Method of making highly doped surface layer for negative electron affinity devices

Abstract

A negative electron affinity device has acceptor dopant concentration increased proximate the emitter face of the III-V semiconductor layer and within the depletion zone effected by an overlying CsO negative electron affinity coating. Methods to accomplish dopant concentration include diffusion, ion implantation and doping during crystal growth.

Description

FIELD OF THE INVENTION

The present invention relates to negative electron affinity devices, such as photocathodes and photomultiplier tubes and more particularly to such a device having a primary electron emitting layer composed of a semiconductor with a tailored concentration gradient of dopant and methods for producing same.

DESCRIPTION OF THE PRIOR ART

Negative electron affinity (NEA) devices such as vacuum tube photodetectors, photocathodes, photomultiplier tubes, and image intensifier tubes convert incoming photons into electrons, and then emit the electrons into vacuum, where they are accelerated by an electric field to increase their energy. The number of electrons are multiplied by secondary emitters. For negative electron affinity action a very thin (monolayer) of Cs or Cs:O is applied to the surface of a III-V semiconductor such as In.sub.x Ga.sub.1-x As. The work function energy should be as small as the choice of the coating material will allow, and the processing should be such that the band bending is as large as possible.

Reflection mode NEA photocathodes have the light incident on the cathode vacuum surface as in photomultiplier tubes, whereas transmission mode photocathodes are thin film structures with the light incident from the rear as for image tubes. NEA action can also be achieved in p+Si. See a text entitled "SEMICONDUCTOR DEVICES AND INTEGRATED ELECTRONICS" by A. G. Milnes, chapter 13 entitled "LIGHT DETECTING SEMICONDUCTOR DEVICES," at page 783 entitled NEGATIVE ELECTRON AFFINITY EMITTERS, published by Van Norstrand Reinhold Company, New York (1980).

In devices such as the Generation III image intensifier, a relatively thick (1-5 .mu.m) semiconductor layer such as gallium arsenide (GaAs), indium phosphate (InP), gallium indium phosphate (GaInP) or other III-V compound is used for absorbing the photons to generate the primary electrons. The emitting surface of this semiconductor is coated with a relatively thin (0.001-0.002 .mu.m) Negative Electron Affinity (NEA) coating such as cesium oxide (CsO). This helps create a depletion layer of intermediate thickness in the semiconductor near the emitting surface. The NEA coating also serves to create a more positively charged surface, so that electrons entering the depletion layer are accelerated toward the surface and thereby have a higher escape probability. The semiconductor matrix is typically doped with an electron acceptor such as zinc (Zn) to yield a P-type material. See U.S. Pat. No. 5,114,373 issued on May 19, 1992 entitled METHOD FOR OPTIMIZING PHOTOCATHODE PHOTO-RESPONSE to R. Peckman and assigned to ITT Corporation, the assignee herein. The patent discusses the fabrication of photocathodes using CsO layers. For descriptions of some differences between Generation II and Generation III image intensifier tubes, see U.S. Pat. No. 5,029,963 issued on Jul. 9, 1991 entitled REPLACEMENT DEVICE FOR A DRIVER VIEWER by C. Naselli et al., and assigned to ITT Corporation, the assignee herein.

In negative electron affinity devices, primary electrons will diffuse to the depletion layer if they are generated sufficiently close. The typical distance an electron will diffuse in the material is characterized by the diffusion length. The diffusion length depends on acceptor doping concentration, High doping levels reduce the diffusion length and the probability that an electron will reach the depletion layer, and thus decreases the photoresponse.

Once an electron reaches the depletion layer, it is accelerated toward the NEA coating. If the semiconductor has sufficiently low work function, and the NEA coating produces a depletion layer with sufficient potential, then the primary electrons can have enough energy to escape into the vacuum. The escape probability depends on the depletion layer thickness, which depends on the doping concentration. Low doping gives a thicker depletion layer, which increases the probability that an electron will collide, lose some of its kinetic energy and be unable to escape into the vacuum. This decreases photoresponse.

Thus there is a tradeoff in the doping concentration: high doping decreases photoresponse by degrading diffusion length, while low doping decreases photoresponse by reducing escape probability. In practice, a compromise value of doping, at around 5.times.10.sup.18 atoms per cm.sup.3, is used.

It is therefore an object of the present invention to provide a negative electron affinity device having enhanced photoresponse.

It is a further object to provide improved photoresponse in a simple and economical manner.

SUMMARY OF THE INVENTION

The problems and disadvantages associated with the conventional techniques and devices utilized to convert electromagnetic radiation to a flow of electrons are overcome by the present invention which includes a negative electron affinity device with a semiconductor layer doped with an electron acceptor dopant. The semiconductor layer has an emitter face from which electrons are emitted. A coating of material to produce or enhance negative electron affinity is deposited over the semiconductor layer emitter face and sets up a depletion band within the semiconductor. Unlike conventional devices of this type, the present invention has a tailored doping profile in which the dopant is concentrated proximate the emitter face. In a corresponding method the enhanced concentration of dopant proximate the emitter face is achieved.

BRIEF DESCRIPTION OF THE FIGURES

For a better understanding of the present invention, reference is made to the following detailed description of an exemplary embodiment considered in conjunction with the accompanying drawings, in which:

FIG. 1 is a schematic cross-sectional view of a negative electron affinity device in accordance with the prior art; and

FIG. 2 is a schematic cross-sectional view of a negative electron affinity device in accordance with the present invention.

DETAILED DESCRIPTION OF THE FIGURES

FIG. 1 shows a negative electron affinity device 10 in accordance with the prior art. The device has a transparent faceplate 12 which would typically be formed from glass, upon which is deposited or attached a semiconductor photon-to-electron conversion layer 14 comprised of, for example, gallium arsenide (GaAs). The semiconductor layer 14 is doped with a doping material 16, such as zinc (Zn) to yield a P-type material. A Negative Electron Affinity (NEA) coating, such as cesium oxide (CsO) 18 is deposited over the GaAs layer 14. The area 20 immediately adjacent to the photocathode structure comprised of the GaAs layer 14 and CsO coating 18 is typically evacuated to permit the uninterrupted traversal of electrons to an electron multiplier, such as a microchannel plate (not shown). The Negative Electron Affinity (NEA) coating 18 creates an electron depletion layer 22 which is illustrated in FIG. 1 as starting at the dashed line 23 and ending at the emitter surface 24 of the semiconductor layer 14 which abuts the CsO layer 18. In known devices, the concentration of the doping particles 16 within the semiconductor layer matrix 14 is homogeneous, or perhaps even reduced near the emitter surface 24 due to dopant evaporation during processing. For this reason, the above-described tradeoff in doping concentration and photoresponse appertains in known devices.

The present invention calls for increasing the doping at the emitter surface 24 of the conversion layer 14, in particular, within the depletion layer 22. This shrinks the depletion layer 22 width without affecting diffusion in the bulk of the semiconductor layer 14. Conversely, the doping of the conversion layer 14 (with the exception of the depletion layer region 22), can be reduced for higher diffusion length without affecting escape probability. The increased doping concentration should be confined to the depletion layer 22 as much as possible. High acceptor concentrations outside the depletion layer 22 (and specifically a doping gradient) can cause diffusion of holes away from the conversion layer region near the depletion layer, which in turn sets up an electric field which tends to confine electrons to the conversion layer. This reduces the probability of electrons reaching the depletion layer.

FIG. 2 illustrates a negative electron affinity device 110 in accordance with the foregoing strategy and with the present invention. Elements illustrated in FIG. 2, which correspond to the elements described above with respect to FIG. 1, have been designated by corresponding reference numerals increased by one hundred. The embodiments of FIG. 1 and FIG. 2 operate in the same manner unless otherwise stated. In the embodiment illustrated in FIG. 2, the doping gradient is completely confined to the depletion layer 122 at the emitting surface. Thus, the doping particles 116 of FIG. 2 are highly concentrated in a narrow band proximate to the CsO layer 118 in contrast to the even dispersion of the doping particles 16, shown in FIG. 1, which are essentially homogeneous within the GaAs layer 14. The depletion layer 122 is therefore much smaller in FIG. 2 then it is in FIG. 1. In the depletion layer of the present invention, there are no holes to diffuse and set up a charge imbalance to push electrons away. In fact, the whole depletion layer is a region of extreme charge imbalance, with electric field accelerating electrons forward, toward the NEA coating. With no grading in the non-depleted part of the active layer, there is no retarding field produced. When extra doping is added exclusively in the depletion layer, the primary theoretical effect is to shorten the length of the depletion zone, thus increasing the escape probability. This provides the above-described advantages and constitute a novel aspect of the present invention.

The aforementioned increase in escape probability and other advantages achieved by employing the novel depletion layer configuration of the present invention, though theoretically predictable, have heretofore been thought impossible in practice because of the difficulty in confining the dopant to such a thin region. The depletion layer is estimated to be on the order of 0.01 to 0.02 .mu.m for current state-of-the-art conventional GEN-3 devices. The effect of extra doping is to make this layer even thinner, so the dopant must be applied only within 0.005 .mu.m of the emitting surface. While zinc (the standard GEN-3 dopant) and most other dopants p-type dopants diffuse quickly except at relatively low temperatures, standard diffusion processes require high temperatures to get a high surface concentration as required for this invention. This is because standard zinc diffusions rely on a solid zinc source such as Zn.sub.3 As.sub.2 or ZnAs.sub.2, which is converted to vapor at high temperature. The high temperatures are required to get the high Zn partial pressures needed to increase the surface concentration of Zn in the GaAs. Under these conditions, however, it would be impossible to confine the diffusion depth to 0.005 .mu.m or less. Furthermore, even if such a thinly doped layer could be achieved using prior art techniques, the standard heatclean process required to prepare the GaAs surface for the NEA coating would drive the dopant much deeper into the active layer. For a detailed description of such a heatclean process, see U.S. Pat. No. 4,890,933 issued to A. Amith et al.

The limitations and disadvantages associated with the aforementioned prior art techniques are overcome in accordance with the inventive process of the present invention, which will now be described. In accordance with a first technique of the present invention, high concentrations of acceptor dopant are diffused into a thin layer at the emitter surface by exposing the GaAs to DiEthylZinc (DEZ) or DiMethylZinc (DMZ) vapor at the relatively low temperature of 350.degree. C. The high vapor pressure of the DEZ or DEZ vapor at such a low temperature allows an extremely highly doped depletion layer to be obtained at the emitter surface which is on the order of between 0.001 and 0.005 .mu.m thick. The DEZ or DMZ diffusion also gives a high surface concentration with a very abrupt concentration profile (which reduces the doping gradient outside of the depletion layer). Preferably, the diffusion is performed after all other high temperature steps have been performed, so that the added zinc does not diffuse deeper. Thus, the bonded cathode is preferably exposed briefly to the DEZ or DMZ vapor as it is cooling from heatclean, before the CsO deposition.

In addition to enhancing the escape probability by reducing the length of the depletion zone, this invention makes it possible to separately dope the active layer and the depletion zone. Therefore, the active layer doping can be reduced, improving the electron diffusion length and the probability electrons will diffuse to the emitting surface. This will further allow the thickness of the active layer to be increased, so that more of the "red" photons (near bandgap energy) can be captured. Dopant is then added to the depletion zone only, using the diffusion technique described above. It is thus possible to increase the surface concentration well above that for state of the art GEN-3, especially considering the suspected loss of zinc from the surface during GEN-3 heatclean processing.

In accordance with another embodiment of the inventive method, diffusion of Zn.sub.3 As.sub.2 or ZnAs.sub.2 is performed at relatively low temperatures (400.degree.-600.degree. C.) to give thinly doped layer width (.about.100 A). 100 A diffusions of zinc require about 25 minutes of exposure at 400.degree. C. Further processing at 400.degree. C. or higher should be avoided with zinc, which is a fast diffuser. The diffusion should occur after the last high temperature process step, or a slower diffusing dopant should be used. Diffusion, per se, is known in the art as can be appreciated by examining the above-noted text which further has an extensive bibliography concerning semiconductor process.

Ion implantation of the acceptor dopant is an alternative to diffusion. Its main advantage is independent control of the depth of implant and the dose (or doping concentration). Like diffusion, ion implantation, per se, is described in the prior art. It is well known to provide selective doping profiles by control of the implantion depth and dose. Ion-implantation forms layers by accelerating impurity ions in an electric field to a high speed. The depth of penetration is determined by the speed before impact. In diffusion the impurity concentration increases in the direction of entrance of the impurities. Ion-implantation allows one to control the impurity profile by varying the acceleration of ions.

Another method is to build in a thin doped layer during crystal growth. This would work best in reflection mode cathodes, because GaAs transmission mode cathodes are usually fabricated by attaching the cathode material and etching the surface where the NEA coating would be applied. It would be difficult to control the etch process precisely enough to leave the thin, highly doped layer required for optimum results. However, for transmission cathodes fabricated by direct deposition of the cathode material, a thin doped layer could be built in during the deposition process.

A photocathode has been described in which the photoresponse is increased by applying higher doping to the emitting surface than to the bulk of the light collecting region. Optimum results should be obtained when the higher doping is confined to the thin depletion region near the emitting surface. Several methods have been described for applying the higher doping.

The present invention is particularly useful in GEN III photocathodes and night vision devices and Negative Electron Affinity photodetectors.

It should be understood that the embodiments described herein are merely exemplary and that a person skilled in the art may make many variations and modifications without departing from the spirit and scope of the invention as defined in the appended claims.

Claims

1. A method for increasing the photoresponse of a negative electron affinity device having a semiconductor layer doped with an electron acceptor dopant, said semiconductor layer having an emitter face having a negative electron affinity coating thereover, said coating setting up a depletion band in said semiconductor layer, comprising the steps of:

doping said semiconductor layer in a manner such that said diopant has an increased concentration with respect to said electron acceptor dopant concentration proximate said emitter face within said depletion band.

2. The method of claim 1, wherein said doping step is by diffusion.

3. The method of claim 2, wherein said diffusion is zinc diffusion conducted at temperatures less than 700 degrees Centigrade.

4. The method of claim 3, wherein said zinc diffusion is conducted at temperatures from about 400 to 600 degrees Centigrade for from about 10 to 40 minutes.

5. The method of claim 2, wherein said diffusion step is diffusing a vaporized dopant selected from the class consisting of DiMethylZinc and DiEthylZinc.

6. The method of claim 5, wherein said method further includes a heatclean step, said diffusion step being conducted while said semiconductor layer is cooling after said heatclean step.

7. The method of claim 5, wherein said diffusion step is performed at 350.degree. C.

8. The method of claim 5, wherein said method further includes a step of depositing a layer of CsO on said semiconductor layer, said diffusing step being conducted before said depositing step.

9. The method of claim 1, wherein said step of doping is by ion implantation.

10. The method of claim 1, wherein said step of doping is conducted during crystal growth of said semiconductor layer.

11. The method of claim 4, wherein said zinc diffusion is produced by exposing the semiconductor surface to vapor a zinc compound selected from Zn.sub.3 As.sub.2, ZnA.sub.2, Zn(CH.sub.3).sub.2, or Zn(C.sub.2 H.sub.5).sub.2.