US2468527A - Blocking-layer cell - Google Patents
Blocking-layer cell Download PDFInfo
- Publication number
- US2468527A US2468527A US661022A US66102246A US2468527A US 2468527 A US2468527 A US 2468527A US 661022 A US661022 A US 661022A US 66102246 A US66102246 A US 66102246A US 2468527 A US2468527 A US 2468527A
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- United States
- Prior art keywords
- selenium
- layer
- blocking
- blocking layer
- cell
- Prior art date
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- Expired - Lifetime
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- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 52
- 229910052711 selenium Inorganic materials 0.000 description 52
- 239000011669 selenium Substances 0.000 description 52
- 230000000903 blocking effect Effects 0.000 description 40
- 239000007788 liquid Substances 0.000 description 11
- 238000000034 method Methods 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 8
- 230000001376 precipitating effect Effects 0.000 description 7
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 230000004048 modification Effects 0.000 description 6
- 238000012986 modification Methods 0.000 description 6
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 4
- 239000000956 alloy Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- 238000010849 ion bombardment Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000009834 vaporization Methods 0.000 description 3
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- 238000004544 sputter deposition Methods 0.000 description 2
- FRWYFWZENXDZMU-UHFFFAOYSA-N 2-iodoquinoline Chemical compound C1=CC=CC2=NC(I)=CC=C21 FRWYFWZENXDZMU-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- LTPBRCUWZOMYOC-UHFFFAOYSA-N beryllium oxide Inorganic materials O=[Be] LTPBRCUWZOMYOC-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000001427 coherent effect Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002068 genetic effect Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/06—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising selenium or tellurium in uncombined form other than as impurities in semiconductor bodies of other materials
- H01L21/10—Preliminary treatment of the selenium or tellurium, its application to the foundation plate, or the subsequent treatment of the combination
- H01L21/105—Treatment of the surface of the selenium or tellurium layer after having been made conductive
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02365—Forming inorganic semiconducting materials on a substrate
- H01L21/02367—Substrates
- H01L21/0237—Materials
- H01L21/02425—Conductive materials, e.g. metallic silicides
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02365—Forming inorganic semiconducting materials on a substrate
- H01L21/02436—Intermediate layers between substrates and deposited layers
- H01L21/02439—Materials
- H01L21/02441—Group 14 semiconducting materials
- H01L21/02444—Carbon, e.g. diamond-like carbon
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02365—Forming inorganic semiconducting materials on a substrate
- H01L21/02518—Deposited layers
- H01L21/02521—Materials
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02365—Forming inorganic semiconducting materials on a substrate
- H01L21/02656—Special treatments
- H01L21/02664—Aftertreatments
- H01L21/02667—Crystallisation or recrystallisation of non-monocrystalline semiconductor materials, e.g. regrowth
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/06—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising selenium or tellurium in uncombined form other than as impurities in semiconductor bodies of other materials
- H01L21/10—Preliminary treatment of the selenium or tellurium, its application to the foundation plate, or the subsequent treatment of the combination
- H01L21/101—Application of the selenium or tellurium to the foundation plate
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/06—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising selenium or tellurium in uncombined form other than as impurities in semiconductor bodies of other materials
- H01L21/10—Preliminary treatment of the selenium or tellurium, its application to the foundation plate, or the subsequent treatment of the combination
- H01L21/108—Provision of discrete insulating layers, i.e. non-genetic barrier layers
Definitions
- This invention relates to a method of applying a blocking layer, more particularly consisting of selenium, onto an electrode for a blocking layer cell, and to a blocking layer cell comprising such a blocking layer.
- non-genetic blocking layers consist of a synthetic resin and were precipitated from a solution on to' the surface to be coated.
- Such a method has first of all the drawback that only those materials can be provided that are soluble in a suitable medium.
- it appears that such layers are not always very homogeneous of composition and thickness in regard to the blocking effect.
- the present invention has for its object to avoid the aforesaid drawbacks and to obtain other advantages. It is characterized in that the blocking layer material is applied by disintegration, through ion bombardment, of the material to be applied (sputtering) and is precipitated on the carrier for the blocking layer.
- a blocking layer applied by means of the method according to the invention is very homogeneous. This is visible even with the naked eye when observing a plate carrying a blocking layer thus established under an inclined beam of light. In this case one definite interference colour is observed.
- Another advantage, which is more particularly inherent to a selenium blocking layer consists in that the selenium thus applied is highly resistant to chemical attack. At variance with selenium layers provided in the usual way, which are attacked even at a normal temperature by various substances, notably nitric acid, a layer applied by means of the method according to the invention only dissolves at a high temperature in nitric acid.
- blockin layer cells can be obtained which have a high and well reproducible breakdown voltage which is to be ascribed to the high homogeneity and compactness of the layer; in addition the forward current has a suitable value.
- a blocking layer cell in which one of the electrodes consists of selenium first of all a blocking layer is formed by making a liquid act upon the surface of the selenium layer, followed by another blocking-layer forming treatment according to the aforesaid method of disintegration.
- a layer of selenium 3 is applied on to an aluminium carrier plate I which is roughened and furnished with a layer of carbon 2.
- a volatile halide e. g. tin chloride.
- the selenium surface is smoothed by means of a press, the surface of the pressing plate having previously been coated with a resin-forming liquid e. g. quinoline. After this the plate is heated in a furnace at about 200 C., the selenium being converted into the conducting crystalline modification.
- a resin forming liquid for instance triethanolamine, is sprayed on to the selenium surface, thus forming a layer of resin 4 having a thickness of several tenths of a micron.
- the assembly is placed in a space in front of a plateshaped selenium electrode (cathode), the latter being connected to the negative side of asource of potential of several kilovolts, whereas another plate-shaped electrode is connected to the positive side of the same source.
- the selenium-coated plate is now placed in the field between the two electrodes, the free selenium side of the plate I, 2 facing the cathode.
- the space is exhausted down to-a pressure of about 100 units.
- the current amounts to several times ten ma.
- the thickness of the selenium layer disintegrated by ion bombardment depends on the time during which the distintegration is effected.
- the disintegration is continued until the thickness'amounts to several .tenths of a micron.
- This thickness may be adjusted in accordance with the purpose for Before formation After formation
- the reverse voltage is the voltage to be applied to make a current of 100 ma. flow in the blocking direction. All measurements have been made on cells having a diameter of 45 mm. It is remarkablethat, in contradistinction to hitherto manufactured blocking layer cells, which after formation exhibit, it is true. a higher reverse voltage but a reduced forward current, cells made by means of the method according to the invention exhibit an increased forward current after formation. Furthermore, it has been found that cells established by means of the method according to the invention retain their electrical properties during operation.
- a method of manufacturing a blocking layer cell comprising the steps of ionically disintegrating an element selected from the group consisting of selenium and sulfur, and precipitating said disintegrated element on a selenium electrade to form a blocking layer thereon.
- a method of manufacturing a blocking layer cell which comprises the steps of ionically disintegrating an element from the group consisting of selenium and sulfur in air, and precipitating said disintegrated element on a selenium electrode to form a blocking layer thereon.
- a method of manufacturing a blocking layer cell which comprises the steps of forming a layer of selenium on a base, converting the selenium into a conducting crystalline modification,
- a method of manufacturing a blocking layer cell which comprises the steps of forming a layer of selenium on a base, converting the selenium into a conducting crystalline modification, applying a liquid to said selenium layer to form a' blocking layer thereon, ionically disintegrating selenium, and precipitating said disintegrated selenium onsaid selenium layer to form a blocking layer thereon.
- a method of manufacturing a blocking layer cell which comprises the steps of forming a layer of selenium on a base, converting the selenium into a conducting crystalline modification, applying a resin-forming liquid to said selenium layer 5 to form a layer of resin, ionically disintegrating 40 cell which comprises the steps of forming a layer same.
- a method of manufacturing a blocking layer of selenium on a base converting the selenium into a conducting crystalline modification, applying a resin-forming liquid to said selenium layer to form a layer of resin, ionically disintegrating sulfur, and precipitating said disintegrated sulfur on said selenium layer to form a blocking layer thereon.
- a method of manufacturing a blocking layer cell which comprises the steps of forming a layer of selenium on a base, applying quinoline to said selenium layer, heating said selenium layer to convert the selenium to the conducting crystalline modification thereof, applying triethanolamine to said selenium layer to form a resinous layer, ionically disintegrating selenium, and precipitating said disintegrated selenium on said resinous layer to form a blocking layer thereon.
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- Engineering & Computer Science (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Manufacturing & Machinery (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biotechnology (AREA)
- Materials Engineering (AREA)
- Crystallography & Structural Chemistry (AREA)
- Photoreceptors In Electrophotography (AREA)
- Physical Vapour Deposition (AREA)
- Electrolytic Production Of Metals (AREA)
- Electrodes For Compound Or Non-Metal Manufacture (AREA)
Description
P 6, 1949. w. c. VAN GEEL ETAL 2,468,527
BLOCKING-LAYER CELL Filed April 10, 1945 WILLEM-CHRISTIAAN VAN GEEL LUDOVICUS AUGUSTINUS LAMBERTUS ESSELING INVENTOR S ATTORNEY Patented Apr. 26, 1949 UNITED STATES PATENT OFFICE BLOCKING -LAYER CELL Application April 10, 1946, Serial No. 661,022 In the Netherlands August 8, 1944 Section 1, Public Law 690, August 8, 1946 Patent expires August 8, 1964 This invention relates to a method of applying a blocking layer, more particularly consisting of selenium, onto an electrode for a blocking layer cell, and to a blocking layer cell comprising such a blocking layer.
Various methods of applying a blocking layer have already been proposed. Thus, for instance, non-genetic blocking layers have come to be known, which consist of a synthetic resin and were precipitated from a solution on to' the surface to be coated. Such a method, however, has first of all the drawback that only those materials can be provided that are soluble in a suitable medium. Secondly, it appears that such layers are not always very homogeneous of composition and thickness in regard to the blocking effect.
Furthermore it has already been proposed to precipitate, by vaporisation, materials such as quartz, magnesium-or beryllium oxide. Particularly if the materials have a low vapour pressure it is diiiicult to apply them, since in this case very high temperatures have to be used. In addition these layers are not sufficiently homogeneous for the required effect.
Again it is known to vaporise sulphur on to selenium electrodes. This took place by means of a thermal treatment, during which the selenium was converted into the conducting crystallinemodification. Such a method is complicated and expensive.
The present invention has for its object to avoid the aforesaid drawbacks and to obtain other advantages. It is characterized in that the blocking layer material is applied by disintegration, through ion bombardment, of the material to be applied (sputtering) and is precipitated on the carrier for the blocking layer.
A blocking layer applied by means of the method according to the invention is very homogeneous. This is visible even with the naked eye when observing a plate carrying a blocking layer thus established under an inclined beam of light. In this case one definite interference colour is observed. Another advantage, which is more particularly inherent to a selenium blocking layer, consists in that the selenium thus applied is highly resistant to chemical attack. At variance with selenium layers provided in the usual way, which are attacked even at a normal temperature by various substances, notably nitric acid, a layer applied by means of the method according to the invention only dissolves at a high temperature in nitric acid.
All of the selenium layers applied in a known manner have the drawback of contracting on 7 Claims. (Cl. 175366) 2 being heated above their melting point. The novel layer perfectly retains its coherence upon heating.
It appears that the last-mentioned two advantages are obtained more particularly if the sputtering takes place in the air. When providing the blocking layer by vaporisation, it often appears, at variance with disintegration, that a film forms under these conditions, which is liable to chemical attack. Consequently, these drawbacks, are also inherent to the vaporisation of sulphur or selenium.
It has turned out that according to the invention blockin layer cells can be obtained which have a high and well reproducible breakdown voltage which is to be ascribed to the high homogeneity and compactness of the layer; in addition the forward current has a suitable value.
In an extremely suitable example of the method according to the invention, used for the manufacture of a blocking layer cell in which one of the electrodes consists of selenium, first of all a blocking layer is formed by making a liquid act upon the surface of the selenium layer, followed by another blocking-layer forming treatment according to the aforesaid method of disintegration.
By making a liquid act upon the surface of a selenium layer a blocking layer or at least a layer having a very low conductivity is obtained, it is true, but it appears that when providing a counter-electrode on such a blocking layer, for instance by sprayin of an alloy having a low melting point. the alloy material and the liquid residue left on the blocking layer form an insulating compound. Owing to the presence of a layer of this compound the forward cur-rent decreases after formation of a blocking layer cell. If, however, after a blocking-layer forming treatment by the action of a liquid, another treatment is used, in which the blocking layer material is applied by disintegration thereof through ion bombardment on to the available insulating layer, it is not feasible for the alloy to combine with the liquid residue, this residue being separated from the alloy material by the blocking layer applied by disintegration.
It is advantageous to carry out the aforesaid first treatment for the formation of a blocking layerby means of a liquid from which a layer of a resin is formed which is precipitated on the surface of the selenium layer. In fact, this yields a more or less coherent blocking layer.
Hereinafter an example is given of the method according to the invention, the advantages ob- 3 tained by the invention appearing from the measuring results.
A layer of selenium 3 is applied on to an aluminium carrier plate I which is roughened and furnished with a layer of carbon 2. To the selenium is added, for increasing its conductivity, a volatile halide e. g. tin chloride. The selenium surface is smoothed by means of a press, the surface of the pressing plate having previously been coated with a resin-forming liquid e. g. quinoline. After this the plate is heated in a furnace at about 200 C., the selenium being converted into the conducting crystalline modification. At the same time a resin forming liquid, for instance triethanolamine, is sprayed on to the selenium surface, thus forming a layer of resin 4 having a thickness of several tenths of a micron. The assembly is placed in a space in front of a plateshaped selenium electrode (cathode), the latter being connected to the negative side of asource of potential of several kilovolts, whereas another plate-shaped electrode is connected to the positive side of the same source. The selenium-coated plate is now placed in the field between the two electrodes, the free selenium side of the plate I, 2 facing the cathode. The space is exhausted down to-a pressure of about 100 units. The current amounts to several times ten ma. The thickness of the selenium layer disintegrated by ion bombardment (denoted by 5 in the drawing) depends on the time during which the distintegration is effected. As a rule, the disintegration is continued until the thickness'amounts to several .tenths of a micron. This thickness may be adjusted in accordance with the purpose for Before formation After formation Forward Reverse Forward Reverse current voltage 1 current voltage 1 Amperes Volts Ampere: Volts The reverse voltage is the voltage to be applied to make a current of 100 ma. flow in the blocking direction. All measurements have been made on cells having a diameter of 45 mm. It is remarkablethat, in contradistinction to hitherto manufactured blocking layer cells, which after formation exhibit, it is true. a higher reverse voltage but a reduced forward current, cells made by means of the method according to the invention exhibit an increased forward current after formation. Furthermore, it has been found that cells established by means of the method according to the invention retain their electrical properties during operation.
For applying by distintegration a different What we claim is:
1. A method of manufacturing a blocking layer cell comprising the steps of ionically disintegrating an element selected from the group consisting of selenium and sulfur, and precipitating said disintegrated element on a selenium electrade to form a blocking layer thereon.
2. A method of manufacturing a blocking layer cell which comprises the steps of ionically disintegrating an element from the group consisting of selenium and sulfur in air, and precipitating said disintegrated element on a selenium electrode to form a blocking layer thereon.
3. A method of manufacturing a blocking layer cell which comprises the steps of forming a layer of selenium on a base, converting the selenium into a conducting crystalline modification,
' ionically disintegrating selenium, and precipitating said disintegrated selenium on said selenium layer.
4. A method of manufacturing a blocking layer cell which comprises the steps of forming a layer of selenium on a base, converting the selenium into a conducting crystalline modification, applying a liquid to said selenium layer to form a' blocking layer thereon, ionically disintegrating selenium, and precipitating said disintegrated selenium onsaid selenium layer to form a blocking layer thereon.
5. A method of manufacturing a blocking layer cell which comprises the steps of forming a layer of selenium on a base, converting the selenium into a conducting crystalline modification, applying a resin-forming liquid to said selenium layer 5 to form a layer of resin, ionically disintegrating 40 cell which comprises the steps of forming a layer same.
selenium, .and precipitating said disintegrated selenium on said resinous layer to form a blocking layer thereon.
6. A method of manufacturing a blocking layer of selenium on a base, converting the selenium into a conducting crystalline modification, applying a resin-forming liquid to said selenium layer to form a layer of resin, ionically disintegrating sulfur, and precipitating said disintegrated sulfur on said selenium layer to form a blocking layer thereon.
7. A method of manufacturing a blocking layer cell which comprises the steps of forming a layer of selenium on a base, applying quinoline to said selenium layer, heating said selenium layer to convert the selenium to the conducting crystalline modification thereof, applying triethanolamine to said selenium layer to form a resinous layer, ionically disintegrating selenium, and precipitating said disintegrated selenium on said resinous layer to form a blocking layer thereon.
WILLEM CHRISTIAAN VAN GEEL. LUDOVICUS AUGUSTINUS LAMBERTUS ESSELING.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 2,221,596 Lorenz Nov. 12, 1940 2,223,203 Brunke Nov. 26, 1940 2,303,522 Addink et al Dec. 1. 1942
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL253109X | 1944-08-08 |
Publications (1)
Publication Number | Publication Date |
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US2468527A true US2468527A (en) | 1949-04-26 |
Family
ID=19781189
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US661022A Expired - Lifetime US2468527A (en) | 1944-08-08 | 1946-04-10 | Blocking-layer cell |
Country Status (7)
Country | Link |
---|---|
US (1) | US2468527A (en) |
BE (1) | BE467879A (en) |
CH (1) | CH253109A (en) |
DE (1) | DE915593C (en) |
FR (1) | FR942904A (en) |
GB (1) | GB637736A (en) |
NL (2) | NL118416B (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2892136A (en) * | 1957-09-09 | 1959-06-23 | Int Rectifier Corp | Rectifier with multiple barrier layers |
DE1090768B (en) * | 1957-05-11 | 1960-10-13 | Licentia Gmbh | Process for the production of selenium dry rectifiers |
US3250964A (en) * | 1961-04-28 | 1966-05-10 | Ibm | Semiconductor diode device and method of making it |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE516590A (en) * | 1951-10-29 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2221596A (en) * | 1938-01-22 | 1940-11-12 | Fides Gmbh | Method of manufacturing dry rectifiers |
US2223203A (en) * | 1938-09-09 | 1940-11-26 | Gen Electric | Dry plate element and method of forming same |
US2303522A (en) * | 1939-03-15 | 1942-12-01 | Hartford Nat Bank & Trust Co | Method of manufacturing blockinglayer electrode systems |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AT153134B (en) * | 1936-06-13 | 1938-04-11 | Aeg | Process for the manufacture of dry plate rectifiers. |
BE434337A (en) * | 1938-06-07 |
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0
- NL NL66146D patent/NL66146C/xx active
- BE BE467879D patent/BE467879A/xx unknown
- NL NL118416D patent/NL118416B/xx unknown
-
1946
- 1946-04-10 US US661022A patent/US2468527A/en not_active Expired - Lifetime
- 1946-08-30 CH CH253109D patent/CH253109A/en unknown
- 1946-11-18 FR FR942904D patent/FR942904A/en not_active Expired
-
1947
- 1947-04-15 GB GB10007/47A patent/GB637736A/en not_active Expired
-
1948
- 1948-10-23 DE DEP19306A patent/DE915593C/en not_active Expired
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2221596A (en) * | 1938-01-22 | 1940-11-12 | Fides Gmbh | Method of manufacturing dry rectifiers |
US2223203A (en) * | 1938-09-09 | 1940-11-26 | Gen Electric | Dry plate element and method of forming same |
US2303522A (en) * | 1939-03-15 | 1942-12-01 | Hartford Nat Bank & Trust Co | Method of manufacturing blockinglayer electrode systems |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1090768B (en) * | 1957-05-11 | 1960-10-13 | Licentia Gmbh | Process for the production of selenium dry rectifiers |
US2892136A (en) * | 1957-09-09 | 1959-06-23 | Int Rectifier Corp | Rectifier with multiple barrier layers |
US3250964A (en) * | 1961-04-28 | 1966-05-10 | Ibm | Semiconductor diode device and method of making it |
Also Published As
Publication number | Publication date |
---|---|
NL118416B (en) | 1900-01-01 |
BE467879A (en) | 1900-01-01 |
GB637736A (en) | 1950-05-24 |
FR942904A (en) | 1949-02-22 |
NL66146C (en) | 1900-01-01 |
CH253109A (en) | 1948-02-15 |
DE915593C (en) | 1954-07-26 |
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