Composition for encapsulating organic electronic element

US11295999B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11295999-B2
Application numberUS-201816606182-A
CountryUS
Kind codeB2
Filing dateApr 20, 2018
Priority dateApr 21, 2017
Publication dateApr 5, 2022
Grant dateApr 5, 2022

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

Provided is a composition for encapsulating an organic electronic element and an organic electronic device comprising the same, and an encapsulating composition that can form a structure capable of effectively blocking moisture or oxygen introduced from the outside into an organic electronic device, thereby securing a lifetime of the organic electronic device, and that can be applied to a top-emitting organic electronic device to prevent physical and chemical damage of organic electronic elements, while having excellent optical properties and processability, and an organic electronic device comprising the same.

First claim

Opening claim text (preview).

The invention claimed is: 1. A composition for encapsulating an organic electronic element, comprising: a curable compound comprising a compound having an oxetane group; a thermal initiator; and a hardening retarder, and satisfying Equation 1 below, 0.03< R/P< 0.6  [Equation 1] wherein R is a part by weight of the hardening retarder relative to 100 parts by weight parts of the curable compound, and P is a part by weight of the thermal initiator relative to 100 parts by weight of the curable compound. 2. The composition according to claim 1 , wherein the curable compound comprises at least one or more curable functional groups. 3. The composition according to claim 2 , wherein the curable functional group is one or more selected from a glycidyl group, an isocyanate group, a hydroxyl group, a carboxyl group, an amide group, an epoxide group, a cyclic ether group, a sulfide group, an acetal group and a lactone group. 4. The composition according to claim 1 , wherein the curable compound further comprises an epoxy compound having a cyclic structure in the molecular structure. 5. The composition according to claim 4 , wherein the epoxy compound having a cyclic structure in the molecular structure has 3 to 10 ring constituent atoms. 6. The composition according to claim 4 , wherein the epoxy compound having a cyclic structure in the molecular structure is an alicyclic epoxy compound. 7. The composition according to claim 4 , wherein an amount of the compound having an oxetane group in the curable compound is in a range of 3 to 50 parts by weight relative to 100 parts by weight of the epoxy compound. 8. The composition according to claim 1 , wherein the curable compound has a weight average molecular weight of 300 g/mol or less. 9. The composition according to claim 1 , wherein the thermal initiator is a thermal cationic initiator. 10. The composition according to claim 1 , wherein the thermal initiator comprises a sulfonium salt, a phosphonium salt, a quaternary ammonium salt, a diazonium salt or a iodonium salt, which has BF 4 − , ASF 6 − , PF 6 − , SbF 6 − , or (BX 4 ) − as an anion, where X is a phenyl substituted with at least two fluorine or trifluoromethyl groups. 11. The composition according to claim 1 , wherein the thermal initiator is included in an amount of 0.01 to 1 part by weight relative to 100 parts by weight of the curable compound. 12. The composition according to claim 1 , wherein the hardening retarder comprises one or more selected from the group consisting of an amine-based compound, a polyether-based compound, boric acid, phenylboric acid, salicylic acid, hydrochloric acid, sulfuric acid, oxamic acid, tetraphthalic acid, isophthalic acid, phosphoric acid, acetic acid, and lactic acid. 13. The composition according to claim 1 , wherein R/P is in a range of more than 0.1 and less than 0.5 when the hardening retarder is a polyether-based compound, and R/P is in a range of more than 0.03 and 0.1 or less when the hardening retarder is an amine-based compound. 14. The composition according to claim 1 , wherein the hardening retarder is included in an amount of 0.002 to 0.12 parts by weight relative to 100 parts by weight of the curable compound. 15. An organic electronic device, comprising: a substrate; an organic electronic element formed on the substrate; and a top encapsulating layer which seals the top surface of the organic electronic element and comprises the composition for encapsulating an organic electronic element according to claim 1 . 16. The organic electronic device according to claim 15 , further comprising a side encapsulating layer formed so as to surround the side surfaces of the organic electronic element on the substrate, wherein the side encapsulating layer and the top encapsulating layer are present on the same plane. 17. A method for manufacturing an organic electronic device comprising steps of: applying the composition for encapsulating an organic electronic element of claim 1 on a substrate, on which the organic electronic element is formed, so as to seal the top surface of the organic electronic element; and curing the composition.

Assignees

Inventors

Classifications

  • the semiconductor body being only partially enclosed · CPC title

  • comprising organic materials, e.g. plastics or resins · CPC title

  • characterised by their materials · CPC title

  • C08G59/24Primary

    carbocyclic · CPC title

  • use in electrical or conductive gadgets · CPC title

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What does patent US11295999B2 cover?
Provided is a composition for encapsulating an organic electronic element and an organic electronic device comprising the same, and an encapsulating composition that can form a structure capable of effectively blocking moisture or oxygen introduced from the outside into an organic electronic device, thereby securing a lifetime of the organic electronic device, and that can be applied to a top-e…
Who is the assignee on this patent?
Lg Chemical Ltd
What technology area does this patent fall under?
Primary CPC classification C08G59/24. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Apr 05 2022 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 4 related publications on this page (citations in our corpus or others sharing the same primary CPC).