Low shrinkage dielectric films

Information

  • Patent Grant
  • 9018108
  • Patent Number
    9,018,108
  • Date Filed
    Friday, March 15, 2013
    11 years ago
  • Date Issued
    Tuesday, April 28, 2015
    9 years ago
Abstract
Methods of forming a dielectric layer on a substrate are described, and may include introducing a first precursor into a remote plasma region fluidly coupled with a substrate processing region of a substrate processing chamber A plasma may be formed in the remote plasma region to produce plasma effluents. The plasma effluents may be directed into the substrate processing region. A silicon-containing precursor may be introduced into the substrate processing region, and the silicon-containing precursor may include at least one silicon-silicon bond. The plasma effluents and silicon-containing precursor may be reacted in the processing region to form a silicon-based dielectric layer that is initially flowable when formed on the substrate.
Description
TECHNICAL FIELD

The present technology relates to semiconductor processes and equipment. More specifically, the present technology relates to forming dielectric materials.


BACKGROUND

As integrated circuit chipmakers continue increasing the density of circuit elements on each chip, filling the gaps that separate those elements becomes more challenging. The increased circuit element density has necessitated shorter widths between adjacent elements. As the width of these gaps shrink faster than their height, the ratio of height to width (known as the aspect ratio) proportionally increases. It is more difficult to fill a tall and narrow gap (i.e., a high aspect ratio gap) with a uniform film of dielectric material than a shallow and wide gap (i.e., a low aspect ratio gap).


One commonly encountered difficulty with filling high aspect ratio gaps is the formation of voids. In high aspect ratio gaps, there is a tendency of the dielectric material filling the gap to deposit at a faster rate around the top end of the gap. Often the dielectric material will close the top before the gap has been completely filled, leaving a void. Even when the top of the gap does not close prematurely, the uneven growth rate of the dielectric film down the sidewalls of the gap can create a weak seam in the middle of the gapfill. These seams can later result in cracks that adversely affect the physical integrity and dielectric properties of the device.


One technique to avoid the formation of voids and weak seams in dielectric gapfills is to fill the gap at a lower deposition rate. Lower deposition rates can give the dielectric material more time to redistribute on the inside surfaces of the gap to reduce the chances of excessive topside growth. A lower deposition rate may also be the result of increased etching or sputtering that occur at the same time as the dielectric deposition. For example, in HDPCVD dielectric material at the top corners of the gap etch away faster than material on the sidewalls and bottom portion of the gap. This increases the chances that the topside of the gap will remain open so the sidewalls and bottom can completely fill with dielectric material. However, reducing the dielectric deposition rate also results in the deposition taking longer to complete. The longer deposition times decrease the rate at which substrate wafers are processed through the deposition chamber, resulting in a reduced efficiency for chamber.


Thus, there is a need for improved systems and methods for filling short-width, high aspect ratio gaps with a void free dielectric film. These and other problems are addressed by the systems and methods of the present invention.


SUMMARY

Methods of forming a dielectric layer on a substrate are described, and may include introducing a first precursor into a remote plasma region fluidly coupled with a substrate processing region of a substrate processing chamber A plasma may be formed in the remote plasma region to produce plasma effluents. The plasma effluents may be directed into the substrate processing region. A silicon-containing precursor may be introduced into the substrate processing region, and the silicon-containing precursor may include at least one silicon-silicon bond. The plasma effluents and silicon-containing precursor may be reacted in the processing region to form a silicon-based dielectric layer that is initially flowable when formed on the substrate.


The silicon-containing precursors may include at least two silicon-silicon bonds, and may include three or more. The first precursor may include one or more precursors selected from the group including ammonia, nitrogen, H2, Ar, and He, and may include additional carrier gases or combinations of precursors as well. The plasma effluents and silicon-containing precursor may be introduced into the processing region through a showerhead configured to maintain separation of the precursors so that they do not contact each other until they enter the substrate processing region. The substrate may be maintained at a distance less than or at about 3 inches from the showerhead, and may be maintained closer or further away in disclosed embodiments. The substrate processing region may be plasma-free during the deposition process, and in alternative arrangements a direct plasma may be provided within the processing region.


The silicon-containing precursor may have the formula SixHy, where x is greater than or equal to 2, and y is 2x+n or greater, where n is any number less than or equal to 2. The silicon-containing precursor may also be introduced into the processing region in a substantially vapor phase. The method for deposition may be performed at a temperature of less than or equal to about 30° C., and the pressure during the process may be less than or equal to about 5 Torr. The as-formed film produced by the described processes may have a density greater than or equal to about 1.4 g/cc.


The methods may also include stopping the introduction of the silicon-containing precursor after the silicon-based dielectric layer is formed. The plasma effluents may be continuously directed into the substrate processing region, however, in order to densify the formed dielectric layer. The methods may further include annealing the formed silicon-based dielectric layer, and during the anneal, the formed silicon-based dielectric layer may shrink by less than about 20%.


Methods are also described for forming a dielectric layer on a substrate in a substrate processing region of a processing chamber. The methods may include introducing a first precursor into a remote plasma region fluidly coupled with the substrate processing region while forming a plasma in the remote plasma region to produce plasma effluents. The methods may also include directing the plasma effluents into the substrate processing region, and introducing a silicon-containing precursor into the substrate processing region. The silicon-containing precursor may include at least one silicon-silicon bond in disclosed embodiments. The methods may also include reacting the plasma effluents and silicon-containing precursor in the substrate processing region to form a silicon-based dielectric layer that is initially flowable when formed on the substrate. The methods may further include curing the formed silicon-based dielectric layer with at least one additional precursor.


The at least one additional precursor utilized may include an oxygen-containing precursor, a nitrogen-containing precursor, or a carbon-containing precursor. The methods may also include directing the plasma effluents into the substrate processing region to densify the cured dielectric layer. The silicon-containing precursor utilized may have the formula SixHy, where x is greater than or equal to 2, and y is 2x+n or greater, where n is any number less than or equal to 2, and where the silicon-containing precursor is introduced into the processing region in a substantially vapor phase. The precursors introduced into the processing chamber to form the silicon-based dielectric layer may include one or more inert precursors and a silicon-containing precursor having silicon-silicon and silicon-hydrogen containing bonds. The methods may also include the step of annealing the formed silicon-based dielectric layer. When performed, the annealing may shrink the formed dielectric layer by less than about 20% during the annealing.


Such technology may provide numerous benefits over conventional techniques. For example, the deposition processes disclosed may produce denser and higher quality films. As such, film shrinkage may be reduced or prevented during annealing or post-formation operations. These and other embodiments, along with many of their advantages and features, are described in more detail in conjunction with the below description and attached figures.





BRIEF DESCRIPTION OF THE DRAWINGS

A further understanding of the nature and advantages of the disclosed technology may be realized by reference to the remaining portions of the specification and the drawings.



FIG. 1 shows a flow chart of a process for forming a dielectric film according to disclosed embodiments.



FIG. 2 shows another flow chart of a process for forming a dielectric film according to disclosed embodiments.



FIG. 3A shows a schematic cross-sectional view of a portion of a substrate processing chamber according to the disclosed technology.



FIG. 3B shows a bottom plan view of a showerhead according to the disclosed technology.



FIG. 4 shows a top plan view of an exemplary substrate processing system according to the disclosed technology.





In the appended figures, similar components and/or features may have the same numerical reference label. Further, various components of the same type may be distinguished by following the reference label by a letter that distinguishes among the similar components and/or features. If only the first numerical reference label is used in the specification, the description is applicable to any one of the similar components and/or features having the same first numerical reference label irrespective of the letter suffix.


DETAILED DESCRIPTION

The present technology includes improved processes and chemistry profiles for depositing silicon-based materials on substrates. While conventional processes may deposit films of similar materials, the films may suffer from reduced quality and density. Accordingly, when lower quality films are densified to produce a higher quality film, film shrinkage may occur that may have an adverse effect on the underlying device. For example, as device geometries are reduced, the silicon or device base may have thinner wall profiles. When a film is deposited within the structures and densified, the shrinking film may exert stress on the underlying structures that can deform the patterning. The present technology, however, may form flowable films that fundamentally shrink less than conventional films. In so doing, more intricate patterns can be covered. For example, trenches within the device may have very high aspect ratios, such as having a height:width ratio greater than or about 5:1, 8:1, 10:1, etc. or more, and as such a flowable dielectric film may be required to provide a bottom-up fill profile. If these films also shrink less when densified, less stress is exerted on the underlying structure, and overall process quality may be improved.


Methods of forming a dielectric layer on a substrate are described, and may include introducing a first precursor into a remote plasma region fluidly coupled with a substrate processing region of a substrate processing chamber A plasma may be formed in the remote plasma region to produce plasma effluents. The plasma effluents may be directed into the substrate processing region. A silicon-containing precursor may be introduced into the substrate processing region, and the silicon-containing precursor may include at least one silicon-silicon bond. The plasma effluents and silicon-containing precursor may be reacted in the processing region to form a silicon-based dielectric layer that is initially flowable when formed on the substrate.


Precursors used in deposition of silicon-based films may include a variety of additional molecules that affect the quality of the deposited film. For example, the presence of hydroxyl groups may increase the flowability of a deposited film. However, it may be desirable to remove these groups in the final film to produce higher quality films. The removal of these groups, or the substitution with other materials including oxygen, nitrogen, and carbon, for example, may reduce the overall density of the deposited or formed film. Accordingly, when later processing steps used to densify the film are performed, the film may shrink, which may produce unwanted stresses on the underlying structure. The inventors have advantageously determined that by reducing the inclusion of materials beyond silicon in the utilized precursors, the resulting film may have improved quality and may have reduced shrinking as compared to conventional films based on more varied precursor groups.


In order to better understand and appreciate the invention, reference is now made to FIG. 1, which shows a flow chart of a process for forming a dielectric film according to disclosed embodiments. Prior to the first operation, a substrate may be delivered into a process chamber, such as those described below. The substrate may be previously patterned or relatively clean. Various front end processing may have been performed including the formation of gates, vias, trenches, and other structures. These structures may be on the nanometer scale, and for example, trenches or gaps that require filling may have widths of less than about 100 nm, and may alternatively be less than or about 75 nm, 50 nm, 40 nm, 30 nm, 25 nm, 20 nm, 10 nm, etc. or less. The patterned substrate may then be delivered to a substrate processing region for deposition of a dielectric material. In disclosed embodiments, the substrate may already be located in the processing region if a previous operation was performed in the same chamber in which the deposition process is to occur. At operation 110, a first precursor may be introduced into a plasma region of the processing chamber that is separate or removed from the processing region of the chamber in which the substrate resides. The first precursor may include one of several precursor materials. For example, the first precursor may be one or more inert gases including argon, helium, nitrogen, etc. Additional gases may alternatively or additionally be used, and may include ammonia (NH3), hydrogen, or nitrogen and/or hydrogen-containing gases. In disclosed embodiments, the first precursor may exclusively include inert gases, and in an exemplary process argon or helium is delivered to the plasma region.


The separate plasma region may be referred to as a remote plasma region herein and may be within a distinct module separate from the processing chamber, or as a compartment within the processing chamber. A plasma may be formed within the remote plasma region thereby generating plasma effluents from the first precursor. At operation 120, the generated plasma effluents are directed into the substrate processing region. This may be effected in a number of ways, including with a pressure differential, generated electric field, or some other known mechanism for directing the flow of ions and/or electrons into the processing region. Before, after, or concurrently with operation 120, a silicon-containing precursor may be introduced into the substrate processing region. In disclosed embodiments, the silicon-containing precursor includes at least one silicon-silicon bond.


The plasma effluents and silicon-containing precursor may be reacted in the substrate processing region to form a silicon based dielectric layer on the substrate. The formed material may be initially flowable when formed or when deposited initially, which may allow the material to flow down into trenches to fill defined patterns on the substrate. The dielectric material may be based on reactions between the plasma species and the silicon-containing precursor. The precursors may begin reacting directly upon contacting one another, and accordingly the precursors may be separated until entering the substrate processing region. Such separation may be performed by components such as a dual-channel showerhead as described further below. The showerhead may be configured to maintain separation of the precursors so as to prevent the precursors from contacting one another until they enter or are delivered into the substrate processing region. Previous technologies may have relied on the inclusion of water or hydroxyl groups in the as deposited film to potentially impart the flowability of the film. As previously stated, though, these groups may produce weaker films that may shrink unacceptably upon densification. The present technology, however, utilizes a variety of parameters that may synergistically allow flowability to occur.


Without being bound to a particular theory, the number of silicon-silicon bonds in the deposited film may directly correspond to the amount of shrinking of the produced film. For example, the more silicon-silicon bonds in the film, the less shrinking may occur as a result of densification because less additional polymerization may be imparted along with less removal of unwanted species. Such as when a silicon oxide film is being formed, after the initial deposition, the formed film may be oxidized or reacted with additional material so as to incorporate oxygen into the polymer matrix, and remove residual materials such as hydrogen, nitrogen, carbon, etc. The more materials that are removed from the film may leave pores within the film that are removed during densification, such as annealing. The removal of these pores may compress the film imparting stress along surfaces contacted by the film. These stresses may overcome a threshold that allows the structure to deform, which may destroy the underlying structure. Accordingly, the present technology may utilize silicon-containing precursors that maximize the number of silicon-silicon bonds, and minimize additional molecular bonding. In this way, less material may need to be removed during curing or other operations, which may reduce the amount of shrinking of the final film.


In disclosed embodiments, the technology may utilize silanes and polysilanes as the silicon-containing precursor. These materials may include or exclusively consist of silicon-silicon and silicon-hydrogen bonds. Exemplary precursors may include at least one silicon-silicon bond, at least two silicon-silicon bonds, at least three silicon-silicon bonds, etc. For example, the precursors may be selected from any of the polysilane homologues beginning with disilane. The silicon-containing precursor may also be selected from a variety of isomers of the polysilanes. For example, if the silicon-containing precursor has five silicon atoms, the composition could include any of n-pentasilane, isopentasilane, neopentasilane, 2-silyltetrasilane, 2,2-disilyltrisilane, etc. The silicon-containing precursors may include cyclic forms or cyclosilanes, such as cyclohexasilane, for example. The polysilanes may also include any saturated or unsaturated compound such as silenes and silynes. The silicon-containing precursor may also be of a general formula such as SixHy. X may be any number of two or greater up to infinity, and Y may be any number of two or greater up to infinity. For example, such a minimal formula would denote disilyne (Si2H2). Y may also be any factor based on X. For example, Y may be 2X, or 2X+N, where n=2, 0, −2, −4, −6, etc., or N may be any number less than or equal to 2. Exemplary silanes used in the technology can include disilane, tetrasilane, cyclohexasilane, etc.


The vapor pressure of many of these disclosed materials is such that the materials may be in a substantially liquid phase under many operating conditions. Although the silicon-containing precursors may be used in liquid form in the disclosed technology, in embodiments the silicon-containing precursors may be introduced into the processing chamber in a vapor or substantially vapor form. However, this may require the use of additional components to ensure that the materials are introduced in a vapor form. Many different mechanisms may be employed to deliver vapor phase silicon-containing precursors. For example, vapor draw with or without a heated ampoule, a bubbler, or direct liquid injection may be utilized among a variety of other technology. However, depending on the precursor utilized, additional issues may occur. For example, if higher order silanes are delivered in liquid phase to an injection nozzle, the injection nozzle may be heated to deliver the material into the substrate processing region as a vapor. However, the vaporization temperature of higher order silanes and the polymerization temperature of higher order silanes may be relatively close, such that the technique may clog the nozzle. Additionally, a bubbler may utilize an inert gas in the delivery of the vapor, but also introduces the additional inert gas. In so doing, further mechanisms may be needed to ensure that an adequate flow of the actual silicon-containing precursor is delivered to provide adequate film formation rates. Higher order silicon-containing precursors or silanes have more silicon-silicon bonds which may lead to less shrinking of the films, but may additionally have very low vapor pressures which may require additional components or mechanisms to provide a vapor phase silicon-containing precursor to the substrate processing region.


Again without being bound to any particular theory, flowability of the dielectric material with the disclosed technology may be based on a combination of process parameters including the temperature and pressure of the process in relation to the silicon-containing precursor, plasma power used, and distance between the showerhead or mechanism delivering the precursors and the substrate on which the films are to be formed. During the processing, the substrate processing region may be relatively, substantially, or completely plasma-free during the deposition. Although the plasma effluents of the first precursor may be delivered into the substrate processing region, the plasma used to generate the effluents may be contained externally to the substrate processing region. The greatest amount of reactions may occur directly under the showerhead, or where the precursors initially interact. The plasma effluents may have had the least amount of time to recombine, and thus greater reactions between the precursors may occur. These gas phase reactions may be affected further by the material used. Silicon-silicon bonds may be weaker bonds than silicon-hydrogen, silicon-oxygen, and other silicon-based bonds. Accordingly, where these greater reactions occur, or where a higher plasma power is utilized, for the silicon-containing precursors of the present technology, a greater number of bonds may be broken. As a possible result, the dielectric material formed in this region may have reduced or no flowability when deposited on the substrate. As the distance of the substrate from the showerhead increases, the amount of interactions may be reduced slightly or more substantially. For example, potentially only one out of two or one out of three silicon-silicon bonds may be broken, and thus the polymerization may include longer chains of silicon groups, which may at least partially impart flowability to the deposited material.


Accordingly, the substrate may be maintained at a distance from the showerhead, or region where the interactions between the precursors begin, that is less than or about three inches. The substrate may be maintained at least 0.1 inches from the showerhead in disclosed embodiments. The substrate may also be maintained at a distance less than or about 2 inches, 1 inch, 0.9, 0.8, 0.7, 0.6, 0.5, 0.4, 0.3, 0.2, 0.1, or less inches, or be maintained between about 3 inches and about 0.01 inches, 2 and 0.1 inches, 1 and 0.2 inches, 0.8 and 0.2 inches, etc. The distance may also be determined in conjunction with the process parameters and silicon-containing precursor or precursors being used.


During the deposition process, the substrate may be maintained at or below about 400° C., and may be maintained at or below about 300° C., 200° C., 100° C., 80° C., 75° C., 50° C., 25° C., 10° C., 0° C., −10° C., −20° C., −30° C., or less, between about 30° C. and −30° C., etc. The processing chamber may be maintained at or below about 100 Torr during the processes, and may be maintained at or below about 50 Torr, 25 Torr, 15 Torr, 5 Torr, 1 Torr, 0.1 Torr, etc., or between about 0.1 mTorr and about 10 Torr. The temperature and pressure may also be set based at least partially on the vapor pressure of the silicon-containing precursor or precursors being used. As one non-limiting example, if tetrasilane is used as the silicon-containing precursor, and the chamber temperature is about −10° C., the vapor pressure of tetrasilane may be below about 3 Torr. As such, if the chamber pressure is greater than about 3 Torr, then condensation of the tetrasilane may occur. The interaction of the plasma effluents with the tetrasilane may also impart energy that overcomes the condensation point. Additionally, as the distance from the plasma source increases, and the plasma power decreases either or both from distance or actual generation power, the amount of silicon-silicon bond breaking may be reduced, which may allow longer polymer chains to be formed. The combination of improved polymerization, i.e. longer silicon-silicon chains, along with the benefit of operations at or near the condensation point of the precursors may at least partially impart flowability to the films. The process may also create longer silicon polymer chains with reduced additional material, which may reduce the amount of shrinking of the final film. The plasma source used in the technology may include plasma generated in the chamber, but remote from and fluidly coupled with the substrate processing region, or alternatively generated in a module separate from but fluidly coupled with the processing chamber. The plasma may be from any known or later developed technology, and may produce plasma power between about 0 and 2000 Watts. In disclosed embodiments, the plasma power may be less than or about 1000 Watts, or about 500, 300, 250, 200, 150, 100, 80, 60, 40, 20 Watts, etc. or less.


Utilizing the described processes, a synergistic combination may be produced where an amount of condensation and an amount of polymerization occur to produce flowable films from silicon-containing precursors that may only include silicon and hydrogen bonding. The resultant films may have flowability when initially formed on the substrate, but may be composed of mostly silicon-silicon and silicon-hydrogen bonds. These films that may have more silicon atoms in the matrix, and more silicon-silicon bonding in the deposited film, may shrink less than conventional films. Advantageously, the inventors have additionally determined that these films may have increased density as formed over conventional films. The as-deposited films may have a density greater than or equal to about 1.2 g/cc. The films may also have densities greater than or equal to about 1.3 g/cc, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2.0, 2.1, etc. or greater.


After an amount of dielectric material has been formed on the substrate, additional processes may be performed. One or more densifying operations may be performed to increase the quality of the dielectric material. In disclosed embodiments, once a determined amount of dielectric material has been formed, the introduction and flow of the silicon-containing precursor may be stopped. However, the plasma effluents may be continued to be produced and directed into the substrate processing region at the formed dielectric layer to densify the formed dielectric material. Additionally or alternatively, the formed silicon-based dielectric layer may be annealed to further densify the film. The annealing may be a dry anneal, such as with nitrogen, or a steam anneal that may occur at temperatures between about 200° C. and higher, above or about 400° C., above or about 900° C., etc. or greater. During the anneal, the amount or film shrinking may be less than conventional films. For example, the film may shrink by less than 50% during the anneal. Additionally, the films produced by the disclosed technology may shrink by less than or about 40%, 30%, 25%, 20%, 15%, 10%, 5%, 0%, −5%, −10%, etc. or less. In exemplary methods and processes, the inventors have determined that negative shrinking may occur. This negative shrinking may imply that the film expands during the processing.


The above example process as described in conjunction with FIG. 1 may produce a substantially silicon based film, and may be used to produce polysilicon films of various structure and characteristics. The processes may be further adjusted to incorporate additional materials to produce oxides, nitrides, carbides, and other compositions useful in semiconductor processing. A further example of the disclosed technology incorporating additional materials is described with respect to FIG. 2. FIG. 2 shows another flow chart of a process for forming a dielectric film according to disclosed embodiments. The process may include similar operations as described with respect to FIG. 1. In disclosed embodiments, at operation 210 a first precursor may be introduced into a remote plasma region fluidly coupled with a substrate processing region while forming a plasma in the remote plasma region to produce plasma effluents. The first precursor may include one or more of any of the previously described precursors, and may consist exclusively of one or more inert precursors such as argon, helium, or nitrogen. At operation 220, the plasma effluents may be directed into the substrate processing region.


A silicon-containing precursor may be introduced into the substrate processing region at operation 230, and the silicon-containing precursor may have at least one silicon-silicon bond. The silicon-containing precursor may include one or more of any of the previously discussed precursors. For example, the silicon-containing precursor may have the formula SixHy, where x may be greater than or equal to 2, and y is 2x+n or greater, and where n may be any number less than or equal to 2. Additionally, the silicon-containing precursor may be introduced into the processing region in a substantially vapor phase. In disclosed embodiments, the precursors introduced into the processing chamber to form the silicon-based dielectric layer may consist of one or more inert precursors and a silicon-containing precursor consisting or silicon-silicon and silicon-hydrogen containing bonds. For example, the first precursor may consist of argon or helium. At operation 240, the plasma effluents and silicon-containing precursors may be reacted to form a silicon-based dielectric layer on the substrate. These operations may be performed in any of the ways previously described. After the initial film has been formed, a curing operation may optionally be performed at operation 250 that cures the formed silicon-based dielectric layer with at least one additional precursor.


The additional precursor may include one or more of an oxygen-containing precursor, such as ozone, a nitrogen-containing precursor, or a carbon-containing precursor. The precursors may be introduced or utilized with or without the plasma effluents directed into the substrate processing region. The additional precursors may be used to additionally substitute material into the silicon-based dielectric material. For example, ozone or another oxygen-containing precursor may be used to provide oxygen that is incorporated into the silicon matrix to produce a silicon oxide film. This may help pack the formed matrix with additional material that may further help reduce shrinkage on annealing or densifying operations. A variety of films may be formed in this way, including oxides, nitrides, carbides, oxycarbides, oxynitrides, carbonitrides, etc. The additional precursors may be flowed after the formation of the silicon-based dielectric, near the end of the formation, and may be introduced with or without the silicon-containing precursors and/or the first precursor. The temperature and/or pressure of the chamber may be changed during the curing operation. For example, if the temperature of the film forming operation is less than 30° C., for example, the chamber temperature may be raised to above or about 30° C., 50° C., 100° C., 200° C., etc., or higher.


Subsequent to the optional introduction of additional precursor material, the cured or otherwise formed dielectric may be optionally densified at operation 260. The flow of the silicon-containing precursor and/or the additional precursor may be stopped, and then the flow of the first precursor may be performed, or continued in various embodiments. Plasma effluents developed from the first precursor may be directed into the substrate processing region to densify the formed or cured dielectric layer. In disclosed embodiments the densifying operation may be performed prior to the curing operation such that operation 260 is performed prior to operation 250. Additional operations may be performed optionally in the process including an anneal at operation 270. The formed, cured, and/or densified dielectric may be annealed as previously discussed to improve the final quality of the film. Further post-deposition treatments may be performed that may include one or more of a variety of operations including UV, e-beam, and other curing or annealing type operations. During the anneal, the silicon-based dielectric layer may shrink by less than or about 50%. The films produced by the disclosed technology may shrink by less than or about 40%, 30%, 25%, 20%, 15%, 10%, 5%, etc. or less. All optional operations may be performed in the same or a different chamber than the film forming or deposition operation. By maintaining the substrate in a chamber without breaking vacuum, moisture and other effects on the formed film may be reduced or prevented.


The technology also encompasses delivery of the silicon-containing precursor into the remote plasma region. Alternatively, the silicon-containing precursor may be activated by a direct plasma applied either in a remote region of the chamber, or alternatively in the processing region of the chamber, where the silicon-containing precursor is delivered to the area in which a plasma is developed. In disclosed embodiments, a silicon-containing precursor may be delivered into a processing region or a plasma region of a chamber and activated with a plasma, such as a type of plasma previously defined. The silicon-containing precursor may be delivered with additional fluids such as inert carriers that may include argon and may include hydrogen in disclosed embodiments as well. The process may be performed at a variety of the temperatures, pressures, and plasma powers previously described. For example, the plasma power applied directly may be less than 500 W, and may also be less than or about 300 W, 200 W, 100 W, 80 W, 70 W, 60 W, 50 W, etc. or less, and the temperatures may be below or about 100° C., and may also be less than or about 75° C., 50° C., 25° C., 15° C., 10° C., 5° C., 0° C., −5° C., etc. or less. Additionally, in this and other disclosed embodiments, the pedestal on which the substrate resides may be electrically biased. Biasing of the pedestal may provide an electrical field that may be used to direct radical species to the surface of the substrate.


The described processes synergistically utilize silicon-containing precursors having silicon-silicon bonding, temperature, pressure, plasma, and deposition distances to produce flowable films of improved qualities and reduced shrinking By accounting for the phase transition profiles of the silicon-containing precursors, the technology advantageously may remove nitrogen, carbon, water, hydroxyl groups, and other additional materials that may reduce the density, and increase the shrinking of the formed films. As would be understood, additional modifications to chamber parameters and plasma power may be used to further tune the deposition processes as may be required. Advantageously, tuning these processes may be performed without the need to break vacuum conditions or move the substrate to an additional chamber. This may reduce overall processing times and save costs over conventional techniques. Additional examples of deposition process parameters, chemistries, and components are disclosed in the course of describing an exemplary processing chamber and system below.


Exemplary Processing System


Deposition chambers that may implement embodiments of the present invention may include high-density plasma chemical vapor deposition (HDP-CVD) chambers, plasma enhanced chemical vapor deposition (PECVD) chambers, sub-atmospheric chemical vapor deposition (SACVD) chambers, and thermal chemical vapor deposition chambers, among other types of chambers. Specific examples of CVD systems that may implement embodiments of the invention include the CENTURA ULTIMA® HDP-CVD chambers/systems, and PRODUCER® PECVD chambers/systems, available from Applied Materials, Inc. of Santa Clara, Calif.


Examples of substrate processing chambers that can be used with exemplary methods of the invention may include those shown and described in co-assigned U.S. Provisional Patent App. No. 60/803,499 to Lubomirsky et al, filed May 30, 2006, and titled “PROCESS CHAMBER FOR DIELECTRIC GAPFILL,” the entire contents of which is herein incorporated by reference for all purposes. Additional exemplary systems may include those shown and described in U.S. Pat. Nos. 6,387,207 and 6,830,624, which are also incorporated herein by reference for all purposes.



FIG. 3A shows a schematic cross-sectional view of a portion of a substrate processing chamber 301 according to the disclosed technology. A remote plasma system (RPS) 310 may process a gas which then travels through a gas inlet assembly 311. Two distinct gas supply channels may be present within the gas inlet assembly 311. A first channel 312 may carry a gas that passes through the remote plasma system (RPS) 310, while a second channel 313 may bypass the RPS 310. The first channel 312 may be used for the process gas and the second channel 313 may be used for a treatment gas in disclosed embodiments. The lid or conductive top portion 321 and a perforated partition, such as showerhead 353, are shown with an insulating ring 324 disposed between, which may allow an AC potential to be applied to the lid 321 relative to showerhead 353. The process gas may travel through first channel 312 into chamber plasma region 320 and may be excited by a plasma in chamber plasma region 320 alone or in combination with RPS 310. The combination of chamber plasma region 320 and/or RPS 310 may be referred to as a remote plasma system herein. The perforated partition or showerhead 353 may separate chamber plasma region 320 from a substrate processing region 370 beneath showerhead 353. Showerhead 353 may allow a plasma present in chamber plasma region 320 to avoid directly exciting gases in substrate processing region 370, while still allowing excited species to travel from chamber plasma region 320 into substrate processing region 370.


Showerhead 353 may be positioned between chamber plasma region 320 and substrate processing region 370 and allow plasma effluents or excited derivatives of precursors or other gases created within chamber plasma region 320 to pass through a plurality of through-holes 356 that traverse the thickness of the plate or plates included in the showerhead. The showerhead 353 may also have one or more hollow volumes 351 that can be filled with a precursor in the form of a vapor or gas, such as a silicon-containing precursor, and pass through small holes 355 into substrate processing region 370, but not directly into chamber plasma region 320. Showerhead 353 may be thicker than the length of the smallest diameter 350 of the through-holes 356 in disclosed embodiments. In order to maintain a significant concentration of excited species penetrating from chamber plasma region 320 to substrate processing region 370, the length 326 of the smallest diameter 350 of the through-holes may be restricted by forming larger diameter portions of through-holes 356 part way through the showerhead 353. The length of the smallest diameter 350 of the through-holes 356 may be the same order of magnitude as the smallest diameter of the through-holes 356 or less in disclosed embodiments.


In the embodiment shown, showerhead 353 may distribute, via through-holes 356, process gases which contain a plasma vapor/gas such as argon, for example. Additionally, the showerhead 353 may distribute, via smaller holes 355, a silicon-containing precursor that is maintained separately from the plasma region 320. The process gas or gases and the silicon-containing precursor may be maintained fluidly separate via the showerhead 353 until the precursors separately enter the processing region 370. The precursors may contact one another once they enter the processing region and react to form a flowable dielectric material on a substrate 380.


In embodiments, the number of through-holes 356 may be between about 60 and about 2000. Through-holes 356 may have a variety of shapes but may be made round. The smallest diameter 350 of through-holes 356 may be between about 0.5 mm and about 20 mm or between about 1 mm and about 6mm in disclosed embodiments. There is also latitude in choosing the cross-sectional shape of through-holes, which may be made conical, cylindrical or a combination of the two shapes. The number of small holes 355 used to introduce a gas into substrate processing region 370 may be between about 100 and about 5000 or between about 500 and about 2000 in different embodiments. The diameter of the small holes 355 may be between about 0.1 mm and about 2 mm.



FIG. 3B shows a bottom plan view of a showerhead 353 according to the disclosed technology. Showerhead 353 corresponds with the showerhead shown in FIG. 3A. Through-holes 356 are depicted with a larger inner-diameter (ID) on the bottom of showerhead 353 and a smaller ID at the top. Small holes 355 are distributed substantially evenly over the surface of the showerhead, even amongst the through-holes 356 which may help to provide more even mixing than other embodiments described herein.


An additional dual channel showerhead, as well as this processing system and chamber, are more fully described in patent application Ser. No. 13/251,714 filed on Oct. 3, 2011, which is hereby incorporated by reference for all purposes to the extent not inconsistent with the claimed features and description herein.


An exemplary film may be created on a substrate supported by a pedestal, such as pedestal 375 having a substrate 380 disposed thereon, within substrate processing region 370 when plasma effluents arriving through through-holes 356 in showerhead 353 combine with a silicon-containing precursor arriving through the small holes 355 originating from hollow volumes 351. Though substrate processing region 370 may be equipped to support a plasma for other processes such as curing, no plasma may be present during the growth or deposition of the exemplary films.


A plasma may be ignited either in chamber plasma region 320 above showerhead 353 or substrate processing region 370 below showerhead 353. Alternatively, no plasma may be formed in any portion of the chamber, and may be only formed in RPS unit 310. A plasma may be present in chamber plasma region 320 to produce the radical plasma effluents, such as from an inflow of one or more of argon, helium, hydrogen, or ammonia. An AC voltage typically in the radio frequency (RF) range is applied between the conductive top portion, such as lid 321, of the processing chamber and showerhead 353 to ignite a plasma in chamber plasma region 320 during deposition. An RF power supply generates a high RF frequency of 13.56 MHz but may also generate other frequencies alone or in combination with the 13.56 MHz frequency.


The top plasma may be left at low or no power when the bottom plasma in the substrate processing region 370 may be turned on during the formation of the dielectric layer or while cleaning the interior surfaces bordering substrate processing region 370. A plasma in substrate processing region 370 may be ignited by applying an AC voltage between showerhead 353 and the pedestal 375 or bottom of the chamber. A cleaning gas may be introduced into substrate processing region 370 while the plasma is present.


The pedestal 375 may be moveable, and may be configured to be raised or lowered in disclosed embodiments, and may similarly be configured to rotate. The pedestal 375 may have a heat exchange channel through which a heat exchange fluid flows to control the temperature of the substrate. This configuration allows the substrate temperature to be cooled or heated to maintain relatively low temperatures, such as from about 0° C. or lower up to about 200° C. or higher. The heat exchange fluid may comprise ethylene glycol, water, or some other fluid capable of introducing or removing heat from the system. The wafer support platter of the pedestal may also be resistively heated in order to achieve relatively high temperatures from about 200° C. or lower up to about 1100° C. or higher using an embedded resistive heating element. An outer portion of the heater element may run adjacent to a perimeter of the support platter, while an inner portion runs on the path of a concentric circle having a smaller radius. The resistive heating element may additionally be coiled through the platter to provide more uniform temperatures. The wiring to the heater element may pass through the stem of the pedestal.


The chamber plasma region or a region in an RPS may be referred to as a remote plasma region. In embodiments, the radical precursor, e.g. an argon precursor, may be created in the remote plasma region and travel into the substrate processing region to combine with the silicon-containing precursor. In embodiments, the silicon-containing precursor is excited only by the radical-argon precursor. Plasma power may essentially be applied only to the remote plasma region, in embodiments, to ensure that the radical-argon precursor provides the dominant excitation to the silicon-containing precursor.


In embodiments employing a chamber plasma region, the excited plasma effluents may be generated in a section of the substrate processing region partitioned from a deposition region. The deposition region, also known herein as the substrate processing region, may be where the plasma effluents mix and react with the silicon-containing precursor to deposit dielectric material on the substrate, e.g., a semiconductor wafer. The excited plasma effluents may also be accompanied by additional gases including other inert gases or ammonia, for example. The silicon-containing precursor may not pass through a plasma before entering the substrate plasma region, in embodiments. The substrate processing region may be described herein as “plasma-free” during the deposition of the dielectric material. “Plasma-free” does not necessarily mean the region is devoid of plasma. Ionized species and free electrons created within the plasma region may travel through pores or apertures in the partition or showerhead, but the silicon-containing precursor may not be substantially excited by the plasma power applied to the plasma region. The borders of the plasma in the chamber plasma region are hard to define and may encroach upon the substrate processing region through the apertures in the showerhead. In the case of an inductively-coupled plasma, a small amount of ionization may be effected within the substrate processing region directly. Furthermore, a low intensity plasma may be created in the substrate processing region without eliminating desirable features of the forming film. All causes for a plasma having much lower intensity ion density than the chamber plasma region, or a remote plasma region, during the creation of the excited plasma effluents do not deviate from the scope of “plasma-free” as used herein.


Plasma power can be a variety of frequencies or a combination of multiple frequencies. In the exemplary processing system, the plasma may be provided by RF power delivered to lid 321 relative to showerhead 353. The RF power may be between about 10 watts and about 2000 watts, between about 100 watts and about 2000 watts, between about 200 watts and about 1500 watts, less than or about 100 Watts, or less than or about 500 watts in different embodiments. The RF frequency applied in the exemplary processing system may be low RF frequencies less than about 200 kHz, high RF frequencies between about 10 MHz and about 15 MHz, or microwave frequencies greater than or about 1 GHz in different embodiments. The plasma power may be capacitively-coupled (CCP) or inductively-coupled (ICP) into the remote plasma region.


Substrate processing region 370 can be maintained at a variety of pressures during the flow of precursors, any carrier gases, and plasma effluents into substrate processing region 370. The pressure may be maintained between about 0.1 mTorr and about 100 Torr, between about 1 Torr and about 20 Torr, less than about 5 Torr, or less than about 3 Torr in different embodiments.


Embodiments of the deposition systems may be incorporated into larger fabrication systems for producing integrated circuit chips. FIG. 3 shows one such system 400 of deposition, etching, baking, and curing chambers according to disclosed embodiments. In the figure, a pair of front opening unified pods (FOUPs) 402 supply substrates of a variety of sizes that are received by robotic arms 404 and placed into a low pressure holding area 406 before being placed into one of the substrate processing chambers 408a-f. A second robotic arm 410 may be used to transport the substrate wafers from the holding area 406 to the substrate processing chambers 408a-f and back. Each substrate processing chamber 408a-f, can be outfitted to perform a number of substrate processing operations including the deposition processes described herein in addition to cyclical layer deposition (CLD), atomic layer deposition (ALD), chemical vapor deposition (CVD), physical vapor deposition (PVD), etch, pre-clean, degas, orientation, and other substrate processes.


The substrate processing chambers 408a-f may include one or more system components for depositing, annealing, curing and/or etching a dielectric film on the substrate wafer. In one configuration, two pairs of the processing chambers, e.g., 408c-d and 408e-f, may be used to deposit dielectric material on the substrate, and the third pair of processing chambers, e.g., 408a-b, may be used to etch the deposited dielectric. In another configuration, all three pairs of chambers, e.g., 408a-f, may be configured to deposit, cure, and densify a dielectric film on the substrate. Any one or more of the processes described may be carried out in chamber(s) separated from the fabrication system shown in different embodiments.


In the preceding description, for the purposes of explanation, numerous details have been set forth in order to provide an understanding of various embodiments of the present invention. It will be apparent to one skilled in the art, however, that certain embodiments may be practiced without some of these details, or with additional details.


Having disclosed several embodiments, it will be recognized by those of skill in the art that various modifications, alternative constructions, and equivalents may be used without departing from the spirit of the disclosed embodiments. Additionally, a number of well-known processes and elements have not been described in order to avoid unnecessarily obscuring the present invention. Accordingly, the above description should not be taken as limiting the scope of the invention.


Where a range of values is provided, it is understood that each intervening value, to the smallest fraction of the unit of the lower limit, unless the context clearly dictates otherwise, between the upper and lower limits of that range is also specifically disclosed. Each smaller range between any stated value or intervening value in a stated range and any other stated or intervening value in that stated range is encompassed. The upper and lower limits of those smaller ranges may independently be included or excluded in the range, and each range where either, neither, or both limits are included in the smaller ranges is also encompassed within the invention, subject to any specifically excluded limit in the stated range. Where the stated range includes one or both of the limits, ranges excluding either or both of those included limits are also included.


As used herein and in the appended claims, the singular forms “a”, “an”, and “the” include plural references unless the context clearly dictates otherwise. Thus, for example, reference to “an aperture” includes a plurality of such apertures, and reference to “the plate” includes reference to one or more plates and equivalents thereof known to those skilled in the art, and so forth.


Also, the words “comprise(s)”, “comprising”, “contain(s)”, “containing”, “include(s)”, and “including”, when used in this specification and in the following claims, are intended to specify the presence of stated features, integers, components, or steps, but they do not preclude the presence or addition of one or more other features, integers, components, steps, acts, or groups.

Claims
  • 1. A method of forming a dielectric layer on a substrate in a substrate processing region of a processing chamber, the method comprising: introducing a first precursor into a remote plasma region fluidly coupled with the substrate processing region while forming a plasma in the remote plasma region to produce plasma effluents;directing the plasma effluents into the substrate processing region;introducing a silicon-containing precursor into the substrate processing region, wherein the silicon-containing precursor includes at least one silicon-silicon bond; andreacting the plasma effluents and silicon-containing precursor in the substrate processing region to form a silicon-based dielectric layer that is initially flowable when formed on the substrate, wherein the processing chamber is maintained at a temperature from about 30° C. to about −30° C., and wherein the pressure within the processing chamber is maintained so the reacting operation occurs at or about the condensation point of the silicon-containing precursor.
  • 2. The method of claim 1, wherein the silicon-containing precursor includes at least two silicon-silicon bonds.
  • 3. The method of claim 1, wherein the first precursor includes one or more precursors selected from the group consisting of ammonia, nitrogen, H2, Ar, and He.
  • 4. The method of claim 1, wherein the plasma effluents and silicon-containing precursor are introduced into the processing region through a showerhead configured to maintain separation of the precursors so that they do not contact each other until they enter the substrate processing region.
  • 5. The method of claim 4, wherein the substrate is maintained at a distance less than or at about 3 inches from the showerhead.
  • 6. The method of claim 1, wherein the substrate processing region is plasma-free during the deposition process.
  • 7. The method of claim 1, wherein the silicon-containing precursor has the formula SixHy, wherein x is greater than or equal to 2, and y is 2x+n or greater, wherein n is any number less than or equal to 2, and wherein the silicon-containing precursor is introduced into the processing region in a substantially vapor phase.
  • 8. The method of claim 1, wherein the method is performed at a temperature of less than or equal to about 30° C.
  • 9. The method of claim 1, wherein the method is performed at a pressure of less than or equal to about 5 Torr.
  • 10. The method of claim 1, whrerein the as-formed film has a density greater than or equal to about 1.4 g/cc.
  • 11. The method of claim 1, further comprising stopping the introduction of the silicon-containing precursor after the silicon-based dielectric layer is formed, and continuing to direct the plasma effluents of the first precursor into the substrate processing region to densify the formed dielectric layer.
  • 12. The method of claim 1, further comprising annealing the formed silicon-based dielectric layer.
  • 13. The method of claim 12, wherein the formed silicon-based dielectric layer shrinks by less than about 20% during the annealing.
  • 14. A method of forming a dielectric layer on a substrate in a substrate processing region of a processing chamber, the method comprising: introducing a first precursor into a remote plasma region fluidly coupled with the substrate processing region while forming a plasma in the remote plasma region to produce plasma effluents;directing the plasma effluents into the substrate processing region;introducing a silicon-containing precursor into the substrate processing region, wherein the silicon-containing precursor includes at least one silicon-silicon bond;reacting the plasma effluents and silicon-containing precursor in the substrate processing region to form a silicon-based dielectric layer that is initially flowable when formed on the substrate, wherein the processing chamber is maintained at a temperature from about 30° C. to about −30° C., and wherein the pressure within the processing chamber is maintained so the reacting operation occurs at or about the condensation point of the silicon-containing precursor; andcuring the formed silicon-based dielectric layer with at least one additional precursor.
  • 15. The method of claim 14, wherein the at least one additional precursor comprises an oxygen-containing precursor, a nitrogen-containing precursor, or a carbon-containing precursor.
  • 16. The method of claim 14, further comprising directing the plasma effluents into the substrate processing region to densify the cured dielectric layer.
  • 17. The method of claim 14, wherein the silicon-containing precursor has the formula SixHy, wherein x is greater than or equal to 2, and y is 2x+n or greater, wherein n is any number less than or equal to 2, and wherein the silicon-containing precursor is introduced into the processing region in a substantially vapor phase.
  • 18. The method of claim 14, wherein the precursors introduced into the processing chamber to form the silicon-based dielectric layer consist of one or more inert precursors and a silicon-containing precursor consisting of silicon-silicon and silicon-hydrogen containing bonds.
  • 19. The method of claim 14, further comprising annealing the formed silicon-based dielectric layer.
  • 20. The method of claim 14, wherein the formed silicon-based dielectric layer shrinks by less than about 20% during the annealing.
CROSS-REFERENCES TO RELATED APPLICATIONS

This application claims the benefit of U.S. Provisional Application No. 61/756,762, filed Jan. 25, 2013, entitled “Low Shrinkage Dielectric Films.” The entire disclosure of which is incorporated herein by reference for all purposes.

US Referenced Citations (1624)
Number Name Date Kind
2861009 Rubner Nov 1958 A
2889704 Pekarek Aug 1959 A
3046177 Hankins Jul 1962 A
3048888 Shockley et al. Aug 1962 A
3109703 Politzer et al. Nov 1963 A
3142714 Politzer et al. Jul 1964 A
3166454 Voelker Jan 1965 A
3451840 Hough Jun 1969 A
3720784 Maydan et al. Mar 1973 A
3806223 Keck et al. Apr 1974 A
RE28375 Maydan et al. Mar 1975 E
3999918 Landsman Dec 1976 A
4147571 Stringfellow et al. Apr 1979 A
4151008 Kirkpatrick Apr 1979 A
4185252 Gerlach Jan 1980 A
4200666 Reinberg Apr 1980 A
4212663 Aslami Jul 1980 A
4233537 Limpaecher Nov 1980 A
4297162 Mundt et al. Oct 1981 A
4309225 Fan et al. Jan 1982 A
4351658 Olshansky Sep 1982 A
4374158 Taniguchi et al. Feb 1983 A
4378987 Miller et al. Apr 1983 A
4385802 Blaszyk et al. May 1983 A
4402571 Cowan et al. Sep 1983 A
4425146 Izawa et al. Jan 1984 A
4425907 Younghouse Jan 1984 A
4468413 Bachmann Aug 1984 A
4469551 Laude Sep 1984 A
4496216 Cowan Jan 1985 A
4507588 Asmussen et al. Mar 1985 A
4511520 Bowen Apr 1985 A
4520472 Reno May 1985 A
4521447 Ovshinsky et al. Jun 1985 A
4525733 Losee Jun 1985 A
4528009 Sarkar Jul 1985 A
4545646 Chern et al. Oct 1985 A
4557561 Schneider et al. Dec 1985 A
4565157 Brors Jan 1986 A
4566403 Fournier Jan 1986 A
4568631 Badami et al. Feb 1986 A
4571819 Rogers et al. Feb 1986 A
4572841 Kaganowicz et al. Feb 1986 A
4590042 Drage May 1986 A
4619680 Nourshargh et al. Oct 1986 A
4656052 Satou et al. Apr 1987 A
4690746 McInerney et al. Sep 1987 A
4690830 Dickson et al. Sep 1987 A
4704367 Alvis et al. Nov 1987 A
4715921 Maher et al. Dec 1987 A
4732761 Machida et al. Mar 1988 A
4734345 Nomura et al. Mar 1988 A
4737379 Hudgens et al. Apr 1988 A
4738748 Kisa Apr 1988 A
4747367 Posa May 1988 A
4762808 Sharp et al. Aug 1988 A
4792378 Rose et al. Dec 1988 A
4808258 Otsubo et al. Feb 1989 A
4816098 Davis et al. Mar 1989 A
4818326 Liu et al. Apr 1989 A
4830705 Loewenstein et al. May 1989 A
4830890 Kanai May 1989 A
4834831 Nishizawa et al. May 1989 A
4835005 Hirooka et al. May 1989 A
4844945 Bhaskar et al. Jul 1989 A
4848400 Grant et al. Jul 1989 A
4848902 Schickle et al. Jul 1989 A
4851370 Doklan et al. Jul 1989 A
4854263 Chang et al. Aug 1989 A
4856859 Imoto Aug 1989 A
4868005 Ehrlich et al. Sep 1989 A
4872947 Wang et al. Oct 1989 A
4877757 York et al. Oct 1989 A
4878994 Jucha et al. Nov 1989 A
4885471 Telfair et al. Dec 1989 A
4890575 Ito et al. Jan 1990 A
4892753 Wang et al. Jan 1990 A
4894352 Lane et al. Jan 1990 A
4898557 Engemann Feb 1990 A
4910043 Freeman et al. Mar 1990 A
4927704 Reed et al. May 1990 A
4931354 Wakino et al. Jun 1990 A
4932749 Haidle et al. Jun 1990 A
4946593 Pinigis Aug 1990 A
4951601 Maydan et al. Aug 1990 A
4953498 Hashizume et al. Sep 1990 A
4960488 Law et al. Oct 1990 A
4962063 Maydan et al. Oct 1990 A
4989541 Mikoshiba et al. Feb 1991 A
4990374 Keeley et al. Feb 1991 A
5000113 Wang et al. Mar 1991 A
5003178 Livesay Mar 1991 A
5006218 Yoshida et al. Apr 1991 A
5013691 Lory et al. May 1991 A
5016332 Reichelderfer et al. May 1991 A
5032435 Biefeld et al. Jul 1991 A
5051380 Maeda et al. Sep 1991 A
5059231 Ackermann et al. Oct 1991 A
5078922 Collins et al. Jan 1992 A
5081069 Parker et al. Jan 1992 A
5089442 Olmer Feb 1992 A
5093149 Doehler et al. Mar 1992 A
5110407 Ono et al. May 1992 A
5112439 Reisman et al. May 1992 A
5124014 Foo et al. Jun 1992 A
5125360 Nakayama et al. Jun 1992 A
5133986 Blum et al. Jul 1992 A
5142385 Anderson et al. Aug 1992 A
5148714 McDiarmid Sep 1992 A
5149375 Matsuyama Sep 1992 A
5156881 Okano et al. Oct 1992 A
5160408 Long Nov 1992 A
5167558 Duchek et al. Dec 1992 A
5178739 Barnes et al. Jan 1993 A
5186120 Ohnishi et al. Feb 1993 A
5204288 Marks et al. Apr 1993 A
5204314 Kirlin et al. Apr 1993 A
5212119 Hah et al. May 1993 A
5215787 Homma Jun 1993 A
5236562 Okumura et al. Aug 1993 A
5242530 Batey et al. Sep 1993 A
5242561 Sato Sep 1993 A
5242566 Parker Sep 1993 A
5244841 Marks et al. Sep 1993 A
5246744 Matsuda et al. Sep 1993 A
5252178 Moslehi Oct 1993 A
5253319 Bhagavatula Oct 1993 A
5264040 Geyling Nov 1993 A
5266502 Okada et al. Nov 1993 A
5269847 Anderson et al. Dec 1993 A
5270125 America et al. Dec 1993 A
5270264 Andideh et al. Dec 1993 A
5271972 Kwok et al. Dec 1993 A
5273930 Steele et al. Dec 1993 A
5275977 Otsubo et al. Jan 1994 A
5279784 Bender et al. Jan 1994 A
5279865 Chebi et al. Jan 1994 A
5288518 Homma Feb 1994 A
5290993 Kaji et al. Mar 1994 A
5294285 Masahiro et al. Mar 1994 A
5294286 Nishizawa et al. Mar 1994 A
5295220 Heming et al. Mar 1994 A
5298365 Okamoto et al. Mar 1994 A
5302233 Kim et al. Apr 1994 A
5302555 Yu Apr 1994 A
5304250 Sameshima et al. Apr 1994 A
5304277 Ohara et al. Apr 1994 A
5304279 Coultas et al. Apr 1994 A
5306530 Strongin et al. Apr 1994 A
5314724 Tsukune et al. May 1994 A
5314845 Lee et al. May 1994 A
5316804 Tomikawa et al. May 1994 A
5317900 Bergquist Jun 1994 A
5319247 Matsuura Jun 1994 A
5323269 Walker et al. Jun 1994 A
5326725 Sherstinsky et al. Jul 1994 A
5328558 Kawamura Jul 1994 A
5334552 Homma Aug 1994 A
5345079 French et al. Sep 1994 A
5348774 Golecki et al. Sep 1994 A
5356722 Nguyen et al. Oct 1994 A
5357365 Ipposhi et al. Oct 1994 A
5362526 Wang et al. Nov 1994 A
5364488 Minato et al. Nov 1994 A
5365057 Morley et al. Nov 1994 A
5369464 Kamon Nov 1994 A
5369722 Heming et al. Nov 1994 A
5372860 Fehlner et al. Dec 1994 A
5374570 Nasu et al. Dec 1994 A
5384008 Sinha et al. Jan 1995 A
5385763 Okano et al. Jan 1995 A
5387288 Shatas Feb 1995 A
5393708 Hsia et al. Feb 1995 A
5399529 Homma Mar 1995 A
5401350 Patrick et al. Mar 1995 A
5403434 Moslehi Apr 1995 A
5408569 Nishimoto Apr 1995 A
5412180 Coombs May 1995 A
5413967 Matsuda et al. May 1995 A
5415835 Brueck et al. May 1995 A
5416048 Blalock et al. May 1995 A
5420075 Homma et al. May 1995 A
5426076 Moghadam Jun 1995 A
5429995 Nishiyama et al. Jul 1995 A
5434109 Geissler et al. Jul 1995 A
5434434 Kasahara et al. Jul 1995 A
5439524 Cain et al. Aug 1995 A
5443647 Aucoin et al. Aug 1995 A
5447570 Schmitz et al. Sep 1995 A
5459565 Aharon et al. Oct 1995 A
5463534 Raven Oct 1995 A
5468342 Nulty et al. Nov 1995 A
5468595 Livesay Nov 1995 A
5468687 Carl et al. Nov 1995 A
5469806 Mochizuki et al. Nov 1995 A
5474589 Ohga et al. Dec 1995 A
5474955 Thakur Dec 1995 A
5480687 Heming et al. Jan 1996 A
5480818 Matsumoto et al. Jan 1996 A
5483920 Pryor Jan 1996 A
5484749 Maeda et al. Jan 1996 A
5485420 Lage et al. Jan 1996 A
5492858 Bose et al. Feb 1996 A
5494523 Steger et al. Feb 1996 A
5503875 Imai et al. Apr 1996 A
5507881 Sichanugrist et al. Apr 1996 A
5508067 Sato et al. Apr 1996 A
5518805 Ho et al. May 1996 A
5521126 Okamura et al. May 1996 A
5522957 Weling et al. Jun 1996 A
5525550 Kato Jun 1996 A
5527391 Echizen et al. Jun 1996 A
5527733 Nishizawa et al. Jun 1996 A
5529630 Imahashi et al. Jun 1996 A
5530293 Cohen et al. Jun 1996 A
5534070 Okamura et al. Jul 1996 A
5534072 Mizuno et al. Jul 1996 A
5536323 Kirlin et al. Jul 1996 A
5536360 Nguyen et al. Jul 1996 A
5547703 Camilletti et al. Aug 1996 A
5558717 Zhao et al. Sep 1996 A
5562952 Nakahigashi et al. Oct 1996 A
5563105 Dobuzinsky et al. Oct 1996 A
5567267 Kazama et al. Oct 1996 A
5569350 Osada et al. Oct 1996 A
5571576 Qian et al. Nov 1996 A
5578532 van de Ven et al. Nov 1996 A
5587014 Iyechika et al. Dec 1996 A
5589002 Su Dec 1996 A
5589233 Law et al. Dec 1996 A
5593741 Ikeda Jan 1997 A
5597439 Salzman Jan 1997 A
5599740 Jang et al. Feb 1997 A
5604151 Goela et al. Feb 1997 A
5607725 Goodman Mar 1997 A
5612251 Lee Mar 1997 A
5614055 Fairbairn et al. Mar 1997 A
5620525 van de Ven et al. Apr 1997 A
5621241 Jain Apr 1997 A
5621497 Terasawa et al. Apr 1997 A
5622784 Okaue et al. Apr 1997 A
5624582 Cain Apr 1997 A
5626922 Miyanaga et al. May 1997 A
5629043 Inaba et al. May 1997 A
5629217 Miwa et al. May 1997 A
5630881 Ogure et al. May 1997 A
5635409 Moslehi Jun 1997 A
5641581 Nishiyama et al. Jun 1997 A
5643638 Otto et al. Jul 1997 A
5645645 Zhang et al. Jul 1997 A
5648175 Russell et al. Jul 1997 A
5660472 Peuse et al. Aug 1997 A
5661093 Ravi et al. Aug 1997 A
5665167 Deguchi et al. Sep 1997 A
5665643 Shin Sep 1997 A
5669975 Ashtiani Sep 1997 A
5672211 Mai et al. Sep 1997 A
5672861 Fairley et al. Sep 1997 A
5674304 Fukada et al. Oct 1997 A
5679606 Wang et al. Oct 1997 A
5683518 Moore et al. Nov 1997 A
5686734 Hamakawa et al. Nov 1997 A
5688357 Hanawa Nov 1997 A
5688382 Besen et al. Nov 1997 A
5691009 Sandhu Nov 1997 A
5693139 Nishizawa et al. Dec 1997 A
5702532 Wen et al. Dec 1997 A
5705321 Brueck et al. Jan 1998 A
5709757 Hatano et al. Jan 1998 A
5710079 Sukharev Jan 1998 A
5711816 Kirlin et al. Jan 1998 A
5712185 Tsai et al. Jan 1998 A
5719085 Moon et al. Feb 1998 A
5728223 Murakami et al. Mar 1998 A
5728260 Brown et al. Mar 1998 A
5728631 Wang Mar 1998 A
5736423 Ngo Apr 1998 A
5739898 Ozawa et al. Apr 1998 A
5749966 Shates May 1998 A
5753044 Hanawa et al. May 1998 A
5755859 Brusic et al. May 1998 A
5756400 Ye et al. May 1998 A
5759744 Brueck et al. Jun 1998 A
5766360 Sato et al. Jun 1998 A
5766365 Umotoy et al. Jun 1998 A
5767628 Keller et al. Jun 1998 A
5769951 van de Ven et al. Jun 1998 A
5770100 Fukuyama et al. Jun 1998 A
5776557 Okano et al. Jul 1998 A
5782980 Allen et al. Jul 1998 A
5786039 Brouquet Jul 1998 A
5786263 Perera Jul 1998 A
5789322 Brown et al. Aug 1998 A
5792261 Hama et al. Aug 1998 A
5792272 Van Os et al. Aug 1998 A
5796116 Nakata et al. Aug 1998 A
5804259 Robles Sep 1998 A
5807785 Ravi Sep 1998 A
5807792 Ilg et al. Sep 1998 A
5811325 Lin et al. Sep 1998 A
5811356 Murugesh et al. Sep 1998 A
5812403 Fong et al. Sep 1998 A
5817562 Chang et al. Oct 1998 A
5822479 Napier et al. Oct 1998 A
5824375 Gupta Oct 1998 A
5835677 Li et al. Nov 1998 A
5840631 Kubo et al. Nov 1998 A
5843233 van de Ven et al. Dec 1998 A
5843837 Baek et al. Dec 1998 A
5844684 Maris et al. Dec 1998 A
5849092 Xi et al. Dec 1998 A
5849455 Ueda et al. Dec 1998 A
5850105 Dawson et al. Dec 1998 A
5853607 Zhao et al. Dec 1998 A
5855681 Maydan et al. Jan 1999 A
5858876 Chew Jan 1999 A
RE36113 Brueck et al. Feb 1999 E
5869149 Denison et al. Feb 1999 A
5872052 Iyer Feb 1999 A
5872058 Van Cleemput et al. Feb 1999 A
5874350 Nakagawa Feb 1999 A
5876503 Roeder et al. Mar 1999 A
5882414 Fong et al. Mar 1999 A
5882417 van de Ven et al. Mar 1999 A
5886864 Dvorsky Mar 1999 A
5888304 Umotoy et al. Mar 1999 A
5888591 Gleason Mar 1999 A
5897751 Makowiecki Apr 1999 A
5900699 Samukawa et al. May 1999 A
5902134 Egashira May 1999 A
5902407 deBoer et al. May 1999 A
5903106 Young et al. May 1999 A
5904491 Ojha et al. May 1999 A
5906680 Meyerson May 1999 A
5907435 Ang May 1999 A
5910342 Hirooka et al. Jun 1999 A
5911834 Fairbairn et al. Jun 1999 A
5913140 Roche et al. Jun 1999 A
5915190 Pirkle Jun 1999 A
5916365 Sherman et al. Jun 1999 A
5920792 Lin Jul 1999 A
5922617 Wang et al. Jul 1999 A
5925189 Nguyen et al. Jul 1999 A
5925411 van de Ven et al. Jul 1999 A
5926722 Jang et al. Jul 1999 A
5926737 Ameen et al. Jul 1999 A
5932283 Kaneyama Aug 1999 A
5935283 Sweeney et al. Aug 1999 A
5935340 Xia et al. Aug 1999 A
5937308 Gardner et al. Aug 1999 A
5937323 Orczyk et al. Aug 1999 A
5939763 Hao et al. Aug 1999 A
5939831 Fong et al. Aug 1999 A
5944049 Beyer et al. Aug 1999 A
5944902 Redeker et al. Aug 1999 A
5946592 Lin Aug 1999 A
5953635 Andideh Sep 1999 A
5961850 Satou et al. Oct 1999 A
5965203 Gabric et al. Oct 1999 A
5965246 Guiselin et al. Oct 1999 A
5966499 Hinkle et al. Oct 1999 A
5966595 Thakur et al. Oct 1999 A
5968587 Frankel Oct 1999 A
5968610 Liu et al. Oct 1999 A
5969409 Lin Oct 1999 A
5970383 Lee Oct 1999 A
5976257 Kanai et al. Nov 1999 A
5976261 Moslehi et al. Nov 1999 A
5976327 Tanaka Nov 1999 A
5980686 Goto Nov 1999 A
5981354 Spikes et al. Nov 1999 A
5985102 Leiphart Nov 1999 A
5986234 Matthews et al. Nov 1999 A
5990000 Hong et al. Nov 1999 A
5990013 Berenguer et al. Nov 1999 A
5990984 Meredith et al. Nov 1999 A
6001175 Maruyama et al. Dec 1999 A
6004831 Yamazaki et al. Dec 1999 A
6008515 Hsia et al. Dec 1999 A
6009827 Robles Jan 2000 A
6009830 Li et al. Jan 2000 A
6013191 Nasser-Faili et al. Jan 2000 A
6013584 M'Saad Jan 2000 A
6014979 Van Autryve et al. Jan 2000 A
6017791 Wang et al. Jan 2000 A
6019839 Achutharaman et al. Feb 2000 A
6020035 Gupta et al. Feb 2000 A
6021785 Grutzediek et al. Feb 2000 A
6024044 Law et al. Feb 2000 A
6024799 Chen et al. Feb 2000 A
6025627 Forbes et al. Feb 2000 A
6026053 Satorius Feb 2000 A
6027601 Hanawa Feb 2000 A
6027705 Kitsuno et al. Feb 2000 A
6030460 Sukharev Feb 2000 A
6030666 Lam et al. Feb 2000 A
6030881 Papasouliotis et al. Feb 2000 A
6037018 Jang et al. Mar 2000 A
6039851 Iyer Mar 2000 A
6040022 Chang et al. Mar 2000 A
6042654 Comita et al. Mar 2000 A
6042901 Denison et al. Mar 2000 A
6043136 Jang et al. Mar 2000 A
6050506 Guo et al. Apr 2000 A
6051503 Bhardwaj et al. Apr 2000 A
6054739 Yamazaki et al. Apr 2000 A
6057242 Kishimoto May 2000 A
6059643 Hu et al. May 2000 A
6061077 Kashiwaya et al. May 2000 A
6070551 Li et al. Jun 2000 A
6071573 Koemtzopoulos et al. Jun 2000 A
6074696 Sato Jun 2000 A
6074959 Wang et al. Jun 2000 A
6077412 Ting et al. Jun 2000 A
6077764 Sugiarto et al. Jun 2000 A
6077786 Chakravarti et al. Jun 2000 A
6079353 Leksell et al. Jun 2000 A
6079356 Umotoy et al. Jun 2000 A
6080683 Faur et al. Jun 2000 A
6080965 Osawa Jun 2000 A
6083822 Lee Jul 2000 A
6087243 Wang Jul 2000 A
6088505 Hobbs Jul 2000 A
6090442 Klaus et al. Jul 2000 A
6090718 Soga et al. Jul 2000 A
6090723 Thakur et al. Jul 2000 A
6095085 Agarwal Aug 2000 A
6095643 Cook et al. Aug 2000 A
6096389 Kanai Aug 2000 A
6096646 Lee et al. Aug 2000 A
6099647 Yieh et al. Aug 2000 A
6103014 Lei et al. Aug 2000 A
6106663 Kuthi et al. Aug 2000 A
6106678 Shufflebotham et al. Aug 2000 A
6109065 Atkins et al. Aug 2000 A
6110838 Loewenstein Aug 2000 A
6110845 Seguchi et al. Aug 2000 A
6114219 Spikes, Jr. et al. Sep 2000 A
6114235 Foote et al. Sep 2000 A
6114253 Jang et al. Sep 2000 A
6114704 Buck et al. Sep 2000 A
6117772 Murzin et al. Sep 2000 A
6121130 Chua et al. Sep 2000 A
6121161 Rossman et al. Sep 2000 A
6121930 Grangeat et al. Sep 2000 A
6122934 Narita et al. Sep 2000 A
6124158 Dautartas et al. Sep 2000 A
6125859 Kao et al. Oct 2000 A
6132814 Livesay et al. Oct 2000 A
6133160 Komiyama et al. Oct 2000 A
6136680 Lai et al. Oct 2000 A
6136685 Narwankar et al. Oct 2000 A
6140242 Oh et al. Oct 2000 A
6144060 Park et al. Nov 2000 A
6146970 Witek et al. Nov 2000 A
6147009 Grill et al. Nov 2000 A
6148761 Majewski et al. Nov 2000 A
6149730 Matsubara et al. Nov 2000 A
6149976 Matsuki et al. Nov 2000 A
6149986 Shibata et al. Nov 2000 A
6149987 Perng et al. Nov 2000 A
6150070 Minter et al. Nov 2000 A
6150209 Sun et al. Nov 2000 A
6150286 Sun et al. Nov 2000 A
6151446 Hunter et al. Nov 2000 A
6153269 Gleason Nov 2000 A
6154582 Bazylenko et al. Nov 2000 A
6156114 Bell et al. Dec 2000 A
6156394 Schultz Yamasaki et al. Dec 2000 A
6156435 Gleason Dec 2000 A
6156483 McCoy et al. Dec 2000 A
6156581 Vaudo et al. Dec 2000 A
6158852 Nuttall et al. Dec 2000 A
6165834 Agarwal et al. Dec 2000 A
6167834 Wang et al. Jan 2001 B1
6168668 Yudovsky Jan 2001 B1
6170428 Redeker et al. Jan 2001 B1
6171901 Blair et al. Jan 2001 B1
6171917 Sun et al. Jan 2001 B1
6174808 Jang et al. Jan 2001 B1
6179277 Huston et al. Jan 2001 B1
6179925 Schmitt et al. Jan 2001 B1
6180490 Vassiliev et al. Jan 2001 B1
6182602 Redeker et al. Feb 2001 B1
6184155 Yu et al. Feb 2001 B1
6184158 Shufflebotham et al. Feb 2001 B1
6186092 Tsai et al. Feb 2001 B1
6187682 Denning et al. Feb 2001 B1
6189483 Ishikawa et al. Feb 2001 B1
6190233 Hong et al. Feb 2001 B1
6190973 Berg et al. Feb 2001 B1
6191004 Hsiao Feb 2001 B1
6191026 Rana et al. Feb 2001 B1
6192712 Saito et al. Feb 2001 B1
6194037 Terasaki et al. Feb 2001 B1
6194038 Rossman Feb 2001 B1
6195246 Livesay Feb 2001 B1
6197705 Vassiliev Mar 2001 B1
6200412 Kilgore et al. Mar 2001 B1
6200893 Sneh et al. Mar 2001 B1
6203657 Collison et al. Mar 2001 B1
6203863 Liu et al. Mar 2001 B1
6204200 Shieh et al. Mar 2001 B1
6204201 Ross Mar 2001 B1
6204483 Fair et al. Mar 2001 B1
6206972 Dunham Mar 2001 B1
6207353 Armacost et al. Mar 2001 B1
6207487 Kim et al. Mar 2001 B1
6207555 Ross Mar 2001 B1
6207587 Li et al. Mar 2001 B1
6211040 Liu et al. Apr 2001 B1
6215106 Boas et al. Apr 2001 B1
6217658 Orczyk et al. Apr 2001 B1
6218057 Cirelli et al. Apr 2001 B1
6218090 Minter et al. Apr 2001 B1
6218268 Xia et al. Apr 2001 B1
6221791 Wang et al. Apr 2001 B1
6223540 Egermeier May 2001 B1
6224950 Hirata May 2001 B1
6228751 Yamazaki et al. May 2001 B1
6230650 Yamazaki May 2001 B1
6231674 Chen et al. May 2001 B1
6232196 Raaijmakers et al. May 2001 B1
6232580 Sandhu May 2001 B1
6233044 Brueck et al. May 2001 B1
6236105 Kariya May 2001 B1
6238527 Sone et al. May 2001 B1
6239002 Jang et al. May 2001 B1
6239044 Kashiwagi et al. May 2001 B1
6239909 Hayashi et al. May 2001 B1
6240874 Pike Jun 2001 B1
6242292 Yamazaki et al. Jun 2001 B1
6245192 Lenz et al. Jun 2001 B1
6245689 Hao et al. Jun 2001 B1
6248397 Ye Jun 2001 B1
6248628 Halliyal et al. Jun 2001 B1
6252665 Williams et al. Jun 2001 B1
6255035 Minter et al. Jul 2001 B1
6255038 Hobbs Jul 2001 B1
6255207 Jang et al. Jul 2001 B1
6258690 Zenke Jul 2001 B1
6261374 Bang et al. Jul 2001 B1
6261857 Alam et al. Jul 2001 B1
6267074 Okumura Jul 2001 B1
6268274 Wang et al. Jul 2001 B1
6268297 Nag et al. Jul 2001 B1
6270572 Kim et al. Aug 2001 B1
6270859 Zhao et al. Aug 2001 B2
6271146 Ross Aug 2001 B1
6274058 Rajagopalan et al. Aug 2001 B1
6274500 Xuechun et al. Aug 2001 B1
6276072 Morad et al. Aug 2001 B1
6284646 Leem Sep 2001 B1
6284686 Marlor Sep 2001 B1
6287962 Lin Sep 2001 B1
6287965 Kang et al. Sep 2001 B1
6290865 Fu Sep 2001 B1
6291319 Yu et al. Sep 2001 B1
6291367 Kelkar Sep 2001 B1
6296255 Hashimoto Oct 2001 B1
6296712 Guo et al. Oct 2001 B1
6302964 Umotoy et al. Oct 2001 B1
6302965 Umotoy et al. Oct 2001 B1
6304318 Matsumoto Oct 2001 B1
6304362 Zheludev et al. Oct 2001 B1
6305314 Sneh et al. Oct 2001 B1
6305531 Sneh et al. Oct 2001 B1
6306265 Fu et al. Oct 2001 B1
6311638 Ishii et al. Nov 2001 B1
6313010 Nag et al. Nov 2001 B1
6319655 Wong et al. Nov 2001 B1
6319849 Oda et al. Nov 2001 B1
6323457 Jung Nov 2001 B1
6326064 Denison et al. Dec 2001 B1
6326246 Yamamoto Dec 2001 B1
6326248 Ohtani et al. Dec 2001 B1
6326325 Dawson-Elli et al. Dec 2001 B1
6328808 Tsai et al. Dec 2001 B1
6331494 Olson et al. Dec 2001 B1
6332470 Fishkin et al. Dec 2001 B1
6335280 Van der Jeugd Jan 2002 B1
6335288 Kwan et al. Jan 2002 B1
6337256 Shim Jan 2002 B1
6337467 Sik Jan 2002 B1
6339997 Nakagawa et al. Jan 2002 B1
6340417 Krivokapic Jan 2002 B1
6340435 Bjorkman et al. Jan 2002 B1
6340556 Wong Jan 2002 B1
6342277 Sherman Jan 2002 B1
6344892 Sugita et al. Feb 2002 B1
6345642 Yoshidome et al. Feb 2002 B1
6346302 Kishimoto et al. Feb 2002 B2
6348389 Chou et al. Feb 2002 B1
6348403 Raina et al. Feb 2002 B1
6348410 Ngo et al. Feb 2002 B1
6348420 Raaijmakers et al. Feb 2002 B1
6348421 Shu et al. Feb 2002 B1
6349887 Pyo Feb 2002 B1
6352945 Matsuki et al. Mar 2002 B1
6355108 Won et al. Mar 2002 B1
6355571 Huang et al. Mar 2002 B1
6355581 Vassiliev et al. Mar 2002 B1
6357385 Ohmi et al. Mar 2002 B1
6358323 Schmitt et al. Mar 2002 B1
6358670 Wong Mar 2002 B1
6358829 Yoon et al. Mar 2002 B2
6360685 Xia et al. Mar 2002 B1
6365518 Lee et al. Apr 2002 B1
6365870 Petring et al. Apr 2002 B1
6368948 Ngo et al. Apr 2002 B1
6372291 Hua et al. Apr 2002 B1
6374770 Lee et al. Apr 2002 B1
6375753 Tolia et al. Apr 2002 B1
6376806 Yoo Apr 2002 B2
6383896 Kirimura et al. May 2002 B1
6383954 Wang et al. May 2002 B1
6383955 Matsuki et al. May 2002 B1
6384437 Tee et al. May 2002 B1
6387207 Janakiraman et al. May 2002 B1
6391777 Chen et al. May 2002 B1
6391785 Satta et al. May 2002 B1
6391803 Kim et al. May 2002 B1
6393042 Tanaka May 2002 B1
6393043 Fuchs May 2002 B1
6395150 Van Cleemput et al. May 2002 B1
6398430 Jeoung et al. Jun 2002 B1
6399489 M'Saad et al. Jun 2002 B1
6399491 Jeon et al. Jun 2002 B2
6399520 Kawakami et al. Jun 2002 B1
6402126 Vaartstra et al. Jun 2002 B2
6406677 Carter et al. Jun 2002 B1
6407399 Livesay Jun 2002 B1
6408125 Akwani et al. Jun 2002 B1
6409839 Sun et al. Jun 2002 B1
6410457 M'Saad et al. Jun 2002 B1
6410463 Matsuki et al. Jun 2002 B1
6413583 Moghadam et al. Jul 2002 B1
6413871 M'Saad et al. Jul 2002 B2
6413886 Kersch et al. Jul 2002 B1
6416823 Li et al. Jul 2002 B2
6418960 Mintz et al. Jul 2002 B1
6423384 Khazeni et al. Jul 2002 B1
6424298 Nishikawa et al. Jul 2002 B1
6426015 Xia et al. Jul 2002 B1
6426127 Ross Jul 2002 B1
6426289 Farrar Jul 2002 B1
6432479 Chang et al. Aug 2002 B2
6433911 Chen et al. Aug 2002 B1
6436193 Kasai et al. Aug 2002 B1
6441491 Grill et al. Aug 2002 B1
6444039 Nguyen et al. Sep 2002 B1
6444551 Ku et al. Sep 2002 B1
6447651 Ishikawa et al. Sep 2002 B1
6448187 Yau et al. Sep 2002 B2
6450117 Murugesh et al. Sep 2002 B1
6451119 Sneh et al. Sep 2002 B2
6451686 Ngai et al. Sep 2002 B1
6454860 Metzner et al. Sep 2002 B2
6458718 Todd Oct 2002 B1
6465044 Jain et al. Oct 2002 B1
6468853 Balasubramanian et al. Oct 2002 B1
6468924 Lee et al. Oct 2002 B2
6469283 Burkhart et al. Oct 2002 B1
6475284 Moore et al. Nov 2002 B1
6479098 Yoo et al. Nov 2002 B1
6479405 Lee et al. Nov 2002 B2
6482688 Hu et al. Nov 2002 B2
6486437 Tanabe Nov 2002 B2
6486487 Tanabe Nov 2002 B2
6489225 Ross Dec 2002 B1
6489241 Thilderkvist et al. Dec 2002 B1
6489254 Kelkar et al. Dec 2002 B1
6492283 Raaijmakers et al. Dec 2002 B2
6500771 Vassiliev et al. Dec 2002 B1
6503557 Joret Jan 2003 B1
6503799 Horita et al. Jan 2003 B2
6503843 Xia et al. Jan 2003 B1
6506253 Sakuma Jan 2003 B2
6508879 Hashimoto Jan 2003 B1
6509283 Thomas Jan 2003 B1
6511539 Raaijmakers et al. Jan 2003 B1
6511718 Paz de Araujo et al. Jan 2003 B1
6511923 Wang et al. Jan 2003 B1
6512264 Ogle, Jr. et al. Jan 2003 B1
6514339 Jung Feb 2003 B1
6522433 Kelsey et al. Feb 2003 B2
6524931 Perera Feb 2003 B1
6527910 Rossman Mar 2003 B2
6528332 Mahanpour et al. Mar 2003 B2
6528412 Wang et al. Mar 2003 B1
6531193 Fonash et al. Mar 2003 B2
6531377 Knorr et al. Mar 2003 B2
6531681 Markle et al. Mar 2003 B1
6534395 Werkhoven et al. Mar 2003 B2
6535535 Yamazaki et al. Mar 2003 B1
6537929 Cheung et al. Mar 2003 B1
6541367 Mandal Apr 2003 B1
6541398 Grill et al. Apr 2003 B2
6541401 Herner et al. Apr 2003 B1
6544345 Mayer et al. Apr 2003 B1
6544900 Raaijmakers et al. Apr 2003 B2
6548416 Han et al. Apr 2003 B2
6548899 Ross Apr 2003 B2
6551926 Ross Apr 2003 B1
6551940 Ko Apr 2003 B1
6555423 Wada et al. Apr 2003 B2
6556280 Kelsey et al. Apr 2003 B1
6559026 Rossman et al. May 2003 B1
6559520 Matsuki et al. May 2003 B2
6561498 Tompkins et al. May 2003 B2
6562720 Thilderkvist et al. May 2003 B2
6565661 Nguyen et al. May 2003 B1
6566278 Harvey et al. May 2003 B1
6567219 Tanaka May 2003 B1
6573030 Fairbairn Jun 2003 B1
6573181 Srinivas et al. Jun 2003 B1
6582777 Ross Jun 2003 B1
6583048 Vincent et al. Jun 2003 B1
6583063 Khan et al. Jun 2003 B1
6583069 Vassiliev et al. Jun 2003 B1
6584987 Cheng et al. Jul 2003 B1
6586886 Katz et al. Jul 2003 B1
6589610 Li et al. Jul 2003 B2
6589611 Li et al. Jul 2003 B1
6589868 Rossman Jul 2003 B2
6596627 Mandal Jul 2003 B2
6596653 Tan et al. Jul 2003 B2
6596654 Bayman et al. Jul 2003 B1
6599839 Gabriel et al. Jul 2003 B1
6602792 Hsu Aug 2003 B2
6602806 Xia et al. Aug 2003 B1
6607983 Chun et al. Aug 2003 B1
6607991 Livesay Aug 2003 B1
6614181 Harvey et al. Sep 2003 B1
6614977 Johnson et al. Sep 2003 B2
6616767 Zhao et al. Sep 2003 B2
6617259 Jung et al. Sep 2003 B2
6618537 Temkin et al. Sep 2003 B2
6620296 Gogh et al. Sep 2003 B2
6624064 Sahin et al. Sep 2003 B1
6624091 Yuan Sep 2003 B2
6626188 Fitzsimmons et al. Sep 2003 B2
6628692 Kasamatsu Sep 2003 B2
6630413 Todd Oct 2003 B2
6632279 Ritala et al. Oct 2003 B1
6633076 Krishnaraj et al. Oct 2003 B2
6635575 Xia et al. Oct 2003 B1
6645303 Frankel et al. Nov 2003 B2
6652924 Sherman Nov 2003 B2
6653203 Huang et al. Nov 2003 B1
6656540 Sakamoto et al. Dec 2003 B2
6656804 Tsujikawa et al. Dec 2003 B2
6660391 Rose et al. Dec 2003 B1
6660662 Ishikawa et al. Dec 2003 B2
6667553 Cerny et al. Dec 2003 B2
6670284 Yin Dec 2003 B2
6673722 Yamazaki et al. Jan 2004 B1
6676751 Solomon et al. Jan 2004 B2
6677601 Shiraishi Jan 2004 B2
6677712 Katz et al. Jan 2004 B2
6682659 Cho et al. Jan 2004 B1
6682969 Basceri et al. Jan 2004 B1
6683364 Oh et al. Jan 2004 B2
6703328 Tanaka et al. Mar 2004 B2
6705124 Zhong et al. Mar 2004 B2
6706634 Seitz et al. Mar 2004 B1
6709715 Lang et al. Mar 2004 B1
6713127 Subramony et al. Mar 2004 B2
6713390 M'Saad et al. Mar 2004 B2
6716770 O'Neill et al. Apr 2004 B2
6720097 Ohkawa et al. Apr 2004 B2
6727190 Srinivasan et al. Apr 2004 B2
6733955 Geiger et al. May 2004 B1
6734101 Bao et al. May 2004 B1
6734115 Cheung et al. May 2004 B2
6740601 Tan et al. May 2004 B2
6747245 Talwar et al. Jun 2004 B2
6756085 Waldfried et al. Jun 2004 B2
6758224 Nogami Jul 2004 B2
6759100 Toda et al. Jul 2004 B2
6759261 Shimokohbe et al. Jul 2004 B2
6759662 Li Jul 2004 B1
6762126 Cho et al. Jul 2004 B2
6770134 Maydan et al. Aug 2004 B2
6780574 Kawashima Aug 2004 B2
6787191 Hanahata et al. Sep 2004 B2
6789789 Randive et al. Sep 2004 B2
6792181 Sasaki Sep 2004 B2
6793733 Janakiraman et al. Sep 2004 B2
6794290 Papasouliotis et al. Sep 2004 B1
6794713 Mizushima et al. Sep 2004 B2
6796148 Borrelli et al. Sep 2004 B1
6797558 Nuttall et al. Sep 2004 B2
6800571 Cheung et al. Oct 2004 B2
6805779 Chistyakov Oct 2004 B2
6806651 Chistyakov Oct 2004 B1
6807662 Toublan et al. Oct 2004 B2
6808748 Kapoor et al. Oct 2004 B2
6808991 Tung Oct 2004 B1
6809012 Yamazaki et al. Oct 2004 B2
6812134 Lu et al. Nov 2004 B1
6812153 Hua et al. Nov 2004 B2
6812157 Gadgil Nov 2004 B1
6818389 Fritze et al. Nov 2004 B2
6818517 Maes Nov 2004 B1
6819886 Runkowske et al. Nov 2004 B2
6821577 Rossman Nov 2004 B2
6821825 Todd et al. Nov 2004 B2
6830624 Janakiraman et al. Dec 2004 B2
6833052 Li et al. Dec 2004 B2
6833322 Anderson et al. Dec 2004 B2
6833578 Tu et al. Dec 2004 B1
6835278 Selbrede et al. Dec 2004 B2
6835638 Forbes et al. Dec 2004 B1
6841341 Fairbairn et al. Jan 2005 B2
6846742 Rossman Jan 2005 B2
6846745 Papasouliotis et al. Jan 2005 B1
6849520 Kim et al. Feb 2005 B2
6853142 Chistyakov Feb 2005 B2
6858523 DeBoer et al. Feb 2005 B2
6858533 Chu et al. Feb 2005 B2
6867086 Chen et al. Mar 2005 B1
6868800 Moroz Mar 2005 B2
6870982 Maheshwari Mar 2005 B1
6872323 Entley et al. Mar 2005 B1
6875558 Gaillard et al. Apr 2005 B1
6875687 Weidman et al. Apr 2005 B1
6876086 Sekine et al. Apr 2005 B2
6882477 Schattenburg et al. Apr 2005 B1
6884685 Luo et al. Apr 2005 B2
6888096 Hamada May 2005 B1
6890403 Cheung et al. May 2005 B2
6896773 Chistyakov May 2005 B2
6900067 Kobayashi et al. May 2005 B2
6903031 Karim et al. Jun 2005 B2
6905542 Samoilov et al. Jun 2005 B2
6905940 Ingle et al. Jun 2005 B2
6916398 Chen et al. Jul 2005 B2
6919279 Rulkens et al. Jul 2005 B1
6919282 Sakama et al. Jul 2005 B2
6926926 Cho et al. Aug 2005 B2
6929831 Patel et al. Aug 2005 B2
6935466 Lubomirsky et al. Aug 2005 B2
6943091 Yu et al. Sep 2005 B2
6946358 Doris et al. Sep 2005 B2
6949447 Ahn et al. Sep 2005 B2
6953609 Carollo Oct 2005 B2
6955836 Kumagai et al. Oct 2005 B2
6958112 Karim et al. Oct 2005 B2
6958175 Sakamoto et al. Oct 2005 B2
6961361 Tanaka et al. Nov 2005 B1
6974781 Timmermans et al. Dec 2005 B2
6987240 Jennings et al. Jan 2006 B2
6989337 Chu et al. Jan 2006 B2
6998355 Ohmi et al. Feb 2006 B2
7004012 Liu et al. Feb 2006 B2
7005601 Jennings Feb 2006 B2
7018902 Visokay et al. Mar 2006 B2
7022561 Huang et al. Apr 2006 B2
7024105 Fodor et al. Apr 2006 B2
7037859 Ingle et al. May 2006 B2
7041543 Varadarajan et al. May 2006 B1
7049211 Karim et al. May 2006 B2
7055127 Pierrat et al. May 2006 B2
7056560 Yim et al. Jun 2006 B2
7074690 Gauri et al. Jul 2006 B1
7077904 Cho et al. Jul 2006 B2
7078651 Jennings Jul 2006 B2
7080528 M'Saad et al. Jul 2006 B2
7081414 Zhang et al. Jul 2006 B2
7084061 Sun et al. Aug 2006 B2
7084076 Park et al. Aug 2006 B2
7087497 Yuan et al. Aug 2006 B2
7091411 Falk et al. Aug 2006 B2
7109051 Cave et al. Sep 2006 B2
7109114 Chen et al. Sep 2006 B2
7115419 Suzuki Oct 2006 B2
7122222 Xiao et al. Oct 2006 B2
7122281 Pierrat Oct 2006 B2
7129185 Aoyama et al. Oct 2006 B2
7132134 Rossman Nov 2006 B2
7141483 Yuan et al. Nov 2006 B2
7142282 Borodovsky Nov 2006 B2
7148155 Tarafdar et al. Dec 2006 B1
7166661 Kuramoto et al. Jan 2007 B2
7172792 Wang et al. Feb 2007 B2
7176144 Wang et al. Feb 2007 B1
7182528 Mori Feb 2007 B2
7183177 Al-Bayati et al. Feb 2007 B2
7183204 Sayama et al. Feb 2007 B2
7183214 Nam et al. Feb 2007 B2
7183227 Rasheed et al. Feb 2007 B1
7192626 Dussarrat et al. Mar 2007 B2
7205240 Karim et al. Apr 2007 B2
7205248 Li et al. Apr 2007 B2
7208389 Tipton et al. Apr 2007 B1
7208425 Ingle et al. Apr 2007 B2
7217658 Bayman et al. May 2007 B1
7220461 Hasebe et al. May 2007 B2
7241690 Pavone et al. Jul 2007 B2
7253124 Lu et al. Aug 2007 B2
7273808 Lin Sep 2007 B1
7288284 Li et al. Oct 2007 B2
7294588 Karim et al. Nov 2007 B2
7297608 Papasouliotis et al. Nov 2007 B1
7309659 Subramanian et al. Dec 2007 B1
7325419 M'Saad et al. Feb 2008 B2
7335609 Ingle et al. Feb 2008 B2
7371427 Rajagopalan et al. May 2008 B2
7390573 Korevaar et al. Jun 2008 B2
7393561 Paranjpe Jul 2008 B2
7399388 Moghadam et al. Jul 2008 B2
7419903 Haukka et al. Sep 2008 B2
7435661 Miller et al. Oct 2008 B2
7440088 Thomas et al. Oct 2008 B2
7456116 Ingle et al. Nov 2008 B2
7459182 Xiong et al. Dec 2008 B2
7479210 Mullapudi et al. Jan 2009 B2
7498273 Mallick et al. Mar 2009 B2
7505647 Goebel et al. Mar 2009 B2
7514375 Shanker et al. Apr 2009 B1
7521378 Fucsko et al. Apr 2009 B2
7524735 Gauri et al. Apr 2009 B1
7524750 Nemani et al. Apr 2009 B2
7540920 Singh et al. Jun 2009 B2
7541297 Mallick et al. Jun 2009 B2
7561252 Sewell et al. Jul 2009 B2
7566655 Balseanu et al. Jul 2009 B2
7582555 Lang et al. Sep 2009 B1
7608300 Bencher et al. Oct 2009 B2
7622369 Lee et al. Nov 2009 B1
7629227 Wang et al. Dec 2009 B1
7642041 Wago Jan 2010 B2
7642171 Ingle et al. Jan 2010 B2
7645339 Singh et al. Jan 2010 B2
7674727 Yuan et al. Mar 2010 B2
7691753 Zhang et al. Apr 2010 B2
7723228 Rajagopalan et al. May 2010 B2
7732342 Balseanu et al. Jun 2010 B2
7745350 Wang et al. Jun 2010 B2
7745352 Mallick et al. Jun 2010 B2
7749574 Mahajani et al. Jul 2010 B2
7758697 Comita et al. Jul 2010 B2
7790634 Munro et al. Sep 2010 B2
7799698 Zhang et al. Sep 2010 B2
7803722 Liang Sep 2010 B2
7815982 Iwanaga Oct 2010 B2
7825038 Ingle et al. Nov 2010 B2
7825044 Mallick et al. Nov 2010 B2
7867921 Wang et al. Jan 2011 B2
7867923 Mallick et al. Jan 2011 B2
7869672 Goebel et al. Jan 2011 B2
7872209 Jennings et al. Jan 2011 B2
7875829 Jennings et al. Jan 2011 B2
7902080 Chen et al. Mar 2011 B2
7910491 Soo Kwon et al. Mar 2011 B2
7915139 Lang et al. Mar 2011 B1
7935643 Liang et al. May 2011 B2
7943514 West May 2011 B2
7943531 Nemani et al. May 2011 B2
7964040 Rasheed et al. Jun 2011 B2
7989365 Park et al. Aug 2011 B2
7993733 Stowell et al. Aug 2011 B2
7994019 Kweskin et al. Aug 2011 B1
8023782 Goebel et al. Sep 2011 B2
8057649 Stowell et al. Nov 2011 B2
8119544 Hasebe et al. Feb 2012 B2
8129555 Cheng et al. Mar 2012 B2
8232176 Lubomirsky et al. Jul 2012 B2
8236708 Kweskin et al. Aug 2012 B2
8242031 Mallick et al. Aug 2012 B2
8264066 Lo et al. Sep 2012 B2
8304351 Wang et al. Nov 2012 B2
8318584 Li et al. Nov 2012 B2
8329587 Liang et al. Dec 2012 B2
8445078 Liang et al. May 2013 B2
8449942 Liang et al. May 2013 B2
8466067 Liang et al. Jun 2013 B2
8466073 Wang et al. Jun 2013 B2
20010000866 Sneh et al. May 2001 A1
20010006070 Shang et al. Jul 2001 A1
20010008742 Jen et al. Jul 2001 A1
20010019860 Adachi et al. Sep 2001 A1
20010020712 Raaijmakers et al. Sep 2001 A1
20010020722 Yang Sep 2001 A1
20010021595 Jang Sep 2001 A1
20010024387 Raaijmakers et al. Sep 2001 A1
20010024691 Kimura et al. Sep 2001 A1
20010024871 Yagi Sep 2001 A1
20010025607 Lebar et al. Oct 2001 A1
20010027964 Isaji et al. Oct 2001 A1
20010028922 Sandhu Oct 2001 A1
20010028924 Sherman Oct 2001 A1
20010029114 Vulpio et al. Oct 2001 A1
20010029892 Cook et al. Oct 2001 A1
20010033900 M'Saad et al. Oct 2001 A1
20010034123 Jeon et al. Oct 2001 A1
20010038919 Berry et al. Nov 2001 A1
20010040099 Pedersen et al. Nov 2001 A1
20010041250 Sneh et al. Nov 2001 A1
20010042511 Liu et al. Nov 2001 A1
20010046567 Matsuki et al. Nov 2001 A1
20010048980 Kishimoto et al. Dec 2001 A1
20010054387 Frankel et al. Dec 2001 A1
20010055672 Todd Dec 2001 A1
20010055877 Vaartstra Dec 2001 A1
20010055889 Iyer Dec 2001 A1
20020000195 Bang et al. Jan 2002 A1
20020000196 Park Jan 2002 A1
20020000202 Yuda et al. Jan 2002 A1
20020000598 Kang et al. Jan 2002 A1
20020004282 Hong Jan 2002 A1
20020006729 Geiger et al. Jan 2002 A1
20020007790 Park Jan 2002 A1
20020011210 Satoh et al. Jan 2002 A1
20020011215 Tel et al. Jan 2002 A1
20020016084 Todd Feb 2002 A1
20020027286 Sundararajan et al. Mar 2002 A1
20020031618 Sherman Mar 2002 A1
20020031725 Sugita et al. Mar 2002 A1
20020034645 Kondo et al. Mar 2002 A1
20020037132 Sercel et al. Mar 2002 A1
20020040847 Ohmi et al. Apr 2002 A1
20020041044 Saito et al. Apr 2002 A1
20020047151 Kim et al. Apr 2002 A1
20020048969 Suzuki et al. Apr 2002 A1
20020050605 Jenq May 2002 A1
20020052077 Tee et al. May 2002 A1
20020052128 Yu et al. May 2002 A1
20020068416 Hsieh et al. Jun 2002 A1
20020068458 Chiang et al. Jun 2002 A1
20020068466 Lee et al. Jun 2002 A1
20020074588 Lee Jun 2002 A1
20020076317 Reimer et al. Jun 2002 A1
20020076837 Hujanen et al. Jun 2002 A1
20020079523 Zheng et al. Jun 2002 A1
20020081817 Bhakta et al. Jun 2002 A1
20020081842 Sambucetti et al. Jun 2002 A1
20020086166 Hendricks et al. Jul 2002 A1
20020090818 Thilderkvist et al. Jul 2002 A1
20020092766 Lampkin Jul 2002 A1
20020093042 Oh et al. Jul 2002 A1
20020094483 Hattori et al. Jul 2002 A1
20020098627 Pomarede et al. Jul 2002 A1
20020098712 Mavoori et al. Jul 2002 A1
20020102358 Das et al. Aug 2002 A1
20020119607 Miyasaka et al. Aug 2002 A1
20020125423 Ebeling et al. Sep 2002 A1
20020127350 Ishikawa et al. Sep 2002 A1
20020127841 Horita et al. Sep 2002 A1
20020129769 Kim et al. Sep 2002 A1
20020139307 Ryding et al. Oct 2002 A1
20020142585 Mandal Oct 2002 A1
20020145168 Bojarczuk, Jr. et al. Oct 2002 A1
20020145712 Kochi Oct 2002 A1
20020146512 Rossman Oct 2002 A1
20020146879 Fu et al. Oct 2002 A1
20020149751 Bloomstein et al. Oct 2002 A1
20020155722 Satta et al. Oct 2002 A1
20020160585 Park Oct 2002 A1
20020163028 Zheng Nov 2002 A1
20020163637 Rossman et al. Nov 2002 A1
20020164421 Chiang et al. Nov 2002 A1
20020164429 Gaillard et al. Nov 2002 A1
20020164890 Kwan et al. Nov 2002 A1
20020164891 Gates et al. Nov 2002 A1
20020168828 Cheng et al. Nov 2002 A1
20020168840 Hong et al. Nov 2002 A1
20020168868 Todd Nov 2002 A1
20020170487 Zehavi et al. Nov 2002 A1
20020172768 Endo et al. Nov 2002 A1
20020173113 Todd Nov 2002 A1
20020173130 Pomerede et al. Nov 2002 A1
20020177298 Konishi et al. Nov 2002 A1
20020182342 Ouellet et al. Dec 2002 A1
20020182893 Ballantine et al. Dec 2002 A1
20020185067 Upham Dec 2002 A1
20020187655 Tan et al. Dec 2002 A1
20020189760 Park Dec 2002 A1
20020189940 Tsai et al. Dec 2002 A1
20020192370 Metzner et al. Dec 2002 A1
20020192393 Ouellet et al. Dec 2002 A1
20020192396 Wang et al. Dec 2002 A1
20020197823 Yoo et al. Dec 2002 A1
20020197831 Todd et al. Dec 2002 A1
20020197849 Mandal Dec 2002 A1
20020197881 Ramdani et al. Dec 2002 A1
20030001201 Yuzuriha et al. Jan 2003 A1
20030003610 Yamazaki et al. Jan 2003 A1
20030013320 Kim et al. Jan 2003 A1
20030015764 Raaijmakers et al. Jan 2003 A1
20030019428 Ku et al. Jan 2003 A1
20030022523 Irino et al. Jan 2003 A1
20030022528 Todd Jan 2003 A1
20030023113 Druzkowski et al. Jan 2003 A1
20030032207 Rengarajan et al. Feb 2003 A1
20030032281 Werkhoven et al. Feb 2003 A1
20030036268 Brabant et al. Feb 2003 A1
20030040199 Agarwal Feb 2003 A1
20030049942 Haukka et al. Mar 2003 A1
20030054670 Wang et al. Mar 2003 A1
20030056900 Li et al. Mar 2003 A1
20030057432 Gardner et al. Mar 2003 A1
20030059535 Luo et al. Mar 2003 A1
20030060057 Raaijmakers et al. Mar 2003 A1
20030064154 Laxman et al. Apr 2003 A1
20030068437 Nakamura et al. Apr 2003 A1
20030068890 Park Apr 2003 A1
20030068902 Wang et al. Apr 2003 A1
20030070451 Ouellet et al. Apr 2003 A1
20030071304 Ogle, Jr. et al. Apr 2003 A1
20030071312 Oana et al. Apr 2003 A1
20030072695 Ruelke et al. Apr 2003 A1
20030072884 Zhang et al. Apr 2003 A1
20030072932 Gandon Apr 2003 A1
20030072975 Shero et al. Apr 2003 A1
20030073290 Ramkumar et al. Apr 2003 A1
20030073310 Olgado et al. Apr 2003 A1
20030077918 Wu et al. Apr 2003 A1
20030082300 Todd et al. May 2003 A1
20030089308 Raaijmakers May 2003 A1
20030089314 Matsuki et al. May 2003 A1
20030089942 Bhattacharyya May 2003 A1
20030091938 Fairbairn May 2003 A1
20030094773 Lerner May 2003 A1
20030101927 Raaijmakers Jun 2003 A1
20030101938 Ronsse et al. Jun 2003 A1
20030104677 Park et al. Jun 2003 A1
20030107079 Iwata et al. Jun 2003 A1
20030110808 M'Saad et al. Jun 2003 A1
20030111961 Katz et al. Jun 2003 A1
20030113085 M'Saad et al. Jun 2003 A1
20030113992 Yau et al. Jun 2003 A1
20030116804 Visokay et al. Jun 2003 A1
20030118748 Kumagai et al. Jun 2003 A1
20030123040 Almogy Jul 2003 A1
20030124873 Xing et al. Jul 2003 A1
20030128543 Rekow Jul 2003 A1
20030128925 Wickman Jul 2003 A1
20030129826 Werkhoven et al. Jul 2003 A1
20030134038 Paranjpe Jul 2003 A1
20030138562 Subramony et al. Jul 2003 A1
20030140851 Janakiraman et al. Jul 2003 A1
20030143328 Chen et al. Jul 2003 A1
20030143410 Won et al. Jul 2003 A1
20030143841 Yang et al. Jul 2003 A1
20030150846 Ishii et al. Aug 2003 A1
20030155234 Feltsman et al. Aug 2003 A1
20030159656 Tan et al. Aug 2003 A1
20030160277 Bhattacharyya Aug 2003 A1
20030165749 Fritze et al. Sep 2003 A1
20030168006 Williams Sep 2003 A1
20030168172 Glukhoy Sep 2003 A1
20030172872 Thakur et al. Sep 2003 A1
20030173586 Moriwaki et al. Sep 2003 A1
20030180458 Sneh Sep 2003 A1
20030183518 Glocker et al. Oct 2003 A1
20030185980 Endo Oct 2003 A1
20030188682 Tois et al. Oct 2003 A1
20030189208 Law et al. Oct 2003 A1
20030194853 Jeon et al. Oct 2003 A1
20030194881 Totsuka et al. Oct 2003 A1
20030196995 Jennings Oct 2003 A1
20030196996 Jennings et al. Oct 2003 A1
20030197831 Kim et al. Oct 2003 A1
20030199151 Ho et al. Oct 2003 A1
20030201723 Katz et al. Oct 2003 A1
20030203515 Lin et al. Oct 2003 A1
20030203637 Hua et al. Oct 2003 A1
20030203653 Buchanan et al. Oct 2003 A1
20030205729 Basceri et al. Nov 2003 A1
20030207033 Yim Nov 2003 A1
20030207530 Yu et al. Nov 2003 A1
20030207561 Dubin et al. Nov 2003 A1
20030207580 Li et al. Nov 2003 A1
20030209323 Yokogaki Nov 2003 A1
20030209422 Wang et al. Nov 2003 A1
20030216006 Li et al. Nov 2003 A1
20030217693 Rattner et al. Nov 2003 A1
20030219540 Law et al. Nov 2003 A1
20030223681 Frick Dec 2003 A1
20030224217 Byun et al. Dec 2003 A1
20030228770 Lee et al. Dec 2003 A1
20030230385 Bach et al. Dec 2003 A1
20030232495 Moghadam et al. Dec 2003 A1
20030235994 Pan et al. Dec 2003 A1
20040003873 Chen et al. Jan 2004 A1
20040008334 Sreenivasan et al. Jan 2004 A1
20040009678 Asai et al. Jan 2004 A1
20040011466 Matsumoto et al. Jan 2004 A1
20040015300 Ganguli et al. Jan 2004 A1
20040018699 Boyd et al. Jan 2004 A1
20040020601 Zhao et al. Feb 2004 A1
20040029323 Shimizu et al. Feb 2004 A1
20040029352 Beyer et al. Feb 2004 A1
20040029353 Zheng et al. Feb 2004 A1
20040029398 Lee et al. Feb 2004 A1
20040033639 Chinn et al. Feb 2004 A1
20040033674 Todd Feb 2004 A1
20040038529 Soininen et al. Feb 2004 A1
20040043626 San et al. Mar 2004 A1
20040045577 Ji et al. Mar 2004 A1
20040048485 Min et al. Mar 2004 A1
20040048492 Ishikawa et al. Mar 2004 A1
20040050492 Lun et al. Mar 2004 A1
20040052969 Lee et al. Mar 2004 A1
20040053450 Sposili et al. Mar 2004 A1
20040058517 Padmapani et al. Mar 2004 A1
20040060514 Janakiraman et al. Apr 2004 A1
20040061229 Moslehi Apr 2004 A1
20040063290 Jennings et al. Apr 2004 A1
20040065253 Tois et al. Apr 2004 A1
20040079118 M'Saad et al. Apr 2004 A1
20040082131 Tsujikawa et al. Apr 2004 A1
20040083964 Ingle et al. May 2004 A1
20040083967 Yuda et al. May 2004 A1
20040084680 Ruelke et al. May 2004 A1
20040090194 Gesley May 2004 A1
20040094091 Yang et al. May 2004 A1
20040096672 Lukas et al. May 2004 A1
20040097030 Hirokazu et al. May 2004 A1
20040101633 Zheng et al. May 2004 A1
20040110092 Lin Jun 2004 A1
20040110354 Natzle et al. Jun 2004 A1
20040113217 Chidambarrao et al. Jun 2004 A1
20040113227 Goto et al. Jun 2004 A1
20040115898 Moghadam et al. Jun 2004 A1
20040115954 Todd Jun 2004 A1
20040118519 Soovo Jun 2004 A1
20040126952 Gondhalekar et al. Jul 2004 A1
20040134773 Pedersen et al. Jul 2004 A1
20040139983 Lakshmanan et al. Jul 2004 A1
20040144490 Zhao et al. Jul 2004 A1
20040145029 Adetutu et al. Jul 2004 A1
20040146661 Kapoor et al. Jul 2004 A1
20040152342 Li et al. Aug 2004 A1
20040159343 Kaoru et al. Aug 2004 A1
20040159834 Huang et al. Aug 2004 A1
20040161899 Luo et al. Aug 2004 A1
20040161903 Yuan et al. Aug 2004 A1
20040163590 Tran et al. Aug 2004 A1
20040163762 Iizuka et al. Aug 2004 A1
20040166680 Miyajima et al. Aug 2004 A1
20040166694 Won et al. Aug 2004 A1
20040166695 Yuan et al. Aug 2004 A1
20040166696 Lee Aug 2004 A1
20040175501 Lukas et al. Sep 2004 A1
20040175883 Kim Sep 2004 A1
20040175957 Lukas et al. Sep 2004 A1
20040180557 Park et al. Sep 2004 A1
20040183202 Usami Sep 2004 A1
20040185641 Tanabe et al. Sep 2004 A1
20040192061 Sasaki et al. Sep 2004 A1
20040194706 Wang et al. Oct 2004 A1
20040197474 Vrtis et al. Oct 2004 A1
20040197843 Chou et al. Oct 2004 A1
20040200499 Harvey et al. Oct 2004 A1
20040206305 Choi et al. Oct 2004 A1
20040206621 Li et al. Oct 2004 A1
20040206729 Shinohara Oct 2004 A1
20040211664 Wang Oct 2004 A1
20040212036 Li et al. Oct 2004 A1
20040216844 Janakiraman et al. Nov 2004 A1
20040219780 Ohuchi Nov 2004 A1
20040224534 Beulens et al. Nov 2004 A1
20040224537 Lee et al. Nov 2004 A1
20040226911 Dutton et al. Nov 2004 A1
20040229051 Schaepkens et al. Nov 2004 A1
20040231590 Ovshinsky Nov 2004 A1
20040231795 Rajagopalan et al. Nov 2004 A1
20040231799 Lee et al. Nov 2004 A1
20040235292 Rajagopalan et al. Nov 2004 A1
20040241342 Karim et al. Dec 2004 A1
20040245091 Karim et al. Dec 2004 A1
20040248374 Belyansky et al. Dec 2004 A1
20040249006 Gleason et al. Dec 2004 A1
20040251236 Zhang et al. Dec 2004 A1
20040253776 Hoffmann et al. Dec 2004 A1
20040253791 Min-Chui et al. Dec 2004 A1
20040253826 Ivanov et al. Dec 2004 A1
20040259042 Fritze et al. Dec 2004 A1
20040265507 Xiong et al. Dec 2004 A1
20040266083 Hareland et al. Dec 2004 A1
20050001556 Hoffman et al. Jan 2005 A1
20050008790 Bikram et al. Jan 2005 A1
20050014354 Ozawa et al. Jan 2005 A1
20050016956 Liu et al. Jan 2005 A1
20050019494 Moghadam et al. Jan 2005 A1
20050026443 Goo et al. Feb 2005 A1
20050032321 Huang et al. Feb 2005 A1
20050040460 Chidambarrao et al. Feb 2005 A1
20050042889 Lee et al. Feb 2005 A1
20050048801 Karim et al. Mar 2005 A1
20050062165 Saenger et al. Mar 2005 A1
20050064297 Wago Mar 2005 A1
20050064730 Ingle et al. Mar 2005 A1
20050070100 Yamasaki et al. Mar 2005 A1
20050073671 Borodovsky Apr 2005 A1
20050074698 Borodovsky Apr 2005 A1
20050078953 Fodor et al. Apr 2005 A1
20050079691 Kim et al. Apr 2005 A1
20050083497 Borodovsky Apr 2005 A1
20050085085 Borodovsky Apr 2005 A1
20050087140 Yuda et al. Apr 2005 A1
20050088633 Borodovsky Apr 2005 A1
20050093078 Chan et al. May 2005 A1
20050095859 Chen et al. May 2005 A1
20050098829 Doris et al. May 2005 A1
20050103266 Chandran et al. May 2005 A1
20050112901 Ji et al. May 2005 A1
20050118428 Bicker et al. Jun 2005 A1
20050118794 Babayan et al. Jun 2005 A1
20050121145 Du Bois et al. Jun 2005 A1
20050121835 Herod et al. Jun 2005 A1
20050124166 Krishnaraj et al. Jun 2005 A1
20050129404 Kim et al. Jun 2005 A1
20050136610 Kitagawa et al. Jun 2005 A1
20050139872 Chidambaram et al. Jun 2005 A1
20050142895 Ingle et al. Jun 2005 A1
20050150452 Sen et al. Jul 2005 A1
20050153519 Lu et al. Jul 2005 A1
20050153574 Mandal Jul 2005 A1
20050160383 Lin Jul 2005 A1
20050160974 Ivanov et al. Jul 2005 A1
20050164517 Karim et al. Jul 2005 A1
20050167742 Challa et al. Aug 2005 A1
20050181555 Haukka et al. Aug 2005 A1
20050186731 Derderian et al. Aug 2005 A1
20050186755 Smythe et al. Aug 2005 A1
20050186789 Agarwal Aug 2005 A1
20050196533 Hasebe et al. Sep 2005 A1
20050196935 Ishitsuka et al. Sep 2005 A1
20050196971 Sen et al. Sep 2005 A1
20050196977 Saito et al. Sep 2005 A1
20050211170 Hanawa et al. Sep 2005 A1
20050214454 Yang et al. Sep 2005 A1
20050214477 Hanawa et al. Sep 2005 A1
20050217578 Gurary et al. Oct 2005 A1
20050218124 Jennings et al. Oct 2005 A1
20050224866 Higashi et al. Oct 2005 A1
20050227017 Senzaki et al. Oct 2005 A1
20050227499 Park et al. Oct 2005 A1
20050230350 Kao et al. Oct 2005 A1
20050233595 Choi et al. Oct 2005 A1
20050238965 Tyrrell et al. Oct 2005 A1
20050250340 Chen et al. Nov 2005 A1
20050257890 Park et al. Nov 2005 A1
20050260347 Narwankar et al. Nov 2005 A1
20050266323 Raulea Dec 2005 A1
20050266655 Nemani et al. Dec 2005 A1
20050271812 Myo et al. Dec 2005 A1
20050272254 Ding et al. Dec 2005 A1
20050274128 Kishorenath et al. Dec 2005 A1
20050285140 Ko et al. Dec 2005 A1
20050287775 Hasebe et al. Dec 2005 A1
20060011984 Currie Jan 2006 A1
20060012938 Park Jan 2006 A1
20060014399 Joe Jan 2006 A1
20060017910 Borodovsky Jan 2006 A1
20060019486 Yu et al. Jan 2006 A1
20060021702 Kumar et al. Feb 2006 A1
20060030151 Ding et al. Feb 2006 A1
20060030165 Ingle et al. Feb 2006 A1
20060045986 Hochberg et al. Mar 2006 A1
20060046156 Amako et al. Mar 2006 A1
20060046160 Wallace et al. Mar 2006 A1
20060046427 Ingle et al. Mar 2006 A1
20060046506 Fukiage Mar 2006 A1
20060046508 Nemani et al. Mar 2006 A1
20060055004 Gates et al. Mar 2006 A1
20060068599 Baek et al. Mar 2006 A1
20060075966 Chen et al. Apr 2006 A1
20060075967 Lu et al. Apr 2006 A1
20060078717 Yamaya et al. Apr 2006 A1
20060084236 Vogt Apr 2006 A1
20060088985 Haverkort et al. Apr 2006 A1
20060090694 Cho et al. May 2006 A1
20060091104 Takeshita et al. May 2006 A1
20060096540 Choi May 2006 A1
20060102977 Fucsko et al. May 2006 A1
20060105106 Balseanu et al. May 2006 A1
20060110939 Joshi et al. May 2006 A1
20060110943 Swerts et al. May 2006 A1
20060121394 Chi Jun 2006 A1
20060148270 Lu et al. Jul 2006 A1
20060148273 Ingle et al. Jul 2006 A1
20060158101 Camilletti et al. Jul 2006 A1
20060159847 Porter et al. Jul 2006 A1
20060160314 Arghavani Jul 2006 A1
20060160372 Dorfman Jul 2006 A1
20060162661 Jung et al. Jul 2006 A1
20060166515 Karim et al. Jul 2006 A1
20060178018 Olsen Aug 2006 A1
20060191478 Gondhalekar et al. Aug 2006 A1
20060196766 Chen Sep 2006 A1
20060199305 Chen et al. Sep 2006 A1
20060205150 Dong Sep 2006 A1
20060207294 M'Saad et al. Sep 2006 A1
20060207504 Hasebe et al. Sep 2006 A1
20060208634 Schaepkens et al. Sep 2006 A1
20060211265 Trott Sep 2006 A1
20060216651 Ho et al. Sep 2006 A1
20060223290 Belyansky et al. Oct 2006 A1
20060223315 Yokota et al. Oct 2006 A1
20060224451 Kerschbrock et al. Oct 2006 A1
20060225648 Rasheed et al. Oct 2006 A1
20060228903 McSwiney et al. Oct 2006 A1
20060240232 Faris Oct 2006 A1
20060251499 Lunday et al. Nov 2006 A1
20060252240 Gschwandtner et al. Nov 2006 A1
20060263522 Byun Nov 2006 A1
20060264062 Ingle et al. Nov 2006 A1
20060269692 Balseanu et al. Nov 2006 A1
20060269693 Balseanu et al. Nov 2006 A1
20060274295 Brueck et al. Dec 2006 A1
20060281496 Cedraeus Dec 2006 A1
20060286774 Singh et al. Dec 2006 A1
20060286776 Ranish et al. Dec 2006 A1
20060292894 Vellaikal et al. Dec 2006 A1
20070004170 Kawasaki et al. Jan 2007 A1
20070007548 Conti et al. Jan 2007 A1
20070010072 Bailey et al. Jan 2007 A1
20070020392 Kobrin et al. Jan 2007 A1
20070020875 Hsu et al. Jan 2007 A1
20070026689 Nakata et al. Feb 2007 A1
20070031598 Okuyama et al. Feb 2007 A1
20070031609 Kumar et al. Feb 2007 A1
20070032054 Ramaswamy et al. Feb 2007 A1
20070045103 Lee et al. Mar 2007 A1
20070048509 Yoneyama et al. Mar 2007 A1
20070049044 Marsh Mar 2007 A1
20070059896 Yuan et al. Mar 2007 A1
20070065578 McDougall Mar 2007 A1
20070066005 Katsuhiko et al. Mar 2007 A1
20070066022 Chen et al. Mar 2007 A1
20070077777 Gumpher Apr 2007 A1
20070080056 German et al. Apr 2007 A1
20070080057 Yasuhiro et al. Apr 2007 A1
20070092661 Ryuzaki et al. Apr 2007 A1
20070098916 Stowell May 2007 A1
20070099438 Ye et al. May 2007 A1
20070102634 Frey et al. May 2007 A1
20070108166 Jennings et al. May 2007 A1
20070108404 Stewart et al. May 2007 A1
20070111546 Iyer et al. May 2007 A1
20070119546 Collins et al. May 2007 A1
20070128864 Ma et al. Jun 2007 A1
20070134433 Dussarrat et al. Jun 2007 A1
20070139633 Bleeker et al. Jun 2007 A1
20070160822 Bristow et al. Jul 2007 A1
20070166892 Hori Jul 2007 A1
20070173073 Weber Jul 2007 A1
20070181145 Ishizuka et al. Aug 2007 A1
20070181966 Watatani et al. Aug 2007 A1
20070197028 Byun et al. Aug 2007 A1
20070207590 Kiyotoshi et al. Sep 2007 A1
20070212850 Ingle et al. Sep 2007 A1
20070218264 Gueneau et al. Sep 2007 A1
20070221127 Tran et al. Sep 2007 A1
20070232071 Balseanu et al. Oct 2007 A1
20070232082 Balseanu et al. Oct 2007 A1
20070235062 Naozumi et al. Oct 2007 A1
20070240631 Nijhawan et al. Oct 2007 A1
20070253881 Maekawa et al. Nov 2007 A1
20070254093 Nijhawan et al. Nov 2007 A1
20070254100 Nijhawan et al. Nov 2007 A1
20070275569 Moghadam et al. Nov 2007 A1
20070277734 Lubomirsky et al. Dec 2007 A1
20070281106 Lubomirsky et al. Dec 2007 A1
20070281448 Chen et al. Dec 2007 A1
20070281495 Mallick et al. Dec 2007 A1
20070281496 Ingle et al. Dec 2007 A1
20070289534 Lubomirsky et al. Dec 2007 A1
20070298585 Lubomirsky et al. Dec 2007 A1
20080000423 Fukiage Jan 2008 A1
20080014711 Choi et al. Jan 2008 A1
20080014759 Chua et al. Jan 2008 A1
20080020591 Balseanu et al. Jan 2008 A1
20080026597 Munro et al. Jan 2008 A1
20080038486 Treichel et al. Feb 2008 A1
20080041831 Jennings et al. Feb 2008 A1
20080063809 Lee et al. Mar 2008 A1
20080070409 Park et al. Mar 2008 A1
20080081104 Hasebe et al. Apr 2008 A1
20080085607 Yu et al. Apr 2008 A1
20080096364 Wilson et al. Apr 2008 A1
20080099431 Kumar et al. May 2008 A1
20080102223 Wagner et al. May 2008 A1
20080102650 Adams et al. May 2008 A1
20080115726 Ingle et al. May 2008 A1
20080118734 Goodwin et al. May 2008 A1
20080124084 Goebel et al. May 2008 A1
20080152838 Sen et al. Jun 2008 A1
20080173402 Suzuki et al. Jul 2008 A1
20080176390 Cheng Jul 2008 A1
20080178805 Paterson et al. Jul 2008 A1
20080182382 Ingle et al. Jul 2008 A1
20080188087 Chen et al. Aug 2008 A1
20080206954 Choi et al. Aug 2008 A1
20080216958 Goto et al. Sep 2008 A1
20080226924 Okubo et al. Sep 2008 A1
20080241358 Joe et al. Oct 2008 A1
20080251016 Cunning et al. Oct 2008 A1
20080260969 Dussarrat et al. Oct 2008 A1
20080292798 Huh et al. Nov 2008 A1
20080305648 Fukazawa et al. Dec 2008 A1
20080318429 Ozawa et al. Dec 2008 A1
20090031953 Ingle et al. Feb 2009 A1
20090035917 Ahn et al. Feb 2009 A1
20090046263 Liu et al. Feb 2009 A1
20090047604 Stoeldraijer et al. Feb 2009 A1
20090053901 Goto et al. Feb 2009 A1
20090054674 Lukas et al. Feb 2009 A1
20090061647 Mallick et al. Mar 2009 A1
20090075490 Dussarrat et al. Mar 2009 A1
20090085096 Park et al. Apr 2009 A1
20090093132 Xu et al. Apr 2009 A1
20090095714 Chen et al. Apr 2009 A1
20090104755 Mallick et al. Apr 2009 A1
20090104789 Mallick et al. Apr 2009 A1
20090104790 Liang Apr 2009 A1
20090104791 Nemani et al. Apr 2009 A1
20090104798 Hirano Apr 2009 A1
20090111056 Hendel et al. Apr 2009 A1
20090117491 Hendel et al. May 2009 A1
20090120368 Lubomirsky et al. May 2009 A1
20090120464 Muhammad et al. May 2009 A1
20090120584 Lubomirsky et al. May 2009 A1
20090142935 Fukuzawa et al. Jun 2009 A1
20090170282 Dong Jul 2009 A1
20090181550 Hasebe et al. Jul 2009 A1
20090194809 Cho Aug 2009 A1
20090203225 Gates et al. Aug 2009 A1
20090206409 Arisumi et al. Aug 2009 A1
20090208715 Stowell et al. Aug 2009 A1
20090209081 Matero et al. Aug 2009 A1
20090215251 Vellaikal et al. Aug 2009 A1
20090224374 Bhatia et al. Sep 2009 A1
20090232977 Morinaga et al. Sep 2009 A1
20090232985 Dussarrat et al. Sep 2009 A1
20090238993 Stowell et al. Sep 2009 A1
20090238998 Stowell et al. Sep 2009 A1
20090242957 Ma et al. Oct 2009 A1
20090252495 Goebel et al. Oct 2009 A1
20090277587 Lubomirsky et al. Nov 2009 A1
20090277778 Stowell et al. Nov 2009 A1
20090280650 Lubomirsky et al. Nov 2009 A1
20090283400 Stowell et al. Nov 2009 A1
20090289284 Goh et al. Nov 2009 A1
20090294925 Lin et al. Dec 2009 A1
20090298257 Lee et al. Dec 2009 A1
20090325391 De Vusser et al. Dec 2009 A1
20100002210 Hendel et al. Jan 2010 A1
20100052066 Yu et al. Mar 2010 A1
20100059889 Gosset et al. Mar 2010 A1
20100078315 Stowell et al. Apr 2010 A1
20100078320 Stowell Apr 2010 A1
20100081094 Hasebe et al. Apr 2010 A1
20100081293 Mallick et al. Apr 2010 A1
20100098884 Balseanu et al. Apr 2010 A1
20100099236 Kwon et al. Apr 2010 A1
20100136313 Shimizu et al. Jun 2010 A1
20100140756 Kozasa et al. Jun 2010 A1
20100143609 Fukazawa et al. Jun 2010 A1
20100184302 Lee et al. Jul 2010 A1
20100190317 Iwasawa et al. Jul 2010 A1
20100190348 Akae et al. Jul 2010 A1
20100221428 Dussarrat Sep 2010 A1
20100221925 Lee et al. Sep 2010 A1
20100227276 Mizuno Sep 2010 A1
20100230052 Iizuka Sep 2010 A1
20100255655 Mallick et al. Oct 2010 A1
20100261318 Feng et al. Oct 2010 A1
20100283097 Endoh et al. Nov 2010 A1
20110014798 Mallick et al. Jan 2011 A1
20110034035 Liang et al. Feb 2011 A1
20110034039 Liang et al. Feb 2011 A1
20110045676 Park et al. Feb 2011 A1
20110076420 Stowell Mar 2011 A1
20110076422 Stowell Mar 2011 A1
20110081782 Liang et al. Apr 2011 A1
20110095007 Jennings et al. Apr 2011 A1
20110097517 Stowell et al. Apr 2011 A1
20110111137 Liang et al. May 2011 A1
20110129616 Ingle et al. Jun 2011 A1
20110136347 Kovarsky et al. Jun 2011 A1
20110151677 Wang et al. Jun 2011 A1
20110159213 Cai et al. Jun 2011 A1
20110159703 Liang et al. Jun 2011 A1
20110165347 Miller et al. Jul 2011 A1
20110165781 Liang et al. Jul 2011 A1
20110186990 Mawatari et al. Aug 2011 A1
20110187000 West Aug 2011 A1
20110212620 Liang et al. Sep 2011 A1
20110217851 Liang et al. Sep 2011 A1
20110223774 Kweskin et al. Sep 2011 A1
20120003840 Wang et al. Jan 2012 A1
20120009802 LaVoie et al. Jan 2012 A1
20120045631 Stowell et al. Feb 2012 A1
20120073501 Lubomirsky et al. Mar 2012 A1
20120074387 King Mar 2012 A1
20120079982 Lubomirsky et al. Apr 2012 A1
20120083133 Solis et al. Apr 2012 A1
20120094468 Bhatia et al. Apr 2012 A1
20120094476 Tanaka et al. Apr 2012 A1
20120111831 Ha May 2012 A1
20120122302 Weidman et al. May 2012 A1
20120142192 Li et al. Jun 2012 A1
20120145079 Lubomirsky et al. Jun 2012 A1
20120161405 Mohn et al. Jun 2012 A1
20120177846 Li et al. Jul 2012 A1
20120180954 Yang et al. Jul 2012 A1
20120190178 Wang et al. Jul 2012 A1
20120193778 Mawatari Aug 2012 A1
20120213940 Mallick Aug 2012 A1
20120225565 Bhatia et al. Sep 2012 A1
20120238108 Chen et al. Sep 2012 A1
20120269989 Liang et al. Oct 2012 A1
20120292720 Chen et al. Nov 2012 A1
20120309205 Wang et al. Dec 2012 A1
20130062736 Brighton et al. Mar 2013 A1
20130084711 Liang et al. Apr 2013 A1
20130149462 Liang et al. Jun 2013 A1
20130193578 Yu et al. Aug 2013 A1
Foreign Referenced Citations (76)
Number Date Country
1830072 Sep 2006 CN
19654737 Jul 1997 DE
0892083 Jan 1999 EP
1095958 May 2001 EP
1469509 Oct 2004 EP
1717848 Nov 2006 EP
1791161 May 2007 EP
2022087 May 2007 EP
57-75738 Oct 1980 JP
61-234534 Oct 1986 JP
64-048425 Feb 1989 JP
1-198033 Aug 1989 JP
01-235259 Sep 1989 JP
01241826 Sep 1989 JP
03-197684 Aug 1991 JP
03-286531 Dec 1991 JP
04-328825 Nov 1992 JP
05-259156 Oct 1993 JP
05-304147 Nov 1993 JP
06-077150 Mar 1994 JP
6-168930 Jun 1994 JP
07-014826 Jan 1995 JP
07-169762 Jul 1995 JP
07-316823 Dec 1995 JP
08-236518 Sep 1996 JP
08-288286 Nov 1996 JP
09-008014 Jan 1997 JP
09-237785 Sep 1997 JP
10-163183 Jun 1998 JP
11-274285 Oct 1999 JP
2001-148382 May 2001 JP
2002-370059 Dec 2002 JP
2003-179054 Jun 2003 JP
2004-012315 Jan 2004 JP
2004-327639 Nov 2004 JP
2004-536444 Dec 2004 JP
2005-142448 Jun 2005 JP
2005-268396 Sep 2005 JP
2005-302848 Oct 2005 JP
2006-041539 Feb 2006 JP
2006-210878 Aug 2006 JP
2007-019067 Jan 2007 JP
2007-191728 Aug 2007 JP
2007-324154 Dec 2007 JP
2008-159824 Jul 2008 JP
2008218684 Sep 2008 JP
2011-220127 Nov 2011 JP
10-1999-0010957 Feb 1999 KR
0204793 Mar 1999 KR
1020000011360 Feb 2000 KR
1020020013383 Feb 2002 KR
10-2004-0091978 Nov 2004 KR
1020040104533 Dec 2004 KR
10-2005-0003758 Jan 2005 KR
10-2005-0072332 Jul 2005 KR
10-2005-0085838 Aug 2005 KR
10-2005-0094183 Sep 2005 KR
1020060081350 Jul 2006 KR
1020060103640 Oct 2006 KR
10-2009-0011765 Feb 2009 KR
10-2009-0121361 Nov 2009 KR
10-2009-0122860 Dec 2009 KR
10-2010-0085743 Jul 2010 KR
200514163 Apr 2005 TW
200707582 Feb 2007 TW
02077320 Oct 2002 WO
03066933 Aug 2003 WO
2005078784 Aug 2005 WO
2006014034 Feb 2006 WO
2007040856 Apr 2007 WO
2007140376 Dec 2007 WO
2007140377 Dec 2007 WO
2009055340 Apr 2009 WO
2010080216 Jul 2010 WO
2012145148 Oct 2012 WO
2013025336 Feb 2013 WO
Non-Patent Literature Citations (172)
Entry
U.S. Appl. No. 12/050,373 filed Mar. 18, 2008, Stowell et al.
U.S. Appl. No. 12/070,660, filed Feb. 20, 2008, Stowell et al.
U.S. Appl. No. 12/077,375, filed Mar. 19, 2008, Stowell et al.
U.S. Appl. No. 12/115,717, filed May 6, 2008, Stowell et al.
U.S. Appl. No. 12/120,391, filed May 14, 2008, Stowell et al.
U.S. Appl. No. 12/238,664, filed Sep. 26, 2008, Stowell.
U.S. Appl. No. 12/238,685, filed Sep. 26, 2008, Stowell.
U.S. Appl. No. 12/833,473, filed Jul. 9, 2010, Stowell.
U.S. Appl. No. 12/833,524, filed Jul. 9, 2010, Stowell.
U.S. Appl. No. 12/833,571, filed Jul. 9, 2010, Stowell et al.
Alexandrov, et al., “Formation of Silicon Nitride Films by Remote Plasma-enhanced Chemical Vapour Deposition”. Advanced Materials for Optics and Electronics, vol. 2, 301-312 (1993).
Aylett, B. J. et al., “Silicon-Nitrogen Compounds. Part V. Diphenylamino-derivatives of Silane,” J. Chem. Soc. (A), Apr. 1969, pp. 636-638.
Aylett, B. J. et al., “Silicon-Nitrogen Compounds. Part VI.1 The Preparation and Properties of Disilazane,” J. Chem. Soc. (A), Apr. 1969, pp. 639-642.
Aylett, B. J. et al., “The Preparation and Some Properties of Disilylamine-Correspondence,” Inorganic Chemistry, Jan. 1966, p. 167.
Beach, “Infrared and Mass Spectroscopic Study of the Reaction of Silyl Iodide and Ammonia. Infrared Spectrum to Silylamine,” Inorganic Chemistry, Sep. 1992, pp. 4174-4177, vol. 31 No. 20.
Bowen, C., et al., “New Processing Techniques: Sweeping of Quartz Wafers and a Practical Method for Processing Quartz Resonators Under Controlled Conditions,” Proceedings of the 1992 IEEE Frequency Control Symposium, pp. 648-656.
Burg, et al. “Silyl-Amino Boron Compounds,” J. Amer. Chem. Soc., Jul. 1950, pp. 3103-3107, vol. 72.
Coltrin, M.E., et al., “Chemistry of AIGaN Particulate Formation,” National Nuclear Security Administration, Physical, Chemical, & Nano Sciences Center, Research Briefs, 2005, pp. 42-43.
Davison, A et al., “The Raman Spectra of Manganese and Rhenium Carbonyl Hydrides and Some Related Species,” Inorganic Chemistry, Apr. 1967, pp. 845-847, vol. 6 No. 4.
Dussarrat, C. et al., “Low Pressure Chemical Vapor Deposition of Silicon Nitride Using Mono—and Disilylamine,” Chemical Vapor Deposition XVI and EUROCVD 14 vol. 2 Proceedings of the International Symposium, Part of the 203rd Electrochemical Society Meeting in Paris France, Apr. 27-May 2, 2003, 11 pages.
Franz, et al., “Conversion of silicon nitride into silicon dioxide through the influence of oxygen,” Solid-State Electronics, Jun. 1971, pp. 449-505, vol. 14, Issue 6, Germany. Abstract Only.
Gulleri, G. et al., “Deposition Temperature Determination of HDPCVD Silicon Dioxide Films,” 2005, Microelectronic Engineering, vol. 82, pp. 236-241.
International Search Report and Written Opinion of PCT/US2011/054635, mailed Jul. 9, 2012, 11 pages.
International Search Report and Written Opinion of PCT/US2011/054981, mailed May 9, 2012, 10 pages.
International Search Report and Written Opinion of PCT/US2011/054984, mailed May 11, 2012, 10 pages.
International Search Report and Written Opinion of PCT/US2011/066275, mailed Sep. 24, 2012, 9 pages.
International Search Report and Written Opinion of PCT/US2011/066281, mailed Jul. 19, 2012, 10 pages.
International Search Report and Written Opinion of PCT/US2011/066601, mailed Jul. 20, 2012, 10 pages.
International Search Report and Written Opinion of PCT/US2012/026786, mailed Jan. 2, 2013, 7 pages.
International Search Report and Written Opinion of PCT/US2012/044679, mailed Jan. 10, 2013, 9 pages.
International Search Report and Written Opinion of PCT/US2012/053999, mailed Feb. 27, 2013, 12 pages.
International Search Report and Written Opinion of PCT/US2012/031640 mailed Oct. 18, 2012, 10 pages.
International Search Report and Written Opinion of PCT/US2012/039629, mailed Dec. 26, 2012, 6 pages.
International Search Report and Written Opinion of PCT/US2012/059400, mailed Mar. 26, 2013, 11 pages.
International Search Report and Written Opinion of PCT/US2012/065086, mailed Mar. 25, 2013, 10 pages.
International Search Report and Written Opinion of PCT/US2013/050906, mailed Jan. 13, 2014, 10 pages.
Kang, “A Study of the Nucleation and Formation of Multi-functional Nanostructures using GaN-Based Materials for Device Applications,” Georgia Institute of Technology, Doctor of Philosophy in the School of Electrical & Computer Engineering Dissertation, Dec. 2006, 187 pages.
Lee, Eun Gu, et al., “Effects of Wet Oxidation on the Electrical Properties of sub-10 nm thick silicon nitride films”, Thin Solid Films, Elsevier-Sequoia S.A. Lausanne, CH. vol. 205, No. 2, Dec. 1, 1991, pp. 246-251.
Loboda, M.J., et al., “Chemical influence of inert gas on the thin film stress in plasma-enhanced chemical vapor deposited a—SiN:H films”. Journal of Materials Research, vol. 11, No. 2, Feb. 1996, pp. 391-398.
Lucovsky, G. et al., “Deposition of silicon dioxide and silicon nitride by remote plasma enhanced chemical vapor deposition,” Journal of Vacuum Science & Technology, vol. 4, No. 3, May-Jun. (1986), pp. 681-688.
Norman, et al., “Reaction of Silylphosphine with Ammonia,” Inorganic Chemistry, Jun. 1979, pp. 1594-1597, vol. 18 No. 6.
Search Report mailed Sep. 4, 2012, European Application No. 07811964, now patent No. 2022087, 8 pages.
Sujishi, Sei et al., “Effect of Replacement of Carbon by Silicon in Trimethylamine on the Stabilities of the Trimethylboron Addition Compounds. Estimation of the Resonance Energy for Silicon-Nitrogen Partial Double Bond,” Amer. Chem. Soc., Sep. 20, 1954, pp. 4631-4636, vol. 76.
Tripp, et al., “The Anodic Oxidation of Silicon Nitride Films on Silicon,” Journal of the Electrochemical Society, 1970, pp. 157-159, 117(2).
Tsu, D. V. et al., “Silicon Nitride and Silicon Diimide Grown by Remote Plasma Enhanced Chemical Vapor Deposition”, Journal of Vacuum Science and Technology: Part a, AVS/AIP, Melville, NY, US, vol. 4, No. 3, Part 01, May 1, 1986, pp. 480-485.
Usenko, et al., “Silicon Nitride Surface Conversion into Oxide to Enable Hydrophilic Bonding,” ECS Meeting Abstracts, 2010, 1 page, Abstract #1716, 218th ECS Meeting.
Wang Li et al., “Properties of Hydrogenated Amorphous Silicon Caarbide Films Irradiated by Excimer Pulse Laser,” 1998.
Ward, L. G. L. et al., “The Preparation and Properties of Bis-Disilanyl Sulphide and Tris-Disilanylamine,” J. Inorg. Nucl. Chem., Dec. 1961, pp. 287-293, vol. 21, Pergamon Press Ltd., Northern Ireland.
Ward, Laird G. L., “Bromosilane, Iodosilane, and Trisilylamine,” Inorganic Syntheses, 1968, pp. 159-170, vol. 11.
Ying-Yu et al., “Preparation of SiC Thin Film Using Organosilicon by Remote Plasma CVD Method,” 1999.
Zuckerman, J.J., “Inorganic Reactions and Methods,” Formation of Bonds to N, P, As, Sb, Bi (Part 1), ISBN-0-89573-250-5, Jan. 1998, 5 pages, vol. 7, VCH Publishers, Inc., New York.
Abraham, Tom, “Reactive Facet Tapering of Plasma Oxide for Multilevel Interconnect Applications,” V-MIC Conference, IEEE, pp. 115-121, Jun. 15-16, 1987.
Agarwal et al., “Challenges in Integrating the High-K Gate Dielectric Film to the Conventional CMOS Process Flow,” Mat. Sec. Soc. Sump. Proc. vol. 670 (2001).
Alonso, J.C. et al., “Fluorinated-chlorinated SiO2 films prepared at low-temperature by remote plasma-enhanced chemical vapor deposition using mixtures of SiF4 and SiF14,” JVST V. 19, No. 2 Mar. 2001, pp. 507-514; XP012005495 ISSN: 0734-2101.
Alonso, J.C. et al., “High rate—low temperature deposition of silicon dioxide films by remote plasma enhanced chemical vapor deposition using silicon tetrachloride.” Journal of Vacuum Science & Technology A: Vacuum, Surfaces, and Films, Nov. 1995, vol. 13, Issue 6, pp. 2924-2929. [Abstract Only].
Applied Materials Website Printout: “SACVD (Sub-Atmospheric Chemical Vapor Deposition)” from www.appliedmaterials.com/products/sacvd.html, printed Jun. 20, 2003.
Author Unknown, “Ultrafine Zinc Oxide,” Sumitomo Osaka Cement Co., Ltd., 2 pages, no date.
Author Unknown, “Zinc Oxide Profile,” obtained on Oct. 15, 2007 from website http://www.mountainroseherbs.com/learn/zinc—oxide.php, Mar. 3, 2005, 2 pages.
Author Unknown, “Vortek Impulse™ Anneal,” Vortek Industries Ltd., 2000 [retrieved on Nov. 3, 2008], 2 pages. Retrieved from: http://web.archive.org/web/20020207191545/http://vortek.com/semi.htm.
Baker, F. et al. “STI TEOS Densification for Furnaces and RTP Tools” 1999 IEEE/SEMI Advanced Semiconductor Manufacturing Conference, 1999, pp. 394-399.
Banerjee et al., “Characterization of CVD Deposited Amorphous Fluorocarbons for Low k Interlayer Dielectrics”, 1 Electrochem. Soc vol. 146, 2219 (1999).
Bang et al. (Jan. 3, 2002). US Patent Application Publication US-2002-0000195 A1.
Bapin et al., “Deposition of SiO2 films from different organosilicon/O2 plasmas under continuous wave and pulsed modes”, Surface and Coatings Technology, Jul. 2001, pp. 649-654.
Bar-Ilan et al., “A comparative study of sub-micron gap filling and planarization techniques”, SPIE vol. 2636, Oct. 1995, 277-288.
Bedair, “Atomic Layer Epitaxy Deposition Processes,” J. Vac. Sci. Technol. B., vol. 12, No. 1, Jan./Feb. 1994.
Boisse-Laporte, “New Type of plasma reactor for thin film deposition: magnetron plasma process assisted by microwaves to ionise sputter vapour,” Surface and Coatings Technology, 2004, 179, 176-181.
Broomfield et al., “HDP Dielectric BEOL Gapfill: A Process for Manufacturing”, IEEE/SEMI Advanced Semiconductor Manufacturing Conference 1996, pp. 255-258.
Chang, Chorng-Ping et al., “Frequency Effects And Properties Of Plasma Deposited Fluorinated Silicon Nitride,” J. Vac. Sci. Technol. B., vol. 6, No. 2, pp. 524-532, Mar./Apr. 1988.
Charles, Christine, “Role of ions in SiO 2 deposition with pulsed and continuous helicon plasma”, Pure and Applied Chemistry, 2002—vol. 74, No. 3, pp. 401-405, 2002. IUPAC 401.
Chen, K.X. et al., “ESCE Course of MOCVD Bubblers,” no page numbers or date available, 2 pages.
Choi et al., “Stability of TIB2 as a Diffusion Barrier on Silicon,” J. Electrochem. Soc., vol. 138, No. 10, Oct. 1991.
Choi et al., “The Effect of Annealing on Resistivity of Low Pressure Chemical Vapor Deposited Titanium Diboride,” J. Appl. Phys. 69 (11), Jun. 1, 1991.
Conti et al., “Processing methods to fill High aspect ratio gaps without premature constriction,” DUMIC Conference, Feb. 8-9, 1999, pp. 201-209.
Cruden et al., “Thermal Decomposition of Low-k Pulsed Plasma Fluorocarbon Films. I. Effects of Precursors and Substrate Temperature”, J. Electrochem. Soc. vol. 146,4590 (1999).
Cruden et al., “Thermal Decomposition of Low-k Pulsed Plasma Fluorocarbon Films. II. Effect of Post-Deposition Annealing and Ambients”J. Electrochem. Soc. 146,4597 (1999).
Definitions of “furnace”, Merriam-Webster Online, 2006.
Derbyshire, “Applications of Integrated Processing,” Solid State Technology, Dec. 1994.
Dharmadhikari et al., “UV-assisted Processing for Advanced Dielectric Films,” Solid State Technology, Mar. 2005, pp. 43-44, 46, 48.
Dickson, M. et al., “Radial uniformity of an external-coil ionized physical vapor deposition source,” J. Vac. Sci. Technol. B 16(2), Mar./Apr. 1998, pp. 523-531.
Ehrlich, D. J. et al., “Submicrometer Patterning by Projected Excimer-Laser-Beam Induced Chemistry,” J. Vac. Sci. Technol. B, vol. 3, No. 1, pp. 1-8, Jan./Feb. 1985.
Elers et al., “NbCI5 as a Precursor in Atomic Layer Epitaxy,” Applied Surface Science 82/83 (1994) 468-474.
Erlat, Ahmet G., et al., “Morphology and gas barrier properties of thin SiOx coatings and polycarbonate: Correlations with plasma-enhanced chemical vapor deposition conditions,” J. Mater. Res., vol. 15, No. 3, Mar. 2000, pp. 704-717.
Farsari, M. et al., “Fabrication of Three-Dimensional Structures by Three-Photon Polymerization,” Optics Letters, vol. 30, No. 23, pp. 3180-3182, Dec. 1, 2005.
Fritze, m. et al., “High-Throughput Hybrid Optical Maskless Lithography: All-Optical 32-nm Node Imaging,” Emerging Lithographic Technologies IX, edited by Scott Mackay, Proceedings of the SPIE, vol. 5751, (SPIE, Bellingham, WA, 2005), pp. 1058-1068.
Fujino, K. et al., “Dependence of Deposition Characteristics on Base Materials in TEOS and Ozone CVD At Atmospheric Pressure,” J. Electrochem. Soc., vol. 138, No. 2, pp. 550-554, Feb. 1991.
Fukada, Takashi et al., “Preparation of SiOF Films With Low Dielectric Constant by ECR Plasma CVD,” DUMIC Conference, ISMIC, pp. 43-49, Feb. 21-22, 1995.
Galiano, M. et al., “Stress-Temperature Behavior of Oxide Films Used for Intermetal Dielectric Applications,” VMIC Conference, ISMIC, pp. 100-106, Jun. 9-10, 1992.
Gelbart, Dan et al., “UV Thermoresists: Sub 100nm Imaging Without Proximity Effects,” SPIE, vol. 3676, pp. 786-793, Mar. 1999.
George et al., “Surface Chemistry for Atomic Layer Growth,” J. Phys. Chem. 1996, 100, 13121-13131.
Goto, Hiroshi et al., “Atomic layer controlled deposition of silicon nitride with self-limiting mechanism,” Applied Physics Letters, AIP, American Institute of Physics, Melville, NY, US vol. 68, No. 23, Jun. 3, 1996, pp. 3257-3259.
Haberland, K. et al., “MOVPE Growth of (Al, Ga) InP-Based Laser Structures Monitored by Real-Time Reflectance Anisotrophy Spectroscopy,” Journal of Electronic Materials, vol. 29, No. 1, 2000, pp. 94-98.
Hayasaka, N. et al., “High-Quality and Low Dielectric Constant SiO2 CVD Using High Density Plasma,” Dry Process Symposium, pp. 163-168, 1993.
Horiike et al., “High rate and highly selective SiO2 etching employing inductively coupled plasma and discussion on reaction kinetics”, JVST A 13(3) May/Jun. 1995, pp. 801-809.
Hwang et al., “Nanometer-Size a-PbO2-type TiO2 in Garnet: A Thermobarometer for Ultrahigh-Pressure Metamorphism,” Science vol. 288 (Apr. 14, 2000).
Iijima, Yukio et al., “Highly Selective SiO2 Etch Employing Inductively Coupled Hydro-Fluorocarbon Plasma Chemistry for Self Aligned Contact Etch”, Jpn. J. Appl. Phys., vol. 36, Part 1, No. 9A, Sep. 1997, pp. 5498-5501.
Imai et al., a Novel Atomic Layer Epitaxy Method of Silicon, Jpn. J. Appl. Phys., vol. 30, No. 12B, Dec. 1991, pp. 3646-3651.
International Search Report and Written Opinion of PCT/US2012/028310, mailed Oct. 18, 2012, 8 pages.
Jeong et al., “Growth and Characterization of Aluminum OxideAI2O3 Thin Films by Plasma-Assisted Atomic Layer Controlled Deposition,” J. Korean Inst. Met. Mater., vol. 38, No. 10, Oct. 2000.
Jeong et al., “Plasma-Assisted Atomic Layer Growth of High-Quality Aluminum Oxide Thin Films,” Jpn. J. Appl. Phys. 1, Regul. Pap. Short Notes, vol. 40, No. 1, Jan. 2001.
Kamins et al., “Kinetics of Selective Epitaxial Deposition of SiGe,” Applied Physics Letters, American Institute of Physics, New York, US, vol. 61, No. 6, Aug. 10, 1992, pp. 669-671.
Kawazu, Satoru et al., “Effects of Oxygen Concentration and Annealing Sequence on Microstructure of Separation by Implanted Oxygen Wafer with High-Temperature Annealing,” Japanese Journal of Applied Physics, vol. 30, No. 1, 1991, pp. 112-115, Publication Office Japanese Journal of Applied Physics, Tokyo, Japan.
Kim, Hwa-Mok, et al., “High-Brightness Light Emitting Diodes using Dislocation-Free Indium Gallium Nitride/Gallium Nitride Multiquantum-Well Nanorod Arrays,” Nano Letters, vol. 4, No. 6, 2004, pp. 1059-1062.
Kuo, Yue, “Etch Mechanism in the Low Refractive Index Silicon Nitride Plasma-Enhanced Chemical Vapor Deposition Process,” Appl. Phys. Lett., vol. 63, No. 2, pp. 144-146, Jul. 12, 1993.
Kwok, K. et al., “Surface Related Phenomena in Integrated PECVD/Ozone-TEOS SACVD Processes for Sub-Half Micron Gap Fill: Electrostatic Effects,” J. Electrochem. Soc., vol. 141, No. 8, pp. 2172-2177, Aug. 1994.
Labelle et al., “Fourier Transform Infrared Spectroscopy of Effluents from Pulsed Plasmas of 1,I,2,2—Tetrafluoroethane, Hexafluoropropylene, and Difluoromethane”, T. Vac. Sci. Techno!. A. 76, 3419 (1999).
Labelle et al., “Pulsed Plasma Enhanced Chemical Vapor Deposition from CH2F2, C2H2F4, and CHCIF/”T. Vac. Sci. Techno!. A, 17, 445 (1999).
Lassig, Stephan E. et al., “Intermetal Dielectric Deposition by Electron Cyclotron Resonance Chemical Vapor Deposition (ECR CVD),” pp. cover and 1-21, no date.
Lau et al., “Solid-State NMR of Low Dielectric Constant Films from Pulsed Hydrofluorocarbon Plasmas”, T. Electrochem. Soc. vol. 146, No. 2652 (1999).
Laxman, Ravi K., “Low e Dielectrics: CVD Fluorinated Silicon Dioxides,” Semiconductor International, pp. 71, 72, 74, May 1995.
Lee et al., “Cyclic Technique for the Enhancement of Highly Oriented Diamond Film Growth,” Thin Solid Films 303 (1997) 264-269.
Lee, B. et al., “Dielectric Planarization Techniques for Narrow Pitch Multilevel Interconnects,” V-MIC Conference, IEEE, pp. 85-92, Jun. 15-16, 1987.
Li, Junling et al., “Modeling Studies of the Mechanisms in Biased ECR CVD,” 3 pages, no date.
Lim et al., “Gap-fill Performance and Film properties of PMD Films for the 65 nm device Technology”, IEEE International Symposium on Semiconductor Manufacturing, Sep. 30-Oct. 2, 2003, pp. 435-438.
Limb et al.,“Molecular Design of Fluorocarbon Film Architecture by Pulsed Plasma Enhanced and Pyrolytic Chemical Vapor Deposition”, Plasmas and Polymers 4(1), 21 (1999).
Lin, Chih-Lang et al., “Velocimetry Microsensors Driven by Linearly Polarized Optical Tweezers,” Optics Letters, vol. 31, No. 3, pp. 329-331, Feb. 1, 2006.
Liop et al., “Molecular orientation in plastic optical fibres,” Jan. 14, 1994, Journal of Physics D: Applied Physics, 27, 25-28.
Lubben et al., “Mechanisms and Kinetics of Si Atomic-Layer Epitaxy on Si(001)2X1 from Si2H6,” J. Vac. Sci. Technol. A 9 (6), Nov./Dec. 1991, 3003-3011.
Ma et al. “Investigation on processing of industrial set-up plasma enhanced chemical vapor deposition with pulsed d.c. power”, Surface and Coatings Technology, vol. 131, No. 1, Sep. 2000, pp. 131-135(5).
Ma et al. “Parametric effects of residual stress in pulsed d.c. plasma enhanced CVD TiN coatings”, Surface & Coatings Technology, vol. 142, 2001, pp. 1023-1027.
Machida, Katsuyuki et al., “SiO2 Planarization Technology With Biasing and Electron Cyclotron Resonance Plasma Deposition for Submicron Interconnections,” J Vac. Sci. Technol. B, vol. 4, No. 4, pp. 818-821, Jul./Aug. 1986.
Masaka, Katsuyuki et al., “Single Step Gap Filling Technology for Subhalf Micron Metal Spacings on Plasma Enhanced TEOS/O2 Chemical Vapor Deposition System”, Extened Abstracts of the 1993 International Conference on Solid State Devices and Materals, Makuhari, 1993, pp. 5110-512 (Applied Materials Japan Inc. Technology Center, 14-3 Shinzumi Narita, Chiba 286 Japan).
Matsuda, Tetsuo et al., “Dual Frequency Plasma CVD Fluorosilicate Glass Deposition for 0.25 um Interlevel Dielectrics,” DUMIC Conference, ISMIC, pp. 22-28, Feb. 21-22, 1995.
Meeks, Ellen et al., “Modeling of SiO2 Deposition in High Density Plasma Reactors and Comparisons of Model Predictions With Experimental Measurements,” J. Vac. Sci. Technol. A, vol. 16, No. 2, pp. 544-563, Mar./Apr. 1998.
Menon et al., “Loading Effect in SiGe Layers grown by Dichlorosilane and Silane-based epitaxy,” Journal of Applied Physics, American Institute of Physics, New York, US, vol. 90, No. 9, Nov. 1, 2001, pp. 4805-4809.
Meyerson et al., “Experimental and chemical kinetic modeling study of silicon CVC from monosilane and disilane,” Chemtronics, vol. 1, Dec. 1989, pp. 150-155.
Min et al., “Chemical Vapor Deposition of Ti-Si-N Films with Alternating Source Supply,” Mat. Res. Soc. Symp. Proc. vol. 564, 1999.
Min et al., “Metal-Organic Atomic-Layer Deposition of Titanium-Silicon-Nitride Films,” Applied Physics Letters, vol. 75, No. 11 (Sep. 11, 1999).
Moore, Darren L. et al., “Reaction of Hydrogen Peroxide with Organosilanes Under Chemical Vapour Deposition Conditions,” Dalton (2000), (16), 2673-2677, 2000, XP002276265.
Musaka, Katsuyuki et al., “Single Step Gap Filling Technology for Subhalf Micron Metal Spacings on Plasma Enhanced TEOS/O2 Chemical Vapor Deposition System,” Extended Abstracts of the International Conference on Solid State Devices and Materials, pp. 510-512, 1993.
Nag et al., “Comparative Evaluation of gap-fill dielectrics in shallow trench isolation for sub-0.25 micron Technologies” IEDM 1996, 841-844.
Pai, “High quality voids free oxide deposition”, Materials Chemistry and Physics, 44, 1996, pp. 1-8.
Pang, S. W. et al., “Aluminum Oxides As Imaging Materials for 193-nm Excimer Laser Lithography,” J. Vac. Sci. Technol. B., vol. 7, No. 6, pp. 1624-1628, Nov./Dec. 1989.
Pankov et al., “The effect of hydrogen addition on the fluorine doping level of SiO2 films prepared by remote plasma enhanced chemical vapor deposition using SiF4-based plasmas”, Japanese Journal of Applied Physics part 1,37 (11) Nov. 1998, pp. 6135-6141.
Paranjpe et al., “Atomic Layer Deposition of AIO for Thin Film Head Gap Applications,” J. Electrochem. Soc., vol. 148, No. 9, Sep. 2001.
Patil et al., “Deposition of Silicon Films in Presence of Nitrogen Plasma Feasibility Study,” Bulletin of Materials Science Indian Acad. Sci. India, vol. 25, No. 5, Oct. 2002, pp. 399-402.
PCT International Search Report and Written Opinion mailed Dec. 30, 2010; International Application No. PCT/US2010/038713, 10 pages.
Pedrow, “Deposition of Plasma-Polymerized Acetylene by an Intense Pulsed RF Plasma Source”, IEEE Transactions on Plasma Science, vol. 18, No. 6, Dec. 1990.
Peters, “Choices and challenges for shallow trench isolation”, Semiconductor International, Apr. 1999, pp. 69-76.
Poonawala, Amyn et al., “ILT for Double Exposure Lithography With Conventional and Novel Materials,” Proc. Of SPIE, vol. 6520, pp. 65202Q-1-65202Q-14, 2007.
Qian, L. Q. et al., “High Density Plasma Deposition and Deep Submicron Gap Fill With Low Dielectric Constant SiOF Films,” DUMIC Conference, ISMIC, pp. 50-56, 1995.
Ritala et al., “Atomic Layer Deposition of Oxide Thin Films With Metal Alkoxides as Oxygen Sources,” Science vol. 288, Apr. 14, 2000.
Robles, S. et al., “Effects of RF Frequency and Deposition Rates on the Moisture Resistance of PECVD TEOS-Based Oxide Films,” ECS Extended Abstracts, vol. 92, No. 1, pp. 215-216, May 1992.
Romanelli, Alex, Semiconductor International website article: AMD Details 45nm Technology, at www.e-insite.net/semiconductor/; Jun. 12, 2003.
Rothschild, M. et al., “A Review of Excimer Laser Projection Lithography,” J. Vac. Sci. Technol. B, vol. 6, No. 1, pp. 1-17, Jan./Feb. 1988.
Saito et al., “A Study of Low Temperature Formation of Stress-Free Silicon Nitride Films,” Record of Electrical and Communication Engineering Converzione Tohoku University, Tokuku Japan, vol. 72, No. 1, Nov. 2003, pp. 302-303.
Sedgwick et al., “Selective SiGe and Heavily As doped Si deposited at low temperature by atmospheric pressure chemical vapor deposition,” Journal of Vacuum Science and Technology: Part B, American Institute of Physics, New York, US, vol. 11, No. 3, May 1, 1993, pp. 1124-1128.
Shapiro, M. J. et al., “Dual Frequency Plasma CVD Fluorosilicate Glass Water Absorption and Stability,” DUMIC Conference, ISMIC, pp. 118-123, Feb. 21-22, 1995.
Shimoda, et al., “Chemical Vapor Deposition of a Silicon Nitride Layer with an Excellent Interface by NH3 Plasma Treatment,” Applied Physics Letters, 52(13);1068-1070 (1988).
Smith, “Mechanism of SiNxHy deposition from N2—SiH4 plasma”Journal of Vacuum Science & Technology B: Microelectronics and Nanometer Structures—May 1990—vol. 8, Issue 3, pp. 551-557.
Stringfellow, G.B. et al., “High Brightness Light-Emitting Diodes”, Semiconductors and Semimetals, vol. 48, Academic Press, San Diego, 1997, pp. 97-107.
Suda et al., “Adsorption and Thermal Dissociation of Disilane (Si2H6) on Si(100)2X1,” J. Vac. Sci. Technol. A8 (1), Jan./Feb. 1990, 61-67.
Takahashi et al., “The Effect of Gas-phase additives C2H4, C2H6 and C2H2 on SiH4/O2 chemical vapor deposition”. Journal of the Electrochemical Society, 143 (4) Apr. 1996, pp. 1355-1361.
Takeishi et al., “Fluorocarbon films deposited by PECVD with high thermal resistance and low dielectric constants.” DUMIC 1996, pp. 71-77.
Takeishi et al., “Stabilizing Dielectric Constants on Fluorine-Doped—SiO2 Films by N2O-Plasma Annealing,” DUMIC Conf. 1995 ISMIC, Executive Summary and Extended Abstract, Feb. 21-22, 1995, pp. 257-259.
Tomar, V.K., et al., “Depositions and characterization of SiOn using HMDS for Photonics applications,” abstract, Feb. 2007, obtained on Oct. 16, 2007 from website http://www.iop.org/EJ/abstract/0268-1242/22/2/008, 2 pages.
Uchino et al., “A Raised Source/Drain Technology Using In-situ P-doped SiGe and B-doped Si for 0.1 CMOS ULSis,” Electron Devices Meeting, 1997, Technical Digest, International Washington, DC, USA, Dec. 7-10, 1991, New York, NY, USA, IEEE, US, Dec. 7, 1997, pp. 479-482.
Usami, Takashi et al., “Low Dielectric Constant Interlayer Using Fluorine-Doped Silicon Oxide,” Jpn. J. Appl. Phys., vol. 33, Part 1, No. 1B, pp. 408-412, Jan. 1994.
V.Y. Vassiliev, et al., “Trends in void-free pre-metal CVD dielectrics”, Solid State Technology, Mar. 2001, pp. 129-136.
Van den hove, Luc et al., “Lithography Options for the 32nm Half Pitch Node,” imec, 50 pages, 2006.
Vassiliev, V. Y. et al., “Trends in Void-Free Pre-Metal CVD Dielectrics,” Solid State Technology, pp. 129-130, 132, 134, 136, Mar. 2001.
Walsh, Michael E., “Nanostructuring Magnetic Thin Films Using Interference Lithography,” Massachusetts Institute of Technology, 86 pages, Aug. 2000.
Walsh, Michael E., “On the Design of Lithographic Interferometers and Their Application,” Massachusetts Institute of Technology, 300 pages, Sep. 2004.
Webster, John G., “Wiley Encyclopedia of Electrical and Electronics Engineering,” vol. 6, pp. 565-566, 1999.
Wikipedia, “Microstrip”, obtained online at http://en.wikipedia.org/wiki/Microstrip on Jan. 25, 2008, 5 pages.
Wikipedia, “Microwave”, obtained online at http://en.wikipedia.org/wiki/Microwave on Dec. 13, 2007, 7 pages.
Wolf et al., “Silicon Processing for the VLSI Era,” vol. 1, 2nd ed., p. 199, Lattice Press, Sunset Beanch, CA, 2000.
Yin, Xiaobo et al., “Near-Field Two-Photon Nanolithography Using An Apertureless Optical Probe,” Applied Physics Letters, vol. 81, No. 19, pp. 3663-3665, Nov. 4, 2002.
Yota et al., “Advanced passivation layer using high-density plasma CVD oxide for 0.25 micron CMOS Technology” DUMIC, Feb. 16-17, 1998, pp. 185-192.
Yota et al., “Extendibility of ICP high-density plasma CVD for use as intermetal dielectric and passivation layers for 0.18 micron technology,” DUMIC Feb. 8-9, 1999, pp. 71-82.
Yu, D. et al., “Step Coverage Study of Peteos Deposition for Intermetal Dielectric Applications,” VMIC Conference, IEEE, pp. 166-172, Jun. 12-13, 1990.
Zajickova, “Deposition of Protective Coatings in RF Organosilicon Discharges,” Jan. 31, 2007, Institute of Physics Publishing, pp. 123-132.
Zajickova, L. et al., “Deposition of protective coatings in rf organosilicon discharges,” abstract, Jan. 2007, obtained on Oct. 16, 2007 on website http://www.iop.org.EJ/abstract/0963-0252/16/1/S14, 2 pages.
Related Publications (1)
Number Date Country
20140213070 A1 Jul 2014 US
Provisional Applications (1)
Number Date Country
61756762 Jan 2013 US