Phosphor and LED light emitting device using the same

Abstract

An LED light emitting device is provided that has high color rendering properties and is excellent color uniformity and, at the same time, can realize even luminescence unattainable by conventional techniques. A phosphor having a composition represented by formula: (Sr.sub.2-X-Y-Z-Ba.sub.XMg.sub.YMn.sub.ZEu.sub.)SiO.sub.4 wherein x, y, z, and are respectively coefficients satisfying 0.1<x<1, 0<y<0.5, 0<z<0.1, y>z, and 0.01<<0.2 is provided. The phosphor is used in combination with ultraviolet and blue light emitting diodes having a luminescence peak wavelength of 360 to 470 nm to form an LED light emitting device.

Claims

1. A europium-manganese-activated alkaline earth magnesium silicate phosphor comprising a composition represented by the following chemical formula:
(Sr.sub.2-X-Y-Z-Ba.sub.XMg.sub.YMn.sub.ZEu.sub.)SiO.sub.4 wherein x, y, z, and are respectively coefficients satisfying 0.1<x<1, 0<y<0.5, 0<z<0.1, y>z, and 0.01<<0.2, and being capable of emitting luminescent components of three colors of blue, green and red.

2. The europium-manganese-activated alkaline earth magnesium silicate phosphor according to claim 1, wherein the phosphor is excited by a light having a peak in an ultraviolet-to-blue region, the phosphor emits light having: a peak in a blue region at a wavelength of 400 to 500 nm, a peak in a green-to-yellow region at a wavelength of 500 to 600 nm, and a peak in a red region at a wavelength of 600 to 700 nm.

3. An LED light emitting device comprising an ultraviolet to blue light emitting diode and a phosphor, said light emitting diode having a luminescence peak wavelength of 360 to 470 nm, and said phosphor is a europium-manganese-activated alkaline earth magnesium silicate phosphor according to claim 1, wherein said phosphor emits white light consisting of blue, green and red light by excitation from said ultraviolet to blue light emitting diode.

4. The LED white light emitting device according to claim 3, further comprising one or more of phosphors that emit blue or red light by excitation from the ultraviolet to blue light emitting diode.

5. An LED light emitting device comprising an ultraviolet light emitting diode and a phosphor, said light emitting diode having a luminescence peak wavelength of 370 to 430 nm, and said phosphor is a europium-manganese-activated alkaline earth magnesium silicate phosphor according to claim 1, wherein said phosphor emits white light consisting of blue, green and red light by excitation from said ultraviolet to blue light emitting diode.

6. The LED white light emitting device according to claim 5, further comprising one or more of phosphors that emit blue or red light by excitation from the ultraviolet to blue light emitting diode.

Description

BRIEF DESCRIPTION OF DRAWINGS

(1) FIG. 1 is a diagram showing a fluorescence distribution spectrum that has characteristics of a phosphor according to the present invention.

(2) FIG. 2 is a cross-sectional view showing the construction of an LED light emitting device according to the present invention.

(3) FIG. 3 is an example of a luminescence spectrum in an LED light emitting device according to the present invention.

(4) FIG. 4 is a diagram showing a method for measuring an azimuthal color difference in such a state that an LED light emitting device is turned on.

DESCRIPTION OF REFERENCE CHARACTERS

(5) 1: Luminescence Spectrum of Phosphor (Sr.sub.1.02Ba.sub.0.45Mg.sub.0.455Mn.sub.0.045Eu.sub.0.03)SiO.sub.4 according to the present invention 2: Luminescence spectrum of phosphor (Sr.sub.1.02Ba.sub.0.44Mg.sub.0.44Mn.sub.0.06Eu.sub.0.04)SiO.sub.4)SiO.sub.4 according to the present invention 3: Light emitting diode 4: Phosphor layer embedded in resin 5: Resin frame 6: White LED 7: Light receiving part in measuring machine

BEST MODE FOR CARRYING OUT THE INVENTION

(6) FIG. 1 shows a luminescence spectrum of a phosphor according to the present invention. The spectrum was obtained by excitation with an ultraviolet light having a luminescence peak wavelength of 395 nm. In FIG. 1, spectrum 1 corresponds to a phosphor composition of (Sr.sub.1.02Ba.sub.0.45Mg.sub.0.455Mn.sub.0.045Eu.sub.0.03)SiO.sub.4, and spectrum 2 corresponds to a phosphor composition of (Sr.sub.1.02Ba.sub.0.44Mg.sub.0.44Mn.sub.0.06Eu.sub.0.04)SiO.sub.4. As is apparent from FIG. 1, the phosphor according to the present invention exhibits a spectrum having a peak in a blue region at a wavelength of 400 to 500 nm, a peak in a green to yellow region at a wavelength of 500 to 600 nm, and a peak in a red region at a wavelength of 600 to 700 nm and emits white light despite a single phosphor.

(7) In FIG. 1, white light that was emitted from the phosphor having spectrum 1 had a luminescent chromaticity (CIE chromaticity value) of (0.324, 0.404), and white light that was emitted from the phosphor having spectrum 2 had a luminescent chromaticity of (0.331, 0.373). The luminescent chromaticity can be varied in a wide range by varying the composition of the phosphor. Specifically, in Eu-activated strontium silicate phosphor (Sr.sub.2SiO.sub.4:Eu), the luminescence intensity of the yellow region can be varied by replacing a part (0.1 to 1 mole) of Sr with Ba; the luminescence intensity of the blue region can be varied by replacing a part (less than 0.5 mole) of Sr with Mg; and the luminescence intensity of the red region can be varied by replacing a part (less than 0.1 mole) of Sr with Mn, whereby the peak height in each of the wavelength ranges can be increased or decreased as desired.

(8) The lower limit of the addition amount of each element is a limit value that, when the addition amount of the element is smaller than the limit value, an effective change in the luminescence spectrum is not observed, and the upper limit of the addition amount has been set as a value that provides a satisfactory effect of a change in spectrum and while taking into consideration a concentration balance between the elements. Regarding the molar ratio between magnesium (Mg) and manganese (Mn), Mg is preferably higher than Mn. This is so because, when Mn is higher than Mg, a colored crystal powder is obtained, resulting in lowered brightness.

(9) The phosphor according to the present invention may be prepared, for example, by the following method. At the outset, strontium carbonate, barium carbonate, magnesium oxide, manganese carbonate, silicon oxide, and europium oxide are weighed as starting materials at a predetermined molar ratio and are thoroughly mixed together in a ball mill. In this case, for example, a halide which has flux action may be added. The resulting starting material mixture is filled into an aluminum crucible and is fired at a temperature of 1100 to 1300 C. for 4 to 6 hr. The firing is preferably carried out in a reducing atmosphere obtained by introducing nitrogen containing a few percentage of hydrogen into a furnace. The fired phosphor is ground in a mortar and may be again fired in a reducing atmosphere. The fired product is ground in a mortar, is poured into water, is washed by decantation, is further milled, is washed, and is then subjected to filtration, drying, and sieving to obtain a phosphor according to the present invention.

(10) The LED light emitting device according to the present invention comprises a combination of a light emitting diode having a luminescence wavelength of 360 to 470 nm with one or more phosphors according to the present invention. Further, in the present invention, the phosphor may be used in combination with an ultraviolet light emitting diode having a luminescence wavelength of 370 to 430 nm. The LED light emitting device may have a construction having a cross section, for example, as shown in FIG. 2 In FIG. 2, numeral 3 designates a light emitting diode, numeral 4 a phosphor layer embedded in a resin, and numeral 5 a resin frame that supports a luminescent part. Electric energy applied to the LED light emitting device is converted to ultraviolet or blue light by the light emitting diode, a part of these lights is converted by the phosphor layer located on the upper part of the light emitting diode to light having a longer wavelength, and the ultraviolet or blue light is combined with the longer-wavelength light to constitute white light that is then radiated to the outside of the LED light emitting device.

(11) FIG. 3 shows an example of a luminescence spectrum of an LED light emitting device obtained by combining an LED light emitting device having a construction as shown in FIG. 2 with a phosphor according to the present invention. Light is emitted from an ultraviolet light emitting diode at a current value of 20 mA and a peak value of 395 nm, and light that has been emitted from the LED light emitting device and has been converted to white light having a chromaticity of (0.280 to 0.380, 0.280 to 0.380) by the phosphor exhibits a spectrum having a very small peak, attributable to an ultraviolet excitation light component, at 395 nm and having luminescence peaks attributable to respective luminescent components of blue, green, and red, whereby property values of a brightness of not less than 400 mcd and an average color rendering index (Ra), which represents the quality of white light in use for illumination, of not less than 75.

(12) The brightness and average color rendering index (Ra) of the LED light emitting device according to the present invention each are on a practical level, but are not significantly improved over LED light emitting devices of type 1 or type 2 that are currently used on an experiment basis in the world. The LED light emitting device according to the present invention is characterized in that the color difference (azimuthal color difference) is very small when LED which emits light is viewed in different azimuths. An azimuthal variation in color causes color unevenness of an object when light from LED is projected onto the object. Accordingly, in order to eliminate the color variation, a mechanism for mixing the white light by a diffusing plate or the like should be incorporated in the device, and this method is not favorable from a practical viewpoint. In the present invention, white light free from a color variation can be realized without adding the mixing mechanism.

(13) The azimuthal color difference can be evaluated, for example, by the following method. LED has a cross section as shown in FIG. 2 and, as viewed from above, has such a shape that a reflective layer is formed in a mortar form within a cylindrical resin frame. As shown in FIG. 4, the color difference in light emitted from the LED light emitting device is determined by first disposing a light receiving part 7 in measuring equipment just above white LED 6, measuring a chromaticity (x, y), then changing angle of the light receiving part 7, measuring a luminescent chromaticity (x, y), determining the maximum value of absolute values of the difference between these values, and regarding the maximum value as an azimuthal color difference (x, y). The azimuthal color difference of the white LED shown in FIG. 3 was evaluated by this method and was found to be a very small and (x, y)=(0.001, 0.002).

(14) The LED light emitting device according to the present invention comprises a phosphor according to the present invention coated onto a light emitting diode. For example, the LED light emitting device can be produced by adding a phosphor to a resin composition to prepare a coating liquid, coating the coating liquid onto a light emitting diode, and curing the resin. The phosphor according to the present invention may be solely used as the phosphor to be used in the LED light emitting device or alternatively may be used as a mixture comprised of the phosphor according to the present invention as a base with other phosphor(s). It has been found that, even when a phosphor prepared by further adding other phosphor such as blue or red phosphor to the phosphor according to the present invention is used, an LED light emitting device which has a smaller azimuthal color difference than conventional LED can be obtained.

EXAMPLES

(15) Next, embodiments of the present invention is further illustrated by the following Examples that are not intended as a limitation of the invention.

(16) The LED light emitting device according to the present invention has been evaluated as follows. The LED light emitting device had a construction having a cross section shown in FIG. 2. The LED light emitting device comprised a light emitting diode comprising a chip having a size of 300 m square, and light was emitted at a current value of 20 mA to evaluate characteristics of the light emitting device. The light emitting diode had a luminescence wavelength of 380 to 420 nm (a luminescence peak wavelength of 400 nm) and had an output of 20 mW (20 mA). Some types of phosphors emitted brighter light upon exposure to short-wavelength excitation light. In this case, the light emitting diode had a luminescence wavelength of 360 to 400 nm (a luminescence peak wavelength of 380 nm). The light emitting diode had an output of 19 mW (20 mA). The luminescence characteristics of the LED light emitting device were evaluated using CAS 140 COMPACT ARRAY SPECTROMETER manufactured by Instrument Systems Inc. and an MCPD device manufactured by Otsuka Electronics Co., Ltd.

(17) <Preparation of LED Light Emitting Device>

(18) Two or more phosphors were separately mixed with a silicone resin at a mixing ratio of 10 to 20% by mass to prepare slurries. These slurries were blended so that the chromaticity of the LED light emitting device was x=0.280 to 0.380 and y=0.280 to 0.380. A part of the resulting slurry was extracted, was dropped on an LED light emitting device disposed as shown in FIG. 2, and was heat treated at a temperature of 100 to 150 C. to cure the silicone resin and thus to obtain an LED light emitting device.

Example 1

(19) Starting materials were weighed and mixed together at a mixing ratio of 1.02 moles of strontium carbonate, 0.44 mole of barium carbonate, 0.44 mole of magnesium oxide, 0.06 mole of manganese carbonate, 0.02 mole of europium oxide, and 1.00 mole of silicon oxide. Further, 0.5% by mass, based on the starting materials, of ammonium chloride as a flux was added thereto, followed by mixing for one hr in a ball mill. The mixture thus obtained was filled into an alumina crucible, was fired for 5 hr in a reducing atmosphere containing 5% of hydrogen to obtain a phosphor. The phosphor thus synthesized was ground in a mortar and was passed through a mesh. Further, a decantation procedure consisting of stirring the phosphor in water, stopping the stirring, and discarding the supernatant was carried out five times. The slurry was then filtered, and the residue was dried. The dried product was passed through 200 meshes to obtain phosphor 1. Subsequently, 30% by mass of phosphor 1 was mixed with a silicone resin, and the slurry was coated onto the light emitting diode. The coated light emitting diode was heat treated at 140 C. to cure the resin and thus to obtain an LED light emitting device.

Example 2

(20) Phosphor 2 was obtained by the same treatment as in Example 1, except that starting materials were weighed and mixed together at a mixing ratio of 1.02 moles of strontium carbonate, 0.45 mole of barium carbonate, 0.455 mole of magnesium oxide, 0.045 mole of manganese carbonate, 0.015 mole of europium oxide, and 1.00 mole of silicon oxide. An LED light emitting device was then obtained in the same manner as in Example 1, except that phosphor 2 was used.

Example 3

(21) Phosphor 3 was obtained by the same treatment as in Example 1, except that starting materials were weighed and mixed together at a mixing ratio of 1.1 moles of strontium carbonate, 0.41 mole of barium carbonate, 0.4 mole of magnesium oxide, 0.05 mole of manganese carbonate, 0.02 mole of europium oxide, and 1.00 mole of silicon oxide. An LED light emitting device was then obtained in the same manner as in Example 1, except that phosphor 3 was used.

Example 4

(22) Phosphor 4 was obtained by the same treatment as in Example 1, except that starting materials were weighed and mixed together at a mixing ratio of 1.02 moles of strontium carbonate, 0.53 mole of barium carbonate, 0.35 mole of magnesium oxide, 0.055 mole of manganese carbonate, 0.0255 mole of europium oxide, and 1.00 mole of silicon oxide. An LED light emitting device was then obtained in the same manner as in Example 1, except that phosphor 4 was used.

Example 5

(23) Phosphor 5 was obtained by the same treatment as in Example 1, except that starting materials were weighed and mixed together at a mixing ratio of 0.796 mole of strontium carbonate, 0.73 mole of barium carbonate, 0.37 mole of magnesium oxide, 0.06 mole of manganese carbonate, 0.022 mole of europium oxide, and 1.00 mole of silicon oxide. An LED light emitting device was then obtained in the same manner as in Example 1, except that phosphor 5 was used.

Example 6

(24) Phosphor 6 was obtained by the same treatment as in Example 1, except that starting materials were weighed and mixed together at a mixing ratio of 0.82 mole of strontium carbonate, 0.65 mole of barium carbonate, 0.42 mole of magnesium oxide, 0.05 mole of manganese carbonate, 0.03 mole of europium oxide, and 1.00 mole of silicon oxide. An LED light emitting device was then obtained in the same manner as in Example 1, except that phosphor 6 was used.

Example 7

(25) Phosphor 7 was obtained by the same treatment as in Example 1, except that starting materials were weighed and mixed together at a mixing ratio of 0.965 mole of strontium carbonate, 0.55 mole of barium carbonate, 0.4 mole of magnesium oxide, 0.045 mole of manganese carbonate, 0.02 mole of europium oxide, and 1.00 mole of silicon oxide. An LED light emitting device was then obtained in the same manner as in Example 1, except that phosphor 7 was used.

Example 8

(26) Phosphor 8 was obtained by the same treatment as in Example 1, except that starting materials were weighed and mixed together at a mixing ratio of 0.98 mole of strontium carbonate, 0.6 mole of barium carbonate, 0.3 mole of magnesium oxide, 0.02 mole of manganese carbonate, 0.05 mole of europium oxide, and 1.00 mole of silicon oxide. A phosphor was prepared by mixing phosphor 8 thus obtained, a blue phosphor represented by Sr.sub.5(PO.sub.4)Cl:Eu and a red phosphor represented by Y.sub.2O.sub.2S:Eu at a mass ratio of 0.2:1.0:0.4.

(27) Subsequently, 30% by mass of the phosphor was mixed with a silicone resin, and the slurry was coated onto the light emitting diode. The coated light emitting diode was heat treated at 140 C. to cure the resin and thus to obtain an LED light emitting device.

Example 9

(28) Phosphor 9 was obtained by the same treatment as in Example 1, except that starting materials were weighed and mixed together at a mixing ratio of 0.945 mole of strontium carbonate, 0.7 mole of barium carbonate, 0.2 mole of magnesium oxide, 0.005 mole of manganese carbonate, and 0.075 mole of europium oxide. A phosphor was prepared by mixing phosphor 9 thus obtained, a blue phosphor represented by (Sr,Ba).sub.5(PO.sub.4)Cl:Eu and a red phosphor represented by La.sub.2O.sub.2S:Eu,Sm at a mass ratio of 0.2:1.0:0.3.

(29) Subsequently, 30% by mass of the phosphor was mixed with a silicone resin, and the slurry was coated onto the light emitting diode. The coated light emitting diode was heat treated at 140 C. to cure the resin and thus to obtain an LED light emitting device.

Example 10

(30) Phosphor 10 was obtained by the same treatment as in Example 1, except that starting materials were weighed and mixed together at a mixing ratio of 1.247 moles of strontium carbonate, 0.5 mole of barium carbonate, 0.15 mole of magnesium oxide, 0.003 mole of manganese carbonate, 0.05 mole of europium oxide, and 1.00 mole of silicon oxide. A phosphor was prepared by mixing phosphor 10 thus obtained, a blue phosphor represented by BaMgAl.sub.10O.sub.17:Eu and a red phosphor represented by La.sub.2O.sub.2S:Eu at a mass ratio of 0.1:1.0:0.4.

(31) Subsequently, 30% by mass of the phosphor was mixed with a silicone resin, and the slurry was coated onto the light emitting diode. The coated light emitting diode was heat treated at 140 C. to cure the resin and thus to obtain an LED light emitting device.

Comparative Example 1

(32) A phosphor was prepared by mixing a blue phosphor represented by (Sr,Ba).sub.5(PO.sub.4).sub.3Cl:Eu, a green phosphor represented by BaMgAl.sub.10O.sub.17:Eu,Mn and a red phosphor represented by La.sub.2O.sub.2S:Eu at a mass ratio of 0.2:1.0:0.3.

(33) Subsequently, 30% by mass of the phosphor was mixed with a silicone resin, and the slurry was coated onto the light emitting diode. The coated light emitting diode was heat treated at 140 C. to cure the resin and thus to obtain a conventional LED light emitting device.

Comparative Example 2

(34) A slurry prepared by mixing 15% by mass of a europium-activated strontium-barium-orthosilicate, which is a yellow phosphor represented by (Sr,Ba).sub.2SiO.sub.4:Eu, with a silicone resin was coated onto the light emitting diode. The coated light emitting diode was heat treated at 140 C. to cure the resin and thus to obtain a conventional LED light emitting device.

(35) A current of 20 mA was allowed to flow into each of the LED light emitting devices thus obtained to emit light. In this case, the brightness and azimuthal color difference of the luminescence were as shown in Table 1.

(36) TABLE-US-00001 TABLE 1 Characteristics of Wavelength light emitting device of excitation Azimuthal Phosphor by diode Brightness color difference Chemical composition (nm) (mcd) (x, y) Ex. 1 (Sr.sub.1.02, Ba.sub.0.44, Mg.sub.0.44, Mn.sub.0.06, Eu.sub.0.04)SiO.sub.4 400 400 (0.001, 0.002) Ex. 2 (Sr.sub.1.02, Ba.sub.0.45, Mg.sub.0.455, Mn.sub.0.045, Eu.sub.0.03)SiO.sub.4 400 410 (0.002, 0.002) Ex. 3 (Sr.sub.1.1, Ba.sub.0.41, Mg.sub.0.4, Mn.sub.0.05, Eu.sub.0.04)SiO.sub.4 400 420 (0.001, 0.001) Ex. 4 (Sr.sub.1.02, Ba.sub.0.53, Mg.sub.0.35, Mn.sub.0.055, Eu.sub.0.045)SiO.sub.4 400 400 (0.002, 0.002) Ex. 5 (Sr.sub.0.796, Ba.sub.0.73, Mg.sub.0.37, Mn.sub.0.06, Eu.sub.0.044)SiO.sub.4 400 410 (0.001, 0.002) Ex. 6 (Sr.sub.0.82, Ba.sub.0.65, Mg.sub.0.42, Mn.sub.0.05, Eu.sub.0.06)SiO.sub.4 400 440 (0.002, 0.002) Ex. 7 (Sr.sub.0.965, Ba.sub.0.55, Mg.sub.0.4, Mn.sub.0.045, Eu.sub.0.04)SiO.sub.4 380 440 (0.002, 0.002) Ex. 8 (Sr.sub.0.98, Ba.sub.0.6, Mg.sub.0.3, Mn.sub.0.02, Eu.sub.0.1)SiO.sub.4 380 410 (0.002, Sr.sub.5(PO.sub.4).sub.3Cl: Eu 0.003) Y.sub.2O.sub.2S: Eu Ex. 9 (Sr.sub.0.945, Ba.sub.0.7, Mg.sub.0.2, Mn.sub.0.005, Eu.sub.0.15)SiO.sub.4 400 420 (0.001, (Sr, Ba).sub.5(PO.sub.4).sub.3Cl: Eu 0.003) La.sub.2O.sub.2S: Eu, Sm Ex. 10 (Sr.sub.1.247, Ba.sub.0.5, Mg.sub.0.15, Mn.sub.0.003, Eu.sub.0.1)SiO.sub.4 400 430 (0.003, BaMgAl.sub.10O.sub.17: Eu 0.002) La.sub.2O.sub.2S: Eu Comp. (Sr, Ba).sub.5(PO.sub.4).sub.3Cl: Eu 400 400 (0.010, Ex. 1 BaMgAl.sub.10O.sub.17: Eu, Mn 0.008) La.sub.2O.sub.2S: Eu, Sm Comp. (Sr, Ba).sub.2SiO.sub.4: Eu 460 490 (0.020, Ex. 2 0.020)

(37) As is apparent from Table 1, according to the present invention, LED light emitting devices having a significantly improved azimuthal color difference can be obtained. Further, the phosphor according to the present invention comprises luminescent components of three colors of red, blue, and green and thus has high color rendering properties and can emit bright light.