1. Field of the Invention
The present invention relates to an electron-emitting device used for a display or the like.
2. Description of the Related Art
A field-emission electron-emitting device is known as an electron-emitting device used for a display or the like. PTL 1 discloses a field-emission electron-emitting device that includes fine protrusions on which an electric field is concentrated. PTL 2 discloses an electron-emitting device in which projections and depressions are formed on the surface of a conductive film. PTL 3 discloses an electron-emitting device that includes an insulating layer between a pair of conductive films, depressions being formed in the surface of the insulating layer.
To form as many electron emission sites as possible in a controlled manner in order to improve electron emission characteristics, it is important to form protrusions in a controlled manner. However, in some cases, it was conventionally insufficient to form as many protrusions as possible that contribute to electron emission in a controlled manner or to easily form the protrusions over a large area in a controlled manner. Accordingly, an aspect of the present invention is to provide a method for easily producing fine protrusions with high controllability to achieve satisfactory electron emission characteristics.
According to an aspect of the present invention, a method for producing an electron-emitting device including a cathode having a plurality of protrusions is provided, the method at least including a step of forming a conductive film composed of a material constituting the cathode on a base by sputtering at a total pressure of 1.0 Pa or more and 2.8 Pa or less; and a step of performing etching treatment on the conductive film to form a cathode having a plurality of protrusions on a surface thereof.
Further aspects of the present invention will become apparent from the following description of exemplary embodiments with reference to the attached drawings.
Various exemplary embodiments of the present invention will now be described in detail with reference to the attached drawings. The sizes, materials, shapes, relative configurations, and the like of constituent elements described in this embodiment are not intended to limit the scope of the present invention unless otherwise specified.
An example of an electron-emitting device to which the production method according to the present invention is suitably applied will be described with reference to
The electron-emitting device includes an insulating member 3 stacked on the surface of a substrate 1 and a gate 5 disposed on the upper face of the insulating member 3 so that the insulating member 3 is sandwiched between the substrate 1 and the gate 5. The electron-emitting device further includes a cathode 6 disposed on the side face of the insulating member 3. The cathode 6 partially extends to part of the upper face of the insulating member 3 and includes a plurality of protrusions 16. The plurality of protrusions 16 are arranged along a corner 32 that is a boundary portion between the side face (3f in
The steps of the production method of this embodiment will now be briefly described with reference to
Step 1
An insulating layer 30 to be a first insulating layer 3a is formed on the surface of the substrate 1. An insulating layer 40 to be a second insulating layer 3b is then stacked on the upper face of the insulating layer 30. A conductive layer 50 to be a gate 5 is stacked on the upper face of the insulating layer 40 (
The insulating layer 40 is composed of a material different from that of the insulating layer 30 so that the amount of the insulating layer 40 etched with an etching solution (etchant) used in the step 3 described below is larger than that of the insulating layer 30 etched.
Step 2
Next, etching treatment (first etching treatment) is performed on the conductive layer 50, the insulating layer 40, and the insulating layer 30 (
In the first etching treatment, specifically, a resist pattern is formed on the conductive layer 50 by photolithography or the like, and the conductive layer 50, the insulating layer 40, and the insulating layer 30 are then etched. Through the step 2, a first insulating layer 3a and a gate 5 that constitute the electron-emitting device shown in
Step 3
Subsequently, etching treatment (second etching treatment) is performed on the insulating layer 40 (
Through the step 3, a second insulating layer 3b that constitutes the electron-emitting device shown in
Step 4
The conductive film 60A composed of a conductive material that constitutes a cathode 6 is deposited by sputtering so as to extend at least from the oblique face 3f, which is the side face of the first insulating layer 3a on a cathode electrode 2 side, to part of the upper face 3e of the first insulating layer 3a (
Herein, although described below in detail, the conductive film 60A is formed by sputtering at a total pressure of 1.0 Pa or more and 2.8 Pa or less. By performing the film formation under such a condition, the conductive film 60A that includes grain portions and grain boundary portions and is suitable for forming effective protrusions 16 by etching performed in the step 5 described below can be formed.
The conductive film 60A is formed so as to cover at least part of the corner 32 of the first insulating layer 3a and extend from the side face 3f of the first insulating layer 3a to the upper face 3e of the first insulating layer 3a. At the same time, a conductive film 60B composed of a material that constitutes the cathode 6 is also deposited on the gate 5. In
Step 5
Subsequently, etching treatment (third etching treatment) is performed on at least the conductive film 60A to form the cathode 6 (
The main purpose of the third etching treatment is to form a plurality of protrusions 16. In the case where the conductive film 60A and the conductive film 60B are formed so as to be in contact with each other in the step 4, a gap 8 is formed therebetween in this step. In the case where the conductive film 60A and the conductive film 60B are formed so as not to be in contact with each other in the step 4, the distance d between the gate 5 and the cathode 6 in the gap 8 is increased in this step.
Through the step 5, as shown in
Step 6
A cathode electrode 2 for supplying electrons to the cathode 6 is formed (
Basically, the electron-emitting device that includes the cathode 6 having the plurality of protrusions 16 and is shown in
In the case where the conductive film 60B deposited on the gate 5 in the step 4 is left on the gate 5 as the conductive film 6B without completely removing the conductive film 60B, the conductive film 6B left can be regarded as part of the gate 5.
In the case where a step of increasing the resistance of the cathode 6 is performed after the step 5, for example, the resistance of the cathode 6 can be increased by oxidizing the cathode 6 after the step 5.
Each of the steps will now be described in detail.
Regarding Step 1
The substrate 1 is a substrate used for supporting the electron-emitting device. The substrate 1 can be composed of quartz glass, glass obtained by reducing the content of impurities such as Na, soda-lime glass, or the like. The substrate 1 needs to have not only high mechanical strength, but also the resistance to dry etching, wet etching, and an alkali or an acid such as a developer. When the electron-emitting device is used for an image display apparatus, the difference in coefficient of thermal expansion between the substrate 1 and the components stacked thereon is desirably as small as possible because a heating step or the like is performed. In consideration of heat treatment, the substrate 1 is desirably composed of a material whose alkali element does not easily diffuse into the electron-emitting device from the inside of the glass.
The insulating layer 30 (first insulating layer 3a) and the insulating layer 40 (second insulating layer 3b) are each composed of a material that is excellent in terms of workability, such as silicon nitride (typically Si3N4) or silicon oxide (typically SiO2). The insulating layer 30 and the insulating layer 40 can be formed by CVD, vacuum deposition, or a typical vacuum film formation method such as sputtering. The thickness of the insulating layer 30 is set to several nanometers to several tens of micrometers and preferably several tens of nanometers to several hundreds nanometers. The thickness of the insulating layer 40 is smaller than that of the insulating layer 30 and is set to several nanometers to several hundreds nanometers and preferably several nanometers to several tens of nanometers.
In the case where the insulating layer 30 and the insulating layer 40 are stacked on the substrate 1 and then the depression 7 is formed in the step 3, the amount of the insulating layer 40 etched needs to be larger than the amount of the insulating layer 30 etched in the second etching treatment. The ratio of the etching amount of the insulating layer 40 to the etching amount of the insulating layer 30 is preferably 10 or more and more preferably 50 or more.
To achieve such a ratio of etching amounts, for example, the insulating layer 30 can be formed of a silicon nitride film and the insulating layer 40 can be formed of a silicon oxide film, a PSG film having a high concentration of phosphorus, or a BSG film having a high concentration of boron. Herein, PSG is phosphosilicate glass and BSG is boron-silicate glass.
The conductive layer 50 (gate 5) has conductivity and is formed by vapor deposition or a typical vacuum film formation method such as sputtering. The conductive layer 50 to be the gate 5 is suitably composed of a material having conductivity, high thermal conductivity, and a high melting point. Examples of the material include metals such as Be, Mg, Ti, Zr, Hf, V, Nb, Ta, Mo, W, Al, Cu, Ni, Cr, Au, Pt, and Pd and alloys thereof. Furthermore, carbides, borides, and nitrides can be used. The thickness of the conductive layer 50 (gate 5) is set to several nanometers to several hundreds nanometers and preferably several tens of nanometers to several hundreds nanometers. Since the conductive layer 50 to be the gate 5 sometimes has a thickness smaller than that of the cathode electrode 2, the conductive layer 50 is desirably composed of a material with lower resistance than the material of the cathode electrode 2.
Regarding Step 2
In the first etching treatment, RIE (reactive ion etching) is preferably used. Through RIE, a material can be precisely etched by applying an etching gas in the plasma state to the material.
In the case where the component to be processed is composed of a material that forms a fluoride, a fluorine gas such as CF4, CHF3, or SF6 is selected as gas used for RIE. In the case where the component to be processed is composed of a material such as Si or Al that forms a chloride, a chlorine gas such as Cl2 or BCl3 is selected. Furthermore, at least one of hydrogen gas, oxygen gas, and argon gas is preferably added to the etching gas to ensure the selection ratio of the material to a resist and to ensure the smoothness of the etched surface or increase the etching rate.
Through the step 2, the first insulating layer 3a and the gate 5 each having the same shape or substantially the same shape as that shown in
The angle (indicated by θ in
Since the insulating layer 3a is formed on the surface of the substrate 1 by a typical film formation method, the upper face 3e of the insulating layer 3a is parallel (substantially parallel) to the surface of the substrate 1. In other words, the upper face 3e of the insulating layer 3a is sometimes completely parallel to the surface of the substrate 1, but the upper face 3e is normally considered to be slightly inclined depending on the film formation environment and conditions. They can be said to be parallel with each other including such a slightly inclined case.
Regarding Step 3
In the step 3, an etching solution (etchant) is selected so that the amount of the insulating layer 3a etched with the etching solution is sufficiently smaller than the amount of the insulating layer 40 etched with the etching solution.
In the above-described second etching treatment, for example, when the insulating layer 40 is composed of silicon oxide and the first insulating layer 3a (insulating layer 30) is composed of silicon nitride, so-called buffered hydrofluoric acid (BHF) may be used as the etching solution. Buffered hydrofluoric acid (BHF) is a mixed solution of ammonium fluoride and hydrofluoric acid. When the insulating layer 40 is composed of silicon nitride and the first insulating layer 3a (insulating layer 30) is composed of silicon oxide, a hot phosphoric acid etching solution may be used as the etchant.
Through the step 3, the second insulating layer 3b having the same or substantially the same pattern as that shown in
The depth (the distance in the depth direction) of the depression 7 is deeply related to the leakage current of the electron-emitting device. A value of the leakage current is decreased as the depth of the depression 7 is increased. However, the depression 7 with an excessive depth poses a problem in that the gate 5 is deformed or the like. Thus, the depth of the depression 7 is practically set to 30 nm or more and 200 nm or less. The depth of the depression 7 can also be rephrased as the distance from the side face 3f (or the corner 32) of the insulating layer 3a to the side face 3d of the insulating layer 3b.
The upper face 3e and the side face 3f of the insulating member 3 are not necessarily connected to each other so as to form a right angle, and can be connected to each other so as to form an obtuse angle. As shown in
Regarding Step 4
The conductive films (60A and 60B) are formed of a material constituting the cathode 6 by sputtering.
Any material can be used as the material (that is, the material constituting the cathode 6) of the conductive films (60A and 60B) as long as the material has conductivity and causes the field emission of electrons. The material preferably has a high melting point of 2000° C. or higher. The conductive material is preferably a material that has a work function of 5 eV or lower and whose oxide is easily etched. Suitable examples of the conductive material include metals such as Hf, V, Nb, Ta, Mo, W, Au, Pt, and Pd and alloys thereof. In consideration of the etching treatment performed in the step 5, the conductive material is particularly preferably Mo or W.
The film formation of the conductive films (60A and 60B) by sputtering is performed at a total pressure of 1.0 Pa or more and 2.8 Pa or less.
By performing such film formation, a conductive film including a region with high film density (grain portion) and a region with low film density (grain boundary portion) can be formed in a controlled manner. The density and composition of the conductive films (60A and 60B) are normally measured by XRR, XPS, or the like, but it is sometimes difficult to measure the density and composition of the actual electron-emitting device. In such a case, for example, the following method can be employed as the measurement method of density and composition. The quantitative analysis of elements is performed using a high-resolution electron energy loss electron microscope in which a TEM (transmission electron microscope) is combined with EELS (electron energy loss spectroscopy), to calculate density and composition.
When the conductive films (60A and 60B) were formed at various total pressures during sputtering, it was found that, as shown in
Argon (Ar) gas, krypton (Kr) gas, xenon (Xe) gas, or the like can be used as gas for sputtering, and argon gas is particularly desired in terms of manufacturing cost. A DC power supply or an RF power supply with an industrial power frequency of 13.56 MHz or the like can be used as a power supply for sputtering. The power during sputtering is a value obtained by dividing discharge power by the area of the target. The value is normally set to, for example, 1 W/cm2 or more and 5 W/cm2 or less. The distance between the sputtering target and the substrate 1 is normally set to, for example, 50 mm or more and 200 mm or less.
In some cases, a second conductive film is formed between the step 3 and the step 4 at a pressure lower than the above-described pressure range, so as to extend from the side face 3f to the upper face 3e of the first insulating layer 3a. In the electron-emitting device produced by forming a second conductive film with high film density below the conductive film 60A that later becomes the cathode 6, the wiring line and the cathode electrode 2 that drive the electron-emitting device can be connected to each of the protrusions 16 (electron emission portions) at a low resistance. Thus, a situation in which a desired electron emission current Ie is not obtained because of the voltage drop caused when the electron-emitting device is driven can be avoided. Furthermore, the adhesiveness of the conductive film 60A to the insulating member 3 can be improved.
Alternatively, in some cases, a second conductive film is formed on the surface (at least the plurality of protrusions 16) of the cathode 6, which has been formed in the step 5, at a pressure lower than the above-described pressure range. By covering the surface of the cathode 6 with the second conductive film having high film density, the resistance of the cathode 6 to processing and the stability during the operation can be improved. In addition, even if the resistance of the cathode 6 is increased through the step 5, the occurrence of a voltage drop described above can be suppressed.
The conductive film 60A and the conductive film 60B may be composed of the same material or different materials. However, the conductive film 60A and the conductive film 60B are preferably composed of the same material and formed at the same time in terms of the ease of production and the controllability of etching. The above-described second conductive film and the conductive film 60A may be composed of the same material or different materials. However, the second conductive film and the conductive film 60A are preferably composed of the same material in terms of the ease of production.
In this step, the conductive film 60A and the conductive film 60B may be formed so as to be in contact with each other or so as not to be in contact with each other. When the conductive film 60A and the conductive film 60B are formed so as to be in contact with each other, the gap 8 can be formed through the step 5. Therefore, the conductive film 60A and the conductive film 60B are desirably formed so as to be in contact with each other because the controllability of the gap 8 is improved.
When the electron-emitting device shown in
In the directional sputtering method, for example, the angle between the substrate 1 and the sputtering target is set and a shielding plate is disposed between the substrate 1 and the sputtering target. A so-called collimation sputtering method, which uses a collimator that gives directivity to sputtered particles, is also in the category of directional sputtering methods. In such a manner, only sputtered particles (sputtered atoms) with restricted angles are incident upon the surface on which a film is to be formed. In particular, the incident angle of the sputtered particles (film formation material) relative to the oblique face 3f of the first insulating layer 3a is preferably smaller than the incident angle of the sputtered particles (film formation material) relative to the upper face 3e (corner 32) of the first insulating layer 3a. Herein, the incident angle of the sputtered particles relative to the upper face 3e of the first insulating layer 3a is set to be closer to 90 degrees than the incident angle of the sputtered particles relative to the oblique face 3f of the first insulating layer 3a is. In this case, the sputtered particles can be incident upon the upper face 3e of the first insulating layer 3a at an angle closer to vertical compared with the case where the sputtered particles are incident upon the oblique face 3f of the first insulating layer 3a. By performing such film formation, the protrusions 16 can be formed on the corner 32 of the first insulating layer 3a with high controllability.
Regarding Step 5
The third etching treatment may be performed by either dry etching or wet etching, but wet etching is preferably selected to easily set the etching selection ratio with respect to other materials.
The combination of the material of the conductive films (60A and 60B) with the etchant used in the third etching treatment is not particularly limited. However, for example, if the material of the conductive films (60A and 60B) is molybdenum (Mo), an alkali solution such as TMAH (tetramethylammonium hydroxide) or ammonia water is preferably used as the etchant. Alternatively, a mixture of 2-(2-n-butoxyethoxy)ethanol and alkanolamine, DMSO (dimethyl sulfoxide), or the like can also be used as the etchant. If the material of the conductive films (60A and 60B) is tungsten (W), a solution of nitric acid, hydrofluoric acid, sodium hydroxide, or the like is preferably used as the etchant.
Since the number of atoms removed per unit time in the etching treatment is uniquely determined in accordance with the material of the conductive films (60A and 60B) and the etching solution, the film density and the etching rate are inversely proportional to each other. The etching rate means the rate of change in thickness per unit time.
As described above, the conductive films (60A and 60B) formed in the pressure range described in the step 4 are conductive films each including grain portions that are suitable for forming effective protrusions 16 and grain boundary portions. There is a difference in etching selection ratio between the grain portions and the grain boundary portions. Therefore, when the etching treatment of the step 5 is performed on the conductive films (60A and 60B) formed in the above-described pressure range, it is believed that the grain boundary portions are preferentially etched rather than the grain portions, whereby the cathode 6 having effective protrusions 16 that are mainly composed of the grain portions can be formed.
For example, the standard deviation σ of the distance d can be obtained by measuring the distances d between the cathode and the gate 5 in the gap 8 in the direction in which the gap 8 extends (the direction in which the corner 32 of the insulating member 3 extends). Specifically, the distance d is measured by observing the gap 8 using a SEM in the direction indicated by an arrow of
The distance d (the shape of the protrusions 16) between the cathode 6 and the gate 5 is dependent on the etching time.
The characteristics shown in
As shown in
When the film formation is performed at a pressure higher than the above-described pressure range, the change in σ becomes more sensitive with respect to etching time. Thus, the controllability is significantly degraded compared with the case where the film formation is performed in the above-described pressure range. This may be because many grain boundary portions are formed compared with the case where the film formation is performed in the above-described pressure range, whereby it becomes difficult to form the protrusions 16 by the etching of the step 5 with high stability and controllability. Moreover, the maximum value of σ obtained becomes small compared with the case where the film formation is performed in the above-described pressure range.
When the film formation is performed at a pressure lower than the above-described pressure range, the standard deviation σ hardly changes even if the etching time in the step 5 is increased. In other words, the formation of the protrusions 16 in the step 5 is substantially not performed. This may be because many grain portions are formed compared with the case where the film formation is performed in the above-described pressure range, whereby effective etching for forming the protrusions 16 is not performed in the step 5.
As described above, by performing the etching described in the step 5 on the conductive films (60A and 60B) formed in the pressure range described in the step 4, the protrusions 16 having a high value of σ can be formed with high stability and controllability.
Regarding Step 6
The cathode electrode 2 has conductivity as with the gate 5, and can be formed by vapor deposition, a typical vacuum film formation method such as sputtering, or photolithography. The cathode electrode 2 and the gate 5 may be composed of the same material or different materials. The thickness of the cathode electrode 2 is set to several tens of nanometers to several micrometers and more preferably several hundreds nanometers to several micrometers.
Next, the peripheral structure of the protrusions 16 of the electron-emitting device produced by the above-described production method will now be described.
The cathode 6 includes the plurality of protrusions 16 arranged along the corner 32 (refer to
In the case where the cathode 6 includes the protrusions 16, the distance between the periphery of the protrusions 16 and the gate 5 is larger than the distance between the protrusions 16 and the gate 5. As a result, electrons emitted from the protrusions 16 are scattered at the gate 5 in an isotropic manner, and the electrons scattered to both sides of each of the protrusions 16 can reach the anode through the regions where the distance to the gate 5 is large. Thus, the electron emission efficiency η can be improved compared with the case where a flat cathode 6 is formed along the corner 32, that is, compared with the case where the distance between the gate and the cathode is constant along the corner 32.
As shown in
When the protrusions 16 are enlarged as shown in
The protrusions 16 cover part of the upper face 3e of the insulating member 3, whereby the four advantages below are considered. The first advantage is that, since the protrusions 16 serving as electron emission portions are in contact with the insulating member 3 in a large area, mechanical adhesion is increased (adhesive strength is increased). The second advantage is that the thermal contact area between the protrusions 16 serving as electron emission portions and the insulating member 3 is increased, and thus the heat generated in the electron emission portions can be efficiently released to the insulating member 3 (thermal resistance is reduced). The third advantage is that, since the protrusions 16 are in contact with the upper face of the insulating member 3 with a gentle slope, the electric field strength at a triple junction that is generated at a boundary between an insulator, a vacuum, and a metal is decreased, whereby the occurrence of a discharge phenomenon caused by the generation of an abnormal electric field can be suppressed. The fourth advantage is that the electron emission efficiency is increased by providing a shape in which the surface of each of the protrusions 16 on the second insulating layer 3b side is inclined with respect to the normal to the rear face 5b of the gate 5.
Herein, the advantage achieved from the structure in which the protrusions 16 cover not only the side face 3f of the insulating member 3 but also part of the upper face 3e of the insulating member 3 will be further described in detail.
Initial Ie and the time variation in Ie were measured at various lengths x of the end (protrusion 16) of the cathode 6 on the gate 5 side, the end entering the depression 7 from the side face 3f of the insulating member 3. The amount of decrease in Ie from the initial Ie tended to become larger as the length x was decreased. Herein, the length x corresponds to x in
The amount of decrease in Ie from the initial Ie became larger as the length x was decreased. However, when x was more than 20 nm, the dependence of Ie on x tended to be reduced.
It is believed from the results that, since the protrusions 16 are brought into contact with the insulating member 3 in a large area by increasing x, thermal resistance is reduced. Furthermore, this may be because the heat capacity is increased due to an increase in the volume of protrusions 16 and the temperature of the edge of each of the protrusions 16 is decreased, whereby the initial variation is decreased.
It is not necessarily preferable that the length x be larger. Practically, the length x is set to 10 nm or more and 30 nm or less. The length x can be controlled by controlling the angle of the material of the cathode 6 during vapor deposition, the thickness of the second insulating layer 3b, and the thickness of the gate 5. If x is more than 30 nm, leakage is generated between the cathode 6 and the gate 5 through the upper face of the insulating member 3, and thus leakage current is increased.
The edge of each of the protrusions 16 of the cathode 6 is desirably kept as far apart from the gate 5 as possible (the distance d is increased). In this case, the scattering of electrons is decreased at the gate 5, and thus the electron emission efficiency η and the amount of emission current Ie are improved.
As shown in
Next, description of a triple junction will be made. A site where three types of materials such as a vacuum, an insulator, and a metal having different dielectric constants are connected to one another is normally called a triple junction. In some cases, the electric field strength at a triple junction becomes excessively higher than that at the periphery of the triple junction and thus discharge or the like is caused. Therefore, when the angle θ (refer to
Next, modifications of an electron-emitting device that is produced by applying the production method of this embodiment will now be described.
To stabilize electron emission characteristics and particularly to stabilize emission current, it is desired that the plurality of protrusions 16 of the cathode 6 do not interfere with each other as much as possible.
The following configuration is desired. As shown in
In addition to the configuration described above, the following configuration is desired. A resistor element is disposed in all or part of each of the portions (the portions that connect the cathode electrode 2 and the protrusions 16) denoted by 6a in
When the side face 3f of the insulating member 3 is flat, it is desired that the portions denoted by 6a have a thickness larger than that of the portions denoted by 6b. In this case, the creepage distance between the plurality of protrusions 16 serving as electron emission portions can be increased compared with the case where the thickness of the portions denoted by 6a is equal to that of the portions denoted by 6b. At the same time, the portions denoted by 6b have a resistance higher than that of the portions denoted by 6a, and therefore the mutual influence of the plurality of protrusions 16 can be reduced as described above. Moreover, the configuration shown in
In the configuration shown in
The emission current can be stabilized by simply increasing the resistance of the conductive film 6 including the protrusions 16, instead of increasing the resistance of only the portions denoted by 6b in
In the example above, the configuration in which the cathode 6 is formed on the side face of the insulating member 3 has been described as an electron-emitting device. However, the configuration of the electron-emitting device to which the production method of this embodiment is applied is not limited to such a configuration. For example, the following configuration shown in
Next, a measurement method of electron emission characteristics of the electron-emitting device produced by the production method of this embodiment and the efficiency at which electrons emitted from the cathode 6 reach the anode, that is, the electron emission efficiency (η) will now be described. The electron emission efficiency η is given as η=Ie/(If+Ie), where If is a current detected when a voltage is applied to the electron-emitting device and Ie is a current extracted into a vacuum when a voltage is applied to the electron-emitting device (current that reaches the anode). The electron emission characteristics can be measured using the configuration shown in
An electron source obtained by arranging, on a substrate, a plurality of the electron-emitting devices produced by the production method of this embodiment and a display panel that uses the electron source will now be described with reference to
The X-direction wiring lines 62 are connected to scanning signal application means (not shown) configured to apply scanning signals for selecting a row of the electron-emitting devices 64 arranged in the X direction. The Y-direction wiring lines 63 are connected to modulating signal generation means (not shown) configured to modulate each column of the electron-emitting devices 64 arranged in the Y direction in response to input signals. A driving voltage applied to each electron-emitting device is fed as the differential voltage between the scanning signals and the modulating signals applied to each electron-emitting device.
In the above-described configuration, each device can be made independently operational by selecting each device with simple matrix wiring.
In
Next, a display 25 including the above-described display panel 77 and a television apparatus 27 will now be described with reference to a block diagram of
A receiving circuit 20 receives television signals of satellite broadcasting, terrestrial broadcasting, or the like and various signals of data broadcasting or the like using a network and outputs the decoded video data to an image-processing unit 21. Herein, the above-described “received signal” can be rephrased as an “input signal”. The image-processing unit 21 includes a γ correction circuit, a resolution conversion circuit, and an I/F circuit. The image-processing unit 21 converts the video data subjected to image processing into a display format of the display (image display apparatus) 25 and outputs the video data to the display (image display apparatus) 25 as an image signal.
The display 25 includes at least the above-described display panel 77 and further includes a driving circuit 108 and a control circuit 22 configured to control the driving circuit 108. The control circuit 22 performs signal processing such as correction processing on input image signals and outputs the image signals and various control signals to the driving circuit 108. The control circuit 22 includes a sync-signal separation circuit, an RGB conversion circuit, a luminance signal conversion unit, and a timing control circuit. The driving circuit 108 outputs driving signals to the electron-emitting devices inside the display panel 77 in accordance with the input image signals, and thus a television image is displayed in accordance with the driving signals. The driving circuit 108 includes a scanning circuit, a modulation circuit, and a high-voltage power supply circuit configured to supply an anode potential. The receiving circuit 20 and the image-processing unit 21 may be accommodated in a housing different from the display 25, that is, in a set-top box (STB 26) or may be accommodated in a housing that is integral with the display 25. Herein, an example in which the television apparatus 27 displays a television image has been described. However, if the receiving circuit 20 is a circuit configured to receive an image distributed through a network such as the Internet, the television apparatus 27 functions as an image display apparatus that can display not only a television image but also various images.
More specific examples based on the above-described embodiment will now be described.
A method for producing an electron-emitting device of this Example will be described with reference to
First, as shown in
The insulating layer 30 was obtained by forming a silicon nitride film by sputtering so as to have a thickness of 500 nm. The insulating layer 40 was obtained by forming a silicon oxide film by sputtering so as to have a thickness of 30 nm. The conductive layer 50 was obtained by forming a tantalum nitride film by sputtering so as to have a thickness of 30 nm.
As shown in
After the resist was removed, as shown in
As shown in
In such a manner, the conductive film 60A and a conductive film 60B were formed at the same time so as to be in contact with each other.
As shown in
Finally, as shown in
As shown in
In Comparative Example 1, an electron-emitting device was produced in the same manner as in Example 1, except that the total pressure during sputtering in Example 1 was changed to 0.1 Pa. The electron emission characteristics of the electron-emitting device were measured in the same manner as in Example 1. When a driving voltage applied between the cathode electrode 2 and the gate 5 was 23 V, the electron emission current Ie was 1 μA. The distance d of the gap 8 of the electron-emitting device in this Comparative Example was slightly smaller than that of the electron-emitting device in Example 1 on average. The standard deviation σ of the distance d in the electron-emitting device of this Comparative Example was obviously smaller than the standard deviation σ of the distance d in the electron-emitting device of Example 1. After the electron emission characteristics were confirmed, the electron-emitting device was observed with a SEM. Consequently, the distance d between the protrusions 16 and the gate 5 was almost constant along the corner 32, and a plurality of effective protrusions 16 arranged along the corner 32 (in a Y direction) as shown in
In Comparative Example 2, an electron-emitting device was produced in the same manner as in Example 1, except that the total pressure during sputtering in Example 1 was changed to 3.0 Pa. The electron emission characteristics of the electron-emitting device were measured in the same manner as in Example 1. When a driving voltage applied between the cathode electrode 2 and the gate 5 was 23 V, the electron emission current Ie was 1.5 μA. The distance d of the gap 8 of the electron-emitting device in this Comparative Example was larger than that of the electron-emitting device in Example 1 on average. The standard deviation σ of the distance d in the electron-emitting device of this Comparative Example was larger than the standard deviation σ of the distance d in the electron-emitting device of Comparative Example 1. However, the standard deviation σ in the electron-emitting device of this Comparative Example was smaller than the standard deviation σ in the electron-emitting device of Example 1.
In this Example, an electron-emitting device was produced basically in the same manner as in Example 1, except that a second conductive film was formed before the conductive films (60A and 60B) were formed. The second conductive film was also formed by sputtering Mo.
In this Example, the second conductive film was formed so as to have a thickness of 20 nm under the same sputtering conditions as in Example 1, except that the total pressure during the sputtering of the conductive films (60A and 60B) in Example 1 was changed to 0.1 Pa. The second conductive film was immersed in BHF (high-purity buffered hydrofluoric acid LAL100 available from STELLA CHEMIFA CORPORATION) for 30 seconds and then cleaned with running water for 5 minutes. After the second conductive film was formed in such a manner, the conductive films (60A and 60B) were formed under the same conditions as in Example 1 so as to each have a thickness of 20 nm. Subsequently, the electron-emitting device of this Example was produced by performing the same processes as in Example 1.
The electron emission characteristics of the electron-emitting device of this Example were measured in the same manner as in Example 1. A driving voltage Vf required to obtain the same emission current Ie was decreased.
In this Example, an electron-emitting device was produced basically in the same manner as in Example 1, except that a second conductive film was formed after the conductive films (60A and 60B) were formed. The second conductive film was also formed by sputtering Mo.
In this Example, the conductive films (60A and 60B) were formed under the same conditions as in Example 1 so as to each have a thickness of 20 nm, and then etched under the same conditions as in Example 1. Subsequently, a second conductive film was formed. In this Example, the second conductive film was formed under the same conditions as those of the second conductive film formed in Example 2 so as to have a thickness of 15 nm. However, in this Example, the etching treatment performed on the second conductive film in Example 2 was not performed. Subsequently, a cathode electrode 2 was formed in the same manner as in Example 1 to produce the electron-emitting device of this Example.
The electron emission characteristics of the electron-emitting device of this Example were measured in the same manner as in Example 1. The rate of decline in emission current Ie was decreased compared with the electron-emitting device of Example 1.
In this Example, an electron source was produced by arranging the electron-emitting devices of Example 1 in a matrix, and a display panel was manufactured using the electron source. Specifically, 1080 row wiring lines and 3×1920 column wiring lines were formed on a rear plate 71 composed of a glass substrate by screen printing with silver paste. Subsequently, an electron-emitting device was formed beside each of the intersecting portions of the row wiring lines and the column wiring lines by the same method as the production method of Example 1. Furthermore, 1080×3×1920 fluorescent members 74 (1080×1920 pixels) were formed on the surface of a glass substrate 73, and a metal back 75 made of aluminum was stacked thereon to form a face plate 76. Inside a vacuum chamber, a supporting frame 72 including frit glass provided in advance was disposed between the rear plate 71 and the face plate 76 to hermetically seal the rear plate 71 and the supporting frame with each other and also the face plate 76 and the supporting frame with each other using frit glass. Through the processes described above, an FED display (display panel 77) in which a vacuum is maintained was produced. The television apparatus 27 shown in
According to the present invention, an electron-emitting device that includes fine protrusions and has satisfactory electron emission characteristics can be formed by a simple method with high controllability.
While the present invention has been described with reference to exemplary embodiments, it is to be understood that the invention is not limited to the disclosed exemplary embodiments. The scope of the following claims is to be accorded the broadest interpretation so as to encompass all such modifications and equivalent structures and functions.
This application claims the benefit of International Application No. PCT/JP2009/067498, filed Oct. 7, 2009, which is hereby incorporated by reference herein in its entirety.
Number | Date | Country | Kind |
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PCT/JP2009/067498 | Oct 2009 | JP | national |