Optoelectronic devices containing a converter carrier layer, and methods of producing an optoelectronic device containing a converter carrier layer
US-2015115302-A1 · Apr 30, 2015 · US
US9840647B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9840647-B2 |
| Application number | US-201415036534-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 5, 2014 |
| Priority date | Nov 20, 2013 |
| Publication date | Dec 12, 2017 |
| Grant date | Dec 12, 2017 |
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An optoelectronic component and a method for manufacturing an optoelectronic component are provided. In an embodiment, the optoelectronic component includes a layer sequence having an active layer configured to emit electromagnetic primary radiation, a converter lamina disposed in a beam path of the electromagnetic primary radiation and a bonding layer disposed between the layer sequence and the converter lamina, wherein the bonding layer comprises an inorganic-organic hybrid material having Si—O—Al bonds and/or Si—O—Zr bonds.
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The invention claimed is: 1. A method for producing a bonding layer comprising an inorganic-organic hybrid material between a layer sequence having an active layer and a converter lamina in an optoelectronic component, the method comprising: providing the layer sequence having the active layer and the converter lamina; producing an adhesive; applying the adhesive to the layer sequence or to the converter lamina; positioning the converter lamina atop the layer sequence or positioning the layer sequence atop the converter lamina; and curing the adhesive to form the bonding layer, wherein producing the adhesive comprises: providing a first reaction mixture comprising at least one compound of the formula III or at least one compound of the formula III and a compound of the formula IV: wherein, in formula III: R′ is hydrogen and/or an organic radical, and R″ is an organic radical having an epoxy group or an organic radical having an isocyanate group, and wherein, in formula IV: M′=Si or Zr, m′=0, 1, 2, 3, 4 or 5, R′″ is hydrogen and/or an organic radical, adding a solution comprising a compound of the formula I and a compound of the formula II dropwise to the first reaction mixture to form a second reaction mixture: wherein, in formula I: M=Al or Zr, R is hydrogen and/or an organic radical, and x=3 or 4, and wherein, in formula II: R 1 and R 2 may be chosen identically or differently and are each hydrogen and/or an organic radical. 2. The method according to claim 1 , wherein the compound of the formula I and the at least one compound of the formula III are used in a molar ratio of 1:1 to 1:10. 3. The method according to claim 1 , further comprising adding an acid to the second reaction mixture to form a third reaction mixture after adding the solution. 4. The method according to claim 1 , wherein the following applies to the at least one compound of the formula III: R′ is selected from a group comprising hydrogen, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, cyclohexyl and phenyl radicals and combinations thereof. 5. The method according to claim 1 , wherein the at least one compound of the formula III has the following formula IIIa: wherein m=0, 1, 2, 3, 4 or 5. 6. The method according to claim 1 , wherein, while providing the first reaction mixture, the first reaction mixture comprises a first compound and a second compound of the formula III or a first compound and a second compound of the formula III and a compound of the formula IV, and wherein the following applies to the first compound of the formula III: R″ is an organic radical having an epoxy group, and the following applies to the second compound of the formula III: R″ is an organic radical having an isocyanate group. 7. The method according to claim 6 , wherein the first compound of the formula III has the following formula IIIa and the second compound of the formula III has the following formula IIId: wherein R′ is independently selected from the group consisting of hydrogen, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, cyclohexyl and phenyl radicals and combinations thereof, n=1, 2, 3, 4 or 5, and m=0, 1, 2, 3, 4 or 5. 8. The method according to claim 1 , wherein the compound of the formula I has the following formula Ia or Ib: Al(OR) 3 Formula Ia Zr(OR) 4 Formula Ib, wherein R is selected from the group consisting of hydrogen, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, cyclohexyl and phenyl radicals and combinations thereof. 9. The method according to claim 1 , wherein the following applies to the compound of the formula I: M=Al, x= 3 , and R is selected from a group comprising hydrogen, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, cyclohexyl and phenyl radicals and combinations thereof.
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