GB2111299A - High current density photoelectron generators - Google Patents
High current density photoelectron generators Download PDFInfo
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- GB2111299A GB2111299A GB08231900A GB8231900A GB2111299A GB 2111299 A GB2111299 A GB 2111299A GB 08231900 A GB08231900 A GB 08231900A GB 8231900 A GB8231900 A GB 8231900A GB 2111299 A GB2111299 A GB 2111299A
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y10/00—Nanotechnology for information processing, storage or transmission, e.g. quantum computing or single electron logic
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y40/00—Manufacture or treatment of nanostructures
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J1/00—Details of electrodes, of magnetic control means, of screens, or of the mounting or spacing thereof, common to two or more basic types of discharge tubes or lamps
- H01J1/02—Main electrodes
- H01J1/34—Photo-emissive cathodes
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
- H01J37/02—Details
- H01J37/04—Arrangements of electrodes and associated parts for generating or controlling the discharge, e.g. electron-optical arrangement, ion-optical arrangement
- H01J37/06—Electron sources; Electron guns
- H01J37/073—Electron guns using field emission, photo emission, or secondary emission electron sources
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J37/00—Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
- H01J37/30—Electron-beam or ion-beam tubes for localised treatment of objects
- H01J37/317—Electron-beam or ion-beam tubes for localised treatment of objects for changing properties of the objects or for applying thin layers thereon, e.g. for ion implantation
- H01J37/3174—Particle-beam lithography, e.g. electron beam lithography
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J9/00—Apparatus or processes specially adapted for the manufacture, installation, removal, maintenance of electric discharge tubes, discharge lamps, or parts thereof; Recovery of material from discharge tubes or lamps
- H01J9/02—Manufacture of electrodes or electrode systems
- H01J9/12—Manufacture of electrodes or electrode systems of photo-emissive cathodes; of secondary-emission electrodes
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J2201/00—Electrodes common to discharge tubes
- H01J2201/34—Photoemissive electrodes
- H01J2201/342—Cathodes
- H01J2201/3421—Composition of the emitting surface
- H01J2201/3423—Semiconductors, e.g. GaAs, NEA emitters
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J2201/00—Electrodes common to discharge tubes
- H01J2201/34—Photoemissive electrodes
- H01J2201/342—Cathodes
- H01J2201/3421—Composition of the emitting surface
- H01J2201/3426—Alkaline metal compounds, e.g. Na-K-Sb
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J2237/00—Discharge tubes exposing object to beam, e.g. for analysis treatment, etching, imaging
- H01J2237/06—Sources
- H01J2237/061—Construction
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J2237/00—Discharge tubes exposing object to beam, e.g. for analysis treatment, etching, imaging
- H01J2237/06—Sources
- H01J2237/063—Electron sources
- H01J2237/06325—Cold-cathode sources
- H01J2237/06333—Photo emission
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J2237/00—Discharge tubes exposing object to beam, e.g. for analysis treatment, etching, imaging
- H01J2237/30—Electron or ion beam tubes for processing objects
- H01J2237/317—Processing objects on a microscale
- H01J2237/3175—Lithography
- H01J2237/31777—Lithography by projection
- H01J2237/31779—Lithography by projection from patterned photocathode
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Abstract
An electron beam generator particularly suitable for direct-write semiconductor lithography applications comprises a photoemissive cathode (16), a continuous wave laser (10) for illuminating the photoemissive cathode, a modulator (11) for varying the intensity of or deflecting the laser beam, and light optics (12) to create an optical pattern on the cathode. The photoemissive cathode (16) comprises a light transmissive substrate (40) onto which is deposited an optically semi-transparent, electrically conductive film (46), e.g. of chromium. This film (46) in turn is coated with a thin layer (48) of a photoemissive substance comprising cesium antimonide, sodium potassium antimonide, cesiated gallium phosphide, or cesiated gallium arsenide phosphide, and this photoemissive layer (48) will emit an intense and substantially monochromatic beam of electrons upon illumination with laser light of appropriate wavelength and energy, e.g. from an argon ion continuous wave laser. The emitted electron beam is configured in accordance with the optical pattern created on the cathode, and, if intended for use in lithographically generating very large scale integrated (VLSI) circuits on semiconductors, is passed through successive electron optical devices to further shape and size the beam as appropriate. A method of manufacturing a photoemitter is also described. <IMAGE>
Description
SPECIFICATION
Improvements relating to high current density photoelectron generators
This invention relates to a photoemissive electron beam generator which is capable of producing a high current density beam of electrons and is suitable for use in electron beam semiconductor lithography, and also relates to a photoemissive electron source for the generator and to a method of making the source.
As more and more elements are placed on semi-conducting chips, lithography systems for making the chips must be developed having ever greater resolution in order to generate the increased number of elements on the chips.
Optical lithographic systems operating at visible wavelengths have resolution limits approximating 1.25 micrometers, but electron beams have been proposed and successfully used to reduce feature size below this limit. Such systems can have resolutions well below 1 micrometer because of the shorter wavelengths associated with high energy electrons.
Since modern semiconductor lithographic systems must achieve fast writing times (high throughput rates) in addition to high resolutions, their electron energy beams must also have a high brightness, which means a high current density. This property is particularly important for so called direct-write systems wherein the electron beam is rapidly steered and modulated so as to effect an exposure of the highly complex circuit pattern directly onto a semiconducting chip. Direct-write methods contrast with conventional projection lithographic techniques in which a mask is used to define the entire pattern for simultaneous exposure onto the chip.
Bright electron sources for use in semiconductor lithography are known. For example, tungsten and LaB6 thermionic cathodes, barium dispenser cathodes, and heated W/O/Zr field emitters have been used. Such field emitters have attained a nominal brightness value of 5 x 107 A/cm2/sr (amperes/square centimeter/steradian).
However, each of these electron sources has some drawback. The tungsten filament suffers from a high evaporation rate at its operating temperature. LaB6 is easily poisoned by environmental impurities, has difficulty in remaining stably bonded at operating temperatures and forms undesirable current intensity lobes. Dispenser cathodes tend to evaporate at operating temperatures and are, moreover, easily poisoned. Furthermore, the support systems of heated cathodes are subject to high temperature distortions, which are likely to cause configurational changes in the electron beams. Finally, field emitters are also easily poisoned, may suffer from spot migration or flicker, require frequent unpredictable reprocessing and, if heated, may similarly introduce beam errors through geometrical distortions caused by the hot support system.Hot emitters are further limited by the finite time required to heat them, thereby precluding rapid intensity modulation of such electron sources. For semiconductor lithographic systems with heated emitters, beam modulation at the target plane is effected electrostatically and requires the additional complexity of blanking electrodes located in the lithographic column.
Cold electron emitters, such as environmentally stable cesium iodide and palladium photocathodes, are also known. Such photocathodes have been irradiated by ultraviolet light to provide electrons for lithography columns operating at a vacuum in the range of 10-4 to 10-5 torr, but the low brightness (approximately 10-50 A/cm2/sr) of the electron beams from these cathodes has restricted their use to projection lithography.
Another criterion for high resolution lithography is that the electron source exhibits uniform and substantially monochromatic (low spread in electron energy) emission. A low spread in electron energy is necessary to provide high resolution imaging by allowing the electron beam to be focussed to a minimum sized spot.
According to the invention, an electron beam generator for an electron beam semiconductor lithography system comprises a continuous wave laser, a modulator for varying the intensity of, or deflecting, the optical output beam of the laser, a photoemissive cathode which has a semitransparent film of a photoemissive substance comprising any one or more of cesium antimonide, sodium potassium antimonide, cesiated gallium phosphide, and cesiated gallium arsenide phosphide, and which is positioned for illumination by the output beam of the laser so that the film of the photoemissive substance is caused to emit electrons, and a light optical train positioned between the laser and the cathode for producing with the output beam of the laser a pattern of laser light on the photoemissive cathode such that the electrons emitted by the film form an electron image which is determined by the pattern and which is suitable for semiconductor lithography.
Such a generator is capable of producing a high current density electron beam from a photoemissive source (i.e. the cathode) operated at low temperatures, the electrons in the generated electron beam being substantially monochromatic (monoenergetic), thus permitting high resolution imaging by allowing the electron beam to be focussed to a minimum sized spot.
Furthermore the intensity of the electron beam may be modulated by modulating the activating laser beam, thereby avoiding the need for electron beam blanking and reducing proximity effects.
Also, the emitted electron beam is spatially uniform and is shapable by shaping the optical illuminating beam.
In a preferred embodiment the laser is an argon ion continuous wave laser operable at a discrete wavelength between 454.5 and 514.5 nanometers, and the photoemissive cathode for generating the electron beam upon illumination by the laser light comprises a substrate which is optically transmissive at the lasing wavelength and which has a back face facing towards the optical output beam of the laser and a front face facing away from the optical output beam of the laser, and an electrically conductive, optically semitransparent film deposited on the front face of the substrate, and the semitransparent film of photoemissive substance is deposited on the electrically conductive film. The photoemissive cathode is operated within a high vacuum environment and is preferably oriented such that the photoemissive surface will emit electrons upon back-illumination by the laser light.
Although the back-illuminated cathode is preferred for lithographic applications, a frontilluminated cathode formed by deposition of the photoemissive surface film onto an opaque, electrically rona'uctive substrate is an alternative configuration.
The construction of the cathode in fact forms another aspect of the present invention, according to which a photoemissive electron source for generating, in response to suitable laser light illumination, a substantially monochromatic high intensity electron beam which can be modulated and shaped, comprises an optically transmissive substrate, an eGectrically conduc.ive, optically semitransparent film deposited upon the substrate, and a semitransparent film of a photoemissive substance deposited on the electrically conductive film, the photoemissive substance comprising any one or more of cesium antimonide, sodium potassium antimonide, cesiated gallium phosphide, and cesiated gallium arsenide phosphide, and being operable to emit electrons upon illumination by suitable laser light
The substrate of the photoemissive source may be made of quartz, glass, or sapphire, and the semitransparent electrically conductive film may be of an electrically conductive metallic material, such as chromium. The preferred photoemissive surface film is cesium antimonide (Cs3Sb) formed by consecutive depositions of antimony and cesium. Other suitable photoemissive surface films for the source may be formed of sodium potassium antimonide (Na2KSb), or of single crystal compounds composed of gallium, phosphorus, and arsenic coated with cesium or cesium and oxygen.
A preferred method of making a Cs3Sb photoemissive cathode in accordance with the invention includes the formation of electrical connections to the cathode by the deposition onto a transparent substrate of a thick electrically conductive metallic coating of, for example, chromium. The metallic coating covers the substrate surface except for a portion thereof, for example a small central region, which is masked prior to deposition of the coating. This region will subsequently contain the photoemissive surface.
The mask is removed after deposition of the thick metallic layer, and a thinner coating of chromium or other electrically conductive material, semitransparent to the illuminating laser wavelength, is deposited over at least the unmasked region and preferably over the entire substrate surface. A thin layer of antimony is then deposited onto the thin electrically conductive film, and cesium is vapour-deposited onto the antimony to complete the manufacture of the
Cs3Sb photoemissive cathode. A Na2KSb photoemissive cathode may be made in the same way except that sodium and potassium are vapour deposited onto the antimony layer in a predetermined ratio instead of cesium.
Photoemissive electron sources in accordance with the invention have a spectral response which is compatible with existing optically monochromatic visible light continuous wave lasers. Also, they possess a photoemissive surface which is easy both to prepare and to restore.
Examples of an electron beam generator in accordance with the invention and of a photoemissive electron source for use therein, will now be described with reference to the accompanying drawings, in which: Figure 1 is a schematic representation of the essential components of an electron beam lithography system employing an electron beam generator in accordance with the invention;
Figure 2 is a graph illustrating the spectral response of various photoemissive materials, sensitive to visible and near infrared radiation, as a function of the irradiating wavelength, with appropriate stimulating laser wavelengths indicated;
Figure 3 is a cross-sectional view of a photoemissive cathode in accordance with the invention and suitable for use in the system shown in Figure 1; and,
Figure 4 illustrates a method of fabricating the photoemissive cathode of Figure 3.
The electron beam lithography system represented in Figure 1 includes a laser 10, such as an argon ion laser which is operable to generate a beam of coherent light at one of several radiating frequencies, namely 454.5, 457.9,465.8, 472.7, 476.5, 488.0, 496.5, 501.7, and 514.5 nanometers. The strongest radiating frequencies are 488.0 and 514.5 nanometers, and a suitable laser is a series 550 argon ion laser available from Control Laser
Corporation of Orlando, Florida.
Positioned in the lasing cavity of the laser 10 or at another location near the laser is a beam modulator 11. The modulator 11 may be any optical, electro-optical, or acousto-optical device suitable for regulating the intensity of the beam or deflecting it.
The light beam radiating from the laser 10 is guided by a light optical train 12 including a plate 1 3 having an aperture 14 of specified geometry, for example, a square. A lens 1 5 focuses the laser light as an image of the aperture 14 onto a photoemissive cathode 1 6 which will be described in detail hereinafter. The photoemissive cathode 1 6 and electron optical components for processing the electrons emitted by the cathode 16 are housed within a vacuum chamber schematically illustrated by the dotted enclosure 18. A high vacuum such as a pressure of 10-9 torr or less is maintained in the vacuum chamber 18.
On the opposite side of the photoemissive cathode 16 from the laser 10 is an anode 20 which operates to accelerate electrons emitted by the cathode 1 6. An additional negatively charged
Whenelt electrode (not shown) may be positioned between the photoemissive cathode 1 6 and the anode 20. From the anode 20 the electron beam next passes through various known electron optical components, which shape and position the electron beam as it is directed towards a target 21. After being accelerated by the anode 20, the electron beam passes through an electron lens 22 and then through an electrostatic beam shaping deflector 26 and a beam-shaping aperture 28.
The beam shaping defiector 26 operates to alter the position of the electron image of the photoemissive electron source on the beam shaping aperture 28 to create a variably shaped and sized electron beam. The beam next passes through a demagnification lens 29, and subsequently through a beam limiting aperture 30. Immersed in a final projection lens 32 are dynamic focussing coiis 34 which focus the beam onto the target 21, dynamic stigmators 36 which provide astigmatic correction to the beam, and a deflection yoke 38 which scans the beam over the target.
Because the photoemissive cathode 1 6 responds instantaneously to illumination by the laser 10, the electron beam intensity can be modulated by modulating the laser beam intensity. Modulation of this optical beam is facilitated by location of the beam modulator 11 outside of the high vacuum chamber 18. In prior art lithographic electron beam devices, beam
modulation is accomplished by special blanking electrodes which must be located between an
electron source and a target within a vacuum
enclosure. The lithography system incorporating
an electron beam generator of the present
invention takes advantage of the general
proposition that replacing any component located
in the vacuum enclosure by a similar functional
element positioned outside the vacuum enclosure
simplifies the overall lithographic column fabrication and operation.
As will be described in greater detail below, the
photoemissive cathode 16 includes a
photoemissive surface formed, for example, of
cesium antimonide, Cs3Sb, which emits electrons when illuminated by the argon ion laser light.
Figure 2 is a graph of the spectral response
(milliamperes of electron current per watt of
illuminating radiation) of various photoemissive
materials as a function of the wavelength of
illumination. Note that at the strongest argon ion
laser illuminating wavelengths of 488.0 and
514.5 nanometers, cesium antimonide has high sensivities with quantum efficiencies of 6 percent or more. The combination of strong
monochromatic optical emission from the argon ion laser and the good match of the argon ion laser wavelengths to the spectral response of cesium antimonide result in the high current density emission from this photocathode. Other lasers operating at wavelengths below approximately 520 nanometers would also be suited for this application.
Another suitable photoemissive surface for the cathode 16 is the "bialkali" sodium potassium antimonide (Na2KSb). Although this surface is more difficult to fabricate than a Cs3Sb surface because a well-defined ratio of sodium to potassium is required, this cathode does not need any highly volatile cesium, and thus is more stable. The preferred method of making the
Na2KSb cathode is basically similar to that to be described hereinafter for Cs3Sb, and the spectral response of these two surfaces is similar as is indicated in Figure 2. Consequently, the Na2KSb cathode is also sensitive to argon ion laser irradiation.
Other suitable photoemissive surfaces may be formed from single crystals composed of elements from groups Ill and V of the Periodic
Table such as gallium, phosphorus, and arsenic coated with either cesium or cesium and oxygen.
Such surfaces can be made to have a negative electron affinity and therefore substantially increased electron escape depths. This characteristic results in an emission of electrons with especialiy low energy spread. The easiest of these compounds to fabricate into photoemissive surfaces for lithographic applications are gallium phosphide (GaP), or gallium arsenide phosphide (Ga(As,P,,)), which require only cesium (instead of cesium and oxygen) for activation. In one manner of fabricating these surfaces, a transmissive layer of GaP is first grown on an optically transparent substrate, with the photoemissive surface grown on this layer. Either an argon ion laser or an appropriate semiconductor injection laser can be used to stimulate electron emission.The argon ion laser emits energy at a radiative wavelength near the optimum quantum efficiency for photoemissive surfaces of gallium phosphide and gallium arsenide phosphide thereby maximizing the emission of electrons. An injection laser will emit energy at much lower power levels but can be constructed to operate near the long wavelength threshold of these photoemissive materials, thereby minimizing the emitted electron energy spread. The superior characteristics of cathodes having photoemissive surfaces composed of compounds from elements of groups Ill and V are, however, balanced by the increased difficulty in fabricating such surfaces for use in the transmissive mode.
The back-illuminated photoemissive cathode disclosed herein and a preferred method of fabricating the cathode will now be described with reference to Figures 3 and 4. With reference first to Figure 3, the photoemissive cathode 1 6 includes a light transmissive substrate 40 which is preferably quartz or sapphire, but which may instead be glass. As will be discussed more completely with reference to Figure 4, a thick metallic coating 42 is deposited onto one face of the substrate 40. Suitable materials are, for example, chromium, tungsten, and aluminium. As can be seen in these figures, the layer 42 does not extend into a central region 44, a structure achieved by keeping the region 44 masked during deposition of the coating 42.A thin semitransparent electrically conducting layer 46 of, for example, chromium is next deposited on top of the layer 42 and the region 44. (This electrically conducting layer may not be necessary for cathodes which utilize gallium phosphide or gallium arsenic phosphide as photoemissive surfaces). Finally, a layer 48 of the photoemissive material, such as cesium antimonide, is produced within the region 44.
The fabrication of the cathode 1 6 will now be discussed with reference to Figure 4. First, a suitable transparent substrate 40 such as quartz, sapphire or glass is selected. Onto one selected face of the substrate 40 is deposited in vacuum a coating of, for example, chromium, sufficiently thick to allow the attachment of external electrical leads and to act as a low resistance electrical path to the central region 44. This deposition may be performed by evaporating chromium from a resistance--heated nichrome wire 52. The central region 44, which may have an area of approximately 0.02 square millimeters or more, is masked to prevent the thick chromium layer from being deposited in the region 44.Thereafter the mask is removed and a thin electrically conductive, optically semitransparent layer 46 of chromium is deposited in vacuum on the entire selected substrate face, including the previously masked central region 44. This chromium may also be supplied by the nichrome wire 52, resistance heated to evaporate chromium onto the substrate 40. The nichrome wire 52 is heated until the electrically conductive, optically semitransparent chromium layer 46 is deposited in the region 44. A suitable thickness for this thin layer of chromium is about 100 angstroms or less, and such a layer 46 will reduce the transmission of visible light through the central region 44 to, for example between 40 and 50% of that passing through the transparent substrate 40
The thin chromium layer 46 serves as an electrical path between the thick annular coating 42 and the central region 44.Next, an antimony bead 54 melted onto a nichrome supporting wire 56 is resistance heated in vacuum so as to evaporate a thin layer or antimony onto the portion of the chromium layer 46 in the region 44. Evaporation of antimony onto the part of the chromium layer 46 outside of the central region 44 will not affect the photoemissive behaviour of the system. The thickness of the antimony film should be such as to reduce the overall transmission of visible light in the central region 44 to, for example, about 30 to 40% of that passing through the transparent substrate 40.Next the substrate 40 with the chromium and antimony coatings and kept under vacuum is positioned in a high vacuum chamber 50 pumped to pressures below 2 x 10-9 torr which is, or will become, that component of the lithography column containing the photoemissive cathode 1 6. The substrate 40 in the high vacuum chamber 50 is then heated to approximately 1 00CC by means of a nichrome heater wire 58 wrapped around the periphery of the substrate 40. Also disposed within the vacuum chamber 50 is a cesium source "channel" 60 which contains, for example, a mixture of cesium chromate and a reducing agent such as silicon. The channel 60 is resistance-heated by means of an electrical connecting wire 62 to evaporate pure cesium onto the heated antimony film in the region 44.
Evaporation of cesium onto the antimony film or chromium layer outside the region 44 will not affect the photoemissive behaviour of the system.
In this way a thin layer or film 48 of cesium antimonide is produced in the region 44. During the foregoing cesium evaporation process, the photoemissive cathode 1 6 is illuminated by, for example, the argon ion laser and the photongenerated current is measured by collecting the emitted electrons with the nichrome wire 52.
When the photocurrent reaches a maximum value, the currents through the wire 62 and through the substrate-heating nichrome heater wire 58 are stopped so that no more cesium is deposited in the region 44. Should the photocurrent drop during cooling of the substrate, additional cesium is evaporated onto the cold surface 44. If the additional cesium evaporated onto the region 44 does not cause the photocurrent to return to its maximum value, more antimony may be evaporated onto the substrate followed by the deposition of additional cesium until the maximum value is re-attained.
Over a period of time, both with and without photoemission from its surface, the Cs3Sb cathode may degrade due to either the loss of cesium or contamination of the antimony by impurities. Such degradation can be reversed by additional evaporation of antimony and cesium onto the region 44 as detailed above.
In operation of the system, a laser beam from the laser 10 passes through the transparent substrate 40 and through the semitransparent chromium layer 46 and penetrates into the cesium antimonide layer 48, causing electrons to be emitted from the cesium antimonide. The electron beam thus emitted from the photoemissive cathode 1 6 has a high current density in the range of one to one hundred milliamperes per square centimeter. Current densities in the beam at the plane of the target 21 will be several hundred amperes per square centimeter. Values in this range are well suited for direct-write lithography systems in which the electron beam is steered to generate a complex pattern on a semiconducting chip. Such electron beams may also be used in making masks for projection lithography or in non-lithographic applications such as electron beam microscopy.
It will thus be appreciated that there has been disclosed a photoemissive cathode 1 6 which, when back-illuminated through a chromium layer with 50 to 60% optical loss, has a quantum efficiency of 3% or more and which upon degradation may be easily restored in situ by the deposition of additional cesium or cesium and antimony. The photoemissive cathode 1 6 is capable of generating a high current density in the range of one to one hundred milliamperes per square centimeter to provide current densities at a target 21 of hundreds of amperes per square centimeter. In addition, there is a low energy spread among the electrons in the range of a few tenths or less of an electron volt.This small spread is a direct consequence of the low energy of the emitted electrons once they have lost most of their initial energy during their transitions from the bound valence states to the vacuum level. The maximum magnitude of the emitted electrons' energy is dependent on the difference of the laser's photon energy and the electron emission threshold energy, defined by an electronic transition between the top of the photoemissive material's valence band and its vacuum level. For argon ion laser light of 514.5 nanometers (2.43 electron volts) and a threshold of photoemission of Cs3Sb of approximately 2.0 electron volts, the maximum emission energy of the electrons is 0.43 electron volts, which is, therefore, the maximum energy spread of the electrons. The nominal energy spread, commonly based on the half-width of the distribution curve of numbers of emitted electrons versus their energy, will be substantially lower than this.
The cathode operates at a low temperature such as room temperature so that there are no support problems as would be the case with a heated cathode. Furthermore, no heating up time is required because the electrons are generated instantaneously in response to illumination by the laser light. Modulation of the electron beam can conveniently be accomplished by modulating the laser beam outside the vacuum chamber 18. In addition, beam shaping or patterning into complex shapes is easily accomplished by apertures or masks in the optical train between the laser 10 and the photoemissive cathode 16 outside of the vacuum enclosure 1 8.
Claims (16)
1. An electron beam generator for an electron beam semiconductor lithography system, the generator comprising a continuous wave laser, a
modulator for varying the intensity of, or deflecting, the optical output beam of the laser, a
photoemissive cathode which has a semitransparent film ot a photoemissive
substance comprising any one or more of cesium
antimonide, sodium potassium antimonide,
cesiated gallium phosphide, and cesiated gallium
arsenide phosphide, and which is positioned for
illumination by the output beam of the laser so
that the film of the photoemissive substance is
caused to emit electrons, and a light optical train
positioned between the laser and the cathode for producing with the output beam of the laser a pattern of laser light on the photoemissive cathode such that the electrons emitted by the film form an electron image which is determined by the pattern and which is suitable for semiconductor lithography.
2. An electron beam generator according to claim 1, in which the photoemissive cathode is arranged to be back illuminated, and the light optical train includes at least one optical lens to focus the output beam of the laser through the back of the photoemissive cathode onto the film.
3. An electron beam generator according to claim 2, in which the optical lens is operable to focus the output beam of the laser onto the film in a manner to form substantially a point source of electrons.
4. An electron beam generator according to any one of claims 1 to 3, in which the laser is an argon ion laser operable at a wavelength between 454.5 and 514.5 nanometers.
5. An electron beam generator according to any one of the preceding claims, in which the photoemissive cathode is positioned within a vacuum chamber, and the laser, the modulator, and the light optical train are positioned outside the vacuum chamber.
6. An electron beam generator according to any one of the preceding claims, in which the modulator is an acousto-optical device.
7. An electron beam generator according to
any one of claims 1 to 5, in which the modulator is an electro-optical device.
8. An electron beam generator according to any one of the preceding claims, in which the photoemissive cathode comprises a substrate which is optically transmissive to the laser light, and which has a back face facing towards the optical output beam of the laser and a front face facing away from the optical output beam of the laser, and an electrically conductive, optically semitransparent film deposited on the front face of the substrate, and the semitransparent film of photoemissive substance is deposited on the electrically conductive film.
9. A photoemissive electron source for generating, in response to suitable laser light illumination, a substantially monochromatic high intensity electron beam which can be modulated and shaped, the source comprising an optically transmissive substrate, an electrically conductive, optically semitransparent, film deposited upon the substrate, and a semitransparent film of a photoemissive substance deposited on the electrically conductive film, the photoemissive substance comprising any one or more of cesium antimonide, sodium potassium antimonide, cesiated gallium phosphide, and cesiated gallium arsenide phosphide, and being operable to emit electrons upon illumination by suitable laser light.
10. An electron source according to claim 9, in which the substrate is formed of quartz or sapphire.
11. An electron source according to claim 9, or claim 10, in which the semitransparent electrically conductive film is of chromium.
12. A method of making a photoemissive cathode capable of high intensity electron emission, comprising, in the order given, the steps of providing a transparent substrate, masking a selected portion of one face of the substrate, depositing a thick metallic coating upon all of said face of the substrate except the masked portion to create a low-resistance electrical path, unmasking the selected portion of the substrate, depositing a semitransparent, electrically conductive film over at least the selected portion of the substrate, depositing a semitransparent layer of antimony over the electrically conductive film, and evaporating onto the antimony layer either cesium, or sodium and potassium in a predetermined ratio.
13. A method according to claim 12, in which during the deposition of cesium or sodium and potassium onto the antimony layer, the partiallyfabricated cathode is illuminated with a laser beam and the current generated by the partiallyfabricated cathode is measured, the deposition of cesium or sodium and potassium being terminated when the current reaches a maximum value.
14. A semiconductor lithography system including an electron beam generator according to claim 1 and substantially as described with reference to Figure 1 of the accompanying drawings.
1 5. A photoemissive electron source according to claim 9, substantially as described with reference to Figure 3 of the accompanying drawings.
16. A method according to claim 12, substantially as described with reference to Figure 4 of the accompanying drawings.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US32596081A | 1981-11-30 | 1981-11-30 |
Publications (2)
Publication Number | Publication Date |
---|---|
GB2111299A true GB2111299A (en) | 1983-06-29 |
GB2111299B GB2111299B (en) | 1986-07-09 |
Family
ID=23270181
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB08231900A Expired GB2111299B (en) | 1981-11-30 | 1982-11-09 | High current density photoelectron generators |
GB08511180A Expired GB2157884B (en) | 1981-11-30 | 1985-05-02 | Photoemissive cathode for high current density photoelectron generators |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB08511180A Expired GB2157884B (en) | 1981-11-30 | 1985-05-02 | Photoemissive cathode for high current density photoelectron generators |
Country Status (4)
Country | Link |
---|---|
JP (2) | JPS58108639A (en) |
DE (1) | DE3241766A1 (en) |
FR (1) | FR2517470B1 (en) |
GB (2) | GB2111299B (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0147009A2 (en) * | 1983-12-28 | 1985-07-03 | Kabushiki Kaisha Toshiba | X-ray scanner |
GB2164787A (en) * | 1984-09-11 | 1986-03-26 | Texas Instruments Ltd | Electron beam apparatus |
EP0182665A2 (en) * | 1984-11-20 | 1986-05-28 | Fujitsu Limited | Method of projecting a photoelectron image |
GB2173635A (en) * | 1985-03-15 | 1986-10-15 | Secr Defence | Photoemissive electron source |
GB2260666A (en) * | 1991-09-20 | 1993-04-21 | Sharp Kk | Time division multiplexed diode lasers |
EP0873573A2 (en) * | 1995-07-10 | 1998-10-28 | Intevac, Inc. | Electron sources utilizing negative electron affinity photocathodes with ultra-small emission areas |
WO2002015223A1 (en) * | 2000-08-17 | 2002-02-21 | Applied Materials, Inc. | An electron beam lithography system using a photocathode with a pattern of apertures for creating a transmission resonance |
CN100394654C (en) * | 2003-01-16 | 2008-06-11 | 松下电器产业株式会社 | Photoelectronic discharge plate and negative particle generator charged clear device and the like equipment using the plate |
CN1788682B (en) * | 2004-11-02 | 2010-09-01 | 通用电气公司 | Electron emitter assembly and method for generating electron beams |
US20180319040A1 (en) * | 2012-11-09 | 2018-11-08 | Denis Beaupre | Methods and systems using concrete mix temperature measurement |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6037633A (en) * | 1983-08-09 | 1985-02-27 | Hamamatsu Photonics Kk | Photoelectron gun |
JPS6347928A (en) * | 1986-08-18 | 1988-02-29 | Fujitsu Ltd | Mask for photoelectron image transfer |
US4963823A (en) * | 1988-06-27 | 1990-10-16 | Siemens Aktiengesellschaft | Electron beam measuring instrument |
DE68916870D1 (en) * | 1988-07-01 | 1994-08-25 | Ibm | Optical fiber photocathode. |
JPH0936025A (en) * | 1995-07-14 | 1997-02-07 | Nec Corp | Method and apparatus for electron beam exposure |
DE10245052A1 (en) * | 2002-09-26 | 2004-04-08 | Leo Elektronenmikroskopie Gmbh | Electron beam source and electron optical apparatus with one |
JP6664223B2 (en) * | 2016-01-12 | 2020-03-13 | 株式会社荏原製作所 | Electron gun and inspection device having the same |
JP6867568B2 (en) * | 2016-11-07 | 2021-04-28 | 国立大学法人東京工業大学 | Nanoscale photocathode electron source |
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GB812403A (en) * | 1954-08-06 | 1959-04-22 | Emi Ltd | Improvements in or relating to the formation of evaporated layers |
GB714054A (en) * | 1950-03-17 | 1954-08-25 | Emi Ltd | Improvements relating to the manufacture of photo-electric devices |
GB1005708A (en) * | 1960-12-14 | 1965-09-29 | Emi Ltd | Improvements relating to photo electrically sensitive devices |
CH391912A (en) * | 1961-11-09 | 1965-05-15 | Trueb Taeuber & Co Ag | Process for visualization and recording of electron-optical images |
FR1345063A (en) * | 1962-10-23 | 1963-12-06 | Thomson Houston Comp Francaise | Photoelectric cathode |
DE1464594A1 (en) * | 1963-07-18 | 1968-12-19 | Forschungslaboratorium Dr Ing | Photocathode |
GB1117759A (en) * | 1964-12-16 | 1968-06-26 | Matsushita Electric Ind Co Ltd | Photoemissive device |
US4097761A (en) * | 1966-02-16 | 1978-06-27 | Rca Corporation | Image tube cathode |
GB1205129A (en) * | 1967-03-10 | 1970-09-16 | Rca Radio Corp Of America | Photocathodes containing antimony and method of making the same |
FR1566316A (en) * | 1968-01-31 | 1969-05-09 | ||
DE1963740A1 (en) * | 1969-12-19 | 1971-07-08 | Max Planck Gesellschaft | Pulse electron source |
FR2076604A5 (en) * | 1970-01-21 | 1971-10-15 | Commissariat Energie Atomique | |
US3821778A (en) * | 1972-12-04 | 1974-06-28 | Hughes Aircraft Co | Infrared photocathode |
JPS573182B2 (en) * | 1973-08-08 | 1982-01-20 | ||
JPS5224385A (en) * | 1975-08-20 | 1977-02-23 | Sanki Eng Co Ltd | Single filter press |
US4039810A (en) * | 1976-06-30 | 1977-08-02 | International Business Machines Corporation | Electron projection microfabrication system |
DE2719799A1 (en) * | 1977-04-28 | 1978-11-02 | Siemens Ag | Mask imaging photoelectronic projector - has mask as positive electrode of acceleration field between photocathode and semiconductor wafer |
JPS5469953A (en) * | 1977-11-15 | 1979-06-05 | Toshiba Corp | Electron emission device |
JPS54146952A (en) * | 1978-05-10 | 1979-11-16 | Hitachi Denshi Ltd | Photoelectric surface |
US4313072A (en) * | 1979-10-10 | 1982-01-26 | The United States Of America As Represented By The United States Department Of Energy | Light modulated switches and radio frequency emitters |
-
1982
- 1982-11-09 GB GB08231900A patent/GB2111299B/en not_active Expired
- 1982-11-11 DE DE19823241766 patent/DE3241766A1/en active Granted
- 1982-11-26 FR FR8219870A patent/FR2517470B1/en not_active Expired
- 1982-11-30 JP JP57208747A patent/JPS58108639A/en active Pending
-
1985
- 1985-05-02 GB GB08511180A patent/GB2157884B/en not_active Expired
-
1990
- 1990-05-29 JP JP13731790A patent/JPH03176953A/en active Pending
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0147009A2 (en) * | 1983-12-28 | 1985-07-03 | Kabushiki Kaisha Toshiba | X-ray scanner |
EP0147009A3 (en) * | 1983-12-28 | 1987-05-13 | Kabushiki Kaisha Toshiba | X-ray scanner |
GB2164787A (en) * | 1984-09-11 | 1986-03-26 | Texas Instruments Ltd | Electron beam apparatus |
EP0182665A2 (en) * | 1984-11-20 | 1986-05-28 | Fujitsu Limited | Method of projecting a photoelectron image |
EP0182665A3 (en) * | 1984-11-20 | 1987-04-22 | Fujitsu Limited | Method of projecting a photoelectron image |
GB2173635A (en) * | 1985-03-15 | 1986-10-15 | Secr Defence | Photoemissive electron source |
GB2173635B (en) * | 1985-03-15 | 1989-11-01 | Secr Defence | An electron capture detector |
GB2260666B (en) * | 1991-09-20 | 1995-12-20 | Sharp Kk | Time division multiplexed diode lasers |
GB2260666A (en) * | 1991-09-20 | 1993-04-21 | Sharp Kk | Time division multiplexed diode lasers |
EP0873573A2 (en) * | 1995-07-10 | 1998-10-28 | Intevac, Inc. | Electron sources utilizing negative electron affinity photocathodes with ultra-small emission areas |
EP0873573A4 (en) * | 1995-07-10 | 2000-03-01 | Intevac Inc | Electron sources utilizing negative electron affinity photocathodes with ultra-small emission areas |
WO2002015223A1 (en) * | 2000-08-17 | 2002-02-21 | Applied Materials, Inc. | An electron beam lithography system using a photocathode with a pattern of apertures for creating a transmission resonance |
US6538256B1 (en) | 2000-08-17 | 2003-03-25 | Applied Materials, Inc. | Electron beam lithography system using a photocathode with a pattern of apertures for creating a transmission resonance |
CN100394654C (en) * | 2003-01-16 | 2008-06-11 | 松下电器产业株式会社 | Photoelectronic discharge plate and negative particle generator charged clear device and the like equipment using the plate |
CN1788682B (en) * | 2004-11-02 | 2010-09-01 | 通用电气公司 | Electron emitter assembly and method for generating electron beams |
US20180319040A1 (en) * | 2012-11-09 | 2018-11-08 | Denis Beaupre | Methods and systems using concrete mix temperature measurement |
Also Published As
Publication number | Publication date |
---|---|
DE3241766A1 (en) | 1983-06-09 |
FR2517470A1 (en) | 1983-06-03 |
GB8511180D0 (en) | 1985-06-12 |
GB2111299B (en) | 1986-07-09 |
GB2157884B (en) | 1986-07-23 |
JPS58108639A (en) | 1983-06-28 |
FR2517470B1 (en) | 1989-01-20 |
JPH03176953A (en) | 1991-07-31 |
GB2157884A (en) | 1985-10-30 |
DE3241766C2 (en) | 1987-04-09 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19921109 |