US3611073A - Diode comprising zinc oxide doped with gallium oxide used as a voltage variable resistor - Google Patents

Diode comprising zinc oxide doped with gallium oxide used as a voltage variable resistor Download PDF

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Publication number
US3611073A
US3611073A US880759A US3611073DA US3611073A US 3611073 A US3611073 A US 3611073A US 880759 A US880759 A US 880759A US 3611073D A US3611073D A US 3611073DA US 3611073 A US3611073 A US 3611073A
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United States
Prior art keywords
percent
silver
oxide
voltage variable
variable resistor
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Expired - Lifetime
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US880759A
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English (en)
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Kazuo Hamamoto
Michio Matsuoka
Takeshi Masuyama
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Panasonic Holdings Corp
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Matsushita Electric Industrial Co Ltd
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    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/06—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
    • H01B1/08—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances oxides
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01C—RESISTORS
    • H01C17/00—Apparatus or processes specially adapted for manufacturing resistors
    • H01C17/28—Apparatus or processes specially adapted for manufacturing resistors adapted for applying terminals
    • H01C17/281—Apparatus or processes specially adapted for manufacturing resistors adapted for applying terminals by thick film techniques
    • H01C17/283—Precursor compositions therefor, e.g. pastes, inks, glass frits
    • H01C17/285—Precursor compositions therefor, e.g. pastes, inks, glass frits applied to zinc or cadmium oxide resistors
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01C—RESISTORS
    • H01C7/00—Non-adjustable resistors formed as one or more layers or coatings; Non-adjustable resistors made from powdered conducting material or powdered semi-conducting material with or without insulating material
    • H01C7/10—Non-adjustable resistors formed as one or more layers or coatings; Non-adjustable resistors made from powdered conducting material or powdered semi-conducting material with or without insulating material voltage responsive, i.e. varistors
    • H01C7/105—Varistor cores
    • H01C7/108—Metal oxide
    • H01C7/112—ZnO type

Definitions

  • At least one of said two electrodes being a silver paint electrode.
  • This invention relates to voltage variable resistors having nonohmic resistance and more particularly relates to varistors comprising zinc oxide and having silver electrodes applied thereto.
  • n a numerical value greater than 1. The value of n is calculated by the following equation:
  • V,and V are the voltages at given currents I and 1 respectively.
  • I, and I are 2 are 10 ma. and 100 ma; respectively.
  • the desired value of C depends upon the use to which the resistor is to be put. It is ordinarily desired that the value of n be as large as possible since this exponent determines the degree to which the resistors depart from ohmic characteristics.
  • Silicon carbide varistors are most widely used as voltage variable resistors and are manufactured by mixing fine particles of silicon carbide with water, a ceramic binder and/or conductive material such a graphite or metal powder, pressing the mixture in a mold to the desired shape, and then drying and firing the pressed body in air or a nonoxidizing atmosphere.
  • Silicon carbide varistors with conductive materials are characterized by a low electric resistance, Le. a low valve of C and a low value of n whereas silicon carbide varistors without conductive materials have a high electric resistance, Le. a high value of C and a high value of n. It has been difficult to manufacture silicon carbide varistors characterized by a high n and a low C.
  • silicon carbide varistors with graphite have been known to exhibit n-valves from 2.5 to 3.3 and C-values from 6 to 13 at a given current of 100 ma. and silicon carbide varistors without graphite shown n-values from 4 to 7 and C-values from 30 to 800 at a given current of 1 ma. with respect for a given size of varistor, e.g. 30 mm. in diameter and 1 mm. in thickness.
  • Conventional rectifiers comprising selenium or cuprous oxide have an n-value of to 10 and a C-valve less than 2 at a given current of mo ma. with respect for a rectifier size of 20 mm. in diameter. In this case, the thickness of the rectifier does not effect the C-value.
  • a germanium or silicon PN junction resistor has an extremely high value of n but its C-value is constant, e.g. on the order of 0.3 or 0.7 at a given current of I00 ma. because its diffusion voltage in the V-l characteristic is constant and cannot be changed greatly. It is necessary for obtaining a desirable C-value to combine several diodes in series and/or in parallel. Another disadvantage of such diodes is the complicated steps involved in their manufacture, with resultant high cost. As a practical matter, the use of diode resistors is not widespread at the present because of their high cost even though they may have a high value of n.
  • An object of this invention is to provide a voltage variable resistor having a high value of n and a low value of C.
  • a further object of this invention is to provide a voltage variable resistor capable of being made by a simple manufacturing method at a low cost.
  • a further object of this invention is to provide a voltage variable resistor characterized by a high stability with respect to temperature, humidity and electric load.
  • Another object of this invention is to provide a voltage variable resistor, the C-value of which can be controlled.
  • reference character 10 designates, as a whole, a voltage variable resistor having, as its active element, a sintered wafer l of electrically conductive ceramic material according to the present invention.
  • Sintered wafer l is prepared in a manner hereinafter set forth, and is provided with a pair of electrodes 2 and 3 having specified compositions and applied in a suitable manner hereinafter set forth, on two opposite surfaces of the wafer.
  • the wafer l is a sintered plate having any one of various shapes such as circular square, rectangular, etc.
  • Wire leads 5 and 6 are attached in conductive relationship to the electrodes 2 and 3, respectively, by a connection means 4 (solder or the like).
  • sintered wafer 1 consists essentially of zinc oxide (ZnO) and a minor portion of an additive of gallium oxide (6320 It is preferable that said sintered wafer have further a minor proportion of an additive of bismuth oxide (Bi O It has been discovered according to the invention that said sintered body 1 has electrical characteristics of superior nonlinearity when it is provided with silver electrodes prepared by applying silver paint to at least one of the opposite surfaces thereof and firing at 300 C. to 900 C. in an oxidizing atmosphere such as air or oxygen. The n-valve and C-value of voltage variable resistors produced in this manner vary with the compositions of the sintered body and the electrodes, and the method of their preparation.
  • the nonlinearity of the novel resistors is attributed to the nonohmic contact between said sintered body 1 and electrodes 2 and 3, it is necessary for obtaining a desirable C-value and n-value to control the compositions of the sintered body I and the electrodes 2 and 3.
  • the control of the C-value and the n-value can also be obtained by applying an ohmic electrode as the electrode 3 in place of the silver electrode.
  • the sintered body have an electrical resistivity less than 10 ohm-cm., said electrical resistivity being measured by a four point method in a per se conventional way.
  • a voltage variable resistor with low C and high n can be obtained when said resistor comprises a sintered wafer consisting essentially of to 99.95 mole percent of zinc oxide (ZnO) and 0.05 to l0.0 mole percent of gallium oxide 03.0, and two electrodes are applied to opposite surfaces of said sintered wafer, at least one of said two electrodes being a silver paint electrode.
  • ZnO zinc oxide
  • gallium oxide 03.0 two electrodes are applied to opposite surfaces of said sintered wafer, at least one of said two electrodes being a silver paint electrode.
  • the C-value is further lowered when one of said electrodes applied to said sintered wafer is a silver paint electrode and the other is an ohmic electrode
  • the n-value is further elevated when said sintered wafer is 99.9 to 97.0 mole percent of zinc oxide (ZnO) and 0.1 to 3.0 mole percent of gallium oxide.
  • the combination of a lower C and a higher n can be obtained when said sintered wafer is 99.9 to 82.0 mole percent of zinc oxide (ZnO), 0.05 to 10.0 mole percent of gallium oxide (Ga,0,) and gallium to 8.0 mole percent of bismuth oxide (Bi 0
  • ZnO zinc oxide
  • Ga,0, gallium oxide
  • Bi 0 gallium to 8.0 mole percent of bismuth oxide
  • the stability during an electric load life test and at ambient temperature is improved when said silver electrode or electrodes has a composition of 70 to 99.5 wt. percent of silver 0.3 to 27 wt. percent of lead oxide (PbO), 0.1 to 15 wt. percent of silicon dioxide (SiO and 0.05 to 15 wt.
  • B 0 percent of boron trioxide
  • the stability during electric load life test and at ambient temperature is also improved when said silver electrode or electrodes have a composition of 70 to 99.5 wt. percent of silver, 0.3 to 27 wt. percent of bismuth oxide (Bi O 0.3 to 15 wt. percent of silicon dioxide (SiO and 0.05 to l5 wt. percent of boron trioxide (B lt has been discovered according to the invention that the n-value and the stability during an electric load life test and at ambient temperature of the resistors are greatly improved when said silver electrodes have a composition of 70 to 99.5 wt. percent silver, 0.3 to 27 wt. percent of bismuth oxide (Bi- 0 0.03 to 15 wt.
  • silicon dioxide SiO 0.05 to 15 wt. percent of boron trioxide (B 0 and 0.05 to 6 wt. percent of at lest one member selected from the group of consisting of cobalt oxide (C00) and of manganese oxide (MnO).
  • n-value and the stability during an electric load life test and at ambient temperature are further improved when said silver electrodes have a composition of 70 to 99.5 wt. percent of silver, 0.3 to 27 wt. percent of lead oxide (PbO), 0.1 to 15 wt. percent of silicon dioxide (SiO 0.05 to 15 wt. percent of boron trioxide (B 0 and 0.05 to 6 wt. percent of at least one member selected from the group of consisting'of cobalt oxide (C00) and manganese oxide (MnO).
  • PbO lead oxide
  • SiO 0.05 to 15 wt. percent of silicon dioxide SiO 0.05 to 15 wt. percent of boron trioxide
  • the sintered body 1 can be prepared by a per se well-known ceramic technique.
  • the starting materials in the compositions described in the foregoing description are mixed in a wet mill so as to produce a homogeneous mixtures.
  • the mixtures are dried and pressed in a mold into desired shapes at a pressure from 100 kg./cm. to 1000 kg./cm
  • the pressed bodies are sintered in air at l l00to l450 C. for l to 3 hours, and then furnace-cooled to room temperature (about lto about 30 C.
  • the pressed bodies are preferably sintered in a nonoxidizing atmosphere such as nitrogen and argon when it is desired to reduce the electrical resistivity.
  • the electrical resistivity also can be reduced by air-quenching from the sintering temperature to room temperature even when the pressed bodies are fired in air.
  • the mixtures may be preliminarily calcined at 600to 1000 C. and pulverized for easy fabrication in the subsequent pressing step.
  • the mixture to be pressed can be admixed with a suitable binder such as water, polyvinyl alcohol, etc.
  • the sintered body have the opposite surfaces lapped with an abrasive powder such as silicon carbide having a particle size of 300 mesh to lSOO mesh.
  • the sintered bodies are coated on one or both surfaces thereof by a silver electrode paint in a per se conventional manner such as by a spray method, screen printing method or brushing method.
  • Solid ingredients having compositions described in the foregoing description can be prepared in a per se conventional manner by mixing commercially available powders with organic resin such as epoxy, vinyl and phenol resin in an organic solvent such as butyl acetate, toluene or the like so as to produce silver electrode paints.
  • the silver powder can be in the form of metallic silver, or in the form of silver carbonate or silver oxide, or in any other form which in firing at the temperatures employed will be converted to metallic silver. Therefore, the term silver" as used throughout this specification and the claims appended hereto in connection with the silver composition before it is fired, is meant to include silver in any form which on firing will be converted to metallic silver.
  • the viscosity of the resultant silver electrode paints can be controlled by the amounts of resin and solvent. Particle size of solid ingredients also are required to be controlled so as to be in the range of 0. l p. to 5,u..
  • the sintered bodies with a silver electrode on only one surface thereof have applied to another surfaces an ohmic electrode in a manner such as by a spray method using Al, Zn and Sn, a vacuum evaporation method using Al. In on Zn and an electrolytic or electroless method using Ni, Cu and Sn.
  • Lead wires can be applied to the silver electrodes in a per se conventional manner byusing conventional solder having a low melting point. It is convenient to employ a conductive adhesive comprising silver powder and resin in an organic solvent for connecting the lead wires to the silver electrodes.
  • Voltage variable resistors according to this invention have a high stability with respect to temperature and in a load life test, which is carried out at 70 C. at a rating powder for 500 hours.
  • the n-value and C-value do not change greatly after heating cycles and the load life test.
  • the method of curing the applied silver electrode paint has a great effect on the n-value of the nonlinear resistors.
  • the n-value will not be optimal when the applied silver electrode paint is heated in a nonoxidizing atmosphere such as nitrogen and hydrogen for curing. It is necessary for obtaining a high nvalue that the applied silver electrode paint be cured by heating in an oxidizing atmosphere such as air or oxygen.
  • Silver electrodes prepared by any other method than by silver painting result in poor n-value.
  • the voltage variable resistor is not produced when the sintered body is provided with silver electrodes on the opposite surfaces by .electroless plating or electrolytic plating in a conventional manner.
  • Silver electrodes prepared by vacuum evaporation or chemical deposition result in an n-value less than 3.
  • Example 1 and then quenched to room temperature (about 15 to about 30 C.).
  • the sintered disc has the opposite surfaces thereof 'lapping using silicon carbide having a particle size of 600 mesh.
  • the thus produced sintered disc is 10 mm. in diameter and 1.5 mm. in thickness.
  • the sintered disc is coatedon the" opposite surfaces thereof with a silver electrode paint by a conventional brushing method.
  • the silver electrode paint employed is composed of solid ingredient according to table 25 and is prepared by mixing with vinyl resin in amyl acetate.
  • the coated disc is fired at the temperature listed in table 2 for 30- minutes in air. 3
  • Lead wires are attached to the silver electrodes by means of; silver paint.
  • the electric characteristics of the resultant resistor and of other similarly prepared resistors are shown in table 1.
  • the zinc oxide sintered body having gallium oxide therein in has a low C value and a high N-value and combined additions of gallium oxide and bismuth oxide will produce a higher n-value.
  • Silver paint B G530 B1103 ZnO (mol (mol (mol 0 (at C (at percent) percent) percent) ma.) n 100 mu.) n
  • the silver pie 1 is paints are composed at ingredient as shown in table 4 and are the same silver electrode prepared by mixing 100 weight parts of said solid ingredient y a conventional brushing compositions with l to 20 weight parts of epoxy resin in 20 to the temperature listed on 40 weight parts of butyl alcohol.
  • the resultant resistors exhibit s in air
  • the fired disc is provided on desirable C-values and n-values as indicated in table 4.
  • the coated disc is fired at table 2 for minute another surface thereof with an oh with aluminum or evapora silver paint.
  • the electric characteristics of the thu one of said electrodes is a silver paint electrode and' the other is an ohmic electrode.
  • a voltage variable resistor according to claim 1 wherem said sintered wafer consists essentially of 99.9 to 97.0 mole percent of zinc oxide (ZnO) and 0.1 to 3.0 mole percent of gallium oxide (Ga O 4.
  • a voltage variable resistor according to claim I wherein said sintered wafer consists essentially of 99.8 to 94.0 mole percent of zinc oxide (ZnO), 0.l T 3.0 mole percent of gallium oxide (Ga-,0 and 0.1 T0 3.0 mole percent of bismuth oxide (BigOa).
  • a voltage variable resistor according to claim 1 wherein said silver electrode has a composition comprising 70 to 99.5 wt. percent of silver, 0.3 to 27 wt. percent of load oxide (P- bO), 0.1 to 15 wt. percent of silicon dioxide (SiO and 0.05 to 15 wt. percent of boron trioxide (B 0 6.
  • a voltage variable resistor according to claim 1, wherein said silver electrode has a composition comprising 70 to 99.5 wt. percent of silver, 0.3 to 27 wt. percent of bismuth oxide (Bi- 0 0.03 to 15 wt. percent of silicon dioxide (SiO 0.05 to 15 wt. percent of boron trioxide (B 0 and 0.05 to 6.0 wt. percent of at least one member selected from the group consisting of cobalt oxide (C00) and manganese oxide (MnO).
  • bismuth oxide Bi- 0 0.03 to 15 wt. percent of silicon dioxide
  • SiO 0.05 to 15 wt. percent of boron trioxide B 0 and 0.05 to 6.0 wt. percent of at least one member selected from the group consisting of cobalt oxide (C00) and manganese oxide (MnO).

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  • Engineering & Computer Science (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Manufacturing & Machinery (AREA)
  • Physics & Mathematics (AREA)
  • Electromagnetism (AREA)
  • Thermistors And Varistors (AREA)
US880759A 1968-12-02 1969-11-28 Diode comprising zinc oxide doped with gallium oxide used as a voltage variable resistor Expired - Lifetime US3611073A (en)

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JP43088826A JPS4814351B1 (nl) 1968-12-02 1968-12-02

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US (1) US3611073A (nl)
JP (1) JPS4814351B1 (nl)
DE (1) DE1961679C3 (nl)
FR (1) FR2025000A1 (nl)
GB (1) GB1291471A (nl)
NL (1) NL144419B (nl)

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3689863A (en) * 1969-12-08 1972-09-05 Matsushita Electric Ind Co Ltd Voltage dependent resistors in a surface barrier type
US3711794A (en) * 1971-10-21 1973-01-16 Gen Electric Surge suppression transmission means
US3719933A (en) * 1970-04-02 1973-03-06 Matsushita Electric Ind Co Ltd Memory device having lead dioxide particles therein
US3754200A (en) * 1971-10-13 1973-08-21 Gen Electric Metal oxide varistor with selectively positionable intermediate electrode
US3818411A (en) * 1971-10-13 1974-06-18 Gen Electric Metal oxide varistor with selectively positionable intermediate electrode
US3838378A (en) * 1972-07-26 1974-09-24 Matsushita Electric Ind Co Ltd Voltage-nonlinear resistors
US3863111A (en) * 1973-06-29 1975-01-28 Gen Electric Polycrystalline varistor surge protective device for high frequency applications
US3999159A (en) * 1974-04-05 1976-12-21 Matsushita Electric Industrial Co., Ltd. Voltage-dependent resistor
US4316171A (en) * 1979-02-09 1982-02-16 Tdk Electronics Co., Ltd. Non-linear resistance elements and method for manufacturing same
EP0070468A2 (en) * 1981-07-16 1983-01-26 Kabushiki Kaisha Toshiba Metal Oxide varistor
US4383237A (en) * 1980-05-07 1983-05-10 Matsushita Electric Industrial Co., Ltd. Voltage-dependent resistor
US4400683A (en) * 1981-09-18 1983-08-23 Matsushita Electric Industrial Co., Ltd. Voltage-dependent resistor
US20150158737A1 (en) * 2012-06-05 2015-06-11 Korea Institute Of Ceramic Engineering And Technology Production method for zinc oxide having improved power factor due to increased gallium doping

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2749489A (en) * 1950-12-04 1956-06-05 Int Standard Electric Corp Dry contact rectifiers
US2940941A (en) * 1953-05-26 1960-06-14 R daltqn
US3033907A (en) * 1957-05-20 1962-05-08 Erie Resistor Corp Substitution type tio2 semi-conductors
US3299332A (en) * 1961-07-10 1967-01-17 Murata Manufacturing Co Semiconductive capacitor and the method of manufacturing the same
US3481874A (en) * 1965-10-19 1969-12-02 Nippon Electric Co Piezoelectric ceramic composition
US3503029A (en) * 1968-04-19 1970-03-24 Matsushita Electric Ind Co Ltd Non-linear resistor
US3505574A (en) * 1966-07-08 1970-04-07 Globe Union Inc Ceramic composition for barrier layer capacitors
US3529218A (en) * 1967-07-28 1970-09-15 Matsushita Electric Ind Co Ltd Ceramic rectifier and a method for preparing the same

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2749489A (en) * 1950-12-04 1956-06-05 Int Standard Electric Corp Dry contact rectifiers
US2940941A (en) * 1953-05-26 1960-06-14 R daltqn
US3033907A (en) * 1957-05-20 1962-05-08 Erie Resistor Corp Substitution type tio2 semi-conductors
US3299332A (en) * 1961-07-10 1967-01-17 Murata Manufacturing Co Semiconductive capacitor and the method of manufacturing the same
US3481874A (en) * 1965-10-19 1969-12-02 Nippon Electric Co Piezoelectric ceramic composition
US3505574A (en) * 1966-07-08 1970-04-07 Globe Union Inc Ceramic composition for barrier layer capacitors
US3529218A (en) * 1967-07-28 1970-09-15 Matsushita Electric Ind Co Ltd Ceramic rectifier and a method for preparing the same
US3503029A (en) * 1968-04-19 1970-03-24 Matsushita Electric Ind Co Ltd Non-linear resistor

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3689863A (en) * 1969-12-08 1972-09-05 Matsushita Electric Ind Co Ltd Voltage dependent resistors in a surface barrier type
US3719933A (en) * 1970-04-02 1973-03-06 Matsushita Electric Ind Co Ltd Memory device having lead dioxide particles therein
US3754200A (en) * 1971-10-13 1973-08-21 Gen Electric Metal oxide varistor with selectively positionable intermediate electrode
US3818411A (en) * 1971-10-13 1974-06-18 Gen Electric Metal oxide varistor with selectively positionable intermediate electrode
US3711794A (en) * 1971-10-21 1973-01-16 Gen Electric Surge suppression transmission means
US3838378A (en) * 1972-07-26 1974-09-24 Matsushita Electric Ind Co Ltd Voltage-nonlinear resistors
US3863111A (en) * 1973-06-29 1975-01-28 Gen Electric Polycrystalline varistor surge protective device for high frequency applications
US3999159A (en) * 1974-04-05 1976-12-21 Matsushita Electric Industrial Co., Ltd. Voltage-dependent resistor
US4316171A (en) * 1979-02-09 1982-02-16 Tdk Electronics Co., Ltd. Non-linear resistance elements and method for manufacturing same
US4383237A (en) * 1980-05-07 1983-05-10 Matsushita Electric Industrial Co., Ltd. Voltage-dependent resistor
EP0070468A2 (en) * 1981-07-16 1983-01-26 Kabushiki Kaisha Toshiba Metal Oxide varistor
EP0070468A3 (en) * 1981-07-16 1983-08-24 Kabushiki Kaisha Toshiba Metal oxide varistor
US4516105A (en) * 1981-07-16 1985-05-07 Tokyo Shibaura Denki Kabushiki Kaisha Metal oxide varistor with non-diffusable electrodes
US4400683A (en) * 1981-09-18 1983-08-23 Matsushita Electric Industrial Co., Ltd. Voltage-dependent resistor
US20150158737A1 (en) * 2012-06-05 2015-06-11 Korea Institute Of Ceramic Engineering And Technology Production method for zinc oxide having improved power factor due to increased gallium doping

Also Published As

Publication number Publication date
JPS4814351B1 (nl) 1973-05-07
FR2025000A1 (nl) 1970-09-04
DE1961679C3 (de) 1979-05-10
GB1291471A (en) 1972-10-04
DE1961679A1 (de) 1970-07-09
DE1961679B2 (de) 1978-08-31
NL144419B (nl) 1974-12-16
NL6918098A (nl) 1970-06-04

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