JP2003086357A - Light emitting element and manufacturing method of the same - Google Patents
Light emitting element and manufacturing method of the sameInfo
- Publication number
- JP2003086357A JP2003086357A JP2001271307A JP2001271307A JP2003086357A JP 2003086357 A JP2003086357 A JP 2003086357A JP 2001271307 A JP2001271307 A JP 2001271307A JP 2001271307 A JP2001271307 A JP 2001271307A JP 2003086357 A JP2003086357 A JP 2003086357A
- Authority
- JP
- Japan
- Prior art keywords
- light emitting
- film
- buffer layer
- emitting device
- layer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 230000004888 barrier function Effects 0.000 claims abstract description 49
- 239000010408 film Substances 0.000 claims description 102
- 238000000034 method Methods 0.000 claims description 39
- 239000000758 substrate Substances 0.000 claims description 39
- 229910052751 metal Inorganic materials 0.000 claims description 22
- 239000002184 metal Substances 0.000 claims description 22
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 10
- 229910052814 silicon oxide Inorganic materials 0.000 claims description 10
- 239000010409 thin film Substances 0.000 claims description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 150000004767 nitrides Chemical class 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 3
- 239000012298 atmosphere Substances 0.000 claims description 2
- 230000006866 deterioration Effects 0.000 abstract description 6
- 150000002894 organic compounds Chemical class 0.000 abstract description 5
- 238000010521 absorption reaction Methods 0.000 abstract description 4
- 238000010030 laminating Methods 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 112
- 239000011521 glass Substances 0.000 description 20
- 239000000463 material Substances 0.000 description 12
- 239000011368 organic material Substances 0.000 description 12
- 238000002347 injection Methods 0.000 description 11
- 239000007924 injection Substances 0.000 description 11
- 230000000694 effects Effects 0.000 description 9
- 238000004544 sputter deposition Methods 0.000 description 9
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 8
- 239000012044 organic layer Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 229910052782 aluminium Inorganic materials 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 230000006378 damage Effects 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- 230000001681 protective effect Effects 0.000 description 6
- 238000007740 vapor deposition Methods 0.000 description 6
- -1 InO3 Chemical compound 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 238000005566 electron beam evaporation Methods 0.000 description 5
- 238000001704 evaporation Methods 0.000 description 5
- 230000005525 hole transport Effects 0.000 description 5
- 229910003437 indium oxide Inorganic materials 0.000 description 5
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 5
- 230000015556 catabolic process Effects 0.000 description 4
- 239000004020 conductor Substances 0.000 description 4
- 230000008020 evaporation Effects 0.000 description 4
- 238000007789 sealing Methods 0.000 description 4
- 238000000576 coating method Methods 0.000 description 3
- 238000010894 electron beam technology Methods 0.000 description 3
- 239000007769 metal material Substances 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 229910001316 Ag alloy Inorganic materials 0.000 description 2
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 2
- KLZUFWVZNOTSEM-UHFFFAOYSA-K Aluminium flouride Chemical compound F[Al](F)F KLZUFWVZNOTSEM-UHFFFAOYSA-K 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 101100321669 Fagopyrum esculentum FA02 gene Proteins 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 229910004298 SiO 2 Inorganic materials 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 239000011231 conductive filler Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- PMHQVHHXPFUNSP-UHFFFAOYSA-M copper(1+);methylsulfanylmethane;bromide Chemical compound Br[Cu].CSC PMHQVHHXPFUNSP-UHFFFAOYSA-M 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 238000005401 electroluminescence Methods 0.000 description 2
- 230000009545 invasion Effects 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 239000004926 polymethyl methacrylate Substances 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 229940100890 silver compound Drugs 0.000 description 2
- 150000003379 silver compounds Chemical class 0.000 description 2
- 238000000638 solvent extraction Methods 0.000 description 2
- 229910001887 tin oxide Inorganic materials 0.000 description 2
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 description 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
- SULWTXOWAFVWOY-PHEQNACWSA-N 2,3-bis[(E)-2-phenylethenyl]pyrazine Chemical class C=1C=CC=CC=1/C=C/C1=NC=CN=C1\C=C\C1=CC=CC=C1 SULWTXOWAFVWOY-PHEQNACWSA-N 0.000 description 1
- MVWPVABZQQJTPL-UHFFFAOYSA-N 2,3-diphenylcyclohexa-2,5-diene-1,4-dione Chemical class O=C1C=CC(=O)C(C=2C=CC=CC=2)=C1C1=CC=CC=C1 MVWPVABZQQJTPL-UHFFFAOYSA-N 0.000 description 1
- ZYASLTYCYTYKFC-UHFFFAOYSA-N 9-methylidenefluorene Chemical class C1=CC=C2C(=C)C3=CC=CC=C3C2=C1 ZYASLTYCYTYKFC-UHFFFAOYSA-N 0.000 description 1
- 229910001148 Al-Li alloy Inorganic materials 0.000 description 1
- 229910017109 AlON Inorganic materials 0.000 description 1
- 229910001020 Au alloy Inorganic materials 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 229910019015 Mg-Ag Inorganic materials 0.000 description 1
- 229910017911 MgIn Inorganic materials 0.000 description 1
- 229910001252 Pd alloy Inorganic materials 0.000 description 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical class C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
- 238000003848 UV Light-Curing Methods 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 150000008425 anthrones Chemical class 0.000 description 1
- 238000004380 ashing Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000001718 carbodiimides Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000004696 coordination complex Chemical class 0.000 description 1
- 238000001723 curing Methods 0.000 description 1
- 239000012769 display material Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000001227 electron beam curing Methods 0.000 description 1
- 150000008376 fluorenones Chemical class 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- 238000007733 ion plating Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- MHCFAGZWMAWTNR-UHFFFAOYSA-M lithium perchlorate Chemical compound [Li+].[O-]Cl(=O)(=O)=O MHCFAGZWMAWTNR-UHFFFAOYSA-M 0.000 description 1
- 229910001486 lithium perchlorate Inorganic materials 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000002912 oxalic acid derivatives Chemical class 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 150000004322 quinolinols Chemical class 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- IBBLKSWSCDAPIF-UHFFFAOYSA-N thiopyran Chemical compound S1C=CC=C=C1 IBBLKSWSCDAPIF-UHFFFAOYSA-N 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
Landscapes
- Devices For Indicating Variable Information By Combining Individual Elements (AREA)
- Electroluminescent Light Sources (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、一対の電極間に正
孔輸送層、発光層、電子注入層からなる有機材料を含む
発光領域を備え、両電極から発光層にキャリアを注入す
ることによって発光層を発光させる有機エレクトロルミ
ネッセンス素子(以下、有機EL素子という)に関す
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention comprises a light emitting region containing an organic material consisting of a hole transport layer, a light emitting layer and an electron injection layer between a pair of electrodes, and by injecting carriers from both electrodes into the light emitting layer. The present invention relates to an organic electroluminescence device (hereinafter, referred to as an organic EL device) that causes a light emitting layer to emit light.
【0002】[0002]
【従来の技術】有機EL素子を利用した平面ディスプレ
イや、平面光源は、次世代のディスプレイ材料として研
究、開発が盛んに行われている。2. Description of the Related Art A flat panel display using an organic EL device and a flat panel light source have been actively researched and developed as next-generation display materials.
【0003】有機EL素子は、例えば、図3に示すよう
に、ガラス基板10上に陽極を構成する透明導電材料
(ITO、SnO2、InO3、ZnO)が用いられた
透明電極12が形成され、この透明電極12上に有機材
料を含む有機材料を含む発光領域18(正孔輸送層1
4、発光層16、電子輸送層17)、発光領域18上
に、陰極を構成するMgAg,Ca,Al、MgInな
どからなる金属電極50が形成されている。そして、透
明電極12から発光層16に注入された正孔と、金属電
極50から発光層に注入される電子とが、発光層16で
再結合することにより発光する。図3に示すように、発
光層16で発光した光は、透明電極を通過し、ガラス基
板10を通じて外部に出る。また、不透明な金属電極5
0側へ進んだ光は、透明電極50で反射され、これより
ガラス基板側へ進んでガラス基板を通って外部へ出る。
しかし、このようなEL素子内で発生した発光光がガラ
ス基板10を通して外部へ射出される場合は、射出割合
は約20%程度であり、残りの80%近くは、発光層1
8やガラス基板10を導波して金属面で吸収されたり基
板の端から放出されてしまう。In an organic EL element, for example, as shown in FIG. 3, a transparent electrode 12 is formed on a glass substrate 10 using a transparent conductive material (ITO, SnO2, InO3, ZnO) which constitutes an anode. On the transparent electrode 12, the light emitting region 18 containing the organic material containing the organic material (the hole transport layer 1
4, a metal electrode 50 made of MgAg, Ca, Al, MgIn or the like, which constitutes a cathode, is formed on the light emitting layer 16, the electron transport layer 17) and the light emitting region 18. Then, the holes injected from the transparent electrode 12 into the light emitting layer 16 and the electrons injected from the metal electrode 50 into the light emitting layer recombine in the light emitting layer 16 to emit light. As shown in FIG. 3, the light emitted from the light emitting layer 16 passes through the transparent electrode and goes out through the glass substrate 10. Also, an opaque metal electrode 5
The light that has traveled to the 0 side is reflected by the transparent electrode 50, travels from there to the glass substrate side, passes through the glass substrate, and exits to the outside.
However, when the emitted light generated in such an EL element is emitted to the outside through the glass substrate 10, the emission rate is about 20%, and the remaining 80% is about the emission layer 1.
8 and the glass substrate 10 are guided and absorbed by the metal surface or emitted from the edge of the substrate.
【0004】素子内で発生した発光を効率良く素子外部
に取り出すして発光効率を改善するために提案されたE
L素子の構成が図4に示すものである。E has been proposed in order to efficiently take out the light emission generated in the device to the outside of the device to improve the light emission efficiency.
The structure of the L element is shown in FIG.
【0005】図4に示すように、ガラス基板10上に電
極を構成する透明導電材料(ITO、SnO2、InO
3、ZnO等)、あるいはMgAg,Ca,Al、Mg
Inなどからなる金属材料が用いられた電極12が形成
され、この電極12上に有機材料を含んだ発光領域18
(正孔輸送層14、発光層16、電子輸送層17)、発
光領域18上に透明電極51が形成されている。この透
明電極60は、図3に示すように不透明な金属材料では
なく、ITO、SnO2、InO3、ZnO、あるいは
これらの酸化物の複合体からなる透明導電膜材料が用い
られている。As shown in FIG. 4, a transparent conductive material (ITO, SnO2, InO) forming an electrode is formed on a glass substrate 10.
3, ZnO, etc.) or MgAg, Ca, Al, Mg
An electrode 12 made of a metal material such as In is formed, and a light emitting region 18 containing an organic material is formed on the electrode 12.
A transparent electrode 51 is formed on (the hole transport layer 14, the light emitting layer 16, the electron transport layer 17) and the light emitting region 18. The transparent electrode 60 is not made of an opaque metal material as shown in FIG. 3, but is made of a transparent conductive film material made of ITO, SnO2, InO3, ZnO, or a complex of these oxides.
【0006】透明電極51に透明導電膜材料を用いるこ
とで、素子の上部電極となる陰極電極側から発光領域1
8で発生した発光光を取り出すことが可能となる。図4
に示すように、発光層16で発光した光は、透明な陰極
電極51を通過し、外部に出る。電極12が不透明な金
属材料である場合は、陽極電極12側へ進んだ光は陽極
電極12で反射され、これより透明電極60側へ進んで
透明電極60を通って外部へ出る。また、電極が透明導
電膜材料からなる場合、例えばガラス上に反射層(散乱
層)(図示せず)と組み合わせることにより、発光層1
6で発光し陽極電極12側へ進んだ光は陽極電極12で
反射され、これより透明電極51側へ進んで透明電極6
0を通って外部へ出ることになる。By using a transparent conductive film material for the transparent electrode 51, the light emitting region 1 is formed from the side of the cathode electrode which is the upper electrode of the device.
The emitted light generated in 8 can be taken out. Figure 4
As shown in, the light emitted from the light emitting layer 16 passes through the transparent cathode electrode 51 and goes out. When the electrode 12 is made of an opaque metal material, the light that has traveled to the anode electrode 12 side is reflected by the anode electrode 12, travels to the transparent electrode 60 side, and passes through the transparent electrode 60 to the outside. When the electrode is made of a transparent conductive film material, for example, by combining it with a reflective layer (scattering layer) (not shown) on glass, the light emitting layer 1
The light emitted at 6 and traveling to the anode electrode 12 side is reflected by the anode electrode 12 and proceeds to the transparent electrode 51 side from this, and the transparent electrode 6
It goes out through 0.
【0007】このような有機EL素子内で発生した発光
光は、ガラス基板10を通して外部へ射出されないた
め、図3の構成に比べて、外部への射出割合は増えるの
である。Since the emitted light generated in such an organic EL element is not emitted to the outside through the glass substrate 10, the emission rate to the outside is increased as compared with the configuration of FIG.
【0008】[0008]
【発明が解決しようとする課題】しかし、図3、図4に
示すような有機EL素子は、例えば、電子注入層や発光
領域を構成する有機層などへの水分や酸素の進入による
素子劣化が発生するといった問題がある。水分や酸素と
の反応により構造変化を生じるため、素子の一部分が発
光しないダークスポットが発生、成長したり、発光効率
が低下を招く原因となり、例えばEL素子を用いたディ
スプレイの場合、表示品位が悪化するのである。したが
って、有機EL素子の耐久性や信頼性を高めるには、電子
注入層や有機層に用いる材料と水分や酸素との反応を防
止するために、有機EL素子全体が封止されている必要
がある。However, in the organic EL device as shown in FIGS. 3 and 4, for example, device deterioration due to entry of moisture or oxygen into the electron injection layer or the organic layer constituting the light emitting region. There is a problem that it will occur. Since a structural change occurs due to the reaction with moisture or oxygen, a dark spot where a part of the element does not emit, grows, or causes a decrease in luminous efficiency. For example, in the case of a display using an EL element, the display quality is It gets worse. Therefore, in order to improve the durability and reliability of the organic EL element, the entire organic EL element must be sealed in order to prevent the reaction between the material used for the electron injection layer and the organic layer and moisture and oxygen. is there.
【0009】図3,4に示されるようにガラスやアルミ
からなるキャップ51、52を発光素子に被せることに
より、水分の侵入を防止されているが、発光素子の小型
化(薄化)の妨げとなり、かつ発光光の外部への射出割
合の低下を引き起すといった問題がある。As shown in FIGS. 3 and 4, by covering the light emitting element with the caps 51 and 52 made of glass or aluminum, invasion of water is prevented, but the miniaturization (thinning) of the light emitting element is hindered. In addition, there is a problem that the ratio of emitted light to the outside is reduced.
【0010】従来、有機EL素子の封止については、これ
まで主に二つの方法による検討が行われてきた。その一
つは、ガラス製キャップ等を有機EL素子に封着するも
のであり、他方は蒸着法等の真空成膜技術を用いて、有
機EL素子の外表面に保護膜を形成するものである。Conventionally, two methods have been mainly studied so far regarding the sealing of the organic EL element. One is to seal a glass cap or the like to the organic EL element, and the other is to form a protective film on the outer surface of the organic EL element by using a vacuum film forming technique such as a vapor deposition method. .
【0011】ガラス製キャップ等を封着して有機EL素
子を封止する方法としては、無機エレクトロルミネッセ
ンス素子で既に用いられているように、背面電極の外側
にガラス板を設け、背面電極とガラス板の間にシリコー
ンオイルを封入する方法等がある。As a method for sealing an organic EL element by sealing a glass cap or the like, a glass plate is provided outside the back electrode and the back electrode and the glass are used, as already used in the inorganic electroluminescence element. There is a method of enclosing silicone oil between the plates.
【0012】保護膜を形成して有機EL素子を封止する
方法については、例えば特開平6−96858号公報に
GeO、SiO、AlF3等をイオンプレーティング法
を用いて有機EL素子の外表面に形成する方法が開示さ
れている。Regarding the method of forming a protective film and sealing the organic EL element, for example, in JP-A-6-96858, GeO, SiO, AlF3 or the like is applied to the outer surface of the organic EL element by the ion plating method. A method of forming is disclosed.
【0013】また、特開平7−211455号公報にお
いては、吸水率1%以下の吸水物質と吸水率0.1%以
下の防湿性物質からなる保護膜を形成する方法が形成さ
れている。Further, Japanese Patent Application Laid-Open No. 7-212455 discloses a method of forming a protective film composed of a water-absorbing substance having a water absorption rate of 1% or less and a moisture-proof substance having a water absorption rate of 0.1% or less.
【0014】また、特開平10−41067号公報にお
いては、有機EL素子の外表面に、最下層に絶縁性化合
物を有する少なくとも2層以上の積層膜からなる膜厚3
μm〜30μmの保護膜を形成する方法が開示されてい
る。Further, in JP-A-10-41067, a film thickness 3 comprising a laminated film of at least two layers having an insulating compound as the lowermost layer is formed on the outer surface of the organic EL element.
A method of forming a protective film of μm to 30 μm is disclosed.
【0015】一般的に有機EL素子を用いたディスプレ
イ等を製造する場合、基板上には有機EL素子を構成す
る積層体の他、スイッチング素子や発光色の異なる発光
領域を区分して形成するための有機材料(リブ)等が形
成される。この場合、基板表面上には多数の凹凸ができ
ることは避けられない。水分や酸素の侵入を防ぐべく、
基板上に有機EL素子を構成積層構造体上に保護膜を形成
した場合、基板上に形成されたスイッチング素子、電
極、有機EL素子といった基板上の凹凸のため、膜応力に
起因するバリア膜のクラックや剥がれ、素子破壊を引き
起こすといった課題があった。膜応力は多層に積層され
ることにより増加する。 また、基板上に付着したダス
トに起因するバリア膜のクラックや剥がれ、素子破壊を
引き起こすといった課題もあった。Generally, when a display or the like using an organic EL element is manufactured, a switching element and a light emitting region having a different emission color are separately formed on a substrate in addition to a laminated body constituting the organic EL element. The organic material (rib) and the like are formed. In this case, it is inevitable that many irregularities are formed on the substrate surface. To prevent the invasion of water and oxygen,
When an organic EL element is formed on the substrate and a protective film is formed on the laminated structure, the barrier film caused by the film stress is generated due to the unevenness on the substrate such as the switching element, the electrode, and the organic EL element formed on the substrate. There were problems such as cracking, peeling, and element destruction. Membrane stress increases by being laminated in multiple layers. Further, there is a problem that the barrier film is cracked or peeled off due to the dust adhering to the substrate, and the device is destroyed.
【0016】EL素子上に保護膜を形成する場合に、バ
リア膜の形成方法によっては、有機EL素子にダメージ
を与えたり、静電破壊が発生するといった課題があっ
た。When forming a protective film on an EL element, there are problems that the organic EL element may be damaged or electrostatic breakdown may occur depending on the method of forming the barrier film.
【0017】本発明は上記課題を解決するためになされ
たものであり、基板上に少なくとも電極、有機発光層、
対向電極を形成した積層構造体上に有機化合物からなる
緩衝層を形成することにより、積層構造体上に直接バリ
ア膜を形成することが可能になり、水分や酸素の進入に
よる有機EL素子劣化や、膜応力によるバリア膜クラッ
ク、及び発光素子劣化のない耐久性、信頼性の高い有機
EL素子及びそれを用いた表示装置、照明装置を実現す
ることを目的とする。The present invention has been made to solve the above-mentioned problems, and at least an electrode, an organic light emitting layer, and
By forming a buffer layer made of an organic compound on the laminated structure on which the counter electrode is formed, it becomes possible to directly form the barrier film on the laminated structure, and deterioration of the organic EL element due to entry of moisture or oxygen and It is an object of the present invention to realize a highly reliable and reliable organic EL element free from cracks in a barrier film due to film stress and deterioration of a light emitting element, and a display device and a lighting device using the same.
【0018】[0018]
【課題を解決するための手段】本発明の発光素子は、基
板上に形成された電極と、有機発光層と対向電極と、を
備えた発光素子であって、前記対向電極上に形成された
緩衝層と、前記緩衝層上に少なくとも1層以上のバリア
膜とが形成されていることを特徴とする。A light emitting device of the present invention is a light emitting device having an electrode formed on a substrate, an organic light emitting layer, and a counter electrode, the light emitting device being formed on the counter electrode. The invention is characterized in that a buffer layer and at least one barrier film are formed on the buffer layer.
【0019】本発明の好ましい態様において、緩衝層
は、有機物を有する。In a preferred embodiment of the present invention, the buffer layer has an organic material.
【0020】また、本発明の好ましい態様において、緩
衝層は、0.3μm以上5μm以下の膜厚である。In a preferred embodiment of the present invention, the buffer layer has a film thickness of 0.3 μm or more and 5 μm or less.
【0021】また、本発明の好ましい態様において、緩
衝層は、基板上に形成された積層体構造の凹凸の2倍以
上の膜厚である。Further, in a preferred aspect of the present invention, the buffer layer has a film thickness that is at least twice as large as the unevenness of the laminate structure formed on the substrate.
【0022】また、本発明の好ましい態様において、緩
衝層は、前記積層構造体を覆い、前記積層構造体の表面
の凹凸を0.5μm以下である。Further, in a preferred aspect of the present invention, the buffer layer covers the laminated structure and the unevenness of the surface of the laminated structure is 0.5 μm or less.
【0023】また、本発明の好ましい態様において、緩
衝層は導電性を有し、体積抵抗値が1012Ω・cm以下
である。In a preferred embodiment of the present invention, the buffer layer has conductivity and has a volume resistance value of 10 12 Ω · cm or less.
【0024】また、本発明の好ましい態様において、バ
リア膜は、酸化膜や窒化膜、金属薄膜、及びダイヤモン
ドライクカーボン膜を少なくとも1種以上含む。なお、
酸化膜はSi又はAlを有する。In a preferred embodiment of the present invention, the barrier film contains at least one kind of oxide film, nitride film, metal thin film and diamond-like carbon film. In addition,
The oxide film has Si or Al.
【0025】また、本発明の好ましい態様において、緩
衝層は、酸化膜を有する。Further, in a preferred embodiment of the present invention, the buffer layer has an oxide film.
【0026】また、本発明の好ましい態様において、酸
化膜はSiOxからなる。In a preferred embodiment of the present invention, the oxide film is made of SiOx.
【0027】また、本発明の好ましい態様において、S
iOx層は、15nm以上1000nm以下の膜厚であ
る。In a preferred embodiment of the present invention, S
The iOx layer has a film thickness of 15 nm or more and 1000 nm or less.
【0028】本発明の表示装置は、上記に記載のいずれ
かの発光素子を用いた表示装置。The display device of the present invention is a display device using any one of the light emitting elements described above.
【0029】本発明の証明装置は、上記に記載のいずれ
かの発光素子を用いた照明装置。The certifying device of the present invention is an illuminating device using any one of the light emitting elements described above.
【0030】本発明の発光素子の製造方法は、基板上に
電極を形成する工程と、前記電極上に有機発光層を形成
する工程と、前記有機発光層上に対向電極を形成する工
程からなる発光素子の製造方法であって、少なくとも前
記対向電極の表面に緩衝層を形成する工程と、前記緩衝
層上に少なくとも1層以上のバリア膜を形成する工程と
を有するこを特徴とする。The method for manufacturing a light emitting device of the present invention comprises a step of forming an electrode on a substrate, a step of forming an organic light emitting layer on the electrode, and a step of forming a counter electrode on the organic light emitting layer. A method of manufacturing a light emitting device, characterized in that it comprises at least a step of forming a buffer layer on the surface of the counter electrode and a step of forming at least one barrier film on the buffer layer.
【0031】本発明の好ましい態様において、一度も大
気中に取り出すことなく、真空中で連続して行われる。In a preferred embodiment of the present invention, it is continuously carried out in a vacuum without being taken out into the atmosphere even once.
【0032】また、本発明の好ましい態様において、前
記対向電極上に緩衝層を形成する工程と、前記緩衝層上
に少なくとも1層以上のバリア膜を形成する工程とは、
100℃以下の温度条件下で行われる。In a preferred embodiment of the present invention, the step of forming a buffer layer on the counter electrode and the step of forming at least one barrier film on the buffer layer include:
It is carried out under a temperature condition of 100 ° C. or lower.
【0033】[0033]
【発明の実施の形態】以下、本発明の実施の形態につい
て、図面に基づいて説明する。BEST MODE FOR CARRYING OUT THE INVENTION Embodiments of the present invention will be described below with reference to the drawings.
【0034】(実施の形態1)以下本発明の実施の形態
1について説明する。図1は本発明に係る発光素子の実
施の形態1を示す断面図である。図1において、101
は基板、102は電極、103は発光層、104は対向
電極、105は緩衝層、106はバリア性を有するバリ
ア膜、107はスイッチング素子をリブで覆ったもので
ある。(First Embodiment) The first embodiment of the present invention will be described below. 1 is a sectional view showing a first embodiment of a light emitting device according to the present invention. In FIG. 1, 101
Is a substrate, 102 is an electrode, 103 is a light emitting layer, 104 is a counter electrode, 105 is a buffer layer, 106 is a barrier film having a barrier property, and 107 is a switching element covered with ribs.
【0035】本実施の形態において、薄膜トランジスタ
からなるスイッチング素子107及びITOからなる画
素電極102が形成されたガラス基板上に、少なくとも
有機EL素子の発光領域103、対向電極104を蒸着法
により形成した積層構造体を形成する。発光領域103
は例えばAlq3等からなる発光層(膜厚500A)と
TPDからなる正孔輸送層(膜厚500A)(図示せ
ず)からなる。対向電極104は、この場合、反射率が
高く、発光層を効率良く発光させる機能を備えているA
l層(膜厚1000A)からなる。In this embodiment, at least a light emitting region 103 of an organic EL element and a counter electrode 104 are formed by vapor deposition on a glass substrate on which a switching element 107 made of a thin film transistor and a pixel electrode 102 made of ITO are formed. Form a structure. Light emitting area 103
Is composed of, for example, a light emitting layer (thickness 500A) made of Alq 3 or the like and a hole transport layer (thickness 500A) (not shown) made of TPD. In this case, the counter electrode 104 has a high reflectance and has a function of causing the light emitting layer to efficiently emit light.
1 layer (thickness 1000 A).
【0036】スイッチング素子107上には、異なる発
光領域を区分するため有機材料が覆っている場合があ
り、この場合、基板表面からおよそ1.5μmの高低差
がある。The switching element 107 may be covered with an organic material for partitioning different light emitting regions, and in this case, there is a height difference of about 1.5 μm from the substrate surface.
【0037】緩衝層105は、ポリアニリンスルホン酸
(PAS)からなる有機導電性材料をスピンコート法に
より対向電極104上に3μm程度形成した後、熱処理
を施こすことにより硬化している。これにより、積層構
造体表面の高低差は約0.5μm程度である。The buffer layer 105 is formed by forming an organic conductive material of polyaniline sulfonic acid (PAS) on the counter electrode 104 to a thickness of about 3 μm by a spin coating method, and then heat treating it to harden it. As a result, the height difference on the surface of the laminated structure is about 0.5 μm.
【0038】また緩衝層のシート抵抗値は106Ω・c
m程度である。The sheet resistance of the buffer layer is 10 6 Ω · c.
It is about m.
【0039】衝層上にはバリア膜106が形成されてい
る。バリア膜は窒化アルミニウムからなりスパッタ法に
て3000A形成されている。バリア膜106は、水蒸
気バリア性に優れ、0.5以下g/m2/dayであ
る。A barrier film 106 is formed on the barrier layer. The barrier film is made of aluminum nitride and is formed at 3000 A by the sputtering method. The barrier film 106 has an excellent water vapor barrier property, and is 0.5 or less g / m 2 / day.
【0040】また、本発明に用いられる素子構成は特に
限定されるものではなく、次のような構成をとることが
出来る。例えば、
陽極/発光層/陰極
陽極/正孔注入層/発光層/陰極
陽極/発光層/電子注入層/陰極
陽極/正孔注入層/発光層/陰極
等をあげることができる。これらの構成の素子において
は各層が複数の層の積層体であってもよいし、また複数
の材料の混合体であってもよい。これらの構成を、基板
/電極/発光領域(正孔注入層、発光層)/対向電極と
大別する。The element structure used in the present invention is not particularly limited, and the following structure can be adopted. For example, there may be mentioned anode / light emitting layer / cathode anode / hole injection layer / light emitting layer / cathode anode / light emitting layer / electron injection layer / cathode anode / hole injection layer / light emitting layer / cathode. In the device having these configurations, each layer may be a laminate of a plurality of layers, or may be a mixture of a plurality of materials. These structures are roughly divided into substrate / electrode / light emitting region (hole injection layer, light emitting layer) / counter electrode.
【0041】発光層に使用される材料としては、ベンゾ
イミダゾール系、ベンゾチアゾール系、ベンゾオキサゾ
ール系の材料、金属キレート化オキシノイド系化合物、
スチルヘルゼン系化合物等をあげることができる。正孔
注入層としては、フルオレノン誘導体、アントラキノジ
メタン誘導体、ジフェニルキノン誘導体、チオピランジ
オキシド誘導体、複素環テトラカルボン酸、カルボジイ
ミド、フルオレニリデンメタン誘導体、アントラキノジ
メタン誘導体、アントロン誘導体、オキサジアゾール誘
導体、キノリノール誘導体の金属錯体、フタロシアニ
ン、ジスチリルピラジン誘導体等が考えられる。Materials used for the light emitting layer include benzimidazole-based, benzothiazole-based, benzoxazole-based materials, metal chelated oxinoid-based compounds,
Examples thereof include stilhelsen compounds. The hole injection layer includes a fluorenone derivative, an anthraquinodimethane derivative, a diphenylquinone derivative, a thiopyran dioxide derivative, a heterocyclic tetracarboxylic acid, a carbodiimide, a fluorenylidene methane derivative, an anthraquinodimethane derivative, an anthrone derivative, and an oxalic acid derivative. A diazole derivative, a metal complex of a quinolinol derivative, a phthalocyanine, a distyrylpyrazine derivative and the like are considered.
【0042】有機EL素子の場合、発光層の形成は主に
抵抗加熱蒸着法を用いるが、エレクトロンビーム蒸着
法、スパッタ法等を用いてもよい。In the case of an organic EL element, the light emitting layer is mainly formed by a resistance heating vapor deposition method, but an electron beam vapor deposition method, a sputtering method or the like may be used.
【0043】有機EL素子は、有機発光層が付着した基
板を高温に加熱すると、有機層が劣化してしまうため、
対向電極104は低温成膜する必要がある。さらに、対
向電極としてITO等、金属薄膜を蒸着法、スパッタ法
やエレクトロンビーム蒸着法等により有機発光層上に形
成する場合、有機層へのダメージを軽減するため、有機
層上にバッファ層を形成してから透明電極を形成するの
が好ましい。バッファ層としては、銅フタロシアニン等
の熱的に安定な有機化合物等を用いればよい。In the organic EL element, when the substrate to which the organic light emitting layer is attached is heated to a high temperature, the organic layer is deteriorated.
The counter electrode 104 needs to be formed at a low temperature. Further, when a metal thin film such as ITO is formed on the organic light emitting layer as a counter electrode by an evaporation method, a sputtering method, an electron beam evaporation method, or the like, a buffer layer is formed on the organic layer in order to reduce damage to the organic layer. It is preferable to form the transparent electrode after that. For the buffer layer, a thermally stable organic compound such as copper phthalocyanine may be used.
【0044】対向電極104は低温で形成されるため、
対向電極104と下地膜の密着性は悪く、対向電極10
4の剥がれが発生しやすい。対向電極と下地膜との密着
性を向上するため、プラズマアッシングといった表面処
理を施した表面に対向電極形成することが好ましい。Since the counter electrode 104 is formed at a low temperature,
The adhesion between the counter electrode 104 and the base film is poor, and the counter electrode 10
4 peeling is likely to occur. In order to improve the adhesion between the counter electrode and the base film, it is preferable to form the counter electrode on the surface that has been subjected to a surface treatment such as plasma ashing.
【0045】対向電極104は、この場合、反射率が高
く、発光層を効率良く発光させる機能を備えていればよ
く、AlあるいはAl化合物、銀あるいは銀化合物等の
金属膜を用いることが好ましい。さらに、銀化合物とし
ては、銀・パラジウム・銅(AgPdCu)の合金ある
いは銀・金・銅(AgAuCu)の合金を用いるのが好
ましい。また、有機化合物を発光層として用いるいわゆ
る電流注入型の有機EL素子の場合、通常反射電極は陰
極となり、電子の注入効率のよい材料、すなわち仕事関
数の低い材料を用いることが多い。有機EL素子の陰極
としては例えばAl−Li合金、Mg−Ag合金等の、
仕事関数が低いが反応性の高い金属(Li、Mg等)と
反応性が低く安定な金属(Al、Ag等)との合金を用
いればよい。あるいは、Li/Al、LiF/Al等の
仕事関数の低い金属あるいはその化合物と仕事関数の高
い金属の積層電極、ITO/Al/ITOといった金属
と透明導電膜の積層電極などを用いることができる。In this case, the counter electrode 104 has only to have a high reflectance and a function of efficiently emitting light from the light emitting layer, and it is preferable to use a metal film of Al or an Al compound, silver or a silver compound. Further, as the silver compound, it is preferable to use an alloy of silver / palladium / copper (AgPdCu) or an alloy of silver / gold / copper (AgAuCu). Further, in the case of a so-called current injection type organic EL element in which an organic compound is used as a light emitting layer, the reflective electrode usually serves as a cathode, and a material having a high electron injection efficiency, that is, a material having a low work function is often used. As the cathode of the organic EL element, for example, an Al-Li alloy, a Mg-Ag alloy, or the like,
An alloy of a metal having a low work function but high reactivity (Li, Mg, etc.) and a metal having a low reactivity and stable (Al, Ag, etc.) may be used. Alternatively, a laminated electrode of a metal having a low work function such as Li / Al or LiF / Al or a compound thereof and a metal having a high work function, a laminated electrode of a metal such as ITO / Al / ITO and a transparent conductive film, and the like can be used.
【0046】また、対向電極側から、発光考を取り出す
光上取り出しの場合は、対向電極は透明あるいは半透明
であることが好ましい。この場合、例えばITO、Zn
Oといった酸化物からなる電極や、MgAg金属薄膜、
酸化物膜とメッシュ状に形成された金属薄膜との積層電
極なども用いることが出来る。When light is extracted from the counter electrode side to extract light, the counter electrode is preferably transparent or semitransparent. In this case, for example, ITO, Zn
Electrodes made of oxides such as O, MgAg metal thin films,
A laminated electrode including an oxide film and a metal thin film formed in a mesh shape can also be used.
【0047】電極102の形成方法としては、酸化イン
ジウムの他、酸化インジウムに酸化錫を含むITOや、
ZnOといった透明導電膜やAl等の金属電極であって
もよく、スパッタ、エレクトロンビーム蒸着、抵抗加熱
蒸着等の方法を用いればよい。As the method of forming the electrode 102, indium oxide, ITO containing tin oxide in indium oxide, or
A transparent conductive film such as ZnO or a metal electrode such as Al may be used, and a method such as sputtering, electron beam evaporation, or resistance heating evaporation may be used.
【0048】基板1は,本発明の発光素子を嘆じ出来るも
のであれば良く,ガラス或いはポリカー簿ねート、ポリ
メチルメタクリレート、ポリエチレンテレフタレートな
どの樹脂フィルム、またはシリコン基板等を用いること
ができる。Any substrate can be used as long as it can be used for the light emitting device of the present invention, and a glass or polycarbonate sheet, a resin film such as polymethylmethacrylate, polyethylene terephthalate, or a silicon substrate can be used.
【0049】緩衝層105は、上記材料に限らないもの
とし、例えば有機材料に導電性フィラーを混合したもの
であっても構わない。The buffer layer 105 is not limited to the above materials, and may be, for example, an organic material mixed with a conductive filler.
【0050】また、緩衝層105の形成方法も、上記方
法に限らないものとし、印刷法等の塗布型の他、真空蒸
着法などを用いてもよい。また硬化方法も熱硬化に限ら
ず、UV照射によるUV硬化、電子線照射によるEB硬
化法等を用いてもよい。The method of forming the buffer layer 105 is not limited to the above method, and a vacuum evaporation method or the like may be used in addition to a coating method such as a printing method. Further, the curing method is not limited to heat curing, and UV curing by UV irradiation, EB curing by electron beam irradiation, or the like may be used.
【0051】緩衝層の膜厚は、0.3μm以上5μm以
下であることが好ましく、さらに好ましいくは0.3μ
m以上10μm以下であることが好ましい。The thickness of the buffer layer is preferably 0.3 μm or more and 5 μm or less, more preferably 0.3 μm.
It is preferably m or more and 10 μm or less.
【0052】また、基板上に形成された積層構造体の高
低差の2倍以上であることが好ましい。Further, it is preferable that the height difference of the laminated structure formed on the substrate is twice or more.
【0053】表1に、本実施の形態における耐久テスト
結果を示す。Table 1 shows the results of the durability test in the present embodiment.
【0054】バリア膜106は、窒化アルミニウムに限
らず、SiOx、Al2O3といった酸化物、窒化物から
なる無機膜、ダイヤモンドライクカーボン膜(DLC
膜)の他、Alなどの金属膜であっても構わない。The barrier film 106 is not limited to aluminum nitride, but an inorganic film made of oxides or nitrides such as SiO x and Al 2 O 3 and a diamond-like carbon film (DLC).
Other than the film, a metal film such as Al may be used.
【0055】また、有機層と無機層の多層膜、または無
機膜の積層膜であっても構わない。Further, it may be a multilayer film of an organic layer and an inorganic layer, or a laminated film of inorganic films.
【0056】また、バリア膜106の形成方法も、上記
方法に限らないものとし、スパッタ、エレクトロンビー
ム蒸着、抵抗加熱蒸着、CVD、塗布型等、真空アーク
法、電子シャワー法、陽極酸化法などを用いればよい。Further, the method of forming the barrier film 106 is not limited to the above method, and sputtering, electron beam evaporation, resistance heating evaporation, CVD, coating type, etc., vacuum arc method, electron shower method, anodic oxidation method, etc. You can use it.
【0057】本実施の形態1においては、基板上に形成
された積層構造体上に、緩衝層105を形成することに
より、前記積層構造体の表面凹凸が低減し、その上に形
成されるバリア膜のクラックを防止することができる。
また、バリア膜が積層構造体にあたえる応力及びその他
外的要因によって引き起こされる応力が積層構造体に与
える影響を低減すること可能になり、対向電極の剥がれ
などといった素子破壊を防止することが出来る。In the first embodiment, by forming the buffer layer 105 on the laminated structure formed on the substrate, the unevenness of the surface of the laminated structure is reduced and the barrier formed thereon. It is possible to prevent the film from cracking.
Further, it is possible to reduce the influence of the stress applied to the laminated structure by the barrier film and the stress caused by other external factors on the laminated structure, and it is possible to prevent element destruction such as peeling of the counter electrode.
【0058】緩衝層105が有する導電性は、1012Ω
・cm以下が好ましい。さらに好ましくは、1010Ω・
cm以下である。The conductivity of the buffer layer 105 is 10 12 Ω.
-It is preferably not more than cm. More preferably, 10 10 Ω
cm or less.
【0059】緩衝層105が導電性を有することにより
対向電極の補助電極としての効果の他、例えば、バリア
膜成膜時のダメージを防止するなど、EL素子の静電破
壊を防止出来ると言った効果もある。It is said that the buffer layer 105 having electroconductivity can prevent the electrostatic breakdown of the EL element in addition to the effect as the auxiliary electrode of the counter electrode and the damage at the time of forming the barrier film, for example. There is also an effect.
【0060】これより、薄型、軽量、高寿命、かつ信頼
性の高い発光素子、表示装置及び照明装置を得ることが
出来る。As a result, it is possible to obtain a thin, lightweight, long-lifetime and highly reliable light emitting element, display device and lighting device.
【0061】(実施の形態2)以下本発明の実施の形態
2について説明する。図2は本発明に係る発光素子の実
施の形態2を示す断面図である。図2において、201
は基板、202は電極、203は発光層、204は対向
電極、205は緩衝層、206はバリア性を有するバリ
ア膜、207はスイッチング素子、208はSiO
2層、209は反射層である。(Second Embodiment) The second embodiment of the present invention will be described below. 2 is a sectional view showing a second embodiment of a light emitting device according to the present invention. In FIG. 2, 201
Is a substrate, 202 is an electrode, 203 is a light emitting layer, 204 is a counter electrode, 205 is a buffer layer, 206 is a barrier film having a barrier property, 207 is a switching element, and 208 is SiO.
Two layers, 209 are reflective layers.
【0062】本実施の形態において、発光素子を形成す
る工程は、一度も大気中に取り出すことなく、真空中で
行われる。In this embodiment mode, the step of forming a light-emitting element is performed in a vacuum without being taken out into the air even once.
【0063】本実施の形態において、反射層209、薄
膜トランジスタからなるスイッチング素子207及びI
TOからなる画素電極202が形成されたガラス基板上
に、少なくとも有機EL素子の発光領域203、対向電極
204を蒸着法により形成した積層構造体を形成する。In this embodiment mode, the reflective layer 209, the switching element 207 including a thin film transistor, and I
A laminated structure in which at least a light emitting region 203 of an organic EL element and a counter electrode 204 are formed by a vapor deposition method is formed on a glass substrate on which a pixel electrode 202 made of TO is formed.
【0064】発光領域203は例えばAlq3等からな
る発光層(膜厚500A)とTPDからなる正孔輸送層
(膜厚500A)(図示せず)からなる。対向電極20
4は、この場合、MgAgからなる金属薄膜(50A)
上に透明あるいは半透明である酸化インジウム(膜厚1
000A)を積層した積層電極からなる。The light emitting region 203 is composed of, for example, a light emitting layer (thickness 500A) made of Alq 3 or the like and a hole transport layer (thickness 500A) (not shown) made of TPD. Counter electrode 20
4 is a metal thin film (50A) made of MgAg in this case.
Transparent or translucent indium oxide (film thickness 1
000A) is laminated.
【0065】スイッチング素子207上には、異なる発
光領域を区分するため有機材料が覆っており、基板表面
からおよそ1μm程度の高低差がある。The switching element 207 is covered with an organic material for partitioning different light emitting regions and has a height difference of about 1 μm from the substrate surface.
【0066】対向電極上に形成されたSiO2層(20
0A)は、スパッタ法にて無加熱に形成されており、緩
衝層205との密着性を向上することが出来る。The SiO 2 layer (20
0A) is formed by a sputtering method without heating and can improve the adhesiveness with the buffer layer 205.
【0067】緩衝層205は、アクリル系材料に例えば
ポリアルキレングリコールを主成分とするポリマーに過
塩素酸リチウムなどの過塩素酸塩を複合化させたイオン
伝導性の導電性付与剤を添加した有機導電性材料を、印
刷法によりSiO2上に208上に5μm形成した後、
電子線照射を施こすことにより硬化している。これによ
り、積層構造体表面の高低差は約20nm程度である。
緩衝層205を形成することにより基板上の表面形状を
平坦化するといった効果がある。また緩衝層のシート抵
抗値は105Ω・cm程度である。The buffer layer 205 is an organic material obtained by adding an ion-conductive conductivity-imparting agent obtained by compounding an acrylic material, for example, a polymer containing polyalkylene glycol as a main component with a perchlorate such as lithium perchlorate. After forming a conductive material on SiO 2 by 5 μm on 208 by a printing method,
It is cured by electron beam irradiation. As a result, the height difference on the surface of the laminated structure is about 20 nm.
The formation of the buffer layer 205 has an effect of flattening the surface shape on the substrate. The sheet resistance of the buffer layer is about 10 5 Ω · cm.
【0068】衝層上にはバリア膜206が形成されてい
る。バリア膜はSiOxとアクリル系樹脂を交互に20
層程度積層した多層膜からなる。SiOxはバリア性を
有し、スパッタ法にて800A形成されている。アクリ
ル系樹脂は蒸着重合により0.3μm程度形成されてい
る。バリア膜206は、水蒸気バリア性に優れ、0.0
5以下g/m2/dayである。A barrier film 206 is formed on the barrier layer. For the barrier film, SiOx and acrylic resin are alternately used.
It is composed of a multi-layer film in which layers are laminated. SiOx has a barrier property, and 800 A is formed by the sputtering method. The acrylic resin is formed to a thickness of about 0.3 μm by vapor deposition polymerization. The barrier film 206 has an excellent water vapor barrier property and is 0.0
It is 5 or less g / m 2 / day.
【0069】有機材料からなる発光領域203は、耐熱
性が悪く、発光領域203上に形成する対向電極20
3、SiOx層208、及び緩衝層206、バリア膜2
06は、100℃以下の温度で形成することが好まし
い。The light emitting region 203 made of an organic material has poor heat resistance and the counter electrode 20 formed on the light emitting region 203.
3, SiOx layer 208, buffer layer 206, and barrier film 2
06 is preferably formed at a temperature of 100 ° C. or lower.
【0070】対向電極204は低温で形成されるため、
対向電極104と下地膜の密着性は悪く、対向電極20
4の剥がれが発生しやすい。また対向電極204上に形
成された緩衝層、バリア膜といった各積層膜も低温で形
成するため、各層界面の密着性も悪く、各膜応力による
各膜界面の剥がれが発生しやすい。対向電極204と緩
衝層205との間にSiOx膜を形成することにより、
対向電極204と緩衝層205の密着性が向上するとい
った効果がある。Since the counter electrode 204 is formed at a low temperature,
The adhesion between the counter electrode 104 and the base film is poor, and the counter electrode 20
4 peeling is likely to occur. Further, since each laminated film such as the buffer layer and the barrier film formed on the counter electrode 204 is also formed at a low temperature, the adhesiveness of the interface between the respective layers is poor, and the film interface is likely to be peeled off due to the stress of each film. By forming a SiOx film between the counter electrode 204 and the buffer layer 205,
This has the effect of improving the adhesion between the counter electrode 204 and the buffer layer 205.
【0071】発光光を対向電極側から取り出す、光上取
り出しの場合は、対向電極は透明あるいは半透明である
ことが好ましい。この場合、例えばITO、ZnOとい
った酸化物からなる電極や、MgAg金属薄膜、酸化物
膜とメッシュ状に形成された金属薄膜との積層電極など
も用いることが出来る。In the case of taking out emitted light from the counter electrode side and taking out the light above, the counter electrode is preferably transparent or semitransparent. In this case, for example, an electrode made of an oxide such as ITO or ZnO, a MgAg metal thin film, or a laminated electrode of an oxide film and a metal thin film formed in a mesh shape can be used.
【0072】電極202の形成方法としては、酸化イン
ジウムの他、酸化インジウムに酸化錫を含むITOや、
ZnOといった透明導電膜やAl等の金属電極であって
もよく、スパッタ、エレクトロンビーム蒸着、抵抗加熱
蒸着等の方法を用いればよい。As a method of forming the electrode 202, indium oxide, ITO containing tin oxide in indium oxide, or
A transparent conductive film such as ZnO or a metal electrode such as Al may be used, and a method such as sputtering, electron beam evaporation, or resistance heating evaporation may be used.
【0073】基板201は,本発明の発光素子を嘆じ出
来るものであれば良く,ガラス或いはポリカー簿ねー
ト、ポリメチルメタクリレート、ポリエチレンテレフタ
レートなどの樹脂フィルム、またはシリコン基板等を用
いることができる。Any substrate can be used as long as it can be used for the light emitting device of the present invention, and glass or resin sheet such as polycarbonate sheet, polymethylmethacrylate, polyethylene terephthalate, or silicon substrate can be used.
【0074】緩衝層205は、上記材料に限らないもの
とし、例えば有機材料に導電性フィラーを混合したもの
であっても構わない。The buffer layer 205 is not limited to the above materials, and may be, for example, an organic material mixed with a conductive filler.
【0075】また、緩衝層205の形成方法も、上記方
法に限らない。The method of forming the buffer layer 205 is not limited to the above method.
【0076】発光光を対向電極側から取り出す、光上取
り出しの場合は、緩衝層やバリア膜は透明あるいは半透
明であることが好ましい。In the case of taking out emitted light from the counter electrode side and taking out light, it is preferable that the buffer layer and the barrier film are transparent or semitransparent.
【0077】発光光を対向電極側から取り出す、光上取
り出しの場合は、緩衝層やバリア膜は透明あるいは半透
明であることが好ましい。In the case of taking out the emitted light from the counter electrode side and taking out the light above, it is preferable that the buffer layer and the barrier film are transparent or semitransparent.
【0078】本実施の形態において、発光素子を形成す
る工程は、一度も大気中に取り出すことなく、真空中で
行われることが好ましい。これにより水分、酸素等が取
り込まれることなく、信頼性の高い発光素子が得ること
が可能になる。In this embodiment mode, the step of forming a light-emitting element is preferably performed in a vacuum without being taken out into the air even once. This makes it possible to obtain a highly reliable light emitting element without taking in water, oxygen, and the like.
【0079】例えば、バリア膜206は、SiOxに限
らず、AlON、Al2O3といった酸化物、窒化物から
なる無機膜、ダイヤモンドライクカーボン(DLC)膜
であっても構わない。For example, the barrier film 206 is not limited to SiOx, but may be an inorganic film made of an oxide such as AlON or Al 2 O 3 , a nitride, or a diamond-like carbon (DLC) film.
【0080】また、有機層と無機層の多層膜、または無
機膜の積層膜であっても構わない。Further, it may be a multilayer film of an organic layer and an inorganic layer, or a laminated film of an inorganic film.
【0081】また、バリア膜206の形成方法も、上記
方法に限らないものとし、スパッタ、エレクトロンビー
ム蒸着、抵抗加熱蒸着、CVD、塗布型等、真空アーク
法、電子シャワー法、陽極酸化法などを用いればよい。The method for forming the barrier film 206 is not limited to the above method, and sputtering, electron beam evaporation, resistance heating evaporation, CVD, coating type, vacuum arc method, electron shower method, anodic oxidation method, etc. may be used. You can use it.
【0082】[0082]
【表1】 [Table 1]
【0083】表1に、本実施の形態における耐久テスト
結果を示す。Table 1 shows the result of the durability test in the present embodiment.
【0084】また、ガラスキャップ等を被うことによ
り、さらにバリア性を向上するこが出来る。By covering with a glass cap or the like, the barrier property can be further improved.
【0085】本実施の形態2においては、基板上に形成
された積層構造体上に、SiOx膜、緩衝層205を形
成することにより、前記積層構造体の表面凹凸が低減
し、その上に形成されるバリア膜のクラックを防止する
ことができる。また、バリア膜が積層構造体にあたえる
応力及びその他外的要因によって引き起こされる応力が
積層構造体に与える影響を低減すること可能になり、対
向電極の剥がれなどといった素子破壊を防止することが
出来る。また、緩衝層205が導電性を有することによ
り対向電極の補助電極としての効果の他、素子の静電破
壊を防止出来ると言った効果もある。In the second embodiment, by forming the SiOx film and the buffer layer 205 on the laminated structure formed on the substrate, surface irregularities of the laminated structure are reduced and formed on it. It is possible to prevent cracks in the barrier film. Further, it is possible to reduce the influence of the stress applied to the laminated structure by the barrier film and the stress caused by other external factors on the laminated structure, and it is possible to prevent element destruction such as peeling of the counter electrode. Further, since the buffer layer 205 has conductivity, there is an effect that the electrostatic breakdown of the element can be prevented in addition to the effect as the auxiliary electrode of the counter electrode.
【0086】これより、薄型、軽量、高寿命、かつ信頼
性の高い発光素子、表示装置及び照明装置を得ることが
出来る。As a result, it is possible to obtain a thin, lightweight, long-lifetime and highly reliable light emitting element, display device and lighting device.
【0087】[0087]
【発明の効果】本発明によれば、基板上に少なくとも電
極、有機発光層、対向電極を形成した積層構造体上に有
機化合物からなる緩衝層を形成することにより、積層構
造体上に直接バリア膜を形成することが可能になり、吸
湿による有機EL素子劣化や、膜応力によるバリア膜ク
ラック、及び発光素子劣化のない信頼性の高い有機EL
素子及びそれを用いた表示装置、照明装置を実現するこ
とを目的とする。According to the present invention, a barrier layer made of an organic compound is formed on a laminated structure in which at least an electrode, an organic light emitting layer and a counter electrode are formed on a substrate, so that a barrier is directly formed on the laminated structure. It becomes possible to form a film, and a highly reliable organic EL device that is free from deterioration of the organic EL device due to moisture absorption, cracks of the barrier film due to film stress, and deterioration of the light emitting device.
An object is to realize an element, a display device using the element, and a lighting device.
【0088】また、従来、水分の侵入を防止するべく有
機EL発光素子に被せられてきたガラスやアルミからな
るキャップ52を設ける必要がなくなり、発光素子の小
型化が可能となり、かつ発光光の外部への射出割合の低
下をなくすことができる。Further, it is no longer necessary to provide the cap 52 made of glass or aluminum, which has been conventionally covered on the organic EL light emitting element in order to prevent the entry of moisture, so that the light emitting element can be downsized and the outside of the emitted light can be eliminated. It is possible to eliminate the decrease in the injection rate to the.
【0089】これより、薄型、軽量、高寿命、かつ信頼
性の高い発光素子、表示装置及び照明装置を得ることが
出来る。As a result, it is possible to obtain a thin, lightweight, long-lifetime and highly reliable light emitting element, display device and lighting device.
【0090】また、緩衝層105が導電性を有すること
により対向電極の補助電極としての効果の他、例えば、
バリア膜成膜時のダメージを防止するなど、EL素子の
静電破壊を防止か可能となり、歩留まりが向上出来ると
言った効果もある。Further, in addition to the effect of the buffer layer 105 having conductivity as an auxiliary electrode of the counter electrode, for example,
There is also an effect that it is possible to prevent electrostatic breakdown of the EL element, such as preventing damage at the time of forming the barrier film, and improve the yield.
【0091】また、対向電極204と緩衝層205との
間にSiOx膜を形成することにより、対向電極204
と緩衝層205の密着性が向上するといった効果があ
る。By forming a SiOx film between the counter electrode 204 and the buffer layer 205, the counter electrode 204
This has the effect of improving the adhesion of the buffer layer 205.
【0092】これより、各膜応力による各膜界面の剥が
れが発生しない信頼性の高い有機EL素子及びそれを用
いた表示装置、照明装置を実現することを目的とする。Therefore, it is an object of the present invention to realize a highly reliable organic EL element in which peeling of each film interface due to each film stress does not occur, and a display device and a lighting device using the same.
【図1】本発明の実施の形態1における発光素子の断面
図FIG. 1 is a sectional view of a light emitting device according to a first embodiment of the present invention.
【図2】本発明の実施の形態2における発光素子の断面
図FIG. 2 is a sectional view of a light emitting device according to a second embodiment of the present invention.
【図3】従来の一般的な有機EL発光素子を示す断面図FIG. 3 is a cross-sectional view showing a conventional general organic EL light emitting device.
【図4】従来の一般的な有機EL発光素子を示す断面図FIG. 4 is a cross-sectional view showing a conventional general organic EL light emitting device.
101 基板 102 電極 103 発光領域 104 対向電極 105 緩衝層 106 バリア膜 101 substrate 102 electrodes 103 light emitting area 104 counter electrode 105 buffer layer 106 barrier film
───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 3K007 AB11 AB15 AB18 BA06 BB07 CB01 CB02 CC01 DA01 DB03 EB00 FA01 FA02 5C094 AA15 AA31 AA36 AA42 AA43 BA03 BA27 CA19 DA07 DA09 DA13 EA04 EA05 EA06 EA07 EA10 FA01 FA02 FA04 FB01 FB02 FB12 FB15 FB20 GB10 JA05 JA08 JA20 5G435 AA14 AA17 AA18 BB05 CC09 GG32 GG42 HH01 HH12 HH20 KK05 ─────────────────────────────────────────────────── ─── Continued front page F term (reference) 3K007 AB11 AB15 AB18 BA06 BB07 CB01 CB02 CC01 DA01 DB03 EB00 FA01 FA02 5C094 AA15 AA31 AA36 AA42 AA43 BA03 BA27 CA19 DA07 DA09 DA13 EA04 EA05 EA06 EA07 EA10 FA01 FA02 FA04 FB01 FB02 FB12 FB15 FB20 GB10 JA05 JA08 JA20 5G435 AA14 AA17 AA18 BB05 CC09 GG32 GG42 HH01 HH12 HH20 KK05
Claims (15)
と対向電極と、を備えた発光素子であって、前記対向電
極上に形成された緩衝層と、前記緩衝層上に少なくとも
1層以上のバリア膜とが形成されていることを特徴とす
る発光素子。1. A light emitting device comprising an electrode formed on a substrate, an organic light emitting layer and a counter electrode, wherein a buffer layer formed on the counter electrode and at least 1 on the buffer layer. A light-emitting element having a barrier film of at least one layer formed.
する請求項1記載の発光素子。2. The light emitting device according to claim 1, wherein the buffer layer contains an organic substance.
膜厚であることを特徴とする請求項1又は2に記載の発
光素子。3. The light emitting device according to claim 1, wherein the buffer layer has a film thickness of 0.3 μm or more and 5 μm or less.
造の凹凸の2倍以上の膜厚であることを特徴とする請求
項1から3のいずれか1項に記載の発光素子。4. The light emitting device according to claim 1, wherein the buffer layer has a film thickness that is at least twice as large as the unevenness of the laminate structure formed on the substrate.
構造体の表面の凹凸を0.5μm以下にしていることを
特徴とする請求項4に記載の発光素子。5. The light emitting device according to claim 4, wherein the buffer layer covers the laminated structure, and the unevenness of the surface of the laminated structure is 0.5 μm or less.
012Ω・cm以下であることを特徴とする請求項1から
5のいずれか1項に記載の発光素子。6. The buffer layer has conductivity and has a volume resistance value of 1
The light emitting device according to claim 1, wherein the light emitting device has a resistance of 0 12 Ω · cm or less.
膜、及びダイヤモンドライクカーボン膜を少なくとも1
種以上含むことを特徴とする請求項1から6のいずれか
1項に記載の発光素子。7. The barrier film is at least one of an oxide film, a nitride film, a metal thin film, and a diamond-like carbon film.
7. The light emitting device according to claim 1, comprising at least one kind.
する請求項1から7のいずれか1項に記載の発光素子。8. The light emitting device according to claim 1, wherein the buffer layer has an oxide film.
する請求項8記載の発光素子。9. The light emitting device according to claim 8, wherein the oxide film is made of SiOx.
nm以下の膜厚であることを特徴とする請求項8又は9
に記載の発光素子。10. The SiOx layer has a thickness of 15 nm or more and 1000 or more.
The film thickness is less than or equal to nm.
The light emitting device according to.
光素子を用いた表示装置。11. A display device using the light emitting device according to claim 1.
発光素子を用いた照明装置。12. An illuminating device using the light emitting device according to claim 1.
電極上に有機発光層を形成する工程と、前記有機発光層
上に対向電極を形成する工程からなる発光素子の製造方
法であって、少なくとも前記対向電極の表面に緩衝層を
形成する工程と、前記緩衝層上に少なくとも1層以上の
バリア膜を形成する工程とを有することを特徴とする発
光素子の製造方法。13. A method of manufacturing a light emitting device, comprising the steps of forming an electrode on a substrate, forming an organic light emitting layer on the electrode, and forming a counter electrode on the organic light emitting layer. And a step of forming a buffer layer at least on the surface of the counter electrode, and a step of forming at least one barrier film on the buffer layer.
空中で連続して行われることを特徴とする請求項13記
載の発光素子の製造方法。14. The method for manufacturing a light emitting device according to claim 13, wherein the process is continuously performed in a vacuum without being taken out into the atmosphere even once.
と、前記緩衝層上に少なくとも1層以上のバリア膜を形
成する工程とは、100℃以下の温度条件下で行われる
ことを特徴とする請求項13記載の発光素子の製造方
法。15. The step of forming a buffer layer on the counter electrode and the step of forming at least one barrier film on the buffer layer are performed under a temperature condition of 100 ° C. or lower. The method for manufacturing a light emitting device according to claim 13.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001271307A JP2003086357A (en) | 2001-09-07 | 2001-09-07 | Light emitting element and manufacturing method of the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2001271307A JP2003086357A (en) | 2001-09-07 | 2001-09-07 | Light emitting element and manufacturing method of the same |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2003086357A true JP2003086357A (en) | 2003-03-20 |
Family
ID=19096833
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2001271307A Pending JP2003086357A (en) | 2001-09-07 | 2001-09-07 | Light emitting element and manufacturing method of the same |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2003086357A (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005038833A (en) * | 2003-06-16 | 2005-02-10 | Semiconductor Energy Lab Co Ltd | Light emitting device and manufacturing method thereof |
JP2006024421A (en) * | 2004-07-07 | 2006-01-26 | Seiko Epson Corp | Electro-optical device and manufacturing method of electro-optical device, and electronic apparatus |
WO2006018914A1 (en) * | 2004-08-20 | 2006-02-23 | Japan Science And Technology Agency | Organic semiconductor laser device and organic electroluminescence device |
WO2006051649A1 (en) * | 2004-11-10 | 2006-05-18 | Idemitsu Kosan Co., Ltd. | Organic electroluminescent element |
JP2006222070A (en) * | 2005-01-17 | 2006-08-24 | Seiko Epson Corp | Light emitting device, manufacturing method thereof, and electronic equipment |
JP2006278021A (en) * | 2005-03-28 | 2006-10-12 | Pioneer Electronic Corp | Inspection method and structure of organic function element sealing film |
KR100692458B1 (en) | 2004-02-18 | 2007-03-09 | 세이코 엡슨 가부시키가이샤 | Organic electroluminescent device and electronic apparatus |
US7683225B2 (en) | 2004-06-16 | 2010-03-23 | Idemitsu Kosan Co., Ltd. | Fluorene-based derivative and organic electroluminescence device employing the same |
US7956355B2 (en) | 2004-10-22 | 2011-06-07 | Seiko Epson Corporation | Method of manufacturing organic electroluminescent device and organic electroluminescent device |
JP2012230913A (en) * | 2003-06-16 | 2012-11-22 | Semiconductor Energy Lab Co Ltd | Light-emitting device |
WO2015015762A1 (en) * | 2013-08-01 | 2015-02-05 | パナソニック株式会社 | Organic light emitting element, organic light emitting display panel, and organic light emitting display apparatus |
-
2001
- 2001-09-07 JP JP2001271307A patent/JP2003086357A/en active Pending
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005038833A (en) * | 2003-06-16 | 2005-02-10 | Semiconductor Energy Lab Co Ltd | Light emitting device and manufacturing method thereof |
JP2014032976A (en) * | 2003-06-16 | 2014-02-20 | Semiconductor Energy Lab Co Ltd | Light-emitting device |
US8609181B2 (en) | 2003-06-16 | 2013-12-17 | Semiconductor Energy Laboratory Co., Ltd. | Light emitting device and method for fabricating light emitting device |
JP2012230913A (en) * | 2003-06-16 | 2012-11-22 | Semiconductor Energy Lab Co Ltd | Light-emitting device |
JP4519532B2 (en) * | 2003-06-16 | 2010-08-04 | 株式会社半導体エネルギー研究所 | LIGHT EMITTING DEVICE AND ELECTRONIC DEVICE USING LIGHT EMITTING DEVICE |
KR100692458B1 (en) | 2004-02-18 | 2007-03-09 | 세이코 엡슨 가부시키가이샤 | Organic electroluminescent device and electronic apparatus |
US8013160B2 (en) | 2004-06-16 | 2011-09-06 | Idemitsu Kosan Co., Ltd. | Fluorene-based derivative and organic electroluminescence device employing the same |
US7683225B2 (en) | 2004-06-16 | 2010-03-23 | Idemitsu Kosan Co., Ltd. | Fluorene-based derivative and organic electroluminescence device employing the same |
US7781628B2 (en) | 2004-06-16 | 2010-08-24 | Idemitsu Kosan Co., Ltd. | Fluorene-based derivative and organic electroluminescence device employing the same |
JP2006024421A (en) * | 2004-07-07 | 2006-01-26 | Seiko Epson Corp | Electro-optical device and manufacturing method of electro-optical device, and electronic apparatus |
WO2006018914A1 (en) * | 2004-08-20 | 2006-02-23 | Japan Science And Technology Agency | Organic semiconductor laser device and organic electroluminescence device |
US7956355B2 (en) | 2004-10-22 | 2011-06-07 | Seiko Epson Corporation | Method of manufacturing organic electroluminescent device and organic electroluminescent device |
JP2006140235A (en) * | 2004-11-10 | 2006-06-01 | Idemitsu Kosan Co Ltd | Organic electroluminescence element |
WO2006051649A1 (en) * | 2004-11-10 | 2006-05-18 | Idemitsu Kosan Co., Ltd. | Organic electroluminescent element |
JP4631683B2 (en) * | 2005-01-17 | 2011-02-16 | セイコーエプソン株式会社 | Light emitting device and electronic device |
JP2006222070A (en) * | 2005-01-17 | 2006-08-24 | Seiko Epson Corp | Light emitting device, manufacturing method thereof, and electronic equipment |
JP2006278021A (en) * | 2005-03-28 | 2006-10-12 | Pioneer Electronic Corp | Inspection method and structure of organic function element sealing film |
WO2015015762A1 (en) * | 2013-08-01 | 2015-02-05 | パナソニック株式会社 | Organic light emitting element, organic light emitting display panel, and organic light emitting display apparatus |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6597111B2 (en) | Protected organic optoelectronic devices | |
US6765351B2 (en) | Organic optoelectronic device structures | |
US6414432B1 (en) | Organic EL device and method for manufacturing same | |
US9343709B2 (en) | Light-emitting device and a method of manufacturing light-emitting device | |
TWI578588B (en) | Organic light emitting diode device and method for manufacturing the same | |
US20050023974A1 (en) | Protected organic electronic devices and methods for making the same | |
JP2004031324A (en) | Organic electroluminescence element | |
KR100771464B1 (en) | Organic el display and production method thereof | |
JPH10275680A (en) | Organic el element | |
JPWO2005027582A1 (en) | Display device and manufacturing method thereof | |
US20040070334A1 (en) | Encapsulated electrode | |
KR100477105B1 (en) | Organic el device and method of manufacturing organic el device | |
JP2003168556A (en) | Organic el element structure | |
JP2004319103A (en) | Organic electroluminescent element | |
JP2003086357A (en) | Light emitting element and manufacturing method of the same | |
TWI226026B (en) | Organic electroluminescent display panel and manufacturing method therefor | |
US20050062052A1 (en) | Panel of organic electroluminescent display | |
CN1592510A (en) | EL device | |
JPH08222373A (en) | Organic thin-film electroluminescent element | |
JP2002359070A (en) | Organic light emitting element and display panel using this element | |
US8129903B2 (en) | Organic electroluminescent display device | |
JP2003297554A (en) | Light-emitting element, and display device and lighting apparatus using the same | |
JP2000012237A (en) | Manufacture of organic electroluminescent display element | |
JP2007080600A (en) | Organic el element, and light emitting device | |
JP2003123967A (en) | Method for producing light emitting element |