crystal 17 and the die 9 can also be performed by using the die 9 in which a part of the slope 30 of each partition plate 18 is cut out.

FIG. 9 is a photomicrograph showing the surface of the ceramic composite 2 obtained by the above-mentioned EFG method. As shown in FIG. 9, in the ceramic composite 2 of the present embodiment, the Y ₃ Al ₅ O ₁₂ phase, which is the first phase, and the Al ₂ O ₃ phase, which is the second phase, are present as eutectic. The first phase and the second phase have a lamellar structure in which they are three-dimensionally entwined with each other. In the figure, the region shown in dark color is the Y ₃ Al ₅ O ₁₂ phase, and the region shown in light color is the Al ₂ O ₃ phase. In addition, the first phase and the second phase are rarely separated in an island shape independently, and have continuous regions in the three-dimensional direction.

_{The composition ratio of the Y 3} Al ₅ O ₁₂ phase contained in the ceramic composite 2 is 19.72 ± 2.00 mol% in the vicinity of the eutectic composition. If _{the composition ratio of the Y 3} Al ₅ O ₁₂ phase is out of this range, it is difficult to uniformly form a lamellar structure by eutectic _{with the Al 2} O _{3 phase.}

The Ce content in the Y ₃ Al ₅ O ₁₂ phase is preferably in the range of 0.01 mol% or more and 5.0 mol% or less. If it is less than 0.01 mol%, the effective strength of the ceramic composite 2 becomes weak and it becomes unsuitable for lighting equipment applications. On the other hand, if it exceeds 5.0 mol%, other compounds other than desired are generated and do not contribute to the emission of white light. By Y ₃ Al ₅ O ₁₂ phase of Y is substituted partially _Ce, Y ₃ Al _{5 O 12} phase functions as a phosphor material, the secondary light by absorbing blue light is the primary light It emits yellow light. The thermal conductivity of Al ₂ O ₃ phase is as large as about 4 times the thermal conductivity of _Y 3 _Al 5 _{O 12 phase,} when converting the primary light in the Y ₃ Al _{5 O 12} phase in the secondary of the yellow light Heat can be dissipated efficiently. In the Y ₃ Al ₅ O ₁₂ phase, the absorption wavelength and the emission wavelength change depending on the Ce concentration, but the ceramic composite of the present embodiment uniformly has a fine lamellar structure even if the Ce content is relatively large, as will be described later. Can be formed.

Further, the ceramic composite 2 contains MgO in the range of 10 ppm or more and 500 ppm or less. By containing MgO in this range, the conversion efficiency from blue light to white light can be enhanced, and the emission intensity of white light can be increased.

Further, in the ceramic composite 2 of the present embodiment, in the lamellar structure of _{the Y 3} Al ₅ O ₁₂ phase and the Al ₂ O _{3 phase, the average value of the lamellar intervals in the Y 3} Al ₅ O ₁₂ phase is 0.5 μm or more and 20 μm or less. Is. Here _Y 3 The _Al 5 lamellar spacing _{O 12} phase, and the width of the _Y 3 _Al 5 _{O 12} phase sandwiched _Al 2 _{O 3} phase, longitudinal continuous _Y 3 _Al 5 _{O 12} phase Shows the width across. If lamellar spacing is less than 0.5μm is, Y ₃ Al ₅ size O ₁₂ phase becomes uniformly blue light becomes several times the wavelength of the blue light is difficult to wavelength-converted into yellow light It ends up. Further, when the lamellar spacing is larger than 20 μm, the lamellar structure is insufficiently dense, and the Y ₃ Al ₅ O ₁₂ phase and the Al ₂ O ₃ phase are formed while the blue light is transmitted through the ceramic composite 2. The number of times the light is incident on the interface is reduced, the light is not sufficiently scattered, and the efficiency of wavelength conversion and color mixing is reduced.

The shape and size of the ceramic composite 2 are not limited, but from the viewpoint of preventing deterioration of workability of the ceramic composite 2, a square shape or diameter having a width of 0.5 mm or more and 300 mm or less and a length of 10 mm or more and 1000 mm or less. It is desirable that the shape is 0.5 mm or more and 2 mm or less. As described above, since the ceramic composite 2 of the present embodiment is manufactured by using the EFG method, it is possible to easily obtain a large-area ceramic composite 2 by increasing the width of the die 9 and the length to be pulled up. Is. In addition, since the average value of the lamella spacing is in the range of 0.5 μm or more and 20 μm or less and has a fine structure, light is likely to be scattered at the interface _{between the Y 3} Al ₅ O ₁₂ phase and the Al ₂ O _{3 phase.} Even if the area is large, light can be uniformly scattered over the entire in-plane area, and uniform white light can be obtained.

The thickness of the ceramic composite 2 is not limited, but is preferably 0.1 mm or more and 4.0 mm or less, and more preferably 0.5 mm or more and 2.0 mm or less. When the thickness of the ceramic composite 2 is less than 0.1 mm, it becomes difficult to control the growth by the EFG method, and the influence of the thickness due to the manufacturing error and the influence of the thickness unevenness in the plane become large. It becomes difficult to obtain white light uniformly over the entire area. Further, since the thermal conductivity of the _{Y 3} Al ₅ O ₁₂ phase contained in the ceramic composite 2 is _{only about 1/4 of that of the Al 2} O ₃ phase, the heat dissipation property deteriorates when the crystal is thickened, and the temperature on the surface and inside deteriorates. Differences are likely to occur. Therefore, when the thickness of the ceramic composite 2 is larger than 4.0 mm, a temperature difference between the outside and the inside in the thickness direction is likely to occur when the ceramic composite 2 is pulled up by the EFG method, a colony structure is likely to occur, and the lamella spacing is increased. It is not preferable because the uniformity is impaired.

10 to 12 are micrographs showing the lamellar structure when the pulling speed by the EFG method is changed, FIG. 10 shows the case where the pulling speed is changed at a small speed, and FIG. 11 shows the case where the pulling speed is changed at a medium speed. The case is shown, and FIG. 12 shows the case of pulling up at a large speed. The range shown in each photograph is a square with a side of 129 μm.
(Comparison example)

The concentration of Ce contained in the ceramic composite 2 was 0.5 mol%, and the pulling speed was 0.035 inch / hour (about 0.9 mm / hour). The result of measuring the average of the lamella intervals of the _{Y 3} Al ₅ O _{12 phase was 26.6 μm.} When blue light with a wavelength of 450 nm was irradiated to a comparative example of a ceramic composite 2 having a thickness of 0.2 mm, the blue light was not sufficiently wavelength-converted, and the white light irradiated to the outside had a strong bluish tint and color. The unevenness was also large.
(Example 1)

The concentration of Ce contained in the ceramic composite 2 was 0.5 mol%, and the pulling speed was 0.2 inch / hour (about 5 mm / hour). The result of measuring the average of the lamella intervals of the _{Y 3} Al ₅ O _{12 two-phase was 15.2 μm.}
(Example 2)

The concentration of Ce contained in the ceramic composite 2 was 0.3 mol%, and the pulling speed was 1.0 inch / hour (about 25 mm / hour). The result of measuring the average of the lamella intervals of the _{Y 3} Al ₅ O _{12 phase was 6.0 μm.}
(Example 3)

The concentration of Ce contained in the ceramic composite 2 was 0.5 mol%, and the pulling speed was 1.0 inch / hour (about 25 mm / hour). The result of measuring the average of the lamella intervals of the _{Y 3} Al ₅ O _{12 phase was 5.5 μm.}
(Example 4)

The concentration of Ce contained in the ceramic composite 2 was 0.3 mol%, and the pulling speed was 2.0 inches / hour (about 50 mm / hour). The result of measuring the average of the lamella intervals of the _{Y 3} Al ₅ O _{12 phase was 3.5 μm.}
(Example 5)

The concentration of Ce contained in the ceramic composite 2 was 0.5 mol%, and the pulling speed was 2.0 inches / hour (about 50 mm / hour). The result of measuring the average of the lamella intervals of the _{Y 3} Al ₅ O _{12 phase was 4.6 μm.}
(Example 6)

The concentration of Ce contained in the ceramic composite 2 was 1.0 mol%, and the pulling speed was 2.0 inches / hour (about 50 mm / hour). The result of measuring the average of the lamella intervals of the _{Y 3} Al ₅ O _{12 phase was 5.1 μm.}
(Example 7)

The concentration of Ce contained in the ceramic composite 2 was 0.3 mol%, and the pulling speed was 4.0 inches / hour (about 100 mm / hour). The result of measuring the average of the lamella intervals of the _{Y 3} Al ₅ O _{12 phase was 2.6 μm.}
(Example 8)

The concentration of Ce contained in the ceramic composite 2 was 0.5 mol%, and the pulling speed was 4.0 inches / hour (about 100 mm / hour). The result of measuring the average of the lamella intervals of the _{Y 3} Al ₅ O _{12 phase was 3.0 μm.}
(Example 9)

The concentration of Ce contained in the ceramic composite 2 was 1.0 mol%, and the pulling speed was 4.0 inches / hour (about 100 mm / hour). The result of measuring the average of the lamella intervals of the _{Y 3} Al ₅ O _{12 phase was 4.4 μm.}
(Example 10)

The concentration of Ce contained in the ceramic composite 2 was 0.5 mol%, and the pulling speed was 8.0 inches / hour (about 200 mm / hour). The result of measuring the average of the lamella intervals of the _{Y 3} Al ₅ O _{12 phase was 4.4 μm.}

When blue light having a wavelength of 450 nm was irradiated to Examples 1 to 10 of the ceramic composite 2 having a thickness of 0.5 mm, the light irradiated to the outside was uniform white light in all the examples.

As shown in FIGS. 10 to 12, in the comparative example in which the average lamella spacing of the _{Y 3} Al ₅ O ₁₂ phases exceeds 20 μm, the light in the _{Y 3} Al ₅ O ₁₂ phases and the Al ₂ O _{3 phases} While the scattering was insufficient, in Examples 1 to 10, uniform wavelength conversion efficiency and uniformity of white light could be obtained. Further, by increasing the pulling speed of the ceramic composite body 2 in the EFG _process, the lamellar spacing of Y ₃ Al _{5 O 12} phase is confirmed tends to become smaller. Furthermore, it was confirmed that the miniaturization of the lamellar structure was maintained even when the Ce concentration was in the range of 0.01 mol% or more and 5.0 mol% or less. It can also be seen that the lower the Ce concentration, the smaller the lamella interval.

As described above, the ceramic composite 2 of the present embodiment has at least _{two oxide phases of Y 3} Al ₅ O ₁₂ phase and Al ₂ O ₃ phase as a lamellar structure, and Y ₃ Al ₅ O ₁₂ Since the average value of the lamellar spacing in the phase is 0.5 μm or more and 20 μm or less and MgO is contained in an amount of 10 ppm or more and 500 ppm or less, the primary light and the secondary light can be uniformly scattered to improve the wavelength conversion efficiency. It will be possible.

Further, in the present invention, by growing and growing the ceramic composite 2 by the EFG method, the pulling speed of the seed crystal is varied within the range of 0.9 mm / hour or more and 400 mm / hour or less, and Ce is converted into the ceramic composite 2. Even if it is contained, the occurrence of colony structure can be prevented. The colony structure is a structure in which a portion of a lamellar structure in which a plurality of phases having a short phase interval are densely present is surrounded by a portion in which a plurality of phases having a long phase interval are sparsely present. As shown in FIGS. 9 to 12, no such colony structure was confirmed to occur in the present embodiment and the examples. Therefore, uneven emission of white light in the ceramic composite 2 can be prevented.

The present invention is not limited to the above-described embodiments, and various modifications can be made within the scope of the claims, and the embodiments obtained by appropriately combining the technical means disclosed in the different embodiments. Is also included in the technical scope of the present invention.

1 ... Manufacturing equipment 2 ... Ceramic composite 3 ... Growing container 4 ... Pulling container 5 ... Crucible 6 ... Crucible drive 7 ... Heater 8 ... Electrode 9 ... Die 10 ... Insulation material 11 ... Atmospheric gas inlet 12 ... Exhaust port 13 ... Shaft 14 ... Shaft drive 15 ... Gate valve 16 ... Substrate entrance 17 ... Seed crystal 18 ... Partition plate 19 ... Slit 21 ... Melt 23 ... Notch 24 ... Notch hole 26 ... Straight body 30 ... Slope

Claims (5)

It has at least _{two oxide phases, Y 3} Al ₅ O ₁₂ phase and Al ₂ O ₃ phase, as a lamellar structure.
The average value of the lamella spacing in the Y ₃ Al ₅ O ₁₂ phase is 0.5 μm or more and 20 μm or less.
A ceramic composite containing 10 ppm or more and 500 ppm or less of MgO. The ceramic composite according to claim 1, wherein the Y ₃ Al ₅ O _{12 phase is activated by Ce.} The ceramic composite according to claim 2, wherein the content of Ce is 0.01 mol% or more and 5.0 mol% or less. The ceramic composite according to any one of claims 1 to 3, wherein the thickness is 0.5 mm or more and 2.0 mm or less. The shape of the ceramic composite in the plane direction is
The invention according to any one of claims 1 to 4, wherein the width is 0.5 mm or more and 300 mm or less and the length is 10 mm or more and 1000 mm or less, or the diameter is 0.5 mm or more and 2 mm or less. Ceramic composite.