This invention relates generally to electron emission areas, and more particularly to electron emission devices and methods for generating an emission current.
Carbon nanotubes are quasi-one-dimensional nanostructures and were first reported in an article by Sumio Iijima entitled “Helical Microtubules of Graphitic Carbon” (Nature, Vol. 354, Nov. 7, 1991, pp. 56-58). Carbon nanotubes have been highlighted as a new functional material expected to have many microscopic and macroscopic applications. Extensive research has been conducted into using carbon nanotubes in various applications, for example in electron emission devices, etc.
Typical electron emission devices incorporating carbon nanotubes each includes a cathode with carbon nanotubes acting as electron emitter formed thereon, and a counter anode with a phosphor layer formed thereon. Emission current can be obtained by applying a voltage difference of a few hundred volts to a thousand volts between the cathode and the counter anode which are received in a vacuum space. The strength of an emission current can be varied with the variation of the magnitude of the voltage difference.
Generally, it is impractical to adjust the strength of the emission current due to the large voltage difference applied between the cathode and counter anode. In addition, molecules accumulated at the carbon nanotubes may contaminate the carbon nanotubes which results in large fluctuation in the emission current, even causes the loss of the electron emission capability of the carbon nanotubes. Therefore in order to achieve an emission current with relatively high stability, it is necessary to operate the carbon nanotubes formed on the cathode at a much higher vacuum ranging from 1×10−9 to 1×10−8 millibars (1 millibar=100 pascals). However, this high vacuum maintenance will inevitably result in the increase of cost of the electron emission devices.
What is needed is to provide an electron emission device with a practically adjustable and relatively stable emission current, and method for generating such an emission current.
A preferred embodiment provides an electron emission device including: an electron emitter, an anode opposite to and spaced apart from the electron emitter, a first power supply circuit, and a second power supply circuit. The first power supply circuit is configured for electrically connecting the electron emitter and the anode with a power supply to generate an electric field between the electron emitter and the anode. The second power supply circuit is configured for electrically connecting the electron emitter with a power supply to supply a heating current for heating the electron emitter whereby electrons emit therefrom.
In another preferred embodiment, a method for generating an emission current includes the steps of: providing an electron emitter; disposing an anode opposite to and spaced apart from the electron emitter; applying a first voltage between the electron emitter and the anode configured for generating an electric field therebetween; and applying a second voltage on the electron emitter configured for generating a current to heat the electron emitter whereby electrons emit therefrom, to form the emission current.
Other advantages and novel features will become more apparent from the following detailed description of embodiments when taken in conjunction with the accompanying drawings.
Many aspects of the present electron emission device and method for generating an emission current can be better understood with reference to the following drawings. The components in the drawings are not necessarily drawn to scale, the emphasis instead being placed upon clearly illustrating the principles of the present electron emission device and method. Moreover, in the drawings, like reference numerals designate corresponding parts throughout the several views.
The exemplifications set out herein illustrate various preferred embodiments, in various forms, and such exemplifications are not to be construed as limiting the scope of the present electron emission device and method in any manner.
Referring to
The electron emitter 102 is a carbon nanotube yarn. As shown in
The anode 104 is disposed opposite to and spaced apart from the electron emitter 102. Usually, a phosphor layer (not shown) is formed on a surface of the anode 104 facing toward the electron emitter 102. When electrons emitted from the electron emitter 102 strike the phosphor layer, light can be emitted from the phosphor layer.
When the electron emission device 100 is in operation, the first power supply circuit 106 is connected to terminals 1062a and 1062b of a power supply 1062 to generate an electric field between the electron emitter 102 and the anode 104. Preferably, the electric field is about 0.6 volts per micrometer. For example, when a distance between the electron emitter 102 and the anode 104 is about 1 millimeter, an output voltage of the power supply 1062 can be about 600 volts correspondingly.
When the electron emission device 100 is in operation, the second power supply circuit 108 is connected to terminals 1082a and 1082b of a power supply 1082 to supply a heating voltage/current for heating the electron emitter 102 to emit electrons therefrom steadily, whereby a steady emission current can be formed. The heating voltage is preferably in the range from about 15 to 100 volts, which can heat the electron emitter 102 up to a temperature ranging from about 1500 to 2000 kelvins (K) correspondingly. Generally, the heating voltage is related to the length of the carbon nanotube yarn (i.e. the electron emitter 102), the shorter of the length of the carbon nanotube yarn, the lower of the heating voltage required. Furthermore, the emission current can be readily adjusted by way of varying the magnitude of the heating voltage due to the relatively lower heating voltage.
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Referring to
The electron emitter 202 includes a refractory metal wire 2022 and a plurality of one-dimensional nanostructures 2024 formed on and electrically connected with the refractory metal wire 2022. When a heating voltage supplied by the power supply 2082 and applied on the refractory metal wire 2022 via the second power supply circuit 208, the one-dimensional nanostructures 2024 are heated to thereby emit electrons therefrom. The one-dimensional nanostructures can be formed on the refractory metal wire 2022 by way of a coating process. The refractory metal wire 2022 usually has a diameter of no less than 1 micrometer, and preferably has a melting point of no less than 1,600 degrees Celsius (° C.). The refractory metal wire 2022 can be a titanium wire (melting point of 1,668° C.), a molybdenum wire (melting point of 2,600° C.), a tantalum wire (melting point of 2,996° C.) or a tungsten wire (melting point of 3,380° C.). The one-dimensional nanostructures 1024 can be tubular, bacilliform, needle-like shaped, cone-shaped, or a mixture thereof. The one-dimensional nanostructures can be composed of carbon nanotubes or refractory metal materials, such as tungsten, molybdenum, titanium, tantalum or an oxide thereof. In the illustrated example, the one-dimensional nanostructures 1024 are composed of tubular carbon nanotubes.
The anode 204, the first power supply circuit 206 and the second power supply circuit 208 are respectively similar to the anode 104, the first power supply circuit 106 and the second power supply circuit 108 as above described in the first embodiment of the present invention. In the second embodiment, the first power supply circuit 206 electrically connects the anode 104 with the refractory metal wire 2022 of the electron emitter 202. The second power supply 208 is electrically connected with the refractory metal wire 2022 of the electron emitter 202. When the electron emission device 200 is in operation, the first power supply circuit 206 is electrically connected to terminals 2062a and 2062b of a power supply 2062, and the second power supply circuit 208 is electrically connected to terminals 2082a and 2082b of a power supply 2082.
Referring to
The electron emitter 302 includes a sleeve 3022 defining an opening (not labeled) therein, one-dimensional nanostructures 3024 formed on an outside surface of the sleeve 3022 and electrically connected therewith, and a filament 3026 placed in the opening and configured for indirectly heating the one-dimensional nanostructures 3024 to emit electrons therefrom. The sleeve can be made of a thermally conductive refractory metal, such as titanium, molybdenum, tantalum, tungsten or an oxide thereof. The one-dimensional nanostructure 3024 is similar to the one-dimensional nanostructure 2024 as described above. The filament 3026 can be a refractory metal filament, such as a tungsten filament, a titanium filament or a molybdenum filament.
The anode 304, the first power supply circuit 306 and the second power supply circuit 308 are respectively similar to the anode 104, the first power supply circuit 106 and the second power supply circuit 108 as above described in the first embodiment of the present invention. In the third embodiment, the first power supply circuit 306 electrically connects the anode 304 with the sleeve 3022 of the electron emitter 302. The second power supply circuit 308 is electrically connected with two terminals of the filament 3026. When the electron emission device 300 is in operation, the first power supply circuit 306 is electrically connected to terminals 3062a and 3062b of a power supply 3062, and the second power supply circuit 308 is electrically connected to terminals 3082a and 3082b of a power supply 3082.
In summary, in various embodiments of the electron emission device, the second power supply circuit thereof is used to supply a heating voltage/current to heat the electron emitter to emit electrons therefrom, whereby an emission current can be achieved. Because the heating voltage is relatively lower, preferably ranging from about 15˜100 volts, and the emission current is related to the heating voltage, accordingly the emission current can be readily adjusted by way of varying the magnitude of the heating voltage. Furthermore, molecules accumulated at the electron emitter can be substantially removed via the heating voltage/current; consequently, the electron emission device can achieve an emission current with a relatively higher stability, even though the electron emitter thereof operated at relatively low vacuum.
It is believed that the present embodiments and their advantages will be understood from the foregoing description, and it will be apparent that various changes may be made thereto without departing from the spirit and scope of the invention or sacrificing all of its material advantages, the examples hereinbefore described merely being preferred or exemplary embodiments of the invention.
Number | Date | Country | Kind |
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200510100365.2 | Oct 2005 | CN | national |