Patent Application
20080160866
1. Field of the Invention
The invention relates to methods for manufacturing field emission cathodes and, particularly, to a method for manufacturing a field emission cathode including a carbon nanotube array.
2. Discussion of Related Art
Carbon nanotubes (CNTs) produced by means of arc discharge between graphite rods were first discovered and reported in an article by Sumio Iijima, entitled “Helical Microtubules of Graphitic Carbon” (Nature, Vol. 354, Nov. 7, 1991, pp. 56-58). Carbon nanotubes are electrically conductive along their length, are chemically stable, and can have, individually, very small diameters (much less than 100 nanometers) and large aspect ratios (length/diameter). Due to these and other properties, it has been suggested that carbon nanotubes can play an important role in fields such as microscopic electronics, field emission devices, thermal interface materials, etc.
Generally, a CNT field emission device includes a field emission cathode, and the field emission cathode includes a conductive electrode and a carbon nanotube array formed on the conductive electrode. The method for manufacturing the field emission cathode mainly includes the following steps: firstly, providing a silicon or silicon dioxide substrate; secondly, forming a conductive electrode on the substrate; thirdly, forming a catalyst layer on the conductive electrode; fourthly, heating the substrate with the catalyst layer formed thereon in air at a temperature in the approximate range from 300° C. to 500° C. for 10 minutes to 12 hours, then annealing the substrate to obtaining catalyst particles; fifthly, placing the substrate with the catalyst particles disposed thereon in a reaction device, introducing a protection gas thereinto, and heating the substrate to a temperature in the approximate range from 400° C. to 750° C.; and introducing a reaction gas into the reaction device for 0.5 minutes to 2 hours to grow a carbon nanotube array on the substrate.
As the field emission cathode is used, an insulative layer can, beneficially, be adopted/incorporated among adjacent carbon nanotubes to avoid the electromagnetic shielding among the carbon nanotubes. However, the typical method for manufacturing the insulative layer is relatively complex and, thus, is not fit for mass production. Furthermore, the toughness and pliability of the field emission cathode is relatively poor and is generally not fit for flexible display devices.
What is needed, therefore, is a method for manufacturing a field emission cathode which includes an electrode and an insulating film incorporated therewith. What is further needed is a field emission cathode that is fit for flexible display devices. Furthermore, what is needed is a method for producing such that is relatively easy and that can be used in mass production.
In one embodiment, a method for manufacturing a field emission cathode includes the following steps:
A method for manufacturing a carbon nanotube/polymer composite, the method comprises the steps of:
Other advantages and novel features of the present method for manufacturing a field emission cathode will become more apparent from the following detailed description of preferred embodiments when taken in conjunction with the accompanying drawings.
Many aspects of the present method for manufacturing a field emission cathode can be better understood with reference to the following drawings. The components in the drawings are not necessarily to scale, the emphasis instead being placed upon clearly illustrating the principles of the present manufacturing method.
Corresponding reference characters indicate corresponding parts throughout the several views. The exemplifications set out herein illustrate at least one preferred embodiment of the present method for manufacturing a field emission cathode, in one form, and such exemplifications are not to be construed as limiting the scope of the invention in any manner.
Reference will now be made to the drawings to describe embodiments of the present method for manufacturing a field emission cathode, in detail.
Referring to
In step (a), the carbon nanotube array is manufactured by means of chemical vapor deposition (CVD), and a height thereof is advantageously in the approximate range from 10 micormeters to 1000 micrometers. Step (a) comprises the steps of:
(a1) providing a substrate;
(a2) forming a catalyst layer on the substrate;
(a3) heating the substrate with the catalyst layer formed thereon and annealing the substrate to obtaining catalyst particles;
(a4) placing the substrate with the catalyst particles disposed thereon in a reaction device, introducing a protection gas thereinto, and heating the substrate to a predetermined temperature; and
(a5) introducing a reaction gas into the reaction device to grow the carbon nanotube array on the substrate.
In step (a1), the substrate can be made of glass, quartz, silicon, or alumina. In step (a2), the catalyst layer can be disposed on the substrate by chemical vapor deposition, thermal disposition, electron-beam disposition, or sputtering. The catalyst layer can be selected from a group consisting of iron (Fe), cobalt (Co), nickel (Ni), or an alloy thereof. A thickness of the catalyst layer is determined by the material of the catalyst layer. In one useful embodiment, the catalyst layer is made of iron (Fe), and the thickness thereof is in the approximate range from 3 nanometers to 10 nanometers. Quite usefully, the thickness of the iron catalyst layer is about 5 nanometers.
In step (a3), the substrate with the iron catalyst layer formed thereon is heated in air at a temperature in the approximate range from 300° C. to 500° C. for about 10 minutes to 12 hours. After the process of annealing, ferric oxide particles are formed on the substrate. In step (a4), the predetermined temperature is chosen according to the material of the catalyst layer and is beneficially in the approximate range from 400° C. to 750° C. When using iron as the catalyst material, the predetermined temperature is opportunely about 650° C. Furthermore, the protection gas can be an inert gas and/or nitrogen gas. Advantageously, the protection gas is argon gas. In step (a5), the reaction gas is a carbon source gas and is introduced into the reaction device for 0.5 minutes to 2 hours. One appropriate carbon source gas is a hydrocarbon such as acetylene or ethene. Quite suitably, the carbon source gas is ethene.
Step (b) includes the steps of:
(b1) mixing methyl methacrylate (MMA), aodiisobutyronitrile (AIBN) and dibutyl phthalate (DBP);
(b2) milling the mixture formed in step (b1) for about 5 minutes to 30 minutes in a water bath of 80° C. to 100° C., thereby polymerizing the MMA; and
(b3) cooling the mixture.
In step (b1), the MMA is used as a main body, and a mass percent thereof in the mixture is advantageously in the approximate range from 95% to 100%. Meanwhile, the AIBN is used as an initiator, and a mass percent thereof in the mixture is usefully in the approximate range from 0.02% to 1%. Lastly, the DBP is used as a plasticizer, and a mass percent thereof in the mixture is beneficially in the approximate range from 0% to 5%. In step (b2), the mixture is suitably milled for 10 minutes in the water bath at 92° C. The polymerized MMA has a working viscosity, so as to be readily placed on the substrate yet be able to generally hold its position until cured.
Before step (c), the air in the carbon nanotube array is removed in advance. The step of removing the air in the carbon nanotube array can be provided after step (a), and the step is executed by evacuating the container, advantageously to a vacuum level of at least about 5×10−2 torr. Alternatively, the step of removing/evacuating the air in the carbon nanotube array can be provided after step (b). In step (c), the goal is to achieve sufficient settling of the prepolymer within the carbon nanotube array, such that each adjacent carbon nanotube pair has prepolymer material therebetween, at least along the length portion thereof to remain within the PMMA layer (e.g., to properly insulate and reinforce adjacent nanotubes). Thus, step (c) yields an initial prepolymer film within the carbon nanotube array, the final thickness of which is then determined by the parameters associated with step (d). It is to be further understood that the settling process of step (c) could be aided by the application of vibrations to the container and/or ultrasonic vibrations within the prepolymer carrier employed in such step.
In step (d), the part of the prepolymer covering an upper end of the carbon nanotube array (i.e., not the portion able to settle deeper into the array) is removed by application of a centrifugal force, along with any amount of prepolymer settled on top of the upper distal end of the carbon nanotube array. Thus, the top/upper end of the carbon nanotube array extends from the prepolymer, with the prepolymer film thereby existing therewithin. In step (e), the polymer film is particularly a composite CNT-PMMA film.
Referring to
It is to be understood that, in instances where the upper end of the carbon nanotube array 120 need not be exposed (e.g., thermal conduction interface, mechanical composite usage, etc.), the polymer of PMMA 110 could be permitted to extend the length of the nanotubes (i.e., to the distal ends thereof) within the array (e.g., step (d) could be skipped). Such full-length extension would facilitate maximum support and protection by the polymer while still allowing an electrical and/or thermal connection to be made with a given distal end of the array. Thus, it is to be understood that the CNT-PMMA film 10 could be easily modified to fulfill other uses, than just for field emission devices. In light of the potential uses for the CNT-PMMA film 10, it is further understood that a temporary/removable substrate could be employed initially (e.g., as per step (e)) or the substrate could instead be chosen in conjunction with the ultimate desired use for the composite (i.e., to remain as part of the final structure).
Compared with the conventional field emission cathode, the field emission cathode manufactured by the present method includes an electrode and a CNT-PMMA polymer film attached on the electrode thereby having the following virtues. Firstly, the CNT-PMMA polymer film has relatively good toughness and pliability, allowing the CNT-PMMA polymer to be bent freely. Therefore, a field emission cathode adopting the CNT-PMMA polymer is fit for flexible display devices. Secondly, the top and bottom ends of the carbon nanotube array in the CNT-PMMA polymer film extend to or even from the top and bottom surfaces of the polymer of PMMA respectively, and, thus, the CNT-PMMA film has double-faced conductive performance. Thirdly, the air in the carbon nanotube array is removed in advance. As such, thus the polymer of PMMA sufficiently fills in the clearance of the carbon nanotube array. Therefore, electromagnetic shielding among the carbon nanotubes can be avoided. Therefore, the present method is relatively easy to carry out and can be used in mass production.
Finally, it is to be understood that the above-described embodiments are intended to illustrate rather than limit the invention. Variations may be made to the embodiments without departing from the spirit of the invention as claimed. The above-described embodiments illustrate the scope of the invention but do not restrict the scope of the invention.
| Number | Date | Country | Kind |
|---|---|---|---|
| 200610061705.X | Jul 2006 | CN | national |
