This application is cross referenced to a related co-pending application filed on the same date, entitled “An electron emitter and a display apparatus utilizing the same”, naming Takehisa Ishida as the inventor.
The present invention relates to an electron emitter and a display apparatus utilizing the same, particularly though not exclusively to a field effect electron emitting apparatus, a method of manufacturing an field effect electron emitting apparatus, a field effect display and a method of manufacturing a field effect display.
Recently Flat Panel Displays (FPD) have become popular due to their smaller footprint and larger flatter screen compared to conventional technology. For example, Liquid Crystal Displays (LCD) and Plasma Display Panels (PDP) are replacing Cathode Ray Tubes (CRT) in many domestic applications. However some types of FPD technology have disadvantages compared to conventional CRT technology. For example LCDs have a slow response rate, which degrades the quality of fast-moving images and PDPs have a reduced life expectancy.
An alternative technology to LCD or PDP is a Field Emission Display (FED). A typical FED incorporates a large array of fine metal tips or carbon nano-tubes (CNT), which emit electrons through a process known as field emission. Since a FED works based on a similar principle to a CRT, namely an electron emitter and a phosphor, it gives a sufficient fast response rate. However, the fabrication of so-called Spindt-type emitters, which are utilized for most FED systems, requires complex processes and increases the cost of the FED.
It would therefore be desirable to provide an emitter which has fast response rate, and/or low production cost.
It is therefore an objective of at least one embodiment to provide an electron emitter that overcomes at least one of the above mentioned problems.
In general terms, in a first aspect the invention proposes that in a field effect electron emitting apparatus using nano-wire electron emitters, each nano-wire electron emitter may be grown in a pore of an insulating layer. This may have the advantage that a simpler process such as electrochemical plating can be used in the fabrication process thus reducing the production cost.
In a second, independent aspect, it is proposed that a portion of the insulating layer may be removed, so that each nano-wire electron emitter may have at least a portion exposed from the pore. This may have the advantage that a simpler process such as etching can be used in the fabrication process thus reducing the production cost.
In a first specific expression of the invention there is provided a field effect electron emitting apparatus comprising
a cathode,
an insulating layer on or adjacent to the cathode having an array of pores, and
a grown nano-wire electron emitter in each pore, each nano wire electron emitter connected to the cathode.
In a second specific expression of the invention there is provided a field effect electron emitting apparatus comprising
a cathode,
an insulating layer on or adjacent to the cathode having an array of pores,
a nano-wire electron emitter in each pore having at least a portion exposed from the pore, each nano-wire electron emitter connected to the cathode, and
a gate electrode on or spaced parallel to the insulating layer.
In a third specific expression of the invention there is provided a method of manufacturing an field effect electron emitting apparatus comprising
providing a cathode,
providing an insulating layer having an array of pores on or adjacent to the cathode, and
growing a nano-wire electron emitter in each pore, each nano wire connected to the cathode.
In a forth specific expression of the invention there is provided a method of manufacturing an field effect electron emitting apparatus comprising
providing a cathode,
providing an insulating layer having an array of pores on or adjacent to the cathode, and
providing a nano-wire electron emitter in each pore having at least a portion exposed from the pore, each nano-wire electron emitter connected to the cathode.
In a fifth specific expression of the invention there is provided a method of manufacturing a field effect display comprising
providing an field effect electron emitting apparatus according to the method as claimed in any of the methods described above, and
providing a phosphor coated screen on or spaced parallel to the field effect electron emitting apparatus.
In a sixth specific expression of the invention there is provided a field effect display comprising
a field effect electron emitting apparatus as described in any of the apparatuses above, and
a phosphor coated screen on or spaced parallel to the field effect electron emitting apparatus.
One or more example embodiments of the invention will now be described, with reference to the following figures, in which:
FIGS. 5(a) to 5(d) are schematics of an implementation of the fabrication process in
FIGS. 6(a) to 6(e) are schematics of an alternative implementation of the fabrication process in
FIGS. 7(a) to 7(e) are schematics of a further alternative implementation of the fabrication process in
FIGS. 8(a) to 8(e) are schematics of a still further alternative implementation of the fabrication process in
Referring to
Referring now to
The substrate 200 is typically rectangular in shape, and may for example be made from a sheet of glass typically 1 mm thick.
The insulating layer 202 is bonded to the substrate 200 by an adhesive 204, or otherwise deposited. The insulating layer 202 may be made of, for example, Anodized Aluminium Oxide (AAO) or Etched Track Membrane (ETM). The insulating layer 202 has a substantially uniform array of pores, each pore 206 being of sufficient width to accommodate the nano-wire electron emitter 216. Pore density of more than 105/mm2, for example 106/mm2, may result in good uniformity and good luminous intensity.
The cathode 214 lies on the substrate and forms base 208 of each pore. The nano-wire electron emitter 216 has a portion in the pore and a portion exposed from the pore. The nano-wire electron emitter 216 is connected to the cathode 214 at the base 208. On top of the insulating layer 202, are spacers 207. The gate electrode 220 lies on top of the spacers 207.
The cathode 214 may be a series of strips which may be independently energised. Alternatively the cathode 214 may simply be a single element. Each strip is typically rectangular in cross section and 100 nm in thickness. Each strip is provided with an external electrical connection at the edge of the substrate.
The spacers 207 may be at either end of the insulating layer 202, or at intermediate locations across the insulating layer 202. The spacers 207 ensure the distance between the gate electrode 220 and the nano-wire electron emitters 216 is kept constant. The gate electrode 220 may either be supported between adjacent spacers 207, or located on top of each spacer. Typically the spacer is made from insulating material such as a polymer.
The gate electrode 220 may be a series of strips which may be independently energised. Alternatively the gate electrode 220 may simply be a single element. Each strip is typically rectangular in cross section and 100 μm in thickness. Each strip is provided with an external electrical connection at the edge of the insulating layer. Each strip has a uniform array of holes, which correspond to each pore or groups of pores in the insulating layer. Various combinations of size in cathode width, aperture of gate electrode, and anode are appropriate depending on the application.
The strips of the gate electrode may for example be arranged generally perpendicularly to the strips of the cathode. This patterning of the strips to intersect perpendicularly, also known as passive matrix electrode configuration, enables the display of moving pictures. Thus the emitter array is thereby divided into independently controllable pixels by the intersection of the strips. Each pixel may cover a plurality of emitters. To activate each pixel the respective strip of the gate electrode is energised with a positive voltage with respect to the corresponding strip of the cathode.
Each nano-wire electron emitter 216 may be made of conductive material such as metal. Material such as Co, Ni, Cr, Ag, Cu, W, Mo or Fe (or their oxides) which have a low work function, high conductivity and high melting point are suitable. Typically the nano-wire is grown in situ (rather than being placed) by electrochemical plating. Typically each nano-wire electron emitter 216 does not extend past the gate electrode. For example each nano-wire electron emitter 216 may include a portion exposed from the pore, such as an exposed portion the length of the pore. Typically, the length of the exposed nano-wire is several micrometers. In the document the term nano-wire is used to mean an elongate conductor less than 500 nm in width. Experiments carried out by the inventors indicate that metal nano-wire less than 200 nm in diameter gives a reasonable threshold voltage.
Referring now to
The anode 302 may be a conductive transparent sheet like electrode 302 between the phosphor layer 300 and the glass plate 304 as shown in
A voltage Vg is applied by variable voltage source 308 between the cathode 214 and the gate electrode 220. The voltage between the cathode 214 and the anode 302 is kept at Va by voltage source 310. The voltage Va is much higher than Vg.
In operation, Vg is applied between the gate electrode 220 and the cathode 214 so that the gate electrode has a positive potential and the cathode has a negative potential. The electron emitter 216 is electrically conductive so the potential of the electron emitter 216 is equal to that of the cathode. The electric field concentrates on the tip of the electron emitter 216 and electrons are emitted from the tip of the electron emitter 216 and accelerated toward the gate electrode 220.
The phosphor coated screen 104 is energised at a higher potential than the gate electrode. The accelerated electrons collide against the phosphor and fluorescent light is generated. By controlling the voltage Vg, the energy and/or density of the electron stream, and therefore the intensity of the fluorescent light, can be adjusted. This may be in terms of the average brightness of the display, or brightness of specific emitters or pixels as required in display of dynamic images.
Method of Fabrication
Referring to
Step 402 may be implemented by depositing cathode 214 made of Cu, Au, Ni or Ti onto a rigid substrate 200, as seen in
Step 404 may be implemented by bonding the insulating layer 501 on top of the cathode 214 using an adhesive layer 204, as seen in
A sheet of anodized aluminium oxide (AAO), is suitable for the insulating layer. AAO is formed by anodizing an aluminium sheet in acid. Pores are generated and self-assembled like lattice and honeycomb-like porous sheet is easily obtained without using a complicated photolithographic process. Furthermore, pore density greater than 106/mm2 (which is impossible by photolithography) can be achieved. Higher emitter density gives more uniformity of electron irradiation. The pore density can be varied by selection of the anodizing conditions.
Alternatively an Etched Track Membrane (ETM) is suitable for the insulating layer. The ETM may be formed in a two-step process. Firstly, a thin, plastic film (e.g. polycarbonate or polyester) is exposed to charged particles (e.g. ion of Se, Pb or Bi). As these particles pass through the plastic film, they create damage tracks, which consist of broken molecular bonds of the polymer. Therefore, the plastic film is partially weakened along the path that the particle traveled. The density of tracks is controlled primarily by the amount of time the film is exposed to the charged particles.
Secondly the actual pores into the film are formed by an etching process. The tracks left by the atomic particles are etched by hot, caustic baths. The hot caustic etches the thin plastic film, dissolving away material from both sides. The areas where the charged particles passed through the film are dissolved many times quicker than the rest of the material where a charged particle did not pass. Thus, uniform, cylindrical and fine pores are created.
Step 406 may be implemented by growing a nano-wire 216 in each pore by electrochemical plating. The substrate and a counter electrode (e.g. a platinum wire) are put into a plating electrolyte (e.g. mixed solution of 0.1 M boric acid H3BO3, 0.2 M Hydrated Copper Sulfate CuSO4-5H2O and a small amount of surfactant) and a plating current is applied between the cathode and the counter electrode. Then plated metal (e.g. copper) is deposited in the pores of insulating layer, as seen in
Step 408 may be implemented by etching the insulating layer by a solution (e.g. 6 M NaOH) and thinned down so that the plated nano-wires are partially exposed, as seen in
Step 410 may be implemented by placing spacers 507 above the nano-wire emitters 216, and placing gate electrode 220 on the spacers 507, as seen in
Step 402 may be implemented by depositing cathode 214 made of metal such as Cu, Au, Ni or Ti on a rigid substrate 200
Step 404 may be implemented by bonding the insulating layer 601 (using AAO or ETM as described above) on top of the cathode 214 by using an adhesive layer 204, as seen in
Step 406 may be implemented by growing a conductive nano-wire 216 in each pore by electrochemical plating. The substrate and counter electrode are put into a plating electrolyte and a plating current is applied between the cathode and the counter electrode. Then plated metal is deposited in the pores of insulating layer as the nano-wire emitters, as seen in
In this example step 410 precedes step 408.
Step 410 may be implemented by screen printing a spacer layer 607 on the insulating layer 601, as seen in
Step 408 may be implemented by etching and thinning down the insulating layer so that the nano-wires emitters 216 are partially exposed, as seen in
Step 402 may be implemented by depositing cathode 214 made of Cu, Au, Ni, Ti or other conductive material onto a rigid substrate 200, as seen in
Step 404 may be implemented by bonding or depositing the insulating layer 702 on top of the cathode 214, as seen in
Step 406 may be implemented by growing a nano-wire 216 in each pore of the insulating layer 702 by electrochemical plating, as seen in
In this example step 410 precedes step 408.
Step 410 may be implemented by placing a shadow mask 704 on the insulating layer 702, as seen in
After removing the shadow mask 704, step 408 may be implemented by etching and thinning down the insulating layer 702 so that the nano-wires emitters 216 are partially exposed, as seen in
In this example the order of the steps is as follows: step 410, step 404, step 402, step 406, and then step 408.
Step 410 may be implemented by depositing and patterning gate electrode 802 on top of an aluminium sheet 804 by screen printing or vacuum evaporation through a shadow mask, as seen in
Step 404 may be implemented by anodizing the aluminium sheet 804 in acid to form a sheet of anodized aluminium oxide (AAO) 806, suitable for the insulating layer. The array of pores is thereby formed in the insulating layer, as seen in
Step 402 may be implemented by depositing cathode 808 made of Cu, Au, Ni, Ti or other conductive material onto the bottom of insulating layer 806, as seen in
Step 406 may be implemented by growing a nano-wire 216 in each pore by electrochemical deposition, as seen in
Step 408 may be implemented by etching and thinning down the insulating layer 806 so that the nano-wires emitters 216 are partially exposed, as seen in
The emitter array, fabricated according to the above, may then be installed into a housing, together with the spacers, anode and screen. Control electronics are provided to energize the cathode, gate electrode and anode according to an input signal and/or stored instructions. Thus each electron emitter can be selectively energised, and the energization varied to achieve the desired display. The skilled reader will also readily appreciate other applications for one or more embodiments, such as in a Scanning Electron Microscope, Back-light of Liquid Crystal Display or a Stepper for semiconductor production.
When inexpensive processes such as plating, etching and/or screen printing, are used to the costs of production can be reduced.
When the gate electrode is used to control the intensity of the electrons emitted from each nano-wire, the response rate is fast enough to display a moving picture with good quality.
Number | Date | Country | Kind |
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200605691-5 | Aug 2006 | SG | national |