1. Field of the Invention
The present invention relates generally to the field of semiconductor packaging and more particularly to methods for forming structures that employ carbon nanotubes for thermal dissipation.
2. Description of the Prior Art
A carbon nanotube is a molecule composed of carbon atoms arranged in the shape of a cylinder. Carbon nanotubes are very narrow, on the order of nanometers in diameter, but can be produced with lengths on the order of hundreds of microns. The unique structural, mechanical, and electrical properties of carbon nanotubes make them potentially useful in electrical, mechanical, and electromechanical devices. In particular, carbon nanotubes possess both high electrical and thermal conductivities in the direction of the longitudinal axis of the cylinder. For example, thermal conductivities of individual carbon nanotubes of 3000 W/m-° K and higher at room temperature have been reported.
The high thermal conductivity of carbon nanotubes makes them very attractive materials for use in applications involving heat dissipation. For example, in the semiconductor industry, devices that consume large amounts of power typically produce large amounts of heat. Following Moore's Law, chip integration combined with die size reduction results in an ever increasing need for managing power density. The heat must be efficiently dissipated to prevent these devices from overheating and failing. Presently, such devices are coupled to large heat sinks, often through the use of a heat spreader. Additionally, to allow for differences in coefficients of thermal expansion between the various components and to compensate for surface irregularities, thermal interface materials such as thermal greases are used between the heat spreader and both the device and the heat sink. However, thermal greases are both messy and require additional packaging, such as spring clips or mounting hardware, to keep the assembly together, and thermal greases have relatively low thermal conductivities.
Therefore, what is needed are better methods for attaching heat sinks, sources, and spreaders that provides both mechanical integrity and improved thermal conductivity.
An exemplary method of forming a thermal pad comprises providing a substrate having a planar surface, forming a release layer on the planar surface, forming a catalyst layer on the release layer, forming an array of vertically aligned carbon nanotubes on the catalyst layer, and releasing the array of carbon nanotubes from the substrate. Releasing the array can include, for example, lifting the array off of the substrate with an adhesive layer, applying a shear force across the separation layer, or dissolving the release layer. Where releasing the array includes applying a shear force, the shear force can be applied mechanically or thermally by changing the temperature. Here, a difference in the coefficients of thermal expansion between the release layer and either the substrate, the catalyst layer, or some other layer between the two, creates the necessary shear force with the change of temperature to delaminate the array from the substrate. Advantageously, when the array is released, the newly freed surface is essentially as smooth as the planar surface of the substrate. The method can also comprise forming a surface layer, such as of copper, on the release layer before forming the catalyst layer. After release, the surface layer becomes one side of the thermal pad.
Another exemplary method of forming a thermal pad comprises providing a substrate having a planar surface, forming a surface layer on the planar surface, forming a catalyst layer on the surface layer, forming an array of vertically aligned carbon nanotubes on the catalyst layer, and dissolving the substrate. The surface layer, in some embodiments, can include copper, zinc, aluminum, nickel, or silicon carbide, depending on the intended use of the thermal pad. For example, the surface composition can be selected to match a composition of a surface to which the thermal pad is intended to be mated. Dissolving the substrate can include etching the substrate with an acid such as hydrofluoric acid. In some embodiments, the substrate is segmented into coupons before the substrate is dissolved, and in some of these embodiments the coupon is attached to a heat management aid, such as a heat spreader or heat sink, or to a semiconductor die before dissolving the substrate.
Still another exemplary method of forming a thermal pad comprises providing a substrate having a planar surface, forming a catalyst layer on the planar surface, forming an array of vertically aligned carbon nanotubes on the catalyst layer, and detaching the first end of the array from the catalyst layer. Detaching the first end of the array from the catalyst layer can include etching the carbon nanotubes at the first end of the array. Etching the carbon nanotubes can include subjecting the array to a heated atmosphere including hydrogen gas and water vapor.
Each of the various exemplary methods can further comprise additional steps relating to forming the catalyst layer, such as forming a barrier layer and/or an interface layer before forming the catalyst layer. Likewise, each exemplary method can include steps such as infiltrating the array with a matrix material, patterning the catalyst layer, metallizing the exposed end of the array, or attaching the exposed end to a foil. These and other variations are disclosed in the following detailed description.
The present invention provides methods for fabricating free-standing carbon nanotube-based thermal pads. The various methods described herein provide free-standing thermal pads by forming the pads on a substrate from which the thermal pads can be later released. The thermal pads are characterized by an array of generally aligned carbon nanotubes where the direction of alignment is essentially perpendicular to the surfaces of array. The alignment of the nanotubes allows the array to provide excellent thermal conduction in the direction of alignment. Accordingly, a thermal pad between a heat source and a heat sink provides a thermally conductive interface therebetween.
Some thermal pads are characterized by at least one, and in some instances, two very smooth surfaces. A thermal pad with a sufficiently smooth surface can adhere to another very smooth surface, such as the backside surface of semiconductor die, much like two microscope slides will adhere to each other. Surfaces of thermal pads, whether very smooth or not, can also be attached to an opposing surface with a metal layer, for example with solder, indium, or silver. Advantageously, some thermal pads are also characterized by a degree of flexibility and pliability. This can make it easier to work with the thermal pads in assembly operations and allows the thermal pads to conform to opposing surfaces that are curved or irregular.
Next, a catalyst layer 160 is formed. The catalyst layer 160 can be formed either directly on the separation layer 130, on the barrier layer 140, or on the interface layer 150. After the catalyst layer 160 has been formed, an array 170 of carbon nanotubes is formed on the catalyst layer 160. The array 170 is formed such that the carbon nanotubes are generally aligned in a direction 175 perpendicular to the planar surface 120. The array 170 includes a first end 180 attached to the catalyst layer 170 and a second end 190 opposite the first end 170.
Examples of a suitable substrate 110 include polished silicon and gallium arsenide wafers. Either can provide an atomically smooth planar surface 120 on which to form the successive layers 130-170. An example of a suitable separation layer 130 is nickel oxide. A nickel oxide separation layer 130 can be formed by depositing and then passivating a nickel thin film to form a dense and continuous oxide film. The passivation can be achieved, for instance, by thermal oxidation, exposure to an oxygen plasma, or by exposure to a strong acid such as chromic acid. A suitable thickness for the nickel oxide separation layer 130 is about 100 Å.
Another suitable separation layer 130, where the substrate 110 is gallium arsenide, is aluminum arsenide. An aluminum arsenide separation layer 130 can be formed, for example, by metal oxide CVD (MOCVD), and a suitable thickness for such a film is about 500 Å. As an alternative to forming the separation layer 130 by deposition, the separation layer 130 can be formed by ion implantation into the substrate 110. For example, hydrogen ions can be implanted into silicon to form a silicon hydride layer that can readily delaminate from the silicon.
The purpose of the barrier layer 140 is to prevent diffusion between the substrate 110 and/or the separation layer 130 and the catalyst layer 160. Preventing such diffusion is desirable in those embodiments where either the substrate 110 or the separation layer 130 includes one or more elements that can poison the catalyst of the catalyst layer 160 and prevent nanotube growth. Examples of elements that are known to poison nanotube catalysis include nickel, iron, cobalt, molybdenum, and tungsten. Other materials, such as silicon, are not known to poison nanotube catalysis. An example of a suitable barrier layer 140 is a sputtered film of aluminum oxide with a thickness of at least 50 Å, and more preferably 100 Å. An appropriate thickness for the barrier layer 140 will depend both on the permeability of the selected material to the elements to be impeded and on the roughness of the planar surface 120, as rougher finishes require a thicker barrier layers 140.
The interface layer 150 is provided, where needed, to improve the catalyst layer 160 which, in turn, provides for higher quality nanotubes characterized by higher wall crystallinities and fewer defects. In some embodiments, a single layer can serve as both the barrier layer 140 and the interface layer 150. Again, a sputtered film of aluminum oxide with a thickness of at least 50 Å, and more preferably 100 Å, can be a suitable interface layer 150. Another suitable interface layer 150 includes silicon dioxide. It should be noted that too thick of an interface layer 150 can lead to cracking during thermal cycling due to mismatches in coefficients of thermal expansion between the interface layer 150 and the layer beneath.
In various embodiments, the catalyst layer 160 is formed either directly on the separation layer 130, on the barrier layer 140, or on the interface layer 150. After the catalyst layer 160 has been formed, an array 170 of carbon nanotubes is formed on the catalyst layer 160. The array 170 is formed such that the carbon nanotubes are generally aligned in a direction 175 perpendicular to the planar surface 120. The array 170 includes a first end 180 attached to the catalyst layer 160 and a second end 190 opposite the first end 180. Depending on the growth conditions and choice of catalyst, the carbon nanotubes can be single-walled or multi-walled. The density, diameter, length, and crystallinity of the carbon nanotubes can also be varied to suit various applications.
One general method for achieving carbon nanotube growth is to heat the catalyst layer 160 in the presence of a carbon-bearing gas. Examples of suitable catalysts and process conditions are taught, for example, by Erik T. Thostenson et al. in “Advances in the Science and Technology of Carbon Nanotubes and their Composites: a Review,” Composites Science and Technology 61 (2001) 1899-1912, and by Hongjie Dai in “Carbon Nanotubes: Opportunities and Challenges,” Surface Science 500 (2002) 218-214. It will be appreciated, however, that the present invention does not require preparing the carbon nanotubes by the catalysis methods of either of these references, and any method that can produce generally aligned carbon nanotubes extending from a surface is acceptable.
After the carbon nanotube array 170 has been formed, the thermal pad is removed from the substrate 110 at the separation layer 130, as shown in
Separation can be accomplished mechanically, chemically, or through a combination of techniques. For instance, where the separation layer comprises nickel oxide and an adjoining layer includes copper, separation can occur by the application of a shear force. Some embodiments take advantage of differences in the coefficients of thermal expansion between the array 170 and the separation layer 130. In these embodiments, after the array 170 is formed and begins to cool, the mismatch in the coefficients of thermal expansion causes a stress to develop along the interface that can cause the array 170 to spontaneously detach, or to detach upon the application of very little force.
An adhesive tape can be applied to the second end 190, in some embodiments, to both pull the array 170 away from the separation layer 130 and to give the released thermal pad a backing layer. In some embodiments the adhesive tape becomes part of the completed thermal pad. In these thermal pads, suitable adhesive tapes can be either electrically insulating, such as with a Kapton backing, or metallized to be conductive, to allow the thermal pad to either electrically isolate a device or component, or provide a path to ground.
Alternatively, the separation layer 130 can be removed chemically by wet etching or a thermal treatment. Thermal treatments take advantage of differences in coefficients of thermal expansion between layers to cause delamination at the separation layer 130. Wet etching can be achieved with strong acids such as hydrofluoric acid to dissolve either silicon or silicon dioxide. For some applications less aggressive and more environmentally acceptable solvents are desirable. Water, for instance, can be used where the separation layer 130 comprises a water-soluble salt.
As shown in
In the example of
Although the method of
In some of the embodiments represented generally by
Yet another method for forming free-standing carbon nanotube thermal pads is illustrated in
An example of such a gas is a mixture of water vapor and hydrogen gas. In one embodiment, the array 170 is grown in a tube furnace. 50 standard cubic centimeters per minute (sccm) of argon gas is bubbled through a water bubbler to saturate the argon with water vapor. The argon saturated with water vapor is then mixed with 400 sccm of hydrogen gas and introduced into the tube furnace which is maintained at a temperature of 700° C. This atmosphere is maintained in the tube furnace for 5 minutes and causes the thermal pad to lift off of the substrate 110, as shown in
The array 170 in any of the above embodiments can be further processed by the methods described below either prior to, or after, release from the substrate 110. In the following examples the embodiment shown in
In some embodiments, forming the metal layer 800 includes applying a conformal coating to the ends of the carbon nanotubes with a wetting layer of a metal that promotes improved wetting of the metal layer 800 to the carbon nanotubes. Suitable wetting layer materials include palladium, chromium, titanium, vanadium, hafnium, niobium, tantalum, magnesium, tungsten, cobalt, zirconium, and various alloys of the listed metals. The wetting layer can be further coated by a thin protective layer, such as of gold, to prevent oxidation of the wetting layer. The wetting and protection layers may be achieved by evaporation, sputtering, or electroplating, for example. It should be noted that these conformal coatings merely conform to the ends of the carbon nanotubes and are not continuous films across the second end 190 of the array 170. Wetting and protection layers are described in more detail in U.S. non-provisional patent application Ser. No. 11/107,599 filed on Apr. 14, 2005 and titled “Nanotube Surface Coatings for Improved Wettability,” incorporated herein by reference in its entirety.
The metal layer 800 can be polished to increase the smoothness of the surface.
As shown in
Copper and silver foils are examples of suitable foils 1000. The foil 1000 can be joined to the attachment layer 1010 by heating the foil 1000 while in contact with the attachment layer 1010 to briefly melt the attachment layer 1010 at the interface. In some embodiments, such as those in which the low melting point metal comprises indium, it can be advantageous to strip the native oxide layer from the attachment layer 1010 by cleaning the attachment layer 1010 with an acid such as hydrochloric acid prior to attaching the foil 1000.
Each of the thermal pads shown in
For example, in
It should be noted that a continuous catalyst layer 160, as shown for example in
Any of these thermal pads can include a matrix material 1100 that fills the interstitial space between the ends 180, 190 of the array 170. Similarly, any can include a base metal layer 1200 that only partially fills the interstitial space of the array 170 around the carbon nanotubes at the first end 180. Also, the interstitial space of any of these thermal pads can be left empty. As noted above, keeping the interstitial space empty improves flexibility. It should also be noted that keeping the interstitial space empty also improves compliance of the thermal pad to differential thermal expansion between opposing surfaces of two objects. The flexibility and pliability of some thermal pads allows them to be attached to curved surfaces in addition to generally flat surfaces.
Some thermal pads are fixedly attached to inflexible substrates, such as heat spreaders, where the second end 190 of the array 170 is meant to be attached to the surface of some other object. Other such thermal pads are free-standing components meant to be disposed between the opposing surfaces of a heat source and a heat sink.
A thermal pad having a second end 190 with exposed nanotubes can be joined to a surface of an object with a low melting point metal or eutectic alloy or a solder. One advantage of this method of joining the thermal pad to the surface is that neither the surface nor the second end 190 needs to be particularly smooth. Irregularities in either are filled by the low melting point metal, eutectic alloy, or solder. Reworking can be easily accomplished by low temperature heating.
A thermal pad having a second end 190 with exposed nanotubes can also be joined to a surface of an object simply by pressing the two together, known herein as “dry-pressing.” Dry pressing can be accomplished with or without the addition of pressure and heat. Modest elevated temperatures (e.g. 200-300° C.) and pressures (e.g., 10 to 100 psi) can be used. In some embodiments, sufficient heat is applied to soften or melt the surface of the object, for example, the copper surface of a heat sink, so that the ends of the carbon nanotubes push into the surface. In these embodiments it can be advantageous to perform the dry-pressing in a non-oxidizing environment such as an oxygen-free atmosphere. Dry-pressing can also comprise making the ends of the carbon nanotubes temporarily reactive. Here, plasma etching can be used, for example, to etch away amorphous carbon and/or any catalyst materials. Plasma etching can also create reactive dangling bonds on the exposed ends of the carbon nanotubes that can form bonds with the opposing surface. Dry pressing can also comprise anodic bonding, where a strong electric field pulls ions from the interface to create a strong bond.
Either end of a thermal pad that comprises a thin substrate, a foil 1000, an unfinished metal layer 800 (
In other instances, where both the surface of the object and the exposed surface of the thin substrate or foil are very smooth, the two can be held together by van der Waals attractions. In still other instances, both the surface of the object and the exposed surface of the thin substrate or foil are compositionally the same or very similar, for example where both comprise silicon. In this example, Si—Si bonds can spontaneously form between the two surfaces.
In the foregoing specification, the invention is described with reference to specific embodiments thereof, but those skilled in the art will recognize that the invention is not limited thereto. Various features and aspects of the above-described invention may be used individually or jointly. Further, the invention can be utilized in any number of environments and applications beyond those described herein without departing from the broader spirit and scope of the specification. The specification and drawings are, accordingly, to be regarded as illustrative rather than restrictive. It will be recognized that the terms “comprising,” “including,” and “having,” as used herein, are specifically intended to be read as open-ended terms of art.
This application claims the benefit of U.S. Provisional Patent Application No. 60/680,262 filed on May 11, 2005 and entitled “Carbon Nanotube-Based Thermal Pad,” U.S. Provisional Patent Application No. 60/691,673 filed on Jun. 17, 2005 and entitled “Carbon Nanotube-Based Thermal Pad,” and U.S. Provisional Patent Application No. 60/709,611 filed on Aug. 19, 2005 and entitled “Carbon Nanotube Based Interface Materials for Heat Dissipation Applications,” each of which is incorporated herein by reference in its entirety. This application is related to U.S. non-provisional patent application Ser. No. 11/______ filed on even date herewith and entitled “Methods for Forming Carbon Nanotube Thermal Pads” (attorney docket number PA3283US). This application is also related to U.S. non-provisional patent application Ser. No. 11/______ filed on even date herewith and entitled “Carbon Nanotube Thermal Pads” (attorney docket number PA3396US). This application is further related to U.S. non-provisional patent application Ser. No. 11/______ filed on even date herewith and entitled “Devices Incorporating Carbon Nanotube Thermal Pads” (attorney docket number PA3728US).
This invention was made with United States Government support under Cooperative Agreement No. 70NANB2H3030 awarded by the Department of Commerce's National Institute of Standards and Technology. The United States has certain rights in the invention.
Number | Date | Country | |
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60680262 | May 2005 | US | |
60691673 | Jun 2005 | US |
Number | Date | Country | |
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Parent | 60709611 | Aug 2005 | US |
Child | 11433184 | May 2006 | US |