1. Field of the Invention
This invention relates to the field of substrate device integration for electronic energy transfer, optical energy transfer and thermal energy transfer from one substrate to another.
2. Description of the Related Art
In the past decade, nanometer scale particles or nano-dots or quantum-dots that self-assembled on a surface have been studied for a variety of applications, particularly in quantum electronics or optoelectronics. For example, it is known that Ge nano-dots form naturally on Si (100) surfaces during deposition of Ge thereon in order to reduce the build-up of elastic strain and minimize the energy. The effect is known in the art by the Stromski-Krastanov (SK) growth mode.
Ge nano-dots of height 4 to 15 nm with widths or diameter of 20-30 nm have been grown. Ge nano-dots in the range of 4 nm size have been grown on SixGe1-x oxide films. Ge nano-dots on Si have also been demonstrated using an anodic alumina membrane mask as well as through deposition of Ge with latex nano-spheres as a mask. Ge nano-dots in the height range of 8 nm have been produced using an anodic alumina membrane. Nano-sphere lithography has produced Ge dots in the 30 nm size range. These approaches, while are not as attractive as self-assembled approaches, can lead to better control of spatial and size distribution of nano-dots than the self-assembled approaches. Thus, technology has come to exist recently for the formation of controlled spatially small (˜50 nm in height or less) nano-dots of Ge on Si.
Nano-dots in other material systems have also been demonstrated. For example, self-organized iron silicide nano-dots have been demonstrated on SixGe1-x or strained Si. Recently, silicide nano-dots as small as 3 nm, in height or diameter, have been grown on oxidized Si. GaN, a high-band-gap material, has been grown as 2-3 nm dots on Al0.15Ga0.85N using Si as anti-surfactant. Similarly, InAs nano-dots have been grown on GaAs substrates.
Despite the development of materials growth and understanding of nano-dot formation, the application of nano-dots has been directed primarily to electronic and optoelectronic devices where the nano-dots are the active elements.
In one embodiment of the invention, there is provided a device structure for electronic transfer between substrates. The device structure includes first and second substrates separated from one another, a plurality of localized spacers connecting the first and second substrates together and at least one of the localized spacers having a lateral dimension less than 350 nm. A sub-micron separation distance between the first and second substrates is configured to provide tunneling of carriers between the first and second substrates.
In one embodiment of the invention, there is provided a device structure for photonic transfer between substrates. The device structure includes first and second substrates separated from one another, a plurality of localized spacers connecting the first and second substrates together and at least one of the localized spacers having a lateral dimension less than 350 nm. A sub-micron separation distance between the first and second substrates is configured to provide tunneling of photons between the first and second substrates.
In one embodiment of the invention, there is provided a device structure for heat transfer between substrates. The device structure includes first and second substrates separated from one another, a plurality of localized spacers connecting the first and second substrates together and at least one of the localized spacers having a lateral dimension less than 350 nm. A sub-micron separation distance between the first and second substrates is configured to provide heat transfer between the first and second substrates.
In one embodiment of the invention, there is provided a substrate-to-substrate coupling structure. The coupling structure includes a first substrate and a second substrate separated from the first substrate by a sub-micron distance configured to couple electrical carriers or heat between one of the first and second substrates to the other. The coupling structure includes a plurality of self-assembled nanodots connecting the first and second substrates together. The self-assembled nanodots are formed by growth of a material of the nanodot on the first substrate.
In one embodiment of the invention, there is provided a method for transferring electronic charge between substrates including (1) providing charge carriers to a first substrate, the first substrate separated from a second substrate by at least one localized spacer having a lateral dimension less than 350 nm, and (2) tunneling the charge carriers from the first substrate to the second substrate across a sub-micron gap between the first and second substrates formed by the at least one localized spacer.
In one embodiment of the invention, there is provided a method for transferring heat between substrates including (1) providing heat to a first substrate, the first substrate separated from a second substrate by at least one localized spacer having a lateral dimension less than 350 nm, and 2) coupling the heat from the first substrate to the second substrate across a sub-micron gap of between the first and second substrates formed by the at least one localized spacer.
It is to be understood that both the foregoing general description of the invention and the following detailed description are exemplary, but are not restrictive of the invention.
A more complete appreciation of the invention and many of the attendant advantages thereof will be readily obtained as the same becomes better understood by reference to the following detailed description when considered in connection with the accompanying drawings, wherein:
In one embodiment of the invention, self-assembled and/or non-self-assembled nano-dots are provided as “localized spacers” to achieve a nano-gap separation for a variety of electronic and energy conversion applications. Referring now to the drawings, wherein like reference numerals designate identical or corresponding parts throughout the several views, in
In one embodiment of the invention, the nano-dots 4 have a lateral dimension that is less than 1000 nm. In another embodiment of the invention, the nano-dots 4 have a lateral dimension that is less than 100 nm. In another embodiment of the invention, the nano-dots 4 have a lateral dimension that is less than 10 nm. In another embodiment of the invention, the nano-dots 4 have a lateral dimension that is less than 5 nm. Thus, in general, the lateral dimension can be in a range from 1 to 1000 nm, 1 to 500 nm, 1 to 300 nm, 1 to 200 nm, 1 to 100 nm, 1 to 50 nm, 1 to 20 nm, or 1 to 10 nm.
In one embodiment of the invention, the nano-dots 4 can be formed from intrinsically high band-gap materials (e.g., as in GaN nano-dots) or through an increase of an effective band-gap from quantum confinement (e.g., as in Ge nano-dots). Accordingly, the nanodots in one embodiment can be a relatively poor electrical conductor as compared to macroscopic Ge. In one embodiment of the invention, the nano-dots 4 can be formed from III-V materials such as InAs or InGasAs formed on GaAs. U.S. Pat. Appl. Publ. No. 2007/0215857 (the contents of which are incorporated herein in its entirety) describes methods for forming InGaAs nanodots. In addition, materials such as Ge, Si, PbTe, Bi2Te3 in small dimensions are known to have low thermal conductivity, especially in the length scales 1 to 10 nm. Thus, in one embodiment of the invention, a plurality of self-assembled and non-self-assembled nano-dots can form thermal and electrically insulating spacers for a variety of device applications discussed below. These self-assembled and non-self-assembled nano-dots form a gap separating two substrates with the gap being small enough to promote electron tunneling, hole tunneling, infrared coupling, and/or convective heat transfer across the gap without imposing on the respective substrates stress related defects associated normally with the joining integrally or by bonding two substrates or substrate materials together.
The nano-dots 4 (formed by self-assembly or surfactant-assisted or through masks on a variety of substrates) can be preformed as Ge nanodots on silicon and subsequently trimmed by selective reactive ion etching to reduce the height of the Ge nanodots. In one embodiment, lithography is used to remove a percentage of the nano-dots on the surface to create a hybrid structure where self-assembly and patterning are used to form the localized spacers of the invention. In this embodiment, a set of nanodots remain on the substrate after etch removal of selected ones of the nanodots initially formed on the substrate.
In one embodiment, the nano-dots 4 can have a height for example from 1 nm to 20 nm in one embodiment. In one embodiment, the nano-dots 4 can have a width in a range of 20-30 nm. These dimensions are considered illustrative and not limiting the invention. In one embodiment, nanodots of Si (or Ge) can be formed by epitaxially overgrowing a thin oxide (e.g., 1-2 nm thick) and then using lithographic techniques to remove the region of Si that was not the overgrown part. U.S. Pat. No. 6,730,531 (the contents of which are incorporated herein in its entirety) describes such a method for the overgrowth of Si on thicker oxides than those described above.
In one embodiment of the invention, the substrates 8 and 10 in
The structure shown in
In this application, the Ge nano-dots (if of a macroscopic size) would electrically “short” charge across the gap. Yet, as noted above, the quantum confinement effects make Ge nano-dots more electrically insulating than bulk macroscopic Ge. Furthermore, in one embodiment of the invention, the Ge nano-dots can be oxidized at temperatures below which the Si surfaces will oxidize, thereby making the Ge nano-dots even more insulating. In some cases, Ge can be replaced by higher bandgap materials such as GaAs, GaN or other spacer materials to reduce the dark current further. Such approaches to reducing dark current can be even more advantageous for organic photovoltaic junctions, where large leakage currents are a significant problem.
Moreover, the “shorting” effect can be controlled by reducing the density and placement of the nanodots. A reduced density reduces the number of places for one substrate to “short” to another. For example, in a self-assembled nanodot (SAND) configuration, the nano-dots 4 have a density of approximately 1010 cm−2. In a non-self-assembled nanodot (NSAND) configuration, where the density of the nanodots has been reduced, the nano-dots 4 have a density of approximately 108 cm−2. Thus, lithographic patterning and etching can be used to reduce the density of nano-dots 4 and thereby control of the spatial and/or size distribution of nano-dots. In one embodiment of the invention, the nano-dot density can be reduced to 104 cm−2.
At 610, the nano-dot material is deposited to a predetermined thickness one or the other of the substrates 8, 10. Owing to stress between the Ge lattice constant and the Si lattice constant, the Ge deposits in “islands” forming Ge nano-dots on the Si surface (i.e., the Ge does not conformally deposit on the Si surface but preferentially coalesces on itself). Other materials systems as described above in the background section can be used in various embodiments of the invention to form nano-dots 4 on substrate 8 or substrate 10.
At 630, optionally, lithographic patterning using conventional masking techniques and materials can be used to remove a percentage of the nano-dots. The percentage of nano-dots removed will depend on the application. In some applications, over 99.999% of the nano-dots are removed to reduce a pathway for inadvertent conduction (heat or thermal) through the gap between the first and second substrates. In other applications, only 10% or fewer of the nano-dots are removed, for example in heat transfer applications where any pathway for heat from the first substrate to be dissipated to the second substrate is beneficial.
At 640, a second substrate is prepared for subsequent bonding to the first substrate by way of connection to the nano-dots. If the second substrate is of the same material as the first substrate, the surface of the second substrate will typically be cleaned using at least some or similar procedures as with the first substrate. If the second substrate is not of the same material as the first substrate, the surface of the second substrate will typically be cleaned using procedures appropriate for the second substrate.
At 640, the second substrate after or before the cleaning may have selected regions of the substrate oxidized or nitrided. For example, a mask material such as for example silicon oxide, silicon nitride, or a photoresist material is used to cover the portion of the second substrate. A low energy oxygen (or nitrogen) ion bombardment process or a plasma oxidation (or nitrification) assisted process, for example, is then used to form an oxide (or nitride) in a nearby surface region of the second substrate exposed to the oxidation process. The mask material is then removed.
At 650, the second substrate is joined to the first substrate by way of the nano-dots. At 650, the nano-dots become bonded to the second substrate using known bonding techniques such as for example solder-eutectic bonding, ultrasonic bonding, hydrogen bonding, van der Waal forces assisted bonding etc. The solder or eutectic metal could be applied as part of the masking process to create NSAND structures, as shown in
In the processes described above, a predetermined array or packing fraction of nano-dots, predetermined height of nano-dots, predetermined shape of nano-dots, predetermined materials in nano-dots, and predetermined attachments between two surfaces (e.g., one with nano-dot spacers coated thereon and the other without) can be used to achieve predetermined gaps ranging from a nm to hundreds of nm.
In various embodiments of the invention, the SAND and NSAND nano-gaps are utilized between two surfaces of bulk materials forming tunneling junctions across the nano-gaps, thereby permitting unique combinations of materials electrically coupled across the gap by tunneling but structurally “isolated” and thereby avoiding traditional heterostructure problems such as stress and thermal mismatch, and the defects resulting therefrom. Such nano-gap heterostructures according to the invention have applications in areas such as for example refrigeration, energy conversion, thermal compliant interfaces, displays, proximity lithography, single junction on organic PV materials and multi-junction solar cells using free-space tunneling structures, electronics packaging and nano-electro-mechanical systems (to be discussed in more detail below).
In another embodiment of the invention, self-assembled nano-dots (SAND) and/or non-self-assembled nano-dots (NSAND) form spacers in an electrically “insulating” and thermally “insulating” structure. “Insulating” in this embodiment implies significantly reduced conduction of electricity and/or heat as compared to bulk macroscopic materials of the same material as the SAND and/or NSAND spacers. Accordingly, these spacers could be used in electronics packaging such as for example the joining “thermally” of a conductive Cu heat sink to a Si device chip. Typically, the thermal expansion differences between Si and Cu are so large that the direct attachment of even a few hundreds of microns of Cu to a bulk Si device chip induces catastrophic coefficient of thermal expansion CTE-difference induced damage to the Si device chip.
In one embodiment of the invention, nano-dots are used to “join” different substrates together that normally would not have been amenable to joining due to disparate thermal expansion differences.
In one embodiment of the invention, nano-dots are used to “join” different types of organic semiconductor materials. Direct formation of different types of organic materials historically has been frustrated due to the formation of defect states at the interface as these different materials are joined. In this embodiment, the SAND and NSAND configurations permit “bulk” type performance of the respective materials without the prolific formation of defect states at the interface of, for example, what would have been between a n-type organic material to a p-type organic material.
In one embodiment of the invention, self-assembled nano-dots (SAND) and/or non-self-assembled nano-dots (NSAND) form spacers in thermo-tunneling devices for refrigeration and energy conversion.
In one embodiment of the invention, the electron wavelength (λe)>>d (the separation distance) and phonon wavelength (λph)<<d. As shown in the embodiment of
In another embodiment of the invention, self-assembled nano-dots (SAND) and/or non-self-assembled nano-dots (NSAND) form spacers in thermo photovoltaic devices. In these devices, the small gap separation permits where the evanescent infra-red blackbody radiation waves from a hot-body to be “optically” coupled to a p-n junction's emitter surface of another body across the gap.
In this way, the thermo-photovoltaic device 90 potentially couples photons over and above the blackbody spectrum emitted by the blackbody, which in turn is dictated by Planck's radiation law. The coupling of photons in such a manner utilizes coupled evanescent modes to transfer heat from upper substrate 96 to the lower substrate 98. Thus, in one embodiment of the invention, Planck's radiation and the photon-tunneling improve the thermophotovoltaic conversion efficiency with the use of SAND and NSAND spacers.
The separation and electrical isolation by electrical insulator 99 allows the thermal isolation of the blackbody emitter, from the p-n junction cell, and thereby achieve two things. Firstly, the blackbody remains hotter and emits more photons as dictated by Planck's law. Secondly, the p-n junction remains colder and the leakage current of the p-n junction is kept low as it increases exponentially with temperature. The reduction of leakage current leads to higher open circuit voltage, fill-factor and conversion efficiency of the thermo-photovoltaic cell.
In another embodiment of the invention, self-assembled nano-dots (SAND) and/or non-self-assembled nano-dots (NSAND) form spacers for gaps to couple heat from a heat-source in one body to a hot-side of a thermionic emitter device, thereby minimizing-induced mechanical stress.
In one embodiment of the invention, the enhanced electric field emission will also be aided by the following condition where the electron wavelength (λe)>>d and phonon wavelength (λp)<<d thereby preventing phonon travel from the hot emitter to cold collector. Thus, in one embodiment of the invention, the thermal energy of the emitter is used more effectively, for causing electrons to be emitted and creating external electric power rather than dissipation by thermal conduction with phonons. In another embodiment of the invention, self-assembled nano-dots (SAND) and/or non-self-assembled nano-dots (NSAND) form spacers in the device of
In another embodiment shown in
Numerous modifications and variations of the invention are possible in light of the above teachings. It is therefore to be understood that within the scope of the appended claims, the invention may be practiced otherwise than as specifically described herein.
This application is related to and claims priority under 35 U.S.C. 119(e) to U.S. provisional patent application 61/304,382, filed Feb. 12, 2010, the entire contents of which are hereby incorporated by reference.
Number | Date | Country | |
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61304382 | Feb 2010 | US |