Ceramic composite for light conversion and light-emitting device using same

Abstract

A ceramic composite for light conversion, which can make the fluorescence dominant wavelength longer up to 580 nm, further arbitrarily adjust the wavelength in the range of 570 to 580 nm, and undergoes no decrease in fluorescence intensity even when the fluorescence dominant wavelength is made longer, with luminescence unevenness suppressed. A light-emitting device comprising ceramic composite mentioned above. The ceramic composite for light conversion is a solidified body including a composition expressed by the following formula (1), where the composition has a structure where at least two oxide phases of a first phase and a second phase are continuously and three-dimensionally entangled mutually, and the ceramic composite for light conversion is characterized in that the first phase is a (Tb, Y).sub.3Al.sub.5O.sub.12 phase activated with Ce for producing fluorescence, whereas the second phase is an Al.sub.2O.sub.3 phase.

Claims

1. A ceramic composite for light conversion, which is formed of a solidified body comprising a composition expressed by the following formula (1), the composition having a structure where at least two oxide phases of a first phase and a second phase are continuously and three-dimensionally entangled mutually, the first phase being a (Tb, Y).sub.3Al.sub.5O.sub.12 phase activated with Ce for producing fluorescence, and the second phase being an Al.sub.2O.sub.3 phase, [Formula 1]
AlO.sub.3/2x.Math.(a.Math.TbO.sub.7/4b.Math.YO.sub.3/2c.Math.CeO.sub.2)(1) in which x satisfies 0.23<x<0.30, and a, b, and c represent mole fractions, and satisfy 0b/a4, 0<c0.025, and a+b+c=1.

2. The ceramic composite for light conversion according to claim 1, wherein c in the formula (1) satisfies 0.002c0.02, and which has a plate shape and a thickness of 80 m or more and 400 m or less in a light-emitting direction.

3. The ceramic composite for light conversion according to claim 1, wherein the composite absorbs light having a peak at a wavelength of 420 to 500 nm and emits fluorescence having a dominant wavelength at 570 to 580 nm.

4. The ceramic composite for light conversion according to claim 2, wherein the composite absorbs light having a peak at a wavelength of 420 to 500 nm and emits fluorescence having a dominant wavelength at 570 to 580 nm.

5. The ceramic composite for light conversion according to claim 3, wherein the composite receives light having a peak at a wavelength of 420 to 500 nm, emits fluorescence converted from some of the light as excitation light, and transmits some of the light to emit transmitted light, and the fluorescence and the transmitted light are mixed to emit white light.

6. The ceramic composite for light conversion according to claim 4, wherein the white light has chromaticity in a region surrounded by (0.30, 0.32), (0.34, 0.30), (0.42, 0.41), and (0.38, 0.45) in CIE chromaticity coordinates (Cx, Cy).

7. A light-emitting device comprising a light-emitting element and the ceramic composite for light conversion according to claim 1.

8. A light-emitting device comprising a light-emitting element having a peak at a wavelength 420 to 500 nm, and the ceramic composite for light conversion according to claim 1 for emitting fluorescence having a dominant wavelength between 570 nm and 580 nm.

9. The light-emitting device according to claim 6, wherein the light-emitting element is a light-emitting diode element.

10. The light-emitting device according to claim 7, wherein the light-emitting element is a light-emitting diode element.

Description

BRIEF DESCRIPTION OF DRAWINGS

(1) FIG. 1 is an optical micrograph showing a cross section of a ceramic composite for light conversion according to Example 1.

(2) FIG. 2 is a schematic cross-sectional view illustrating an embodiment of a light-emitting device according to the present invention.

(3) FIG. 3 is an X-ray diffraction diagram of a ceramic composite for light conversion according to Example 1.

(4) FIG. 4 is fluorescence spectra of ceramic composites for light conversion according to Example 1 and Comparative Example 1.

(5) FIG. 5 is a CIE chromaticity diagram illustrating CIE chromaticity Cx and Cy of the total luminous flux emitted from a light-emitting device using a ceramic composite for light conversion according to the present invention.

(6) FIG. 6 is a luminance line analysis diagram on light-emitting surface during light emission from light-emitting device according to Example 3 and Comparative Example 3.

DESCRIPTION OF EMBODIMENTS

(7) A ceramic composite for light conversion and a light-emitting device using the composite according to the present invention will be described below in detail with reference to a preferred embodiment.

(8) (Ceramic Composite for Light Conversion)

(9) The ceramic composite for light conversion according to the present embodiment is a solidified body including a composition expressed by the following formula (1), which has a structure where at least two oxide phases of a first phase and a second phase are continuously and three-dimensionally entangled mutually, and the first phase is a (Tb, Y).sub.3Al.sub.5O.sub.12 phase activated by Ce that emits fluorescence, whereas the second phase is an Al.sub.2O.sub.3 phase.

(10) [Mathematical Formula 2]
AlO.sub.3/2x.Math.(a.Math.TbO.sub.7/4b.Math.YO.sub.3/2c.Math.CeO.sub.2)(1)
(x satisfies 0.23<x<0.30, and a, b, and c represent mole fractions, and satisfy 0b/a4, 0<c0.025, and a+b+c=1)

(11) In the present embodiment, the structure where the two oxide phases are continuously and three-dimensionally entangled mutually takes on a structure as shown in section in FIG. 1, rather than a structure where the two types of oxide particles coupled to each other. In this structure, the oxide phases are in direct contact with each other, without any boundary phase such as an amorphous phase between the respective phases.

(12) The formula (1) has therein x, a, b, and c which can be determined by the following method. First, a ground product of the ceramic composite for light conversion according to the present embodiment is melted by heating together with sodium carbonate and boric acid, and then dissolved by heating with the addition of hydrochloric acid and sulfuric acid. The dissolved matter obtained is subjected to inductively-coupled plasma atomic emission spectrometry (ICP-AES) to determine the contents of Al, Tb, Y, and Ce in terms of relative weight, and from the results, x, a, b, and c can be calculated.

(13) x in the formula (1) satisfies 0.23<x<0.30, preferably 0.238x0.294. When x in the formula (1) is 0.23 or less or 0.30 or more, a coarsened region of the first phase or second phase is generated extensively in the solidified body, thereby making the solidified body likely to be cracked. In addition, even when cracking is not generated, coarsening of the first phase or second phase unfavorably causes the fluorescence dominant wavelength to vary significantly, or results in the presence of samples with luminescence unevenness unsuppressed, thus making a white light-emitting device including the ceramic composite for light conversion according to the present embodiment inappropriate as a white light-emitting device.

(14) b/a in the formula (1) satisfies 0b/a4. When b/a in the formula (1) exceeds 4, the fluorescence dominant wavelength becomes unfavorably less than 570 nm, thereby resulting in failure to achieve the effect of the increased wavelength.

(15) c in the formula (1) satisfies 0<c0.025, preferably 0.002c0.02. When c in the formula (1) is 0, the first phase of the ceramic composite fails to function as a fluorescent phase, because there is no activation element for producing fluorescence. Alternatively, when c is larger than 0.025, there is a need to significantly reduce the thickness of the ceramic composite for light conversion for the purpose of achieving a white light emission, for example, to a thickness less than 50 m depending on the chromaticity range of an intended white region in applying the ceramic composite for light conversion to a white light-emitting device. In this case, it becomes difficult to achieve an appropriate white color, due to a slight difference in sample thickness. Therefore, in order to keep, at constant chromaticity, the light emission from a white light-emitting device including the ceramic composite for light conversion according to the present embodiment, which has a plate shape as will be described later, a need is created to keep the thickness of the ceramic composite for light conversion, which has a plate shape, constant with a high degree of accuracy, which is unfavorable from the perspective of quality stability. It is to be noted that the appropriate white color mentioned above refers to a white color in which blue light and yellow light are mixed in appropriate proportions and which does not contain an excessively intense yellow or blue color.

(16) The constituent phases of the ceramic composite for light conversion according to the present embodiment can be confirmed by identifying peaks of an X-ray diffraction diagram on a powder obtained by grinding the ceramic composite for light conversion. In addition, the elements Y and Ce contained in the first phase can be confirmed through the element analysis of a mirror-like cross section by means of a field-emission scanning electron microscope. In the reflection electron image photographed in the element analysis, the first phase ((Tb, Y).sub.3Al.sub.5O.sub.12 phase) and the second phase (Al.sub.2O.sub.3 phase) can be definitely identified from a difference in brightness of a monochrome image. From a constituent element mapping diagram in the same field of view as the reflection electron image, it can be determined that the distribution regions of the elements Y and Ce correspond with the region identified as the first phase and the Tb element distribution region in the reflection electron image. These indicate that Y or Ce is present in the (Tb, Y).sub.3Al.sub.5O.sub.12 phase.

(17) In the present embodiment, oxide phases other than the first and second phases, very few if any, may be present in some cases to the extent that fluorescence characteristics will not be affected. The oxide phases other than the first and second phase typically include complex oxide phases such as a CeAlO.sub.3 phase, a CeAl.sub.11O.sub.18 phase, and a (Y, Ce)AlO.sub.3 phase.

(18) The ceramic composite for light conversion according to the present embodiment can efficiently emit fluorescence with a dominant wavelength of 570 to 580 m by absorbing light (excitation light) with a peak at a wavelength of 420 to 500 nm. Because of this, yellow fluorescence can be efficiently obtained. The ceramic composite for light conversion according to the present embodiment can emit fluorescence even when the excitation light has a wavelength of 400 to 419 nm or 501 to 530 nm, while the efficiency is decreased. Moreover, even when the excitation light is near-ultraviolet light with a wavelength of 300 to 360 nm, the composite can emit fluorescence.

(19) In the present embodiment, the dominant wavelength refers to a wavelength obtained from the intersection point of a line through two points, which are a point represented by the coordinates of a white point: Cx=0.33 and Cy=0.33 in the CIE chromaticity diagram and a point represented by the coordinate on a luminescence spectrum of the sample (ceramic composite for light conversion), and a monochromatic locus, and refers to a representative wavelength of the light. The dominant wavelength of the fluorescence can be measured by a solid quantum efficiency measurement system of FP6500 from JASCO Corporation in combination with an integrating sphere. The fluorescence dominant wavelength emitted by the ceramic composite for light conversion according to the present embodiment hardly varies depending on the proportion of CeO.sub.2, that is, c in the formula (1), but can be arbitrarily adjusted in the range of 570 to 580 nm depending on x and b/a in the formula (1).

(20) Furthermore, the ceramic composite for light conversion according to the present embodiment can receive light with a peak at a wavelength of 420 to 500 nm, emit fluorescence converted from some of the light as excitation light, and further transmit the other light to emit the transmitted light, thereby emitting white light obtained from mixture of the fluorescence and transmitted light.

(21) The chromaticity range of the white color is not able to be rigorously defined in general because the visibility of the colors varies from individual to individual, but light in the following chromaticity range is regarded as a white color in the present embodiment. The chromaticity range is the region on the chromaticity diagram, which is located above and below a blackbody locus plotted in the range of 2500 to 15000 K of black body color temperature, and in which the deviation (uv) from the blackbody locus is located within approximately 0.02. The uv herein refers to the distance from the blackbody locus drawn on the uv chromaticity diagram to the uv chromaticity which is converted from xy chromaticity values of light. More specifically, light corresponding to 2500 to 15000 K in correlated color temperature is regarded as the white light.

(22) The chromaticity of white light emitted by the ceramic composite for light conversion according to the present embodiment preferably falls within the region surrounded by (0.30, 0.32), (0.34, 0.30), (0.42, 0.41), and (0.38, 0.45) in CIE chromaticity coordinates (Cx, Cy), that is, within the white region in a warm color system. The ceramic composite for light conversion according to the present embodiment can emit a white color in the previously mentioned region by receiving light with a peak at a wavelength from 420 to 500 nm, and thus constitute a white light-emitting device which emits a white color in a warm color system with little luminescence unevenness.

(23) The ceramic composite for light conversion according to the present embodiment can convert some of the received light into light of another wavelength, and emit the converted light from a light-emitting surface other than the light-receiving surface, and directly transmit the unconverted light and emit the light from the light-emitting surface other than the light-receiving surface, thus allowing the composite to serve as a light conversion member for a light-emitting device just by processing the composite. The light emission from the light-emitting device exhibits the chromaticity of the mixture of the converted fluorescence and transmitted light. The chromaticity can fall within the range of the white region.

(24) The ceramic composite for light conversion according to the present embodiment preferably has the plate shape, because an emission surface of a light-emitting element configured in a planar surface and a principal surface of the ceramic composite for light conversion can be easily aligned to be substantially parallel to each other. In addition, the substantially fixed thickness of the ceramic composite for light conversion in a plate shape can stabilize the proportions of color mixture with a substantially uniform amount of wavelength conversion of light being transmitted, thereby suppressing luminescence unevenness at the light-emitting surface. Where the thickness of the ceramic composite for light conversion of a plate shape is increased, it is possible to increase fluorescence emitted by the first phase of the ceramic composite for light conversion, which receives excitation light emitted by the light-emitting element, thus adjusting the chromaticity of light of the excitation light and fluorescence synthesized to intended chromaticity values in the range of the white region.

(25) Where the ceramic composite for light conversion according to the present embodiment has a plate shape, the thickness of the ceramic composite for light conversion in the light emission direction is preferably 80 m or more and 400 m or less. The thickness less than 80 m in the light emission direction may not be preferred, because the thickness may make it difficult to adjust the combined light of excitation light and light emitted by the ceramic composite for light conversion to chromaticity in the range the white region, and may make luminescence unevenness likely to be caused without succeeding in obtaining an adequate mixed color due to the short optical path length. The thickness in excess of 400 m in the light emission direction may not be preferred, because depending on the surface condition of aside surface of the ceramic composite for light conversion, light reflected by the side surface may be mixed with the emitted light to cause luminance unevenness or chromaticity unevenness (luminescence unevenness) at the light-emitting surface. In addition, the thickness in excess of 400 m in the light emission direction may not be preferred, because depending on the configuration of the light-emitting device, light that has a relatively high proportion of the fluorescence (the proportion of yellow light is relatively high with respect to blue light) and is not white, is leaked to the side of the ceramic composite for light conversion, and the light from the side may unfavorably cause unevenness in some cases.

(26) In the present embodiment, in particular, when the ceramic composite for light conversion having a composition represented by formula (1) where c satisfies 0.002c0.02, being of a plate shape, and having a thickness of 80 m or more and 400 m or less in the light emission direction, is applied to a white light-emitting device, an appropriate white light emission can be obtained in which blue light and yellow light are mixed in appropriate proportions, and thus, the ceramic composite for light conversion is particularly preferred, which has the composition represented by the formula (1) where c satisfies 0.002c0.02, and has a plate shape and a thickness of 80 m or more and 400 m or less in the light emission direction.

(27) In the present embodiment, when a white light-emitting device using the ceramic composite for light conversion emits a light, the state in which unevenness in luminance distribution and chromaticity distribution generates in the light emission surface (light-emitting surface) is referred to as luminescence unevenness. Substantial luminescence unevenness refers to a condition in which a plurality of spots or linear regions, which substantially varies in luminance or chromaticity, are observed, where optical measuring instrument such as a two-dimensional luminance meter is focused on the light-emitting surface of the light-emitting device emitting light to measure the light, and chromatically display the result as a luminance distribution or a chromaticity distribution. In the case of this condition, when the light-emitting surface is subjected to a line analysis, there is an increased difference in luminance or chromaticity from the average on the line. On the other hand, insignificant luminescence unevenness refers to a condition in which a difference between luminance or chromaticity in a spot or linear region and the average value is small on an analysis line, or the regions are indistinguishable clearly from each other. In the case of this condition, when the light-emitting surface is subjected to a line analysis, there is a small difference in luminance or chromaticity from the average on the line.

(28) The luminescence unevenness of the ceramic composite for light conversion is believed to be caused by segregation of a substitution element, in particular, Ce in the first phase as a fluorescent phase. The segregation refers to the local presence of a target element in a region of the crystal phase, rather than uniform distribution of the element in the phase. When there is a region with segregation of Ce as an activation element in the first phase, strong fluorescence will be produced more than necessary in the region. This fluorescence component will serve as a region that exhibits high luminance or high chromaticity at a light-emitting surface when a light-emitting element is formed, and observed as luminance unevenness or chromaticity unevenness.

(29) Therefore, in the case of the ceramic composite for light conversion according to the present embodiment, luminescence unevenness is assumed to be suppressed because the presence of Tb makes Ce likely to be incorporated in (Tb, Y).sub.3Al.sub.5O.sub.12 phase as the first phase during the production of the composite as compared with conventional ceramic composites for light conversion, thereby increasing the uniformity element distribution in the first phase, and reducing the development of segregation.

(30) When Gd that is larger in ionic radius than Y is added for the purpose of making the fluorescence dominant wavelength longer in a conventional ceramic composite for light conversion, luminescence unevenness will be increased as in Comparative Examples 3 and 4 as will be described later. In a conventional ceramic composite for light conversion in which Y is substituted with Gd that has an intermediate ionic radius in size between Y and Ce that are respectively smaller and larger in ionic radius, the uniformity of Ce distribution in the first phase will be reduced to increase luminescence unevenness, in exchange for the longer fluorescence dominant wavelength.

(31) Since Tb has an intermediate ionic radius in size between Y and Ce that are respectively smaller and larger in ionic radius as in the case of Gd, and the difference in ionic radius between Tb and Gd is slight as compared with the difference between Y and Gd, it is inconceivable that Tb has an entirely different influence, rather an opposite influence from Gd on the partition (how to be incorporated from the melt into the crystal phase) of the substitution element, in light of technical common sense regarding solidification of common single crystals (materials of single crystal phases). In the present embodiment, although it is not known exactly why the presence of Tb in the melt or the first phase acted to enhance the uniformity of Ce distribution in the first phase, which is not developed by the presence of Gd, the solidification of the ceramic composite for light conversion according to the present embodiment is assumed to be accompanied by a reaction of one liquid phase (melt) and two solid phases (first phase and second phase) in equilibrium with each other, unlike solidification of common single crystals, and related to the presence of the second phase to which no activation element is distributed. Moreover, in a special reaction system such as the solidification in the present embodiment, the influence of some sort of factor other than the ionic radius on the partition of the constituent element from the liquid phase to the solid phase is believed to possibly become larger than in a reaction system of common single crystal solidification with one liquid phase and one solid phase in equilibrium with each other.

(32) Accordingly, because the ceramic composite for light conversion according to the present embodiment is produced by a characteristic production method including solidifying a single dissolved matter homogeneously containing the activation element to form an oxide phase (first phase) in which an activation element is distributed and an oxide phase (second phase) in which no activation element is distributed, Ce is considered to be made likely to be incorporated into a (Tb, Y).sub.3Al.sub.5O.sub.12 phase as the first phase by solidifying a dissolved matter in which Ce coexists with a specific proportion of Tb in the production of the ceramic composite for light conversion according to the present embodiment. Thus, the segregation of Ce in the first phase is considered to be suppressed to suppress luminescence unevenness.

(33) (Method for Producing Ceramic Composite for Light Conversion)

(34) Next, a method will be described for producing the ceramic composite for light conversion according to the present embodiment.

(35) The ceramic composite for light conversion according to the present embodiment can be prepared by melting a raw oxide that is identical to the formula (1) in composition, and solidifying the melted matter through a unidirectional solidification method under a predetermined condition. For example, a solidified body can be obtained in such a simple way that a melted matter of a raw oxide put in a crucible maintained at a predetermined temperature equal to or higher than the melting temperature (approximately 1800 C.) is condensed by cooling (solidified) while controlling the cooling rate. The unidirectional solidification method refers to a method of achieving solidification by applying an optimal temperature gradient to a solid phase/liquid phase interface to unidirectionally control crystal growth. In the unidirectional solidification method, a crystal phase included grows sequentially in a single-crystal state.

(36) As long as the raw oxide has at least one oxide phase that is a fluorescent phase, and can prepare the composition expressed by the formula (1), the ceramic composite materials previously disclosed by the applicant (JP 7-149597 A, JP 7-187893 A, JP 8-81257 A, JP 8-253389 A, JP 8-253390 A, and JP 9-67194 A, as well as corresponding US applications (U.S. Pat. Nos. 5,569,547, 5,484,752, and 5,902,963)) can be used. The disclosures in these applications and patents are to be considered incorporated by reference herein.

(37) The unidirectional solidification method controls the temperature decrease gradient applied in the solidification direction and the transfer rate in the solidification direction. The temperature decrease gradient refers to a temperature difference for each 1 cm of a heating means, which is measured with thermocouples or the like provided at regular intervals in a direction parallel to the solidification direction, for example, in the case of implementing the unidirectional solidification method by transferring a crucible with a melted matter contained therein, or pulling up or down the melted matter. The temperature decrease gradient is preferably 20 C./cm or more, and more preferably 25 C./cm or more. This is effective to suppress the production of oxide phases other than the first and second phases. When the temperature gradient is lower than 20 C./cm, complex oxide phases such as a CeAlO.sub.3 phase and a CeAl.sub.11O.sub.19 phase may be produced which are high in percentage by volume, and when a white light-emitting device is constructed from a blue light-emitting element and the ceramic composite for light conversion according to the present invention, the total radiant flux obtained from the white light-emitting device may be reduced in some cases. In addition, the complex oxide phases described above contain Ce, and thus may decrease the amount of Ce contained in the first phase in some cases.

(38) In addition, the transfer rate refers to the rate of transferring a crucible or the like in a direction parallel to the solidification direction, for example, in the case of implementing the unidirectional solidification method by transferring the crucible, or pulling up or down the melted matter. The transfer rate is preferably 25 mm/hour or less, more preferably 1 to 15 mm/hour. This is effective to suppress the production of oxide phases other than the first and second phases. When the transfer rate exceeds 25 mm/hour, complex oxide phases such as a CeAlO.sub.3 phase and a CeAl.sub.11O.sub.19 phase may be produced which are high in percentage by volume as described previously, and when a white light-emitting device is constructed from a blue light-emitting element and the ceramic composite for light conversion according to the present invention, the total radiant flux obtained from the white light-emitting device may be reduced in some cases. In addition, the complex oxide phases containing Ce as described above are produced which are high in percentage by volume, and thus may decrease the amount of Ce contained in the first phase in some cases.

(39) The unidirectional solidification under the condition as described above is preferred for the production of a solidified body which serves as the ceramic composite for light conversion according to the present embodiment. However, even under conditions other than the previously described condition, a solidified body which serves as the ceramic composite for light conversion according to the present embodiment can be produced as long as the first and second phase are solidified in coexistence with each other.

(40) (Light-Emitting Device)

(41) Next, a light-emitting device according to the present embodiment will be described.

(42) The light-emitting device according to the present embodiment is a light-emitting device which irradiates a ceramic composite for light conversion with light emitted from a light-emitting element, and utilizes light transmitted through the ceramic composite for light conversion and fluorescence with a wavelength converted by the ceramic composite for light conversion.

(43) Examples of the light-emitting device according to the present embodiment include, for example, the light-emitting device 1 shown in FIG. 2. The light-emitting device 1 includes ceramic composite 3 for light conversion, which has a fluorescence dominant wavelength at a wavelength of 570 to 580 nm, and a light-emitting element 4 which emits light with a peak at 420 to 500 nm. The ceramic composite 3 for light conversion is formed in a plate shape. A single crystal substrate 2 is arranged under the ceramic composite 3 for light conversion so as to be parallel to the ceramic composite 3 for light conversion. The light-emitting element 4 is formed on the single crystal substrate 2, and connected through electrodes 5, 6 to a package 7 at another surface opposite to the substrate side. The light-emitting element 4 is an element that emits light ranging from violet to blue, and so as to obtain a white color in tune with the wavelength, light ranging violet to blue emitted from the light-emitting element 4 is transmitted through the single crystal substrate 2, and then allowed to enter the ceramic composite 3 for light conversion with a fluorescence peak wavelength adjusted. Then, yellow luminescence from the excited first phase (fluorescent phase) and transmitted light ranging violet to blue from the second phase (non-fluorescent phase) can pass through the solidified body structured so that the first phase and the second phase are continuously and three-dimensionally entangled mutually and distributed uniformly to homogeneously mix the light and obtain a white color with little luminescence unevenness.

(44) As described above, the ceramic composite for light conversion according to the present embodiment includes the respective oxide phases containing the phosphorescent phase, which are continuously and three-dimensionally entangled mutually. Therefore, homogeneous yellow fluorescence adjusted to any fluorescence dominant wavelength of 570 to 580 nm can be efficiently and stably obtained from the ceramic composite for light conversion according to the present embodiment. Furthermore, the composite is excellent in heat resistance and durability because it is made of the oxide ceramic.

(45) Furthermore, the light-emitting device according to the present embodiment includes the ceramic composite for light conversion according to the present embodiment, and the homogeneous yellow fluorescence with a wavelength adjusted thus makes it possible to emit white light in any color tone, and emit high-luminance homogeneous white light with little luminescence unevenness, in combination with a blue light-emitting element. Furthermore, the light-emitting device according to the present embodiment includes the ceramic composite for light conversion according to the present embodiment, and the ceramic composite for light conversion is thus per se a bulk body, which requires no sealing resin, thereby making it possible to increase the output and increase the efficiency without deterioration by heat or light.

(46) In addition, the light-emitting device according to the present embodiment preferably includes a light-emitting diode element as the light-emitting element thereof. The ceramic composite for light conversion according to the present embodiment can be combined with a blue light-emitting diode element to constitute a highly-efficient light-emitting device.

EXAMPLES

(47) The present invention will be described below in more detail with reference to examples. First, a method for measuring the fluorescence dominant wavelength and fluorescence intensity of the ceramic composite for light conversion, a method for identifying the constituent phases of the ceramic composite for light conversion, and a method for determining luminescence unevenness in a light-emitting device and at a light-emitting surface thereof will be described.

(48) (Method for Measurement of Fluorescence Dominant Wavelength and Fluorescence Intensity)

(49) On a disk-shaped sample of 16 mm0.2 mm obtained from the ceramic composite for light conversion, a fluorescence characteristic evaluation was made at an excitation light wavelength of 460 nm by means of a solid quantum efficiency measurement system from JASCO Corporation, to measure the fluorescence dominant wavelength. In addition, the fluorescence intensity was regarded as relative fluorescence intensity corresponding to a relative value in the case of regarding, as 100, the maximum fluorescence intensity in Comparative Example 1 as will be described later.

(50) (Method for Identifying Constituent Phase of Ceramic Composite for Light Conversion)

(51) The constituent phases of the ceramic composite for light conversion were confirmed by identifying peaks of an X-ray diffraction diagram on a powder obtained by grinding the ceramic composite for light conversion. In addition, the elements Y and Ce contained in the first phase were confirmed through the element analysis of a mirror-like cross section by means of a field-emission scanning electron microscope. Furthermore, from a constituent element mapping diagram in the same field of view as the reflection electron image, the presence of Y or Ce in the (Tb, Y).sub.3Al.sub.5O.sub.12 phase was confirmed by confirming that the distribution region of the elements Y and Ce correspond with the region identified as the first phase and the Tb element distribution region in the reflection electron image.

(52) (Method for Measuring Chromaticity of Light Emission from Light-Emitting Device)

(53) The light-emitting device 1 was prepared as shown in FIG. 2. The ceramic composite 3 for light conversion was the shape of a plated sample of 1 mm1 mm0.08 to 0.5 mm, which was obtained from the solidified body. The light-emitting element 4 was an LED for emitting blue light with a wavelength of 463 nm. The LED was allowed to emit light to irradiate the bottom of the plate-shaped sample with the blue light, and the radiant flux radiated from the surface on the side opposite to the bottom was measured in a commercially available LED measurement system with an integrating sphere. It was confirmed that the measured radiant flux indicated a value reflecting the fluorescence characteristics of the ceramic composite for light conversion. The light-emitting device was allowed to emit light to measure the chromaticity from the total luminous flux of the emitted light taken into the integrating sphere. From the chromaticity measured, it was confirmed that white light is obtained with the light-emitting device including the ceramic composite for light conversion in the shape of a plate varied in thickness.

(54) (Method for Evaluation of Luminescence Unevenness)

(55) Luminescence unevenness of the ceramic composite for light conversion was evaluated by the following method. Because the luminescence unevenness varies with the chromaticity of light emitted by the ceramic composite for light conversion, the chromaticity Cy to be evaluated was defined in a whiter region, and luminescence unevenness was evaluated with a light-emitting device including a ceramic composite for light conversion in the shape of a plate which was thick to emit light with the chromaticity.

(56) The values for chromaticity Cx and Cy of light emitted by the light-emitting device are increased with the increased thickness of the ceramic composite for light conversion. For that reason, a graph with Cx and Cy as variables on two axes and a graph with the thickness of the ceramic composite for light conversion and Cy as variables on two axes were prepared to determine, from approximate lines thereof, the thickness of the ceramic composite for light conversion in a plate shape when chromaticity Cy becomes 0.35.

(57) The light-emitting surface of the light-emitting device 1 including a ceramic composite for light conversion of a plate shape having a size of 1 mm1 mm with a thickness selected so that the chromaticity Cy of the total luminous flux of light emitted by the light-emitting device fallen within the range of 0.350.005 was subjected to measurement of luminance distribution and chromaticity distribution at the light-emitting surface by means of a measurement system for luminance, illuminance, and chromaticity from Cybernet Systems Co., Ltd. The measured luminance distribution and chromaticity distribution at the light-emitting surface were subjected to line analyses (18 lines in total) of 9 lines for each of the horizontal and vertical directions at intervals of 0.1 mm, and the difference (variation) between the luminance or chromaticity on the line and the average value for the luminance or chromaticity at the surface was measured to figure out the maximum variation (largest variation). FIG. 6 shows an example of line analyses. The horizontal axis in the figure indicates a distance from the center of the light-emitting element, whereas the horizontal axis therein indicates a variation (%) in luminance when the average value for the luminance at the surface is used as a reference value (0). Where the maximum variation of the luminance or chromaticity on the line from the average value within 10% is defined as a standard, it was determined that luminescence unevenness was suppressed unless there was a plurality of non-standard lines in which the maximum variation exceeds 10%. In the light-emitting device including the ceramic composite for light conversion according to the present invention, the maximum value of the luminance distribution was larger than the maximum value of the chromaticity distribution. For that reason, the measurement result of the luminance line distribution was used for the determination of luminescence unevenness in all of examples and comparative examples of the present invention.

Example 1

(58) An -Al.sub.2O.sub.3 powder (purity: 99.99%), a Tb.sub.4O.sub.7 powder (purity: 99.9%), and a CeO.sub.2 powder (purity: 99.9%) were weighed respectively to be 0.773 mol in terms of Al.sub.3/2, 0.2270.997 mol in terms of TbO.sub.7/4, and 0.2270.003 mol. These powders were subjected to wet mixing in ethanol for 16 hours by means of a ball mill, and the ethanol as a solvent was then removed by means of an evaporator to obtain a raw material powder. The raw material powder was preliminarily melted in a vacuum furnace, which was regarded as a raw material for unidirectional solidification.

(59) Next, this raw material was directly put in a molybdenum crucible, set in a melting retention zone of an unidirectional solidification system including the melting retention zone in the upper part thereof and a cooling zone in the lower part thereof in which a temperature gradient of 50 C./cm was set in a vertical direction (solidification direction), and melted under a pressure of 1.3310.sup.3 Pa (10.sup.5 Torr). Next, in the same atmosphere, the molybdenum crucible was lowered at a rate of 5 mm/hour to cool the molybdenum crucible from the bottom, thereby obtaining a ceramic composite for light conversion according to Example 1, including Tb.sub.3Al.sub.5O.sub.12 phase: Ce phase and an Al.sub.2O.sub.2 phase. Table 1 shows the fluorescence dominant wavelength and relative fluorescence intensity of the obtained ceramic composite for light conversion.

(60) Furthermore, FIG. 3 shows an X-ray diffraction diagram on a powder obtained by grinding the ceramic composite for light conversion according to Example 1. It has been confirmed that the ceramic composite for light conversion according to Example 1 has peaks for Tb.sub.3Al.sub.5O.sub.12 and Al.sub.2O.sub.3. In addition, a cross section perpendicular to the solidification direction was subjected to an element analysis with a field-emission scanning electron microscope to confirm the presence of Ce in the Tb.sub.3Al.sub.5O.sub.12 phase, and it has been thus confirmed that the ceramic composite for light conversion according to. Example 1 is formed of the Tb.sub.3Al.sub.5O.sub.12 phase activated with Ce and the Al.sub.2O.sub.3 phase. FIG. 1 shows a photograph of a cross-sectional structure perpendicular to the solidification direction of the ceramic composite for light conversion according to Example 1. In FIG. 1 a white section A refers to the second phase (Al.sub.2O.sub.3 phase), whereas a white black section B refers to the first phase (the Tb.sub.3Al.sub.5O.sub.12 phase activated with Ce).

(61) Next, ceramic composites for light conversion of a plate shape and a size of 1 mm1 mm of varying thickness were obtained from the ceramic composite for light conversion according to Example 1, and light-emitting devices including the ceramic composite for light conversion of a plate shape and a light-emitting element for emitting light with a peak at 463 nm were prepared for each thickness of the ceramic composites for light conversion. Then, chromaticity was measured from the total luminous fluxes taken into the integrating sphere when the light-emitting devices were allowed to emit light. The chromaticity plotted in FIG. 5 has chromaticity examples of light emitted by the light-emitting devices in the case of adjusting a thickness of the ceramic composites for light conversion of a plate shape to 0.15 mm, 0.20 mm, and 0.24 mm respectively in the order of chromaticity value from smallest to largest. It has been confirmed that when the thickness of the ceramic composite for light conversion of a plate shape falls at least within the range between 0.15 mm and 0.24 mm, the light-emitting device including the composite falls into the chromaticity of a white region. More specifically, it has been successfully confirmed through chromaticity that white light is achieved by the light-emitting device using the ceramic composite for light conversion according to Example 1. In addition, from the variation in chromaticity due to the thickness, it has been determined that the chromaticity Cy of light emitted by the light-emitting device can be adjusted to the chromaticity range of 0.30 to 0.41 as shown in FIG. 5 by adjusting the thickness of the ceramic composite for light conversion used in the light-emitting device.

(62) Next, a graph with the chromaticity Cx and Cy as variables on two axes (graph 1) and a graph with the thickness of the sample and Cy as variables on two axes (graph 2) were drawn from the measured chromaticity Cx and Cy of light emitted by the light-emitting device and the thickness of the ceramic composite for light conversion of a plate shape. The thickness of the ceramic composite for light conversion of the plate shape and the chromaticity Cx in the case of chromaticity Cy=0.35 were respectively 0.22 mm and 0.37 which were obtained from an approximate line of the graph 1 and the graph 2.

(63) Then, a ceramic composite for light conversion of a plate shape having a thickness for the chromaticity Cy: 0.35 of light emitted by the light-emitting device, that is, a thickness of 0.22 mm and a size of 1 mm1 mm was obtained from the ceramic composite for light conversion according to Example 1. And then, a light-emitting device was prepared which was provided with the ceramic composite for light conversion of a plate shape and a light-emitting element for emitting light with a peak at 463 nm. Next, this light-emitting device was allowed to emit light for measuring luminance distribution and chromaticity distribution at the light-emitting surface, and evaluating luminescence unevenness. The results are shown in Table 1.

Example 2

(64) Raw materials, an -Al.sub.2O.sub.3 powder (purity: 99.99%), a Tb.sub.4O.sub.7 powder (purity: 99.9%), and a CeO.sub.2 powder (purity: 99.9%) were weighed respectively to be 0.773 mol in terms of Al.sub.3/2, 0.2270.994 mol in terms of TbO.sub.7/4, and 0.2270.006 mol. As for the rest, except that the transfer rate of the molybdenum crucible was adjusted to 10 mm/hour, a ceramic composite for light conversion according to Example 2 was obtained in the same way as in Example 1. In the same way as in Example 1, it was confirmed that the ceramic composite for light conversion according to Example 2 is formed of a Tb.sub.3Al.sub.5O.sub.12 phase activated with Ce and an Al.sub.2O.sub.3 phase. Table 1 shows the fluorescence dominant wavelength and relative fluorescence intensity of the obtained ceramic composite for light conversion.

(65) Except for adjusting the thicknesses of the ceramic composites for light conversion of a plate shape to 0.14 mm, 0.19 mm, and 0.24 mm, light-emitting devices were prepared for each thickness of the ceramic composites for light conversion in the same way as in Example 1, and the chromaticity Cx and Cy of light emitted by the light-emitting devices was measured in the same way as in Example 1. The thickness of the ceramic composite for light conversion of a plate shape and the chromaticity Cx in the case of chromaticity Cy=0.35 were obtained in the same way as in Example 1, and luminescence unevenness was determined in the same way as in Example 1. Table 1 shows the thickness of the ceramic composite for light conversion of a plate shape and the chromaticity Cx in the case of chromaticity Cy=0.35, as well as the result of determining luminescence unevenness.

Example 3

(66) An -Al.sub.2O.sub.2 powder (purity: 99.99%), a Tb.sub.4O.sub.7 powder (purity: 99.9%), and a CeO.sub.2 powder (purity: 99.9%) were weighed respectively to be 0.773 mol in terms of AlO.sub.3/2, 0.2270.99 mol in terms of TbO.sub.7/4, and 0.2270.01 mol. As for the rest, except that the transfer rate of the molybdenum crucible was adjusted to 10 mm/hour, a ceramic composite for light conversion was obtained in the same way as in Example 1. In the same way as in Example 1, it was confirmed that the ceramic composite for light conversion according to Example 3 is formed of a Tb.sub.3Al.sub.5O.sub.12 phase activated with Ce and an Al.sub.2O.sub.3 phase. Table 1 shows the fluorescence dominant wavelength and relative fluorescence intensity of the obtained ceramic composite for light conversion.

(67) In addition, except that the thicknesses of the ceramic composites for light conversion of the plate shape were adjusted to 0.10 mm, 0.15 mm, and 0.19 mm to prepare light-emitting devices, the thickness of the ceramic composite for light conversion of the plate shape and the chromaticity Cx in the case of chromaticity Cy=0.35, as well as luminescence unevenness were determined in the same way as in Example 1. The results are shown in Table 1.

Example 4

(68) An -Al.sub.2O.sub.3 powder (purity: 99.99%), a Tb.sub.4O.sub.7 powder (purity: 99.9%), a Y.sub.2O.sub.3 powder (purity: 99.9%), and a CeO.sub.2 powder (purity: 99.9%) were weighed respectively to be 0.773 mol in terms of AlO.sub.3/2, 0.2270.990.4 mol in terms of TbO.sub.7/4, 0.2270.990.6 mol in terms of YO.sub.3/2, and 0.2270.01 mol. As for the rest, except that the transfer rate of the molybdenum crucible was adjusted to 10 mm/hour, a ceramic composite for light conversion was obtained in the same way as in Example 1. In the same way as in Example 1, it was confirmed that the ceramic composite for light conversion according to Example 4 is formed of a (Tb, Y).sub.3Al.sub.5O.sub.12 phase activated with Ce and an Al.sub.2O.sub.3 phase. Table 1 shows the fluorescence dominant wavelength and relative fluorescence intensity of the obtained ceramic composite for light conversion.

(69) In addition, the thickness of the ceramic composite for light conversion of the plate shape and the chromaticity Cx in the case of chromaticity Cy=0.35, as well as luminescence unevenness were determined in the same way as in Example 3. The results are shown in Table 1.

Example 5

(70) Except that an -Al.sub.2O.sub.3 powder (purity: 99.99%), a Tb.sub.4O.sub.7 powder (purity: 99.9%), a Y.sub.2O.sub.3 powder (purity: 99.9%), and a CeO.sub.2 powder (purity: 99.9%) were weighed respectively to be 0.808 mol in terms of AlO.sub.3/2, 0.1920.9980.3 mol in terms of TbO.sub.7/4, 0.1920.9980.7 mol in terms of YO.sub.3/2, and 0.1920.002 mol, a ceramic composite for light conversion was obtained in the same way as in Example 1. In the same way as in Example 1, it was confirmed that the ceramic composite for light conversion according to Example 5 is formed of a (Tb, Y).sub.3Al.sub.5O.sub.12 phase activated with Ce and an Al.sub.2O.sub.3 phase. Table 1 shows the fluorescence dominant wavelength and relative fluorescence intensity of the obtained ceramic composite for light conversion.

(71) In addition, except that the thicknesses of the ceramic composites for light conversion of the plate shape were adjusted to 0.20 mm, 0.35 mm, and 0.50 mm to prepare light-emitting devices, the thickness of the ceramic composite for light conversion of the plate shape and the chromaticity Cx in the case of chromaticity Cy=0.35, as well as luminescence unevenness were determined in the same way as in Example 1. The results are shown in Table 1.

Example 6

(72) Except that raw materials, an -Al.sub.2O.sub.3 powder (purity: 99.99%), a Tb.sub.4O.sub.7 powder (purity: 99.9%), a Y.sub.2O.sub.3 powder (purity: 99.9%), and a CeO.sub.2 powder (purity: 99.9%) were weighed respectively to be 0.800 mol in terms of AlO.sub.3/2, 0.2000.9980.225 mol in terms of TbO.sub.7/4, 0.2000.9980.775 mol in terms of YO.sub.3/2, and 0.2000.002 mol, a ceramic composite for light conversion was obtained in the same way as in Example 1. In the same way as in Example 1, it was confirmed that the ceramic composite for light conversion according to Example 6 is formed of a (Tb, Y).sub.3Al.sub.5O.sub.12 phase activated with Ce and an Al.sub.2O.sub.3 phase. Table 1 shows the fluorescence dominant wavelength and relative fluorescence intensity of the obtained ceramic composite for light conversion.

(73) In addition, the thickness of the ceramic composite for light conversion of the plate shape and the chromaticity Cx in the case of chromaticity Cy=0.35, as well as luminescence unevenness were determined in the same way as in Example 5. The results are shown in Table 1.

Example 7

(74) Except that raw materials, an -Al.sub.2O.sub.3 powder (purity: 99.99%), a Tb.sub.4O.sub.7 powder (purity: 99.9%), a Y.sub.2O.sub.3 powder (purity: 99.9%), and a CeO.sub.2 powder (purity: 99.9%) were weighed respectively to be 0.788 mol in terms of AlO.sub.3/2, 0.2120.9820.4 mol in terms of TbO.sub.7/4, 0.2120.9820.6 mol in terms of YO.sub.3/2, and 0.2120.018 mol, a ceramic composite for light conversion was obtained in the same way as in Example 1. In the same way as in Example 1, it was confirmed that the ceramic composite for light conversion according to Example 7 is formed of a (Tb, Y).sub.3Al.sub.5O.sub.12 phase activated with Ce and an Al.sub.2O.sub.3 phase. Table 1 shows the fluorescence dominant wavelength and relative fluorescence intensity of the obtained ceramic composite for light conversion.

(75) In addition, except that the thicknesses of the ceramic composites for light conversion of the plate shape were adjusted to 0.08 mm, 0.14 mm, and 0.18 mm to prepare light-emitting devices, the thickness of the ceramic composite for light conversion of the plate shape and the chromaticity Cx in the case of chromaticity Cy=0.35, as well as luminescence unevenness were determined in the same way as in Example 1. The results are shown in Table 1.

Example 8

(76) Except that raw materials, an -Al.sub.2O.sub.3 powder (purity: 99.99%), a Tb.sub.4O.sub.7 powder (purity: 99.9%), and a CeO.sub.2 powder (purity: 99.9%) were weighed respectively to be 0.808 mol in terms of AlO.sub.3/2, 0.1920.985 mol in terms of TbO.sub.7/4, and 0.1920.015 mol, a ceramic composite for light conversion was obtained in the same way as in Example 1. In the same way as in Example 1, it was confirmed that the ceramic composite for light conversion according to Example 8 is formed of a Tb.sub.3Al.sub.5O.sub.12 phase activated with Ce and an Al.sub.2O.sub.3 phase. Table 1 shows the fluorescence dominant wavelength and relative fluorescence intensity of the obtained ceramic composite for light conversion.

(77) In addition, the thickness of the ceramic composite for light conversion of the plate shape and the chromaticity Cx in the case of chromaticity Cy=0.35, as well as luminescence unevenness were determined in the same way as in Example 7. The results are shown in Table 1.

Example 9

(78) Except that raw materials, an -Al.sub.2O.sub.3 powder (purity: 99.99%), a Tb.sub.4O.sub.7 powder (purity: 99.9%), and a CeO.sub.2 powder (purity: 99.9%) were weighed respectively to be 0.773 mol in terms of AlO.sub.3/2, 0.2270.9770.4 mol in terms of TbO.sub.7/4, and 0.2270.023 mol, a ceramic composite for light conversion was obtained in the same way as in Example 1. In the same way as in Example 1, it was confirmed that the ceramic composite for light conversion according to Example 9 is formed of a Tb.sub.3Al.sub.5O.sub.12 phase activated with Ce and an Al.sub.2O.sub.3 phase. Table 1 shows the fluorescence dominant wavelength and relative fluorescence intensity of the obtained ceramic composite for light conversion.

(79) In addition, the thickness of the ceramic composite for light conversion of the plate shape and the chromaticity Cx in the case of chromaticity Cy=0.35, as well as luminescence unevenness were determined in the same way as in Example 7. The results are shown in Table 1.

Example 10

(80) Except that raw materials, an -Al.sub.2O.sub.3 powder (purity: 99.99%), a Tb.sub.4O.sub.7 powder (purity: 99.9%), a Y.sub.2O.sub.3 powder (purity: 99.9%), and a CeO.sub.2 powder (purity: 99.9%) were weighed respectively to be 0.808 mol in terms of AlO.sub.3/2, 0.1920.980.225 mol in terms of TbO.sub.7/4, 0.1920.980.775 mol in terms of YO.sub.3/2, and 0.1920.02 mol, a ceramic composite for light conversion was obtained in the same way as in Example 1. In the same way as in Example 1, it was confirmed that the ceramic composite for light conversion according to Example 10 is formed of a (Tb, Y).sub.3Al.sub.5O.sub.12 phase activated with Ce and an Al.sub.2O.sub.3 phase. Table 1 shows the fluorescence dominant wavelength and relative fluorescence intensity of the obtained ceramic composite for light conversion.

(81) In addition, except that the thicknesses of the ceramic composites for light conversion of the plate shape were adjusted to 0.08 mm, 0.10 mm, and 0.13 mm to prepare light-emitting devices, the thickness of the ceramic composite for light conversion of the plate shape and the chromaticity Cx in the case of chromaticity Cy=0.35, as well as luminescence unevenness were determined in the same way as in Example 1. The results are shown in Table 1. In addition, the chromaticity plotted in FIG. 5 has chromaticity examples of the light-emitting devices in the case of adjusting the samples to 0.08 mm, 0.10 mm, and 0.13 mm in thickness respectively in the order of chromaticity value from smallest to largest.

Example 11

(82) Except that raw materials, an -Al.sub.2O.sub.3 powder (purity: 99.99%), a Tb.sub.4O.sub.7 powder (purity: 99.9%), a Y.sub.2O.sub.3 powder (purity: 99.9%), and a CeO.sub.2 powder (purity: 99.9%) were weighed respectively to be 0.800 mol in terms of AlO.sub.3/2, 0.2000.997 0.2 mol in terms of TbO.sub.7/4, 0.2000.9970.8 mol in terms of YO.sub.3/2, and 0.2000.003 mol, a ceramic composite for light conversion was obtained in the same way as in Example 1. In the same way as in Example 1, it was confirmed that the ceramic composite for light conversion according to Example 11 is formed of a (Tb, Y).sub.3Al.sub.5O.sub.12 phase activated with Ce and an Al.sub.2O.sub.3 phase. Table 1 shows the fluorescence dominant wavelength and relative fluorescence intensity of the obtained ceramic composite for light conversion. The obtained fluorescence dominant wavelength was 570 nm.

(83) In addition, the thickness of the ceramic composite for light conversion of the plate shape and the chromaticity Cx in the case of chromaticity Cy=0.35, as well as luminescence unevenness were determined in the same way as in Example 5. The results are shown in Table 1.

Example 12

(84) An -Al.sub.2O.sub.3 powder (purity: 99.99%), a Tb.sub.4O.sub.7 powder (purity: 99.9%), and a CeO.sub.2 powder (purity: 99.9%) were weighed respectively to be 0.773 mol in terms of AlO.sub.3/2, 0.2270.975 mol in terms of TbO.sub.7/4, and 0.2270.025 mol. As for the rest, except that the transfer rate of the molybdenum crucible was adjusted to 10 mm/hour, a ceramic composite for light conversion was obtained in the same way as in Example 1. In the same way as in Example 1, it was confirmed that the ceramic composite for light conversion according to Example 12 is formed of a Tb.sub.3Al.sub.5O.sub.12 phase activated with Ce and an Al.sub.2O.sub.3 phase. Table 1 shows the fluorescence dominant wavelength and relative fluorescence intensity of the obtained ceramic composite for light conversion.

(85) In addition, the thickness of the ceramic composite for light conversion of the plate shape and the chromaticity Cx in the case of chromaticity Cy=0.35, as well as luminescence unevenness were determined in the same way as in Example 7. The results are shown in Table 1. The thickness less than 80 m produce a difference in chromaticity due to a slight variation in sample thickness, thus, in order to keep light emitted by the white light-emitting device at constant chromaticity, there is a need to equalize the thicknesses of the plate-like ceramic composites for light conversion with a high degree of precision, and there is a need to control, with a high degree of precision, processing for adjusting the thicknesses of the plate-like ceramic composites for light conversion.

Comparative Example 1

(86) Except that raw materials, an -Al.sub.2O.sub.3 powder (purity: 99.99%), a Y.sub.2O.sub.3 powder (purity: 99.9%), and a CeO.sub.2 powder (purity: 99.9%) were weighed respectively to be 0.813 mol in terms of AlO.sub.3/2, 0.1870.997 mol in terms of YO.sub.3/2, and 0.187 0.003 mol, a ceramic composite for light conversion was obtained in the same way as in Example 1. A cross section perpendicular to the solidification direction was subjected to an element analysis with a field-emission scanning electron microscope to confirm the presence of Ce in a Y.sub.3Al.sub.5O.sub.12 phase, and it has been thus confirmed that the ceramic composite for light conversion according to Comparative Example 1 is formed of the Y.sub.3Al.sub.5O.sub.12 phase activated with Ce and an Al.sub.2O.sub.3 phase. Table 1 shows the fluorescence dominant wavelength, relative fluorescence intensity of the obtained ceramic composite for light conversion, the thickness and chromaticity Cx of the ceramic composite for light conversion at chromaticity Cy=0.35 in the case of a LED, and the result of determining luminescence unevenness. In spite of little luminescence unevenness of the obtained ceramic composite for light conversion, the fluorescence dominant wavelength was 568 nm.

Comparative Example 2

(87) Except that raw materials, an -Al.sub.2O.sub.3 powder (purity: 99.99%), a Y.sub.2O.sub.3 powder (purity: 99.9%), and a CeO.sub.2 powder (purity: 99.9%) were weighed respectively to be 0.808 mol in terms of AlO.sub.3/2, 0.1920.99 mol in terms of YO.sub.3/2, and 0.1920.01 mol, a ceramic composite for light conversion was obtained in the same way as in Example 1. In the same way as in Comparative Example 1, it was confirmed that the ceramic composite for light conversion according to Comparative Example 2 is formed of a Y.sub.3Al.sub.5O.sub.12 phase activated with Ce and an Al.sub.2O.sub.3 phase. Table 1 shows the fluorescence dominant wavelength, relative fluorescence intensity of the obtained ceramic composite for light conversion, the thickness and chromaticity Cx of the ceramic composite for light conversion at chromaticity Cy=0.35 in the case of a LED, and the result of determining luminescence unevenness. The fluorescence dominant wavelength of the obtained ceramic composite for light conversion was 571 nm. While the fluorescence dominant wavelength was 570 nm or more under the influence of the high Ce proportion, the luminescence unevenness was significant.

Comparative Example 3

(88) Except that raw materials, an -Al.sub.2O.sub.3 powder (purity: 99.99%), a Y.sub.2O.sub.3 powder (purity: 99.9%), a Gd.sub.2O.sub.3 powder (purity: 99.9%), and a CeO.sub.2 powder (purity: 99.9%) were weighed respectively to be 0.808 mol in terms of AlO.sub.3/2, 0.1920.89 mol in terms of YO.sub.3/2, 0.1920.10 mol in terms of GdO.sub.3/2, and 0.1870.01 mol, a ceramic composite for light conversion was obtained in the same way as in Example 1. A cross section perpendicular to the solidification direction was subjected to an element analysis with a field-emission scanning electron microscope to confirm the presence of Ce in a (Y, Gd).sub.3Al.sub.5O.sub.12 phase, and it has been thus confirmed that the ceramic composite for light conversion according to Comparative Example 3 is formed of the (Y, Gd).sub.3Al.sub.5O.sub.12 phase activated with Ce and an Al.sub.2O.sub.3 phase.

(89) It is to be noted that the compositions of the Gd-containing ceramic composite for light conversion according to Comparative Examples 3 and 4 are expressed by the following formula (2), and the ratio between GdO.sub.3/2 and YO.sub.3/2 is shown as a/b in Table 1.
[Formula 3]
AlO.sub.3/2x.Math.(a.Math.GdO.sub.3/2b.Math.YO.sub.3/2c.Math.CeO.sub.2)(2)

(90) Table 1 shows the fluorescence dominant wavelength, relative fluorescence intensity of the obtained ceramic composite for light conversion, the thickness and chromaticity Cx of the ceramic composite for light conversion at chromaticity Cy=0.35 in the case of a LED, and the result of determining luminescence unevenness. While the fluorescence dominant wavelength of the obtained ceramic composite for light conversion was increased to 574 nm under the influence of Gd, the luminescence unevenness was more significant than in Comparative Example 2.

Comparative Example 4

(91) Except that raw materials, an -Al.sub.2O.sub.3 powder (purity: 99.99%), a Y.sub.2O.sub.3 powder (purity: 99.9%), a Gd.sub.2O.sub.3 powder (purity: 99.9%), and a CeO.sub.2 powder (purity: 99.9%) were weighed respectively to be 0.808 mol in terms of AlO.sub.3/2, 0.1920.86 mol in terms of YO.sub.3/2, 0.1920.10 mol in terms of GdO.sub.3/2, and 0.1920.04 mol, a ceramic composite for light conversion was obtained in the same way as in Example 1. In the same way as in Comparative Example 3, it was confirmed that the ceramic composite for light conversion according to Comparative Example 4 is formed of a (Y, Gd).sub.3Al.sub.5O.sub.12 phase activated with Ce and an Al.sub.2O.sub.3 phase. Table 1 shows the fluorescence dominant wavelength, relative fluorescence intensity of the obtained ceramic composite for light conversion, the thickness and chromaticity Cx of the ceramic composite for light conversion at chromaticity Cy=0.35 in the case of a LED, and the result of determining luminescence unevenness. While the fluorescence dominant wavelength of the obtained ceramic composite for light conversion was increased to 575 nm under the influence of Gd, the luminescence unevenness was far more significant than in Comparative Example 3 with the Gd proportion lower than in Comparative Example 4.

Comparative Example 5

(92) Except that raw materials, an -Al.sub.2O.sub.3 powder (purity: 99.99%), a Tb.sub.4O.sub.7 powder (purity: 99.9%), and a CeO.sub.2 powder (purity: 99.9%) were weighed respectively to be 0.813 mol in terms of AlO.sub.3/2, 0.1870.99 mol in terms of TbO.sub.7/4, and 0.187 0.01 mol, a ceramic composite for light conversion was obtained in the same way as in Example 1. Table 1 shows the fluorescence dominant wavelength, relative fluorescence intensity of the obtained ceramic composite for light conversion, the thickness and chromaticity Cx of the ceramic composite for light conversion at chromaticity Cy=0.35 in the case of a LED, and the result of determining luminescence unevenness. The obtained ceramic composite for light conversion, including a non-uniform structure with coarse initial crystals of Al.sub.2O.sub.3 produced extensively, varied significantly in chromaticity for each sample, and thus, was not appropriate as a ceramic composite for light conversion for use in a white light-emitting device.

Comparative Example 6

(93) Except that raw materials, an -Al.sub.2O.sub.3 powder (purity: 99.99%), a Tb.sub.4O.sub.7 powder (purity: 99.9%), a Y.sub.2O.sub.3 powder (purity: 99.9%), and a CeO.sub.2 powder (purity: 99.9%) were weighed respectively to be 0.769 mol in terms of AlO.sub.3/2, 0.2310.990.25 mol in terms of TbO.sub.7/4, 0.2310.990.75 mol in terms of YO.sub.3/2, and 0.2310.01 mol, a ceramic composite for light conversion was obtained in the same way as in Example 1. The solidified body obtained had a plurality of cracks, thereby resulting in failure to obtain any disk-shaped sample of 16 mm0.2 mm as shown in Table 1.

Comparative Example 7

(94) Except that raw materials, an -Al.sub.2O.sub.3 powder (purity: 99.99%), a Tb.sub.4O.sub.7 powder (purity: 99.9%), and a CeO.sub.2 powder (purity: 99.9%) were weighed respectively to be 0.76 mol in terms of AlO.sub.3/2, 0.240.98 mol in terms of TbO.sub.7/4, and 0.240.02 mol, a ceramic composite for light conversion was obtained in the same way as in Example 1. Table 1 shows the fluorescence dominant wavelength, relative fluorescence intensity of the obtained ceramic composite for light conversion, the thickness and chromaticity Cx of the ceramic composite for light conversion at chromaticity Cy=0.35 in the case of a LED, and the result of determining luminescence unevenness. There were a plurality of non-standard lines, and it was determined that the suppression of luminescence unevenness was not sufficient.

Comparative Example 8

(95) Except that raw materials, an -Al.sub.2O.sub.3 powder (purity: 99.99%), a Tb.sub.4O.sub.7 powder (purity: 99.9%), a Y.sub.2O.sub.3 powder (purity: 99.9%), and a CeO.sub.2 powder (purity: 99.9%) were weighed respectively to be 0.808 mol in terms of AlO.sub.3/2, 0.1920.970.5 mol in terms of TbO.sub.7/4, 0.1920.970.5 mol in terms of YO.sub.3/2, and 0.1920.03 mol, a ceramic composite for light conversion was obtained in the same way as in Example 1. While the fluorescence dominant wavelength and the relative fluorescence intensity were able to be measured in regard to the disk-shaped sample obtained, the high chromaticity Cx and Cy of the total luminous fluxes emitted from the light-emitting devices in regard to all of the plate-shaped samples failed to fall into any white region as shown in Table 1. For this reason, it was not possible to calculate the thickness or chromaticity Cx of the ceramic composite for light conversion at chromaticity Cy=0.35 in the case of a LED.

(96) TABLE-US-00001 TABLE 1 Fluorescece Intensity The (Comparative White Chromaticity Number of Dominant Example 1 Thickness for Cx Non- Wavelength Regarded as LED (mm) (at (at Cy = Standard x b/a a/b c (nm) 100) Cy = 0.36) 0.35) Lines Example 1 0.294 0.0 0.003 577 125 0.22 0.37 0/18 Example 2 0.294 0.0 0.006 577 135 0.18 0.37 0/18 Example 3 0.294 0.0 0.01 577 141 0.12 0.37 0/18 Example 4 0.294 1.5 0.01 576 139 0.14 0.86 0/18 Example 5 0.238 2.3 0.002 573 103 0.40 0.34 0/18 Example 6 0.250 2.4 0.002 572 101 0.40 0.33 0/18 Example 7 0.269 1.5 0.018 576 148 0.09 0.36 1/18 Example 8 0.238 0.0 0.015 576 140 0.11 0.36 0/18 Example 9 0.294 0.0 0.023 577 144 0.08 0.37 0/18 Example 10 0.258 2.4 0.02 572 142 0.08 0.33 0/18 Example 11 0.250 0.0 0.003 575 99 0.40 0.32 0/18 Example 12 0.294 0.0 0.025 677 146 0.02 0.37 1/18 Comparative 0.248 0.0 0.003 568 100 1.10 0.31 0/18 Example 1 Comparative 0.263 0.0 0.01 571 139 0.18 0.92 4/18 Example 2 Comparative 0.269 0.1 0.01 574 128 0.16 0.54 18/18 Example 3 Comparative 0.263 0.1 0.04 575 138 0.08 0.30 18/18 Example 4 Comparative 0.230 0.0 0.01 significant variations Example 5 Comparative 0.300 3.0 0.01 unmeasurable Example 6 Comparative 0.316 0.0 0.02 577 144 0.08 0.37 8/18 Example 7 Comparative 0.238 1.0 0.03 575 150 failure to calculate Example 8 (outside white region)

(97) From the foregoing, it is found that the range for white light emissions obtained by adjusting the thicknesses of the ceramic composites for light conversion according to the examples has a region surrounded by (0.30, 0.32), (0.34, 0.30), (0.42, 0.41), and (0.38, 0.45) in the CIE chromaticity (Cx, Cy) shown in FIG. 5 in the case of the light-emitting device using the ceramic composite for light conversion according to the present invention.

(98) Furthermore, FIG. 4 shows a fluorescence spectrum of the ceramic composite for light conversion according to Example 1, in conjunction with a fluorescence spectrum of the ceramic composite for light conversion according to Comparative Example 1 with a fluorescence dominant wavelength of 568 nm. It is found that the fluorescence spectrum of the ceramic composite for light conversion according to Example 1 with a long fluorescence dominant wavelength is shifted to the long wavelength side with respect to the fluorescence spectrum of the ceramic composite for light conversion according to Comparative Example 1 with a short fluorescence dominant wavelength.

(99) Furthermore, FIG. 6 is a diagram showing an example of a line analysis on the luminance at a light-emitting surface of a light-emitting device including the ceramic composite for light conversion according to Example 3, in conjunction with an example according to Comparative Example 3. It is found that Example 3 varies insignificantly from place to place, and has the maximum variation within the standards, as compared with Comparative Example 3. As just described, it has been confirmed that luminescence unevenness is suppressed with the maximum variation within the standards in the line analysis for all of the 18 lines in Example 3.

(100) Accordingly, it is found that the ceramic composite for light conversion according to the present invention is a ceramic composite for light conversion, which is able to arbitrarily adjust the fluorescence dominant wavelength through x and/or b/a in the formula (1), and high in relative fluorescence intensity even when the fluorescence dominant wavelength is a long wavelength, further with luminescence unevenness suppressed, and used in a preferred manner in a white light-emitting device.

REFERENCE SIGNS LIST

(101) 1 light-emitting device 2 single crystal substrate 3 ceramic composite for light conversion 4 light-emitting element (light-emitting diode element) 5, 6 electrode 7 package