EP0501785A2 - Structure pour émettre des électrons et procédé de fabrication - Google Patents

Structure pour émettre des électrons et procédé de fabrication Download PDF

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Publication number
EP0501785A2
EP0501785A2 EP92301632A EP92301632A EP0501785A2 EP 0501785 A2 EP0501785 A2 EP 0501785A2 EP 92301632 A EP92301632 A EP 92301632A EP 92301632 A EP92301632 A EP 92301632A EP 0501785 A2 EP0501785 A2 EP 0501785A2
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EP
European Patent Office
Prior art keywords
layer
aperture
electrically conductive
combination
layers
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Application number
EP92301632A
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German (de)
English (en)
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EP0501785A3 (en
Inventor
Wolfgang M. Feist
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Raytheon Co
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Raytheon Co
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Publication of EP0501785A3 publication Critical patent/EP0501785A3/en
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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J9/00Apparatus 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
    • H01J9/02Manufacture of electrodes or electrode systems
    • H01J9/022Manufacture of electrodes or electrode systems of cold cathodes
    • H01J9/025Manufacture of electrodes or electrode systems of cold cathodes of field emission cathodes
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05BELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
    • H05B33/00Electroluminescent light sources
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J3/00Details of electron-optical or ion-optical arrangements or of ion traps common to two or more basic types of discharge tubes or lamps
    • H01J3/02Electron guns
    • H01J3/021Electron guns using a field emission, photo emission, or secondary emission electron source
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J31/00Cathode ray tubes; Electron beam tubes
    • H01J31/08Cathode ray tubes; Electron beam tubes having a screen on or from which an image or pattern is formed, picked up, converted, or stored
    • H01J31/10Image or pattern display tubes, i.e. having electrical input and optical output; Flying-spot tubes for scanning purposes
    • H01J31/12Image or pattern display tubes, i.e. having electrical input and optical output; Flying-spot tubes for scanning purposes with luminescent screen
    • H01J31/123Flat display tubes
    • H01J31/125Flat display tubes provided with control means permitting the electron beam to reach selected parts of the screen, e.g. digital selection
    • H01J31/127Flat display tubes provided with control means permitting the electron beam to reach selected parts of the screen, e.g. digital selection using large area or array sources, i.e. essentially a source for each pixel group
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J2329/00Electron emission display panels, e.g. field emission display panels
    • H01J2329/86Vessels
    • H01J2329/8625Spacing members

Definitions

  • This invention relates generally to electron emitting structures and manufacturing methods and, more particularly, to electric field-producing electron emitting structures and to methods of fabricating such structures.
  • a cold cathode is formed by providing an electron emitting structure in the shape of a cone having a tip.
  • An electrically conductive gate electrode arrangement is positioned adjacent the tip portion of the cone to generate and control the electron emission from the tip portion.
  • An electric field may be produced between the electron emitting structure and a spaced-apart anode, by the application of a potential therebetween. The electric field is concentrated at the tip portion of the cone with sufficient intensity that electrons are emitted from the tip and are collected by the anode.
  • An anode display screen for such a flat panel display may be formed in accordance with conventional cathode-ray tube (CRT) technology, and may comprise a thin, optically transparent electrode affixed to the inside surface of a glass layer.
  • the electrode is coated with luminescing means, illustratively a phosphor material, which emits optical energy such as visible light in response to electron bombardment.
  • the emitted electrons are accelerated toward the anode by a potential, typically between 500 volts and 10 kilovolts, depending on the maximum brightness required, to illuminate the pixels of the phosphor-coated anode screen, typically mounted in close proximity to the tips.
  • a highly collimated beam of vaporized metal illustratively molybdenum, impinges normally onto a substrate, having a metal film (the control grid electrode) having micron-sized apertures over small cavities.
  • a second beam illustratively aluminum oxide vapor, impinges simultaneously onto the substrate, but at a very shallow angle.
  • the substrate is rotated about its central axis.
  • the net effect is that the apertures are gradually closed by the deposition of composite material (the molybdenum and aluminum oxide) while the metal cones (the cathode electrodes) are formed within the microcavities by the molybdenum vapor beam.
  • the composite material surrounding the cones and closing the apertures is later removed by selective chemical etching.
  • the vapor beams must be highly collimated, i.e., they must be evaporated from a considerable distance, typically 70 cm or more.
  • the process described by Spindt et al. is complicated and moreover, the apparatus needed to produce the process would be expensive, particularly for useful-sized displays.
  • wedge-shaped structures wherein a sharp edge portions of the wedge structure extends upward from a substrate, adjacent a gate electrode, toward an anode. See, for example, “Self-Aligned Silicon-Strip Field Emitter Array,” by J.P. Spallas, et al., and “Simulation and Design of Field Emitters,” by R.B. Marcus, et al., both papers presented at the 2d Int. Conf. on Vac. Microelectronics, at Bath, England, in 1989. It is suggested that such wedge emitters may provide certain advantages over comparably sized cone emitters.
  • wedge emitters provide the advantage of utilizing a greater fraction of the available substrate surface area for the support of the emitting devices.
  • heat may be dissipated more readily through wedges due to their larger mass or volume, and thus temperature increases are much smaller, than in comparable cone emitters.
  • wedge emitters share the same manufacturing problems and technical concerns of cone emitters. That is, with either approach, it is difficult to obtain uniformity among all of the emitting tips or wedges over an array of such emitters. As such, the manufacturing yields of these devices is generally less than satisfactory.
  • an electron emitting structure including a sheet of electrically conductive material having an edge. With such an arrangement, electron emission can be provided from the edge of a sheet of conductive material. Such a structure is simpler to fabricate than the prior approaches of wedges and cones having tip portions.
  • the surface conditions and geometrical aspects of the minute field emission tips are subject to change during their assembly with the anode in a closely fitted, vacuum envelope, and during their activation cycle, which serves to desorb surface contamination and to stabilize the microscopic tip geometry which can change due to field-induced atomic migration.
  • These tips are also subject to change over their operating life because of further atomic migration and ion bombardment.
  • the wedges may have similar problems.
  • the macroscopic and microscopic conditions of the edge of a sheet of conductive material used as an electron emitter are easier to control than the tip or wedge type emitters. Such edges are less susceptible to changes during subsequent manufacturing processes. Moreover, the edges of the sheet of conductive material are less subject to contamination during fabrication of the emission structure.
  • an electron emitting structure includes a first layer of electrically conductive material having an aperture disposed therein and a second layer of electrically conductive material spaced from the first layer.
  • a voltage potential coupled to the first layer provides a flow of electrons from peripheral edge portions of the aperture in the first layer.
  • a voltage potential is also coupled to the second electrode for controlling the rate of the flow of electrons.
  • the second layer of electron emitting structure has an aperture disposed in alignment with the aperture disposed in the first layer.
  • the potential is disposed between peripheral edges of the aperture in the second layer to control the rate of electron flow.
  • the electron flow is through the first aperture in the second layer in another embodiment flow of electrons occurs beyond the aperture in the second layer.
  • a third layer of electrically conductive material spaced from said first and second electrically conductive layers, the third electrically conductive layer having an aperture disposed therein substantially aligned with the apertures disposed in the first and second electrically conductive layers.
  • the tip-like and wedge electron emitting structures of the prior art have been replaced with a structure wherein electrons are emitted from a peripheral edge, preferably a peripheral edge of an aperture, thus alleviating fabrication difficulties and changes and degradation associated with a tip-like and generally wedge-shaped electron emitting structures.
  • a method of forming an electron emitting structure comprises the steps of forming a first sheet of electrically conductive material and forming a second sheet of electrically conductive material spaced from the first sheet.
  • a first one of said sheets has an aperture and a second one of said sheets is disposed to control field emission from peripherial edges of the aperture of said first sheet.
  • an electron emission apparatus 10 is shown to include an electron emitting structure 12 spaced from an anode structure 14, with an intervening gap 13 therebetween being substantially evacuated.
  • Electron emitting structure 12 comprises a first electrically conductive layer 28 spaced from a second electrically conductive layer 32, said layers 28, 32 having a generally circular aperture 34 disposed therethrough.
  • Anode structure 14 comprises an electrically conductive material.
  • an electron beam is drawn from a peripheral edge portion of one of the conductive layers 28 and 32 in accordance with the potential differences among conductive layers 28, 32 and anode 14.
  • one of the peripheral edge portions of the conductive layers 28, 32 within aperture 34 provides a cathode electrode of the electron emitting structure.
  • the other one of the peripheral edge portions of conductive layers 28, 32 may be used as a control or grid electrode of emitting structure 12.
  • emitting structure 12 includes, in addition to electrically conductive layers 24, 28 and 32, electrically insulating layers 22, 26, and 30, and an optional substrate or support layer 20.
  • substrate 20 is typically a silicon wafer, of the type used in conventional integrated circuit technology.
  • substrate 20 can be any other material which can support the structures to be described. If the structures to be described can be supported without the substrate 20 then the substrate 20 can be eliminated. Further, the substrate 20 may also be electrically conductive.
  • an optional electrically insulating layer 22, illustratively silicon dioxide (SiO2) is disposed over substrate 20 and may be grown or deposited thereon. Layer 22 is illustratively 8000 ⁇ (O.8 ⁇ m) in thickness.
  • Electrically conductive layer 24 which may provide a control voltage or a reference voltage, is deposited over layer 22; it is illustratively molybdenum, 3000 ⁇ in thickness.
  • conductive layer 24 functions as the control electrode while one of the overlying apertured layers function as the connection to the cathode electrode and the other layer functions as a focusing electrode.
  • a reference voltage (or control signal) may be coupled to layer 24 via signal lead 54.
  • layer 28 functions as the control electrode.
  • layer 28 is coupled to a signal lead 50 for connection to a cathode or control voltage as desired.
  • Each of the layers 26, 28, 30, and 32 provided in electron emitting structure 12 have a multiplicity of apertures generally denoted as 34, with each aperture 34 here extending through layers 26, 28, 30, and 32, as shown.
  • Apertures 34 are depicted as circular, and this is the preferred configuration; however, other shapes such as ovals, squares, etc. are possible.
  • circular apertures and apertures in general are here preferred to provide electron emission edges, it is also possible to use an edge of a conductive sheet, as will be further described in conjunction with FIG. 11A.
  • the conductive layer need not be a continuous sheet, but could alternatively be a loop of conductive material enclosing a region and thus providing a peripheral edge portion of an aperture from which electron emission can occur.
  • Apertures 34 extend through conductive layers 32 and 28 with a first diameter, illustratively between 1-2 ⁇ m, and through insulating layers 30 and 26 with a second, slightly larger, diameter.
  • the extent by which insulating layers 30 and 26 are undercut with respect to conductive layers 32 and 28 is illustratively 0.5 ⁇ m.
  • an annular peripheral edge surface of conductive layer 28 extends into aperture 34, providing a relatively sharp edge for the formation of a beam of electrons which flow in a generally uniform distribution upward through aperture 34 to anode structure 14 under the control of the voltage applied to conductive layer 32.
  • annular peripheral edge surface of conductive layer 32 extends into aperture 34, providing a relatively sharp edge for the formation of a beam of electrons which flow in a generally uniform distribution upward to anode structure 14 under the control of a voltage applied to conductive layer 28.
  • Electrically conductive layers 24, 28 and 32 have thus far been illustratively described as molybdenum.
  • these electrically conductive layers may be fabricated from a wide variety of materials. Generally, it is desired that these materials are refractory, and have the properties of high conductivity, relatively low work function and provide satisfactory adhesion to the adjacent layers. Examples of more refractory metals which may be used include molybdenum, tungsten, titanium and tantalum. These metals may be coated with a ceramic material, such as lanthanum hexaboride (LaB6) to exhibit substantially lowered work function.
  • the material for use as layers 24, 28 and 32 may also comprise a conductive ceramic which may be a super conductor.
  • Electron emission apparatus 110 includes an electron emitting structure 112 spaced from an anode structure 114, with an intervening gap 113 being substantially evacuated. Electron emitting structure 112 comprises a first plurality of substantially parallel conductors 128a, 128b, . . ., spaced from a second plurality of substantially parallel conductors 132a, 132b, . . ., and a multiplicity of generally circular apertures 134 formed through conductors 128a, 128b, . . ., and 132a, 132b, . . ..
  • Anode structure 114 includes an electrically conductive layer 142 which is disposed between a support 140 and a electroluminescent material layer 144 as will be further described.
  • electrostatic forces resulting from potentials applied to conductors 128a, 128b, . . ., conductors 132a, 132b, . . ., and conductive layer 142, via signal leads 150a, 150b, . . ., 1521, 152b, . . ., and 154, respectively, cause electron beams to be drawn from here peripheral edge portions 127 of corresponding conductors 128a, 128b, . . ., within apertures 134, onto an adjacent surface portion of anode structure 114, with such electron emission here under the control of signals applied between conductors 132a, 132b, . . ., and 128a, 128b, .
  • conductors 132a, 132b here function as control (or grid) electrodes of emitting structure 112, whereas peripheral edges of conductors 128a, 128b, . . ., function as cathodes.
  • Anode structure 114 thus here includes an electroluminescent coating 144 to convert the electrical energy from the electron bombardment into visible light energy.
  • a reference voltage is coupled to layer 124 via signal lead 154.
  • the gap between the anode structure and the emitting structure is essentially evacuated, preferably at a pressure of approximately 10 ⁇ 9 torr.
  • vacuum level may not be necessary.
  • the plurality of electrically conductive stripes 128, 132 are each provided by patterning a layer of material (not shown) or depositing such material as stripes through a patterned region.
  • Each of the plurality of stripes 128, 132 illustratively comprises molybdenum, 3000 ⁇ in thickness, which functions as the connection to the cathode electrode in the electron emission apparatus 110 of the present invention.
  • Individual stripes 128a, 128b . . . are disposed over an insulating layer 126 here of silicon dioxide 8000 ⁇ in thickness.
  • the plurality of stripes 128 is provided as a plurality of parallel stripes, electrically isolated from one another by virtue of spacings 129a, . . ., between them, which extend from the lower-left toward the upper-right in FIG. 2.
  • Each stripe 128a, 128b . . ., of the plurality of stripes 128 is coupled to an individual signal lead 150a, 150b, . . ., respectively, for connections to individually addressable cath
  • Electrically insulating layer 130 overlies the plurality of stripes 128, additionally filling the spacings 129a, . . ., between the individual parallel stripes 128a, 128b . . . thereof.
  • the plurality of electrically conductive stripes 132 are disposed as generally mentioned above over insulating layer 130, and such plurality of stripes 132 illustratively comprises molybdenum, 3000 ⁇ in thickness.
  • the plurality of stripes 132 here function as control electrodes in the electron emission apparatus 110 of the present invention.
  • the plurality of parallel stripes 132 are electrically isolated from one another by virtue of the spacings 131a, . . ., between them, as shown.
  • Each stripe 132a, 132b, . . ., of the plurality of stripes 132 is coupled to an individual signal lead 152a, 152b, . . ., respectively, for connections to individually addressable control voltages.
  • Apertures 134 are positioned at intersections of the parallel stripes 128a, 128b, . . ., with the parallel stripes 132a, 132b, . . ., that is, at the intersections of the individually addressable cathode and control electrodes.
  • Apertures 134 have a first diameter, illustratively between 1-2 ⁇ m through the pluralities of stripes 128, 132, and have a second, slightly larger, diameter through insulating layers 130, 126, here 1 ⁇ m increase in diameter.
  • an annular peripheral edge surface 127a of stripes 128a, 128b extends into aperture 134, providing a sharp edge for the formation of a beam of electrons which flow in a generally uniform distribution upward through the remainder of aperture 134 to anode electrode 142 under the control of the voltage applied to control electrode 132.
  • Anode structure 114 spaced apart from electron emitting structure 112, illustratively by 0.5-2.0 mm, includes an optically transparent substrate layer 140, illustratively glass, onto which is deposited a layer of electrically conductive material 142.
  • Conductive layer 142 is preferably an optically transparent material such as indium-tin-oxide (ITO); alternatively, layer 142 may comprise a metal such as aluminum, gold, or platinum, sufficiently thin so as to be essentially optically transparent.
  • Layer 144 comprising an electroluminescent material, illustratively a light-emitting phosphor, may be coated over layer 142.
  • FIGS. 3A and 3B a portion of electron emitting structure 112 useful in visualizing an arrangement of apertures 134 according to the present invention is shown.
  • the simplified cutaway section illustrated by FIG. 2 depicts only one aperture 134 at each of the intersections of the stripes 128a, 128b, . . ., with the stripes 132a, 132b, . . .
  • the views of FIGS. 3A and 3B imply an arrangement comprising a plurality of apertures 134 disposed at each of a corresporiding plurality of intersections of such plurality of stripes 128, 132. While the arrangement of apertures 134 depicted in FIG.
  • 3A may imply a rectangular array, such arrangement is not intended to be a limitation on the invention.
  • the arrangement of apertures 134 at each intersection of the stripes 128a, 128b, . . ., with the stripes 132a, 132b, . . ., will be selected in accordance with the particular application of the cathode structure. For example, a particular arrangement of phosphors on an opposing surface of anode structure (not shown) for use in a display would influence the exact arrangement of the intersecting stripes and positions of apertures 134.
  • FIGs. 4-11A illustrate various embodiments of the electron emission apparatus of the present invention.
  • FIG. 4 the embodiment of FIG. 4 corresponds in form to that of FIG. 2, and whose electron emission structure 112 is also shown in FIGs. 3A and 3B.
  • the electron emission apparatus of FIG. 4 includes electrically conductive layer 124, and stripes 128a and 132a, electrically insulating layers 122, 126 and 130, and substrate 120, comprising the emitting structure 112.
  • the anode structure 114 includes substrate 140, electrically conductive layer 142 and electroluminescent coating 144. Aperture 134 in emitting structure 112 extends through all layers and stripes down to conductive layer 124.
  • Conductive stripe 128a provides the connection to the peripheral edges 127 in aperture 134 of stripe 128a, that is the cathode electrode from which electron emission occurs within aperture 134.
  • the stripe 128a comprises relatively thick sections 128a′ away from apertures 134, illustratively 3000 ⁇ (0.30 ⁇ m), and relatively thin sections 128a ⁇ in the vicinity of apertures 134, illustratively 200-1000 ⁇ (0.02-0.10 ⁇ m).
  • the portion 128a′ of increased thickness of stripe 128a over the greater portion of its area increases its conductivity and mechanical strength in the contact areas.
  • the thin portion 128a ⁇ of stripe 128a which may be as thin as possible, such as 200 ⁇ , provides a sharp-edged emitting surface 127 for optimal electron emission density characteristics.
  • Annular surface 127 can be made even sharper by a processing technique, to be discussed later, which would provide a taper, as illustrated, to surface 127.
  • the embodiment of electron emission apparatus 210 illustrated in FIG. 5, includes electrically conductive layers 224, 228 and 232, electrically insulating layers 222, 226 and 230, and substrate 220, comprising the emitting structure 212.
  • the anode structure 214 includes substrate 240, electrically conductive layer 242 and electroluminescent coating 244. Aperture 234 in electron emission structure 212 extends through all layers down to conductive layer 224.
  • the structure of the FIG. 5 embodiment differs from the structure of FIG. 4 in that electrically conductive layer 228, functioning as the connection to the cathode electrode, is of uniform thickness throughout.
  • layer 228 is 300 ⁇ (0.03 ⁇ m) in thickness.
  • the form of layer 228 in the FIG. 5 embodiment provides the advantage of simplified manufacturing processing over the FIG. 4 embodiment, but it lacks certain performance characteristics of the other.
  • the thin annular surface 227 of conductive layer 228 within aperture 234, functioning as the cathode electrode may be made even sharper by a processing technique, to be discussed later, which provides a taper to surface 227.
  • the conductive layers 228, 232 may also be patterned to provide individually addressable stripes.
  • the embodiment of electron emission apparatus 310 illustrated in FIG. 6, includes electrically conductive layers 324, 328 and 332, electrically insulating layers 322, 326 and 330, and substrate 320, comprising the emitting structure 312.
  • the anode structure 314 includes substrate 340, electrically conductive layer 342 and electroluminescent coating 344. Aperture 334 in electron emission structure 312 extends through all layers down to conductive layer 324.
  • FIG. 6 embodiment The structure of the FIG. 6 embodiment is similar to that of FIG. 4, but it includes an additional conductive layer 360, illustratively a 0.3 rm layer of molybdenum, disposed over conductive layer 332 and spaced therefrom by an electrically insulating layer 362, illustratively a O.8 ⁇ m layer of SiO2.
  • Layers 360 and 362 include apertures which are substantially identical to apertures 334 formed through layers 326, 328, 330 and 332, and aligned therewith.
  • layer 360 provides improved focusing of the electron beams 336 by attracting those electrons which are directed outward from the cylinder formed by aperture 334.
  • the embodiment of electron emission apparatus 510 illustrated in FIG. 7, includes electrically conductive layers 524, 528 and 532, electrically insulating layers 522, 526 and 530, and substrate 520, comprising the emitting structure 512.
  • the anode structure 514 includes substrate 540, electrically conductive layer 542 and electroluminescent coating 544. Aperture 534 in electron emission structure 512 extends through all layers down to conductive layer 524.
  • the structure of the FIG. 7 embodiment differs from the structure of FIG. 4 in that aperture 534 through electrically conductive layer 532, functioning as the control electrode, is greater in diameter than aperture 534 through electrically conductive layer 528, functioning as the cathode electrode.
  • aperture 534 through layer 532 may illustratively be one ⁇ m greater in diameter than aperture 534 through layer 528.
  • the embodiment of electron emission apparatus 610 illustrated in FIG. 8, includes electrically conductive layers 624, 628 and 632, electrically insulating layers 622, 626 and 630, and substrate 620, comprising the emitting structure 612.
  • the anode structure 614 includes substrate 640, electrically conductive layer 642 and electroluminescent coating 644. Aperture 634 in electron emission structure 612 extends through all layers down to conductive layer 624.
  • the structure of the FIG. 8 embodiment differs significantly from the embodiments thus far described.
  • the upper conductive layer 632 functions as the connection to the cathode electrode while the lower conductive layer 628 functions as the control electrode.
  • the lower conductive layer 628 functions as the control electrode.
  • conductive layer 632, the electron emitting layer is preferably thinner than layer 628; illustratively, layer 632 may be 0.03 ⁇ m in thickness and layer 628 may be 0.3 ⁇ m in thickness.
  • the embodiment of electron emission apparatus 710 includes electrically conductive layers 724 and 72B, electrically insulating layers 722 and 726, and substrate 720, comprising the emitting structure 712.
  • the anode structure 714 includes substrate 740, electrically conductive layer 742 and electroluminescent coating 744. Aperture 734 in electron emission structure 712 extends through layers 728 and 726 down to conductive layer 724.
  • the apertured conductive layer 728 functions as the connection to the cathode electrode while the unapertured conductive layer 724 functions as the control electrode.
  • the apertured conductive layer 728 functions as the connection to the cathode electrode while the unapertured conductive layer 724 functions as the control electrode.
  • FIG. 9A there is shown an embodiment which is a first variation on the structure of FIG. 9.
  • the apertures of conductive layer 728′ are greater in diameter than the corresponding apertures 734′ through insulating layer 726′.
  • electrons are drawn from peripheral edge 727′ of conductive layer 728′ by virtue of the electric field induced as a result of the potential difference applied at terminals 750 and 754.
  • electric field through insulating layer 726′ is sufficient to cause field emission of electrons.
  • FIG. 9B a second variation on the structure of FIG. 9, in which insulating layer 726 ⁇ is unapertured.
  • An electric field through insulating layer 726 ⁇ , induced by the potential difference applied at terminals 750 and 754, results in field emission of electrons from peripheral edge 727 ⁇ of conductive layer 728 ⁇ .
  • conductive layers 728, 728′ and 728 ⁇ , of the embodiments of FIGS. 9, 9A and 9B, respectively, may be stepped in thickness, as shown, for example, in layer 128a of FIG. 4, to provide the advantages described therefor.
  • FIG. 9C there is shown an embodiment which may share the general structure of the FIG. 7 embodiment, but which is similar to the FIG. 9 embodiment in its mode of operation.
  • the unapertured conductive layer 824 functions as the control electrode
  • apertured conductive layer 824 functions as the connection to the cathode electrode
  • apertured conductive layer 832 functions as a focusing layer, to improve the pattern of electron flow from peripheral edge 827 toward anode structure 814.
  • the application of potentials to the several electrodes to produce field emission of electrons from the cathode and current flow of the field-emitted electrons to the anode may be as follows.
  • the conductive layer 142 of anode structure 114 may be set at +1200 volts with respect to emitter layer 128a, and control electrode layer 132a is set between 100-300 volts, illustratively +135 volts with respect to emitter layer 128a.
  • emitter layer 632 is the top layer of emitting structure 612
  • the conductive layer 642 of anode structure 614 is set at +1200 volts with respect to emitter layer 632
  • the potential at control electrode layer 628, with respect to emitter layer 632 may range between +100 and +300 volts, illustratively +135 volts.
  • FIG. 9C having the cathode provided as the intermediate layer, here 828, that the upper layer 832 thereof maybe disposed to provide the anode for the device. That is a relatively high positive potential may be applied between terminals 850 and 852 to draw field emitting electrons towards layer 832 whereas a potential is applied to underlying layer 824 to control emission of electrons from peripheral edge portions 827 of layer 828.
  • layer 832 may be provided as a patterned layer, as shown, having an aperture electrode disposed over layer 832, or alternatively may be provided as continuous non-pattern layer (not shown). This particular structure would be well adapted to vacuum microelectronic microwave type of devices.
  • structure 814 may also have a dielectric coating (not shown) disposed over layer 844 and structure 814 may then rest directly upon layer 832 to provide a more compact display element (not shown).
  • a substrate 720 as generally discussed in conjunction with FIG. 9A and 9B has disposed over a first surface thereof, a layer 722 comprised of, here typically silicon dioxide having a thickness of 3000 ⁇ and having disposed thereover, a layer 724 of a refractory conductive material such as molybdenum with layer 724 having a thickness of 3000 ⁇ .
  • a layer 726 of silicon dioxide having a thickness of 0.8 microns is disposed over layer 724.
  • etch-stop layer 770 of a different insulative type of material as layer 722 is disposed over silicon dioxide layer 726.
  • etch-stop layer 770 is comprised of a material such as silicon nitride and is deposited to a thickness of 500 to 800 ⁇ for example.
  • a second conductive layer 772 Disposed over etchstop layer 770 is a second conductive layer 772, here also comprised of molybdenum.
  • a masking layer (not shown), is disposed over layer 774 and is patterned to provide an aperture (not shown) exposing selective underlying portions of layer 774.
  • Layer 774 is then reactively ion etched to provide an aperture 774a having steep vertical sidewalls in layer 774.
  • Exposed portions of underlying layer 772 are also reactive ion etched to provide an aperture 772a having steep vertical sidewalls through layer 772, thus providing the structure, as generally shown, in conjunction with FIG. 9D.
  • a third layer 776 of molybdenum is disposed over layer 774 and through the apertures 772a and 774a, provided through layers 772 and 774 respectively.
  • Molybdenum layer 776 has a thickness of, here 3000 ⁇ .
  • RIE directive ion reactive etching
  • Such an etch is used to provide a directional etch to etch away in a vertical direction portions of layer 776.
  • Layer 774 is also removed using hydrofloric acid leaving layer 772 and portions 776′ of layer 776 (FIG. 9E). Since the reactive ion etching technique, preferentially etches in the vertical direction a small ridge or raised edge annulus portion 776′ is left of layer 776 along the peripheral edge portions 772′ of layer 772 in the aperture 772a.
  • the structure described above is seen as providing a field emission structure which may preferably provide improved field emission characteristics. That is, the structure provides an annulus as in keeping with many of the prior embodiments and here the annulus 772′ has a raised edge portion 776′. Moreover, such a structure may also be fabricated by providing any of the aforementioned structures discussed in conjunction with FIG.9A or FIG. 9B, for example, by placing a sufficient voltage on said structures such that portions of the field emission electrodes are eroded away during normal field emission to a stabilized point in which this small raised-edge or ear shaped portion is provided as a raised annulus surface over the annulus portion of layer 772 provided by aperture 772a.
  • FIG. 10 there is shown a sketch, in exaggerated scale, of a cross-sectional view of a flat panel display 400 including an electron emission apparatus which may be of the type shown in FIG. 2.
  • the electron emission apparatus of flat panel display 400 includes emitter structure 112, illustrated in greater detail in FIG. 2 and anode structure 114, also shown in greater detail in FIG. 2.
  • anode structure 114 includes an optically-transparent substrate 140, illustratively made of glass.
  • a thin electrode layer 142 illustratively indium-tin-oxide, is affixed to the inner surface of glass substrate 140, and an electroluminescent material 144, illustratively a light-emitting phosphor, is coated on electrode layer 142.
  • Emitter structure 112 is affixed to the inner surface of base substrate 402, typically fabricated of glass.
  • Anode structure 114 and base substrate 402 are assembled such that emitter structure 112 is spaced from, and precisely positioned with respect to, anode structure 114 by spacer element 404, which is affixed to the inner surfaces of substrates 140 and 402 by sealing means 406.
  • anode structure 114 is illustratively spaced from emitter structure 112 by 0.5-2.0 mm.
  • Spacer element 404 may illustratively be fabricated of glass, ceramic or metal, and sealing means 406 shall be appropriately selected to seal such spacer element 404 to the materials of substrates 140 and 402. The seal provided by spacer element 404 and sealing means 406 between substrates 140 and 402 is sufficient to allow cavity 408 to be effectively evacuated.
  • Row and column control voltages provided, as seen in FIG. 2, on signal leads 150a, 150b, . . . and 152a, 152b . . ., respectively, as well as the reference voltage applied to substrate conductor 124 on signal lead 154, as seen in FIG. 2, are coupled to emitter structure 112 from controller and power source 410 via a multiplicity of signal leads 412, which pass under spacer element 404 into evacuated cavity 408, and which form electrical contact with emitter structure 112 via contact means 414.
  • anode voltage is coupled to anode electrode layer 142 from power source 410 via signal lead 416 which passes around spacer element 404 into cavity 408.
  • FIG. 11 a cathode structure in accordance with the present invention which is generally used as the cathodes in the embodiment of FIGs. 1-10 above, or which can also be used as a cathode in any device which uses such a structure, is shown.
  • the cathode as shown in FIG. 11 can alternatively be used in vacuum microelectric devices such as amplifiers, transistors, tubes, and the like.
  • the cathode of the present invention comprises one or more electrically conductive layers 9001, 9002, 9003, . . ., referred to collectively as conductive layers 900, each having one or more apertures 9021, 9022, 9023, . . ., referred to collectively as apertures 902, disposed therein.
  • Electrical potentials V1, V2, V3, . . . selectively applied to terminal means 9041, 9042, 9043, . . ., and coupled, respectively, to layers 9001, 9002, 9003,. . .. ., cause emission of electrons from the peripheral edge portions of conductive layers 900 within apertures 902, which electrons are accelerated toward a more positive electrical potential +V.
  • a sheet 920 comprising an electrically conductive material having here one or alternatively more than one edge 922 adapted for field electron emission is shown disposed on a dielectric layer 926.
  • a potential is coupled to layer 920 via terminal 924.
  • Field-emitted electrons from edge 922 are accelerated towards a more positive potential +V.
  • Edge 922 is preferably a sharp edge as mentioned above to concentrate field emission of electrons therefrom.
  • the disclosure of the fabrication method will be limited to a description of the process for fabricating emitting structure 312.
  • the process of fabricating anode structure 314, including affixing layers of a conductive material and an electroluminescent material on a glass substrate follows conventional cathode-ray tube (CRT) manufacturing technology.
  • CTR cathode-ray tube
  • the process for enclosing emitting structure 312 and anode structure 314 within a chamber capable of evacuation is also deemed to be well known.
  • the exact details of construction would be apparent to one of skill in the art. For example, a simple expedient would be to replace the conventional tip or wedge cathodes with the sheet or layer of conductive material having an edge or an aperture as in the present invention to provide field electron emission therefrom.
  • the process to be described is based generally on techniques of patterning by etching selective portions of a metal layer.
  • Alternative techniques such as depositing metal through a patterned resist layer and lifting off the resist to leave the patterned layer could alternatively be used.
  • a process of fabricating electron emitting structure 312 includes providing a wafer of material for substrate 320, preferably silicon, a semiconducting material, because of its availability and ease of handling.
  • substrate 320 may comprise an insulating material such as glass, ceramic or sapphire.
  • the important characteristic of substrate 320 is that it has an extremely flat and smooth surface for depositions thereon.
  • Substrate 320 is provided to support the remainder of the structure to be fabricated. As such it could also be a metal, or it could be eliminated if the resulting structure had sufficient structural integrity.
  • layer 322 may be grown in a conventional oxidation furnace, or it may be deposited.
  • a layer 324 of a metal having suitable characteristics including work function, resistivity, and stability particularly for subsequent processing and during operation of the resulting device is deposited using conventional techniques such as evaporation or sputtering, for example.
  • suitable metals include gold, platinum, and more refractory metals such as molybdenum, tungsten, titanium, tantalum, and so forth.
  • a layer 324 of molybdenum illustratively 0.1-0.3 ⁇ m in thickness, is deposited on SiO2 layer 322.
  • Molybdenum layer 324 may be deposited by evaporation or by sputter deposition; the latter process is preferred for its enhanced adhesion qualities.
  • a photoresist may be appropriately coated onto the exposed surface of layer 324 and the device etched, typically by standard wet chemical etch or by reactive ion etch.
  • "lift off” processing could be used.
  • the structure thus far assembled is placed in an oven, illustratively a commercial rapid thermal anneal (RTA) equipment, and heated quickly, typically at an average rate of 50-100°C per second, to approximately 1000°C, held at this temperature for approximately 10 seconds, then allowed to cool.
  • RTA rapid thermal anneal
  • this heating step tends to reduce the resistance of an electrically conductive thin film layer, and is preferably repeated in this illustrative process after each subsequent metal deposition, here of a molybdenum layer.
  • the RTA process step may be performed after all layers of molybdenum have been deposited.
  • LPCVD low pressure chemical vapor deposition
  • layer 326 may then be masked and etched to provide windows to access contact pads (not shown) associated with the underlying molybdenum layer 324.
  • layer 328 of a metal here molybdenum, illustratively 0.1-0.3 ⁇ m in thickness.
  • Layer 328 is deposited on SiO2 layer 326, preferably by sputter deposition, alternatively by evaporation.
  • Layer 328 is masked with a layer 372 of photoresist which is patterned to expose generally circular areas 375 where apertures 334 (FIG. 6) will eventually be located.
  • each such exposed circular area 375 has a diameter 2-5 ⁇ m greater than the diameter of aperture 334 (FIG. 6).
  • molybdenum layer 328 is then etched, using standard wet chemical or reactive ion etch, to remove the molybdenum from these areas.
  • Photoresist layer 372 (FIG. 12B) is removed and an additional layer 328a of molybdenum 0.01-0.03 rm thickness is then sputter deposited to provide a layer portion 328′ slightly increased in thickness and a very thin layer portion 328 ⁇ of molybdenum in the previously etched-away areas surrounding the eventual locations of apertures 334.
  • Molybdenum layer 328 is then masked with photoresist (not shown) to pattern the stripes comprising layer 328 (as seen in FIG. 3A) and contact pads (not shown) for each stripe, and etched, using standard wet chemical or reactive ion etch, to create such pattern in the molybdenum.
  • a thin layer 228 of molybdenum is deposited on SiO2 layer 226, preferably by sputter deposition, alternatively by evaporation.
  • Molybdenum layer 228 is then masked with photoresist to pattern the stripes comprising layer 228 (as seen in FIG. 2) and contact pads (not shown) for each stripe, and etched, using wet chemical or reactive ion etch, to create such pattern in the molybdenum.
  • LPCVD low pressure chemical vapor deposition
  • Layer 330 may then be masked and etched to provide windows to access the contact pads (not shown) associated with the underlying molybdenum layers 324 and 328.
  • a layer 332 of molybdenum is deposited on SiO2 layer 330, preferably by sputter deposition, alternatively by evaporation.
  • Layer 332 is masked (not shown) with photoresist to pattern the stripes comprising layer 332 (as seen in FIG. 2) and contact pads (not shown) for each stripe, and etched, using wet chemical or reactive ion etch, to create such a desired pattern in the molybdenum layer 332.
  • LPCVD low pressure chemical vapor deposition
  • Layer 362 may then be masked and etched to provide windows to access the contact pads (not shown) associated with the underlying molybdenum layers 324, 328 and 332.
  • a layer 360 of molybdenum is deposited on SiO2 layer 362, preferably by sputter deposition, alternatively by evaporation.
  • Layer 360 may then be masked with photoresist to pattern the layer and form a contact pad (not shown), and etched, using wet chemical or reactive ion etch, to create such pattern in the molybdenum.
  • the steps involving the depositions of layers 362 and 360 are not required for the embodiments of FIGs. 4-5, 7-9, 9A-9C, and 11, 11A.
  • aperture 334 (FIG. 6) is provided through layers 360, 362, 332, 330, 328 and 326, down to layer 324 to provide the electron emitting structure 312 (FIG. 6).
  • aperture 334 is provided by a series of etching steps.
  • An initial step of this process is to provide a masking layer 374 over layer 360.
  • masking layer 354 is a coating of photoresist of sufficient thickness that it can survive the etching process, illustratively a thickness of 2.0-2.2 ⁇ m.
  • the masking layer 374 is patterned to provide here an aperture which substantially defines the diameters of apertures 334, illustratively 1-2 ⁇ m.
  • Apertures 334 are provided by removing exposed portions of layers 362, 360, 332, 330, 328 and 326.
  • standard reactive ion etch wherein the etchant gases are provided to selectively etch each layer as it becomes exposed is used. It is desirable to complete the total etch process as quickly as possible so as to avoid etching off the photoresist layer covering the regions of layer 362 which are to be protected from the etchant.
  • the assembly is placed in a conventional reactive ion etching chamber and the appropriate etchant gases are pumped therethrough.
  • the etchant gases are selective, i.e., they provide good etch selectivity of either the molybdenum or the SiO2, thereby ensuring uniform etching of each layer over its entire area.
  • the etchant used for the molybdenum layers is a chlorine-based plasma, illustratively a mixture of chlorine and oxygen gases
  • the etchant for the SiO2 layers is a fluorine-based gas, illustratively CHF3.
  • the etchant gas fed into the chamber is alternated so as to etch the subsequently exposed layer.
  • etching process particularly the etching of a layer of molybdenum in a generally circular aperture
  • the etching of the layer is usually fastest at the center of the aperture and proceeds downwardly and outwardly.
  • tapered surface 327 (FIG. 6)
  • Such monitoring may be accomplished by a process of end point detection, i.e., by evaluating the intensity of characteristic spectral emissions associated with the reacting gases in the chamber.
  • a second monitoring process may involve laser deflection from an area on layer 328, such area being remote from, but equivalent in thickness to, those portions of layer 328 within functional apertures 334 of structure 312.
  • This laser deflection monitoring evaluates the reflectivity of layer 328, determining the moment at which the etch of layer 328 is to be terminated. Finally, the monitoring of the progress of the etch of molybdenum layer 328 may involve successive visual inspections based on experience and etch time. Still another method for forming a sharp edge on surface 327 involves chemical or electrochemical etching.

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  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Cold Cathode And The Manufacture (AREA)
  • Cathode-Ray Tubes And Fluorescent Screens For Display (AREA)
  • Electrodes For Cathode-Ray Tubes (AREA)
EP19920301632 1991-03-01 1992-02-26 Electron emitting structure and manufacturing method Withdrawn EP0501785A3 (en)

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US664184 1991-03-01

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EP0660368A1 (fr) * 1993-12-22 1995-06-28 Gec-Marconi Limited Dispositif d'électron à émission de champs
EP0696045A1 (fr) * 1994-08-05 1996-02-07 Pixel International S.A. Cathode d'écran plat de visualisation à résistance d'accès constante
EP0703594A1 (fr) * 1994-09-22 1996-03-27 Canon Kabushiki Kaisha Dispositif émetteur d'électrons et procédé de fabrication, source d'électrons et dispositif de formation d'image, comportant tels dispositifs émetteurs d'électrons
WO1996013848A1 (fr) * 1994-10-31 1996-05-09 Honeywell Inc. Dispositif d'affichage a emetteur de champ
US5577944A (en) * 1994-04-29 1996-11-26 Texas Instruments Incorporated Interconnect for use in flat panel display
US5818166A (en) * 1996-07-03 1998-10-06 Si Diamond Technology, Inc. Field emission device with edge emitter and method for making
EP0871195A1 (fr) * 1997-04-11 1998-10-14 Sony Corporation Elément à émission de champ, procédé de sa fabrication et dispositif d'affichage à émission de champ
EP0930634A1 (fr) * 1998-01-16 1999-07-21 Sony Corporation Dispositif émetteur d'électrons, procédé de fabrication et de fonctionnement
WO1999049492A1 (fr) * 1998-03-21 1999-09-30 Korea Advanced Institute Of Science & Technology Afficheur ligne a emission de champ
US5965971A (en) * 1993-01-19 1999-10-12 Kypwee Display Corporation Edge emitter display device
EP0974998A2 (fr) * 1998-07-23 2000-01-26 Sony Corporation Emetteur de champ à cathode froide et dispositif d'affichage avec de tels émetteurs
KR20000011924A (ko) * 1998-07-23 2000-02-25 이데이 노부유끼 냉음극전계방출소자및냉음극전계방출표시장치
EP1089310A2 (fr) * 1999-09-30 2001-04-04 Kabushiki Kaisha Toshiba Dispositif à émission de champ
EP1868226A1 (fr) * 2005-04-05 2007-12-19 Fuji Jukogyo Kabushiki Kaisha Dispositif emetteur de lumiere
DE202006020357U1 (de) 2006-09-21 2008-10-30 Safetec Gmbh Elektrode und Vorrichtung für Galvano-Fussbad
DE102006060856A1 (de) 2005-11-06 2009-04-16 Safetec Gmbh Vorrichtung und Verfahren zur Dekorporation von Strontium und weiterer radioaktiv strahlender Elemente aus dem Körper
ITMI20130897A1 (it) * 2013-05-31 2014-12-01 St Microelectronics Srl Dispositivo microelettronico a vuoto integrato e relativo metodo di fabbricazione.
US9496392B2 (en) 2014-03-31 2016-11-15 Stmicroelectronics S.R.L. Integrated vacuum microelectronic structure and manufacturing method thereof

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KR100477739B1 (ko) * 1999-12-30 2005-03-18 삼성에스디아이 주식회사 전계 방출 소자 및 그 구동 방법
KR20050086238A (ko) * 2004-02-25 2005-08-30 삼성에스디아이 주식회사 전계 방출 표시장치
KR20050104643A (ko) * 2004-04-29 2005-11-03 삼성에스디아이 주식회사 전자 방출 표시장치용 캐소드 기판, 전자 방출 표시장치및 이의 제조 방법
KR20050111706A (ko) * 2004-05-22 2005-11-28 삼성에스디아이 주식회사 전계방출 표시소자 및 그 제조방법

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US5965971A (en) * 1993-01-19 1999-10-12 Kypwee Display Corporation Edge emitter display device
EP0660368A1 (fr) * 1993-12-22 1995-06-28 Gec-Marconi Limited Dispositif d'électron à émission de champs
US5942849A (en) * 1993-12-22 1999-08-24 Gec-Marconi Limited Electron field emission devices
GB2285168B (en) * 1993-12-22 1997-07-16 Marconi Gec Ltd Electron field emission devices
US5577944A (en) * 1994-04-29 1996-11-26 Texas Instruments Incorporated Interconnect for use in flat panel display
EP0696045A1 (fr) * 1994-08-05 1996-02-07 Pixel International S.A. Cathode d'écran plat de visualisation à résistance d'accès constante
FR2723471A1 (fr) * 1994-08-05 1996-02-09 Pixel Int Sa Cathode d'ecran plat de visualisation a resistance d'acces constante
EP0703594A1 (fr) * 1994-09-22 1996-03-27 Canon Kabushiki Kaisha Dispositif émetteur d'électrons et procédé de fabrication, source d'électrons et dispositif de formation d'image, comportant tels dispositifs émetteurs d'électrons
CN1106656C (zh) * 1994-09-22 2003-04-23 佳能株式会社 电子发射器件、电子源及成像设备
US5847495A (en) * 1994-09-22 1998-12-08 Canon Kabushiki Kaisha Electron-emitting device and image forming apparatus using same
EP1037246A3 (fr) * 1994-09-22 2001-06-13 Canon Kabushiki Kaisha Dispositif émetteur d'électrons et procédé de fabrication, source d'électrons et dispositif de formation d'image, comportant tels dispositifs émetteurs d'électrons
EP1037246A2 (fr) * 1994-09-22 2000-09-20 Canon Kabushiki Kaisha Dispositif émetteur d'électrons et procédé de fabrication, source d'électrons et dispositif de formation d'image, comportant tels dispositifs émetteurs d'électrons
AU712966B2 (en) * 1994-09-22 1999-11-18 Canon Kabushiki Kaisha Electron-emitting device and method of manufacturing the same as well as electron source and image forming apparatus comprising such electron-emitting device
WO1996013848A1 (fr) * 1994-10-31 1996-05-09 Honeywell Inc. Dispositif d'affichage a emetteur de champ
US5818166A (en) * 1996-07-03 1998-10-06 Si Diamond Technology, Inc. Field emission device with edge emitter and method for making
US6522053B1 (en) 1997-04-11 2003-02-18 Sony Corporation Field emission element, fabrication method thereof, and field emission display
EP0871195A1 (fr) * 1997-04-11 1998-10-14 Sony Corporation Elément à émission de champ, procédé de sa fabrication et dispositif d'affichage à émission de champ
US6135839A (en) * 1997-04-11 2000-10-24 Sony Corporation Method of fabricating edge type field emission element
US6489710B1 (en) 1998-01-16 2002-12-03 Sony Corporation Electron emitting apparatus, manufacturing method therefor and method of operating electron emitting apparatus
EP0930634A1 (fr) * 1998-01-16 1999-07-21 Sony Corporation Dispositif émetteur d'électrons, procédé de fabrication et de fonctionnement
WO1999049492A1 (fr) * 1998-03-21 1999-09-30 Korea Advanced Institute Of Science & Technology Afficheur ligne a emission de champ
US6727642B1 (en) 1998-03-21 2004-04-27 Korea Advanced Institute Of Science & Technology Flat field emitter displays
KR20000011924A (ko) * 1998-07-23 2000-02-25 이데이 노부유끼 냉음극전계방출소자및냉음극전계방출표시장치
EP0974998A3 (fr) * 1998-07-23 2003-01-29 Sony Corporation Emetteur de champ à cathode froide et dispositif d'affichage avec de tels émetteurs
EP0974998A2 (fr) * 1998-07-23 2000-01-26 Sony Corporation Emetteur de champ à cathode froide et dispositif d'affichage avec de tels émetteurs
EP1089310A3 (fr) * 1999-09-30 2002-08-28 Kabushiki Kaisha Toshiba Dispositif à émission de champ
EP1089310A2 (fr) * 1999-09-30 2001-04-04 Kabushiki Kaisha Toshiba Dispositif à émission de champ
EP1868226A1 (fr) * 2005-04-05 2007-12-19 Fuji Jukogyo Kabushiki Kaisha Dispositif emetteur de lumiere
EP1868226A4 (fr) * 2005-04-05 2011-03-30 Fuji Heavy Ind Ltd Dispositif emetteur de lumiere
DE102006060856A1 (de) 2005-11-06 2009-04-16 Safetec Gmbh Vorrichtung und Verfahren zur Dekorporation von Strontium und weiterer radioaktiv strahlender Elemente aus dem Körper
DE202006020357U1 (de) 2006-09-21 2008-10-30 Safetec Gmbh Elektrode und Vorrichtung für Galvano-Fussbad
ITMI20130897A1 (it) * 2013-05-31 2014-12-01 St Microelectronics Srl Dispositivo microelettronico a vuoto integrato e relativo metodo di fabbricazione.
US9508520B2 (en) 2013-05-31 2016-11-29 Stmicroelectronics S.R.L. Integrated vacuum microelectronic device and fabrication method thereof
US9496392B2 (en) 2014-03-31 2016-11-15 Stmicroelectronics S.R.L. Integrated vacuum microelectronic structure and manufacturing method thereof
US9865421B2 (en) 2014-03-31 2018-01-09 Stmicroelectronics S.R.L. Integrated vacuum microelectronic structure and manufacturing method thereof

Also Published As

Publication number Publication date
JPH04328222A (ja) 1992-11-17
CA2060809A1 (fr) 1992-09-02
KR920019215A (ko) 1992-10-22
EP0501785A3 (en) 1992-11-19

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