Capacitors

Information

  • Patent Grant
  • 6891215
  • Patent Number
    6,891,215
  • Date Filed
    Thursday, April 17, 2003
    21 years ago
  • Date Issued
    Tuesday, May 10, 2005
    19 years ago
Abstract
A method of forming a capacitor includes forming first and second capacitor electrodes over a substrate. A capacitor dielectric region is formed intermediate the first and second capacitor electrodes, and includes forming a silicon nitride comprising layer over the first capacitor electrode. A silicon oxide comprising layer is formed over the silicon nitride comprising layer. The silicon oxide comprising layer is exposed to an activated nitrogen species generated from a nitrogen-containing plasma effective to introduce nitrogen into at least an outermost portion of the silicon oxide comprising layer. Silicon nitride is formed therefrom effective to increase a dielectric constant of the dielectric region from what it was prior to said exposing. Capacitors and methods of forming capacitor dielectric layers are also disclosed.
Description
TECHNICAL FIELD

This invention relates capacitors, to methods of forming capacitors and to methods of forming capacitor dielectric layers.


BACKGROUND OF THE INVENTION

Capacitors are commonly-used electrical components in semiconductor circuitry, for example in DRAM circuitry. As integrated circuitry density increases, there is a continuing challenge to maintain sufficiently high storage capacitance despite decreasing capacitor area. A typical capacitor is comprised of two conductive electrodes separated by a non-conducting dielectric region. The dielectric region is preferably comprised of one or more materials preferably having a high dielectric constant and low leakage current characteristics. Example materials include silicon oxides, such as SiO2, and Si3N4. Si3N4 is typically preferred due to its higher dielectric constant than SiO2.


Numerous capacitor dielectric materials have been and are being developed in an effort to meet the increasing stringent requirements associated with the production of smaller and smaller capacitor devices used in higher density integrated circuitry. Most of these materials do, however, add increased process complexity or cost over utilization of conventional SiO2 and Si3N4 capacitor dielectric materials.


One dielectric region in use today includes a composite of silicon oxide and silicon nitride layers. Specifically, a first capacitor electrode is formed to have a silicon oxide comprising layer, typically silicon dioxide, of 6 to 10 Angstroms thereover. Such might be formed by deposition, or more typically by ambient or native oxide formation due to oxidation of the first electrode material (for example conductively doped polysilicon) when exposed to clean room ambient atmosphere. Thereafter, a silicon nitride layer is typically deposited by low pressure chemical vapor deposition. This can, however, undesirably produce very small pinholes in the silicon nitride layer, particularly with thin layers of less than 200 Angstroms, with the pinholes becoming particularly problematic in layers of less than or equal to about 75 Angstroms thick. These pinholes can undesirably reduce film density and result in undesired leakage current in operation.


One technique for filling such pinholes is to oxidize the substrate in a manner which fills such pinholes with silicon oxide material. For example, one such manner where the lower electrode material comprises silicon is to expose the substrate to suitable oxidizing conditions to cause silicon from the electrode and silicon from the silicon nitride to oxidize. Such forms silicon oxide material which thereby completely fills the pinholes and forms a silicon oxide layer typically from about 5 Angstroms to about 25 Angstroms thick over the silicon nitride. Wet oxidation conditions are typically used.


A second capacitor electrode is ultimately formed thereover, with the dielectric region in such example comprising an oxide-nitride-oxide composite. Typically achieved dielectric constant for such a capacitor dielectric region is about 5. Higher dielectric constant capacitor dielectric regions are of course desired, and it would be desirable to provide methods which enable utilization of silicon nitride and/or silicon oxide material dielectric regions if practical.


The invention was primarily motivated in improving dielectric constant of silicon nitride comprising capacitor dielectric layers having pinholes formed therein which are filled with silicon oxide material. However the invention is in no way so limited as will be appreciated by the artisan, with the invention only being limited by the accompanying claims as literally worded without narrowing reference to the specification, and in accordance with the doctrine of equivalents.


SUMMARY

The invention includes capacitors, methods of forming capacitors and methods of forming capacitor dielectric layers. In one implementation, a method of forming a capacitor includes forming first and second capacitor electrodes over a substrate. A capacitor dielectric region is formed intermediate the first and second capacitor electrodes, and includes forming a silicon nitride comprising layer over the first capacitor electrode. A silicon oxide comprising layer is formed over the silicon nitride comprising layer. The silicon oxide comprising layer is exposed to an activated nitrogen species generated from a nitrogen-containing plasma effective to introduce nitrogen into at least an outermost portion of the silicon oxide comprising layer. Silicon nitride is formed therefrom effective to increase a dielectric constant of the dielectric region from what it was prior to said exposing.


In one implementation, a method of forming a capacitor dielectric layer includes forming a silicon nitride comprising layer over a substrate. An outer silicon oxide comprising layer is formed over the silicon nitride comprising layer. The substrate is provided with the silicon nitride and the silicon oxide comprising layers within a plasma deposition chamber. The chamber includes a substrate receiver and a powerable electrode spaced therefrom, and the substrate is received by the receiver. A spacing between the receiver and the electrode of at least 0.1 inch is provided, with the substrate being received on the receiver. With such spacing, a nitrogen comprising gas is injected to within the chamber and with the electrode generating a plasma therefrom effective to form an activated nitrogen species which diffuses into the outer silicon oxide comprising layer. Silicon nitride is formed therefrom in only an outermost portion of the silicon oxide comprising layer.


In one implementation, a capacitor includes first and second capacitor electrodes. A capacitor dielectric region is received intermediate the first and second capacitor electrodes. The capacitor dielectric region includes a silicon nitride comprising layer having an outermost surface which contacts the second capacitor electrode. The outermost surface consists essentially of silicon nitride. The silicon nitride comprising layer has a plurality of pinholes therein which are at least partially filled with silicon oxide material which is spaced from the second electrode.





BRIEF DESCRIPTION OF THE DRAWINGS

Preferred embodiments of the invention are described below with reference to the following accompanying drawings.



FIG. 1 is a diagrammatic sectional view of a semiconductor wafer fragment in process in accordance with an aspect of the invention.



FIG. 2 is a view of the FIG. 1 wafer fragment at a processing step subsequent to that shown by FIG. 1.



FIG. 3 is a view of the FIG. 2 wafer fragment at a processing step subsequent to that shown by FIG. 2.



FIG. 4 is an alternate view of the FIG. 2 wafer fragment at a processing step subsequent to that shown by FIG. 2.



FIG. 5 is another alternate view of the FIG. 2 wafer fragment at a processing step subsequent to that shown by FIG. 2.



FIG. 6 is a diagrammatic view of a plasma deposition chamber usable in accordance with an aspect of the invention.



FIG. 7 is a view of the FIG. 3 wafer fragment at a processing step subsequent to that shown by FIG. 3.



FIG. 8 is a view of the FIG. 4 wafer fragment at a processing step subsequent to that shown by FIG. 4.



FIG. 9 is a view of the FIG. 5 wafer fragment at a processing step subsequent to that shown by FIG. 5.





DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

This disclosure of the invention is submitted in furtherance of the constitutional purposes of the U.S. Patent Laws “to promote the progress of science and useful arts” (Article 1, Section 8).


A wafer fragment in process in accordance with a method of forming a capacitor in accordance with an aspect of the invention is indicated generally with reference numeral 10. Such comprises a bulk monocrystalline silicon substrate 12. In the context of this document, the term “semiconductor substrate” or “semiconductive substrate” is defined to mean any construction comprising semiconductive material, including, but not limited to, bulk semiconductive materials such as a semiconductive wafer (either alone or in assemblies comprising other materials thereon), and semiconductive material layers (either alone or in assemblies, comprising other materials). The term “substrate” refers to any supporting structure, including, but not limited to, the semiconductive substrates described above. An insulative layer 14, for example doped or undoped silicon dioxide, or silicon nitride, is formed over bulk substrate 12.


A first capacitor electrode material 16 is formed over insulative layer 14. At this point, or preferably later in the process, electrode material 16 is ultimately patterned/provided into some desired first capacitor electrode shape. Exemplary materials for electrode 16 include silicon (for example polysilicon) metals, conductive metal oxides, and any other conductive layer or layers. An exemplary thickness in one preferred embodiment, and particularly where layer 16 comprises polysilicon, is 600 Angstroms. A first or inner silicon oxide comprising layer 18 is formed over, and “on” as shown, first capacitor electrode 16. An exemplary method for forming layer 18 is by oxidizing an outer portion of electrode material 16, for example by exposure to clean room ambient. This oxide layer is not preferred, but rather an effect of an exposed silicon or other oxidizable substrate. Typical thickness for layer 18 is less than or equal to 15 Angstroms. Layer 18 preferably consists essentially of silicon dioxide.


A silicon nitride comprising layer 20 is formed over first capacitor electrode 16 and in the illustrated preferred embodiment is formed on first or inner silicon oxide comprising layer 18. An exemplary thickness is from 30 Angstroms to 80 Angstroms. In but one embodiment, silicon nitride comprising layer 20 is formed to have a plurality of pinholes 22 formed therein. Such are shown in exaggerated width in the figures for clarity. In the illustrated embodiment, at least some pinholes extend completely through layer 20 to silicon oxide comprising layer 18. Silicon nitride comprising layer 20 might be deposited by any existing or yet-to-be developed technique, with chemical vapor deposition or plasma enhanced chemical vapor deposition being but examples. One exemplary process whereby a silicon nitride layer 20 is deposited by chemical vapor deposition includes NH3 at 300 sccm, dichlorosilane at 100 sccm, 750 mTorr, 600° C., and 60 minutes of processing.


Referring to FIG. 2, a second or outer silicon oxide comprising layer 24 is formed over silicon nitride comprising layer 20, and as shown in the preferred embodiment is formed thereon. In one preferred embodiment, and where silicon nitride comprising layer 20 includes pinholes, silicon oxide comprising layer 24 is formed effective to fill such pinholes with silicon oxide, as shown. Such preferably occurs by an oxidation. One example method of forming silicon oxide comprising layer 24 is to oxidize the substrate effective to both fill said pinholes with silicon oxide derived from at least some silicon of the first capacitor electrode material and form such second silicon oxide comprising layer 24 on silicon nitride comprising layer 20 thereover from at least some silicon of the silicon nitride material. By way of example only, exemplary oxidation conditions include 800° C., 5 slpm H2, 10 slpm O2, at atmospheric pressure for 15 minutes. For purposes of the continuing discussion, second silicon oxide comprising layer 24 upon formation includes a portion 25 which is everywhere received elevationally over silicon nitride comprising layer 20, and which is outside of pinholes 22. An exemplary thickness for portion 25 is from 5 Angstroms to 25 Angstroms.


The silicon oxide comprising layer is exposed to an activated nitrogen species generated from a nitrogen-containing plasma effective to introduce nitrogen into at least an outermost portion of the silicon oxide comprising layer, and silicon nitride is formed therefrom. By way of example only, FIGS. 3, 4 and 5 illustrate different exemplary embodiments of the same where the silicon nitride comprising layer includes pinholes formed therein. FIG. 3 depicts wafer fragment embodiment 10, FIG. 4 an embodiment 10a, and FIG. 5 an embodiment 10b. Like numerals from the first described embodiments are utilized in FIGS. 4 and 5, with differences being indicated by different numerals or by “a” or “b” suffixes, respectively. In each of the depicted preferred embodiments, the exposing and forming of silicon nitride therefrom transforms only an outermost portion of the second silicon oxide comprising layer to silicon nitride. Alternately in accordance with an aspect of the invention, the entirety of a silicon oxide comprising layer received over a silicon nitride comprising layer might be transformed to silicon nitride.


Transformation of the respective illustrated portions of former silicon oxide comprising layer 24 ultimately to silicon nitride is depicted by the stippling intended to show the transformation to silicon nitride. For example, FIG. 3 depicts all of portion 25 of silicon oxide comprising layer 24 as being transformed to silicon nitride. FIG. 4 depicts an embodiment wherein only an outermost part of portion 25a is ultimately transformed to silicon nitride. The FIG. 4 embodiment shows approximately half of portion 25a being transformed to silicon nitride. Of course, more or less of portion 25 might alternately be transformed in connection with the FIG. 4 embodiment. In FIG. 5, the exposing and forming silicon nitride therefrom was also effective to transform an outermost portion 27 of the silicon oxide material within the pinholes to silicon nitride. Such depicts an approximate outermost portion constituting roughly one-third of the pinhole depth in FIG. 5, although more or less transformation of the subject silicon oxide material within the pinholes might be transformed in accordance with the FIG. 5 and similar embodiments. In each of the preferred FIGS. 3-5 embodiments, at least some silicon oxide remains within the previously formed pinholes, with the embodiments of FIGS. 3 and 4 depicting processing whereby no silicon nitride is formed within pinholes 22.


Exemplary preferred processing by which such exposing and transformation to silicon nitride occurs is as described in U.S. patent application Ser. No. 09/633,556 filed Aug. 7, 2000, entitled “Transistor Structures, Methods of Incorporating Nitrogen Into Silicon-Oxide-Containing Layers, and Methods of Forming Transistors”, listing Gurtej S. Sandhu, John T Moore and Neil R. Rueger as inventors, and which is herein fully incorporated by reference. One preferred process for effecting the exposing and formation of silicon nitride is described with reference to FIG. 6. Such diagrammatically depicts a plasma deposition chamber 60. Such preferably constitutes a single wafer processor comprising a powerable electrode 62 and a wafer receiver or chuck 64. Receiver 64 might be heated or cooled from an appropriate power source. Receiver 64 and electrode 62 are received within chamber walls 66. By way of example only, an exemplary such reactor would be a high density plasma chamber from Applied Materials. Electrode 62 and receiver 64 are spaced from one another by a depicted distance 68. Typically and preferably, such spacing is adjustable by the operator. In one preferred embodiment, substrate 10 of FIG. 2 is provided within chamber 60 received by receiver 64.


Nitrogen is injected to within chamber 60, for example from one or more injection ports 70, and with electrode 62 a plasma 72 is generated therefrom effective to form the activated nitrogen species. In one most preferred embodiment, generated plasma 72 is spaced from the outer silicon oxide comprising layer of substrate 10. Such is preferably accomplished by the control of spacing 68 and the powering of electrode 62 to, in the preferred embodiment, preclude plasma 72 from directly being exposed to the outer surface of substrate 10. One reason for preferably avoiding direct plasma exposure is to avoid possible plasma damage to underlying devices. The illustrated plasma 72 constitutes an exemplary remote plasma, wherein the actual plasma species is not provided directly in contact with substrate 10. Plasma generation outside of the chamber could also be utilized to generate the activated nitrogen. Preferred spacing 68 is at least 0.1 inch, more preferably at least 1.0 inch, still more preferably at least 2.0 inches, and even more preferably at least 4.0 inches. Exemplary preferred nitrogen gasses include one or more of N2, NH3 and NOx. Other exemplary processing parameters are as described in U.S. patent application Ser. No. 09/633,556 referred to above. In one preferred embodiment, the activated nitrogen species diffuses into the outer silicon oxide comprising layer 24, and silicon nitride is formed therefrom in only an outermost portion of the silicon oxide comprising layer.


Preferably, the electrode is powered at anywhere from 100 to 3000 watts, with an exemplary preferred pressure range during the processing being, for example, from 10 mTorr to 1 Torr. Chuck temperature is preferably maintained from, for example, room temperature to about 900° C. Preferred exposure times include from 5 seconds to 60 seconds.


The formation of silicon nitride therefrom might occur during such exemplary exposing. Alternately, such might occur afterward from conventional subsequent wafer processing involving thermal exposure of the substrate, or by a dedicated thermal annealing step. For example and by way of example only, if wafer receiver 64 is maintained at a temperature of around 800° C. or higher during the exposing, silicon nitride may inherently form during such exposing by the act of nitrogen diffusion into layer 24. Alternately by way of example only and if processing at lower temperatures, silicon nitride might subsequently be formed from the diffused nitrogen species by thermally annealing the substrate at a temperature of at least 600° C. after the exposing for some suitable period of time to effect silicon nitride transformation.


Referring to FIGS. 7, 8 and 9, a second capacitor electrode 40 is formed over the substrate. In the preferred and illustrated embodiment, second capacitor electrode material 40 is formed on (in contact with) transformed layer 24/24a/24b. An exemplary thickness range for layer 40 is from 300 Angstroms to 600 Angstroms. Second electrode material 40 might comprise the same or different materials from first electrode material 16. In the depicted and preferred embodiment, layers 18, 20 and transformed layer 24/24a/24b constitute a respective capacitor dielectric region which is received intermediate the first and second capacitor electrodes. Most preferably in accordance with the preferred embodiment, the exposing of silicon oxide comprising layer 24 and the transformation to silicon nitride is effective to increase a dielectric constant of the dielectric region from what it was prior to the exposing.


The invention also comprises capacitors independent of the method of fabrication. For example, FIGS. 7, 8 and 9 depict capacitor dielectric regions 18/20/24, 18/20/24a and 18/20/24b. Each comprises a silicon nitride comprising layer 20/24, 20/24a and 20/24b, respectively, having outermost surfaces 45, 45a and 45b, respectively. Surfaces 45, 45a and 45b contact the respective second capacitor electrodes 40. Outermost surfaces 45/45a/45b consist essentially of silicon nitride. Silicon nitride comprising layers 20/24, 20/24a and 20/24b have a plurality of pinholes 22 therein which are at least partially filled with silicon oxide comprising material which is spaced from second electrode material 40. In the embodiments of FIGS. 7 and 8, such provide examples wherein the pinholes are totally filled with silicon oxide material. The embodiment of FIG. 9 depicts but one example wherein the pinholes are only partially filled with silicon oxide material, and in such depicted and preferred embodiment where the pinholes comprise uppermost portions which are filled with silicon nitride material.


In compliance with the statute, the invention has been described in language more or less specific as to structural and methodical features. It is to be understood, however, that the invention is not limited to the specific features shown and described, since the means herein disclosed comprise preferred forms of putting the invention into effect. The invention is, therefore, claimed in any of its forms or modifications within the proper scope of the appended claims appropriately interpreted in accordance with the doctrine of equivalents.

Claims
  • 1. A capacitor comprising: a first capacitor electrode; a second capacitor electrode; and a capacitor dielectric region received intermediate the first and second capacitor electrodes, the capacitor dielectric region comprising a silicon nitride comprising layer having an outermost surface which contacts the second capacitor electrode, said outermost surface consisting essentially of silicon nitride, the silicon nitride comprising layer having a plurality of pinholes therein which are at least partially filled with silicon oxide which is free of silicon nitride and is spaced from the second electrode.
  • 2. The capacitor of claim 1 wherein the pinholes are totally filled with silicon oxide.
  • 3. The capacitor of claim 1 wherein the pinholes are only partially filled with silicon oxide.
  • 4. The capacitor of claim 1 wherein the pinholes comprise uppermost portions filled with silicon nitride material.
  • 5. The capacitor of claim 1 wherein the dielectric region comprises an inner silicon oxide comprising layer received intermediate the first capacitor electrode and the silicon nitride comprising layer.
  • 6. A capacitor comprising: a first capacitor electrode; a second capacitor electrode; and a capacitor dielectric region received intermediate the first and second capacitor electrodes, the capacitor dielectric region comprising: a silicon oxide comprising layer received on the first capacitor electrode; and a silicon nitride comprising layer received on the silicon oxide comprising layer, the silicon nitride comprising layer having an outermost surface which contacts the second capacitor electrode, said outermost surface consisting essentially of silicon nitride, the silicon nitride comprising layer having a plurality of pinholes therein which are at least partially filled with silicon oxide which is free of silicon nitride and is spaced from the second electrode.
  • 7. The capacitor of claim 6 wherein the pinholes are totally filled with silicon oxide.
  • 8. The capacitor of claim 6 wherein the pinholes are only partially filled with silicon oxide.
  • 9. The capacitor of claim 6 wherein the pinholes comprise uppermost portions filled with silicon nitride material.
Parent Case Info

This patent resulted from a divisional application of U.S. patent application Ser. No. 09/943,180, filed Aug. 29, 2001, entitled “Methods of Forming Capacitors”, naming John T. Moore and Scott J. DeBoer as inventors, the disclosure of which is incorporated by reference.

US Referenced Citations (118)
Number Name Date Kind
3627598 McDonald et al. Dec 1971 A
4254161 Kemlage Mar 1981 A
4262631 Kubacki Apr 1981 A
4435447 Ito et al. Mar 1984 A
4605447 Brotherton et al. Aug 1986 A
4882649 Chen et al. Nov 1989 A
4891684 Nishioka et al. Jan 1990 A
4980307 Ito et al. Dec 1990 A
4996081 Ellul et al. Feb 1991 A
5026574 Economu et al. Jun 1991 A
5032545 Doan et al. Jul 1991 A
5051794 Mori Sep 1991 A
5142438 Reinberg et al. Aug 1992 A
5164331 Lin et al. Nov 1992 A
5227651 Kim et al. Jul 1993 A
5237188 Iwai et al. Aug 1993 A
5254489 Nakata Oct 1993 A
5258333 Shappir et al. Nov 1993 A
5318924 Lin et al. Jun 1994 A
5324679 Kim et al. Jun 1994 A
5330920 Soleimani et al. Jul 1994 A
5330936 Ishitani Jul 1994 A
5334554 Lin et al. Aug 1994 A
5350707 Ko et al. Sep 1994 A
5376593 Sandhu et al. Dec 1994 A
5378645 Inoue et al. Jan 1995 A
5382533 Ahmad et al. Jan 1995 A
5393702 Yang et al. Feb 1995 A
5397748 Watanabe et al. Mar 1995 A
5398641 Shih Mar 1995 A
5436481 Egawa et al. Jul 1995 A
5445999 Thakur et al. Aug 1995 A
5449631 Giewont et al. Sep 1995 A
5459105 Matsuura Oct 1995 A
5464792 Tseng et al. Nov 1995 A
5498890 Kim et al. Mar 1996 A
5500380 Kim Mar 1996 A
5504029 Murata et al. Apr 1996 A
5508542 Geiss et al. Apr 1996 A
5518946 Kuroda May 1996 A
5518958 Giewont et al. May 1996 A
5523596 Ohi et al. Jun 1996 A
5596218 Soleimani et al. Jan 1997 A
5612558 Harshfield Mar 1997 A
5619057 Komatsu Apr 1997 A
5620908 Inoh et al. Apr 1997 A
5633036 Seebauer et al. May 1997 A
5663077 Adachi et al. Sep 1997 A
5674788 Wristers et al. Oct 1997 A
5685949 Yashima Nov 1997 A
5716864 Abe Feb 1998 A
5719083 Komatsu Feb 1998 A
5731235 Srinvasan et al. Mar 1998 A
5760475 Cronin et al. Jun 1998 A
5763922 Chau Jun 1998 A
5821142 Sung et al. Oct 1998 A
5834372 Lee Nov 1998 A
5837592 Chang et al. Nov 1998 A
5837598 Aronowitz et al. Nov 1998 A
5840610 Gilmer et al. Nov 1998 A
5844771 Graettinger et al. Dec 1998 A
5851603 Tsai et al. Dec 1998 A
5861651 Brasen et al. Jan 1999 A
5885877 Gardner et al. Mar 1999 A
5939750 Early Aug 1999 A
5960289 Tsui et al. Sep 1999 A
5960302 Ma et al. Sep 1999 A
5970345 Hattangady et al. Oct 1999 A
5972783 Arai et al. Oct 1999 A
5972800 Hasegawa Oct 1999 A
5994749 Oda Nov 1999 A
5998253 Loh et al. Dec 1999 A
6001748 Tanaka Dec 1999 A
6008104 Schrems Dec 1999 A
6033998 Aronowitz et al. Mar 2000 A
6054396 Doan Apr 2000 A
6057220 Ajmera et al. May 2000 A
6080629 Gardner et al. Jun 2000 A
6080682 Ibok Jun 2000 A
6087229 Aronowitz et al. Jul 2000 A
6091109 Hasegawa Jul 2000 A
6091110 Hebert et al. Jul 2000 A
6093661 Trivedi et al. Jul 2000 A
6096597 Tsu et al. Aug 2000 A
6110780 Yu et al. Aug 2000 A
6110842 Okuno et al. Aug 2000 A
6114203 Ghidini et al. Sep 2000 A
6136636 Wu Oct 2000 A
6140187 DeBusk et al. Oct 2000 A
6146948 Wu et al. Nov 2000 A
6174821 Doan Jan 2001 B1
6184110 Ono et al. Feb 2001 B1
6197701 Shue et al. Mar 2001 B1
6201303 Ngo et al. Mar 2001 B1
6207532 Lin et al. Mar 2001 B1
6207586 Ma et al. Mar 2001 B1
6207985 Walker Mar 2001 B1
6225167 Yu et al. May 2001 B1
6228701 Dehm et al. May 2001 B1
6232244 Ibok May 2001 B1
6255703 Hause et al. Jul 2001 B1
6265327 Kobayashi et al. Jul 2001 B1
6268296 Misium et al. Jul 2001 B1
6274442 Gardner et al. Aug 2001 B1
6297162 Jang et al. Oct 2001 B1
6323114 Hattangady et al. Nov 2001 B1
6331492 Misium et al. Dec 2001 B2
6350707 Liu et al. Feb 2002 B1
6362085 Yu et al. Mar 2002 B1
6399445 Hattangady et al. Jun 2002 B1
6399448 Mukhopadhyay et al. Jun 2002 B1
6410991 Kawai et al. Jun 2002 B1
6413881 Aronowitz et al. Jul 2002 B1
6436771 Jang et al. Aug 2002 B1
6450116 Noble et al. Sep 2002 B1
6482690 Shibata Nov 2002 B2
6492690 Ueno et al. Dec 2002 B2
20030034518 Yoshikawa Feb 2003 A1
Foreign Referenced Citations (2)
Number Date Country
0 886 308 Jun 1998 EP
WO 9639713 Jun 1996 WO
Related Publications (1)
Number Date Country
20030209778 A1 Nov 2003 US
Divisions (1)
Number Date Country
Parent 09943180 Aug 2001 US
Child 10418532 US