Patent Application
20120069544
The present invention relates to a light-emitting device, especially to the field of LEDs, comprising a wavelength converting member with a luminescent medium for wavelength conversion (color conversion) of blue light and/or ultraviolet light into red light and/or yellow light and/or green light and a light source emitting blue light and/or ultraviolet light arranged to pump the luminescent medium, said luminescent medium essentially having a main phase of a solid state host material which is doped with Ce3+-ions. The present invention further relates to a corresponding lighting system comprising at least one light emitting device and the corresponding luminescent medium.
A light-emitting device comprising a light source and a wavelength converting member with a luminescent medium for wavelength conversion is known for example as a light-emitting device comprising a Light Emitting Diode (LED) emitting blue light and/or ultraviolet light and a wavelength converting member comprising a phosphor medium in the optical path of the LED for partially converting blue and/or ultraviolet light into yellow and/or green light to generate white light. Said luminescent medium has a main phase of a Ce3+-ions doped sulfide, especially from the group of (Mg, Ca,Sr)S, or a Ce3+-ions doped garnet like Y3Al5O12:Ce (YAG) or (Gd1-xYx)3(Al1-yGay)5O12:Ce (YAGaG:Ce).
Further on light-emitting devices formed as “red-enhanced LEDs” based on additional Eu2+ wideband emitters with high colour rendering but low luminance are known.
It is an object of the present invention to provide light emitting device with an enhanced lumen yield and improved colour rendering.
This object is achieved with the light emitting device with high colour rendering according to claim 1.
The host material comprises ions of a further rare-earth material (Ln: lanthanide), wherein the host material is selected such that the emission energy of the 5d-4f emission on Ce3+-ions is energetically higher than the absorption energy into an upper 4fn state of the further rare-earth material Ln, and wherein the light emission of wavelength converted light is caused by an intra-atomic 4fn-4fn transition within the ions of the further rare-earth material. The Ce3+-ions work as a sensitizer of the further ions of the rare earth material which function as activators, whereby the host material is selected in a way that the (emission) energy difference involving the Ce3+ f1 ground state and the lowest relaxed excited 5d state is larger than the energy difference between the ground- and excited 4f excited states, involved in the emission process, of the Ln3+ ion, to which the energy is transferred. The light-emitting device comprises a wavelength converting member with a luminescent medium for wavelength conversion (color conversion) of blue light and/or ultraviolet light into yellow light and/or green light and/or red light, said luminescent medium essentially having a main phase of a solid state host material which is doped with Ce3+-ions. The pumping scheme involves 4f-5d-transitions in Ce3+-ions, and energy transfer to an upper 4fn state of the trivalent ion of the further rare-earth material, from which additional luminescence emission takes place.
With respect to the present invention, the term “high colour rendering” relates to a light-emitting device with a colour rendering index (CRI) equal to or higher than 70 (CRI≧70).
The light source especially is a Light Emitting Diode (LED), a laser or a discharge lamp and the luminescent medium is a medium for converting the wavelength of one part of the blue and/or ultraviolet light into a red light component caused by the 4fn-4fn transition within the ions of the further rare-earth material and the yellow and/or green and/or red light caused by the main phase of the solid state host material to generate white light. The wavelength of the blue light and/or ultraviolet light is preferably in the spectral region of 300 nm to 480 nm.
A suitable luminescent medium can be found by preparing the Ce-doped solid state host material and measuring the excitation spectrum, the reflection spectrum and the emission spectrum of the resulting luminescent medium in the wavelength region from about 150 nm to about 700 nm.
With respect to the host material according to the invention the term “essentially” means especially that ≧95%, preferably ≧98% and most preferred ≧99.5% of the host material of the gain medium has the desired structure and/or composition.
The term “main phase” implies that there may be further phases, e.g. resulting out of mixture(s) of the above-mentioned materials with additives which may be added e.g. during ceramic processing. These additives may be incorporated fully or in part in the final material, which then may also be a composite of several chemically different species and particularly include such species known to the art as fluxes.
According to a preferred embodiment of the present invention, the further trivalent rare-earth ions are Pr3+, Sm3+, Tb3+, Dy3+ or a mixture thereof to design light-emitting devices emitting light of a different chromaticity, for example with an enhanced red-component of the emitted light. The pumping scheme includes the following steps:
a) Ce3++hν→(Ce3+)*(4f-5d-optical absorption on Ce3+-ions);
b) (Ce3+)*+Ln3+→Ce3++(Ln3+)*(energy transfer); and
c) (Ln3+)*→Ln3++hν (luminescence on Ln3+ ions);
wherein the further trivalent rare-earth ions Ln3+ are Pr3+, Sm3+, Tb3+, Dy3+. The [Xe]4fn-[Xe]4fn transition causing the light emission of wavelength converted light is electric dipole forbidden (e.g. the 5D4-7F5 transition of Tb3+).
According to a preferred embodiment of the present invention, the luminescent medium has a dopant concentration of the Ce3+-ions in the range of 0.01% mol to 5% mol and a concentration of the further rare earth ions, which is between 0.5 and 50 times the dopant concentration of the Ce3+-ions.
According to another preferred embodiment of the present invention, the luminescent medium is selected from the following materials: (Lu1-a-bCeaLnb)3(Al1-x-yGaxScy)5O12 (0.0≦a≦0.1; 0.0≦b≦0.6; 0.0≦x≦0.5; 0.0≦y≦0.5). The luminescent medium preferably is (Lu1-a-bCeaTbb)3AlGa4O12 with 0.0≦a≦0.1; 0.0≦b≦0.6.
According to another preferred embodiment of the present invention, the luminescent medium is selected from the following materials: Ca1-x-y-a-bMgaSrb(Cex/2Lny/2Na(x+y)/2)S (0.0≦a<1.0; 0.0≦b<1.0; and a+b<1; 0.0≦x<0.05; 0.0≦y<0.05).
According to another preferred embodiment of the present invention, the luminescent medium is selected from the following materials: (Y1-x-a-bGdxCeaLnb)2SiO5 (0.0≦a≦0.1; 0.0≦b≦0.1; 0.0≦x≦1.0 and 0.0≦y≦1.0).
According to another preferred embodiment of the present invention, the luminescent medium is selected from the following materials: (Y1-a-bCeaLnb)3(Al1-x-yGaxScy)5O12 (0.0≦a≦0.1; 0.0≦b≦0.1; 0.0≦x≦0.5; 0.0≦y≦0.5). The luminescent medium preferably is (Y1-a-bCeaTbb)3AlGa4O12 with 0.0≦a≦0.1; 0.0≦b≦0.6.
According to another preferred embodiment of the present invention, the luminescent medium is selected from the following materials: Gd1-a-bCeaTbbBO3 (0.0≦a≦0.1; 0.0≦b≦0.6).
According to a preferred embodiment of the present invention, the luminescent medium is a powder or a ceramic or a monocrystalline material. The powder is used to form a wavelength converting member formed as a luminescent screen.
The composition of the luminescent medium formed as a powder and/or ceramic material comprises the following steps: dissolving a metal nitrate in water; inpissating of the resulting dissolution; calcination of the original mixture under CO-atmosphere at 900° C. to 1200° C.; milling and further calcination under CO-atmosphere at 1500° C. to 1700° C.; and braking/milling and sieving the powder, especially with a sieve having 36 microns openings. The resulting powder has an average particle size of about 5 microns (5 μm). The following step is used to produce ceramic material: The milled powders are dried and pressed and subsequently exposed to uniaxial or isostatic pressure to form ceramic compacts of the desired shape.
The present invention further relates to a lighting system comprising at least one aforementioned light emitting device, wherein the system is used in one or more of the following applications:
It is a further object of the present invention to provide a luminescent medium adapted for a light emitting device with an enhanced lumen yield and improved colour rendering.
This object is achieved with the luminescent medium according to claim 11. The luminescent medium for wavelength conversion of blue light and/or ultraviolet light into yellow light and/or green and/or red light essentially has a main phase of a solid state host material which is doped with Ce3+-ions and comprises ions of a further rare-earth material Ln, wherein the host material is selected such that the emission energy of the 5d-4f emission of Ce3+-ions is energetically higher than the absorption energy into an upper 4fn state of the further rare-earth material.
According to a preferred embodiment of the present invention, the ions of the further rare-earth material Ln are Pr3+, Sm3+, Tb3+, Dy3+ or a mixture thereof.
According to a preferred embodiment of the present invention, the host material has a dopant concentration of the Ce3+-ions in the range of 0.01% mol to 5% mol and a concentration of the further rare earth ions, which is between 0.5 and 50 times the dopant concentration of the Ce3+-ions.
According to a preferred embodiment of the present invention, the luminescent medium is selected from the following materials: (Lu1-a-bCeaLnb)3(Al1-x-yGaxScy)5O12 (0.0≦a≦0.1; 0.0≦b≦0.6; 0.0≦x≦0.5; 0.0≦y≦0.5). The luminescent medium preferably is (Lu1-a-bCeaTbb)3AlGa4O12 with 0.0≦a≦0.1; 0.0≦b≦0.6.
According to another preferred embodiment of the present invention, the luminescent medium is selected from the following materials: Ca1-x-y-a-bMgaSrb(Cex/2Lny/2Na(x+y)/2)S (0.0≦a<1.0; 0.0≦b<1.0; and a+b<1; 0.0≦x<0.05; 0.0≦y<0.05).
According to another preferred embodiment of the present invention, the luminescent medium is selected from the following materials: (Y1-x-a-bGdxCeaLnb)2SiO5(0.0≦a≦0.1; 0.0≦b≦0.1; 0.0≦x≦1.0 and 0.0≦y≦1.0).
According to another preferred embodiment of the present invention, the luminescent medium is selected from the following materials: (Y1-a-bCeaLnb)3(Al1-x-yGaxScy)5O12 (0.0≦a≦0.1; 0.0≦b≦0.6; 0.0≦x≦0.5; 0.0≦y≦). The luminescent medium preferably is (Y1-a-bCeaTbb)3AlGa4O12 with 0.0≦a≦0.1; 0.0≦b≦0.6.
According to another preferred embodiment of the present invention, the luminescent medium is selected from the following materials: Gd1-a-bCeaTbbBO3 (0.0≦a≦0.1; 0.0≦b≦0.6).
The aforementioned components, as well as the claimed components and the components to be used in accordance with the invention in the described embodiments, are not subject to any special exceptions with respect to their size, shape, material selection and technical concept such that the selection criteria known in the pertinent field can be applied without limitations.
Additional details, features, characteristics and advantages of the object of the invention are disclosed in the subclaims, the figures and the following description of the respective figure and examples, which—in an exemplary fashion—show one embodiment and example of a light-emitting device according to the invention.
In the drawings:
The wavelength converting member 2 comprises the luminescent medium, which comprises a solid state host material which is doped with rare-earth ions.
The light source 3 is emitting blue light and/or ultraviolet light 10. The blue light and/or ultraviolet light 10 emitted by the light source 3 is used for pumping the wavelength converting member 2 to create white light 11 composed of the blue light and/or ultraviolet light 10 and red and/or yellow and/or green luminescence light 12 leaving the wavelength converting member 2. The light-emitting device 1 is configured as a longitudinally pumped light-emitting device 1, wherein the resulting white light 11 is aligned to the main axis 8 of the optical path 7 of the pumping light 10.
The light emitting device 1 shown in
The luminescent medium is pumped with blue light and/or ultraviolet light 10 emitted by the light source 3. The luminescent medium absorbs the radiation of the blue light and/or ultraviolet light via the dipole allowed 4f-5d transition (arrow 13) in the Ce3+-ion. The excited Ce3+-ion transfers its energy (arrow 14) to the upper lasing state of the Tb3+-ion (or alternatively to the lasing state of another further rare-earth ion) which then emits the desired light 11 with a wavelength around 543 nm through a transition (arrow 14) between the upper lasing state (5D4 state of the Tb3+) and a lower lasing state (7F5 state of the Tb3+) followed by a transition to the ground state (arrow 16).
The excitation spectrum 18 shows a broad structure in the spectral wavelength range between 300 and 400 nm corresponding to the desired absorption of the radiation of the blue light and/or ultraviolet light in the spectral region of 300 nm to 480 nm via the dipole allowed 4f-5d transition (arrow 13) on the Ce3+-ion.
The emission spectrum 17 shows significant structures in the spectral wavelength range between 480 and 630 nm corresponding to green, yellow and red light generating a full color gamut for the human eye. The wavelength with maximum emission intensity is at λmax=543 nm; the colour point parameter are x=0.319, y=0.610; and a high lumen equivalent LE=512 lm/W is reached.
Other variations to the disclosed embodiments can be understood and effected by those skilled in the art in practicing the claimed invention, from a study of the drawings, the disclosure, and the appended claims. In the claims, the word “comprising” does not exclude other elements or steps, and the indefinite article “a” or “an” does not exclude a plurality. The mere fact that certain measures are recited in mutually different dependent claims does not indicate that a combination of these measures cannot be used to advantage. Any reference signs in the claims should not be construed as limiting the scope.
| Number | Date | Country | Kind |
|---|---|---|---|
| 09155914.6 | Mar 2009 | EP | regional |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/IB10/51124 | 3/16/2010 | WO | 00 | 12/7/2011 |
