The present invention relates to semiconductor devices and methods for their manufacture and, more particularly, relates to epitaxial growth of lattice mismatched systems.
Conventional semiconductor device fabrication is generally based on growth of lattice-matched layers. A lattice mismatched epitaxial layer at a semiconductor interface can lead to a high density of dislocations that degrade semiconductor device performance. Over the past several years, however, there has been increased interest in epitaxial growth of lattice-mismatched semiconducting material systems. Lattice mismatched systems can provide a greater range of materials characteristics than silicon. For example, the mechanical stress in a lattice mismatched layer and control of its crystal symmetry can be used to modify the energy-band structure to optimize performance of optoelectronic devices. Comprehensive materials engineering solutions are also needed to integrate high-quality Group III-V and II-VI heteroepitaxial films on Si. For example, lattice mismatched systems can enable compound semiconductor devices to be integrated directly with Si-based complementary metal oxide semiconductor (CMOS) devices. This capability to form multifunction chips will be important to the development of future optical and electronic devices.
Problems arise, however, because an epitaxial layer of a lattice-mismatched material on a substrate is often limited to a critical thickness (hc), before misfit dislocations begin to form in the expitaxial material. For example, hc=2 nm for a germanium epitaxial layer on a silicon substrate. Because of the relatively small hc and the large dislocation densities at thicknesses greater than hc, use of the heteroepitaxial layer is impractical. Conventional solutions include multiple post-growth annealing, liquid-phase epitaxy, epitaxial necking, and graded layers. Conventional solutions, however, require intricate patterning and/or high processing temperatures that can increase fabrication cost and complexity.
Thus, there is a need to overcome these and other problems of the prior art and to provide a method to grow high-quality heteroepitaxial layers of lattice mismatched systems.
According to various embodiments, the present teachings include a method of forming a semiconductor device. The method can include forming an interface layer on a substrate and forming a plurality of touchdown windows in the interface layer. The touchdown windows can be formed using interferometric lithography such that each of the touchdown windows expose a portion of the substrate. The exposed portions of the substrate can then be exposed to a material comprising a semiconductor material to form an island comprising the semiconductor material on each of the exposed portions of the substrate.
According to various other embodiments, the present teachings include another method of forming an epitaxial overgrowth layer. The method can include forming an interface layer on a substrate and using interferometric lithography to form a periodic pattern on the interface layer. The periodically patterned interface layer can be plasma etched to form a template that exposes portions of the substrate. Germanium islands can be selectively grown on the substrate through openings of the template using molecular beam epitaxy. The germanium islands can then coalesce to form a single crystal expitaxial overgrowth layer.
According to various other embodiments, the present teachings can include a semiconductor device. The semiconductor device can include a substrate and a template disposed on the substrate, wherein the template comprises a periodic pattern that exposes portions of the substrate. An epitaxial layer can be disposed over the template and can contacting the exposed portions of the substrate. The semiconductor device can further include a layer disposed on the epitaxial layer, wherein the layer comprises at least one element from Groups III-V and II-VI.
It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory only and are not restrictive of the invention, as claimed.
The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate several embodiments of the invention and together with the description, serve to explain the principles of the invention.
In the following description, reference is made to the accompanying drawings that form a part thereof, and in which is shown by way of illustration specific exemplary embodiments in which the invention may be practiced. These embodiments are described in sufficient detail to enable those skilled in the art to practice the invention and it is to be understood that other embodiments may be utilized and that changes may be made without departing from the scope of the invention. The following description is, therefore, not to be taken in a limited sense.
As used herein, the term “self-directed touchdown” refers to a nucleation and growth process that is initiated without reliance on a photolithographic mask to pattern a substrate or other layer.
As used herein, the term “nanoheteroepitaxy” refers to engineering a heterojunction at the nanoscale to relieve lattice strain.
As used herein, the terms “epitaxial layer” and “epilayer” are used interchangeably to refer to a layer grown upon an underlying layer, where the layer has the same crystalline orientation as the underlying layer. The underlying layer can be, for example, a substrate.
Referring to
An interface layer 20 can be formed on substrate 10. Interface layer 20 can be, for example, an oxide layer, such as, a SiO2 layer, having a thickness of about 1 Å to about 30 Å. The SiO2 layer can be formed by methods known in the art, such as, for example, treating substrate 10 in a Piranha solution or by thermal growth. Other interface materials can include, but are not limited to, Si3N4, Al2O3, and W. In various embodiments, interface layer 20 can comprise an amorphous material.
In various embodiments, properties of interface layer 20, such as surface roughness and thickness, can be controlled to tailor the defect morphology of the epitaxial layer. For example, interface layer 20 can be formed using H2O2 to achieve a monolayer of atomically flat SiO2 on a hydrogenated Si(100) substrate.
After forming interface layer 20 on substrate 10, interface layer 20 can be exposed to a material comprising a semiconductor material. Exposure temperatures can be about 500°0 C. to about 750° C. The semiconductor material can comprise, for example, germanium (Ge). In various embodiments, molecular beam epitaxy can be used to expose interface layer 20 to Ge. As shown in cross-sectional view of
While not intending to be bound by any particular theory, it is believed that interface layer free areas 30 can form through reaction of the Ge with the oxide film as follows: SiO2(s)+Ge(ad)→SiO(g)+GeO(g). Ge can also diffuse through the pinholes or other defects that exist in the interface layer and react with SiO2 in the presence of Si: Si+2SiO2(s)+Ge(ad)→GeO(g)+3SiO(g). Instead of indiscriminately removing a large area of the SiO2, the reaction between Ge and SiO2 can take place in a self-limiting fashion with a well-defined surface density and inter-distance. Interface layer free areas 30 can be randomly distributed to form a remaining portion of interface layer 25, and can be about 2 nm to about 8 nm wide. The spacing between interface layer free areas can be about 2 nm to about 14 nm.
As exposure to Ge continues, the Ge can deposit in interface layer free areas 30. There is generally no deposition on remaining portions of interface layer 25, due to selective deposition. This self-directed touch-down of Ge on Si occurs without lithography to pattern the substrate or interface layer. The regions of Ge growth on Si substrate 10 can form crystalline Ge islands, referred to herein as seed pads 40, shown in
While not intending to be bound by any particular theory, it is believed that selective growth of Ge on Si and over SiO2 results from a different mechanism than the reaction between Ge and SiO2 forming volatile monoxide products. For example, the desorption activation energy (Ed) of Ge from SiO2 is approximately 42±3 kJ/mol, on the order of Van der Waals forces rather than a strong chemical bond. The selectivity of Ge on Si over SiO2 is dominated by the low desorption activation energy of Ge adspecies on the SiO2 surface. At the growth temperature, the low desorption activation energy can give rise to a high desorption flux. When the Ge impingement flux is less than the desorption flux, Ge adspecies evaporate before forming stable nuclei. If the surface temperature is decreased, the desorption flux of Ge adspecies decreases exponentially. When the impingement flux exceeds the desorption flux, net Ge adspecies on the surface leads to formation of stable islands. One of ordinary skill in the art understands that formation of a Ge epilayer on a Si substrate is disclosed for further understanding of the exemplary methods and that other layers can be formed on other substrates.
According to various embodiments and referring to
In an exemplary embodiment, a Ge epilayer was formed on a silicon substrate using the methods disclosed herein. Referring back to
A SiO2 layer 20 was then formed on silicon substrate 10. SiO2 layer 20 was formed by chemical oxidation by immersion of silicon substrate 10 in a fresh Piranha solution for about 10 minutes at about 80° C. The thickness of SiO2 layer 20 was about 1.2 nm. SiO2 layer 20 was rinsed with deionized water, dried with N2 gas, and placed in an ultrahigh vacuum (UHV) molecular beam epitaxy (MBE) chamber. The base pressure of the UHV chamber was about 4×10−10 Torr. After heating substrate 10 to about 510° C. to about 620° ° C., a Ge flux of about 0.24 equivalent monolayers per second was provided by a Ge Knudsen effusion cell operated at about 1200° C. The Ge exposure created a plurality of touchdown windows 30 in SiO2 layer 20 having a width of about 3 nm to about 7 nm. Continued exposure to Ge resulted in the formation of Ge seed pads 40 within touchdown windows 30. Ge seed pads 40 had a density exceeding about 1011cm−2. The inter-touchdown window distance was about 2 nm to about 12 nm.
Further exposure to Ge resulted in the seed pads 40 growing over the top of touchdown windows 30 and coalescing into Ge epilayer 50, for example, as shown in
In various other embodiments, an epilayer can be formed using a template formed in the interface layer by interferometric lithography. Referring back to
As shown in the top view of
After forming template 26, template 26 and the exposed portions of substrate 10 can be exposed to a material comprising a semiconductor material. Exposure temperatures can be about 500°0 C. to about 750° C. The semiconductor material can comprise, for example, germanium (Ge). In various embodiments, molecular beam epitaxy can be used to expose template 26 and the exposed portions of substrate 10 to Ge. Due to selective deposition, Ge can deposit on the exposed portions of substrate 10, but there is generally little or no deposition on template 26. As exposure to Ge continues, Ge growth on exposed portions of substrate 10 can form crystalline Ge islands 41, also referred to herein as seed pads, as shown in
Semiconductor layer 51 can be virtually defect-free having a threading dislocation density of about 1×105 cm−2 or less. Stacking faults can exist over the surface of the remaining template 26, but generally terminate within about 80 nm from the interface, for example, the SiO2-Ge interface. As shown in
In various embodiments, layer 61 can be formed on template 26 prior to coalescing of islands 41 into a continuous layer. As shown in
In an exemplary embodiment, a Ge epilayer was formed on a silicon . substrate using a template as disclosed herein. Referring back to
Contaminants were removed from the surface of silicon substrate 10 and template 26 by immersion in a Piranha solution for about 20 minutes. The Piranha solution was prepared by mixing 4 volumetric parts of 2M H2SO4 with 1 volumetric part of 30 wt % H2O2. Because the Piranha solution is an oxidant, a SiO2 layer formed on the exposed portions of silicon substrate 10. Silicon substrate 10 and template 25 were then rinsed with deionized water, dried with N2 gas, and placed in an ultrahigh vacuum (UHV) molecular beam epitaxy (MBE) chamber. The base pressure of the UHV chamber was about 4×10−10 Torr. Silicon substrate 10 and template 25 were heated to about 900° C. to remove contaminants and to partially remove the oxide formed by the Piranha treatment. The temperature was then reduced to about 650° C. Ge exposure was provided by a Ge Knudsen effusion cell operated at about 1120° C. for a Ge growth rate of about 0.7 ML/min.
The Ge exposure created a plurality of Ge islands within touchdown windows 31. As shown in
Other embodiments of the invention will be apparent to those skilled in the art from consideration of the specification and practice of the invention disclosed herein. It is intended that the specification and examples be considered as exemplary only, with a true scope and spirit of the invention being indicated by the following claims.
This application is a continuation-in-part of U.S. patent application Ser. No. 10/935,228 filed on Sep. 8, 2004, and claims priority to. U.S. Provisional Patent Application Ser. No. 60/622,688 filed on Oct. 28, 2004, the disclosures of which are incorporated by reference in their entirety.
Number | Date | Country | |
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60622688 | Oct 2004 | US |
Number | Date | Country | |
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Parent | 10935228 | Sep 2004 | US |
Child | 11260231 | Oct 2005 | US |