The present invention relates to a heat dissipating structure including a heat source and a heat dissipating part, and manufacture thereof.
Electronic devices including central processing units (CPUs) used in servers and personal computers are provided with a heat spreader or a heat sink of a highly heat conductive material such as copper that is located immediately above a heat-generating semiconductor chip so that heat generated or released from the semiconductor element is dissipated efficiently.
Such a semiconductor chip and a heat spreader have surface roughness of submicron order. Even when they are directly abutted, they cannot form a sufficiently large contact area, and the contact interface will act as a large thermal resistance, which makes effective heat dissipation difficult. To reduce the thermal resistance at the contact, a thermal interface material is commonly disposed between a heat source and a heat spreader.
It is required for such a thermal interface material, in addition to having a high heat conductivity, to be adaptive to the fine surface roughness of a heat source and a heat spreader to ensure a large contact area. Materials commonly used at present include silicone grease, phase change material (PCM), which is a grease with better characteristics than silicone grease, and indium.
Silicone grease and PCM can create good contact with a fine-roughness surface, but their heat conductivity is in the range of about 1 to 5 W/mK. If these materials are to be used, the film thickness has to be decreased to achieve effective heat dissipation. A heat source and a heat spreader generally differ in thermal expansion coefficient, and a relative positional shift will occur as they undergo thermal expansion. The thermal interface material has to absorb this relative positional shift, placing a limit on the minimum thickness.
Indium has a heat conductivity (about 80 W/mK) higher than that of PCM, and can be easily deformed or molten to create good contact. Indium is a rare metal, and the cost of indium is rising rapidly due to largely increasing demands. In addition, its heat conductivity cannot be said to be sufficiently high.
In recent years, attention has been focused on carbon nanotubes (CNTs) as a new electric and thermal conductor. Carbon nanotubes (CNTs) have a long tube-like structure formed of a graphene sheet in which carbon atoms are regularly arranged, and they are categorized into single-walled nanotubes (SWNTs), which are formed of a single wall, and multi-walled nanotubes (MWNTs), which are formed of a plurality of walls. Their diameter ranges from a minimum of 0.4 nm to a maximum of about 4 nm for single-walled ones, and they can be increased as large as several tens of nanometers for multi-layered ones. Their length can be controlled, for instance, in a wide range of 5 μm to 500 μm, by setting up appropriate growth conditions including growth time.
CNTs have very high electric conductivity and very high heat conductivity in their axial (longitudinal axis) direction. The heat conductivity in the axal direction of CNTs can be, for instance, as high as about 1,500 W/mK. CNTs have a thin cylindrical shape with high flexibility. They also have high refractoriness (heat resisting property). A wide range of studies have been carried out aiming to develop applications of CNTs as electric or thermal conductors. To produce carbon nanotubes for use as thermal interface, it is preferable to increase the density and control the orientation of CNTs so as to improve the heat dissipation characteristics.
Japanese Unexamined Patent Publication (Kokai) No. 2006-108377 (Japanese Patent No. 4167212) proposes to prepare a concave portion on one of two wiring layers opposed to each other, form a catalyst layer on the surface of the concave portion, and grow CNTs from the catalyst layer, thereby achieving an increased number density of CNTs and an increased electric conductivity as compared to CNTs grown on a flat plane, and also proposes to prepare many concave portions on a heat sink surface to be located opposite to a semiconductor chip, form a catalyst layer on the surface of each concave portion, and grow CNTs from the catalyst layer thereby achieving a bundle of CNTs with an increased number density, followed by connecting the bundle of CNTs to the semiconductor chip via a thermally conductive adhesion layer made of such material as Au and Sn.
In recent semiconductor integrated circuit devices, integration has been advancing. Increase in electric current density tends to cause increased heat generation and increased thermal expansion. When a semiconductor integrated circuit device is connected to a circuit substrate in fixed manner, difference in thermal expansion causes stress, which may lead to destruction of the device. If a semiconductor integrated circuit device is connected to a heat dissipating part via flexible CNTs, the stress attributable to difference in thermal expansion will be able to be largely reduced.
The growth temperature of CNT is commonly at 600° C. or above in general (common) chemical vapor deposition (CVD). Many semiconductor devices and electronic parts cannot dure or resist heat history of 600° C. or above. Method for growing CNTs at desired locations may impose limitations on the processes depending on the object. Accordingly, it is often difficult to grow CNTs directly at desired positions of a semiconductor device or electronic part.
Japanese Unexamined Patent Publication (Kokai) No. 2006-147801 proposes to grow a high density CNT assembly (sheet) on a substrate via a metal catalyst layer, coat a resin layer on a heat source such as a semiconductor element, bring the CNT assembly immerse into this resin layer, allow the resin to penetrate into spaces between CNTs, cure the resin, and thereafter remove the substrate, thereby leaving a sheet formed of CNTs bonded by a resin layer on a heat source.
The degree of freedom of a process can be increased if a high heat-conductivity component comprising oriented CNT assembly can be prepared separately. In this case, CNTs can be grown on a separate heat resisting substrate, followed by transferring the CNTs to a desired position on a semiconductor device or an electronic part to form a connection component. A CNT sheet comprising assembly of many carbon nanotubes (CNTs) oriented in the thickness direction and bound by resin material will give self-supporting ability to the CNT assembly and accordingly allow the CNT assembly to be handled easily. It is preferable that the resin material fills gaps between CNTs and can form face-to-face contact with a heat source and a heat dissipating part when disposed between the heat source and the heat dissipating part.
Published Japanese Translation of PCT International Publication JP 2007-506642 (WO2005/031864) proposes to mix CNTs with clay formed of aggregates of small plate-like particles, apply a shear force to orient the CNTs in a pull-out direction, and divide into pads after the pull-out procedure to form a thermal interface material having high heat conductivity in the thickness direction, and also proposes to mix CNTs with liquid crystal resin, spread the mixture into a layer, and align the CNTs in the thickness direction by applying an electric field, magnetic field, etc., thereby forming thermal interface material having high heat conductivity in the thickness direction.
Japanese Unexamined Patent Publication (Kokai) No. 2006-290736 proposes to grow high-density CNT assembly on a growth substrate via a metal catalyst, form a protective layer to cover exposed ends of the CNT assembly, remove the substrate, form a protective layer to cover the other exposed ends of the CNT assembly, inject a polymer solution among CNTs in the assembly, which has both ends covered by protective layers, solidify it to produce a substrate, remove the protective layers, form a phase change material layer, embedding the exposed ends of the CNTs, apply pressure and heat to melt the phase change material, bend the ends of the CNTs, and then cool and solidify the phase change material layer. The polymer solution to be used is, for instance, silicone rubber such as Sylgard 160 available from Dow Corning. The phase change material may comprise paraffin and may be softened and liquefied at the phase change temperature, for instance, 20° C. to 90° C.
According to one aspect, a heat dissipating structure includes:
a heat source;
a heat dissipating part disposed to oppose to the heat source;
a concave portion formed in at least one of the opposing surfaces of the heat source and the heat dissipating part; and
a heat conducting structure comprising a filler layer of thermoplastic material disposed between the heat source and the heat dissipating part and contacting with the opposing surfaces of the heat source and the heat dissipating part, and an assembly of carbon nanotubes that are distributed in the thermoplastic material, oriented perpendicularly to the surfaces of the filler layer, contacting, at both end faces, with the opposing surfaces of the heat source and the heat dissipating part, and limited its distribution in the opposing surfaces by the concave portion.
According to another aspect, a method for manufacturing a heat dissipating structure includes:
growing carbon nanotube assembly on a growth substrate;
disposing, on the carbon nanotube assembly, a thermoplastic material sheet having a thickness larger than a length of the carbon nanotubes;
heating and melting the thermoplastic material sheet so as to embed the carbon nanotube assembly, and thereafter cooling and solidifying the thermoplastic material to form a carbon nanotube sheet;
disposing the carbon nanotube sheet between opposing surfaces of a heat source and a heat dissipating part, at least one of which opposing surfaces has a concave portion, constituting a laminated structure;
heating and pressing the carbon nanotube sheet held between the heat source and the heat dissipating part to melt the thermoplastic material and shorten distance between the heat source and the heat dissipating part so as to bring two end faces of the carbon nanotube assembly in contact with the heat source and the heat dissipating part; and
cooling the laminated structure to solidify the thermoplastic material.
The object and advantages of the invention will be realized and attained by means of the elements and combinations particularly pointed out in the claims.
It is to be understood that both the foregoing general description and the following detailed description are exemplary and are not restrictive of the invention, as claimed.
The present inventors have examined possibility of binding oriented CNTs with thermoplastic material into a sheet-like assembly. If the binding material for binding CNTs into a sheet shape is thermoplastic, the contact area of the sheet with the heat source and the heat dissipating part can be maximized as large as possible by heating the binding material to soften or melt it, to let the sheet itself in highly deformable state, while giving each CNT freedom of deformation, etc. If the ends of CNTs are brought into direct contact with the heat source and the heat dissipating part at the surfaces of the sheet and subsequently cooled, it will be possible to fix and maintain the contacting state of the CNT assembly. Processes for producing such a carbon nanotube sheet will be described below.
As illustrated in
The growth substrate 11 will be removed after the formation of carbon nanotubes. To meet this aim, it is preferable that the growth substrate 11 does not change its property at the carbon nanotube formation temperature and that at least the surface in contact with carbon nanotubes is of a material that can be easily peeled off or removed from the carbon nanotubes, or of a material that can be etched selectively against the carbon nanotube.
For instance, Fe (iron) is deposited by sputtering to a thickness of 2.5 nm over the surface of a growth substrate 11 to form a catalyst metal film 12 of Fe. The catalyst metal may be Co (cobalt), Ni (nickel), Au (gold), Ag (silver), Pt (platinum), or an alloy containing at least one material thereof, instead of Fe. Instead of a metal film, the catalyst may be in the form of fine metal particles with controlled size prepared by using differential mobility analyzer (DMA) etc. The same metal species as for thin films may be used in this case.
An underlying film for the catalyst metal may be formed of Mo (molybdenum), Ti (titanium), Hf (hafnium), Zr (zirconium), Nb (niobium), V (vanadium), TaN (tantalum nitride), TiSix (titanium silicide), Al (aluminum), Al2O3 (aluminum oxide), TiOx (titanium oxide), Ta (tantalum), W (tungsten or wolfram), Cu (copper), Au (gold), Pt (platinum), Pd (palladium), TiN (titanium nitride), or an alloy containing at least one of these materials. For instance, a laminated structure of Fe (2.5 nm)/Al (10 nm) or a laminated structure of Co (2.6 nm)/TiN (5 nm) may be adopted. When using fine metal particles, they may be in the form of, for instance, a laminated structure such as Co (average diameter 3.8 nm)/TiN (5 nm thick).
As illustrated in
Here, other film formation methods such as thermal CVD and remote plasma CVD may be used to grow a carbon nanotube 13. The carbon nanotubes to be grown may also be in the form of a monolayer carbon nanotubes. The source material for carbon may be a hydrocarbon such as methane and ethylene, or an alcohol such as ethanol and methanol, instead of acetylene.
A large number of carbon nanotubes 13 oriented perpendicularly to the substrate 11 are formed on the growth substrate 11, in this way. Carbon nanotubes have a property or habit that they will grow perpendicularly to the substrate when the number density is above a certain limit. The in-plane number desnsity of the carbon nanotubes 13 grown under the above growth conditions was about 1×1011/cm2.
As illustrated in
As illustrated in
The filler to be used to form a filler layer is not limited to Micromelt 6239 hot-melt filler, and may be any other material provided that it is in a solid state at room temperature, and becomes liquid when heated and returns back into a solid state, exhibiting adhesive force, when cooled thereafter. For example, polyamide-based hot-melt resin, polyester-based hot-melt resin, polyurethane-based resin, modified polyolefin-based hot-melt resin, ethylene copolymer hot-melt resin, modified SBR hot-melt resin, EVA based hot-melt resin, and butyl rubber-based hot-melt resin, etc. may be employed. The melting point of the hot-melt resin is limited its maximum value by the heatproof temperature of the heat dissipating part on which this CNT sheet will be set. There are no other specific limitations for the melting point of the hot-melt resin, as long as it meets the above-mentioned requirement. For instance, it is from about 60° C. to 250° C. There are no specific limitations on the thickness of the sheet-like hot-melt resin body. It is preferable to determine the sheet thickness according to the length of the carbon nanotubes 13. A preferable sheet thickness is from 5 μm to 500 μm. The shape of the hot-melt resin is preferably a sheet shape, but there are no specific limitations on its shape. There is no problem to use grain shape or rod shape.
Then, after confirming that spaces among the carbon nanotubes 13 have been filled with the hot-melt filler, the sheet is cooled to solidify the hot-melt resin. Heating temperature and heating time or duration are determined considering the melting point of the hot-melt resin, molten-state viscosity, resin sheet thickness, carbon nanotube length, etc.
As illustrated in
When a CNT sheet is disposed between two objects and the filler layer 14 is heated, the filler layer 14 will be molten and increase the contact area with the objects while decreasing its thickness. When the ends of CNTs come in contact with the objects, the CNTs start to deform elastically, depending on the applied pressure, forming good contact with the objects. The CNTs deform to some extent, but they are oriented generally perpendicularly to the surfaces of the CNT sheet, and this direction is also called as perpendicular.
It is also possible to employ such a structure in which the ends of CNTs are coated with a metal layer having a higher heat conductivity than that of the filler layer. When the ends of CNTs are coated with metal, good contact (electrically and thermally) is established between the CNTs and the metal layer and when the metal coat layer is brought in contact with the objects, good contact can also be established easily.
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As illustrated in
A substrate as depicted in
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As depicted in
Thus, it is possible to provide a CNT sheet comprising a CNT assembly 13 having no metal layer on both end faces, a CNT sheet comprising a CNT assembly 13 having a metal layer deposited on one end face, and a CNT sheet comprising a CNT assembly 13 having metal layers deposited on both end faces.
Preliminary experiment will be described in which CNT sheets, each having one end face coated with a metal layer and bound with a filler layer, are used. First, since it is important to take out heat from a heat source, the coating of metal layer is disposed on the heat source (CPU) side.
As depicted in
As depicted in
Causes of generating cracks are studied. When a CNT sheet 3 is disposed between a heat generator 1 and a heat dissipating part 2, the CNTs in the CNT assembly are oriented in the direction perpendicular to the surface of the sheet 3. The thickness of the filler layer 14 is larger than the length of the CNTs 13, and accordingly, the both ends of the CNTs cannot come in contact with the heat source 1 and the heat dissipating part 2. As the thermoplastic resin 14 is heated and molten, the heat source 1 and the heat dissipating part 2 approach each other by applied pressure, and the thermoplastic resin 14 will flow outward, at least until the CNT assembly exhibits supporting force. Here, it can be considered that the CNTs 13 also move together with the thermoplastic resin 14.
It can be considered to provide some structure for preventing movement of CNTs, so that the CNTs will not move even when the thermoplastic resin is molten. Concave portion which accommodates the ends of carbon nanotubes and prevents movement thereof may be formed in either one or both of the heat source and the heat spreader.
When the thermoplastic resin, which is used as filler, is molten and a pressure is applied to combine the CPU chip, i.e. heat source, the CNT sheet, and the heat spreader by thermo-compression bonding, the resin moves in the in-plane direction of the heat spreader, but the carbon nanotubes are limited their movement by the concave portion formed in the heat spreader (or the heat source). As a result, it is expected that no crack is generated in the carbon nanotube assembly, preventing local degradation of heat dissipation.
For example, Micromelt 6239 hot-melt filler (melting temperature 135° C. to 145° C., molten state viscosity 5.5 Pa-s to 8.5 Pa-s at 225° C.) available from Henkel Japan Ltd. may be used as the thermoplastic resin.
A concave portion 4 is provided in that surface of the heat spreader 2 which faces the heat source 1 and is in contact with the CNT sheet 3. The concave portion 4 has a flat bottom, and the concave portion 4 has a rectangular cross section in the thickness direction. The area of the concave portion 4 is designed to accomodate the CNT assembly 13. The depth of the concave portion 4 is designed to be able to prevent movement of the CNTs. To ensure physical contact of the CNTs, the depth of the concave portion 4 should be shorter than the length of the CNTs. The depth of the concave portion 4 may be, for instance, 1 μm to 200 μm, or, for instance, 10 μm to 50 μm. The concave portion 4 is formed by etching or machining. The heat spreader 2 may be of metal, such as copper, in particular, oxygen free copper.
A CNT sheet 3 is disposed on a heat source 1, such as a CPU chip, and a heat spreader 2 is disposed thereabove at a position aligned with the CNT sheet 3. The concave portion 4 faces the CNT sheet 3.
As depicted in
Described above are cases where a concave portion with a rectangular cross section is formed on the surface of a heat spreader. The concave portion may have other shapes. For instance, it may be such a concave portion formed by digging from the surface to give a cross sectional shape in the thickness direction of the bottom surface having a zigzag shape.
In embodiment 1, a concave portion was formed on a heat spreader 2 that faced a heat source 1. A concave portion may be formed on a heat source 1 instead. Described below is embodiment 2 in which a concave portion is formed on a heat source.
In
Formation of a concave portion is not limited to only one of the heat source and the heat dissipating part. Described below is embodiment 3 in which concave portions are formed on both the heat source and the heat dissipating part.
In
In
Description has been made on the case where one end of a CNT assembly is coated with metal and that the metal coating is disposed on the side of a CPU chip 1. Metal coating is effective in depressing heat resistance, but not a requisite. Either a CNT assembly having no metal coating or a CNT assembly with both ends coated with metal may also be used.
Distribution of CNTs in an assembly can also be restricted to prevent cracking when a CNT sheet as depicted in either
In the constitutions in
The present invention has been described above along the embodiments. The invention is not limited thereto. For instance, CNT sheets may be used not only as a heat-conducting component, but also as an electroconductive component such as earth conductor. The metal used to coat the ends of CNTs is not limited to Au, but may also be selected from Au, Sn, Ag, and Al, according to the situation. When it is used as heat conductor, the material that coats the ends of CNTs may not be metal. It may be permissible to use a semiconductor material or insulation material that has a higher heat conductivity than that of the filler layer. Various modifications, substitutions, alterations, improvements, and combinations will be obvious to those skilled in the art.
All examples and conditional language recited herein are intended for pedagogical purposes to aid the reader in understanding the invention and the concepts contributed by the inventor to furthering the art, and are to be construed as being without limitation to such specifically recited examples and conditions, nor does the organization of such examples in the specification relate to a showing of the superiority and inferiority of the invention. Although the embodiments of the present invention have been described in detail, it should be understood that the various changes, substitutions, and alterations could be made hereto without departing from the spirit and scope of the invention.
This application is based upon and claims the benefit of priority of the prior International Patent Application No.PCT/JP2010/001775, filed on Mar. 12, 2010, the entire contents of which are incorporated herein by reference.
Number | Date | Country | |
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Parent | 13603773 | Sep 2012 | US |
Child | 15826555 | US |
Number | Date | Country | |
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Parent | PCT/JP2010/001775 | Mar 2010 | US |
Child | 13603773 | US |