US3346755A - Dark current reduction in photoconductive target by barrier junction between opposite conductivity type materials - Google Patents
Dark current reduction in photoconductive target by barrier junction between opposite conductivity type materials Download PDFInfo
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- US3346755A US3346755A US539107A US53910766A US3346755A US 3346755 A US3346755 A US 3346755A US 539107 A US539107 A US 539107A US 53910766 A US53910766 A US 53910766A US 3346755 A US3346755 A US 3346755A
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- 239000000463 material Substances 0.000 title description 22
- 230000004888 barrier function Effects 0.000 title description 3
- WMWLMWRWZQELOS-UHFFFAOYSA-N bismuth(III) oxide Inorganic materials O=[Bi]O[Bi]=O WMWLMWRWZQELOS-UHFFFAOYSA-N 0.000 claims description 24
- 229910045601 alloy Inorganic materials 0.000 claims description 23
- 239000000956 alloy Substances 0.000 claims description 23
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 claims description 17
- 229910052714 tellurium Inorganic materials 0.000 claims description 16
- UHYPYGJEEGLRJD-UHFFFAOYSA-N cadmium(2+);selenium(2-) Chemical compound [Se-2].[Cd+2] UHYPYGJEEGLRJD-UHFFFAOYSA-N 0.000 claims description 12
- 239000000758 substrate Substances 0.000 claims description 12
- 229910001215 Te alloy Inorganic materials 0.000 claims description 6
- YYDHEZLTMPKETQ-UHFFFAOYSA-N [Te].[Se] Chemical compound [Te].[Se] YYDHEZLTMPKETQ-UHFFFAOYSA-N 0.000 claims 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 26
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 25
- 229910052737 gold Inorganic materials 0.000 description 25
- 239000010931 gold Substances 0.000 description 25
- 229910052711 selenium Inorganic materials 0.000 description 19
- 239000011669 selenium Substances 0.000 description 19
- 239000004065 semiconductor Substances 0.000 description 10
- 229910001370 Se alloy Inorganic materials 0.000 description 8
- 229910052785 arsenic Inorganic materials 0.000 description 7
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 7
- 239000011521 glass Substances 0.000 description 6
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 6
- 238000001704 evaporation Methods 0.000 description 5
- 230000000087 stabilizing effect Effects 0.000 description 5
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 230000008020 evaporation Effects 0.000 description 4
- 229910052732 germanium Inorganic materials 0.000 description 4
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 4
- YBMRDBCBODYGJE-UHFFFAOYSA-N germanium oxide Inorganic materials O=[Ge]=O YBMRDBCBODYGJE-UHFFFAOYSA-N 0.000 description 4
- PVADDRMAFCOOPC-UHFFFAOYSA-N oxogermanium Chemical compound [Ge]=O PVADDRMAFCOOPC-UHFFFAOYSA-N 0.000 description 4
- WUPHOULIZUERAE-UHFFFAOYSA-N 3-(oxolan-2-yl)propanoic acid Chemical compound OC(=O)CCC1CCCO1 WUPHOULIZUERAE-UHFFFAOYSA-N 0.000 description 3
- 229910052980 cadmium sulfide Inorganic materials 0.000 description 3
- 230000031700 light absorption Effects 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229940007424 antimony trisulfide Drugs 0.000 description 2
- NVWBARWTDVQPJD-UHFFFAOYSA-N antimony(3+);trisulfide Chemical compound [S-2].[S-2].[S-2].[Sb+3].[Sb+3] NVWBARWTDVQPJD-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000000903 blocking effect Effects 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 230000002411 adverse Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000005350 fused silica glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical group [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
Images
Classifications
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J29/00—Details of cathode-ray tubes or of electron-beam tubes of the types covered by group H01J31/00
- H01J29/02—Electrodes; Screens; Mounting, supporting, spacing or insulating thereof
- H01J29/10—Screens on or from which an image or pattern is formed, picked up, converted or stored
- H01J29/36—Photoelectric screens; Charge-storage screens
- H01J29/39—Charge-storage screens
- H01J29/45—Charge-storage screens exhibiting internal electric effects caused by electromagnetic radiation, e.g. photoconductive screen, photodielectric screen, photovoltaic screen
- H01J29/451—Charge-storage screens exhibiting internal electric effects caused by electromagnetic radiation, e.g. photoconductive screen, photodielectric screen, photovoltaic screen with photosensitive junctions
- H01J29/456—Charge-storage screens exhibiting internal electric effects caused by electromagnetic radiation, e.g. photoconductive screen, photodielectric screen, photovoltaic screen with photosensitive junctions exhibiting no discontinuities, e.g. consisting of uniform layers
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F99/00—Subject matter not provided for in other groups of this subclass
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S148/00—Metal treatment
- Y10S148/064—Gp II-VI compounds
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S148/00—Metal treatment
- Y10S148/072—Heterojunctions
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S257/00—Active solid-state devices, e.g. transistors, solid-state diodes
- Y10S257/917—Plural dopants of same conductivity type in same region
Definitions
- a vidicon pickup tube generally comprises an evacuated glass bulb within which is mounted an electron gun of any suitable construction for developing a beam of electrons. The electrons so developed are focused and deflected in a desired scanning beam over a photoconductive target.
- the photoconductive target is usually supported on a light-transparent backing which may be the end wall or faceplate of a glass bulb or tube envelope.
- the target usually includes an electrically conductive light-transparent layer serving as a signal plate, and a layer of photoconductive material over the signal plate. The focused and deflected electrons are deposited on the face of the photoconductive target remote from the signal plate to produce a charge thereon.
- a further object is to provide an improved substrate for a photoconductive layer including vitreous selenium. in order to increase the thermal stability of the layer.
- Another object is to provide a target for a photoconductive device containing vitreous selenium and tellurium and in which the dark current is appreciably reduced.
- the smoothness of the substrate on which the vitreous selenium is overlaid contributes appreciably to thermal stabilization of the selenium in the vitreous state.
- the desired smoothness of the substrate is obtained in one example by first depositing a layer of bismuth trioxide on a relatively smooth glass faceplate, then coating the layer of bismuth trioxide with a relatively thin layer of gold, and coating the gold layer with a relatively thin layer of Wide band gap N-type semiconductor material.
- a photoconductive layer of vitreous selenium-tellurium alloy is applied to the relatively smooth surface of the wide band gap N-type semiconductor material.
- the relatively thin layer of wide band gap N-type semiconductor material intermediate the bold and selenium alloy layers,
- an outer stabilizing layer may be applied to the selenium alloy layer.
- FIG. 1 is a fragmentary view, partly in section, of a vidicon tube having a photoconductive target including a vitreous selenium alloy characterized by increased thermal stability of the alloy and reduced dark current; and
- FIGS. 2 and 3 are fragmentary sectional views of plural layer targets that may be used in the vidicon tube shown in FIG. 1.
- FIG. 1 a vidicon tube 10 in which a target 12 incorporates the present invention.
- the tube 10 is conventional except for the target 12.
- the tube 10 comprises an elongated glass envelope 14 closed at one end thereof by a transparent glass faceplate 16.
- the faceplate 16 is sealed across the end referred to by means of an indium ring 18 and a clamping ring 20.
- the target 12 is positioned on the inner surface of the faceplate 16.
- a mesh screen 22 mounted across one end of a tubular focusing electrode 23.
- an electron gun for providing an electron beam.
- the beam is scanned across the target 12 by suitable means such as electromagnetic coils (not shown) disposed outside of the enevelope 14.
- the target 12 is a multilayered structure that may have either of the forms illustrated in FIGS. 2 and In the form shown in FIG. 2, the target 12 comprises four layers supported on the faceplate 16.
- the first layer 24 next to the faceplate 16, comprises bismuth trioxide having a thickness of from about 10 to about 500 microns. The maximum thickness of this layer is not critical, except that it should not be so thick as to objectionably impede light transfer therethrough.
- the gold layer 26 may have a thickness of from about 10 to about 200 Angstroms.
- a third layer 28 of a wide band gap N-type semiconductor material covers the gold layer 26.
- the layer 28 may have a thickness of from about 10 to about 500 Angstroms.
- the materials suitable for the layer 28 are cadmium sulfide, cadmium selenide, bismuth trioxide or tin dioxide. Of these materials I prefer to use cadmium selenide
- a photoconductive layer 30 applied to the layer 28, comprises a vitreous alloy of selenium and tellurium.
- Arsenic may also be included. Although the arsenic may be omitted for satisfactory results, its presence contributes to improved decay.
- the layer 30 may have a thickess of from about 4 to about 7 microns.
- the layer 30 is graded so as to provide a richer concentration of tellurium at the surface of the layer adjacent to the N-type layer 28, than at the opposite surface.
- the amount of tellurium in the layer 30 is preferably gradually reduced towards the surface of the layer remote from the N-type layer 28.
- the vitreous alloy layer 30 may contain at its surface adjacent to the N-type layer 28, from 70 to 82% selenium, 17 to 29% tellurium and about 1% arsenic, all by weight. However, for best results the vitreous alloy layer 30 contained about 76% selenium, about 23% tellurium and about 1% arsenic by weight at its surface adjacent to the gold layer 26. When arsenic is not used, the selenium content may be increased by about 1% by Weight. The tellurium content in the surface region of layer 30 remote from the N-type layer 28, may be from to about by weight. The arsenic when used is uniformly distributed throughout the layer 30.
- the combination of layers 24, 26 and 28 is accompanied by several important advantages.
- One of these advan tages concerns a preservation of thermal stability of the vitreous alloy layer 30.
- Another advantage relates to a reduction in dark current.
- the smoothness of the substrate i.e., the N-type layer 28 on which the vitreous alloy layer is deposited, contributes to improved thermal stability of the vitreous character of the layer 30.
- Such smooth surface of the layer 28 involves an appreciable reduction in surface discontinuities. Since such discontinuities induce crystal growth in the vitreous alloy layer 30, their reduction or elimination by the smooth character of the N-type layer 28 effectively serves to restrain crystal growth and thereby preserve the vitreous form of the alloy layer 30.
- the smoothness of the N-type layer 28 is appreciably enhanced by the smoothness of the layer 24 of bismuth trioxide.
- Such smoothness of the layer 24 of bismuth trioxide is a consequence of several factors including the natural tendency of this material to form a smooth surface and the manner in which the layer 24 is formed, as will be described in the following.
- the junction between the N-type layer 28 and the tellurium rich surface of the vitreous alloy layer 30, restrains hole injection in the junction when reverse biased.
- Such reverse bias occurs when the gold layer 26 serving as a signal electrode is connected to a positive voltage source and the vitreous selenium alloy layer 30 is rendered negative by electrons impinging on the surface thereof remote from the layer 28.
- the junction formed by the N-type layer 28 and the P-type tellurium-rich surface of the layer 30 serves to block hole injection from the layer 28 when so biased and when layer 30 is in the non-conductive state as when in the dark. This junction may thus be termed a blocking junction.
- a stabilizing layer 32 may be provided over the surface of the layer 30 remote from the faceplate 16, as shown in FIG. 3.
- the stabilizing layer 32 may be formed of a material such as germanium, germanium oxide, antimony trisulfide or antimony trioxide. Of these materials, I have found germanium and germanium oxide to be the best.
- the substrate 16 which may be a glass or fused quartz faceplate and on which the layer 24 of bismuth trioxide is to be deposited, is characterized by the best obtainable smoothness and freedom from surface imperfections.
- One Way in which such surface smoothness may be produced is by lapping or fire polishing.
- Bismuth trioxide is then evaporated on the smooth substrate surface in an ambient containing oxygen and having a pressure of about 10 microns of mercury to form the layer 24.
- the layer 24 should have a minimum thickness of 10 microns and may have a maximum thickness determined by its light absorption as indicated before herein. Such light absorption should be sufiiciently small so as not to affect adversely a desired light energization of the target by an image to which the target is exposed. I have found that a thickness of layer 24 up to about 500 microns is not accomplished by light absorption to an objectionable degree.
- the bismuth trioxide may be evaporated from a heated boat, or in any ther suitable known manner.
- the gold signal electrode layer 26 is next applied over the bismuth trioxide layer 24 by heating a gold coated filament to evaporate gold therefrom in known manner.
- the gold evaporation step may be performed in the oxygen-containing ambient in which the layer 26 Was deposited, or in any other desired ambient.
- the gold evaporation is permitted to proceed until the resultant gold layer 26 acquires a thickness of from about 10 to about 200 Angstroms. The thickness may be monitored by a commercially available quartz thickness monitor.
- the faceplate may be removed from the evaporator in which the gold layer was formed and placed in a dust-free container and air baked at temperatures ranging from 50 C. and up to about 300 C. for approximately one hour. While this air baking step is not necessary for satisfactory results, its practice appreciably improves the operation of the finished device as a consequence of desirable changes produced in the bismuth trioxide layer 24 by this step. One of these changes is to increase the smoothness of the surface of layer 24 adjacent to the gold layer 26.
- the layer 28 of wide band gap N-type semiconductor material such as cadmium selenide, is evaporated onto the gold layer 26 to a thickness of from about 10 to about 500 Angstroms.
- the evaporation may be eifected in an ambient having a pressure of about 10 torr.
- the thickness of the layer 28 may be determined by a suitable light interference monitor in known manner.
- the coated substrate may be removed from the evaporator and air baked at temperatures from 50 to 300 C. for approximately one hour. While this step is not necessary for satisfactory results, it is desirable in that it contributes to a further reduction in dark current.
- the vitreous selenium-containing alloy layer 30 is formed to a thickness of from about 4 to about 7 microns.
- a dropping pellet technique may be employed such as is described in copending application Ser. No. 507,728 of William M. Kramer and assigned to the assignee of this application.
- the final stabilizing layer 32 of material such as germanium or germanium oxide, or other material described before herein in connection with layer 32, may be formed over the vitreous selenium alloy layer 30 by suitably evaporating the same and monitoring the thickness to a value of from about 10 to about Angstroms.
- a target for a photoconductive device comprising:
- a relatively thin layer of wide band gap N-type semiconductor material on said gold layer selected from the group consisting of cadmium sulfide, cadmium selenide, bismuth trioxide and tin dioxide, and
- a target for a photoconductive device according to claim 1 and wherein:
- said layer of bismuth trioxide has a thickness of from about to about 500 microns
- said layer of gold has a thickness of from about 10 to about 200 Angstroms
- said layer of wide band gap N-type semiconductor material has a thickness of from about 10 to about 500 Angstroms
- vitreous selenium-containing alloy having a thickness of from about 4 to about 7 microns.
- a target for a photoconductive device comprising:
- the tellurium in said vitreous alloy being graded in content from a maximum at the surface of said alloy adjacent to said layer of cadmium selenide, to a minimum in the opposite surface of said alloy layer.
- vitreous selenium-tellurium alloy includes about 23% tellurium by weight at the surface thereof adjacent to said cadmium selenide layer, and from about 0 to about 10% of tellurium by weight at the opposite surface of said alloy layer.
- a target for a photoconductive device comprising:
- a layer of wide band gap N-type semiconductor material on said signal electrode layer selected from the group consisting of cadmium sulfide, cadmium selenide, bismuth trioxide and tin dioxide,
- said last-named layer having a thickness of from about 10 to about 500 Angstroms whereby the outer surface of said layer remote from said signal electrode layer is characterized by substantially the same relative smoothness as said signal electrode layer, and
- a target for a photoconductive device and wherein said bismuth trioxide layer is relatively smooth and said signal electrode layer is made of gold having a thickness of from about 10 to about 200 Angstroms, whereby the surface of said gold layer remote from said bismuth trioxide layer is substantially as smooth as said bismuth trioxide layer, for improving the thermal stability of said vitreous selenium-tellurium alloy layer.
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- Physics & Mathematics (AREA)
- Electromagnetism (AREA)
- Image-Pickup Tubes, Image-Amplification Tubes, And Storage Tubes (AREA)
- Formation Of Various Coating Films On Cathode Ray Tubes And Lamps (AREA)
Description
Oct. 10, 1967 J. DRESNER 3,346,755 DARK CURRENT REDUCTION IN PHOTOCONDUCTIVE TARGET BY BARRIER JUNCTION BETWEEN OPPOSITE CONDUCTIVITY TYPE MATERIALS Filed March 31, 1966 Z0 gmunl lnllmk @V I a I I 7 i 32 INVENTOR. .bmwDzim/ee.
United States Patent O 3,346,755 DARK CURRENT REDUCTION IN PHOTOCON- DUCTIVE TARGET BY BARRIER JUNCTION BETWEEN OPPOSITE CONDUCTIVITY TYPE MATERIALS Joseph Dresner, Princeton, N.J., assignor to Radio Corporation of America, a corporation of Delaware Filed Mar. 31, 1966, Ser. No. 539,107 7 Claims. (Cl. 313-94) My invention relates to targets for photoconductive devices and particularly to an improved target including vitreous selenium.
One type of photoconductive device in which the target herein disclosed is adapted to be used to advantage is a vidicon pickup tube. A vidicon pickup tube generally comprises an evacuated glass bulb within which is mounted an electron gun of any suitable construction for developing a beam of electrons. The electrons so developed are focused and deflected in a desired scanning beam over a photoconductive target.
The photoconductive target is usually supported on a light-transparent backing which may be the end wall or faceplate of a glass bulb or tube envelope. The target usually includes an electrically conductive light-transparent layer serving as a signal plate, and a layer of photoconductive material over the signal plate. The focused and deflected electrons are deposited on the face of the photoconductive target remote from the signal plate to produce a charge thereon.
One problem in connection with a photoconductor including selenium in the vitreous state is the relatively rapid reversion of the vitreous selenium to the crystalline state. Selenium is objectionably conductive in the crystalline state. Such reversion is particularly pronounced when the photoconductor is heated during fabricati-onand operation of a device in which it is used. While prior attempts to solve this problem have resulted in some improvement with respect to the thermal stability of a selenium-containing photoconductor, further increase in thermal stability is desirable for increased operating life and improved performance of the device.
Another problem arising where a selenium-containing photoconductor is used, concerns dark current. While prior attempts have resulted in appreciable reduction of dark current, a further reduction thereof is desirable for optimum results.
Accordingly, it is an object of the invention to improve the thermal stability of a target for a photoconductive device including vitreous selenium.
A further object is to provide an improved substrate for a photoconductive layer including vitreous selenium. in order to increase the thermal stability of the layer.
Another object is to provide a target for a photoconductive device containing vitreous selenium and tellurium and in which the dark current is appreciably reduced.
I have discovered that where vitreous selenium is used in the target of a photoconductive device, the smoothness of the substrate on which the vitreous selenium is overlaid contributes appreciably to thermal stabilization of the selenium in the vitreous state. As herein disclosed, the desired smoothness of the substrate is obtained in one example by first depositing a layer of bismuth trioxide on a relatively smooth glass faceplate, then coating the layer of bismuth trioxide with a relatively thin layer of gold, and coating the gold layer with a relatively thin layer of Wide band gap N-type semiconductor material. To the relatively smooth surface of the wide band gap N-type semiconductor material is applied a photoconductive layer of vitreous selenium-tellurium alloy. The relatively thin layer of wide band gap N-type semiconductor material intermediate the bold and selenium alloy layers,
not only contributes to thermal stability of the vitreous selenium alloy outer layer but also is accompanied by an appreciable reduction in dark current.
If desired, an outer stabilizing layer may be applied to the selenium alloy layer.
Further objects and features of the invention will become apparent as the present description continues.
In the drawing, to which referece is now made for a description of an embodiment of the invention by way of example: 7
FIG. 1 is a fragmentary view, partly in section, of a vidicon tube having a photoconductive target including a vitreous selenium alloy characterized by increased thermal stability of the alloy and reduced dark current; and
FIGS. 2 and 3 are fragmentary sectional views of plural layer targets that may be used in the vidicon tube shown in FIG. 1.
In FIG. 1 is shown a vidicon tube 10 in which a target 12 incorporates the present invention. The tube 10 is conventional except for the target 12. The tube 10 comprises an elongated glass envelope 14 closed at one end thereof by a transparent glass faceplate 16. The faceplate 16 is sealed across the end referred to by means of an indium ring 18 and a clamping ring 20. The target 12 is positioned on the inner surface of the faceplate 16. Closely spaced from the target 12 is a mesh screen 22 mounted across one end of a tubular focusing electrode 23. In the other end portion (not shown) of the envelope 14 is positioned an electron gun for providing an electron beam. The beam is scanned across the target 12 by suitable means such as electromagnetic coils (not shown) disposed outside of the enevelope 14.
The target 12 is a multilayered structure that may have either of the forms illustrated in FIGS. 2 and In the form shown in FIG. 2, the target 12 comprises four layers supported on the faceplate 16. The first layer 24 next to the faceplate 16, comprises bismuth trioxide having a thickness of from about 10 to about 500 microns. The maximum thickness of this layer is not critical, except that it should not be so thick as to objectionably impede light transfer therethrough. On the bismuth trioxide layer 24, is a relatively thin layer 26 of gold which serves as a signal electrode. The gold layer 26 may have a thickness of from about 10 to about 200 Angstroms. A third layer 28 of a wide band gap N-type semiconductor material covers the gold layer 26. The layer 28 may have a thickness of from about 10 to about 500 Angstroms. Among the materials suitable for the layer 28 are cadmium sulfide, cadmium selenide, bismuth trioxide or tin dioxide. Of these materials I prefer to use cadmium selenide for best results.
A photoconductive layer 30 applied to the layer 28, comprises a vitreous alloy of selenium and tellurium. Arsenic may also be included. Although the arsenic may be omitted for satisfactory results, its presence contributes to improved decay. The layer 30 may have a thickess of from about 4 to about 7 microns.
The layer 30 is graded so as to provide a richer concentration of tellurium at the surface of the layer adjacent to the N-type layer 28, than at the opposite surface. The amount of tellurium in the layer 30 is preferably gradually reduced towards the surface of the layer remote from the N-type layer 28.
For good results the vitreous alloy layer 30 may contain at its surface adjacent to the N-type layer 28, from 70 to 82% selenium, 17 to 29% tellurium and about 1% arsenic, all by weight. However, for best results the vitreous alloy layer 30 contained about 76% selenium, about 23% tellurium and about 1% arsenic by weight at its surface adjacent to the gold layer 26. When arsenic is not used, the selenium content may be increased by about 1% by Weight. The tellurium content in the surface region of layer 30 remote from the N-type layer 28, may be from to about by weight. The arsenic when used is uniformly distributed throughout the layer 30.
The combination of layers 24, 26 and 28 is accompanied by several important advantages. One of these advan tages concerns a preservation of thermal stability of the vitreous alloy layer 30. Another advantage relates to a reduction in dark current.
With respect to thermal stability of the vitreous alloy layer 30, I have found that the smoothness of the substrate, i.e., the N-type layer 28 on which the vitreous alloy layer is deposited, contributes to improved thermal stability of the vitreous character of the layer 30. Such smooth surface of the layer 28 involves an appreciable reduction in surface discontinuities. Since such discontinuities induce crystal growth in the vitreous alloy layer 30, their reduction or elimination by the smooth character of the N-type layer 28 effectively serves to restrain crystal growth and thereby preserve the vitreous form of the alloy layer 30. I have found that the smoothness of the N-type layer 28 is appreciably enhanced by the smoothness of the layer 24 of bismuth trioxide. Such smoothness of the layer 24 of bismuth trioxide is a consequence of several factors including the natural tendency of this material to form a smooth surface and the manner in which the layer 24 is formed, as will be described in the following.
As far as reduced dark current is concerned, I have found that the junction between the N-type layer 28 and the tellurium rich surface of the vitreous alloy layer 30, restrains hole injection in the junction when reverse biased. Such reverse bias occurs when the gold layer 26 serving as a signal electrode is connected to a positive voltage source and the vitreous selenium alloy layer 30 is rendered negative by electrons impinging on the surface thereof remote from the layer 28. The junction formed by the N-type layer 28 and the P-type tellurium-rich surface of the layer 30 serves to block hole injection from the layer 28 when so biased and when layer 30 is in the non-conductive state as when in the dark. This junction may thus be termed a blocking junction.
For further stabilization of the vitreous alloy layer 30 a stabilizing layer 32 may be provided over the surface of the layer 30 remote from the faceplate 16, as shown in FIG. 3. The stabilizing layer 32 may be formed of a material such as germanium, germanium oxide, antimony trisulfide or antimony trioxide. Of these materials, I have found germanium and germanium oxide to be the best.
In making the target herein disclosed I take great care to assure that the substrate 16, which may be a glass or fused quartz faceplate and on which the layer 24 of bismuth trioxide is to be deposited, is characterized by the best obtainable smoothness and freedom from surface imperfections. One Way in which such surface smoothness may be produced is by lapping or fire polishing.
Bismuth trioxide is then evaporated on the smooth substrate surface in an ambient containing oxygen and having a pressure of about 10 microns of mercury to form the layer 24. The layer 24 should have a minimum thickness of 10 microns and may have a maximum thickness determined by its light absorption as indicated before herein. Such light absorption should be sufiiciently small so as not to affect adversely a desired light energization of the target by an image to which the target is exposed. I have found that a thickness of layer 24 up to about 500 microns is not accomplished by light absorption to an objectionable degree. The bismuth trioxide may be evaporated from a heated boat, or in any ther suitable known manner.
The gold signal electrode layer 26 is next applied over the bismuth trioxide layer 24 by heating a gold coated filament to evaporate gold therefrom in known manner. The gold evaporation step may be performed in the oxygen-containing ambient in which the layer 26 Was deposited, or in any other desired ambient. The gold evaporation is permitted to proceed until the resultant gold layer 26 acquires a thickness of from about 10 to about 200 Angstroms. The thickness may be monitored by a commercially available quartz thickness monitor.
After the application of the bismuth trioxide layer 24 and the gold layer 26 to the faceplate 26, the faceplate may be removed from the evaporator in which the gold layer was formed and placed in a dust-free container and air baked at temperatures ranging from 50 C. and up to about 300 C. for approximately one hour. While this air baking step is not necessary for satisfactory results, its practice appreciably improves the operation of the finished device as a consequence of desirable changes produced in the bismuth trioxide layer 24 by this step. One of these changes is to increase the smoothness of the surface of layer 24 adjacent to the gold layer 26.
Following the application of the gold layer 26, and the baking step, the layer 28 of wide band gap N-type semiconductor material, such as cadmium selenide, is evaporated onto the gold layer 26 to a thickness of from about 10 to about 500 Angstroms. The evaporation may be eifected in an ambient having a pressure of about 10 torr. The thickness of the layer 28 may be determined by a suitable light interference monitor in known manner. After evaporation of layer 28, the coated substrate may be removed from the evaporator and air baked at temperatures from 50 to 300 C. for approximately one hour. While this step is not necessary for satisfactory results, it is desirable in that it contributes to a further reduction in dark current.
After the layer 28 has been applied, the vitreous selenium-containing alloy layer 30 is formed to a thickness of from about 4 to about 7 microns. In order to provide a desired grading of the tellurium content of the alloy of from about 17 to about 29% by weight of tellurium in the surface region of the layer 28 adjacent to layer 30, from about 0 to about 10% by weight of tellurium in the opposite surface region of layer 28, and about 1% by weight of arsenic, if desired, a dropping pellet technique may be employed such as is described in copending application Ser. No. 507,728 of William M. Kramer and assigned to the assignee of this application.
The final stabilizing layer 32 of material such as germanium or germanium oxide, or other material described before herein in connection with layer 32, may be formed over the vitreous selenium alloy layer 30 by suitably evaporating the same and monitoring the thickness to a value of from about 10 to about Angstroms.
It is apparent from the foregoing that I have provided an improved vitreous selenium alloy target for a photoconductive device.
I claim:
1. A target for a photoconductive device comprising:
(a) a light transparent substrate,
(b) a relatively thick layer of bismuth trioxide on said substrate,
(c) a relatively thin layer of gold on said bismuth trioxide layer,
(d) a relatively thin layer of wide band gap N-type semiconductor material on said gold layer, selected from the group consisting of cadmium sulfide, cadmium selenide, bismuth trioxide and tin dioxide, and
(e) a relatively thick layer containing vitreous selenium on said layer of wide band gap N-type semiconductor material.
2. A target for a photoconductive device according to claim 1, and wherein said relatively thick layer containing vitreous selenium is overlaid With a stabilizing layer made of a material selected from the group consisting of germanium, germanium oxide, antimony trisulfide and antimony trioxide.
3. A target for a photoconductive device according to claim 1 and wherein:
(a) said layer of bismuth trioxide has a thickness of from about to about 500 microns,
(b) said layer of gold has a thickness of from about 10 to about 200 Angstroms,
(c) said layer of wide band gap N-type semiconductor material has a thickness of from about 10 to about 500 Angstroms, and
(d) said vitreous selenium-containing alloy having a thickness of from about 4 to about 7 microns.
4. A target for a photoconductive device comprising:
(a) an air-baked substrate including a support and succeeding layers of bismuth trioxide and gold on said support,
(b) a layer of cadmium selenide on said gold, and
(c) a layer of vitreous selenium-tellurium alloy on said layer of cadmium selenide,
(l) the tellurium in said vitreous alloy being graded in content from a maximum at the surface of said alloy adjacent to said layer of cadmium selenide, to a minimum in the opposite surface of said alloy layer.
5. A target for a photoconductive device according to claim 4 and wherein said vitreous selenium-tellurium alloy includes about 23% tellurium by weight at the surface thereof adjacent to said cadmium selenide layer, and from about 0 to about 10% of tellurium by weight at the opposite surface of said alloy layer.
6. A target for a photoconductive device comprising:
(a) a substrate having a relatively smooth surfaced outer signal electrode layer thereon, and a layer of bismuth trioxide having a thickness of from about 10 to about 500 microns under said signal electrode layer,
(b) a layer of wide band gap N-type semiconductor material on said signal electrode layer, selected from the group consisting of cadmium sulfide, cadmium selenide, bismuth trioxide and tin dioxide,
6 (1) said last-named layer having a thickness of from about 10 to about 500 Angstroms whereby the outer surface of said layer remote from said signal electrode layer is characterized by substantially the same relative smoothness as said signal electrode layer, and
(c) a relatively thick layer of a vitreous seleniumtellurium alloy on said layer of N-type semiconductor material, said vitreous alloy containing by Weight about 23% tellurium in a surface thereof whereby said surface exhibits P-type conductivity, said surface being adjacent to said N-type layer for forming a blocking junction therewith,
(d) whereby said target is characterized by reduced dark current and the thermal stability of said vitreous alloy is improved.
7. A target for a photoconductive device according to claim 6 and wherein said bismuth trioxide layer is relatively smooth and said signal electrode layer is made of gold having a thickness of from about 10 to about 200 Angstroms, whereby the surface of said gold layer remote from said bismuth trioxide layer is substantially as smooth as said bismuth trioxide layer, for improving the thermal stability of said vitreous selenium-tellurium alloy layer.
References Cited UNITED STATES PATENTS 6/1959 Heijne et a1 3l3--65 3/1967 Dresner et al 313-94 X
Claims (1)
- 4. A TARGET FOR A PHOTOCONDUCTIVE DEVICE COMPRISING: (A) AN AIR-BAKED SUBSTRATE INCLUDING A SUPPORT AND SUCCEEDING LAYERS OF BISMUTH TRIOXIDE AND GOLD ON SAID SUPPORT, (B) A LAYER OF CADMIUM SELENIDE ON SAID GOLD, AND (C) A LAYER OF VITREOUS SELENIUM-TELLURIUM ALLOY ON SAID LAYER OF CADMIUM SELENIDE, (1) THE TELLURIUM IN SAID VITREOUS ALLOY BEING GRADED IN CONTENT FROM A MAXIMUM AT THE SURFACE OF SAID ALLOY ADJACENT TO SAID LAYER OF CADMIUM SELENIDE, TO A MINIMUM IN THE OPPOSITE SURFACE OF SAID ALLOY LAYER.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US539107A US3346755A (en) | 1966-03-31 | 1966-03-31 | Dark current reduction in photoconductive target by barrier junction between opposite conductivity type materials |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US539107A US3346755A (en) | 1966-03-31 | 1966-03-31 | Dark current reduction in photoconductive target by barrier junction between opposite conductivity type materials |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3346755A true US3346755A (en) | 1967-10-10 |
Family
ID=24149810
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US539107A Expired - Lifetime US3346755A (en) | 1966-03-31 | 1966-03-31 | Dark current reduction in photoconductive target by barrier junction between opposite conductivity type materials |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3346755A (en) |
Cited By (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3405298A (en) * | 1965-03-04 | 1968-10-08 | Rca Corp | Photoconductive device having a target including a selenium blocking layer |
| US3519866A (en) * | 1967-09-26 | 1970-07-07 | Rca Corp | Photoconductive pickup tube having opaque gold pattern encapsulated in tin oxide layer |
| US3571646A (en) * | 1967-07-17 | 1971-03-23 | Tokyo Shibaura Electric Co | Photoconductive target with n-type layer of cadmium selenide including cadmium chloride and cuprous chloride |
| US3783324A (en) * | 1972-09-11 | 1974-01-01 | Rca Corp | Photosensitive charge storage electrode having a selectively conducting protective layer of matching valence band on its surface |
| US3816787A (en) * | 1970-08-17 | 1974-06-11 | Tokyo Shibaura Electric Co | Photoconductor comprising cadmium selenide |
| DE2411517A1 (en) * | 1973-03-12 | 1974-09-26 | Hitachi Ltd | METHOD FOR PRODUCING A LIGHT SENSITIVE HETEROGENIC DIODE |
| US3858074A (en) * | 1971-11-09 | 1974-12-31 | Matsushita Electric Industrial Co Ltd | Photoelectric transducer element including a heterojunction formed by a photoelectric transducer film and an intermediate film having a larger energy gap than the photoelectric transducer film |
| JPS5023717A (en) * | 1973-07-02 | 1975-03-14 | ||
| US3890525A (en) * | 1972-07-03 | 1975-06-17 | Hitachi Ltd | Photoconductive target of an image pickup tube comprising graded selenium-tellurium layer |
| US3922579A (en) * | 1970-04-22 | 1975-11-25 | Hitachi Ltd | Photoconductive target |
| US4240006A (en) * | 1977-12-26 | 1980-12-16 | Sony Corporation | Photoconductive layer and target structure for image pickup tube |
| US4307319A (en) * | 1975-10-03 | 1981-12-22 | Hitachi, Ltd. | Semiconductor layer of oxygen depletion type cerium oxide or lead oxide |
| US8322906B2 (en) | 2011-08-08 | 2012-12-04 | XtraLight Manufacturing Partnership Ltd | Versatile lighting units |
| US9644829B2 (en) | 2013-04-25 | 2017-05-09 | Xtralight Manufacturing, Ltd. | Systems and methods for providing a field repairable light fixture with a housing that dissipates heat |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2890359A (en) * | 1953-06-13 | 1959-06-09 | Philips Corp | Camera tube |
| US3310700A (en) * | 1964-05-28 | 1967-03-21 | Rca Corp | Photoconductive device incorporating stabilizing layers on the face of the selenium layer |
-
1966
- 1966-03-31 US US539107A patent/US3346755A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2890359A (en) * | 1953-06-13 | 1959-06-09 | Philips Corp | Camera tube |
| US3310700A (en) * | 1964-05-28 | 1967-03-21 | Rca Corp | Photoconductive device incorporating stabilizing layers on the face of the selenium layer |
Cited By (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3405298A (en) * | 1965-03-04 | 1968-10-08 | Rca Corp | Photoconductive device having a target including a selenium blocking layer |
| US3571646A (en) * | 1967-07-17 | 1971-03-23 | Tokyo Shibaura Electric Co | Photoconductive target with n-type layer of cadmium selenide including cadmium chloride and cuprous chloride |
| US3519866A (en) * | 1967-09-26 | 1970-07-07 | Rca Corp | Photoconductive pickup tube having opaque gold pattern encapsulated in tin oxide layer |
| US3922579A (en) * | 1970-04-22 | 1975-11-25 | Hitachi Ltd | Photoconductive target |
| US3816787A (en) * | 1970-08-17 | 1974-06-11 | Tokyo Shibaura Electric Co | Photoconductor comprising cadmium selenide |
| US3858074A (en) * | 1971-11-09 | 1974-12-31 | Matsushita Electric Industrial Co Ltd | Photoelectric transducer element including a heterojunction formed by a photoelectric transducer film and an intermediate film having a larger energy gap than the photoelectric transducer film |
| US3890525A (en) * | 1972-07-03 | 1975-06-17 | Hitachi Ltd | Photoconductive target of an image pickup tube comprising graded selenium-tellurium layer |
| US3783324A (en) * | 1972-09-11 | 1974-01-01 | Rca Corp | Photosensitive charge storage electrode having a selectively conducting protective layer of matching valence band on its surface |
| DE2411517A1 (en) * | 1973-03-12 | 1974-09-26 | Hitachi Ltd | METHOD FOR PRODUCING A LIGHT SENSITIVE HETEROGENIC DIODE |
| JPS5023717A (en) * | 1973-07-02 | 1975-03-14 | ||
| US4307319A (en) * | 1975-10-03 | 1981-12-22 | Hitachi, Ltd. | Semiconductor layer of oxygen depletion type cerium oxide or lead oxide |
| US4240006A (en) * | 1977-12-26 | 1980-12-16 | Sony Corporation | Photoconductive layer and target structure for image pickup tube |
| US8322906B2 (en) | 2011-08-08 | 2012-12-04 | XtraLight Manufacturing Partnership Ltd | Versatile lighting units |
| US8764236B2 (en) | 2011-08-08 | 2014-07-01 | XtraLight Manufacturing Partnership Ltd | Versatile lighting units |
| US9644829B2 (en) | 2013-04-25 | 2017-05-09 | Xtralight Manufacturing, Ltd. | Systems and methods for providing a field repairable light fixture with a housing that dissipates heat |
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