EP1685581A4 - Well formation - Google Patents
Well formationInfo
- Publication number
- EP1685581A4 EP1685581A4 EP04783947A EP04783947A EP1685581A4 EP 1685581 A4 EP1685581 A4 EP 1685581A4 EP 04783947 A EP04783947 A EP 04783947A EP 04783947 A EP04783947 A EP 04783947A EP 1685581 A4 EP1685581 A4 EP 1685581A4
- Authority
- EP
- European Patent Office
- Prior art keywords
- cnt
- ink
- composition
- carbon nanotubes
- thinner
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B32/00—Carbon; Compounds thereof
- C01B32/15—Nano-sized carbon materials
- C01B32/158—Carbon nanotubes
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y10/00—Nanotechnology for information processing, storage or transmission, e.g. quantum computing or single electron logic
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/04—Carbon
- C08K3/041—Carbon nanotubes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/40—Glass
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/20—Conductive material dispersed in non-conductive organic material
- H01B1/24—Conductive material dispersed in non-conductive organic material the conductive material comprising carbon-silicon compounds, carbon or silicon
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J1/00—Details of electrodes, of magnetic control means, of screens, or of the mounting or spacing thereof, common to two or more basic types of discharge tubes or lamps
- H01J1/02—Main electrodes
- H01J1/30—Cold cathodes, e.g. field-emissive cathode
- H01J1/304—Field-emissive cathodes
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J31/00—Cathode ray tubes; Electron beam tubes
- H01J31/08—Cathode ray tubes; Electron beam tubes having a screen on or from which an image or pattern is formed, picked up, converted, or stored
- H01J31/10—Image or pattern display tubes, i.e. having electrical input and optical output; Flying-spot tubes for scanning purposes
- H01J31/12—Image or pattern display tubes, i.e. having electrical input and optical output; Flying-spot tubes for scanning purposes with luminescent screen
- H01J31/123—Flat display tubes
- H01J31/125—Flat display tubes provided with control means permitting the electron beam to reach selected parts of the screen, e.g. digital selection
- H01J31/127—Flat display tubes provided with control means permitting the electron beam to reach selected parts of the screen, e.g. digital selection using large area or array sources, i.e. essentially a source for each pixel group
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J9/00—Apparatus or processes specially adapted for the manufacture, installation, removal, maintenance of electric discharge tubes, discharge lamps, or parts thereof; Recovery of material from discharge tubes or lamps
- H01J9/02—Manufacture of electrodes or electrode systems
- H01J9/022—Manufacture of electrodes or electrode systems of cold cathodes
- H01J9/025—Manufacture of electrodes or electrode systems of cold cathodes of field emission cathodes
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J2201/00—Electrodes common to discharge tubes
- H01J2201/30—Cold cathodes
- H01J2201/304—Field emission cathodes
- H01J2201/30446—Field emission cathodes characterised by the emitter material
- H01J2201/30453—Carbon types
- H01J2201/30469—Carbon nanotubes (CNTs)
Definitions
- CNTs Uniformly and selectively depositing CNTs over a large substrate is one of the main issues for an FED fabrication process.
- a typical means of growing carbon nanotubes on a substrate is to use chemical vapor deposition (CVD) techniques with catalyst activation. This technique requires a relatively high growth temperature, thereby increasing the production cost. It is also difficult to achieve a film with uniform properties over a large area.
- CVD chemical vapor deposition
- Other methods, such as screen-printing or dispensing have been developed to deposit CNTs in paste or ink composites.
- the composites consist of CNT powder mixed with conductive or non- conductive particles, carriers or vehicles and binders in some cases.
- CNT deposition is the last step in the cathode fabrication procedure, especially for triode structures.
- FIGURE 1(a) illustrates a side view of one embodiment of a well structure
- FIGURE 1(b) illustrates the well structure with integrated gate electrodes
- FIGURE 1(c) illustrates a metal grid electrode mounted after CNT deposition in the wells
- FIGURE 2(a) illustrates cathode electrodes printed using a screen-printing process
- FIGURE 2(b) illustrates an insulator layer printed using a screen-printing process
- FIGURE 3(a) illustrates filling the wells with a CNT ink
- FIGURE 3(b) illustrates spreading of the CNT ink within the wells
- FIGURE 3(c) illustrates
- An embodiment of the present invention provides a process for uniformly depositing CNTs into well structures as shown in FIGURE 1(a).
- Well structures may have four or more walls to form a hole (or one wall if a round hole).
- the well structure may also be employed as gated, triode structures in which the grid electrodes are deposited on the top of an insulator in advance of CNT deposition (as shown in FIGURE 1(b)), or a metal grid is mounted on after CNT deposition in the wells (as shown in FIGURE 1(c)).
- the metal grid can be used to modulate the current from the CNT material placed inside the well structure, as shown in the FIGURE 1(c). Both embodiments (FIGURES 1(b) and 1(c)) require CNT material inside the well structure.
- Each well may correspond to an individual pixel or sub-pixel. In some cases, several well structures may together be part of a pixel or sub-pixel.
- the well structures can be prepared using thick film process for low-resolution applications, such as screen printing (as shown in FIGURES 2(a) and 2(b)), or using thin film process for high-resolution well structures.
- Cathode electrodes are printed using screen- printing.
- a conducting cathode electrode can also be patterned onto a substrate.
- the electrode lines can be defined by etching the pattern from a thin film of conducting metal deposited onto the substrate using many techniques available in the art (e.g., evaporation, sputter, CVD, etc.)
- the etch pattern is defined using one of several lithography techniques (e.g., optical lithography, e-beam lithography, embossing, etc).
- Photo-active pastes such as DuPont FodelTM can be used to form the cathode electrode.
- the insulator layer may be printed using screen- printing.
- the walls of the well structure may also be printed using dispensing (including ink- jet printing) techniques, or they may be formed by sand or bead blasting techniques typically used in the plasma display industry.
- Photo-active pastes such as DuPont FodelTM can be used to form the insulator wall structure.
- FIGURES 2(a) and 2(b) show fabrication of a well structure.
- insulating material such as glass and ceramics
- semiconducting materials such as Si
- conducting materials such as metal sheets or foils, either pure metals or metal alloys
- CNT ink or paste composites such as dispensing, ink-jet printing, screen-printing, dipping, painting, brushing, spraying and spin-coating.
- the dispensing head moves relative to the substrate and is placed in position to dispense one or more drops of the ink or paste using a computer program before moving to the next spot to deposit more material (see FIGURE 3(a)).
- a Musashi SHOT miniTM was used, although other dispensers or ink-jet dispensers may be used.
- the formulations may need adjusting, depending on the model and type of dispenser used.
- This process may require heat or UV (ultraviolet) curing steps, depending on the CNT ink material used.
- CNTs are contained inside the well structure. It is possible to make the well structures very accurate using printing or dispensing techniques or using sand or bead blasting processes. If the well structures are made accurately, then using the process just described will result in uniform CNT deposition for each pixel. The well structures also effectively avoid edge emission issues that may also lead to non-uniform performance.
- the shape of the wells can define the shape and effective emitting area of a CNT cathode for an individual pixel or sub-pixel.
- FIGURE 5 illustrates a vacuum-sealed CNT field emission display configurated with well- formation processes as described herein.
- the sidewall spacer (wall spacer) and the internal spacers hold the gap between the anode plate (phosphor screen) and the cathode plate after the vacuum sealed display is evacuated.
- CNT-based inks with good field emission properties have been developed according to a process(es) of the present invention.
- a dispenser, an inkjet printer, a screen-printer and the like and combinations thereof can be used to fill the wells with a relatively accurate volume of CNT-ink.
- no further post-deposition processes are performed, such as the removal of sacrificial layers, which could damage the CNT ink.
- Such sacrificial layers are central to the processes disclosed in U.S. Patent No. 6,705,910. Such damage to the CNT ink will adversely affect its field emission capabilities.
- Examples of suitable means for filling the CNT-ink into the wells of the pixels include, but are not limited to, dispensing, inkjet printing, screen-printing, spin-on coating, brushing, dipping, and the like and combinations thereof.
- dispensing inkjet printing, screen-printing, spin-on coating, brushing, dipping, and the like and combinations thereof.
- the following examples are presented to further illustrate the present invention and are not to be construed as unduly limiting the scope of the present invention.
- the following illustrate sample formulations of CNT-ink that can be utilized according to a process of the present invention, and the field emission properties obtained with the various formulations.
- SWNTs Single wall carbon nanotubes
- the SWNTs were in a range of from 1 nm (nanometer) to 2 nm in diameter and in a range of from 5 ⁇ m (micrometers) to 20 ⁇ m in length.
- MWNTs multiwall carbon nanotubes
- the other components of the composite that were prepared were contained in an inorganic adhesive material. This inorganic adhesive material was obtained from Cotronics Corp., Brooklyn, New York, under the name/identifier of Resbond 989, that is a mixture of Al 2 O 3 particles, water, and inorganic adhesives.
- Composites that contain other particles may also be used, such as SiO 2 . These particles may be insulating, conducting or semiconducting. The particle sizes may be less than 50 ⁇ m.
- the carrier in the Resbond 989 is believed to be water, but other carrier materials may be used and they may also be organic or inorganic. Other materials that promote other properties of this material, such as binders (e.g., alkali silicates or phosphates) may also be present in the composite in small quantities.
- a Musashi-made dispenser (model: SHOT miniTM) was employed to deposit the CNT ink mixture into the well structures
- Other dispenser machines can be used, including ink-jet approaches.
- the CNT material is placed in each of the well structures by moving the dispensing head and/or the substrate relative to each other and dispensing dots of material at pre-defined locations.
- the substrate was then dried at room temperature in air for 10 minutes, but it can also be dried (cured) in an oven at increased temperature (approximately 100°C or higher) in order to eliminate the water faster. If the solvent contains organic materials, then an even higher temperature may be set to remove the materials. For example, up to 300°C will be set to remove epoxy.
- the oven or curing vessel may contain a vacuum pump to exhaust the air out of the oven and form a vacuum inside the oven during the drying/curing process.
- the oven or curing vessel may also provide a gas environment or flow around the sample that further promotes curing or drying. This gas environment or flow may or may not be partially or completely from inert gases such as the noble gases or nitrogen. Ultraviolet or infrared light may also be used to aid the curing process.
- a surface activation process (as discussed in U.S. Patent Application Serial No. 10/269,577) was applied to the CNT cathodes to improve the field emission properties. 3) The samples were then ready for field emission tests.
- a reference substrate was utilized that had the same thickness of a substrate that was desired to be subjected to a depositing of a CNT-ink of the present invention to determine if the CNT-ink, and dots comprising CNT-ink, could be dispensed consistently.
- the size of the spot of dispensed material comprising CNT-ink depended on the viscosity, nozzle size of the dispenser, and the distance (gap) between the nozzle and substrate. The smaller the nozzle opening, the more sensitive the variable of the gap between the nozzle and substrate.
- the dispenser was programmed to adjust the substrate position to the proper location(s) and to provide for a good alignment.
- the dispensing volume of CNT-ink can be adjusted by, for example, air pressure, distance, suck-back vacuum, viscosity of the dispensing material, and the size of the nozzle opening.
- the distance and the viscosity of dispensing materials are the most important parameters for dispensing consistently because the other parameters are more easy to control.
- the distance control is dependent on how flat the substrate is and the leveling of the X-Y table and also can be accurately controlled by a height sensor.
- Firing Process The following discloses a firing process of the present invention to provide for a removal of organic materials from a CNT cathode of the present invention. After the wells are filled, a firing process is needed to remove the organic materials in the CNT cathode.
- a substrate, comprising a CNT-ink of the present invention was subjected to baking in an oven at 100°C for 10 minutes in air.
- the substrate was placed into another nitrogen-flowing oven for firing.
- the temperature was slowly increased (at a rate of 180°C/hour) to 315°C and maintained at 315°C for 10 minutes.
- the temperature was increased (at the same ramp rate of 180°C/hour) to 450°C and fired at 450°C for 10 minutes. 4) The temperature was slowly decreased to room temperature (at the same ramp rate of 180°C/hour), i.e., the substrate was cooled to room temperature.
- the thinner can be evaporated at 230°C without any remains or residues.
- a 5 mL quantity of thinner (Terpineol) was then added to the jar.
- Other organic materials can also be used to adjust the viscosity of the CNT ink.
- a 1 mL quantity of Kasil® 2135 was then added to the jar. The Kasil was used to improve ink adhesion to the substrate.
- Other inorganic materials such as potassium silicate can also be used.
- FIGURE 6(a) The cathodes prepared with different CNT-inks of the present invention were tested using a diode configuration as illustrated in FIGURE 6(a).
- the spacer thickness between the cathode and anode is about 0.5 mm.
- the anode is ITO glass coated with phosphor.
- a field emission image from a cathode (CNT-ink 2) made by filling the well structure using the process described herein for CNT-ink 2 is shown in FIGURE 6(b). Twenty-two pixels were in the sample.
- FIGURE 7 shows the I-V curves from various cathodes made by the different CNT-inks prepared as previously described.
- a CNT-ink is used to fill the wells of pixels using methods such as, but not limited to, dispensing or screen-printing methods.
- a uniform cathode can be obtained over individual pixels or sub-pixels.
- the edge-emission can also be reduced or eliminated.
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Abstract
Composition of carbon nanotubes (CNTs) are produced into inks that are dispensable via ink jet deposition processes. The CNT ink is dispensed into wells formed in a cathode structure.
Description
WELL FORMATION
This patent application claims priority to U.S. Provisional Patent Application Serial No. 60/502,454, filed September 12, 2003. This patent application is a continuation-in-part of U.S. Patent Application Serial No. 10/269,577, which claims priority to U.S. Provisional Patent Applications Serial Nos. 60/343,642; 60/348,856; and 60/369,794. TECHNICAL FIELD The present invention relates in general to depositing carbon nanotubes with CNT inks into well structures. BACKGROUND INFORMATION Cathode uniformity is a critical factor for commercializing field emission displays (FEDs). Carbon nanotube (CNT) materials have the highest potential as cathode materials for future FEDs. Uniformly and selectively depositing CNTs over a large substrate is one of the main issues for an FED fabrication process. A typical means of growing carbon nanotubes on a substrate is to use chemical vapor deposition (CVD) techniques with catalyst activation. This technique requires a relatively high growth temperature, thereby increasing the production cost. It is also difficult to achieve a film with uniform properties over a large area. Other methods, such as screen-printing or dispensing, have been developed to deposit CNTs in paste or ink composites. The composites consist of CNT powder mixed with conductive or non- conductive particles, carriers or vehicles and binders in some cases. The size and shape of the patterns created by these techniques are often non-uniform from spot to spot resulting in a non- uniform effective emitting area for each pixel or subpixel. Furthermore, edge emission from the printed or dispensed CNT composite ink or paste commonly results in non-uniformity performance of the CNT cathode, making the cathode fabrication process unpredictable. For FED applications, depositing the same amount of CNTs on each pixel or sub-pixel with uniform effective emitting area is a major goal for obtaining uniform emission current from an individual pixel or sub-pixel. On the other hand, ideally, CNT deposition is the last step in the cathode fabrication procedure, especially for triode structures. Once a CNT cathode is prepared, further wet chemical process or etching processes that may degrade the cathode performance should not be applied to the surface of the CNT cathode.
BRIEF DESCRIPTION OF THE DRAWINGS For a more complete understanding of the present invention, the advantages thereof, reference is now made to the following descriptions taken in conjunction with the accompanying drawings, in which: FIGURE 1(a) illustrates a side view of one embodiment of a well structure; FIGURE 1(b) illustrates the well structure with integrated gate electrodes; FIGURE 1(c) illustrates a metal grid electrode mounted after CNT deposition in the wells; FIGURE 2(a) illustrates cathode electrodes printed using a screen-printing process; FIGURE 2(b) illustrates an insulator layer printed using a screen-printing process; FIGURE 3(a) illustrates filling the wells with a CNT ink; FIGURE 3(b) illustrates spreading of the CNT ink within the wells; FIGURE 3(c) illustrates drying of the CNT ink; FIGURE 4(a) illustrates an embodiment of CNT ink inside well structures; FIGURE 4(b) illustrates another example of an alternative embodiment of CNT ink inside well structures; FIGURE 5 illustrates a portion of a field emission display configured in accordance with an embodiment of the present invention; FIGURE 6(a) illustrates a portion of a diode structure configured in accordance with an embodiment of the present invention; FIGURE 6(b) shows a digital image of field emission from a cathode manufactured using an embodiment of the present invention; and FIGURE 7 illustrates I-V characteristics of CNT inks manufactured in accordance with embodiments of the present invention. DETAILED DESCRIPTION In the following description, numerous specific details are set forth to provide a thorough understanding of the present invention. However, it will be obvious to those skilled in the art that the present invention may be practiced without such specific details. In other instances, well-known circuits have been shown in block diagram form in order not to obscure the present invention in unnecessary detail. An embodiment of the present invention provides a process for uniformly depositing CNTs into well structures as shown in FIGURE 1(a). Well structures may have four or more
walls to form a hole (or one wall if a round hole). The well structure may also be employed as gated, triode structures in which the grid electrodes are deposited on the top of an insulator in advance of CNT deposition (as shown in FIGURE 1(b)), or a metal grid is mounted on after CNT deposition in the wells (as shown in FIGURE 1(c)). The metal grid can be used to modulate the current from the CNT material placed inside the well structure, as shown in the FIGURE 1(c). Both embodiments (FIGURES 1(b) and 1(c)) require CNT material inside the well structure. Each well may correspond to an individual pixel or sub-pixel. In some cases, several well structures may together be part of a pixel or sub-pixel. The well structures can be prepared using thick film process for low-resolution applications, such as screen printing (as shown in FIGURES 2(a) and 2(b)), or using thin film process for high-resolution well structures. Cathode electrodes are printed using screen- printing. A conducting cathode electrode can also be patterned onto a substrate. The electrode lines can be defined by etching the pattern from a thin film of conducting metal deposited onto the substrate using many techniques available in the art (e.g., evaporation, sputter, CVD, etc.) The etch pattern is defined using one of several lithography techniques (e.g., optical lithography, e-beam lithography, embossing, etc). Photo-active pastes such as DuPont Fodel™ can be used to form the cathode electrode. The insulator layer may be printed using screen- printing. The walls of the well structure may also be printed using dispensing (including ink- jet printing) techniques, or they may be formed by sand or bead blasting techniques typically used in the plasma display industry. Photo-active pastes such as DuPont Fodel™ can be used to form the insulator wall structure. FIGURES 2(a) and 2(b) show fabrication of a well structure. Many materials can be used for substrates, including both insulating material (such as glass and ceramics), semiconducting materials (such as Si), or conducting materials (such as metal sheets or foils, either pure metals or metal alloys), or combinations of these materials. Low cost glass substrates may be utilized for flat panel display applications. Various methods may be used to fill the well structure with the CNT ink or paste composites, such as dispensing, ink-jet printing, screen-printing, dipping, painting, brushing, spraying and spin-coating. Using the dispensing or ink-jet printing processes, the dispensing head moves relative to the substrate and is placed in position to dispense one or more drops of the ink or paste using a computer program before moving to the next spot to deposit more material (see FIGURE 3(a)). In the following descriptions, a Musashi SHOT mini™ was used, although other dispensers or ink-jet dispensers may be used. The formulations may need
adjusting, depending on the model and type of dispenser used. Once the fluid CNT-ink is placed in the well structure, it can cover the bottom of the well structure completely through a wetting process (see FIGURE 3(b)). After drying or curing the ink or paste, the CNTs remain in the walls of pixels (see FIGURE 3(c)). This process may require heat or UV (ultraviolet) curing steps, depending on the CNT ink material used. As a consequence, CNTs are contained inside the well structure. It is possible to make the well structures very accurate using printing or dispensing techniques or using sand or bead blasting processes. If the well structures are made accurately, then using the process just described will result in uniform CNT deposition for each pixel. The well structures also effectively avoid edge emission issues that may also lead to non-uniform performance. The shape of the wells can define the shape and effective emitting area of a CNT cathode for an individual pixel or sub-pixel. To fill the wells uniformly, preparing a uniform CNT-ink or CNT-paste and controlling the volume of the ink or paste in the well are important factors. Due to hydrophilic or hydrophobia properties of the CNT ink or paste and the surface of the substrate or well structure, the CNTs can be conformed to the wells in different shapes as shown in FIGURES 4(a) and 4(b). FIGURE 5 illustrates a vacuum-sealed CNT field emission display configurated with well- formation processes as described herein. The sidewall spacer (wall spacer) and the internal spacers hold the gap between the anode plate (phosphor screen) and the cathode plate after the vacuum sealed display is evacuated. Different CNT-based inks with good field emission properties have been developed according to a process(es) of the present invention. A dispenser, an inkjet printer, a screen-printer and the like and combinations thereof can be used to fill the wells with a relatively accurate volume of CNT-ink. It is important to note that after the CNT ink is deposited to form a cathode structure, no further post-deposition processes are performed, such as the removal of sacrificial layers, which could damage the CNT ink. Such sacrificial layers are central to the processes disclosed in U.S. Patent No. 6,705,910. Such damage to the CNT ink will adversely affect its field emission capabilities. Examples of suitable means for filling the CNT-ink into the wells of the pixels include, but are not limited to, dispensing, inkjet printing, screen-printing, spin-on coating, brushing, dipping, and the like and combinations thereof. The following examples are presented to further illustrate the present invention and are not to be construed as unduly limiting the scope of the present invention. The following
illustrate sample formulations of CNT-ink that can be utilized according to a process of the present invention, and the field emission properties obtained with the various formulations.
SAMPLE 1 (CNT-ink 1):
1) Source of Materials: Single wall carbon nanotubes (SWNTs) were obtained from CarboLex, Inc., Lexington, Kentucky. The SWNTs were in a range of from 1 nm (nanometer) to 2 nm in diameter and in a range of from 5 μm (micrometers) to 20 μm in length. Single wall, double-wall, or multiwall carbon nanotubes (MWNTs) from other vendors and prepared by other methods can also be used with similar results. The other components of the composite that were prepared were contained in an inorganic adhesive material. This inorganic adhesive material was obtained from Cotronics Corp., Brooklyn, New York, under the name/identifier of Resbond 989, that is a mixture of Al2O3 particles, water, and inorganic adhesives. Composites that contain other particles may also be used, such as SiO2. These particles may be insulating, conducting or semiconducting. The particle sizes may be less than 50 μm. The carrier in the Resbond 989 is believed to be water, but other carrier materials may be used and they may also be organic or inorganic. Other materials that promote other properties of this material, such as binders (e.g., alkali silicates or phosphates) may also be present in the composite in small quantities.
2) Preparation of the mixture of carbon nanotubes with the Resbond 989 and deposition onto substrate: Grinding of the mixture: A 1 gram quantity of CNT powders (40wt.%) and a 1.5 gram quantity of Resbond (60wt.%) were put together into a mortar. The mixture was ground using a pestle for at least half an hour in order that the mixture looked like a gel, meaning that the CNTs and Al2O3 particles did not separate with each other. Please note that different weight ratios of CNTs to Resbond may also work. Additionally, water or other carrier materials may also be added into the mixture to dilute it in order to adjust the viscosity. The mixture was then ready for depositing onto the substrate.
Applying the mixture onto the substrate and curing: A Musashi-made dispenser (model: SHOT mini™) was employed to deposit the CNT ink mixture into the well structures Other dispenser machines can be used, including ink-jet approaches. The CNT material is placed in each of the well structures by moving the
dispensing head and/or the substrate relative to each other and dispensing dots of material at pre-defined locations. The substrate was then dried at room temperature in air for 10 minutes, but it can also be dried (cured) in an oven at increased temperature (approximately 100°C or higher) in order to eliminate the water faster. If the solvent contains organic materials, then an even higher temperature may be set to remove the materials. For example, up to 300°C will be set to remove epoxy. The oven or curing vessel may contain a vacuum pump to exhaust the air out of the oven and form a vacuum inside the oven during the drying/curing process. The oven or curing vessel may also provide a gas environment or flow around the sample that further promotes curing or drying. This gas environment or flow may or may not be partially or completely from inert gases such as the noble gases or nitrogen. Ultraviolet or infrared light may also be used to aid the curing process. A surface activation process (as discussed in U.S. Patent Application Serial No. 10/269,577) was applied to the CNT cathodes to improve the field emission properties. 3) The samples were then ready for field emission tests.
SAMPLE 2 (CNT-ink 2)
1) A 0.9 gram quantity of single- walled CNTs unpurifϊed, from Iljin Nanotech Corp., Ltd., a 5.7 gram quantity of epoxies (including Ethylcellulose, 2-(2-Butoxyethoxy) Ethyl Acetate, and 2-(2-Butoxyethoxy) ethanol), and 0.5 grams of glass frit were weighed and ground in a mortar for 30 minutes with a pestle. Single wall, double wall or multiwall CNT materials may also be used and CNT materials from other vendors may also be used.
2) A 2 mL quantity of thinner (Terpineol) was then added to the mortar. Other organic materials can also be used to adjust the viscosity of the CNT ink.
3) The resulting mixture was then ground in the mortar by hand for 30 minutes.
4) After grinding the mixture in the mortar, a three-roll mill was immediately employed to further mix the resulting paste for another 30 minutes. This process is used to provide for evenly distributing the mixture components and to provide for a consistent viscosity in the resulting paste (CNT-ink 2).
5) The resulting CNT-ink 2 was then added to a syringe that was fitted to a dispenser (Musashi SHOT mini™) and was ready for use.
Dispensing Process The following discloses a process of dispensing a CNT-ink of the present invention.
1) A reference substrate was utilized that had the same thickness of a substrate that was desired to be subjected to a depositing of a CNT-ink of the present invention to determine if the CNT-ink, and dots comprising CNT-ink, could be dispensed consistently.
2) The size of the spot of dispensed material comprising CNT-ink depended on the viscosity, nozzle size of the dispenser, and the distance (gap) between the nozzle and substrate. The smaller the nozzle opening, the more sensitive the variable of the gap between the nozzle and substrate.
3) The dispenser was programmed to adjust the substrate position to the proper location(s) and to provide for a good alignment.
4) Various programs were used for different dot patterns to fill the wells.
5) The dispensing volume of CNT-ink can be adjusted by, for example, air pressure, distance, suck-back vacuum, viscosity of the dispensing material, and the size of the nozzle opening. The distance and the viscosity of dispensing materials are the most important parameters for dispensing consistently because the other parameters are more easy to control. The distance control is dependent on how flat the substrate is and the leveling of the X-Y table and also can be accurately controlled by a height sensor.
Firing Process The following discloses a firing process of the present invention to provide for a removal of organic materials from a CNT cathode of the present invention. After the wells are filled, a firing process is needed to remove the organic materials in the CNT cathode.
1) A substrate, comprising a CNT-ink of the present invention, was subjected to baking in an oven at 100°C for 10 minutes in air.
2) After baking, the substrate was placed into another nitrogen-flowing oven for firing. First, the temperature was slowly increased (at a rate of 180°C/hour) to 315°C and maintained at 315°C for 10 minutes.
3) Then, the temperature was increased (at the same ramp rate of 180°C/hour) to 450°C and fired at 450°C for 10 minutes.
4) The temperature was slowly decreased to room temperature (at the same ramp rate of 180°C/hour), i.e., the substrate was cooled to room temperature.
SAMPLE 3 (CNT-ink 3)
1) A 0.2 gram quantity of CNTs (obtained from Iljin Nanotech Corp., Ltd., single-wall, unpurified) was weighed using a microbalance and put into a jar. Single wall, double wall or multiwall CNT materials may also be used and CNT materials from other vendors may also be used.
2) A 0.2 gram quantity of aluminum oxide nanoparticles was then added to the jar. The size of the particles was in the range of from 0.01-0.02 μm.
3) A 5 mL quantity of thinner (Terpineol), was then added. Other organic materials can also be used to adjust the viscosity of the CNT ink.
4) With a stirrer, the mixture of CNTs, aluminum oxide nanoparticles, and terpineol was stirred for 3 hours.
5) After stirring, a three-roll mill was immediately employed to further mix the resulting ink for 30 minutes to provide for evenly distributing the mixture components and to provide for a consistent viscosity in the resulting mixture (CNT-ink 3).
6) The resulting CNT-ink 3 was then added to a syringe that was fitted to dispenser (Musashi SHOT mini™) and was ready for use.
Baking process The cathode made by dispensing a CNT-ink, such as CNT-ink 3, was baked in an oven at 230°C for 30 minutes in air. The thinner can be evaporated at 230°C without any remains or residues.
SAMPLE 4 (CNT-ink 4)
1 ) A 0.2 gram quantity of CNTs was weighed using a microbalance and put into a jar.
2) A 0.2 gram quantity of aluminum oxide nanoparticles was then added to the jar. The size of the particles was in the range of from 0.01-0.02 μm.
3) A 5 mL quantity of thinner (Terpineol) was then added to the jar. Other organic materials can also be used to adjust the viscosity of the CNT ink.
4) A 1 mL quantity of Kasil® 2135 was then added to the jar. The Kasil was used to improve ink adhesion to the substrate. Other inorganic materials such as potassium silicate can also be used.
5) With a stirrer, the mixture of CNTs, aluminum oxide nanoparticles, Kasil and thinner was stirred for 3 hours.
6) After stirring, a three-roll miller was immediately employed to further mix the resulting ink for 30 minutes to provide for evenly distributing the mixture components and to provide for a consistent viscosity in the resulting mixture (CNT-ink 4).
7) The resulting CNT-ink 4 was ready for use in screen-printing.
Baking process The CNT cathode made by screen printing was baked in an oven at 100-300°C for 30 minutes in air. After baking, generally only inorganic materials remained in the cathode.
Field Emission Results The cathodes prepared with different CNT-inks of the present invention were tested using a diode configuration as illustrated in FIGURE 6(a). The spacer thickness between the cathode and anode is about 0.5 mm. The anode is ITO glass coated with phosphor. A field emission image from a cathode (CNT-ink 2) made by filling the well structure using the process described herein for CNT-ink 2 is shown in FIGURE 6(b). Twenty-two pixels were in the sample. FIGURE 7 shows the I-V curves from various cathodes made by the different CNT-inks prepared as previously described. In summary, a CNT-ink is used to fill the wells of pixels using methods such as, but not limited to, dispensing or screen-printing methods. With this self-filling process, a uniform cathode can be obtained over individual pixels or sub-pixels. In addition, the edge-emission can also be reduced or eliminated. Although the present invention and its advantages have been described in detail, it should be understood that various changes, substitutions and alterations can be made herein without departing from the spirit and scope of the invention as defined by the appended claims.
Claims
WHAT IS CLAIMED IS:
1. A composition comprising carbon nanotube and an inorganic adhesive.
2. A composition comprising carbon nanotubes, an epoxy, glass frit, and thinner.
3. A composition comprising carbon nanotubes, aluminum oxide nanoparticles, and thinner.
4. A composition according to claim 2 wherein said epoxy is selected from the group consisting of ethylcellulose, 2-(2-butoxyethoxy) ethyl acetate, 2-(2-butoxyethoxy) ethanol, and combinations thereof.
5. A process of preparing a composition comprising contacting carbon nanotubes, an inorganic adhesive, and water.
6. A process of preparing a composition comprising contacting carbon nanotubes, an epoxy, glass frit, and thinner.
7. A process of preparing a composition comprising contacting carbon nanotubes, aluminum oxide nanoparticles, and thinner.
8. A process of preparing a composition comprising contacting carbon nanotubes, aluminum oxide nanoparticles, thinner, and Kasil.
9. A process according to claims 5, 6, 7, or 8 further comprising dispensing the composition.
10. A process according to claim 9 wherein said dispensing comprises dispensing, screen printing, ink-jet printing, dipping, painting, brushing, spin-coating, spraying, and combinations thereof.
11. A process of depositing a carbon nanotube (CNT) ink-like composition in wells formed in a cathode structure whereby a post-deposition process is not performed on the cathode structure subsequent to deposition of the CNT ink-like composition.
12. The process as recited in claim 11, wherein the post-deposition process removes a layer of material from the cathode structure.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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US50245403P | 2003-09-12 | 2003-09-12 | |
US10/937,840 US7854861B2 (en) | 2001-10-19 | 2004-09-09 | Well formation |
US10/937,437 US7842522B2 (en) | 2001-10-19 | 2004-09-09 | Well formation |
PCT/US2004/029922 WO2005029528A1 (en) | 2003-09-12 | 2004-09-10 | Well formation |
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EP1685581A1 EP1685581A1 (en) | 2006-08-02 |
EP1685581A4 true EP1685581A4 (en) | 2009-08-26 |
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JP (1) | JP2007505474A (en) |
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JP2006073516A (en) | 2004-08-30 | 2006-03-16 | Samsung Sdi Co Ltd | Electron emitting element and manufacturing method of the same |
WO2007035838A2 (en) * | 2005-09-21 | 2007-03-29 | University Of Florida Research Foundation, Inc. | Low temperature methods for forming patterned electrically conductive thin films and patterned articles therefrom |
KR100752013B1 (en) | 2006-06-28 | 2007-08-28 | 제일모직주식회사 | Composition for preparing an emitter, a method for preparing an emitter, an emitter prepared therefrom, and a flat panel display comprising the same |
KR101336963B1 (en) | 2007-09-04 | 2013-12-04 | 삼성전자주식회사 | A carbon nano-tube(CNT) film with a transformed substrate structure and a manufacturing method thereof |
DE102008008837A1 (en) | 2008-02-13 | 2009-08-27 | Bayer Materialscience Ag | Printable composition for producing electrically conductive coatings and process for their preparation |
CN101712468B (en) * | 2008-09-30 | 2014-08-20 | 清华大学 | Carbon nanotube composite material and preparation method thereof |
CN104192792B (en) | 2008-11-14 | 2016-06-29 | 清华大学 | The preparation method of nanostructured |
KR20170132341A (en) | 2009-04-30 | 2017-12-01 | 유니버시티 오브 플로리다 리서치 파운데이션, 인크. | Single wall carbon nanotube based air cathodes |
CA2821163A1 (en) | 2010-12-17 | 2012-06-21 | University Of Florida Research Foundation, Inc. | Hydrogen oxidation and generation over carbon films |
CA2832072A1 (en) | 2011-04-04 | 2012-10-11 | University Of Florida Research Foundation, Inc. | Nanotube dispersants and dispersant free nanotube films therefrom |
JP2017504547A (en) | 2013-11-20 | 2017-02-09 | ユニバーシティー オブ フロリダ リサーチ ファウンデーション,インコーポレイテッドUniversity Of Florida Research Foundation,Inc. | Reduction of carbon dioxide with carbon-containing materials |
JP7282424B2 (en) * | 2019-12-30 | 2023-05-29 | 高麗大学校産学協力団 | Carbon nanotube (CNT) paste emitter, manufacturing method thereof and X-ray tube device using same |
CN116970314A (en) * | 2023-08-23 | 2023-10-31 | 广东职业技术学院 | Printable conductive coating and preparation method thereof |
Citations (2)
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EP0905737A1 (en) * | 1997-09-30 | 1999-03-31 | Ise Electronics Corporation | Electron-emitting source and method of manufacturing the same |
US20030092207A1 (en) * | 2001-10-19 | 2003-05-15 | Zvi Yaniv | Activation effect on carbon nanotubes |
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US5576162A (en) * | 1996-01-18 | 1996-11-19 | Eastman Kodak Company | Imaging element having an electrically-conductive layer |
US6359383B1 (en) * | 1999-08-19 | 2002-03-19 | Industrial Technology Research Institute | Field emission display device equipped with nanotube emitters and method for fabricating |
US7449081B2 (en) * | 2000-06-21 | 2008-11-11 | E. I. Du Pont De Nemours And Company | Process for improving the emission of electron field emitters |
EP1302312B1 (en) * | 2001-10-15 | 2005-12-28 | Fuji Photo Film Co., Ltd. | Lithographic printing plate precursor |
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- 2004-09-10 JP JP2006526386A patent/JP2007505474A/en active Pending
- 2004-09-10 KR KR1020067006861A patent/KR20060121910A/en not_active Application Discontinuation
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EP0905737A1 (en) * | 1997-09-30 | 1999-03-31 | Ise Electronics Corporation | Electron-emitting source and method of manufacturing the same |
US20030092207A1 (en) * | 2001-10-19 | 2003-05-15 | Zvi Yaniv | Activation effect on carbon nanotubes |
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WO2005029528A1 (en) | 2005-03-31 |
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