JPH0212796A - Forming method for electrode of thin film el element - Google Patents
Forming method for electrode of thin film el elementInfo
- Publication number
- JPH0212796A JPH0212796A JP63162018A JP16201888A JPH0212796A JP H0212796 A JPH0212796 A JP H0212796A JP 63162018 A JP63162018 A JP 63162018A JP 16201888 A JP16201888 A JP 16201888A JP H0212796 A JPH0212796 A JP H0212796A
- Authority
- JP
- Japan
- Prior art keywords
- film
- resist
- electrode
- etching
- thin film
- 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
- 238000000034 method Methods 0.000 title claims abstract description 21
- 239000010409 thin film Substances 0.000 title claims description 7
- 239000010408 film Substances 0.000 claims description 34
- 238000005530 etching Methods 0.000 claims description 29
- 239000000243 solution Substances 0.000 claims description 19
- 239000012670 alkaline solution Substances 0.000 claims description 8
- 238000001259 photo etching Methods 0.000 claims description 2
- 239000002253 acid Substances 0.000 abstract description 6
- CJNBYAVZURUTKZ-UHFFFAOYSA-N hafnium(IV) oxide Inorganic materials O=[Hf]=O CJNBYAVZURUTKZ-UHFFFAOYSA-N 0.000 abstract description 5
- 239000003513 alkali Substances 0.000 abstract 3
- 239000007788 liquid Substances 0.000 abstract 3
- 238000009413 insulation Methods 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- FKTOIHSPIPYAPE-UHFFFAOYSA-N samarium(III) oxide Inorganic materials [O-2].[O-2].[O-2].[Sm+3].[Sm+3] FKTOIHSPIPYAPE-UHFFFAOYSA-N 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 20
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 7
- 229910017604 nitric acid Inorganic materials 0.000 description 7
- WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 description 7
- 239000000463 material Substances 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 238000001035 drying Methods 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 101100389125 Rattus norvegicus Egln3 gene Proteins 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 239000011810 insulating material Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 101100269850 Caenorhabditis elegans mask-1 gene Proteins 0.000 description 1
- 239000004063 acid-resistant material Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000005566 electron beam evaporation Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
Landscapes
- Electroluminescent Light Sources (AREA)
Abstract
Description
【発明の詳細な説明】
[発明の目的]
(産業上の利用分野)
本発明は交流電界の印加によってEL発光を呈する薄J
1%EL素子に関し、特に、その電極形成方法に関する
。[Detailed Description of the Invention] [Object of the Invention] (Industrial Application Field) The present invention provides a thin J
The present invention relates to a 1% EL element, and particularly to a method for forming electrodes thereof.
(従来の技術)
一般に、薄膜EL素子は、ガラス基板上にI n20.
.5n02等から成る多数本の帯状透明電極を形成し、
この上にY、O,。(Prior Art) Generally, a thin film EL device is manufactured by forming an Inn20.
.. A large number of band-shaped transparent electrodes made of 5n02 etc. are formed,
Y, O, on top of this.
TiO2,5in2等から成る第1の絶縁層を形成し、
その上にZnS : Mn焼結ペレットを電子ビーム蒸
着することにより得られる発光層を形成し、この上に第
1の絶縁層と同様の材質からなる第2の絶縁層を形成し
、さらにこの上に透明電極に直交する方向に並設された
A!QMからなる多数本の帯状背面電極を形成して構成
される。また、通常Al膜の上には電極取り出し端子と
してNi膜が形成されている。このような薄膜EL素子
において、背面電極番形成する方法としては例えば特公
昭62−48358号公報等に開示され、第4図に示す
ように、先ず、第2の絶縁層の上全面にAn膜とN1膜
を順次積層する。Forming a first insulating layer made of TiO2, 5in2, etc.
A light emitting layer obtained by electron beam evaporation of ZnS:Mn sintered pellets is formed thereon, a second insulating layer made of the same material as the first insulating layer is formed, and a second insulating layer made of the same material as the first insulating layer is formed. A! are arranged in parallel in the direction perpendicular to the transparent electrode. It is constructed by forming a large number of strip-shaped back electrodes made of QM. Further, a Ni film is usually formed on the Al film as an electrode lead terminal. In such a thin film EL element, a method for forming a back electrode number is disclosed in Japanese Patent Publication No. 62-48358, etc., and as shown in FIG. and N1 film are sequentially stacked.
そして、N1Jll全面にポジタイプのレジスト(例え
ば、東京応化製の0FPR−800)を塗布し、レジス
ト中の溶剤を蒸発させるために85°C程度の温度でプ
レベークを行う。Then, a positive type resist (for example, 0FPR-800 manufactured by Tokyo Ohka Co., Ltd.) is applied to the entire surface of N1Jll, and prebaking is performed at a temperature of about 85° C. in order to evaporate the solvent in the resist.
次いで、帯状のパターンのマスクをレジスト上方に被せ
光りを照射して露光を行ない、現像液を流して光が照射
された部分のレジストを除去する。そして、残った部分
のレジストの付着力を高くするために100℃程度の温
度でボストベークを行なう0次に、常温の希硝酸系のエ
ツチング液を用いてN i I!li、をエツチングし
、さらに、40〜60″Cに加熱したリン酸硝酸混合液
からなるAn膜用のエツチング液を用いてAl膜をエツ
チングし帯状にツチングされたN1FtlA及びAC膜
を得る。なお、レジストは酸系のエツチング液に対して
強(Ni股上に残っている。そして、乾燥させた後、電
極取り出し端子を形成するために、前記端子対応箇所を
覆うパターンのマスクを前記レジスト上方に被せ二重露
光を行ない、その後現像してN1JIA上の不用なレジ
ストを除去する。そして、再度常温の希硝酸系のエツチ
ング液を用いてN1膜をエツチングし、最後にレジスト
を剥離すると、前記透明電極と対向する帯状のAl膜と
、この、/iv/、の上の端部であって外部回路との接
続を行なうための電極取り出し端子となるNi15(と
による背面電極が形成される。Next, a band-shaped patterned mask is placed over the resist and exposed to light, and a developer is flowed to remove the resist in the areas irradiated with light. Then, in order to increase the adhesion of the remaining resist, a post-bake is performed at a temperature of about 100°C, and then NiI! is applied using a dilute nitric acid-based etching solution at room temperature. li, and then etched the Al film using an etching solution for An film made of a phosphoric acid/nitric acid mixture heated to 40 to 60''C to obtain N1FtlA and AC films etched into strips. , the resist is resistant to acid-based etching solutions (remains on the Ni ridge). Then, after drying, in order to form electrode extraction terminals, a mask with a pattern covering the corresponding portions of the terminals is placed above the resist. Overlapping double exposure is performed, and then development is performed to remove unnecessary resist on the N1JIA.Then, the N1 film is etched again using a dilute nitric acid-based etching solution at room temperature, and finally the resist is peeled off. A back electrode is formed by a band-shaped Al film facing the electrode and a Ni 15 film (at the upper end of /iv/, which serves as an electrode extraction terminal for connection to an external circuit).
(発明が解決しようとする課題)
前記従来技術においては、An膜のエツチング液として
リン酸硝酸混合液などの酸系のエツチング液を用いてい
るため、その下地層である第2の絶縁層としてはAl2
03やSiO2等の耐酸性を有する材料しか使用できな
かった。しかしこれらの材料を使用すると耐圧が高くな
り、ELの駆動電圧が高くなる問題があった。また、従
来技術のようにAlII!/N1WAの二層構造の背面
電極では二重露光を用いてAl膜の端部にNi膜を残す
場合、AlWAのエツチングに酸系のエツチング液を用
いると、その工程がかなり複雑となる。(Problems to be Solved by the Invention) In the above-mentioned prior art, since an acid-based etching solution such as a phosphoric acid/nitric acid mixed solution is used as the etching solution for the An film, the second insulating layer which is the underlying layer is used as the etching solution for the An film. is Al2
Only acid-resistant materials such as 03 and SiO2 could be used. However, when these materials are used, there is a problem that the withstand voltage becomes high and the driving voltage of the EL becomes high. Also, like the prior art, AlII! When using double exposure to leave a Ni film on the edge of the Al film in the double-layered back electrode of /N1WA, the process becomes quite complicated if an acid-based etching solution is used to etch the AlWA.
そこで、本発明は前記問題点に基づいて成されたもので
あり、駆動電圧を低くすることができるとともに、工程
を簡略化できる薄膜EL素子の電極形成方法を提供する
ことを目的とするものである。Therefore, the present invention has been made based on the above-mentioned problems, and an object of the present invention is to provide a method for forming electrodes of a thin film EL element, which can lower the driving voltage and simplify the process. be.
[発明の構成]
(課題を解決するための手段)
本発明は背面電極の形成方法において、レジストの現像
液およびAΩ膜のエツチング液として有機アルカリ溶液
を用いたものである。[Structure of the Invention] (Means for Solving the Problems) The present invention uses an organic alkaline solution as a resist developer and an AΩ film etching solution in a method for forming a back electrode.
(作用)
レジストの現像液とAl膜のエツチング液として同じ有
機アルカリ溶液を用いたことにより、レジストの現像と
Alfiのエツチングを同時に行ない、工程の簡略化を
図り、かつ背面電極の下層の絶縁層として酸に弱いSm
20.やHf O2などの材料を使用できる。(Function) By using the same organic alkaline solution as the resist developer and the Al film etching solution, resist development and Alfi etching can be performed at the same time, simplifying the process, and improving the insulating layer below the back electrode. Sm is weak against acids as
20. Materials such as HfO2 and HfO2 can be used.
(実施例)
以下、図面に基づいて本発明の一実施例を詳述する。第
3図において、ガラス基[1上には多数の帯状透明電極
2が形成され、この上にはSm20.やHfO,などの
絶縁材料から成る第1の絶縁層3が形成され、この上に
は発光層4か形成され、さらにその上には第1の絶縁層
3と同じ材料がら成る第2の絶縁層5が形成されている
。そして、第2の絶縁層5の上には基板全体にAlJI
!6およびN1g7を同一真空中にて連続形成する。(Example) Hereinafter, an example of the present invention will be described in detail based on the drawings. In FIG. 3, a large number of band-shaped transparent electrodes 2 are formed on a glass substrate [1], and on top of this are formed Sm20. A first insulating layer 3 made of an insulating material such as or HfO is formed, a light emitting layer 4 is formed on this, and a second insulating layer 3 made of the same material as the first insulating layer 3 is further formed on top of this. Layer 5 is formed. Then, on the second insulating layer 5, AlJI is applied over the entire substrate.
! 6 and N1g7 are formed successively in the same vacuum.
次に、フォトエツチング工程を用い、背面電極用のAn
膜6および電極取り出し端子用のNi膜7をストライプ
に加工する方法を第1図及び第2図を基にして説明する
9先ず、第2図(A)に示すように、Ni膜7の上にポ
ジタイプのレジスト8をスピンナー等の方法にて塗布す
る。そして、レジスト8中の溶剤を蒸発させるなめ85
℃程度の温度でプレベークを行なう。次に、第2図(B
)に示すように、帯状に光透過部9At有するマスク9
をレジスト8の上に被せ、光を照射して露光を行なう、
その後、現像液としてテトラメチルアンモニウムハイド
ロオキサイドと水を主成分とする有機アルカリ溶液(例
えば、東京応化製NMD−3)を用いて現像することに
より、第2図(C)に示すように未露光部のレジスト8
Aだけ残る。尚、このテトラメチルアンモニウムハイド
ロオキサイドの水への混合比は2〜3重1%である。そ
して、リンス、エアブロ−などによる乾燥の後、レジス
ト8Aの付着力を高めるため、ioo’c程度の温度で
ボストベークを行なうが、これまでの工程は第4図の従
来例と同様である。Next, using a photo-etching process, the An
A method for processing the film 6 and the Ni film 7 for the electrode lead terminal into stripes will be explained based on FIGS. 1 and 2.9 First, as shown in FIG. A positive type resist 8 is applied to the surface using a spinner or the like. Then, a lick 85 for evaporating the solvent in the resist 8
Pre-bake is performed at a temperature of about ℃. Next, Figure 2 (B
), a mask 9 having a band-shaped light transmitting portion 9At
is placed on top of the resist 8 and irradiated with light to perform exposure.
Thereafter, by developing using an organic alkaline solution containing tetramethylammonium hydroxide and water as main components (for example, NMD-3 manufactured by Tokyo Ohka) as a developer, the unexposed part resist 8
Only A remains. The mixing ratio of this tetramethylammonium hydroxide to water is 2 to 3 weights and 1%. After rinsing and drying by air blowing, etc., a boss bake is performed at a temperature of approximately IOOC to increase the adhesion of the resist 8A, but the steps up to this point are the same as the conventional example shown in FIG.
次に、電極取り出し端子にのみNi膜7を残すなめに、
第2図(D)に示すようにレジスト8Aの上にマスク1
0を被せ二重露光を行なう、そして、常温の希硝酸系の
エツチング液を用いてNi膜7のエツチングを行なうこ
とにより、第2図(E)に示すように、帯状のNi膜7
か形成される。この際、酸系のエツチング液にはレジス
ト8Aは反応しないので、NiB!A7の上にはそのま
まレジスト8Aが残る。次に、A QJ1!6のエツチ
ングを行なう、このエツチング液としては前記現像液と
同じテトラメチルアンモニウムハイドロオキサイドと水
を主成分とする有機アルカリ溶液を用いる。このエツチ
ングにより、第2図(F)に示すようにA IQ膜6が
帯状にエツチングされるとともに、二重露光による未露
光部のレジスト8Bだけが残る現像が同時に行われる0
次に、再度希硝酸系のエツチング溶液を用いてNi17
のエツチングを行なうことにより、第2図(G)に示す
ように電極取り出し端子対応箇所のNi膜7だけが残り
、最後にレジスト9Bの剥離を行なって背面電極が形成
される。Next, in order to leave the Ni film 7 only on the electrode extraction terminal,
As shown in FIG. 2(D), mask 1 is placed on resist 8A.
By performing double exposure and etching the Ni film 7 using a dilute nitric acid-based etching solution at room temperature, a band-shaped Ni film 7 is formed as shown in FIG. 2(E).
or is formed. At this time, the resist 8A does not react with the acid-based etching solution, so NiB! The resist 8A remains on A7. Next, etching of AQJ1!6 is carried out. As the etching solution, an organic alkaline solution containing tetramethylammonium hydroxide and water as the main components, which is the same as the developer described above, is used. As a result of this etching, the A IQ film 6 is etched into a band shape as shown in FIG.
Next, using dilute nitric acid-based etching solution again, Ni17 was etched.
By performing this etching, only the Ni film 7 corresponding to the electrode lead terminal remains as shown in FIG. 2(G), and finally, the resist 9B is peeled off to form a back electrode.
以上のように本発明によればレジストの現像液およびA
lM6のエツチング液として有機アルカリ溶液を用いて
いる。このため、A QM、6の下地層としての第2の
絶縁層5に酸に弱いSm20.やHf O2などの絶縁
材料を使用することができる。これらの材料を用いると
駆動電圧が低くなり、EL素子の低電圧駆動が可能とな
る。また、有機アルカリ溶液を用いることにより、前半
のNi膜7のエツチングの前に二重露光を行ない、この
Ni膜7のエツチングの後に、A I;:LH6のエツ
チングとレジスト8Aの現象とを同時に行なうことがで
きるとともに、従来のようにAl膜のエツチングの後、
二重露光するために乾燥を行なう工程も不用となるため
、大幅に工程の簡略化を図ることができる。尚、後半の
N1M7のエツチング工程において、希硝酸のエツチン
グ液が第2の絶縁層5に流れるが、このエツチング液は
酸性度が弱いので第2の絶縁層5への影響はほとんどな
い。As described above, according to the present invention, the resist developer and A
An organic alkaline solution is used as the 1M6 etching solution. For this reason, the second insulating layer 5 as the underlying layer of A QM, 6 is made of Sm20. Insulating materials such as HfO2 and HfO2 can be used. When these materials are used, the driving voltage becomes low, and it becomes possible to drive the EL element at a low voltage. Furthermore, by using an organic alkaline solution, double exposure is performed before etching the Ni film 7 in the first half, and after etching the Ni film 7, the etching of A I;:LH6 and the phenomenon of the resist 8A are simultaneously performed. In addition, after etching the Al film as in the conventional method,
Since the step of drying for double exposure is also unnecessary, the process can be greatly simplified. In the latter half of the N1M7 etching step, an etching solution of dilute nitric acid flows onto the second insulating layer 5, but this etching solution has weak acidity and therefore has almost no effect on the second insulating layer 5.
以上、本発明の一実施例について詳述したが、本発明の
要旨の範囲内で適宜変形できる。Although one embodiment of the present invention has been described in detail above, it can be modified as appropriate within the scope of the gist of the present invention.
例えば、前記実施例は、IllとNi膜との二層構造の
背面電極について詳述したが、Al膜の一層構造にも同
様に適用できる。For example, in the above embodiments, the back electrode has a two-layer structure of Ill and Ni films, but the present invention can be similarly applied to a single-layer structure of Al films.
[発明の効果]
以上詳述したように本発明によれば、レジストの現像液
およびAl膜のエツチング液として有機アルカリ溶液と
用いたことにより、EL素子の低電圧駆動を図れるとと
もに、工程を簡略化できるri膜EL素子の電極形成方
法を提供することができる。[Effects of the Invention] As detailed above, according to the present invention, by using an organic alkaline solution as a resist developer and an Al film etching solution, it is possible to drive the EL element at a low voltage, and the process can be simplified. It is possible to provide a method for forming electrodes of an RI film EL element that can be
4、4,
第1図は本発明の一実施例の工程を示すフロチャート、
第2図(A)〜(G)は工程に沿った概略説明図、第3
図は断面図、第4図は従来の工程を示すフロチャートで
ある。
6・・・Al膜
8・・・レジスト
第4図
手
続
?m
正
書1
(自
発
昭和63年8月10日
事件の表示
昭和63年特許願第1
62018号
2、発明の名称
i[EL素子の電極形成方法
3、補正をする者FIG. 1 is a flowchart showing the steps of an embodiment of the present invention;
Figures 2 (A) to (G) are schematic explanatory diagrams along the process;
The figure is a sectional view, and FIG. 4 is a flowchart showing a conventional process. 6...Al film 8...Resist figure 4 procedure? m Official document 1 (Indication of the incident August 10, 1988 Patent application No. 1 62018 2, Title of the invention i [Electrode formation method for EL element 3, Person making the amendment
Claims (1)
膜を積層し、このAl膜を所定の形状にフオトエッチン
グにより加工する薄膜EL素子の電極形成方法において
、前記Al膜上に塗布されるレジストの現像液およびA
l膜のエッチング液として有機アルカリ溶液を用いるこ
とを特徴とする薄膜EL素子の電極形成方法。(1) At least Al is used as the back electrode of the thin film EL element.
In a method for forming electrodes of a thin film EL element, in which films are laminated and the Al film is processed into a predetermined shape by photo-etching, a developer for a resist applied on the Al film and A
1. A method for forming electrodes of a thin film EL device, characterized in that an organic alkaline solution is used as an etching solution for the film.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63162018A JPH0212796A (en) | 1988-06-29 | 1988-06-29 | Forming method for electrode of thin film el element |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63162018A JPH0212796A (en) | 1988-06-29 | 1988-06-29 | Forming method for electrode of thin film el element |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0212796A true JPH0212796A (en) | 1990-01-17 |
Family
ID=15746493
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63162018A Pending JPH0212796A (en) | 1988-06-29 | 1988-06-29 | Forming method for electrode of thin film el element |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0212796A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2017112361A (en) * | 2015-12-15 | 2017-06-22 | 株式会社リコー | Manufacturing method of field-effect transistor |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2017112361A (en) * | 2015-12-15 | 2017-06-22 | 株式会社リコー | Manufacturing method of field-effect transistor |
US20170186626A1 (en) * | 2015-12-15 | 2017-06-29 | Ricoh Company, Ltd. | Method for manufacturing a field-effect transistor |
US10204799B2 (en) * | 2015-12-15 | 2019-02-12 | Ricoh Company, Ltd. | Method for manufacturing a field-effect transistor |
US20190148168A1 (en) * | 2015-12-15 | 2019-05-16 | Ricoh Company, Ltd. | Method for manufacturing a field-effect transistor |
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