Epitaxial process

Information

  • Patent Grant
  • 8853060
  • Patent Number
    8,853,060
  • Date Filed
    Monday, May 27, 2013
    11 years ago
  • Date Issued
    Tuesday, October 7, 2014
    9 years ago
Abstract
An epitaxial process includes the following step. A recess is formed in a substrate. A seeding layer is formed to cover a surface of the recess. A buffer layer is formed on the seeding layer. An etching process is performed on the buffer layer to homogenize and shape the buffer layer. An epitaxial layer is formed on the homogenized flat bottom shape buffer layer.
Description
BACKGROUND OF THE INVENTION

1. Field of the Invention


The present invention relates generally to an epitaxial process, and more specifically to an epitaxial process, wherein a homogenized buffer layer with a flat bottom shape was formed below an epitaxial layer.


2. Description of the Prior Art


For decades, chip manufacturers have made metal-oxide-semiconductor (MOS) transistors faster by making them smaller. As the semiconductor processes advance to very deep sub micron era such as 65-nm node or beyond, how to increase the driving current for MOS transistors has become a critical issue. In order to improve the devices performances, crystal strain technology has been developed. Crystal strain technology is becoming more and more attractive as a means for getting better performances in the field of MOS transistor fabrication. Putting a strain on a semiconductor crystal alters the speed at which charges move through that crystal. Strain makes CMOS transistors work better by enabling electrical charges, such as electrons, to pass more easily through the silicon lattice of the gate channel. In the known arts, attempts have been made to use a strained silicon layer, which was grown epitaxially on a silicon substrate with a silicon germanium (SiGe) structure or a silicon carbide structure disposed therebetween. In this type of MOS transistor, a biaxial tensile strain occurs in the epitaxy silicon layer due to the silicon germanium structure or the silicon carbide structure which has a larger or smaller lattice constant than silicon, thereby altering the band structure, and the carrier mobility increases. This enhances the speed performances of the MOS transistors.


Moreover, the performance of an epitaxial layer is related to its size, ingredients, the distribution of the ingredients and its position, even the relative position to a gate. Improving the performance of an epitaxial layer to enhance the performances or achieve specific electrical requirements for formed semiconductor structure has therefore become an important issue in the industry.


SUMMARY OF THE INVENTION

The present invention provides an epitaxial process, wherein a homogenized flat bottom shape buffer layer was formed in a recess for forming an epitaxial layer to control the volume and the cross-sectional profile of the epitaxial layer formed on the buffer layer.


The present invention provides an epitaxial process including the following steps. A recess is formed in a substrate. A seeding layer is formed to cover a surface of the recess. A buffer layer is formed on the seeding layer. An etching process is performed on the buffer layer for forming a homogenized and shaped buffer layer. The center and edge thickness of the buffer layer is substantially the same after the etching process. An epitaxial layer is formed on the buffer layer.


According to the above, the present invention provides an epitaxial process, which forms a seeding layer, forms a buffer layer, performs an etching process to homogenize the buffer layer to have a flat bottom shape, and then forms an epitaxial layer on the homogenized flat bottom shape buffer layer. In this way, the homogenized flat bottom shape buffer layer is easier for the epitaxial layer to be grown thereon, and defects such as dislocations can be reduced. Moreover, the volume and the cross-sectional profile of the epitaxial layer can be adjusted by controlling the flatness and the remaining thickness of the homogenized and shaped buffer layer, thereby achieving specific electrical requirements with controlled stress caused by followed epitaxy steps. Preferably, the volume of the epitaxial layer can be enlarged by forming a thinner buffer layer through etching and shaping, thereby increasing the stresses induced by the epitaxial layer. Therefore, the stress effect induced by the epitaxial layer can be enhanced by the method of forming the homogenized flat bottom shape buffer layer of the present invention.


These and other objectives of the present invention will no doubt become obvious to those of ordinary skill in the art after reading the following detailed description of the preferred embodiment that is illustrated in the various figures and drawings.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 schematically depicts a flow chart of an epitaxial process according to an embodiment of the present invention.



FIGS. 2-8 schematically depicts cross-sectional views of an epitaxial process according to an embodiment of the present invention.





DETAILED DESCRIPTION


FIG. 1 schematically depicts a flow chart of an epitaxial process according to an embodiment of the present invention. FIGS. 2-8 schematically depict cross-sectional views of an epitaxial process according to an embodiment of the present invention. Two gates are depicted in this embodiment, which discloses an epitaxial process of the present invention, but the number of the gates is not restricted to it. An epitaxial layer is formed beside the gates in this embodiment, but it is not limited thereto. In this embodiment, germanium (Ge) is implanted/imported to form a silicon germanium (SiGe) layer or a silicon germanium (SiGe) epitaxial layer to form a PMOS transistor, but it is not limited thereto. In another embodiment, other elements may be implanted or imported to form the epitaxial layers; for example, P-type ions such as boron may be implanted or imported to form an epitaxial layer for forming a PMOS transistor, or carbon or N-type ions such as phosphorous may be implanted or imported to form an epitaxial layer for forming a NMOS transistor.


Please refer to FIG. 1 and FIGS. 2-3. According to a step K1 of FIG. 1, a recess is formed in a substrate. More precisely, as shown in FIG. 2, a substrate 110 is provided. The substrate 110 may be a semiconductor substrate such as a silicon substrate, a silicon containing substrate, a III-V group-on-silicon (such as GaN-on-silicon) substrate, a graphene-on-silicon substrate or a silicon-on-insulator (SOI) substrate.


A plurality of gates 120, such as two gates 120, is formed on the substrate 110. The gates 120 may include a dielectric layer 122, an electrode layer 124 and a cap 126. The dielectric layer 122 may be a buffer layer on and a dielectric layer having a high dielectric constant etc, depending upon the paired semiconductor process. For example, when the present invention is applied in a polysilicon gate process, the dielectric layer 122 is a dielectric suitable for a polysilicon gate such as an oxide layer; when the present invention is applied in a gate-first process or a gate-last for high-K first process, the dielectric layer 122 may include a buffer layer and a dielectric layer having a high dielectric constant; when the present invention is applied in a gate-last for high-K last with a buffer layer first process, the dielectric layer 122 may include a buffer layer and a sacrificial dielectric layer, wherein the sacrificial dielectric layer will be replaced by a dielectric layer having a high dielectric constant in a later performed metal gate replacement process; when the present invention is applied in a gate-last for high-K last with a buffer layer last process, the dielectric layer 122 may be a sacrificial dielectric layer, wherein the sacrificial dielectric layer will be replaced by a buffer layer and a dielectric layer having a high dielectric constant in a later performed metal gate replacement process. In this embodiment, the present invention is applied in a gate-last for high-K first process, and the dielectric layer 122 may include a buffer layer and a dielectric layer having a high dielectric constant. The buffer layer may be an oxide layer, which may be formed through a chemical oxide process, a thermal oxide process, or other processes, for buffering the dielectric layer having a high dielectric constant and the substrate 110. The dielectric layer having a high dielectric constant may be the group selected from hafnium oxide (HfO2), hafnium silicon oxide (HfSiO4), hafnium silicon oxynitride (HfSiON), aluminum oxide (Al2O3), lanthanum oxide (La2O3), tantalum oxide (Ta2O5), yttrium oxide (Y2O3), zirconium oxide (ZrO2), strontium titanate oxide (SrTiO3), zirconium silicon oxide (ZrSiO4), hafnium zirconium oxide (HfZrO4), strontium bismuth tantalite (SrBi2Ta2O9, SBT), lead zirconate titanate (PbZrxTi1-xO3, PZT) and barium strontium titanate (BaxSr1-xTiO3, BST). The electrode layer 124 may be a polysilicon layer to serve as a sacrificial gate, which is replaced by a metal gate through performing a replacement metal gate (RMG) process. The cap layer 126 may be a single layer or multilayer structure composed of nitride or oxide etc.


Two spacers 130 are formed on the substrate 110 beside the gates 120 respectively to define the position of a later formed epitaxial layer in the substrate 110 beside the gates 120, wherein the relative position between the epitaxial layer and the gates 120 will directly affect the stresses induced by the epitaxial layer in a gate channel C below each of the gates 120. The spacers 130 may be single layer or dual layers structures composed of an oxide layer, a nitride layer or an oxynitride layer etc. For simplifying the illustration, the spacers 130 are nitride spacers, and other spacers may be formed before or after the spacers 130 are formed. For instance, a spacer (not shown) may be formed before the spacers 130 are formed to define the position of a lightly doped source/drain (not shown) desired to be formed in the substrate 110 beside the gate 120; or a spacer (not shown) may be formed after the spacers 130 are formed to define the position of a source/drain (not shown) desired to be formed in the substrate 110 beside the gate 120. The formation sequence order of the spacers 130 and other spacers may be changed, and each of these spacers may be partially removed or completely removed after the corresponding epitaxial layer, lightly doped source/drain or source/drain is formed, depending upon a desired formed semiconductor structure.


Thereafter, an etching process P1 is performed to form at least a recess R beside each of the gates 120. Preferably, a recess R is respectively formed in the substrate 110 beside two sides of each of the gates 120. As shown in FIG. 2, only one recess R is formed in the substrate 110 beside the two spacers 130 for clarity purposes. The etching process P1 may be a dry etching process or/and a wet etching process. For instance, the etching process P1 may include performing a dry etching process to form the recess R with a predetermined depth dl and then performing a wet etching process to adjust the size and the shape of the recess R. In this embodiment, the recess R has a diamond shaped cross-sectional profile, but it is not limited thereto. In another embodiment, the recess R may have a differently shaped cross-sectional profile such as a U-shaped cross-sectional profile, a hexagonal-shaped cross-sectional profile or an octagonal-shaped cross-sectional profile. The epitaxial process presented in the present invention is suited for being applied to the recess R having various cross-sectional profiles (or a later formed epitaxial layer having various cross-sectional profiles in the recess R).


According to a step K2 of FIG. 1, a seeding layer is formed to cover a surface of the recess. As shown in FIG. 4, a seeding layer 140 is formed to cover a surface S1 of the recess R. The seeding layer may be formed through a chemical vapor deposition (CVD) process with silicon containing source gas, but it is not limited thereto. In this embodiment, the method for forming the seeding layer may have only dichlorosilane (DCS) gas imported to form a pure silicon layer on the surface S1 of the recess R, but it is not limited thereto. Moreover, the method for forming the seeding layer may further include importing other gases to form a silicon-containing layer on the surface S1 of the recess R, depending upon the processing needs or a desired formed structure. For example, hydrogen chloride (HCl) gas may be imported to form a silicon layer, wherein the forming ratio of the specific positions can be controlled by adjusting the dichlorosilane (DCS) gas and hydrogen chloride (HCl) gases quantities. In other words, partial areas may be removed by etching when the seeding layer 140 is formed through importing dichlorosilane (DCS) gas and hydrogen chloride (HCl) gas simultaneously. As a result, the seeding layer 140 having a desired profile can be controlled precisely in a macroscopic view.


According to a step K3 of FIG. 1, a buffer layer is formed on the seeding layer after the seeding layer 140 is formed. As shown in FIG. 5, a buffer layer 150 is formed on the seeding layer 140. The buffer layer 150 may be a silicon germanium (SiGe) layer with a low germanium concentration for buffering the seeding layer 140 of a pure silicon or a surface of the recess R and a later formed epitaxial layer with a high germanium concentration on the buffer layer 150, thereby reducing the quantity of structural defects such as substrate dislocations caused by the epitaxial layer. Thus, the seeding layer 140 and the buffer layer 150 may include different materials, or the same materials with different concentrations. Preferably, the germanium (Ge) content of the buffer layer 150 is lower than 50%. Still preferably, the germanium (Ge) content of the buffer layer 150 has a gradient distribution with a concentration increasing from the outer side (which substantially contacts the seeding layer 140) toward the inner side. The seeding layer 150 may be a chemical vapor deposition (CVD) process with silicon source gas, but it is not limited thereto. For instance, the seeding layer 150 may have hydrogen chloride (HCl), dichlorosilane (DCS) and germanium (Ge) gases imported, wherein germanium (Ge) gas may be germane (GeH4) gas, but it is not limited thereto. For example, under a pressure of 10 torrs, dichlorosilane (DCS) gas maybe imported at 50 sccm (Standard Cubic Centimeter per Minute) and germanium (Ge) gas maybe imported at 250 sccm, or germanium (Ge) gas maybe imported at 70˜380 sccm instead. Furthermore, hydrogen chloride (HCl) gas may be further imported to remove some areas by etching under the same deposition circumstance. Thus, in a macroscopic view, the buffer layer 150 can be formed at specific positions.


The buffer layer 150 may selectively have boron implanted. One of the purposes of the buffer layer 150 is to prevent boron in a boron-containing epitaxial layer formed thereon from diffusing outward to the substrate 110, and this purpose can be achieved by adjusting the boron content in the buffer layer 150 or even without boron in the buffer layer 150. It is emphasized that the buffer layer 150 at this time has a non-homogeneous and rough surface S2. If an epitaxial layer is directly formed on the buffer layer 150, structural defects in the epitaxial layer will occur and the volume and the cross-sectional profile of the epitaxial layer will be hard to control, thereby degrading the overall device performances.


Therefore, according to a step K4 of FIG. 1, an etching process is performed on the buffer layer to homogenize and shape the surface of the buffer layer. As shown in FIG. 6, an etching process P2 is performed to homogenize and shape buffer layer 150, thereby forming a liner buffer layer 150′, which has a homogeneous flat bottom surface S3 with substantially same thickness at recessed bottom center and edge. In this way, the aforesaid problem can be solved, which means that defects of a later formed epitaxial layer on the buffer layer 150′ can be reduced and the volume and the cross-sectional profile of the epitaxial layer can be well controlled. Moreover, as a part of (the surface S2 of) the buffer layer 150 is removed and the flat bottom surface S3 is formed, the volume of the epitaxial layer can be enlarged, thereby improving the stress performance induced in the gate channel C.


The etching process P2 may include at least an etching gas imported to etch specific areas or specific crystal planes of the buffer layer 150. In one embodiment, the etching gas may be hydrogen chloride (HCl) gas, which can etch specific crystal planes of the buffer layer 150 to remove non-homogeneous areas, so that the buffer layer 150′ can be formed with a flat bottom shape, but it is not limited thereto. Moreover, the etching process P2 may further include having at least a depositing gas imported to compensate areas that were over-etched during the etching process; that is, the etching rates of specific positions can be controlled. The depositing gas may include silane (SiH4), dichlorosilane (DCS) or/and germane (GeH4), but it is not limited thereto. It is emphasized that due to the etching rate of the etching process P2 being larger than the depositing rate of the etching process P2, the characteristic of etching and the buffer layer 150 with a homogenized flat bottom shape can be maintained in a macroscopic view. Moreover, the total flow rate of the etching gas of the etching process P2 may be larger than the total flow rate of the depositing gas of the etching process P2, so that the characteristic of etching and smooth surface can be maintained. For instance, when hydrogen chloride (HCl) gas is imported to serve as an etching gas during the etching process P2, and dichlorosilane (DCS) gas and germane (GeH4) gases are imported to serve as depositing gases during the etching process P2, hydrogen chloride (HCl) gas is preferably imported at 200 sccm, dichlorosilane (DCS) gas is preferably imported at 50 sccm and germane (GeH4) gas is preferably imported at 120 sccm. Therefore, the total flow rate of the etching gas (i.e. hydrogen chloride gas) of the etching process P2 is larger than the total flow rate of the depositing gas (i.e. dichlorosilane and germane gases) of the etching process P2, thereby having suitable etching rates for specific areas, but is it not limited thereto. Moreover, the etching process P2 is preferred to be performed at a low pressure to have different etching rates in different crystal planes, and the homogenization and shaping step of the buffer layer 150 can therefore be controlled precisely and the thickness of the buffer layer 150′ can also be controlled. The process pressure can be at 0.1 torrs to 200 torrs. Preferably, the process pressure can be at 1 torrs to 100 torrs, or 5-50 torrs still preferably.


The etching process P2 is preferably performed in-situ, so that oxidation and pollution of the buffer layer 150′ and other layers caused by exposing them to the air can be avoided. In other words, the etching process P2 may be performed in the same processing chamber as the one where the seeding layer, the buffer layer and the epitaxial layer are formed. Preferably, the etching process P2 is performed by importing different gases or the same gases with different ratios in the same processing chamber as one where the seeding layer, the buffer layer and the epitaxial layer are formed, depending upon the needs. Thus, the qualities of a formed semiconductor component can be ensured, processes can be simplified and costs can be reduced.


According to a step K5 of FIG. 1, an epitaxial layer is formed on the buffer layer. As shown in FIGS. 7-8, an epitaxial layer 160 is formed on the buffer layer 150′. In an embodiment, the epitaxial layer 160 may include a silicon germanium (SiGe) epitaxial layer, but it is not limited thereto. In this embodiment, the epitaxial layer 160 includes a bulk epitaxial layer 162 and a cap epitaxial layer 164 from bottom to top.


More precisely, as shown in FIG. 7, the bulk epitaxial layer 162 is formed on the buffer layer 150′. At this time, the bulk epitaxial layer 162 fills up the recess R of FIG. 3. Preferably, a top surface T1 of the bulk epitaxial layer 162 is at least on the same level as a top surface T2 of the substrate 110, thereby exerting fully the stress performance of the bulk epitaxial layer 162 and divots on the bulk epitaxial layer 162 will not form, which would lead to coverage difficulty when forming structures thereon. The bulk epitaxial layer 162 may be a silicon germanium (SiGe) epitaxial layer and its germanium (Ge) content is higher than 15% to have a high enough concentration for inducing stresses in the gate channel C because the stresses induced by the epitaxial layer originate mainly from the bulk epitaxial layer 162. The bulk epitaxial layer 162 may be a vapor deposition process, but it is not limited thereto. For instance, dichlorosilane gas at a flow rate of 50 sccm and germane gas at a flow rate of 600 sccm are imported under a pressure of 10 torrs, or germane gas at a flow rate of 380˜800 sccm may be imported instead. Moreover, the bulk epitaxial layer 162 may have ions such as boron imported to increase conductivity, such that diborane (B2H6) at a flow rate of 220 sccm can be imported or diborane (B2H6) at a flow rate of 70˜280 sccm can be imported instead, but it is not limited thereto.


As shown in FIG. 8, the cap epitaxial layer 164 is formed on the bulk epitaxial layer 162. A top surface T3 of the cap epitaxial layer 164 is higher than the top surface T2 of the substrate 110. In this embodiment, the cap epitaxial layer 164 may be a silicon layer to prevent ingredients such as germanium in the bulk epitaxial layer 162 from diffusing outwards. The cap epitaxial layer 164 may be a silicon germanium (Ge) layer with a germanium concentration decreasing from bottom to top. Preferably, the maximum germanium content of the cap epitaxial layer 164 (i.e. the germanium content in a bottom surface T4) is lower than the germanium content of the bulk epitaxial layer 162, and the germanium content in the top surface T3 of the cap epitaxial layer 164 is substantially zero. Furthermore, the cap epitaxial layer 164 may have P-type ions such as boron ions selectively doped to increase conductivity.


Later semiconductor processes such as a source/drain (not shown) implantation process or a salicide process may be performed, which are not described herein. Moreover, implanting source/drain may be performed before the etching process P1 for forming the recess R is performed or at the same time as the bulk epitaxial layer 162 is formed.


To summarize, the present invention provides an epitaxial process, which forms a seeding layer, forms a buffer layer, performs an etching process to homogenize and shape the buffer layer, and then forms an epitaxial layer on the homogenized flat bottom shaped buffer layer. In this way, it is easier for an epitaxial layer to grow on the flat bottom shaped buffer layer, and defects such as dislocations can therefore be reduced. Moreover, the volume and the cross-sectional profile of the epitaxial layer can be adjusted by controlling the flatness and the remaining thickness of the homogenized flat bottom shaped buffer layer, thereby achieving specific electrical requirements. Preferably, the volume of the epitaxial layer can be enlarged by forming a thinner buffer layer through etching and shaping, thereby increasing stresses induced by the epitaxial layer. Therefore, the stress effect induced by the epitaxial layer can be enhanced by the method of forming a homogenized flat bottom shaped buffer layer of the present invention.


Moreover, the etching process of the present invention can etch specific areas or specific crystal planes of the buffer layer, thereby forming the homogenized flat bottom shaped buffer layer. The etching process may include at least an etching gas and at least a selective depositing gas. However, the etching rate of the etching process must be larger than the depositing rate of the etching process to achieve the etching purpose. Intuitively, the total flow rate of the etching gas imported during the etching process is larger than the total flow rate of the depositing gas imported during the etching process to ensure the etching and the shaping characteristics of the etching process. In this way, the purpose of better controlling the etching rates on specific areas can be achieved by importing etching gases and depositing gases simultaneously and by adjusting the compositions and their ratios of these gases; the final thickness at center and edge area of the buffer layer will be substantially the same.


Preferably, the etching process may include importing hydrogen chloride (HCl) gas serving as an etching gas, and selectively further include silane (SiH4), dichlorosilane (DCS) or/and germane (GeH4) gases serving as depositing gases. Moreover, the etching process is performed in the same processing chamber or is performed in-situ when forming the seeding layer, the buffer layer and the epitaxial layer to prevent layers from exposing these layers to the air. Preferably, the etching process is performed by importing different gases or the same gases with different ratios in the same processing chamber as the one for forming the seeding layer, the buffer layer and the epitaxial layer, thereby simplifying the processes and reducing the pollution. In this way, the yields and the quality of a formed semiconductor component are improved.


Moreover, the epitaxial process of the present invention can also be applied in a non-planar MOSFET such as a fin field-effect transistor (FinFET), which includes forming a gate disposed across a fin-shaped structure, forming a recess in the fin-shaped structure by serving the gate and a spacer as a hard mask, forming a seeding layer, forming a buffer layer, performing an etching process to homogenize and shape the buffer layer, and then forming an epitaxial layer on the shaped buffer layer.


Those skilled in the art will readily observe that numerous modifications and alterations of the device and method may be made while retaining the teachings of the invention. Accordingly, the above disclosure should be construed as limited only by the metes and bounds of the appended claims.

Claims
  • 1. An epitaxial process, comprising: forming a recess in a substrate;forming a seeding layer to cover a surface of the recess;forming a buffer layer on the seeding layer;performing an etching process on the buffer layer to homogenize and shape the buffer layer; andforming an epitaxial layer on the buffer layer.
  • 2. The epitaxial process according to claim 1, wherein the seeding layer comprises being formed by importing dichlorosilane (DCS) gas.
  • 3. The epitaxial process according to claim 1, wherein the buffer layer comprises being formed by importing hydrogen chloride (HCl), dichlorosilane (DCS), germane (GeH4) gas.
  • 4. The epitaxial process according to claim 1, wherein the etching process comprises importing at least an etching gas.
  • 5. The epitaxial process according to claim 4, wherein the etching gas comprises hydrogen chloride (HCl) gas.
  • 6. The epitaxial process according to claim 4, wherein the etching process comprises importing at least a depositing gas.
  • 7. The epitaxial process according to claim 6, wherein the depositing gas comprises silane (SiH4), dichlorosilane (DCS) or/and germane (GeH4) gas.
  • 8. The epitaxial process according to claim 6, wherein the total flow rate of the etching gas is larger than the total flow rate of the depositing gas.
  • 9. The epitaxial process according to claim 6, wherein the etching rate of the etching process is larger than the depositing rate of the etching process.
  • 10. The epitaxial process according to claim 1, wherein the etching process is performed in-situ.
  • 11. The epitaxial process according to claim 1, wherein the etching process is performed in the same processing chamber as the one where the seeding layer, the buffer layer and the epitaxial layer are formed.
  • 12. The epitaxial process according to claim 11, wherein the etching process is performed by importing different gases from forming the seeding layer, forming the buffer layer and forming the epitaxial layer.
  • 13. The epitaxial process according to claim 1, wherein the epitaxial layer comprises a silicon germanium (SiGe) epitaxial layer.
  • 14. The epitaxial process according to claim 1, wherein the epitaxial layer comprises a bulk epitaxial layer and a cap epitaxial layer from bottom to top.
  • 15. The epitaxial process according to claim 14, wherein the bulk epitaxial layer comprises a silicon germanium (SiGe) epitaxial layer, and the germanium (Ge) content is higher than 15%.
  • 16. The epitaxial process according to claim 1, wherein the seeding layer and the buffer layer comprise different materials.
  • 17. The epitaxial process according to claim 1, wherein the seeding layer comprises a silicon layer.
  • 18. The epitaxial process according to claim 1, wherein the buffer layer comprises a silicon germanium (SiGe) layer.
  • 19. The epitaxial process according to claim 18, wherein the germanium (Ge) content of the buffer layer is lower than 50%.
US Referenced Citations (146)
Number Name Date Kind
4891303 Garza Jan 1990 A
5217910 Shimizu Jun 1993 A
5273930 Steele Dec 1993 A
5356830 Yoshikawa Oct 1994 A
5372957 Liang Dec 1994 A
5385630 Philipossian Jan 1995 A
5399506 Tsukamoto Mar 1995 A
5625217 Chau Apr 1997 A
5777364 Crabbe Jul 1998 A
5783478 Chau Jul 1998 A
5783479 Lin Jul 1998 A
5960322 Xiang Sep 1999 A
6030874 Grider Feb 2000 A
6048756 Lee Apr 2000 A
6074954 Lill Jun 2000 A
6100171 Ishida Aug 2000 A
6110787 Chan Aug 2000 A
6165826 Chau Dec 2000 A
6165881 Tao Dec 2000 A
6191052 Wang Feb 2001 B1
6228730 Chen May 2001 B1
6274447 Takasou Aug 2001 B1
6274894 Wieczorek et al. Aug 2001 B1
6355533 Lee Mar 2002 B2
6365476 Talwar Apr 2002 B1
6368926 Wu Apr 2002 B1
6444591 Schuegraf Sep 2002 B1
6537370 Hernandez Mar 2003 B1
6544822 Kim Apr 2003 B2
6605498 Murthy Aug 2003 B1
6613695 Pomarede Sep 2003 B2
6621131 Murthy Sep 2003 B2
6624068 Thakar Sep 2003 B2
6632718 Grider Oct 2003 B1
6642122 Yu Nov 2003 B1
6664156 Ang Dec 2003 B1
6676764 Joo Jan 2004 B2
6699763 Grider Mar 2004 B2
6703271 Yeo Mar 2004 B2
6777275 Kluth Aug 2004 B1
6806151 Wasshuber Oct 2004 B2
6809402 Hopper Oct 2004 B1
6858506 Chang Feb 2005 B2
6861318 Murthy Mar 2005 B2
6864135 Grudowski Mar 2005 B2
6869867 Miyashita Mar 2005 B2
6887751 Chidambarrao May 2005 B2
6887762 Murthy May 2005 B1
6891192 Chen May 2005 B2
6930007 Bu Aug 2005 B2
6946350 Lindert Sep 2005 B2
6962856 Park Nov 2005 B2
6972461 Chen Dec 2005 B1
6991979 Ajmera Jan 2006 B2
6991991 Cheng Jan 2006 B2
7037773 Wang May 2006 B2
7060576 Lindert Jun 2006 B2
7060579 Chidambaram Jun 2006 B2
7112495 Ko Sep 2006 B2
7118952 Chen Oct 2006 B2
7132338 Samoilov Nov 2006 B2
7169675 Tan Jan 2007 B2
7183596 Wu Feb 2007 B2
7202124 Fitzgerald Apr 2007 B2
7217627 Kim May 2007 B2
7288822 Ting Oct 2007 B1
7303999 Sriraman Dec 2007 B1
7335959 Curello Feb 2008 B2
7410859 Peidous Aug 2008 B1
7462239 Brabant Dec 2008 B2
7491615 Wu Feb 2009 B2
7494856 Zhang Feb 2009 B2
7494858 Bohr Feb 2009 B2
7592231 Cheng Sep 2009 B2
7667227 Shimamune Feb 2010 B2
7682940 Ye Mar 2010 B2
7691752 Ranade Apr 2010 B2
7838370 Mehta Nov 2010 B2
8367528 Bauer et al. Feb 2013 B2
20020160587 Jagannathan Oct 2002 A1
20020182423 Chu Dec 2002 A1
20030181005 Hachimine Sep 2003 A1
20030203599 Kanzawa Oct 2003 A1
20040045499 Langdo Mar 2004 A1
20040067631 Bu Apr 2004 A1
20040227164 Lee Nov 2004 A1
20050070076 Dion Mar 2005 A1
20050079692 Samoilov Apr 2005 A1
20050082616 Chen Apr 2005 A1
20050139231 Abadie Jun 2005 A1
20050260830 Kwon Nov 2005 A1
20050285193 Lee Dec 2005 A1
20050287752 Nouri Dec 2005 A1
20060051922 Huang Mar 2006 A1
20060057859 Chen Mar 2006 A1
20060076627 Chen Apr 2006 A1
20060088968 Shin Apr 2006 A1
20060115949 Zhang Jun 2006 A1
20060163558 Lee Jul 2006 A1
20060228842 Zhang Oct 2006 A1
20060231826 Kohyama Oct 2006 A1
20060258126 Shiono Nov 2006 A1
20060281288 Kawamura Dec 2006 A1
20060292779 Chen Dec 2006 A1
20060292783 Lee Dec 2006 A1
20070023847 Rhee Feb 2007 A1
20070034906 Wang Feb 2007 A1
20070049014 Chen Mar 2007 A1
20070072353 Wu Mar 2007 A1
20070072376 Chen Mar 2007 A1
20070082451 Samoilov Apr 2007 A1
20070128783 Ting Jun 2007 A1
20070166929 Matsumoto Jul 2007 A1
20070262396 Zhu Nov 2007 A1
20080014688 Thean Jan 2008 A1
20080061366 Liu Mar 2008 A1
20080067545 Rhee Mar 2008 A1
20080076236 Chiang Mar 2008 A1
20080085577 Shih Apr 2008 A1
20080116525 Liu May 2008 A1
20080124874 Park May 2008 A1
20080128746 Wang Jun 2008 A1
20080142886 Liao Jun 2008 A1
20080220579 Pal Sep 2008 A1
20080233722 Liao Sep 2008 A1
20080233746 Huang Sep 2008 A1
20090039389 Tseng Feb 2009 A1
20090045456 Chen Feb 2009 A1
20090075029 Thomas et al. Mar 2009 A1
20090095992 Sanuki Apr 2009 A1
20090117715 Fukuda May 2009 A1
20090124056 Chen May 2009 A1
20090166625 Ting Jul 2009 A1
20090184402 Chen Jul 2009 A1
20090186475 Ting Jul 2009 A1
20090246922 Wu Oct 2009 A1
20090278170 Yang Nov 2009 A1
20090302348 Adam Dec 2009 A1
20100001317 Chen Jan 2010 A1
20100093147 Liao Apr 2010 A1
20110117732 Bauer et al. May 2011 A1
20110212604 Yang et al. Sep 2011 A1
20110278651 Thirupapuliyur et al. Nov 2011 A1
20120138897 Lin et al. Jun 2012 A1
20120295427 Bauer Nov 2012 A1
20130105861 Liao et al. May 2013 A1