Patent Grant
7307379
The present invention relates to an electron emitting element capable of stably operating for a long period of time even in the atmosphere, and an imaging device using the same.
A Spindt-type electrode, a carbon nanotube (CNT)-type electrode and the like have been known as conventional cold cathode-type electron emitting elements, which have been studied on applications to the field of FED (Field Emission Display). The elements are operated in such a manner that a voltage is applied to a pointed end to form a strong electric field of about 1 GV/m and to emit electrons with the help of a tunneling effect.
There has been heretofore present an idea that such an electron emitting element is operated in the atmosphere and applied to a charger or an electrostatic latent image forming device. For example, there has been proposed a method in which a Spindt-type cold cathode is operated in the atmosphere to emit electrons into the atmosphere, to ionize gas molecules into ions as charged particles and to form an electrostatic latent image (see Japanese Laid-Open Patent Publication No. 06-255168). Besides, the result of a research on a carbon nanotube operated in the atmosphere has been reported (see Yamaguchi and three others, “Development of High Efficiency Electron Source for Image Recording with Carbon Nanotube,” Japan Hardcopy 97 articles, The Imaging Society of Japan, July 1997, pp 221-224). As seen from the documents, suggestion has been given on a possibility of applying an electron emission element as an electron source for an electrophotograph charger or electrostatic latent image forming device.
The two types of electron emitting elements, however, have a strong electric field in the vicinity of a surface of an electron emitting section as described above, which makes it easy that emitted electrons acquire energy larger than the electric field to ionize gas molecules. This has resulted in a problem that plus ions generated by ionization of gas molecules are accelerated by the strong electric field in the direction toward the element surface and collide with the element surface, causing element breakdown due to sputtering.
There have been known other type cold cathodes such as an MIM (Metal Insulator Metal) type and an MIS (Metal Insulator Semiconductor) type. Those are a surface emission-type electron emitting element working in a way such that electrons are accelerated using a quantum size effect and a strong electric field and caused to be emitted from a flat element surface. The electron emitting elements have no necessity for a strong electric field outside of the element since electrons are accelerated inside of the element and emitted. Hence, an electron emitting element of the MIM type or the MIS type can solve a problem that the element is broken down by sputtering through ionization of gas molecules, which occurs in the electron emitting element of the Spindt type or the CNT type.
An electron emitting element in which electrons injected into a porous semiconductor are accelerated in an electric field, forced to pass through a surface metal thin film with the help of a tunneling effect and finally emitted into a vacuum has been proposed as an electron emitting element belonging to the MIS type using a quantum size effect of a porous semiconductor (for example, porous silicon) formed by an anodic oxidation treatment on a semiconductor (see Japanese Laid-Open Patent Publication No. 08-250766). A cold cathode made of such a porous semiconductor has a great merit that an element can be fabricated by means of an extremely simple, convenient, low-cost method adopting anodic oxidation.
In a case where such an element is operated in the atmosphere, however, a problem has newly occurred that various gas molecules are adsorbed on a surface of the element to change an electric characteristic or the like of the semiconductor and to thereby reduce an electron emission current.
The surface of a cold cathode of the MIM type or the MIS type inside which element electrons are accelerated is constituted generally of a metal thin film playing a role as an upper electrode applying an electric field to the inside of the element. Since electrons accelerated in the inside of the element, however, are emitted into a vacuum tunneling through the surface metal thin film, an tunneling effect enhanced with a smaller film thickness increases an electron emission quantity. A thickness of the metal film by which the two roles are established simultaneously has been appropriate in the range of from several nm to tens of nm. For example, in Japanese Laid-Open Patent Publication No. 08-250766, there is disclosed an example with a thickness of a metal thin film of 15 nm.
Cold cathodes of the MIM type and the MIS type have difficulty forming a dense metal film because of a very thin film on the surfaces thereof and almost no barrier effect to gas molecules is exerted. Therefore, in a case where an electron emitting element is operated in the atmosphere, a problem arises that gas molecules intrude into an inside semiconductor layer to change an electric characteristic or the like of the semiconductor to thereby reduce an electron emission current.
It is an object of the present invention to provide an electron emitting element capable of stably operating in the atmosphere or in a low vacuum by solving the above problems when being operated in the atmosphere or in the low vacuum, and to provide an imaging device using the electron emitting element.
The electron emitting element according to the present invention, in order to achieve the object, is directed to an electron emitting element of a structure in which a semiconductor layer is formed between an upper electrode and lower electrode, wherein an organic compound adsorption layer is formed on a semiconductor surface of the semiconductor layer by causing the organic compound to be adsorbed on the semiconductor surface. The semiconductor layer here is made of silicon or polysilicon and part or the whole thereof can be made porous. The organic compound can be a straight-chain or branched non-cyclic hydrocarbon having 7 or more carbon atoms in a molecule, a compound obtained by coupling at least an aldehyde group to a non-cyclic hydrocarbon, or a non-cyclic hydrocarbon having at least one unsaturated bond in a molecule.
The imaging device according to the present invention is directed to an imaging device using the electron emitting element according to the present invention as a charger, wherein an electrostatic latent image carrier is charged by emitting electrons from the electron emitting element in the atmosphere. The imaging device according to the present invention is directed to an imaging device using the electron emitting element according to the present invention as a charge feed device, wherein a latent image is formed directly on an electrostatic latent image carrier by emitting electrons from the electron emitting element in the atmosphere.
According to the present invention, as described above, an electron emitting element in which a semiconductor layer is formed between an upper electrode and lower electrode is constructed and an organic compound is caused to be adsorbed on a semiconductor surface of the semiconductor layer, thereby enabling an electron emitting element capable of stably operating even in the atmosphere to be provided and further an imaging device using the electron emitting element to be provided.
With reference to
The semiconductor layer of the electron emitting element according to the present invention can be a porous silicon semiconductor layer or a porous polysilicon semiconductor layer in which part or all of silicon or polysilicon is made porous. A porous silicon semiconductor layer obtains a large emission current, while a porous polysilicon semiconductor layer greatly improves thermal stability. A porous semiconductor layer is high in effect of semiconductor surface stabilization with adsorption of an organic compound. Herein, the term, polysilicon, means polycrystalline silicon.
In a case where a semiconductor layer is porous, a semiconductor surface includes not only a surface of the semiconductor layer, but also a semiconductor surface in the inside of the semiconductor layer on which an organic compound can be adsorbed by way of holes formed inside the semiconductor layer. That is, in a case where semiconductor is porous, an organic compound is adsorbed on the semiconductor layer and thereby, not only is organic compound adsorption layer 15 or 25 formed on a surface of semiconductor layer 14 or 24 shown in
An electron emitting element of the present invention can use a non-cyclic hydrocarbon as the organic compound. A non-cyclic hydrocarbon can be adsorbed on a semiconductor surface of a semiconductor layer to thereby cause hydrophobicity to exerted. Thereby water molecules in the atmosphere can be prevented from intruding into the semiconductor layer and an oxidation reaction of a semiconductor layer with water molecules can also be prevented from occurring, which makes it possible to suppress a change in electric characteristic and reduction in electron emission current of an electron emission element. Since a non-cyclic hydrocarbon is less in steric hindrance as compared with a cyclic hydrocarbon, the non-cyclic hydrocarbon can be adsorbed on a semiconductor surface at a higher density, thereby hydrophobicity of the semiconductor surface can be raised.
An electron emitting element according to the present invention can use a straight-chain or branched non-cyclic hydrocarbon having 7 or more carbon atoms as the non-cyclic hydrocarbon. Such a non-cyclic hydrocarbon is attached to a semiconductor surface and becomes a saturated hydrocarbon to thereby form a chemically stable semiconductor surface extremely low in reactivity with an oxidant, a reductant, an acid or a base. The term, a branched non-cyclic hydrocarbon, means a non-cyclic hydrocarbon having at least one branching.
An electron emitting element according to the present invention can use a compound obtained by coupling at least an aldehyde group to the non-cyclic hydrocarbon as the organic compound. In a case of a non-cyclic hydrocarbon, or especially in a case where a non-cyclic hydrocarbon is a saturated hydrocarbon, the hydrocarbon is poor in reactivity with a surface of semiconductor such as silicon to render chemical adsorption thereof difficult. In such a case, when a compound with an alkyl group coupled with an aldehyde group as a functional group is forced to act on a semiconductor surface such as silicon surface, an aldehyde group with a high reactivity reacts and is adsorbed on the semiconductor surface to enable a structure in which the semiconductor surface is surrounded with alkyl groups to be realized. If a non-cyclic compound having carbon atoms in number exceeding 17 is used, a proportion of aldehyde groups contained in the compound decreases, which in turn, reduces chemical adsorptivity to a semiconductor layer surface.
Examples of compounds obtained by coupling an aldehyde group to the above-mentioned non-cyclic hydrocarbon includes: n-octanal (CH3(CH2)6CHO), n-decanal (CH3(CH2)8CHO), n-dodecanal (CH3(CH2)10CHO), 6-methylpeptanal ((CH3)2CH(CH2)4CHO), 11-methyldodecanal ((CH3)2CH(CH2)10CHO) and others.
An electron emitting element according to the present invention can use a non-cyclic hydrocarbon having at least one unsaturated bond as the non-cyclic hydrocarbon. Especially, in a case where a non-cyclic hydrocarbon is a saturated hydrocarbon, the hydrocarbon is poor in reactivity with a surface of semiconductor such as silicon, resulting in difficulty of chemical adsorption. In such a case, when a non-cyclic hydrocarbon having at least one unsaturated bond such as a double bond or a triple bond having a high reactivity is forced to act on a surface of semiconductor such as silicon, portions of double bonds or triple bonds having a high reactivity react with and are adsorbed on the semiconductor surface to enable a structure in which the semiconductor surface is surrounded with alkyl groups to be realized. If a non-cyclic hydrocarbon, with an unsaturated bond, and having carbon atoms in number exceeding 17 is used, a proportion of unsaturated bonds contained in the non-cyclic hydrocarbon decreases, leading to reduction in chemical absorptivity to a semiconductor surface.
Examples of non-cyclic hydrocarbons having the unsaturated bond include: 1-octene (CH3(CH2)5CH═CH2), 1-decene (CH3(CH2)7CH═CH2), 1-dodecene (CH3(CH2)9CH═CH2), 1-hexadecene (CH3(CH2)13CH═CH2), 6-methyl-1-heptene ((CH3)2CH(CH2)4CH═CH2), 2-methyl-1-nonene (CH3(CH2)6C(CH3)═CH2), 11-methyl-1-tridecene ((CH3)2CH(CH2)8CH═CH2), 2,4-dimethyl-1-heptene (CH3(CH3)2CH (CH3)CH2C(CH3)═CH2), 1,7-octadiene (CH2═CH(CH2)4CH═CH2), 1,3-decadiene (CH3(CH2)5CH═CH—CH═CH2) and others.
An electron emitting element according to the present invention can use a straight chain or branched non-cyclic unsaturated aldehyde compound expressed in a formula of C2H2n−1CHO (n is an integer ranging from 7 to 17) as a compound obtained by coupling an aldehyde group to the above-mentioned non-cyclic hydrocarbon. With the presence of an aldehyde group and an unsaturated bond in a molecule, a reactivity with a semiconductor surface further increases, thereby enabling a stronger chemical adsorption to be realized. Examples of such compounds include: 2-octenal (CH3(CH2)4CH═CHCHO), 2-decenal (CH3(CH2)6CH═CHCHO), 2-dodecenal (CH3(CH2)8CH═CHCHO), 2-hexadecenal (CH3(CH2)12CH═CHCHO), 6-methyl-2-heptenal (CH3)2CH(CH2)2CH═CHCHO), 11-methyl-2-dodecenal ((CH3)2CH(CH2)7CH═CHCHO), 2,6-dimethyl-5-heptenal ((CH3)2C═CH(CH2)2CH (CH3)CHO) and others.
The imaging device according to the present invention is directed to an imaging device using the electron emitting element according to the present invention as a charger, wherein the electron emitting element emits electrons into the atmosphere to charge an electrostatic latent image carrier. The electron emitting element according to the present invention can stabilize a semiconductor surface of a semiconductor layer by causing an organic compound to be adsorbed on the semiconductor surface to prevent gas molecules in the atmosphere from being adsorbed on the semiconductor surface and to thereby enable a change in electric characteristic and reduction in an electron emission current in the electron emitting element caused by the gas molecules to be suppressed; therefore, the element is used as a charger to thereby enable an electrostatic latent image carrier to be charged.
The imaging device according to the present invention is directed to an imaging device using the electron emitting element according to the present invention as a charge feed device, wherein the electron emitting element is caused to emit electrons in the atmosphere to form a latent image directly on the electrostatic latent image carrier. The electron emitting element according to the present invention can stabilize a semiconductor surface of a semiconductor layer by causing an organic compound to be adsorbed on the semiconductor surface to prevent gas molecules in the atmosphere from being adsorbed on the semiconductor surface and to thereby enable a change in electric characteristic and reduction in an electron emission current in the electron emitting element caused by the gas molecules to be suppressed; therefore, the element is used as a charge feed device to thereby enable a latent image to be formed directly on an electrostatic latent image carrier.
Therefore, the imaging device according to the present invention is constructed as a more simplified imaging device without generating ozone, which has been problematic in a conventional discharge-type charger.
Description will be given of embodiments of the present invention in a concrete manner below based on the accompanying drawing.
With reference to
The porous polysilicon layer was prepared by means of the following method. First of all, an undoped polysilicon layer with a thickness of about 1.5 μm was formed on a surface of conductive substrate 13b made of n-type silicon by means of a LPCVD (Low Pressure Chemical Vapor deposition) method. Then, a constant current anodic oxidation treatment was applied to the polysilicon layer in a mixed solution of a 50 mass % hydrofluoric acid aqueous solution and ethanol with a mixing ratio of 1 to 1 with the polysilicon layer as a positive electrode and a platinum electrode as a negative electrode to thereby render part or the whole of the polysilicon layer porous and to obtain the porous polysilicon layer. Pore diameters of the porous polysilicon layer were on the order in the range of about 10 nm to 100 nm. Note that a surface of the polysilicon layer is illuminated with light during anodic oxidation treatment using a tungsten lamp of 500 W. At the last stage, the porous polysilicon layer was applied with an RTO (Rapid Thermal Oxidation) treatment at about 900° C. to form an oxide film.
Then, an organic compound was caused to be adsorbed on the polysilicon surface of the porous polysilicon layer obtained as described above to thereby form organic compound adsorption layer 15. For example, the element with the porous polysilicon layer was sufficiently dehydrated and thereafter, the element was put into n-decanal (CH3(CH2)8CHO) kept at 90° C. The element was kept in n-decanal for about 30 minutes, thereby, as shown in
In addition, as shown in
The electron emitting element fabricated as described above can be driven in a way as described below. That is, with reference to
Measurement was carried out on a diode current Ips flowing between upper electrode 16 and lower electrode 13 and an emission current le flowing into collector electrode 37 by electrons emitted from upper electrode 16 and minus ions in the atmosphere and results are shown in
As shown in
For the sake of reference,
A thickness of a metal thin film of upper electrode of an electron emitting element is about 15 nm. An upper electrode of such a thin film is difficult forming a dense thin film without no clearance, which enables various gas molecules in the atmosphere to pass through the upper electrode. Besides, even if a polysilicon layer of an electron emitting element is rendered porous by anodic oxidation and an oxide film is formed thereon by RTO or the like to cover a surface of the polysilicon layer with a thin film of SiO2, the SiO2 film is not dense because of being a thin film and a polysilicon surface having hydrogen terminals remains. Hence, it is imagined that molecules of oxygen, nitrogen and water present in the atmosphere are adsorbed at the hydrogen terminals on the polysilicon layer surface and then, a chemical reaction such as oxidation occurs under influence of a current generated by driving the element, which degrades element characteristic.
It is imagined that since an organic compound is adsorbed on the semiconductor surface of a semiconductor layer to thereby form an organic compound adsorption layer obtained by replacing hydrogen terminals of polysilicon present on the semiconductor surface with alkyl groups, an electron emission characteristic of the electron emitting element can be stabilized. That is, it is imagined that by causing long chain alkyl groups to be adsorbed on the semiconductor surface of a semiconductor layer, the semiconductor surface of a semiconductor layer can be protected from adsorption of various gas molecules in the atmosphere and the quasi-active semiconductor surface easy to react with gas molecules (hydrogen terminals or the like on the polysilicon semiconductor surface) can be subjected to chemical adsorption with an organic compound and stabilized; therefore, degradation while continuous driving can be overcome. Besides, it is inferred that since long chain alkyl groups exert hydrophobicity, the alkyl groups prevent adsorption of water and excessive progress in oxidation, thereby stabilizing the element.
As described above, by causing an organic compound to be absorbed on a semiconductor surface of a semiconductor layer to form an organic compound adsorption layer, an electron emitting element operating stably for a long time in the atmosphere can be realized.
Another electron emitting element according to the present invention (an inventive element in the example shown in
Electron emitting element 11 according to the present invention was obtained in a similar way to that in Embodiment 1 with the exception that 1-decene (CH3(CH2)7CH═CH2) was used when an organic compound was caused to be adsorbed on a silicon surface of a porous polysilicon layer. By adsorption of 1-decene to the silicon surface of a porous polysilicon layer, a reaction occurs, as shown in
Note that an adsorption state of an organic compound, that is a state of an organic compound adsorption layer, on the silicon surface can be analyzed with DRIFT (Diffuse Reflectance Infrared Fourier-transform), Auger electron spectroscopy, Raman spectroscopy or the like.
With reference to
The porous polysilicon layer on the surface of insulating substrate 22 on which lower electrode 23 was formed was formed according to a method described below. An undoped polysilicon layer with a thickness of about 1.5 μm was formed on a surface of lower electrode 23 formed on the surface of insulating substrate 22 made of glass by means of an LPCVD method. Then, a constant current anodic oxidation treatment was applied on the polysilicon layer in a mixed solution of a 50 mass % hydrogen fluoride aqueous solution and ethanol with a mixing ratio of 1 to 1 with the polysilicon layer as a positive electrode and a platinum electrode as a negative electrode to thereby render part or the whole of the polysilicon layer porous to obtain the porous polysilicon layer. Pore diameters in the porous polysilicon layer were on the order in the range of from about 10 nm to 100 nm. Note that a surface of the silicon layer was illuminated with light from a tungsten lamp with the output of 500 W during anodic oxidation. Finally, a constant current was fed in an about 10% dilute sulfuric acid with the silicon substrate as a positive electrode and a platinum electrode as a negative electrode to thereby apply an ECO (Electrochemical Oxidation) treatment to the silicon substrate and to form an oxide film. In a fabrication process with such an ECO treatment, a process temperature is low, which alleviates a restraint on a substrate material, thereby enabling glass as a substrate material to be used. Besides, since, directly subsequent thereto, the porous polysilicon layer can be oxidized with a wet treatment, the process can be simplified as compared with oxidation in rapid thermal oxidation.
In a similar way to that in Embodiment 1, an organic compound adsorption layer was formed on the polysilicon surface of the porous polysilicon layer and thereafter, the upper electrode was formed thereon.
With reference to
Detailed description will be given of an imaging device using the electron emitting element according to the present invention as a charger.
First of all, with reference to
The devices implementing the imaging process include: a charger 52 charging the surface of photosensitive member 51 uniformly; an optical system in which the surface of photosensitive member 51 is imagewise illuminated with exposure light 53 according to an image not shown; a developing device 54 for visualizing the electrostatic latent image formed on the surface of photosensitive member 51 by exposure with the optical system; a transferring device 55 transferring the developed image (that is, an image of toner 60) onto a sheet-like paper 61 appropriately transported; a cleaning device 56 removing a residual developing agent (residual toner) not transferred onto the surface of photosensitive member 51 after the transfer; and a charge removing device 57 removing electrostatic charge remaining on the surface of photosensitive member 51, which are installed in this order in a rotational direction of photosensitive member 51.
Many of Papers 61 are accommodated in, for example, a tray or a cassette and accommodated papers are fed one piece at a time by a feeding means to a transfer region, opposite photosensitive member 51 at a position where transferring device 55 is installed, so that the paper coincides with the leading edge of the toner image formed on the surface of photosensitive member 51. Paper 61 after the transfer is separated from photosensitive member 51 and further fed to a fixing device 58.
Fixing device 58 fixes an unfixed toner image transferred onto a paper as a permanent image, and includes a heat roller the surface opposite the toner image of which is heated to a temperature melting and fixing the toner, and a press roller bringing paper 61 pressed to the heat roller so as to be in close contact with the heat roller side. Paper 61 passing through the fixing device 58 is discharged outside the imaging device onto a discharge tray not shown through discharging rollers.
The optical system not shown launches an optical image on-off driven according to image data using a semiconductor laser since an imaging device of the present invention is a printer or a digital copying machine. Especially in a digital copying machine, reflecting light from a manuscript for copying is read by an image reading sensor such as a CCD element is inputted to the optical system including the semiconductor laser and then, an optical image according to image data is outputted. In a printer, image data from other processing devices such as a word processor and a personal computer is converted to an optical image and paper is illuminated with the optical image. The conversion to the optical image is carried out using not only a semiconductor laser but also an LED element or a liquid crystal shutter.
In the way described above, if an imaging operation in the imaging device gets started, photosensitive member 51 is rotation-driven in the direction of the arrow mark and the surface of photosensitive member 51 is uniformly charged to a potential with a specific polarity by charger 52. After the charge, an optical image is launched by exposure light 53 in the optical system not shown and an electrostatic latent image according to the optical image is formed on the surface of photosensitive member 51. Developing is carried out in next developing device 54 to visualize the electrostatic latent image. In one imaging device according to the present invention, the developing is one with toner of one component and the toner is selectively attracted by an electrostatic force to an electrostatic latent image formed on the surface of photosensitive member 51 to thereby complete developing.
A toner image thus developed on the surface of photosensitive member 51 is electrostatically transferred onto paper 61 transported properly in synchronism with the rotation of photosensitive member 51 with transferring device 55 disposed in a transfer region. The transfer is performed by causing the toner image to migrate to the paper 61 side while transferring device 55 charges the rear surface of paper 61 with a polarity opposite a polarity of toner charge. After the transfer, part of the toner image not transferred to the surface of photosensitive member 51 is left behind thereon, the residual toner is removed from the surface of photosensitive member 51 with cleaning device 56 and the charge on the surface of photosensitive member 51 is removed to a uniform potential thereon, for example almost zero potential by charge removing device 57 for reuse of photosensitive member 51.
On the other hand, paper 61 on which the transfer has been completed is separated from photosensitive member 51 and paper 61 is transported to fixing device 58. In fixing device 58, the toner image on paper 61 is melted and press-adhered on paper 61 by a pressure acted thereon between the rollers. Paper 61 having passed through fixing device 58 is discharged into a discharge tray or the like installed outside the imaging device as the paper on which imaging is completed.
A charger using corona discharge as a working principle has generally used heretofore as charger 52 of an imaging device of an electrophotography type. To be concrete, there has been known a wire charge scheme using tungsten wire with a diameter of the order of 60 μm to which a high voltage is applied; a saw teeth charger scheme applying a high voltage to a plurality of saw teeth each having a sharply pointed tip; a roller charging scheme applying a high voltage to the roller put into contact with a photosensitive member and others, whereas since any of the schemes is a charger using discharge as a principle, it has been problematic to generate much of ozone. In a case where electron emitting element 11 according to the present invention is used as charger 52 of
Then, detailed description will be given of an imaging device using such an electron emitting element according to the present invention as a charge feeding device. As described above, it has been common that a method in which a photosensitive member is uniformly charged, exposure with a light beam is carried out to thereby form an electrostatic image, while it is also possible that ions are supplied directly onto an insulating material or a photosensitive member with a charge feed device such as Ion Printing Technology to thereby form an electrostatic latent image. Such a direct latent image forming scheme can simplify conventional two processes of charge and exposure into one process, which is advantageous for down sizing of an imaging device. In a case where an electrostatic latent image carrier is a photosensitive member, there are a problem of restraint on material and wear and another problem of dielectric break-down in a film; therefore, design items such as a film thickness and a dielectric item cannot be greatly altered, while in a case where a direct latent image forming scheme with a charge feed device, a photosensitive member is not necessarily required as an electrostatic latent image carrier, but a common insulating material can be used as the carrier. Hence, a freedom in material selection can be enhanced. Thereby, wear resistance and a resolution of an electrostatic latent image carrier can be improved.
With reference to
Since a conventional charge feed device generates ions by discharge as a principle in a similar way to that in a conventional charger, a problem has arisen that generates much of ozone. By using an electron emitting element of the present invention as charge feed device 72 of
An improved number of digits in magnitude of electron emission quantity was checked in a case where an organic compound shown in Table 1 is caused to be adsorbed on a semiconductor surface of a semiconductor layer in conditions similar to those of Embodiment 1. Examples 1, 2 and 4 correspond to Embodiments 1, 2 and 3, respectively.
As shown in Table 1, by causing a compound obtained by coupling at least aldehyde group to a non-cyclic hydrocarbon or a non-cyclic hydrocarbon having at least one unsaturated bond to be adsorbed on a semiconductor surface of a semiconductor layer, an electron emission quantity is increased by 0.37 to 2.02 digits in magnitude.
Although the present invention has been described and illustrated in detail, it is clearly understood that the same is by way of illustration and example only and is not to be taken by way of limitation, the spirit and scope of the present invention being limited only by the terms of the appended claims.
The present invention, as described above, can be widely used in an electron emitting element and an imaging device using the same.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2003-116091 | Apr 2003 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2004/005278 | 4/13/2004 | WO | 00 | 9/23/2005 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2004/095146 | 11/4/2004 | WO | A |
| Number | Name | Date | Kind |
|---|---|---|---|
| 6249080 | Komoda et al. | Jun 2001 | B1 |
| Number | Date | Country |
|---|---|---|
| 06-255168 | Sep 1994 | JP |
| 08-250766 | Sep 1996 | JP |
| 11-329213 | Nov 1999 | JP |
| 2000-019921 | Jan 2000 | JP |
| 2001-313151 | Nov 2001 | JP |
| 2001-357961 | Dec 2001 | JP |
| 2002-174943 | Jun 2002 | JP |
| 2002-258585 | Sep 2002 | JP |
| 2002-311683 | Oct 2002 | JP |
| 2004-265603 | Sep 2004 | JP |
| 2004-266089 | Sep 2004 | JP |
| Number | Date | Country | |
|---|---|---|---|
| 20060186786 A1 | Aug 2006 | US |
