Multilayer electronic component and conductive paste composition for internal electrode
US-2015371728-A1 · Dec 24, 2015 · US
US10062474B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10062474-B2 |
| Application number | US-75005810-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 30, 2010 |
| Priority date | Mar 31, 2009 |
| Publication date | Aug 28, 2018 |
| Grant date | Aug 28, 2018 |
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Disclosed is a conductive layer including photopolymerizable resin having dispersed carbon nanotubes, which is transparent with high electrical conductivity and facilitates the formation of an electrode pattern. A laminate and a transparent electrode, including the conductive layer, are also provided.
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What is claimed is: 1. A transparent electrode comprising a substrate and a conductive layer provided on a surface of the substrate, the conductive layer comprising carbon nanotubes and having at least two pyrolysis onsets showing at least 5% weight reduction in a pyrolysis range of 200-900° C., the pyrolysis range including a first pyrolysis range which initiates pyrolysis at 200-450° C. and shows a weight reduction of W1% and a second pyrolysis range which initiates pyrolysis at 450-700° C. and shows a weight reduction of W2%, and the W1/W2 being 0.1-20; wherein the conductive layer is obtained from a composition comprising an alkali-soluble binder resin, a photopolymerizable compound, a photoinitiator, and carbon nanotubes, in which a ratio of an amount of the carbon nanotubes and a total amount of the alkali-soluble binder resin and the photopolymerizable compound is 1:0.2 to 1:10.0 by weight, and a ratio of an amount of the alkali-soluble binder resin and an amount of the photopolymerizable compound is 1:0.1 to 1:2 by weight; wherein the alkali-soluble binder resin and the photopolyerizable compound are different from each other, and the alkali-soluble binder resin is a copolymer of (meth)acrylic and (meth)acrylic acid ester, or a hydroxypropyl methylcellulose acetate phthalate ester; wherein the substrate is a polyimide film manufactured by polymerizing an aromatic dianhydride and an aromatic diamine to form a polyamic acid, which is then subject to an imidization to give the polyimide film, and wherein the polyimide film has an average coefficient of linear thermal expansion of 35 ppm/° C. or less measured at 50-250° C. using thermomechanical analysis at a film thickness of 50-100 μm; wherein the aromatic dianhydride includes one or more selected from the group consisting of 2,2-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride, 4-(2,5-dioxotetrahydrofuran-3-yl)-1,2,3,4-tetrahydronaphthalene-1,2-dicarboxylic anhydride, 4,4′-(4,4′-isopropylidenediphenoxy)bis(phthalic anhydride), pyromellitic dianhydride, biphenyltetracarboxylic dianhydride, and oxydiphthalic dianhydride; and wherein the aromatic diamine includes one or more selected from the group consisting of 2,2-bis[4-(4-aminophenoxy)-phenyl]propane, 2,2′-bis(trifluoromethyl)-4,4′-diaminobiphenyl, 3,3′-bis(trifluoromethyl)-4,4′-diaminobiphenyl, 4,4′-bis(3-aminophenoxy)diphenylsulfone, bis(3-aminophenyl)sulfone, bis(4-aminophenyl)sulfone, 1,3-bis(3-aminophenoxy)benzene, 1,4-bis(4-aminophenoxy)benzene, 2,2′bis[3(3-aminophenoxy)phenyl]hexafluoropropane, 2,2′-bis[4(4-aminophenoxy)phenyl]hexafluoropropane, 2,2′-bis(3-aminophenyl)hexafluoropropane, 2,2′-bis(4-aminophenyl)hexafluoropropane, and oxydianiline. 2. The transparent electrode as set forth in claim 1 , wherein the conductive layer has a thickness ranging from 10 nm to 5 μm. 3. The transparent electrode as set forth in claim 1 , having a light transmittance of 70% or more at 550 nm and a surface resistivity of 1,000 Ω/sq or less. 4. The transparent electrode as set forth in claim 1 , obtained by patterning the conductive layer using photolithography. 5. The transparent electrode as set forth in claim 1 , wherein the copolymer of (meth) acrylic acid and (meth)acrylic acid ester further comprises a monomeric unit selected from the group consisting of acryl amide, methacryl amide, styrene, and α-methyl styrene. 6. A conductive laminate comprising a substrate and a conductive layer, the conductive layer comprising carbon nanotubes and having at least two pyrolysis onsets showing at least 5% weight reduction in a pyrolysis range of 200-900° C., the pyrolysis range including a first pyrolysis range which initiates pyrolysis at 200-450° C. and shows a weight reduction of W1% and a second pyrolysis range which initiates pyrolysis at 450-700° C. and shows a weight reduction of W2%, and the W1/W2 being 0.1-20; wherein the conductive layer is obtained from a composition comprising an alkali-soluble binder resin, a photopolymerizable compound, a photoinitiator, and carbon nanotubes, in which a ratio of an amount of the carbon nanotubes and a total amount of the alkali-soluble binder resin and the photopolymerizable compound is 1:0.2 to 1:10.0 by weight, and a ratio of an amount of the alkali-soluble binder resin and an amount of the photopolymerizable compound is 1:0.1 to 1:2 by weight; wherein the alkali-soluble binder resin and the photopolyerizable compound are different from each other, and the alkali-soluble binder resin is a copolymer of (meth)acrylic and (meth)acrylic acid ester, or a hydroxypropyl methylcellulose acetate phthalate ester; wherein the substrate is a polyimide film manufactured by polymerizing an aromatic dianhydride and an aromatic diamine to form a polyamic acid, which is then subject to an imidization to give the polyimide film, and wherein the polyimide film has an average coefficient of linear thermal expansion of 35 ppm/° C. or less measured at 50-250 ° C. using thermomechanical analysis at a film thickness of 50-100 μm; wherein the aromatic dianhydride includes one or more selected from the group consisting of 2,2-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride, 4-(2,5-dioxotetrahydrofuran-3-yl)-1,2,3,4-tetrahydronaphthalene-1,2-dicarboxylic anhydride, 4,4′-(4,4 -isopropylidenediphenoxy)bis(phthalic anhydride), pyromellitic dianhydride, biphenyltetracarboxylic dianhydride, and oxydiphthalic dianhydride; and wherein the aromatic diamine includes one or more selected from the group consisting of 2,2-bis[4-(4-aminophenoxy)-phenyl]propane, 2,2′-bis(trifluoromethyl)-4,4′-diaminobiphenyl, 3,3′-bis(trifluoromethyl)-4,4′-diaminobiphenyl, 4,4′-bis(3-aminophenoxy)diphenylsulfone, bis(3-aminophenyl)sulfone, bis(4-aminophenyl)sulfone, 1,3-bis(3-aminophenoxy)benzene, 1,4-bis(4-aminophenoxy)benzene, 2,2′-bis[3(3-aminophenoxy)phenyl]hexafluoropropane, 2,2′-bis[4(4-aminophenoxy)phenyl]hexafluoropropane, 2,2′-bis(3-aminophenyl)hexafluoropropane, 2,2′-bis(4-aminophenyl)hexafluoropropane, and oxydianiline. 7. The conductive laminate as set forth in claim 6 , wherein the conductive layer has a thickness ranging from 10 nm to 5 μm. 8. The conductive laminate as set forth in claim 6 , having a light transmittance of 70% or more at 550 nm and a surface resistivity of 1,000 Ω/sq or less. 9. The conductive laminate as set forth in claim 6 , wherein the copolymer of (meth)acrylic acid and (meth)acrylic acid ester further comprises a monomeric unit selected from the group consisting of acryl amide, methacryl amide, styrene, and α-methyl styrene. 10. A conductive layer comprising carbon nanotubes and having at least two pyrolysis onsets showing at least 5% weight reduction in a pyrolysis range of 200-900° C., the pyrolysis range including a first pyrolysis range which initiates pyrolysis at 200-450° C. and shows a weight reduction of W1% and a second pyrolysis range which initiates pyrolysis at 450-700° C. and shows a weight reduction of W2%, and the W 1/W2 being 0.1-20, said conductive layer being obtained from a composition comprising an alkali-soluble binder resin, a photopolymerizable compound, a photoinitiator, and carbon nanotubes, in which a ratio of an amount of the carbon nanotubes and a total amount of the alkali-soluble binder resin and the photopolymerizable compound is 1:0.2 to 1:10.0 by weight, and a ratio of an amount of the alkali-soluble binder resin and an amount of the photopolymerizable compound is 1:0.1 to 1:2 by weight based on solid content of the composition; wherein the alkali-soluble binder resin and the photopolyerizable compound are different from each other, and the alkali-soluble binder resin is a copolymer of (meth)acrylic and (meth)acrylic acid ester, or a hydroxypropyl methylcellulose a
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