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Publication numberUS3195199 A
Publication typeGrant
Publication date20 Jul 1965
Filing date1 Sep 1961
Priority date1 Sep 1961
Publication numberUS 3195199 A, US 3195199A, US-A-3195199, US3195199 A, US3195199A
InventorsAlbert Ochs Stefan
Original AssigneeRca Corp
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Method of making targets for pickup tubes
US 3195199 A
Abstract  available in
Images(1)
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Claims  available in
Description  (OCR text may contain errors)

July 20, 1965 s. A. OCHS METHOD OF MAKING TARGETS FOR PICKUP TUBES Filed Sept. 1, 1961 ,M s m m R H I N LN mw m w A N m A i F d H J x x W M w H mkwm wxw kmQKRkW NNN 0 g -sw United States Patent 3,195,199 DETHGD 8F MAKENG TARGETS FUR HCKUP TUBE Stefan Albert Ochs, Princeton, NJ, assignor to Radio Glorporation of America, a corporation of Delaware Fiied Sept. 1, 1961, Ser. No. 135,652 4 Claims. (Cl. 22190) This invention relates to television pickup or camera tubes. In particular, this invention relates to a novel method of manufacturing an improved target structure for television pickup tubes.

In the prior art, there are several commercially available tube types known as Image Orthicons. The Image Orthicon tube generally comprises an envelope having an electron gun in one end thereof. In the opposite end of the envelope is a photocathocle. Between the electron gun and the photocathode is a semiconducting storage target electrode.

During operation of the Image Orthicon tube, an image of a scene to be reproduced is directed onto the photocathode which produces photoelectron emission which in turn provides a charge pattern on one side of the target electrode. The electron beam scans the opposite side of the storage target to read off the charge pattern thereon and produces electrical output signals corresponding to the original input scene.

In the prior art, the storage targets for the Image Orthicon type of tube have been made of a thin membrane of glass, thin semiconducting materials, or insulating materials with electrically conducting plugs therein. This invention is particularly related to storage targets of the semiconducting type. The semiconducting type storage target generally comprises an annular support ring having a thin membrane of magnesium oxide supported across the aperture in the support ring.

A storage target of the magnesium oxide type is difl'icult to produce economically. The reasons for this difficulty include the fact that, frequently, the magnesium metal deposit will not properly adhere to an organic film, which temporarily functions as a support membrane, and which is stretched across the support ring during manufacture of the target. Due to this lack of adherence of the magnesium, the resultant target is likely to split during some of the subsequent tube processing.

A further difliculty in manufacturing such a storage target is that the oxidation on the deposited magnesium film requires exposure of the magnesium surface to an oxidizing atmosphere at a relatively high temperature. Such treatment may be undesirably severe for the film, its substrate or other parts of the device. An alternative suggestion is to evaporate directly the desired oxidized material, i.e. magnesium oxide, onto the support membrane. However, with many compounds, particularly the oxides, the evaporation temperatures are too high to be practical. Still further, many materials, such as magnesium oxide, decompose badly when heated to their evaporation temperature.

It is therefore an object of this invention to provide a novel method of manufacturing an improved electrode target structure.

It is another object of this invention to provide a new and improved method of manufacturing magnesium oxide targets for use in Image Orthicon type tubes.

These and other objects are accomplished in accordance with this invention by depositing on the temporary support membrane, an under layer before metallic magnesium is deposited, and then oxidizing the magnesium, or, as an alternative, depositing magnesium metal through a cloud of oxidizing material so that a chemical reaction occurs and magnesium oxide is deposited onto the support membrane or on the underlayer directly.

39 1 53 Patented July 20, l 935 The invention will be more clearly understood by reference to the accompanying single sheet of drawings wherein;

FIG. 1 is a partial sectional view of an Image Orthicon made in accordance with this invention;

FIG. 2 is an annular sectional view of a storage target in the process of being made, in accordance with the invention;

FIG. 3 is a somewhat schematic plan view of apparatus for the novel process of manufacturing a storage type target in accordance with this invention.

Referring now to FIG. 1, there is shown an Image Orthicon tube 10. The tube 10 comprises an evacuated envelope 12 having an electron gun (not shown) positioned in the stem end thereof (to the left as viewed in FIG. 1). Positioned on the inner surface of the face plate, in the opposite end of the envelope, is a photocathode 16. The photocathode may be of any conventional materiais, examples of which are the 8-10 photosurface described in US. Patent No. 2,682,479 issued to Johnson, or the multi-alkali photosurface described in U.S. Patent No. 2,770,561 issued to Sommer.

In the envelope l2, spaced from the photocathode 16 toward the electron gun, is a semiconducting type storage target 13. The storage target 18 comprises an annular metallic support member 23 having a thin film of magnesium oxide thereon.

During operation of the Image Orthicon 10, light from a scene to be reproduced is directed through the transparent face plate onto the photocathode 16 producing a photo-electron image corresponding to the light from the scene. The photo-electron image is focused, and accelerated, by known techniques, and lands on one side of the storage target 18 to provide a charge pattern thereon. An electron beam from the electron gun scans the opposite side of the storage target 18 to remove the charge pattern therefrom. The electron beam is reflected back toward the electron gun where it is fed into a con ventional electron multiplier which produces electrical output signals from the tube. The output signals correspond to the light from the scene to be reproduced.

In order to manufacture a storage target 18, shown more clearly in FIG. 2, a thin film of organic material 24 is first deposited on and across an apertured support member or metallic support ring 20 before one attempts to deposit either magnesium metal, or magnesium oxide. The thin organic film 24 may be any of several known materials. Examples of materials which have been found suitable are collodion. nitrocellulose, or isobutylmethacrylate. The organic film 24 functions as a temporary substrate for a magnesium metal layer, or for the magnesium oxide layer. In accordance with this invention, and due to the fact that it is very difiicult to evaporate a uniform and reasonably thick layer of magnesium metal onto the organic layer 24, a thin underlayer 26 of a material which deposits readily on the organic substrate 24 is provided. The underlayer 26 is selected for its properties of readily depositing onto the organic substrate and its property of readily permitting a uniform and sufficiently thick magnesium layer to be deposited thereon. It was found by applicant that magnesium can be evaporated to the required thickness and uniformity onto an organic film if first a thin underlayer 26 has been deposited.

The underlayer 26 should be too thin to be laterally, electrically conducting after the target has passed through the standard manufacturing process. The underlayer 26 may be deposited by evaporation of the selected material in a vacuum of approximately 10 mm. of mercury. Two materials for the underlayer 26 which have been found to be suitable are aluminum or gold. Many other materials, (metals as well as oxides and salts,) arebe-v lieved to be suitable for use as the underlayer 26 prior to the subsequent magnesium metal deposition.

A particular example of the underlayer 26 is a deposit of gold or aluminum which has been evaporated-onto a nitrocellulose support membrane 24 and which is of a thickness of approximately 20 to 30 Angstrom units. Onto thisunderlayer 26 there is deposited, by evaporation in a good vacuum, a film of magnesium metal that is approximately 1,000 Angstrom units thick.

When this has been done, the support membrane 24 is removed, which results in a self-supporting magnesium film attached to the support ring 20. In the case of many organic support membranes 24, the temporary support membrane can be removed by heating the target in an oxidizingatmosphere, such as air or oxygen, to approximately 200 C. for a period of time of approximately minutes. An oxidizing atmosphere is chosen in order to avoid the formation of carbon deposits on the magnesium film. Another suitable Way of removing the support membrane film 24 comprises exposing the film 24 to the vapor of a liquid in which the film is soluble but which does not attack the magnesium layer. As an example, collodion or isobutyl-methacrylate films can be removed from underneath the magnesium layer, without damaging the magnesium layer, by exposing the film to acetone or amyl-acetate vapor.

The next step in manufacturing the targets involves the oxidation of the thin layer of magnesium metal. This may be accomplished by heating the target in an oxygen atmosphere at a temperature of about 450 C. The oxygen fed into the system should be carefully dried since the secondary electron emission gain of the magnesium film is greatly reduced by exposure of the film to water vapor.

, When the support membrane 24 is removed by heating in an'oxidized atmosphere, the steps of removing the membrane and oxidizing the metallic magnesium may be combined in a single operation by placing the target in an oxygen atmosphere and heating to a temperature of about 450 C. for a period of time of one hour.

Another advantage which is gained by having the underlayer 26 beneath the magnesium oxide film arises from the fact that the underlayer 26 will become the surface layer on one side of the finished magnesium oxide target. This surface layer can, by proper selection of materials, be made to have a lower scattering coefficient for the electrons of the scanning electron beam than the scattering coefiicient of a magnesium oxide surface. Therefore, if the underlayer 26 is positioned on the scanned or gun side of the finished target, in the tube 10, larger values of beam modulation'are to be expected than that found when bare magnesium oxide is used. l

Referring now to FIG. 3, the apparatus there shown for manufacturing targets may be used for targets with or Without the underlayer 26 previously described. There is illustrated a technique for depositing chemical compounds by evaporating one component of the final material through a cloud of another component of the final material. Thus, magnesium metal is evaporated in a high vacuum system, illustrated by the bell jar 30, through an oxygen cloud, from a standard conical tungsten heater or evaporator boat 32. The target ring having its organic film 24 positioned thereon, with'or without the underlayer 26, is positioned a suitable distance above the evaporator 32 to function as a substrate. A small amount of oxygen is introduced into the system at a point between the evaporator 32 and the substrate. In the particular example of this invention shown, a glass bottle 34 with a thin neck 36, having a small orifice at its end was used. The oxygen is formed by heating mercuric oxide in the bottle 34, by means of heating a coil 38 by an electric current from a source not shown, resulting in oxygen gas being forced through the orifice.

Due to the relatively fast pumping speed of the vacuum system and the slow rate of efilux of the oxygen from the bottle 34, an appreciable pressure of oxygen was generated only in the immediate vicinity of the orifice. The pressure in the vacuum system at some distance from the oxygen source did not show any significant increase due the use of standard evaporating techniques.

to the gas influx. Thus, a fairly well localized oxygen cloud was formed above the magnesium evaporator.

As a result of the process illustrated in FIG. 3 a magnesium oxide film is formed in the space above the evaporator 32, and a magnesium oxide film is deposited on the substrate. It is important to note that, when utilizing the apparatus shownin FIGJ3, the evaporator 32 and the oxygen source 34 do not need to be heated above approximately 700 C. to provide the magnesium oxide layer; whereas, to evaporate magnesium oxide directly, temperatures of about 3,000 C. are needed which prohibits The tech nique illustrated in FIG. 3 can, of course, be used for compounds other than the magnesium oxide, for example, other oxides, such as aluminum oxide, may be deposited in thesame manner.

The technique disclosed in FIG. 3 is also suitable for depositing layers of varying composition by changing the conditions of the process while the process is being accomplished. As an example, the rate of oxygen outflow, or the rate the metal is supplied from the evaporator 32 may be altered during progress of deposition of the composition.

Thus, the apparatus shown in FIG. 3 provides a film of magnesium oxide either directly on the support membrane '24 or onto the underlayer 2-6 as described in connection with FIG. 2. In either instance, the organic film 24 may be removed by an air brake at approximately 200 C. leaving a self-supporting magnesium oxide film.

What is claimed is:

1. The method of manufacturing a target electrode assembly for use in a television pickup tube comprising the steps of: a 1

(a) positioning a supporting membrane made of an organic material across an opening in an apertured support member, (b) then evaporating annunde-rlayer of film made of a material selected from the group consisting of gold and aluminum to a thickness of approximately 30 Angstrom units, onto said supporting membrane,

while said film is supported by said membrane,

(c) thereafter evaporating magnesium oxide onto said underlayer him, and (d) then removing said supporting membrane by changing the material of said membrane to a form that is automatically separable from said underlayer 2. The method of manufacturing a target electrode assembly for use in a television pickup tube, comprising the-steps of: v

(a) positioning a removable supporting membrane made of an organic material across an opening in an apertured support-member,

(b) then evaporating an underlayer film of a metal selected from the group consisting of gold and aluminum, to a thinness of approximately 30 Angstrom units,

(c) then evaporating a relatively thick layer of magnesium metal onto said underlayer film,

(d) oxidizing said magnesium metal and converting .said magnesium metal to magnesium oxide, and

(e) oxidizing said membrane and finally removing the same.

' 3. -The method of making a target assembly for use in a television pick-up tube comprising an electron gun, a target assembly and a photocathode spaced in that order in an evacuated envelope, said method comprising the steps of:

(e) positioning across a support ring a membrane made of a material selected from the group consisting of collodion, nitrocellulose and isobutyl methacrylate, said member being sufiicie-ntly thick to serve as a support,

(b) evaporating in an evacuated ambient a layer of metal selected from the group consisting of aluminum and gold, on said support membrane, wherein said layer has a thickness of from about 20 to about 30 Angstrom units,

(c) evaporating in an evacuated ambient a layer of magnesium metal on said layer of material to a thickness of about 1000 Angstrom units,

(d) heating said magnesium metal layer in an oxygen atmosphere at a temperature of about 450 C. to convert said magnesium metal into magnesium oxide, and

(e) finally chemically removing said temporary support member.

4. The method of making a target electrode assembly as claimed in claim 3, wherein the step of heating said magnesium to convert it into magnesium oxide and the step of chemically removing said temporary support membrane, are performed simultaneously by heating said target electrode in an oxiding atmosphere.

References Cited by the Examiner UNITED STATES PATENTS Zworykin et a1 117-222 'F-arnsworth 117-222 Flory 117-211 Wilder 117-210 Gier 117-46 Sheldon 313-65 Janssen et a1 117-106 Dobischek et a1. 117-106 Sternglass et al 313-103 Schneeberger 313-65 Rigot 117-210 X RICHARD D. NEVIUS, Primary Examiner. 20 \VILLIAM D. MARTIN, JOSEPH REBOIJD,

Examiners.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US2205055 *30 Apr 193618 Jun 1940Rca CorpElectric discharge device
US2251124 *10 Aug 193529 Jul 1941Farnsworth Television & RadioCathode ray amplifying tube
US2373752 *25 Jan 194117 Apr 1945Rca CorpPicture transmitter tube mosaic screen
US2579772 *17 Oct 194925 Dec 1951Remington Rand IncMethod of making an image storage screen
US2665220 *26 Feb 19495 Jan 1954Hartford Nat Bank & Trust CoMethod of manufacturing luminescent screens
US2747131 *12 Oct 195122 May 1956Emanuel Sheldon EdwardElectronic system sensitive to invisible images
US2798007 *25 Jun 19542 Jul 1957Philips CorpMethod of applying a light-diffusing layer to a glass surface
US2802127 *3 Feb 19546 Aug 1957Dietrich DobischekDynode coating
US2898499 *23 May 19564 Aug 1959Westinghouse Electric CorpTransmission secondary emission dynode structure
US2928969 *11 May 195615 Mar 1960Westinghouse Electric CorpImage device
US2998331 *9 Jan 195929 Aug 1961CsfMethod of making storage tube targets and resulting article
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3363126 *3 Jun 19669 Jan 1968Army UsaImage orthicon cathode ray tube with copper screen target having a chromium supported magnesium oxide film
US3755865 *17 Sep 19704 Sep 1973Gen ElectricNovel mesh-reinforced sec target for camera tubes
US4481999 *23 Feb 198213 Nov 1984The United States Of America As Represented By The United States Department Of EnergyMethod of forming a thin unbacked metal foil
Classifications
U.S. Classification164/46, 164/131, 164/95, 313/376
International ClassificationH01J29/41, H01J29/10
Cooperative ClassificationH01J29/413
European ClassificationH01J29/41B