Electrolytic solution for aluminum electrolytic capacitor and aluminum electrolytic capacitor using the same
US-2016020036-A1 · Jan 21, 2016 · US
US2017033256A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2017033256-A1 |
| Application number | US-201615217952-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jul 22, 2016 |
| Priority date | Jul 28, 2015 |
| Publication date | Feb 2, 2017 |
| Grant date | — |
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A method of making an ultraviolet sensor includes applying a metal-containing solution to a substrate using a spin coating technique to form a metal-containing coat. The metal-containing coat is baked and pyrolyzed to form a metal-containing oxide film on the substrate. The metal-containing oxide film has a cubic crystalline structure suitable for ultraviolet photodetectors in flame detection applications.
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What is claimed is: 1 . A method of making an ultraviolet (UV) photodetector, comprising: applying a metal-containing solution to a substrate using a spin coat technique to form a metal-containing coat; baking the metal-containing coat; and pyrolyzing the metal-containing coat to form a metal-containing oxide film according to Mg x Zn (1-x) O with a cubic crystalline structure. 2 . The method as recited in claim 1 , wherein applying the metal-containing solution includes applying the metal-containing solution over a metal-containing oxide film. 3 . The method as recited in claim 1 , wherein the metal-containing oxide film is a first metal-containing oxide film, and further including: applying a metal-containing solution having magnesium and zinc to the metal-containing oxide film using a spin coat technique; and pyrolyzing the metal-containing solution to form a second metal-containing oxide film overlaying the first metal-containing oxide film. 4 . The method as recited in claim 1 , further including calcining the metal-containing oxide film to form a metal-containing oxide layer. 5 . The method as recited in claim 1 , wherein the predetermined baking temperature is about 150 degrees Celsius and the predetermined time interval is about five (5) minutes. 6 . The method as recited in claim 1 , wherein pyrolyzing the metal-containing coat includes placing the metal-containing coat in a furnace and flowing an inert gas over the metal-containing coat to decompose, but not oxidize or make volatile organic ligands in the metal-containing coat. 7 . The method as recited in claim 6 , wherein the inert gas includes a gas from a group nitrogen, argon, and helium. 8 . The method as recited in claim 6 , further including pyrolyzing the metal-containing coat at a temperature that is between about 450 degrees Celsius and about 550 degrees Celsius. 9 . The method as recited in claim 6 , further including pyrolyzing the metal-containing coat for a pyrolyzing time interval that is between about five (5) minutes and about thirty (30) minutes. 10 . The method as recited in claim 6 , further including pyrolyzing the metal-containing coat at about 500 degrees Celsius for about five (5) minutes. 11 . The method as recited in claim 1 , wherein calcining includes placing the metal-containing oxide film in a furnace with oxygen-containing atmosphere to oxidize and remove interstitial zinc from the metal-containing oxide film. 12 . The method as recited in claim 11 , wherein the oxygen-containing atmosphere comprises oxygen at a concentration that twenty (20) percent or greater. 13 . The method as recited in claim 4 , wherein calcining includes placing the metal-containing oxide film in a furnace pre-heated to a calcining temperature of between about 650 degrees Celsius and about 750 degrees Celsius. 14 . The method as recited in claim 4 , wherein calcining includes placing the metal-containing oxide film in a furnace for a calcining time interval of between about ten (10) minutes and about thirty (30) minutes. 15 . The method as recited in claim 4 , wherein calcining includes placing the metal-containing oxide film in a furnace pre-heated to about 750 degree Celsius for about ten (10) minutes. 16 . The method as recited in claim 1 , further including annealing the metal-containing oxide film. 17 . The method as recited in claim 16 , wherein annealing includes placing the metal-containing oxide layer in a furnace with a static atmosphere. 18 . The method as recited in claim 16 , wherein annealing includes placing the metal-containing oxide layer in a furnace with a temperature between about 200 degrees Celsius and about 400 degrees Celsius for between about thirty (30) minutes and about four (4) hours. 19 . The method as recited in claim 1 , further including quenching the metal-containing oxide film. 20 . The method as recited in claim 1 , wherein the metal-containing solution includes an organometallic magnesium source, and organometallic zinc source, a solvent, and a stabilizer. 21 . The method as recited in claim 1 , wherein the metal-containing solution includes at least one of diethanolamine, toluene, zinc 2-ethylhexanoate, and magnesium 2-ethylhexanoate. 22 . The method as recited in claim 1 , wherein the metal-containing solution includes magnesium and zinc in a ratio range between about 0.5 to 0.5 and about 0.8 to 0.2. 23 . The method as recited in claim 1 , wherein the metal-containing solution includes magnesium and zinc in a ratio of about 0.72 to 0.28. 24 . A tri-functional chemical solution deposition additive comprising an amino alcohol. 25 . The tri-functional chemical solution deposition additive according to claim 24 , wherein the amino alcohol comprises one or more hydroxyl groups 26 . The tri-functional chemical solution deposition additive according to claim 24 , wherein the amino alcohol comprises a primary amine. 27 . The tri-functional chemical solution deposition additive according to claim 24 , wherein the amino alcohol comprises a secondary amine. 28 . The tri-functional chemical solution deposition additive according to claim 24 , wherein the amino alcohol comprises a tertiary amine. 29 . The tri-functional chemical solution deposition additive according to claim 25 , wherein the amino alcohol is monoethanolamine, diethanolamine, triethanolamine, hetpaminol, isoetarine, noepinephrine, propanolamine, shphingosine, or methanolamine. 30 . A method for stabilizing an organometallic precursor in a chemical solution deposition reaction comprising adding a tri-functional chemical solution deposition additive to a solution of organometallic precursor prior to deposition. 31 . The method for stabilizing an organometallic precursor in a chemical solution deposition reaction according to claim 30 , wherein the organometallic precursor is a metal 2-ethylhexanoate. 32 . The method for stabilizing an organometallic precursor in a chemical solution deposition reaction according to claim 31 , wherein metal 2-ethylhexanoate is magnesium 2-ethylhexanoate or zinc 2-ethylhexanoate. 33 . The method for stabilizing an organometallic precursor in a chemical solution deposition reaction according to claim 32 , wherein the tri-functional chemical solution deposition additive diethanolamine. 34 . The method for stabilizing an organometallic precursor in a chemical solution deposition reaction according to claim 31 , wherein the tri-functional chemical solution deposition additive is added to the organometallic precursor in a ratio of between 0.05 to 1 and 1 to 1 of additive to total weight of all metals in the solution. 35 . The method for stabilizing an organometallic precursor in a chemical solution deposition reaction according to claim 33 , wherein the tri-functional chemical solution deposition additive is added to the organometallic precursor in a 1 to 1 ratio. 36 . A method of increasing crystal growth in a chemical solution deposition reaction comprising adding a tri-functional chemical solution deposition additive to the organometallic precursor prior to deposition. 37 . The method of increasing crystal growth in a film formed
applied to measurement of ultraviolet light (using counting tubes G01T) · CPC title
performed under inert atmosphere · CPC title
Deposition of multilayers of inorganic material · CPC title
performed under reactive atmosphere, e.g. oxidising or reducing atmospheres · CPC title
Coating compositions, e.g. paints, varnishes or lacquers, based on inorganic substances · CPC title
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