WO2004028216A1 - 有機エレクトロ・ルミネッセンス表示装置および有機エレクトロ・ルミネッセンス表示装置の製造方法 - Google Patents
有機エレクトロ・ルミネッセンス表示装置および有機エレクトロ・ルミネッセンス表示装置の製造方法 Download PDFInfo
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- WO2004028216A1 WO2004028216A1 PCT/JP2003/011746 JP0311746W WO2004028216A1 WO 2004028216 A1 WO2004028216 A1 WO 2004028216A1 JP 0311746 W JP0311746 W JP 0311746W WO 2004028216 A1 WO2004028216 A1 WO 2004028216A1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
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Definitions
- the present invention relates to an organic electroluminescent device (hereinafter, abbreviated as “organic EL”), and more particularly, to an organic EL display device capable of high-definition display subjected to color patterning by a dopant and the color pattern
- organic EL organic electroluminescent device
- the present invention relates to a method for manufacturing an organic EL device having been subjected to the above. Background art
- organic EL elements are self-luminous elements having a very fast response speed, they are expected to provide a good flat display device having a wide viewing angle when applied to a display device. For this reason, the application of the organic EL element to a flat display device instead of a liquid crystal display device is being studied.
- a color pattern having R, G, and B characteristics is formed in order to perform color display.
- a patterning method using a shadow mask and a patterning method using an ink jet printer have been proposed. The method of performing color patterning using a shadow mask can perform good patterning.
- a solution containing a dopant when a color pattern is formed by doping an organic EL material, if a solution containing a dopant can be introduced into the organic EL material layer by utilizing a capillary phenomenon, it is easy and reliable. It is based on the idea that high-precision color printing can be performed. That is, in the present invention, a trench is formed adjacent to the organic EL material layer with desired accuracy by photoresist. The wrench is small enough to allow a solution containing dopant to be introduced onto the organic EL material layer by capillary action. You. The introduced dopant is diffused into the organic EL material layer at the same time as the solvent is dried by baking treatment, and the organic EL material layer is doped.
- the accuracy of the color patterning is determined in accordance with the accuracy of the photoresist pattern formed adjacent to the organic EL material layer and the pattern configuration, and patterning for full-color display becomes possible.
- the photoresist pattern is left after doping, the photoresist used in the present invention is optically transparent and colorless, so that even if the pattern of the photoresist layer remains, it is not optically No circumstances arise.
- the trench pattern can be formed so that a wall is formed directly from the electrode before forming the functional layer. Further, in a preferred embodiment of the present invention, a trench pattern can be formed on the functional layer. That is, according to the present invention,
- a first electrode formed on the substrate is formed on the first electrode
- a trench pattern formed adjacent to the functional layer is
- an organic electroluminescent display device including the functional layer and a second electrode layer formed on the trench pattern.
- the functional layer may include a polymer or an oligomer having an amine derivative structure.
- different dopants may be included in regions of the functional layer adjacent to each other across the trench pattern wall.
- the doping concentration in the functional layer below the wall forming the trench pattern is lower than in other portions.
- the step of forming the functional layer and the trench pattern includes: a step of forming the functional layer; a step of forming a photoresist layer on the functional layer; Steps for patterning the trench pattern
- a step of introducing at least a second functional layer having a composition different from that of the functional layer along the trench pattern can be included.
- the method may further include a step of supplying a dopant solution along the trench pattern and performing a dove on the functional layer.
- the step of doping the functional layer by supplying the dopant solution includes:
- the method may include a step of supplying the dopant solution along the trench pattern; and a step of heating the functional layer to diffuse the dopant into the functional layer.
- the step of performing doping may include a step of supplying different dopants across the wall of the trench pattern.
- FIG. 1 is a perspective view of an organic EL display device according to the present invention.
- FIG. 2 is a diagram showing a cross section of the organic EL display device shown in FIG. 1 along the arrow line B—B. C FIG. It is.
- FIG. 4 is a diagram showing a part of a manufacturing process of the organic EL display device of the present invention.
- FIG. 5 is a detailed perspective view of the organic EL display device of the present invention.
- FIG. 6 is a view showing another embodiment of the organic EL display device of the present invention.
- FIG. 7 is a diagram showing a doping pattern of the organic electroluminescent display device of the present invention.
- FIG. 8 is a diagram showing a doping pattern obtained by stamping. BEST MODE FOR CARRYING OUT THE INVENTION
- FIG. 1 is a partially sectional perspective view showing the structure of the organic EL device of the present invention.
- the organic EL element 10 shown in FIG. 1 emits light generated by electoluminescence in the direction of arrow A.
- an anode 14 is deposited and patterned by a transparent conductive film on a substrate 12 such as glass.
- a substrate 12 such as glass.
- FIG. 1 in order to clearly show the patterned anode 14, a part of the structure on the substrate 12 of the organic EL device is partially cut away to show the patterned anode 14.
- a functional layer 16 for generating light emission by electoluminescence is deposited on the anode 14.
- a photoresist layer 18 formed by a photoresist is formed, and the photoresist layer 18 has a trench pattern 1 separated by a wall. 8a and 18 are patterned.
- the trench patterns 18a and 18b are formed in parallel to and substantially perpendicular to the patterned anode 14.
- a reflective electrode (not shown) is formed on the photoresist layer 18 to emit light in the direction of arrow A.
- the material for forming the anode 14 is described in the present invention.
- any configuration can be used as long as it is transparent and conductive.
- the anode 14 does not necessarily have to be transparent, and AI, Ni, Ni / AI, Cr, Ag, etc. are used as the anode. can do.
- the functional layer 16 that can be used in the present invention is formed by applying a photoresist to form a trench pattern 18a, 18b so that the functional layer 16 can be formed. It preferably has solvent resistance and film strength.
- an oligomeric carrier transporting material or a polymerizable carrier transporting material can be used.
- an oligomeric carrier transporting material is defined as any carrier transporting material having a molecular weight between the following monomolecular carrier transporting materials and polymer carrier transporting materials.
- the following is an example of a polymer-uniform carrier transport material that can be used in the present invention.
- a carrier transporting material in addition to the above-mentioned polymeric carrier transporting material, a carrier transporting material is mixed with a resin having optically favorable properties such as a polymethyl methacrylate resin, a polycarbonate resin, and an epoxy resin.
- Carrier transport materials can be used.
- the carrier transporting material that can be used by mixing with the resin component for example, the following materials can be used.
- Examples of the electron transporting layer that can be used in the present invention include the following materials.
- a light-emitting material can be used if necessary.
- the light-emitting material that can be used in the present invention include complexes such as AIq3, and other known ⁇ A light-emitting low-molecular material or a high-molecular material can also be used.
- luminescent materials that can be used in the present invention will be exemplified.
- the above-described functional layer 16 is described as a single layer 16 in a specific embodiment of the present invention, if necessary, a hole transport layer, a light emitting layer, an electron transport It is also possible to include a plurality of layers such as layers.
- the photoresist that can be used to form the trench pattern any of the positive or negative photoresists known so far can be used. Specifically, the positive photoresist can be used.
- photoresist As a small resin resist, a so-called acid dissociation system using a composition obtained by mixing a photosensitive material with phenol novolak, a polyvinyl phenol alkyl ester, and a photoacid generator mixed Form (Rule 26) Photoresist can be cited.
- the negative type photoresist resist any photoresist can be used as long as it uses photopolymerization.
- an acrylate, epoxy, or acid dissociation photoresist is used. can do.
- a photo-curable epoxy resin-based negative type resist can be used.
- the photoresist that can be used in the present invention a solventless photoresist that does not affect the lower functional layer 16 as much as possible can be used.
- the trench patterns 18a and 18b are provided. Is performed on the functional layer along the line.
- any dopant can be used as long as required light-emitting characteristics can be obtained. Examples thereof include a daylight fluorescent material, a fluorescent brightener, and a laser dye. , Organic scintillation, and dyes for fluorescent analysis reagents.
- the above-mentioned pigments include Nile Blue, Nile Red, TPB, Coumarin 6, Ketocoumarin, Luprene, DCM-1 (Orange Red), Perylene, p-terphenyl, Polyphenyl 1, Stilbene 1 , Stilbene 3, coumarin 2, coumarin 47, coumarin 102, coumarin 30, rhodamine 6G, rhodamine B, rhodamine 700, styryl 9, HITCL, IR140, etc.
- any dye other than these can be used as long as an appropriate emission spectrum can be given. More generally, for example, in order to obtain blue (B) emission, a wavelength of about 420 nm is required.
- a dye that gives a peak in the emission spectrum can be used.
- G green
- R red
- a dye that gives a peak of an emission spectrum at about 600 nm can be used.
- These dyes can be further selected from those having a name and a chemical structure corresponding to the color index (CI) in consideration of the range of the emission spectrum, solubility and the like as appropriate.
- CI color index
- the above solvents further include 2-ethylhexyl chloride, amyl chloride, isopropyl chloride, chlorinated chloride, naphthalene chloride, butyl chloride, hexyl chloride, methyl chloride, methylene chloride, o-chlorotoluene, Toluene, Toluene benzene, Carbon tetrachloride, Dichloroethane, Dichloroethylene, Dichlorotoluene, Dichlorobutane, Dichloropropane, Dichlorobenzene, Dibromoethane, Dibromobutane, Dibromopropane, Dibromobenzene, Dibromopentane, Aryl bromide, Isopropyl bromide , Bromide tyl, bromide octyl, butyl bromide, propyl bromide, methyl bromide, lauryl bromide,
- solvents examples include amyl alcohol, aryl alcohol, isoamyl alcohol, isobutyl alcohol, isopropyl alcohol, pendanol, ether, 2-ethylbutanol, 2-ethylhexanol, and 2-butanol.
- n-octanol glycidol, cyclohexanol, 3,5,1-dimethyl-1-hexyne-3-nitro, n-decanol, tetrahydrofurfuryl alcohol, ⁇ -terbineol, neopentyl alcohol, nonanol, fusel oil , Butanol, furfuryl alcohol, propargyl alcohol, propanol, hexanol, heptanol, benzyl alcohol, pentanol, methanol, methylcyclohexanol, 2-methyl-1-butanol, 3-methyl-2-buta Lumpur, three to methyl one 1-butyne one 3- ol, 4-methyl-one 2- pen evening Nord, 3-methyl-one 1 one pentyne - can also be mentioned alcohols such as 3-ol.
- solvent examples include anisol, ethyl isoamyl ether, ethyl t-butyl ether, ethyl benzyl ether, epoxybutane, crown ethers, cresyl methyl ether, diisoamyl ether, diisopropyl ether, and getyl acetal.
- Ether phenyl ether, furan, furfural, methylal, methyl t-butyl ether, methylfuran, monochloroethyl ether
- examples of the above-mentioned solvents include acetylacetone, acetoaldehyde, acetophenone, acetone, isophorone, ethyl-n-butylketone, diacetonealcohol, diisopropylketone, diisopropylketone, getylketone, cyclohexanone, Di-n-propyl ketone, xylon, mesityl methoxide, methyl-n-amyl ketone, methyl isobutyl ketone, methyl ethyl ketone, methyl cyclohexanone, methyl n-butyl ketone, methyl n-propyl ketone, Ketone / aldehyde solvents such as
- Solvents that can be used in the present invention further include getyl adipate, dioctyl adipate, triethyl acetylquenate, tributyl acetylquenate, ethylacetylacetate, arylarylacetate, methylacetoacetate, and abietin.
- solvents examples include ethylene glycol, ethylene glycol dibutyl ether, ethylene glycol diacetate, ethylene glycol dibutyl ether, ethylene glycol dimethyl ether, ethylene glycol monoacetate, ethylene glycol monoisopropyl ether, and ethylene glycol dibutyl ether.
- Tylene glycol monoethyl ether ethylene glycol monoethyl ether acetate, ethylene glycol monophenyl ether, ethylene glycol monobutyl ether, ethylene glycol monobutyl ether, ethylene glycol monohexyl ether, ethylene blender Monomethyl ether, Ethylene glycol monomethyl ether acetate, Ethylene glycol monomethoxymethyl ether, Ethylene Lolohydrin, 1,3-butylene glycol, glycerin, glycerin 1,3-diacetate, glycerin dialkyl ether, glycerin fatty acid ester, glycerin triacetate, glycerin trilaurate, glycerin monoacetate, 2- Black mouth — 1,3-propanediol, 3-chloro-1,2-propanediol, poly (ethylene glycol), diethylene glycol ethyl methyl ether, and polyhydric alcohol such as poly
- solvents examples include isovaleric acid, isobutyric acid, itaconic acid, 2-ethylhexanoic acid, 2-ethylethylacetic acid, oleic acid, caprylic acid, caproic acid, formic acid, valeric acid, acetic acid, lactic acid, and vivarin.
- Carboxylic acid derivatives such as acid, propionic acid, and ethyl Phenol, octyl phenol, catechol, guaiacol, xylenol, P
- FIG. 2 is a cross-sectional view of the organic EL display device of the present invention shown in FIG. 1 taken along a line BB (a position where the anode 14 cut in the pattern is cut).
- the organic EL display device of the present invention can be configured as a transistor array in which a plurality of thin film transistors (TFTs) are formed on a substrate 12, but FIG. For simplification, the TFT structure is omitted. As shown in FIG.
- an anode 14 is deposited on a substrate 12, and a film-forming functional layer 16 is formed on the anode 14.
- trench patterns 18 a and 18 b formed by photo resist are formed, and the dopant can be supplied to the functional layer 16 by capillary action. It is configured.
- adjacent trench patterns are doped with different dopants.
- the trench pattern 18a is doped with a dopant such as Nile pellets.
- the R region is formed, and the G pattern is formed in the trench pattern 18b by doping perylene.
- the doped dopant is diffused into the functional layer 16 by a baking process to provide a desired light emission.
- a force sword 20 is deposited on the upper part of the trench patterns 18a and 18b, so that a current can be supplied to the functional layer 16 in cooperation with the anode 14. It is said to be done.
- the material used as the force sword 20 is preferably reflective in a bottom emission configuration, but essentially any conductive material can be used, for example, Al, C a, S r, L i A and N i, N i / AKC r, A g, M g Ag can be used.
- an organic conductive film using an alkali metal element or an alkaline earth metal element can be used as a force source.
- a conductive film such as a metal such as A, ITO, Ag, Ni, or Cr can be used as the auxiliary conductive layer.
- a force sword shown as an upper electrode in FIG. 2 is provided on the substrate 12 side and formed from a light-transmitting or non-transmitting conductive film, and an anode is used as a functional layer. It can also be formed from a light-reflective or light-transmissive conductive film as the structure of the upper electrode in FIG. FIG.
- FIG. 3 is a diagram showing a part of the manufacturing process of the organic EL display device of the present invention.
- a transparent anode 14 such as ITO is formed on a substrate 12 and a functional layer 16 is formed on the anode 14, for example, by a method such as spin coating. And baking.
- a photoresist layer 18 is formed on the formed functional layer 16 using, for example, an epoxy-based photoresist.
- the trench patterns 18a and .18b are formed on the photoresist layer 18.
- the surface of the photoresist layer 18 and the surface of the functional layer 16 are subjected to assing treatment to change the chemical affinity of the dopant with respect to the solvent. You can do it.
- the trench patterns 18a and 18b are separated from each other by walls 22 so that different dopants Do can be introduced. Thereafter, as shown in FIG. 3 (c), the solution of dopant Do is applied to the trench patterns 18a and 18b formed on the photoresist layer 18 using the capillary phenomenon. Introduce.
- the same dopant Do can be introduced into the trench patterns 18a and 18b, or different dopants Do can be introduced. Thereafter, as shown in FIG.
- a baking process is performed to diffuse the dopant into the functional layer 16 to obtain a desired color patterning.
- Nile Red is introduced into the wrench 18a to form an R region
- Perylene is introduced into the wrench 18b to form a G region.
- the dopant does not penetrate during baking, does not emit light, or has a specific shape according to the present invention.
- emission of blue (B) due to polyvinyl carbazole is observed. Thereafter, in the present invention, as shown in FIG.
- FIG. 5 is a perspective view showing the element structure of the organic EL display device of the present invention. As shown in FIG.
- the organic EL display device 10 of the present invention can have a configuration in which TFTs 32 are arranged in a matrix on a substrate 30 and can be driven by an active matrix. You. A pixel electrode 34 is formed adjacent to the TFT 32, and a functional layer 16 is formed on the pixel electrode 34. Further, the functional layer 16 is doped according to the present invention, and the end positions of both side walls forming the trench pattern for doping are indicated by 36 a and 36 b. . As shown in FIG. 5, the doping in the present invention is performed using a trench pattern formed by photolithography, so that it is possible to perform the doping with extremely high precision in pixel units.
- FIG. 6 is a diagram showing a cross-sectional configuration of another embodiment of the organic EL display device of the present invention.
- a transparent conductive electrode 14 is formed on a substrate 12, and a first functional layer 16 a is formed on the conductive electrode 14. Are formed.
- a photoresist layer 18 is formed, and on this photoresist layer 18, trench patterns 18a and 18b are formed. Further, in the organic EL display device 10 shown in FIG. 6, a second functional layer 16b and a third functional layer 16c are formed along the trench patterns 18a and 18b. Materials have been introduced. In the present invention, the functional layers 16b and 16c introduced into the trench patterns 18a and 18b may be the same or different. When different functional layers 16b and 16c are introduced, a functional layer that gives a different light emission spectrum for each of the trench patterns 18a and 18b can be introduced. Inning can also be terminated at the manufacturing stage. Further, in the embodiment shown in FIG.
- a dopant D 0 can be further introduced by using a capillary phenomenon in order to obtain a desired light emission.
- a dopant Do is introduced into the trench pattern # 8d according to the present invention, so that a desired light emission can be obtained.
- An ITO film was formed on a glass substrate by sputtering to a thickness of about 50 nm to form a pixel electrode.
- a functional layer with a thickness of about 100 nm was formed.
- a photoresist layer is formed on the obtained functional layer using an epoxy-based photoresist (SU-8: manufactured by Microchem), and after baking, the pitch becomes 190 ppi and 340 ppi.
- the trench pattern was patterned. After the polishing, the surface of the trench pattern and the exposed functional layer were subjected to 02 ashes to impart hydrophilicity to the surface.
- FIG. 8 shows the state of the dopant solution that penetrates the trench pattern during doping.
- the doping example shown in FIG. 8 was obtained when a dopant solution was introduced using a capillary phenomenon to a trench pattern of 190 ppi.
- FIG. 8 according to the present invention, it is shown that doping can be favorably performed along the trench pattern.
- baking was performed at 130 ° C for 30 min, the solvent was dried, the dopant was diffused, and MgAg was deposited again by sputtering to form a force sword.
- a protective layer was formed under an N 2 atmosphere to produce an organic EL display device of the present invention. When a DC voltage was applied to the manufactured organic EL device, good B light emission was obtained.
- a dopant solution having the composition shown in Table 1 below was prepared, and the organic EL display was performed in the same manner as in Example 1.
- Example 4 doping was performed using the capillary phenomenon in the same manner as in Example 1 except that the wrench pattern was formed at a size of 330 ppi. It was possible.
- a wrench pattern was formed in the shape of a comb as shown in Fig. 1, a 2% by weight solution of nylon was introduced from one end, and a 2% by weight solution of perylene was injected from the opposite end. Except for the doping, an organic EL device was formed in the same manner as in Example 1, and the emission characteristics were observed. As a result, R, G, and B emissions were observed. Nile red and perylene have higher luminous efficiencies than polyvinylcarbazole, so they emit light in R and G preferentially, and dopant is not doped in the region where the trench wall is formed. This is because light emission was observed. Table 2 shows the results obtained for the dopants and emission characteristics of Examples 1 to 4 described above.
- the present invention As described above, according to the present invention, it is shown that a high-definition color patterning can be easily and inexpensively formed on an organic EL display device. So far, the present invention has been described in detail with reference to the embodiment shown in the drawings. However, the present invention is not limited to the embodiment shown in the drawing, Any configuration, material, manufacturing process order, and the like can be applied as appropriate as long as a similar configuration can be obtained. In the present invention, when the trench pattern is formed in a color filter shape so as to correspond to each pixel, it is possible to perform good color patterning.
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Abstract
Description
Claims
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JP2004537560A JPWO2004028216A1 (ja) | 2002-09-17 | 2003-09-12 | 有機エレクトロ・ルミネッセンス表示装置および有機エレクトロ・ルミネッセンス表示装置の製造方法 |
AU2003261602A AU2003261602A1 (en) | 2002-09-17 | 2003-09-12 | Organic electroluminescent display and method for manufacturing organic electroluminescent display |
US10/528,756 US20060145163A1 (en) | 2002-09-17 | 2003-09-12 | Organic elctroluminescent display and method for manufacturing organic electroluminescent display |
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PCT/JP2003/011746 WO2004028216A1 (ja) | 2002-09-17 | 2003-09-12 | 有機エレクトロ・ルミネッセンス表示装置および有機エレクトロ・ルミネッセンス表示装置の製造方法 |
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US (1) | US20060145163A1 (ja) |
JP (1) | JPWO2004028216A1 (ja) |
KR (1) | KR100754309B1 (ja) |
CN (1) | CN100573900C (ja) |
AU (1) | AU2003261602A1 (ja) |
TW (1) | TWI232695B (ja) |
WO (1) | WO2004028216A1 (ja) |
Cited By (9)
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WO2006025612A1 (en) * | 2004-09-02 | 2006-03-09 | Seiko Epson Corporation | Material composition for conductive layers in electronic devices |
JP2006241309A (ja) * | 2005-03-03 | 2006-09-14 | Seiko Epson Corp | 塗布液組成物、薄膜形成方法および有機薄膜 |
JP2008294401A (ja) * | 2007-04-25 | 2008-12-04 | Mitsubishi Chemicals Corp | 有機電界発光素子用組成物、有機電界発光素子および有機電界発光素子の製造方法 |
WO2014092194A1 (en) * | 2012-12-14 | 2014-06-19 | Canon Kabushiki Kaisha | Electrophotographic photosensitive member, process cartridge, electrophotographic apparatus and phthalocyanine crystal |
US9093399B2 (en) | 2009-05-28 | 2015-07-28 | Sharp Kabushiki Kaisha | Organic electroluminescence display device, method for producing same, color filter substrate and method for producing same |
JP2016108374A (ja) * | 2014-12-02 | 2016-06-20 | セイコーエプソン株式会社 | 成膜用インク、成膜方法、膜付きデバイスおよび電子機器 |
JP2018520479A (ja) * | 2015-06-12 | 2018-07-26 | メルク パテント ゲーエムベーハー | Oled調合物のための溶媒としての非芳香族環を含むエステル |
JP2020520049A (ja) * | 2017-05-03 | 2020-07-02 | メルク パテント ゲーエムベーハー | 有機機能材料の調合物 |
JP2022023039A (ja) * | 2015-08-28 | 2022-02-07 | メルク パテント ゲーエムベーハー | エポキシ基含有溶媒を含む有機機能性材料の調合物 |
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JP4762630B2 (ja) * | 2005-08-03 | 2011-08-31 | 東京応化工業株式会社 | レジスト組成物およびレジストパターン形成方法 |
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CN100444699C (zh) * | 2006-01-26 | 2008-12-17 | 友达光电股份有限公司 | 双面显示装置 |
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WO2017080326A1 (zh) * | 2015-11-12 | 2017-05-18 | 广州华睿光电材料有限公司 | 印刷组合物、包含其的电子器件及功能材料薄膜的制备方法 |
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KR20220153375A (ko) * | 2021-05-11 | 2022-11-18 | 삼성에스디아이 주식회사 | 잉크 조성물, 이를 이용한 막, 이를 포함하는 전기영동 장치 및 디스플레이 장치 |
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- 2003-07-30 TW TW092120807A patent/TWI232695B/zh not_active IP Right Cessation
- 2003-09-12 AU AU2003261602A patent/AU2003261602A1/en not_active Abandoned
- 2003-09-12 CN CNB038219581A patent/CN100573900C/zh not_active Expired - Fee Related
- 2003-09-12 WO PCT/JP2003/011746 patent/WO2004028216A1/ja active Application Filing
- 2003-09-12 KR KR1020057002013A patent/KR100754309B1/ko not_active IP Right Cessation
- 2003-09-12 US US10/528,756 patent/US20060145163A1/en not_active Abandoned
- 2003-09-12 JP JP2004537560A patent/JPWO2004028216A1/ja active Pending
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JPH11185968A (ja) * | 1997-12-17 | 1999-07-09 | Sanyo Electric Co Ltd | 有機エレクトロルミネッセンス装置及びその製造方法 |
JP2000294379A (ja) * | 1999-04-07 | 2000-10-20 | Casio Comput Co Ltd | 有機el発光装置 |
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Cited By (13)
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WO2006025612A1 (en) * | 2004-09-02 | 2006-03-09 | Seiko Epson Corporation | Material composition for conductive layers in electronic devices |
JP2006241309A (ja) * | 2005-03-03 | 2006-09-14 | Seiko Epson Corp | 塗布液組成物、薄膜形成方法および有機薄膜 |
JP2008294401A (ja) * | 2007-04-25 | 2008-12-04 | Mitsubishi Chemicals Corp | 有機電界発光素子用組成物、有機電界発光素子および有機電界発光素子の製造方法 |
US9093399B2 (en) | 2009-05-28 | 2015-07-28 | Sharp Kabushiki Kaisha | Organic electroluminescence display device, method for producing same, color filter substrate and method for producing same |
WO2014092194A1 (en) * | 2012-12-14 | 2014-06-19 | Canon Kabushiki Kaisha | Electrophotographic photosensitive member, process cartridge, electrophotographic apparatus and phthalocyanine crystal |
JP2016108374A (ja) * | 2014-12-02 | 2016-06-20 | セイコーエプソン株式会社 | 成膜用インク、成膜方法、膜付きデバイスおよび電子機器 |
JP2018520479A (ja) * | 2015-06-12 | 2018-07-26 | メルク パテント ゲーエムベーハー | Oled調合物のための溶媒としての非芳香族環を含むエステル |
JP2021153053A (ja) * | 2015-06-12 | 2021-09-30 | メルク パテント ゲーエムベーハー | Oled調合物のための溶媒としての非芳香族環を含むエステル |
JP7309778B2 (ja) | 2015-06-12 | 2023-07-18 | メルク パテント ゲーエムベーハー | Oled調合物のための溶媒としての非芳香族環を含むエステル |
JP2022023039A (ja) * | 2015-08-28 | 2022-02-07 | メルク パテント ゲーエムベーハー | エポキシ基含有溶媒を含む有機機能性材料の調合物 |
JP7293298B2 (ja) | 2015-08-28 | 2023-06-19 | メルク パテント ゲーエムベーハー | エポキシ基含有溶媒を含む有機機能性材料の調合物 |
JP2020520049A (ja) * | 2017-05-03 | 2020-07-02 | メルク パテント ゲーエムベーハー | 有機機能材料の調合物 |
JP7330898B2 (ja) | 2017-05-03 | 2023-08-22 | メルク パテント ゲーエムベーハー | 有機機能材料の調合物 |
Also Published As
Publication number | Publication date |
---|---|
US20060145163A1 (en) | 2006-07-06 |
JPWO2004028216A1 (ja) | 2006-01-19 |
AU2003261602A1 (en) | 2004-04-08 |
CN100573900C (zh) | 2009-12-23 |
KR100754309B1 (ko) | 2007-09-03 |
KR20050054495A (ko) | 2005-06-10 |
CN1682573A (zh) | 2005-10-12 |
TWI232695B (en) | 2005-05-11 |
TW200420172A (en) | 2004-10-01 |
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