Semiconductor device structures and methods of forming semiconductor structures

Abstract
A method of patterning a semiconductor film is described. According to an embodiment of the present invention, a hard mask material is formed on a silicon film having a global crystal orientation wherein the semiconductor film has a first crystal plane and second crystal plane, wherein the first crystal plane is denser than the second crystal plane and wherein the hard mask is formed on the second crystal plane. Next, the hard mask and semiconductor film are patterned into a hard mask covered semiconductor structure. The hard mask covered semiconductor structured is then exposed to a wet etch process which has sufficient chemical strength to etch the second crystal plane but insufficient chemical strength to etch the first crystal plane.
Description
BACKGROUND OF THE INVENTION

1. Field of the Invention


The present invention relates to the field of semiconductor processing and more particularly to semiconductor structures and their methods of fabrication.


2. Discussion of Related Art


In order to increase the performance of modern integrated circuits, such as microprocessors, silicon on insulator (SOI) transistors have been proposed. Silicon on insulator (SOI) transistors have an advantage in that they can be operated in a fully depleted manner. Fully depleted transistors have an advantage of ideal subthreshold gradients for optimized on current/off current ratios. An example of a proposed SOI transistor which can be operated in a fully depleted manner is that of a tri-gate transistor 100, such as illustrated in FIG. 1. Tri-gate transistor 100 includes a silicon body 104 formed on insulating substrate 102 having buried oxide layer 103 formed on a monocrystalline silicon substrate 105. A gate dielectric layer 106 is formed on the top and sidewalls of the silicon body 104 as shown in FIG. 1. A gate electrode 108 is formed on the gate dielectric layer and surrounds the body 104 on three sides essentially providing a transistor 100 having three gate electrodes (G1, G2, G3) one on each of the sidewalls of the silicon body 104 and one on the top surface of the silicon body 104. A source region 110 and a drain region 112 are formed in silicon body 104 on opposite sides of gate electrode 108 as shown in FIG. 1. The active channel region is the region of the silicon body located beneath gate electrode 108 and between the source region 110 and drain region 112. An advantage of a tri-gate transistor 100 is that it exhibits good short channel effects (SCEs). One reason tri-gate transistors 100 exhibit good short channel effects is that the nonplanarity of such devices places the gate electrode 108 in such a way as to surround the active channel region on all three sides.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 illustrates a nonplanar or tri-gate transistor.



FIGS. 2A-2E illustrate a method of forming a semiconductor structure in accordance with embodiments of the present invention.



FIG. 2F is an illustration of a nonplanar transistor formed from the structure of FIG. 2E.



FIGS. 3A-3C illustrate a method of forming a semiconductor structure in accordance with embodiments of the present invention.



FIG. 3D is an illustration of a nonplanar transistor utilizing a semiconductor structure of FIG. 3C.



FIGS. 4A-4C illustrate a method of forming a semiconductor structure in accordance with embodiments of the present invention.



FIG. 4D is an illustration of a nonplanar transistor utilizing the semiconductor structure of FIG. 4C.



FIG. 5 is an illustration of a portion of an integrated circuit which includes an n type field effect transistor and a p type field effect transistor with a non parallel orientation on a substrate.





DETAILED DESCRIPTION OF THE PRESENT INVENTION

Embodiments of the present invention describe semiconductor structures and methods of forming semiconductor structures. In the following description numerous specific details are set forth in order to provide a thorough understanding of the present invention. In other instances, well known semiconductor processes and manufacturing techniques have not been described in particular detail in order to not unnecessarily obscure the present invention.


The present invention utilizes atomic layer control of single crystalline semiconductor structures to maximize performance of semiconductor devices. In embodiments of the present invention, hard mask covered single crystalline structures are exposed to anisotropic wet etches. The wet etch has sufficient chemical strength to overcome the activation energy barrier of the chemical etching reaction in order to etch less dense planes of the semiconductor structure, but insufficient chemical strength to overcome the activation energy barrier of the chemical etching reaction, thereby not etching high density planes. By choosing proper crystal orientation and by forming a hard mask over the less dense planes of the structure and by using a wet etch chemistry with the appropriate chemical strength, one can form semiconductor structures with desired faceting, crystal orientation and sidewall smoothing. In embodiments of the present invention, natural facets in epitaxial silicon are exploited to negate edge roughness in three-dimensional silicon channel structures. In an embodiment of the present invention, natural facets are exploited to form a three-dimensional channel structure which enables good gate control of the channel region. In yet other embodiments of the present invention, semiconductor bodies of PMOS and NMOS transistors are formed with specific arrangement on single crystalline semiconductors to exploit the crystal orientation and achieve increased mobility for both holes and electrons. Other aspects of the present invention will become obvious from the detailed description which follows.


A method of forming a three-dimensional semiconductor structure utilizing a self limiting etch and natural faceting is illustrated in FIGS. 2A-2F in accordance with embodiments of the present invention. The fabrication of a semiconductor structure begins with a substrate 200. In an embodiment of the present invention, substrate 200 is a silicon on insulator (SOI) substrate. A SOI substrate 200 includes a lower monocrystalline silicon substrate 202. An insulating layer 204, such as silicon dioxide or silicon nitride, is formed on monocrystalline substrate 202. A single crystalline silicon film 206 is formed on the top of the insulating layer 204. Insulating layer 204 is sometimes referred to as a “buried oxide” or a “buried insulating” layer and is formed to a thickness sufficient to isolate single crystalline silicon film 206 from lower monocrystalline silicon substrate 202. In an embodiment of the present invention, the insulating layer is a buried oxide layer formed to a thickness between 200-2000 Å. In an embodiment of the present invention, the silicon film 206 is an intrinsic (i.e., undoped) silicon epitaxial film. In other embodiments, the single crystalline silicon film 206 is doped to a p type or n type conductivity with a concentration level between 1×1016-1×1019 atom/cm3. Silicon film 206 can be in situ doped (i.e., doped while it is deposited) or doped after it is formed on insulating layer 204 by, for example, ion implantation. Doping silicon film 206 after it is deposited enables both n type devices and p type devices to be fabricated on the same substrate. In an embodiment of the present invention, silicon film 206 is formed to a thickness which is approximately equal to the height desired of the subsequently formed silicon structure. In an embodiment of the present invention, the single crystalline silicon film 206 has a thickness of less than 30 nanometers and ideally around 20 nanometers or less.


A silicon on insulator (SOI) substrate 200 can be formed in any well known method. In one method of forming the silicon on insulator substrate, known as the SIMOX technique, oxygen atoms are implanted at a high dose into a single crystalline silicon substrate and then annealed to form buried oxide 204 within the substrate. The portion of the single crystalline silicon substrate above the buried oxide becomes the silicon film 206. Another technique currently used to form SOI substrates is an epitaxial silicon film transfer technique which is generally referred to as “bonded SOI”. In this technique, a first silicon wafer has a thin oxide grown on its surface that will later serve as the buried oxide 204 in the SOI structure. Next, a high dose hydrogen implant is made into the first silicon wafer to form a stress region below the silicon surface of the first wafer. The first wafer is then flipped over and bonded to the surface of a second silicon wafer. The first wafer is then cleaved along the high stress plane created by the hydrogen implant. The cleaving results in a SOI structure with a thin silicon layer on top, the buried oxide underneath, all on top of the second single crystalline silicon wafer. Well known smoothing techniques, such as HCl smoothing or chemical mechanical polishing (CMP) can be used to smooth the top surface of the silicon film 206 to its desired thickness.


Although the present invention will be described with respect to silicon structures formed on silicon on insulator (SOI) substrates, the present invention can be carried out on standard monocrystalline silicon wafers or substrates to form a “bulk” device. The silicon structures can be formed directly from the monocrystalline silicon wafer or formed from epitaxial silicon films formed on a monocrystalline silicon substrate. Additionally, although embodiments of the present invention are illustrated with respect to the formation of single crystalline silicon structures and devices formed therefrom, the methods and structures of the present invention are equally applicable to other types of semiconductors, such as but not limited to germanium (Ge), a silicon germanium alloy (SixGey), gallium arsenide (GaAs), indium antimonide (InSb), gallium phosphide (GaP), and gallium antimonide (GaSb). Accordingly, embodiments of the present invention include semiconductor structures and methods of forming semiconductor structures utilizing semiconductors, such as but not limited to germanium (Ge), a silicon germanium alloy (SixGey), gallium arsenide (GaAs), indium antimonide (InSb), gallium phosphide (GaP), and gallium antimonide (GaSb).


In FIG. 2A, single crystalline silicon film 206 has a (100) global crystal orientation, as defined by the xy plane. A silicon film with a (100) global crystal orientation has a <100> plane which is planar with the surface of the film. That is, as illustrated in FIG. 2A, a single crystalline silicon film with a (100) global crystal orientation has a <100> plane which lies in the xy plane with a normal axis in the z direction.


In the following description round brackets ( ) are used to illustrate the global crystal orientation of the film, as defined by the xy plane and along the z direction, while pointed brackets < > are used to describe specific local planes within said globally defined crystalline film.


Additionally, as illustrated in FIG. 2A, a single crystalline silicon with a (100) crystal orientation has a pair of <110> planes which are perpendicular to one another. That is, the (100) single crystalline silicon has a <110> plane which lies in the zx plane with a normal axis extending in the y direction and has a <110> plane which lies in the zy plane and with a normal axis in the x direction. In an embodiment of the present invention, silicon film 206 with a (100) global crystal orientation is etched to form a silicon structure which has a pair of laterally opposite sidewalls which are formed from the <110> plane and a second pair of laterally opposite sidewalls, perpendicular thereto, which lie in the <110> plane.


In order to etch silicon film 206 into a silicon body, a hard mask material 208 can be formed on the top surface 219 of silicon film 206. Hard mask material 208 is a material which can provide a hard mask for etching of silicon film 206. Hard mask material 208 is a material which can retain its profile during the etching of silicon film 206. Hard mask material 208 is a material which will not etch or will only slightly etch during the etching of silicon film 206. In an embodiment of the present invention, the hard mask material is formed of a material such that the etchant used to etch silicon film 206 will etch silicon film 206 at least 5 times faster than the hard mask material and ideally at least 10 times faster. That is, in an embodiment of the present invention, the silicon film and the hard mask are chosen to provide an etch selectivity of at least 5:1 and ideally at least 10:1. In an embodiment of the present invention, hard mask material 208 is formed from silicon nitride or silicon oxynitride. In an embodiment of the present invention, hard mask material 208 is formed from a silicon nitride film with between 0-5% carbon, formed by a low pressure chemical vapor deposition (LPCVD) process. Hard mask material 208 is formed to a thickness sufficient to retain its profile during the entire etch of silicon film 206 but not too thick to cause difficulties in patterning. In an embodiment of the present invention, the hard mask material 208 is formed to a thickness between 3 nanometers to 50 nanometers and ideally to a thickness around 10 nanometers.


Next, as also shown in FIG. 2B, a photoresist mask 210 is formed on hard mask material 208. Photoresist mask 210 contains the feature pattern to be transferred into silicon film 206. Photoresist mask 210 can be formed by any well known technique, such as by blanket depositing photoresist material and then masking, exposing and developing the photoresist material into a photoresist mask 210 having the desired pattern for a silicon film 206. Photoresist mask 210 is typically formed of an organic compound. Photoresist mask 210 is formed to a thickness sufficient to retain its profile while patterning hard mask film 208 but yet is not formed too thick to prevent its lithographic patterning into the smallest dimensions (i.e., critical dimensions) possible with the photolithography system and process used. In an embodiment of the present invention, photoresist mask 210 is orientated on single crystalline silicon film 206 so as to define a photoresist mask with a pair of laterally opposite sidewalls aligned with a <110> crystal plane and a second pair of laterally opposite sidewalls, perpendicular to the first, aligned with the <110> plane.


Next, as shown in FIG. 2C, hard mask material 208 is etched in alignment with photoresist mask 210 to form a hard mask 212 as shown in FIG. 2C. Photoresist mask 210 prevents the underlying portion of hard mask material 208 from being etched. In an embodiment of the present invention, the hard mask material 208 is etched with an etchant which can etch the hard mask material but does not etch the underlying silicon film 206. In an embodiment of the present invention, the hard mask material is etched with an etchant that has almost perfect selectivity to the underlying silicon film 206. That is, in an embodiment of the present invention, the hard mask etchant etches the hard mask material 208 at least 20 times faster than the underlying silicon film 206 (i.e., etchant has a hard mask to silicon film selectivity of at least 20:1). When hard mask material 208 is a silicon nitride or silicon oxynitride film, hard mask material 208 can be etched into a hard mask 212 utilizing a dry etch process, such as a reactive ion etching. In an embodiment of the present invention, a silicon nitride or silicon oxynitride hard mask is reactively ion etched utilizing a chemistry comprising CHF3 and O2 and Ar.


Next, as also shown in FIG. 2C, after hard mask film 208 has been patterned into a hard mask 212, photoresist mask 210 may be removed by well known techniques. For example, photoresist mask 210 may be removed utilizing “piranha” clean solution which includes sulfuric acid and hydrogen peroxide. Additionally, residue from the photoresist mask 210 may be removed with an O2 ashing.


Although not required, it is desirable to remove photoresist mask 210 prior to patterning silicon film 206 so that a polymer film from the photoresist does not form on the sidewalls of the patterned silicon film 206. For example, when silicon film 206 is used as a semiconductor body or fin in a nonplanar device, it is desirable to first remove the photoresist mask prior to etching the silicon film because dry etching processes can erode the photoresist mask and cause polymer films to develop on the sidewalls of the silicon body which can be hard to remove and which can detrimentally affect device performance.


Next, as shown in FIG. 2D, silicon film 206 is etched in alignment with hard mask 212 to form a patterned silicon film 214 which has a first pair of laterally opposite sidewalls 218 aligned with the <110> crystal plane and a second pair of laterally opposite sidewalls 220 aligned with the <110> crystal plane. Hard mask 212 prevents the underlying portion of silicon film 206 from being etched during the etch process. In an embodiment of the present invention, the etch is continued until the underlying buried oxide layer 204 is reached. Silicon film 206 is etched with an etchant which etches silicon film 206 without significantly etching hard mask 212. In an embodiment of the present invention, silicon film 206 is etched with an etchant which enables silicon film 206 to be etched at least 5 times and ideally 10 times faster than hard mask 212 (i.e., etchant has a silicon film 206 to hard mask 212 etch selectivity of at least 5:1 and ideally at least 10:1). Silicon film 206 can be etched utilizing any suitable process. In an embodiment of the present invention, silicon film 206 is anisotropically etched so that the silicon body 214 has nearly vertical sidewalls 218 formed in alignment with the sidewalls of hard mask 212. When hard mask 212 is a silicon nitride or silicon oxynitride film, silicon film 206 can be etched utilizing a dry etch process, such as a reactive ion etch (RIE) or plasma etch with a chemistry comprising Cl2 and HBr.


After etching silicon film 206 to form silicon body or structure 214, the sidewalls 218 will typically have a line edge roughness 222 of about 2-4 nanometers. When forming a silicon body or structure with a width between sidewalls 218 of only 20-30 nanometers, such a surface roughness is unacceptably large and can detrimentally affect device performance.


Accordingly, in an embodiment of the present invention, the silicon structure 214 is exposed to a wet etch or a “faceting” etch while hard mask 212 is present on structure 214 in order to remove the edge roughness and/or to tailor the shape of the structure to enhance device performance. In an embodiment of the present invention, the hard mask 212 capped silicon structure 214, is exposed to an anisotropic wet etch. The wet etchant has sufficient chemical strength to overcome the activation energy barrier of the chemical etching reaction in order to etch less dense planes of the semiconductor structure, but insufficient chemical strength to overcome the activation energy barrier of the chemical etching reaction, thereby not etching high density planes.


In an embodiment of the present invention, a wet etch chemistry and process are used which can etch the less dense <100> and <110> planes but which cannot etch the higher density <111> planes. Because hard mask 212 covers the less dense <100> plane on the top surface of the silicon structure 214, said less dense plane is protected from etching. Because the less dense plane <100> on the top surface is shielded and because the etch does not have a sufficient chemical strength to etch the <111> plane, the wet etch stops on the first total intact or contiguous <111> plane as shown in FIG. 2E. In this way, the “faceting” or wet etch is self limiting. Thus, upon self-limitation of the wet etch, only <111> planes and etch-resistant films used to shield the less dense <110> and <100> planes remain exposed. The faceting etch of the present invention can be said to be an anisotropic etch because it etches in one direction at one rate while etching in other directions at a second slower rate or not at all. Because the etch process etches the <100> and <110> planes but not the <111> planes, the faceting or wet etch forms a silicon structure 230 having sidewalls 232 defined by the <111> plane as shown in FIG. 2E. The anisotropic wet etch removes the surface roughness 222 from sidewalls 218 (FIG. 2D) and generates optically smooth sidewalls 232 as shown in FIG. 2E. Additionally, after exposing the structure 214 to the faceting etch for a sufficient period of time, sidewalls 218 are defined by the <111> plane and generate a structure 230 with a v-shape or inwardly tapered sidewalls 232. The sidewalls 232 angle inward from the top surface 219 of structure 230 at an angle alfa of 62.5 degrees. In an embodiment of the present invention, the top surface 219 of structure 230 has a width (W1) between laterally opposite sidewalls 232 of between 20-30 nm and the bottom surface has a width (W2) between laterally opposite sidewalls of between 10-15 nm.


In an embodiment of the present invention, the wet etch or “faceting” etch is a hydroxide based etch with a sufficiently low hydroxide concentration and nucleophillicity (i.e. chemical strength) so that there is no etching of the fully intact <111> planes. In an embodiment of the present invention, structure 214 is exposed to a faceting or wet etch which comprises less than 1% ammonia hydroxide (NH4OH) by volume. In an embodiment of the present invention, structure 214 is exposed to a wet etchant comprising between 0.2-1% NH4OH by volume at a temperature range between 5-25° C. In an embodiment of the present invention, sonic energy at the frequency range between 600-800 kilohertz dissipating between 0.5-3 watts/cm2 is applied to the etch solution during the faceting etch. In an embodiment of the present invention, the hard mask capped silicon structure is exposed to the faceting etch for between 15 seconds-5 minutes.


In another embodiment of the present invention, the faceting or wet etch can comprise ultra-dilute (<0.1% by volume) aqueous solutions of tetraalkylammonium hydroxides (e.g. tetraethylammonium hydroxide and tetramethylammonium hydroxide at a temperature between 5 and 20° C.).


The fabricated silicon structure 230 can be used to fabricate semiconductor devices, such as transistors and capacitors, as well as micro-electrical mechanical systems (MEMS) and opto-electronic devices. In an embodiment of the present invention, semiconductor structure 230 is used as a semiconductor body or fin for a nonplanar or three-dimensional transistor, such as but not limited to a tri-gate transistor, a dual gate transistor, a FINFET, an omega-FET or a pi-FET.


In an embodiment of the present invention, silicon structure 230 provides a silicon body or fin for a tri-gate transistor 240 illustrated in FIG. 2F. In order to fabricate a tri-gate transistor 240 as illustrated in FIG. 2F, hard mask 212 is removed from silicon structure 230. In an embodiment of the present invention, when hard mask 212 is a silicon nitride or silicon oxynitride film, a wet etch comprising phosphoric acid in de-ionized water may be used to remove the hard mask. In an embodiment of the present invention, the hard mask etchant comprises an aqueous solution of between 80-90% phosphoric acid (by volume) heated to a temperature between 150-170° C. and ideally to 160° C. In an embodiment of the present invention, after removing hard mask 212, the substrate can be cleaned utilizing standard SC1 and SC2 cleans. It is desirable to clean the substrate after removal of the hard mask with phosphoric acid because phosphoric acid typically includes many metallic impurities which can affect device performance or reliability. It is to be appreciated that if one desires to form a FINFET or a dual gate device, the hard mask 212 may be left on silicon structure 230 in order to isolate the top surface of the semiconductor structure 230 from control by a subsequently formed gate electrode.


Next, a gate dielectric layer 250 is formed on the sidewalls 232 as well as on the top surface of semiconductor body 230. Gate dielectric layer 250 can be any well known and suitable gate dielectric layer, such as but not limited to a silicon dioxide or silicon nitride gate dielectric layer. Additionally, gate dielectric layer 250 can be a high-k gate dielectric layer, such as but not limited to hafnium oxide, zirconium oxide, titanium oxide and tantalum oxide. Any well known technique, such as but not limited to chemical vapor deposition and atomic layer deposition may be utilized to form gate dielectric layer 250.


Next, a gate electrode 260 is formed on gate dielectric layer 250 on the top surface and sidewalls of semiconductor structure 230 as illustrated in FIG. 2F. Gate electrode 260 is formed perpendicular to sidewalls 232. The gate electrode can be formed from any well known gate electrode material, such as but not limited to doped polycrystalline silicon, as well as metal films, such as but not limited to tungsten, tantalum, titanium, and their nitrides. Additionally, it is to be appreciated that a gate electrode need not necessarily be a single material and can be a composite stack of thin films, such as but not limited to a lower metal film formed on the gate dielectric layer with a top polycrystalline silicon film. The gate dielectric layer and gate electrode may be formed by blanket depositing or growing the gate dielectric layer over the semiconductor body and then blanket depositing a gate electrode material over the gate dielectric layer. The gate dielectric layer and gate electrode material may then be patterned with well know photolithography and etching techniques to form gate electrode 260 and gate dielectric layer 250 as illustrated in FIG. 2F. Alternatively, the gate dielectric layer and gate electrode may be formed utilizing a well known replacement gate process. A source region 272 and a drain region 274 are formed in silicon body 230 on opposite sides of gate electrode 260 as illustrated in FIG. 2F. Any well known and suitable technique, such as solid source diffusion or ion implantation may be used to form source and drain regions. In an embodiment of the present invention, the source region 272 and drain region 274 are formed to a concentration between 1×1019-1×1021 atoms/cm3.


The fabricated nonplanar transistor 240 includes a semiconductor body 230 surrounded by gate dielectric layer 250 and gate electrode 260 as shown in FIG. 2F. The portion of the semiconductor body 230 located beneath the gate dielectric and gate electrode is the channel region of the device. In an embodiment of the present invention the source and drain region are doped to a first conductivity type (n type or p type) while the channel region is doped to a second opposite conductivity type (p type or n type) or is left undoped. When a conductive channel is formed by gate electrode 260 in the channel region of silicon body 230, charges (i.e., holes or electrons) flow between the source and drain region along the <110> plane in silicon body 230. That is, in transistor 240, charge migration is along the <110> crystal plane in structure 240. Is has been found that charge migration in the <110> direction provides good hole mobility. Accordingly, in an embodiment of the present invention, device 240 is a p type device where the source and drain regions are formed to a p type conductivity and where the carriers are holes. Additionally, by inwardly tapering the sidewalls of silicon body 230, gate electrode 260 has good control over the channel region of body 230 enabling fast turn “on” and turn “off” of transistor 240.



FIGS. 3A-3D illustrate a method of forming a monocrystalline silicon body or structure in accordance with another embodiment of the present invention. As shown in FIG. 3A, a hard mask 312 is formed on a single crystalline silicon film 306 having a (100) global crystal orientation. Hard mask 312 can be formed as described above. In FIG. 3A, however, the hard mask 312 is orientated on silicon film 306 to produce a pair of sidewalls which are aligned with the <100> plane and a second pair of sidewalls which are also aligned to the <100> plane. (It is to be appreciated that the orientation of hard mask 312 is rotated approximately 45° in the xy plane from the orientation of hard mask 212 in FIG. 2A.)


Next, as illustrated in FIG. 3B, the (100) global crystal orientation silicon film 306 is etched in alignment with the hard mask 312 to produce a silicon structure 314 which has a pair of laterally opposite sidewalls 318 which are aligned with the <100> plane and a second pair of sidewalls 320, which are perpendicular to the first pair and which are also aligned with the <100> plane. Silicon film 306 can be etched as described above.


Next, the silicon structure 314 is exposed to a faceting wet etch while hard mask 312 is present on the top surface 319 of silicon structure 314. The faceting wet etch has a sufficient chemical strength to etch the less dense <110> and <100> planes but insufficient strength to etch the high density <111> plane. Because the less dense <100> plane on the top surface 319 of the silicon structure 314 is covered by the hard mask 312 and because the etch does not have sufficient chemical strength to etch the <111> plane, the silicon structure 314 is transformed into a silicon structure 330 having a pair of sidewalls 332 having a “V” notched shape formed by intersecting <111> planes as illustrated in FIG. 3C. As before, the faceting etch is self limiting, and stops at the first contiguous <111> planes. The <111> planes of sidewalls 332 meet at an angle β of approximate 55°. A combination of crystal orientation, atom shielding, and a well-controlled anisotropic wet etch enables the formation of silicon structure 330 with “V” notch sidewalls 332.


As discussed above, the silicon structure 330 can be used to create silicon nonplanar or three-dimensional devices as well as micro-machines and MEMS devices. In an embodiment of the present invention, the silicon structure 330 is used to form a nonplanar transistor, such as a tri-gate transistor 330 as illustrated in FIG. 3D. Gate electrode 360 is formed perpendicular to sidewalls 332 as shown in FIG. 3D. The nonplanar device has a gate dielectric layer 350 and a gate electrode 360 formed over and around a portion of silicon body 330 as illustrated in FIG. 3D. A source region 372 and a drain region 374 are formed in the silicon body 330 on opposite sides of the gate electrode. The charge migration from the source to the drain region in transistor 340 is parallel to or in alignment with the <100> plane. Because charge migration is along the <100> plane, the silicon structure 330 provides good electron mobility and is therefore ideal for use in the fabrication of an n type field effect transistor (NFET) where the carriers are electrons and the source region 372 and drain regions 374 are n type conductivity.



FIGS. 4A-4D illustrates a method of forming a semiconductor body or structure in accordance with another embodiment of the present invention. As shown in FIG. 4A, a substrate 400, such as a silicon on insulator (SOI) substrate which includes a lower monocrystalline silicon substrate 402, a buried oxide layer 404 and a single crystalline silicon film 406 is provided. Although, a silicon on insulator substrate 400 is ideally used, other well known semiconductor substrates can be used as set forth above. In an embodiment of the present invention, single crystalline silicon film 406 has a (110) global crystal orientation as shown in FIG. 4A. A single crystalline silicon film with a (110) global crystal orientation has a <110> plane of the silicon lattice which is planar to or parallel with the surface of the film. That is, as illustrated in FIG. 4A, a single crystalline silicon film with a (110) global crystal orientation has a <110> plane in the xy plane with a normal axis in the z direction. Additionally, a single crystalline silicon film with a (110) global crystal orientation has <111> planes and <110> planes which are orthogonal to each other and orthogonal to a <110> plane. That is, in a single crystalline silicon film 406 with (110) global crystal orientation there are <111> planes which lie in the xz plane with normal axis in the y direction and there are <110> planes which lie in the zy plane and have a normal axis in the x direction as shown in FIG. 4A. Next, a hard mask 412, as shown in FIG. 4A, is formed on single crystalline silicon film 406 having a (110) crystal orientation as described above. Hard mask 412 is orientated on silicon film 406 to produce a pair of sidewalls aligned with <110> plane and a second pair of perpendicular sidewalls which are aligned with the <111> plane. Hard mask 412 can be formed of materials and by methods described above.


Next, as illustrated in FIG. 4B, the (110) silicon film is etched in alignment with hard mask 412 to produce a silicon structure 414 which has a pair of laterally opposite sidewalls 418 which are parallel with or aligned with the <110> plane and a second pair of sidewalls 420, which are perpendicular to the first pair 418 which are parallel with or aligned with a <111> plane. Hard mask 412 capped silicon structure 414 is then exposed to a faceting wet etch. The faceting wet etch has sufficient chemical strength to etch the less dense <110> plane, but insufficient chemical strength to etch the higher density <111> plane. Because the less dense <110> plane of the top surface 419 is covered by hard mask 412 and because the etch does not have sufficient chemical strength to etch the <111> plane, structure 414 is transformed into structure 430 having a pair of laterally opposite sidewalls 432 defined by <111> planes as illustrated in FIG. 4C. After exposing structure 414 to the faceting etch for a sufficient period of time, the sidewalls 432 are defined by the <111> planes and generate a structure with a v-shape or inwardly tapered sidewalls. The sidewalls 432 angle inward from the top surface 419 of structure 430 at an angle gamma of approximately 62.5 degrees. In an embodiment of the present invention, the top surface 419 has a width (W1) between laterally opposite sidewalls 430 of between 20-30 nm and a bottom surface has width (W2) between laterally opposite sidewalls 440 of between 10-15 nm. A combination of crystal orientation, hard mask shielding, and a wet etch with the appropriate chemical strength enables the formation of silicon structure 430 with inwardly tapered sidewalls 432.


As discussed above, structure 430 can be used to create a variety of well known semiconductor devices, such as silicon nonplanar or three-dimensional devices, as well as opto-electronic devices and MEMS devices. In an embodiment of the present invention, the silicon structure 430 is used to form a silicon body of nonplanar transistor, such as a tri-gate transistor 440, as illustrated in FIG. 4D. The tri-gate transistor 440 has a gate dielectric layer 450 and a gate electrode 460 formed over and around a portion of silicon body 430 as illustrated in FIG. 4D. The gate electrode 460 runs in a direction perpendicular to sidewalls 432 as shown in FIG. 4D. The gate dielectric layer 450 and gate electrode 460 may be formed of any suitable material and suitable known method, such as described above. A source region 472 and a drain 474 are formed in silicon body 430 on opposite sides of gate electrode 460 as illustrated in FIG. 4D. The charge migration from the source region 472 to the drain region 474 in silicon body 430 is parallel to or in alignment with the <110> plane. The inwardly tapered sidewalls 432 of silicon body 430 provide good gate control 460 of the channel region of the device which enables the fast turn “on” and turn “off” of device 440.


Although the present invention thus far has been described with respect to the shaping or “faceting” of single crystalline silicon structures utilizing a combination of crystal orientation, hard mask shielding, and well controlled wet etchants, concepts of the present invention are equally applicable to other types of single crystalline semiconductor films, such as but not limited to germanium (Ge), a silicon germanium alloy (SixGey), gallium arsenide (GaAs), indium antimonide (InSb), gallium phosphide (GaP), and gallium antimonide (GaSb). For example, a single crystalline indium antimonide (InSb) structure can be faceted utilizing a wet etchant comprising an aqueous solution of 0.05-0.1 mol/L citric acid at a temperature range between 5-15° C. Similarly, a single crystalline gallium arsenide (GaAs) structure can be faceted by exposing a hard mask covered gallium arsenide structure to a wet etchant comprising an aqueous solution of less than 0.05 mol/L citric acid at a temperature range between 5-15° C.


Additionally, in an embodiment of the present invention, an integrated circuit is formed from a p type transistor and an n type transistor 520 which are orientated and/or shaped to optimize the performance of each type of transistor. For example, as illustrated in FIG. 5, in an embodiment of the present invention a single crystalline silicon film having a (100) global crystal orientation is patterned as described with respect to FIGS. 2A-2F to form a silicon body 512 for a p type nonplanar transistor 510 wherein the charge (hole) migration is parallel with a <110> plane and is also patterned as described with respect to FIGS. 3A-3D to form a silicon body 522 for a n type nonplanar transistor 520 wherein charge (electron) migration is parallel with a <100> plane. Accordingly, in an embodiment of the present invention, a p type nonplanar transistor and an n type nonplanar transistor are orientated in a non-parallel (e.g., 45° C. offset) manner with respect to one another on a substrate in order to optimize the hole mobility for the p type transistor and the electron mobility for the n type transistor. In other embodiments of the present invention, the semiconductor bodies of the p type device and the n type device are oriented with respect to one another to enable the faceting etch to shape the bodies into structures which optimize performance for each device type. In this way, the performance of an integrated circuit which includes both an n type nonplanar transistor and a p type nonplanar transistor can be greatly improved.

Claims
  • 1. A nonplanar transistor, comprising: a semiconductor body disposed on and continuous with a bulk monocrystalline silicon substrate, the semiconductor body comprising inwardly tapered sidewalls that each taper inward from the top of the semiconductor body at an angle of approximately 62.5 degrees, wherein charge migration in the semiconductor body is along a direction perpendicular to the sidewalls; anda gate electrode disposed over the semiconductor body and orthogonal to the direction of charge migration.
  • 2. The nonplanar transistor of claim 1, wherein each sidewall is flat from the top of the semiconductor body to the bottom of the semiconductor body.
  • 3. The nonplanar transistor of claim 1, wherein the nonplanar transistor is a p type field effect transistor, and wherein the direction perpendicular to the sidewalls is parallel to a <110> plane of the bulk monocrystalline silicon substrate.
  • 4. The nonplanar transistor of claim 1, further comprising: a high-k gate dielectric layer disposed between the semiconductor body and the gate electrode.
  • 5. The nonplanar transistor of claim 1, wherein the gate electrode is a metal gate electrode.
  • 6. A nonplanar transistor, comprising: a semiconductor body disposed on and continuous with a bulk monocrystalline silicon substrate, the semiconductor body comprising inwardly tapered sidewalls, wherein charge migration in the semiconductor body is along a direction perpendicular to the sidewalls; anda gate electrode disposed over the semiconductor body and orthogonal to the direction of charge migration, wherein the nonplanar transistor is a p type field effect transistor, and wherein the direction perpendicular to the sidewalls is parallel to a <110> plane of the bulk monocrystalline silicon substrate.
  • 7. The nonplanar transistor of claim 6, wherein each sidewall is flat from the top of the semiconductor body to the bottom of the semiconductor body.
  • 8. The nonplanar transistor of claim 6, further comprising: a high-k gate dielectric layer disposed between the semiconductor body and the gate electrode.
  • 9. The nonplanar transistor of claim 6, wherein the gate electrode is a metal gate electrode.
CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No. 13/277,897, filed Oct. 20, 2011, which is a divisional of U.S. patent application Ser. No. 12/463,309, filed May 8, 2009, now U.S. Pat. No. 8,071,983, issued on Dec. 6, 2011, which is a divisional of U.S. patent application Ser. No. 11/158,661, filed Jun. 21, 2005, now U.S. Pat. No. 7,547,637, issued on Jun. 16, 2009, the entire contents of which are hereby incorporated by reference herein.

US Referenced Citations (536)
Number Name Date Kind
4231149 Chapman et al. Nov 1980 A
4487652 Almgren Dec 1984 A
4711701 McLevige Dec 1987 A
4751201 Nottenburg et al. Jun 1988 A
4818715 Chao Apr 1989 A
4871692 Lee et al. Oct 1989 A
4872046 Morkoc et al. Oct 1989 A
4905063 Beltram et al. Feb 1990 A
4906589 Chao Mar 1990 A
4907048 Huang Mar 1990 A
4914059 Nissim et al. Apr 1990 A
4994873 Madan Feb 1991 A
4996574 Shirasaka et al. Feb 1991 A
5023203 Choi Jun 1991 A
5120666 Gotou Jun 1992 A
5124777 Lee Jun 1992 A
5179037 Seabaugh Jan 1993 A
5216271 Takagi et al. Jun 1993 A
5278102 Horie Jan 1994 A
5308999 Gotou et al. May 1994 A
5328810 Lowrey et al. Jul 1994 A
5338959 Kim et al. Aug 1994 A
5346836 Manning et al. Sep 1994 A
5346839 Sundaresan Sep 1994 A
5357119 Wang et al. Oct 1994 A
5371024 Hieda et al. Dec 1994 A
5391506 Tada et al. Feb 1995 A
5398641 Shih Mar 1995 A
5428237 Yuzurihara et al. Jun 1995 A
5466621 Hisamoto et al. Nov 1995 A
5475869 Gomi et al. Dec 1995 A
5479033 Baca et al. Dec 1995 A
5482877 Rhee Jan 1996 A
5495115 Kudo et al. Feb 1996 A
5514885 Myrick May 1996 A
5521859 Ema et al. May 1996 A
5543351 Hirai et al. Aug 1996 A
5545586 Koh Aug 1996 A
5554870 Fitch et al. Sep 1996 A
5563077 Ha Oct 1996 A
5576227 Hsu Nov 1996 A
5578513 Maegawa Nov 1996 A
5595919 Pan Jan 1997 A
5595941 Okamoto et al. Jan 1997 A
5652454 Iwamatsu et al. Jul 1997 A
5658806 Lin et al. Aug 1997 A
5665203 Lee et al. Sep 1997 A
5682048 Shinohara et al. Oct 1997 A
5698869 Yoshimi et al. Dec 1997 A
5701016 Burroughes et al. Dec 1997 A
5716879 Choi et al. Feb 1998 A
5739544 Yuki et al. Apr 1998 A
5760442 Shigyo et al. Jun 1998 A
5770513 Okaniwa et al. Jun 1998 A
5773331 Solomon et al. Jun 1998 A
5776821 Haskell et al. Jul 1998 A
5793088 Choi et al. Aug 1998 A
5804848 Mukai Sep 1998 A
5811324 Yang Sep 1998 A
5814545 Seddon et al. Sep 1998 A
5814895 Hirayama et al. Sep 1998 A
5821629 Wen et al. Oct 1998 A
5827769 Aminzadeh et al. Oct 1998 A
5844278 Mizuno et al. Dec 1998 A
5856225 Lee et al. Jan 1999 A
5859456 Efland et al. Jan 1999 A
5880015 Hata Mar 1999 A
5883564 Partin Mar 1999 A
5888309 Yu Mar 1999 A
5889304 Watanabe Mar 1999 A
5899710 Mukai May 1999 A
5905285 Garnder et al. May 1999 A
5908313 Chau et al. Jun 1999 A
5952701 Bulucea Sep 1999 A
5965914 Miyamoto Oct 1999 A
5976767 Li Nov 1999 A
5981400 Lo Nov 1999 A
5985726 Yu et al. Nov 1999 A
6013926 Oku et al. Jan 2000 A
6018176 Lim Jan 2000 A
6031249 Yamazaki et al. Feb 2000 A
6051452 Shigyo et al. Apr 2000 A
6054355 Inumiya et al. Apr 2000 A
6063675 Rodder May 2000 A
6063677 Rodder et al. May 2000 A
6066869 Noble et al. May 2000 A
6087208 Krivokapic et al. Jul 2000 A
6093621 Tseng Jul 2000 A
6114201 Wu Sep 2000 A
6114206 Yu Sep 2000 A
6117697 Seaford et al. Sep 2000 A
6117741 Chatterjee et al. Sep 2000 A
6120846 Hintermaier et al. Sep 2000 A
6133593 Boos et al. Oct 2000 A
6144072 Iwamatsu et al. Nov 2000 A
6150222 Gardner et al. Nov 2000 A
6153485 Pey et al. Nov 2000 A
6163053 Kawashima Dec 2000 A
6165880 Yaung et al. Dec 2000 A
6174820 Habermehl et al. Jan 2001 B1
6190975 Kubo et al. Feb 2001 B1
6200865 Gardner et al. Mar 2001 B1
6218309 Miller et al. Apr 2001 B1
6251729 Montree et al. Jun 2001 B1
6251763 Inumiya et al. Jun 2001 B1
6252262 Jonker et al. Jun 2001 B1
6252284 Muller et al. Jun 2001 B1
6259135 Hsu et al. Jul 2001 B1
6261921 Yen et al. Jul 2001 B1
6262456 Yu et al. Jul 2001 B1
6274503 Hsieh Aug 2001 B1
6287924 Chao et al. Sep 2001 B1
6294416 Wu Sep 2001 B1
6307235 Forbes et al. Oct 2001 B1
6310367 Yagishita et al. Oct 2001 B1
6317444 Chakrabarti et al. Nov 2001 B1
6319807 Yeh et al. Nov 2001 B1
6320212 Chow Nov 2001 B1
6335251 Miyano et al. Jan 2002 B2
6358800 Tseng Mar 2002 B1
6359311 Colinge et al. Mar 2002 B1
6362111 Laaksonen et al. Mar 2002 B1
6368923 Huang Apr 2002 B1
6376317 Forbes et al. Apr 2002 B1
6383882 Lee et al. May 2002 B1
6387820 Sanderfer May 2002 B1
6391782 Yu May 2002 B1
6396108 Krivokapic et al. May 2002 B1
6399970 Kubo et al. Jun 2002 B2
6403434 Yu Jun 2002 B1
6403981 Yu Jun 2002 B1
6406795 Hwang et al. Jun 2002 B1
6407442 Inoue et al. Jun 2002 B2
6413802 Hu et al. Jul 2002 B1
6413877 Annapragada Jul 2002 B1
6424015 Ishibashi et al. Jul 2002 B1
6437550 Andoh et al. Aug 2002 B2
6457890 Kohlruss et al. Oct 2002 B1
6458662 Yu Oct 2002 B1
6459123 Enders et al. Oct 2002 B1
6465290 Suguro et al. Oct 2002 B1
6472258 Adkisson et al. Oct 2002 B1
6475869 Yu Nov 2002 B1
6475890 Yu Nov 2002 B1
6479866 Xiang Nov 2002 B1
6483146 Lee et al. Nov 2002 B2
6483151 Wakabayashi et al. Nov 2002 B2
6483156 Adkisson et al. Nov 2002 B1
6495403 Skotnicki et al. Dec 2002 B1
6498096 Bruce et al. Dec 2002 B2
6500767 Chiou et al. Dec 2002 B2
6501141 Leu Dec 2002 B1
6506692 Andideh Jan 2003 B2
6525403 Inaba et al. Feb 2003 B2
6526996 Chang et al. Mar 2003 B1
6534807 Mandelman et al. Mar 2003 B2
6537862 Song Mar 2003 B2
6537885 Kang et al. Mar 2003 B1
6537901 Cha et al. Mar 2003 B2
6541829 Nishinohara et al. Apr 2003 B2
6555879 Krivokapic et al. Apr 2003 B1
6562665 Yu May 2003 B1
6562687 Deleonibus et al. May 2003 B1
6566734 Sugihara et al. May 2003 B2
6583469 Fried et al. Jun 2003 B1
6605498 Murthy et al. Aug 2003 B1
6607948 Sugiyama et al. Aug 2003 B1
6610576 Nowak Aug 2003 B2
6611029 Ahmed et al. Aug 2003 B1
6630388 Ishii et al. Oct 2003 B2
6635909 Clark et al. Oct 2003 B2
6642090 Fried et al. Nov 2003 B1
6642114 Nakamura Nov 2003 B2
6645797 Buynoski et al. Nov 2003 B1
6645826 Yamazaki et al. Nov 2003 B2
6645861 Cabral et al. Nov 2003 B2
6656853 Ito Dec 2003 B2
6657259 Fried et al. Dec 2003 B2
6660598 Hanafi et al. Dec 2003 B2
6664160 Park et al. Dec 2003 B2
6680240 Maszara Jan 2004 B1
6686231 Ahmed et al. Feb 2004 B1
6689650 Gambino et al. Feb 2004 B2
6693324 Maegawa et al. Feb 2004 B2
6696366 Flanner et al. Feb 2004 B1
6706571 Yu et al. Mar 2004 B1
6709982 Buynoski et al. Mar 2004 B1
6713396 Anthony Mar 2004 B2
6716684 Krivokapic et al. Apr 2004 B1
6716686 Buynoski et al. Apr 2004 B1
6716690 Wang et al. Apr 2004 B1
6730964 Horiuchi May 2004 B2
6744103 Snyder Jun 2004 B2
6756657 Zhang et al. Jun 2004 B1
6762469 Mocuta et al. Jul 2004 B2
6764884 Yu et al. Jul 2004 B1
6765303 Krivokapic et al. Jul 2004 B1
6770516 Wu et al. Aug 2004 B2
6774390 Sugiyama et al. Aug 2004 B2
6780694 Doris et al. Aug 2004 B2
6784071 Chen et al. Aug 2004 B2
6784076 Gonzalez et al. Aug 2004 B2
6787402 Yu Sep 2004 B1
6787406 Hill et al. Sep 2004 B1
6787439 Ahmed et al. Sep 2004 B2
6787845 Deleonibus Sep 2004 B2
6787854 Yang et al. Sep 2004 B1
6790733 Natzle et al. Sep 2004 B1
6794313 Chang Sep 2004 B1
6794718 Nowak et al. Sep 2004 B2
6798000 Luyken et al. Sep 2004 B2
6800885 An et al. Oct 2004 B1
6800910 Lin et al. Oct 2004 B2
6803631 Dakshina-Murthy et al. Oct 2004 B2
6812075 Fried et al. Nov 2004 B2
6812111 Cheong et al. Nov 2004 B2
6815277 Fried et al. Nov 2004 B2
6821834 Ando Nov 2004 B2
6825506 Chau et al. Nov 2004 B2
6830998 Pan et al. Dec 2004 B1
6831310 Mathew et al. Dec 2004 B1
6833588 Yu et al. Dec 2004 B2
6835614 Hanafi et al. Dec 2004 B2
6835618 Dakshina-Murthy et al. Dec 2004 B1
6838322 Pham et al. Jan 2005 B2
6844238 Yeo et al. Jan 2005 B2
6849556 Takahashi Feb 2005 B2
6849884 Clark et al. Feb 2005 B2
6852559 Kwak et al. Feb 2005 B2
6855606 Chen et al. Feb 2005 B2
6855990 Yeo et al. Feb 2005 B2
6858478 Chau et al. Feb 2005 B2
6864540 Divakaruni et al. Mar 2005 B1
6867433 Yeo et al. Mar 2005 B2
6867460 Anderson et al. Mar 2005 B1
6869868 Chiu et al. Mar 2005 B2
6869898 Inaki et al. Mar 2005 B2
6870226 Maeda et al. Mar 2005 B2
6884154 Mizushima et al. Apr 2005 B2
6885055 Lee Apr 2005 B2
6890811 Hou et al. May 2005 B2
6891234 Connelly et al. May 2005 B1
6897527 Dakshina-Murthy et al. May 2005 B2
6902947 Chinn et al. Jun 2005 B2
6902962 Yeo et al. Jun 2005 B2
6909147 Aller et al. Jun 2005 B2
6909151 Hareland et al. Jun 2005 B2
6919238 Bohr Jul 2005 B2
6921691 Li et al. Jul 2005 B1
6921702 Ahn et al. Jul 2005 B2
6921963 Krivokapic et al. Jul 2005 B2
6921982 Joshi et al. Jul 2005 B2
6924190 Dennison Aug 2005 B2
6949443 Ke et al. Sep 2005 B2
6955961 Chung Oct 2005 B1
6956281 Smith et al. Oct 2005 B2
6960517 Rios et al. Nov 2005 B2
6967351 Fried et al. Nov 2005 B2
6969878 Coronel et al. Nov 2005 B2
6970373 Datta et al. Nov 2005 B2
6974738 Hareland et al. Dec 2005 B2
6975014 Krivokapic et al. Dec 2005 B1
6977415 Matsuo Dec 2005 B2
6982433 Hoffman et al. Jan 2006 B2
6998301 Yu et al. Feb 2006 B1
6998318 Park Feb 2006 B2
7005366 Chau et al. Feb 2006 B2
7013447 Mathew et al. Mar 2006 B2
7018551 Beintner et al. Mar 2006 B2
7045401 Lee et al. May 2006 B2
7045407 Keating et al. May 2006 B2
7045441 Chang et al. May 2006 B2
7056794 Ku et al. Jun 2006 B2
7060539 Chidambarrao et al. Jun 2006 B2
7061055 Sekigawa et al. Jun 2006 B2
7071064 Doyle et al. Jul 2006 B2
7074623 Lochtefeld et al. Jul 2006 B2
7074656 Yeo et al. Jul 2006 B2
7074662 Lee et al. Jul 2006 B2
7084018 Ahmed et al. Aug 2006 B1
7105390 Brask et al. Sep 2006 B2
7105891 Visokay Sep 2006 B2
7105894 Yeo et al. Sep 2006 B2
7105934 Anderson et al. Sep 2006 B2
7112478 Grupp et al. Sep 2006 B2
7115945 Lee et al. Oct 2006 B2
7119402 Kinoshita et al. Oct 2006 B2
7122463 Ohuchi Oct 2006 B2
7132360 Schaeffer et al. Nov 2006 B2
7138320 Van Bentum et al. Nov 2006 B2
7141480 Adam et al. Nov 2006 B2
7141856 Lee et al. Nov 2006 B2
7154118 Lindert Dec 2006 B2
7163851 Abadeer et al. Jan 2007 B2
7163898 Mariani et al. Jan 2007 B2
7172943 Yeo et al. Feb 2007 B2
7183137 Lee et al. Feb 2007 B2
7187043 Arai et al. Mar 2007 B2
7214991 Yeo et al. May 2007 B2
7235822 Li Jun 2007 B2
7238564 Ko et al. Jul 2007 B2
7241653 Hareland et al. Jul 2007 B2
7247547 Zhu et al. Jul 2007 B2
7247578 Brask Jul 2007 B2
7250367 Vaartstra et al. Jul 2007 B2
7250645 Wang et al. Jul 2007 B1
7268024 Yeo et al. Sep 2007 B2
7273785 Dennard et al. Sep 2007 B2
7291886 Doris et al. Nov 2007 B2
7297600 Oh et al. Nov 2007 B2
7304336 Cheng et al. Dec 2007 B2
7323710 Kim et al. Jan 2008 B2
7329913 Brask et al. Feb 2008 B2
7339241 Orlowski et al. Mar 2008 B2
7341902 Anderson et al. Mar 2008 B2
7348284 Doyle et al. Mar 2008 B2
7348642 Nowak Mar 2008 B2
7354817 Watanabe et al. Apr 2008 B2
7358121 Chau et al. Apr 2008 B2
7388259 Doris et al. Jun 2008 B2
7396730 Li Jul 2008 B2
7439120 Pei Oct 2008 B2
7452778 Chen et al. Nov 2008 B2
7456471 Anderson et al. Nov 2008 B2
7456476 Hareland et al. Nov 2008 B2
7479421 Kavalieros et al. Jan 2009 B2
7573059 Hudait et al. Aug 2009 B2
7585734 Kang et al. Sep 2009 B2
7612416 Takeuchi et al. Nov 2009 B2
7655989 Zhu et al. Feb 2010 B2
7701018 Yamagami et al. Apr 2010 B2
20010019886 Bruce et al. Sep 2001 A1
20010026985 Kim et al. Oct 2001 A1
20010040907 Chakrabarti Nov 2001 A1
20020011612 Hieda Jan 2002 A1
20020036290 Inaba et al. Mar 2002 A1
20020037619 Sugihara et al. Mar 2002 A1
20020048918 Grider et al. Apr 2002 A1
20020058374 Kim et al. May 2002 A1
20020074614 Furuta et al. Jun 2002 A1
20020081794 Ito Jun 2002 A1
20020096724 Liang et al. Jul 2002 A1
20020142529 Matsuda et al. Oct 2002 A1
20020149031 Kim et al. Oct 2002 A1
20020160553 Yamanaka et al. Oct 2002 A1
20020166838 Nagarajan Nov 2002 A1
20020167007 Yamazaki et al. Nov 2002 A1
20020177263 Hanafi et al. Nov 2002 A1
20020177282 Song Nov 2002 A1
20020185655 Fahimulla et al. Dec 2002 A1
20030036290 Hsieh et al. Feb 2003 A1
20030042542 Maegawa et al. Mar 2003 A1
20030057477 Hergenrother et al. Mar 2003 A1
20030057486 Gambino et al. Mar 2003 A1
20030067017 Ieong et al. Apr 2003 A1
20030080332 Phillips May 2003 A1
20030080384 Takahashi et al. May 2003 A1
20030085194 Hopkins, Jr. May 2003 A1
20030098479 Murthy et al. May 2003 A1
20030098488 O'Keeffe et al. May 2003 A1
20030102497 Fried et al. Jun 2003 A1
20030102518 Fried et al. Jun 2003 A1
20030111686 Nowak Jun 2003 A1
20030122186 Sekigawa et al. Jul 2003 A1
20030143791 Cheong et al. Jul 2003 A1
20030151077 Mathew et al. Aug 2003 A1
20030174534 Clark et al. Sep 2003 A1
20030190766 Gonzalez et al. Oct 2003 A1
20030201458 Clark et al. Oct 2003 A1
20030203636 Anthony Oct 2003 A1
20030227036 Sugiyama et al. Dec 2003 A1
20040016968 Coronel et al. Jan 2004 A1
20040029345 Deleonibus et al. Feb 2004 A1
20040029393 Ying et al. Feb 2004 A1
20040031979 Lochtefeld et al. Feb 2004 A1
20040033639 Chinn et al. Feb 2004 A1
20040036118 Abadeer et al. Feb 2004 A1
20040036126 Chau et al. Feb 2004 A1
20040036127 Chau et al. Feb 2004 A1
20040038436 Mori et al. Feb 2004 A1
20040038533 Liang Feb 2004 A1
20040061178 Lin et al. Apr 2004 A1
20040063286 Kim et al. Apr 2004 A1
20040070020 Fujiwara et al. Apr 2004 A1
20040075141 Maeda et al. Apr 2004 A1
20040075149 Fitzgerald et al. Apr 2004 A1
20040082125 Hou Apr 2004 A1
20040092062 Ahmed et al. May 2004 A1
20040092067 Hanafi et al. May 2004 A1
20040094807 Chau et al. May 2004 A1
20040099903 Yeo et al. May 2004 A1
20040099966 Chau et al. May 2004 A1
20040108523 Chen et al. Jun 2004 A1
20040108558 Kwak et al. Jun 2004 A1
20040110097 Ahmed et al. Jun 2004 A1
20040110331 Yeo et al. Jun 2004 A1
20040113181 Wicker Jun 2004 A1
20040119100 Nowak et al. Jun 2004 A1
20040124492 Matsuo Jul 2004 A1
20040126975 Ahmed et al. Jul 2004 A1
20040132236 Doris Jul 2004 A1
20040145000 An et al. Jul 2004 A1
20040145019 Dakshina-Murthy et al. Jul 2004 A1
20040166642 Chen et al. Aug 2004 A1
20040169221 Ko et al. Sep 2004 A1
20040169269 Yeo et al. Sep 2004 A1
20040180491 Arai et al. Sep 2004 A1
20040191980 Rios et al. Sep 2004 A1
20040195624 Liu et al. Oct 2004 A1
20040198003 Yeo et al. Oct 2004 A1
20040203254 Conley et al. Oct 2004 A1
20040209463 Kim et al. Oct 2004 A1
20040217420 Yeo et al. Nov 2004 A1
20040219711 Wu et al. Nov 2004 A1
20040219722 Pham et al. Nov 2004 A1
20040219780 Ohuchi Nov 2004 A1
20040222473 Risaki Nov 2004 A1
20040227187 Cheng et al. Nov 2004 A1
20040238887 Nihey Dec 2004 A1
20040238915 Chen et al. Dec 2004 A1
20040256647 Lee et al. Dec 2004 A1
20040262683 Bohr et al. Dec 2004 A1
20040262699 Rios et al. Dec 2004 A1
20040266076 Doris et al. Dec 2004 A1
20050019993 Lee et al. Jan 2005 A1
20050020020 Collaert et al. Jan 2005 A1
20050023633 Yeo et al. Feb 2005 A1
20050035415 Yeo et al. Feb 2005 A1
20050040429 Uppal Feb 2005 A1
20050040444 Cohen Feb 2005 A1
20050059214 Cheng et al. Mar 2005 A1
20050062082 Bucher et al. Mar 2005 A1
20050073060 Datta et al. Apr 2005 A1
20050093028 Chambers May 2005 A1
20050093067 Yeo et al. May 2005 A1
20050093075 Bentum et al. May 2005 A1
20050093154 Kottantharayil et al. May 2005 A1
20050104055 Kwak et al. May 2005 A1
20050110082 Cheng et al. May 2005 A1
20050116289 Boyd et al. Jun 2005 A1
20050118790 Lee et al. Jun 2005 A1
20050127362 Zhang et al. Jun 2005 A1
20050127632 Gehret Jun 2005 A1
20050133829 Kunii et al. Jun 2005 A1
20050133866 Chau et al. Jun 2005 A1
20050136584 Boyanov et al. Jun 2005 A1
20050139860 Snyder et al. Jun 2005 A1
20050145894 Chau et al. Jul 2005 A1
20050145941 Bedell et al. Jul 2005 A1
20050145944 Murthy et al. Jul 2005 A1
20050148131 Brask Jul 2005 A1
20050148137 Brask et al. Jul 2005 A1
20050153494 Ku et al. Jul 2005 A1
20050156171 Brask et al. Jul 2005 A1
20050156202 Rhee et al. Jul 2005 A1
20050156227 Jeng Jul 2005 A1
20050161739 Anderson et al. Jul 2005 A1
20050162928 Rosmeulen Jul 2005 A1
20050167766 Yagishita Aug 2005 A1
20050170593 Kang et al. Aug 2005 A1
20050184316 Kim Aug 2005 A1
20050189583 Kim et al. Sep 2005 A1
20050199919 Liu Sep 2005 A1
20050202604 Cheng et al. Sep 2005 A1
20050215014 Ahn et al. Sep 2005 A1
20050215022 Adam et al. Sep 2005 A1
20050224797 Ko et al. Oct 2005 A1
20050224800 Lindert et al. Oct 2005 A1
20050227498 Furkawa et al. Oct 2005 A1
20050230763 Huang et al. Oct 2005 A1
20050233156 Senzaki Oct 2005 A1
20050239252 Ahn et al. Oct 2005 A1
20050255642 Liu et al. Nov 2005 A1
20050266645 Park Dec 2005 A1
20050272192 Oh et al. Dec 2005 A1
20050277294 Schaefer et al. Dec 2005 A1
20050280121 Doris et al. Dec 2005 A1
20050287752 Nouri et al. Dec 2005 A1
20060014338 Doris et al. Jan 2006 A1
20060040054 Pearlstein et al. Feb 2006 A1
20060043500 Chen et al. Mar 2006 A1
20060046521 Vaartstra et al. Mar 2006 A1
20060063469 Talieh et al. Mar 2006 A1
20060068591 Radosavljevic et al. Mar 2006 A1
20060071275 Brask et al. Apr 2006 A1
20060071299 Doyle et al. Apr 2006 A1
20060086977 Shah et al. Apr 2006 A1
20060148182 Datta et al. Jul 2006 A1
20060154478 Hsu et al. Jul 2006 A1
20060170066 Mathew et al. Aug 2006 A1
20060172479 Furukawa et al. Aug 2006 A1
20060172480 Wang et al. Aug 2006 A1
20060172497 Hareland et al. Aug 2006 A1
20060180859 Radosavljevic et al. Aug 2006 A1
20060202270 Son et al. Sep 2006 A1
20060204898 Gutsche et al. Sep 2006 A1
20060205164 Ko et al. Sep 2006 A1
20060211184 Boyd et al. Sep 2006 A1
20060220131 Kinoshita et al. Oct 2006 A1
20060227595 Chuang et al. Oct 2006 A1
20060240622 Lee et al. Oct 2006 A1
20060244066 Yeo et al. Nov 2006 A1
20060263699 Abatchev et al. Nov 2006 A1
20060281325 Chou et al. Dec 2006 A1
20060286729 Kavalieros et al. Dec 2006 A1
20070001219 Radosavljevic et al. Jan 2007 A1
20070004117 Yagishita Jan 2007 A1
20070023795 Nagano et al. Feb 2007 A1
20070029624 Nowak Feb 2007 A1
20070045735 Orlowski et al. Mar 2007 A1
20070045748 Booth, Jr. et al. Mar 2007 A1
20070048930 Figura et al. Mar 2007 A1
20070052041 Sorada et al. Mar 2007 A1
20070069293 Kavalieros et al. Mar 2007 A1
20070069302 Jin et al. Mar 2007 A1
20070090416 Doyle et al. Apr 2007 A1
20070093010 Mathew et al. Apr 2007 A1
20070108514 Inoue et al. May 2007 A1
20070145487 Kavalieros et al. Jun 2007 A1
20070187682 Takeuchi et al. Aug 2007 A1
20070241414 Narihiro Oct 2007 A1
20070259501 Xiong et al. Nov 2007 A1
20070262389 Chau et al. Nov 2007 A1
20080017890 Yuan et al. Jan 2008 A1
20080017934 Kim et al. Jan 2008 A1
20080111163 Russ et al. May 2008 A1
20080116515 Gossner et al. May 2008 A1
20080128796 Zhu et al. Jun 2008 A1
20080128797 Dyer et al. Jun 2008 A1
20080212392 Bauer Sep 2008 A1
20080237655 Nakabayashi et al. Oct 2008 A1
20080258207 Radosavljevic et al. Oct 2008 A1
20090061572 Hareland et al. Mar 2009 A1
20090090976 Kavalieros et al. Apr 2009 A1
20090099181 Wurster et al. Apr 2009 A1
20100200923 Chen et al. Aug 2010 A1
Related Publications (1)
Number Date Country
20140035009 A1 Feb 2014 US
Divisions (2)
Number Date Country
Parent 12463309 May 2009 US
Child 13277897 US
Parent 11158661 Jun 2005 US
Child 12463309 US
Continuations (1)
Number Date Country
Parent 13277897 Oct 2011 US
Child 14048923 US