[go: up one dir, main page]

TW201000603A - Light emitting device comprising a ceramic material with line emitter activators and an interference filter - Google Patents

Light emitting device comprising a ceramic material with line emitter activators and an interference filter Download PDF

Info

Publication number
TW201000603A
TW201000603A TW098104098A TW98104098A TW201000603A TW 201000603 A TW201000603 A TW 201000603A TW 098104098 A TW098104098 A TW 098104098A TW 98104098 A TW98104098 A TW 98104098A TW 201000603 A TW201000603 A TW 201000603A
Authority
TW
Taiwan
Prior art keywords
ceramic material
lighting
light
ceramic
illuminating device
Prior art date
Application number
TW098104098A
Other languages
Chinese (zh)
Inventor
Cornelis Reinder Ronda
Original Assignee
Koninkl Philips Electronics Nv
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Koninkl Philips Electronics Nv filed Critical Koninkl Philips Electronics Nv
Publication of TW201000603A publication Critical patent/TW201000603A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/08Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials
    • C09K11/77Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals
    • C09K11/7766Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals containing two or more rare earth metals
    • C09K11/7767Chalcogenides
    • C09K11/7769Oxides
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/50Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on rare-earth compounds
    • C04B35/505Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on rare-earth compounds based on yttrium oxide
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/515Shaped 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
    • C04B35/553Shaped 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 fluorides
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/64Burning or sintering processes
    • C04B35/645Pressure sintering
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/08Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials
    • C09K11/61Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing fluorine, chlorine, bromine, iodine or unspecified halogen elements
    • C09K11/615Halogenides
    • C09K11/616Halogenides with alkali or alkaline earth metals
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3201Alkali metal oxides or oxide-forming salts thereof
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3201Alkali metal oxides or oxide-forming salts thereof
    • C04B2235/3203Lithium oxide or oxide-forming salts thereof
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3224Rare earth oxide or oxide forming salts thereof, e.g. scandium oxide
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3224Rare earth oxide or oxide forming salts thereof, e.g. scandium oxide
    • C04B2235/3225Yttrium oxide or oxide-forming salts thereof
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3231Refractory metal oxides, their mixed metal oxides, or oxide-forming salts thereof
    • C04B2235/3232Titanium oxides or titanates, e.g. rutile or anatase
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/44Metal salt constituents or additives chosen for the nature of the anions, e.g. hydrides or acetylacetonate
    • C04B2235/444Halide containing anions, e.g. bromide, iodate, chlorite
    • C04B2235/445Fluoride containing anions, e.g. fluosilicate
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/60Aspects relating to the preparation, properties or mechanical treatment of green bodies or pre-forms
    • C04B2235/604Pressing at temperatures other than sintering temperatures
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/65Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
    • C04B2235/66Specific sintering techniques, e.g. centrifugal sintering
    • C04B2235/661Multi-step sintering
    • C04B2235/662Annealing after sintering
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/65Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
    • C04B2235/66Specific sintering techniques, e.g. centrifugal sintering
    • C04B2235/661Multi-step sintering
    • C04B2235/662Annealing after sintering
    • C04B2235/663Oxidative annealing
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/74Physical characteristics
    • C04B2235/77Density
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/96Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance
    • C04B2235/9607Thermal properties, e.g. thermal expansion coefficient
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10HINORGANIC LIGHT-EMITTING SEMICONDUCTOR DEVICES HAVING POTENTIAL BARRIERS
    • H10H20/00Individual inorganic light-emitting semiconductor devices having potential barriers, e.g. light-emitting diodes [LED]
    • H10H20/80Constructional details
    • H10H20/84Coatings, e.g. passivation layers or antireflective coatings
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10HINORGANIC LIGHT-EMITTING SEMICONDUCTOR DEVICES HAVING POTENTIAL BARRIERS
    • H10H20/00Individual inorganic light-emitting semiconductor devices having potential barriers, e.g. light-emitting diodes [LED]
    • H10H20/80Constructional details
    • H10H20/85Packages
    • H10H20/851Wavelength conversion means
    • H10H20/8511Wavelength conversion means characterised by their material, e.g. binder
    • H10H20/8512Wavelength conversion materials

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Manufacturing & Machinery (AREA)
  • Structural Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Luminescent Compositions (AREA)
  • Led Device Packages (AREA)

Abstract

The invention relates to an improved light emitting device comprising a ceramic with line-emitting activators in optical contact with an interference filter. This light emitting device has a greatly increased light efficiency towards a preferred light-emitting direction.

Description

201000603 六、發明說明: 【發明所屬之技術領域】 本發明係關於發光裝置,尤其係LED。 【先前技術】 本發明係關於發光裝置,尤其係諸如填光體轉換的發光 二極體(pcLED)之LED。其亦涉及此等pCLED在用於LCD背 光、汽車照明、投影及發信目的之光源中之應用。 目前所應用的pcLED為用於照明目的之白色pcLED或所201000603 VI. Description of the Invention: TECHNICAL FIELD OF THE INVENTION The present invention relates to a light-emitting device, particularly an LED. [Prior Art] The present invention relates to a light-emitting device, particularly an LED such as a light-filled light-emitting diode (pcLED). It also relates to the use of such pCLEDs in light sources for LCD backlighting, automotive lighting, projection and signaling purposes. Currently used pcLED is a white pcLED or a place for lighting purposes.

〇月的全轉換pcLED。後者被應用為綠色及紅色光源,其中 色點係由半導體所發射之藍色輻射之加色混合的結果,其 不被磷光體及受到藍色LED光所激發之螢光屏之綠色至紅 色發射吸收。這係由於難以在不犧牲光源的總輻射效率 下,完全抑制藍色輻射透過螢光屏之洩漏之故。出於此目 的,例如在WO2007/039849已提出陶究材料,該案以引用 的方式併入本文中。 然而’對於-些應用,先前技術之LED之發光不能被認 為係令人滿意的。因此,存在對可提供滿意度增加的發光 分布之發光裝置的需要。 【發明内容】 本發明之一目的係提供一種發光裝置,其可在 . ^ m —X…衣夏,具可在眉 用中使用且,其提供一令人滿意之增加的發光分布。 解E :措&amp; &gt;本發明之技術方案1之發光裝置予以 ,決。因&amp;,提供-種發光裝置,其包括至少一主要為陶 瓷之材料及至少一盥 為旬 /、β亥陶究材料光學接觸之干涉濾光器, 137813 201000603 ψ 其中該陶瓷材料包括作為用於發射光之活化劑之&amp;3+、 Tb3+、Ho3+及Mn4+中之至少一者。 術浯「主要」尤其意謂該材料之&gt;9〇%、較佳三95%及最 佳299%具有理想結構及/或组成。應」主意的是(取決於製 耘)諸如黏合劑或助熔劑之一些添加劑可存在於該陶瓷 材料中。Λ冑添加劑可全部或部分併入最終材#中,該材 料因此亦可為若干化學性質不同的物種之複合物且尤其包 含在本技術中被稱為助熔劑及/或黏合劑之此等物種。合 適的助熔劑及/黏合劑包含鹼土金屬氧化物或鹼金屬氧化 物(例如Mg〇)及氟化物、Si02等。 八術5吾「陶瓷材料」在本發明之意義上尤其意謂及,或包 3 、、’口日日或多晶岔霄材料或具有一經控制的孔量或無孔之 複合材料。 人術語「多晶材料」在本發明之意義上尤其意謂及/或包 3具有一大於主要成分之9〇%之體積密度之一材料,其由 ^於80%的單晶B壽組成,每個單晶缚之直徑大於⑴$微米且 可具有不同的結晶取向(crystall〇graphic 〇七价如⑽)。此 等早晶疇可藉由非晶系材料或玻璃狀材料或藉由額外的結 晶成分而連接。 人術5吾「光學接觸」在本發明之意義上特別意謂及/或包 3右干裝置,其中干涉濾光器與發光層之間的距離如此 J以致於無干涉圖案形成於干涉濾光器與發光層之 間。此可減少該裝置之實體尺寸及不想要的光洩漏。 ,— 干以’慮光裔」尤其意謂及/或包含一光學組件, J378J3 201000603 其係由複數個具有交替的高低折射率之層所組成。 已顯示在本發明内可作廣泛應用之此種發光裝置之使用 具有以下優點之至少一者: 由於在包括在—側上之所述活化劑之H與在另-侧上 之干涉濾光器之間的增效效應’可發現朝向一較佳方向 之一極大增加的發光; 允許在一較大的溫度範圍内使用該陶瓷材料;Haoyue's full conversion pcLED. The latter is applied as a green and red light source, where the color point is the result of additive color mixing of the blue radiation emitted by the semiconductor, which is not emitted by the phosphor and the green to red emission of the phosphor screen excited by the blue LED light. absorb. This is because it is difficult to completely suppress the leakage of blue radiation through the fluorescent screen without sacrificing the total radiation efficiency of the light source. For this purpose, ceramic materials have been proposed, for example, in WO 2007/039849, which is incorporated herein by reference. However, for some applications, the illumination of prior art LEDs cannot be considered satisfactory. Therefore, there is a need for a light-emitting device that can provide an increased luminous distribution of satisfaction. SUMMARY OF THE INVENTION One object of the present invention is to provide a light-emitting device that can be used in an eyebrow and that provides a satisfactory increased illumination distribution. Solution E: Measure &&gt; The illuminating device of the first aspect of the present invention is determined. </ RTI> </ RTI> </ RTI> </ RTI> </ RTI> </ RTI> </ RTI> </ RTI> </ RTI> </ RTI> </ RTI> </ RTI> </ RTI> </ RTI> </ RTI> </ RTI> </ RTI> </ RTI> </ RTI> </ RTI> </ RTI> At least one of &amp; 3+, Tb3+, Ho3+, and Mn4+ of the activator that emits light. The term "main" in particular means that &gt;9%, preferably three 95% and preferably 299% of the material have an ideal structure and/or composition. It should be understood that (depending on the sputum) some additives such as binders or fluxes may be present in the ceramic material. The cerium additive may be incorporated, in whole or in part, into the final material #, which may therefore also be a composite of several chemically distinct species and in particular such species known in the art as fluxing and/or binders. . Suitable fluxes and/or binders include alkaline earth metal oxides or alkali metal oxides (e.g., Mg oxime) and fluorides, SiO 2 and the like. In the sense of the present invention, "ceramic material" means, in particular, or a composite material having a controlled amount of pores or no pores. The term "polycrystalline material" in the sense of the present invention means, in particular, and/or that the package 3 has a material density greater than 9 % by weight of the main component, which consists of 80% of the single crystal B lifetime. Each of the single crystals has a diameter greater than (1) $ microns and may have a different crystallographic orientation (crystall〇graphic 〇 seven prices such as (10)). These early crystal domains may be joined by an amorphous material or a glassy material or by an additional crystalline component. Human "5" "optical contact" in the sense of the present invention particularly means and / or package 3 right-hand device, wherein the distance between the interference filter and the luminescent layer is such that the interference-free pattern is formed in the interference filter Between the device and the luminescent layer. This reduces the physical size of the device and unwanted light leakage. ,—Drying into a 'lighting man' especially means and/or including an optical component, J378J3 201000603 consists of a plurality of layers having alternating high and low refractive indices. The use of such a illuminating device which has been shown to be widely applicable in the present invention has at least one of the following advantages: due to the H of the activator included on the side and the interference filter on the other side The synergistic effect between 'can be found to greatly increase the luminescence towards one of the preferred directions; allowing the ceramic material to be used over a wide temperature range;

未觀察到發射偏移(如在包括寬頻發射器之許多應用中 所觀察到的)。 根據本發明之-較佳實施例,該陶兗材料内之活化心 摻雜程度為㈣1%(莫耳··莫耳)且$25%(莫耳:莫引較 佳為n%(莫耳:莫耳)且训(莫耳:莫耳),最佳為 :莫耳)W耳:莫耳)。在本文中,術 、 '耳」表不以莫耳表示的活化劑之摻雜程度, ,、係與以莫耳表示的陶莞材料相比較。 根據本發明之一較伟眚你办,丨 ^ 2-. — “ 孕又佳只^例,该至少一干涉濾光器包括 1具有々多子層之濾光11。子層之數目較佳為⑽且;^30,No transmission offset was observed (as observed in many applications including wideband transmitters). According to a preferred embodiment of the invention, the degree of doping of the activated core in the ceramic material is (4) 1% (mole·moule) and $25% (mole: m is preferably n% (mole: Moer) and training (Mor: Moer), the best is: Moer) W ear: Moer). In this paper, the degree of doping of the activator, which is not expressed by Mohr, is compared with the pottery material expressed by Mohr. According to one of the present inventions, 丨^ 2-. — "Pregnant and good example, the at least one interference filter comprises a filter 11 having a plurality of sub-layers. The number of sub-layers is preferably For (10) and; ^30,

Hi子層之平均厚度為⑽奈米且侧奈米,較佳為 100奈米且$3〇〇奈米。 岸5亥至少一干涉層之材料較佳經選擇使得該至少一個干涉 層包括—具有折射率差異之交替分層,结構。 9 根據本發明之一較佳實施例,該至少 —選自群組 Ti〇2/Si〇2、Si〇2/Zn〇 2〇3/ZnO &gt; Hf02/Si〇2 . Hf〇2/Al203 一干涉濾光器包括 、Al2〇3/Ti〇2、 ' Y2〇3/Ti〇2 , 137813 201000603The Hi sublayer has an average thickness of (10) nanometers and side nanometers, preferably 100 nanometers and $3 nanometers. Preferably, the material of at least one of the interference layers is selected such that the at least one interference layer comprises - alternating layers having a refractive index difference. According to a preferred embodiment of the present invention, the at least one selected from the group consisting of Ti〇2/Si〇2, Si〇2/Zn〇2〇3/ZnO &gt; Hf02/Si〇2. Hf〇2/Al203 An interference filter includes, Al2〇3/Ti〇2, 'Y2〇3/Ti〇2, 137813 201000603

Zr〇2/Ti〇2或其等之混合物之材料。 替代地及/或此外,該至少一干涉濾光器包括基本上由 樹脂製成之若干層,該等樹脂可視情況包括具有一高折射 率之材料之奈米粒子(較佳的材料包含氾〇2及办〇)。 根據本發明之一較佳實施例,該陶瓷材料包括一選自以 下群組之材料,該群組包括: -Ln203:Er ’ Ln係選自包括sc、γ、Gd、Lu及其等之混合 物之群組; -Ln203:Ho ; -Ln203:Tb ;及 _ ,Ml係選自包括u、κ、仏或其等之混合物 之群組,Μ1!係選自包括Si、Ge、丁卜☆、財及其等之 混合物之群組; 或其混合物。 陶兗材料較佳包括基本上由此材料製成的材料。然而, 在-些應用中,添加劑之微量亦可存在於塊狀組合物中。 此等添加劑尤其包含在本技術中被稱為助熔劑之此等物 種。合適的助熔劑包含鹼土金屬氧化物或鹼金屬氧化物及 氟化物、Si〇2等及其等之混合物。 根據本發明之一較佳實施例,該至少一陶究材料之折射 率為21.4 ’較佳為d.7 ,最佳為n 已顯示此對於本發明内之許多應用有利。令人驚譯的發 現係’對於許多應用,折射率可隨陶瓷材料之組合物而自 動改變,使得該陶㈣料與該發光裝置之其他組份的「折 »37813 201000603 射率匹配」在許多情況下係可能的。 根據本發明之—較佳實施例,在以一 10 W/cm2之光功率密 度及一2.75 eV的平均光能量,於20crc下將陶瓷材料曝光 1000小時後’該陶瓷材料之光熱穩定性為280%至y0〇%。 術語「光熱穩定性」在本發明之意義上尤其意謂及/或 . 包含在同時施加熱量及高強度激發下之特定吸收特性之守 艮’亦即一 100%的光熱穩定性表示該材料事實上不受同 時幸S射及加熱之影響。 (、 ' 根據本發明之一較佳實施例,在以一 1〇 w/cm2之光功率密 度及一2.75 eV的平均光能量,於2〇〇它下將陶瓷材料曝光 1000小時後,該陶瓷材料之光熱穩定性為^82.5%至 $95%,較佳為 &gt;85%至$97%。 根據本發明之一較佳實施例,該陶瓷材料在室溫下的熱 導率為 20.005 Wcrr^iC1 至 $0.75 Wcm·丨 1C1。 根據本發明之一實施例,該陶瓷材料對於波長範圍在 u 上650奈米至$800奈米之光表現一在空氣中的法線入射為 210%至5°/。之透明度。 對於波長範圍在2550奈米至$1〇〇〇奈米之光,在空氣中 的法線入射之透明度較佳為3〇%至3〇%,對於在波長範 圍在2650奈米至S800奈米之光較佳為&gt;3〇%至巧5%及最佳 為 &gt;40°/。至 &lt;70%。 術語「透明度」在本發明之意義上尤其意謂對於在空氣 中的法線入射,不可被該材料吸收之一波長之入射光之 -。車乂佳&gt;20/〇,更佳230%,最佳240%且$85°/。透射穿 137813 201000603 過枚αα。對於紅色及、綠色陶究材料,此波長較佳係分別在 Μ70奈米且$8〇〇奈米或y1〇奈米且$57〇奈米之範圍内。 根據本發明之„較佳實施例’該陶究材料具有理論密度 之 395% 且 —密度。 根據本發明之—較佳實施例,該陶瓷材料具有理論密度 之297°/。且$100%之—密度。 根據所述的本發明之較佳實施例之低於丨〇〇%之密度較 係藉由將„亥材料燒結達到一個階段而獲得,其中仍然有 孔存在於陶瓷基體中。最佳的係密度在&gt;98 〇%且99 之 f圍内’在該陶兗基體中之總的孔體積在20.2% — £2%之 =圍内。一較佳的平均孔徑係在y〇〇奈米—2兄〇奈米之 範圍内。 此外,本發明係關於一種用以製造根據本發明之發光裝 置之陶竟材料所用的一材料之方法,肖方法包括一燒結步 驟。 乡術语「燒結步驟」在本發明之意義上尤其意謂在熱量影 響下,一前驅體粉末之緻密化,其可在不達到該經燒結材 枓之主要成分之液態下,與單向塵力或等歷壓力之施加結 合。 據本發明之一實施例,該燒結步驟並無額外的壓力, 車父佳係在還原氛圍或惰性氛圍中。 根據本發明之一實施例,該方法進—步包括以下步驟: 在燒結前對該(等)前驅體材料加壓達到其理想密度之β〇% 至g〇%,根據本發明之一實施例係達到其理想密度之 *37813 201000603 255%至$60%。在實務上已經顯示的係此可改良本發明所 描述之大多數材料之燒結步驟。 根據本發明之-實施例’製造用於根據本發明之—發光 裝置之一材料之方法包括以下步驟: (a) 混合該材料之前驅體材料; (b) 選擇性地燒成該等前驅體材料,較佳在一 至 S150(TC的溫度下,以移除揮發性材料; 、 (c)選擇性地研磨及洗淨; (d) —第一加壓步驟,較佳為一在kN〒之單向加壓步 驟,其使用具有一理想形狀(例如桿狀或小球狀)之模 具之合適粉末壓實工具;及/或一冷等壓加壓步 驟,其較佳在23000巴至$3500巴下; (e) —燒結步驟,其係在巧㈧它至^^⑻艺而無額外的壓 力下; (f) 一熱加壓步驟,其較佳為一熱等壓加壓步驟,較佳在 / &gt;100巴至$2500巴且較佳在一 25〇〇。(3至S2000°C之溫 度;及/或一熱單向加壓步驟,較佳在&gt;1〇〇巴至^25〇〇 巴且較佳在一 2500°C至S2000°C之溫度; (g) 一後退火步驟(視情況),其係在惰性氛圍或空氣中於 &gt;500°C 至 &lt;1700°C 下進行。 此外,本發明係關於一種發光裝置,尤其係一種包括一 本發明之陶瓷材料之LED。 根據本發明之一化合物及/或一陶瓷材料可用於許多系 統及/或應用中’以下係其中之一者或多者: 137813 -9- 201000603 - 辦公室照明系統; 家用系統; - 商店照明系統; - 家用照明系統; 重點照明(accent lighting)系統, - 聚光照明系統; - 劇場照明系統; ' 光纖應用系統; ' 投影系統; ' 自我照明顯示系統; • 像素化顯示系統; &quot; 分段顯示系統; &quot; 警告標誌系統; - 醫學照明應用系統; - 指示標誌系統;及 - 裝飾性照明系統; - 攜帶式系統; ' 汽車應用; - 溫室照明系統; ' 廣告照明系統。 上述成分,及所主張成分及根據所述實施射之本發明 而使用之成分,就其大小、形狀、化合物選擇及技術概念 而5不叉任何特別例外限制,使得可應用在相關領域中已 知的選擇準則而無限制。 137813 201000603 【實施方式】 附之目的之額外細節、特點、特徵及優點被揭示於 一太:射’且以下以例示性方式對實例進行之描述顯 不本發明之發光裝置之若干實施例及實例。A material of Zr〇2/Ti〇2 or a mixture thereof. Alternatively and/or additionally, the at least one interference filter comprises a plurality of layers substantially made of a resin, which may optionally comprise nanoparticles having a high refractive index material (preferably comprising ubiquinone) 2 and do not know). According to a preferred embodiment of the present invention, the ceramic material comprises a material selected from the group consisting of: -Ln203:Er 'Ln is selected from the group consisting of sc, γ, Gd, Lu, and the like. a group of -Ln203:Ho; -Ln203:Tb; and _, Ml is selected from the group consisting of a mixture of u, κ, 仏 or the like, Μ1! is selected from the group consisting of Si, Ge, Dingbu ☆, a group of wealth and its mixture; or a mixture thereof. The ceramic material preferably comprises a material that is substantially made of the material. However, in some applications, minor amounts of additives may also be present in the bulk composition. Such additives include, inter alia, such species known in the art as fluxing agents. Suitable fluxing agents include alkaline earth metal oxides or alkali metal oxides and fluorides, SiGe2, and the like, and mixtures thereof. According to a preferred embodiment of the invention, the at least one ceramic material has a refractive index of 21.4 Å, preferably d.7, and preferably n, which has been shown to be advantageous for many applications within the invention. The surprising finding is that for many applications, the refractive index can be automatically changed with the composition of the ceramic material, so that the ceramic (four) material matches the other components of the illuminating device with a "Folding»37813 201000603 radiance" in many The situation is possible. According to a preferred embodiment of the present invention, the photothermal stability of the ceramic material is 280 after exposure of the ceramic material at 20 crc for 1000 hours at an optical power density of 10 W/cm 2 and an average light energy of 2.75 eV. % to y0〇%. The term "photothermal stability" in the sense of the present invention means, in particular, and/or. The inclusion of a specific absorption characteristic under simultaneous application of heat and high-intensity excitation, that is, a 100% photothermal stability indicates the fact of the material. It is not affected by the simultaneous S-shot and heating. (, ' According to a preferred embodiment of the present invention, after exposing the ceramic material to an underlying light energy density of 1 〇 w/cm 2 and an average light energy of 2.75 eV for 1000 hours, the ceramic The photothermal stability of the material is from 82.5% to $95%, preferably &gt; 85% to $97%. According to a preferred embodiment of the invention, the thermal conductivity of the ceramic material at room temperature is 20.005 Wcrr^iC1 Up to $0.75 Wcm·丨1C1. According to one embodiment of the invention, the ceramic material exhibits a normal incidence in air of 210% to 5°/ for light having a wavelength range of 650 nm to $800 nm on u. Transparency. For light with a wavelength range from 2550 nm to $1 nm, the normal incidence of incidence in air is preferably 3〇% to 3〇% for wavelengths ranging from 2650 nm to S800. The light of the nanometer is preferably &gt;3〇% to 5% and optimally &gt;40°/. to &lt;70%. The term "transparency" in the sense of the present invention means especially for in the air. Normal incidence, can not be absorbed by the material at one wavelength of incident light - 乂佳佳 > 20 / 〇, better 230%, best 240% and $ 85 Transmitted through 137813 201000603 over αα. For red and green ceramic materials, this wavelength is preferably within the range of Μ70 nm and $8〇〇Ny or y1〇Nano and $57〇N. The preferred embodiment of the present invention has a theoretical density of 395% and density. According to a preferred embodiment of the invention, the ceramic material has a theoretical density of 297°/. and a density of $100%. The density of less than 丨〇〇% according to the preferred embodiment of the invention described above is obtained by sintering the material into a stage in which holes are still present in the ceramic matrix. The density is in the range of &gt;98% and 99%. The total pore volume in the ceramic matrix is in the range of 20.2% to £2%. A preferred average pore size is in y〇〇n. Further, the present invention relates to a method for producing a material for use in the ceramic material of the light-emitting device according to the present invention, and the method includes a sintering step. In the sense of the invention, it means especially in the heat The densification of a precursor powder can be combined with the application of a one-way dust force or an equal pressure in a liquid state that does not reach the main component of the sintered crucible. According to an embodiment of the present invention, There is no additional pressure in the sintering step, and the owner is in a reducing atmosphere or an inert atmosphere. According to an embodiment of the invention, the method further comprises the steps of: pressurizing the (etc.) precursor material prior to sintering. To achieve a desired density of β〇% to g〇%, according to an embodiment of the invention, it reaches its ideal density of *37813 201000603 255% to $60%. This has been shown in practice to improve the sintering step of most of the materials described herein. A method for fabricating a material for a light-emitting device according to the present invention includes the following steps: (a) mixing the precursor material of the material; (b) selectively firing the precursors The material is preferably at a temperature of from 1 to S150 (TC to remove volatile materials; (c) selectively ground and washed; (d) - a first pressurizing step, preferably one at kN a one-way pressurization step using a suitable powder compacting tool having a mold of a desired shape (e.g., rod or pellet); and/or a cold isostatic pressing step, preferably from 23,000 to $3,500 bar (e) - a sintering step, which is carried out in the art (8) to no additional pressure; (f) a hot pressurization step, preferably a hot isostatic pressing step, preferably At / &gt; 100 bar to $2500 bar and preferably at 25 〇〇. (3 to S2000 ° C temperature; and / or a hot one-way pressurization step, preferably in &gt; 1 〇〇巴至^25 〇〇巴 and preferably at a temperature of from 2500 ° C to S 2000 ° C; (g) a post-annealing step (as appropriate) in an inert atmosphere or air at &gt; 500 ° C to Furthermore, the invention relates to a light-emitting device, in particular to an LED comprising a ceramic material according to the invention. A compound according to the invention and/or a ceramic material can be used in many systems and/or In the application 'One of the following or more: 137813 -9- 201000603 - office lighting system; home system; - store lighting system; - home lighting system; accent lighting system, - spotlighting system; - Theater lighting system; 'Fiber application system; 'Projection system; 'Self-illuminated display system; • Pixelated display system; &quot; Segmented display system; &quot; Warning sign system; - Medical lighting application system; - Indicator system; And - decorative lighting systems; - portable systems; 'automobile applications; - greenhouse lighting systems; ' advertising lighting systems. The above ingredients, and the claimed ingredients and the ingredients used in accordance with the invention according to the implementation, the size , shape, compound selection and technical concepts without any special exception restrictions, making it applicable The selection criteria are known in the art without limitation. 137813 201000603 [Embodiment] Additional details, features, features and advantages of the present invention are disclosed in the description of the present invention. Several embodiments and examples of the illumination device of the present invention.

實例I 根據一第一本發明之實例之一lED之製備: Y2〇3:Ho係藉由混合及燒成技術製備。該等氧化物係在 乙酵中混合且在戰下乾燥。加熱係在3小時期間於 00 C下進行。;gr濃度為1莫耳%(相對於γ)。 合成之粉末係在24小時期間内,使用在作為液體媒質之 異丙醇中之Zr〇2球予以球磨24小時。在乾燥後,該材料在 赋於空氣中予以熱處理8小時。或者,亦可使用造成小 很多的初級磷光體粒子之沈積技術以避免耗時的研磨步 驟。藉由一熱加壓製程’在一 Ar氛圍中以一 3〇购的愿力 於150(TC持續4小時將該所製備的粉末燒結成透明陶变。EXAMPLE I Preparation according to one of the first examples of the invention, lED: Y2〇3: Ho was prepared by mixing and firing techniques. These oxides are mixed in the yeast and dried under the war. The heating was carried out at 00 C over a period of 3 hours. The gr concentration is 1 mol% (relative to γ). The synthesized powder was ball milled for 24 hours using a Zr〇2 ball in isopropanol as a liquid medium over a period of 24 hours. After drying, the material was heat treated for 8 hours in air. Alternatively, deposition techniques that result in much smaller primary phosphor particles can be used to avoid time consuming grinding steps. The prepared powder was sintered to a transparent ceramic change by a heat pressurization process of '150 TC for 4 hours in an Ar atmosphere.

此步驟亦可藉由添加一如LiF之助熔劑予以執行,該之 濃度較佳在0.01-5%之間。 將具有尺寸1χ1χ0·5 mm3之樣品從鑄錠切下,並將其 所有側拋光且放置於一具有lxl mm2大小、於44〇奈米發射 之LED晶片上。該樣品之厚度係經選擇使得幾乎無藍光洩 漏通過(小於2%)。接通LED導致綠光。 在該透明陶瓷磷光體層之頂部上施用一干涉濾光器(由 20個交替的Si〇2及Ti〇2層組成),導致在前向方向上之光強 度增加超過因數1.7。 137813 11 201000603 比較性實例i : 作為一比較性實例’製備一 LED,該LED包括具有與本 發明貫例相同之厚度及h〇3+濃度之—Y2〇3:H〇(顆粒大小2 微米至8微米)的粉末層。 然而’根據該比較性實例I之led之應用不會導致有效 率產生綠光。幾乎無藍光及綠光往前向方向離開粉末層, 大部分光被反射回到LED且因在不想要的方向上之散射及 在LED及填光體層中之吸收而損失。This step can also be carried out by adding a flux such as LiF, which is preferably between 0.01 and 5%. A sample having a size of 1 χ 1 χ 0·5 mm 3 was cut from the ingot, and all sides thereof were polished and placed on an LED wafer having a size of lxl mm 2 and emitted at 44 Å. The thickness of the sample was chosen such that there was almost no blue light leakage (less than 2%). Turning on the LED causes green light. An interference filter (consisting of 20 alternating Si〇2 and Ti〇2 layers) was applied on top of the transparent ceramic phosphor layer, resulting in an increase in light intensity in the forward direction of more than a factor of 1.7. 137813 11 201000603 Comparative Example i: As a comparative example, an LED is prepared which comprises the same thickness and h〇3+ concentration as the example of the invention - Y2〇3:H〇 (particle size 2 microns to 8 micron) powder layer. However, the application of the led according to the comparative example I did not cause the efficiency to produce green light. Almost no blue and green light exits the powder layer in the forward direction, and most of the light is reflected back to the LED and is lost due to scattering in unwanted directions and absorption in the LED and fill layer.

比較性實例II 、作為另一比較性實例,以類似於本發明之實例ί之一方 式’-陶£磷光體材料係由YAG:Ce(寬頻發射)組成。 將- 1 X1X0.5 mms之樣品應用於一發射藍光之咖(發射 440奈米)。調整厚度及濃度以獲得藍光穿過陶变:一 約2%的透射。接通LED導致黃光。 在該透明陶瓷磷光體層之頂部 以上=曙致在前向方向之光強度二::與 之二:本發明之實例1之光學增^ ’其使得本發明 之LED對於在前向方向 月 之襄置特別有用。上之冗度增盈有所必要及/或有利 是,亦觀察到當引進該干涉渡光器 之發射譜部分被藍偏移,大約偏 此效果係根據本發明之任何㈣所:水。 為係本發明之另一優點。 $不到的,其被認Comparative Example II As another comparative example, in a manner similar to the example of the present invention, the phosphor material is composed of YAG:Ce (wideband emission). A sample of -1 X1X0.5 mms was applied to a blue-emitting coffee (transmitting 440 nm). Adjust the thickness and concentration to obtain blue light through the ceramic change: a transmission of about 2%. Turning on the LED causes yellow light. Above the top of the transparent ceramic phosphor layer = the light intensity in the forward direction is two:: and two: the optical enhancement of the inventive example 1 which makes the LED of the present invention for the moon in the forward direction This is especially useful. It is necessary and/or advantageous to increase the redundancy in the above, and it is also observed that the portion of the emission spectrum when the introduction of the interference irradiator is blue-shifted, approximately the effect of any (4) according to the present invention: water. It is another advantage of the present invention. Less than $, it is recognized

本發明實例H 137813 -12· 201000603 摻雜有Mn4+(5莫耳%)之LTiF6係藉由在加熱與燒結期 間’在例如由鐵氟龍(Teflon)製成之耐氫氟酸器皿中將氫 氧化物溶於稀氫氟酸(3〇%至5〇%)中予以製備。發光材料 係藉由對反應混合物進行蒸鍍而隔離以接收一乾燥粉末。 6亥磷光體係以如上所述之方式予以研磨。一陶瓷層係藉由 在—6〇(TC之溫度,於100 Mpa下進行熱加壓24小時而製 備0Inventive Example H 137813 -12· 201000603 LTiF6 doped with Mn4+ (5 mol%) is made by hydrogen in a hydrofluoric acid resistant vessel made of, for example, Teflon during heating and sintering. The oxide is prepared by dissolving in dilute hydrofluoric acid (3% to 5% by weight). The luminescent material is isolated by evaporation of the reaction mixture to receive a dry powder. The 6-G phosphor system was ground as described above. A ceramic layer is prepared by heat-pressing at a temperature of TC for 20 hours at 100 MPa for 24 hours.

在該透明陶竟石舞《體層 &lt;頂部上之一干涉渡%器(舆以 上所述相同)之施用,導致在前向方向上之光強度增加約 因數1.6。 在以上之詳細實施例中之元件及特徵之特定組合僅為例 :性;亦明確期望此等教示與在本文中及在以引用的方式 併入之專利/申請案中之其他教示可互換及替代。如孰習 1 匕項技術者所認知,在不脫離所主張的本發明之精神及範 :二!1此項技術者可思及對本文所述内容之變更、修 飾及,、他貫施。因此,先前p、+、没认 在丨士 &amp; 无引描述僅為例示性且不旨在限 制。本發明之範圍係在以 — 月衣項及其等效物十予以界 疋。此外,本描述及請求項中The application of the transparent ceramic stone dance "body layer" on top of one of the interferences, resulting in an increase in light intensity in the forward direction of about 1.6. The specific combinations of the elements and features in the above detailed description are merely exemplary; and the teachings are to be interpreted as being interchangeable with other teachings herein and in the patents/applications incorporated by reference. Alternative. As understood by those skilled in the art, the spirit and scope of the claimed invention are not deviated from the following: 1 The person skilled in the art can think about the changes, modifications, and implementations of the contents described herein. Therefore, the previous p, +, and unrecognized gentlemen &amp; descriptions are for illustrative purposes only and are not intended to be limiting. The scope of the invention is defined by the term "moon clothing" and its equivalent. In addition, in this description and in the request

Afr ± PM. ^ 用之多考符號並未限制Afr ± PM. ^ Multiple test symbols are not restricted

所主張之本發明之範圍。 J 137813The scope of the claimed invention. J 137813

Claims (1)

201000603 七、申請專利範圍: 1. 2.201000603 VII. Patent application scope: 1. 2. 3. 一種發光裝置,1句括5小 一 八 ^一主要為陶瓷之材料及至少 甘士 : ’該干㈣光器與該陶㈣料光學接觸, '该陶竞材料包括作為用於發射光之活化劑之玢3+、 Tb +、H〇3+及Mn4+中之至少一者。 其中在該陶瓷材料内之該等活 %(莫耳:莫耳)及&lt;25%(莫耳: 如請求項1之發光裝置, 化劑之摻雜程度為20.01 莫耳)。 如β青求項1至2中任一項之获杏壯g 貝心t光衣置,其中該陶瓷材料包 括一選自以下群組之材料,該群組包括: Ln2〇3:Er ’ Ln係選自包括Sc、γ、別、&amp;及其等之混 合物之群組; Ln203:Ho ; Ln203:Tb ;及3. A illuminating device consisting of 5 small ones and eight ones mainly composed of ceramic material and at least Gans: 'The dry (four) optical device is in optical contact with the ceramic (four) material, 'The Tao Jing material is included as a light for emission At least one of 活化3+, Tb+, H〇3+, and Mn4+ of the activator. The activity % (mole: mole) and &lt; 25% (mole: the light-emitting device of claim 1 , the doping degree of the chemical agent is 20.01 mol) in the ceramic material. For example, in the case of any one of the items 1 to 2, the apricot is provided, wherein the ceramic material comprises a material selected from the group consisting of: Ln2〇3: Er 'Ln Is selected from the group consisting of a mixture of Sc, γ, 、, &amp; and the like; Ln203: Ho; Ln203: Tb; M 2M F6:Mn ’ Mi係選自包括u、κ、Na或其等之混合 物之群組,M11係選自包括Si、Ge、Ti ' Zr、Hf及其等之 混合物之群組; 或其混合物。 4. 如請求項1至3中任一項之發光裝置,其中該至少一陶瓷 材料之折射率為21.4。 5. 如請求項1至4中任一項之發光裝置,其中以一 1〇 W/cm2 之光功率密度及一2·75 eV的平均光能量,於:⑼它下將 該陶瓷材料曝光1000小時後’該陶瓷材料之光熱穩定性 為 &gt;80%至 00%。 137813 201000603 6. 如請求項1至5中任一項之發光裝置,其中該陶瓷材料之 熱導率為 20.005 W crn^K-1 至 $0.75 W cm—ifT1。 7. 如請求項1至6中任一項之發光裝置,其中該陶瓷材料具 有理論密度之295%且5101%之一密度。 8. 一種系統,其包括一如請求項1至7中任一項之發光裝 置,該系統被用於以下應用中之一者或多者: 辦公室照明系統; 家用系統; 商店照明系統; 家用照明系統; 重點照明系統; 聚光照明系統; 劇場照明系統; 光纖應用系統; 投影系統; 自我照明顯示系統; 像素化顯示系統; 分段顯示系統; 警告標認糸統, 醫學照明應用系統; 指不標誌、糸統,及 裝飾性照明系統; 攜帶式系統; 汽車應用; 137813 201000603 溫室照明系統; 廣告照明系統。M 2M F6: Mn 'Mi is selected from the group consisting of a mixture of u, κ, Na or the like, and M11 is selected from the group consisting of Si, Ge, Ti 'Zr, Hf, and the like; mixture. 4. The illuminating device of any one of claims 1 to 3, wherein the at least one ceramic material has a refractive index of 21.4. 5. The illuminating device according to any one of claims 1 to 4, wherein the ceramic material is exposed to 1000 at a light power density of 1 〇W/cm 2 and an average light energy of 2.75 eV. After a while, the photothermal stability of the ceramic material was &gt; 80% to 00%. The illuminating device of any one of claims 1 to 5, wherein the ceramic material has a thermal conductivity of 20.005 W crn^K-1 to $0.75 W cm-ifT1. 7. The illuminating device of any of claims 1 to 6, wherein the ceramic material has a density of 295% and 5101% of the theoretical density. 8. A system comprising a lighting device according to any one of claims 1 to 7, the system being used in one or more of the following applications: office lighting system; home system; store lighting system; home lighting System; key lighting system; spotlighting system; theater lighting system; fiber optic application system; projection system; self-illumination display system; pixelated display system; segment display system; warning standard system, medical lighting application system; Signs, systems, and decorative lighting systems; portable systems; automotive applications; 137813 201000603 greenhouse lighting systems; advertising lighting systems. 137813. 201000603 四、指定代表圖: (一) 本案指定代表圖為:(無) (二) 本代表圖之元件符號簡單說明: 五、本案若有化學式時,請揭示最能顯示發明特徵的化學式: (無) 137813137813. 201000603 IV. Designation of representative drawings: (1) The representative representative of the case is: (none) (2) The symbol of the symbol of the representative figure is simple: 5. If there is a chemical formula in this case, please disclose the chemical formula that best shows the characteristics of the invention. : (none) 137813
TW098104098A 2008-02-12 2009-02-09 Light emitting device comprising a ceramic material with line emitter activators and an interference filter TW201000603A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP08101519 2008-02-12

Publications (1)

Publication Number Publication Date
TW201000603A true TW201000603A (en) 2010-01-01

Family

ID=40527536

Family Applications (1)

Application Number Title Priority Date Filing Date
TW098104098A TW201000603A (en) 2008-02-12 2009-02-09 Light emitting device comprising a ceramic material with line emitter activators and an interference filter

Country Status (2)

Country Link
TW (1) TW201000603A (en)
WO (1) WO2009101578A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109072075A (en) * 2016-05-09 2018-12-21 通用电气公司 Additive Mn phosphor material for high power density application

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8491816B2 (en) 2008-02-07 2013-07-23 Mitsubishi Chemical Corporation Semiconductor light emitting device, backlight, color image display device and phosphor to be used for them
JP5795771B2 (en) 2009-12-17 2015-10-14 コーニンクレッカ フィリップス エヌ ヴェ Illumination device including light source and wavelength conversion component
WO2011073871A2 (en) 2009-12-17 2011-06-23 Koninklijke Philips Electronics N.V. Light emitting diode device with luminescent material
US11862758B2 (en) 2018-11-28 2024-01-02 Lawrence Livermore National Security, Llc Systems and methods for fluoride ceramic phosphors for LED lighting

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10217552A1 (en) * 2002-04-19 2003-11-06 Philips Intellectual Property Plasma screen with terbium (III) activated phosphor
US7497973B2 (en) * 2005-02-02 2009-03-03 Lumination Llc Red line emitting phosphor materials for use in LED applications
KR20080056258A (en) * 2005-09-30 2008-06-20 코닌클리즈케 필립스 일렉트로닉스 엔.브이. Light-Emitting Element Having Ceramic SiAONON Material
JP2009512130A (en) * 2005-10-05 2009-03-19 コーニンクレッカ フィリップス エレクトロニクス エヌ ヴィ Fluorescence conversion type electroluminescent device with absorption filter

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109072075A (en) * 2016-05-09 2018-12-21 通用电气公司 Additive Mn phosphor material for high power density application

Also Published As

Publication number Publication date
WO2009101578A1 (en) 2009-08-20

Similar Documents

Publication Publication Date Title
TWI486254B (en) Luminous ceramic laminate and manufacturing method thereof
CN101605866B (en) Lighting systems incorporating composite monolithic ceramic luminescence converters
JP5631745B2 (en) Light emitting device having translucent ceramic plate
JP5833547B2 (en) Luminescent ceramic and light emitting device using the same
JP5083211B2 (en) Composite for light conversion, light emitting device using the same, and color tone control method
CN109467453B (en) Fluorescent ceramic with characteristic microstructure and preparation method and application thereof
CN102106003B (en) Optical element for light-emitting device and manufacturing method thereof
CN101405368B (en) Electroluminescent device
TW200932886A (en) Light emitting device comprising a multiphase SiAlON-based ceramic material
JP5454473B2 (en) Phosphor ceramics, method for producing the same, and light emitting device
CN101305072B (en) There is the luminescent device of the CaAlSiN light-converting material of improvement
TW200840404A (en) Illumination system comprising monolithic ceramic luminescence converter
TW200804720A (en) Fluorescent lighting creating white light
JPWO2016117623A1 (en) Sintered phosphor, light emitting device, lighting device, vehicle headlamp, and method for manufacturing sintered phosphor
TW201135985A (en) Light emissive ceramic laminate and method of making same
TW201038718A (en) Co-doped 2-5-8 nitrides
TWI428309B (en) A ceramic composite for optical conversion and a light-emitting device using the ceramic composite
KR101747015B1 (en) Polycrystalline ceramics, production thereof, and uses thereof
TW201244165A (en) Light emitting composite with phosphor components
TW200927884A (en) Light emitting device comprising a composite sialon-based ceramic material
TW201000603A (en) Light emitting device comprising a ceramic material with line emitter activators and an interference filter
TW200949308A (en) Color filter for a light emitting device