Optoelectronic component comprising a bonding layer and method for producing a bonding layer in an optoelectronic component

US9840647B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9840647-B2
Application numberUS-201415036534-A
CountryUS
Kind codeB2
Filing dateNov 5, 2014
Priority dateNov 20, 2013
Publication dateDec 12, 2017
Grant dateDec 12, 2017

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  1. Title

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  2. Abstract

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  5. First independent claim

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Abstract

Official abstract text for this publication.

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.

First claim

Opening claim text (preview).

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.

Assignees

Inventors

Classifications

  • Electricity · mapped topic

  • Metal-containing linkages · CPC title

  • Electricity · mapped topic

  • C09J183/14Primary

    in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms (C09J183/10 takes precedence) · CPC title

  • Electricity · mapped topic

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What does patent US9840647B2 cover?
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 th…
Who is the assignee on this patent?
Osram Opto Semiconductors Gmbh
What technology area does this patent fall under?
Primary CPC classification C09J183/14. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Dec 12 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).