Heterojunction tunneling diodes and process for fabricating same

Information

  • Patent Grant
  • 7105866
  • Patent Number
    7,105,866
  • Date Filed
    Thursday, August 5, 2004
    19 years ago
  • Date Issued
    Tuesday, September 12, 2006
    17 years ago
Abstract
High quality epitaxial layers of compound semiconductor materials can be grown overlying large silicon wafers by first growing an accommodating buffer layer on a silicon wafer. The accommodating buffer layer is a layer of monocrystalline oxide spaced apart from the silicon wafer by an amorphous interface layer of silicon oxide. The amorphous interface layer dissipates strain and permits the growth of a high quality monocrystalline oxide accommodating buffer layer. Any lattice mismatch between the accommodating buffer layer and the underlying silicon substrate is taken care of by the amorphous interface layer.
Description
FIELD OF THE INVENTION

This invention relates generally to semiconductor structures and devices and to a method for their fabrication, and more specifically to the fabrication and use of resonant heterojunction tunnel diodes that include a monocrystalline compound semiconductor material.


BACKGROUND OF THE INVENTION

The vast majority of semiconductor discrete devices and integrated circuits are fabricated from silicon, at least in part because of the availability of inexpensive, high quality monocrystalline silicon substrates. Other semiconductor materials, such as the so-called compound semiconductor materials, have physical attributes, including wider bandgap and/or higher mobility than silicon, or direct bandgaps that make these materials advantageous for certain types of semiconductor devices. Unfortunately, compound semiconductor materials are generally much more expensive than silicon and are not available in large wafers as is silicon. Gallium arsenide (GaAs), the most readily available compound semiconductor material, is available in wafers only up to about 150 millimeters (mm) in diameter. In contrast, silicon wafers are available up to about 300 mm and are widely available at 200 mm. The 150 mm GaAs wafers are many times more expensive than are their silicon counterparts. Wafers of other compound semiconductor materials are even less available and are more expensive than GaAs.


Because of the desirable characteristics of compound semiconductor materials, and because of their present generally high cost and low availability in bulk form, for many years attempts have been made to grow thin films of the compound semiconductor materials on a foreign substrate. To achieve optimal characteristics of the compound semiconductor material, however, a monocrystalline film of high crystalline quality is desired. Attempts have been made, for example, to grow layers of a monocrystalline compound semiconductor material on germanium, silicon, and various insulators. These attempts have generally been unsuccessful because lattice mismatches between the host crystal and the grown crystal have caused the resulting thin film of compound semiconductor material to be of low crystalline quality.


If a large area thin film of high quality monocrystalline compound semiconductor material was available at low cost, a variety of semiconductor devices could advantageously be fabricated in that film at a low cost compared to the cost of fabricating such devices on a bulk wafer of compound semiconductor material or in an epitaxial film of such material on a bulk wafer of compound semiconductor material. In addition, if a thin film of high quality monocrystalline compound semiconductor material could be realized on a bulk wafer such as a silicon wafer, an integrated device structure, such as, for example, a resonant heterojunction tunnel diode, could be achieved that took advantage of the best properties of both the silicon and the compound semiconductor material.


Tunnel diodes, where carriers tunnel through the band gap of a doped p-n junction, have taken many forms since first proposed in about 1958. Tunnel diodes provide very fast switching time and low power dissipation. The first tunnel diode, called an Esaki tunneling diode (after its originator), comprised two silicon regions of different conductivity types with both being highly doped. When bias is applied to the Esaki-type diode, the available states for electrons in the contact layer align with available states for holes in the valence band of the injection layer and tunneling occurs. Traditional Esaki diodes formed in silicon-based material systems, however, exhibit low peak current densities, low peak-to-valley current ratios, and low operational frequencies, which make them unsuitable for present-day demands for enhanced performance in areas such as high frequency circuits, portable communications systems, and digital applications. Thus, present-day Esaki-type diodes may comprise germanium, gallium arsenide, or other semiconductor materials, which exhibit more suitable electrical properties. For example, tunnel diodes having the most favorable electrical properties are currently manufactured in compound semiconductor material systems comprising materials such as indium aluminum arsenide (InAlAs), indium gallium arsenide (InGaAs), indium phosphide (InP), gallium arsenide (GaAs), and aluminum arsenide (AlAs). Unfortunately, as stated above, such compound semiconductor substrates tend to be expensive and extremely fragile.


Accordingly, a need exists for a semiconductor structure that provides a high quality monocrystalline compound semiconductor film over another monocrystalline material and for a process for making such a structure.





BRIEF DESCRIPTION OF THE DRAWINGS

The present invention is illustrated by way of example and not limitation in the accompanying figures, in which like references indicate similar elements, and in which:



FIGS. 1–3 illustrate schematically, in cross section, device structures in accordance with various embodiments of the invention;



FIG. 4 illustrates graphically the relationship between maximum attainable film thickness and lattice mismatch between a host crystal and a grown crystalline overlayer;



FIG. 5 illustrates a high resolution Transmission Electron Micrograph of a structure including a monocrystalline accommodating buffer layer;



FIG. 6 illustrates an x-ray diffraction spectrum of a structure including a monocrystalline accommodating buffer layer;



FIG. 7 illustrates a high resolution Transmission Electron Micrograph of a structure including an amorphous oxide layer;



FIG. 8 illustrates an x-ray diffraction spectrum of a structure including an amorphous oxide layer;



FIG. 9 illustrates schematically, in cross section, a monolithic integrated circuit in accordance with one embodiment of the invention; and



FIGS. 10–17 illustrate schematically, in cross section, device structures in accordance with further exemplary embodiments of the invention.





Skilled artisans will appreciate that elements in the figures are illustrated for simplicity and clarity and have not necessarily been drawn to scale. For example, the dimensions of some of the elements in the figures may be exaggerated relative to other elements to help to improve understanding of embodiments of the present invention.


DETAILED DESCRIPTION OF THE DRAWINGS


FIG. 1 illustrates schematically, in cross section, a portion of a semiconductor structure 20 in accordance with an embodiment of the invention. Semiconductor structure 20 includes a monocrystalline substrate 22, accommodating buffer layer 24 comprising a monocrystalline material, and a layer 26 of a monocrystalline compound semiconductor material. In this context, the term “monocrystalline” shall have the meaning commonly used within the semiconductor industry. The term shall refer to materials that are a single crystal or that are substantially a single crystal and shall include those materials having a relatively small number of defects such as dislocations and the like as are commonly found in substrates of silicon or germanium or mixtures of silicon and germanium and epitaxial layers of such materials commonly found in the semiconductor industry.


In accordance with one embodiment of the invention, structure 20 also includes an amorphous intermediate layer 28 positioned between substrate 22 and accommodating buffer layer 24. Structure 20 may also include a template layer 30 between the accommodating buffer layer and compound semiconductor layer 26. As will be explained more fully below, the template layer helps to initiate the growth of the compound semiconductor layer on the accommodating buffer layer. The amorphous intermediate layer helps to relieve the strain in the accommodating buffer layer and by doing so, aids in the growth of a high crystalline quality accommodating buffer layer.


Substrate 22, in accordance with an embodiment of the invention, is a monocrystalline semiconductor wafer, preferably of large diameter. The wafer can be of a material from Group IV of the periodic table, and preferably a material from Group IVA. Examples of Group IV semiconductor materials include silicon, germanium, mixed silicon and germanium, mixed silicon and carbon, mixed silicon, germanium and carbon, and the like. Preferably substrate 22 is a wafer containing silicon or germanium, and most preferably is a high quality monocrystalline silicon wafer as used in the semiconductor industry. Accommodating buffer layer 24 is preferably a monocrystalline oxide or nitride material epitaxially grown on the underlying substrate. In accordance with one embodiment of the invention, amorphous intermediate layer 28 is grown on substrate 22 at the interface between substrate 22 and the growing accommodating buffer layer by the oxidation of substrate 22 during the growth of layer 24. The amorphous intermediate layer serves to relieve strain that might otherwise occur in the monocrystalline accommodating buffer layer as a result of differences in the lattice constants of the substrate and the buffer layer. As used herein, lattice constant refers to the distance between atoms of a cell measured in the plane of the surface. If such strain is not relieved by the amorphous intermediate layer, the strain may cause defects in the crystalline structure of the accommodating buffer layer. Defects in the crystalline structure of the accommodating buffer layer, in turn, would make it difficult to achieve a high quality crystalline structure in monocrystalline compound semiconductor layer 26.


Accommodating buffer layer 24 is preferably a monocrystalline oxide or nitride material selected for its crystalline compatibility with the underlying substrate and with the overlying compound semiconductor material. For example, the material could be an oxide or nitride having a lattice structure substantially matched to the substrate and/or to the subsequently applied semiconductor material. Materials that are suitable for the accommodating buffer layer include metal oxides such as the alkaline earth metal titanates, alkaline earth metal zirconates, alkaline earth metal hafnates, alkaline earth metal tantalates, alkaline earth metal ruthenates, alkaline earth metal niobates, alkaline earth metal vanadates, perovskite oxides such as alkaline earth metal tin-based perovskites, lanthanum aluminate, lanthanum scandium oxide, and gadolinium oxide. Additionally, various nitrides such as gallium nitride, aluminum nitride, and boron nitride may also be used for the accommodating buffer layer. Most of these materials are insulators, although strontium ruthenate, for example, is a conductor. Generally, these materials are metal oxides or metal nitrides, and more particularly, these metal oxide or nitrides typically include at least two different metallic elements. In some specific applications, the metal oxides or nitride may include three or more different metallic elements.


Amorphous interface layer 28 is preferably an oxide formed by the oxidation of the surface of substrate 22, and more preferably is composed of a silicon oxide. The thickness of layer 28 is sufficient to relieve strain attributed to mismatches between the lattice constants of substrate 22 and accommodating buffer layer 24. Typically, layer 28 has a thickness in the range of approximately 0.5–5 nm.


The compound semiconductor material of layer 26 can be selected, as needed for a particular semiconductor structure, from any of the Group IIIA and VA elements (III–V semiconductor compounds), mixed III–V compounds, Group II(A or B) and VIA elements (II–VI semiconductor compounds), and mixed II–VI compounds. Examples include gallium arsenide (GaAs), gallium indium arsenide (GaInAs), gallium aluminum arsenide (GaAlAs), indium phosphide (InP), cadmium sulfide (CdS), cadmium mercury telluride (CdHgTe), zinc selenide (ZnSe), zinc sulfur selenide (ZnSSe), and the like. Suitable template materials chemically bond to the surface of the accommodating buffer layer 24 at selected sites and provide sites for the nucleation of the epitaxial growth of the subsequent compound semiconductor layer 26. Appropriate materials for template 30 are discussed below.



FIG. 2 illustrates, in cross section, a portion of a semiconductor structure 40 in accordance with a further embodiment of the invention. Structure 40 is similar to the previously described semiconductor structure 20, except that an additional buffer layer 32 is positioned between accommodating buffer layer 24 and layer of monocrystalline compound semiconductor material 26. Specifically, the additional buffer layer is positioned between template layer 30 and the overlying layer of compound semiconductor material. The additional buffer layer, formed of a semiconductor or compound semiconductor material, serves to provide a lattice compensation when the lattice constant of the accommodating buffer layer cannot be adequately matched to the overlying monocrystalline compound semiconductor material layer.



FIG. 3 schematically illustrates, in cross section, a portion of a semiconductor structure 34 in accordance with another exemplary embodiment of the invention. Structure 34 is similar to structure 20, except that structure 34 includes an amorphous layer 36, rather than accommodating buffer layer 24 and amorphous interface layer 28, and an additional semiconductor layer 38.


As explained in greater detail below, amorphous layer 36 may be formed by first forming an accommodating buffer layer and an amorphous interface layer in a similar manner to that described above. Monocrystalline semiconductor layer 38 is then formed (by epitaxial growth) overlying the monocrystalline accommodating buffer layer. The accommodating buffer layer is then exposed to an anneal process to convert the monocrystalline accommodating buffer layer to an amorphous layer. Amorphous layer 36 formed in this manner comprises materials from both the accommodating buffer and interface layers, which amorphous layers may or may not amalgamate. Thus, layer 36 may comprise one or two amorphous layers. Formation of amorphous layer 36 between substrate 22 and semiconductor layer 38 (subsequent to layer 38 formation) relieves stresses between layers 22 and 38 and provides a true compliant substrate for subsequent processing—e.g., compound semiconductor layer 26 formation.


The processes previously described above in connection with FIGS. 1 and 2 are adequate for growing monocrystalline compound semiconductor layers over a monocrystalline substrate. However, the process described in connection with FIG. 3, which includes transforming a monocrystalline accommodating buffer layer to an amorphous oxide layer, may be better for growing monocrystalline compound semiconductor layers because it allows any strain in layer 26 to relax.


Semiconductor layer 38 may include any of the materials described throughout this application in connection with either of compound semiconductor material layer 26 or additional buffer layer 32. For example, layer 38 may include monocrystalline Group IV or monocrystalline compound semiconductor materials.


In accordance with one embodiment of the present invention, semiconductor layer 38 serves as an anneal cap during layer 36 formation and as a template for subsequent semiconductor layer 26 formation. Accordingly, layer 38 is preferably thick enough to provide a suitable template for layer 26 growth (at least one monolayer) and thin enough to allow layer 38 to form as a substantially defect free monocrystalline semiconductor compound.


In accordance with another embodiment of the invention, semiconductor layer 38 comprises compound semiconductor material (e.g., a material discussed above in connection with compound semiconductor layer 26) that is thick enough to form devices within layer 38. In this case, a semiconductor structure in accordance with the present invention does not include compound semiconductor layer 26. In other words, the semiconductor structure in accordance with this embodiment only includes one compound semiconductor layer disposed above amorphous oxide layer 36.


The following non-limiting, illustrative examples illustrate various combinations of materials useful in structures 20, 40, and 34 in accordance with various alternative embodiments of the invention. These examples are merely illustrative, and it is not intended that the invention be limited to these illustrative examples.


EXAMPLE 1

In accordance with one embodiment of the invention, monocrystalline substrate 22 is a silicon substrate oriented in the (100) direction. The silicon substrate can be, for example, a silicon substrate as is commonly used in making complementary metal oxide semiconductor (CMOS) integrated circuits having a diameter of about 200–300 mm. In accordance with this embodiment of the invention, accommodating buffer layer 24 is a monocrystalline layer of SrzBa1-zTiO3 where z ranges from 0 to 1 and the amorphous intermediate layer is a layer of silicon oxide (SiOx) formed at the interface between the silicon substrate and the accommodating buffer layer. The value of z is selected to obtain one or more lattice constants closely matched to corresponding lattice constants of the subsequently formed layer 26. The accommodating buffer layer can have a thickness of about 2 to about 100 nanometers (nm) and preferably has a thickness of about 10 nm. In general, it is desired to have an accommodating buffer layer thick enough to isolate the compound semiconductor layer from the substrate to obtain the desired electrical and optical properties. Layers thicker than 100 nm usually provide little additional benefit while increasing cost unnecessarily; however, thicker layers may be fabricated if needed. The amorphous intermediate layer of silicon oxide can have a thickness of about 0.5–5 nm, and preferably a thickness of about 1.5–2.5 nm.


In accordance with this embodiment of the invention, compound semiconductor material layer 26 is a layer of gallium arsenide (GaAs) or aluminum gallium arsenide (AlGaAs) having a thickness of about 1 nm to about 100 micrometers (μm) and preferably a thickness of about 0.5 μm to 10 μm. The thickness generally depends on the application for which the layer is being prepared. To facilitate the epitaxial growth of the gallium arsenide or aluminum gallium arsenide on the monocrystalline oxide, a template layer is formed by capping the oxide layer. The template layer is preferably 1–10 monolayers of Ti—As, Sr—O—As, Sr—Ga—O, or Sr—Al—O. By way of a preferred example, 1–2 monolayers of Ti—As or Sr—Ga—O have been shown to successfully grow GaAs layers.


EXAMPLE 2

In accordance with a further embodiment of the invention, monocrystalline substrate 22 is a silicon substrate as described above. The accommodating buffer layer is a monocrystalline oxide of strontium or barium zirconate or hafnate in a cubic or orthorhombic phase with an amorphous intermediate layer of silicon oxide formed at the interface between the silicon substrate and the accommodating buffer layer. The accommodating buffer layer can have a thickness of about 2–100 nm and preferably has a thickness of at least 5 nm to ensure adequate crystalline and surface quality and is formed of a monocrystalline SrZrO3, BaZrO3, SrHfO3, BaSnO3 or BaHfO3. For example, a monocrystalline oxide layer of BaZrO3 can grow at a temperature of about 700 degrees C. The lattice structure of the resulting crystalline oxide exhibits a 45 degree rotation with respect to the substrate silicon lattice structure.


An accommodating buffer layer formed of these zirconate or hafnate materials is suitable for the growth of compound semiconductor materials in the indium phosphide (InP) system. The compound semiconductor material can be, for example, indium phosphide (InP), indium gallium arsenide (InGaAs), aluminum indium arsenide, (AlInAs), or aluminum gallium indium arsenic phosphide (AlGaInAsP), having a thickness of about 1.0 nm to 10 μm. A suitable template for this structure is 1–10 monolayers of zirconium-arsenic (Zr—As), zirconium-phosphorus (Zr—P), hafnium-arsenic (Hf—As), hafnium-phosphorus (Hf—P), strontium-oxygen-arsenic (Sr—O—As), strontium-oxygen-phosphorus (Sr—O—P), barium-oxygen-arsenic (Ba—O—As), indium-strontium-oxygen (In-Sr—O), or barium-oxygen-phosphorus (Ba—O—P), and preferably 1–2 monolayers of one of these materials. By way of an example, for a barium zirconate accommodating buffer layer, the surface is terminated with 1–2 monolayers of zirconium followed by deposition of 1–2 monolayers of arsenic to form a Zr—As template. A monocrystalline layer of the compound semiconductor material from the indium phosphide system is then grown on the template layer. The resulting lattice structure of the compound semiconductor material exhibits a 45 degree rotation with respect to the accommodating buffer layer lattice structure and a lattice mismatch to (100) InP of less than 2.5%, and preferably less than about 1.0%.


EXAMPLE 3

In accordance with a further embodiment of the invention, a structure is provided that is suitable for the growth of an epitaxial film of a II–VI material overlying a silicon substrate. The substrate is preferably a silicon wafer as described above. A suitable accommodating buffer layer material is SrxBa1-xTiO3, where x ranges from 0 to 1, having a thickness of about 2–100 nm and preferably a thickness of about 5–15 nm. The II–VI compound semiconductor material can be, for example, zinc selenide (ZnSe) or zinc sulfur selenide (ZnSSe). A suitable template for this material system includes 1–10 monolayers of zinc-oxygen (Zn—O) followed by 1–2 monolayers of an excess of zinc followed by the selenidation of zinc on the surface. Alternatively, a template can be, for example, 1–10 monolayers of strontium-sulfur (Sr—S) followed by the ZnSeS.


EXAMPLE 4

This embodiment of the invention is an example of structure 40 illustrated in FIG. 2. Substrate 22, monocrystalline oxide layer 24, and monocrystalline compound semiconductor material layer 26 can be similar to those described in example 1. In addition, an additional buffer layer 32 serves to alleviate any strains that might result from a mismatch of the crystal lattice of the accommodating buffer layer and the lattice of the monocrystalline semiconductor material. Buffer layer 32 can be a layer of germanium or a GaAs, an aluminum gallium arsenide (AlGaAs), an indium gallium phosphide (InGaP), an aluminum gallium phosphide (AlGaP), an indium gallium arsenide (InGaAs), an aluminum indium phosphide (AlInP), a gallium arsenide phosphide (GaAsP), or an indium gallium phosphide (InGaP) strain compensated superlattice. In accordance with one aspect of this embodiment, buffer layer 32 includes a GaAsxP1-x superlattice, wherein the value of x ranges from 0 to 1. In accordance with another aspect, buffer layer 32 includes an InyGa1-yP superlattice, wherein the value of y ranges from 0 to 1. By varying the value of x or y, as the case may be, the lattice constant is varied from bottom to top across the superlattice to create a match between lattice constants of the underlying oxide and the overlying compound semiconductor material. The compositions of other materials, such as those listed above, may also be similarly varied to manipulate the lattice constant of layer 32 in a like manner. The superlattice can have a thickness of about 50–500 nm and preferably has a thickness of about 100–200 nm. The template for this structure can be the same of that described in example 1. Alternatively, buffer layer 32 can be a layer of monocrystalline germanium having a thickness of 1–50 nm and preferably having a thickness of about 2–20 nm. In using a germanium buffer layer, a template layer of either germanium-strontium (Ge—Sr) or germanium-titanium (Ge—Ti) having a thickness of about one monolayer can be used as a nucleating site for the subsequent growth of the monocrystalline compound semiconductor material layer. The formation of the oxide layer is capped with either a monolayer of strontium or a monolayer of titanium to act as a nucleating site for the subsequent deposition of the monocrystalline germanium. The monolayer of strontium or titanium provides a nucleating site to which the first monolayer of germanium can bond.


EXAMPLE 5

This example also illustrates materials useful in a structure 40 as illustrated in FIG. 2. Substrate material 22, accommodating buffer layer 24, monocrystalline compound semiconductor material layer 26 and template layer 30 can be the same as those described above in example 2. In addition, a buffer layer 32 is inserted between the accommodating buffer layer and the overlying monocrystalline compound semiconductor material layer. The buffer layer, a further monocrystalline semiconductor material, can be, for example, a graded layer of indium gallium arsenide (InGaAs) or indium aluminum arsenide (InAlAs). In accordance with one aspect of this embodiment, buffer layer 32 includes InGaAs, in which the indium composition varies from 0 to about 47%. The buffer layer preferably has a thickness of about 10–30 nm. Varying the composition of the buffer layer from GaAs to InGaAs serves to provide a lattice match between the underlying monocrystalline oxide material and the overlying layer of monocrystalline compound semiconductor material. Such a buffer layer is especially advantageous if there is a lattice mismatch between accommodating buffer layer 24 and monocrystalline compound semiconductor material layer 26.


EXAMPLE 6

This example provides exemplary materials useful in structure 34, as illustrated in FIG. 3. Substrate material 22, template layer 30, and monocrystalline compound semiconductor material layer 26 may be the same as those described above in connection with example 1.


Amorphous layer 36 is an amorphous oxide layer which is suitably formed of a combination of amorphous intermediate layer materials (e.g., layer 28 materials as described above) and accommodating buffer layer materials (e.g., layer 24 materials as described above). For example, amorphous layer 36 may include a combination of SiOx and SrzBa1-z TiO3 (where z ranges from 0 to 1),which combine or mix, at least partially, during an anneal process to form amorphous oxide layer 36.


The thickness of amorphous layer 36 may vary from application to application and may depend on such factors as desired insulating properties of layer 36, type of semiconductor material comprising layer 26, and the like. In accordance with one exemplary aspect of the present embodiment, layer 36 thickness is about 2 nm to about 100 nm, preferably about 2–10 nm, and more preferably about 5–6 nm.


Layer 38 comprises a monocrystalline compound semiconductor material that can be grown epitaxially over a monocrystalline oxide material such as material used to form accommodating buffer layer 24. In accordance with one embodiment of the invention, layer 38 includes the same materials as those comprising layer 26. For example, if layer 26 includes GaAs, layer 38 also includes GaAs. However, in accordance with other embodiments of the present invention, layer 38 may include materials different from those used to form layer 26. In accordance with one exemplary embodiment of the invention, layer 38 is about 1 monolayer to about 100 nm thick.


Referring again to FIGS. 1–3, substrate 22 is a monocrystalline substrate such as a monocrystalline silicon substrate. The crystalline structure of the monocrystalline substrate is characterized by a lattice constant and by a lattice orientation. In similar manner, accommodating buffer layer 24 is also a monocrystalline material and the lattice of that monocrystalline material is characterized by a lattice constant and a crystal orientation. The lattice constants of the accommodating buffer layer and the monocrystalline substrate must be closely matched or, alternatively, must be such that upon rotation of one crystal orientation with respect to the other crystal orientation, a substantial match in lattice constants is achieved. In this context the terms “substantially equal” and “substantially matched” mean that there is sufficient similarity between the lattice constants to permit the growth of a high quality crystalline layer on the underlying layer.



FIG. 4 illustrates graphically the relationship of the achievable thickness of a grown crystal layer of high crystalline quality as a function of the mismatch between the lattice constants of the host crystal and the grown crystal. Curve 42 illustrates the boundary of high crystalline quality material. The area to the right of curve 42 represents layers that has a large number of defects. With no lattice mismatch, it is theoretically possible to grow an infinitely thick, high quality epitaxial layer on the host crystal. As the mismatch in lattice constants increases, the thickness of achievable, high quality crystalline layer decreases rapidly. As a reference point, for example, if the lattice constants between the host crystal and the grown layer are mismatched by more than about 2%, monocrystalline epitaxial layers in excess of about 20 nm cannot be achieved.


In accordance with one embodiment of the invention, substrate 22 is a (100) or (111) oriented monocrystalline silicon wafer and accommodating buffer layer 24 is a layer of strontium barium titanate. Substantial matching of lattice constants between these two materials is achieved by rotating the crystal orientation of the titanate material by 45° with respect to the crystal orientation of the silicon substrate wafer. The inclusion in the structure of amorphous interface layer 28, a silicon oxide layer in this example, if it is of sufficient thickness, serves to reduce strain in the titanate monocrystalline layer that might result from any mismatch in the lattice constants of the host silicon wafer and the grown titanate layer. As a result, in accordance with an embodiment of the invention, a high quality, thick, monocrystalline titanate layer is achievable.


Still referring to FIGS. 1–3, layer 26 is a layer of epitaxially grown monocrystalline material and that crystalline material is also characterized by a crystal lattice constant and a crystal orientation. In accordance with one embodiment of the invention, the lattice constant of layer 26 differs from the lattice constant of substrate 22. To achieve high crystalline quality in this epitaxially grown monocrystalline layer, the accommodating buffer layer must be of high crystalline quality. In addition, in order to achieve high crystalline quality in layer 26, substantial matching between the crystal lattice constant of the host crystal, in this case, the monocrystalline accommodating buffer layer, and the grown crystal is desired. With properly selected materials this substantial matching of lattice constants is achieved as a result of rotation of the crystal orientation of the grown crystal with respect to the orientation of the host crystal. If the grown crystal is gallium arsenide, aluminum gallium arsenide, zinc selenide, or zinc sulfur selenide and the accommodating buffer layer is monocrystalline SrxBa1-xTiO3, substantial matching of crystal lattice constants of the two materials is achieved, wherein the crystal orientation of the grown layer is rotated by 45° with respect to the orientation of the host monocrystalline oxide. Similarly, if the host material is a strontium or barium zirconate or a strontium or barium hafnate or barium tin oxide and the compound semiconductor layer is indium phosphide or gallium indium arsenide or aluminum indium arsenide, substantial matching of crystal lattice constants can be achieved by rotating the orientation of the grown crystal layer by 45° with respect to the host oxide crystal. In some instances, a crystalline semiconductor buffer layer between the host oxide and the grown compound semiconductor layer can be used to reduce strain in the grown monocrystalline compound semiconductor layer that might result from small differences in lattice constants. Better crystalline quality in the grown monocrystalline compound semiconductor layer can thereby be achieved.


The following example illustrates a process, in accordance with one embodiment of the invention, for fabricating a semiconductor structure such as the structures depicted in FIGS. 1–3. The process starts by providing a monocrystalline semiconductor substrate comprising silicon or germanium. In accordance with a preferred embodiment of the invention, the semiconductor substrate is a silicon wafer having a (100) orientation. The substrate is preferably oriented on axis or, at most, about 0.5° off axis. At least a portion of the semiconductor substrate has a bare surface, although other portions of the substrate, as described below, may encompass other structures. The term “bare” in this context means that the surface in the portion of the substrate has been cleaned to remove any oxides, contaminants, or other foreign material. As is well known, bare silicon is highly reactive and readily forms a native oxide. The term “bare” is intended to encompass such a native oxide. A thin silicon oxide may also be intentionally grown on the semiconductor substrate, although such a grown oxide is not essential to the process in accordance with the invention. In order to epitaxially grow a monocrystalline oxide layer overlying the monocrystalline substrate, the native oxide layer must first be removed to expose the crystalline structure of the underlying substrate. The following process is preferably carried out by molecular beam epitaxy (MBE), although other epitaxial processes may also be used in accordance with the present invention. The native oxide can be removed by first thermally depositing a thin layer of strontium, barium, a combination of strontium and barium, or other alkali earth metals or combinations of alkali earth metals in an MBE apparatus. In the case where strontium is used, the substrate is then heated to a temperature of about 750° C. to cause the strontium to react with the native silicon oxide layer. The strontium serves to reduce the silicon oxide to leave a silicon oxide-free surface. The resultant surface, which exhibits an ordered 2×1 structure, includes strontium, oxygen, and silicon. The ordered 2×1 structure forms a template for the ordered growth of an overlying layer of a monocrystalline oxide. The template provides the necessary chemical and physical properties to nucleate the crystalline growth of an overlying layer.


In accordance with an alternate embodiment of the invention, the native silicon oxide can be converted and the substrate surface can be prepared for the growth of a monocrystalline oxide layer by depositing an alkali earth metal oxide, such as strontium oxide, strontium barium oxide, or barium oxide, onto the substrate surface by MBE at a low temperature and by subsequently heating the structure to a temperature of about 750° C. At this temperature a solid state reaction takes place between the strontium oxide and the native silicon oxide causing the reduction of the native silicon oxide and leaving an ordered 2×1 structure with strontium, oxygen, and silicon remaining on the substrate surface. Again, this forms a template for the subsequent growth of an ordered monocrystalline oxide layer.


Following the removal of the silicon oxide from the surface of the substrate, in accordance with one embodiment of the invention, the substrate is cooled to a temperature in the range of about 200–800° C. and a layer of strontium titanate is grown on the template layer by molecular beam epitaxy. The MBE process is initiated by opening shutters in the MBE apparatus to expose strontium, titanium and oxygen sources. The ratio of strontium and titanium is approximately 1:1. The partial pressure of oxygen is initially set at a minimum value to grow stoichiometric strontium titanate at a growth rate of about 0.3–0.5 nm per minute. After initiating growth of the strontium titanate, the partial pressure of oxygen is increased above the initial minimum value. The overpressure of oxygen causes the growth of an amorphous silicon oxide layer at the interface between the underlying substrate and the growing strontium titanate layer. The growth of the silicon oxide layer results from the diffusion of oxygen through the growing strontium titanate layer to the interface where the oxygen reacts with silicon at the surface of the underlying substrate. The strontium titanate grows as an ordered monocrystal with the crystalline orientation rotated by 45° with respect to the ordered 2×1 crystalline structure of the underlying substrate. Strain that otherwise might exist in the strontium titanate layer because of the small mismatch in lattice constant between the silicon substrate and the growing crystal is relieved in the amorphous silicon oxide intermediate layer.


After the strontium titanate layer has been grown to the desired thickness, the monocrystalline strontium titanate is capped by a template layer that is conducive to the subsequent growth of an epitaxial layer of a desired compound semiconductor material. For the subsequent growth of a layer of gallium arsenide, the MBE growth of the strontium titanate monocrystalline layer can be capped by terminating the growth with 1–2 monolayers of titanium, 1–2 monolayers of titanium-oxygen or with 1–2 monolayers of strontium-oxygen. Following the formation of this capping layer, arsenic is deposited to form a Ti—As bond, a Ti—O—As bond or a Sr—O—As. Any of these form an appropriate template for deposition and formation of a gallium arsenide monocrystalline layer. Following the formation of the template, gallium is subsequently introduced to the reaction with the arsenic and gallium arsenide forms. Alternatively, gallium can be deposited on the capping layer to form a Sr—O—Ga bond, and arsenic is subsequently introduced with the gallium to form the GaAs.



FIG. 5 is a high resolution Transmission Electron Micrograph (TEM) of semiconductor material manufactured in accordance with the present invention. Single crystal SrTiO3 accommodating buffer layer 24 was grown epitaxially on silicon substrate 22. During this growth process, amorphous interfacial layer 28 is formed which relieves strain due to lattice mismatch. GaAs compound semiconductor layer 26 was then grown epitaxially using template layer 30.



FIG. 6 illustrates an x-ray diffraction spectrum taken on structure including GaAs compound semiconductor layer 26 grown on silicon substrate 22 using accommodating buffer layer 24. The peaks in the spectrum indicate that both the accommodating buffer layer 24 and GaAs compound semiconductor layer 26 are single crystal and (100) orientated.


The structure illustrated in FIG. 2 can be formed by the process discussed above with the addition of an additional buffer layer deposition step. The buffer layer is formed overlying the template layer before the deposition of the monocrystalline compound semiconductor layer. If the buffer layer is a compound semiconductor superlattice, such a superlattice can be deposited, by MBE for example, on the template described above. If instead the buffer layer is a layer of germanium, the process above is modified to cap the strontium titanate monocrystalline layer with a final layer of either strontium or titanium and then by depositing germanium to react with the strontium or titanium. The germanium buffer layer can then be deposited directly on this template.


Structure 34, illustrated in FIG. 3, may be formed by growing an accommodating buffer layer, forming an amorphous oxide layer over substrate 22, and growing semiconductor layer 38 over the accommodating buffer layer, as described above. The accommodating buffer layer and the amorphous oxide layer are then exposed to an anneal process sufficient to change the crystalline structure of the accommodating buffer layer from monocrystalline to amorphous, thereby forming an amorphous layer such that the combination of the amorphous oxide layer and the now amorphous accommodating buffer layer form a single amorphous oxide layer 36. Layer 26 is then subsequently grown over layer 38. Alternatively, the anneal process may be carried out subsequent to growth of layer 26.


In accordance with one aspect of this embodiment, layer 36 is formed by exposing substrate 22, the accommodating buffer layer, the amorphous oxide layer, and semiconductor layer 38 to a rapid thermal anneal process with a peak temperature of about 700° C. to about 1000° C. and a process time of about 10 seconds to about 10 minutes. However, other suitable anneal processes may be employed to convert the accommodating buffer layer to an amorphous layer in accordance with the present invention. For example, laser annealing or “conventional” thermal annealing processes (in the proper environment) may be used to form layer 36. When conventional thermal annealing is employed to form layer 36, an overpressure of one or more constituents of layer 30 may be required to prevent degradation of layer 38 during the anneal process. For example, when layer 38 includes GaAs, the anneal environment preferably includes an overpressure of arsenic to mitigate degradation of layer 38.


As noted above, layer 38 of structure 34 may include any materials suitable for either of layers 32 or 26. Accordingly, any deposition or growth methods described in connection with either layer 32 or 26 may be employed to deposit layer 38.



FIG. 7 is a high resolution Transmission Electron Micrograph (TEM) of semiconductor material manufactured in accordance with the embodiment of the invention illustrated in FIG. 3. In accordance with this embodiment, a single crystal SrTiO3 accommodating buffer layer was grown epitaxially on silicon substrate 22. During this growth process, an amorphous interfacial layer forms as described above. Next, GaAs layer 38 is formed above the accommodating buffer layer and the accommodating buffer layer is exposed to an anneal process to form amorphous oxide layer 36.



FIG. 8 illustrates an x-ray diffraction spectrum taken on a structure including GaAs compound semiconductor layer 38 and amorphous oxide layer 36 formed on silicon substrate 22. The peaks in the spectrum indicate that GaAs compound semiconductor layer 38 is single crystal and (100) orientated and the lack of peaks around 40 to 50 degrees indicates that layer 36 is amorphous.


The process described above illustrates a process for forming a semiconductor structure including a silicon substrate, an overlying oxide layer, and a monocrystalline gallium arsenide compound semiconductor layer by the process of molecular beam epitaxy. The process can also be carried out by the process of chemical vapor deposition (CVD), metal organic chemical vapor deposition (MOCVD), migration enhanced epitaxy (MEE), atomic layer epitaxy (ALE), physical vapor deposition (PVD), chemical solution deposition (CSD), pulsed laser deposition (PLD), or the like. Further, by a similar process, other monocrystalline accommodating buffer layers such as alkaline earth metal titanates, zirconates, hafnates, tantalates, vanadates, ruthenates, and niobates, perovskite oxides such as alkaline earth metal tin-based perovskites, lanthanum aluminate, lanthanum scandium oxide, and gadolinium oxide can also be grown. Further, by a similar process such as MBE, other III–V and II–VI monocrystalline compound semiconductor layers can be deposited overlying the monocrystalline oxide accommodating buffer layer.


Each of the variations of compound semiconductor materials and monocrystalline oxide accommodating buffer layer uses an appropriate template for initiating the growth of the compound semiconductor layer. For example, if the accommodating buffer layer is an alkaline earth metal zirconate, the oxide can be capped by a thin layer of zirconium. The deposition of zirconium can be followed by the deposition of arsenic or phosphorus to react with the zirconium as a precursor to depositing indium gallium arsenide, indium aluminum arsenide, or indium phosphide respectively. Similarly, if the monocrystalline oxide accommodating buffer layer is an alkaline earth metal hafnate, the oxide layer can be capped by a thin layer of hafnium. The deposition of hafnium is followed by the deposition of arsenic or phosphorous to react with the hafnium as a precursor to the growth of an indium gallium arsenide, indium aluminum arsenide, or indium phosphide layer, respectively. In a similar manner, strontium titanate can be capped with a layer of strontium or strontium and oxygen and barium titanate can be capped with a layer of barium or barium and oxygen. Each of these depositions can be followed by the deposition of arsenic or phosphorus to react with the capping material to form a template for the deposition of a compound semiconductor material layer comprising indium gallium arsenide, indium aluminum arsenide, or indium phosphide.



FIG. 9 illustrates schematically, in cross section, a device structure 900 in accordance with a further embodiment of the invention. Device structure 900 includes a monocrystalline semiconductor substrate 901, preferably a monocrystalline silicon wafer. Monocrystalline semiconductor substrate 901 includes two regions, 902 and 903. An electrical semiconductor component generally indicated by the dashed line 909 is formed in region 902. Electrical component 909 can be a resistor, a capacitor, an active semiconductor component such as a diode or a transistor or an integrated circuit such as a MOS integrated circuit. For example, electrical component 909 can be a MOS circuit configured to perform digital signal processing or another function for which silicon integrated circuits are well suited. The electrical semiconductor component in region 902 can be formed by conventional semiconductor processing as well known and widely practiced in the semiconductor industry. A layer of insulating material 904 such as a layer of silicon dioxide or the like may overlie electrical semiconductor component 909.


Insulating material 904 and any other layers that may have been formed or deposited during the processing of semiconductor component 909 in region 902 are removed from the surface of region 903 to provide a bare substrate surface in that region, for example, a bare silicon surface. As is well known, bare silicon surfaces are highly reactive and a native silicon oxide layer can quickly form on the bare surface. A layer of barium or barium and oxygen may be deposited onto the native oxide layer on the surface of region 903 and then reacted with the oxidized surface to form a first template layer (not shown). In accordance with one embodiment of the invention, a monocrystalline oxide layer 906 is formed overlying the template layer by a process of molecular beam epitaxy. In one aspect of this exemplary embodiment, reactants including barium, titanium, and oxygen are deposited onto the template layer to form the monocrystalline oxide layer. Initially during the deposition, the partial pressure of oxygen is kept near the minimum necessary to fully react with the barium and titanium to form a monocrystalline barium titanate layer 906. The partial pressure of oxygen is then increased to provide an overpressure of oxygen and to allow oxygen to diffuse through the growing monocrystalline oxide layer. The oxygen diffusing through the barium titanate reacts with silicon at the surface of region 903 to form an amorphous layer 905 is silicon oxide on the second region and at the interface between the silicon substrate and the monocrystalline oxide.


In accordance with an embodiment of the invention, the step of depositing the monocrystalline oxide layer 906 is followed by depositing a second template layer (not shown), which can be 1–10 monolayers of titanium, barium, strontium, barium and oxygen, titanium and oxygen, or strontium and oxygen. A buffer layer 907 of a monocrystalline semiconductor material is then deposited overlying the second template layer by a process of molecular beam epitaxy. The deposition of buffer layer 907 may be initiated, for example, by depositing a layer of arsenic onto the template. This initial step is then followed by depositing gallium and arsenic to form monocrystalline gallium arsenide. Alternatively, strontium may be substituted for barium in the above example. Further, layer 907 may comprise any suitable monocrystalline semiconductor material, as described herein.


In accordance with one aspect of the present embodiment, after monocrystalline oxide layer 906 formation, the monocrystalline titanate layer and the silicon oxide layer, which is interposed between substrate 901 and the titanate layer, are exposed to an anneal process such that the titanate and oxide layers form an amorphous oxide layer 905. An additional compound semiconductor layer 908 is then epitaxially grown over layer 907, using the techniques described above in connection with layer 907. Alternatively, the above-described anneal process can be performed after formation of additional compound semiconductor layer 908.


In accordance with a further embodiment of the invention, a semiconductor component, generally indicated by a dashed line 910, is formed in compound semiconductor layer 908. Semiconductor component 910 can be formed by processing steps conventionally used in the fabrication of gallium arsenide or other III–V compound semiconductor material devices. Semiconductor component 910 may be any active or passive component, and preferably is a tunneling diode, light emitting diode, semiconductor laser, photodetector, heterojunction bipolar transistor (HBT), high frequency MESFET, or other component that utilizes and takes advantage of the physical properties of compound semiconductor materials. A metallic conductor schematically indicated by the line 911 can be formed to electrically couple device 910 and device 909, thus implementing an integrated device that includes at least one component formed in the silicon substrate and one device formed in the monocrystalline semiconductor material layer. Although illustrative structure 900 has been described as a structure formed on a silicon substrate 901 and having a barium (or strontium) titanate layer 906 and a gallium arsenide layer 908, similar devices can be fabricated using other monocrystalline substrates, monocrystalline oxide layers and other monocrystalline compound semiconductor layers as described elsewhere in this disclosure.



FIG. 10 illustrates a semiconductor structure 1000 in accordance with a further embodiment of the invention. In this embodiment, structure 1000 is a resonant interband tunnel diode formed of monocrystalline epitaxial layers of compound semiconductor material on a monocrystalline silicon substrate. Structure 1000 includes a monocrystalline semiconductor substrate 1001, such as a monocrystalline silicon wafer. An amorphous oxide layer 1002 is preferably formed overlying substrate 1001, in accordance with the process described above. An accommodating buffer layer 1003 is formed overlying substrate 1001 and amorphous oxide layer 1002. As described above, amorphous oxide layer 1002 may be grown at the interface between substrate 1001 and the growing accommodating buffer layer 1003 by the oxidation of substrate 1001 during the growing of layer 1003. Accommodating buffer layer 1003 is preferably a monocrystalline oxide or nitride material selected for its crystalline compatibility with the underlying substrate and with the overlying compound semiconductor material. In this embodiment, wherein substrate 1001 is monocrystalline silicon and the overlying compound semiconductor material layer is monocrystalline GaAs, layer 1003 may comprise, for example, an alkali earth metal titanate such as barium titanate or strontium titanate.


An additional buffer layer 1004 is preferably formed overlying layer 1003 to alleviate any strains that might result from a mismatch of the crystal lattice of accommodating buffer layer 1003 and the lattice of the monocrystalline semiconductor material layer. In this exemplary embodiment, buffer layer 1004 is a layer of GaAs and can have a thickness of about 500 to about 2000 nanometers (nm) and preferably a thickness of about 500 to about 1000 nm. The thickness generally depends on the application for which the layer is being prepared. To facilitate the epitaxial growth of the gallium arsenide on the monocrystalline oxide, a template layer (not shown) may be formed by capping the oxide layer. The template layer is preferably 1–10 monolayers of Ti—As, Sr—O—As, Sr—Ga—O, or Sr—Al—O.


In accordance with this embodiment of the invention, carrier supply layer 1005 is a layer of n+ doped GaAs having a thickness of about 500 nanometers (nm). A first quantum well layer 1006, a barrier layer 1007, and a second quantum well layer 1008 are epitaxially grown, in succession, on carrier supply layer 1005. In accordance with this embodiment of the invention, quantum well layers 1006 and 1008 are layers of indium gallium arsenide (InGaAs) having a thickness of about 4 to about 5 nanometers (nm). Barrier layer 1007 is a layer of GaAs having a thickness of about 2 to about 4 nanometers (nm). Quantum well layers 1006, 1008 and barrier layer 1007 are not intentionally doped. After formation of layers 1006, 1007, and 1008, a second carrier supply layer 1009 is grown on second quantum well layer 1008. In accordance with this embodiment of the invention, carrier supply layer 1009 is a layer of p+ doped GaAs having a thickness of about 50 nanometers (nm).



FIG. 11 illustrates a semiconductor structure 1100 in accordance with a further embodiment of the invention. In this embodiment, structure 1100 is a resonant interband tunnel diode formed of monocrystalline epitaxial layers of compound semiconductor material on a monocrystalline silicon substrate. Structure 1100 includes a monocrystalline semiconductor substrate 1101, such as a monocrystalline silicon wafer. An amorphous oxide layer 1102 is preferably formed overlying substrate 1101, in accordance with the process described above. An accommodating buffer layer 1103 is formed overlying substrate 1101 and amorphous oxide layer 1102. As described above, amorphous oxide layer 1102 may be grown at the interface between substrate 1101 and the growing accommodating buffer layer 1103 by the oxidation of substrate 1101 during the growing of layer 1103. Accommodating buffer layer 1103 is preferably a monocrystalline oxide or nitride material selected for its crystalline compatibility with the underlying substrate and with the overlying compound semiconductor material. In this embodiment, wherein substrate 1101 is monocrystalline silicon and the overlying compound semiconductor material layer is monocrystalline InP, layer 1103 may comprise, for example, an alkali earth metal zirconate such as strontium zirconate or barium zirconate, or an alkali earth metal hafnate such as strontium hafnate or barium hafnate.


An additional buffer layer 1104 is preferably formed overlying layer 1103 to alleviate any strains that might result from a mismatch of the crystal lattice of accommodating buffer layer 1103 and the lattice of the monocrystalline semiconductor material layer. In this exemplary embodiment, buffer layer 1104 is a layer of InP or indium aluminum arsenide (InAlAs) and can have a thickness of about 50 nanometers (nm). To facilitate the epitaxial growth of the InP or InAlAs on the monocrystalline oxide, a template layer (not shown) may be formed by capping the oxide layer. The template layer may be 1–10 monolayers of Zr—As, Hf—As, Zr—P, Hf—P, Sr—O—As, Sr—O—P, Ba—O—As, Ba—O—P, or In—Sr—O. For example, where layer 1103 is barium zirconate, the template layer may be 1–2 monolayers of zirconium followed by deposition of 1–2 monolayers of arsenic to form a Zr—As template.


In accordance with this embodiment of the invention, a first carrier supply layer having first and second layers 1105 and 1106 of doped monocrystalline semiconductor material is formed overlying buffer layer 1104. Layers 1105 and 1106 are n+ doped InGaAs having a thickness of about 50 to about 100 nanometers (nm) and n+ doped InAlAs having a thickness of about 50 to about 100 nm, respectively. If tunnel diode structure 1100 is later electrically coupled to a second semiconductor device, layer 1105 may serve as a contact layer for the electrical interconnects.


A first quantum well layer 1107, a barrier layer 1108, and a second quantum well layer 1109 are epitaxially grown, in succession, on carrier supply layer 1106. In accordance with this embodiment of the invention, quantum well layers 1107 and 1109 are layers of InGaAs having a thickness of about 4 nm. Barrier layer 1108 is a layer of InAlAs having a thickness of about 2 nm. Quantum well layers 1107, 1109 and barrier layer 1108 are not intentionally doped. After formation of layers 1107, 1108 and 1109, a second carrier supply layer having first and second layers 1110 and 1111 of doped monocrystalline semiconductor material is grown on second quantum well layer 1109. Layers 1110 and 1111 are p+ doped InAlAs having a thickness of about 50 to about 100 nanometers (nm) followed by a p+ doped InGaAs layer having a thickness of about 50 to about 100 nm. If tunnel diode structure 1100 is later electrically coupled to a second semiconductor device, layer 1111 may serve as a contact layer for the electrical interconnects.



FIG. 12 illustrates a semiconductor structure 1200 in accordance with a further embodiment of the invention. In this embodiment, structure 1200 is a resonant intraband tunnel diode formed of monocrystalline epitaxial layers of compound semiconductor material on a monocrystalline silicon substrate. Structure 1200 includes a monocrystalline semiconductor substrate 1201, such as a monocrystalline silicon wafer. An amorphous oxide layer 1202 is preferably formed overlying substrate 1201, in accordance with the process described above. An accommodating buffer layer 1203 is formed overlying substrate 1201 and amorphous oxide layer 1202. As described above, amorphous oxide layer 1202 may be grown at the interface between substrate 1201 and the growing accommodating buffer layer 1203 by the oxidation of substrate 1201 during the growing of layer 1203. Accommodating buffer layer 1203 is preferably a monocrystalline oxide or nitride material selected for its crystalline compatibility with the underlying substrate and with the overlying compound semiconductor material. In this embodiment, wherein substrate 1201 is monocrystalline silicon and the overlying compound semiconductor material layer is monocrystalline GaAs, layer 1203 may comprise, for example, an alkali earth metal titanate such as barium titanate or strontium titanate.


An additional buffer layer 1204 is preferably formed overlying layer 1203 to alleviate any strains that might result from a mismatch of the crystal lattice of accommodating buffer layer 1203 and the lattice of the monocrystalline semiconductor material layer. In this exemplary embodiment, buffer layer 1204 is a layer of GaAs and can have a thickness of about 500 to about 2000 of about 50 to about 100 nanometers (nm) and preferably a thickness of about 500 to about 1000 nm. To facilitate the epitaxial growth of the gallium arsenide on the monocrystalline oxide, a template layer (not shown) may be formed by capping the oxide layer. The template layer is preferably 1–10 monolayers of Ti—As, Sr—O—As, Sr—Ga—O, or Sr—Al—O.


In accordance with a preferred embodiment of the invention, a first contact layer 1205 is formed on buffer layer 1204 and comprises a layer of n+ doped GaAs having a thickness of about 50 nm. A collection layer 1206 is then formed overlying contact layer 1205, and comprises a layer of n− doped GaAs having a thickness of about 50 nm.


Following formation of collection layer 1206, a first tunnel barrier layer 1207, a quantum well layer 1208, and a second tunnel barrier layer 1209 are epitaxially grown, in succession, on the collection layer. In accordance with this embodiment of the invention, tunnel barrier layers 1207 and 1209 are layers of aluminum gallium arsenide (AlGaAs) or aluminum arsenide (AlAs) having a thickness of about 5 nm. Quantum well layer 1208 is a layer of GaAs having a thickness of about 5 nm. Quantum well layer 1208 and tunnel barrier layers 1207 and 1209 are not intentionally doped. After formation of layers 1207, 1208, and 1209, an injection layer 1210 is grown on second tunnel barrier layer 1209. In accordance with this embodiment of the invention, injection layer 1210 is a spacer layer of n doped GaAs having a thickness of about 50 nm. In accordance with a preferred embodiment of the invention, a second contact layer 1211 is formed on injection layer 1210 and comprises a layer of n+ doped GaAs having a thickness of about 50 nm.



FIG. 13 illustrates a semiconductor structure 1300 in accordance with a further embodiment of the invention. In this embodiment, structure 1300 is a resonant intraband tunnel diode formed of monocrystalline epitaxial layers of compound semiconductor material on a monocrystalline silicon substrate. Structure 1300 includes a monocrystalline semiconductor substrate 1301, such as a monocrystalline silicon wafer. An amorphous oxide layer 1302 is preferably formed overlying substrate 1301, in accordance with the process described above. An accommodating buffer layer 1303 is formed overlying substrate 1301 and amorphous oxide layer 1302. As described above, amorphous oxide layer 1302 may be grown at the interface between substrate 1301 and the growing accommodating buffer layer 1303 by the oxidation of substrate 1301 during the growing of layer 1303. Accommodating buffer layer 1303 is preferably a monocrystalline oxide or nitride material selected for its crystalline compatibility with the underlying substrate and with the overlying compound semiconductor material. In this embodiment, wherein substrate 1301 is monocrystalline silicon and the overlying compound semiconductor material layer is monocrystalline InP, layer 1303 may comprise, for example, an alkali earth metal zirconate such as strontium zirconate or barium zirconate, or an alkali earth metal hafnate such as strontium hafnate or barium hafnate.


An additional buffer layer 1304 is preferably formed overlying layer 1303 to alleviate any strains that might result from a mismatch of the crystal lattice of accommodating buffer layer 1303 and the lattice of the monocrystalline semiconductor material layer. In this exemplary embodiment, buffer layer 1304 is a layer of InP or InAlAs and can have a thickness of about 500 to about 2000 nanometers (nm) and preferably a thickness of about 500 to about 1000 nm. To facilitate the epitaxial growth of the InP or InAlAs on the monocrystalline oxide, a template layer (not shown) may be formed by capping the oxide layer. The template layer may be 1–10 monolayers of Zr—As, Hf—As, Zr—P, Hf—P, Sr—O—As, Sr—O—P, Ba—O—As, Ba—O—P, or In—Sr—O. For example, where layer 1303 is barium zirconate, the template layer may be 1–2 monolayers of zirconium followed by deposition of 1–2 monolayers of arsenic to form a Zr—As template.


In accordance with a preferred embodiment of the invention, a first contact layer 1305 is formed on buffer layer 1304 and comprises a layer of n+ doped InGaAs having a thickness of about 50 nm. A spacer layer 1306 is then formed overlying contact layer 1305, and comprises a layer of InGaAs having a thickness of about 50 nm.


Following formation of spacer layer 1306, a first tunnel barrier layer 1307, a quantum well layer 1308, and a second tunnel barrier layer 1309 are epitaxially grown, in succession, on the spacer layer. In accordance with this embodiment of the invention, tunnel barrier layers 1307 and 1309 are layers of AlAs or InAlAs having a thickness of about 5 nm. Quantum well layer 1308 is a layer of InGaAs having a thickness of about 5 nm. Quantum well layer 1308 and tunnel barrier layers 1307 and 1309 are not intentionally doped. After formation of layers 1307, 1308, and 1309, a spacer layer 1310 is grown on second tunnel barrier layer 1309. In accordance with this embodiment of the invention, spacer layer 1310 is a layer of n− InGaAs having a thickness of about 5 nm. Preferably, injection layer 1310 is not intentionally doped. In accordance with a preferred embodiment of the invention, a contact layer 1311 is formed overlying injection layer 1310 and comprises n+ doped InGaAs having a thickness of about 50 nm.


Referring now to FIG. 14, a monolithic integrated circuit is provided in accordance with one embodiment of the present invention. Monolithic integrated circuit 1400 generally includes a MOS circuit 1401 electrically coupled to a tunnel diode. In FIG. 14, for illustration purposes only, and without limitation, MOS circuit 1401 is electrically coupled to an intraband tunnel diode 1300, such as that exhibited in FIG. 13. Composite layers 1302 through 1311, as presented in FIG. 14, are identical to those illustrated and described above with reference to FIG. 13. In this embodiment, semiconductor substrate 1301 is a monocrystalline silicon substrate, such as a silicon wafer.


In accordance with the present embodiment of the invention, MOS circuit 1401 is first formed in semiconductor substrate 1301 using conventional processing steps and techniques well known to those skilled in the art. MOS circuit 1401 generally comprises a gate electrode 1402, a gate dielectric layer 1403, and n+ doped regions 1404. Gate dielectric layer 1403 is formed over a portion of substrate 1301, and gate electrode 1402 is then formed over gate dielectric layer 1403. Selective n-type doping is performed to form n+ doped regions 1404 within substrate 1301 along adjacent sides of gate electrode 1402 and are source, drain, or source/drain regions for the MOS transistor. The n+ doped regions 1404 have a doping concentration of at least about 1E19 atoms per cubic centimeter to allow one or more ohmic contacts to be formed. In this embodiment, n+ doped region 1404 is a drain region for the MOS transistor. After formation of MOS portion 1401 of the integrated circuit, all of the layers formed during processing are removed from the surface of substrate 1301 in the region where tunnel diode 1300 will be formed. A bare silicon surface is thus provided for the subsequent processing of tunnel diode 1300, for example in the manner set forth above.


After formation of both MOS circuit 1401 and tunnel diode 1300 on substrate 1301, processing continues to form a substantially completed integrated circuit 1400. Ohmic contacts 1405 and 1406 may be formed on drain region 1404 and contact layer 1312, respectively, using standard processing techniques well known in the art. An insulating layer 1408 is formed over substrate 1301, MOS circuit 1401, and tunnel diode 1300. Portions of insulating layer 1408 are then removed to define contact openings where the devices are to be interconnected. Interconnect trenches are formed within insulating layer 1408 to provide the lateral connections between the contacts. As illustrated in FIG. 14, interconnect 1407 connects a drain region of the MOS circuit to the uppermost contact layer 1312 of tunnel diode 1300. A passivation layer 1409 is formed over the interconnect 1407 and insulating layer 1408. Other electrical connections may be made to the devices and/or other electrical or electronic components within the integrated circuit 1400 but not illustrated in the figure according to conventional techniques available to those skilled in the art.


Referring now to FIG. 15, a monolithic integrated circuit is provided in accordance with one embodiment of the present invention. Monolithic integrated circuit 1500 generally includes a MOS circuit 1401 electrically coupled in series to first and second tunnel diodes. In FIG. 15, for illustration purposes only, and without limitation, MOS circuit 1401 is electrically coupled to first and second intraband tunnel diodes 1200 and 1501 of the type illustrated and described with reference to FIG. 12. Composite layers 1202 through 1210, as presented in FIG. 15, are identical to those illustrated and described above with reference to FIG. 12. In this embodiment, semiconductor substrate 1201 is a monocrystalline silicon substrate, such as a silicon wafer.


In accordance with the present embodiment of the invention, MOS circuit 1401 is first formed in semiconductor substrate 1301 using conventional processing steps and techniques well known to those skilled in the art, in accordance with the above description in reference to FIG. 14. First tunnel diode 1200 is formed in accordance with FIG. 12 and its accompanying description, except that second contact layer 1211 is omitted, leaving injection layer 1210 as the top layer of first tunnel diode 1200.


Second tunnel diode 1501 is formed overlying injection layer 1210 of first tunnel diode 1200, beginning with formation of a collection layer 1506. In the present embodiment of the invention, collection layer 1506 is a layer of n-doped GaAs. Following formation of collection layer 1506, a first tunnel barrier layer 1507, a quantum well layer 1508, and a second tunnel barrier layer 1509 are grown, in succession, on the collection layer. In accordance with this embodiment of the invention, tunnel barrier layers 1507 and 1509 are layers of AlGaAs or AlAs. Quantum well layer 1508 is a layer of GaAs. Quantum well layer 1508 and tunnel barrier layers 1507 and 1509 are not intentionally doped. After formation of layers 1507, 1508, and 1509, a spacer layer 1510 comprising n doped GaAs is grown on second tunnel barrier layer 1509. Finally, a contact layer 1511 is formed on spacer layer 1510 and comprises a layer of n+ doped GaAs.


As detailed with reference to FIG. 14, after formation of both MOS circuit 1401 and tunnel diodes. 1200 and 1501 on substrate 1301, processing continues to form a substantially completed integrated circuit 1500. Ohmic contacts 1405 and 1406 may be formed on drain region 1404 and contact layer 1512, respectively. An insulating layer 1408 is formed over substrate 1301, MOS circuit 1401, and tunnel diodes 1200 and 1501. Portions of insulating layer 1408 are then removed to define contact openings where the devices are to be interconnected. Interconnect trenches are formed within insulating layer 1408 to provide the lateral connections between the contacts. As illustrated in FIG. 15, interconnect 1407 connects a drain region of the MOS circuit to the uppermost contact layer 1512 of tunnel diode 1501. A passivation layer 1409 is formed over the interconnect 1407 and insulating layer 1408. Other electrical connections may be made to the devices and/or other electrical or electronic components within the integrated circuit 1500 (not illustrated in the figure) according to conventional techniques available to those skilled in the art.


Referring now to FIG. 16, a monolithic integrated circuit is provided in accordance with one embodiment of the present invention. Monolithic integrated circuit 1600 generally includes a MOS circuit 1401 having a drain region 1604 and a tunnel diode 1300 formed overlying and electrically coupled to the drain region. In FIG. 16, for illustration purposes only, and without limitation, MOS circuit 1401 is electrically coupled to an intraband tunnel diode 1300 of the type illustrated and described with reference to FIG. 13. Composite layers 1303 through 1311, as presented in FIG. 16, are identical to those illustrated and described above with reference to FIG. 13. In this embodiment, semiconductor substrate 1301 is a monocrystalline silicon substrate, such as a silicon wafer.


In this embodiment, no amorphous layer is formed between substrate 1301 and monocrystalline layer 1303. Rather, monocrystalline oxide layer 1303 is formed overlying drain region 1604 and is selectively doped to render the oxide electrically conductive. Intraband tunnel diode 1300 is then formed in accordance with the above description in electrical contact with the electrically conductive oxide of layer 1303.


In FIG. 17, a monolithic integrated circuit 1700 generally includes a MOS transistor having a gate electrode and a tunnel diode formed overlying and electrically coupled to the gate electrode. In FIG. 17, for illustration purposes only, and without limitation, an interband tunnel diode generally of the type illustrated and described with reference to FIG. 10 is formed overlying the gate electrode of the MOS transistor. In this embodiment, semiconductor substrate 1701 is a monocrystalline silicon substrate, such as a silicon wafer. N+ doped regions 1702 represent the source, drain, or source/drain regions of the MOS transistor, and are formed via ion implantation in substrate 1701.


An amorphous oxide layer 1709 is preferably formed overlying substrate 1701, in accordance with the process described above. In accordance with this embodiment of the present invention, a monocrystalline oxide layer 1703 is formed overlying amorphous layer 1709. Gate electrode 1704 is then formed overlying monocrystalline oxide layer 1703 in accordance with the above-described techniques. In this embodiment, gate electrode 1704 is a layer of n+ doped GaAs and can have a thickness of about 50 to about 500 nanometers (nm) and preferably a thickness of about 50 to about 100 nm.


A first quantum well layer 1705, a barrier layer 1706, and a second quantum well layer 1707 are grown, in succession, on gate electrode 1704. In accordance with this embodiment of the invention, quantum well layers 1705 and 1707 are InGaAs and barrier layer 1706 is GaAs, none of which are intentionally doped. After formation of layers 1705, 1706, and 1707, a p+ doped GaAs carrier supply layer 1708 is epitaxially grown on second quantum well layer 1707.


Clearly, these embodiments of integrated circuits having compound semiconductor portions and Group IV semiconductor portions are meant to illustrate embodiments of the present invention and do not limit the present invention. There are a multiplicity of other combinations of semiconductor devices and other embodiments of the present invention that come within the present disclosure. For example, the compound semiconductor portion may include light emitting diodes, photodetectors, diodes, or the like, and the Group IV semiconductor portions can include digital logic, memory arrays, and most structures that can be formed in conventional MOS integrated circuits. By using embodiments of the present invention, it is now simpler to integrate devices that work better in compound semiconductor materials with other components that work better or are easily and/or inexpensively formed within Group IV semiconductor materials. This allows the device size to decrease, the manufacturing costs to decrease, and yield and reliability to increase.


As contemplated in the above description, a monocrystalline Group IV wafer can also be used in forming only compound semiconductor electrical components over the wafer. In this manner, the wafer is essentially a “handle” wafer used during the fabrication of the compound semiconductor electrical components within a monocrystalline compound semiconductor layer overlying the wafer. Therefore, electrical components can be formed within II–V or II–IV semiconductor materials over a wafer of at least approximately 200 millimeters in diameter and possibly at least approximately 300 millimeters.


By the use of this type of substrate, a relatively inexpensive “handle” wafer overcomes the fragile nature of the compound semiconductor wafers by placing them over a relatively more durable and easy to fabricate base material. Therefore, an integrated circuit can be formed such that all electrical components, and particularly all active electronic devices, can be formed within the compound semiconductor material even though the substrate itself may include a Group IV semiconductor material Fabrication costs for compound semiconductor devices should decrease because larger substrates can be processed more economically and more readily compared to relatively smaller and more fragile conventional compound semiconductor wafers.


In the foregoing specification, the invention has been described with reference to specific embodiments. However, one of ordinary skill in the art appreciates that various modifications and changes can be made without departing from the scope of the present invention as set forth in the claims below. Accordingly, the specification and figures are to be regarded in an illustrative rather than a restrictive sense, and all such modifications are intended to be included within the scope of present invention. For example, use of Sb-based materials, such as indium antimonide (InSb), aluminum antimonide (AlSb), indium aluminum antimonide (InAlSb), gallium antimonide (GaSb), indium gallium antimonide (InGaSb), and aluminum gallium antimonide (InGaSb), is possible in accordance with the present invention. As those skilled in the art will appreciate, the present invention may be applicable to any heterojunction interband tunnel diode, resonant tunnel diode, or other tunnel diode structures in any III–V or compound semiconductor that can lattice-matched to silicon using a perovskite or other appropriate oxide.


Benefits, other advantages, and solutions to problems have been described above with regard to specific embodiments. However, the benefits, advantages, solutions to problems, and any element(s) that may cause any benefit, advantage, or solution to occur or become more pronounced are not to be construed as a critical, required, or essential features of elements of any or all the claims. As used herein, the terms “comprises,” “comprising,” or any other variation thereof, are intended to cover a non-exclusive inclusion, such that a process, method, article, or apparatus that comprises a list of elements does not expressly listed or inherent to such process, method, article, or apparatus.

Claims
  • 1. A monolithic integrated circuit comprising: an MOS circuit formed at least partially in a monocrystalline substrate;a monocrystalline compound semiconductor layer overlying the monocrystalline substrate; anda tunnel diode formed at least partially in the monocrystalline compound semiconductor layer, the tunnel diode electrically coupled to the MOS circuit.
  • 2. The monolithic integrated circuit of claim 1 wherein the MOS circuit comprises an MOS transistor having a drain region and the tunnel diode is electrically coupled to the drain region.
  • 3. The monolithic integrated circuit of claim 2 further comprising a second tunnel diode coupled to the drain region in series with the tunnel diode.
  • 4. The monolithic integrated circuit of claim 1 wherein the MOS circuit comprises an MOS transistor having a drain region and the tunnel diode is formed overlying and electrically coupled to the drain region.
  • 5. The monolithic integrated circuit of claim 1 wherein the MOS circuit comprises an MOS transistor having a gate electrode and the tunnel diode is formed overlying and electrically coupled to the gate electrode.
  • 6. The monolithic integrated circuit of claim 1 wherein the MOS circuit comprises a digital circuit.
  • 7. The monolithic integrated circuit of claim 1 wherein the tunnel diode comprises an interband tunnel diode.
  • 8. The monolithic integrated circuit of claim 1 wherein the tunnel diode comprises an intraband tunnel diode.
Parent Case Info

This application is a continuation of application Ser. No. 09/624,691 filed Jul. 24, 2000, now abandoned.

US Referenced Citations (587)
Number Name Date Kind
3617951 Anderson Nov 1971 A
3670213 Nakawaga et al. Jun 1972 A
3758199 Thaxter Sep 1973 A
3766370 Walther Oct 1973 A
3802967 Ladany et al. Apr 1974 A
3818451 Coleman Jun 1974 A
3914137 Huffman et al. Oct 1975 A
3935031 Adler Jan 1976 A
4006989 Andringa Feb 1977 A
4084130 Holton Apr 1978 A
4120588 Chaum Oct 1978 A
4146297 Alferness et al. Mar 1979 A
4174422 Matthews et al. Nov 1979 A
4174504 Chenausky et al. Nov 1979 A
4177094 Kroon Dec 1979 A
4242595 Lehovec Dec 1980 A
4284329 Smith et al. Aug 1981 A
4289920 Hovel Sep 1981 A
4297656 Pan Oct 1981 A
4298247 Michelet et al. Nov 1981 A
4378259 Hasegawa et al. Mar 1983 A
4392297 Little Jul 1983 A
4398342 Pitt et al. Aug 1983 A
4404265 Manasevit Sep 1983 A
4424589 Thomas et al. Jan 1984 A
4439014 Stacy et al. Mar 1984 A
4442590 Stockton et al. Apr 1984 A
4447116 King et al. May 1984 A
4452720 Harada et al. Jun 1984 A
4459325 Nozawa et al. Jul 1984 A
4482422 McGinn et al. Nov 1984 A
4482906 Hovel et al. Nov 1984 A
4484332 Hawrylo Nov 1984 A
4503540 Nakashima et al. Mar 1985 A
4523211 Morimoto et al. Jun 1985 A
4525871 Foyt et al. Jun 1985 A
4594000 Falk et al. Jun 1986 A
4626878 Kuwano et al. Dec 1986 A
4629821 Bronstein-Bonte et al. Dec 1986 A
4661176 Manasevit Apr 1987 A
4667088 Kramer May 1987 A
4667212 Nakamura May 1987 A
4681982 Yoshida Jul 1987 A
4695120 Holder Sep 1987 A
4723321 Saleh Feb 1988 A
4748485 Vasudev May 1988 A
4756007 Qureshi et al. Jul 1988 A
4772929 Manchester et al. Sep 1988 A
4773063 Hunsperger et al. Sep 1988 A
4774205 Choi et al. Sep 1988 A
4777613 Shahan et al. Oct 1988 A
4793872 Meunier et al. Dec 1988 A
4801184 Revelli Jan 1989 A
4802182 Thornton et al. Jan 1989 A
4804866 Akiyama Feb 1989 A
4815084 Scifres et al. Mar 1989 A
4841775 Ikeda et al. Jun 1989 A
4843609 Ohya et al. Jun 1989 A
4845044 Ariyoshi et al. Jul 1989 A
4846926 Kay et al. Jul 1989 A
4855249 Akasaki et al. Aug 1989 A
4866489 Yokogawa et al. Sep 1989 A
4868376 Lessin et al. Sep 1989 A
4872046 Morkoc et al. Oct 1989 A
4876208 Gustafson et al. Oct 1989 A
4876218 Pessa et al. Oct 1989 A
4876219 Eshita et al. Oct 1989 A
4882300 Inoue et al. Nov 1989 A
4885376 Verkade Dec 1989 A
4888202 Murakami et al. Dec 1989 A
4889402 Reinhart Dec 1989 A
4891091 Shastry Jan 1990 A
4896194 Suzuki Jan 1990 A
4901133 Curran et al. Feb 1990 A
4910164 Shichijo Mar 1990 A
4912087 Aslam et al. Mar 1990 A
4928154 Umeno et al. May 1990 A
4934777 Jou et al. Jun 1990 A
4952420 Walters Aug 1990 A
4959702 Moyer et al. Sep 1990 A
4963508 Umeno et al. Oct 1990 A
4963949 Wanlass et al. Oct 1990 A
4965649 Zanio et al. Oct 1990 A
4981714 Ohno et al. Jan 1991 A
4984043 Vinal Jan 1991 A
4999842 Huang et al. Mar 1991 A
5018816 Murray et al. May 1991 A
5028563 Feit et al. Jul 1991 A
5028976 Ozaki et al. Jul 1991 A
5051790 Hammer Sep 1991 A
5053835 Horikawa et al. Oct 1991 A
5055445 Belt et al. Oct 1991 A
5055835 Sutton Oct 1991 A
5057694 Idaka et al. Oct 1991 A
5060031 Abrokwah et al. Oct 1991 A
5063081 Cozzette et al. Nov 1991 A
5063166 Mooney et al. Nov 1991 A
5064781 Cambou et al. Nov 1991 A
5067809 Tsubota Nov 1991 A
5073981 Giles et al. Dec 1991 A
5075743 Behfar-Rad Dec 1991 A
5081062 Vasudev et al. Jan 1992 A
5081519 Nishimura et al. Jan 1992 A
5087829 Ishibashi et al. Feb 1992 A
5103494 Mozer Apr 1992 A
5116461 Lebby et al. May 1992 A
5119448 Schaefer et al. Jun 1992 A
5122679 Ishii et al. Jun 1992 A
5122852 Chan et al. Jun 1992 A
5127067 Delcoco et al. Jun 1992 A
5130762 Kulick Jul 1992 A
5132648 Trinh et al. Jul 1992 A
5140387 Okazaki et al. Aug 1992 A
5140651 Soref et al. Aug 1992 A
5141894 Bisaro et al. Aug 1992 A
5143854 Pirrung et al. Sep 1992 A
5144409 Ma Sep 1992 A
5148504 Levi et al. Sep 1992 A
5155658 Inam et al. Oct 1992 A
5159413 Calviello et al. Oct 1992 A
5163118 Lorenzo et al. Nov 1992 A
5166761 Olson et al. Nov 1992 A
5173474 Connell et al. Dec 1992 A
5173835 Cornett et al. Dec 1992 A
5181085 Moon et al. Jan 1993 A
5185589 Krishnaswamy et al. Feb 1993 A
5188976 Kume et al. Feb 1993 A
5191625 Gustavsson Mar 1993 A
5194397 Cook et al. Mar 1993 A
5194917 Regener Mar 1993 A
5198269 Swartz et al. Mar 1993 A
5208182 Narayan et al. May 1993 A
5210763 Lewis et al. May 1993 A
5216359 Makki et al. Jun 1993 A
5216729 Berger et al. Jun 1993 A
5221367 Chisholm et al. Jun 1993 A
5225031 McKee et al. Jul 1993 A
5227196 Itoh Jul 1993 A
5238877 Russell Aug 1993 A
5244818 Jokers et al. Sep 1993 A
5248564 Ramesh Sep 1993 A
5260394 Tazaki et al. Nov 1993 A
5262659 Grudkowski et al. Nov 1993 A
5266355 Wernberg et al. Nov 1993 A
5268327 Vernon Dec 1993 A
5270298 Ramesh Dec 1993 A
5280013 Newman et al. Jan 1994 A
5281834 Cambou et al. Jan 1994 A
5283462 Stengel Feb 1994 A
5286985 Taddiken Feb 1994 A
5293050 Chapple-Sokol et al. Mar 1994 A
5306649 Hebert Apr 1994 A
5310707 Oishi et al. May 1994 A
5312765 Kanber May 1994 A
5313058 Friederich et al. May 1994 A
5314547 Heremans et al. May 1994 A
5315128 Hunt et al. May 1994 A
5323023 Fork Jun 1994 A
5326721 Summerfelt Jul 1994 A
5334556 Guldi Aug 1994 A
5352926 Andrews Oct 1994 A
5356509 Terranova et al. Oct 1994 A
5356831 Calviello et al. Oct 1994 A
5357122 Okubora et al. Oct 1994 A
5358925 Neville Connell et al. Oct 1994 A
5362972 Yazawa et al. Nov 1994 A
5362998 Iwamura et al. Nov 1994 A
5365477 Cooper, Jr. et al. Nov 1994 A
5371621 Stevens Dec 1994 A
5371734 Fischer Dec 1994 A
5372992 Itozaki et al. Dec 1994 A
5373166 Buchan et al. Dec 1994 A
5387811 Saigoh Feb 1995 A
5391515 Kao et al. Feb 1995 A
5393352 Summerfelt Feb 1995 A
5394489 Koch Feb 1995 A
5395663 Tabata et al. Mar 1995 A
5397428 Stoner et al. Mar 1995 A
5399898 Rostoker Mar 1995 A
5404581 Honjo Apr 1995 A
5405802 Yamagata et al. Apr 1995 A
5406202 Mehrgardt et al. Apr 1995 A
5410622 Okada et al. Apr 1995 A
5418216 Fork May 1995 A
5418389 Watanabe May 1995 A
5420102 Harshavardhan et al. May 1995 A
5427988 Sengupta et al. Jun 1995 A
5430397 Itoh et al. Jul 1995 A
5436759 Dijaii et al. Jul 1995 A
5438584 Paoli et al. Aug 1995 A
5441577 Sasaki et al. Aug 1995 A
5442191 Ma Aug 1995 A
5442561 Yoshizawa et al. Aug 1995 A
5444016 Abrokwah et al. Aug 1995 A
5446719 Yoshida et al. Aug 1995 A
5450812 McKee et al. Sep 1995 A
5452118 Maruska Sep 1995 A
5453727 Shibasaki et al. Sep 1995 A
5466631 Ichikawa et al. Nov 1995 A
5473047 Shi Dec 1995 A
5473171 Summerfelt Dec 1995 A
5477363 Matsuda Dec 1995 A
5478653 Guenzer Dec 1995 A
5479033 Baca et al. Dec 1995 A
5479317 Ramesh Dec 1995 A
5480829 Abrokwah et al. Jan 1996 A
5481102 Hazelrigg, Jr. Jan 1996 A
5482003 McKee et al. Jan 1996 A
5484664 Kitahara et al. Jan 1996 A
5486406 Shi Jan 1996 A
5491461 Partin et al. Feb 1996 A
5492859 Sakaguchi et al. Feb 1996 A
5494711 Takeda et al. Feb 1996 A
5504035 Rostoker et al. Apr 1996 A
5504183 Shi Apr 1996 A
5508554 Takatani et al. Apr 1996 A
5510665 Conley Apr 1996 A
5511238 Bayraktaroglu Apr 1996 A
5512773 Wolf et al. Apr 1996 A
5514484 Nashimoto May 1996 A
5514904 Onga et al. May 1996 A
5515047 Yamakido et al. May 1996 A
5515810 Yamashita et al. May 1996 A
5516725 Chang et al. May 1996 A
5519235 Ramesh May 1996 A
5523602 Horiuchi et al. Jun 1996 A
5528057 Yanagase et al. Jun 1996 A
5528067 Farb et al. Jun 1996 A
5528209 Macdonald et al. Jun 1996 A
5528414 Oakley Jun 1996 A
5530235 Stefik et al. Jun 1996 A
5538941 Findikoglu et al. Jul 1996 A
5540785 Dennard et al. Jul 1996 A
5541422 Wolf et al. Jul 1996 A
5548141 Morris et al. Aug 1996 A
5549977 Jin et al. Aug 1996 A
5551238 Prueitt Sep 1996 A
5552547 Shi Sep 1996 A
5553089 Seki et al. Sep 1996 A
5556463 Guenzer Sep 1996 A
5559368 Hu et al. Sep 1996 A
5561305 Smith Oct 1996 A
5569953 Kikkawa et al. Oct 1996 A
5570226 Ota Oct 1996 A
5572052 Kashihara et al. Nov 1996 A
5574296 Park et al. Nov 1996 A
5574589 Feuer et al. Nov 1996 A
5574744 Gaw et al. Nov 1996 A
5576879 Nashimoto Nov 1996 A
5578162 D'Asaro et al. Nov 1996 A
5585167 Satoh et al. Dec 1996 A
5585288 Davis et al. Dec 1996 A
5588995 Sheldon Dec 1996 A
5589284 Summerfelt et al. Dec 1996 A
5596205 Reedy et al. Jan 1997 A
5596214 Endo Jan 1997 A
5602418 Imai et al. Feb 1997 A
5603764 Matsuda et al. Feb 1997 A
5606184 Abrokwah et al. Feb 1997 A
5608046 Cook et al. Mar 1997 A
5610744 Ho et al. Mar 1997 A
5614739 Abrokwah et al. Mar 1997 A
5619051 Endo Apr 1997 A
5621227 Joshi Apr 1997 A
5623439 Gotoh et al. Apr 1997 A
5623552 Lane Apr 1997 A
5629534 Inuzuka et al. May 1997 A
5633724 King et al. May 1997 A
5635433 Sengupta Jun 1997 A
5635453 Pique et al. Jun 1997 A
5640267 May et al. Jun 1997 A
5642371 Tohyama et al. Jun 1997 A
5650646 Summerfelt Jul 1997 A
5656382 Nashimoto Aug 1997 A
5659180 Shen et al. Aug 1997 A
5661112 Hatta et al. Aug 1997 A
5666376 Cheng Sep 1997 A
5667586 Ek et al. Sep 1997 A
5668048 Kondo et al. Sep 1997 A
5670798 Schetzina Sep 1997 A
5670800 Nakao et al. Sep 1997 A
5674366 Hayashi et al. Oct 1997 A
5674813 Nakamura et al. Oct 1997 A
5679947 Doi et al. Oct 1997 A
5679965 Schetzina Oct 1997 A
5682046 Takahashi et al. Oct 1997 A
5684302 Wersing et al. Nov 1997 A
5686741 Ohori et al. Nov 1997 A
5689123 Major et al. Nov 1997 A
5693140 McKee et al. Dec 1997 A
5696392 Char et al. Dec 1997 A
5719417 Roeder et al. Feb 1998 A
5725641 MacLeod Mar 1998 A
5729394 Sevier et al. Mar 1998 A
5729641 Chandonnet et al. Mar 1998 A
5731220 Tsu et al. Mar 1998 A
5733641 Fork et al. Mar 1998 A
5734672 McMinn et al. Mar 1998 A
5735949 Mantl et al. Apr 1998 A
5741724 Ramdani et al. Apr 1998 A
5745631 Reinker Apr 1998 A
5753300 Wessels et al. May 1998 A
5753928 Krause May 1998 A
5753934 Yano et al. May 1998 A
5754319 Van De Voorde et al. May 1998 A
5754714 Suzuki et al. May 1998 A
5760426 Marx et al. Jun 1998 A
5760427 Onda Jun 1998 A
5760740 Blodgett Jun 1998 A
5764676 Paoli et al. Jun 1998 A
5767543 Ooms et al. Jun 1998 A
5770887 Tadatomo et al. Jun 1998 A
5772758 Collins et al. Jun 1998 A
5776359 Schultz et al. Jul 1998 A
5776621 Nashimoto Jul 1998 A
5777350 Nakamura et al. Jul 1998 A
5777762 Yamamoto Jul 1998 A
5778018 Yoshikawa et al. Jul 1998 A
5778116 Tomich Jul 1998 A
5780311 Beasom et al. Jul 1998 A
5789733 Jachimowicz et al. Aug 1998 A
5789845 Wadaka et al. Aug 1998 A
5790583 Ho Aug 1998 A
5792569 Sun et al. Aug 1998 A
5792679 Nakato Aug 1998 A
5796648 Kawakubo et al. Aug 1998 A
5801072 Barber Sep 1998 A
5801105 Yano et al. Sep 1998 A
5807440 Kubota et al. Sep 1998 A
5810923 Yano et al. Sep 1998 A
5812272 King et al. Sep 1998 A
5814583 Itozaki et al. Sep 1998 A
5825055 Summerfelt Oct 1998 A
5825799 Ho et al. Oct 1998 A
5827755 Yonehara et al. Oct 1998 A
5828080 Yano et al. Oct 1998 A
5830270 McKee et al. Nov 1998 A
5831960 Jiang et al. Nov 1998 A
5833603 Kovacs et al. Nov 1998 A
5834362 Miyagaki et al. Nov 1998 A
5838035 Ramesh Nov 1998 A
5838053 Bevan et al. Nov 1998 A
5844260 Ohori Dec 1998 A
5846846 Suh et al. Dec 1998 A
5852687 Wickham Dec 1998 A
5857049 Beranek et al. Jan 1999 A
5858814 Goossen et al. Jan 1999 A
5861966 Ortel Jan 1999 A
5863326 Nause et al. Jan 1999 A
5864171 Yamamoto et al. Jan 1999 A
5869845 Vander Wagt et al. Feb 1999 A
5872493 Ella Feb 1999 A
5873977 Desu et al. Feb 1999 A
5874860 Brunel et al. Feb 1999 A
5878175 Sonoda et al. Mar 1999 A
5879956 Seon et al. Mar 1999 A
5880452 Plesko Mar 1999 A
5882948 Jewell Mar 1999 A
5883564 Partin Mar 1999 A
5883996 Knapp et al. Mar 1999 A
5886867 Chivukula et al. Mar 1999 A
5888296 Ooms et al. Mar 1999 A
5889296 Imamura et al. Mar 1999 A
5896476 Wisseman et al. Apr 1999 A
5905571 Butler et al. May 1999 A
5907792 Droopad et al. May 1999 A
5912068 Jia Jun 1999 A
5919515 Yano et al. Jul 1999 A
5919522 Baum et al. Jul 1999 A
5926493 O'Brien et al. Jul 1999 A
5926496 Ho et al. Jul 1999 A
5937115 Domash Aug 1999 A
5937274 Kondow et al. Aug 1999 A
5937285 Abrokwah et al. Aug 1999 A
5948161 Kizuki Sep 1999 A
5953468 Finnila et al. Sep 1999 A
5955591 Imbach et al. Sep 1999 A
5959308 Shichijo et al. Sep 1999 A
5959879 Koo Sep 1999 A
5962069 Schindler et al. Oct 1999 A
5963291 Wu et al. Oct 1999 A
5966323 Chen et al. Oct 1999 A
5976953 Zavracky et al. Nov 1999 A
5977567 Verdiell Nov 1999 A
5981400 Lo Nov 1999 A
5981976 Murasato Nov 1999 A
5981980 Miyajima et al. Nov 1999 A
5984190 Nevill Nov 1999 A
5985404 Yano et al. Nov 1999 A
5986301 Fukushima et al. Nov 1999 A
5987011 Toh Nov 1999 A
5987196 Noble Nov 1999 A
5990495 Ohba Nov 1999 A
5995359 Klee et al. Nov 1999 A
5995528 Fukunaga et al. Nov 1999 A
5997638 Copel et al. Dec 1999 A
5998781 Vawter et al. Dec 1999 A
5998819 Yokoyama et al. Dec 1999 A
6002375 Corman et al. Dec 1999 A
6008762 Nghiem Dec 1999 A
6011641 Shin et al. Jan 2000 A
6011646 Mirkarimi et al. Jan 2000 A
6013553 Wallace et al. Jan 2000 A
6020222 Wollesen Feb 2000 A
6022140 Fraden et al. Feb 2000 A
6022410 Yu et al. Feb 2000 A
6022671 Binkley et al. Feb 2000 A
6022963 McGall et al. Feb 2000 A
6023082 McKee et al. Feb 2000 A
6028853 Haartsen Feb 2000 A
6039803 Fitzgerald et al. Mar 2000 A
6045626 Yano et al. Apr 2000 A
6046464 Schetzina Apr 2000 A
6048751 D'Asaro et al. Apr 2000 A
6049110 Koh Apr 2000 A
6049702 Tham et al. Apr 2000 A
6051858 Uchida et al. Apr 2000 A
6051874 Masuda Apr 2000 A
6055179 Koganei et al. Apr 2000 A
6058131 Pan May 2000 A
6059895 Chu et al. May 2000 A
6064078 Northrup et al. May 2000 A
6064092 Park May 2000 A
6064783 Congdon et al. May 2000 A
6078717 Nashimoto et al. Jun 2000 A
6080378 Yokota et al. Jun 2000 A
6083697 Beecher et al. Jul 2000 A
6087681 Shakuda Jul 2000 A
6088216 Laibowitz et al. Jul 2000 A
6090659 Laibowitz et al. Jul 2000 A
6093302 Montgomery Jul 2000 A
6096584 Ellis-Monaghan et al. Aug 2000 A
6100578 Suzuki Aug 2000 A
6103008 McKee et al. Aug 2000 A
6103403 Grigorian et al. Aug 2000 A
6107653 Fitzgerald Aug 2000 A
6107721 Lakin Aug 2000 A
6108125 Yano Aug 2000 A
6110813 Ota et al. Aug 2000 A
6110840 Yu Aug 2000 A
6113225 Miyata et al. Sep 2000 A
6113690 Yu et al. Sep 2000 A
6114996 Nghiem Sep 2000 A
6121642 Newns Sep 2000 A
6121647 Yano et al. Sep 2000 A
6128178 Newns Oct 2000 A
6134114 Ungermann et al. Oct 2000 A
6136666 So Oct 2000 A
6137603 Henmi Oct 2000 A
6139483 Seabaugh et al. Oct 2000 A
6140746 Miyashita et al. Oct 2000 A
6143072 McKee et al. Nov 2000 A
6143366 Lu Nov 2000 A
6146906 Inoue et al. Nov 2000 A
6150239 Goesele et al. Nov 2000 A
6151240 Suzuki Nov 2000 A
6153010 Kiyoku et al. Nov 2000 A
6153454 Krivokapic Nov 2000 A
6156581 Vaudo et al. Dec 2000 A
6171905 Morita et al. Jan 2001 B1
6173474 Conrad Jan 2001 B1
6174755 Manning Jan 2001 B1
6175497 Tseng et al. Jan 2001 B1
6175555 Hoole Jan 2001 B1
6180252 Farrell et al. Jan 2001 B1
6180486 Leobandung et al. Jan 2001 B1
6181920 Dent et al. Jan 2001 B1
6184044 Sone et al. Feb 2001 B1
6184144 Lo Feb 2001 B1
6191011 Gilboa et al. Feb 2001 B1
6194753 Seon et al. Feb 2001 B1
6197503 Vo-Dinh et al. Mar 2001 B1
6198119 Nabatame et al. Mar 2001 B1
6204525 Sakurai et al. Mar 2001 B1
6204737 Ella Mar 2001 B1
6208453 Wessels et al. Mar 2001 B1
6210988 Howe et al. Apr 2001 B1
6211096 Allman et al. Apr 2001 B1
6222654 Frigo Apr 2001 B1
6224669 Yi et al. May 2001 B1
6225051 Sugiyama et al. May 2001 B1
6229159 Suzuki May 2001 B1
6232242 Hata et al. May 2001 B1
6232806 Woeste et al. May 2001 B1
6232910 Bell et al. May 2001 B1
6233435 Wong May 2001 B1
6235145 Li et al. May 2001 B1
6238946 Ziegler May 2001 B1
6239012 Kinsman May 2001 B1
6239449 Fafard et al. May 2001 B1
6253649 Kawahara et al. May 2001 B1
6241821 Yu et al. Jun 2001 B1
6242686 Kishimoto et al. Jun 2001 B1
6248459 Wang et al. Jun 2001 B1
6248621 Wilk et al. Jun 2001 B1
6252261 Usui et al. Jun 2001 B1
6255198 Linthicum et al. Jul 2001 B1
6256426 Duchet Jul 2001 B1
6265749 Gardner et al. Jul 2001 B1
6268269 Lee et al. Jul 2001 B1
6271619 Yamada et al. Aug 2001 B1
6275122 Speidell et al. Aug 2001 B1
6277436 Stauf et al. Aug 2001 B1
6278054 Ho et al. Aug 2001 B1
6278137 Shimoyama et al. Aug 2001 B1
6278138 Suzuki Aug 2001 B1
6278523 Gorecki Aug 2001 B1
6278541 Baker Aug 2001 B1
6291319 Yu et al. Sep 2001 B1
6291866 Wallace Sep 2001 B1
6297598 Wang et al. Oct 2001 B1
6297842 Koizumi et al. Oct 2001 B1
6300615 Shinohara et al. Oct 2001 B1
6306668 McKee et al. Oct 2001 B1
6307996 Nashimoto et al. Oct 2001 B1
6312819 Jia et al. Nov 2001 B1
6313486 Kencke et al. Nov 2001 B1
6316785 Nunoue et al. Nov 2001 B1
6316832 Tsuzuki et al. Nov 2001 B1
6319730 Ramdani et al. Nov 2001 B1
6320238 Kizilyalli et al. Nov 2001 B1
6326637 Parkin et al. Dec 2001 B1
6326645 Kadota Dec 2001 B1
6326667 Sugiyama et al. Dec 2001 B1
6329277 Liu et al. Dec 2001 B1
6338756 Dietze Jan 2002 B1
6339664 Farjady et al. Jan 2002 B1
6340788 King et al. Jan 2002 B1
6341851 Takayama et al. Jan 2002 B1
6343171 Yoshimura et al. Jan 2002 B1
6345424 Hasegawa et al. Feb 2002 B1
6348373 Ma et al. Feb 2002 B1
6355945 Kadota et al. Mar 2002 B1
6359330 Goudard Mar 2002 B1
6362017 Manabe et al. Mar 2002 B1
6362558 Fukui Mar 2002 B1
6367699 Ackley Apr 2002 B1
6372356 Thornton et al. Apr 2002 B1
6372813 Johnson et al. Apr 2002 B1
6376337 Wang et al. Apr 2002 B1
6389209 Suhir May 2002 B1
6391674 Ziegler May 2002 B1
6392253 Saxena May 2002 B1
6392257 Ramdani et al. May 2002 B1
6393167 Davis et al. May 2002 B1
6404027 Hong et al. Jun 2002 B1
6410941 Taylor et al. Jun 2002 B1
6410947 Wada Jun 2002 B1
6411756 Sadot et al. Jun 2002 B1
6415140 Benjamin et al. Jul 2002 B1
6417059 Huang Jul 2002 B1
6419849 Qiu et al. Jul 2002 B1
6427066 Grube Jul 2002 B1
6432546 Ramesh et al. Aug 2002 B1
6438281 Tsukamoto et al. Aug 2002 B1
6445724 Abeles Sep 2002 B1
6452232 Adan Sep 2002 B1
6461927 Mochizuki et al. Oct 2002 B1
6462360 Higgins, Jr. et al. Oct 2002 B1
6477285 Shanley Nov 2002 B1
6496469 Uchizaki Dec 2002 B1
6498358 Lach et al. Dec 2002 B1
6501121 Yu et al. Dec 2002 B1
6504189 Matsuda et al. Jan 2003 B1
6524651 Gan et al. Feb 2003 B1
6528374 Bojarczuk, Jr. et al. Mar 2003 B1
6538359 Hiraku et al. Mar 2003 B1
6589887 Dalton et al. Jul 2003 B1
20010013313 Droopad et al. Aug 2001 A1
20010020278 Saito Sep 2001 A1
20010036142 Kadowaki et al. Nov 2001 A1
20010055820 Sakurai et al. Dec 2001 A1
20020006245 Kubota et al. Jan 2002 A1
20020008234 Emrick Jan 2002 A1
20020021855 Kim Feb 2002 A1
20020030246 Eisenbeiser et al. Mar 2002 A1
20020047123 Ramdani et al. Apr 2002 A1
20020047143 Ramdani et al. Apr 2002 A1
20020052061 Fitzgerald May 2002 A1
20020072245 Ooms et al. Jun 2002 A1
20020076878 Wasa et al Jun 2002 A1
20020079576 Seshan Jun 2002 A1
20020131675 Litvin Sep 2002 A1
20020140012 Droopad Oct 2002 A1
20020145168 Bojarczuk, Jr. et al. Oct 2002 A1
20020179000 Lee et al. Dec 2002 A1
20020195610 Klosowiak Dec 2002 A1
Foreign Referenced Citations (162)
Number Date Country
196 07 107 Aug 1997 DE
197 12 496 Oct 1997 DE
198 29 609 Jan 2000 DE
100 17 137 Oct 2000 DE
0 247 722 Dec 1987 EP
0 250 171 Dec 1987 EP
0 300 499 Jan 1989 EP
0 309 270 Mar 1989 EP
0 331 338 Sep 1989 EP
0 331 467 Sep 1989 EP
0 342 937 Nov 1989 EP
0 392 714 Oct 1990 EP
0 412 002 Feb 1991 EP
0 455 526 Jun 1991 EP
0 483 993 May 1992 EP
0 494 514 Jul 1992 EP
0 514 018 Nov 1992 EP
0 538 611 Apr 1993 EP
0 581 239 Feb 1994 EP
0 600 658 Jun 1994 EP
0 602 568 Jun 1994 EP
0 607 435 Jul 1994 EP
0 614 256 Sep 1994 EP
0 619 283 Oct 1994 EP
0 630 057 Dec 1994 EP
0 661 561 Jul 1995 EP
0 860 913 Aug 1995 EP
0 682 266 Nov 1995 EP
0 711 853 May 1996 EP
0 766 292 Apr 1997 EP
0 777 379 Jun 1997 EP
0 810 666 Dec 1997 EP
0 828 287 Mar 1998 EP
0 852 416 Jul 1998 EP
0 875 922 Nov 1998 EP
0 881 669 Dec 1998 EP
0 884 767 Dec 1998 EP
0 926 739 Jun 1999 EP
0 957 522 Nov 1999 EP
0 964 259 Dec 1999 EP
0 964 453 Dec 1999 EP
0 993 027 Apr 2000 EP
0 999 600 May 2000 EP
1 001 468 May 2000 EP
1 035 759 Sep 2000 EP
1 037 272 Sep 2000 EP
1 043 426 Oct 2000 EP
1 043 427 Oct 2000 EP
1 043 765 Oct 2000 EP
1 054 442 Nov 2000 EP
1 069 605 Jan 2001 EP
1 069 606 Jan 2001 EP
1 085 319 Mar 2001 EP
1 089 338 Apr 2001 EP
1 109 212 Jun 2001 EP
1 176 230 Jan 2002 EP
2 779 843 Dec 1999 FR
1 319 311 Jun 1970 GB
2 152 315 Jul 1985 GB
2 335 792 Sep 1999 GB
52-88354 Jul 1977 JP
52-89070 Jul 1977 JP
52-135684 Nov 1977 JP
54-134554 Oct 1979 JP
55-87424 Jul 1980 JP
58-075868 May 1983 JP
58-213412 Dec 1983 JP
59-044004 Mar 1984 JP
59-073498 Apr 1984 JP
59066183 Apr 1984 JP
60-161635 Aug 1985 JP
60-210018 Oct 1985 JP
60-212018 Oct 1985 JP
61-36981 Feb 1986 JP
61-63015 Apr 1986 JP
61-108187 May 1986 JP
62-245205 Oct 1987 JP
63-34994 Feb 1988 JP
63-131104 Jun 1988 JP
63-198365 Aug 1988 JP
63-289812 Nov 1988 JP
64-50575 Feb 1989 JP
64-52329 Feb 1989 JP
1-102435 Apr 1989 JP
1-179411 Jul 1989 JP
01-196809 Aug 1989 JP
03-149882 Nov 1989 JP
HE. 2-391 Jan 1990 JP
02051220 Feb 1990 JP
3-41783 Feb 1991 JP
03046384 Feb 1991 JP
3-171617 Jul 1991 JP
03-188619 Aug 1991 JP
5-48072 Feb 1993 JP
5-086477 Apr 1993 JP
5-152529 Jun 1993 JP
05150143 Jun 1993 JP
05 221800 Aug 1993 JP
5-232307 Sep 1993 JP
5-238894 Sep 1993 JP
5-243525 Sep 1993 JP
5-291299 Nov 1993 JP
06-069490 Mar 1994 JP
6-232126 Aug 1994 JP
6-291299 Oct 1994 JP
6-334168 Dec 1994 JP
0812494 Jan 1996 JP
9-67193 Mar 1997 JP
9-82913 Mar 1997 JP
10-256154 Sep 1998 JP
10-269842 Oct 1998 JP
10-303396 Nov 1998 JP
10-321943 Dec 1998 JP
11135614 May 1999 JP
11-238683 Aug 1999 JP
11-260835 Sep 1999 JP
01 294594 Nov 1999 JP
11340542 Dec 1999 JP
2000-068466 Mar 2000 JP
2 000 1645 Jun 2000 JP
2000-278085 Oct 2000 JP
2000-349278 Dec 2000 JP
2000-351692 Dec 2000 JP
2001-196892 Jul 2001 JP
2002-9366 Jan 2002 JP
WO 9210875 Jun 1992 WO
WO 9307647 Apr 1993 WO
WO 9403908 Feb 1994 WO
WO 9502904 Jan 1995 WO
WO 9745827 Dec 1997 WO
WO 9805807 Jan 1998 WO
WO 9820606 May 1998 WO
WO 9914797 Mar 1999 WO
WO 9914804 Mar 1999 WO
WO 9919546 Apr 1999 WO
WO 9963580 Dec 1999 WO
WO 9967882 Dec 1999 WO
WO 0006812 Feb 2000 WO
WO 0016378 Mar 2000 WO
WO 0033363 Jun 2000 WO
WO 0048239 Aug 2000 WO
WO 0104943 Jan 2001 WO
WO 0116395 Mar 2001 WO
WO 0133585 May 2001 WO
WO 0137330 May 2001 WO
WO 0159814 Aug 2001 WO
WO 0159820 Aug 2001 WO
WO 0159821 Aug 2001 WO
WO 0159837 Aug 2001 WO
WO 02 01648 Jan 2002 WO
WO 0203113 Jan 2002 WO
WO 0203467 Jan 2002 WO
WO 0203480 Jan 2002 WO
WO 0208806 Jan 2002 WO
WO 02009150 Jan 2002 WO
WO 0209160 Jan 2002 WO
WO 0211254 Feb 2002 WO
WO 0233385 Apr 2002 WO
WO 0247127 Jun 2002 WO
WO 0250879 Jun 2002 WO
WO 02099885 Dec 2002 WO
WO 03012874 Feb 2003 WO
Related Publications (1)
Number Date Country
20050056210 A1 Mar 2005 US
Continuations (1)
Number Date Country
Parent 09624691 Jul 2000 US
Child 10911624 US