Alkanolamine semiconductor process residue removal composition and process

Information

  • Patent Grant
  • 6564812
  • Patent Number
    6,564,812
  • Date Filed
    Tuesday, June 4, 2002
    22 years ago
  • Date Issued
    Tuesday, May 20, 2003
    21 years ago
Abstract
A two carbon atom linkage alkanolamine compound composition comprises the two carbon atom linkage alkanolamine compound, gallic acid or catechol, and optionally, an aqueous hydroxylamine solution. The balance of the composition is made up of water, preferably high purity deionized water, or another suitable polar solvent. A process for removing photoresist or other residue from a substrate, such as an integrated circuit semiconductor wafer including titanium metallurgy, comprises contacting the substrate with the composition for a time and at a temperature sufficient to remove the photoresist or other residue from the substrate. Use of the two carbon atom linkage alkanolamine compound in the composition and process provides superior residue removal without attacking titanium or other metallurgy, oxide or nitride layers on the substrate.
Description




BACKGROUND OF THE INVENTION




1. Field of the Invention




The present invention relates generally to a cleaning composition and process for removal of organic, organometallic and metal oxide residues from substrates. More particularly, it relates to such a composition and process for removing semiconductor device fabrication residues from semiconductor device substrates, such as etching residues after plasma etching processes in the fabrication of integrated circuits on silicon wafers and similar processes. Most especially, it relates to such a composition and process which is effective for the removal of these materials while avoiding substantial attack on metal or insulation layers employed in integrated circuits, including titanium layers.




2. Description of the Prior Art




As integrated circuit manufacturing has become more complex and the dimensions of circuit elements fabricated on silicon or other semiconductor wafers have become smaller, continued improvement in techniques used to remove residues formed from such materials has been required. Oxygen plasma oxidation is often used for removal of photoresist or other polymeric materials after their use during the fabrication process has been completed. Such high energy processes typically result in the formation of organometallic and other residues on sidewalls of the structures being formed in the fabrication process.




A variety of metal and other layers are commonly employed in integrated circuit fabrication, including aluminum, aluminum/silicon/copper, titanium, titanium nitride, titanium/tungsten, tungsten, silicon oxide, polysilicon crystal, and the like. The use of such different layers results in the formation of different organometallic residues in the high energy processes. In addition to being effective for removing such residues, stripping and cleaning compositions should also not attack the different metallurgies or insulation layers used in integrated circuit fabrication.




A variety of residue removal compositions and processes suitable for integrated circuit fabrication have been developed and marketed by EKC Technology, Inc., the assignee of the present application. Some of these compositions and processes are also useful for stripping photoresist, polyimide or other polymeric layers from substrates in integrated circuit fabrication, and EKC has also developed a variety of compositions and processes for stripping such polymeric layers from substrates in integrated circuit fabrication. Such compositions and processes are disclosed in the following commonly assigned issued patents: U.S. Pat. No. 5,482,566, issued Jan. 9, 1996 to Lee; U.S. Pat. No. 5,399,464, issued Mar. 21, 1995 to Lee; U.S. Pat. No. 5,381,807, issued Jan. 17, 1995 to Lee; U.S. Pat. No. 5,334,332, issued Aug. 2, 1994 to Lee; U.S. Pat. No. 5,279,771, issued Jan. 18, 1994 to Lee; U.S. Pat. No. 4,824,763, issued Apr. 25, 1989 to Lee and U.S. Pat. No. 4,395,348, issued Jul. 26, 1983 to Lee. These compositions have achieved substantial success in integrated circuit fabrication applications. However, further development of integrated circuits and their fabrication processes have created a need for improvement in residue removal compositions and processes.




As a result of a continuous effort to decrease critical dimension size in the integrated circuit industry, such as in the fabrication of sub-micron size devices, etching residue removal and substrate compatibility with chemicals employed in wet processing is becoming more and more critical for obtaining acceptable yield in very large scale integration (VLSI) and ultra large scale integration (ULSI) processes. The composition of such etching residue is generally made up of the etched substrates, underlying substrate, photoresist and etching gases. The substrate compatibility of the wafers with wet chemicals is highly dependent on the processing of the polysilicon, multilevel interconnection dielectric layers and metallization in thin film deposition, etching and post-etch treatment of the wafers, which are often quite different from one fabrication process to another. Some of the above compositions have produced corrosion on certain metal substrates, such as those including a titanium metal layer. Titanium has become more widely used in semiconductor manufacturing processes. It is employed both as a barrier layer to prevent electromigration of certain atoms and as an antireflector layer on top of other metals.




SUMMARY OF THE INVENTION




Accordingly, it is an object of this invention to provide an improved composition for residue removal and process using such a composition suitable for meeting current semiconductor fabrication requirements.




It is another object of the invention to provide such a composition and process which is suitable for removing residues from wafers and other substrates including one or more titanium metal layers without substantial attack on such titanium layers.




The attainment of these and related objects may be achieved through use of the residue removal composition and process herein disclosed. A residue removal composition in accordance with this invention comprises a two carbon atom linkage alkanolamine compound, gallic acid or catechol, optionally, an aqueous hydroxylamine solution, and desirably a balance of water or another suitable polar solvent. A process for removing a residue from a substrate in accordance with this invention comprises contacting the substrate with a composition that contains a two carbon atom linkage alkanolamine compound for a time and at a temperature sufficient to remove the residue from the substrate.




In practice, we have found that use of a two carbon atom linkage alkanolamine compound gives a residue removing composition that attacks titanium substantially less than prior compositions. At the same time, the two carbon atom linkage alkanolamine compound containing composition gives equivalent performance as a residue removing composition.




The attainment of the foregoing and related objects, advantages and features of the invention should be more readily apparent to those skilled in the art, after review of the following more detailed description of the invention, taken together with the drawings, in which:











BRIEF DESCRIPTION OF THE DRAWINGS





FIGS. 1-8

are scanning electron microscope (SEM) photographs showing comparative results achieved using the composition and process of the present invention.











DETAILED DESCRIPTION OF THE INVENTION




The two carbon atom linkage alkanolamine compounds suitable for use in the invention have the structural formula,











wherein X and Y are, independently in each ease, hydrogen, methyl or ethyl, and R is hydrogen or an alkyl group containing from 1 to 4 carbon atoms. The two carbon atom linkage alkanolamine compounds useful in the present invention preferably have relatively high boiling points, such as for example, 75° C. or above. Preferred specific examples of such two carbon atom linkage alkanolamine compounds include monoethanolamine and monoisopropanolamine.




The composition desirably contains at least about 10% by weight of at least one two carbon atom linkage alkanolamine compound, from about 5% to about 40% by weight of gallic acid, catechol or other chelating agent, and optionally, up to about 50 percent by weight of a 50% by weight aqueous hydroxylamine solution. The balance of the composition is desirably made up of water, preferably high purity deionized water, or another suitable polar solvent. The solvents can be used singly or as mixtures. The composition preferably includes from about 10% to about 80% by weight of at least one two carbon atom linkage alkanolamine compound, from about 5% to about 30% by weight of the gallic acid or catechol, from about 10% to about 30% of the hydroxylamine solution, with the remaining balance preferably being water or other suitable polar solvent.




In practice, it appears that the catechol or gallic acid enhances the ability of the two carbon atom linkage alkanolamine compound to remove the residue. At the same time, the presence of the catechol, gallic acid or other chelating agent helps to prevent attack on titanium metallurgy.




Suitable examples of polar solvents for the composition, in addition to water, include dimethyl sulfoxide, ethylene glycol, ethylene glycol alkyl ether, diethylene glycol alkyl ether, triethylene glycol alkyl ether, propylene glycol, propylene glycol alkyl ether, dimethyl sulfoxide, N-substituted pyrrolidone, ethylenediamine and ethylenetriamine. Additional polar solvents as known in the art can also be used in the composition of the present invention.




The residue cleaning compositions of the present composition are effective in removing organometallic and metal oxide residue from a variety of integrated circuit silicon wafer substrates, including metal layers, such as aluminum or titanium, oxide layers, such as silicon oxides, nitride layers, such as silicon nitride, and the like. The cleaning compositions of the present invention are also effective in removing organometallic and metal oxide residue generated on the substrate of etching equipment utilized in the fabrication of integrated circuits. Examples of commercially available etching equipment include that available from Lam Research, Tegal, Electrotech, Applied Materials, Tokyo Electron, Hitachi and the like.




The method of cleaning a substrate using the cleaning compositions of the present invention involves contacting a substrate having organometallic and metal oxide residue thereon with a stripping and cleaning composition of the present invention for a time and at a temperature sufficient to remove the residue. The substrate is generally immersed in the stripping and cleaning composition. The time and temperature are determined based on the particular material being removed from a substrate. Generally, the temperature is in the range of from about ambient or room temperature to about 120° C. and the contact time is from about 2 to 60 minutes.




The substrate may then be rinsed in a polar solvent, such as isopropyl alcohol, followed by a deionized water rinse. The substrate is then mechanically dried, such as with a spin drier, or nitrogen blow dried.




The following represent non-limiting examples and describe the invention further.




Examples of cleaning compositions according to the present invention suitable for removing resist or other organic residues from a substrate are set forth in Table I below.
















TABLE 1









Cleaning




Alkanolamine




Gallic Acid/Catechol




Hydroxyl-




Additional






Composition




Wt. %




Wt. %




Amine Wt. %




Solvent Wt. %











A




60% DGA




 5% Catechol




30% (50 Wt










% Aq. Sol'n)






B




55% MIPA




10% gallic acid




30% (50 Wt




5% Water









% Aq. Sol'n.)






C




60% MEA





35% (50 Wt




5% Water









% Aq. Sol'n.)






D




60% MEA




 5% gallic acid




35% (50 Wt









% Aq. Sol'n.)






E




60% MIPA




 5% Catechol




35% (50 Wt









% Aq. Sol'n.)






F




30% MEA




10% Catechol




30% (50 Wt




5% Water







25% MIPA





% Aq. Sol'n.)






G




30% MEA




10% gallic acid




30% (50 Wt




5% Water







25% MIPA





% Aq. Sol'n.)






H




55% DGA




10% gallic acid




30% (50 Wt




5% Water









% Aq. Sol'n.)











Abbreviations:










DGA = diglycolamine










MEA = monoethanolamine










MIPA = monoisopropanolamine













EXAMPLE 1




A semiconductor wafer having a patterned metal stack consisting of TiN/Al/Ti/TiN/SiO


2


was treated with composition A at 75° C. for 30 minutes to remove process reside from the wafer, for comparative purposes.

FIG. 1

is a scanning electron microscope (S EM) photograph of the wafer after this treatment. Substantial undercutting of both Ti layers are visible in this photograph.




EXAMPLE 2




A semiconductor wafer having a patterned metal stack consisting of TiN/Al/Ti/TiN/Ti/SiO


2


was treated with composition B at 75° C. for 30 minutes to remove process reside from the wafer.

FIG. 2

is a SEM photograph of the wafer after this treatment. No undercutting of the lower Ti layer is visible, and a slight undercutting of the upper Ti layer is visible.




EXAMPLE 3




A semiconductor wafer having a patterned metal stack consisting of TiN/Al/Ti/TiN/Ti/SiO


2


was treated with composition C at 75° C. for 30 minutes to remove process reside from the wafer, as a control.

FIG. 3

is a SEM photograph of the wafer after this treatment Undercutting of both Ti layers is visible.




EXAMPLE 4




A semiconductor wafer having a patterned metal stack consisting of TiN/Al/Ti/TiN/Ti/SiO


2


was treated with composition D at 75° C. for 30 minutes to remove process reside from the wafer.

FIG. 4

is a SEM photograph of the wafer after this treatment A slight undercutting of the lower Ti layer is visible, and no undercutting of the upper Ti layer is visible.




EXAMPLE 5




A semiconductor wafer having a patterned metal stack consisting of W/Ti/SiO


2


was treated with composition E at 75° C. for 30 minutes to remove process reside from the wafer.

FIG. 5

is a SEM photograph of the wafer after this treatment. No undercutting of the Ti layer is visible.




EXAMPLE 6




A semiconductor wafer having a patterned metal stack consisting of TiN/Ti/Al/Ti/TiN/BPSG (boron phosphosilicate glass) was treated with composition F at 75° C. for 30 minutes to remove process reside from the wafer.

FIG. 6

is a SEM photograph of the wafer after this treatment No undercutting of the Ti layers is visible.




EXAMPLE 7




A semiconductor wafer having a patterned metal stack consisting of TiN/Al/Ti/TiN/SiO


2


was treated with composition G at 75° C. for 30 minutes to remove process reside from the wafer.

FIG. 7

is a SEM photograph of the wafer after this treatment No undercutting of the Ti layers is visible.




EXAMPLE 8




A semiconductor wafer having a patterned metal stack consisting of TiN/Al/Ti/TiN/Ti/SiO


2


was treated with composition H at 75° C. for 30 minutes to remove process reside from the wafer, for comparative purposes.

FIG. 8

is SEM photograph of the wafer after this treatment Undercutting of the Ti layers is visible.




The above examples show that compositions B, D, E, F and G successfully remove residues from substrates having a titanium metallurgy while reducing or eliminating attack on the titanium metallurgy. Increased amounts of catechol or gallic acid produce an improved reduction of attack on the titanium metallurgy. The comparative compositions A, C and H all show substantial attack on the titanium metallurgy, even when a two carbon atom linkage alkanolamine compound is used in the absence of gallic acid or catechol. When gallic acid or catechol is used with an alkanolamine compound other than a two carbon atom linkage alkanolamine compound, the gallic acid or catechol does not show a similar reduction of attack of the composition on the titanium metallurgy.




It should now be readily apparent to those skilled in the art that a novel composition and process capable of achieving the stated objects of the invention has been provided. The improved two carbon atom linkage alkanolamine compound based composition and process using such a composition of this invention is suitable for meeting current semiconductor fabrication requirements. The composition and process is suitable for removing photoresist residues and other residues from wafers and other substrates including one or more titanium metal layers without substantial attack on such titanium layers.




It should further be apparent to those skilled in the art that various changes in form and details of the invention as shown and described may be made. It is intended that such changes be included within the spirit and scope of the claims appended hereto.



Claims
  • 1. A process for removal of residue from a semiconductor substrate, which comprises:contacting the semiconductor substrate with a composition comprising: a two carbon atom linkage alkanolamine compound; a chelating agent; an aqueous hydroxylamine solution; and a polar organic solvent for a time and at a temperature sufficient to remove the residue from the substrate without damaging the substrate so that the semiconductor substrate can undergo continued fabrication of an integrated circuit, wherein the residue comprises residue from etching or plasma oxidation of the semiconductor substrate during fabrication of an integrated circuit; and rinsing the composition from the semiconductor substrate.
  • 2. The process of claim 1, wherein the substrate comprises titanium.
  • 3. The process of claim 1, wherein the polar organic solvent is selected from the group consisting of dimethyl sulfoxide, ethylene glycol, ethylene glycol alkyl ether, diethylene glycol alkyl ether, triethylene glycol alkyl ether, propylene glycol, propylene glycol alkyl ether, N-substituted pyrrolidone, ethylenediamine, and ethylenetriamine.
  • 4. The process of claim 3, wherein the two carbon atom linkage alkanolamine compound has the formula: wherein X and Y are independently in each case, hydrogen, methyl or ethyl, and R is hydrogen or an alkyl group containing from 1 to 4 carbons.
  • 5. The process of claim 1, wherein the chelating agent is catechol.
  • 6. The process of claim 5, wherein the catechol is present in an amount of from about 5 percent to 30 percent by weight.
  • 7. The process of claim 3, wherein the contact time is from about 2 to 60 minutes.
  • 8. The process of claim 1 wherein the composition comprises a second two carbon atom linkage alkanolamine compound which is different than the first two carbon atom linkage alkanolamine.
  • 9. The process of claim 1 wherein the composition comprises about 5% by weight hydroxylamine and about 5% of a chelating agent.
  • 10. The process of claim 1 wherein the residue comprises organometallic and metal oxide residue.
  • 11. A process for removal of residue from a semiconductor substrate, which comprises:contacting the semiconductor substrate with a composition consisting essentially of: at least one two carbon atom linkage alkanolamine compound; at least one chelating agent; an aqueous hydroxylamine solution; and at least one polar organic solvent for a time and at a temperature sufficient to remove the residue from the substrate without damaging the substrate so that the semiconductor substrate can undergo continued fabrication of an integrated circuit, wherein the residue comprises residue from etching or plasma oxidation of the semiconductor substrate during fabrication of an integrated circuit; and rinsing the composition from the semiconductor substrate.
  • 12. The process of claim 11, wherein the semiconductor substrate comprises aluminum.
  • 13. The process of claim 11, wherein the semiconductor substrate comprises titanium.
  • 14. The process of claim 11, wherein the polar organic solvent is selected from the group consisting of dimethyl sulfoxide, ethylene glycol, ethylene glycol alkyl ether, diethylene glycol alkyl ether, triethylene glycol alkyl ether, propylene glycol, propylene glycol alkyl ether, N-substituted pyrrolidone, ethylenediamine, and ethylenetriamine.
  • 15. The process of claim 11, wherein the composition comprises about 5% by weight hydroxylamine and about 5% of the chelating agent.
  • 16. The process of claim 11, herein the semiconductor substrate comprises tungsten.
  • 17. The process of claim 11, wherein the semiconductor substrate comprises silicon oxide.
  • 18. The process of claim 11, wherein the semiconductor substrate comprises polysilicon.
  • 19. The process of claim 11, wherein the semiconductor substrate comprises TiN.
  • 20. The process of claim 11, wherein the semiconductor substrate comprises Cu metal.
  • 21. The process of claim 11, wherein the semiconductor substrate comprises TiW.
  • 22. The process of claim 11, wherein the semiconductor substrate comprises SiN.
  • 23. The process of claim 11, wherein the semiconductor substrate comprises Al/Si/Cu.
  • 24. The process of claim 11, wherein the substrate comprises aluminum metal.
  • 25. The process of claim 11, wherein the substrate comprises titanium metal.
  • 26. The process of claim 11, wherein the semiconductor substrate comprises tungsten metal.
  • 27. The process of claim 1, wherein the semiconductor substrate comprises tungsten.
  • 28. The process of claim 1, wherein the semiconductor substrate comprises aluminum.
  • 29. The process of claim 1, wherein the semiconductor substrate comprises silicon oxide.
  • 30. The process of claim 1, wherein the semiconductor substrate comprises polysilicon.
  • 31. The process of claim 1, wherein the semiconductor substrate comprises TiN.
  • 32. The process of claim 1, wherein the semiconductor substrate comprises Cu metal.
  • 33. The process of claim 1, wherein the semiconductor substrate comprises TiW.
  • 34. The process of claim 1, wherein the semiconductor substrate comprises SiN.
  • 35. The process of claim 1, wherein the semiconductor substrate comprises Al/Si/Cu.
  • 36. The process of claim 1, wherein the substrate comprises tungsten metal.
  • 37. The process of claim 1, wherein the substrate comprises titanium metal.
  • 38. The process of claim 1, wherein the substrate comprises aluminum metal.
  • 39. A process for removal of residue from a semiconductor substrate, which comprises;contacting the semiconductor substrate with a composition comprising: a two carbon atom linkage alkanolamine compound; a chelating agent; an aqueous hydroxylamine solution; and a polar organic solvent for a time and at a temperature sufficient to remove the residue from the substrate without damaging the substrate so that the semiconductor substrate can undergo continued fabrication of an integrated circuit, wherein the residue comprises organometallic material; and rinsing the composition from the semiconductor substrate.
  • 40. The process of claim 39, wherein the polar organic solvent is selected from the group consisting of dimethyl sulfoxide, ethylene glycol, ethylene glycol alkyl ether, diethylene glycol alkyl ether, triethylene glycol alkyl ether, propylene glycol, propylene glycol alkyl ether, N-substituted pyrrolidone, ethylenediamine, and ethylenetriamine.
  • 41. The process of claim 39, wherein the semiconductor substrate comprises aluminum.
  • 42. The process of claim 39, wherein the semiconductor substrate comprises titanium.
  • 43. The process of claim 39, wherein the semiconductor substrate comprises tungsten.
  • 44. The process of claim 39, wherein the semiconductor substrate comprises silicon oxide.
  • 45. The process of claim 39, wherein the semiconductor substrate comprises polysilicon.
  • 46. The process of claim 39, wherein the semiconductor substrate comprises TiN.
  • 47. The process of claim 39, wherein the semiconductor substrate composes copper metal.
  • 48. The process of claim 39, wherein the semiconductor substrate comprises TiW.
  • 49. The process of claim 39, wherein the semiconductor substrate poses SiN.
  • 50. The process of claim 39, wherein the semiconductor substrate comprises Al/Si/Cu.
  • 51. The process of claim 39, wherein the substrate comprises titanium metal.
  • 52. The process of claim 39, wherein the substrate comprises tungsten metal.
  • 53. The process of claim 39, wherein the substrate comprises aluminum metal.
CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No. 09/444,548 filed Nov. 22, 1999, now U.S. Pat. No. 6,399,551, which is a divisional of application Ser. No. 08/815,616 filed Mar. 11, 1997, now U.S. Pat. No. 6,121,217, which is a continuation-in-part of application Ser. No. 08/628,060 filed Apr. 17, 1996, now U.S. Pat. No. 6,187,730, which is a continuation-in-part of application Ser. No. 08/078,657 filed Jun. 21, 1993, now abandoned, the disclosures of which are incorporated herein by reference thereto.

US Referenced Citations (75)
Number Name Date Kind
3160539 Hall et al. Dec 1964 A
3530186 Greco Sep 1970 A
3582401 Berilla et al. Jun 1971 A
3649395 Lee Mar 1972 A
3753933 Olstowski et al. Aug 1973 A
4111767 Kawagishi et al. Sep 1978 A
4155866 Berkenblit et al. May 1979 A
4165294 Vander Mey Aug 1979 A
4168989 Edelman et al. Sep 1979 A
4221674 Vander Mey Sep 1980 A
4238275 Shih Dec 1980 A
4239661 Muraoka et al. Dec 1980 A
4242218 Vander Mey Dec 1980 A
4264716 Vincent et al. Apr 1981 A
4268406 O'Brien et al. May 1981 A
4276185 Martin Jun 1981 A
4278635 Kerst Jul 1981 A
4279870 Natansohn et al. Jul 1981 A
RE30714 Harriman et al. Aug 1981 E
4282111 Ciuba Aug 1981 A
4284435 Fox Aug 1981 A
4289645 Muccitelli Sep 1981 A
4294729 Bakos et al. Oct 1981 A
RE30796 Lesinski Nov 1981 E
4395348 Lee Jul 1983 A
4482626 Twist et al. Nov 1984 A
4487708 Muccitelli Dec 1984 A
4539230 Shimizu et al. Sep 1985 A
4549968 Muccitelli Oct 1985 A
4595519 Takano et al. Jun 1986 A
4617251 Sizensky Oct 1986 A
4626411 Nemes et al. Dec 1986 A
4699868 Sabongi Oct 1987 A
4732887 Obanawa et al. Mar 1988 A
4737195 Carandang et al. Apr 1988 A
4765844 Merrem et al. Aug 1988 A
4824763 Lee Apr 1989 A
4824949 Lachhein et al. Apr 1989 A
4834912 Hodgens, et al. May 1989 A
4861386 Hoy Aug 1989 A
4873136 Foust et al. Oct 1989 A
4888244 Masubuchi et al. Dec 1989 A
4895703 Zupanovich et al. Jan 1990 A
4929301 Beechko May 1990 A
4941941 Austin et al. Jul 1990 A
4980077 Morris et al. Dec 1990 A
5015298 Arrington May 1991 A
5022926 Kreh et al. Jun 1991 A
5049201 Cheng et al. Sep 1991 A
5073622 Wojtech et al. Dec 1991 A
5091103 Dean et al. Feb 1992 A
5185235 Sato et al. Feb 1993 A
5279771 Lee Jan 1994 A
5288332 Pastilnik et al. Feb 1994 A
5290361 Hayashida et al. Mar 1994 A
5308745 Schwartzkopf May 1994 A
5334332 Lee Aug 1994 A
5381807 Lee Jan 1995 A
5399464 Lee Mar 1995 A
5407788 Fang Apr 1995 A
5417877 Ward May 1995 A
5419779 Ward May 1995 A
5482566 Lee Jan 1996 A
5496491 Ward et al. Mar 1996 A
5554312 Ward Sep 1996 A
5556482 Ward et al. Sep 1996 A
5563119 Ward Oct 1996 A
5672577 Lee Sep 1997 A
5902780 Lee May 1999 A
5911835 Lee et al. Jun 1999 A
5928430 Ward et al. Jul 1999 A
5981454 Small Nov 1999 A
6000411 Lee Dec 1999 A
6187730 Lee Feb 2001 B1
6399551 Lee Jun 2002 B1
Foreign Referenced Citations (10)
Number Date Country
1144481 Mar 1969 GB
55-52379 Apr 1980 JP
56-5899 Jan 1981 JP
62-49355 Mar 1987 JP
62-95531 May 1987 JP
63-183445 Jul 1988 JP
64-21088 Jan 1989 JP
1-105949 Apr 1989 JP
1-159388 Jun 1989 JP
5-259066 Oct 1993 JP
Non-Patent Literature Citations (6)
Entry
MSDS, Experimental Stripper, WMX-225 (1 sheet) (1995).
MSDS, Experimental Stripper, WMX-230 (1 sheet) (1995).
Large Diameter Silicon Wafer Cleaning Technology, Semicon/West 1944.
Ultraclean Technology: ULSI Processing's Crucial Factor, T. Ohmi, Microcontamination, Oct. 1988, pp. 49-52.
Photoresist: Materials and Processes, pp. 63, 64, and 246 (1993).
ACT 935 Technical Bulletin, ACT, Inc, 1994.
Continuations (1)
Number Date Country
Parent 09/444548 Nov 1999 US
Child 10/160035 US
Continuation in Parts (2)
Number Date Country
Parent 08/628060 Apr 1996 US
Child 08/815616 US
Parent 08/078657 Jun 1993 US
Child 08/628060 US