Patent Grant
7459842
This application claims the priority benefit of Japanese Patent Application No. 2004-017709 filed on Jan. 26, 2004.
Not Applicable.
1. Field of the Invention
The present invention relates to self-luminous elements including a fluorescent substance layer having fluorescent substances in a hermetic enclosure, where a fluorescent substance light-emits due to electron beam excitation. Particularly, the present invention relates to self-luminous elements, each having a new gas occlusion material for occluding unnecessary gases, which is disposed in an envelope to make and maintain a high degree of vacuum degree inside the enclosure.
2. Description of the Prior Art
In self-luminous elements, an envelope is hermetically sealed to maintain the inside thereof in a hermetic state. Such a closed space is maintained to a high degree of vacuum, such as less than 1×10−3 Pa. To realize such a state, high-melting point metal materials, such as Ti, Mo, Ba, Zr, and the equivalents, each which has the function of absorbing residual gases and removing them from the gas phase, have been used as getter materials (hereinafter, referred to as getter).
A fluorescent display tube, shown in
In conventional self-luminous elements employing the electron beam excitation emission, an expensive getter ring 110, which has a metal container filled with a getter material such as Ba—Al alloy, is used to maintain the inner surface of the vacuum hermetic envelope in a high degree of vacuum and to maintain the inner surface of the envelope and the surface of the fluorescent substance in a clean state.
In plasma display devices being self-luminous elements, unnecessary gases, other than the display gas such as a plasma excitation gas, that form within or enter the envelope after it has been evacuated to a high degree of vacuum, adversely affect the operational life of the device. Therefore, it is required to remove unnecessary gases inside the plasma display device.
In order to maintain the luminous characteristics of an EL display device being a self-luminous element, after the luminous elements have been sealed inside the envelope, the inside thereof must be maintained to minimize the formation or introduction of unnecessary gases.
As to the getters for fluorescent display tubes, various techniques have been developed to prevent harmful effects due to the high-frequency induction heating. For example, as shown in
A technique has been disclosed for preventing the problem of forming an evaporation film through the r-f induction heating of the getter ring and of effectively using the man-power and the space (for example, refer to Patent Publication No. WO00/54307). In this technique, a non-evaporation type getter (NEG) formed of metals of one or more types or an alloy of them, on the upper surface of an insulating substrate constituting a display element is fabricated through a printing method or sputtering method. The metals are selected from the group consisting of Ti, Cr, Al, V, Nb, Ta, W, Mo, Th, Ni, Fe, and Mn. The non-evaporation type getter (NEG), however, is expensive and requires the activation workability.
Moreover, there is a technique for preventing the trouble occurring when an evaporation film is formed by h-f heating a getter ring being a getter material for a fluorescent display tube and effectively using the man-power and the space. In this technique, a Ba—Al alloy or Mg—Al alloy, which does not contain an additive metal such as Ni, is press molded in a disk, oval, or rectangular shaped getter. Then, the getter is mounted in the electron tube such as a fluorescent display tube, using metal wires or fritted glass. The technique of flushing the getter through the laser beam heating and thus forming a getter mirror film has been disclosed (for example, refer to Japanese Patent Laid-open Publication No. Tokkai-hei No. 2002-343233).
In addition to the technique of using a metal having the getter effect and maintaining a clean atmosphere in the vacuum envelope, the technique of using TiO2 or ZnO2 as an auxiliary getter material is disclosed as described below. TiO2 and ZnO2 are used as a getter material. However, if a material absorbs O or H, other chemicals may be mixed in a getter material. Such materials are dissolved in a fixing solution to make a solution, and then the solution is coated on support members. The concentration of the getter material in the coating solution is set to 2 to 5 wt %. However, the fixing solution evaporates during the sealing step and is drawn out. Finally, the titanium oxide remains as a getter material.
In order to effectively derive the absorption effect of the getter mixed in the fixing material 10, it is effective to bake the substrate above at least 400° C. That is, the technique is disclosed of improves the getter effect by deoxidizing TiO2 into TiO or Ti through the baking step (refer to Japanese Patent Laid-open Publication No. Tokkai No. 2000-340140). However, this technique has a problem in a practical use because only an auxiliary effect of creating and maintaining a high degree of vacuum degree was confirmed.
In order to maintain a high degree of vacuum such as 1×10−3 Pa in the closed space, such as the vacuum display device of the present invention, materials, having the function of absorbing residual gas molecules and removing them from the gas phase, for example, high melting point metal materials, such as Ti, Mo, Ba, and Zr, have been employed as getter materials. The Ba series getters have been practically used as getters generally usable in a temperature range of 140° C. to 120° C. However, a high melting point metal material, such as Ti, Mo, or Zr, has not been used practically as a getter material. Powders of high melting point metal, being the getter material, may generally be unstable because it can catch fire when in contact with the air. Moreover, the metal powders do not often have a sufficient gas occlusion capability.
Various techniques have been developed to obtain getter materials, which are safe and easy to handle, and to improve the occlusion efficiency of residual gases of a getter material. The problem, however, is that any one of those techniques requires a room for disposing a getter material and requires the step of activating the surface of the metal getter material though h-f induction heating or resistance heating after the getter material has been placed in the envelope.
The present invention is made to solve the above-mentioned problems.
An object of the present invention is to provide a gas occlusion material, which is safe, easy to handle, saves space, and absorbs residual gases inside a hermetic envelope to maintain the hermetic envelope in high vacuum degree, in place of the conventional metal getter.
Another object of the present invention is to provide a display device using the gas occlusion material to solve the following problems.
In self-luminous elements using the electron beam excitation emission, the vacuum hermetic enclosure is maintained in high vacuum degree while both the inner surface of the enclosure and the surface of the fluorescent substance are maintained clean.
In the plasma display devices being self-luminous elements, it is said that unnecessary gases, other than gas for displaying such as plasma generation gas, generated and invaded after an enclosure has been evacuated in high vacuum adversely affect the operational life of the device. Accordingly, the unnecessary gases inside the plasma display device are removed.
In order to maintain the luminous characteristics of an EL display device, or a self-luminous element, the cleaning degree is maintained so as to exclude internal unnecessary gases after luminous elements are sealed inside the enclosure.
In order to solve the above-mentioned problems, the present invention uses a relatively safe ZrOx (where 1≦x≦2). According to the present invention, a gas occlusion material containing a zirconium dioxide is disposed in a hermetic envelope so as to be exposed in an atmosphere in the hermetic envelope. Thus, the gas occlusion material absorbs undesired gases inside the hermetic envelope of a self-luminous element, thus improving the reliability of the self-luminous element.
In another aspect of the present invention, a self-luminous element comprises a gas occlusion material containing a zirconium dioxide; a member on which the gas occlusion material is coated, the member being disposed in a hermetic envelope so as to be exposed in an atmosphere in the hermetic envelope.
In further another aspect of the present invention, a self-luminous element comprises a vacuum hermetic envelope; an electron source disposed inside the vacuum hermetic envelope; a fluorescent substance layer disposed inside the vacuum hermetic envelope, for light emitting in response to electrons irradiated from the electron source; and a gas occlusion material disposed inside the vacuum envelope, the gas occlusion material containing ZrOx (where 1≦x≦2); the gas occlusion material being disposed so as to be exposed to an atmosphere in the hermetic enclosure.
In the self-luminous element according to the present invention, the electron source comprises a filament-like electron source.
In the electron tube according to the present invention, the electron source comprises a field emission electron source.
In the electron tube according to the present invention, the gas occlusion material having a conductivity and containing ZrOx (where 1≦x≦2) is exposed in an atmosphere inside the hermetic enclosure.
In the self-luminous element according to the present invention, the gas occlusion material containing ZrOx (where 1≦x≦2) is formed in a film state over an inner surface of the hermetic enclosure.
In the self-luminous element according to the present invention, the gas occlusion material containing ZrOx (where 1≦x≦2) is formed in a film state on the upper surface of an insulating layer overlying an inner surface of the hermetic enclosure.
In the self-luminous element according to the present invention, the gas occlusion material containing ZrOx (where 1≦x≦2) is formed to a grid member disposed above the fluorescent substance layer.
In the self-luminous element according to the present invention, the gas occlusion material containing ZrOx (where 1≦x≦2) is coated on a filament support member disposed on an inner surface of the hermetic enclosure.
In the self-luminous element according to the present invention, the gas occlusion material containing ZrOx (where 1≦x≦2) is coated on a core line disposed in a space on an inner surface of the hermetic enclosure.
In the self-luminous element according to the present invention, the gas occlusion material containing ZrOx (where 1≦x≦2) comprises an anode electrode acting as a base electrode formed on an inner surface of the hermetic enclosure.
In the self-luminous element according to the present invention, the gas occlusion material containing ZrOx (where 1≦x≦2) is formed a spacer member for a flat grid disposed around the fluorescent layer.
In further another aspect of the present invention, a method for producing a self-luminous element comprises the steps of disposing a gas occlusion material containing ZrOx (where 1≦x≦2) at a portion of a vacuum envelope; forming a display device envelope which contains the gas occlusion material; and raising the display device envelope to a temperature of 120° C. to 600° C.
In still further aspect of the present invention, a method for producing a self-luminous element comprises the steps of disposing a gas occlusion material containing ZrOx (where 1≦x≦2) at a portion of a vacuum envelope; forming a display device envelope which contains the gas occlusion material; and hermetically sealing the display device envelope in vacuum at a temperature of 300° C. to 400° C.
The present invention can provide a gas occlusion material, which is safer than the conventional metal getter, is easy to handle, saves the space, and absorbs residual gases inside a hermetic envelope to maintain the hermetic envelope in high vacuum degree. The gas occlusion material containing ZrOx (where 1≦x≦2), which is a safe material, can be disposed as various members, constituting a self-luminous element, inside a hermetic envelope. Thus, in an atmosphere of the hermetic envelope, the gas occlusion material can effectively maintain the inside of the hermetic envelope in a clean state.
In self-luminous elements using electron beam excitation emission, the gas occlusion material can maintain the inside of the vacuum hermetic envelope in high vacuum degree and can clean the inner surface of the envelope and the fluorescent substance surface.
In plasma display devices being self-luminous elements, it is generally accepted that after the inside of an envelope is evacuated in high vacuum, the generation and/or invasion of gases, other than gases needed for display, such as plasma generation gas, adversely affect the operational life of the fluorescent display. Undesired gases inside the plasma display device must be removed to maintain the safe hermetic envelope atmosphere.
In order to maintain the luminous characteristics of EL display devices being self-luminous elements, after luminous elements are sealed inside an envelope, the gas occlusion material can effectively maintain the envelope in no existence of internal unnecessary gases.
This and other objects, features, and advantages of the present invention will become more apparent upon reading of the following detailed description and drawings, in which:
A distributed type getter and a contact-type getter are known as means for achieving a high vacuum degree using a getter. The distributed type getter absorbs gas molecules by reacting and combining with gas molecules with a vapor of the getter generated through chiefly evaporating or sputtering Ba, Mg, Ca, and others and then by evaporating them onto a solid surface. In the contact-type getter, a getter is evaporated onto the surface of a solid such as Ti, Ta, Zr, or V and then the resultant clean getter surface captures gas molecules.
The metal, Zr, used as the contact-type getter material makes an oxide film indicating a strong corrosion resistance on the surface thereof in air. However Zr is characterized in that the powder thereof catches fire easily.
It is believed that any one of the distributed-type getter and the contact-type getter works as a gas occlusion material, which occludes gaseous molecules and atoms through the chemical reaction of a metal or metal alloy and gas molecules.
Zirconium oxide has two types, that is, a low temperature type (monoclinic system) and a high temperature type (pyramidal quadratic system). It is known that the transition temperature occurs in vicinity of 1000° C. reversibly and endothermically. Moreover, it is known that zirconium has a high oxygen defect. For that reason, the present inventor supposed that because the oxygen defect transmits oxygen ions at high temperatures, it would have the mechanism of absorbing gas molecules. It was considered to use ZrOx (where 1≦x≦2) as a gas occlusion material equivalent to the getter material for the display device.
Fluorescent display tubes, using a getter ring as a gas occlusion material acting as both the distributed-type getter and the contact-type getter, were fabricated as comparative objects.
Zeolite series molecular sieve (synthetic zeolite having fine pores of 4 nm industrially manufactured by Linde Co.), used as an absorbent material having a high physical absorption capability such as moisture absorbent or carbon dioxide, is known in public as a physical gas occlusion material. The getter material using the zeolite series molecular sieve was built in a fluorescent display tube. Thus, it was evaluated whether or not the trial getter material can be used as a gas occlusion material for fluorescent display tubes.
Comparative example 1 is an example of a fluorescent display tube using a conventional getter ring. As shown in
Thereafter, a fluorescent substance layer 400 for low velocity electron beams is formed on the upper surface of the anode conductor through the screen printing process. Then, the intermediate structure is baked at 450° C. to complete an anode substrate.
The anode substrate, a conventional getter ring 110, a filament 600, and a grid electrode 500 are integrated. A boat container 700 is assembled with the glass substrate 000 (of 25 mm in width×50 mm in length). A complete envelope is fabricated by sealing the boat container of 25 mm in width×50 mm in length×3 mm in height with a low melting point glass in an atmosphere of 400° C. to 500° C.
Next, gases remaining in the envelope are drawn out in an atmosphere of 400° C. to 500° C., so that a fluorescent display tube hermetically sealed in vacuum is fabricated. Thereafter, the getter was heated through h-f induction heating so that a sample in a high vacuum state was fabricated. Moreover, the fluorescent display tube hermetically sealed in vacuum was stored in an oven at 100° C. to 300° C. and then was subjected to aging. Thus, a fluorescent display tube was completely produced.
Comparative example 2 shows an example in that a gas occlusion material containing zeolite series molecular sieve is disposed as an occlusion layer on the upper surface of the insulating layer of the anode substrate. Zeolite series molecular sieve (synthetic zeolite having fine pores of 4 nm industrially manufactured by Linde Co.) is used as an absorbent material having a high physical absorption capability such as moisture absorbent or carbon dioxide. Various products are used according to sizes of fine pores.
The following fluorescent display tubes were prepared for comparison to examine whether or not the above mentioned materials can be used as gas occlusion materials for fluorescent display tubes.
Specifically, in the fluorescent display tube shown in
Thereafter, a boat container (of 25 mm in width×50 mm in length×3 mm in height) is hermetically sealed with a low melting point glass in an atmosphere of 400° C. to 500° C. to make a fluorescent display tube.
The following examples 3A, 4A, 5A, and 13X were used as the zeolite series molecular sieve.
A gas occlusion material forming paste containing the zeolite series molecular sieve is prepared by mixing a mixed solvent of butyl-carbitol and terpinenol in a vehicle in which ethyl cellulose is dissolved.
3A: A product having an effective diameter of less than 0.3 nm, which absorbs H2O, NH3, and He.
4A: A product having an effective diameter of less than 0.4 nm, which absorbs H3S, CO2, C2H2, C3H3OH, and C6H6.
5A: A product having an effective diameter of less than 1.0 nm, which absorbs n-paraffin, n-olefin, and n-C4H9OH, C3H3OH, and C6H6.
13x: A product having an effective diameter of less than 1.0 nm, which absorbs iso-paraffin, iso-olefin, and di-n-butylamin aromatic series.
In the embodiment 1,
As shown in
Thereafter, a fluorescent substance layer 400 for low velocity electron beam is formed on the upper surface of the anode conductor through the screen printing process. Then the intermediate structure is baked at about 450° C. to complete an anode substrate.
Thereafter, the fluorescent substance layer 400 for low velocity electron beam is formed on the upper surface of the anode conductor through the screen printing process. Then, a gas occlusion material forming paste of 15 mm×30 mm containing zirconium dioxide is printed in the area where the anode conductors are not disposed and on the upper surface of the glass substrate 000 of 25 mm in width×50 mm in length. In succession, the printed structure is baked in an air atmosphere at about 450° C. After baking, the weight of the gas occlusion layer 100 was about 6 mg.
Thereafter, the boat container of 25 mm in width×50 mm in length×3 mm in height is sealed in vacuum with a low melting point glass in an atmosphere of 400° C. to 500° C. to fabricate a fluorescent display tube.
The gas occlusion material forming paste containing the zirconium dioxide is prepared by mixing a mixed solvent of butyl-carbitol and terpinenol in a vehicle in which ethyl cellulose is dissolved.
The fluorescent display tubes produced in the comparative examples 1 and 2 and in the embodiment were evaluated according to the following methods.
As to the electron emission capability of a filament in a fluorescent display tube:
As the anode voltage increases from a negative value to a positive value, more electrons emitted from the cathode are accelerated toward the anode. The space between the anode and the cathode is filled with the emitted electrons, so that the state where the cathode is shielded by the electrons is balanced. The region II is called a space charge limited region. As the anode voltage is further increases, the state becomes the temperature-limited region III where the anode current is limited due to the electron emission capability of the cathode. The total current Is from the cathode is represented by the following equation (I) of Richardson and Dushman.
Is=SATn exp(−eΦ/KT) (1)
Accordingly, by measuring Is at a constant temperature T in the temperature limited region, the quality of cathode can be evaluated. The measured current Is is used as a pulse emission value for evaluating the electron emission capability of a filament of a fluorescent display tube. Generally, it is targeted that the measured current value exceeds 100%, with respect to standard values being values obtained by a normally operable filament fluorescent display tube (and so forth).
As to gas current:
Here, the electron emission capability of a filament in a fluorescent display device will be explained. In the fluorescent display device, the inside of the hermetic envelope must be maintained at a high vacuum degree of less than 1×10−3 Pa but a minute amount of gas still exists in the envelope. In the means for measuring the vacuum degree necessary to maintain the function of a fluorescent display tube, a minute amount of ions are generated when a predetermined positive voltage is applied to the grid in the fluorescent display tube while electrons are emitted from the energized filament.
A current due to the minute ions in the fluorescent display tube is measured when a predetermined positive voltage is applied to the anode disposed in the fluorescent display tube. This value corresponds to a numerical value to evaluate a vacuum degree and is called an ion current. Generally, values obtained by a normally operable fluorescent display device are set as standard values. An ion current less than 100% with respect to a standard value is used as an index of the vacuum degree of a fluorescent display tube (and so forth)
In the fluorescent display tube of the embodiment 1, the initial value of the pulse emission being a target value of the electron emission capability of a filament is 120% to the value of the standard fluorescent display tube. However, in the comparative example 1, the electron emission capability is about 60% of the pulse emission when a voltage is applied to a filament and glowing is made with the thermal electrons for 100 hours. However, the electron emission capability was about 200% with respect to the pulse emission of the fluorescent display tube using the standard Ba—Al getter. This value was equivalent to the Ba—Al getter.
In the fluorescent display tube of the embodiment 1, the initial value of gas current, being an index of vacuum degree, is 110% with respect to that of the standard fluorescent display tube. However, when a filament in the fluorescent display tube is driven with a voltage and emits thermal electrons for 100 hours, the initial value drops to about 80%. This was equivalent to the value in the fluorescent display tube using the standard Ba—Al getter 110.
The gas occlusion layer 100 containing zirconium dioxide is disposed at a portion in an envelope. Thus, it was ascertained that there is the possibility that a gas occlusion effect close to that of the conventional Ba—Al getter 110 can be obtained.
Next, using the fluorescent display devices in the comparative example 1, the comparative example 2, and the embodiment 1, the pulse emission, being an index of the electron emission capability of a filament, and the gas current, being an index of vacuum degree, were evaluated. Thus, it was confirmed whether or not the zirconium dioxide and the zeolite series molecular sieve could be used as the gas occlusion material for a fluorescent display tube.
Referring to
Judging from data mentioned above, it is understood that there is a possibility that the fluorescent display tube in the embodiment 1, in which a zirconium dioxide gas occlusion material is disposed at a portion in a vacuum envelope, can provide a gas occlusion effect close to that of the fluorescent display tube in the comparative example 1 using the conventional Ba—Al getter.
The fluorescent display tube is usually used at a room temperature (about 25° C.), but may be often stored at 85° C. or more according to the specification. In the fluorescent display tube in the embodiment 1, the gas current was measured at 25° C., 50° C., 85° C., and 120° C. and then evaluated at 25° C.
The gas currents at 25° C., 50° C., 85° C., and 120° C., which indicate the vacuum degree of the fluorescent display tube in the embodiment 1, were compared with that of the fluorescent display tube in the comparative example 1 using the conventional Ba—Al getter. At 25° C., the gas current was about 100% of that of the comparative example 1. At 50° C., the gas current was about 150% of that of the comparative example 1. At 85° C., the gas current was about 200% of that of the comparative example 1. At 120° C., the gas current was about 200% of that of the comparative example 1. However, the gas current was about 90% of that of the comparative example 1 when the fluorescent display tube settles to 25° C. after leaving it in an atmosphere at 120° C.
Judging from the results, it was ascertained that zirconium dioxide used as a gas occlusion material can provide the effect identical to that of the conventional Ba—Al getter at normal temperatures. It was ascertained that when the fluorescent display tube settles to a room temperature of 25° C. after storing at 50° C. or more, it can provide a gas occlusion effect identical to that of the fluorescent display tube in the comparative example 1.
The problem arises that when the fluorescent display tube is generally stored at 85° C., brightness decreases due to gases released from the fluorescent substance surface in the fluorescent display tube. When the fluorescent display tube using the conventional Ba—Al getter is driven at a normal temperature (25° C.), the Ba—Al getter absorbs gases unnecessary for the fluorescent display tube, so that stable display is recovered.
The pulse emission indicating the electron emission capability of the fluorescent display tube in the embodiment 1 was compared with that of the fluorescent display tube using the Ba—Al getter in the comparative example 1. At a normal temperature of 25° C., the pulse emission value was about 20%. After the fluorescent display tube was left in an atmosphere of 120° C. for 24 hours, the pulse emission value was about 110%. After the fluorescent display tube was illuminated for 4 hours at 25° C., the pulse emission value was about 90%. After the fluorescent display tube was further illuminated for 16 hours at 25° C., the pulse emission value was about 130%.
By disposing zirconium dioxide in a portion of a vacuum envelope, it is understood there is a possibility that a gas occlusion effect close to that of the conventional Ba—Al getter can be obtained.
Ascertainment of gas occlusion of zirconium dioxide:
In the fluorescent display tube in the embodiment 1, types of gas mainly absorbed were ascertained whether or not the gas occlusion layer containing zirconium dioxide can be used as a gas occlusion material for a fluorescent display tube.
Referring to
Judging from the above description, by disposing zirconium dioxide as a gas occlusion layer in a portion of the vacuum envelope, it is understood that a gas occlusion effect close to that of the conventional Ba—Al getter can be obtained.
The operational life characteristics when the fluorescent display tube in the comparative example 1 and the fluorescent display tube in the embodiment 1 are driven for 500 hours at normal temperatures were ascertained. Moreover, the operational life characteristics when the fluorescent display tube in the comparative example 1 and the fluorescent display tube in the embodiment 1 are driven for 500 hours in an atmosphere at 85° C. were ascertained.
Referring to
It was ascertained that the gas occlusion layer, acting as a gas occlusion material, containing zirconium dioxide can be used as a substitute for the conventional Ba—Al getter.
Zirconium suboxide ZrO, acting as a catalyst, has many unsolved points in the detail principle. Recently, zirconium suboxide ZrO, being a stable oxide, has been reviewed as to applications as catalyst and can be considered as an effective gas occlusion material. It is known that zirconium dioxide has high oxide defects. It is said that because zirconium dioxide has the property of transmitting oxygen ions at high temperatures, there may be the mechanism in which oxygen defects absorb gas molecules. Hence, it can be considered that zirconium dioxide is effective as a gas occlusion material.
An embodiment of a fluorescent display tube, or a self-luminous element, using a filament electron source, will be described below, in which zirconium dioxide is disposed therein. Moreover, an embodiment of a fluorescent display tube, or a self-luminous element, using a field emission electron source, will be described below, in which zirconium dioxide is disposed in a vacuum hermetic envelope.
In the embodiment 2, the gas occlusion layer is disposed such that the surface thereof is exposed in the vacuum atmosphere. Thus, an effect similar to that in the embodiment 1 was obtained.
In the embodiment 3, the fluorescent display tube in the embodiment 2, which does not use the Ba—Al getter, and which is disposed such that the surface of the gas occlusion layer is exposed in a vacuum atmosphere, showed an effect similar to that in the embodiment 1.
The fluorescent display tube in the embodiment 4 exhibited an effect similar to that in the embodiment 1.
By forming the pattern as shown in
A paste is prepared by mixing graphite acting as a conductive material of 1 wt % to 30 wt % and a solid content such as zirconium dioxide, with a vehicle in which ethyl cellulose is dissolved in a mixed solvent of organic titanium, butyl-carbitol, and tarpinenol. As shown in
The rib spacer 511, into which zirconium dioxide is mixed, is formed through printing a paste. The paste was prepared by mixing a low melting point glass of 30 wt % to 50 wt % and a solid content such as ZrO2 into a vehicle. The vehicle is made by dissolving an organic binder such as ethyl cellulose in a mixed solvent of organic titanium, butyl-carbitol, and terpinenol. In the embodiment 10, an effect similar to that in the embodiment 1 was obtained.
The metal material on which zirconium dioxide is electro-deposited is mounted in a fluorescent display tube, for example, in parallel to the filament cathode. In other structure, the fluorescent display tube was fabricated in a manner similar to that in the embodiment 1. The metal material having the gas occlusion layer 100, electro-deposited in the completed fluorescent display tube, is separated from the filament and thus can be activated externally through resistance heating such as electric conduction.
In the embodiment 11, a combination of the metal material and the Ba—Al getter resulted in a fluorescent display tube having the reliability higher than the embodiment 1.
An exhaust hole (not shown) is formed at a corner of the cathode substrate 2 to evacuate gases remaining in the envelope. After evacuation, the exhaust hole is sealed and the inside of the envelope 2 is maintained at a high vacuum degree of 1×10−3 Pa or less.
Vertical field emission elements 620, each acting as an electron source, are formed on the cathode surface confronting the anode substrate in the envelope. Each field emission element 620 has a cathode electrode formed on the inner surface of the cathode substrate, a resistance layer formed on the cathode electrode, an insulating layer such as silicon oxide formed on the resistance layer, a gate electrode formed on the insulating layer, and a cone emitter formed on the cathode electrode within an opening formed through both the insulating layer and the gate electrode. Some field emission devices (FEDs) do not have a resistance layer between the cathode electrode 5 and the insulating layer.
An anode electrode acting as a display section is formed on the inner surface of the anode substrate in the envelope 3 and at a position confronting a field emission element. The anode electrode is formed of a translucent anode conductor 300 such as ITO formed on the anode substrate 1 and a fluorescent substance layer 400 coated in a predetermined shape, for example, in a dot matrix, on the anode conductor.
Gas occlusion layers 100, spaced at small intervals, are coated on the inner surface of the anode substrate in the envelope and around fluorescent substance layers respectively forming display sections. The surface of each gas occlusion layer 100 is exposed in the atmosphere in the envelope 3. The gas occlusion layer 100 absorbs gases released in the envelope, or specifically, gases generated when the fluorescent substance layer 400 glows in response to impingement of electrons from a field emission element.
In the twelfth embodiment, when electrons emitted from the field emission element 620 glows strike the fluorescent substance layer 400 on the anode electrode, thus causing excitation light emission. The light emission is observed via the anode conductor and via the translucent anode substrate. Part of the energy when the electrons strike the fluorescent substance layer 400 is converted into heat while the fluorescent substance layer 400 is decomposed to generate gases. The gas occlusion layer 100 surrounding the corresponding fluorescent substance layer 400 occludes the generated gases. At this time, the gas occlusion layer 100 works as a shielding member when light emission of the fluorescent substance layer 400 is viewed from the anode substrate side.
According to the twelfth embodiment, gases drifting above the display section during the light emission by excitation of the fluorescent substance layer 400 are efficiently absorbed with the gas occlusion layer 100 surrounding the fluorescent substance layer 400. Therefore, the gas occlusion layer 400 can absorb gases uniformly all over the display sections in the envelope, thus maintaining the inside of the envelope in high vacuum degree. A reduction of gases drifting above the display section enables reduced contamination of the emitter of the field emission element due to the gasses. As a result, the emission and luminous brightness can be maintained, so that the operational life of the fluorescent display can be prolonged, compared with that of the conventional one.
In the twelfth embodiment, the gas occlusion layers 100 are formed on the inner surface of the anode substrate at small intervals so as to surround the fluorescent substance layer 400. However, the gas occlusion layers 100 may be formed in contact with the anode conductor and without any spacing, such that the gas occlusion material 100 is at the same potential as that of the anode conductor when a positive voltage is applied to the anode conductor. In this case, the gas occlusion material layer 100 is activated with impingement of electrons, so that the gas occlusion capability can be improved.
In embodiment 13, a display element, in which zirconium dioxide acting as a gas occlusion material of the present invention, is fabricated. The display element uses carbon type electron emission elements, each having a carbon electron source, in place of the Spint-type electron sources. This configuration exhibited an effect similar to that in the twelfth embodiment.
In embodiment 14, a display element, in which zirconium dioxide acting as a gas occlusion material of the present invention, is formed. The display element uses MIM type electron emission elements, each in a metal/insulating thin film/metal structure, in place of the Spint-type electron sources. This configuration exhibited an effect similar to that in the twelfth embodiment.
In the embodiments described above, the gas occlusion material is applied to display elements having electron sources and fluorescent substance layers in a vacuum hermetic envelope. Here, as the display elements are enumerated fluorescent display tubes including filament cathodes as electron sources, Spint-type field emission display devices, display elements using carbon electron emission sources, and display elements using MIM-type electron emission elements. However, the gas occlusion material containing ZrOx (where 1≦x≦2) according to the present invention can be applied to display devices in which the atmosphere in a hermetic envelope must be maintained in an initial state, in addition to the case where the inside of an envelope is maintained in vacuum.
Unlike the conventional fluorescent display tube using the Ba—Al getter, an electron beam excitation fluorescent substance, being a kind of self-luminous element using a novel gas occlusion material of the present invention, can provide an inexpensive, long-life fluorescent display tube, without constraints in the Ba—Al getter installation space. Accordingly, the industrial applicability is that new applications for fluorescent display tubes usable more easily can be broadened.
As described above, the gas occlusion material containing ZrOx (where 1≦x≦2) according to the present invention is made as a paste, together with various materials. The paste may be disposed as a gas occlusion layer to a self-luminous element. Furthermore, aerosol is prepared by dispersing the paste in ethanol, acetone, water, or other solvent. Thus, the aerosol can be applied on the surfaces of column supports or other members of a display element.
Even in elements such as fluorescent display tubes, plasma display devices, EL elements, which require a vacuum hermetic vessel, the new gas occlusion material can be used as an inexpensive, long-life gas occlusion material. This, needless to say, can broaden new applications of self-luminous elements.
| Number | Name | Date | Kind |
|---|---|---|---|
| 2023707 | Spanner et al. | Dec 1935 | A |
| 6686678 | Suk et al. | Feb 2004 | B2 |
| 6838822 | Yonezawa et al. | Jan 2005 | B2 |
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