WO2018095211A1 - 发光陶瓷结构及其制备方法、相关发光装置和投影装置 - Google Patents
发光陶瓷结构及其制备方法、相关发光装置和投影装置 Download PDFInfo
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- WO2018095211A1 WO2018095211A1 PCT/CN2017/109330 CN2017109330W WO2018095211A1 WO 2018095211 A1 WO2018095211 A1 WO 2018095211A1 CN 2017109330 W CN2017109330 W CN 2017109330W WO 2018095211 A1 WO2018095211 A1 WO 2018095211A1
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F21—LIGHTING
- F21V—FUNCTIONAL FEATURES OR DETAILS OF LIGHTING DEVICES OR SYSTEMS THEREOF; STRUCTURAL COMBINATIONS OF LIGHTING DEVICES WITH OTHER ARTICLES, NOT OTHERWISE PROVIDED FOR
- F21V7/00—Reflectors for light sources
- F21V7/22—Reflectors for light sources characterised by materials, surface treatments or coatings, e.g. dichroic reflectors
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/515—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
- C04B35/58—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides
- C04B35/581—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides based on aluminium nitride
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/009—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone characterised by the material treated
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
- C04B41/52—Multiple coating or impregnating multiple coating or impregnating with the same composition or with compositions only differing in the concentration of the constituents, is classified as single coating or impregnation
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
- C04B41/80—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only ceramics
- C04B41/81—Coating or impregnation
- C04B41/89—Coating or impregnation for obtaining at least two superposed coatings having different compositions
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F21—LIGHTING
- F21K—NON-ELECTRIC LIGHT SOURCES USING LUMINESCENCE; LIGHT SOURCES USING ELECTROCHEMILUMINESCENCE; LIGHT SOURCES USING CHARGES OF COMBUSTIBLE MATERIAL; LIGHT SOURCES USING SEMICONDUCTOR DEVICES AS LIGHT-GENERATING ELEMENTS; LIGHT SOURCES NOT OTHERWISE PROVIDED FOR
- F21K9/00—Light sources using semiconductor devices as light-generating elements, e.g. using light-emitting diodes [LED] or lasers
- F21K9/60—Optical arrangements integrated in the light source, e.g. for improving the colour rendering index or the light extraction
- F21K9/68—Details of reflectors forming part of the light source
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F21—LIGHTING
- F21V—FUNCTIONAL FEATURES OR DETAILS OF LIGHTING DEVICES OR SYSTEMS THEREOF; STRUCTURAL COMBINATIONS OF LIGHTING DEVICES WITH OTHER ARTICLES, NOT OTHERWISE PROVIDED FOR
- F21V29/00—Protecting lighting devices from thermal damage; Cooling or heating arrangements specially adapted for lighting devices or systems
- F21V29/85—Protecting lighting devices from thermal damage; Cooling or heating arrangements specially adapted for lighting devices or systems characterised by the material
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F21—LIGHTING
- F21V—FUNCTIONAL FEATURES OR DETAILS OF LIGHTING DEVICES OR SYSTEMS THEREOF; STRUCTURAL COMBINATIONS OF LIGHTING DEVICES WITH OTHER ARTICLES, NOT OTHERWISE PROVIDED FOR
- F21V29/00—Protecting lighting devices from thermal damage; Cooling or heating arrangements specially adapted for lighting devices or systems
- F21V29/85—Protecting lighting devices from thermal damage; Cooling or heating arrangements specially adapted for lighting devices or systems characterised by the material
- F21V29/86—Ceramics or glass
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F21—LIGHTING
- F21V—FUNCTIONAL FEATURES OR DETAILS OF LIGHTING DEVICES OR SYSTEMS THEREOF; STRUCTURAL COMBINATIONS OF LIGHTING DEVICES WITH OTHER ARTICLES, NOT OTHERWISE PROVIDED FOR
- F21V7/00—Reflectors for light sources
- F21V7/22—Reflectors for light sources characterised by materials, surface treatments or coatings, e.g. dichroic reflectors
- F21V7/24—Reflectors for light sources characterised by materials, surface treatments or coatings, e.g. dichroic reflectors characterised by the material
Definitions
- the present invention relates to the field of illumination and display technologies, and in particular, to a luminescent ceramic structure, a method of fabricating the same, a related illuminating device, and a projection device.
- the packaging method of the phosphor is mainly composed of an organic silicone package and an inorganic glass package, and the thermal conductivity of the two packages is low (lW/(mK) or less), and the heat damage resistance temperature is not high.
- the withstand temperature of silica gel is generally below 200 ° C, and the temperature of glass is generally below 500 ° C.
- TW201023405A discloses a light-emitting structure including a light-emitting ceramic layer and a porous ceramic reflective layer, wherein the porous ceramic reflective layer is a porous YAG reflective layer, and the technical solution utilizes heat resistance of the ceramic structure and excellent mechanical mechanism.
- the performance is much better than the technical solutions of the above-mentioned silicone packaging and inorganic glass packaging.
- this technical solution is generated in the LED lighting period. The intensity of the excitation light emitted by the LED is far less than that of the current laser.
- the luminescent ceramic layer Under the illumination of the laser, the luminescent ceramic layer emits a large amount of heat, and the porous structure of the porous ceramic reflective layer makes the heat difficult. To pass it out, a heat sink substrate needs to be placed on the back side to improve heat dissipation.
- the constituent material of the porous ceramic reflective layer is usually different from the constituent material of the heat dissipation substrate, which makes it difficult for the two to enhance the bonding force by co-sintering.
- the present invention provides a luminescent ceramic structure, which has the characteristics of high thermal conductivity, strong adhesive force, and high reliability.
- the present invention provides a luminescent ceramic structure comprising a luminescent ceramic layer, a porous ceramic reflective layer and a ceramic heat dissipation substrate which are sequentially laminated and bonded together; wherein the porous ceramic reflective layer is catalyzed by oxidation Alumina porous ceramics of zinc and/or magnesia, miscellaneous zinc oxide and/or magnesium oxide for bonding to ceramic heat sink substrates; and at least part of the cumbersome zinc oxide is present in the form of Zn x Al y O, and At least part of the cumbersome magnesium oxide is present in the form of Mg X A1 y O; the ceramic heat dissipating substrate is an aluminum nitride ceramic substrate.
- Zn x Al y O is specifically ZnAl 2 0 4
- Mg X A1 y O is specifically MgAl 2 0 4 .
- porous ceramic reflective layer is further miscible with at least one of zirconia, titanium oxide and cerium oxide.
- the proportion of the oxides in the porous ceramic reflective layer is 1% to 10 ⁇ 3 ⁇ 4 of the total mass.
- the luminescent ceramic layer is a Ce miscellaneous YAG ceramic.
- the luminescent ceramic layer has a thickness of 0.05 to 1 mm
- the porous ceramic reflective layer has a thickness of 0.1 to 2 mm
- the ceramic heat dissipation substrate has a thickness of 0.5 to 5 mm.
- the surface of the luminescent ceramic layer is coated with an anti-reflection film, or the surface of the luminescent ceramic layer has a rough microstructure.
- the present invention provides a method of fabricating a luminescent ceramic structure according to the first aspect, comprising: sequentially casting a casting paste for forming a porous ceramic reflective layer and a luminescent ceramic layer, respectively
- the above-described luminescent ceramic structure is formed on a ceramic heat-dissipating substrate, followed by lamination and sintering in sequence.
- a light emitting device comprising the luminescent ceramic structure of the first aspect, further comprising an excitation light source for generating excitation light, wherein the luminescent ceramic structure is located on the optical path of the excitation light .
- the invention provides a projection system comprising the illumination device of the third aspect, further comprising a projection imaging device.
- the luminescent ceramic structure provided by the present invention utilizes alumina porous ceramic as the reflective layer, and also bonds the luminescent ceramic layer and the ceramic heat dissipation substrate as a bonding layer to achieve higher efficiency. , higher reliability.
- the alumina reflective ceramic layer is a non-dense porous structure, this knot The structure can ensure a high reflectance even when the thickness is thin, and the non-dense porous structure can achieve the adhesion of the alumina ceramic and the aluminum nitride ceramic with inconsistent thermal expansion coefficients.
- zinc oxide and/or magnesium oxide is added to the alumina porous ceramic to chemically react with a trace amount of alumina layer on the surface of the aluminum nitride ceramic substrate to form Zn X A1 y O and/or Mg X A1 y O, The adhesion to the aluminum nitride ceramic substrate is further enhanced.
- FIG. 1 is a schematic structural view of an embodiment of a luminescent ceramic structure of the present invention.
- FIG. 2 is a schematic structural view of another embodiment of a luminescent ceramic structure of the present invention.
- FIG. 3 is a schematic structural view of still another embodiment of the luminescent ceramic structure of the present invention.
- the luminescent ceramic structure includes a luminescent ceramic layer (first layer), a porous ceramic reflective layer (second layer), and a ceramic heat dissipation substrate (third layer), which are sequentially laminated and bonded together, wherein the porous ceramic reflection
- the layer is an alumina porous ceramic
- the ceramic heat dissipation substrate is an aluminum nitride ceramic substrate.
- the oxide in the porous alumina ceramic layer can react with the aluminum oxide layer on the surface of the aluminum nitride to form a composite product.
- the composite product is used to improve the bonding of the porous ceramic reflective layer to the ceramic heat sink substrate.
- the porous ceramic reflective layer is an alumina porous ceramic, its own alumina is difficult to react with aluminum oxide on the surface of aluminum nitride or aluminum nitride, so the present invention utilizes an extra cumbersome oxide to participate in the reaction and becomes a porous ceramic reflection.
- the connection bridge between the layer and the ceramic heat dissipation substrate is the main inventive concept of the present invention.
- the first layer of the luminescent ceramic layer functions to receive the irradiation of the excitation light, and The excitation light is converted into a laser beam of a different wavelength.
- the excitation light here may be light emitted by a solid-state light source, such as L ED light, laser diode light, laser light, or any other source light of the present invention. Since the luminescent ceramic layer is a ceramic structure, its thermal stability and thermal conductivity are far superior to those of a glass or silica-based phosphor layer (that is, the phosphor is encapsulated in continuous glass or silica gel), and can withstand high-power excitation light. Irradiation can be applied to high-intensity laser fluorescent lighting/display fields.
- the luminescent ceramic layer may be a pure phase fluorescent ceramic, specifically a variety of oxide ceramics, nitride ceramics or oxynitride ceramics, by injecting trace amounts of activator elements (such as lanthanides) into the ceramic preparation process. ), forming a luminescent center. Since the general activator element has a small amount of impurities (generally less than 1%), the fluorescent ceramic is usually a transparent or translucent luminescent ceramic, and the excitation light is easily emitted directly through the luminescent ceramic layer, so that the luminescent ceramic layer is The luminous efficiency is not high, and it is more suitable for lower power excitation light application scenarios.
- the luminescent ceramic layer is a Ce miscellaneous YAG ceramic; in another embodiment of the invention, the luminescent ceramic layer is a Ce miscellaneous LuAG ceramic.
- the luminescent ceramic layer may also be a composite ceramic layer with a transparent/translucent ceramic as a matrix, and luminescent ceramic particles (such as phosphor particles) are distributed in the ceramic matrix.
- the transparent/translucent ceramic substrate may be various oxide ceramics (such as alumina ceramics, Y 3 A1 5 0 12 ceramics), nitride ceramics (such as aluminum nitride ceramics) or oxynitride ceramics, and the role of the ceramic matrix is to Light and heat conduct, so that the excitation light can be incident on the luminescent ceramic particles, and the laser light can be emitted from the luminescent ceramic layer; the luminescent ceramic particles bear the main illuminating function of the luminescent ceramic layer, and are used to absorb the excitation light and convert it.
- the luminescent ceramic particles have a large grain size, and the activator element has a large amount of impurities (such as 1 to 5%), so that the luminescent efficiency is high; and the luminescent ceramic particles are dispersed in the ceramic matrix, thereby avoiding the luminescent ceramics.
- the luminescent ceramic particles in the deeper layer cannot be irradiated by the excitation light, and the poisoning of the activator element concentration caused by the large amount of the pure phase fluorescent ceramics is avoided, thereby improving the luminous efficiency of the luminescent ceramic layer. .
- scattering particles may be added to the luminescent ceramic layer to distribute the scattering particles in the ceramic matrix.
- the function of the scattering particles is to enhance the scattering of the excitation light in the luminescent ceramic layer, thereby increasing the optical path of the excitation light in the luminescent ceramic layer, so that the light utilization efficiency of the excitation light is greatly improved, and the light conversion efficiency of the luminescent ceramic layer is improved.
- the scattering particles may be scattering particles such as alumina, cerium oxide, zirconium oxide, cerium oxide, titanium oxide, zinc oxide, barium sulfate, etc., either as scattering particles of a single material or Two or more combinations, characterized by an apparent white color, are capable of scattering visible light, are stable in material, can withstand high temperatures, and have a particle size that is of the same order of magnitude or an order of magnitude lower than the wavelength of the excitation light.
- the scattering particles may be replaced by pores of the same size, and total reflection is achieved by the difference in refractive index between the pores and the ceramic matrix to scatter the excitation light or the laser.
- the luminescent ceramic layer may also be another composite ceramic layer which differs from the composite ceramic layer described above only in the ceramic matrix.
- the ceramic substrate is a pure phase fluorescent ceramic, i.e., the ceramic substrate itself has an activator capable of emitting a laser light upon irradiation with excitation light.
- the technical scheme combines the advantages of the above-mentioned composite ceramic layer luminescent ceramic particles with high luminous efficiency and the above-mentioned pure phase fluorescent ceramics having the luminescent property, and simultaneously illuminating the luminescent ceramic particles and the ceramic matrix to further improve the luminescent ceramic layer.
- the luminous efficiency, and the ceramic matrix has a certain amount of activator, but the amount of impurities is low, which can ensure that the ceramic substrate has sufficient light transmittance.
- the luminescent ceramic layer it is also possible to increase the internal scattering of the scattering particles or the pore-enhanced luminescent ceramic layer.
- a typical but non-limiting choice of luminescent ceramic particles is a garnet luminescent ceramic with a lanthanide complex, such as Ca 3(Al,Sc) 2 Si 3 0 12 , or an aluminate such as (Gd, Tb, Y, Lu) 3 (Al, Ga) 5 0 12 and the composite component of ⁇ ⁇ ⁇ 2 1 2 0 12 , etc., wherein the elements separated by commas in parentheses such as (Al, Ga) refer to A1 and Ga
- the ratio can be arbitrarily selected, but the total amount of the two elements is equivalent to 1, in the chemical formula, for example, A 7 Ga. . 3 , A1
- Ce miscellaneous YAG garnet that is, ( ⁇ , - x Ce J 3 Al 5 0 12 ) is preferred.
- the luminescent ceramic particles are Ce miscellaneous LuAG pomegranate Stone structure.
- the thickness of the luminescent ceramic layer is 0.05 to 1 mm. If the luminescent ceramic layer is too thin, the efficiency is lowered. If the luminescent ceramic layer is too thick, the thermal resistance is too large, which is disadvantageous for heat dissipation.
- the second layer of the porous ceramic reflective layer is used for scattering reflection of the laser light or the mixed light of the laser light and the unabsorbed excitation light.
- the porous ceramic reflective layer is specifically an alumina porous ceramic, and the reflection principle is to utilize the refractive index difference between the pore and the alumina to cause the incident light to be totally reflected at the interface between the alumina and the pore to achieve a reflection effect.
- the refractive index of alumina is generally about 1.7, and the pores are considered to be air inside, and the refractive index is about 1. When light is incident from the inside of alumina to the interface between alumina and air, the incident angle is small. Total reflection occurs.
- the reflectivity of the porous ceramic reflective layer can be controlled by controlling the thickness of the porous ceramic reflective layer by adding a pore former or controlling the temperature rise rate.
- the alumina porous ceramic of the invention is resistant to high temperature and oxidation, and is suitable for high-power illuminating luminescent ceramic structure, and the pores are more easily distributed uniformly, which is favorable for uniform reflection of the reflective layer.
- a metal reflective layer in the prior art is easy to oxidize and vulcanize, especially in a high temperature environment; another prior art uses a bonding agent such as glass to bond white scattering particles into a layer, and the technical solution is defective.
- the adhesive is viscous, and the white scattering particles have a small particle size and are easily agglomerated, and it is difficult to uniformly disperse them. Since the reflective functional material of the reflective layer is white scattering particles, it cannot be uniformly dispersed. Causes uneven reflectance.
- an oxide is additionally mixed in the porous alumina ceramic layer, and some of the oxide may react with the alumina at a high temperature to form a new composite oxide in the form of the composite oxide.
- M x Al y O where M is an element of a poor oxide.
- a typical feature is: at least one of zinc oxide and magnesium oxide.
- zinc oxide is at least partially Zn x Al y
- magnesium oxide is present at least partially in the form of Mg x Al y O.
- the cumbersome oxides are intensively mixed with the raw material of the alumina porous ceramic layer during the preparation process, and during the sintering process, the cumbersome oxide partially reacts with the alumina.
- the alumina porous ceramic layer is directly fired on the ceramic heat dissipation substrate, and the ceramic heat dissipation substrate is a prepared aluminum nitride ceramic substrate, and the surface of the aluminum nitride ceramic substrate is usually oxidized to produce an aluminum oxide film.
- the impurity oxide in the raw material ie, magnesium oxide or zinc oxide as described above
- the aluminum oxide film on the surface of the aluminum nitride ceramic substrate to form a composite oxide.
- the composite oxide allows the alumina porous ceramic layer to be more closely bonded to the aluminum nitride ceramic heat sink substrate, thereby improving the reliability of the product.
- Zn x Al y O is specifically ZnAl 2 0 4
- Mg X A1 y O is specifically MgAl 2
- the composite oxide is a spinel structure and has a stable structure, which is beneficial to the combination of the porous ceramic layer and the ceramic heat dissipation layer.
- the presence of the substance can be confirmed by detecting the combination of the alumina porous ceramic layer and the aluminum nitride ceramic heat-dissipating substrate and performing component analysis and characterization.
- the diffraction peak card of the X-ray diffraction spectrum is PDF #21-1152
- the diffraction peak card of the ray diffraction spectrum of ZnAl 2 0 4 is PDF #05-0669.
- the element ratio of Zn to A1 or Mg to A1 is not particularly limited, and in an actual luminescent ceramic structure product, The ratio of elements may not appear at a fixed value, but there are many possible forms of compounds. The proportions of the elements in different compound forms are different.
- the bases X and y are used to indicate any zinc-aluminum oxidation that satisfies the equilibrium of the compound.
- magnesium aluminum oxide may also be a composite oxide having a molar ratio of other elements such as Zn 2 A1 2 0 5 or the like, and the presence of the composite oxide may be confirmed by elemental analysis or X-ray diffraction spectrum.
- At least one of zirconia, titanium oxide and cerium oxide is further complicated, and they are all
- a high refractive index ceramic powder, in combination with a relatively low refractive index alumina, is advantageous for increasing its reflectivity.
- zirconia also has a toughening function, and the mechanical properties of the porous alumina ceramic layer can be improved by the zirconia.
- the proportion of oxides in the porous ceramic reflective layer is total mass
- the hetero-oxide further comprises at least one of cerium oxide, titanium oxide and cerium oxide, at least one of magnesium oxide or zinc oxide and at least one of zirconia, titanium oxide and cerium oxide.
- the mass ratio of the reflective layer is 1 ⁇ 3 ⁇ 4 ⁇ 10 ⁇ 3 ⁇ 4.
- 1% ⁇ 10 ⁇ 3 ⁇ 4 represents the mass fraction of the oxides in the preparation process, and there is no loss in the reaction, so in the final product, the mass fraction of 1% ⁇ 10 ⁇ 3 ⁇ 4 is Including oxides, including the mass fraction after Zn X A1 y O and/or Mg X A1 y O is converted into an oxide, which is the sum of the two.
- the proportion of the impurity oxide should not be too low, otherwise it will result in insufficient composite oxide production, and the effect of enhancing the combination of the porous ceramic reflective layer and the ceramic heat dissipation substrate is not achieved.
- the thermal conductivity of the cumbersome oxide is low and the coefficient of thermal expansion is deviated from the alumina, the excessively high temperature may cause the thermal conductivity to be low, and the co-firing stability with the YAG ceramic may be deteriorated.
- a relatively good amount of 1% to 10% of the total mass can be obtained, but the basic embodiment of the present invention is not limited to this mass ratio.
- the alumina porous ceramic layer and the luminescent ceramic layer are connected by sintering, and the slurry constituting the alumina porous ceramic layer and the slurry constituting the luminescent ceramic layer are successively coated on the heat dissipation substrate to form the luminescent ceramic layer and the alumina porous ceramic.
- the ceramic layers are firmly bonded together.
- the alumina porous ceramic layer and the luminescent ceramic layer may be separately formed and joined by an adhesive layer, and the adhesive layer may be a glass bonding layer or an organic bonding layer (such as silica gel, epoxy resin, etc.).
- the thickness of the porous ceramic reflective layer is 0.1 to 2 mm. If the porous ceramic reflective layer is too thin, the reflectance is lowered; if the porous ceramic reflective layer is too thick, the thermal resistance is too large, Conducive to heat dissipation.
- the third layer of the ceramic heat dissipation substrate functions to dissipate heat transferred from the reflective layer into the air or further divergence through other heat dissipating members.
- the ceramic heat dissipating substrate is made of an aluminum nitride ceramic substrate because the aluminum nitride ceramic has excellent thermal conductivity and good mechanical properties.
- the third layer uses an aluminum nitride ceramic substrate as the heat dissipation substrate, the surface thereof must have oxidized alumina, and the second layer of alumina porous ceramic is oxidized.
- the composite oxide reference may be made to the description in the above porous ceramic reflective layer, and the description thereof will not be repeated here.
- the ceramic heat sink substrate has a thickness of 0.5 to 5 mm. If the ceramic heat sink substrate is too thin, the strength is too low; if the ceramic heat sink substrate is too thick, it will be too heavy and the substrate cost is too high.
- the surface of the luminescent ceramic layer is coated with an anti-reflection film, specifically, a high-refractive-index film, a low-refractive-index film, and an anti-reflection film for alternately improving the incident light transmission. Excess rate and improved light extraction efficiency.
- the surface of the luminescent ceramic layer has a rough microstructure, and specifically, a sawtooth structure is etched on the surface of the luminescent ceramic layer to further improve the excitation efficiency and the light extraction efficiency.
- a method for preparing a luminescent ceramic structure comprising: casting a casting slurry respectively for forming a porous ceramic reflective layer and a luminescent ceramic layer on a ceramic heat dissipation substrate, and then sequentially The luminescent ceramic structure is formed by lamination and sintering.
- a luminescent ceramic layer is prepared by Ce miscellaneous YAG (YAG:Ce), and a porous ceramic reflective layer is prepared by dissolving zinc oxide and/or magnesium oxide of alumina to aluminum nitride. Ceramic (thermal conductivity exceeding 80W/mK) is used as a ceramic heat sink substrate.
- YAG casting slurry and porous alumina casting slurry are prepared.
- the porous alumina casting slurry is cast on the ceramic heat dissipation substrate, and the casting tape is dried to obtain a green sheet; the YAG casting slurry is continuously cast on the porous alumina green sheet to form a ceramic heat dissipation substrate.
- the YAG ceramic has a high thermal conductivity (14 W/m/K at 20 ° C, 10.5 W/m/K at 100 ° C) and a high melting point of YAG (1970 ° C), It can greatly improve the heat dissipation efficiency and thermal destruction temperature of the phosphor package, and meet the use of high-power blue LEDs, especially blue lasers.
- the reflective layer is made of a porous alumina ceramic co-fired with the YAG ceramic layer, which can ensure better reflectivity, and its thermal conductivity is higher than that of the glass ceramic, and the interfacial heat of the co-firing method. The resistance is lower.
- a luminescent ceramic structure in which a reflective ceramic and a luminescent ceramic are co-fired is formed on a ceramic heat-dissipating substrate by a casting method, and various shapes such as a square or a ring can be realized, and since the casting thickness can be controlled, light can be realized.
- the process provided by the present invention is compared to the process of separately fabricating the luminescent ceramic layer, followed by cutting, thinning, polishing, plating the reflective layer, and soldering the reflective layer onto the thermally conductive substrate. It can be sintered at one time, and the process is simpler, and the fabrication of a large-diameter luminescent ceramic structure can be realized. Therefore, it is a low-cost and high-efficiency mass production preparation method.
- Embodiments of the present invention further provide a light emitting device comprising the luminescent ceramic structure of the embodiment of the present invention, further comprising an excitation light source for generating excitation light, wherein the luminescent ceramic structure is located on the optical path of the excitation light.
- the luminescent ceramic layer is for absorbing excitation light to generate a laser beam
- the porous ceramic reflective layer is for scattering and reflecting the laser light or the mixed light of the laser light and the unabsorbed excitation light
- the ceramic heat dissipation substrate is used for conducting the reflection layer. The heat is emitted.
- the illuminating device can be applied to general lighting, such as various luminaires, searchlights, stage lights, car headlights, and can also be applied to display systems such as projectors, televisions, and the like.
- the illuminating device has the advantages of energy saving (electroluminescence source is LD), high brightness, and long life.
- Embodiments of the present invention further provide a projection system including the illumination device of the embodiment of the present invention, further comprising a projection imaging device.
- the projection system adopts the above-mentioned illuminating device, the maximum brightness of the emitted light is significantly improved, and the small projection of the home, the projection of the living room, the projection of the project, and the projection of the cinema can be competent. Moreover, the increase in brightness also contributes to the improvement of the contrast of the projector.
- the luminescent ceramic structure of the present embodiment includes: a luminescent ceramic layer 110, a porous ceramic reflective layer 120, and a ceramic heat dissipation substrate 130 laminated in series; wherein the luminescent ceramic layer 110 includes a fluorescent crystal grain 111 And the scattering medium 112, the porous ceramic reflective layer 120 comprises an alumina porous ceramic 122, which is miscible with zinc oxide 121; and the ceramic heat dissipation substrate 130 is an aluminum nitride ceramic substrate.
- the luminescent ceramic structure of the embodiment is prepared by a casting method, and specifically includes the following steps:
- alumina ball Tetraethyl orthosilicate
- PVB polyvinyl butyral
- BBP benzyl butyrate
- P EG polyethylene glycol
- the binder and plasticizer may be added directly and mixed with the slurry, or previously dissolved in a solvent and then added to the slurry.
- porous alumina casting slurry First, the synthetic raw material alumina, the miscellaneous zinc oxide, and the pore forming agent are mixed and added to the ethanol solvent, and the pore forming agent may be starch, or PMMA microspheres ( Polymethyl methacrylate), then milled with a ball of alumina ball for a while.
- the ball mill slurry is mixed with a polymeric binder such as, but not limited to, polyvinyl butyral (PVB), a plasticizer such as, but not limited to, benzyl butyrate. (BBP), polyethylene glycol (PEG).
- the binder and plasticizer may be added directly and mixed with the slurry, or previously dissolved in a solvent and then added to the slurry.
- a porous alumina casting slurry having a suitable viscosity was cast on an aluminum nitride ceramic substrate with a doctor blade having an adjustable gap. The thickness of the cast strip is adjusted by the wiper gap, slurry viscosity and casting rate.
- the casting belt is dried under an air or oxygen atmosphere, and the substrate may or may not be heated during the process. After evaporating the solvent and the pore former from the casting belt, green sheets of different thicknesses are obtained.
- a doctor blade having an adjustable gap to form a porous alumina stacked on the heat conductive substrate And YAG raw layer.
- the green sheet is heated in air to decompose organic components such as a binder and a plasticizer. After removal of the binder, the green sheet is in a vacuum, H 2 /N 2 , 11 2 and/or ⁇ 3"/11 2 atmosphere, at 1200 ° C to 1900 ° C, preferably 1500 ° C to 1800 ° C More preferably, it is sintered in a temperature range of 1600 ° C to 1700 ° C for 1 hour to 100 hours, preferably 2 to 10 hours.
- the binder removal and sintering process can be carried out independently or together. In the formation of defects such as vacancies, laminated green sheets sintered under a reducing atmosphere usually have a brown or dark brown color during sintering. It is usually necessary to perform reoxidation under air or oxygen atmosphere so that the ceramic sheets are in the visible wavelength range. It has high luminous efficiency inside.
- the basic composition of the luminescent ceramic structure of the present embodiment is the same as that of the first embodiment, and the only difference is that: the aluminum oxide porous ceramic is cumbersome with magnesium oxide instead of zinc oxide.
- the basic composition of the luminescent ceramic structure of the present embodiment is the same as that of the first embodiment, and the only difference is that: the aluminum oxide porous ceramic is cumbersome with magnesium oxide and zinc oxide.
- ZnAl 2 0 4 and MgAl 2 0 4 are formed between the porous ceramic reflective layer 120 and the ceramic heat dissipation substrate 130.
- the basic composition of the luminescent ceramic structure of the present embodiment is the same as that of the first embodiment, and the only difference is that: in the porous ceramic reflective layer 120, the zirconia and the zirconia are further complicated on the basis of the zinc oxide and/or magnesium oxide. Yttrium oxide.
- the basic composition of the luminescent ceramic structure of this embodiment is the same as that of the first embodiment, and the only difference is that: the luminescent ceramic layer 110 is plated with a high refractive index film, and the low refractive index film is alternately multilayered. AR coating 14 0, used to further increase the blue light transmittance and improve the light extraction efficiency.
- the basic composition of the luminescent ceramic structure of the present embodiment is the same as that of the first embodiment, except that a sawtooth structure 150 is etched on the luminescent ceramic layer 110 to further improve light extraction efficiency.
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Abstract
一种发光陶瓷结构及其制备方法、相关发光装置和投影装置。发光陶瓷结构,包括依次层叠结合在一起的发光陶瓷层(110)、多孔陶瓷反射层(120)和氮化铝陶瓷散热基板(130);其中多孔陶瓷反射层(120)为掺杂氧化锌和/或氧化镁(121)的氧化铝多孔陶瓷(122),掺杂的氧化锌和/或氧化镁(121)用于与陶瓷散热基板(130)结合,并且掺杂的氧化锌和/或氧化镁(121)至少部分以Zn xAl yO和/或Mg xAl yO的形式存在,以增强与氮化铝陶瓷基板(130)的粘接力。本发明的发光陶瓷结构具有导热率高、粘接力强、可靠性高的特点,可以作为相关发光装置和投影装置的光学器件。
Description
发光陶瓷结构及其制备方法、 相关发光装置和投影装置
技术领域
[0001] 本发明涉及照明和显示技术领域, 特别涉及一种发光陶瓷结构及其制备方法、 相关发光装置和投影装置。
背景技术
[0002] 利用激光或者 LED等光源激发荧光粉以获得预定单色光或者多色光, 是一种广 泛应用于照明光源、 投影显示等领域的技术方案。 这种技术方案往往是利用激 光或者 LED出射光入射到高速旋转的荧光粉色轮上, 以实现良好的散热。
技术问题
[0003] 目前荧光粉的封装方式主要为有机硅胶封装和无机玻璃封装两种, 这两种封装 方式的热导率均较低 (lW/(m.K)以下) , 且抗热破坏温度不高, 硅胶的耐受温 度一般在 200°C以下, 玻璃的耐受温度一般在 500°C以下。
[0004] 为了解决热导率及耐热性问题, 本领域技术人员进一步幵发了陶瓷结构的荧光 发光结构。 现有技术中, TW201023405A公幵了一种发光结构, 包括发光陶瓷层 和多孔陶瓷反射层, 其中多孔陶瓷反射层为多孔 YAG反射层, 该技术方案利用 了陶瓷结构的耐热性和优良的机械性能, 较上述有机硅胶封装和无机玻璃封装 的技术方案有很大的进步。 然而该技术方案产生于 LED照明吋期, LED发出的激 发光的光强远不及现如今激光, 在激光的照射下, 发光陶瓷层发出大量的热, 多孔陶瓷反射层自身的多孔结构使得热量难以传递出去, 需要在其背面设置散 热基板以改善散热。
[0005] 现有技术中, 多孔陶瓷反射层的组成材料通常与散热基板的组成材料不同, 导 致两者难以通过共同烧结的方式增强结合力。
问题的解决方案
技术解决方案
[0006] 为解决现有技术中存在的技术问题, 本发明提供了一种发光陶瓷结构, 具有导 热率高、 粘接力强、 可靠性高的特点。
[0007] 根据本发明的第一方面, 本发明提供一种发光陶瓷结构, 包括依次层叠结合在 一起的发光陶瓷层、 多孔陶瓷反射层和陶瓷散热基板; 其中上述多孔陶瓷反射 层为惨杂氧化锌和 /或氧化镁的氧化铝多孔陶瓷, 惨杂的氧化锌和 /或氧化镁用于 与陶瓷散热基板结合; 并且惨杂的氧化锌的至少部分以 Zn xAl yO的形式存在, 以 及惨杂的氧化镁的至少部分以 Mg XA1 yO的形式存在; 上述陶瓷散热基板为氮化 铝陶瓷基板。
[0008] 进一步地, 上述 Zn xAl yO具体是 ZnAl 20 4, Mg XA1 yO具体是 MgAl 20 4。
[0009] 进一步地, 上述多孔陶瓷反射层还惨杂氧化锆、 氧化钛和氧化钇中的至少一种
[0010] 进一步地, 上述多孔陶瓷反射层中惨杂的氧化物比例是总质量的 1%~10<¾。
[0011] 进一步地, 上述发光陶瓷层是 Ce惨杂 YAG陶瓷。
[0012] 进一步地, 上述发光陶瓷层的厚度为 0.05~lmm, 上述多孔陶瓷反射层的厚度 为 0.1~2mm, 上述陶瓷散热基板的厚度为 0.5~5mm。
[0013] 进一步地, 上述发光陶瓷层表面镀有增透膜, 或发光陶瓷层表面有粗糙微结构
[0014] 根据本发明的第二方面, 本发明提供一种如第一方面的发光陶瓷结构的制备方 法, 包括: 将分别用于形成多孔陶瓷反射层和发光陶瓷层的流延浆料先后浇注 在陶瓷散热基板上, 然后依次经过层压和烧结形成上述发光陶瓷结构。
[0015] 根据本发明的第三方面, 本发明提供一种发光装置, 包括第一方面的发光陶瓷 结构, 还包括用于产生激发光的激发光源, 上述发光陶瓷结构位于上述激发光 的光路上。
[0016] 根据本发明的第四方面, 本发明提供一种投影系统, 包括第三方面的发光装置 , 还包括投影成像装置。
发明的有益效果
有益效果
[0017] 本发明提供的发光陶瓷结构, 一方面, 利用氧化铝多孔陶瓷作为反射层的同吋 , 也作为粘接层将发光陶瓷层和陶瓷散热基板粘接起来, 实现更高效率的同吋 , 可靠性更高。 另一方面, 由于氧化铝反射陶瓷层是非致密的多孔结构, 此结
构能够在厚度较薄的情况下, 仍能够保证有较高的反射率, 并且这种非致密的 多孔结构能够实现热膨胀系数不一致的氧化铝陶瓷与氮化铝陶瓷的粘接。 更重 要的是, 在氧化铝多孔陶瓷中添加氧化锌和 /或氧化镁, 与氮化铝陶瓷基板表层 的微量氧化铝层发生化学反应生成 Zn XA1 yO和 /或 Mg XA1 yO, 进一步增强与氮化 铝陶瓷基板的粘接力。
[0018]
对附图的简要说明
附图说明
[0019] 图 1为本发明的发光陶瓷结构的一个实施例的结构示意图;
[0020] 图 2为本发明的发光陶瓷结构的另一个实施例的结构示意图;
[0021] 图 3为本发明的发光陶瓷结构的又一个实施例的结构示意图。
本发明的实施方式
[0022] 下面通过具体实施方式结合附图对本发明作进一步详细说明。
[0023] 在本发明中, 发光陶瓷结构包括依次层叠结合在一起的发光陶瓷层 (第一层) 、 多孔陶瓷反射层 (第二层) 和陶瓷散热基板 (第三层) , 其中多孔陶瓷反射 层为氧化铝多孔陶瓷, 陶瓷散热基板为氮化铝陶瓷基板。 本发明的技术方案, 为提高多孔陶瓷反射层与氮化铝陶瓷基板的结合力, 在氧化铝多孔陶瓷层中惨 杂了氧化物。 由于氮化铝陶瓷基板的表面容易产生薄薄的一层氧化铝, 惨杂在 氧化铝多孔陶瓷层中的氧化物可以与氮化铝表面的氧化铝层发生反应, 生成一 种复合产物, 从而利用该复合产物提高多孔陶瓷反射层与陶瓷散热基板的结合 。 由于多孔陶瓷反射层为氧化铝多孔陶瓷, 其本身的氧化铝难以与氮化铝或者 氮化铝表面的氧化铝发生任何反应, 因此本发明利用额外惨杂的氧化物参与反 应, 成为多孔陶瓷反射层与陶瓷散热基板的连结桥梁, 这是本发明的主要发明 构思。
[0024] 以下对本发明发光陶瓷结构的各个层进行逐一描述。
[0025] <发光陶瓷层 >
[0026] 在本发明实施方式中, 第一层发光陶瓷层的作用在于接收激发光的照射, 并将
激发光转换为波长不同的受激光。 这里的激发光可以为固态光源发出的光, 如 L ED光、 激光二极管光、 激光器光, 也可以为其他任何本发明申请前公幵的光源 光。 由于发光陶瓷层为陶瓷结构, 其热稳定性及导热性能远远优于以玻璃或硅 胶为基质的荧光粉层 (即将荧光粉封装在连续的玻璃或硅胶中) , 能够承受大 功率激发光的照射, 可以适用于高亮度激光荧光照明 /显示领域。
[0027] 发光陶瓷层可以是纯相的荧光陶瓷, 具体可以是各种氧化物陶瓷、 氮化物陶瓷 或氮氧化物陶瓷, 通过在陶瓷制备过程中惨入微量的激活剂元素 (如镧系元素 ) , 形成发光中心。 由于一般激活剂元素的惨杂量较小 (一般小于 1%) , 该类 荧光陶瓷通常是透明或半透明发光陶瓷, 激发光容易直接穿过该发光陶瓷层后 出射, 因此该发光陶瓷层的发光效率不高, 更适于较低功率的激发光应用场景 。 在本发明的一个实施方式中, 发光陶瓷层是 Ce惨杂 YAG陶瓷; 在本发明的另 一个实施方式中, 发光陶瓷层为 Ce惨杂 LuAG陶瓷。
[0028] 发光陶瓷层还可以是复合陶瓷层, 其以透明 /半透明陶瓷作为基质, 在陶瓷基 质内分布着发光陶瓷颗粒 (如荧光粉颗粒) 。 透明 /半透明陶瓷基质可以是各种 氧化物陶瓷 (如氧化铝陶瓷、 Y 3A1 50 12陶瓷) 、 氮化物陶瓷 (如氮化铝陶瓷) 或氮氧化物陶瓷, 陶瓷基质的作用在于对光和热进行传导, 使得激发光能够入 射到发光陶瓷颗粒上, 并使受激光能够从发光陶瓷层中出射; 发光陶瓷颗粒承 担发光陶瓷层的主要发光功能, 用于吸收激发光并将其转换为受激光。 发光陶 瓷颗粒的晶粒粒径较大, 而且激活剂元素的惨杂量较大 (如 1~5%) , 使得其发 光效率高; 而且发光陶瓷颗粒分散于陶瓷基质中, 避免了位于发光陶瓷层较深 位置的发光陶瓷颗粒无法被激发光照射到的情况, 还避免了纯相荧光陶瓷整体 惨杂量较大而导致的激活剂元素浓度中毒的情况, 从而提高了发光陶瓷层的发 光效率。
[0029] 进一步的, 上述发光陶瓷层中还可以增加散射颗粒, 使散射颗粒分布于陶瓷基 质中。 散射颗粒的作用在于增强激发光在发光陶瓷层内的散射, 从而增大激发 光在发光陶瓷层内的光程, 使得激发光的光利用率大大提高, 提高了发光陶瓷 层的光转换效率。 散射颗粒可以是散射粒子, 如氧化铝, 氧化钇, 氧化锆, 氧 化镧, 氧化钛, 氧化锌, 硫酸钡等, 既可以是单一材料的散射颗粒, 也可以是
两种或两种以上的组合, 其特点为表观白色, 能够对可见光进行散射, 而且材 料稳定, 能够承受高温, 粒径与激发光波长处于同一数量级或低一个数量级。 在另外一些实施方式中, 散射颗粒还可以替换为同尺寸的气孔, 利用气孔与陶 瓷基质的折射率差实现全反射从而对激发光或受激光进行散射。
[0030] 发光陶瓷层还可以是另外一种复合陶瓷层, 该复合陶瓷层与上述复合陶瓷层的 区别仅在于陶瓷基质不同。 在本实施方式中, 陶瓷基质是纯相的荧光陶瓷, 即 陶瓷基质本身具有激活剂, 能够在激发光的照射下发出受激光。 该技术方案综 合了上述复合陶瓷层的发光陶瓷颗粒具有高发光效率的优势以及上述纯相的荧 光陶瓷具有发光性能的优势, 同吋利用发光陶瓷颗粒与陶瓷基质进行发光, 进 一步提高了发光陶瓷层的发光效率, 而且该陶瓷基质虽然具有一定的激活剂惨 杂量, 但是惨杂量较低, 能够保证该陶瓷基质具有足够的透光性。 在该发光陶 瓷层中, 同样可以增加散射颗粒或气孔增强发光陶瓷层的内部散射。
[0031] 发光陶瓷颗粒典型但非限定性的选择是镧系元素惨杂的石榴石发光陶瓷, 如 Ca 3(Al,Sc) 2Si 30 12, 也可以是铝酸盐, 如 (Gd,Tb,Y,Lu) 3(Al,Ga) 50 12以及复合组分 的¥ ^§ 2 1 20 12等, 其中括号里用逗号隔幵的元素如 (Al,Ga) 是指 A1与 Ga的 比例可以任意选择, 但是该两元素总量在化学式中相当于 1, 例如 A 7Ga。.3、 A1
。 在本发明的一个实施方式中, 优选 Ce惨杂 YAG石榴石, 即 (Υ ,— xCe J 3Al 50 12 。 在本发明的另一个实施方式中, 发光陶瓷颗粒为 Ce惨杂 LuAG石榴石结构。
[0032] 在本发明的一个实施方式中, 发光陶瓷层的厚度为 0.05~ lmm, 如果发光陶瓷 层过薄, 效率下降; 如果发光陶瓷层过厚, 热阻太大, 不利于散热。
[0033] <多孔陶瓷反射层>
[0034] 在本发明实施例中, 第二层多孔陶瓷反射层用于对受激光或者受激光与未被吸 收的激发光的混合光进行散射反射。 多孔陶瓷反射层具体为氧化铝多孔陶瓷, 其反射原理是利用孔隙与氧化铝的折射率差, 使入射光在氧化铝与孔隙的界面 发生全反射而实现反射效果。 氧化铝的折射率一般为 1.7左右, 而孔隙可认为其 内为空气, 折射率为 1左右, 当光从氧化铝内部入射到氧化铝与空气的界面吋, 入射角较小的情况下即可发生全反射。 通过控制气孔的大小 (如通过在制备过
程中添加造孔剂或控制升温速率等) 以及控制多孔陶瓷反射层的厚度即可控制 多孔陶瓷反射层的反射率。 本发明的氧化铝多孔陶瓷耐高温、 抗氧化, 适于大 功率发光的发光陶瓷结构, 而且气孔较容易分布均匀, 有利于反射层各处的反 射率均匀。 一种现有技术中的金属反射层易氧化、 硫化, 尤其在高温环境中寿 命短; 另外一种现有技术中利用玻璃等粘接剂将白色散射颗粒粘结成层, 该技 术方案的缺陷在于, 在制备过程中, 粘接剂是粘稠的, 而白色散射颗粒粒径较 小, 容易团聚, 难以将其均匀分散, 由于该反射层的反射功能材料为白色散射 颗粒, 不能分散均匀将导致反射率不均匀。
[0035] 在本发明实施方式中, 氧化铝多孔陶瓷层中额外惨杂了氧化物, 部分该氧化物 可以与氧化铝在高温下发生反应, 生成新的复合氧化物, 该复合氧化物的形式 为M xAl yO, 其中 M为惨杂的氧化物的元素。 本发明的一个实施方式中, 典型特 点是: 惨杂有氧化锌和氧化镁中至少一种。 在惨杂有氧化锌的情况下, 氧化锌 至少部分以 Zn xAl y
0的形式存在, 在惨杂有氧化镁的情况下, 氧化镁至少部分以 Mg xAl yO的形式存 在。 惨杂的氧化物在制备过程中以与氧化铝多孔陶瓷层的原料混合的方式惨入 , 在烧结过程中, 惨杂的氧化物部分地与氧化铝反应。 氧化铝多孔陶瓷层是在 陶瓷散热基板上直接烧制的, 而陶瓷散热基板是预先准备好的氮化铝陶瓷基板 , 该氮化铝陶瓷基板的表面通常会受到氧化而产生一层氧化铝薄膜, 当烧制氧 化铝多孔陶瓷层吋, 原料中的惨杂氧化物 (即如上述的氧化镁或氧化锌) 极易 与氮化铝陶瓷基板表面的氧化铝薄膜反应, 生成复合氧化物, 该复合氧化物使 得氧化铝多孔陶瓷层与氮化铝陶瓷散热基板更加紧密的结合在一起, 从而提高 了产品的可靠性。
[0036] 在本发明的一些实施例中, Zn xAl yO具体是 ZnAl 20 4, Mg XA1 yO具体是 MgAl 2
0 4, 该类复合氧化物为尖晶石结构, 结构稳定, 利于多孔陶瓷层与陶瓷散热层 的结合。 可以通过检测氧化铝多孔陶瓷层与氮化铝陶瓷散热基板的结合部, 进 行成分分析表征来确认该物质的存在。 MgAl 20 4
的 X射线衍射谱的衍射峰卡片是 PDF#21-1152, ZnAl 20 4的 射线衍射谱的衍射 峰卡片是 PDF#05-0669。
[0037] 当然, 值得说明的是, 本发明的 Zn xAl yO和 Mg xAl yO中, Zn与 A1或 Mg与 A1的 元素比例没有特别限定, 并且在实际的发光陶瓷结构产品中, 元素比例可能并 不是以一个固定的值出现, 而是有多种可能的化合物形式, 不同化合物形式中 元素比例有差异, 采用底标 X和 y意在表示满足化合物的价位平衡的任何锌铝氧 化物或镁铝氧化物。 例如, 复合氧化物也可能是其他元素摩尔比的复合氧化物 如 Zn 2A1 20 5等, 同样可以通过元素分析或 X射线衍射谱确认该复合氧化物存在
[0038] 在本发明的另一实施方式中, 除了惨杂有氧化锌和氧化镁中至少一种以外, 还 进一步惨杂有氧化锆、 氧化钛和氧化钇中的至少一种, 它们都是高折射率的陶 瓷粉末, 与相对低折射率的氧化铝配合有利于提高其反射率。 此外, 氧化锆还 具有增韧的功能, 通过惨杂氧化锆能够提高氧化铝多孔陶瓷层的机械性能。
[0039] 在本发明的实施方式中, 多孔陶瓷反射层中惨杂的氧化物比例是总质量的
1%~10%。 即, 当惨杂的氧化物只有氧化镁或氧化锌的至少一种吋, 该氧化镁或 氧化锌的至少一种的总质量占多孔陶瓷反射层的比例为 1%~10<¾; 当惨杂的氧化 物进一步包括氧化锆、 氧化钛和氧化钇中的至少一种吋, 氧化镁或氧化锌的至 少一种与氧化锆、 氧化钛和氧化钇中的至少一种的总质量占多孔陶瓷反射层的 质量比例为 1<¾~10<¾。 值得说明的是, 1%~10<¾所表示的是制备过程中惨杂的氧 化物的质量分数, 在反应中没有损失, 因此在最终的产品中, 1%~10<¾的质量分 数既包括氧化物, 又包括 Zn XA1 yO和 /或 Mg XA1 yO折合成氧化物之后的质量分数 , 为两者之和。
[0040] 惨杂氧化物的比例不宜过低, 否则将导致没有足够的复合氧化物产生, 达不到 增强多孔陶瓷反射层与陶瓷散热基板结合的作用。 此外, 由于惨杂的氧化物的 热导率偏低, 且热膨胀系数与氧化铝有偏差, 过高的惨杂会造成热导率偏低, 与 YAG陶瓷的共烧稳定性会变差。 而相当于总质量的 1%~10%的惨杂量能取得较 好的效果, 但本发明的基本实施方式不限于此质量比例。
[0041] 氧化铝多孔陶瓷层与发光陶瓷层通过烧结连接, 构成氧化铝多孔陶瓷层的浆料 与构成发光陶瓷层的浆料先后涂覆在散热基板上, 构成发光陶瓷层、 氧化铝多 孔陶瓷层和散热基板的层叠式三层结构, 通过烧结使氧化铝多孔陶瓷层与发光
陶瓷层牢固地结合在一起。 此外, 氧化铝多孔陶瓷层与发光陶瓷层还可以各自 成型后通过粘接层连接, 粘接层可以为玻璃粘接层、 有机粘接层 (如硅胶、 环 氧树脂等) 。
[0042] 在本发明的一个搜实施方式中, 多孔陶瓷反射层的厚度为 0.1~2mm, 如果多孔 陶瓷反射层过薄, 反射率降低; 如果多孔陶瓷反射层过厚, 热阻太大, 不利于 散热。
[0043] <陶瓷散热基板 >
[0044] 在本发明实施例中, 第三层陶瓷散热基板的作用在于将反射层传导过来的热量 散发到空气中或进一步通过其他散热件发散。 陶瓷散热基板选用氮化铝陶瓷基 板, 是由于氮化铝陶瓷具有优良的导热性能, 而且其机械性能也较好。
[0045] 本发明的发光陶瓷结构, 由于第三层采用氮化铝陶瓷基板作为散热基板, 其表 面必然有被氧化后的氧化铝, 而在第二层的氧化铝多孔陶瓷中惨杂有氧化锌和 氧化镁中至少一种, 这样在第二层与第三层的界面处会形成 Zn XA1 yO和 Mg XA1 y O中至少一种, 用于结合第二层和第三层, 从而提高了两层之间的结合力。 关于 该复合氧化物的描述, 可以参照上述多孔陶瓷反射层中的描述, 此处不再赘述
[0046] 在本发明的一个实施例中, 陶瓷散热基板的厚度为 0.5~5mm。 如果陶瓷散热基 板过薄, 则强度太低; 如果陶瓷散热基板过厚, 会过重且基板成本过高。
[0047] 在本发明的其它实施例中, 发光陶瓷层表面镀有增透膜, 具体可以是镀高折射 率膜、 低折射率膜多层交替的增透膜, 用来进一步提高入射光透过率以及提高 出光效率。 或者发光陶瓷层表面有粗糙微结构, 具体可以是在发光陶瓷层表面 刻蚀出锯齿状结构, 用来进一步提高激发效率和出光效率。
[0048] 在本发明的实施例中还提供了发光陶瓷结构的制备方法, 包括: 将分别用于形 成多孔陶瓷反射层和发光陶瓷层的流延浆料先后浇注在陶瓷散热基板上, 然后 依次经过层压和烧结形成发光陶瓷结构。
[0049] 在本发明的一个实施例中, 以 Ce惨杂 YAG (YAG:Ce) 制备发光陶瓷层, 以惨 杂氧化锌和 /或氧化镁的氧化铝制备多孔陶瓷反射层, 以氮化铝陶瓷 (热导率超 过 80W/mK) 作为陶瓷散热基板。 首先, 准备 YAG流延浆料和多孔氧化铝流延浆
料; 然后, 将多孔氧化铝流延浆料浇注在陶瓷散热基板上, 干燥浇注带以获得 生片材; 继续将 YAG流延浆料浇注在多孔氧化铝生片材上, 形成陶瓷散热基板 上堆叠多孔氧化铝和 YAG生片层; 最后, 通过层压和烧结得到发光陶瓷结构成
P
ΡΠ °
[0050] 在上述实施例中, 由于 YAG陶瓷热导率较高 (20°C为 14W/m/K, 100°C为 10.5 W/m/K) 且 YAG熔点很高 (1970°C) , 可以大大提高荧光粉封装散热效率和抗 热破坏温度, 满足大功率蓝光 LED尤其是蓝光激光的使用。
[0051] 在上述实施例中, 反射层采用与 YAG陶瓷层共烧的多孔氧化铝陶瓷, 能够保证 较好的反射率, 其热导率也较玻璃陶瓷更高, 且共烧的方式界面热阻更低。 另 夕卜, 采用流延法在陶瓷散热基板上制作反射陶瓷和发光陶瓷共烧的发光陶瓷结 构, 能够实现各种形状, 如方形或圆环, 且由于流延厚度可以控制, 因而能够 实现发光层和反射层厚度可控的结构, 因而相比于单独制作发光陶瓷层, 然后 进行切割、 减薄、 抛光、 镀反射层、 焊接反射层到导热基板上的制作方式, 本 发明提供的工艺, 能够一次烧结成型, 且工艺更简单, 且能够实现大直径发光 陶瓷结构的制作。 因此是一种低成本高效率的量产制备方式。
[0052] 本发明实施例进一步提供一种发光装置, 包括本发明实施例的发光陶瓷结构, 还包括用于产生激发光的激发光源, 发光陶瓷结构位于激发光的光路上。 发光 陶瓷层用于吸收激发光以产生受激光, 多孔陶瓷反射层用于对该受激光或者受 激光与未被吸收的激发光的混合光进行散射反射, 陶瓷散热基板用于将反射层 传导过来的热量散发。 该发光装置可以应用到一般的照明上, 如各种灯具一 路灯、 探照灯、 舞台灯、 汽车大灯, 也可以应用到显示系统上, 如投影机、 电 视机等。 该发光装置的优势在于, 节能 (电致发光光源为 LD) 、 高亮度、 长寿 命。
[0053] 本发明实施例进一步提供一种投影系统, 包括本发明实施例的发光装置, 还包 括投影成像装置。 该投影系统采用了上述发光装置后, 出射光的最大亮度有了 明显提高, 小至家庭微型投影、 客厅投影, 大至工程投影、 影院投影, 都可以 胜任。 而且亮度的提高也有利于投影机对比度的提高。
[0054] 以下通过具体实施例详细说明本发明的技术方案, 应当理解, 这些实施例仅是
示例性的, 不能理解为对本发明保护范围的限制。
[0055] 实施例一
[0056] 如图 1所示, 本实施例的发光陶瓷结构包括: 依次层叠结合在一起的发光陶瓷 层 110、 多孔陶瓷反射层 120和陶瓷散热基板 130; 其中发光陶瓷层 110包括荧光 晶粒 111和散射介质 112, 多孔陶瓷反射层 120包括氧化铝多孔陶瓷 122, 惨杂有 氧化锌 121 ; 陶瓷散热基板 130为氮化铝陶瓷基板。 在制备发光陶瓷结构的过程 中, 由于氮化铝陶瓷基板的表面必然有被氧化后的氧化铝, 而在多孔陶瓷反射 层 120中惨杂有氧化锌, 这样会形成 Zn xAl yO, 从而提高了多孔陶瓷反射层 120和 陶瓷散热基板 130之间的结合力。
[0057] 本实施例的发光陶瓷结构采用流延法制备, 具体可以包括如下步骤:
[0058] 1.
YAG流延浆料的制备: 首先将合成原料氧化钇、 氧化铝、 氧化铈和助熔剂 TEOS
(正硅酸乙酯) 混合加入乙醇溶剂中, 然后用氧化铝球球磨一段吋间。 将该球 磨浆料与聚合物粘结剂及增塑剂混合, 聚合物粘结剂诸如但不限于聚乙烯醇缩 丁醛 (PVB) , 增塑剂诸如但不限于邻苯二甲酸苄丁酯 (BBP) 、 聚乙二醇 (P EG) 。 粘结剂和增塑剂可直接加入并与浆料混合, 或预先在溶剂中溶解然后加 入浆料中。
[0059] 2.多孔氧化铝流延浆料的制备: 首先将合成原料氧化铝、 惨杂的氧化锌, 以及 造孔剂混合加入乙醇溶剂中, 造孔剂可以是淀粉, 或 PMMA微球 (聚甲基丙烯 酸甲酯) , 然后用氧化铝球球磨一段吋间。 将该球磨浆料与聚合物粘结剂及增 塑剂混合, 聚合物粘结剂诸如但不限于聚乙烯醇缩丁醛 (PVB) , 增塑剂诸如但 不限于邻苯二甲酸苄丁酯 (BBP) 、 聚乙二醇 (PEG) 。 粘结剂和增塑剂可直接 加入并与浆料混合, 或预先在溶剂中溶解然后加入浆料中。
[0060] 3.浇注: 具有适当粘度的多孔氧化铝流延浆料用具有可调间隙的刮片浇注在氮 化铝陶瓷基板上。 通过刮片间隙、 浆料粘度和浇注速率调整浇注带的厚度。 在 空气或氧气气氛下, 干燥该浇注带, 过程中可加热或不加热基体。 从浇注带蒸 发掉溶剂和造孔剂之后, 获得不同厚度的生片材。 继续将 YAG流延浆料用具有 可调间隙的刮片浇注在多孔氧化铝生片材上, 形成导热基板上堆叠多孔氧化铝
和 YAG生片层。
[0061] 4.层压: 浇注带的堆叠被置于由诸如不锈钢的金属制成的金属模具之间, 加热 浇注带堆叠至粘结剂的 Tg温度 (玻璃化温度) 之上, 然后进行单轴压紧, 之后 释放压力。 该过程中, 生片材上的图案诸如孔、 柱或粗糙表面通过在层压中使 用具有设计图案的模具形成在生片材上。 这种图案可提高光耦合, 以及通过波 导效应减少侧向光传播, 从而促进光输出方向上的光萃取。
[0062] 5.烧结: 在空气中加热生片材以分解有机组分, 如粘结剂、 增塑剂。 脱除粘结 剂之后, 生片材在真空、 H 2/N 2、 11 2和/或八3"/11 2气氛中, 在 1200°C至 1900°C, 优选 1500°C至 1800°C, 更优选 1600°C至 1700°C的温度范围内烧结, 并持续 1小吋 至 100小吋, 优选 2至 10小吋。 脱除粘结剂和烧结工序可独立进行或一起进行。 由于氧空位等缺陷的形成, 还原性气氛下烧结的层压生片材在烧结期间通常颜 色呈褐色或深褐色。 通常有必要在空气或氧气气氛下进行再氧化, 以便使陶瓷 片材在可见光波长范围内具有较高发光效率。
[0063] 实施例二
[0064] 本实施例的发光陶瓷结构的基本组成与实施例一相同, 唯一不同点在于: 氧化 铝多孔陶瓷中惨杂有氧化镁, 代替氧化锌。
[0065] 实施例三
[0066] 本实施例的发光陶瓷结构的基本组成与实施例一相同, 唯一不同点在于: 氧化 铝多孔陶瓷中惨杂有氧化镁和氧化锌。
[0067] 经分析, 本实施例在多孔陶瓷反射层 120和陶瓷散热基板 130之间有 ZnAl 20 4 和 MgAl 20 4生成。
[0068] 实施例四
[0069] 本实施例的发光陶瓷结构的基本组成与实施例一相同, 唯一不同点在于: 多孔 陶瓷反射层 120中, 在惨杂氧化锌和 /或氧化镁的基础上进一步惨杂氧化锆和氧化 钇。
[0070] 实施例五
[0071] 如图 2所示, 本实施例的发光陶瓷结构的基本组成与实施例一相同, 唯一不同 点在于: 在发光陶瓷层 110上镀有高折射率膜、 低折射率膜多层交替的增透膜 14
0, 用以进一步提高蓝光透过率和提高出光效率。
[0072] 实施例六
[0073] 如图 3所示, 本实施例的发光陶瓷结构的基本组成与实施例一相同, 唯一不同 点在于: 在发光陶瓷层 110上刻蚀出锯齿状结构 150, 用以进一步提高出光效率
[0074] 以上内容是结合具体的实施方式对本发明所作的进一步详细说明, 不能认定本 发明的具体实施只局限于这些说明。 对于本发明所属技术领域的普通技术人员 来说, 在不脱离本发明构思的前提下, 还可以做出若干简单推演或替换, 都应 当视为属于本发明的保护范围。
Claims
权利要求书
一种发光陶瓷结构, 其特征在于, 包括依次层叠结合在一起的发光陶 瓷层、 多孔陶瓷反射层和陶瓷散热基板; 其中所述多孔陶瓷反射层为 惨杂氧化锌和 /或氧化镁的氧化铝多孔陶瓷, 惨杂的氧化锌和 /或氧化 镁用于与所述陶瓷散热基板结合; 并且惨杂的氧化锌的至少部分以 Z n XA1 y0的形式存在, 以及惨杂的氧化镁的至少部分以 Mg XA1 y0的形 式存在; 所述陶瓷散热基板为氮化铝陶瓷基板。
根据权利要求 1所述的发光陶瓷结构, 其特征在于, 所述 Zn xAl yO具 体是 ZnAl 20 4, Mg XA1 y0具体是 MgAl 20 4。
根据权利要求 1所述的发光陶瓷结构, 其特征在于, 所述多孔陶瓷反 射层还惨杂氧化锆、 氧化钛和氧化钇中的至少一种。
根据权利要求 1所述的发光陶瓷结构, 其特征在于, 所述多孔陶瓷反 射层中惨杂的氧化物比例是总质量的 1 %~ 10%。
根据权利要求 1所述的发光陶瓷结构, 其特征在于, 所述发光陶瓷层 是 Ce惨杂 YAG陶瓷。
根据权利要求 1-5任一项所述的发光陶瓷结构, 其特征在于, 所述发 光陶瓷层的厚度为 0.05~lmm, 所述多孔陶瓷反射层的厚度为 0.1~2m m, 所述陶瓷散热基板的厚度为 0.5~5mm。
根据权利要求 1所述的发光陶瓷结构, 其特征在于, 所述发光陶瓷层 表面镀有增透膜, 或所述发光陶瓷层表面有粗糙微结构。
一种如权利要求 1-7任一项所述的发光陶瓷结构的制备方法, 其特征 在于, 所述方法包括: 将分别用于形成多孔陶瓷反射层和发光陶瓷层 的流延浆料先后浇注在陶瓷散热基板上, 然后依次经过层压和烧结形 成所述发光陶瓷结构。
一种发光装置, 其特征在于, 包括权利要求 1-7任一项所述的发光陶 瓷结构, 还包括用于产生激发光的激发光源, 所述发光陶瓷结构位于 所述激发光的光路上。
一种投影系统, 其特征在于, 包括权利要求 9中所述的发光装置, 还
包括投影成像装置。
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CN111393151A (zh) * | 2020-03-26 | 2020-07-10 | 郑州中瓷科技有限公司 | 一种掺杂氧化锆的氧化铝陶瓷基板及其制备工艺 |
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Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN203489180U (zh) * | 2013-10-15 | 2014-03-19 | 深圳市光峰光电技术有限公司 | 波长转换装置及其光源系统、投影系统 |
US20140239196A1 (en) * | 2013-02-28 | 2014-08-28 | Konica Minolta, Inc. | Deposition substrate and scintillator panel |
CN104100933A (zh) * | 2013-04-04 | 2014-10-15 | 深圳市绎立锐光科技开发有限公司 | 一种波长转换装置及其制作方法、相关发光装置 |
CN104595852A (zh) * | 2013-10-30 | 2015-05-06 | 深圳市绎立锐光科技开发有限公司 | 一种波长转换装置、漫反射层、光源系统及投影系统 |
CN105322433A (zh) * | 2014-05-28 | 2016-02-10 | 深圳市绎立锐光科技开发有限公司 | 波长转换装置及其相关发光装置 |
WO2016091107A1 (zh) * | 2014-12-11 | 2016-06-16 | 深圳市光峰光电技术有限公司 | 漫反射材料、漫反射层、波长转换装置以及光源系统 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4847954B2 (ja) * | 2005-03-29 | 2011-12-28 | 京セラ株式会社 | 反射部材、これを用いた発光装置および照明装置 |
US7514721B2 (en) * | 2005-11-29 | 2009-04-07 | Koninklijke Philips Electronics N.V. | Luminescent ceramic element for a light emitting device |
JP2008153075A (ja) * | 2006-12-18 | 2008-07-03 | Sharp Corp | 表示装置用照明装置、表示装置 |
WO2009074919A1 (en) * | 2007-12-11 | 2009-06-18 | Koninklijke Philips Electronics N.V. | Side emitting device with hybrid top reflector |
JP6394144B2 (ja) * | 2013-11-08 | 2018-09-26 | 日本電気硝子株式会社 | プロジェクター用蛍光ホイール及びプロジェクター用発光デバイス |
CN105278225B (zh) * | 2014-07-21 | 2018-05-15 | 深圳市光峰光电技术有限公司 | 波长转换装置及其制备方法、相关发光装置和投影装置 |
CN107209302A (zh) * | 2015-02-03 | 2017-09-26 | 日本电气硝子株式会社 | 波长转换部件及使用其的发光装置 |
-
2016
- 2016-11-25 CN CN201611053227.8A patent/CN108105604B/zh active Active
-
2017
- 2017-11-03 WO PCT/CN2017/109330 patent/WO2018095211A1/zh active Application Filing
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20140239196A1 (en) * | 2013-02-28 | 2014-08-28 | Konica Minolta, Inc. | Deposition substrate and scintillator panel |
CN104100933A (zh) * | 2013-04-04 | 2014-10-15 | 深圳市绎立锐光科技开发有限公司 | 一种波长转换装置及其制作方法、相关发光装置 |
CN203489180U (zh) * | 2013-10-15 | 2014-03-19 | 深圳市光峰光电技术有限公司 | 波长转换装置及其光源系统、投影系统 |
CN104595852A (zh) * | 2013-10-30 | 2015-05-06 | 深圳市绎立锐光科技开发有限公司 | 一种波长转换装置、漫反射层、光源系统及投影系统 |
CN105322433A (zh) * | 2014-05-28 | 2016-02-10 | 深圳市绎立锐光科技开发有限公司 | 波长转换装置及其相关发光装置 |
WO2016091107A1 (zh) * | 2014-12-11 | 2016-06-16 | 深圳市光峰光电技术有限公司 | 漫反射材料、漫反射层、波长转换装置以及光源系统 |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP4015483A4 (en) * | 2019-11-26 | 2023-09-20 | Shenzhen Lighting Institute | FLUORESCENT CERAMIC AND PREPARATION METHOD THEREFOR, LUMINESCENT DEVICE AND PROJECTION DEVICE |
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