US20060138388A1 - Phosphor for light sources and associated light source - Google Patents

Phosphor for light sources and associated light source Download PDF

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US20060138388A1
US20060138388A1 US11/359,267 US35926706A US2006138388A1 US 20060138388 A1 US20060138388 A1 US 20060138388A1 US 35926706 A US35926706 A US 35926706A US 2006138388 A1 US2006138388 A1 US 2006138388A1
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phosphor
oxide
garnet
emission
mixture
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Franz Kummer
Franz Zwaschka
Andries Ellens
Alexandra Debray
Guenther Waitl
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Priority claimed from DE19934126A external-priority patent/DE19934126A1/en
Priority claimed from DE19951790A external-priority patent/DE19951790A1/en
Priority claimed from DE19963791A external-priority patent/DE19963791A1/en
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Priority to US11/359,267 priority Critical patent/US20060138388A1/en
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    • 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
    • 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
    • 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
    • C09K11/7715—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals containing cerium
    • 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
    • C09K11/7766—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals containing two or more rare earth metals
    • C09K11/7767—Chalcogenides
    • C09K11/7769—Oxides
    • 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
    • C09K11/7766—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals containing two or more rare earth metals
    • C09K11/7774—Aluminates
    • H—ELECTRICITY
    • H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
    • H05B33/00—Electroluminescent light sources
    • H05B33/12—Light sources with substantially two-dimensional radiating surfaces
    • H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
    • 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
    • H01L33/504—Elements with two or more wavelength conversion materials

Definitions

  • the invention relates in particular to a yellow-emitting garnet phosphor for excitation by a light source with short wavelengths in the visible blue spectral region, with the result that white light is generated.
  • a lamp primarily a fluorescent lamp
  • an LED light-emitting diode
  • WO 98/05078 has already disclosed a phosphor for light sources and an associated light source.
  • the phosphor used is a garnet of the structure A 3 B 5 O 12 , the host lattice of which, as first component A, comprises at least one of the rare earths Y, Lu, Sc, La, Gd or Sm. Furthermore, one of the elements Al, Ga or In is used for the second component B. The only dopant used is Ce.
  • a very similar phosphor is known from WO 97/50132.
  • the dopant used in that document is either Ce or Tb. While Ce emits in the yellow spectral region, the emission from Tb is in the green spectral region. In both cases, the complementary color principle (blue-emitting light source and yellow-emitting phosphor) is used to achieve a white luminous color.
  • EP-A 124 175 describes a fluorescent lamp which, in addition to a mercury fill, contains a plurality of phosphors. These are excited by UV radiation (254 nm) or also by short-wave radiation at 460 nm. Three phosphors are selected in such a way that they add up to form white (color mixture).
  • a phosphor which has a garnet structure A 3 B 5 O 12 and which is doped with Ce is used, the second component B representing at least one of the elements Al and Ga and the first component A containing terbium.
  • the process for producing the phosphor is characterized by the following process steps: (a) comminution of the oxides and addition of a flux; (b) first firing in forming gas; (c) milling and screening; and (d) second firing.
  • terbium is suitable as a constituent of the host lattice (first component of the garnet) for a yellow-emitting phosphor, the activator of which is cerium.
  • Tb has only been considered as an activator or coactivator, together with cerium, for emission in the green region, if excitation is produced by cathode rays (electrons) or short-wave UV photons (GB-A 1 600 492 and EP-A 208 713).
  • terbium as the principal constituent of the first component A of the garnet, can be used on its own or together with at least one of the rare earths Y, Gd, La and/or Lu.
  • At least one of the elements Al or Ga is used as the second component.
  • the second component B may additionally contain In.
  • the activator is cerium.
  • a garnet of the structure (Tb 1-x-y RE x Ce y ) 3 (Al, Ga) 5 O 12 where
  • the phosphor absorbs in the range from 420 to 490 nm and can thus be excited by the radiation from a blue light source, which is in particular the radiation source for a lamp or LED. Good results have been achieved with a blue LED whose emission peak was at 430 to 470 nm.
  • the emission peak of the Tb-garnet: Ce phosphor is at approximately 550 nm.
  • This phosphor is particularly useful for use in a white LED based on the combination of a blue LED with the Tb-garnet-containing phosphor, which is excited by absorption of part of the emission from the blue LED and the emission from which supplements a remaining radiation from the LED, to form white light.
  • a Ga(In)N-LED is particularly suitable as the blue LED, but any other route for producing a blue LED which emits in the range from 420 to 490 nm is also suitable. 430 to 470 nm is particularly recommended as the principal emission region, since this is where efficiency is highest.
  • the particularly preferred range for y is 0.02 ⁇ y ⁇ 0.06.
  • the phosphor according to the invention is also suitable for combination with other phosphors.
  • 0 ⁇ y ⁇ 0.1 has proven particularly suitable as the phosphor.
  • Y frequently lies in the range from 0.01 to 0.05.
  • Tb in the host lattice serve primarily to improve the properties of known cerium-activated phosphors, while the addition of relatively large amounts of Tb can be used in a controlled way in particular to shift the wavelength of the emission from known cerium-activated phosphors. Therefore, a high proportion of Tb is particularly suitable for white LEDs with a low color temperature of below 5000 K.
  • FIG. 1 shows an emission spectrum of a first Tb-garnet phosphor
  • FIG. 2 shows the reflectance spectrum of this Tb-garnet phosphor
  • FIG. 3 shows emission spectra of further Tb-garnet phosphors
  • FIG. 4 shows reflectance spectra of the Tb-garnet phosphors from FIG. 3 ;
  • FIG. 5 shows emission spectra for further Tb-garnet phosphors
  • FIG. 6 shows reflectance spectra for the Tb-garnet phosphors from FIG. 5 ;
  • FIG. 7 shows an emission spectrum for a white LED with Tb-garnet phosphor.
  • the phosphor obtained corresponds to the composition (Y 0.29 Tb 0.67 Ce 0.04 ) 3 Al 5 O 12 . It has a strong yellow body color. An emission spectrum for this phosphor when excited at 430 nm and a reflectance spectrum for the phosphor between 300 and 800 nm are shown in FIGS. 1 and 2 .
  • the components 43.07 g Terbium oxide Tb 4 O 7 1.65 g Cerium oxide CeO 2 21.13 g Aluminum oxide Al 2 O 3 0.12 g Barium fluoride BaF 2 0.062 g Boric acid H 3 BO 3 are intimately mixed and processed as described under Example 1.
  • the phosphor obtained corresponds to the overall composition (Tb0.96Ce 0.04 ) 3 Al 5 O 12 or, in the representation which illustrates the host lattice, Tb 3 Al 5 O 12 :Ce. It has a strong yellow body color.
  • the X-ray diffraction diagram shows that there is a cubic garnet phase.
  • the emission spectrum and reflectance spectrum for this phosphor are shown in FIGS. 3 and 4 , respectively.
  • the components 32.18 g Yttrium oxide Y 2 O 3 0.56 g Terbium oxide Tb 4 O 7 2.07 g Cerium oxide CeO 2 26.41 g Aluminum oxide Al 2 O 3 0.077 g Boric acid H 3 BO 3 are intimately mixed and processed as described under Example No. 1.
  • the phosphor obtained corresponds to the composition (Y 0.95 Tb 0.01 Ce 0.04 ) 3 Al 5 O 12 . It has a strong yellow body color.
  • the emission spectrum and reflectance spectrum for this phosphor are shown in FIGS. 3 and 4 , respectively.
  • the components 26.76 g Yttrium oxide Y 2 O 3 9.53 g Terbium oxide Tb 4 O 7 2.07 g Cerium oxide CeO 2 26.41 g Aluminum oxide Al 2 O 3 0.149 g Barium fluoride BaF 2 0.077 g Boric acid H 3 BO 3 are intimately mixed and processed as described under Example No. 1.
  • the phosphor obtained corresponds to the composition (Y 0.79 Tb 0.17 Ce 0.04 ) 3 Al 5 O 12 . It has a strong yellow body color.
  • the emission spectrum and reflectance spectrum for this phosphor are shown in FIGS. 3 and 4 , respectively.
  • the components 30.82 g Yttrium oxide Y 2 O 3 0.56 g Terbium oxide Tb 4 O 7 4.13 g Cerium oxide CeO 2 26.41 g Aluminum oxide Al 2 O 3 0.149 g Barium fluoride BaF 2 0.077 g Boric acid H 3 BO 3 are intimately mixed and processed as described under Example No. 1.
  • the phosphor obtained corresponds to the composition (Y 0.91 Tb 0.01 Ce 0.08 ) 3 Al 5 O 12 . It has a strong yellow body color.
  • the components 43.07 g Terbium oxide Tb 4 O 7 1.65 g Cerium oxide CeO 2 21.13 g Aluminum oxide Al 2 O 3 0.062 g Boric acid H 3 BO 3 are intimately mixed and processed as described under Example 1, except that the temperature during the two firings is lower by 50° C. in each case.
  • the phosphor obtained corresponds to the composition (Tb0.96Ce 0.04 ) 3 Al 5 O 12 . It has a strong yellow body color.
  • the emission spectrum and reflectance spectrum for this phosphor are shown in FIGS. 5 and 6 , respectively.
  • the components 43.07 g Terbium oxide Tb 4 O 7 1.65 g Cerium oxide CeO 2 17.05 g Aluminum oxide Al 2 O 3 7.50 g Gallium oxide Ga 2 O 3 0.062 g Boric acid H 3 BO 3 are intimately mixed and processed as described under Example 1, except that the temperature for the two firings is lower by 50° C. in each case.
  • the phosphor obtained corresponds to the composition (Tb 0.96 Ce 0.04 )Al 4 GaO 12 . It has a strong yellow body color.
  • the emission spectrum and reflectance spectrum for this phosphor are shown in FIGS. 5 and 6 , respectively.
  • the components 43.07 g Terbium oxide Tb 4 O 7 1.65 g Cerium oxide CeO 2 12.97 g Aluminum oxide Al 2 O 3 15.00 g Gallium oxide Ga 2 O 3 0.062 g Boric acid H 3 BO 3 are intimately mixed and processed as described under Example 1, except that the temperature for the two firings is lower by 50° C. in each case.
  • the phosphor obtained corresponds to the composition (Tb 0.96 Ce 0.04 ) 3 Al 3 Ga 2 O 12 . It has a yellow body color.
  • the emission spectrum and reflectance spectrum of this phosphor are shown in FIGS. 5 and 6 , respectively.
  • the components 4.88 kg Yttrium oxide Y 2 O 3 7.05 kg Gadolinium oxide Gd 2 O 3 161.6 g Terbium oxide Tb 4 O 7 595 g Cerium oxide CeO 2 7.34 kg Aluminum oxide Al 2 O 3 5.50 g Boric acid H 3 BO 3 are mixed for 24 hours in a 60 l polyethylene vessel. The mixture is introduced into crucibles made from aluminum oxide with a capacity of approx. 1 l and is fired in a pushed-bat kiln for 6 hours at 1550° C. under forming gas. The fired material is milled in an automatic mortar mill and then finely screened. The phosphor obtained has the composition (Y 0.50 Gd 0.45 Tb 0.01 Ce 0.04 ) 3 Al 5 O 12 . It has a strong yellow body color. The emission spectrum and reflectance spectrum for this phosphor are shown in FIGS. 3 and 4 , respectively.
  • the phosphors described above generally have a yellow body color. They emit in the yellow spectral region. When Ga is added or used on its own instead of Al, the emission shifts more toward green, so that it is also possible in particular to achieve higher color temperatures.
  • Ga-containing (or Ga,Al-containing) Tb-garnets and purely Al-containing Tb-garnets can be used in mixed form in order to be able to adapt to desired color loci.

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Abstract

A phosphor for light sources, the emission from which lies in the short-wave optical spectral region, as a garnet structure A3B5O12. It is activated with Ce, the second component B representing at least one of the elements Al and Ga, and the first component A is terbium or terbium together with at least one of the elements Y, Gd, La and/or Lu.
In a preferred embodiment, a phosphor having a garnet of structure (Tb1-x-yRExCey)3(Al,Ga)5O12, where
RE=Y, Gd, La and/or Lu;
0≦x≦0.5−y;
0<y<0.1 is used.

Description

    CROSS REFERENCES TO RELATED APPLICATIONS
  • This application is a continuation of copending application Ser. No. 10/687,436, filed Oct. 16, 2003, which is a continuation of Ser. No. 09/787,208, filed Mar. 15, 2001, now U.S. Pat. No. 6,669,866.
    • TECHNICAL FIELD
  • The invention relates in particular to a yellow-emitting garnet phosphor for excitation by a light source with short wavelengths in the visible blue spectral region, with the result that white light is generated. A lamp (primarily a fluorescent lamp) or an LED (light-emitting diode) is particularly suitable as the light source.
    • PRIOR ART
  • WO 98/05078 has already disclosed a phosphor for light sources and an associated light source. In that document, the phosphor used is a garnet of the structure A3B5O12, the host lattice of which, as first component A, comprises at least one of the rare earths Y, Lu, Sc, La, Gd or Sm. Furthermore, one of the elements Al, Ga or In is used for the second component B. The only dopant used is Ce.
  • A very similar phosphor is known from WO 97/50132. The dopant used in that document is either Ce or Tb. While Ce emits in the yellow spectral region, the emission from Tb is in the green spectral region. In both cases, the complementary color principle (blue-emitting light source and yellow-emitting phosphor) is used to achieve a white luminous color.
  • Finally, EP-A 124 175 describes a fluorescent lamp which, in addition to a mercury fill, contains a plurality of phosphors. These are excited by UV radiation (254 nm) or also by short-wave radiation at 460 nm. Three phosphors are selected in such a way that they add up to form white (color mixture).
    • SUMMARY OF THE INVENTION
  • According to the invention, for light sources from which the emission lies in the short-wave optical spectral region, a phosphor which has a garnet structure A3B5O12 and which is doped with Ce is used, the second component B representing at least one of the elements Al and Ga and the first component A containing terbium. The process for producing the phosphor is characterized by the following process steps: (a) comminution of the oxides and addition of a flux; (b) first firing in forming gas; (c) milling and screening; and (d) second firing. Surprisingly, it has been found that under particular circumstances, namely under blue excitation in the range from 420 to 490 nm, terbium (Tb) is suitable as a constituent of the host lattice (first component of the garnet) for a yellow-emitting phosphor, the activator of which is cerium. Previously, in this context Tb has only been considered as an activator or coactivator, together with cerium, for emission in the green region, if excitation is produced by cathode rays (electrons) or short-wave UV photons (GB-A 1 600 492 and EP-A 208 713).
  • In this case, terbium, as the principal constituent of the first component A of the garnet, can be used on its own or together with at least one of the rare earths Y, Gd, La and/or Lu.
  • At least one of the elements Al or Ga is used as the second component. The second component B may additionally contain In. The activator is cerium. In a particularly preferred embodiment, a garnet of the structure
    (Tb1-x-yRExCey)3(Al, Ga)5O12, where
  • RE=Y, Gd, La and/or Lu;
  • 0≦x≦0.5-y;
  • 0<y<0.1 is used.
  • The phosphor absorbs in the range from 420 to 490 nm and can thus be excited by the radiation from a blue light source, which is in particular the radiation source for a lamp or LED. Good results have been achieved with a blue LED whose emission peak was at 430 to 470 nm. The emission peak of the Tb-garnet: Ce phosphor is at approximately 550 nm.
  • This phosphor is particularly useful for use in a white LED based on the combination of a blue LED with the Tb-garnet-containing phosphor, which is excited by absorption of part of the emission from the blue LED and the emission from which supplements a remaining radiation from the LED, to form white light.
  • A Ga(In)N-LED is particularly suitable as the blue LED, but any other route for producing a blue LED which emits in the range from 420 to 490 nm is also suitable. 430 to 470 nm is particularly recommended as the principal emission region, since this is where efficiency is highest.
  • By selecting the type and quantity of rare earths, it is possible to fine-tune the location of the absorption and emission bands, in a similar way to that which is known from the literature for other phosphors of type YAG:Ce. In conjunction with light-emitting diodes, it is particularly suitable for x to be 0.25≦x≦0.5-y.
  • The particularly preferred range for y is 0.02<y<0.06.
  • The phosphor according to the invention is also suitable for combination with other phosphors.
  • A garnet of structure
    (TbxRE1-x-yCey)3(Al, Ga)5O12,
  • where RE=Y, Gd, La and/or Lu;
  • 0≦x≦0.02, in particular x=0.01;
  • 0<y<0.1 has proven particularly suitable as the phosphor. Y frequently lies in the range from 0.01 to 0.05.
  • Generally, relatively small amounts of Tb in the host lattice serve primarily to improve the properties of known cerium-activated phosphors, while the addition of relatively large amounts of Tb can be used in a controlled way in particular to shift the wavelength of the emission from known cerium-activated phosphors. Therefore, a high proportion of Tb is particularly suitable for white LEDs with a low color temperature of below 5000 K.
    • BRIEF DESCRIPTION OF THE DRAWINGS
  • The invention is to be explained in more detail below with reference to a number of exemplary embodiments. In the drawing:
  • FIG. 1 shows an emission spectrum of a first Tb-garnet phosphor;
  • FIG. 2 shows the reflectance spectrum of this Tb-garnet phosphor;
  • FIG. 3 shows emission spectra of further Tb-garnet phosphors;
  • FIG. 4 shows reflectance spectra of the Tb-garnet phosphors from FIG. 3;
  • FIG. 5 shows emission spectra for further Tb-garnet phosphors;
  • FIG. 6 shows reflectance spectra for the Tb-garnet phosphors from FIG. 5;
  • FIG. 7 shows an emission spectrum for a white LED with Tb-garnet phosphor.
    • DETAILED DESCRIPTION OF THE INVENTION Exemplary Embodiment No. 1
  • The components
    9.82 g Yttrium oxide Y2O3
    2.07 g Cerium oxide CeO2
    37.57 g Terbium oxide Tb4O7
    26.41 g Aluminum oxide Al2O3
    0.15 g Barium fluoride BaF2
    0.077 g Boric acid H3BO3

    are mixed and comminuted together for two hours in a 250 ml polyethylene wide-necked bottle using 150 g of aluminum oxide balls with a diameter of 10 mm. Barium fluoride and boric acid serve as fluxes. The mixture is fired for three hours in a covered corundum crucible at 1550° C. in forming gas (nitrogen containing 2.3% by volume hydrogen) and then milled in an automatic mortar mill and screened through a screen with a mesh width of 53 μm. This is followed by a second firing for three hours at 1500° C. under forming gas (nitrogen containing 0.5% by volume hydrogen). Then, milling and screening is carried out as after the first firing. The phosphor obtained corresponds to the composition (Y0.29Tb0.67Ce0.04)3Al5O12. It has a strong yellow body color. An emission spectrum for this phosphor when excited at 430 nm and a reflectance spectrum for the phosphor between 300 and 800 nm are shown in FIGS. 1 and 2.
    • Exemplary Embodiment No. 2
  • The components
    43.07 g Terbium oxide Tb4O7
    1.65 g Cerium oxide CeO2
    21.13 g Aluminum oxide Al2O3
    0.12 g Barium fluoride BaF2
    0.062 g Boric acid H3BO3

    are intimately mixed and processed as described under Example 1. The phosphor obtained corresponds to the overall composition (Tb0.96Ce0.04)3Al5O12 or, in the representation which illustrates the host lattice, Tb3Al5O12:Ce. It has a strong yellow body color. The X-ray diffraction diagram shows that there is a cubic garnet phase. The emission spectrum and reflectance spectrum for this phosphor are shown in FIGS. 3 and 4, respectively.
    • Exemplary Embodiment No. 3
  • The components
    32.18 g Yttrium oxide Y2O3
    0.56 g Terbium oxide Tb4O7
    2.07 g Cerium oxide CeO2
    26.41 g Aluminum oxide Al2O3
    0.077 g Boric acid H3BO3

    are intimately mixed and processed as described under Example No. 1. The phosphor obtained corresponds to the composition (Y0.95Tb0.01Ce0.04)3Al5O12. It has a strong yellow body color. The emission spectrum and reflectance spectrum for this phosphor are shown in FIGS. 3 and 4, respectively.
    • Exemplary Embodiment No. 4
  • The components
    26.76 g Yttrium oxide Y2O3
    9.53 g Terbium oxide Tb4O7
    2.07 g Cerium oxide CeO2
    26.41 g Aluminum oxide Al2O3
    0.149 g Barium fluoride BaF2
    0.077 g Boric acid H3BO3

    are intimately mixed and processed as described under Example No. 1. The phosphor obtained corresponds to the composition (Y0.79Tb0.17Ce0.04)3Al5O12. It has a strong yellow body color. The emission spectrum and reflectance spectrum for this phosphor are shown in FIGS. 3 and 4, respectively.
    • Exemplary Embodiment No. 5
  • The components
    30.82 g Yttrium oxide Y2O3
    0.56 g Terbium oxide Tb4O7
    4.13 g Cerium oxide CeO2
    26.41 g Aluminum oxide Al2O3
    0.149 g Barium fluoride BaF2
    0.077 g Boric acid H3BO3

    are intimately mixed and processed as described under Example No. 1. The phosphor obtained corresponds to the composition (Y0.91Tb0.01Ce0.08)3Al5O12. It has a strong yellow body color.
    • Exemplary Embodiment No. 6
  • The components
    43.07 g Terbium oxide Tb4O7
    1.65 g Cerium oxide CeO2
    21.13 g Aluminum oxide Al2O3
    0.062 g Boric acid H3BO3

    are intimately mixed and processed as described under Example 1, except that the temperature during the two firings is lower by 50° C. in each case. The phosphor obtained corresponds to the composition (Tb0.96Ce0.04)3Al5O12. It has a strong yellow body color. The emission spectrum and reflectance spectrum for this phosphor are shown in FIGS. 5 and 6, respectively.
    • Exemplary Embodiment No. 7
  • The components
    43.07 g Terbium oxide Tb4O7
    1.65 g Cerium oxide CeO2
    17.05 g Aluminum oxide Al2O3
    7.50 g Gallium oxide Ga2O3
    0.062 g Boric acid H3BO3

    are intimately mixed and processed as described under Example 1, except that the temperature for the two firings is lower by 50° C. in each case. The phosphor obtained corresponds to the composition (Tb0.96Ce0.04)Al4GaO12. It has a strong yellow body color. The emission spectrum and reflectance spectrum for this phosphor are shown in FIGS. 5 and 6, respectively.
    • Exemplary Embodiment No. 8
  • The components
    43.07 g Terbium oxide Tb4O7
    1.65 g Cerium oxide CeO2
    12.97 g Aluminum oxide Al2O3
    15.00 g Gallium oxide Ga2O3
    0.062 g Boric acid H3BO3

    are intimately mixed and processed as described under Example 1, except that the temperature for the two firings is lower by 50° C. in each case. The phosphor obtained corresponds to the composition (Tb0.96Ce0.04)3Al3Ga2O12. It has a yellow body color. The emission spectrum and reflectance spectrum of this phosphor are shown in FIGS. 5 and 6, respectively.
    • Exemplary Embodiment No. 9
  • The components
    4.88 kg Yttrium oxide Y2O3
    7.05 kg Gadolinium oxide Gd2O3
    161.6 g Terbium oxide Tb4O7
    595 g Cerium oxide CeO2
    7.34 kg Aluminum oxide Al2O3
    5.50 g Boric acid H3BO3

    are mixed for 24 hours in a 60 l polyethylene vessel. The mixture is introduced into crucibles made from aluminum oxide with a capacity of approx. 1 l and is fired in a pushed-bat kiln for 6 hours at 1550° C. under forming gas. The fired material is milled in an automatic mortar mill and then finely screened. The phosphor obtained has the composition (Y0.50Gd0.45Tb0.01Ce0.04)3Al5O12. It has a strong yellow body color. The emission spectrum and reflectance spectrum for this phosphor are shown in FIGS. 3 and 4, respectively.
    • Exemplary Embodiment 10 (LED)
  • When these phosphors are used in a white LED together with GaInN, a structure similar to that described in WO 97/50132 is employed. By way of example, identical fractions of phosphor in accordance with Example 1 and of phosphor in accordance with Example 4 are dispersed in epoxy resin and a LED with an emission peak of approximately 450 nm (blue) is encapsulated by this resin mixture. The emission spectrum of a white LED obtained in this way is shown in FIG. 7. In this case, the mixture of the blue LED radiation with the yellow phosphor emission results in a color locus of x=0.359/y=0.350, corresponding to white light of color temperature 4500 K.
  • The phosphors described above generally have a yellow body color. They emit in the yellow spectral region. When Ga is added or used on its own instead of Al, the emission shifts more toward green, so that it is also possible in particular to achieve higher color temperatures. In particular, Ga-containing (or Ga,Al-containing) Tb-garnets and purely Al-containing Tb-garnets can be used in mixed form in order to be able to adapt to desired color loci.

Claims (9)

1-11. (canceled)
12. A process for producing an Al-containing Tb-garnet phosphor, a Ga-containing Tb-garnet phosphor, or a Ga,Al-containing Tb-garnet phosphor, the process comprising:
(a) intimately mixing an oxide of cerium, an oxide of terbium or terbium and at least one of Y, Gd, La, and/or Lu, at least one oxide of Al and Ga, and at least one flux to form a mixture; and
(b) firing the mixture in forming gas to form the phosphor.
13. The process of claim 12 wherein the flux is BaF2, HBO3, or both.
14. The process of claim 12 wherein the forming gas is a mixture of nitrogen and hydrogen gases wherein the hydrogen is 2.3% by volume.
15. The process of claim 12 wherein a stoichiometric excess of aluminum oxide is used to form the mixture.
16. The process of claim 12 wherein the mixture is fired at a temperature from 1450° C. to 1550° C.
17. The process of claim 12 wherein the mixture is milled after firing and then fired for a second time in forming gas.
18. The process of claim 17 wherein the firings are performed at a temperature from 1450° C. to 1550° C.
19. The process of claim 18 wherein the firings are each for three hours.
US11/359,267 1999-07-23 2006-02-22 Phosphor for light sources and associated light source Abandoned US20060138388A1 (en)

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DE19934126A DE19934126A1 (en) 1999-07-23 1999-07-23 Fluorescent oxide for forming white LEDs, includes cerium-activated garnet-based oxide with terbium addition
DE19934126.5 1999-07-23
DE19951790.8 1999-10-27
DE19951790A DE19951790A1 (en) 1999-10-27 1999-10-27 Fluorescent for light sources and associated light source
DE19963791A DE19963791A1 (en) 1999-12-30 1999-12-30 Fluorescent oxide for forming white LEDs, includes cerium-activated garnet-based oxide with terbium addition
DE19963791.1 1999-12-30
US09/787,208 US6669866B1 (en) 1999-07-23 2000-07-08 Luminous substance for a light source and light source associates therewith
PCT/DE2000/002241 WO2001008452A1 (en) 1999-07-23 2000-07-08 Luminous substance for a light source and light source associated therewith
US10/687,436 US7115217B2 (en) 1999-07-23 2003-10-16 Phosphor for light sources and associated light source
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EP1116418B1 (en) 2003-10-22
CN100344728C (en) 2007-10-24
HUP0103863A3 (en) 2004-08-30
CA2345114A1 (en) 2001-02-01
CN1654594A (en) 2005-08-17
JP2003505582A (en) 2003-02-12
US7063807B2 (en) 2006-06-20
US20040079956A1 (en) 2004-04-29
US6669866B1 (en) 2003-12-30
WO2001008452A1 (en) 2001-02-01
HU228953B1 (en) 2013-07-29
HUP0103863A2 (en) 2002-03-28
CN1190997C (en) 2005-02-23
KR20010079912A (en) 2001-08-22
EP1378556A3 (en) 2004-01-28
DE50004145D1 (en) 2003-11-27
EP1116418A1 (en) 2001-07-18
DE20023590U1 (en) 2005-02-24
KR100431398B1 (en) 2004-05-14
US7115217B2 (en) 2006-10-03
CN1318271A (en) 2001-10-17
EP1378556A2 (en) 2004-01-07
US20050145868A1 (en) 2005-07-07

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