WO2020085049A1 - 表面被覆蛍光体粒子、複合体および発光装置 - Google Patents
表面被覆蛍光体粒子、複合体および発光装置 Download PDFInfo
- Publication number
- WO2020085049A1 WO2020085049A1 PCT/JP2019/039348 JP2019039348W WO2020085049A1 WO 2020085049 A1 WO2020085049 A1 WO 2020085049A1 JP 2019039348 W JP2019039348 W JP 2019039348W WO 2020085049 A1 WO2020085049 A1 WO 2020085049A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- phosphor particles
- phosphor
- electrical conductivity
- coating layer
- coated
- Prior art date
Links
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 title claims abstract description 203
- 239000002245 particle Substances 0.000 title claims abstract description 149
- 239000002131 composite material Substances 0.000 title claims description 11
- 239000011247 coating layer Substances 0.000 claims abstract description 47
- 229910000000 metal hydroxide Inorganic materials 0.000 claims abstract description 43
- 150000004692 metal hydroxides Chemical class 0.000 claims abstract description 43
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 30
- 229910044991 metal oxide Inorganic materials 0.000 claims abstract description 21
- 150000004706 metal oxides Chemical class 0.000 claims abstract description 21
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 6
- 150000004767 nitrides Chemical class 0.000 claims abstract description 6
- 229910052727 yttrium Inorganic materials 0.000 claims abstract description 5
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 4
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims abstract description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910052735 hafnium Inorganic materials 0.000 claims abstract description 4
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 4
- 239000010936 titanium Substances 0.000 claims abstract description 4
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910052726 zirconium Inorganic materials 0.000 claims abstract description 4
- 238000003809 water extraction Methods 0.000 claims description 19
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims description 17
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 7
- 230000005284 excitation Effects 0.000 claims description 6
- 238000004364 calculation method Methods 0.000 claims description 5
- 239000003566 sealing material Substances 0.000 claims description 5
- 238000000034 method Methods 0.000 abstract description 13
- 239000000203 mixture Substances 0.000 abstract description 3
- 239000008367 deionised water Substances 0.000 abstract 3
- 229910021641 deionized water Inorganic materials 0.000 abstract 3
- 238000000605 extraction Methods 0.000 abstract 3
- 239000002002 slurry Substances 0.000 description 32
- 238000004519 manufacturing process Methods 0.000 description 29
- 239000000843 powder Substances 0.000 description 25
- 239000000126 substance Substances 0.000 description 20
- 238000003756 stirring Methods 0.000 description 19
- 238000010438 heat treatment Methods 0.000 description 17
- 230000000052 comparative effect Effects 0.000 description 10
- 238000002360 preparation method Methods 0.000 description 10
- 239000011248 coating agent Substances 0.000 description 9
- 238000000576 coating method Methods 0.000 description 9
- 239000002253 acid Substances 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 238000001914 filtration Methods 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 238000001878 scanning electron micrograph Methods 0.000 description 6
- 239000013078 crystal Substances 0.000 description 5
- 150000002500 ions Chemical class 0.000 description 5
- 238000004381 surface treatment Methods 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000008393 encapsulating agent Substances 0.000 description 4
- 238000010979 pH adjustment Methods 0.000 description 4
- 239000002243 precursor Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 229910052581 Si3N4 Inorganic materials 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000004833 X-ray photoelectron spectroscopy Methods 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000010828 elution Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000004065 semiconductor Substances 0.000 description 3
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 3
- 229910052582 BN Inorganic materials 0.000 description 2
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical compound N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 2
- 229910052693 Europium Inorganic materials 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- 238000010306 acid treatment Methods 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 150000004645 aluminates Chemical class 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 229910001940 europium oxide Inorganic materials 0.000 description 2
- AEBZCFFCDTZXHP-UHFFFAOYSA-N europium(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Eu+3].[Eu+3] AEBZCFFCDTZXHP-UHFFFAOYSA-N 0.000 description 2
- 230000004907 flux Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000011812 mixed powder Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- 102100032047 Alsin Human genes 0.000 description 1
- 101710187109 Alsin Proteins 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910052684 Cerium Inorganic materials 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- 230000004931 aggregating effect Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004993 emission spectroscopy Methods 0.000 description 1
- OGPBJKLSAFTDLK-UHFFFAOYSA-N europium atom Chemical compound [Eu] OGPBJKLSAFTDLK-UHFFFAOYSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000017525 heat dissipation Effects 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 229910052747 lanthanoid Inorganic materials 0.000 description 1
- 150000002602 lanthanoids Chemical class 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 238000000634 powder X-ray diffraction Methods 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000000967 suction filtration Methods 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/02—Use of particular materials as binders, particle coatings or suspension media therefor
- C09K11/025—Use of particular materials as binders, particle coatings or suspension media therefor non-luminescent particle coatings or suspension media
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/08—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/08—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials
- C09K11/64—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing aluminium
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/08—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials
- C09K11/77—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals
- C09K11/7728—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals containing europium
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L33/00—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L33/48—Semiconductor devices having potential barriers specially adapted for light emission; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof characterised by the semiconductor body packages
- H01L33/50—Wavelength conversion elements
Definitions
- the present invention relates to surface-coated phosphor particles, a composite, and a light emitting device.
- a light-emitting device that combines a semiconductor light-emitting element such as an LED and a phosphor that absorbs a part of light from the semiconductor light-emitting element and converts the absorbed light into long-wavelength wavelength-converted light to emit light Is being promoted.
- a nitride phosphor or an oxynitride phosphor having a relatively stable crystal structure has been attracting attention.
- Patent Document 1 discloses that the surface of the ⁇ -sialon phosphor is coated with a metal hydroxide in order to improve the brightness of the ⁇ -sialon phosphor.
- Patent Document 2 discloses, as a conventional technique, coating the surface of phosphor particles with a glass material for the purpose of suppressing the hydrolysis of a phosphor containing a sulfide by reacting with moisture in the air. Then, after pointing out the effect of the coating on the dispersibility of the phosphor particles in the encapsulant, in order to improve the dispersibility of the phosphor in the encapsulant, the surface of the phosphor particles contains a metal oxide. Techniques for coating with coating material particles are disclosed.
- Patent Document 3 in order to improve the gas barrier property of the coating layer provided on the surface of the phosphor particle, the glass powder adhered to the surface of the phosphor particle is melted by heating, thereby the surface of the phosphor particle. It is disclosed that a continuous film is formed on.
- the inventors have examined the characteristics of a light emitting device in which a composite body in which a phosphor is sealed with a sealing material is incorporated with an LED, and as a result, they have found that the emission intensity slightly decreases with time.
- the water that moved through the encapsulant contacted the phosphor, and the metal component in the phosphor was ionized and eluted into the water, and the crystal of the phosphor gradually. It has been found that the change in the structure lowers the wavelength conversion efficiency of the phosphor, which in turn leads to a decrease in the emission intensity of the light emitting device.
- a composite provided with the above-mentioned surface-coated phosphor particles and an encapsulant for encapsulating the surface-coated phosphor particles.
- a light emitting device including a light emitting element that emits excitation light, and the above-mentioned composite body that converts the wavelength of the excitation light.
- 3 is an SEM image of the surface-coated phosphor particles of Example 1.
- 3 is an SEM image of the surface-coated phosphor particles of Example 2.
- 3 is an SEM image of phosphor particles of Comparative Example 1.
- the inventors of the present invention have extensively studied a technique for suppressing the elution of metal components constituting the phosphor particles as ions in water, and as a result, highly advanced the morphology of the coating layer formed on the surface of the phosphor particles. It is important to control, and in particular, the inventors have found that the material forming the coating layer is selected, and have completed the present invention.
- embodiments of the present invention will be described in detail.
- the surface-coated phosphor particles according to the embodiment include phosphor particles and a coating layer provided on the surface of the phosphor particles.
- phosphor particles and a coating layer provided on the surface of the phosphor particles.
- the phosphor particles are made of an oxynitride phosphor or a nitride phosphor.
- the oxynitride phosphor include an ⁇ -sialon phosphor containing Eu and a ⁇ -sialon phosphor containing Eu.
- nitride phosphors examples include Eu-containing CASN phosphors and Eu-containing SCASN phosphors.
- the Eu-containing CASN phosphor is, for example, a red phosphor that is represented by the formula CaAlSiN 3 : Eu 2+ , has Eu 2+ as an activator, and has a crystal of alkaline earth silicon nitride as a host.
- the definition of the Eu-containing CASN phosphor in the present specification excludes the Eu-containing SCASN phosphor.
- the SCASN phosphor containing Eu is, for example, a red phosphor represented by the formula (Sr, Ca) AlSiN 3 : Eu 2+ , having Eu 2+ as an activator, and a crystal composed of an alkaline earth silicon nitride as a matrix.
- the phosphor particles of the present embodiment are composed of the above-mentioned ⁇ -sialon phosphor containing Eu, ⁇ -sialon phosphor containing Eu, CASN phosphor containing Eu, or SCASN phosphor containing Eu. Is preferred.
- the particle size of the phosphor particles is not particularly limited, and is appropriately adjusted so as to obtain the dispersibility in the sealing material described below and the desired wavelength conversion efficiency.
- a coating layer composed of a metal hydroxide or a metal oxide containing one or more elements selected from the group consisting of aluminum, titanium, zirconium, yttrium and hafnium is provided on the surface of the phosphor particles. It is provided.
- the metal hydroxide or metal oxide is excellent in transparency and stability, and among them, aluminum hydroxide or aluminum oxide is preferable from the viewpoints of moisture barrier property, cost control property, coatability for phosphor particles, and the like. Used.
- the coating layer may be an aggregate formed by aggregating a plurality of particles of a metal hydroxide or a metal oxide, but is composed of a metal hydroxide or a metal oxide, phosphor particles
- a continuous coating layer that continuously coats is preferable.
- the continuous coating layer has a layered structure in which a metal hydroxide or a metal oxide is formed as a continuous film, and a plurality of particles as in the invention described in Patent Document 2 are densely aggregated. The structure is different from that of the formed aggregate.
- the continuous coating layer may have a concavo-convex structure in which a large number of non-penetrating recesses are formed.
- the surface coverage of the phosphor particles with the coating layer is preferably 50% or more, more preferably 70% or more. By setting the surface coverage by the coating layer as described above, the amount of the metal component of the phosphor particles eluted as ions can be further suppressed.
- the coating layer preferably covers the entire surface of the phosphor particles.
- the surface coverage of the coating layer can be evaluated by X-ray photoelectron spectroscopy (XPS) measurement. Specifically, focusing on Si, which is an element contained in the phosphor particles and not included in the metal hydroxide or the metal oxide forming the coating layer, XPS measurement shows that the Si on the phosphor particle surface Obtain the content (atm%: atomic percent).
- the content of Si in the phosphor particles without the metal hydroxide or the coating with the metal oxide, which is not subjected to the surface treatment described below, is A1, and the content of Si in the phosphor particles to be the target of the surface coverage calculation is When A2 is set, the surface coverage by the coating layer can be calculated by the following formula. Surface coverage (%) (A1-A2) / A1 ⁇ 100
- the lower limit of the thickness of the coating layer is preferably 0.01 ⁇ m or more, more preferably 0.1 ⁇ m or more.
- the upper limit of the thickness of the coating layer is preferably 10 ⁇ m or less, more preferably 5 ⁇ m or less.
- the surface-coated phosphor particles of the present embodiment have a hot water extraction electrical conductivity index ⁇ of 2.0 mS / m or less defined below.
- (Calculation method of hot water extraction electrical conductivity index) (1) The electrical conductivity ⁇ 0 of ion-exchanged water at 25 ° C. is measured. (2) Disperse 1 g of the surface-coated phosphor particles in 30 ml of the above ion-exchanged water using a dispersing device such as an ultrasonic disperser, put in a pressure vessel and heat at 150 ° C for 16 hours, and then add 20 ml of ion-exchanged water.
- the electrical conductivity ⁇ 1 is measured in a state of being cooled to 25 ° C. (3)
- Method for producing surface-coated phosphor particles As an example of a method for producing surface-coated phosphor particles provided with a coating layer composed of a metal oxide, (1) a step of forming a coating layer of a substance (such as particles) containing a metal hydroxide on the surface of the phosphor particles (2) The heat treatment is performed to change the metal hydroxide into a metal oxide and to convert the coating layer into a continuous coating layer to obtain surface-coated phosphor particles having a continuous coating layer containing a metal oxide. And a manufacturing method including the steps. In this manufacturing method, it is important to make the coating layer of particles containing a metal hydroxide a dense coating so that it can be converted into a continuous coating layer by heat treatment. As a method for producing such surface-coated phosphor particles, three examples of production method examples 1 to 3 will be described below.
- Manufacturing method example 1 has a slurry preparing step, a stirring step, a pH adjusting step, a stirring / washing / filtering step, a drying step and a heating step. Details of each step will be described below.
- Phosphor powder, ion-exchanged water, and a substance containing metal hydroxide are mixed in appropriate amounts to prepare a phosphor-containing slurry.
- the pH of the slurry obtained here is preferably within a range in which both the surface potential of the phosphor particles and the surface potential of the substance containing the metal hydroxide have positive values.
- Each surface potential of the substance containing the phosphor particles and the metal hydroxide can be measured by, for example, a zeta potential measuring device.
- aluminum hydroxide is used as the substance containing a metal hydroxide, it can be used in the form of aluminum hydroxide in a sol state (sometimes customarily called alumina sol) or an aqueous solution of aluminum hydroxide.
- the slurry obtained in the slurry preparation step is stirred using a stirring means such as a stirrer or a stirring device so that the substance containing the phosphor powder and the metal hydroxide is sufficiently dispersed.
- the pH of the obtained slurry is adjusted to 9 or more by dropping the alkaline agent at a predetermined dropping rate.
- the alkaline agent include alkaline aqueous solutions such as NH 3 aqueous solution and NaOH aqueous solution.
- the surface potential of the substance containing the metal hydroxide becomes positive and the surface potential of the phosphor particles becomes negative. As a result, the substance containing the metal hydroxide easily adheres to the surface of the phosphor particles densely.
- ⁇ -sialon phosphor particles are used as the phosphor particles and alumina sol is used as the substance containing metal hydroxide
- the surface potential of aluminum hydroxide becomes positive at pH 6.5 or higher.
- the surface potential of the ⁇ -sialon phosphor particles becomes negative.
- an electrostatic attractive force acts between the two, so that the substance containing aluminum hydroxide easily adheres to the surface of the ⁇ -sialon phosphor particles.
- the concentration of the alkaline aqueous solution, the dropping speed and the dropping time are adjusted to adjust the concentration of the substance containing the metal hydroxide attached to the surface of the phosphor particles.
- the thickness and surface coverage can be controlled.
- the slurry obtained by the pH adjusting step is stirred using a stirring means such as a stirrer so that the phosphor particles are sufficiently dispersed, and washed with a cleaning liquid such as ion-exchanged water. Then, the phosphor powder (phosphor particles coated with a substance containing a metal hydroxide) is taken out by a filtration means such as suction filtration.
- a stirring means such as a stirrer
- the layer containing the metal hydroxide that densely coats the surface of the phosphor particles is oxidized and converted into a metal oxide, and a continuous metal oxide is formed. It creates a continuous film-like morphology called the coating layer.
- the temperature for heating the phosphor powder is preferably 500 ° C. or higher and 1000 ° C. or lower, and particularly when alumina sol is used as the substance containing metal hydroxide, the heating temperature may be 500 ° C. or higher and 600 ° C. or lower. preferable.
- Manufacturing method example 2 has a slurry preparation step, a stirring step, a stirring / washing / filtering step, a drying step, and a heating step.
- the alkaline agent is added to adjust the pH after the stirring step, but in Manufacturing Method Example 2, the alkaline agent is added to adjust the pH in the slurry preparation step.
- the coating layer made of a substance containing a metal hydroxide can be made a more dense coating layer. It is also possible to adjust the rate at which the alkaline agent is added, which makes it possible to further improve the denseness of the coating. With such a dense coating layer, a continuous coating layer can be stably obtained by the subsequent heat treatment. On the other hand, if the pH is adjusted in the slurry preparation step as in Production Method Example 2, the production step can be shortened.
- Manufacturing method example 3 has a slurry preparing step, a stirring step, a pH adjusting step, a stirring / washing / filtering step, a drying step and a heating step. Details of each step will be described below.
- a substance containing a metal hydroxide is used as a starting material for the continuous coating layer, but in Production Method Example 3, a metal hydroxide is used as a starting material for the continuous coating layer. Precursors are used.
- a phosphor powder, ion-exchanged water, and a precursor of a metal hydroxide are mixed in appropriate amounts to prepare a phosphor-containing slurry.
- the metal hydroxide is aluminum hydroxide, Na aluminate is used as its precursor.
- the obtained slurry is usually strongly alkaline, and specifically, a pH of 12 or more is preferable, and a pH of 13 or more is more preferable.
- a metal hydroxide is deposited by adding an acid such as hydrochloric acid or sulfuric acid to this slurry. As a result, a phosphor-containing slurry containing the phosphor powder, ion-exchanged water, and metal hydroxide is obtained.
- the pH of the phosphor-containing slurry obtained here is within a range in which both the surface potential of the phosphor particles and the surface potential of the metal hydroxide have negative values, and specifically, pH 11 or higher is preferable, and pH 12 or higher. Is more preferable.
- the slurry obtained in the slurry preparation step is stirred using a stirring means such as a stirrer or a stirring device so that the phosphor powder and the metal hydroxide are sufficiently dispersed.
- the pH adjusting step the pH is adjusted to 9 or less by dropping an acid such as hydrochloric acid or sulfuric acid at a predetermined dropping rate into the obtained slurry.
- an acid such as hydrochloric acid or sulfuric acid
- one of the surface potentials of the metal hydroxide and the surface potential of the phosphor particles becomes positive and the other surface potential becomes negative, so that the phosphor becomes The metal hydroxide tends to be densely attached to the surface of the particles.
- ⁇ -sialon phosphor particles are used as phosphor particles and aluminum hydroxide is deposited from a slurry containing Na aluminate, the surface potential of aluminum hydroxide becomes positive at a pH of 10 or less.
- the surface potential of the ⁇ -sialon phosphor particles becomes negative. As a result, an electrostatic attractive force acts between the two, so that aluminum hydroxide easily adheres to the surface of the ⁇ -sialon phosphor particles.
- the pH adjusting step by adjusting the concentration of the acid dropped into the slurry, the dropping speed and the dropping time, the thickness and surface coverage of the metal hydroxide attached to the surface of the phosphor particles can be controlled. .
- the stirring step, the pH adjusting step, the stirring / washing / filtering step, the drying step, and the heating step are carried out in the same manner as in the manufacturing method example 1, so that the surface of the phosphor particles is made of a metal oxide.
- the surface-coated phosphor particles on which the continuous coating layer is formed are manufactured.
- the stirring step is performed, and the acid is further added to adjust the pH. .
- a slurry preparation step and a stirring step are carried out in parallel, and an acid is continuously added from the slurry preparation step to adjust the pH, whereby the surface potential of the metal hydroxide and the phosphor particles are increased.
- One of the surface potentials may be positive and the other surface potential may be negative.
- the hot water extraction electrical conductivity index can be controlled by appropriately selecting the type and amount of the metal oxide, the method of attaching the metal oxide to the surface of the phosphor particles, and the like. .
- the heating conditions for converting into a substance can be mentioned as factors for setting the above-mentioned hot water extraction electric conductivity index within a desired numerical range.
- a coating layer made of a metal oxide is formed on the surface of the phosphor particles so that the hot water extraction electric conductivity index ⁇ becomes 2.0 mS / m or less.
- FIG. 1 is a schematic cross-sectional view showing the structure of the light emitting device according to the embodiment.
- the light emitting device 10 includes a light emitting element 20, a heat sink 30, a case 40, a first lead frame 50, a second lead frame 60, a bonding wire 70, a bonding wire 72, and a composite body 80.
- the light emitting element 20 is mounted in a predetermined area on the upper surface of the heat sink 30. By mounting the light emitting element 20 on the heat sink 30, the heat dissipation of the light emitting element 20 can be improved.
- a package substrate may be used instead of the heat sink 30.
- the light emitting element 20 is a semiconductor element that emits excitation light.
- One electrode (not shown) disposed on the upper surface side of the light emitting element 20 is connected to the surface of the first lead frame 50 via a bonding wire 70 such as a gold wire.
- the other electrode (not shown) formed on the upper surface of the light emitting element 20 is connected to the surface of the second lead frame 60 via a bonding wire 72 such as a gold wire.
- the case 40 has a generally funnel-shaped recess whose hole diameter gradually increases from the bottom surface upward.
- the light emitting element 20 is provided on the bottom surface of the recess.
- the wall surface of the recess surrounding the light emitting element 20 serves as a reflection plate.
- the composite 80 is filled in the above-mentioned concave portion whose wall surface is formed by the case 40.
- the composite 80 is a wavelength conversion member that lengthens the wavelength of the excitation light emitted from the light emitting element 20.
- the composite of the present embodiment is used as the composite 80, and the surface-coated phosphor particles 82 of the present embodiment are dispersed in a sealing material 84 such as a resin.
- the light emitting device 10 emits a mixed color of the light of the light emitting element 20 and the light generated from the surface-coated phosphor particles 82 that are excited by absorbing the light of the light emitting element 20. It is preferable that the light emitting device 10 emits white light by mixing the light of the light emitting element 20 and the light generated from the surface-coated phosphor particles 82.
- the surface-coated phosphor particles 82 having a hot water extraction electric conductivity index ⁇ of 2.0 mS / m or less fluorescence is generated in the sealing material 84 due to moisture. Ions can be prevented from eluting from the body particles, and by suppressing the emission intensity of the light emitting device 10 from decreasing, the reliability of the light emitting device 10 can be improved.
- FIG. 1 a surface mount type LED is illustrated as the light emitting device according to the embodiment, but the light emitting device according to the embodiment may be a cannonball type LED.
- Example 1 The phosphor particles ( ⁇ -sialon phosphor powder) of Production Example 1 were surface-treated by the following procedure.
- FIG. 2 is an SEM image of the surface-coated phosphor particles of Example 1. As shown in FIG. 2, it was confirmed that the continuous coating layer was formed by continuously coating aluminum oxide without scattering aluminum oxide on the surface of the phosphor particles.
- Example 2 Regarding the phosphor particles of Production Example 1, 4.74 g of AERODISP W 630 (manufactured by Evonik Resource Efficiency GmbH) was added in place of the alumina sol of (1) in the above surface treatment, and the pH of the obtained slurry was 5.0.
- the surface-coated phosphor particles of Example 2 were subjected to the same surface treatment as in Example 1 except that When the surface potential of aluminum hydroxide and the surface potential of the phosphor particles at pH 5.0 were measured using a zeta potential measuring device, the surface potential of aluminum hydroxide was 42 mV and the surface potential of the phosphor particles was 11 mV. It was The surface-coated phosphor particles of Example 2 were observed using SEM.
- FIG. 3 is an SEM image of the surface-coated phosphor particles of Example 1. As shown in FIG. 3, it was confirmed that the continuous coating layer was formed by continuously coating aluminum oxide without scattering aluminum oxide on the surface of the phosphor particles.
- Comparative Example 1 Regarding the phosphor particles of Production Example 1, those not subjected to the above-mentioned surface treatment were set as Comparative Example 1.
- the phosphor particles of Comparative Example 1 were observed using SEM.
- FIG. 4 is an SEM image of the phosphor particles of Comparative Example 1. As shown in FIG. 4, all the surfaces of the phosphor particles of Comparative Example 1 are exposed.
- the electrical conductivity ⁇ 1 was measured in a state of being cooled to 25 ° C. (3)
- the phosphor particles were cured at 120 ° C., and then post-cured at 110 ° C. for 10 hours to perform sealing.
- the LED used had an emission peak wavelength of 448 nm and a chip size of 1.0 mm ⁇ 0.5 mm.
- the acceptance condition of the reliability test is that the reliability coefficient M is 95% or more. This is a value that cannot be achieved without using highly reliable phosphor particles. It was confirmed that the LED packages equipped with the surface-coated phosphor particles of Example 1 and Example 2 satisfied the above-mentioned passing conditions. This result indicates that in the surface-coated phosphor particles of Example 1 and Example 2, the coating layer formed on the surface of the phosphor particles suppressed the elution of the metal component forming the phosphor particles into water. It is speculated that
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Manufacturing & Machinery (AREA)
- Computer Hardware Design (AREA)
- Power Engineering (AREA)
- Luminescent Compositions (AREA)
- Led Device Packages (AREA)
Abstract
Description
特許文献2には、硫化物を含む蛍光体が空気中の水分と反応して加水分解することを抑制する目的で蛍光体粒子の表面をガラス材料でコーティングすることを従来技術として挙げている。そして、蛍光体粒子の封止材への分散性に被膜が与える影響を指摘した上で、蛍光体の封止材への分散性を向上させるべく、蛍光体粒子の表面を金属酸化物を含むコーティング材料粒子で被覆する手法が開示されている。
特許文献3には、蛍光体粒子の表面に設けられた被覆層のガスバリア性を向上させるために、蛍光体粒子の表面に付着させたガラス粉を加熱により溶融することにより、蛍光体粒子の表面に連続な皮膜を形成することが開示されている。
(熱水抽出電気伝導指数の算出方法)
(1)25℃のイオン交換水の電気伝導率Ω0を測定する。
(2)前記イオン交換水30mlに前記表面被覆蛍光体粒子1gを分散させ、耐圧容器に入れて150℃で16時間加熱した後、イオン交換水20mlを追加し25℃に冷却した状態で電気伝導率Ω1を測定する。
(3)電気伝導率Ω1と電気伝導率Ω0との差分ΔΩ(=電気伝導率Ω1-電気伝導率Ω0)を熱水抽出電気伝導指数ΔΩとする。
実施形態に係る表面被覆蛍光体粒子は、蛍光体粒子と、当該蛍光体粒子の表面に設けられた被覆層とを備える。以下、本実施形態の表面被覆蛍光体粒子の各構成について説明する。
酸窒化物蛍光体として、Euを含有するα型サイアロン蛍光体、Euを含有するβ型サイアロン蛍光体などが挙げられる。
本実施形態では、上記蛍光体粒子の表面に、アルミニウム、チタン、ジルコニウム、イットリウムおよびハフニウムよりなる群より選ばれる1種以上の元素を含む金属水酸化物または金属酸化物により構成される被覆層が設けられている。当該金属水酸化物または金属酸化物は、透明性や安定性に優れており、この中でも、水分遮断性、コスト抑制性、蛍光体粒子に対する被覆性などの点から水酸化アルミニウムまたは酸化アルミニウムが好ましく用いられる。
当該被覆層は、金属水酸化物または金属酸化物からなる複数の粒子が凝集して形成される集合体であってもよいが、金属水酸化物または金属酸化物により構成され、蛍光体粒子を連続的に被覆する連続被覆層であることが好ましい。ここで、連続被覆層は、金属水酸化物または金属酸化物が連続膜となって形成される層状の構造であり、特許文献2に記載の発明のような複数の粒子が密に凝集して形成される集合体とは異なる構造である。連続被覆層は、未貫通凹部が多数形成された凹凸構造を有してもよい。
表面被覆率(%)=(A1-A2)/A1×100
本実施形態の表面被覆蛍光体粒子は、以下に定義される熱水抽出電気伝導指数ΔΩが2.0mS/m以下である。
(熱水抽出電気伝導指数の算出方法)
(1)25℃のイオン交換水の電気伝導率Ω0を測定する。
(2)上記イオン交換水30mlに表面被覆蛍光体粒子1gを超音波分散機などの分散装置を用いて分散させ、耐圧容器に入れて150℃で16時間加熱した後、イオン交換水20mlを追加し、25℃に冷却した状態で電気伝導率Ω1を測定する。
(3)電気伝導率Ω1と電気伝導率Ω0との差分ΔΩ(=電気伝導率Ω1-電気伝導率Ω0)を熱水抽出電気伝導指数ΔΩとする。
上記熱水抽出電気伝導指数は、値が小さいほど、蛍光体粒子から水へ溶出した金属イオンの量が少ないことを示す指標となる。
金属酸化物で構成される被覆層を備える表面被覆蛍光体粒子の製造方法の一例として、(1)蛍光体粒子表面に金属水酸化物を含む物質(粒子など)による被覆層を形成する工程と、(2)加熱処理を施すことにより、金属水酸化物を金属酸化物に変化させるとともに被覆層を連続被覆層に変換し、金属酸化物を含む連続被覆層を備える表面被覆蛍光体粒子を得る工程と、を含む製造方法が挙げられる。この製造方法においては加熱処理によって連続被覆層に変換できるように、金属水酸化物を含む粒子による被覆層を緻密な被覆とすることが重要となる。
このような表面被覆蛍光体粒子の製造方法として、以下、製造方法例1乃至3の3例を挙げて説明する。
製造方法例1は、スラリー調製工程、攪拌工程、pH調整工程、撹拌・洗浄・濾過工程、乾燥工程および加熱工程を有する。各工程の詳細を以下に説明する。
蛍光体粉末、イオン交換水、および金属水酸化物を含む物質をそれぞれ適量混合し、蛍光体含有スラリーを調製する。ここで得られるスラリーのpHは、蛍光体粒子の表面電位と金属水酸化物を含む物質の表面電位が共に正の値をとる範囲内とすることが好ましい。蛍光体粒子および金属水酸化物を含む物質の各表面電位は、たとえば、ゼータ電位測定装置により測定することができる。なお、金属水酸化物を含む物質として水酸化アルミニウムを用いる場合には、ゾル状態の水酸化アルミニウム(慣習的にアルミナゾルと呼ばれる場合がある)や水酸化アルミニウム水溶液の形態で使用することができる。
スラリー調製工程で得られたスラリーを、スターラーなどの攪拌手段や攪拌装置を用いて、蛍光体粉末および金属水酸化物を含む物質が十分に分散するように攪拌する。
pH調整工程では、得られたスラリーにアルカリ剤を所定の滴下速度で滴下することにより、pHが9以上になるように調整される。アルカリ剤としては、NH3水溶液、NaOH水溶液などのアルカリ性水溶液が挙げられる。アルカリ剤の添加によりpH値が増加する過程で、金属水酸化物を含む物質の表面電位が正となり、蛍光体粒子の表面電位が負となる。このことにより、蛍光体粒子の表面に金属水酸化物を含む物質が緻密に付着しやすくなる。
具体的には、蛍光体粒子としてβ型サイアロン蛍光体粒子を用い、金属水酸化物を含む物質としてアルミナゾルを用いた場合には、pHが6.5以上で水酸化アルミニウムの表面電位が正となり、β型サイアロン蛍光体粒子の表面電位が負となる。このことにより、両者の間に静電引力が働くため、β型サイアロン蛍光体粒子の表面に水酸化アルミニウムを含む物質が密に付着しやすくなる。
上記pH調整工程により得られたスラリーを、スターラーなどの攪拌手段を用いて蛍光体粒子が十分に分散するように攪拌し、イオン交換水などの洗浄液を用いて洗浄する。その後、吸引濾過などの濾過手段により、蛍光体粉末(金属水酸化物を含む物質で被覆された蛍光体粒子)を取り出す。
得られた蛍光体粉末が十分に乾燥するように所定時間の加熱処理を実行し、表面が金属水酸化物を含む物質で密に被覆された複数の蛍光体粒子からなる蛍光体粉末を得る。
得られた蛍光体粉末に加熱処理を施すことにより、蛍光体粒子の表面を密に被覆する金属水酸化物を含む層を酸化して金属酸化物に変えるとともに、金属酸化物で構成される連続被覆層という連続的な膜状の形態を作り出す。蛍光体粉末を加熱する際の温度は、500℃以上1000℃以下が好ましく、特に、金属水酸化物を含む物質としてアルミナゾルを用いる場合には、加熱温度を500℃以上600℃以下とすることが好ましい。以上の工程により、蛍光体粒子の表面に金属酸化物で構成される連続被覆層が形成された表面被覆蛍光体粒子が製造される。
製造方法例2は、スラリー調製工程、攪拌工程、撹拌・洗浄・濾過工程、乾燥工程および加熱工程を有する。製造方法例1では、攪拌工程の後にアルカリ剤を添加してpHを調整したが、製造方法例2では、スラリー調製工程においてアルカリ剤を添加してpHを調整する。
一方、製造方法例2のように、スラリー調製工程においてpHを調整すれば、製造工程の短縮化を図ることができる。
製造方法例3は、スラリー調製工程、攪拌工程、pH調整工程、撹拌・洗浄・濾過工程、乾燥工程および加熱工程を有する。各工程の詳細を以下に説明する。
製造方法例1および製造方法例2では、連続被覆層の出発原料として金属水酸化物を含む物質が用いられているが、製造方法例3では、連続被覆層の出発原料として、金属水酸化物の前駆物質が用いられる。
本例では、蛍光体粉末、イオン交換水、および金属水酸化物の前駆物質をそれぞれ適量にて混合し、蛍光体含有スラリーを調製する。金属水酸化物が水酸化アルミニウムである場合には、その前駆物質としてアルミン酸Naが用いられる。得られるスラリーは、通常は強アルカリ性であり、具体的には、pH12以上が好ましく、pH13以上がより好ましい。このスラリーに、塩酸、硫酸などの酸を添加することにより、金属水酸化物を析出させる。これにより、蛍光体粉末、イオン交換水、および金属水酸化物を含む蛍光体含有スラリーが得られる。ここで得られる蛍光体含有スラリーのpHは、蛍光体粒子の表面電位と金属水酸化物の表面電位が共に負の値をとる範囲内であり、具体的には、pH11以上が好ましく、pH12以上がより好ましい。
スラリー調製工程で得られたスラリーを、スターラーなどの攪拌手段や攪拌装置を用いて、蛍光体粉末および金属水酸化物が十分に分散するように攪拌する。
pH調整工程では、得られたスラリーに塩酸、硫酸などの酸を所定の滴下速度で滴下することにより、pHが9以下になるように調整される。酸の添加によりpH値が低下する過程で、金属水酸化物の表面電位および蛍光体粒子の表面電位のうち、一方の表面電位が正となり、他方の表面電位が負となることにより、蛍光体粒子の表面に金属水酸化物が緻密に付着しやすくなる。
具体的には、蛍光体粒子としてβ型サイアロン蛍光体粒子を用い、アルミン酸Naを含むスラリーから水酸化アルミニウムを析出させた場合には、pHが10以下で水酸化アルミニウムの表面電位が正となり、β型サイアロン蛍光体粒子の表面電位が負となる。このことにより、両者の間に静電引力が働くため、β型サイアロン蛍光体粒子の表面に水酸化アルミニウムが密に付着しやすくなる。
なお、pH調整工程において、スラリーに滴下する酸の濃度、滴下速度や滴下時間を調節することにより、蛍光体粒子の表面に付着する金属水酸化物の厚さや表面被覆率を制御することができる。
なお、製造方法例3では、スラリー調製工程(前駆物質から金属水酸化物を析出させる工程)での酸の添加の後、攪拌工程を実施し、さらに酸を添加してpHを調整している。これとは別の方法として、スラリー調製工程と攪拌工程を並行して行い、スラリー調製工程から連続的に酸を添加してpHを調整することにより、金属水酸化物の表面電位および蛍光体粒子の表面電位のうち、一方の表面電位を正とし、他方の表面電位を負としてもよい。
図1は、実施形態に係る発光装置の構造を示す概略断面図である。図1に示すように、発光装置10は、発光素子20、ヒートシンク30、ケース40、第1リードフレーム50、第2リードフレーム60、ボンディングワイヤ70、ボンディングワイヤ72および複合体80を備える。
たとえば、図1では、実施形態に係る発光装置として表面実装型のLEDが例示されているが、実施形態に係る発光装置は砲弾型のLEDとしてもよい。
宇部興産社製α型窒化ケイ素粉末(SN-E10グレード、酸素含有量1.0質量%)95.43質量%、トクヤマ社製窒化アルミニウム粉末(Fグレード、酸素含有量0.8質量%)3.04質量%、大明化学社製酸化アルミニウム粉末(TM-DARグレード)0.74質量%、信越化学工業社製酸化ユーロピウム粉末(RUグレード)0.79質量%をV型混合機(筒井理化学器械社製S-3)を用い混合し、さらに目開き250μmの篩を全通させ凝集を取り除き、原料混合粉末を得た。ここでの配合比(質量%)は、β型サイアロンの一般式:Si6-zAlzOzN8-zにおいて、酸化ユーロピウムを除いて、Si/Al比から算出してz=0.25となるように設計したものである。
製造例1の蛍光体粒子(β型サイアロン蛍光体粉末)に以下の手順により表面処理を実施した。
(1)製造例1の蛍光体粒子10g、イオン交換水150ml、アルミナゾル(アルミナゾル520-A、日産化学社製)7.11gを混合し、スラリーを調製した。得られたスラリーのpHは4.1であった。pH4.1における、水酸化アルミニウムの表面電位および蛍光体粒子の表面電位をそれぞれゼータ電位測定装置を用いて測定したところ、水酸化アルミニウムの表面電位が44mV、蛍光体粒子の表面電位が16mVであった。
(2)スターラーを用いて、上記スラリーを15分間攪拌した。
(3)上記スラリーに0.05重量%アンモニア水を徐々に滴下し、滴下時間3分後にpHが9になるように調整した。pHが9における、水酸化アルミニウムの表面電位および蛍光体粒子の表面電位をそれぞれゼータ電位測定装置を用いて測定したところ、水酸化アルミニウムの表面電位が13mV、蛍光体粒子の表面電位が-25mVであった。
(4)スターラーを用いて、上記スラリーを60分間攪拌し、イオン交換水を用いて洗浄した後、吸引濾過を行い、蛍光体粉末を得た。
(5)得られた蛍光体粉末を105℃で15時間乾燥した。
(6)乾燥処理後の蛍光体粉末に、電気炉を用いて600℃、1時間の加熱処理を施し、実施例1の表面被覆蛍光体粒子を得た。
実施例1の表面被覆蛍光体粒子について、走査型電子顕微鏡(SEM)を用いて観察を行った。図2は、実施例1の表面被覆蛍光体粒子のSEM像である。図2に示すように、蛍光体粒子の表面に酸化アルミニウムが点在することなく、酸化アルミニウムが連続的に被覆することにより連続被覆層が形成されていることが確認された。
製造例1の蛍光体粒子について、上記表面処理のうち(1)のアルミナゾルの代わりにAERODISP W 630(Evonik Resource Efficiency GmbH社製)4.74gを添加し、得られたスラリーのpHが5.0になったことを除いて、実施例1と同様な表面処理を実施したものを実施例2の表面被覆蛍光体粒子とした。pH5.0における、水酸化アルミニウムの表面電位および蛍光体粒子の表面電位をそれぞれゼータ電位測定装置を用いて測定したところ、水酸化アルミニウムの表面電位が42mV、蛍光体粒子の表面電位が11mVであった。
実施例2の表面被覆蛍光体粒子について、SEMを用いて観察を行った。図3は、実施例1の表面被覆蛍光体粒子のSEM像である。図3に示すように、蛍光体粒子の表面に酸化アルミニウムが点在することなく、酸化アルミニウムが連続的に被覆することにより連続被覆層が形成されていることが確認された。
製造例1の蛍光体粒子について、上記表面処理を実施しないものを比較例1とした。比較例1の蛍光体粒子について、SEMを用いて観察を行った。図4は、比較例1の蛍光体粒子のSEM像である。図4に示すように、比較例1の蛍光体粒子は表面が全て露出している。
各実施例の表面被覆蛍光体粒子および比較例1の蛍光体粒子の熱水抽出電気伝導指数を以下の要領で算出した。熱水抽出電気伝導指数について得られた結果を表2に示す。
(1)25℃のイオン交換水の電気伝導率Ω0を測定した。
(2)上記イオン交換水30mlに表面被覆蛍光体粒子(または蛍光体粒子)1gを超音波分散機により分散させ、耐圧容器に入れて150℃で16時間加熱した後、イオン交換水20mlを追加し25℃に冷却した状態で電気伝導率Ω1を測定した。
(3)電気伝導率Ω1と電気伝導率Ω0との差分ΔΩ(=電気伝導率Ω1-電気伝導率Ω0)を熱水抽出電気伝導指数ΔΩとした。
各実施例の表面被覆蛍光体粒子および比較例1の蛍光体粒子を搭載したLEDパッケージの信頼性試験を以下の要領で評価した。信頼性試験によって得られた結果を表2に示す。
LEDパッケージは図1に示した発光装置の構造に準じたものを用いた。
蛍光体のLEDパッケージへの搭載は、ケース凹型の底部に設置されたLED上面の電極とリードフレームとをワイヤボンディングした後、液体状のシリコーン樹脂(OE6656、東レダウコーニング株式会社製)に混合した蛍光体粒子をマイクロシリンジからケース凹部に注入して行った。蛍光体粒子の搭載後、120℃で硬化させた後、110℃×10時間のポストキュアを施して封止した。LEDは、発光ピーク波長448nmで、チップ1.0mm×0.5mmの大きさのものを用いた。
Claims (6)
- 酸窒化物蛍光体または窒化物蛍光体からなる蛍光体粒子と、
前記蛍光体粒子の表面に設けられ、アルミニウム、チタン、ジルコニウム、イットリウムおよびハフニウムよりなる群より選ばれる1種以上の元素を含む金属水酸化物または金属酸化物により構成される被覆層と、
を備え、
以下に定義される熱水抽出電気伝導指数ΔΩが2.0mS/m以下である、表面被覆蛍光体粒子。
(熱水抽出電気伝導指数の算出方法)
(1)25℃のイオン交換水の電気伝導率Ω0を測定する。
(2)前記イオン交換水30mlに前記表面被覆蛍光体粒子1gを分散させ、耐圧容器に入れて150℃で16時間加熱した後、イオン交換水20mlを追加し25℃に冷却した状態で電気伝導率Ω1を測定する。
(3)電気伝導率Ω1と電気伝導率Ω0との差分ΔΩ(=電気伝導率Ω1-電気伝導率Ω0)を熱水抽出電気伝導指数ΔΩとする。 - 前記被覆層が前記蛍光体粒子の表面を連続的に被覆する連続被覆層である請求項1に記載の表面被覆蛍光体粒子。
- 前記被覆層が水酸化アルミニウムまたは酸化アルミニウムにより構成される請求項1または2に記載の表面被覆蛍光体粒子。
- 前記蛍光体粒子が、Euを含有するα型サイアロン蛍光体、Euを含有するβ型サイアロン蛍光体、Euを含有するCASN蛍光体またはEuを含有するSCASN蛍光体からなる請求項1乃至3のいずれか1項に記載の表面被覆蛍光体粒子。
- 請求項1乃至4のいずれか1項に記載の表面被覆蛍光体粒子と、前記表面被覆蛍光体粒子を封止する封止材と、
を備える複合体。 - 励起光を発する発光素子と、
前記励起光の波長を変換する請求項5に記載の複合体と、
を備える発光装置。
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020217014423A KR20210080427A (ko) | 2018-10-24 | 2019-10-04 | 표면 피복 형광체 입자, 복합체 및 발광 장치 |
CN201980069479.5A CN112888762A (zh) | 2018-10-24 | 2019-10-04 | 表面覆盖荧光体粒子、复合体和发光装置 |
JP2020553071A JP7436380B2 (ja) | 2018-10-24 | 2019-10-04 | 表面被覆蛍光体粒子の製造方法、複合体の製造方法および発光装置の製造方法 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2018-200304 | 2018-10-24 | ||
JP2018200304 | 2018-10-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2020085049A1 true WO2020085049A1 (ja) | 2020-04-30 |
Family
ID=70330972
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2019/039348 WO2020085049A1 (ja) | 2018-10-24 | 2019-10-04 | 表面被覆蛍光体粒子、複合体および発光装置 |
Country Status (5)
Country | Link |
---|---|
JP (1) | JP7436380B2 (ja) |
KR (1) | KR20210080427A (ja) |
CN (1) | CN112888762A (ja) |
TW (1) | TW202028415A (ja) |
WO (1) | WO2020085049A1 (ja) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2023189046A1 (ja) * | 2022-03-31 | 2023-10-05 | 三井金属鉱業株式会社 | 蛍光体及びその製造方法 |
WO2024101040A1 (ja) * | 2022-11-07 | 2024-05-16 | デンカ株式会社 | 蛍光体粉末および発光装置 |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TWI805458B (zh) * | 2022-07-24 | 2023-06-11 | 逢甲大學 | 高緻密性複合發光材料、其製備方法及發光裝置 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006265506A (ja) * | 2005-02-28 | 2006-10-05 | Denki Kagaku Kogyo Kk | 蛍光体とその製造方法、およびそれを用いた発光素子 |
JP2009256558A (ja) * | 2007-05-22 | 2009-11-05 | Showa Denko Kk | 蛍光体及びその製造方法、並びにそれを用いた発光装置 |
JP2011503266A (ja) * | 2007-11-12 | 2011-01-27 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | 適合された屈折率を有する被覆された蛍光体粒子 |
JP2013229438A (ja) * | 2012-04-25 | 2013-11-07 | Nichia Chem Ind Ltd | 発光装置及びその製造方法 |
JP2014197635A (ja) * | 2013-03-29 | 2014-10-16 | 三菱化学株式会社 | 発光装置と、それに用いるβサイアロン蛍光体 |
JP2016108496A (ja) * | 2014-12-09 | 2016-06-20 | パナソニックIpマネジメント株式会社 | アルカリ土類金属蛍光体、波長変換部材及び発光装置 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101128564B (zh) * | 2005-02-28 | 2012-07-25 | 电气化学工业株式会社 | 荧光体及其制造方法及使用了该荧光体的发光元件 |
JP2008291251A (ja) | 2007-04-26 | 2008-12-04 | Sharp Corp | 蛍光体の製造方法、波長変換部材および発光装置 |
JP2009013186A (ja) | 2007-06-29 | 2009-01-22 | Mitsubishi Chemicals Corp | 被覆蛍光体粒子、被覆蛍光体粒子の製造方法、蛍光体含有組成物、発光装置、画像表示装置、および照明装置 |
-
2019
- 2019-10-04 WO PCT/JP2019/039348 patent/WO2020085049A1/ja active Application Filing
- 2019-10-04 JP JP2020553071A patent/JP7436380B2/ja active Active
- 2019-10-04 KR KR1020217014423A patent/KR20210080427A/ko not_active Application Discontinuation
- 2019-10-04 CN CN201980069479.5A patent/CN112888762A/zh active Pending
- 2019-10-15 TW TW108137027A patent/TW202028415A/zh unknown
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2006265506A (ja) * | 2005-02-28 | 2006-10-05 | Denki Kagaku Kogyo Kk | 蛍光体とその製造方法、およびそれを用いた発光素子 |
JP2009256558A (ja) * | 2007-05-22 | 2009-11-05 | Showa Denko Kk | 蛍光体及びその製造方法、並びにそれを用いた発光装置 |
JP2011503266A (ja) * | 2007-11-12 | 2011-01-27 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | 適合された屈折率を有する被覆された蛍光体粒子 |
JP2013229438A (ja) * | 2012-04-25 | 2013-11-07 | Nichia Chem Ind Ltd | 発光装置及びその製造方法 |
JP2014197635A (ja) * | 2013-03-29 | 2014-10-16 | 三菱化学株式会社 | 発光装置と、それに用いるβサイアロン蛍光体 |
JP2016108496A (ja) * | 2014-12-09 | 2016-06-20 | パナソニックIpマネジメント株式会社 | アルカリ土類金属蛍光体、波長変換部材及び発光装置 |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2023189046A1 (ja) * | 2022-03-31 | 2023-10-05 | 三井金属鉱業株式会社 | 蛍光体及びその製造方法 |
WO2024101040A1 (ja) * | 2022-11-07 | 2024-05-16 | デンカ株式会社 | 蛍光体粉末および発光装置 |
Also Published As
Publication number | Publication date |
---|---|
JPWO2020085049A1 (ja) | 2021-09-16 |
CN112888762A (zh) | 2021-06-01 |
JP7436380B2 (ja) | 2024-02-21 |
TW202028415A (zh) | 2020-08-01 |
KR20210080427A (ko) | 2021-06-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP1854864B1 (en) | Fluorescent substance and process for producing the same, and luminescent element using the same | |
US8398892B2 (en) | Phosphor, method for producing the same and light-emitting device using the same | |
WO2020085049A1 (ja) | 表面被覆蛍光体粒子、複合体および発光装置 | |
US9708492B2 (en) | LED device and coating liquid used for production of same | |
KR101553086B1 (ko) | 표면-개질된 변환 발광성 물질 | |
KR101577081B1 (ko) | 표면-개질된 인광체 | |
JP5748028B2 (ja) | 複合波長変換粉体、複合波長変換粉体含有樹脂組成物及び発光装置 | |
JP6485467B2 (ja) | 蛍光体、発光装置及び蛍光体の製造方法 | |
EP2903040A1 (en) | Wavelength conversion member, light-emitting device, and method for producing wavelength conversion member | |
KR20190131089A (ko) | 개선된 열전도율을 갖는 파장 변환기들 및 이를 포함하는 조명 디바이스들 | |
EP2017322A1 (en) | Luminescent material | |
EP2128219A1 (en) | Fluorescent substance, method for production thereof, and wavelength converter, light-emitting device and lighting device | |
JP2013529244A (ja) | 発光物質 | |
WO2009096082A1 (en) | Luminescent material | |
TWI660526B (zh) | 發光元件、發光裝置及彼等之製造方法 | |
TWI829904B (zh) | 螢光體粉末、複合體及發光裝置 | |
JP2020066677A (ja) | 表面被覆蛍光体粒子、複合体、発光装置および表面被覆蛍光体粒子の製造方法 | |
JP6068473B2 (ja) | 波長変換粒子、波長変換部材及び発光装置 | |
JP6974781B2 (ja) | 発光装置の製造方法 | |
TW202043435A (zh) | 螢光體粉末、複合體及發光裝置 | |
CN111849480A (zh) | 红外线荧光粉、包含其的荧光粉复合材料与发光装置、以及荧光粉复合材料的制备方法 | |
WO2022255219A1 (ja) | フッ化物蛍光体、その製造方法及び発光装置 | |
JP7361968B1 (ja) | α型サイアロン蛍光体、発光装置およびα型サイアロン蛍光体の製造方法 | |
US10407615B2 (en) | Fluorescent material, method of producing same, and light emitting device | |
JP2022184763A (ja) | フッ化物蛍光体、その製造方法及び発光装置 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 19876516 Country of ref document: EP Kind code of ref document: A1 |
|
ENP | Entry into the national phase |
Ref document number: 2020553071 Country of ref document: JP Kind code of ref document: A |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
ENP | Entry into the national phase |
Ref document number: 20217014423 Country of ref document: KR Kind code of ref document: A |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 19876516 Country of ref document: EP Kind code of ref document: A1 |