JPH01265493A - Manufacture of thin film el element - Google Patents
Manufacture of thin film el elementInfo
- Publication number
- JPH01265493A JPH01265493A JP63094815A JP9481588A JPH01265493A JP H01265493 A JPH01265493 A JP H01265493A JP 63094815 A JP63094815 A JP 63094815A JP 9481588 A JP9481588 A JP 9481588A JP H01265493 A JPH01265493 A JP H01265493A
- Authority
- JP
- Japan
- Prior art keywords
- film
- electrode group
- extraction electrode
- signal electrode
- group
- 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 abstract description 11
- 239000010409 thin film Substances 0.000 title claims description 12
- 239000000758 substrate Substances 0.000 claims abstract description 14
- 239000011521 glass Substances 0.000 claims abstract description 12
- 238000000034 method Methods 0.000 claims abstract description 8
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000010408 film Substances 0.000 claims description 69
- 238000000605 extraction Methods 0.000 claims description 26
- 238000010030 laminating Methods 0.000 claims description 3
- 238000005530 etching Methods 0.000 abstract description 2
- 239000007788 liquid Substances 0.000 abstract 2
- 239000002075 main ingredient Substances 0.000 abstract 2
- 238000001771 vacuum deposition Methods 0.000 abstract 1
- 239000005394 sealing glass Substances 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 238000004904 shortening Methods 0.000 description 2
- 238000004544 sputter deposition Methods 0.000 description 2
- 238000007738 vacuum evaporation Methods 0.000 description 2
- 238000003466 welding Methods 0.000 description 2
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- BJXXCWDIBHXWOH-UHFFFAOYSA-N barium(2+);oxygen(2-);tantalum(5+) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Ba+2].[Ba+2].[Ba+2].[Ba+2].[Ba+2].[Ta+5].[Ta+5].[Ta+5].[Ta+5] BJXXCWDIBHXWOH-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 238000000206 photolithography Methods 0.000 description 1
- 238000005476 soldering Methods 0.000 description 1
- VEALVRVVWBQVSL-UHFFFAOYSA-N strontium titanate Chemical compound [Sr+2].[O-][Ti]([O-])=O VEALVRVVWBQVSL-UHFFFAOYSA-N 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
この発明は、キャラクタやグラフィクスなどの表示に用
いる薄膜ICL素子の製造方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application This invention relates to a method of manufacturing a thin film ICL element used for displaying characters, graphics, etc.
従来の技術
従来より電場発光蛍光体を用いた固体映像装置としてX
−Yマトリックス表示装置が知られている。この装置は
、電場発光体層(以下EL発光体層と略称する)の両面
に水平平行電極群(以下走査電極群と略称する)と垂直
平行電極群(以下信号電極群と略称する)とを互いに直
交するように配置し、それぞれの電極群に接続された給
’+1f線に依り切り替え装置を通して信号を加えて、
両−]Zl&の交点部分のEL発光体層を発光させ(こ
の交点の発光部分面を絵素と称する)、発光した絵素の
組み合わせに依って文字記号1図形などを表示させるも
のである。Conventional technology X
-Y matrix display devices are known. This device has a horizontal parallel electrode group (hereinafter referred to as a scanning electrode group) and a vertical parallel electrode group (hereinafter referred to as a signal electrode group) on both sides of an electroluminescent layer (hereinafter referred to as an EL emitter layer). A signal is applied through the switching device by the supply '+1f line arranged so as to be orthogonal to each other and connected to each electrode group,
The EL light emitter layer at the intersection of Zl& is caused to emit light (the light emitting surface at this intersection is called a picture element), and characters, symbols, figures, etc. are displayed depending on the combination of the emitted picture elements.
第4図は従来例の構造を示すもので、また第5図はその
製造工程を示すものである。ここで用いられる固体映像
表示装置の表示板としては通常、ガラスなどの透光性基
板1上に透明な信号電極群2及び第1の取り出し電極群
3を形成し、その上に第1誘電体層膜4.ICL発光体
層膜6.第2誘電体層膜6を順次積層し、第4図に示す
ように前記信号電極群にかからない箇所にCr膜?、N
i膜s 、 Cr膜9.Au膜10をストライプ状に順
次積層し、第2の取りだし電極群11として、Al膜1
2を信号電極群2に直交し第2の取り出し電極群11に
かかるような配置で積層して成膜する。FIG. 4 shows the structure of a conventional example, and FIG. 5 shows its manufacturing process. The display plate of the solid-state image display device used here usually has a transparent signal electrode group 2 and a first extraction electrode group 3 formed on a transparent substrate 1 such as glass, and a first dielectric layer Layer film 4. ICL light emitter layer film 6. The second dielectric layer film 6 is sequentially laminated, and as shown in FIG. 4, a Cr film is placed on a portion not covering the signal electrode group. , N
i film s, Cr film 9. Au films 10 are sequentially laminated in a stripe shape, and the Al film 1 is stacked as a second extraction electrode group 11.
2 are stacked in such a manner that they are perpendicular to the signal electrode group 2 and extend over the second extraction electrode group 11 to form a film.
一般に透明な信号電極群2としては平滑なガラス基板上
に酸化錫添加インジウム(以下ITOと略する)を被着
し、所望の形状にパターンニングするなどにより形成さ
れる。これに直交し、対向する走査7t[群12として
はアルミニウムなどの金属膜が真空蒸着などにより形成
される。Generally, the transparent signal electrode group 2 is formed by depositing indium tin oxide (hereinafter abbreviated as ITO) on a smooth glass substrate and patterning it into a desired shape. Scanning 7t perpendicular to and opposite to this [group 12] a metal film of aluminum or the like is formed by vacuum evaporation or the like.
発明が解決しようとする課題 ところがil述した方法では2つの問題点があった。Problems that the invention aims to solve However, the method described above has two problems.
まず取り出し電極群と外部回路を接続する方法に直接圧
接により接続する直接圧接方式においては、接触面(最
上層)に用いることのできる金属は限られておりAuの
ように酸化被膜を作りにくい材料でなければならない。First, in the direct pressure welding method, which connects the extraction electrode group and the external circuit by direct pressure welding, there are only a limited number of metals that can be used for the contact surface (top layer), and materials such as Au that are difficult to form an oxide film. Must.
しかし、各積層膜を湿度などから保護するためにシール
ガラスを取付けなければならない、このためにシールガ
ラスと接触する最上層の人Uでは密着性が弱いなどの面
からNiなどの金属がよい。However, in order to protect each laminated film from humidity etc., a sealing glass must be attached, and for this reason, the uppermost layer U, which comes into contact with the sealing glass, has weak adhesion, so a metal such as Ni is preferable.
このだめには第2のセリ出し電極群のCr膜。This tank is covered with a Cr film of the second soldering electrode group.
Ni膜を成膜後−慶大気圧にしてシールガラスと接触す
る部分に人Uが付かないようにマスクなどを取付は再度
真空中にて第2の取り出し電極群人Uを成膜しなければ
ならないため過大な時間の浪費であった。さらにこの時
−慶大気圧にするとNi膜と人U膜の密着性が弱くなる
ためNi膜とAu膜の間にCr膜を一層追加しなければ
ならないという課題があった。After forming the Ni film, the second take-out electrode group U must be deposited in a vacuum again at atmospheric pressure and a mask etc. is attached to prevent U from getting on the part that comes into contact with the sealing glass. It was a huge waste of time because it didn't work. Furthermore, at this time, there was a problem in that if the atmospheric pressure was set to 1000, the adhesion between the Ni film and the U film became weaker, so a further Cr film had to be added between the Ni film and the Au film.
本発明は上記欠点を除去した薄膜ICL素子の製造方法
を提供することを目的とする。An object of the present invention is to provide a method for manufacturing a thin film ICL element that eliminates the above-mentioned drawbacks.
課題を解決するための手段
本発明によれば、透光性基板上に透明な信号電極群と前
記信号電極群の取り出し部である第1の取り出し電極群
を成膜する工程と前記第1取り出し電極群にかからない
範囲に第1誘電体層膜。Means for Solving the Problems According to the present invention, a step of forming a transparent signal electrode group and a first take-out electrode group, which is a take-out portion of the signal electrode group, on a transparent substrate, and the first take-out step are performed. The first dielectric layer film is placed in a range that does not cover the electrode group.
EL発光体層膜、第2誘電体層膜を順次積層する工程と
il記信号電甑群にかからない箇所にCr膜。In the process of sequentially laminating the EL light emitting layer film and the second dielectric layer film, a Cr film is applied to areas not covered by the signal wire group.
Ni膜、Au膜をストライプ状に順次積層し、第2の取
り出し電極群とする工程と前記第2の取り出し電極群の
シールガラス接触面と重なりかつ前記第1の取り出し電
極群にかさならない範囲に人e膜を成膜する工程と、ス
トライプパターンを形成する工程からなる薄膜EL素子
においてテトラ・メチル・アンモニウムを主成分とする
現像液を用いることによりシールガラス接触面の人U膜
を除去するようにしたものである。A step of sequentially laminating a Ni film and an Au film in a stripe shape to form a second extraction electrode group, and an area that overlaps the sealing glass contact surface of the second extraction electrode group and does not overlap the first extraction electrode group. In the thin film EL device, which consists of a step of forming a film and a step of forming a stripe pattern, the film of the film on the contact surface of the seal glass is removed by using a developer containing tetramethyl ammonium as a main component. This is what I did.
作用
本発明は薄膜ICL素子の走査電極群のストライプパタ
ーン形成時にシールガラス接触面のAu膜が除去できる
ことにより薄膜EL素子作成上時間の短縮に寄与するこ
とができる。Function The present invention can contribute to shortening the manufacturing time of a thin film EL element by removing the Au film on the contact surface of the seal glass when forming the stripe pattern of the scanning electrode group of the thin film ICL element.
実施例
以下に本発明の一実施例について説明する。第1図にお
いて1は透光性基板であり、2は信号電極群、4は第1
誘電体層、5は発光体層、6は第2誘′准体層、11は
第2の取り出し電極群(第2図)として7はCr膜、8
はNi膜、1oは人U膜であり第2の取り出し電極群の
最上層に形成されている。12は走査電極群であり、1
3はレジストである。EXAMPLE An example of the present invention will be described below. In FIG. 1, 1 is a transparent substrate, 2 is a signal electrode group, and 4 is a first
Dielectric layer, 5 is a light emitter layer, 6 is a second dielectric layer, 11 is a second extraction electrode group (Fig. 2), 7 is a Cr film, 8 is a dielectric layer;
is a Ni film, and 1o is a human U film, which are formed on the top layer of the second extraction electrode group. 12 is a scanning electrode group;
3 is a resist.
次にさらに具体的に説明する。透光性基板1はガラス基
板であり、コーニング7o59ガラスを用いた。なお基
板1の大きさは240jffX180IIMで厚さは2
.4nである。基板1上に直流スパッタリング法により
ガス圧0,5Pa(アルゴン対酸素の分圧比6:4)で
厚さ600HのITO膜を形成した。このときのITO
膜の抵抗率は、2.2×10−4Ω・1*であった。そ
の後!TO膜をフォトリソ技術によりストライプ状に加
工し信号電極群にすると同時に第1の取り出し電極群と
した(第1図a)。なおパターン間隔は300μmで、
230μm幅のパターンを形成した。エツチングは塩化
第二鉄の塩酸水溶液で行った。Next, it will be explained more specifically. The transparent substrate 1 is a glass substrate, and Corning 7o59 glass is used. The size of the board 1 is 240jff x 180IIM and the thickness is 2
.. It is 4n. An ITO film with a thickness of 600 H was formed on the substrate 1 by direct current sputtering at a gas pressure of 0.5 Pa (partial pressure ratio of argon to oxygen: 6:4). ITO at this time
The resistivity of the film was 2.2×10 −4 Ω·1*. after that! The TO film was processed into stripes by photolithography to form a signal electrode group and at the same time a first extraction electrode group (FIG. 1a). Note that the pattern spacing is 300 μm,
A pattern with a width of 230 μm was formed. Etching was performed with an aqueous solution of ferric chloride in hydrochloric acid.
その上にチタン酸ジルコン酸ストロンチウム[5r(T
ixZriz)03) を基板温度400°Cでスパ
ックリングすることにより、厚さeoonmの第1誘電
体膜4を形成した。その上に蒸着法により基板温度20
0℃で厚さsoonmのマンガン添加硫化亜鉛膜からな
るEL発光体層膜6を形成した。真空中450’Cで1
時間熱処理の後、その上にタンタル酸バリウム[Ba’
ra2061焼結体を、基板温度150’Cでスパッタ
リングする事により厚さ200nmの第2誘電体膜6を
形成した(第3図b)。On top of that, strontium titanate zirconate [5r(T
The first dielectric film 4 having a thickness of eonm was formed by spuckling the ixZriz)03) at a substrate temperature of 400°C. On top of that, the substrate temperature is 20℃ by vapor deposition method.
An EL luminescent layer film 6 made of a manganese-doped zinc sulfide film having a thickness of soon m was formed at 0°C. 1 at 450'C in vacuum
After time heat treatment, barium tantalate [Ba'
A second dielectric film 6 having a thickness of 200 nm was formed by sputtering the RA2061 sintered body at a substrate temperature of 150'C (FIG. 3b).
次に信号電極群2と第1の取り出し電極群3の成膜範囲
以外の箇所に第2の取り出し電極群11゜Cr膜7.N
1膜8.最上層にAu膜10を真空蒸着により積層した
。この時の基板温度は150°Cで膜厚は両方とも30
0nEIlである。Next, a second extraction electrode group 11°Cr film 7. N
1 membrane8. An Au film 10 was laminated on the top layer by vacuum evaporation. At this time, the substrate temperature was 150°C and the film thickness was 30°C.
0nEIl.
最後に膜厚160nmのAl膜を真空蒸着し走査’、t
i: I’iff群12とした。成膜範囲は、前記第2
の取り出し電極群のシールガラスと接触する面まで重な
りかつ前記第1取り出し電極群にかからない範囲である
、こうして成膜した走査電極群12にレジスト13を塗
布し、露光する、露光する範囲は前記第2の取り出し電
極群の一部と重なりシールガラス接触面にかからない範
囲かつ前記第1の取り出し電極群にかからない範囲であ
る。このようにして形成したレジストパターンをテトラ
・メチル・アンモニウムを主成分とする現像液を用いて
、信号電極群6とは直交する方向にストライプ状にエツ
チング加工し走査電極群12とした。同時にシールガラ
スと接触する而の走査電極群と前記第2の取り出し電極
群の最上属人U膜10がテトラ・メチル・アンモニウム
を主成分とする現像液で溶かされる。このようにして本
発明の薄膜EL素子を完成した。Finally, an Al film with a thickness of 160 nm is vacuum deposited and scanned ', t.
i: I'iff group 12. The film forming range is the second
A resist 13 is coated on the thus formed scanning electrode group 12, which overlaps up to the surface contacting the seal glass of the extraction electrode group and does not cover the first extraction electrode group, and is exposed. This is a range that overlaps a part of the second extraction electrode group and does not cover the sealing glass contact surface, and a range that does not cover the first extraction electrode group. The resist pattern thus formed was etched into stripes in a direction perpendicular to the signal electrode group 6 using a developer containing tetramethyl ammonium as a main component to form a scanning electrode group 12. At the same time, the uppermost membranes 10 of the scanning electrode group and the second extraction electrode group which are in contact with the sealing glass are dissolved with a developer containing tetramethyl ammonium as a main component. In this way, the thin film EL device of the present invention was completed.
作成したELデイスプレィの第2の取り出し電極群部分
の信頼性を冷熱試験(−20’C〜70’C。The reliability of the second extraction electrode group portion of the produced EL display was tested by thermal testing (-20'C to 70'C).
100サイクル)の場合AlとAuの接続部の抵抗値を
測定したが、初期値とほとんど変化せず非常に信頼性が
高いことが確認できた。In the case of 100 cycles), the resistance value of the connection between Al and Au was measured, and it was confirmed that the resistance value hardly changed from the initial value and was extremely reliable.
なお、本実施例ではAuの下地の層としてN1膜を用い
たがこれに限定されるものではなくcrなどの金属でも
よい。In this embodiment, the N1 film is used as the underlying layer of Au, but the layer is not limited to this, and metals such as Cr may also be used.
発明の効果
以上のように本発明によれば、走査電極群のパターン形
成時に第2の取り出し電極群のシールガラス接触面のA
u膜が除去用、来ることにより薄膜EL素子作成上時間
の短縮に寄与することができるとともにシールガラス接
触面の密着力が向上する。Effects of the Invention As described above, according to the present invention, when forming the pattern of the scanning electrode group, the A of the sealing glass contact surface of the second extraction electrode group is
By removing the U film, it is possible to contribute to shortening the time required to produce a thin film EL element, and the adhesion of the sealing glass contact surface is improved.
第1図は本発明にかかる薄膜EL素子の製造方法を用い
て製造した薄膜EL素子の構成を示す断面図、第2図は
同平面図、第3図は同製造工程図、第4図は従来用いら
れている薄膜EL素子の構成を示す断面図、第6図はそ
の製造工程図である。
1・・・・・・透光性基板、2・・・・・・信号重囲群
、3・・・・・・第1の単り出し電極群、4・・・・・
・第1誘電体膜、6・・・・・・EL発光体層膜、6・
・・・・・第2誘電体膜、7・・・・・・Cr膜、8・
・・・・・N1膜、9・・・・・・Cr膜、1o・・・
・・・Au膜、11・・・・・・第2の取り出し電極群
、12・・・・・・Al膜(走査電極群)、13・・・
・・・レジスト、14・・・・・・シールガラス。
代理人の氏名、弁理士 中 尾 敏 男 ほか1名1−
区尤+ひ級
e−−762訪tあ1ゴ
!4−−−シール刀・ラス
第 2 図FIG. 1 is a cross-sectional view showing the structure of a thin film EL device manufactured using the method for manufacturing a thin film EL device according to the present invention, FIG. 2 is a plan view of the same, FIG. 3 is a diagram of the manufacturing process, and FIG. A cross-sectional view showing the structure of a conventionally used thin film EL element, and FIG. 6 is a manufacturing process diagram thereof. DESCRIPTION OF SYMBOLS 1...Transparent substrate, 2...Signal overlap group, 3...First single electrode group, 4...
・First dielectric film, 6... EL light emitting layer film, 6.
...Second dielectric film, 7...Cr film, 8.
...N1 film, 9...Cr film, 1o...
...Au film, 11...second extraction electrode group, 12...Al film (scanning electrode group), 13...
...Resist, 14... Seal glass. Name of agent, patent attorney Toshio Nakao and 1 other person1-
Gu Yu + Hi-class e--762 visit t a 1 go! 4---Seal sword/lass Fig. 2
Claims (1)
トライプ状に加工し信号電極群と前記信号電極群の取り
出し部である第1の取り出し電極群とを同時に形成する
工程と、前記第1の取り出し電極群にかからない範囲に
第1誘電体層膜、発光体層膜、第2誘電体層膜からなる
積層膜を形成する工程と、前記信号電極群にかからない
箇所にCr膜、Ni膜、Au膜をストライプ状に順次積
層し第2の取り出し電極群を形成する工程と、前記第2
の取り出し電極群の前記積層膜を保護するためのシール
ガラスとの接触面を覆いかつ前記第1の取り出し電極群
にかからない範囲にAl膜を成膜する工程と、前記Al
膜上に前記信号電極群と直交しかつ前記第2の取り出し
電極群の一部とかさなりかつ前記シールガラスとの接触
面に成膜された前記Al膜が露出するようなストライプ
状にレジストパターンを形成する工程と、テトラ・メチ
ル・アンモニウムを主成分とする現像液を用いることに
より前記Al膜を前記信号電極群と直交するようレジス
トパターンに沿ってストライプ状にエッチング加工し走
査電極群とすると同時に前記露出したAl膜と下層のA
u膜を同時に除去できる工程からなることを特徴とする
薄膜EL素子の製造方法。forming a transparent conductive film at a predetermined location on a light-transmitting substrate and processing it into a stripe shape to simultaneously form a signal electrode group and a first extraction electrode group that is an extraction portion of the signal electrode group; a step of forming a laminated film consisting of a first dielectric layer film, a light emitting layer film, and a second dielectric layer film in an area not covered by the first extraction electrode group; a Cr film in a part not covered by the signal electrode group; a step of sequentially laminating a Ni film and an Au film in a stripe shape to form a second extraction electrode group;
forming an Al film in a range that covers the contact surface with the seal glass for protecting the laminated film of the extraction electrode group and does not cover the first extraction electrode group;
A resist pattern is formed on the film in the form of a stripe, which is perpendicular to the signal electrode group, overlaps a part of the second extraction electrode group, and exposes the Al film formed on the contact surface with the seal glass. At the same time, the Al film is etched into stripes along the resist pattern perpendicular to the signal electrode group to form a scanning electrode group by using a developer containing tetra-methyl ammonium as a main component. The exposed Al film and the lower layer A
A method for manufacturing a thin film EL device, comprising a step in which the u film can be removed at the same time.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63094815A JPH01265493A (en) | 1988-04-18 | 1988-04-18 | Manufacture of thin film el element |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63094815A JPH01265493A (en) | 1988-04-18 | 1988-04-18 | Manufacture of thin film el element |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01265493A true JPH01265493A (en) | 1989-10-23 |
Family
ID=14120553
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63094815A Pending JPH01265493A (en) | 1988-04-18 | 1988-04-18 | Manufacture of thin film el element |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01265493A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009026770A (en) * | 2008-10-02 | 2009-02-05 | Seiko Epson Corp | Display device |
-
1988
- 1988-04-18 JP JP63094815A patent/JPH01265493A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009026770A (en) * | 2008-10-02 | 2009-02-05 | Seiko Epson Corp | Display device |
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