This application contains subject matter related to U.S. application Ser. No. 10/218,179, filed Aug. 12, 2002, entitled LOW LOSS RE BIAS ELECTRODE FOR A PLASMA REACTOR WITH ENHANCED WAFER EDGE RF COUPLING AND HIGHLY EFFICIENT WAFER COOLING, by Hiroji Hanawa et al.; U.S. application Ser. No. 10/646,458, filed Aug. 22, 2003, entitled PLASMA IMMERSION ION IMPLANTATION APPARATUS INCLUDING A PLASMA SOURCE HAVING LOW DISSOCIATION AND LOW MINIMUM PLASMA VOLTAGE, by Kenneth Collins et al.; U.S. application Ser. No. 10/646,533, filed Aug. 22, 2003, entitled PLASMA IMMERSION ION IMPLANTATION PROCESS USING A PLASMA SOURCE HAVING LOW DISSOCIATION AND MINIMUM PLASMA VOLTAGE, by Kenneth Collins et al.; U.S. application Ser. No. 10/646,532, filed Aug. 22, 2003, entitled PLASMA IMMERSION ION IMPLANTATION APPARATUS INCLUDING A CAPACITIVELY COUPLED RF PLASMA SOURCE HAVING LOW DISSOCIATION AND LOW MINIMUM PLASMA VOLTAGE, by Kenneth Collins et al.; U.S. application Ser. No. 10/646,612, filed Aug. 22, 2003, entitled PLASMA IMMERSION ION IMPLANTATION PROCESS USING A CAPACITIVELY COUPLED PLASMA SOURCE HAVING LOW DISSOCIATION AND LOW MINIMUM PLASMA VOLTAGE, by Kenneth Collins et al.; U.S. application Ser. No. 10/646,528, filed Aug. 22, 2003, entitled PLASMA IMMERSION ION IMPLANTATION PROCESS USING A PLASMA SOURCE HAVING LOW DISSOCIATION AND LOW MINIMUM PLASMA VOLTAGE, by Kenneth Collins et al.; U.S. application Ser. No. 10/646,467, filed Aug. 22, 2003, entitled PLASMA IMMERSION ION IMPLANTATION PROCESS USING AN INDUCTIVELY COUPLED PLASMA SOURCE HAVING LOW DISSOCIATION AND LOW MINIMUM PLASMA VOLTAGE, by Kenneth Collins et al.; U.S. application Ser. No. 10/646,527, filed Aug. 22, 2003, entitled PLASMA IMMERSION ION IMPLANTATION SYSTEM INCLUDING A PLASMA SOURCE HAVING LOW DISSOCIATION AND LOW MINIMUM PLASMA VOLTAGE, by Kenneth Collins et al.; U.S. application Ser. No. 10/646,526, filed Aug. 22, 2003, entitled PLASMA IMMERSION ION IMPLANTATION SYSTEM INCLUDING AN CAPACITIVELY COUPLED PLASMA SOURCE HAVING LOW DISSOCIATION AND LOW MINIMUM PLASMA VOLTAGE, by Kenneth Collins et al.; and U.S. application Ser. No. 10/646,460, filed Aug. 22, 2003, entitled PLASMA IMMERSION ION IMPLANTATION SYSTEM INCLUDING AN INDUCTIVELY COUPLED PLASMA SOURCE HAVING LOW DISSOCIATION AND LOW MINIMUM PLASMA VOLTAGE, by Kenneth Collins et al., all of which are assigned to the present assignee.
Semiconductor wafer processing requires more strict control of wafer temperature to reduce wafer temperature excursion during processing, as device geometries shrink to ever smaller dimensions. For example, high temperatures can adversely affect the sharp semiconductor junction profiles required for small feature sizes. Limiting workpiece (or semiconductor wafer) temperature during processing is also necessary whenever processing is carried out using photoresist masking of device features, in order to avoid heat-induced degradation of the photoresist.
In plasma processing of wafers, the wafer temperature can exceed many hundreds of degrees C., particularly where large RF bias power levels are employed at low chamber pressure, where heat transfer by gas convection and conduction is poor (and radiation heat transfer is also poor). For example, in plasma immersion ion implantation reactors, RF bias power applied to the wafer may be many kWatts, particularly where deep implant depths are required. The wafer must be actively cooled to limit temperature rise to maintain photoresist integrity or avoid material degradation. Typically electrostatic chucks are used to clamp the wafer to a cooled or temperature controlled surface. In a conventional Unipolar or Monopolar electrostatic chuck, a voltage is applied across a dielectric layer between wafer and electrode. The “dielectric” layer may be a near ideal insulator or may be a semiconductor. The “dielectric” layer may be a deposited film or a bulk solid material, such as ceramic or semiconducting material. The electrostatic field across the structure formed by the wafer, dielectric layer, air or vacuum gap and the electrode produces an attractive force between the wafer and the dielectric layer. Alternatively, conventional Bipolar electrostatic chucks have more than one electrode. A voltage is applied across two or more electrodes separated from the wafer by the dielectric layer. The electrostatic fields across the structure formed by the wafer, dielectric layer, air or vacuum gap and each electrode produces an attractive force between wafer and dielectric layer.
Typical electrostatic chucks employ a heat transfer gas between the wafer and the electrostatic chuck surface to promote heat transfer. Helium is a preferred gas due to its high thermal conductivity, but other gases are sometimes used. For high RF power levels (high heat load on the wafer), the helium pressure must be correspondingly high to provide a sufficient heat transfer rate. Unfortunately, such high gas pressure reduces the threshold RF power level (or RF voltage level) at which arcing, gas breakdown, or dielectric breakdown occurs within the helium gas passages in the chuck, in the interface between electrostatic chuck and wafer, or in the wafer support pedestal. Such problems have become more critical as greater demands are placed on processes such as plasma immersion ion implantation processes. For example, certain implantation processes may require implant doses in excess of 1017 cm−3, requiring the exposure of the wafer to high RF power levels for several minutes, during which the wafer temperature can reach over 400° C. without active cooling or over 200° C. with conventional electrostatic chucks. Similar problems can occur in other applications, such as plasma or reactive ion etching etching, plasma chemical vapor deposition, physical vapor deposition, etc.
Another problem is that the top surface of the electrostatic chuck must have many open channels (channels machined into the chuck top surface) through which the helium cooling gas is pumped to provide thermal conductance between the wafer and the chuck. Such channels have many sharp edges, which create contamination of particles on the wafer backside or contamination of the process. These edges may have radii on the order of microns, so as to be very sharp. Contamination is caused by scratching the wafer backside over the sharp edges of the channels and/or by the deleterious effects of high electric fields in the vicinity of each sharp edge, which can lead to arcing about the sharp edges, removing material from the chuck surface into the plasma. A goal of wafer processing in fabricating extremely small features on the wafer is to limit the number of contaminant particles on each wafer backside to not more than tens of thousands or less. The contaminants either contaminate the current wafer or are passed along to contaminate other processes or reactors that handle the same lot of wafers.
The use of high pressure gas to cool the wafer makes the electrostatic chuck so vulnerable to arcing, gas breakdown or dielectric breakdown, that the applied RF bias voltage cannot exceed several kV in typical cases. Moreover, the ability of a conventional electrostatic chuck to cool the wafer is inadequate for many of the future processes being contemplated, its heat transfer coefficient for the wafer being less than about 1000 Watts/m2° K. What is needed is an electrostatic chuck (wafer support pedestal) which can withstand about 10 kV of RF bias voltage without arcing, gas breakdown, or dielectric breakdown, which has a heat transfer coefficient of at least 1000 Watts/m2° K (between wafer and electrostatic chuck) and has a heat transfer coefficient of at least 5000 Watts/m2° K (between electrostatic chuck dielectric surface and heat sink or cooling circuit), minimizes scratching and particle formation at wafer backside, does not contaminate the wafer backside, and has material properties compatible with the plasma processing environment (consumption rate, non-source of contaminants).
A method of electrostatically chucking a workpiece such as a semiconductor wafer, while controlling workpiece temperature during plasma processing requiring application of a high level of RF power, includes providing a polished surface on a puck in the reactor, placing the workpiece on the polished surface of the puck and cooling the puck. Plasma processing is carried out by either coupling RF plasma bias power through the puck or applying RF plasma source power to plasma in the reactor. Furthermore, during plasma processing, a chucking voltage is applied to a chucking electrode of the puck to pull the workpiece into direct contact with the surface of the puck with sufficient electrostatic force to remove heat from the workpiece through directly contacting surfaces of the puck and workpiece at about the rate at which the workpiece is heated either directly by the RF plasma bias power or indirectly through the plasma from the RF plasma source power. The chucking voltage is sufficient to remove heat at the rate at which heat is deposited in the workpiece, or to maintain the workpiece temperature below a certain temperature or to limit the rate of rise of the workpiece temperature.
Alternatively, the chucking voltage is selected to provide a sufficient force to attain a selected heat transfer coefficient between contacting surfaces of the puck and wafer such that the wafer temperature or the rate of temperature rise is controlled. The chucking voltage is typically specified relative to the DC bias on the wafer (the time average voltage on the wafer with respect to the plasma ground reference, typically the chamber wall). The chucking voltage may be a positive or negative voltage with respect to the DC bias on the wafer. The chucking voltage may be adjusted during processing to accommodate varying heat load, RF bias voltage or target wafer temperature.
The foregoing eliminates the need for any coolant gas in the electrostatic chuck, so that far more RF bias voltage may be applied through the chuck without arcing, gas breakdown or dielectric breakdown. Moreover, the contact cooling of the wafer provides superior cooling. And, the polished surface of the puck reduces contamination.
RF bias power is applied to the chuck 14 by an RF bias power generator 44 through an impedance match circuit 46. A D.C. chucking voltage is applied to the chuck 14 from a chucking voltage source 48 isolated from the RF bias power generator 44 by an isolation capacitor 50. The RF power delivered to the wafer 40 from the RF bias power generator 44 can heat the wafer 40 to temperatures beyond 400 degrees C., depending upon the level and duration of the applied RF plasma bias power from the generator 44. It is believed that about 80% or more of the RF power from the bias power generator 44 is dissipated as heat in the wafer 40.
In other implementations, there may be little or no bias delivered by the bias power generator 44 (or there may be no bias power generator), in which case the wafer 40 is heated (indirectly) by power from the source power generator 30 via interaction between the wafer 40 and the plasma in the chamber. This interaction can include bombardment of the wafer by plasma ions, electrons and neutrals, with wafer heating arising from the kinetic energy of the ions, electrons and neutrals, as well as electrical effects arising from the interaction of the charged particles with electric fields in the vicinity of the wafer, as is well-known in the art. The wafer may be heated by radiation emitted by plasma species, such as ultraviolet, visible or infrared radiation emitted by excited atomic or molecular species (ions or neutrals) during relaxation, as is well known in the art. The wafer may be heated by other means, such as by hot surfaces in or adjacent the process chamber, by thermal radiation, convection or conduction, as is well known in the art. Thus, the wafer 40 is heated directly by RF power from the bias power generator 44 or indirectly (via wafer-plasma interaction) by RF power from the source power generator 30.
Conventionally, the wafer temperature was regulated to avoid overheating by providing coolant gas at a selected pressure between the wafer 40 and the chuck 14 and removing heat from the gas. Such gas introduction requires open gas channels in the chuck surface on which the wafer is mounted. The presence of such open coolant gas channels in the chuck surface creates two problems. First, the RF bias power applied to the chuck can cause the gas to break down in the channels. This problem is solved by either limiting the coolant gas pressure (which reduces the heat transfer from the wafer) or by limiting the RF bias voltage, e.g., to below 1 kV (which can negatively impact plasma processing). A second problem is that the many sharp edges defining the open gas channels in the chuck surface lead to contamination, either by the breaking off of material forming the sharp edges or by arcing near those edges, or by scratching of the wafer backside. A related problem is that in applications requiring very high RF bias power levels, the coolant gas breaks down (preventing operation) and the coolant gas system may have an insufficient heat transfer coefficient for the high heat load on the wafer.
The electrostatic chuck 14 of
Referring to
RF bias power from the RF bias power generator 44 may be applied to the electrode 62 or, alternatively, to the metal layer 64 for RF coupling through the semi-insulative puck layer 60.
A very high heat transfer coefficient between the wafer 40 and the puck 60 is realized by maintaining a very high chucking force. A suitable range for this force depends upon the anticipated heat loading of the wafer, and will be discussed later in this specification. The heat transfer coefficient (having units of Watts/m2° K or heat flux density for a given temperature difference) of the wafer-to-puck contacting surfaces is adequate to remove heat at the rate heat is deposited on the wafer. Specifically, the heat transfer coefficient is adequate because during plasma processing it either limits the wafer temperature below a specified maximum temperature or limits the time rate of rise of the wafer temperature below a maximum rate of rise. The maximum wafer temperature may be selected to be anywhere in a practical range from on the order to 100 degrees C. or higher, depending upon the heat load. The maximum rate of heat rise during processing may be anywhere in a range from 3 to 20 degrees per second. Specific examples may be 20 degrees per second, or 10 degrees per second or 3 degrees per second. By comparison, if the wafer is uncooled, the rate of heat rise may be 86.7 degrees per second in the case of a typical 300 mm silicon wafer with a heat load of 7500 Watts, 80% of which is absorbed by the wafer. Thus, the rate of temperature rise is reduced to one-fourth of the un-cooled rate of heat rise in one embodiment of the invention.
Such performance is accomplished, first, by maintaining the puck at a sufficiently low temperature (for example, about 80° C. below the target wafer temperature), and second, by providing the top surface of the puck 60 with a sufficiently smooth finish (e.g., on the order of ten's of micro-inches RMS deviation, or preferably on the order of micro-inches RMS deviation). For this purpose, the top surface 60a of the puck 60 can be highly polished to a finish on the order of about 2 micro-inches RMS deviation, for example. Furthermore, heat is removed from the puck 60 by cooling the metal layer 64. For this reason, internal coolant passages 70 are provided within the metal layer 64 coupled to a coolant pump 72 and heat sink or cooling source 74. In an alternative embodiment, the internal cooling passages 70 may extend into the puck 60 or adjacent its back surface in addition or instead of extending through the metal layer 64. In any case, the coolant passages 70 are thermally coupled to the puck 60, either directly or through the metal layer 64, and are for cooling the puck 60. The coolant liquid circulating through the internal passages 70 can be water, ethylene glycol or a mixture, for example. Alternatively, the coolant may be a perfluorinated heat transfer liquid such as “fluorinert” (made by 3M company). Unlike the internal gas coolant passages of conventional chucks, this feature presents little or no risk of arcing in the presence of high RF bias power applied to the chuck 14 by the RF bias power generator 44.
One advantage of such contact-cooling of the wafer over the conventional method employing a coolant gas is that the thermal transfer efficiency between the coolant gas and each of the two surfaces (i.e., the puck surface and the wafer bottom surface) is very limited, in accordance with the thermal accommodation coefficient of the gas with the materials of the two surfaces. The heat transfer rate is attenuated by the product of the gas-to-wafer thermal accommodation coefficient and the gas-to-puck thermal accommodation coefficient. If both coefficients are about 0.5 (as a high rough estimate), then the wafer-gas-puck thermal conductance is attenuated by a factor of about 0.25. In contrast, the contact-cooling thermal conductance in the present invention has virtually no such attenuation, the thermal accommodation coefficient being in effect unity for the chuck 14 of
The heat transfer coefficient between the wafer 40 and the puck 60 in the wafer contact-cooling electrostatic chuck 14 is affected by the puck top surface finish and the chucking force. These parameters can be adjusted to achieve the requisite heat transfer coefficient for a particular environment. An important environmental factor determining the required heat transfer coefficient is the applied RF bias power level. It is believed that at least 80% of the RF bias power from the bias generator 44 is dissipated as heat in the wafer 40. Therefore, for example, if the RF bias power level is 7500 Watts and 80% of the RF bias power from the bias generator 44 is dissipated as heat in the wafer 40, if the wafer area is 706 cm2 (300 mm diameter wafer) and if a 80 degrees C. temperature difference is allowed between the wafer 40 and the puck 60, then the required heat transfer coefficient is h=7500×80% Watts/(706 cm2×80 degrees K), which is 1071 Watts/m2° K. For greater RF bias power levels, the heat transfer coefficient can be increased by augmenting any one or both of the foregoing factors, namely the temperature drop across the puck, the chucking force or the smoothness of the puck surface. Such a high heat transfer coefficient, rarely attained in conventional electrostatic chucks, is readily attained in the electrostatic chuck 14 of
In addition, the heat transfer is improved by providing more puck surface area available for direct contact with the wafer backside. In a conventional chuck, the puck surface available for wafer contact is greatly reduced by the presence of open coolant gas channels machined, ground or otherwise formed in the puck surface. These channels occupy a large percentage of the puck surface. In the puck 60 of
The opposite case is illustrated in
Also, if the wafer heat loading is center-low (as in
Another way of obtaining a center-high radial distribution of heat transfer coefficient is to make the puck surface slightly bowed with a center-high contour, as illustrated in
The chucking voltage required to attain a particular heat transfer coefficient is increased if an insulating (oxide or nitride, for example) layer is added to the wafer backside. Therefore, the chucking voltage must be determined empirically each time a new batch of wafers is to be processed. This is inconvenient and reduces productivity. One way around this problem is to mask the difference between wafers with and without a backside oxide layer. The difference is masked by adding a thin insulating layer 60b on the top puck surface 60a. The presence of such a thin insulating layer increases the requisite chucking voltage to reach a particular heat transfer coefficient value. The advantage is that the chucking voltage required remains at least nearly the same whether or not the wafer backside has an insulating layer.
Another problem is that of contamination. Contamination is nearly prevented prior to processing of the wafer by seasoning both the chamber interior surfaces and the puck top surface 60a simultaneously (in the absence of the wafer) by depositing a thin layer consisting of a material that is compatible with the plasma process that is to be performed. Such a seasoning layer, in addition to suppressing contamination, may also serve as the high resistance insulating layer 60b on the puck top surface 60a that masks differences between wafers with and without an oxide on their backside. A thin (e.g., on the order of a thousand angstroms or up to one micron or more) seasoning layer 60b may be deposited on the puck top surface 60a. The seasoning layer 60b may be formed of silicon dioxide or germanium dioxide, silicon nitride or germanium nitride, silicon carbide, aluminum nitride or aluminum oxide, a fluorocarbon polymer, a fluorohydrocarbon polymer, a nitride of a silicon hydride, a hydrocarbon, or (less desirably) hydrides of silicon or germanium. The seasoning layer 60b is deposited by forming a plasma containing precursors of the desired material for a sufficient length of time to deposit a layer having a thickness on the order of about a thousand angstroms or up to one micron or more on the interior chamber surfaces, including the puck top surface 60a. This forms the seasoning layer 60b over the puck 60 as well as a seasoning layer over all internal chamber surfaces and is done before the wafer is placed on the chuck 14. Thereafter, the wafer is placed on the surface of the seasoning layer 60b, and plasma processing is performed. After the wafer is removed (or after a large number of wafers has been processed in similar fashion), the seasoning layer 60b is removed. Removal of the seasoning layer 60b is performed by either furnishing radicals into the chamber or by reactive ion etching. For example, if the seasoning layer is silicon dioxide, then NF3 or F radicals may be used to remove it. If the seasoning layer is a fluorocarbon, fluorohydrocarbon or a hydrocarbon, then oxygen may be used in the form of either atomic oxygen or reactive oxygen ions, to remove the seasoning layer. The radicals (or ions) used to remove the seasoning layer may be produced in another external plasma reactor and then transferred into the reactor of
The wafer contact cooling electrostatic chuck of
The invention is applicable to etch, CVD (low-temperature), plasma immersion ion implantation (as applied to junction formation or doping, materials modification) beamline ion implantation, physical vapor deposition, chamber pre-cleaning and the like. With the electrostatic chuck of
RF Powered Process Kit
Thus, the high dielectric constant of the ceramic ring 405 provides greater capacitive coupling of RF power from the ESC base 215 to plasma overlying the wafer periphery. The effective capacitance per unit area near the wafer pedestal will be the series combination of the capacitances per unit area of the ceramic ring (a large capacitance) and of the collar 400 (a smaller capacitance). By thus increasing the electric field over the wafer periphery, the problems encountered at the wafer periphery in conventional reactors, such as poor etch profile due to non-perpendicular electric fields, poor etch rate and depth, tendency toward etch stopping in high aspect ratio openings
The degree to which the capacitive coupling of RF power from the ESC base 215 to plasma over the wafer periphery needs to be enhanced can be determined empirically for each process that is to be performed. This need can arise from a number of factors. For example, the portion of the wafer 130 overhanging the edge of the puck 205 overlies the silicon (or silicon carbide) collar but is separated therefrom by an air gap of about 3 to 7 mils, the air gap having relatively low dielectric constant (e.g., 1). This aspect suppresses capacitive coupling of RF power to plasma over the peripheral portion of the wafer 130. The needed increase in capacitive coupling at the wafer periphery may be determined on the basis of the radial distribution of etch rate, or the radial distribution of etch profile, or other parameters, for example. Once the determination is made, the capacitive coupling by the ceramic ring 405 that provides the requisite enhancement can be found for example by trial and error, or possibly by analytical methods. This capacitive coupling of the ring 405 can be controlled by appropriate selection of the dielectric constant of the ceramic ring 405, of the axial thickness of the ceramic ring 405 and of the radial thickness of the axial ring 405. The axial thickness can be greatly reduced from that illustrated in
A low capacitance quartz cover 430 (dielectric constant of about 4) overlies the quartz spacer 410 and the cathode liner 275. The quartz spacer 430 has a first leg 431 nesting in an outer corner 411 of the quartz spacer 410 and a second leg 432 extending axially between the quartz spacer 410 on one side and the collar 400 and ring 405 on the other side. A portion of the second leg 432 extends below an outer portion of the collar 400, so that the gap between the cover 430 and the components 275, 410, 215 underlying it meanders to prevent plasma leakage therethrough. It should be noted that this approach is followed throughout the design of the entire wafer support pedestal 135, so that contiguous air (or vacuum) gaps or passages tend to meander in order to suppress plasma leakage and promote recombination.
In summary, the radial and axial thicknesses of the ceramic ring 405 and its dielectric constant are selected to achieve a radial distribution of capacitance per unit area over the aluminum ESC base 215 that is sufficiently greater at the periphery than at the center to compensate for inherent factors that would otherwise tend to distort process performance. For example, the capacitance per unit area provided by the ceramic ring 405 is sufficiently greater than that of the ESC puck 205 so as to achieve a more nearly uniform radial distribution of etch rate or etch profile, for example. Since the ESC base 215 is driven with the bias RF power generator, it is spaced from the grounded cathode liner 275 by the quartz spacer 410. The spacing provided by the quartz spacer 410 is sufficiently large and the dielectric constant of the quartz spacer 410 is sufficiently small to avoid or prevent arcing and/or gas breakdown between the base 215 and the liner 275.
The RF potential of the ESC base 215 with respect to the ESC electrode 210 is governed by the manner in which it is coupled to the RF power output of the impedance match element 46. In one case, it is connected directly to the RF power output and is therefore at maximum RF potential. In another case, optional reactive elements are connected between the ESC base 215 and the ESC electrode 210 so that the RF potential is divided between the ESC electrode 210 and the ESC base 215. This latter option reduces the RF potential on the ESC base 215 and therefore reduces the amount of RF power that can be coupled from the ESC base 215 via the ceramic ring 405 to plasma at the wafer periphery to compensate for roll-off of the electric field beyond the edge of the puck 205.
The high voltage electrostatic chuck of
While the invention has been described in detail with specific reference to preferred embodiments, it is understood that variations and modifications thereof may be made without departing from the true spirit and scope of the invention.
Number | Name | Date | Kind |
---|---|---|---|
2344138 | Drummond | Mar 1944 | A |
3109100 | Gecewicz | Oct 1963 | A |
3385356 | Dalin | May 1968 | A |
3576685 | Swann et al. | Apr 1971 | A |
3907616 | Wiemer | Sep 1975 | A |
4116791 | Zega | Sep 1978 | A |
4184188 | Briglia | Jan 1980 | A |
4382099 | Legge et al. | May 1983 | A |
4384918 | Abe | May 1983 | A |
4385946 | Finegan et al. | May 1983 | A |
4434036 | Hoerschelmann et al. | Feb 1984 | A |
4465529 | Arima et al. | Aug 1984 | A |
4481229 | Suzuki et al. | Nov 1984 | A |
4500563 | Ellenberger et al. | Feb 1985 | A |
4521441 | Flowers | Jun 1985 | A |
4539217 | Farley | Sep 1985 | A |
4565588 | Seki et al. | Jan 1986 | A |
4584026 | Wu et al. | Apr 1986 | A |
4638858 | Chu | Jan 1987 | A |
4692836 | Suzuki | Sep 1987 | A |
4698104 | Barker et al. | Oct 1987 | A |
4764394 | Conrad | Aug 1988 | A |
4771730 | Tezuka | Sep 1988 | A |
4778561 | Ghanbari | Oct 1988 | A |
4867859 | Harada et al. | Sep 1989 | A |
4871421 | Ogle et al. | Oct 1989 | A |
4892753 | Weng et al. | Jan 1990 | A |
4912065 | Mizuno et al. | Mar 1990 | A |
4937205 | Nakayama et al. | Jun 1990 | A |
4948458 | Ogle | Aug 1990 | A |
5040046 | Chhabra et al. | Aug 1991 | A |
5061838 | Lane et al. | Oct 1991 | A |
5074456 | Degner et al. | Dec 1991 | A |
5106827 | Borden et al. | Apr 1992 | A |
5107201 | Ogle | Apr 1992 | A |
5250137 | Arami et al. | Oct 1993 | A |
5270250 | Murai et al. | Dec 1993 | A |
5277751 | Ogle | Jan 1994 | A |
5288650 | Sandow | Feb 1994 | A |
5290382 | Zarowin et al. | Mar 1994 | A |
5312778 | Collins et al. | May 1994 | A |
5345999 | Hosokawa | Sep 1994 | A |
5354381 | Sheng | Oct 1994 | A |
5423945 | Marks et al. | Jun 1995 | A |
5435881 | Ogle | Jul 1995 | A |
5463525 | Barnes et al. | Oct 1995 | A |
5467249 | Barnes et al. | Nov 1995 | A |
5505780 | Dalvie et al. | Apr 1996 | A |
5510011 | Okamura et al. | Apr 1996 | A |
5514603 | Sato | May 1996 | A |
5515167 | Ledger et al. | May 1996 | A |
5520209 | Goins et al. | May 1996 | A |
5542559 | Kawakami et al. | Aug 1996 | A |
5561072 | Saito | Oct 1996 | A |
5569363 | Bayer et al. | Oct 1996 | A |
5572038 | Sheng et al. | Nov 1996 | A |
5581874 | Aoki et al. | Dec 1996 | A |
5587038 | Cecchi et al. | Dec 1996 | A |
5627435 | Jansen et al. | May 1997 | A |
5643838 | Dean et al. | Jul 1997 | A |
5648701 | Hooke et al. | Jul 1997 | A |
5653811 | Chan | Aug 1997 | A |
5654043 | Shao et al. | Aug 1997 | A |
5660895 | Lee et al. | Aug 1997 | A |
5665640 | Foster et al. | Sep 1997 | A |
5674321 | Pu et al. | Oct 1997 | A |
5683517 | Shan | Nov 1997 | A |
5711812 | Chapek et al. | Jan 1998 | A |
5718798 | Deregibus | Feb 1998 | A |
5764471 | Burkhart | Jun 1998 | A |
5770982 | Moore | Jun 1998 | A |
5880923 | Hausmann | Mar 1999 | A |
5883778 | Sherstinsky et al. | Mar 1999 | A |
5888413 | Okumura et al. | Mar 1999 | A |
5897752 | Hong et al. | Apr 1999 | A |
5911832 | Denholm et al. | Jun 1999 | A |
5923521 | Burkhart | Jul 1999 | A |
5935077 | Ogle | Aug 1999 | A |
5944942 | Ogle | Aug 1999 | A |
5948168 | Shan et al. | Sep 1999 | A |
5985742 | Henley et al. | Nov 1999 | A |
5994207 | Henley et al. | Nov 1999 | A |
5994236 | Ogle | Nov 1999 | A |
5998933 | Shun'Ko | Dec 1999 | A |
6000360 | Koshimuzu | Dec 1999 | A |
6013567 | Henley et al. | Jan 2000 | A |
6020592 | Liebert et al. | Feb 2000 | A |
6022418 | Iwabuchi | Feb 2000 | A |
6028762 | Kamitani | Feb 2000 | A |
6033482 | Parkhe | Mar 2000 | A |
6041735 | Murzin et al. | Mar 2000 | A |
6050218 | Chen et al. | Apr 2000 | A |
6072685 | Herchen | Jun 2000 | A |
6076483 | Shintani et al. | Jun 2000 | A |
6081414 | Flanigan et al. | Jun 2000 | A |
6096661 | Ngo et al. | Aug 2000 | A |
6101971 | Denholm et al. | Aug 2000 | A |
6103599 | Henley et al. | Aug 2000 | A |
6132552 | Donohoe et al. | Oct 2000 | A |
6139697 | Chen et al. | Oct 2000 | A |
6150628 | Smith et al. | Nov 2000 | A |
6151203 | Shamouilian et al. | Nov 2000 | A |
6153524 | Henley et al. | Nov 2000 | A |
6155090 | Rubenson | Dec 2000 | A |
6164241 | Chen et al. | Dec 2000 | A |
6165376 | Miyake et al. | Dec 2000 | A |
6174450 | Patrick et al. | Jan 2001 | B1 |
6174743 | Pangrle et al. | Jan 2001 | B1 |
6182604 | Goeckner et al. | Feb 2001 | B1 |
6187110 | Henley et al. | Feb 2001 | B1 |
6188564 | Hao | Feb 2001 | B1 |
6207005 | Henley et al. | Mar 2001 | B1 |
6237527 | Kellerman et al. | May 2001 | B1 |
6239553 | Barnes et al. | May 2001 | B1 |
6246567 | Parkhe | Jun 2001 | B1 |
6248642 | Donlan et al. | Jun 2001 | B1 |
6265328 | Henley et al. | Jul 2001 | B1 |
6291313 | Henley et al. | Sep 2001 | B1 |
6291939 | Dolan et al. | Sep 2001 | B1 |
6300643 | Fang et al. | Oct 2001 | B1 |
6303519 | Hsiao et al. | Oct 2001 | B1 |
6305316 | DiVergilio et al. | Oct 2001 | B1 |
6335536 | Goeckner et al. | Jan 2002 | B1 |
6339297 | Sugai et al. | Jan 2002 | B1 |
6341574 | Bailey, III et al. | Jan 2002 | B1 |
6348126 | Hanwa et al. | Feb 2002 | B1 |
6350697 | Richardson et al. | Feb 2002 | B1 |
RE37580 | Barnes et al. | Mar 2002 | E |
6392351 | Shun'Ko | May 2002 | B1 |
6395150 | Van Cleemput et al. | May 2002 | B1 |
6403453 | Ono et al. | Jun 2002 | B1 |
6410449 | Hanawa et al. | Jun 2002 | B1 |
6413321 | Kim et al. | Jul 2002 | B1 |
6417078 | Dolan et al. | Jul 2002 | B1 |
6418874 | Cox et al. | Jul 2002 | B1 |
6426015 | Xia et al. | Jul 2002 | B1 |
6433553 | Goeckner et al. | Aug 2002 | B1 |
6453842 | Hanawa et al. | Sep 2002 | B1 |
6461972 | Kabansky | Oct 2002 | B1 |
6468388 | Hanawa et al. | Oct 2002 | B1 |
6494986 | Hanawa et al. | Dec 2002 | B1 |
6500686 | Katata et al. | Dec 2002 | B2 |
6511899 | Henley et al. | Jan 2003 | B1 |
6513538 | Chung et al. | Feb 2003 | B2 |
6514838 | Chan | Feb 2003 | B2 |
6528391 | Henley et al. | Mar 2003 | B1 |
6535371 | Kayamoto et al. | Mar 2003 | B1 |
6551446 | Hanwa et al. | Apr 2003 | B1 |
6559408 | Smith et al. | May 2003 | B2 |
6579805 | Bar-Gadda | Jun 2003 | B1 |
6582999 | Henley et al. | Jun 2003 | B2 |
6593173 | Anc et al. | Jul 2003 | B1 |
6679981 | Pan et al. | Jan 2004 | B1 |
6687113 | Saito et al. | Feb 2004 | B2 |
6800559 | Bar-Gadda | Oct 2004 | B2 |
6811448 | Paton et al. | Nov 2004 | B1 |
6838695 | Doris et al. | Jan 2005 | B2 |
20010042827 | Fang et al. | Nov 2001 | A1 |
20020047543 | Sugai et al. | Apr 2002 | A1 |
20020088776 | Nakano et al. | Jul 2002 | A1 |
20030013260 | Gossman et al. | Jan 2003 | A1 |
20030013314 | Ying et al. | Jan 2003 | A1 |
20030047283 | Parkhe et al. | Mar 2003 | A1 |
20030085205 | Lai et al. | May 2003 | A1 |
20040045813 | Kanno et al. | Mar 2004 | A1 |
20050183669 | Parkhe et al. | Aug 2005 | A1 |
Number | Date | Country |
---|---|---|
0 546 852 | Jun 1993 | EP |
0 836 218 | Apr 1998 | EP |
0 964 074 | Dec 1999 | EP |
1 111 084 | Jun 2001 | EP |
1 158 071 | Nov 2001 | EP |
1 191 121 | Mar 2002 | EP |
59-86214 | May 1984 | JP |
59-218728 | Dec 1984 | JP |
62-120041 | Jun 1987 | JP |
070455542 | Feb 1995 | JP |
2000150908 | May 2000 | JP |
WO 9900832 | Jan 1999 | WO |
WO 0030149 | May 2000 | WO |
WO 0111650 | Feb 2001 | WO |
WO 0225694 | Mar 2002 | WO |
WO 9318201 | Sep 2003 | WO |
Number | Date | Country | |
---|---|---|---|
20060043065 A1 | Mar 2006 | US |