WO1992000924A1 - Compositions de verre de tellurite - Google Patents
Compositions de verre de tellurite Download PDFInfo
- Publication number
- WO1992000924A1 WO1992000924A1 PCT/GB1991/001123 GB9101123W WO9200924A1 WO 1992000924 A1 WO1992000924 A1 WO 1992000924A1 GB 9101123 W GB9101123 W GB 9101123W WO 9200924 A1 WO9200924 A1 WO 9200924A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- low melting
- glass composition
- glass
- oxide
- composition
- 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.)
- Ceased
Links
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/02—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of inorganic substances
- H01B3/08—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of inorganic substances quartz; glass; glass wool; slag wool; vitreous enamels
- H01B3/085—Particles bound with glass
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C14/00—Glass compositions containing a non-glass component, e.g. compositions containing fibres, filaments, whiskers, platelets, or the like, dispersed in a glass matrix
- C03C14/004—Glass compositions containing a non-glass component, e.g. compositions containing fibres, filaments, whiskers, platelets, or the like, dispersed in a glass matrix the non-glass component being in the form of particles or flakes
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C3/00—Glass compositions
- C03C3/12—Silica-free oxide glass compositions
- C03C3/122—Silica-free oxide glass compositions containing oxides of As, Sb, Bi, Mo, W, V, Te as glass formers
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C8/00—Enamels; Glazes; Fusion seal compositions being frit compositions having non-frit additions
- C03C8/24—Fusion seal compositions being frit compositions having non-frit additions, i.e. for use as seals between dissimilar materials, e.g. glass and metal; Glass solders
-
- 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
- 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
- H01B1/14—Conductive material dispersed in non-conductive inorganic material
-
- 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
- H01B1/14—Conductive material dispersed in non-conductive inorganic material
- H01B1/16—Conductive material dispersed in non-conductive inorganic material the conductive material comprising metals or alloys
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/02—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of inorganic substances
- H01B3/08—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of inorganic substances quartz; glass; glass wool; slag wool; vitreous enamels
- H01B3/087—Chemical composition of glass
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L23/00—Details of semiconductor or other solid state devices
- H01L23/28—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection
- H01L23/29—Encapsulations, e.g. encapsulating layers, coatings, e.g. for protection characterised by the material, e.g. carbon
- H01L23/291—Oxides or nitrides or carbides, e.g. ceramics, glass
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L23/00—Details of semiconductor or other solid state devices
- H01L23/48—Arrangements for conducting electric current to or from the solid state body in operation, e.g. leads, terminal arrangements ; Selection of materials therefor
- H01L23/482—Arrangements for conducting electric current to or from the solid state body in operation, e.g. leads, terminal arrangements ; Selection of materials therefor consisting of lead-in layers inseparably applied to the semiconductor body (electrodes)
- H01L23/4827—Materials
- H01L23/4828—Conductive organic material or pastes, e.g. conductive adhesives, inks
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C2214/00—Nature of the non-vitreous component
- C03C2214/04—Particles; Flakes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
- H01L2924/0001—Technical content checked by a classifier
- H01L2924/0002—Not covered by any one of groups H01L24/00, H01L24/00 and H01L2224/00
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L2924/00—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
- H01L2924/095—Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00 with a principal constituent of the material being a combination of two or more materials provided in the groups H01L2924/013 - H01L2924/0715
- H01L2924/097—Glass-ceramics, e.g. devitrified glass
- H01L2924/09701—Low temperature co-fired ceramic [LTCC]
Definitions
- the present invention relates to novel glass compositions and, in particular, to novel low temperature glasses which are useful as sealing glasses or solder glasses, and in electronic paste formulations.
- solder glass or "sealing glass” is a term which is used to describe glasses which form an adhesive bond between two glasses, or between a combination of glass, metal, or a ceramic material. It is well known in the art that commercially available solder glasses capable of sealing ceramic and electrical component parts, such as television tube and semiconductor devices, are practical in the 400° to 500°C range. These solder glasses are generally based upon the lead oxide-boron oxide binary system. The lead oxide-boron oxide eutectic comprises 13% by weight of boron oxide and 87% by weight of lead oxide and represents the most fluid glass in that binary system. It is the starting point from which most commercial solder glasses have been derived. Whilst these glasses, with the addition of certain fillers, have been very successful, there is a need in the art for a solder glass which will seal at temperatures below the lower limit of the range of use for the lead oxide-boron oxide based glasses.
- a second useful feature of these glasses is their high thermal expansion which can be modified to be comparable with high expansion materials including copper, silver and aluminium.
- a solder glass In order for a glass to qualify as a solder glass it has to meet certain physical criteria. These criteria will depend to a great extent upon the properties of the materials which the solder glass is to unite. Thus, in general, a solder glass should possess the following characteristics: i) a low viscosity in the melting phase; ii) a thermal expansion which will match the thermal expansion of the workpiece; iii) a sealing temperature which is below the lowest annealing and strain points of the materials to which it is to be sealed, iv) good physical and chemical stability; and v) a good adhesion to the workpiece.
- W087/05006 describes a solder glass for low temperature applications which is based upon the addition of bismuth oxide, zinc oxide and phosphorus pentoxide to the lead oxide-vanadium oxide eutectic.
- US-A-3408212 describes the effect of adding large quantities of lead fluoride to lead oxide-vanadium oxide mixtures. A narrow glass forming region was found to exist in the centre of the lead oxide-lead fluoride-vanadium pentoxide ternary diagram, with improved glass life stability.
- US-A-3837866 describes the addition of arsenic oxides to both the lead oxide-vanadium pentoxide and caesium oxide-vanadium pentoxide eutectics to prevent early recrystallization. However, the addition of arsenic oxide tends to increase the viscosity of the resulting glasses.
- US-A-4186023 describes lead borate and lead zinc borate glasses containing from 0.1 to 10% by weight of cuprous oxide and a non-volatile metal fluoride, the mol ratio of cuprous oxide to the fluoride content of the metal fluoride being in the range of from 1:0.25 to 1:10.
- solder glass compositions some of which have dilatometric softening temperatures of below 350°C, which are capable of wetting and bonding to a wide range of glasses, metals and ceramics including typical electronic substrates such as alumina, metallised alumina and silicon, and which are not derived from the lead oxide-boron oxide eutectic or the lead oxide- vanadium pentoxide eutectic mixtures.
- the present invention provides a low melting glass composition which comprises in mol percent calculated on an oxide basis i) from 50 to 85% of Te0 2 , or an appropriate amount of a precursor for Te0 2 , ii) from 0.1 to 30% of an oxide of silver, or an appropriate amount of a precursor therefor, iii) from 5 to 30% of an oxide of lead and/or an oxide of zinc, or an appropriate amount of a precursor for the said oxide, and iv) optionally from 0.1 to 44.9% of one or more oxides of Mg, Ti, Ta, Mo, B, W, Tl, V, Li, Na, K, Rb, Cs, Ca, Sr, Zr, Hf, Si, Ge, Al, Ga, In, P, Sn, Sb, Bi, La or a rare earth metal, or an appropriate amount of a precursor for one or more of the chosen oxides, provided that when V is included in the composition it is present in an amount of less than 5 mol %, and the glass composition having a dilato
- the low melting glass composition of the present invention thus contain Te0 2 as the major component in an amount of from 50-85 mol %, preferably 60 to 80 mol %, more preferably 65-75 mol %.
- the low melting glass composition of the present invention may be a three oxide system, the first oxide comprising Te0 2 , with the second and third oxides comprising components (ii) and (iii) as defined above.
- the second oxide, component (ii) will generally be present in an amount of at least 1.0 mol %, preferably 10 to 25 mol %, whilst the third oxide, component (iii) will generally be present in an amount of from 10 to 20 mol %.
- the low melting glass composition may be a four or more component system, in which the additional components are as defined above for component (iv) .
- Component (iv) is preferably an oxide of Mo, W, Mg, Tl, B or V, most preferably M0O 3 or W0 3 .
- the preferred low melting glass compositions of the present invention have a dilatometric softening point, Ts, in the range of from 210 to 380°C, preferably 350°C or below and more preferably
- a composition having a thermal coefficient of expansion of greater than 190 x 10 -7 is preferred for sealing to high expansion.
- the low melting glass compositions of the present invention may additionally contain at least one solid halide of low volatility, such as lithium or sodium fluoride, in an amount of ⁇ 5% by weight.
- at least one solid halide of low volatility such as lithium or sodium fluoride
- a further and surprising attribute of many of the glasses of the present invention is their good water and chemical durability. It is the combination of this property with either or both the high expansion and low melting temperature that makes the glasses of this invention such good sealing/bonding materials.
- the various oxides used in the preparation of the compositions of the present invention are usually in the form of fine powders. Precursors of these oxides can also be useful, providing that they decompose to form the required oxides at a temperature below the melting temperature of the glass. Suitable precursors are the nitrites, nitrates, carbonates, metal organic salts, for example citrates, acetates, etc. and telluric acid.
- the invention also includes within its scope a mixture of the above-described glass compositions of the invention with from 1 to 50% by weight, based on the mixture, of an inert refractory filler material having a thermal coefficient of expansion below that of the glass composition.
- the filler should be insoluble or only slightly soluble in the glass composition.
- the filler material is preferably used in an amount of from 5 to 30% by weight, based on the mixture, but the amount will depend upon the thermal expansion of the substrate or parts which the composition is intended to join, and on the specific gravity of the materials, a larger amount of filler resulting in a greater decrease in the thermal coefficient of expansion of the composition.
- the filler materials are used in order to modify the thermal coefficient of expansion of the glass composition, without effecting significantly the bonding temperature, of the glass.
- the filler material may thus be added to the glass composition of the invention as a means of controlling the overall thermal expansion and contraction of the resulting solder glass mixture. Increased amounts of a low thermal expansion filler will correspondingly decrease the linear expansion of the glass composite.
- Suitable filler materials include amorphous Si0 2 , zircon, aluminium titanate, corderite, Nb ⁇ 5, a ⁇ 5 and lithium aluminium silicates e.g. jS-spodumene.
- the fillers are mixed with the glass composition in amounts in the range of from 1 to 50% by weight based on the mixture.
- the mixtures may be prepared, for example, by ball milling in a conventional manner to produce a finely divided, uniformly mixed material.
- the low melting glass compositions of the present invention optionally in admixture with a filler as described above, may be applied to the substrate surfaces which are to be bonded together either as a molten glass, or as a shaped preform, or the powdered glass may be admixed with an organic vehicle to form a glass paste which is used to coat the substrate.
- the substrate is then heated initially to a temperature at which the organic vehicle will "burn off” and then at a temperature sufficient to melt the glass and form the seal.
- the composite is heated to a temperature in the range of from 300° to 450°C to melt the glass and form the bond.
- the organic vehicle may be any synthetic organic solvent which preferably boils or decomposes at a temperature below the softening point of the glass composition.
- the glasses of this invention may also successfully be employed in passivating, dielectric, resistor, conducting, die attach or similar electronic paste formulations in which the glass acts wholely or in part as the adhesive bond.
- the invention includes within its scope the use of a filler to modify mechanical properties such as thermal expansion. It is also intended to provide, where appropriate, for the use of fillers to modify electrical properties such as conductivity, resistivity and dielectric constant by the inclusion of; high and low resistivity metals, semiconducting oxides, nitrides, borides and carbides and dielectrics such as barium titanate or other insulating oxide materials.
- a metal flake or powder filler such as silver, gold, copper, aluminium or a solder alloy may be admixed with the low melting glass composition of the present invention in an amount of from 25% to 95% by weight based on the total dry weight of the composition, preferably 60 to 95% by weight based on the total dry weight of the composition.
- the metal-glass mixture may be formulated into a paste by admixture with an organic vehicle.
- the organic vehicle will generally be used in an amount such that the total solids content of the metal-filled glass paste is in the range of from 70 to 90% solids.
- the metal-glass mixture is particularly suitable for electronic applications, such as "thick film" conducting pastes and die attach applications in bonding semiconductor devices to a ceramic substrate, such as alumina.
- solder glasses and pastes of the present invention may be coated onto metal-glass or ceramic substrates at any chosen thickness but usually at thicknesses in the range of from about 0.5 to 500 micrometres.
- the paste will generally be applied to the substrate surface in a conventional manner, for example by brush coating, screen printing, stencilling or stamping.
- the paste is typically syringe dispensed.
- the die is attached by placing it in the centre of the wet paste and setting it by the application of pressure so that the paste flows up the side of the die and leaves a thin film beneath the die.
- the structure is then heat treated to "burn off" the organic vehicle and the temperature then raised to melt the low melting glass composition.
- a range of three oxide tellurite based glasses were made of the composition Te0 2 :X:Y, investigating the tellurite rich glass region.
- the compositions which were made are given, in mol %, as points 1 to 6 on Figure 1 of the accompanying drawings which is a phase diagram of the compositions.
- the oxides X and Y which were incorporated into the tellurite glass systems were selected from the following:
- composition TXY1 85:7.5:7.5 mol %
- composition TXY2 80:15:5 mol %
- composition TXY3 ⁇ * ⁇ 80:5:15 mol %
- a four oxide tellurite based glass was made from the following components by fusing at a temperature of 775°C for 10 minutes in a platinum crucible:
- Two four oxide tellurite based glasses were made from the following components by fusing at a temperature of 775°C for 10 minutes in a platinum crucible:
- a tellurite glass was selected to fuse to an Al/Mg alloy.
- the glass selected for bonding purposes had a slightly lower TCE value than that of the metal to be bonded so that the glass was put into compression on sealing.
- the glass was ground to sub 38 micrometre particle size, suspended in heptane and spread thinly and evenly onto the flat metal surface.
- Another piece of metal was placed over the top of the glass to create a "sandwich" which was heated to 300° to 450°C to bond the two metal pieces together. A manual inspection indicated that a good bond had been obtained.
- Table 4 The results are given in Table 4 below:
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Inorganic Chemistry (AREA)
- Materials Engineering (AREA)
- Geochemistry & Mineralogy (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Physics & Mathematics (AREA)
- Ceramic Engineering (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Glass Compositions (AREA)
Abstract
Une composition de verre à bas point de fusion contient un pourcentage molaire de TeO2 compris entre 50 to 85 %, un pourcentage molaire d'oxyde d'argent compris entre 0,1 et 30 %, un pourcentage molaire d'un oxyde de plomb et/ou de zinc compris entre 5 et 30 %, et éventuellement jusqu'à 44,9 % d'un ou plusieurs autre(s) oxyde(s), la composition de verre présentant une température de ramollissement dilatométrique typique (Ts), de 380 °C au moins.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB909015072A GB9015072D0 (en) | 1990-07-09 | 1990-07-09 | Glass composition |
| GB9015072.3 | 1990-07-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO1992000924A1 true WO1992000924A1 (fr) | 1992-01-23 |
Family
ID=10678825
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/GB1991/001124 Ceased WO1992000925A1 (fr) | 1990-07-09 | 1991-07-09 | Compositions de verre |
| PCT/GB1991/001123 Ceased WO1992000924A1 (fr) | 1990-07-09 | 1991-07-09 | Compositions de verre de tellurite |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/GB1991/001124 Ceased WO1992000925A1 (fr) | 1990-07-09 | 1991-07-09 | Compositions de verre |
Country Status (2)
| Country | Link |
|---|---|
| GB (1) | GB9015072D0 (fr) |
| WO (2) | WO1992000925A1 (fr) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2378700A (en) * | 2001-08-15 | 2003-02-19 | Agilent Technologies Inc | Tellurite glass |
| EP1617721A4 (fr) * | 2003-04-14 | 2012-04-18 | Bromine Compounds Ltd | Formulations biocides solides |
| WO2012129554A3 (fr) * | 2011-03-24 | 2013-02-28 | E. I. Du Pont De Nemours And Company | Composition de pâte conductrice et dispositifs à semi-conducteurs réalisés avec celle-ci |
| CN102971268A (zh) * | 2010-05-04 | 2013-03-13 | E·I·内穆尔杜邦公司 | 包含铅-碲-锂-氧化物的厚膜浆料以及它们在半导体装置制造中的用途 |
| CN103730538A (zh) * | 2009-10-28 | 2014-04-16 | 昭荣化学工业株式会社 | 用于形成太阳能电池电极的导电膏 |
| DE102013226636A1 (de) * | 2013-12-19 | 2015-06-25 | Friedrich-Schiller-Universität Jena | Glaszusammensetzung, Bauelement und Verfahren zur Herstellung eines Bauelements |
| US10084100B2 (en) | 2010-10-07 | 2018-09-25 | Shoei Chemical Inc. | Solar cell element and method for manufacturing same |
| US10658528B2 (en) | 2017-04-18 | 2020-05-19 | Dupont Electronics, Inc. | Conductive paste composition and semiconductor devices made therewith |
| CN112174522A (zh) * | 2014-08-29 | 2021-01-05 | 日立化成株式会社 | 无铅低熔点玻璃组合物以及使用组合物的玻璃材料和元件 |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0718249A1 (fr) * | 1994-11-29 | 1996-06-26 | Ube Industries, Ltd. | Matériau composite à matrice vitreuse ayant une résistance et une tenacité élevée, poudre composite vitreuse, et procédés pour leur production |
| US6344425B1 (en) * | 1999-11-19 | 2002-02-05 | Corning Incorporated | Fluorotellurite, amplifier glasses |
| US20130049148A1 (en) * | 2011-02-22 | 2013-02-28 | E I Du Pont De Nemours And Company | Conductive paste composition and semiconductor devices made therewith |
| US8512463B2 (en) | 2011-04-05 | 2013-08-20 | E I Du Pont De Nemours And Company | Thick film paste containing bismuth-tellurium-oxide and its use in the manufacture of semiconductor devices |
| US20130186463A1 (en) * | 2011-12-06 | 2013-07-25 | E I Du Pont De Nemours And Company | Conductive silver paste for a metal-wrap-through silicon solar cell |
| EP2654086B1 (fr) * | 2012-04-17 | 2018-10-03 | Heraeus Precious Metals North America Conshohocken LLC | Pâte pour film épais conducteur pour contacts de cellule solaire |
| BR102013009339A2 (pt) * | 2012-04-17 | 2015-06-30 | Heraeus Precious Metals North America Conshohocken Llc | Sistema de reação inorgânica, composição de pasta eletrocondutora, célula solar |
| US8845932B2 (en) | 2012-04-26 | 2014-09-30 | E I Du Pont De Nemours And Company | Thick film paste containing bismuth-tellurium-oxide and its use in the manufacture of semiconductor devices |
| US9087937B2 (en) * | 2012-05-10 | 2015-07-21 | E I Du Pont De Nemours And Company | Glass composition and its use in conductive silver paste |
| WO2014045900A1 (fr) * | 2012-09-18 | 2014-03-27 | 株式会社村田製作所 | Pâte conductrice et cellule solaire |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61242927A (ja) * | 1985-04-20 | 1986-10-29 | Agency Of Ind Science & Technol | 感湿性ガラス粉末焼結体の製造方法 |
| JPS6236040A (ja) * | 1985-08-08 | 1987-02-17 | Iwaki Glass Kk | 低融点封着用硝子 |
| US4652536A (en) * | 1985-06-28 | 1987-03-24 | Hoya Corporation | Tellurite glass |
| WO1987005006A1 (fr) * | 1986-02-19 | 1987-08-27 | Dumesnil Maurice E | COMPOSITION VITREUSE A FAIBLE POINT DE FUSION CONTENANT DU PbO ET DU V2O5 |
| US4945071A (en) * | 1989-04-19 | 1990-07-31 | National Starch And Chemical Investment Holding Company | Low softening point metallic oxide glasses suitable for use in electronic applications |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3423326A (en) * | 1967-02-20 | 1969-01-21 | Kennecott Copper Corp | Zinc tellurite glasses |
| SU552311A1 (ru) * | 1974-12-30 | 1977-03-30 | Предприятие П/Я Р-6681 | Стекло |
-
1990
- 1990-07-09 GB GB909015072A patent/GB9015072D0/en active Pending
-
1991
- 1991-07-09 WO PCT/GB1991/001124 patent/WO1992000925A1/fr not_active Ceased
- 1991-07-09 WO PCT/GB1991/001123 patent/WO1992000924A1/fr not_active Ceased
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61242927A (ja) * | 1985-04-20 | 1986-10-29 | Agency Of Ind Science & Technol | 感湿性ガラス粉末焼結体の製造方法 |
| US4652536A (en) * | 1985-06-28 | 1987-03-24 | Hoya Corporation | Tellurite glass |
| JPS6236040A (ja) * | 1985-08-08 | 1987-02-17 | Iwaki Glass Kk | 低融点封着用硝子 |
| WO1987005006A1 (fr) * | 1986-02-19 | 1987-08-27 | Dumesnil Maurice E | COMPOSITION VITREUSE A FAIBLE POINT DE FUSION CONTENANT DU PbO ET DU V2O5 |
| US4945071A (en) * | 1989-04-19 | 1990-07-31 | National Starch And Chemical Investment Holding Company | Low softening point metallic oxide glasses suitable for use in electronic applications |
Non-Patent Citations (3)
| Title |
|---|
| CHEMICAL ABSTRACTS, vol. 106, no. 18, May 1987, Columbus, Ohio, US; abstract no. 142782N, page 285 ; see abstract & JP,A,61 242 927 (AGENCY OF INDUSTRIAL SCIENCE AND TECHNOLOGY) October 29, 1986 * |
| CHEMICAL ABSTRACTS, vol. 107, no. 16, October 1987, Columbus, Ohio, US; abstract no. 139474D, page 331 ; see abstract & JP,A,62 036 040 (IWASHIRO GLASS K.K.) February 17, 1987 * |
| CHEMICAL ABSTRACTS, vol. 93, no. 6, August 11, 1980, Columbus, Ohio, US; abstract no. 52442K, page 366 ; see abstract & STROIT. MATER. SILIK. PROM-ST. vol. 21, no. 1, 1980, BULG. pages 22 - 25; * |
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Also Published As
| Publication number | Publication date |
|---|---|
| GB9015072D0 (en) | 1990-08-29 |
| WO1992000925A1 (fr) | 1992-01-23 |
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