US3631303A - Iii-v cathodes having a built-in gradient of potential energy for increasing the emission efficiency - Google Patents

Iii-v cathodes having a built-in gradient of potential energy for increasing the emission efficiency Download PDF

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US3631303A
US3631303A US3948A US3631303DA US3631303A US 3631303 A US3631303 A US 3631303A US 3948 A US3948 A US 3948A US 3631303D A US3631303D A US 3631303DA US 3631303 A US3631303 A US 3631303A
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active layer
iii
cathode
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layer
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George A Antypas
Ronald L Bell
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Varian Medical Systems Inc
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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J1/00Details 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
    • H01J1/02Main electrodes
    • H01J1/34Photo-emissive cathodes
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J2201/00Electrodes common to discharge tubes
    • H01J2201/34Photoemissive electrodes
    • H01J2201/342Cathodes
    • H01J2201/3421Composition of the emitting surface
    • H01J2201/3423Semiconductors, e.g. GaAs, NEA emitters
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S148/00Metal treatment
    • Y10S148/042Doping, graded, for tapered etching
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S148/00Metal treatment
    • Y10S148/049Equivalence and options
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S148/00Metal treatment
    • Y10S148/065Gp III-V generic compounds-processing
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S148/00Metal treatment
    • Y10S148/067Graded energy gap
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S148/00Metal treatment
    • Y10S148/072Heterojunctions
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S148/00Metal treatment
    • Y10S148/12Photocathodes-Cs coated and solar cell
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S438/00Semiconductor device manufacturing: process
    • Y10S438/936Graded energy gap

Definitions

  • This invention relates to photocathodes and more particularly to photocathodes having a gradient of potential energy thereaeross for establishing electron drift towards the emissive surface.
  • a substrate means preferably a binary or compound III-V crystalline solid, upon which is grown a Ill-V semiconductor crystalline solid active layer formed by: a first constituent which is at least one element listed under column III of the periodic table; a second constituent which is at least one element listed under column V of the periodic table; and a third or additional material which is at least one nonunifonnly present element which progressively changes in concentration across the active layer for establishing the gradient of potential energy.
  • the gradient of potential energy across the graded active layer biases the movement of free electrons therein towards the emissive surface.
  • the gradient is established by progressively decreasing the bandgap energy of the active layer, from the substrate side to the emissive surface side by progressively altering the concentrations of elements forming the compound semiconductor crystal.
  • the gradient may be established by nonuniformly doping the active layer with heavy concentrations of a suitable P-type dopant near the substrate region of the active layer and decreasing concentrations of the dopant toward the emissive surface. The dopant captures free electrons from the balance band, causing a nonuniformly distributed negative charged across the active layer.
  • the simultaneously created holes in the the valance band of the semiconductor are mobile and by diffusion tend to distribute themselves evenly across the active layer.
  • the negative charge concentration toward the substrate side of the active layer tends to prevent this diffusion of the positive holes.
  • a sufficient diffusion of holes does take place to establish an electric field across the active layer which is positive on the emissive surface and negative adjacent to the substrate.
  • the gradient of electron energy potential created by the graded band energy and dopant concentrations establish a unidirectional flow of electrons toward the emissive surface. This bias on the electron diffusion minimizes the loss of electrons into the substrate and the interior region of the active layer.
  • the enhanced electron diffusion increases the emissive efficiency of the photocathode and establishes a faster response time between photon absorption and electron emissron.
  • FIG. I is a schematic diagram, in section, of an infrared image converter showing the inventive photocathode, employed in a reflective optical system,
  • FIG. 2 is an enlarged sectional view of the inventive photocathode taken along lines 2-2 of FIG. 1,
  • FIG. 3 is an energy level diagram for the graded bandgap embodiment of the photocathode.
  • FIG. 4 is an energy level diagram of the graded dopant embodiment of the photocathode.
  • FIG. I there is shown an infrared image intensifier tube 10, representing one of the uses of the present invention.
  • An object 12 to be viewed gives off or reflects optical radiation in the near infrared spectrum. Rays emanating from object 12 are focused on the photosensitive surface of photocathode 14 through a lens 16 and a 45 mirror 18 disposed within an evacuated envelope 20. Vacuum envelope 20 is preferably evacuated to a suitably low pressure such as 10* Torr. The image of object 12 is reflected from mirror 18 onto photocathode 14 which converts the near infrared image into a corresponding electron image emitted from photocathode 14.
  • the emitted electrons are accelerated by a relatively high voltage such as 30 kv. via accelerating electrodes 22, and focused onto a fluorescent screen 24.
  • the optical image appearing on fluorescent screen 24 is a greatly intensified image of object 12 and is viewed through fluorescent screen 24 by the eye or a suitable optical pickup device.
  • a reflection optical system is depicted in FIG. I; however, a transmission optical system may be employed with a suitably thin photocathode active layer grown on a suitably transparent substrate.
  • Photocathode I4 is shown in greater detail.
  • Photocathode 14 includes a heavily doped P- type semiconductor substrate 32 with a graded active layer 34 thereover, both supported on a conductive electrode 36.
  • a layer 38 of alkali metal up to 5 monolayers thick is formed on the clean surface of graded active layer 34 for filling the surface energy states of active layer 34.
  • a layer 40 of cesium oxide [c520] is then preferably formed on alkali metal layer 38 for lowering the work function of the photocathode as described by Ronald L. Bell in application Ser. No. 698, 941, filed Jan. 18, 1968, entitled Photoemitter Having A P-Type Semiconductor Substrate Overlaid with Cesium and N-Type Cesium Oxide Layers, and assigned to the present assignee.
  • optical radiation in the near infrared range and forming the image to be convened falls onto the emissive surface of photocathode I4 and passes through cesium oxide layer 40 and alkali metal layer 38 and is absorbed in P- semiconductor active layer 34. Upon absorption, the infrared radiation produces an electron hole pair pattern corresponding to the optical image. The electrons drift toward the cesium oxide emissive surface under the influence of the gradient of potential energy developed by the graded bandgap levels or graded dopant concentration in graded layer 34. The electrons so accelerated pass through alkali metal layer 38 and cesium oxide layer 40 and are emitted into the vacuum to form an electron image which is then accelerated to fluorescent screen 24.
  • graded active layer 34 is selected to have a semiconductive energy bandgap preferably equal to or slightly greater than the work function of cesium oxide layer 40.
  • the junction of active layer 34 with cesium layer 38 and cesium oxide layer 40 causes severe band bending of the conduction band level 50 and the valance band level 52in active layer 34.
  • Substrate 32 is heavily doped with P-dopants such as Zn or Be to bring the fermi level within the semiconductive material near to the top of valance band 52.
  • the preferred cesium oxide layer 40 is N- type to bring its fermi level near the bottom of its conduction band 54.
  • Conduction band 50 across active layer 34 is shown sloping downward to the right toward the emissive surface as dictated by the progressively changing composition of active layer 34.
  • the effect of the gradient will become particularly noticeable with a downwards slope of several times KT [thermal energy for the operating temperature] in a distance which is the inverse of the absorption depth for photon energies of greatest interest.
  • a gradient energy potential of 1,000 volts per centimeter may easily be established in this embodiment.
  • greater electric fields may be established if required, subject to the breakdown limitations of the graded layer material.
  • conduction level 50 at about 1 ev. adjacent to emissive layer 40. This boundary condition limits the steepness of the slope in graded active layer 34.
  • Another consideration in determining the maximum slope of the gradient is how much shift in response frequency caused by the decreasing bandgap is permissible.
  • bandgap could be gradually lowered by incorporating an increased fraction of the bandgap lowering element into the growth of the compound active layer 34 on substrate layer 32. All of the techniques available must allow for controlled variation of the bandgap by variation of the growth parameters. Some variations in growth parameters occur naturally, such as the depletion of one component of the melt in the case of liquid epitaxy, or different incorporation rates from a given environment with varying temperature in the case of liquid or vapor epitaxy. Another possibility involving the dynamics of growth initiation is that a composition and bandgap gradient may be induced in the base layer simply by growing from an environment of constant composition onto a substrate of higher bandgap than the equilibrium solid deposited. Further, films of these materials formed by evaporation of compounds or their elements in high vacuum may be deposited in a controlled way to produce graded properties of the types discussed above.
  • GaAs,, ,,,,Sb, was grown on GaAs substrates by liquid phase epitaxy resulting in the epitaxial layer having a bandgap gradient which varies from about 700 volts per centimeter near the substrate [l-Zyfrom the substrate] to about 20 voltsper centimeter at a distance greater than p. from the substrate.
  • GaAs Sb photocathode was grown on a GaAs substrate resulting in a bandgap gradient of approximately 200 volts per centimeter. This example had a surprisingly good performance comparable to highly cleaned GaAs.
  • the first and second constituents were Ga and As respectively, while the third or additional material was Sb.
  • the above examples had a measured sensitivity of approximately 700 ramps per meter, with the second example having a lower threshold.
  • the column lll elements Ga, In, and Al; and the column V elements As, Sb, and P are the preferred constituents of the lll-V crystal because they may be combined in many combinations and proportions to produce binary or compound substrates and active layers.
  • the remaining lll-V elements B, Tl, N, and B may also be used.
  • FIG. 4 shows the energy level diagram for the graded dopant concentration embodiment. Except for the dopant, the composition of the lll-V semiconductor remains constant throughout the active layer which in this embodiment may be a binary lll-V crystalline solid. The concentration of the P-dopant, heaviest near substrate 32 and lightest near the emissive surface, causes conduction band 50 to slope downward toward the emissive surface. Thermal electrons from valance band 52 are captured by the dopant centers producing a nonuniform negative charge distribution across active layer 34. The positive holes generated by the escaping thermal electrons tend to diffuse themselves uniformly across the thickness of the active layer. An electric field develops between the stationary negatively charged dopants and the diffusing positively charged holes.
  • a gradient of dopant could be effected by reducing the dopant content of the growth atmosphere, for example, by reducing the rate of injection of an organozinc vapor into the growth area, or by lowering the temperature of a zinc metallic or alloy doping source, during the growth process.
  • the structure and embodiments shown herein without departing from the concept of the present invention.
  • other lll-V semiconductor materials and dopants may be employed.
  • the cesium layer may be employed along without the cesium oxide or both layers eliminated altogether.
  • Thin active layers are preferably grown on a lll-V substrate; however a thick active layer could be mounted on glass or other suitable material.
  • the features and advantages of each modification may be employed with the other modifications.
  • the graded bandgap and graded dopants embodiments may be used separately or combined in a single photocathode.
  • a lll-V semiconductor cathode for providing free electrons and having a built-in gradient of potential energy for enhancing the flow of free electrons therethrough towards an emissive surface, the combination comprising:
  • an active layer supported by the support means and formed by a lll-V semiconductor crystalline solid comprising a first constituent which is at least one element listed under column ll] of the periodic table and a second constituent which is at least one element listed under column V of the periodic table and a third constituent which is at least one additional element for determining the conduction band profile of the active layer in accordance with the concentration of the third constituent, the concentration of the third constituent being higher proximate one major surface of the active layer and lower proximate the other major surface of the active layer causing a decrease in the conduction band across the active layer thereby establishing the gradient of energy potential which promotes free electron drift toward the emissive surface.
  • the third constituent is a P-dopant material which decreases in concentration across the active layer from about 10 atoms/cc. near the support means to about 10" atoms/cc. near the emissive surface.

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Abstract

A gradient of potential energy was established in the active layer of a III-V photocathode for enhancing free electron diffusion toward the emissive surface of the cathode. The energy gradient was provided by decreasing the bandgap energy across the active layer which caused the conduction level to slope downwards from the substrate to the emissive surface through progressive changes in the concentration of the III-V elements forming the active layer. Alternatively, a nonuniform concentration of active layer dopant-heavy on the substrate side and light on the emissive side of the active layer-established a built-in electric field across the active layer. The graded bandgap and/or dopant levels promote free electron drift toward the outer surface of the active layer. Layers of cesium, cesium oxide, or both, were provided over the active layer to lower the work function of the photocathode emissive surface.

Description

United States Patent [72] Inventors George A. Antypas Mountain View; Ronald L. Bell, Woodslde, both of Calif.
[21 Appl. No. 3,948
[22] Filed Jan. 19, 1970 [45] Patented Dec. 28, 1971 [73] Assignee Varlnn Associates Palo Alto, Calil.
[54] Ill-V CATHODES HAVING A BUILT-1N GRADIENT OF POTENTIAL ENERGY FOR INCREASING THE EMISSION EFFICIENCY 8 Claims, 4 Drlwlng Flgl.
[52] U.S.Cl 317/234 R,
317/235 N, 317/235 AN, 317/235 AG, 313/346 [51] Int. CL. I 1101115/00 [50] Field ofsearch 317/235 [56] References Clted UNITED STATES PATENTS 3,387,161 6/1968 Van Laar 331/94 3,478,213 11/1969 Simon 250/207 3,059,123 10/1962 Pfann 307/885 3,304,445 2/1967 Weddell 310/3 3,132,057 5/1964 Greenberg 148/33 Primary Examiner-John W. l-luckert Assistant Examiner-Martin H. Edlow Attorneys- Stanley Z. Cole and Leon F. Herbert ABSTRACT: A gradient of potential energy was established in the active layer of a III-V photocathode for enhancing free electron diffusion toward the emissive surface of the cathode. The energy gradient was provided by decreasing the bandgap energy across the active layer which caused the conduction level to slope downwards from the substrate to the emissive surface through progressive changes in the concentration of the Ill-V elements forming the active layer. Alternatively, a nonuniform concentration of active layer dopantheavy on the substrate side and light on the emissive side of the active layer-established a built-in electric field across the active layer. The graded bandgap and/or dopant levels promote free electron drift toward the outer surface of the active layer. Layers of cesium, cesium oxide, or both, were provided over the active layer to lower the work function of the photocathode emissive surface.
g cowoucn M050 FERMI LEVEL VALENCE VACUUM BAND s2 NEWTON/1 cs o LAYER 40 A 1 SUBSTRATE cs LAYER ss DlSTANCE mom ELECTRODE as PATENTEB DEC28 197:
@ ATTORNEY DISTANCE FROM ELECTRODE 5 Mm I.- mma WAB ED 3 MM m 1m 4 mm Q ll EL GD. Y F D G m H L W C E E V mm H H R .U. M v: M V v I .l. 0 4 L U IL R A 0 rr m C 04 E V e F. R cw K N m f A m 4 f 5/ TRIM M W M m W X\ m. m 1 w a mz w WRZVD H MD EL W m M m L m m M A M R WM 2 V 5 G CL P n /6 TV! II. E w Tr A An eT J G m2 5 l E N B AT-.|| F SEE w SEE SUBSTRATE 52 Cs LAYER 58 III-V CATI-IODES HAVING A BUILT-IN GRADIENT OF POTENTIAL ENERGY FOR INCREASING THE EMISSION EFFICENCY The invention herein described was made in the course of Government Contract No. F336l-68-C-l 396 with the United States Air Force.
BACKGROUND OF THE INVENTION 1. Field of the Invention This invention relates to photocathodes and more particularly to photocathodes having a gradient of potential energy thereaeross for establishing electron drift towards the emissive surface.
2. Description of the Prior Art Heretofore, the application of external electric fields across cathodes to increase electron emission has been limited. Generally these fields are generated by applying a voltage across a pair of space SnO layers positioned on either side of the cathode. An inherent limitation in this structure is that electrons of low energy cannot penetrate the thin conductive layer placed over the emissive surface.
Internal electric fields established by nonuniform doping have been employed in the drift transistor art as described in John N. Shives book entitled The Properties, Physics, and Design of Semiconductor Devices" page 231.. The purpose of the built-in electric field in this application was to accelerate minority carriers across the transistor junction. Further, the concept of a graded bandgap layer is known in the graded bandgap base (GBGB) transistor art. However, these sources of internal fields or potential energy gradients have not heretofore been employed to increase the emission efiiciency of Ill-V photocathodes.
SUMMARY OF THE INVENTION It is therefore an object of this invention to provide a more efficient Ill-V semiconductor cathode.
It is a further object of this invention to provide a III-V semiconductor cathode having a faster response time.
It is another object of this invention to provide a III-V semiconductor cathode having a unidirectional electron flow for avoiding the loss of free electrons in the interior portion of the active layer.
Briefly these and other objects are achieved by providing a substrate means, preferably a binary or compound III-V crystalline solid, upon which is grown a Ill-V semiconductor crystalline solid active layer formed by: a first constituent which is at least one element listed under column III of the periodic table; a second constituent which is at least one element listed under column V of the periodic table; and a third or additional material which is at least one nonunifonnly present element which progressively changes in concentration across the active layer for establishing the gradient of potential energy. The gradient of potential energy across the graded active layer biases the movement of free electrons therein towards the emissive surface. In one embodiment the gradient is established by progressively decreasing the bandgap energy of the active layer, from the substrate side to the emissive surface side by progressively altering the concentrations of elements forming the compound semiconductor crystal. In another embodiment, the gradient may be established by nonuniformly doping the active layer with heavy concentrations of a suitable P-type dopant near the substrate region of the active layer and decreasing concentrations of the dopant toward the emissive surface. The dopant captures free electrons from the balance band, causing a nonuniformly distributed negative charged across the active layer. The simultaneously created holes in the the valance band of the semiconductor are mobile and by diffusion tend to distribute themselves evenly across the active layer. The negative charge concentration toward the substrate side of the active layer tends to prevent this diffusion of the positive holes. However, a sufficient diffusion of holes does take place to establish an electric field across the active layer which is positive on the emissive surface and negative adjacent to the substrate. The gradient of electron energy potential created by the graded band energy and dopant concentrations establish a unidirectional flow of electrons toward the emissive surface. This bias on the electron diffusion minimizes the loss of electrons into the substrate and the interior region of the active layer. The enhanced electron diffusion increases the emissive efficiency of the photocathode and establishes a faster response time between photon absorption and electron emissron.
BRIEF DESCRIPTION OF THE DRAWINGS Further objects and advantages of the present invention and the cause and operation of the gradient of energy potential will become apparent from the following description taken in conjunction with the drawings in which:
FIG. I is a schematic diagram, in section, of an infrared image converter showing the inventive photocathode, employed in a reflective optical system,
FIG. 2 is an enlarged sectional view of the inventive photocathode taken along lines 2-2 of FIG. 1,
FIG. 3 is an energy level diagram for the graded bandgap embodiment of the photocathode, and
FIG. 4 is an energy level diagram of the graded dopant embodiment of the photocathode.
DESCRIPTION OF THE PREFERRED EMBODIMENTS Referring now to FIG. I there is shown an infrared image intensifier tube 10, representing one of the uses of the present invention. An object 12 to be viewed, gives off or reflects optical radiation in the near infrared spectrum. Rays emanating from object 12 are focused on the photosensitive surface of photocathode 14 through a lens 16 and a 45 mirror 18 disposed within an evacuated envelope 20. Vacuum envelope 20 is preferably evacuated to a suitably low pressure such as 10* Torr. The image of object 12 is reflected from mirror 18 onto photocathode 14 which converts the near infrared image into a corresponding electron image emitted from photocathode 14. The emitted electrons are accelerated by a relatively high voltage such as 30 kv. via accelerating electrodes 22, and focused onto a fluorescent screen 24. The optical image appearing on fluorescent screen 24 is a greatly intensified image of object 12 and is viewed through fluorescent screen 24 by the eye or a suitable optical pickup device. A reflection optical system is depicted in FIG. I; however, a transmission optical system may be employed with a suitably thin photocathode active layer grown on a suitably transparent substrate.
Referring now to FIG. 2, photocathode I4 is shown in greater detail. Photocathode 14 includes a heavily doped P- type semiconductor substrate 32 with a graded active layer 34 thereover, both supported on a conductive electrode 36. Preferably, a layer 38 of alkali metal up to 5 monolayers thick is formed on the clean surface of graded active layer 34 for filling the surface energy states of active layer 34. A layer 40 of cesium oxide [c520] is then preferably formed on alkali metal layer 38 for lowering the work function of the photocathode as described by Ronald L. Bell in application Ser. No. 698, 941, filed Jan. 18, 1968, entitled Photoemitter Having A P-Type Semiconductor Substrate Overlaid with Cesium and N-Type Cesium Oxide Layers, and assigned to the present assignee.
In operation, optical radiation in the near infrared range and forming the image to be convened, falls onto the emissive surface of photocathode I4 and passes through cesium oxide layer 40 and alkali metal layer 38 and is absorbed in P- semiconductor active layer 34. Upon absorption, the infrared radiation produces an electron hole pair pattern corresponding to the optical image. The electrons drift toward the cesium oxide emissive surface under the influence of the gradient of potential energy developed by the graded bandgap levels or graded dopant concentration in graded layer 34. The electrons so accelerated pass through alkali metal layer 38 and cesium oxide layer 40 and are emitted into the vacuum to form an electron image which is then accelerated to fluorescent screen 24.
Referring now to the energy level diagram shown in FIG. 3, graded active layer 34 is selected to have a semiconductive energy bandgap preferably equal to or slightly greater than the work function of cesium oxide layer 40. The junction of active layer 34 with cesium layer 38 and cesium oxide layer 40 causes severe band bending of the conduction band level 50 and the valance band level 52in active layer 34. Substrate 32 is heavily doped with P-dopants such as Zn or Be to bring the fermi level within the semiconductive material near to the top of valance band 52. The preferred cesium oxide layer 40 is N- type to bring its fermi level near the bottom of its conduction band 54. Conduction band 50 across active layer 34 is shown sloping downward to the right toward the emissive surface as dictated by the progressively changing composition of active layer 34. The effect of the gradient will become particularly noticeable with a downwards slope of several times KT [thermal energy for the operating temperature] in a distance which is the inverse of the absorption depth for photon energies of greatest interest. A gradient energy potential of 1,000 volts per centimeter may easily be established in this embodiment. Of course, greater electric fields may be established if required, subject to the breakdown limitations of the graded layer material. For emission purposes it is desirable to maintain conduction level 50 at about 1 ev. adjacent to emissive layer 40. This boundary condition limits the steepness of the slope in graded active layer 34. Another consideration in determining the maximum slope of the gradient is how much shift in response frequency caused by the decreasing bandgap is permissible.
A number of techniques exist for making the graded bandgap embodiment. For instance bandgap could be gradually lowered by incorporating an increased fraction of the bandgap lowering element into the growth of the compound active layer 34 on substrate layer 32. All of the techniques available must allow for controlled variation of the bandgap by variation of the growth parameters. Some variations in growth parameters occur naturally, such as the depletion of one component of the melt in the case of liquid epitaxy, or different incorporation rates from a given environment with varying temperature in the case of liquid or vapor epitaxy. Another possibility involving the dynamics of growth initiation is that a composition and bandgap gradient may be induced in the base layer simply by growing from an environment of constant composition onto a substrate of higher bandgap than the equilibrium solid deposited. Further, films of these materials formed by evaporation of compounds or their elements in high vacuum may be deposited in a controlled way to produce graded properties of the types discussed above.
More specifically, GaAs,, ,,,,Sb,, was grown on GaAs substrates by liquid phase epitaxy resulting in the epitaxial layer having a bandgap gradient which varies from about 700 volts per centimeter near the substrate [l-Zyfrom the substrate] to about 20 voltsper centimeter at a distance greater than p. from the substrate. As another example, a 2p. GaAs Sb photocathode was grown on a GaAs substrate resulting in a bandgap gradient of approximately 200 volts per centimeter. This example had a surprisingly good performance comparable to highly cleaned GaAs. In both of these examples, the first and second constituents were Ga and As respectively, while the third or additional material was Sb. The above examples had a measured sensitivity of approximately 700 ramps per meter, with the second example having a lower threshold. Generally, the column lll elements Ga, In, and Al; and the column V elements As, Sb, and P, are the preferred constituents of the lll-V crystal because they may be combined in many combinations and proportions to produce binary or compound substrates and active layers. In some applications the remaining lll-V elements B, Tl, N, and B, may also be used.
FIG. 4 shows the energy level diagram for the graded dopant concentration embodiment. Except for the dopant, the composition of the lll-V semiconductor remains constant throughout the active layer which in this embodiment may be a binary lll-V crystalline solid. The concentration of the P-dopant, heaviest near substrate 32 and lightest near the emissive surface, causes conduction band 50 to slope downward toward the emissive surface. Thermal electrons from valance band 52 are captured by the dopant centers producing a nonuniform negative charge distribution across active layer 34. The positive holes generated by the escaping thermal electrons tend to diffuse themselves uniformly across the thickness of the active layer. An electric field develops between the stationary negatively charged dopants and the diffusing positively charged holes. The presence of this electric field limits the diffusion process resulting in an equilibrium condition. Thus substantial electric fields are generated causing conduction band 50 and valance band 52 to slope as shown. More specifically, a field of 750 volts/cm. was developed across a Z-micron active layer due to a Zn dopant gradient of from 10 atoms/cc. on the substrate side to 10 atoms/cc. on the vacuum side of the active layer. As the net bandgap between conduction band 50 and valance band 52 remains constant throughout the sloping region, no shift in response peaks is notice in the graded dopant embodiment. Many possibilities are available for accomplishing this gradiation of concentration. In the case of vapor phase epitaxy, a gradient of dopant could be effected by reducing the dopant content of the growth atmosphere, for example, by reducing the rate of injection of an organozinc vapor into the growth area, or by lowering the temperature of a zinc metallic or alloy doping source, during the growth process.
Clearly, various changes may be made in the structure and embodiments shown herein without departing from the concept of the present invention. For example, other lll-V semiconductor materials and dopants may be employed. In some cases, the cesium layer may be employed along without the cesium oxide or both layers eliminated altogether. Thin active layers are preferably grown on a lll-V substrate; however a thick active layer could be mounted on glass or other suitable material. Further, the features and advantages of each modification may be employed with the other modifications. For instance, the graded bandgap and graded dopants embodiments may be used separately or combined in a single photocathode.
It will be apparent to those skilled in the art that the objects of this invention have been achieved by providing a gradient of potential energy across the active layer for accelerating the free electrons thereacross and improving the response time of the cathode. The force generated by the gradient of energy potential biases the free electron motion toward the emissive surface and avoids electron loss in the substrate and interior regions of the active layer.
What is claimed is:
1. In a lll-V semiconductor cathode for providing free electrons and having a built-in gradient of potential energy for enhancing the flow of free electrons therethrough towards an emissive surface, the combination comprising:
support means; and
an active layer supported by the support means and formed by a lll-V semiconductor crystalline solid comprising a first constituent which is at least one element listed under column ll] of the periodic table and a second constituent which is at least one element listed under column V of the periodic table and a third constituent which is at least one additional element for determining the conduction band profile of the active layer in accordance with the concentration of the third constituent, the concentration of the third constituent being higher proximate one major surface of the active layer and lower proximate the other major surface of the active layer causing a decrease in the conduction band across the active layer thereby establishing the gradient of energy potential which promotes free electron drift toward the emissive surface.
2. The lllV cathode as specified in claim 1, wherein a thin cesium layer is formed over the emissive surface of the active layer to decrease the work function of the cathode.
3. The Iii-V cathode as specified in claim 2 wherein a cesium oxide layer is provided over the cesium layer to further reduce the work function.
6. The Ill-V cathode as specified in claim 5, wherein the additional material is at least one element selected from either of the two groups of claim 5.
7. The iii-V cathode as described in claim 1 wherein the cathode is a photocathode, and the changing composition of the active layer causes the conduction band to have a slope at least [(T in a distance which is the inverse of the absorption depth for the incident photons.
8. The photocathode as described in claim 1 wherein the third constituent is a P-dopant material which decreases in concentration across the active layer from about 10 atoms/cc. near the support means to about 10" atoms/cc. near the emissive surface.

Claims (7)

  1. 2. The III-V cathode as specified in claim 1, wherein a thin cesium layer is formed over the emissive surface of the active layer to decrease the work function of the cathode.
  2. 3. The III-V cathode as specified in claim 2 wherein a cesium oxide layer is provided over the cesium layer to further reduce the work function.
  3. 4. The III-V cathode as specified in claim 1, wherein the support means is a III-V crystalline solid substrate upon which the active layer is grown by epitaxy.
  4. 5. The III-V cathode as described in claim 1 wherein the first constituent is at least one element selected from the group consisting of Al, Ga, and In, and the second constituent is at least one element selected from the group consisting of P, As, and Sb.
  5. 6. The III-V cathode as specified in claim 5, wherein the additional material is at least one element selected from either of the two groups of claim 5.
  6. 7. The III-V cathode as described in claim 1 wherein the cathode is a photocathode, and the changing composition of the active layer causes the conduction band to have a slope at least KT in a distance which is the inverse of the absorption depth for the incident photons.
  7. 8. The photocathode as described in claim 1 wherein the third constituent is a P-dopant material which decreases in concentration across the active layer from about 1020 atoms/cc. near the support means to about 1018 atoms/cc. near the emissive surface.
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US3958143A (en) * 1973-01-15 1976-05-18 Varian Associates Long-wavelength photoemission cathode
US3981755A (en) * 1972-11-24 1976-09-21 U.S. Philips Corporation Photocathode manufacture
US3986065A (en) * 1974-10-24 1976-10-12 Rca Corporation Insulating nitride compounds as electron emitters
US3992233A (en) * 1975-03-10 1976-11-16 The Secretary Of State For Defence In Her Britannic Majesty's Government Of The United Kingdom Of Great Britain And Northern Ireland Surface treatment of III-V compound crystals
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US4096511A (en) * 1971-11-29 1978-06-20 Philip Gurnell Photocathodes
US4107564A (en) * 1974-05-21 1978-08-15 Alexandr Ivanovich Klimin Photoemitter
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US5404026A (en) * 1993-01-14 1995-04-04 Regents Of The University Of California Infrared-sensitive photocathode
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US20100128203A1 (en) * 2008-11-27 2010-05-27 Jung-Han Shin Lamp, method for manufacturing the same and liquid crystal display apparatus having the same
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US4096511A (en) * 1971-11-29 1978-06-20 Philip Gurnell Photocathodes
US3981755A (en) * 1972-11-24 1976-09-21 U.S. Philips Corporation Photocathode manufacture
US3958143A (en) * 1973-01-15 1976-05-18 Varian Associates Long-wavelength photoemission cathode
US3901745A (en) * 1973-02-06 1975-08-26 Int Standard Electric Corp Gallium arsenide photocathode
US4107564A (en) * 1974-05-21 1978-08-15 Alexandr Ivanovich Klimin Photoemitter
US3986065A (en) * 1974-10-24 1976-10-12 Rca Corporation Insulating nitride compounds as electron emitters
US3992233A (en) * 1975-03-10 1976-11-16 The Secretary Of State For Defence In Her Britannic Majesty's Government Of The United Kingdom Of Great Britain And Northern Ireland Surface treatment of III-V compound crystals
US4066483A (en) * 1976-07-07 1978-01-03 Western Electric Company, Inc. Gate-controlled bidirectional switching device
US4344803A (en) * 1979-03-14 1982-08-17 Licentia Patent-Verwaltungs-G.M.B.H. Photo cathode made from composite semiconductor/glass material
US4518980A (en) * 1981-06-03 1985-05-21 U.S. Philips Corporation Semiconductor device for the vacuum-emission of electrons
US4871911A (en) * 1985-02-14 1989-10-03 U.S. Philips Corporation Electron beam apparatus comprising a semiconductor electron emitter
FR2592217A1 (en) * 1985-12-20 1987-06-26 Thomson Csf INTERNAL AMPLIFICATION PHOTOCATHODE
EP0230818A1 (en) * 1985-12-20 1987-08-05 Thomson-Csf Photo cathode with internal amplification
US4829355A (en) * 1985-12-20 1989-05-09 Thomson-Csf Photocathode having internal amplification
US5315126A (en) * 1992-10-13 1994-05-24 Itt Corporation Highly doped surface layer for negative electron affinity devices
US5354694A (en) * 1992-10-13 1994-10-11 Itt Corporation Method of making highly doped surface layer for negative electron affinity devices
US5404026A (en) * 1993-01-14 1995-04-04 Regents Of The University Of California Infrared-sensitive photocathode
EP0789935A1 (en) * 1994-11-01 1997-08-20 Intevac, Inc. Heterojunction energy gradient structure
EP0789935A4 (en) * 1994-11-01 1998-08-19 Intevac Inc Heterojunction energy gradient structure
US5908699A (en) * 1996-10-11 1999-06-01 Skion Corporation Cold cathode electron emitter and display structure
US5712490A (en) * 1996-11-21 1998-01-27 Itt Industries, Inc. Ramp cathode structures for vacuum emission
US7015467B2 (en) 2002-10-10 2006-03-21 Applied Materials, Inc. Generating electrons with an activated photocathode
US20040069960A1 (en) * 2002-10-10 2004-04-15 Applied Materials, Inc. Electron beam pattern generator with photocathode comprising low work function cesium halide
US20040140432A1 (en) * 2002-10-10 2004-07-22 Applied Materials, Inc. Generating electrons with an activated photocathode
US7446474B2 (en) 2002-10-10 2008-11-04 Applied Materials, Inc. Hetero-junction electron emitter with Group III nitride and activated alkali halide
US7161162B2 (en) * 2002-10-10 2007-01-09 Applied Materials, Inc. Electron beam pattern generator with photocathode comprising low work function cesium halide
US20060055321A1 (en) * 2002-10-10 2006-03-16 Applied Materials, Inc. Hetero-junction electron emitter with group III nitride and activated alkali halide
US7005637B2 (en) 2003-01-31 2006-02-28 Intevac, Inc. Backside thinning of image array devices
US20040180462A1 (en) * 2003-01-31 2004-09-16 Intevac, Inc. Backside thinning of image array devices
US20060138322A1 (en) * 2003-01-31 2006-06-29 Costello Kenneth A Backside imaging through a doped layer
US20040245593A1 (en) * 2003-01-31 2004-12-09 Costello Kenneth A. Backside thinning of image array devices
US7042060B2 (en) 2003-01-31 2006-05-09 Intevac, Inc. Backside thinning of image array devices
US7479686B2 (en) 2003-01-31 2009-01-20 Intevac, Inc. Backside imaging through a doped layer
US20070034987A1 (en) * 2005-06-01 2007-02-15 Intevac Inc. Photocathode structure and operation
US7531826B2 (en) 2005-06-01 2009-05-12 Intevac, Inc. Photocathode structure and operation
EP1939917A3 (en) * 2006-12-28 2008-07-23 Hamamatsu Photonics K.K. Photocathode, photomultiplier abnd electron tube
US20100096985A1 (en) * 2006-12-28 2010-04-22 Hamamatsu Photonics K.K. Photocathode, photomultiplier and electron tube
CN101211730B (en) * 2006-12-28 2011-11-09 浜松光子学株式会社 Photocathode, photomultiplier and electron tube
US8421354B2 (en) 2006-12-28 2013-04-16 Hamamatsu Photonics K.K. Photocathode, photomultiplier and electron tube
US20100128203A1 (en) * 2008-11-27 2010-05-27 Jung-Han Shin Lamp, method for manufacturing the same and liquid crystal display apparatus having the same
US8362678B2 (en) * 2008-11-27 2013-01-29 Samsung Display Co., Ltd. Lamp structure and liquid crystal display apparatus having the same
CN111627821A (en) * 2020-06-05 2020-09-04 温州大学 Electron-hole reversible doping method for multilayer molybdenum ditelluride field effect transistor
CN111627821B (en) * 2020-06-05 2023-09-12 温州大学 Electron-hole reversible doping method for multi-layer molybdenum ditelluride field effect transistor

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