JPS61161691A - Field light emitting lamp - Google Patents
Field light emitting lampInfo
- Publication number
- JPS61161691A JPS61161691A JP60001924A JP192485A JPS61161691A JP S61161691 A JPS61161691 A JP S61161691A JP 60001924 A JP60001924 A JP 60001924A JP 192485 A JP192485 A JP 192485A JP S61161691 A JPS61161691 A JP S61161691A
- Authority
- JP
- Japan
- Prior art keywords
- thin film
- transparent conductive
- high dielectric
- conductive film
- 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
- 239000010408 film Substances 0.000 claims description 37
- 239000010409 thin film Substances 0.000 claims description 32
- 239000000463 material Substances 0.000 claims description 19
- 229920003002 synthetic resin Polymers 0.000 claims description 12
- 239000000057 synthetic resin Substances 0.000 claims description 12
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 16
- 239000000843 powder Substances 0.000 description 13
- 238000000034 method Methods 0.000 description 11
- 239000012190 activator Substances 0.000 description 8
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 7
- 229910052782 aluminium Inorganic materials 0.000 description 7
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 7
- -1 allyl ester Chemical class 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 239000000853 adhesive Substances 0.000 description 5
- 230000001070 adhesive effect Effects 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 238000002834 transmittance Methods 0.000 description 5
- KXJGSNRAQWDDJT-UHFFFAOYSA-N 1-acetyl-5-bromo-2h-indol-3-one Chemical compound BrC1=CC=C2N(C(=O)C)CC(=O)C2=C1 KXJGSNRAQWDDJT-UHFFFAOYSA-N 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 239000003822 epoxy resin Substances 0.000 description 4
- 239000011888 foil Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 4
- 229920000647 polyepoxide Polymers 0.000 description 4
- 229910001928 zirconium oxide Inorganic materials 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- JRPBQTZRNDNNOP-UHFFFAOYSA-N barium titanate Chemical compound [Ba+2].[Ba+2].[O-][Ti]([O-])([O-])[O-] JRPBQTZRNDNNOP-UHFFFAOYSA-N 0.000 description 3
- 229910002113 barium titanate Inorganic materials 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 239000003989 dielectric material Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 229920001807 Urea-formaldehyde Polymers 0.000 description 2
- 239000005083 Zinc sulfide Substances 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005566 electron beam evaporation Methods 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 229910003437 indium oxide Inorganic materials 0.000 description 2
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 2
- 229910052981 lead sulfide Inorganic materials 0.000 description 2
- 229940056932 lead sulfide Drugs 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000007650 screen-printing Methods 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 2
- 229910001887 tin oxide Inorganic materials 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- 229920006337 unsaturated polyester resin Polymers 0.000 description 2
- 229910052984 zinc sulfide Inorganic materials 0.000 description 2
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 2
- PFNQVRZLDWYSCW-UHFFFAOYSA-N (fluoren-9-ylideneamino) n-naphthalen-1-ylcarbamate Chemical compound C12=CC=CC=C2C2=CC=CC=C2C1=NOC(=O)NC1=CC=CC2=CC=CC=C12 PFNQVRZLDWYSCW-UHFFFAOYSA-N 0.000 description 1
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
- WUPHOULIZUERAE-UHFFFAOYSA-N 3-(oxolan-2-yl)propanoic acid Chemical compound OC(=O)CCC1CCCO1 WUPHOULIZUERAE-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 101100327917 Caenorhabditis elegans chup-1 gene Proteins 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004695 Polyether sulfone Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229910001128 Sn alloy Inorganic materials 0.000 description 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 229910052980 cadmium sulfide Inorganic materials 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000012461 cellulose resin Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000011889 copper foil Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 229940113088 dimethylacetamide Drugs 0.000 description 1
- 229920006332 epoxy adhesive Polymers 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 238000001755 magnetron sputter deposition Methods 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 238000005240 physical vapour deposition Methods 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006393 polyether sulfone Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 238000001552 radio frequency sputter deposition Methods 0.000 description 1
- 238000005546 reactive sputtering Methods 0.000 description 1
- 150000003377 silicon compounds Chemical class 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 150000003609 titanium compounds Chemical class 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は、液晶のバックライト或いは各種形状の表示装
置等に使用できる電場発光灯に関するものである。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to an electroluminescent lamp that can be used for liquid crystal backlights, display devices of various shapes, and the like.
(従来の技術)
従来、電場発光灯としては、光透過性を有する合成樹脂
基材の表面に、透明導電膜、発光体層および背面電極を
順次形成した構造のものが知られている。この電場発光
灯は透明導電膜と背面電極の間に電圧を印加することに
より、電気ルミネセンス螢光体を励起せしめて発光させ
るものである。(Prior Art) Conventionally, as an electroluminescent lamp, one having a structure in which a transparent conductive film, a light-emitting layer, and a back electrode are sequentially formed on the surface of a synthetic resin base material having light transparency is known. This electroluminescent lamp excites an electroluminescent phosphor to emit light by applying a voltage between a transparent conductive film and a back electrode.
(発明が解決しようとする問題点)
而して、上記従来品においては、透明導電膜と発光体層
との密着力が弱く、両者の界面で剥離現象(所謂「電極
剥離」 )を生ずることがあった。(Problems to be Solved by the Invention) However, in the conventional product described above, the adhesion between the transparent conductive film and the luminescent layer is weak, and a peeling phenomenon (so-called "electrode peeling") occurs at the interface between the two. was there.
透明導電膜と発光体層との界面で剥離を生じた場合には
、例えそれが局部的なものであっても、接触面積が減少
することにより電極間の電気抵抗が大きくなり、その結
果、発光灯の発光探度の低下を招くという不都合がある
。If peeling occurs at the interface between the transparent conductive film and the light emitting layer, even if it is only local, the electrical resistance between the electrodes will increase due to the decrease in the contact area, and as a result, This has the disadvantage of causing a decrease in the light emission detection rate of the light emitting lamp.
(問題点を解決するための手段)
本発明者達は上記現状に鑑み鋭意検討の結果、透明導電
膜と発光体1mの間に高誘電体層を介在せしめることに
より、透明導電膜と発光体層の密着力を向上でき、電極
剥離を防止し得ることを見出し、本発明を完成するに至
ったものである。(Means for Solving the Problems) In view of the above-mentioned current situation, the inventors of the present invention have made extensive studies and found that by interposing a high dielectric layer between the transparent conductive film and the light emitting material, the transparent conductive film and the light emitting material can be It was discovered that the adhesion of the layers could be improved and electrode peeling could be prevented, leading to the completion of the present invention.
即ち、本発明は光透過性を有する合成樹脂基材の表面上
に、透明導電膜、高誘電体薄膜、発光体層および背面電
極が順次積層されていることを特徴とする電場発光灯に
係るものである。That is, the present invention relates to an electroluminescent lamp characterized in that a transparent conductive film, a high dielectric thin film, a light emitter layer, and a back electrode are sequentially laminated on the surface of a synthetic resin base material having light transparency. It is something.
本発明において用いる光透過性を有する合成樹脂基材は
、厚さが通常約50〜200μm のフィルム状或いは
シート状のもので、光透過率は約60%以上に設定する
のが好適であるが、場合によりこれよりも光透過率の小
さなものも使用し得る。The light-transmitting synthetic resin base material used in the present invention is usually in the form of a film or sheet with a thickness of about 50 to 200 μm, and the light transmittance is preferably set to about 60% or more. However, in some cases, a material with a smaller light transmittance than this may also be used.
この合成樹脂基材は、ポリエステル、ポリカーボネート
、ポリエーテルスルホン、ポリアミド、ポリスチレン、
ポリアセタール、ポリオレフィン、ポリアクリロニトリ
ル、ABS[脂、ポリウレタン等の熱可塑性樹脂または
溶剤可溶性樹脂、或いはエポキシ樹脂、アリルエステル
樹脂、シリコーンフェノール樹脂、不飽和ポリエステル
樹脂、メラミン樹脂、尿素樹脂等の熱硬化性樹脂から形
成できる。This synthetic resin base material is made of polyester, polycarbonate, polyethersulfone, polyamide, polystyrene,
Polyacetal, polyolefin, polyacrylonitrile, ABS [fat, thermoplastic resin or solvent-soluble resin such as polyurethane, or thermosetting resin such as epoxy resin, allyl ester resin, silicone phenol resin, unsaturated polyester resin, melamine resin, urea resin, etc. It can be formed from
上記合成樹脂基材の表面とには、酸化インジウム、酸化
スズ、酸化インジウムと酸化スズの混合物、金、銀、銅
、アルミニウム、パラジウム或いは白金等から成り、可
視光線領域で透明であり且つ導電性を有する厚さが通常
約50〜100OAの電極として機能する透明導電膜が
形成される。The surface of the synthetic resin base material is made of indium oxide, tin oxide, a mixture of indium oxide and tin oxide, gold, silver, copper, aluminum, palladium, platinum, etc., and is transparent in the visible light range and conductive. A transparent conductive film functioning as an electrode is formed having a thickness of usually about 50 to 100 OA.
合成樹脂基材表面への透明導電膜の形成は、従来から知
られている真空蒸着法、スパッタリング法、イオンブレ
ーティング法等により行なうことができる。The transparent conductive film can be formed on the surface of the synthetic resin base material by a conventionally known vacuum deposition method, sputtering method, ion blating method, or the like.
本発明においては透明導電膜上に光透過性で且つ高誘電
率の高誘電体薄膜ばか形成される。高誘電体薄膜の光透
過率は、合成樹脂基材のそれに応じて変わり得るが通常
は約70%以上であり、また誘電率は通常約100以上
である。In the present invention, a light-transmissive, high dielectric thin film having a high dielectric constant is formed on a transparent conductive film. The light transmittance of the high dielectric thin film may vary depending on the synthetic resin base material, but it is usually about 70% or more, and the dielectric constant is usually about 100 or more.
この高誘電体薄膜の形成はTi5Si、Zrの反応性蒸
着或いは反応性スパッタリングにより、Ti0z、5i
02、Zr0z R膜を形成する方法、Ti0z、5i
02、ZrO2、Ta205を用いてRFxバッタリン
グ、電子ビーム蒸着の如きPVD法により前記金属酸化
物薄膜を形成する法、アルキルチタネート化合物の如き
有機チタン化合物、テトラエチルシリケートの如き有機
ケイ素化合物、或いは有機ジルコニウム化合物を用いて
コーティング法やCVO法により、金属酸化物薄膜を形
成する方法等に行なうことができる。This high dielectric thin film is formed by reactive vapor deposition or reactive sputtering of Ti5Si and Zr.
02, Method of forming Zr0z R film, Ti0z, 5i
02, a method of forming the metal oxide thin film by a PVD method such as RFx battering or electron beam evaporation using ZrO2 or Ta205, an organic titanium compound such as an alkyl titanate compound, an organic silicon compound such as tetraethyl silicate, or an organic zirconium A method of forming a metal oxide thin film using a compound by a coating method or a CVO method can be used.
上記高誘電体薄膜の厚さは約50A〜5μmとするのが
好適である。この高誘電体薄膜の厚さが薄すぎると連続
した均一膜とならず効果が期待できず、厚すぎると電場
発光灯の発光輝度の低下を招くことがある。The thickness of the high dielectric thin film is preferably about 50 A to 5 μm. If the high dielectric thin film is too thin, it will not be a continuous and uniform film, and no effect can be expected; if it is too thick, the luminance of the electroluminescent lamp may be reduced.
本発明においては、このように透明導電膜上に高誘電体
薄膜が形成されるのであり、該高誘電体薄膜の形成によ
り合成樹脂基材側における光透過率の低下が懸念される
が、実際には光透過率の低下を来たすようなことは殆ん
どない。In the present invention, a high dielectric thin film is formed on the transparent conductive film in this way, and there is a concern that the formation of the high dielectric thin film will reduce the light transmittance on the synthetic resin base material side. There is almost no decrease in light transmittance.
上記高誘電体薄膜上には更に発光体層および背面m極が
順次形成される。A light emitter layer and a rear m-pole are further formed in this order on the high dielectric thin film.
発光体層は電圧の印加により発光するもので、例えば螢
光体とバインダーとしての高分子誘電体の混合物により
形成でき、その厚さは通常約20〜100μmである。The phosphor layer emits light upon application of a voltage, and can be formed, for example, from a mixture of a phosphor and a dielectric polymer as a binder, and its thickness is usually about 20 to 100 μm.
螢光体としては、硫化狸鉛、セレン化亜鉛、硫化亜鉛と
硫化カドミウムの混晶等の主剤に活性剤としての銅、銀
、金、マンガン等の金属粉末詔よび付活性剤としての塩
素、臭素、ヨウ素等のハロゲン或いはアルミニウム、ガ
リウム等の金属粉末を添加した混合物を用いることがで
きる。この場合、主剤、活性剤および付活性剤の混合割
合は、通常、主剤100重量部に対し、活性剤0.01
〜0.1重量部、付活性剤1〜3重量部である。 ”
また、バインダーとしての高分子誘電体としては、シア
ンエチルセルロース等のセルロース系樹脂、ポリフッ化
ビニリデン、フッ化ビニリデンを含む共重合体等のフッ
素樹脂、エポキシ樹脂、不飽和ポリエステル樹脂、有機
ケイ素樹脂、メラミン樹脂、尿素樹脂、ポリウレタン樹
脂等を用いることができる。The phosphor is made of lead sulfide, zinc selenide, mixed crystal of zinc sulfide and cadmium sulfide as a main ingredient, metal powders such as copper, silver, gold, manganese, etc. as an activator, and chlorine as an activator. A mixture containing a halogen such as bromine or iodine or a metal powder such as aluminum or gallium can be used. In this case, the mixing ratio of the base agent, activator, and activator is usually 0.01 parts by weight of the activator to 100 parts by weight of the base agent.
~0.1 part by weight, and 1 to 3 parts by weight of the activator. ”
In addition, examples of polymeric dielectric materials used as binders include cellulose resins such as cyanethyl cellulose, fluororesins such as polyvinylidene fluoride and copolymers containing vinylidene fluoride, epoxy resins, unsaturated polyester resins, organosilicon resins, and melamine. Resin, urea resin, polyurethane resin, etc. can be used.
発光体層形成成分としての螢光体と高分子誘電体の混合
割合は、種々の条件によって変わり得るが通常は高分子
誘電体100重量部に対し、螢光体50〜600重厭部
である。The mixing ratio of the phosphor and the polymeric dielectric as components for forming the phosphor layer may vary depending on various conditions, but is usually 50 to 600 parts by weight of the phosphor to 100 parts by weight of the polymer dielectric. .
発光体層は、例えば高分子誘電体粉末をアセトン、メチ
ルエチルケトン、ジメチルフォルムアミド、ジメチルア
セトアミド、ジメチルスルフォキサイド等の有機溶媒に
溶解せしめ、この溶液中に螢光体粉末を分散せしめ、こ
の液を高誘電体薄膜上に塗布し、その後加熱により溶媒
を除去し、次いで高分子誘電体の融点以上もしくは硬化
温度以上に所定時間加熱せしめ、該誘電体の熱融着もし
くは硬化により、高誘電体薄膜上に層形成する方法によ
り行なうことができる。The phosphor layer is made by dissolving polymeric dielectric powder in an organic solvent such as acetone, methyl ethyl ketone, dimethyl formamide, dimethyl acetamide, dimethyl sulfoxide, etc., dispersing the phosphor powder in this solution, and dispersing the phosphor powder in this solution. is applied onto a high dielectric thin film, the solvent is removed by heating, and the dielectric is heated above the melting point or curing temperature for a predetermined period of time to form a high dielectric material by thermal fusion or curing of the dielectric. This can be done by forming a layer on a thin film.
本発明においては発光体層上に背面[9が形成される。In the present invention, a back surface [9] is formed on the light emitter layer.
背面電極は例えばアルミ済、銅箔等の金属箔を、前記発
光体層形成時において、有機溶媒除去後に発光体形成成
分層tに配置し、その後加熱することにより、発光体層
上に強固に積層一体化できる。The back electrode is formed by, for example, placing a metal foil such as aluminum or copper foil on the luminescent material forming component layer t after removing the organic solvent during the formation of the luminescent layer, and then heating it to firmly place it on the luminescent layer. Can be laminated and integrated.
本発明の電場発光灯は、例えば(a)合成樹脂基材の表
面上に透明導電膜、高誘電体薄膜、発光体層および背面
[極を順次形する方法、或いは(b”1合成樹脂基材の
表面上に透明導電膜、高誘電体薄膜を順次形成させた部
材と、背面電極の表面に発光体層を形成した部材を用意
し、これら両部材を高誘電体薄膜と発光体層が向い合う
ように重ね合わせ、加熱加圧する方法、等により得るこ
とができる。The electroluminescent lamp of the present invention can be produced by, for example, (a) forming a transparent conductive film, a high dielectric thin film, a light emitter layer, and a back surface [pole] in sequence on the surface of a synthetic resin base material; A member in which a transparent conductive film and a high dielectric thin film are sequentially formed on the surface of the material, and a member in which a luminescent layer is formed on the surface of the back electrode are prepared. It can be obtained by stacking them facing each other and applying heat and pressure.
本発明においては、所望により発光体層と背面電極の間
に絶縁層を介在せしめることができる。In the present invention, an insulating layer can be interposed between the light emitting layer and the back electrode if desired.
この絶縁層は、発光体層形成時に用いたと同種の高分子
誘電体により形成する(所望によりチタン酸バリウム、
酸化チタン等の高誘電率を有する材料を混合できる)の
が、絶縁層と発光体層との密着力の点で好適である。This insulating layer is formed of the same type of polymeric dielectric material used in forming the light emitting layer (barium titanate, if desired).
A material having a high dielectric constant such as titanium oxide can be mixed therein is preferable from the viewpoint of adhesion between the insulating layer and the luminescent layer.
次に、図面により本発明の詳細な説明する。図面に示す
電場発光灯において、1は合成樹脂基材であり、その片
面とには、透明導電膜2、高誘電体薄膜3、発光体層4
、絶縁層5および背面電極6が順次積層されている。Next, the present invention will be explained in detail with reference to the drawings. In the electroluminescent lamp shown in the drawing, 1 is a synthetic resin base material, on one side of which are coated a transparent conductive film 2, a high dielectric thin film 3, and a luminescent layer 4.
, an insulating layer 5 and a back electrode 6 are sequentially laminated.
この発光灯は透明導電膜2と背面電極6の間に電圧を印
加すると、発光体層4が発光する。In this light emitting lamp, when a voltage is applied between the transparent conductive film 2 and the back electrode 6, the light emitter layer 4 emits light.
なお、絶縁層5は省略することもできるが、発光体R4
の発光効率、発光輝度および該発光体層4と背面電極6
との密着力向上のために、設けることが望ましい。Note that the insulating layer 5 can be omitted, but the light emitter R4
Luminous efficiency, luminance, and luminescent layer 4 and back electrode 6
It is desirable to provide this in order to improve the adhesion with the
本発明は透明導電膜2と発光体jfi 4の間に高誘電
体薄膜3を介在せしめるものであり、かようにすること
により透明導電膜2と発光体@4の密着力を向上せしめ
ることができる。In the present invention, a high dielectric thin film 3 is interposed between the transparent conductive film 2 and the light emitter 4, and by doing so, the adhesion between the transparent conductive film 2 and the light emitter @4 can be improved. can.
(実施例) 以下、実施例により本発明を更に詳細に説明する。(Example) Hereinafter, the present invention will be explained in more detail with reference to Examples.
実施例1
厚さ75−m の透明なポリエチレンテレフタレート
フィルムの片面上に、Sn含有量が10重景%であるI
n−Sn合金をターゲットとして用い、酸素との反応性
マグネトロンスパンタリング法により、厚さ200Aの
透明導電膜を形成する。Example 1 I was coated on one side of a 75-m thick transparent polyethylene terephthalate film with an Sn content of 10%.
Using an n-Sn alloy as a target, a transparent conductive film with a thickness of 200 A is formed by a reactive magnetron sputtering method with oxygen.
次に、透明導電膜りにアルキルジルコニウム溶液(日本
曹達社製、商品名アトロンNZr ’) を塗布し、
80℃の温度で30分間加熱する。この加熱により、溶
媒が除去されると共にアルキルジルコニウムが分解され
、厚さ2000 Aの酸化ジルコニウム薄膜(高誘電体
薄膜)が形成される。Next, an alkylzirconium solution (manufactured by Nippon Soda Co., Ltd., trade name Atron NZr') is applied to the transparent conductive film.
Heat at a temperature of 80° C. for 30 minutes. This heating removes the solvent and decomposes the alkylzirconium, forming a zirconium oxide thin film (high dielectric thin film) with a thickness of 2000 A.
その後、バインダーとしてのシアノエチルセルロースの
アセトン溶液に、螢光体粉末を分散させ、この液を酸化
ジルコニウム薄膜上にスクリーン印刷法により塗布し、
60℃で120分間加熱し、更に温度を150℃に上昇
せしめ2分間加熱することにより、厚さ60amの発光
体層を形成する。なお、上記螢光体粉末としては硫化炬
鉛を主成分とする粉末を用い、該粉末とシアノエチルセ
ルロースとの配合比(重量比)は84 : 16とした
。Thereafter, the phosphor powder was dispersed in an acetone solution of cyanoethyl cellulose as a binder, and this liquid was applied onto the zirconium oxide thin film by screen printing.
By heating at 60° C. for 120 minutes, and further increasing the temperature to 150° C. and heating for 2 minutes, a phosphor layer with a thickness of 60 am is formed. As the phosphor powder, a powder containing lead sulfide as a main component was used, and the blending ratio (weight ratio) of the powder and cyanoethyl cellulose was 84:16.
次いで、発光体層上に前記と同じシアノエチルセルロー
スのアトセン溶液にチタン酸バリウム粉末を分散せしめ
て塗布する。なお、チタン酸バリウムとシアノエチルセ
ルロースとの配合比c重量比)は1;1とした。Next, barium titanate powder is dispersed in the same atocene solution of cyanoethylcellulose as described above and applied onto the luminescent layer. The blending ratio c (weight ratio) of barium titanate and cyanoethyl cellulose was 1:1.
を載置し、温度を150℃に上昇せしめ、2分間加熱す
ることにより、絶縁層を形成せしめると共に、該絶縁層
ヒにアルミニウム箔(背面電極)を密着させ、図面に示
すのと同構造の電場発光灯を得た。The temperature was raised to 150°C and heated for 2 minutes to form an insulating layer, and an aluminum foil (back electrode) was attached to the insulating layer to form the same structure as shown in the drawing. Obtained an electroluminescent lamp.
この電場発光灯における透明溝wLII膜と発光体層と
の接着力は、200011/ 25 m−幅であり、両
者間の密着強度は大きなものであった。The adhesive force between the transparent groove wLII film and the luminescent layer in this electroluminescent lamp was 200011/25 m-width, and the adhesion strength between them was great.
上記接着力は、電灯発光灯の背面電極をエポキシ系接着
剤により厚さ2+a+の鉄板に接着せしめ、温度25℃
、剥離速度50mn/minの条件で180゜ピーリン
グ法により、発光体層と高誘電体薄膜としての酸化ジル
コニウム薄膜との界面で剥離せしめることにより測定し
た値である。The above adhesive strength was obtained by bonding the back electrode of an electric light emitting lamp to a 2+a+ thick iron plate using epoxy adhesive at a temperature of 25°C.
This value was measured by peeling at the interface between the luminescent layer and the zirconium oxide thin film as a high dielectric thin film using a 180° peeling method at a peeling rate of 50 mn/min.
比較のため、酸化ジルコニウム薄膜(高誘電体薄膜)を
形成しないこと以外は全て上記と同様に作業して電場発
光灯を得、該発光灯における透明導電■膜と発光体層と
の接着力を同様にして測定したところ、700 i/2
5 m幅であり、両者間の密着力は小さなものであった
。For comparison, an electroluminescent lamp was obtained in the same manner as above except that a zirconium oxide thin film (high dielectric thin film) was not formed, and the adhesive strength between the transparent conductive film and the luminescent layer in the lamp was evaluated. When measured in the same way, it was 700 i/2
The width was 5 m, and the adhesion between the two was small.
実施例2
厚さ75μmのポリエチレンテレフタレートフィルム上
の片面とに、1n203(ただし、5n02を5重量%
含育)をターゲットとして用い、電子ビーム蒸着法によ
り、低級酸化物膜を成膜し、これを大気中で170℃の
温度で10分間加熱して焼鈍することにより、透明導電
膜とする。Example 2 One side of a 75 μm thick polyethylene terephthalate film was coated with 1n203 (5% by weight of 5n02).
A lower oxide film is formed by an electron beam evaporation method using a carbonaceous material as a target, and the film is annealed by heating at a temperature of 170° C. for 10 minutes in the air to form a transparent conductive film.
次に、Ta205をターゲットとして RFスパッタリ
ング法により、透明導電膜tに厚さ1000λの高誘電
体薄膜を形成する。Next, a high dielectric thin film with a thickness of 1000λ is formed on the transparent conductive film t by RF sputtering using Ta205 as a target.
一方、これとは別に厚さ200μmのアルミニウム箔辷
に、エポキシ樹脂100重量部と酸化チタン粉末200
重量部から成る混合物を散布し、100℃の温度で1時
間加熱することにより、厚さ10μmの絶縁層を形成す
る。Separately, 100 parts by weight of epoxy resin and 200 parts of titanium oxide powder were added to a 200 μm thick aluminum foil.
A mixture consisting of parts by weight is spread and heated at a temperature of 100° C. for 1 hour to form an insulating layer with a thickness of 10 μm.
この絶縁ahに、バインダーとしてのエポキシ樹脂のア
セトン溶液に、螢光体粉末を分散させた液をシルクスク
リーン印刷法により塗布し、100℃の温度で5分間加
熱せしめることにより、厚さ30μmの発光体層を形成
する。螢光体粉末としては、硫化亜鉛(主剤)、銅(活
性剤)およびアルミニウム(付活性剤)の混合された緑
色発光螢光体を用いた。A liquid prepared by dispersing phosphor powder in an acetone solution of an epoxy resin as a binder is applied to this insulation ah using a silk screen printing method, and heated at a temperature of 100°C for 5 minutes. Forms body layers. As the phosphor powder, a green-emitting phosphor containing a mixture of zinc sulfide (base ingredient), copper (activator), and aluminum (activator) was used.
その後、前記ポリエチレンテレフタレートフィルム、透
明導電膜および高誘電体薄膜から成る部材と、アルミニ
ウム箔、絶縁層および発光体層から成る部材両者を高誘
電体薄膜と発光体層を向き合わせるようにして重ね合わ
せ、ロールラミネーター(温度150℃)により11層
一体化17、電場発光灯を得た。Thereafter, the member consisting of the polyethylene terephthalate film, the transparent conductive film, and the high dielectric thin film, and the member consisting of the aluminum foil, the insulating layer, and the luminescent layer are stacked together with the high dielectric thin film and the luminescent layer facing each other. , 11 layers were integrated using a roll laminator (temperature: 150° C.) to obtain an electroluminescent lamp.
この電場発光灯にお゛ける透明導電膜と発光体層との接
着力は、1800g/25−+幅であり、両者間の密着
強度は大きなものであった。The adhesive force between the transparent conductive film and the luminescent layer in this electroluminescent lamp was 1800 g/25-+ width, and the adhesion strength between the two was high.
比較のため、高誘電体薄膜を形成しないこと以外は全て
上記と同様に作業して電場発光灯を得、該発光灯におけ
る透明導電膜と発光体層との接着力はりρθF/25M
幅であり、両者間の密着力は小さなものであった。For comparison, an electroluminescent lamp was obtained in the same manner as above except that no high dielectric thin film was formed, and the adhesive strength between the transparent conductive film and the luminescent layer in the lamp was ρθF/25M.
The width was small, and the adhesion between the two was small.
(発明の効果)
本発明においては、透明導電膜と発光体層の間に高誘電
体薄膜を介在せしめることにより、両者間の密着力が向
−ヒするので、電極剥離を有効に防止できる。(Effects of the Invention) In the present invention, by interposing a high dielectric thin film between the transparent conductive film and the luminescent layer, the adhesion between the two is improved, so that electrode peeling can be effectively prevented.
図面は本発明に係る電場発光灯の実例を示す正面図であ
る。
1 ・・・・・r・合成樹脂基材 2・・・透明導電
膜3・・・・・・・・・高誘電体薄膜 4・・・・・
・・・・発光体層5 ・・・・・・絶縁層 6
・・・・・・・・背面電極特許出ト雇人
日東電気工業株式会社
代表者土方三部
/−鏝r絹基材
2− 透FIF4導電項
3−−一高妨電俸薄膜
4− あ1杯1
ターーー比#C肩
6− 肯面覧穐The drawing is a front view showing an example of the electroluminescent lamp according to the present invention. 1...r・Synthetic resin base material 2...Transparent conductive film 3...High dielectric thin film 4...
... Luminous layer 5 ... Insulating layer 6
・・・・・・・・・Rear electrode patent issuer Hijikata Mibe, representative of Nitto Electric Industry Co., Ltd. / - Trowel Silk base material 2 - Transparent FIF 4 conductive term 3 - High electromagnetic interference thin film 4 - A 1 Cup 1 Tar-ratio #C Shoulder 6- Kenmen Viewing
Claims (1)
膜、高誘電体薄膜、発光体層および背面電極が順次積層
されていることを特徴とする電場発光灯。An electroluminescent lamp characterized in that a transparent conductive film, a high dielectric thin film, a light emitter layer, and a back electrode are sequentially laminated on the surface of a synthetic resin base material having light transparency.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60001924A JPS61161691A (en) | 1985-01-09 | 1985-01-09 | Field light emitting lamp |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60001924A JPS61161691A (en) | 1985-01-09 | 1985-01-09 | Field light emitting lamp |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS61161691A true JPS61161691A (en) | 1986-07-22 |
Family
ID=11515143
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60001924A Pending JPS61161691A (en) | 1985-01-09 | 1985-01-09 | Field light emitting lamp |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61161691A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5076963A (en) * | 1987-10-30 | 1991-12-31 | Nippon Kasei Chemical Co., Ltd | Pastes for forming a luminescent layer and insulator layer of electroluminescent element and electroluminescent element using such pastes |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5994395A (en) * | 1982-11-19 | 1984-05-31 | 松下電工株式会社 | Method of producing light emitting device |
-
1985
- 1985-01-09 JP JP60001924A patent/JPS61161691A/en active Pending
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5994395A (en) * | 1982-11-19 | 1984-05-31 | 松下電工株式会社 | Method of producing light emitting device |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5076963A (en) * | 1987-10-30 | 1991-12-31 | Nippon Kasei Chemical Co., Ltd | Pastes for forming a luminescent layer and insulator layer of electroluminescent element and electroluminescent element using such pastes |
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