WO2005112135A2 - Diode electroluminescente emettant une lumiere blanche - Google Patents
Diode electroluminescente emettant une lumiere blanche Download PDFInfo
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- WO2005112135A2 WO2005112135A2 PCT/FR2005/000841 FR2005000841W WO2005112135A2 WO 2005112135 A2 WO2005112135 A2 WO 2005112135A2 FR 2005000841 W FR2005000841 W FR 2005000841W WO 2005112135 A2 WO2005112135 A2 WO 2005112135A2
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- Prior art keywords
- doped
- europium
- phosphor
- formula
- diode according
- Prior art date
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- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims abstract description 32
- 239000000203 mixture Substances 0.000 claims abstract description 31
- 230000005855 radiation Effects 0.000 claims abstract description 11
- 239000000126 substance Substances 0.000 claims abstract description 9
- 229910052693 Europium Inorganic materials 0.000 claims description 29
- OGPBJKLSAFTDLK-UHFFFAOYSA-N europium atom Chemical compound [Eu] OGPBJKLSAFTDLK-UHFFFAOYSA-N 0.000 claims description 27
- 239000011777 magnesium Substances 0.000 claims description 19
- 150000001875 compounds Chemical class 0.000 claims description 18
- 229910052749 magnesium Inorganic materials 0.000 claims description 11
- 239000011572 manganese Substances 0.000 claims description 11
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 10
- 229910052771 Terbium Inorganic materials 0.000 claims description 9
- GZCRRIHWUXGPOV-UHFFFAOYSA-N terbium atom Chemical compound [Tb] GZCRRIHWUXGPOV-UHFFFAOYSA-N 0.000 claims description 9
- 229910017639 MgSi Inorganic materials 0.000 claims description 8
- 229910052782 aluminium Inorganic materials 0.000 claims description 8
- 239000002019 doping agent Substances 0.000 claims description 8
- 229910052748 manganese Inorganic materials 0.000 claims description 8
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 7
- 229910052761 rare earth metal Inorganic materials 0.000 claims description 7
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 6
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 6
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 6
- -1 rare earth borate Chemical class 0.000 claims description 6
- 239000011701 zinc Substances 0.000 claims description 6
- 229910052684 Cerium Inorganic materials 0.000 claims description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 5
- 229910004283 SiO 4 Inorganic materials 0.000 claims description 5
- ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 claims description 5
- 229910052802 copper Inorganic materials 0.000 claims description 5
- 239000010949 copper Substances 0.000 claims description 5
- 229910052727 yttrium Inorganic materials 0.000 claims description 5
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 4
- 150000004645 aluminates Chemical class 0.000 claims description 4
- 229910052733 gallium Inorganic materials 0.000 claims description 4
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 claims description 4
- 229910052725 zinc Inorganic materials 0.000 claims description 4
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 claims description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 3
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 claims description 3
- 239000005083 Zinc sulfide Substances 0.000 claims description 3
- 229910052738 indium Inorganic materials 0.000 claims description 3
- 238000004020 luminiscence type Methods 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- GTDCAOYDHVNFCP-UHFFFAOYSA-N chloro(trihydroxy)silane Chemical compound O[Si](O)(O)Cl GTDCAOYDHVNFCP-UHFFFAOYSA-N 0.000 claims description 2
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims 1
- 239000010452 phosphate Substances 0.000 claims 1
- 229910052984 zinc sulfide Inorganic materials 0.000 claims 1
- 230000005284 excitation Effects 0.000 description 10
- 239000007858 starting material Substances 0.000 description 10
- 229910052788 barium Inorganic materials 0.000 description 9
- 238000000295 emission spectrum Methods 0.000 description 8
- 229910052712 strontium Inorganic materials 0.000 description 8
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical class [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 6
- 150000002500 ions Chemical class 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 238000006467 substitution reaction Methods 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- 101100513612 Microdochium nivale MnCO gene Proteins 0.000 description 4
- 229910004298 SiO 2 Inorganic materials 0.000 description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 4
- 238000000227 grinding Methods 0.000 description 4
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 239000010703 silicon Substances 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- 229910052786 argon Inorganic materials 0.000 description 3
- 238000001354 calcination Methods 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 150000002910 rare earth metals Chemical class 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical group [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 229910052765 Lutetium Inorganic materials 0.000 description 2
- 150000001242 acetic acid derivatives Chemical class 0.000 description 2
- 150000001642 boronic acid derivatives Chemical class 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000000695 excitation spectrum Methods 0.000 description 2
- 230000004907 flux Effects 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 150000004679 hydroxides Chemical class 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 150000002823 nitrates Chemical class 0.000 description 2
- 150000003891 oxalate salts Chemical class 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 1
- 229910052688 Gadolinium Inorganic materials 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 229910052769 Ytterbium Inorganic materials 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 238000000975 co-precipitation Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004737 colorimetric analysis Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical group [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011872 intimate mixture Substances 0.000 description 1
- MIDZQLGOZMFQPO-UHFFFAOYSA-N magnesium;barium(2+);dioxido(oxo)silane Chemical compound [Mg+2].[Ba+2].[O-][Si]([O-])=O.[O-][Si]([O-])=O MIDZQLGOZMFQPO-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 238000006862 quantum yield reaction Methods 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 229910052706 scandium Inorganic materials 0.000 description 1
- SIXSYDAISGFNSX-UHFFFAOYSA-N scandium atom Chemical compound [Sc] SIXSYDAISGFNSX-UHFFFAOYSA-N 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 238000002604 ultrasonography Methods 0.000 description 1
- NAWDYIZEMPQZHO-UHFFFAOYSA-N ytterbium Chemical compound [Yb] NAWDYIZEMPQZHO-UHFFFAOYSA-N 0.000 description 1
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
- C09K11/08—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
- C09K11/77342—Silicates
-
- 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
- H01L33/501—Wavelength conversion elements characterised by the materials, e.g. binder
- H01L33/502—Wavelength conversion materials
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02B—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO BUILDINGS, e.g. HOUSING, HOUSE APPLIANCES OR RELATED END-USER APPLICATIONS
- Y02B20/00—Energy efficient lighting technologies, e.g. halogen lamps or gas discharge lamps
Definitions
- the present invention relates to a light-emitting diode emitting a white light.
- Light emitting diodes LEDs
- the present invention meets this need.
- the light-emitting diode according to the invention which emits white light, is characterized in that it comprises:
- the diode emitting in white is characterized in that it comprises:
- a source of emission of radiation in the wavelength range between 370 nm and 420 nm;
- FIG. 1 is a graph which represents the emission spectra of two luminophores according to the invention for an excitation wavelength of 370 nm;
- FIG. 1 is a graph which represents the emission spectra of two luminophores according to the invention for an excitation wavelength of 370 nm;
- FIG. 1 is a graph which represents the emission spectra of two luminophores according to the invention for an excitation wavelength of 370 nm;
- FIG. 2 is a graph which represents the excitation spectrum of a luminophore according to the invention for an emission wavelength of 623 nm
- FIG. 3 is a graph which represents the emission spectrum of a luminophore according to the invention for an excitation wavelength of 370 nm
- FIG. 4 is a graph which represents the emission spectra of three luminophores according to the invention for an excitation wavelength of 370 nm.
- Rare earth means the elements of the group constituted by scandium, yttrium and the elements of the periodic classification of atomic number inclusive between 57 and 71. It is specified for the remainder of the description that, unless otherwise indicated, in the ranges of values that are given, the values at the terminals are included.
- the LED comprises three essential elements which are an emission source and two luminophores. More specifically, the emission source is a source capable of emitting radiation whose wavelength is in the range of about 370 nm to about 420 nm. It is actually a radiation in the range of visible near ultraviolet. Such sources are well known in the art, for example, can be InGaN-type semiconductors,
- the LED comprises a first phosphor which is capable of emitting both blue light and red light.
- This phosphor corresponds to the formula (1) which has been given above.
- This luminophore is a barium magnesium silicate, doped with europium, which can be considered as a partial substitution of barium, and with manganese, which can be considered as a partial substitution of magnesium.
- this product When subjected to UV excitation, ie to radiation in a wavelength range between about 370 nm and about 420 nm, this product has the property of emitting in particular in the red and also in the blue, ie in a wavelength range between 400 nm and 500 nm for blue and between 550 nm and 720 nm, more particularly between 550 nm and 700 nm, for the red with a good performance. More particularly, the phosphor corresponds to the above-mentioned formula (1) in which 0.0001 ⁇ x ⁇ 0.25 and 0.0001 ⁇ y ⁇ 0.25.
- the phosphor corresponds to the above-mentioned formula (1) in which 0.01 ⁇ x ⁇ 0.25 and 0.01 ⁇ y ⁇ 0.25. It may be noted that it is advantageous to have a concentration of europium in the compound of at least 0.01% to obtain an emission of better intensity. It is also advantageous to have a concentration of europium and manganese of at most 25% in order to minimize annoying self-extinction phenomena.
- the percentages indicated above correspond to the molar substitution rates of the Eu 2+ and Mn 2 doping ions respectively to the Ba 2+ and Mg 2+ ions.
- the luminophore of formula (1) satisfies the following x and y values: 0.01 ⁇ x ⁇ 0.03 and 0.04 ⁇ y ⁇ 0.06. For these values of x and y the emission intensity is the largest. According to yet another variant, the luminophore of formula (1) satisfies the following x and y values: 0.01 ⁇ x ⁇ 0.02 and 0.05 ⁇ y ⁇ 0.1. In this case, the phosphors have for each of the blue and red colors emission intensities substantially identical to each other. According to a last variant, the luminophore of formula (1) satisfies the following x and y values: 0.09 ⁇ x ⁇ 0.11 and 0.09 ⁇ y ⁇ 0.11.
- barium, magnesium and silicon may be partially substituted by elements other than those described above.
- the barium may be partially substituted by calcium and / or strontium in a proportion which may be up to about 30%, this proportion being expressed by the atomic ratio substituent (substituent + barium).
- Magnesium may be partially substituted by zinc in a proportion of up to about 30%, this proportion being also expressed by the Zn / (Zn + Mg) atomic ratio.
- silicon can be partially substituted by germanium, aluminum and / or phosphorus in a proportion that can be up to about 10%, this proportion being expressed by the substitute atomic ratio (substituent + silicon).
- this first phosphor is in a phasically pure form.
- the X-ray diagram of this product shows only one phase corresponding to the Ba 3 MgSi 2 O 8 phase.
- the second phosphor of the LED according to the first embodiment is a luminophore emitting a green light. By this is meant a light whose wavelength is between about 500 nm and about 550 nm. This phosphor is capable of emitting this light when subjected to the radiation emitted by the aforementioned source.
- this second phosphor can be chosen from the product families below: ZnS zinc sulfides doped with copper or doped with copper and aluminum; - alkaline earth silicates doped with europium; by this is meant products of the type MSÎ 2 ⁇ 5 : Eu 2+ or M 2 SiO 4 : Eu + , M being an alkaline earth such as barium or strontium; the alkaline earth aluminates doped with europium or europium in combination with manganese, such as the products of the MAI 2 O 4 : Eu 2+ type , M being an alkaline earth metal such as strontium, M 4 Al 1 ⁇ 25: Eu 2+ , M being an alkaline earth metal such as strontium or else of the Mo type, 8 2Ali 2 ⁇ 8) 8 2: Eu 2+ or Mo, ⁇ 2 Ali 2 ⁇ 8j8 2: Eu 2+ , Mn 2
- the products mentioned as doping agents in the above mentioned products are used in combination with the matrix to give it the required properties of luminescence.
- the products mentioned as doping agents in the above mentioned products are used in combination with the matrix to give it the required properties of luminescence.
- a compound based on at least one element A chosen from alkaline earth metals at least one element B chosen from aluminum, gallium or indium, sulfur and a dopant capable of imparting luminescence properties to said compound and which is in the form of a mixture of a majority AB 2 S 4 type crystal -ographic phase and a B 2 S 3 type crystallographic phase.
- element B may be more particularly gallium and element A strontium.
- the dopant may be chosen from divalent manganese, divalent rare earths and the group comprising trivalent rare earths in combination with an alkali, the dopant being more particularly europium II, ytterbium in combination with an alkaline.
- the luminophore of formula (1) used for the invention is generally prepared by a reaction in the solid state at high temperature.
- the oxides of the required metals or organic or inorganic forming these oxides by heating such as carbonates, oxalates, hydroxides, acetates, nitrates, borates of said metals.
- An intimate mixture, especially by grinding, is formed at the appropriate concentrations of all the starting materials in the finely divided state.
- a starting mixture by coprecipitation from solutions of the precursors of the desired oxides, for example in an aqueous medium.
- the mixture of starting materials is then heated at least once for a period of from about one hour to about one hundred hours at a temperature of about 500 ° C to about 1300 ° C; it is preferable to carry out the heating in the presence of a stream, for example of the NH 4 CI type, and at least partly under a reducing atmosphere (hydrogen in argon, for example) to bring the europium completely to the atmosphere. divalent state.
- a stream for example of the NH 4 CI type
- a reducing atmosphere hydrogen in argon, for example
- This composition corresponds to the formula (1) given above with the aforementioned values of x and y. All the more particular values of x and y which have been mentioned above as well as what has been said for possible partial substitutions of barium, magnesium and silicon also apply here for this luminophore. But, unlike the phosphor of the first mode which is phasically pure, it is in the form of a mixture of at least three phases. It consists of at least Ba 2 SiO 1 Ba 2 MgSi 2 ⁇ 7 and Ba 3 MgSi 2 ⁇ 8 phases. An additional phase of the BaCO 3 type may possibly be present. The existence of these phases is evidenced by the X-ray analysis and the resulting diagrams.
- the LED of the invention that emits in the . white includes only a single phosphor.
- the luminophore of the second embodiment may also be prepared by solid / solid reaction at high temperature from the oxides of the required metals or organic or inorganic compounds capable of forming these oxides by heating such as carbonates, oxalates, hydroxides, acetates, nitrates, borates of said metals.
- a homogeneous mixture is formed at the appropriate concentrations of all the starting materials.
- This mixing is done simply by deagglomeration of the powders of the starting products without implementing a grinding. It is then calcined. This calcination can be done without flow. It is preferably carried out at least partly under a reducing atmosphere (hydrogen in argon for example) for the reason given above and at a temperature which is of at least 500 ° C. and at most 1150 ° C. preferably.
- a reducing atmosphere hydrogen in argon for example
- it is preferable to use phosphors whose sizes are at most 20 ⁇ m and preferably at most 10 ⁇ m and whose average size may be for example between 3 ⁇ m and 6 ⁇ m.
- the phosphor (s) are incorporated in a polymer matrix, of the epoxy type, for example, in which the aforementioned radiation emission source is inserted. , the assembly being placed in a housing.
- the white colorimetry of the light emitted by the LED depends on the nature of the two phosphors and their respective proportions. In known manner, these proportions can be defined from the determination of the relative quantum yields of each of the phosphors.
- the invention finally relates to a lighting device which is characterized in that it comprises a diode of the type described above.
- Such devices such as lamps, are well known and consist for example of one or more LEDs, inserted in layers, in housings whose surface is transparent. Examples will now be given.
- EXAMPLE 1 This example relates to a luminophore that can be used for the first embodiment of the invention and corresponds to the composition Ba 3 MgSi 2 O 8 : 2% Eu 2+ .
- the solid process is carried out by mixing the oxides BaCO 3 , Eu 2 O 3 , (MgCO 3 ) Mg (OH) 2.5H 2 O, MnCO 3 and SiO 2 in stoichiometric proportions. 0.4 mole of NH CI is added to the mixture as a flux.
- These starting materials are mixed homogeneously by grinding; the mixture, placed in a crucible, is introduced into an oven where it undergoes two heat treatments. A first heat treatment is carried out at 600 ° C. for 4 hours in air. The mixture, gray in color, is then ground and then returned to the oven in an alumina crucible. After a 4 hour purge of the oven with a 10% Ar / h mixture, the mixture is heated for 4 hours at 1200 ° C. in this reducing atmosphere. A rise and fall ramp of 360 ° C / h is used. The product obtained is in the form of a white powder.
- EXAMPLE 2 This example relates to a luminophore that can be used for the first embodiment of the invention and corresponds to the composition Ba 3 MgSi 2 ⁇ 8 : 2% Eu 2+ , 20% Mn 2+ and corresponding to the formula Ba 2 , 94 Eu 0 , o 6 Mgo, 8 Mno, 2 Si 2 ⁇ 8 .
- the procedure is as in Example 1, solid, by mixing the oxides BaCO 3 , Eu 2 O 3 , (MgCO 3 ) 4 Mg (OH) 2 .5H 2 O, MnCO 3 and SiO 2 in stoichiometric proportions. 0.4 mole of NH 4 CI is added to the mixture as a flux.
- the curves of FIG. 1 give, for the compounds thus obtained, the emission spectrum for an excitation wavelength of 370 nm. It can thus be seen that in response to excitation in the UV range, the compounds emit in the red (peak around 625 nm) and also in the blue (peak around 440 nm).
- the excitation spectrum of the compound of Example 1, for the emission wavelength 623 nm, is represented in FIG. 2. It appears from this figure that the maximum yield is reached for a wavelength of 350nm. Between 350nm and 400nm the relative yield varies between 100% and 78%.
- EXAMPLE 3 A mixture of the luminophore of Example 1 is formed with the compound of formula (S0 g5urj ⁇ ⁇ 5) Ga2 1S4 obtained in the manner described in Example 1 of WO 02/100976, in different mass proportions.
- the trichromatic coordinates of the mixtures obtained are given below. These coordinates are calculated from the emission spectrum of the mixtures and according to standard NF X 08-12 (System x, y CIE 1931).
- EXAMPLE 4 This example relates to a luminophore usable for the second embodiment of the invention.
- the compound prepared is identical to that of Example 1 for its formulation.
- the procedure is as described in Example 1 starting from the same starting materials and in the same quantities. However, these products are simply mixed and deagglomerated without being ground.
- the calcination is then carried out as in Example 1.
- FIG. 3 gives, for the compound thus obtained, the emission spectrum for an excitation wavelength of 370 nm. So we see that in response to excitation in the UV field, the compound emits in the red (peak around 625 nm), in the blue (peak around 440 nm) and also in the green (peak around 510 nm).
- EXAMPLES 5 to 7 These examples relate to luminophores that can be used for the first embodiment of the invention.
- the procedure is as in Example 1 by mixing the starting materials and grinding for 30 minutes.
- a first heat treatment is carried out at 950 ° C for 2 hours in air.
- the product resulting from the calcination is mixed with 1% by weight of NH 4 Cl in 30 minutes.
- the mixture is then heated for 4 hours at 1200 ° C in a reducing atmosphere composed of an Ar / H 2 5% H 2.
- the product is crushed slightly.
- the amounts used of the starting materials (in g) are given in Table 1 and in Table 2 the formulas of the luminophores obtained are given.
- the curves of FIG. 4 give, for the compounds thus obtained, the emission spectrum for an excitation wavelength of 370 nm. It can be seen that the compound of Example 5 has intensities for the blue and the red. substantially similar emissions. On the other hand, the red color is maximized for the compound of Example 6
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- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Luminescent Compositions (AREA)
- Led Device Packages (AREA)
- Electroluminescent Light Sources (AREA)
Abstract
Description
Claims
Priority Applications (9)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL05753855T PL1735404T3 (pl) | 2004-04-16 | 2005-04-06 | Dioda elektroluminescencyjna emitująca światło białe |
EP05753855A EP1735404B1 (fr) | 2004-04-16 | 2005-04-06 | Diode electroluminescente emettant une lumiere blanche |
CN200580011468XA CN1942553B (zh) | 2004-04-16 | 2005-04-06 | 白色发光二极管 |
MXPA06011944A MXPA06011944A (es) | 2004-04-16 | 2005-04-06 | Diodo electroluminescente emitiendo una luz blanca. |
DE602005022846T DE602005022846D1 (de) | 2004-04-16 | 2005-04-06 | Weisses licht emittierende diode |
CA002560470A CA2560470C (fr) | 2004-04-16 | 2005-04-06 | Diode electroluminescente emettant une lumiere blanche |
US11/547,154 US7968005B2 (en) | 2004-04-16 | 2005-04-06 | White light emitting diode |
AT05753855T ATE477316T1 (de) | 2004-04-16 | 2005-04-06 | Weisses licht emittierende diode |
JP2007507812A JP4799549B2 (ja) | 2004-04-16 | 2005-04-06 | 白色発光ダイオード |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0404045A FR2869159B1 (fr) | 2004-04-16 | 2004-04-16 | Diode electroluminescente emettant une lumiere blanche |
FR0404045 | 2004-04-16 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2005112135A2 true WO2005112135A2 (fr) | 2005-11-24 |
WO2005112135A3 WO2005112135A3 (fr) | 2006-01-19 |
Family
ID=34944943
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/FR2005/000841 WO2005112135A2 (fr) | 2004-04-16 | 2005-04-06 | Diode electroluminescente emettant une lumiere blanche |
Country Status (13)
Country | Link |
---|---|
US (1) | US7968005B2 (fr) |
EP (1) | EP1735404B1 (fr) |
JP (1) | JP4799549B2 (fr) |
KR (1) | KR100864124B1 (fr) |
CN (2) | CN1942553B (fr) |
AT (1) | ATE477316T1 (fr) |
CA (1) | CA2560470C (fr) |
DE (1) | DE602005022846D1 (fr) |
FR (1) | FR2869159B1 (fr) |
MX (1) | MXPA06011944A (fr) |
PL (1) | PL1735404T3 (fr) |
TW (1) | TWI481061B (fr) |
WO (1) | WO2005112135A2 (fr) |
Cited By (4)
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WO2008078711A1 (fr) * | 2006-12-25 | 2008-07-03 | Kyocera Corporation | Substance fluorescente, son procédé de fabrication, convertisseur de longueur d'onde, dispositif fluorescent et illuminateur |
JP2008163061A (ja) * | 2006-12-27 | 2008-07-17 | Kyushu Institute Of Technology | 蛍光体及びランプ |
JP2008208203A (ja) * | 2007-02-26 | 2008-09-11 | Kyocera Corp | 蛍光体とその製造方法および波長変換器ならびに発光装置 |
US8057703B2 (en) * | 2007-12-12 | 2011-11-15 | Wei-Hung Lo | Three-band phosphor for multi-layer agricultural plastic film |
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FR2846663B1 (fr) * | 2002-11-05 | 2006-08-11 | Rhodia Elect & Catalysis | Materiau transformant la lumiere, notamment pour parois de serres, comprenant comme additif un silicate de baryum et de magnesium |
JP4949793B2 (ja) * | 2006-09-29 | 2012-06-13 | 京セラ株式会社 | 蛍光体及び波長変換器ならびに発光装置 |
JP4991362B2 (ja) * | 2007-01-29 | 2012-08-01 | 京セラ株式会社 | 蛍光体とその製造方法および波長変換器ならびに発光装置 |
JP5036454B2 (ja) * | 2007-08-29 | 2012-09-26 | 京セラ株式会社 | 蛍光体粒子および波長変換器ならびに発光装置 |
TW200946829A (en) * | 2008-02-21 | 2009-11-16 | Koninkl Philips Electronics Nv | GLS-alike LED light source |
JP2009280793A (ja) * | 2008-04-24 | 2009-12-03 | Kyocera Corp | 蛍光体および波長変換器ならびに発光装置、照明装置 |
EP2446487B1 (fr) * | 2009-06-24 | 2016-07-13 | Seoul Semiconductor Co., Ltd. | Dispositif électroluminescent employant des substances luminescentes dotées de luminophores d oxyorthosilicate |
US8592829B2 (en) * | 2009-08-17 | 2013-11-26 | Osram Sylvania Inc. | Phosphor blend for an LED light source and LED light source incorporating same |
JP5633845B2 (ja) * | 2009-11-30 | 2014-12-03 | 独立行政法人産業技術総合研究所 | フォトクロミック物質及びその製造方法 |
US20120153184A1 (en) * | 2010-12-21 | 2012-06-21 | Honeywell International Inc. | Luminescent phosphor-containing materials, and methods for their production and use in authenticating articles |
JP5689407B2 (ja) * | 2011-12-28 | 2015-03-25 | 宇部マテリアルズ株式会社 | ケイ酸塩緑色発光蛍光体 |
CN102585823A (zh) * | 2012-01-31 | 2012-07-18 | 厦门大学 | 一种紫外led激发三基色氮氧化物荧光粉及其合成方法 |
US8679367B2 (en) * | 2012-08-09 | 2014-03-25 | Intematix Corporation | Green-emitting (oxy)nitride-based phosphors and light-emitting device using the same |
SG11201604518YA (en) * | 2013-12-04 | 2016-07-28 | Merck Patent Gmbh | EU<sp>2+</sp> -ACTIVATED PHOSPHORS |
WO2016001219A1 (fr) * | 2014-06-30 | 2016-01-07 | Rhodia Operations | Suspension d'un silicate de magnésium, procédé pour sa fabrication, et son utilisation en tant que luminophore |
JP5799434B2 (ja) * | 2014-08-27 | 2015-10-28 | 独立行政法人 国立印刷局 | 残光性発光体とその作製方法、残光性発光インキ組成物及び真偽判別印刷物 |
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JP3679695B2 (ja) | 1999-08-12 | 2005-08-03 | 東京エレクトロン株式会社 | 現像装置、基板処理装置及び現像方法 |
JP3515737B2 (ja) * | 2000-06-22 | 2004-04-05 | 松下電器産業株式会社 | 蛍光体およびそれを用いた蛍光ランプ |
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JP4077170B2 (ja) | 2000-09-21 | 2008-04-16 | シャープ株式会社 | 半導体発光装置 |
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- 2004-04-16 FR FR0404045A patent/FR2869159B1/fr not_active Expired - Fee Related
-
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- 2005-04-06 CA CA002560470A patent/CA2560470C/fr not_active Expired - Fee Related
- 2005-04-06 EP EP05753855A patent/EP1735404B1/fr not_active Not-in-force
- 2005-04-06 US US11/547,154 patent/US7968005B2/en not_active Expired - Fee Related
- 2005-04-06 JP JP2007507812A patent/JP4799549B2/ja not_active Expired - Fee Related
- 2005-04-06 KR KR1020067021263A patent/KR100864124B1/ko not_active IP Right Cessation
- 2005-04-06 AT AT05753855T patent/ATE477316T1/de not_active IP Right Cessation
- 2005-04-06 MX MXPA06011944A patent/MXPA06011944A/es active IP Right Grant
- 2005-04-06 CN CN200580011468XA patent/CN1942553B/zh not_active Expired - Fee Related
- 2005-04-06 CN CN201010208223.9A patent/CN101864299B/zh not_active Expired - Fee Related
- 2005-04-06 DE DE602005022846T patent/DE602005022846D1/de active Active
- 2005-04-06 WO PCT/FR2005/000841 patent/WO2005112135A2/fr active Application Filing
- 2005-04-06 PL PL05753855T patent/PL1735404T3/pl unknown
- 2005-04-15 TW TW094112145A patent/TWI481061B/zh not_active IP Right Cessation
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008078711A1 (fr) * | 2006-12-25 | 2008-07-03 | Kyocera Corporation | Substance fluorescente, son procédé de fabrication, convertisseur de longueur d'onde, dispositif fluorescent et illuminateur |
EP2116586A1 (fr) * | 2006-12-25 | 2009-11-11 | Kyocera Corporation | Substance fluorescente, son procédé de fabrication, convertisseur de longueur d'onde, dispositif fluorescent et illuminateur |
JPWO2008078711A1 (ja) * | 2006-12-25 | 2010-04-22 | 京セラ株式会社 | 蛍光体およびその製法ならびに波長変換器、発光装置、照明装置 |
EP2116586A4 (fr) * | 2006-12-25 | 2012-03-07 | Kyocera Corp | Substance fluorescente, son procédé de fabrication, convertisseur de longueur d'onde, dispositif fluorescent et illuminateur |
JP5137850B2 (ja) * | 2006-12-25 | 2013-02-06 | 京セラ株式会社 | 蛍光体およびそれを用いた波長変換器、発光装置、照明装置 |
JP2008163061A (ja) * | 2006-12-27 | 2008-07-17 | Kyushu Institute Of Technology | 蛍光体及びランプ |
JP2008208203A (ja) * | 2007-02-26 | 2008-09-11 | Kyocera Corp | 蛍光体とその製造方法および波長変換器ならびに発光装置 |
US8057703B2 (en) * | 2007-12-12 | 2011-11-15 | Wei-Hung Lo | Three-band phosphor for multi-layer agricultural plastic film |
Also Published As
Publication number | Publication date |
---|---|
CN1942553B (zh) | 2013-05-29 |
EP1735404B1 (fr) | 2010-08-11 |
JP2007533149A (ja) | 2007-11-15 |
CA2560470A1 (fr) | 2005-11-24 |
WO2005112135A3 (fr) | 2006-01-19 |
FR2869159B1 (fr) | 2006-06-16 |
CN101864299B (zh) | 2015-01-14 |
FR2869159A1 (fr) | 2005-10-21 |
TW200605396A (en) | 2006-02-01 |
JP4799549B2 (ja) | 2011-10-26 |
CN101864299A (zh) | 2010-10-20 |
KR100864124B1 (ko) | 2008-10-16 |
KR20070013282A (ko) | 2007-01-30 |
PL1735404T3 (pl) | 2011-02-28 |
CN1942553A (zh) | 2007-04-04 |
US20080035888A1 (en) | 2008-02-14 |
TWI481061B (zh) | 2015-04-11 |
US7968005B2 (en) | 2011-06-28 |
DE602005022846D1 (de) | 2010-09-23 |
CA2560470C (fr) | 2009-12-22 |
MXPA06011944A (es) | 2006-12-15 |
ATE477316T1 (de) | 2010-08-15 |
EP1735404A2 (fr) | 2006-12-27 |
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