EP0993513B1 - Technique electrochimique assistee par impedance et procede electrochimique permettant d'eliminer un materiau, notamment un materiau generateur d'excedents, dans un dispositif emetteur d'electrons - Google Patents

Technique electrochimique assistee par impedance et procede electrochimique permettant d'eliminer un materiau, notamment un materiau generateur d'excedents, dans un dispositif emetteur d'electrons Download PDF

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Publication number
EP0993513B1
EP0993513B1 EP98931401A EP98931401A EP0993513B1 EP 0993513 B1 EP0993513 B1 EP 0993513B1 EP 98931401 A EP98931401 A EP 98931401A EP 98931401 A EP98931401 A EP 98931401A EP 0993513 B1 EP0993513 B1 EP 0993513B1
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Prior art keywords
layer
emitter
impedance
electrode
insulating
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EP98931401A
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German (de)
English (en)
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EP0993513A1 (fr
EP0993513A4 (fr
Inventor
N. Johan Knall
John D. Porter
Christopher J. Spindt
Gabriela S. Chakarova
Duane A. Haven
John C. Macaulay
Roger W. Barton
Maria S. Nikolova
Peter C. Searson
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Canon Inc
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Canon Inc
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Priority claimed from US08/884,701 external-priority patent/US6120674A/en
Priority claimed from US08/884,700 external-priority patent/US5893967A/en
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    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25F—PROCESSES FOR THE ELECTROLYTIC REMOVAL OF MATERIALS FROM OBJECTS; APPARATUS THEREFOR
    • C25F3/00—Electrolytic etching or polishing
    • 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
    • H01J9/022—Manufacture of electrodes or electrode systems of cold cathodes
    • H01J9/025—Manufacture of electrodes or electrode systems of cold cathodes of field emission cathodes

Definitions

  • This invention relates to removing undesired portions of material from partially finished structures without removing desired portions of the same type of material, especially when the structures are electron-emitting devices, commonly referred to as cathodes, suitable for products such as cathode-ray tube (“CRT”) displays of the flat-panel type.
  • CTR cathode-ray tube
  • a field-emission cathode contains a group of electron-emissive elements that emit electrons upon being subjected to an electric field of sufficient strength.
  • the electron-emissive elements are typically situated over a patterned layer of emitter electrodes.
  • a patterned gate layer typically overlies the patterned emitter layer at the locations of the electron-emissive elements. Each electron-emissive element is exposed through an opening in the gate layer.
  • Figs. 1a - 1d illustrate a conventional technique as, for example, disclosed in Spindt et al, U.S. Patent 3,755,704 , for creating conical electron-emissive elements in a gated field emitter for a flat-panel CRT display.
  • the partially finished field emitter consists of an electrically insulating substrate 20, an emitter electrode layer 22, an intermediate dielectric layer 24, and a gate layer 26.
  • Gate openings 28 extend through gate layer 26.
  • Corresponding, somewhat wider dielectric openings 30 extend through dielectric layer 24.
  • a lift-off layer 32 is formed on top of gate layer 26 as depicted in Fig. 1b .
  • Emitter material is deposited on top of the structure and into dielectric openings 30 in such a way that the apertures through which the emitter material enters openings 30 progressively close.
  • a closure material is simultaneously deposited at a grazing angle to help close the deposition apertures.
  • conical electron-emissive elements 34A are thereby formed in composite openings 28/30 over emitter layer 22. See Fig. 1c .
  • a continuous layer 34B of the emitter/closure material forms on top of gate layer 26.
  • Lift-off layer 32 is subsequently removed to lift off excess emitter/closure-material layer 34B.
  • Fig. 1d shows the resultant structure.
  • lift-off layer 32 Utilization of lift-off layer 32 to remove excess emitter/closure-material layer 34B is disadvantageous for various reasons. Portions of the lift-off material invariably accumulate along the side edges of gate layer 26. This reduces the size of the openings through which the emitter material is initially deposited and makes it difficult to scale down electron-emissive elements 34A. The grazing-angle deposition of lift-off layer 32 becomes increasingly difficult as the lateral area of the field emitter increases and thus presents an impediment to scaling up the field-emitter area.
  • the lift-off material deposition must be performed carefully to assure that no lift-off material accumulates on emitter layer 22 and causes cones 34A to be lifted off during the lift-off of excess layer 34B. Since layer 34B is removed as an artifact of removing lift-off layer 32, particles of the removed emitter material can contaminate the field emitter. Furthermore, deposition of the lift-off material takes fabrication time and therefore money.
  • Wilshaw PCT Patent Publication WO 96/06443 , discloses a process for manufacturing a gated field emitter in which each electron-emissive element consists of a molybdenum cone situated on a cylinder. The electron-emissive elements are formed over a bottom metal layer. Using an aqueous electrolytic solution, Wilshaw applies a potential of 2 - 4 volts to a niobium gate layer in order to electrochemically remove a layer of excess molybdenum that accumulated over the gate layer during the deposition of molybdenum through openings in the gate layer to form the conical portions of the electron-emissive elements.
  • Wilshaw removes the bottom metal layer. Consequently, Wilshaw's electron-emissive elements are electrically isolated from one another during the electrochemical removal of the excess emitter material. Inasmuch as some electron-emissive elements may be electrically shorted to the excess molybdenum during the electrochemical removal step, Wilshaw needs this isolation to protect the unshorted electron-emissive elements since they could otherwise be electrically shorted through the back metal layer and the shorted elements to the excess molybdenum and thus could be electrochemically attacked in removing the excess molybdenum. Later, Wilshaw performs an operation on the back surface to nullify the presence of shorted electron-emissive elements. Finally, Wilshaw forms a resistive layer over the bottoms of the electron-emissive elements, and a layer of emitter electrodes over the resistive layer.
  • Wilshaw's electrochemical removal technique avoids the necessity to use to use a lift-off layer for removing the layer of excess emitter material.
  • removing the back metal layer before electrochemically removing the excess molybdenum and then creating emitter electrodes after completing the electrochemical removal is time-consuming and requires several complex processing steps. Performing the additional electrical-short nullification operation further increases the fabrication time and complexity.
  • Wilshaw's use of an aqueous electrolytic solution for removing the excess molybdenum poses difficulties.
  • the high charge-to-radius values of the ions of metals, such as molybdenum (whose normal ionic charge state is plus six) cause these metals to precipitate readily out of aqueous electrolytic solutions as metal hydroxides, metal oxides, and/or hydrated metal oxides.
  • the precipitates coat the electron-emissive elements and destroy their usefulness.
  • Wilshaw's electrochemical removal potential of 2 - 4 volts which presumptively overcomes the precipitation problem without causing electrochemical removal of the niobium in the gate layer is quite high and would result in significant electrochemical attack of many other highly attractive candidates for the gate metal. It is desirable to have an easier, more flexible way to avoid unwanted precipitation.
  • the present invention furnishes an efficient, relatively simple electrochemical procedure for selectively removing certain material from a structure without significantly electrochemically attacking, and thus without significantly removing, certain other material of the same chemical type as the removed material.
  • the electrochemical removal procedure of the invention is normally impedance assisted.
  • the disclosure also furnishes organically based electrochemistry for the electrochemical removal procedure in an unclaimed embodiment.
  • the impedance assistance in the present electrochemical removal technique is implemented with an impedance component that typically constitutes a permanent part of the structure and, in any event, is present in the structure during the electrochemical removal operation.
  • the impedance component has characteristics designed to overcome electrical short problems which occur when one or more portions of the material intended to remain in the structure become electrically coupled to the material intended to be removed. Due to the presence of the impedance component, each such electrical short is normally repaired (i.e., eliminated) automatically during the electrochemical removal without impairing the selectivity of the removal.
  • Wilshaw is there any necessity to perform a separate, potentially complex operation to repair electrically shorted electron-emissive elements.
  • the number of processing steps is reduced in the invention, thereby saving fabrication time and money.
  • the invention alleviates the problems that using a lift-off layer creates in scaling down electron-emissive elements and in scaling up the lateral area of the electron emitter.
  • the possibility of unintentionally lifting off electron-emissive elements due to the use of a lift-off layer is avoided.
  • the invention avoids the emitter-material particulate contamination problem that can occur with use of a lift-off layer. The invention thereby enables fabrication of the electron-emissive elements to be completed in an efficient, economical manner.
  • the first step in the present electrochemical removal procedure is to provide an initial structure containing a first electrically non-insulating region which consists at least partially of first material.
  • electrically non-insulating means electrically conductive or electrically resistive.
  • the first non-insulating region can, for example, be a layer of excess emitter material that accumulates during deposition of emitter material to form electron-emissive elements.
  • the initial structure When the electrochemical removal procedure is impedance assisted, the initial structure includes an impedance component (consisting of one or more impedance elements) electrically coupled to multiple electrically non-insulating members, such as electron-emissive elements.
  • Each non-insulating member like the first non-insulating region, consists at least partially of the first material.
  • An electrode such as an emitter electrode, is typically electrically coupled through the impedance component to the non-insulating members.
  • a small fraction of the non-insulating members may be shorted to the non-insulting region at this point and/or may become shorted to the non-insulating region during the electrochemical removal operation of the invention.
  • the removal step normally entails subjecting the initial structure to an electrolytic solution.
  • the impedance component is of sufficiently high impedance that the first material of each non-insulating member not shorted to the non-insulating region is not significantly attacked.
  • choosing the impedance component to be of the indicated sufficiently high impedance enables the unshorted non-insulating members to be effectively electrically isolated from any non-insulating member shorted to the first non-insulating region.
  • the selected potential i.e., the potential applied to the non-insulating region for electrochemically removing the first material of the non-insulating region, is thus not transmitted to the unshorted non-insulating members.
  • the unshorted non-insulating members are not significantly electrochemically attacked as a consequence of applying the selected potential to the non-insulating region.
  • the first material of any shorted non-insulating member is substantially attacked during the electrochemical removal procedure.
  • the attack terminates when enough of the first material has been removed to eliminate the short. Consequently, a short between the first non-insulating region and any non-insulating member is automatically repaired in the invention without the necessity of removing the impedance component or the underlying electrode.
  • the now-repaired non-insulating member can often perform its intended function.
  • the multiple non-insulating members, along with the impedance component, may broadly be replaced simply with a second electrically non-insulating region consisting at least partially of the first material.
  • the second non-insulating region is typically an electron-emissive element.
  • at least part of the first material of the first non-insulating region is now electrochemically removed by a procedure that entails contacting the first material of the first non-insulating region with an electrolytic solution containing organic solvent and acid.
  • the removing step is done such that the first material of the second non-insulating region is not significantly attacked during the removing step.
  • organic solvent in the electrolytic solution provides a number of advantages over an electrolytic solution, such as that employed in Wilshaw, where water is the solvent.
  • the electrolysis-produced ions of metals, such as molybdenum, which are especially suitable for electron-emissive elements but have high ionic charge-to-radius values are normally highly soluble in organic solvent.
  • metal precipitation difficulties are greatly reduced with the organic solvent used in the invention. There is no need to employ an unduly high electrochemical removal potential which, while avoiding unwanted precipitation, significantly limits the choice of materials for gate or control electrodes.
  • Electrochemical removal can be performed considerably faster with an electrolytic solution that employs organic solvent than with an aqueous electrolytic solution. Specifically, electrolysis proceeds more rapidly at higher temperature due to increased reaction rates, higher ion mobilities, and reduced electrolytic solution viscosity. By appropriately selecting the organic solvent employed in the present electrolytic solution, the organic solvent can have a higher boiling point than water. Accordingly, electrolysis can be performed at a higher temperature with the electrolytic solution of the invention than with an aqueous one. Since higher temperature produces faster electrolysis, processing time is reduced with the present electrolytic solution.
  • the acid utilized in the electrolytic solution can be organic acid.
  • organic acid is formed with a sulfur-containing acid.
  • the electrolytic solution typically includes a salt, normally an organic salt.
  • the electrochemistry provided by the invention is especially useful in selectively removing material from one part of a structure while avoiding the removal of material of the same chemical type in another part of the structure.
  • the removal operation is conducted in a rapid, efficient, and uncomplicated manner.
  • Certain types of electrical shorts are automatically repaired in the invention. There is no need to remove the impedance component, when present, or the emitter electrode before performing the electrochemical removal. Nor is there any need for a lift-off layer. Consequently, the invention provides a significant advance over the prior art.
  • the present invention utilizes an impedance-assisted electrochemical technique to remove excess emitter material in creating electron-emissive elements for a gated field-emission cathode.
  • Each such field emitter is suitable for exciting phosphor regions on a faceplate in a cathode-ray tube of a flat-panel display such as a flat-panel television or a flat-panel video monitor for a personal computer, a lap-top computer, or a workstation.
  • electrically insulating generally applies to materials having a resistivity greater than 10 10 ohm-cm.
  • electrically non-insulating thus refers to materials having a resistivity below 10 10 ohm-cm. Electrically non-insulating materials are divided into (a) electrically conductive materials for which the resistivity is less than 1 ohm-cm and (b) electrically resistive materials for which the resistivity is in the range of 1 ohm-cm to 10 10 ohm-cm. These categories are determined at an electric field of no more than 1 volt/ ⁇ m.
  • electrically conductive materials are metals, metal-semiconductor compounds (such as metal silicides), and metal-semiconductor eutectics. Electrically conductive materials also include semiconductors doped (n-type or p-type) to a moderate or high level. Electrically resistive materials include intrinsic and lightly doped (n-type or p-type) semiconductors. Further examples of electrically resistive materials are (a) metal-insulator composites, such as cermet (ceramic with embedded metal particles), (b) forms of carbon such as graphite, amorphous carbon, and modified (e.g., doped or laser-modified) diamond, (c) and certain silicon-carbon compounds such as silicon-carbon-nitrogen.
  • Figs. 2a - 2c illustrate how an impedance-assisted electrochemical technique is utilized in accordance with the invention to remove excess emitter material during the creation of electron-emissive elements for a gated field emitter.
  • the starting point in the procedure of Fig. 2 is an electrically insulating substrate 40 typically formed with ceramic or glass. See Fig. 2a .
  • Substrate 40 which provides support for the field emitter, is configured as a plate.
  • substrate 40 typically consists of a plate of Schott D263 glass having a thickness of approximately 1 mm.
  • substrate 40 constitutes at least part of the backplate.
  • Emitter region 42 overlies substrate 40.
  • Emitter region 42 consists of (a) a lower electrically conductive layer 42A patterned into emitter electrodes and (b) an upper emitter impedance component 42B.
  • Emitter-electrode layer 42A is situated on top of substrate 40.
  • the emitter electrodes of layer 42A extend generally parallel to one another in the direction of the rows of picture elements (pixels) in the CRT flat-panel display and thus constitute row electrodes.
  • Layer 42A typically consists of a metal such as nickel or aluminum.
  • the thickness of layer 42A is 100 - 500 nm, typically 200 nm.
  • Emitter impedance component 42B lies on top of emitter-electrode layer 42A. At the minimum, impedance component 42B needs to underlie each electron-emissive element. Component 42B need not be present at locations where there are no overlying electron-emissive elements.
  • Impedance component 42B can be constituted and configured in various ways.
  • impedance component 42B typically consists of one or more blanket layers of electrically resistive material.
  • Component 42B can also be formed with one or more patterned layers of electrically resistive material.
  • emitter region 42 is an electrically non-insulating region.
  • the thickness of impedance component 42B depends on the value of its impedance and how component 42B is implemented to achieve the desired impedance value.
  • An electrically insulating layer 44 which serves as the interelectrode dielectric, is provided on top of the structure.
  • the thickness of insulating layer 44 is normally in the range of 0.05 - 3 ⁇ m. More specifically, layer 44 has a thickness of 100 nm - 500 nm, typically 150 nm.
  • Insulating layer 44 typically consists of silicon oxide or silicon nitride. Although not shown in Fig. 2a , parts of insulating layer 44 may contact substrate 40 depending on the configuration of impedance component 42B.
  • a patterned electrically non-insulating gate layer 46 consisting of selected gate material is situated on interelectrode dielectric layer 44.
  • Gate layer 46 normally has a thickness in the range of 30 - 500 nm. More particularly, the gate thickness is 30 - 100 nm, typically 50 nm.
  • the gate material is normally metal, preferably chromium or/and nickel. Alternative candidates for the gate material include molybdenum, platinum, niobium, tantalum, titanium, tungsten, and titanium-tungsten.
  • Gate layer 46 may be patterned in various ways.
  • gate layer 46 can be configured as multiple generally parallel control electrodes for controlling the emission of electrons from the electron-emissive elements.
  • Layer 46 typically forms part of a group of control electrodes having main control portions (not shown here) which contact portions of layer 46 and which extend generally parallel to one another.
  • the control electrodes constitute column electrodes that extend perpendicular to the row electrodes of emitter layer 42A and thus extend along the columns of pixels.
  • a multiplicity of generally circular openings 48 extend through gate layer 46. Although the diameters of gate openings 48 depend on how openings 48 are created, the gate opening diameter is normally in the range of 0.05 - 2 ⁇ m. More specifically, the gate opening diameter is 80 - 400 nm, typically 150 nm.
  • a multiplicity of generally circular dielectric openings (or dielectric open spaces) 50 extend through insulating layer 44 down to impedance component 42B of emitter region 42.
  • Each dielectric opening 50 is vertically aligned to a corresponding one of gate openings 48 to form a composite opening 48/50 that exposes part of impedance component 42B.
  • Each dielectric open space 50 is somewhat wider than corresponding gate opening 48. Consequently, insulating layer 44 undercuts gate layer 46 along composite openings 48/50.
  • openings 48/50 can be formed by etching gate layer 46 through apertures in a mask, typically photoresist, to form gate openings 48 and then etching insulating layer 44 through openings 48 to create dielectric open spaces 50.
  • Composite openings 48/50 can also be created by using etched charged-particle tracks as described in Macaulay et al, PCT Patent Publication WO 95/07543 .
  • openings 48/50 can be formed according to the sphere-based procedure described in Spindt et al, "Research in Micron-Size Field-Emission Tubes," IEEE Conf. Rec. 1966 Eighth Conf. on Tube Techniques, 20 Sept. 1966, pages 143 - 147 .
  • Electrically non-insulating emitter cone material is evaporatively deposited on top of the structure in a direction generally perpendicular to the upper surface of insulating layer 44 (or gate layer 46).
  • the emitter cone material accumulates on gate layer 46 and passes through gate openings 48 to accumulate on impedance component 42B in dielectric open spaces 50. Due to the accumulation of the cone material on gate layer 46, the openings through which the cone material enters open spaces 50 progressively close. The deposition is performed until these openings fully close. As a result, the cone material accumulates in dielectric open spaces 50 to form corresponding conical electron-emissive elements 52A as shown in Fig. 2b .
  • a continuous (blanket) layer 52B of the cone material is simultaneously formed on gate layer 46.
  • the emitter cone material is normally metal, preferably molybdenum when gate layer 46 consists of chromium or/and nickel.
  • Alternative candidates for the cone material include nickel, chromium, platinum, niobium, tantalum, titanium, tungsten, titanium-tungsten, and titanium carbide subject to the cone material differing from the gate material.
  • a suitable photoresist mask (not shown) one or more portions of excess emitter-material layer 52B along the lateral periphery of the partially finished field emitter are removed. Consequently, parts of gate layer 46 and/or (when present) parts of the main control portions that contact gate layer 46 are exposed along the lateral periphery of the field emitter. Selected internal portions of gate layer 46 and/or (when present) the main control portions are also typically exposed during the masked etch.
  • FIG. 3a An electrochemical removal operation is now performed on the so-etched structure of Fig. 2b utilizing a potentiostatic electrochemical system of the type schematically shown in Fig. 3a .
  • Item 52C in Fig. 3a is the portion of excess emitter-material layer 52B remaining after the masked etch described in the preceding paragraph. Excess emitter-material layer 52C is removed during the electrochemical operation.
  • a small fraction of conical electron-emissive elements 52A are electrically shorted to gate layer 46 prior to electrochemically removing excess layer 52C and/or become electrically shorted to gate layer 46 during the electrochemical removal operation. Since excess layer 52C contacts gate layer 46, all of these electron-emissive cones 52C are shorted to excess layer 52C and, as discussed further below, are normally attacked significantly during the removal of layer 52C. The remaining cones 52A--i.e., cones 52A not shorted to layer 52C--are not significantly attacked as layer 52C is being removed. Likewise, the electrochemical removal operation is conducted without substantially attacking patterned gate layer 46 and (when present) the main control portions of the control electrodes.
  • the electrochemical removal system is formed with an electrochemical cell 60 and a control system 62 in the form of a potentiostat that regulates the cell operation.
  • Electrochemical cell 60 consists of an electrolytic solution 64, a cell wall 65, a counter electrode 70, and a reference electrode 72.
  • the partially finished field emitter is immersed in electrolytic solution 64.
  • Counter electrode 70 typically platinized titanium or platinum, is immersed in electrolytic solution 64 and extends parallel to excess emitter-material layer 52C.
  • Reference electrode 72 typically silver/silver chloride or mercury/mercurous chloride (Calomel), is situated in solution 64, preferably close to layer 52C.
  • Control system 62 has a working-electrode terminal WE, a reference-electrode terminal RE, and a counter-electrode terminal CE.
  • Cell 60 is electrically connected to control system 62 by a working-electrode conductor 73, an electrically insulated reference-electrode conductor 74, and a counter-electrode conductor 76.
  • Conductors 73, 74, and 76 all typically consist of platinum wire or electrically insulated copper wire.
  • Working-electrode conductor 73 is electrically coupled to the control electrodes. This coupling is made directly to gate layer 46 as shown in Fig. 3a when layer 46 is patterned into control electrodes, or by way of (when present) the main control portions of the control electrodes. Since gate layer 46 is in contact with excess emitter-material layer 52C, the combination of layers 46 and 52C and the main control portions forms a working anode electrode for cell 60.
  • Reference-electrode conductor 74 is electrically connected to reference electrode 72.
  • Counter-electrode conductor 76 is electrically connected to counter electrode 70.
  • Electrochemical cell 60 is operated in a potentiostatic (constant-potential) mode.
  • Reference electrode 72 provides a highly reproducible fixed reference potential V R .
  • V R is approximately 0.2 volt relative to a Normal Hydrogen Electrode at room temperature.
  • Control system 62 operates as a potentiostat to place working-electrode conductor 73 at a largely constant working-electrode driving potential V WE that normally exceeds reference potential V R on reference-electrode conductor 74 by a largely fixed anodic potential V A . Under some operating conditions, anodic potential can be negative so that working-electrode driving potential V WE is less than V R .
  • potential V A is schematically depicted as being provided by a voltage source 62A in potentiostatic control system 62.
  • Driving potential V WE equals V A + V R referenced to a Normal Hydrogen Electrode. Potential V WE is applied through conductor 73 and through the control electrodes (constituted by gate layer 46 or the combination of layer 46 and the adjoining main control portions) to excess layer 52C for dissolving the excess emitter material during the electrochemical removal procedure.
  • Control system 62 places counter-electrode conductor 76 at a largely constant counter-electrode potential V CE .
  • Reference potential V R exceeds counter-electrode potential V CE by a largely fixed counter potential V C .
  • counter potential V C is schematically depicted as being supplied by a voltage source 62C in control system 62.
  • Counter-electrode potential V C equals V R - V C .
  • emitter-electrode layer 42A can be handled in anyone of three ways, all of which result in (a) excess emitter-material layer 52C being electrochemically removed and (b) any shorted cone 52A typically being attacked sufficiently to repair the short, but without unshorted cones 52A being attacked significantly.
  • the potential on emitter-electrode layer 42A can be left unregulated--i.e., no special action is taken to control the potential of layer 42A.
  • the potential on layer 42A may reach a value close to driving potential V WE on the working electrode formed with gate layer 46, excess layer 52C, and (when present) the separate main control portions of the control electrodes.
  • the minimum value of the impedance provided by impedance component 42B for handling the potential on layer 42A is the highest of the three techniques.
  • emitter-electrode layer 42A can be electrolytically self-biased to a negative potential relative to potential V WE .
  • the emitter-electrode self-biasing technique is implemented by appropriately choosing the electrically non-insulating materials electrically coupled to electron-emissive cones 52A and in contact with electrolytic solution 64. These non-insulating materials consist of the materials which form impedance component 42B, emitter-electrode layer 42A, and further metal regions (not shown) that provide external electrical connections to layer 42A. Since cones 52A are electrically coupled through impedance component 42B to emitter-electrode layer 42A, cones 52A are thus at a negative potential relative to the working electrode.
  • emitter-electrode layer 42A can be actively maintained at a largely constant emitter-electrode potential V EE below working-electrode potential V WE .
  • a largely fixed emitter potential V E is provided by a voltage source 77 connected between working-electrode conductor 73 and a further electrical conductor 79 connected to emitter-electrode layer 42A. Inasmuch as voltage source 77 and further conductor 79 are optional, they are indicated in dotted line in Fig. 3a .
  • Emitter-electrode potential V EE equals V WE - V E . Since working-electrode potential V WE equals V A + V R , potential V EE also equals V A + V R - V E .
  • cones 52A are normally close to emitter-electrode potential V EE and thus are nearly V E below V WE .
  • the magnitude of emitter potential V E should not be so great that the emitter material of excess layer 52C plates out on cones 52A during the electrochemical removal of excess layer 52C.
  • Fig. 3b illustrates an alternative way of implementing the electrochemical removal system of Fig. 3a .
  • Electromechanical cell 60 in Fig. 3b has a surrounding wall 66 and an O-ring 68 rather than cell wall 65.
  • Electrolytic solution 64 contacts only the top of the field emitter in Fig. 3b .
  • O-ring 68 prevents solution 64 from leaking out of cell 60 at the bottom of wall 66.
  • working-electrode conductor 73 and (when used) further conductor 79 make electrical connections to the outside of cell 60.
  • Optional voltage source 77 is electrically connected to counter-electrode conductor 76 rather than to working-electrode conductor 73.
  • potential V E in Fig. 3a differs in value from potential V E in Fig. 3b .
  • electrolytic solution 64 is formed with an organic solvent and an acid electrolyte.
  • the organic solvent in electrolytic solution 64 consists of a polar organic roomtemperature liquid.
  • suitable organic solvents for solution 64 are dimethylsulfoxide ("DMSO"), ethanol, and methanol.
  • DMSO dimethylsulfoxide
  • MO 6+ highly charged molybdenum ions
  • the acid electrolyte in solution 64 can be an inorganic or organic acid. Because sulfur-containing acids have high disassociation constants so as to yield high reaction rates, the acid is typically a sulfur-containing acid. Examples of suitable sulfur-containing inorganic acids are sulfuric acid, sulfurous acid, and sulfamic acid. In the organic-acid case, the sulfur-containing acid is normally a sulfonic acid, typically an aromatic sulfonic acid, particularly one having a benzene ring. An example of a suitable aromatic sulfonic acid having a benzene ring is paratoluenesulfonic acid ("p-TSA").
  • p-TSA paratoluenesulfonic acid
  • Electrolytic solution 64 may also contain a salt electrolyte, either organic or inorganic.
  • the salt electrolyte is normally an organic salt.
  • the organic salt is typically an aromatic sulfonic-acid salt, especially one having a benzene ring.
  • suitable sulfonic-acid salts having benzene rings are tetraethylammonium para-toluenesulfonate ("TEAp-TS"), tetramethylammonium para-toluenesulfonate, and tetrabutylammonium para-tuloene sulfonate.
  • voltage source 62A in control system 60 sets anodic potential V A at a suitable value to fix cell driving potential V WE at a value in the range of 0.2 - 0.9 volt, typically 0.6 volt, referenced to a Normal Hydrogen Electrode.
  • V WE potential in the range of 0.2 - 0.9 volt
  • emitter potential V E equals 0.4 - 2.4 volts, typically 0.5 volt, in order to set emitter-electrode potential V EE at this V E amount below working-electrode potential V E .
  • DMSO has a boiling point of nearly 190°C.
  • the electrolysis with the preceding example of solution 64 can be conducted at a temperature in excess of 100°C, the boiling point of water.
  • the rate of removal of excess emitter-material layer 52C is quite high. Since DMSO is flammable, the electrolysis is performed a safe distance below the DMSO boiling point. With DMSO as the solvent, the electrochemical removal is usually performed at 20 - 120°C, typically 40 - 60°C.
  • the driving force provided by anodic driving potential V WE causes the molybdenum in excess emitter-material layer 52C to be anodically oxidized, and thereby dissolved in electrolytic solution 64, typically as Mo 6+ ions. Accordingly, excess layer 52C is electrochemically removed from the top of the structure.
  • the p-TSA is employed to adjust the rate at which the molybdenum in excess layer 52C is oxidized and thereby removed from the field-emission structure. Increasing the p-TSA concentration increases the rate at which the molybdenum in layer 52C is oxidized at a given value of potential V WE , and vice versa. Hydrogen ions (H + ) are reduced at counter electrode 70 to produce hydrogen gas.
  • a small fraction of electron-emissive cones 52A are electrically short circuited to excess emitter-material layer 52C directly or through gate layer 46.
  • Such an electrical short typically occurs as a result of a cone 52A being forced into contact with gate layer 46, or as a result of one or more electrically conductive particles lodging between that cone 52A and layer 46 or 52C.
  • the conductive particles typically consist of emitter cone material that breaks off excess layer 52C.
  • Each cone 52A shorted to excess layer 52C receives working-electrode potential V WE .
  • V WE working-electrode potential
  • V EE potential below V WE
  • the difference between potential V WE and the emitter-electrode potential during the electrochemical removal operation is largely dropped across the portion of impedance component 42B underlying that shorted cone 52A. Consequently, each shorted cone 52A is electrochemically attacked until a sufficient amount of emitter material has been removed from excess layer 52C and that cone 52A to produce a suitably wide gap between the then-existing remainder of excess layer 52C and any remainder of that cone 52A. When the gap reaches such a width that the potential on originally shorted cone 52A drops below the value needed to electrochemically remove material, the attack on that cone 52A terminates.
  • the electrochemical attack on a shorted cone 52A sometimes terminates when only a relatively small portion of that cone 52A has been removed. Depending on how much of a previously shorted cone 52A remains and how that remainder is shaped, the remaining portion of that cone 52A may be able to function adequately as an electron-emissive element. In any event, shorts between cones 52A and excess layer 52C are eliminated (repaired) by using the present electrochemical procedure to remove layer 52C.
  • the impedance of impedance component 42B is sufficiently high that all of cones 52A not shorted to excess emitter-material layer 52C are effectively electrically isolated from one another and, importantly, from any cone 52A shorted to excess layer 52C.
  • an unshorted cone 52A can be electrochemically attacked only if there is a current path by which electrons generated during the oxidation of that cone's material can reach some part of the expanded working electrode formed with gate layer 46, excess layer 52C, the main control portions (when present), and any shorted cones 52A.
  • the high impedance of component 42B during the electrochemical removal operation virtually closes any current path from an unshorted cone 52A through emitter-electrode layer 42A to a shorted cone 52A.
  • the impedance of component 42B is controlled so that the cumulative short-circuit current of a number of shorted cones 52A, e.g., 1 - 2% of total cones 52A, is insufficient to result in the removal of any significant amount of the material of unshorted cones 52A.
  • a number of shorted cones 52A e.g. 1 - 2% of total cones 52A
  • the high impedance provided by component 42B during the electrochemical removal operation functions largely on its own to prevent the electrochemical removal of unshorted cones 52A.
  • Self biasing or actively maintaining layer 42A at a suitable potential typically in the vicinity of 0.5 volt below V WE provides impedance component 42B with electrolytic assistance in protecting unshorted cones 52A.
  • use of the self-biasing or active-potential-maintenance technique makes it harder for unshorted cones 52A to reach a potential at which they could be electrochemically removed, thereby relaxing the requirements on component 42B. That is, the impedance of component 42B during the electrochemical removal operation can be somewhat lower than with the unregulated technique.
  • impedance component 42B When impedance component 42B consists of electrically resistive material, component 42B provides an impedance Z B of at least 10 6 - 10 11 ohms, typically 10 9 ohms, between emitter-electrode layer 42A and each cone 52A during normal display operation. Component 42B is configured to provide impedance Z B at a considerably higher value during the electrochemical removal of layer 52C. Specifically, component 42B provides high impedance to (positive) current flow upward into an unshorted cone 52A. With the unregulated technique, impedance Z B is typically in the vicinity of 10 11 ohms or more during the removal of excess layer 52C.
  • the minimum value of impedance Z B during the electrochemical removal depends on the number of shorted cones 52A and the specifics of the electrochemistry.
  • the (positive) anodic current I WE that flows through the working electrode is indicative of the rate at which material is electrochemically removed from a structure subjected to the electrolytic solution and driving potential.
  • the removal rate normally increases with increasing anodic current I WE .
  • the preferred V WE potential range given above at the preferred 0.5-mole p-TSA and 0.1-mole TEAp-TS values was determined by experimentally monitoring anodic polarization curves (current I WE as a function of applied driving potential V WE ) for an electrochemical cell separately configured to remove specimens of molybdenum, chromium, and nickel.
  • Fig. 4a illustrates the experimental results, indicating that the removal rates for chromium and nickel are very small compared to the removal rate for molybdenum when driving potential V WE is in the range of 0.2 - 0.9 volt referenced to a Normal Hydrogen Electrode.
  • electrolytic solution 64 that employs an organic solvent when cones 52A and excess layer 52C are formed with molybdenum, while gate layer 46 and (when present) the adjoining main control portions consist of chromium and/or nickel, is:
  • electrolytic solution 64 can alternatively be an aqueous solution containing:
  • electrochemical cell 60 With electrochemical cell 60 being operated at the conditions given in the preceding paragraph, excess layer 52C is electrochemically removed from the structure.
  • the driving force provided by anodic potential V WE causes the molybdenum in layer 52C to be oxidized and dissolved in electrolytic solution 64, typically as Mo (VI) ions.
  • the sodium nitrate is used to adjust the molybdenum oxidation.
  • the NO 3 - ions produced by dissociation of NaNO 3 act as the oxidizing agent. Increasing the NaNO 3 concentration increases the rate at which the molybdenum in layer 52C is oxidized, and vice versa. Reduction of hydrogen ions again occurs at counter electrode 70 to produce hydrogen gas.
  • Figs 5a - 5d illustrate an unclaimed implementation of the process sequence of Fig. 2 for the case in which the field emitter is provided with separate electrically conductive main control portions 80 that contact patterned gate layer 46.
  • Fig. 5a depicts one such main control portion 80 that extends perpendicular to the plane of the figure.
  • the combination of a main control portion 80 and the portion(s) of gate layer 46 adjoining that main portion 80 form a composite control electrode 46/80.
  • a group of large control apertures 82 one of which is shown in Fig. 5a , extend through each main control portion 80.
  • Each large control aperture 82 exposes a multiplicity of composite openings 48/50.
  • the emitter electrodes of non-insulating region 42A in Fig. 5a extend horizontally, parallel to the plane of the figure.
  • Fig. 5c illustrates how the structure appears after performing the masked etch to remove part of excess emitter-material layer 52B, including excess emitter material situated along the lateral periphery of the structure.
  • the remainder of excess layer 52B consists of a group of rectangular islands 52C that overlie corresponding portions of gate layer 46.
  • a layout (plan) view of Fig. 5c is depicted in Fig. 6a .
  • Fig. 5d illustrates the appearance of the structure after electrochemically removing each island 52C using the impedance-assisted technique of the invention.
  • neither gate layer 46 nor main control portions 80 are substantially electrochemically attacked during the removal of layers 52C.
  • unshorted cones 52A are not significantly electrochemically attacked during the removal operation, the attack (if any) on unshorted cones 52A being much less than the (very small) attack on control portions 46 and 80.
  • a layout view corresponding to the structure of Fig. 5a is depicted in Fig. 6b .
  • main control portions 80 are situated on parts of patterned gate layer 46.
  • gate layer 46 can overlie parts of the main control portions.
  • Fig. 7 depicts such an alternative in which gate layer 46 extends partly over a group of electrically conductive main control portions 84 extending perpendicular to the plane of the figure.
  • Item 52D shown in dashed line in Fig. 7 , indicates the remainder of excess emitter-material layer 52B after the masked patterning etch.
  • the shape of excess layer 52D is nearly the same as the shape of excess layer 52C in the process sequence of Fig. 5c .
  • impedance component 42B The impedance characteristics of impedance component 42B are chosen in such a way as to enhance the flat-panel display performance during normal operation of the present field emitter, including providing the display with protection against short circuits, and to enhance the ability to remove excess emitter-material layer 52C without removing any significant amount of the material of unshorted cones 52A.
  • component 42B provides the display with protection against an electrically shorted cone 52A by limiting the resultant short-circuit current to a value low enough to avoid excessive power consumption and to avoid significantly impacting the brightness level achieved with other cones 52A in the same large control 82 as the shorted cone 52A.
  • V GE represent the voltage between gate layer 46 and the emitter electrodes of layer 42A.
  • V Z represent the voltage across the thickness of impedance component 42B below any one of electron-emissive cones 52A.
  • Impedance voltage V Z is one component of gate-to-emitter voltage V GE . Nearly all of the V GE drop for a particular unshorted cone 52A occurs across the gap between gate layer 46 and that cone 52A. Impedance voltage V Z for an unshorted cone 52A is thus much smaller than gate-to-emitter voltage V GE .
  • the picture elements (pixels) in the flat-panel display usually have multiple levels of gray-scale brightness corresponding to different values of gate-to-emitter voltage V GE .
  • V ZL represent the operating V Z value that occurs at the minimum pixel brightness level during normal display operation. At a typical maximum V GE level of 35 volts, lower operating value V ZL is typically 1 volt or less.
  • V ZU represent the upper V Z value that occurs during normal display operation.
  • shorted cones 52A are automatically repaired in using the present invention, some shorted cones 52A are typically present during normal display operation. For a shorted cone 52A, substantially the entire value of its gate-to-emitter voltage V GE is present across impedance component 42B.
  • Upper operating value V ZU is typically the maximum value of voltage V GE . Accordingly, V ZU is typically 35 volts.
  • Impedance Z B is the vertical impedance that component 42B presents to a current I Z flowing through the thickness of component 42B, where current I Z is the current of a single cone 52A.
  • the characteristics of component 42B are chosen so that vertical impedance Z B is high when the magnitude (absolute value) of impedance voltage V Z is in the vicinity of electrochemical removal value V ZR and, compared to the V ZR value, is relatively low when voltage V Z is in the normal operational range from lower operating value V ZL to upper operating value V ZU .
  • impedance Z B is high when voltage V Z is in the vicinity of -Z BR .
  • the field emitter is not normally subjected to V Z values in the vicinity of -V ZU to -V ZL . Accordingly, the characteristics of component 42B at V Z values in the vicinity of -V ZU to -V ZL are not of interest here.
  • the Z B dependence on impedance voltage V Z can be expressed mathematically utilizing a transition V Z value lying between electrochemical removal value V ZR and lower operating value V ZL .
  • V ZT represent this transition value
  • the magnitude of vertical impedance Z B is (a) greater than a transition value Z BT when impedance voltage V Z is between -V ZT and zero and (b) less than transition value Z BT when voltage V Z is between V ZT and V ZU .
  • the magnitude of impedance Z B is also typically, but usually not necessarily, greater than Z BT when voltage V Z is between zero and V ZT . Note that the Z B characteristics are not specified for the region in which impedance voltage V Z is less than -V ZT .
  • impedance Z B for V Z values in the vicinity of -V ZU to - V ZL is not of interest here.
  • the magnitude of impedance Z B is typically largely constant. Since impedance Z B varies with voltage V Z , the current-voltage characteristics ("I-V") characteristics of impedance component 42B are non-linear, normally highly non-linear.
  • the magnitude of impedance Z B is sufficiently low during normal device operation that current I Z can readily reach the values needed to achieve the desired pixel brightness levels.
  • the magnitude of impedance voltage V Z is at the considerably lower value V ZR that occurs during the electrochemical removal of excess layer 52C, the magnitude of impedance Z B increases sufficiently to cause unshorted cones 52A to be effectively electrically isolated from one another and from any shorted cones 52A. Any electrical shorting of cones 52A to excess layer 52C thus does not hinder the electrochemical removal operation or damage unshorted cones 52A.
  • Figs. 8a - 8d illustrate four different ways of implementing impedance component 42B to achieve the preceding I-V characteristics.
  • component 42B consists of a layer 90 of electrically resistive material. Letting R B be the vertical resistance of resistive layer 90, vertical resistance R B is then (a) greater than a transition resistance value R BT when voltage V Z is between -V ZT and zero and (b) less than R BT when voltage V Z is between V ZT and V ZU .
  • the I-V characteristics of resistive layer 90 are normally symmetric about the zero-I Z point. Accordingly, resistance R B is greater than R BT when voltage V Z is between zero on V ZT .
  • Resistive layer 90 can be formed with cermet (i.e., metallic particles embedded in ceramic) or a silicon-carbon compound such as silicon-carbon-nitrogen.
  • cermet i.e., metallic particles embedded in ceramic
  • silicon-carbon compound such as silicon-carbon-nitrogen.
  • Other candidates for layer 90 include lightly doped polycrystalline semiconductor material (such as polycrystalline silicon), intrinsic amorphous semiconductor material (such as intrinsic amorphous silicon), large-bandgap semiconductor material, aluminum nitride, and gallium nitride.
  • Impedance component 42A is configured as a two-layer resistor in Fig. 8b .
  • the two-layer resistor consists of a lower electrically resistive layer 92 and an upper electrically resistive layer 94.
  • Resistor 92/94 has the same basic resistive I-V characteristics as given above for resistive layer 90.
  • Lower resistive layer 92 provides resistor 92/94 with the generally linear I-V characteristics for the I Z range from I ZL to I ZU during normal display operation.
  • Upper resistor 94 which typically consists of cermet, largely provides the increased vertical resistance needed during the electrochemical removal operation. Further information on resistor 92/94 is given in Knall et al, International Patent Application PCT/US98/12461, filed 19 June 1998 ,.
  • impedance component 42B consists of a diode formed with an upper anode layer 96 and a lower cathode layer 98.
  • Diode 96/98 is typically a semiconductor diode having a threshold voltage V T less than 0.9 volt.
  • V T threshold voltage
  • impedance voltage V Z is greater than V T
  • the magnitude of impedance voltage V Z is less than zero (i.e., diode 96/98 is reversed biased), substantially no current flows through diode 96/98. In effect, the internal resistance of diode 96/98 is very high when voltage V Z is negative.
  • Impedance component 42A is configured to implement a capacitor in Fig. 8d .
  • the capacitor consists of an upper electrically conductive plate 100, a dielectric layer 102, and a lower plate formed with emitter electrode 42A. Upper plate 100 could be eliminated. Electron-emissive element 52A then form the upper plate.
  • the I-V characteristics for impedance component 42B are met with capacitor 100/102/104 due to the switching/non-switching nature of how the flat-panel display is utilized during normal display operation and during the electrochemical removal operation.
  • Fig. 9 depicts a typical example of the core active region of a flat-panel CRT display that employs an area field emitter manufactured according to the invention.
  • Substrate 40 forms the backplate for the CRT display.
  • Emitter region 42 is situated along the interior surface of backplate 40.
  • One main control portion 80 is depicted in Fig. 9 .
  • a transparent, typically glass, faceplate 110 is located across from baseplate 40.
  • Light-emitting phosphor regions 112, one of which is shown in Fig. 9 are situated on the interior surface of faceplate 110 directly across from corresponding large control apertures 82.
  • a thin light-reflective layer 114 typically aluminum, overlies phosphor regions 112 along the interior surface of faceplate 110. Electrons emitted by electron-emissive elements 52A pass through light-reflective layer 114 and cause phosphor regions 112 to emit light that produces an image visible on the exterior surface of faceplate 110.
  • the core active region of the flat-panel CRT display typically includes other components not shown in Fig. 9 .
  • a black matrix situated along the interior surface of faceplate 110 typically surrounds each phosphor region 112 to laterally separate it from other phosphor regions 112. Focusing ridges provided over interelectrode dielectric layer 44 help control the electron trajectories. Spacer walls are utilized to maintain a relatively constant spacing between backplate 40 and faceplate 110.
  • a field emitter manufactured according to the invention When incorporated into a flat-panel CRT display of the type illustrated in Fig. 9 , a field emitter manufactured according to the invention operates in the following way.
  • Light-reflective layer 114 serves as an anode for the field-emission cathode.
  • the anode is maintained at high positive potential relative to the gate and emitter lines.
  • the so-selected gate portion extracts electrons from the electron-emissive elements at the intersection of the two selected electrodes and controls the magnitude of the resulting electron current. Desired levels of electron emission typically occur when the applied gate-to-cathode parallel-plate electric field reaches 20 volts/mm or less at a current density of 0.1 mA/cm 2 as measured at the phosphor-coated faceplate in the display when phosphor regions 112 are high-voltage phosphors. Upon being hit by the extracted electrons, phosphor regions 112 emit light.
  • metals different from the preferred ones specified above can be selected for the emitter material of electron-emissive cones 52A and for the gate/column materials of gate layer 46 and (when present) the separate main control portions 80 or 84 by performing electrochemical removal tests on candidate metals using different electrolytic solution compositions and then examining the results, as in Figs. 4a and 4b , to determine appropriate ranges of driving potential V WE .
  • An electrochemical removal system containing a working-electrode conductor, a counter electrode, a counter-electrode conductor analogous to conductor 76, and an optional counter electrode conductor analogous to conductor 79, but no reference electrode (or reference-electrode conductor), can be used in place of the electrochemical removal system of Fig. 3a or 3b .
  • a counter electrode can be provided in the electron emitter itself, as part of substrate 40, instead of being situated in electrolytic solution 64 above excess layer 52C.
  • Optional counter-electrode conductor 79 can be connected to a separate terminals on control system 62 rather than being commonly connected through terminal WE in Fig. 3a or terminal CE in Fig. 3b .
  • a galvanostatic (constant-current) electrochemical removal system can be used in place of the potentiostatic system described above. Potentiostat control system 62 of Fig. 3a or 3b is then replaced with a galvanostatic control system containing a current source that causes a substantially constant current to flow in working-electrode conductor 73 and counter-electrode conductor 76. Because the potential between working-electrode conductor 73 and counter electrode 70 in a galvanostatic system could rise to a value sufficient to electrochemically remove gate layer 46 and/or (when present) the separate main control portions, the electrochemical removal operation is typically terminated after a pre-selected removal time. Alternatively, a potential-measuring device can be included in the system for causing the removal process to terminate upon reaching a pre-selected potential between those of conductors 73 and 76.
  • the electrochemical removal system of Fig. 3a or 3b can be modified to cause a controllable potential to exist between working-electrode conductor 73 and counter-electrode conductor 76 rather than holding conductor 73 at a fixed potential.
  • the potential between conductors 73 and 76 can be set at a fixed value during operation or could be programmably controlled.
  • Impedance component 42B can be formed with three or more electrically resistive layers. Combinations of resistors, capacitors, diodes, and other such basic electrical elements can be employed to form impedance component 42B.
  • Figs. 2 and 5 can be revised to make electron-emissive elements of non-conical shape.
  • the deposition of the emitter material can be terminated before fully closing the openings through which the emitter material enters dielectric openings 52.
  • Electron-emissive elements 52A are then formed generally in the shape of truncated cones.
  • the electrochemical removal operation of the invention is subsequently performed on excess emitter-material layer 52C with truncated cones 52A initially exposed to electrolytic solution 64 through apertures in layer 52C.
  • the organic solvent in electrolytic solution 62 can be formed with two or more organic liquids.
  • the acid can be formed with two or more acids, typically two or more organic acids.
  • Two or more salts, typically organic salt, can likewise be used in solution 62.
  • any one or more of lithium nitrate (LiNO 3 ) potassium nitrate (KNO 3 ), rubidium nitrate (RbNO 3 ), and cesium nitrate (CsNO 3 ) can be substituted for, or utilized in combination with, sodium nitrate as the source of oxidizing ions in an aqueous implementation of electrolytic solution 62.
  • any one or more of lithium hydroxide (LiOH), potassium hydroxide (KOH), or/and rubidium hydroxide (RbOH), and cesium hydroxide (CsOH) can be substituted for, or employed in combination with, sodium hydroxide as the base in solution 64.
  • Any one or more of the oxidizing agents can be used with any one or more of the bases. For any of these substitutions or combinations, the total molar concentrations of the oxidizing agents and bases are then respectively the same as described above for sodium nitrate and sodium hydroxide.
  • Nitrates of one or more Group II metals can be used in an aqueous implementation of electrolytic solution 64 instead of, or in addition to, the Group I metal nitrates described above.
  • hydroxides of one or more of these Group II metals can be used in solution 64 in place of, or in addition to, the Group I metal hydroxides described above.
  • the masked etch can be performed in such a way that (a) substantially all of each main control portion 80 is covered with excess emitter material rather than leaving only islands 52C of excess emitter material on control portions 80 and (b) the excess emitter material is removed from the areas between control portions 80.
  • the electrochemical removal procedure of the invention may be performed long enough to create openings through patterned excess-emitter material layer 52C for exposing electron-emissive cones 52A but not long enough to remove all of layer 52C. By combining the two preceding variations, the remaining excess emitter material situated on control portions 80 can serve as parts of portions 80 to increase their current-conduction capability.
  • electron-emissive cones have tips formed with emitter material, such as refractory metal carbide, that cannot readily be directly electrochemically removed. Titanium carbide is an attractive refractory carbide for the tips of the electron-emissive cones.
  • electrically non-insulating emitter material such as molybdenum
  • the cone formation process is then completed by depositing the non-electrochemically removable material on top of the structure and into openings 50 until the apertures through which the material enters openings 50 fully close.
  • An electrochemical removal operation is then performed in the manner described above to remove the excess electrochemically removable emitter material situated directly on gate layer 46 and (when present) the separate main control portions. During this operation, the excess non-electrochemically removable emitter material located along the top of the structure is lifted off. Consequently, conical electron-emissive elements having bases of electrochemically removable emitter material and tips of non-electrochemically removable emitter material are exposed through gate openings 48.
  • layer 32 in the prior art process of Fig. 1 consists of electrochemically removable material
  • the principles of the invention can be extended to electrochemically removing an intermediate layer, such as layer 32, situated between a gate layer and a layer containing excess emitter material.
  • the excess material layer is typically lifted off as a result of removing the intermediate layer.
  • Any of the electrochemical removal systems described above can be employed in the so-extended process sequence.
  • Substrate 40 can be deleted if emitter region 42 is of sufficient thickness to support the structure.
  • Insulating substrate 40 can be replaced with a composite substrate in which a thin insulating layer overlies a relatively thick non-insulating layer that furnishes structural support.
  • the electrochemical removal technique of the invention can be used in fabricating ungated electron emitters.
  • the electron emitters produced according to the invention can be employed to make flat-panel devices other than flat-panel CRT displays.
  • Various modifications and applications may thus be made by those skilled in the art without departing from the true scope of the invention as defined in the appended claims.

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Claims (12)

  1. Procédé comprenant les étapes de
    réaliser une structure initiale dans laquelle (a) une première région électriquement non-isolante (52B, 52C ou 52D) comprend un premier matériau, (b) un moyen d'impédance (42B) est couplé électriquement à une multiplicité d'éléments électriquement non isolants (52A) et (c) chaque élément non-isolant (52A) comprend le premier matériau; et
    retirer électrochimiquement au moins une partie du premier matériau de la région non-isolante (52B, 52C ou 52D) par une procédure qui implique l'application d'un potentiel sélectionné à la région non-isolante (52B, 52C ou 52D), le moyen d'impédance (42B) fournissant une impédance suffisamment élevée pendant l'étape de retrait pour que le premier matériau de chaque élément non-isolant précité (52A) soit largement découplé électriquement de la région non-isolante (52B, 52C ou 52D) à l'extérieur de la connection électrique par le moyen d'impédance (42B) et à l'extérieur de la connection électrique par toute solution électrolytique d'intervention (64) n'est pas attaquée d'une manière significative électrochimiquement pendant l'étape de retrait.
  2. Procédé selon la revendication 1, où le premier matériau de n'importe quel élément non isolant (52A) couplé électriquement à la région non-isolante (52B, 52C et 52D) à l'extérieur de la connection électrique par le moyen d'impédance (42B) et à l'extérieur de la connection électrique par n'importe quelle solution électrolytique d'intervention (64) est sensiblement attaqué électrochimiquement pendant l'étape de retrait.
  3. Procédé selon la revendication 1 ou 2, où l'étape de retrait entraîne la soumission de la structure initiale à une solution électrolytique (64).
  4. Procédé selon l'une quelconque des revendications 1 à 3, où la structure initiale comprend une électrode électriquement conductrice (42A) couplé électriquement par le moyen d'impédance (42B) aux éléments non-isolants (52A).
  5. Procédé selon la revendication 4, où l'étape de retrait est exécutée, sans appliquer de potentiel autre que le potentiel sélectionné, au moyen d'impédance (42B) ou à l'électrode (42A).
  6. Procédé selon la revendication 4 ou 5, où l'impédance est elle-même suffisamment élevée pendant l'étape de retrait, sans assistance électrolytique significative de l'électrode (42A) et de n'importe quel autre composant électriquement non-isolant (79) couplé électriquement aux éléments non-isolants (52A) pour empêcher largement que chaque élément non-isolant ainsi découplé (52A) soit attaqué d'une manière significative électrochimiquement pendant l'étape de retrait.
  7. Procédé selon la revendication 4 ou 5, où la structure initiale comprend au moins un composant électriquement non-isolant (42A, 79), incluant potentiellement l'électrode (42A), couplée électriquement aux éléments non-isolants (52A) pour assister électrolytiquement le moyen d'impédance (42B) pour empêcher que chaque élément non-isolant ainsi découplé (52A) soit attaqué d'une manière significative électrochimiquement pendant l'étape de retrait.
  8. Procédé selon la revendication 4, où l'étape de retrait implique l'application d'un autre potentiel à l'électrode (42A).
  9. Procédé selon la revendication 8, où l'autre potentiel est suffisamment différent du potentiel sélectionné pour assister le moyen d'impédance (42B) pour empêcher que chaque élément non-isolant ainsi découplé (52A) soit attaqué d'une manière significative électrochimiquement pendant l'étape de retrait.
  10. Procédé selon l'une quelconque des revendications 1 à 9, où le moyen d'impédance (42B) comprend une couche électriquement résistive (90, 92/94).
  11. Procédé selon l'une quelconque des revendications 1 à 9, où le moyen d'impédance (42B) (a) est configuré pour mettre en oeuvre au moins un condensateur (42A/100/102) ou (b) comprend au moins une diode (96/98) configurée pour être conductrice vers l'avant pendant le fonctionnement normal d'une structure finale contenant le moyen d'impédance (42B) et les éléments non-isolants (52A).
  12. Procédé selon l'une quelconque des revendications 1 à 11, où l'impédance (a) est une grandeur inférieure à une valeur de transition ZBT lorsqu'une tension Vz au moyen d'impédance (42B) est entre une valeur de transition VZT et une valeur de fonctionnement supérieure et (b) est une grandeur plus grande que ZBT lorsqu'une tension Vz est approximativement entre - VZT et zéro.
EP98931401A 1997-06-30 1998-06-29 Technique electrochimique assistee par impedance et procede electrochimique permettant d'eliminer un materiau, notamment un materiau generateur d'excedents, dans un dispositif emetteur d'electrons Expired - Lifetime EP0993513B1 (fr)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US08/884,701 US6120674A (en) 1997-06-30 1997-06-30 Electrochemical removal of material in electron-emitting device
US884700 1997-06-30
US884701 1997-06-30
US08/884,700 US5893967A (en) 1996-03-05 1997-06-30 Impedance-assisted electrochemical removal of material, particularly excess emitter material in electron-emitting device
PCT/US1998/012801 WO1999000537A1 (fr) 1997-06-30 1998-06-29 Technique electrochimique assistee par impedance et procede electrochimique permettant d'eliminer un materiau, notamment un materiau generateur d'excedents, dans un dispositif emetteur d'electrons

Publications (3)

Publication Number Publication Date
EP0993513A1 EP0993513A1 (fr) 2000-04-19
EP0993513A4 EP0993513A4 (fr) 2001-04-04
EP0993513B1 true EP0993513B1 (fr) 2009-01-07

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EP (1) EP0993513B1 (fr)
JP (1) JP3648255B2 (fr)
KR (1) KR100621293B1 (fr)
WO (1) WO1999000537A1 (fr)

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NL1014727C2 (nl) * 2000-03-23 2001-09-25 Univ Eindhoven Tech Werkwijze voor het elektrolytisch polijsten van een metaal in aanwezigheid van een elektrolytsamenstelling, alsmede een vormdeel verkregen volgens een dergelijke werkwijze.
JP4803998B2 (ja) * 2004-12-08 2011-10-26 ソニー株式会社 電界放出型電子放出素子の製造方法

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US2928777A (en) * 1950-12-16 1960-03-15 Electro Process Inc Electrolytic polishing of metals
US4385971A (en) * 1981-06-26 1983-05-31 Rca Corporation Electrolytic etch for eliminating shorts and shunts in large area amorphous silicon solar cells
US4629539A (en) * 1982-07-08 1986-12-16 Tdk Corporation Metal layer patterning method
JPH0353099A (ja) * 1989-07-19 1991-03-07 Matsushita Electric Ind Co Ltd Ｔａ基材の加工方法
US5564959A (en) * 1993-09-08 1996-10-15 Silicon Video Corporation Use of charged-particle tracks in fabricating gated electron-emitting devices
GB9416754D0 (en) * 1994-08-18 1994-10-12 Isis Innovation Field emitter structures
US5828288A (en) * 1995-08-24 1998-10-27 Fed Corporation Pedestal edge emitter and non-linear current limiters for field emitter displays and other electron source applications
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JP4195109B2 (ja) * 1996-11-13 2008-12-10 荏原ユージライト株式会社 電解剥離用電解液および電解剥離方法

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Publication number Publication date
JP2001508834A (ja) 2001-07-03
EP0993513A1 (fr) 2000-04-19
EP0993513A4 (fr) 2001-04-04
KR100621293B1 (ko) 2006-09-13
WO1999000537A1 (fr) 1999-01-07
KR20010014008A (ko) 2001-02-26
JP3648255B2 (ja) 2005-05-18

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