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Next Patent: Power surface mount light emitting die package
In particular, a garnet of structure
where
RE=Y, Gd, La and/or Lu;
0≦x≦0.5−y;
0<y<0.1 is used.
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[0001] The invention is based on a phosphor for light sources and an associated light source in accordance with the preamble of claim
[0002] 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 A
[0003] 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.
[0004] 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).
[0005] It is an object of the present invention to provide a phosphor in accordance with the preamble of claim
[0006] This object is achieved through the characterizing features of claim
[0007] 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 A
[0008] 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.
[0009] 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
[0010] where
[0011] RE=Y, Gd, La and/or Lu;
[0012] 0≦x≦0.5−y;
[0013] 0<y<0.1 is used.
[0014] 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.
[0015] 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.
[0016] 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.
[0017] 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.
[0018] The particularly preferred range for y is 0.02<y<0.06.
[0019] The phosphor according to the invention is also suitable for combination with other phosphors.
[0020] A garnet of structure
[0021] where RE=Y, Gd, La and/or Lu;
[0022] 0≦x≦0.02, in particular x=0.01;
[0023] 0<y<0.1 has proven particularly suitable as the phosphor. Y frequently lies in the range from 0.01 to 0.05.
[0024] 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.
[0025] The invention is to be explained in more detail below with reference to a number of exemplary embodiments. In the drawing:
[0026]
[0027]
[0028]
[0029]
[0030]
[0031]
[0032]
[0033] Exemplary Embodiment No. 1:
The components 9.82 g Yttrium oxide Y 2.07 g Cerium oxide CeO 37.57 g Terbium oxide Tb 26.41 g Aluminum oxide Al 0.15 g Barium fluoride BaF 0.077 g Boric acid H
[0034] 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 annealed for three hours in a covered corundum crucible at 1550° C. in forming gas (nitrogen containing 2.3% by volume hydrogen). The annealed material is milled in an automatic mortar mill and screened through a screen with a mesh width of 53 μm. This is followed by a second anneal 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 anneal. The phosphor obtained corresponds to the composition (Y
[0035] Exemplary Embodiment No. 2:
The components 43.07 g Terbium oxide Tb 1.65 g Cerium oxide CeO 21.13 g Aluminum oxide Al 0.12 g Barium fluoride BaF 0.062 g Boric acid H
[0036] are intimately mixed as described under Example No. 1. Two anneals and the further processing of the annealed products take place as described under Example 1. The phosphor obtained corresponds to the overall composition (Tb
[0037] Exemplary Embodiment No. 3:
The components 32.18 g Yttrium oxide Y 0.56 g Terbium oxide Tb 2.07 g Cerium oxide CeO 26.41 g Aluminum oxide Al 0.077 g Boric acid H
[0038] are intimately mixed as described under Example No. 1. Two anneals and processing of the annealed products take place as described under Example No. 1. The phosphor obtained corresponds to the composition (Y
[0039] Exemplary Embodiment No. 4:
The components 26.76 g Yttrium oxide Y 9.53 g Terbium oxide Tb 2.07 g Cerium oxide CeO 26.41 g Aluminum oxide Al 0.149 g Barium fluoride BaF 0.077 g Boric acid H
[0040] are intimately mixed as described under Example No. 1. Two anneals and processing of the annealed products take place as described under Example No. 1. The phosphor obtained corresponds to the composition (Y
[0041] Exemplary Embodiment No. 5
The components 30.82 g Yttrium oxide Y 0.56 g Terbium oxide Tb 4.13 g Cerium oxide CeO 26.41 g Aluminum oxide Al 0.149 g Barium fluoride BaF 0.077 g Boric acid H
[0042] are intimately mixed as described under Example No. 1. Two anneals and processing of the annealed products are carried out as described under Example No. 1. The phosphor obtained corresponds to the composition (Y
[0043] Exemplary Embodiment No. 6:
The components 43.07 g Terbium oxide Tb 1.65 g Cerium oxide CeO 21.13 g Aluminum oxide Al 0.062 g Boric acid H
[0044] are intimately mixed as described under Example No. 1. Two anneals and processing of the annealed products are carried out as described under Example 1, except that the annealing temperature during the two anneals is lower by 50° C. in each case. The phosphor obtained corresponds to the composition (Tb
[0045] Exemplary Embodiment No. 7:
The components 43.07 g Terbium oxide Tb 1.65 g Cerium oxide CeO 17.05 g Aluminum oxide Al 7.50 g Gallium oxide Ga 0.062 g Boric acid H
[0046] are intimately mixed as described under Example No. 1. Two anneals and processing of the annealed products are carried out as described under Example 1, except that the annealing temperature for the two anneals is lower by 50° C. in each case. The phosphor obtained corresponds to the composition (Tb
[0047] Exemplary Embodiment No. 8:
The components 43.07 g Terbium oxide Tb 1.65 g Cerium oxide CeO 12.97 g Aluminum oxide Al 15.00 g Gallium oxide Ga 0.062 g Boric acid H
[0048] are intimately mixed as described under Example No. 1. Two anneals and processing of the annealed products are carried out as described under Example 1, except that the annealing temperature for the two anneals is lower by 50° C. in each case. The phosphor obtained corresponds to the composition (Tb
[0049] Exemplary Embodiment No. 9
The components 4.88 kg Yttrium oxide Y 7.05 kg Gadolinium oxide Gd 161.6 g Terbium oxide Tb 595 g Cerium oxide CeO 7.34 kg Aluminum oxide Al 5.50 g Boric acid H
[0050] are mixed for 24 hours in a 60 l polyethylene vessel. The mixture is introduced into annealing crucibles made from aluminum oxide with a capacity of approx. 1 l and is annealed in a pushed-bat kiln for 6 hours at 1550° C. under forming gas. The annealed material is milled in an automatic mortar mill and then finely screened. The phosphor obtained has the composition (Y
[0051] Exemplary Embodiment 10 (LED):
[0052] 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
[0053] 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.