GB2043991A - Method of fabricating a dispenser cathode - Google Patents
Method of fabricating a dispenser cathode Download PDFInfo
- Publication number
- GB2043991A GB2043991A GB7940153A GB7940153A GB2043991A GB 2043991 A GB2043991 A GB 2043991A GB 7940153 A GB7940153 A GB 7940153A GB 7940153 A GB7940153 A GB 7940153A GB 2043991 A GB2043991 A GB 2043991A
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- United Kingdom
- Prior art keywords
- foil
- substrate
- electron
- pellet
- alkaline earth
- Prior art date
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- Granted
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 14
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 claims abstract description 83
- 239000011888 foil Substances 0.000 claims abstract description 71
- 238000000034 method Methods 0.000 claims abstract description 67
- 239000000463 material Substances 0.000 claims abstract description 65
- 239000000758 substrate Substances 0.000 claims abstract description 43
- 229910052751 metal Inorganic materials 0.000 claims abstract description 42
- 239000002184 metal Substances 0.000 claims abstract description 42
- 239000008188 pellet Substances 0.000 claims abstract description 41
- 239000012260 resinous material Substances 0.000 claims abstract description 12
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 9
- 230000008020 evaporation Effects 0.000 claims abstract description 9
- 238000001704 evaporation Methods 0.000 claims abstract description 9
- 239000001301 oxygen Substances 0.000 claims abstract description 9
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 9
- 230000002000 scavenging effect Effects 0.000 claims abstract description 9
- 238000000151 deposition Methods 0.000 claims abstract description 7
- 238000004544 sputter deposition Methods 0.000 claims abstract description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 4
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910002804 graphite Inorganic materials 0.000 claims abstract description 4
- 239000010439 graphite Substances 0.000 claims abstract description 4
- 229910052726 zirconium Inorganic materials 0.000 claims abstract description 4
- 238000000206 photolithography Methods 0.000 claims abstract description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 22
- 238000000576 coating method Methods 0.000 claims description 21
- 239000011248 coating agent Substances 0.000 claims description 20
- 239000003870 refractory metal Substances 0.000 claims description 12
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 11
- 239000001569 carbon dioxide Substances 0.000 claims description 10
- 230000001681 protective effect Effects 0.000 claims description 10
- 230000008569 process Effects 0.000 claims description 9
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 8
- 238000010438 heat treatment Methods 0.000 claims description 8
- IATRAKWUXMZMIY-UHFFFAOYSA-N strontium oxide Chemical compound [O-2].[Sr+2] IATRAKWUXMZMIY-UHFFFAOYSA-N 0.000 claims description 8
- 238000003466 welding Methods 0.000 claims description 8
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 7
- 229910052721 tungsten Inorganic materials 0.000 claims description 7
- 239000010937 tungsten Substances 0.000 claims description 7
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 6
- CBFCDTFDPHXCNY-UHFFFAOYSA-N icosane Chemical group CCCCCCCCCCCCCCCCCCCC CBFCDTFDPHXCNY-UHFFFAOYSA-N 0.000 claims description 6
- 229910052750 molybdenum Inorganic materials 0.000 claims description 6
- 239000011733 molybdenum Substances 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 5
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 4
- 239000000020 Nitrocellulose Substances 0.000 claims description 4
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims description 4
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 4
- 239000000292 calcium oxide Substances 0.000 claims description 4
- 238000003486 chemical etching Methods 0.000 claims description 4
- 230000008021 deposition Effects 0.000 claims description 4
- 229910052741 iridium Inorganic materials 0.000 claims description 4
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 claims description 4
- 229920001220 nitrocellulos Polymers 0.000 claims description 4
- 238000009713 electroplating Methods 0.000 claims description 3
- 238000003801 milling Methods 0.000 claims description 3
- 229910052762 osmium Inorganic materials 0.000 claims description 3
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- 238000000227 grinding Methods 0.000 claims description 2
- 238000005498 polishing Methods 0.000 claims description 2
- 229910000287 alkaline earth metal oxide Inorganic materials 0.000 claims 10
- 238000005530 etching Methods 0.000 claims 1
- 238000007740 vapor deposition Methods 0.000 claims 1
- 230000004913 activation Effects 0.000 abstract description 5
- 238000005245 sintering Methods 0.000 abstract description 4
- 239000003638 chemical reducing agent Substances 0.000 abstract description 3
- 238000005229 chemical vapour deposition Methods 0.000 abstract description 3
- 238000006722 reduction reaction Methods 0.000 abstract description 2
- AYJRCSIUFZENHW-UHFFFAOYSA-L barium carbonate Chemical compound [Ba+2].[O-]C([O-])=O AYJRCSIUFZENHW-UHFFFAOYSA-L 0.000 description 14
- 239000011148 porous material Substances 0.000 description 6
- 238000001994 activation Methods 0.000 description 5
- 230000003647 oxidation Effects 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 4
- 229910001863 barium hydroxide Inorganic materials 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 3
- 238000013461 design Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- LTPBRCUWZOMYOC-UHFFFAOYSA-N Beryllium oxide Chemical compound O=[Be] LTPBRCUWZOMYOC-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 238000001259 photo etching Methods 0.000 description 2
- 239000011253 protective coating Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000002144 chemical decomposition reaction Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 230000036571 hydration Effects 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000011819 refractory material Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J1/00—Details of electrodes, of magnetic control means, of screens, or of the mounting or spacing thereof, common to two or more basic types of discharge tubes or lamps
- H01J1/02—Main electrodes
- H01J1/13—Solid thermionic cathodes
- H01J1/20—Cathodes heated indirectly by an electric current; Cathodes heated by electron or ion bombardment
- H01J1/28—Dispenser-type cathodes, e.g. L-cathode
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J9/00—Apparatus or processes specially adapted for the manufacture, installation, removal, maintenance of electric discharge tubes, discharge lamps, or parts thereof; Recovery of material from discharge tubes or lamps
- H01J9/02—Manufacture of electrodes or electrode systems
- H01J9/04—Manufacture of electrodes or electrode systems of thermionic cathodes
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Solid Thermionic Cathode (AREA)
Abstract
A dispenser cathode is fabricated by sandwiching a reservoir 12 of electron emitting material between a perforated metal foil 11 and a support structure 13. The electron emitting material is in the form of a pellet of barium oxide impregnated with a wax or resinous material to minimize chemical reduction of the barium oxide in air. During tube bakeout or subsequently during cathode activation, the wax or resinous material evaporates and barium oxide migrates through the apertures to cover the surface of the foil in a uniform manner. The desired pattern of apertures in the foil is achieved by photolithography, or by forming the foil (e.g., by chemical vapor deposition, sputter deposition, evaporation, or sintering) on a substrate containing an array of protruding posts. With either technique for forming the apertures, a shadow grid can also be formed as an integral part of the cathode surface by depositing a layer of oxygen scavenging material such as zirconium or graphite on a selected portion of the cathode surface. <IMAGE>
Description
SPECIFICATION
Method of fabricating a dispenser cathode
BACKGROUND OF THE INVENTION
This invention is a further development in the fabrication of dispenser cathodes, which find application generally in microwave tubes and linear beam devices.
Heretofore, the emitting surfaces of dispenser cathodes have been made either from porous metal matrices whose pores were filled with electron emitting material, or from porous metal plugs covering reservoirs of electron emitting material.
The porous metal bodies of prior art dispenser cathodes, whether they were matrices filled with electron emitting material or porous plugs covering reservoirs of electron emitting material, did not have consistently uniform pore size, pore length, or spacing between pores on the surface.
As a consequence, dispenser cathodes of the prior art tended to exhibit non-uniform electron emission from their surfaces.
U.S. Patent 4,101,800 (issued July 18, 1978) described a dispenser cathode comprising a reservoir of electron emitting material covered by a perforated metal foil. The pattern of perforations was such as to permit migration of electronemitting material from the reservoir to the foil surface in such a way as to coat the surface uniformly, thereby providing a cathode surface of substantialiy uniform emissivity. The prior art has not, however, developed a practicable method for fabricating a perforated metal foil of the kind disclosed in U.S. Patent 4,101,800. Consequently the production of dispenser cathodes having uniform surface porosity has not heretofore been commercially feasible.
SUMMARY OF THE INVENTION
It is an object of the present invention to provide a method for fabricating a dispenser cathode having a uniform surface porosity, whereby uniform electron emission from the surface can be achieved.
It is a concomitant object of this invention to provide a method for controlling the porosity of the surface of a dispenser cathode in order to provide a surface of uniform electron emission.
It is a further object of this invention to fabricate a dispenser cathode having uniform surface porosity by a method that minimizes carburization and oxidation of the cathode surface.
It is a particular object of the present invention to provide a method for fabricating a dispenser cathode having uniform pattern of electron emission from its surface by sandwiching a reservoir of electron emitting material between an apertured foil and a supporting structure using a bonding technique that minimizes carburization of the emitting surface.
In order to accomplish the aforementioned objects of this invention, a quantity of material having a low work function (e.g., barium oxide) is placed on a supporting structure, and a thin foil of refractory or platinum-group metal having a desired pattern of uniformly sized and evenly distributed apertures is placed on the support structure so as to cover the barium oxide. The foil is bonded to the support structure by laser welding so as to localize the heating effects due to the bonding process. In order to prevent chemical reaction of the barium oxide with moisture in the air during fabrication of the cathode, a specially treated pellet of barium oxide is used. This barium oxide pellet is formed by heating a solid pellet of barium carbonate in a vacuum to liberate carbon dioxide, thereby leaving a porous pellet of barium oxide.The porous pellet of barium oxide is then impregnated with a wax, or with a resinous material such as methyl methacrylate or nitrocellulose, to provide a protective coating over the barium oxide. Without such a protective coating, rapid chemical reduction of the barium oxide to barium hydroxide would occur. Barium hydroxide is not usable as an electron emitting material.
In the fabrication of a dispenser cathode according to the present invention, a pellet of barium oxide impregnated with a wax or a resinous material to prevent any rapid chemical reaction in air is placed on the surface a metal supporting member of the cathode structure. The apertured foil is placed over the barium oxide pellet, and is then welded to the metal supporting member. A laser welding technique is preferred because laser welding can be accomplished in areas of limited access, and effectively localizes the heating effects of the welding process. The heat generated during tube bake-out and processing, or during cathode activation, causes the wax or resinous protective material to evaporate from the barium oxide pellet.
The apertured metal foil of uniform pore size and distribution according to this invention may be obtained by a photolithographic technique whereby a pattern of holes is chemically etched in a foil of a refractory metal such as tungsten or molybdenum. After the holes have been formed, the foil is then coated with iridium, osmium or some other platinum-group metal. Typically, the tungsten or molybdenum foil is 0.001 inch thick, and the coating thereon is about one micron thick.
Alternatively, a foil having a desired pattern of uniformly sized and distributed pores according to the present invention could be produced by deposition af a layer of a platinum-group metal onto a substrate having an array of appropriate dimensioned and spaced posts projecting therefrom. After the layer of metal has been deposited upon such a substrate, typically to a thickness in the range from 0.0005 inch to 0.0015, the substrate with its projecting posts is
removed either by chemical etching or by
evaporation. Deposition of the platinum-group
metal layer onto the substate could be
accomplished by chemical vapor deposition,
sputter deposition, electro-plating or evaporation.
Such techniques are well known to those skilled in
the art. Alternatively, the metal layer could be formed by rolling fine particles of the metal (i.e., particles less than one micron in diameter) onto the substrate and subsequently sintering the articles to form a porous layer. The substrate could be made of any material amenable to photoetching or subsequent evaporation, whereby the posts could be formed by a photoetching process, and whereby the entire substrate with its projecting posts could subsequently be removed from the overlying foil by chemical etching and/or evaporation. Suitable substrate materials are molybdenum, aluminum and copper.
It is within the purview of the present invention to provide a shadow grid as an integral part of the foil covering the reservoir of electron emitting material. To accomplish this, the area of the foil destined to function as the shadow grid is coated with a non-emitting material such as zirconium or graphite. The non-emitting material coated onto specific non-perforated areas of the cathode surface suppresses electron emission from these areas and thereby functions in a manner analogous to a shadow grid in a non-intercepting gridded gun.
Other methods for accomplishing the objects of this invention will become apparent to those skilled in the art upon a perusal of the following description of the preferred embodiment together with the accompanying drawing.
DESCRIPTION OF THE DRAWING
FIG. 1 is a cross-sectional view of a dispenser cathode according to the present invention.
FIG. 2 is a pictorial flow diagram illustrating a step-by-step process for fabricating a metallic foil having uniformly sized and spaced apertures for use as the emitting surface of a dispenser cathode
FIG. 3 is a plan view of a dispenser cathode emitting surface fabricated by the process illustrated in FIG. 2, with a shadow grid formed as
an integral part of the emitting surface.
FIG. 4 is a plan view of a dispenser cathode as
in FIG. 3, with an alternative design for the shadow grid.
FIG. 5 is a plan view of another dispenser
cathode as in FIG. 3, with another alternative
design for the shadow grid.
FIG. 6 is a plan view of yet another dispenser
cathode as in FIG. 3, with a further alternative
design for the shadow grid.
FIG. 7 is a flow diagram summarizing the steps
in the fabrication of a reservoir of thermionically
emitting material according to the present
invention.
DESCRIPTION OF THE PREFERRED EMBODIMENT
FIG. 1 shows a dispenser cathode 10 according
to the present invention. The cathode structure comprises an electron-emitting surface 11
covering a reservoir 12 of thermionically emitting
material such as barium oxide, or a mixture of
barium oxide in combination with calcium oxide
and/or strontium oxide.
The electron emitting surface 11 is an
apertured metal foil supported on a hollow elongate member 13, which is mountable within an electron tube such as a klystron or a travelling wave tube. The support member 13 is made of a refractory material, and encloses a heater coil 14 that is made of a material such as tungsten that can dissipate electric power so as to achieve a temperature within the support structure 13 in the range from 8000C to 1 000C. The support structure 1 3 may be made entirely of a refractory metal such as tungsten or molybdenum; or it may be a composite structure whose bottom portion is made of a refractory insulating material such as alumina or beryllia, and whose upper portion is made of a refractory metal.
As shown in FIG. 1, the upper portion of the support structure 13 is configured to retain a block 1 5 of refractory metal such as tungsten, tantalum, or a porous tungsten-impregnated material. The block 1 5 need not be a separate member, but could be fabricated as an integral part of a homogeneous support structure 13.
On the upper surface of the refractory metal block 15, the reservoir 12 of material that emits electrons by thermionic emission at temperatures above 7000C is provided. The reservoir 12 would typically comprise a layer of barium oxide.
However, as discussed above, the reservoir layer 1 2 could also comprise a mixture of barium oxide in combination with calcium oxide and/or strontium oxide, depending upon the particular use intended for the tube in which the dispenser cathode 10 is to be mounted. On top of the reservoir layer 12, the metal foil 11 is disposed.
The foil 11 is arranged as a cap structure retaining the reservoir layer 12 in position. The foil 11 is bonded to the outside vertical wall of the support structure 13 by an appropriate technique such as laser welding, which localizes the heating effects of the bonding technique so as to minimize chemical decomposition of the electron-emitting material constituting the reservoir layer 12.
Barium oxide, when exposed to air, is quickly converted to barium hydroxide by the moisture in the air. Barium hydroxide, which melts at 780C, is ineffective as a thermionic electron-emitting material. Hence, the application of a barium oxide layer to the surface of a cathode has heretofore required rigid control of the environment in which fabrication takes place.
According to the present invention, the barium oxide reservoir layer 1 2 is applied to the top surface of the refractory metal block 1 5 by the following technique. First, a solid pellet of barium carbonate is heated in a vacuum to liberate carbon dioxide, leaving barium oxide according to the equation BaCO3~BaO + CO2. The pellet of barium oxide that remains after the carbon dioxide has been liberated is quite porous. Next, the porous barium oxide pellet, while still under vacuum, is impregnated with a wax such as eicosane, or a resinous material such as methyl methacrylate or nitrocellulose. This wax or resinous coating, which permeates the barium oxide pellet, protects the pellet from hydration in moist air.Such coated pellets can easily be fabricated in desired quantities by well-known techniques: e.g., in an inert atmosphere by back-filling a vacuum chamber with argon.
A wax-impregnated or resin-impregnated barium oxide pellet is then placed on the surface of the refractory metal block 1 5. The apertured metal foil 11 is then disposed to cover the barium oxide pellet; and the perimeter of the foil 11 is then sealed to the outer wall of the support structure 13 by laser welding. Later, during the tube bake-out or during the cathode activation process, the heat thereby produced causes the wax or resinous protective material to evaporate from the pellet through the apertures in the foil 11. By this technique, not only can the barium oxide electron-emitting layer 12 be applied under ordinary atmospheric conditions, but also the layer
12 can be heated to operating temperatures without causing carburization or oxidation of the surface of the foil 15.
Using prior techniques, carburization or oxidation of the emitting surface could be caused by the release of carbon dioxide gas during cathode activation. In the prior art, the conventional method of applying a layer of barium oxide to the surface of a cathode involved covering a quantity of barium carbonate with a porous foil and then welding the foil to a support structure.
Subsequent activation of the cathode by heating to 9000C would convert the barium carbonate to barium oxide, thereby driving off carbon dioxide gas. This carbon dioxide gas would react with adjacent metal surfaces (including the electronemitting surface) to cause carburization or oxidation thereof. Furthermore, the carburized surface would act as a reducing agent for the barium oxide, thereby generating elemental barium that would evaporate at operating temperatures of the cathode. With the technique of the present invention, on the other hand, there is no carbon dioxide to be liberated from the waxor resin-impregnated barium oxide pellet. Thus, the possibility of carburization or oxidation of the surface of the foil 11 by the formation of the barium oxide reservoir layer 1 2 is eliminated.
In order to provide a uniform electron emission density over the surface of the foil 11, a pattern of apertures of uniformed size and of uniform distribution with respect to each other are formed on the foil surface. Such uniform porosity of the foil 11 is achieved according to the present invention by fabricating the foil 11 according to one of the following techniques:
(1) Photolithography: A pattern of uniformly dimensioned and spaced holes is chemically etched through a foil that is made of a refractory metal such as tungsten or molybdenum, preferably about 0.001 inch thick. Thereafter, a coating of iridium, osmium or other platinumgroup metal is deposited to a thickness of about one micron on one surface (i.e., the upper surface) of foil. This coating of iridium or other platinumgroup metal serves to enhance emissivity.
(2) Deposition on a Substrate: A layer of refractory metal or platinum-group metal is
deposited upon a substrate by chemical vapor
deposition, sputter deposition, electro-plating or
evaporation. The material from which the
substrate is made depends upon the deposition technique used. The substrate is configured to
have a flat surface with evenly spaced posts
protruding therefrom, the posts having been
formed by a conveXtional photolithographic and
chemical milling technique. Preferably, the
thickness of the substrate, exclusive of the
protruding posts, is about 0.01 inch. The posts are
generally cylindrical, with a diameter in the range
from 0.0005 inch to 0.0010 inch, and extend
about 0.0010 inch to 0.0015 inch above the flat
surface of the substrate.In the usual embodiment,
the posts are separated by about 0.002 inch from
center to center.
The second technique described above for
fabricating uniformly apertured metal foil for use
in a dispenser cathode is illustrated in the pictorial
flow-diagram of FIG. 2. At step A, a substrate
having an array of posts protruding therefrom is
pictured. The posts are uniformly dimensioned and
uniformly spaced with respect to each other, and
are produced on the substrate by a conventional
lithographic technique and by chemical milling. At
step B, the substrate of step A is shown coated
with a layer of refractory metal or platinum-group
metal. The particular type of coating process used
would depend upon the nature of the substrate
material. At step C, the coated substrate of step B
is shown after having been polished to achieve a
metal layer of uniform thickness with the
substrate posts flush with the upper surface of the
metal layer.Polishing may be done by a
conventional method such as surface grinding. At
step D, the metal layer produced at step C is
shown with the substrate (including its projecting
posts) having been removed. The substrate can be
removed by a conventional method such as
chemical etching or evaporation, depending upon
the nature of the substrate material.
The metal foil remaining after the substrate has
been removed, as pictured at step D in FIG. 2, has
an array of holes of predetermined size and spatial
distribution. This foil is used to cover the barium
oxide reservoir 12, as shown in FIG. 1, and
provides the desired electron-emitting pattern
from the surface of the dispenser cathode. During
cathode activation, barium oxide migrates up
through the apertures in the foil 11 and coats the
entire surface thereof by a diffusion process
known as Knudsen flow. In this way, the-non- perforated surface of the foil 11 becomes a
thermionic electron source of substantially
uniform suface emissivity.
(3) Sintering: The formation of a metallic foil on
the surface of the substrate could also be
accomplished by the sintering of fine particles of a
refractory or platinum-group metal onto the
surface of the substrate.
A porous metallic foil fabricated according to this invention can also be treated so as to provide
a pattern of non-emitting portions on the upper
surface of the foil. Thus, after a foil of uniform porosity has been fabricated according to the process described above in connection with FIG.
2, a pattern of non-emitting surface areas can then be superimposed upon selected portions of the upper surface of the foil to function in a manner analogous to a shadow grid in a nonintercepting gridded gun. These non-emitting areas comprise a coating of an oxygen scavenging material such as zirconium or graphite, which can be deposited upon the surface of the foil by sputter deposition or any other appropriate technique known to those skilled in the art.
The configuration of the shadow grid portion of the foil can be selected in accordance with the application for which the tube is intended. In FIG.
3, the shadow grid is configured as a pattern of circles, which is representative of shadow grid patterns used in klystron tubes. In FIG. 4, the shadow grid is configured as a pattern of hexagons, which represents another type of shadow grid pattern used in klystrons and also in travelling wave tubes. In FIG. 5, a radial vane configuration for the shadow grid pattern is shown, which provides an advantage with respect to thermal conductivity. In FIG. 6, the shadow grid comprises an array of bars.
The steps in the fabrication of the layer 1 2 of thermionically emitting material according to the present invention are summarized in the flow diagram of FIG. 7. First, a quantity of alkaline earth carbonate material is compacted to form a pellet.
This pellet is then heated in a vacuum at 9000C to convert the carbonate to an oxide by driving off carbon dioxide. In the case of a barium carbonate pellet, the heating converts the barium carbonate pellet to a porous pellet of barium oxide. This resulting oxide pellet is then impregnated in a vacuum with a wax or with a resinous material.
Finally, this impregnated oxide pellet is placed on the block 1 5 at the top of the cathode support structure 13, and is covered with the perforated foil 11.
The steps in the fabrication of a dispenser cathode according to the present invention may be summarized as follows;
1) The heater 14 is assembled in the cathode structure 13.
2) The protected (i.e., wax- or resinimpregnated oxide pellet is inserted in place on the support structure 1 3 to form the reservoir 1 2 of electron-emitting material.
3) The perforated foil 11 is placed over the protected oxide pellet.
4) The perimeter of the perforated foil 11 is laser welded to the support structure 1 3 so as to sandwich the oxide pellet between the foil 11 and the support structure 13.
This invention has been described above in terms of a particular embodiment. However, from a reading of the above disclosure, other techniques for optimizing the desired electron emitting pattern from the surface of a dispenser cathode will suggest themselves to those skilled in the art. Consequently, the invention is limited only by the following claims.
Claims (1)
1. A method of fabricating a dispenser cathode, said method comprising the steps of:
a) placing a quantity of electron-emitting material on top of a metal support structure;
b) placing a perforated metallic foil over said electron-emitting material, a non-perforated portion of said foil comprising a coating of an oxygen scavenging material; and
c) affixing said foil to said support structure so as to sandwich said electron-emitting material between said foil and said support structure.
2. The method of claim 1 wherein said foil is affixed to said support structure by laser welding around the periphery of said foil.
3. The method of claim 1 wherein said coating of an oxygen scavenging material comprises a coating of zirconium.
4. The method of claim 1 wherein said coating of an oxygen scavenging material comprises a coating of graphite.
5. The method of claim 1 wherein said coating of an oxygen scavenging material is configured as a pattern of circles.
6. The method of claim 1 wherein said coating of an oxygen scavenging material is configured as a pattern of hexagons.
7. The method of claim 1 wherein said coating of an oxygen scavenging material is configured as a pattern comprising radial vanes.
8. The method of claim 1 wherein said coating of an oxygen scavenging material is configured to comprise an array of bars.
9. A dispenser cathode, said cathode comprising a reservoir of electron-emitting material sandwiched between a support structure and a perforated foil made of a refractory metal, said perforated foil being fabricated by the process of chemically etching a pattern of apertures on the foil.
10. The dispenser cathode of claim 9 wherein said foil is made of tungsten.
1 The dispenser cathode of claim 9 wherein said foil is made of molybdenum.
1 2. The dispenser cathode of claim 9 further comprising a coating of metal on the surface of said foil to enhance electron emissivity, said coating being applied to said foil by the process of deposition after said apertures have been chemically etched on said foil.
13. The dispenser cathode of claim 12 wherein said coating to enhance electron emissivity comprises a layer of iridium.
14. The dispenser cathode of claim 12 wherein said coating to enhance electron emissivity comprises a layer of osmium.
1 5. A method of fabricating a dispenser cathode, said cathode comprising a reservoir of electron-emitting material sandwiched between a support structure and a perforated foil, said perforated foil being fabricated by the steps of:
a) depositing a coating of metal upon a substrate, said substrate being configured to have a flat surface with posts protruding therefrom;
b) polishing said coated substrate in order to obtain a metal layer of uniform thickness with said posts of said substrate being flush with the upper surface of said metal layer; and
c) removing said substrate, including the projecting posts of said substrate.
1 6. The method of claim 1 5 wherein said metal coating deposited upon said substrate comprises a refractory metal.
1 7. The method of claim 1 5 wherein said metal deposited upon said substrate comprises a platinum-group metal.
18. The method of claim 15 wherein said metal is deposited upon said substrate by vapor deposition.
19. The method of claim 15 wherein said metal is deposited upon said substrate by sputter deposition.
20. The method of claim 1 5 wherein said metal is deposited upon said substrate by electroplating.
21. The method of claim 1 5 wherein said metal is deposited upon said substrate by evaporation.
22. The method of claim 1 5 wherein said posts are formed on said substrate by photolithography.
23. The method of claim 15 wherein said posts are formed on said substrate by chemical milling.
24. The method of claim 15 wherein said coated substrate is polished by surface grinding.
25. The method of claim 1 5 wherein said substrate is removed by chemical etching.
26. The method of claim 1 5 wherein said substrate is removed by evaporation.
27. The method of claim 1 5 wherein said reservoir of electron-emitting material comprises barium oxide
28. The method of claim 1 5 wherein said reservoir of electron-emitting material comprises a mixture of barium oxide and calcium oxide.
29. The method of claim 1 5 wherein said reservoir of electron-emitting material comprises a mixture of barium oxide and strontium oxide.
30. The method of claim 1 5 wherein said reservoir of electron-emitting material comprises a mixture of barium oxide, calcium oxide, and strontium oxide.
31. The method of claim 1 5 wherein said reservoir of electron emitting material is formed by placing a quantity of said electron-emitting material upon said support structure, and by covering said quantity of electron-emitting material with said perforated foil to form a layer of said electron-emitting material sandwiched between said foil and said support structure.
32. The method of claim 31 wherein said quantity of electron-emitting material that is placed upon said support structure is in the form of a pellet.
33. The method of claim 32 wherein said pellet comprises an alkaline earth oxide impregnated with a wax.
34. The method of claim 33 wherein said wax is eicosane.
35. The method of claim 32 wherein said pellet comprises an alkaline earth oxide impregnated with a resinous material.
36. The method of claim 35 wherein said resinous material comprises methyl methacrylate.
37. The method of claim 35 wherein said resinous material comprises nitrocellulose.
38. A method of fabricating a pellet of an alkaline earth oxide material for use in the fabrication of a dispenser cathode, said method comprising the steps of:
a) compacting a quantity of alkaline earth carbonate;
b) heating the compacted alkaline earth carbonate to convert said alkaline earth carbonate to an alkaline earth oxide by driving off carbon dioxide; and
c) impregnating the alkaline earth oxide thus formed with a protective material.
39. The method of claim 38 wherein said step of impregnating said alkaline earth oxide with said protective material is performed in a vacuum.
40. The method of claim 38 wherein said protective material is a wax.
41. The method of claim 38 wherein said protective material is a resonance material.
42. A pellet of an alkaline earth oxide material, said pellet being fabricated by the process of:
a) compacting a quantity of alkaline earth carbonate;
b) heating the compacted alkaline earth carbonate to convert said alkaline earth carbonate to an alkaline earth oxide by driving off carbon dioxide; and
c) impregnating the alkaline earth oxide thus formed with a protective material.
43. The pellet of claim 42 wherein said step of impregnating said alkaline earth oxide with said protective material is performed in a vacuum.
44. The pellet of claim 42 wherein said protective material is wax.
45. The pellet of claim 44 wherein said wax is eicosane.
46. The pellet of claim 42 wherein said protective material is a resinous material.
47. The pellet of claim 46 wherein said resinous material is methyl methacrylate.
48. The pellet of claim 46 wherein said resinous material is nitrocellulose.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US96486778A | 1978-11-30 | 1978-11-30 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| GB2043991A true GB2043991A (en) | 1980-10-08 |
| GB2043991B GB2043991B (en) | 1983-05-11 |
Family
ID=25509102
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB8210616A Expired GB2100502B (en) | 1978-11-30 | 1979-11-20 | Dispenser cathodes |
| GB7940153A Expired GB2043991B (en) | 1978-11-30 | 1979-11-20 | Method of fabricating a dispenser cathode |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB8210616A Expired GB2100502B (en) | 1978-11-30 | 1979-11-20 | Dispenser cathodes |
Country Status (4)
| Country | Link |
|---|---|
| JP (1) | JPS5576538A (en) |
| CA (1) | CA1150763A (en) |
| DE (2) | DE2954658C2 (en) |
| GB (2) | GB2100502B (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS56118242A (en) * | 1980-02-23 | 1981-09-17 | New Japan Radio Co Ltd | Thermion emission cathode |
| JPS56130057A (en) * | 1980-03-18 | 1981-10-12 | Matsushita Electric Ind Co Ltd | Hot cathode |
| JPS587740A (en) * | 1981-06-30 | 1983-01-17 | インタ−ナシヨナル・ビジネス・マシ−ンズ・コ−ポレ−シヨン | Electron emission layer |
| WO1984001664A1 (en) * | 1982-10-12 | 1984-04-26 | Hughes Aircraft Co | Controlled porosity dispenser cathode |
| DE4114856A1 (en) * | 1991-05-07 | 1992-11-12 | Licentia Gmbh | STOCK CATHODE AND METHOD FOR THE PRODUCTION THEREOF |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2881512A (en) * | 1954-06-16 | 1959-04-14 | Cie Generale De Telegraphite S | Composition for sintered barium cathodes |
| DE1071849B (en) * | 1955-02-05 | 1959-12-24 | ||
| BE550302A (en) * | 1955-08-15 | |||
| US2874077A (en) * | 1957-10-23 | 1959-02-17 | Rauland Corp | Thermionic cathodes |
| US3159461A (en) * | 1958-10-20 | 1964-12-01 | Bell Telephone Labor Inc | Thermionic cathode |
| NL108689C (en) * | 1959-01-23 | 1900-01-01 | ||
| US3243638A (en) * | 1962-10-31 | 1966-03-29 | Gen Electric | Dispenser cathode |
| DE2010479C3 (en) * | 1970-03-05 | 1973-11-22 | Siemens Ag, 1000 Berlin U. 8000 Muenchen | Metal capillary cathode with a porous emission material carrier protected against humidity |
| US4101800A (en) * | 1977-07-06 | 1978-07-18 | The United States Of America As Represented By The Secretary Of The Navy | Controlled-porosity dispenser cathode |
-
1979
- 1979-11-20 GB GB8210616A patent/GB2100502B/en not_active Expired
- 1979-11-20 GB GB7940153A patent/GB2043991B/en not_active Expired
- 1979-11-21 CA CA000340306A patent/CA1150763A/en not_active Expired
- 1979-11-28 DE DE19792954658 patent/DE2954658C2/de not_active Expired - Lifetime
- 1979-11-28 DE DE19792947919 patent/DE2947919A1/en active Granted
- 1979-11-30 JP JP15449979A patent/JPS5576538A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| CA1150763A (en) | 1983-07-26 |
| DE2947919C2 (en) | 1991-06-20 |
| GB2100502A (en) | 1982-12-22 |
| GB2100502B (en) | 1983-08-03 |
| JPH028413B2 (en) | 1990-02-23 |
| JPS5576538A (en) | 1980-06-09 |
| DE2947919A1 (en) | 1980-06-12 |
| DE2954658C2 (en) | 1991-01-17 |
| GB2043991B (en) | 1983-05-11 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19921120 |