US20030047464A1 - Electrochemically roughened aluminum semiconductor processing apparatus surfaces - Google Patents

Electrochemically roughened aluminum semiconductor processing apparatus surfaces Download PDF

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US20030047464A1
US20030047464A1 US09/918,683 US91868301A US2003047464A1 US 20030047464 A1 US20030047464 A1 US 20030047464A1 US 91868301 A US91868301 A US 91868301A US 2003047464 A1 US2003047464 A1 US 2003047464A1
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aluminum
semiconductor processing
ranges
chamber
aluminum alloy
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US09/918,683
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Jennifer Sun
Clifford Stow
Senh Thach
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Applied Materials Inc
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Applied Materials Inc
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Priority to US09/918,683 priority Critical patent/US20030047464A1/en
Assigned to APPLIED MATERIALS, INC. reassignment APPLIED MATERIALS, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: STOW, CLIFF, SUN, JENNIFER Y., THACH, SENH
Priority to KR10-2003-7015103A priority patent/KR20040030619A/en
Priority to CNB028121333A priority patent/CN1267578C/en
Priority to PCT/US2002/023287 priority patent/WO2003012162A1/en
Priority to EP02768339A priority patent/EP1415016A1/en
Priority to TW091116827A priority patent/TWI223347B/en
Publication of US20030047464A1 publication Critical patent/US20030047464A1/en
Priority to US10/866,470 priority patent/US20040224171A1/en
Abandoned legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/44Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25FPROCESSES FOR THE ELECTROLYTIC REMOVAL OF MATERIALS FROM OBJECTS; APPARATUS THEREFOR
    • C25F3/00Electrolytic etching or polishing
    • C25F3/02Etching
    • C25F3/04Etching of light metals
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/44Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
    • C23C16/4401Means for minimising impurities, e.g. dust, moisture or residual gas, in the reaction chamber
    • C23C16/4404Coatings or surface treatment on the inside of the reaction chamber or on parts thereof
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/26Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
    • Y10T428/263Coating layer not in excess of 5 mils thick or equivalent
    • Y10T428/264Up to 3 mils
    • Y10T428/2651 mil or less

Definitions

  • the present invention pertains to an electrochemically roughened aluminum or aluminum alloy surface for use within a semiconductor processing chamber.
  • the present invention also pertains to a method of electrochemically roughening an aluminum or aluminum alloy surface.
  • the roughened surface is typically anodized to provide a finished surface for use in semiconductor processing.
  • Semiconductor manufacturing processes such as etch and deposition processes, utilize a wide variety of processing gases and substrate materials. Highly volatile process byproducts are typically removed from the processing chamber by application of vacuum. Less volatile byproducts may adhere to the interior surface of the processing chamber or may redeposit on the surface of the semiconductor substrate being processed. Most semiconductor manufacturers prefer to have redepositing byproducts deposit on processing chamber surfaces (rather than the substrate). The processing chamber surfaces are then periodically cleaned. Frequent chamber cleanings are expensive in terms of processing chamber downtime. The more redeposited byproducts which can be held by the processing chamber surfaces, the less frequent the cleaning requirement.
  • FIG. 1 Interior surfaces of semiconductor processing chambers are frequently aluminum.
  • One prior art semiconductor processing chamber includes anodized aluminum surfaces which have been lapped to have a surface roughness of only 4 Ra, which is essentially a mirror finish.
  • the highly polished, anodized aluminum surface developed numerous tiny cracks in the anodized layer, known as craze lines; these are shown in FIG. 1. While the craze lines 100 typically do not penetrate all of the way through the anodized layer to the boundary layer at the base aluminum beneath, they tend to spread across the anodized surface, producing a spider web pattern.
  • the anodized aluminum surface reacts with fluorine gas, causing the craze lines to fill with a self-passivating fluoride.
  • the craze lines may not interfere with the operation of the chamber during a fluorine-based etch process, they are cosmetically unappealing, and the user of the processing chamber tends to worry that fluorine-containing species may be passing through the protective anodized layer and corroding the aluminum surface beneath.
  • the craze lines do not fill with self-passivating fluoride and the anodized surface may eventually fail, exposing the aluminum beneath to corrosion by chlorine-containing species.
  • One method of improving the adhesion of semiconductor processing byproducts to an aluminum surface within a semiconductor processing chamber is to provide a roughened surface to which byproducts generated during processing can stick.
  • aluminum semiconductor chamber surfaces have been roughened by bead blasting.
  • bead blasting often is a manual process, in which it is difficult to control the uniformity and repeatability.
  • bead blasting typically provides a very sharp, jagged surface 200 on the aluminum, as shown in FIG. 2. Tips of the roughened aluminum can curl over, forming hook-shaped projections 202 which can break off or entrap particles 204 , including the bead blast particle itself.
  • the bead blasting media may act as a source of contamination of the aluminum surface.
  • Bead blasting is not useful as a roughening method for some of the softer aluminum alloys, such as the 1000 series, because the bead blasting particles can easily become embedded in the ductile metal. Further, the sharp surface provided by bead blasting may complicate a subsequent anodization process.
  • the roughening method should provide a surface which does not entrap particles, is free from jagged and hooked surface formations, and is easily anodized.
  • Applicants have discovered a uniform, controllable method for electrochemically roughening an aluminum-comprising surface intended for use within a semiconductor processing chamber.
  • the aluminum-comprising surface is aluminum or an aluminum alloy.
  • Applicants have also determined that if they electrochemically roughen an aluminum or aluminum alloy surface, they avoid the formation of jagged and hooked surface topography.
  • the surface which is formed by the electrochemical roughening provides a topography which resembles small rolling hills and valleys.
  • the estimated average height of the hills above the valleys is approximately 16 ⁇ m; the estimated average distance between the hills is approximately 50 ⁇ m, depending on the grade of the aluminum.
  • the height of the hills ranges from about 8 ⁇ m to about 25 ⁇ m, and the distance between the center of one hill and that of an adjacent hill ranges from about 30 ⁇ m to about 100 ⁇ m.
  • the hill and valley topography obtained by electrochemically roughening an aluminum or aluminum alloy surface relieves stress in an anodized finish subsequently produced over the roughened surface, so that the anodized layer does not crack upon thermal cycling up to about 300° C.
  • the amount of redepositing byproduct which can be accumulated over the hills and valleys is drastically increased over that which can be accumulated over a bead-blasted surface.
  • the number of substrate processing cycles prior to cleaning with the new, electrochemically roughened, aluminum or aluminum alloy anodized surface is about 5 times greater than with the bead blasted aluminum anodized surface.
  • Applicants' method for surface roughening can be used on aluminum and aluminum alloys in general, including but not limited to 6061 and LP (available from Alcan Alusuisse). Applicants' method promotes formation of a smooth, rolling-hilled, anodized surface which does not entrap particles. Further, applicants' electrochemically roughened aluminum-comprising surfaces provide increased surface area for collection of redepositing byproducts.
  • FIG. 1 shows a prior art anodized aluminum surface 100 which has been lapped to have a surface roughness of 4 Ra. Note the many craze lines 102 which have formed in the aluminum surface subsequent to exposure to process conditions, producing a spider web pattern.
  • FIG. 2 shows a prior art aluminum surface 200 which has been roughened using bead blasting. Note the many hook-shaped projections 202 which can break off or entrap particles 204 , including the bead blast particle itself.
  • FIG. 3 shows an aluminum surface 300 which has been roughened using applicants' electrochemical roughening method. Note the smooth, rolling topography of applicants' electrochemically roughened aluminum surface.
  • Applicants' invention pertains to a method of electrochemically roughening an aluminum-comprising surface.
  • the aluminum-comprising surface is aluminum or an aluminum alloy.
  • Aluminum is commonly alloyed with elements such as silicon, copper, zinc, magnesium, manganese, iron, titanium, and nickel, by way of example, and not by way of limitation.
  • Applicants' invention has use in semiconductor processing chambers which include electrochemically roughened aluminum surfaces, and particularly roughened surfaces having a protective coating thereover, such as an anodized aluminum coating.
  • Applicants' method for electrochemically roughening an aluminum-comprising surface comprises immersing the aluminum-comprising surface in an aqueous HCl solution having a concentration ranging from about 1 volume % to about 5 volume % at a temperature ranging from about 45° C. to about 80° C., then applying an electrical charge having a charge density ranging from about 80 amps/ft. 2 to about 250 amps/ft. 2 for a time period ranging from about 5 minutes to about 25 minutes.
  • Chelating agents such as, for example, but without limitation, gluconic acid, available from VWR Scientific Products, West Chester, Pa. may be added to the HCl solution to control the bath chemistry and conductivity.
  • Typical processing conditions for electrochemically roughening aluminum and aluminum alloys according to applicants' method are presented in Table One, below. TABLE ONE Typical Process Conditions for Electrochemically Roughening Aluminum and Aluminum Alloys Typical Preferred Optimum Process Process Known Process Process Parameter Conditions Conditions Conditions HCl Concentration (% volume) 1-5 1-3 1-1.5 Chelating Agent (% volume) 0.5-3 0.5-1.5 0.8-1.2 Tank Temperature (° C.) 45-80 50-70 55-65 AC Frequency (Hz) 60-120 80-100 85-95 Charge Density (amps/ft. 2 ) 80-250 120-250 150-250 Time (min.) 4-25 4-20 4-20
  • Unroughened, machined aluminum and aluminum alloy typically has a surface roughness ranging from about 12 Ra to about 32 Ra.
  • the aluminum or aluminum alloy surface typically has a surface roughness ranging from about 100 Ra to about 200 Ra, preferably ranging from about 110 Ra to about 160 Ra.
  • applicants' aluminum and aluminum alloy roughening method provides a surface 300 having a topography resembling small rolling hills and valleys.
  • the estimated average height of the hills above the valleys is approximately 16 ⁇ m; the estimated average distance between the hills is approximately 50 ⁇ m, depending on the grade of the aluminum.
  • the height of the hills ranges from about 8 ⁇ m to about 25 ⁇ m, and the distance between the center of one hill and that of an adjacent hill ranges from about 30 ⁇ m to about 100 ⁇ m.
  • Applicants' electrochemically roughened aluminum or aluminum alloy surface provides increased surface area for collection of redepositing byproducts, but does not entrap particles.
  • Applicants' electrochemical roughening method is particularly useful for roughening aluminum and aluminum alloy surfaces which are subsequently protected by a plasma-resistant coating, for use within semiconductor processing chambers, such as an etch chamber or a deposition chamber.
  • Applicants' method is particularly useful for roughening any apparatus surface which comes into contact with semiconductor processing byproducts.
  • Applicants' electrochemically roughened aluminum or aluminum alloy surface provides pockets in the hills and valleys which provide for the accumulation of semiconductor processing byproducts, such as etch byproducts or CVD deposition byproducts, preventing the byproducts from redepositing on the surface of the semiconductor substrate being processed. It is helpful to use a protective coating applied over the aluminum or aluminum alloy surface which provides for adhesion of depositing byproducts.
  • Example protective coatings include anodic oxide, flame spray-deposited aluminum oxide, and other ceramic coatings which may be conductive or non-conductive.
  • fluorine and carbon from the etch process react to form a polymer which easily adheres to an electrochemically roughened, anodized aluminum surface.
  • Applicants' electrochemically roughened, anodized aluminum or anodized aluminum alloy surfaces can be included in etch chambers which are used for etching dielectric materials (including inorganic dielectric materials, such as silicon oxide, silicon nitride, silicon oxynitride, and tantalum pentoxide, and organic dielectric materials, such as an organic low-k dielectric material), metals (such as aluminum, copper, titanium, tantalum, and tungsten), and polysilicon, by way of example, and not by way of limitation.
  • dielectric materials including inorganic dielectric materials, such as silicon oxide, silicon nitride, silicon oxynitride, and tantalum pentoxide, and organic dielectric materials, such as an organic low-k dielectric material), metals (such as aluminum, copper, titanium, tantalum, and tungsten), and polysilicon, by way of example, and not by way of limitation.
  • Applicants' method can be used to create roughened surfaces for semiconductor processing chamber components such as wall liners, cathode liners, slit valve doors, slit valve liners, buffer inserts, and gas distribution plates, by way of example, and not by way of limitation.
  • Anodization of applicants' electrochemically roughened aluminum and aluminum alloy surfaces can be performed using conventional aluminum anodization techniques known in the art, such as by following Mil Standard No. A-8625F, by way of example, and not by way of limitation. Because applicants' roughening method relieves stress within the aluminum or aluminum alloy surface, the resulting anodized surface does not form craze lines, even when subjected to the temperature cycling which occurs due to particular semiconductor manufacturing processes.
  • Ceramic coatings either conductive or non-conductive, may be applied over a roughened, anodized surface.

Abstract

A uniform, controllable method for electrochemically roughening an aluminum-comprising surface to be used in a semiconductor processing apparatus is disclosed Typically the aluminum-comprising surface is aluminum or an aluminum alloy. The method involves immersing an aluminum-comprising surface in an HCl solution having a concentration ranging from about 1 volume % to about 5 volume %, at a temperature within the range of about 45° C. to about 80° C., then applying an electrical charge having a charge density ranging from about 80 amps/ft.2 to about 250 amps/ft.2 for a time period ranging from about 4 minutes to about 25 minutes. A chelating agent may be added to enhance the roughening process. The electrochemical roughening method can be used on aluminum alloys in general, including but not limited to 6061 and LP. The electrochemical roughening provides a smoothly rolling surface which does not entrap particles and which provides increased surface area for semiconductor process byproduct adhesion. The roughened surface provides an excellent surface for subsequent anodization.

Description

    BACKGROUND OF THE INVENTION
  • 1. Field of the Invention [0001]
  • The present invention pertains to an electrochemically roughened aluminum or aluminum alloy surface for use within a semiconductor processing chamber. The present invention also pertains to a method of electrochemically roughening an aluminum or aluminum alloy surface. The roughened surface is typically anodized to provide a finished surface for use in semiconductor processing. [0002]
  • 2. Brief Description of the Background Art [0003]
  • Semiconductor manufacturing processes, such as etch and deposition processes, utilize a wide variety of processing gases and substrate materials. Highly volatile process byproducts are typically removed from the processing chamber by application of vacuum. Less volatile byproducts may adhere to the interior surface of the processing chamber or may redeposit on the surface of the semiconductor substrate being processed. Most semiconductor manufacturers prefer to have redepositing byproducts deposit on processing chamber surfaces (rather than the substrate). The processing chamber surfaces are then periodically cleaned. Frequent chamber cleanings are expensive in terms of processing chamber downtime. The more redeposited byproducts which can be held by the processing chamber surfaces, the less frequent the cleaning requirement. [0004]
  • Interior surfaces of semiconductor processing chambers are frequently aluminum. One prior art semiconductor processing chamber includes anodized aluminum surfaces which have been lapped to have a surface roughness of only 4 Ra, which is essentially a mirror finish. However, when subjected to the high temperatures and processing conditions used in many semiconductor manufacturing processes, the highly polished, anodized aluminum surface developed numerous tiny cracks in the anodized layer, known as craze lines; these are shown in FIG. 1. While the [0005] craze lines 100 typically do not penetrate all of the way through the anodized layer to the boundary layer at the base aluminum beneath, they tend to spread across the anodized surface, producing a spider web pattern. During a fluorine-based etch process, the anodized aluminum surface reacts with fluorine gas, causing the craze lines to fill with a self-passivating fluoride. Although the craze lines may not interfere with the operation of the chamber during a fluorine-based etch process, they are cosmetically unappealing, and the user of the processing chamber tends to worry that fluorine-containing species may be passing through the protective anodized layer and corroding the aluminum surface beneath. Further, in a non-fluorine-based environment (such as during a chlorine-based etch process), the craze lines do not fill with self-passivating fluoride and the anodized surface may eventually fail, exposing the aluminum beneath to corrosion by chlorine-containing species.
  • During a number of semiconductor processing procedures, byproducts are formed which are not sufficiently volatile to be removed by the vacuum system of the processing chamber. In many instances, it is desirable to provide a surface inside the processing chamber on which these byproducts are capable of adhering, so that they will not fall upon semiconductor workpieces during processing, causing contamination. [0006]
  • One method of improving the adhesion of semiconductor processing byproducts to an aluminum surface within a semiconductor processing chamber is to provide a roughened surface to which byproducts generated during processing can stick. Typically, aluminum semiconductor chamber surfaces have been roughened by bead blasting. However, bead blasting often is a manual process, in which it is difficult to control the uniformity and repeatability. Further, bead blasting typically provides a very sharp, jagged surface [0007] 200 on the aluminum, as shown in FIG. 2. Tips of the roughened aluminum can curl over, forming hook-shaped projections 202 which can break off or entrap particles 204, including the bead blast particle itself. As a result, the bead blasting media may act as a source of contamination of the aluminum surface. Bead blasting is not useful as a roughening method for some of the softer aluminum alloys, such as the 1000 series, because the bead blasting particles can easily become embedded in the ductile metal. Further, the sharp surface provided by bead blasting may complicate a subsequent anodization process.
  • It would therefore be desirable to provide a uniform and controllable method for roughening an aluminum surface which could be used for all aluminum alloys. In particular, the roughening method should provide a surface which does not entrap particles, is free from jagged and hooked surface formations, and is easily anodized. [0008]
  • SUMMARY OF THE INVENTION
  • Applicants have discovered a uniform, controllable method for electrochemically roughening an aluminum-comprising surface intended for use within a semiconductor processing chamber. Typically the aluminum-comprising surface is aluminum or an aluminum alloy. Applicants have also determined that if they electrochemically roughen an aluminum or aluminum alloy surface, they avoid the formation of jagged and hooked surface topography. The surface which is formed by the electrochemical roughening provides a topography which resembles small rolling hills and valleys. The estimated average height of the hills above the valleys is approximately 16 μm; the estimated average distance between the hills is approximately 50 μm, depending on the grade of the aluminum. Typically, the height of the hills ranges from about 8 μm to about 25 μm, and the distance between the center of one hill and that of an adjacent hill ranges from about 30 μm to about 100 μm. [0009]
  • Surprisingly, the hill and valley topography obtained by electrochemically roughening an aluminum or aluminum alloy surface relieves stress in an anodized finish subsequently produced over the roughened surface, so that the anodized layer does not crack upon thermal cycling up to about 300° C. In addition, unexpectedly, the amount of redepositing byproduct which can be accumulated over the hills and valleys (including an anodized surface which mirrors the underlying aluminum surface) is drastically increased over that which can be accumulated over a bead-blasted surface. As a result, the number of substrate processing cycles prior to cleaning with the new, electrochemically roughened, aluminum or aluminum alloy anodized surface is about 5 times greater than with the bead blasted aluminum anodized surface. [0010]
  • Applicants' method for surface roughening can be used on aluminum and aluminum alloys in general, including but not limited to 6061 and LP (available from Alcan Alusuisse). Applicants' method promotes formation of a smooth, rolling-hilled, anodized surface which does not entrap particles. Further, applicants' electrochemically roughened aluminum-comprising surfaces provide increased surface area for collection of redepositing byproducts.[0011]
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 shows a prior art anodized [0012] aluminum surface 100 which has been lapped to have a surface roughness of 4 Ra. Note the many craze lines 102 which have formed in the aluminum surface subsequent to exposure to process conditions, producing a spider web pattern.
  • FIG. 2 shows a prior art aluminum surface [0013] 200 which has been roughened using bead blasting. Note the many hook-shaped projections 202 which can break off or entrap particles 204, including the bead blast particle itself.
  • FIG. 3 shows an [0014] aluminum surface 300 which has been roughened using applicants' electrochemical roughening method. Note the smooth, rolling topography of applicants' electrochemically roughened aluminum surface.
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • Applicants' invention pertains to a method of electrochemically roughening an aluminum-comprising surface. Typically the aluminum-comprising surface is aluminum or an aluminum alloy. Aluminum is commonly alloyed with elements such as silicon, copper, zinc, magnesium, manganese, iron, titanium, and nickel, by way of example, and not by way of limitation. Applicants' invention has use in semiconductor processing chambers which include electrochemically roughened aluminum surfaces, and particularly roughened surfaces having a protective coating thereover, such as an anodized aluminum coating. [0015]
  • Applicants' method for electrochemically roughening an aluminum-comprising surface comprises immersing the aluminum-comprising surface in an aqueous HCl solution having a concentration ranging from about 1 volume % to about 5 volume % at a temperature ranging from about 45° C. to about 80° C., then applying an electrical charge having a charge density ranging from about 80 amps/ft.[0016] 2 to about 250 amps/ft.2 for a time period ranging from about 5 minutes to about 25 minutes. Chelating agents (such as, for example, but without limitation, gluconic acid, available from VWR Scientific Products, West Chester, Pa.) may be added to the HCl solution to control the bath chemistry and conductivity.
  • Typical processing conditions for electrochemically roughening aluminum and aluminum alloys according to applicants' method are presented in Table One, below. [0017]
    TABLE ONE
    Typical Process Conditions for Electrochemically Roughening
    Aluminum and Aluminum Alloys
    Typical Preferred Optimum
    Process Process Known Process
    Process Parameter Conditions Conditions Conditions
    HCl Concentration (% volume) 1-5 1-3   1-1.5
    Chelating Agent (% volume) 0.5-3   0.5-1.5 0.8-1.2
    Tank Temperature (° C.) 45-80 50-70 55-65
    AC Frequency (Hz)  60-120  80-100 85-95
    Charge Density (amps/ft.2)  80-250 120-250 150-250
    Time (min.)  4-25  4-20  4-20
  • Processing conditions will need to be adjusted depending on the specific chemical composition of the particular aluminum alloy being roughened. Applicants have performed electrochemical roughening of several commercially available aluminum alloys. Specific processing conditions used during the electrochemical roughening of these alloys are presented in Table Two, below. [0018]
    TABLE TWO
    Process Conditions for Electrochemically Roughening
    Particular Aluminum Alloys
    Alloy
    Process Condition 6061* LP**
    HCl Concentration (% volume) 1.0-1.5 1.0-1.5
    Gluconic Acid*** (% volume) 0.9-1.1 0.9-1.1
    (Chelating Agent)
    Tank Temperature (° C.) 55-65 55-65
    AC Frequency (Hz) 85-95 85-95
    Charge Density (amps/ft.2) 175-250 175-250
    Time (min.)  6-12 4-8
  • Unroughened, machined aluminum and aluminum alloy typically has a surface roughness ranging from about 12 Ra to about 32 Ra. After performing applicants' electrochemical roughening method, the aluminum or aluminum alloy surface typically has a surface roughness ranging from about 100 Ra to about 200 Ra, preferably ranging from about 110 Ra to about 160 Ra. [0019]
  • As shown in FIG. 3, applicants' aluminum and aluminum alloy roughening method provides a [0020] surface 300 having a topography resembling small rolling hills and valleys. The estimated average height of the hills above the valleys is approximately 16 μm; the estimated average distance between the hills is approximately 50 μm, depending on the grade of the aluminum. Typically, the height of the hills ranges from about 8 μm to about 25 μm, and the distance between the center of one hill and that of an adjacent hill ranges from about 30 μm to about 100 μm. Applicants' electrochemically roughened aluminum or aluminum alloy surface provides increased surface area for collection of redepositing byproducts, but does not entrap particles.
  • Applicants' electrochemical roughening method is particularly useful for roughening aluminum and aluminum alloy surfaces which are subsequently protected by a plasma-resistant coating, for use within semiconductor processing chambers, such as an etch chamber or a deposition chamber. Applicants' method is particularly useful for roughening any apparatus surface which comes into contact with semiconductor processing byproducts. Applicants' electrochemically roughened aluminum or aluminum alloy surface provides pockets in the hills and valleys which provide for the accumulation of semiconductor processing byproducts, such as etch byproducts or CVD deposition byproducts, preventing the byproducts from redepositing on the surface of the semiconductor substrate being processed. It is helpful to use a protective coating applied over the aluminum or aluminum alloy surface which provides for adhesion of depositing byproducts. Example protective coatings include anodic oxide, flame spray-deposited aluminum oxide, and other ceramic coatings which may be conductive or non-conductive. [0021]
  • In particular, during a fluorine-based etch process, fluorine and carbon from the etch process react to form a polymer which easily adheres to an electrochemically roughened, anodized aluminum surface. [0022]
  • Applicants' electrochemically roughened, anodized aluminum or anodized aluminum alloy surfaces can be included in etch chambers which are used for etching dielectric materials (including inorganic dielectric materials, such as silicon oxide, silicon nitride, silicon oxynitride, and tantalum pentoxide, and organic dielectric materials, such as an organic low-k dielectric material), metals (such as aluminum, copper, titanium, tantalum, and tungsten), and polysilicon, by way of example, and not by way of limitation. [0023]
  • Applicants' method can be used to create roughened surfaces for semiconductor processing chamber components such as wall liners, cathode liners, slit valve doors, slit valve liners, buffer inserts, and gas distribution plates, by way of example, and not by way of limitation. [0024]
  • Anodization of applicants' electrochemically roughened aluminum and aluminum alloy surfaces can be performed using conventional aluminum anodization techniques known in the art, such as by following Mil Standard No. A-8625F, by way of example, and not by way of limitation. Because applicants' roughening method relieves stress within the aluminum or aluminum alloy surface, the resulting anodized surface does not form craze lines, even when subjected to the temperature cycling which occurs due to particular semiconductor manufacturing processes. [0025]
  • Other protective, plasma-resistant coatings, such as flame spray-deposited aluminum oxide and other ceramic coatings, can be deposited or applied over a roughened aluminum or aluminum alloy surface using techniques known in the art. Ceramic coatings, either conductive or non-conductive, may be applied over a roughened, anodized surface. [0026]
  • The above described preferred embodiments are not intended to limit the scope of the present invention, as one skilled in the art can, in view of the present disclosure expand such embodiments to correspond with the subject matter of the invention claimed below. [0027]

Claims (45)

We claim:
1. A semiconductor processing chamber having at least one interior surface comprising electrochemically roughened aluminum or aluminum alloy.
2. The semiconductor processing chamber of claim 1, wherein said at least one interior surface has a surface roughness ranging from about 100 Ra to about 200 Ra.
3. The semiconductor processing chamber of claim 2, wherein said surface roughness ranges from about 110 Ra to about 160 Ra.
4. The semiconductor processing chamber of claim 1, wherein said electrochemically roughened aluminum or aluminum alloy surface has the appearance of rolling hills and valleys, when magnified.
5. The semiconductor processing chamber of claim 4, wherein the height of said hills ranges from about 8 μm to about 25 μm.
6. The semiconductor processing chamber of claim 4 or claim 5, wherein the distance between the center of one hill and the center of an adjacent hill ranges from about 30 μm to about 100 μm.
7. The semiconductor processing chamber of claim 1, wherein said electrochemically roughened aluminum or aluminum alloy surface underlies a coating selected from the group consisting of an anodized coating, a flame spray-deposited aluminum oxide coating, a ceramic coating, and an anodized coating having a ceramic coating applied thereover.
8. The semiconductor processing chamber of claim 1, wherein byproducts generated during an etch process or a deposition process adhere to said electrochemically roughened aluminum surface.
9. The semiconductor processing chamber of claim 1, wherein said semiconductor processing chamber is selected from the group consisting of an etch chamber and a deposition chamber.
10. The semiconductor processing chamber of claim 9, wherein said semiconductor processing chamber is an etch chamber which is used for etching a material selected from the group consisting of a dielectric material, a metal, and polysilicon.
11. The semiconductor processing chamber of claim 9, wherein said semiconductor processing chamber is an etch chamber, and wherein fluorine and carbon from an etch process react to form a polymer which adheres to said electrochemically roughened aluminum surface.
12. A processing component for use within a semiconductor processing chamber, wherein said processing component has at least one electrochemically roughen ed aluminum or aluminum alloy surface.
13. The processing component of claim 12, wherein said electrochemically roughened aluminum or aluminum alloy surface has a surface roughness ranging from about 100 Ra to about 200 Ra.
14. The processing component of claim 13, wherein said surface roughness ranges from about 110 Ra to about 160 Ra.
15. The processing component of claim 12, wherein said electrochemically roughened aluminum or aluminum alloy surface has the appearance of rolling hills and valleys, when magnified.
16. The processing component of claim 15, wherein the height of said hills ranges from about 8 μm to about 25 μm.
17. The processing component of claim 15 or claim 16, wherein the distance between the center of one hill and the center of an adjacent hill ranges from about 30 μm to about 100 μm.
18. The processing component of claim 12, wherein said electrochemically roughened aluminum or aluminum alloy surface underlies a coating selected from the group consisting of an anodized coating, a flame spray-deposited aluminum oxide coating, a ceramic coating, and an anodized coating having a ceramic coating applied thereover.
19. The processing component of claim 12, wherein byproducts generated during an etch process or a deposition process adhere to said electrochemically roughened aluminum or aluminum alloy surface.
20. The processing component of claim 12, wherein said processing component is used within a semiconductor processing chamber selected from the group consisting of an etch chamber and a deposition chamber.
21. The processing component of claim 20, wherein said semiconductor processing chamber is an etch chamber which is used for etching a material selected from the group consisting of a dielectric material, a metal, and polysilicon.
22. The processing component of claim 20, wherein said semiconductor processing chamber is an etch chamber, and wherein fluorine and carbon from an etch process react to form a polymer which adheres to said electrochemically roughened surface.
23. The processing component of claim 12, wherein said processing component is selected from the group consisting of: a wall liner, a cathode liner, a slit valve door, a slit valve liner, a buffer insert, and a gas distribution plate.
24. A semiconductor processing apparatus surface, wherein said surface comprises electrochemically roughened aluminum or aluminum alloy.
25. The semiconductor processing apparatus surface of claim 24, wherein said surface has a surface roughness ranging from about 100 Ra to about 200 Ra.
26. The semiconductor processing apparatus surface of claim 25, wherein said surface roughness ranges from about 110 Ra to about 160 Ra.
27. The semiconductor processing apparatus surface of claim 24, wherein said electrochemically roughened aluminum or aluminum alloy surface has the appearance of rolling hills and valleys, when magnified.
28. The semiconductor processing apparatus surface of claim 27, wherein the height of said hills ranges from about 8 μm to about 25 μm.
29. The semiconductor processing apparatus surface of claim 27 or claim 28, wherein the distance between the center of one hill and the center of an adjacent hill ranges from about 30 μm to about 100 μm.
30. The semiconductor processing apparatus surface of claim 24, wherein said surface underlies a coating selected from the group consisting of an anodized coating, a flame spray-deposited aluminum oxide coating, a ceramic coating, and an anodized coating having a ceramic coating applied thereover.
31. The semiconductor processing apparatus surface of claim 24, wherein byproducts generated during an etch process or a deposition process adhere to said electrochemically roughened surface.
32. The semiconductor processing apparatus surface of claim 31, wherein fluorine and carbon from an etch process react to form a polymer which adheres to said surface.
33. The semiconductor processing apparatus surface of claim 24, wherein said surface is present on an apparatus component selected from the group consisting of: a wall liner, a cathode liner, a slit valve door, a slit valve liner, a buffer insert, and a gas distribution plate.
34. A method for electrochemically roughening a surface comprising aluminum or an aluminum alloy, including the steps of:
a) immersing said surface in an HCl solution having a concentration ranging from about 1 volume % to about 5 volume %, at a temperature ranging from about 45 ° C. to about 80° C.; and
b) applying an electrical charge having a charge density ranging from about 80 amps/ft.2 to about 250 amps/ft.2 for a time period ranging from about 4 minutes to about 25 minutes.
35. The method of claim 34, wherein said HCl solution has a concentration ranging from about 1 volume % to about 3 volume %.
36. The method of claim 35, wherein said temperature of said HCl solution ranges from about 50° C. to about 70° C.
37. The method of claim 34, wherein said HCl solution further includes a chelating agent, and wherein said chelating agent is present at a concentration within the range of about 0.5 volume % to about 3 volume %.
38. The method of claim 37, wherein said chelating agent is gluconic acid.
39. The method of claim 34, wherein said charge density ranges from about 120 amps/ft.2 to about 250 amps/ft.2.
40. The method of claim 34, wherein said time period ranges from about 4 minutes to about 20 minutes.
41. The method of claim 34, wherein said aluminum-comprising surface is an aluminum alloy selected from the group consisting of 6061 and LP.
42. The method of claim 41, wherein said HCl solution concentration ranges from about 1 volume % to about 1.5 volume %; wherein said temperature of said HCl solution ranges from about 55° C. to about 65° C.; and wherein said charge density ranges from about 175 amps/ft.2 to about 250 amps/ft.2.
43. The method of claim 42, wherein said HCl solution further includes a gluconic acid chelating agent, which is present at a concentration within the range of about 0.9 volume % to about 1.1 volume %.
44. The method of claim 43, wherein said time period during which said charge density is present ranges from about 6 minutes to about 12 minutes, and the aluminum alloy is 6061.
45. The method of claim 43, wherein said wherein said time period during which said charge density is present ranges from about 4 minutes to about 8 minutes, and the aluminum alloy is LP.
US09/918,683 2001-07-27 2001-07-27 Electrochemically roughened aluminum semiconductor processing apparatus surfaces Abandoned US20030047464A1 (en)

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KR10-2003-7015103A KR20040030619A (en) 2001-07-27 2002-07-22 Electrochemically roughened aluminum semiconductor processing apparatus surfaces
CNB028121333A CN1267578C (en) 2001-07-27 2002-07-22 Electrochemically roughened aluminium semiconductor processing apparatus surface
PCT/US2002/023287 WO2003012162A1 (en) 2001-07-27 2002-07-22 Electrochemically roughened aluminum semiconductor processing apparatus surfaces
EP02768339A EP1415016A1 (en) 2001-07-27 2002-07-22 Electrochemically roughened aluminum semiconductor processing apparatus surfaces
TW091116827A TWI223347B (en) 2001-07-27 2002-07-26 Electrochemically roughened aluminum semiconductor processing apparatus surfaces and method of preparing such surfaces
US10/866,470 US20040224171A1 (en) 2001-07-27 2004-06-10 Electrochemically roughened aluminum semiconductor chamber surfaces

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Cited By (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030057179A1 (en) * 1999-12-28 2003-03-27 Applied Materials, Inc. System level in-situ integrated dielectric etch process particularly useful for copper dual damascene
US20030173526A1 (en) * 2002-03-13 2003-09-18 Applied Materials, Inc. Method of surface texturizing
US20040056211A1 (en) * 2002-03-13 2004-03-25 Applied Materials, Inc. Method of surface texturizing
US20040224171A1 (en) * 2001-07-27 2004-11-11 Sun Jennifer Y. Electrochemically roughened aluminum semiconductor chamber surfaces
US6902627B2 (en) 2002-11-25 2005-06-07 Applied Materials, Inc. Cleaning chamber surfaces to recover metal-containing compounds
WO2005068681A2 (en) * 2003-12-19 2005-07-28 Applied Materials, Inc. Cleaning tantalum-containing deposits from process chamber components
US20050271984A1 (en) * 2004-06-07 2005-12-08 Applied Materials, Inc. Textured chamber surface
US20060032586A1 (en) * 2003-05-09 2006-02-16 Applied Materials, Inc. Reducing electrostatic charge by roughening the susceptor
US20060105182A1 (en) * 2004-11-16 2006-05-18 Applied Materials, Inc. Erosion resistant textured chamber surface
US20060110620A1 (en) * 2004-11-24 2006-05-25 Applied Materials, Inc. Process chamber component with layered coating and method
US20060159940A1 (en) * 2005-01-18 2006-07-20 Applied Materials, Inc. Corrosion-resistant aluminum component having multi-layer coating
US20060185795A1 (en) * 2003-05-09 2006-08-24 Applied Materials, Inc. Anodized substrate support
US20060239471A1 (en) * 2003-08-27 2006-10-26 Sony Computer Entertainment Inc. Methods and apparatus for targeted sound detection and characterization
US20060264259A1 (en) * 2002-07-27 2006-11-23 Zalewski Gary M System for tracking user manipulations within an environment
US20060264258A1 (en) * 2002-07-27 2006-11-23 Zalewski Gary M Multi-input game control mixer
US20060274911A1 (en) * 2002-07-27 2006-12-07 Xiadong Mao Tracking device with sound emitter for use in obtaining information for controlling game program execution
US20060274032A1 (en) * 2002-07-27 2006-12-07 Xiadong Mao Tracking device for use in obtaining information for controlling game program execution
US20060287084A1 (en) * 2002-07-27 2006-12-21 Xiadong Mao System, method, and apparatus for three-dimensional input control
US20060287085A1 (en) * 2002-07-27 2006-12-21 Xiadong Mao Inertially trackable hand-held controller
US20060292310A1 (en) * 2005-06-27 2006-12-28 Applied Materials, Inc. Process kit design to reduce particle generation
US20070021208A1 (en) * 2002-07-27 2007-01-25 Xiadong Mao Obtaining input for controlling execution of a game program
US20070025562A1 (en) * 2003-08-27 2007-02-01 Sony Computer Entertainment Inc. Methods and apparatus for targeted sound detection
US20070059460A1 (en) * 2005-09-09 2007-03-15 Applied Materials, Inc. Flow-formed chamber component having a textured surface
US20070060336A1 (en) * 2003-09-15 2007-03-15 Sony Computer Entertainment Inc. Methods and systems for enabling depth and direction detection when interfacing with a computer program
US20070102286A1 (en) * 2005-10-31 2007-05-10 Applied Materials, Inc. Process kit and target for substrate processing chamber
US20070113783A1 (en) * 2005-11-19 2007-05-24 Applied Materials, Inc. Band shield for substrate processing chamber
US20070173059A1 (en) * 2005-11-25 2007-07-26 Applied Materials, Inc. Process kit components for titanium sputtering chamber
US20070178810A1 (en) * 2006-01-27 2007-08-02 Applied Materials, Inc. Particle reduction on surfaces of chemical vapor deposition processing apparatus
US20070260340A1 (en) * 2006-05-04 2007-11-08 Sony Computer Entertainment Inc. Ultra small microphone array
US20070274535A1 (en) * 2006-05-04 2007-11-29 Sony Computer Entertainment Inc. Echo and noise cancellation
US20070283884A1 (en) * 2006-05-30 2007-12-13 Applied Materials, Inc. Ring assembly for substrate processing chamber
US20080178801A1 (en) * 2007-01-29 2008-07-31 Applied Materials, Inc. Process kit for substrate processing chamber
US20080295872A1 (en) * 2007-05-30 2008-12-04 Applied Materials, Inc. Substrate cleaning chamber and components
US20090084317A1 (en) * 2007-09-28 2009-04-02 Applied Materials, Inc. Atomic layer deposition chamber and components
US20090194414A1 (en) * 2008-01-31 2009-08-06 Nolander Ira G Modified sputtering target and deposition components, methods of production and uses thereof
US7670436B2 (en) 2004-11-03 2010-03-02 Applied Materials, Inc. Support ring assembly
US20110014981A1 (en) * 2006-05-08 2011-01-20 Sony Computer Entertainment Inc. Tracking device with sound emitter for use in obtaining information for controlling game program execution
US7910218B2 (en) 2003-10-22 2011-03-22 Applied Materials, Inc. Cleaning and refurbishing chamber components having metal coatings
US7964085B1 (en) 2002-11-25 2011-06-21 Applied Materials, Inc. Electrochemical removal of tantalum-containing materials
US8617672B2 (en) 2005-07-13 2013-12-31 Applied Materials, Inc. Localized surface annealing of components for substrate processing chambers
US20150064450A1 (en) * 2013-08-29 2015-03-05 Applied Materials, Inc. Anodization architecture for electro-plate adhesion
US9101954B2 (en) 2013-09-17 2015-08-11 Applied Materials, Inc. Geometries and patterns for surface texturing to increase deposition retention
US9460898B2 (en) 2014-08-08 2016-10-04 Applied Materials, Inc. Plasma generation chamber with smooth plasma resistant coating
US9583369B2 (en) 2013-07-20 2017-02-28 Applied Materials, Inc. Ion assisted deposition for rare-earth oxide based coatings on lids and nozzles
US9663870B2 (en) 2013-11-13 2017-05-30 Applied Materials, Inc. High purity metallic top coat for semiconductor manufacturing components
US9711334B2 (en) 2013-07-19 2017-07-18 Applied Materials, Inc. Ion assisted deposition for rare-earth oxide based thin film coatings on process rings
US9725799B2 (en) 2013-12-06 2017-08-08 Applied Materials, Inc. Ion beam sputtering with ion assisted deposition for coatings on chamber components
US9850591B2 (en) 2013-03-14 2017-12-26 Applied Materials, Inc. High purity aluminum top coat on substrate
US9850568B2 (en) 2013-06-20 2017-12-26 Applied Materials, Inc. Plasma erosion resistant rare-earth oxide based thin film coatings
US9869013B2 (en) 2014-04-25 2018-01-16 Applied Materials, Inc. Ion assisted deposition top coat of rare-earth oxide
JP2018502223A (en) * 2014-12-15 2018-01-25 アプライド マテリアルズ インコーポレイテッドApplied Materials,Incorporated Method for texturing a chamber component and chamber component having a textured surface
US10196728B2 (en) 2014-05-16 2019-02-05 Applied Materials, Inc. Plasma spray coating design using phase and stress control
US10336656B2 (en) 2012-02-21 2019-07-02 Applied Materials, Inc. Ceramic article with reduced surface defect density
US10364197B2 (en) 2012-02-22 2019-07-30 Applied Materials, Inc. Heat treated ceramic substrate having ceramic coating
US10730798B2 (en) 2014-05-07 2020-08-04 Applied Materials, Inc. Slurry plasma spray of plasma resistant ceramic coating
US10815562B2 (en) 2014-04-25 2020-10-27 Applied Materials, Inc. Plasma erosion resistant thin film coating for high temperature application
US20210225616A1 (en) * 2018-01-08 2021-07-22 Lam Research Corporation Components and Processes for Managing Plasma Process Byproduct Materials

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI342582B (en) * 2003-07-17 2011-05-21 Applied Materials Inc Method of surface texturizing
DE102010060143A1 (en) 2009-11-05 2011-06-09 Oerlikon Solar Ag, Trübbach Method for producing vacuum-processing chamber that is utilized in e.g. physical vapor deposition, involves defining volume of vacuum-processing chamber through wall, and smoothing and shot blasting inner surface of wall by grinding

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4468295A (en) * 1982-05-10 1984-08-28 Hoechst Aktiengesellschaft Process for electrochemically roughening aluminum for printing plate supports
US5275691A (en) * 1991-02-28 1994-01-04 Fuji Photo Film Co., Ltd. Method for treating a surface of an aluminum substrate for a printing plate
US5565058A (en) * 1992-08-27 1996-10-15 Applied Materials, Inc. Lid and door for a vacuum chamber and pretreatment therefor
US5755887A (en) * 1995-04-06 1998-05-26 Nihon Sinku Gijutsu Kabusiki Components of apparatus for film making and method for manufacturing the same
US5916454A (en) * 1996-08-30 1999-06-29 Lam Research Corporation Methods and apparatus for reducing byproduct particle generation in a plasma processing chamber
US6007673A (en) * 1996-10-02 1999-12-28 Matsushita Electronics Corporation Apparatus and method of producing an electronic device
US6444304B1 (en) * 1998-10-09 2002-09-03 Kabushiki Kaisha Kobe Seiko Sho (Kobe Steel, Ltd.) Anodic oxide layer and ceramic coating for aluminum alloy excellent in resistance to gas and plasma corrosion

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5193984A (en) * 1975-02-14 1976-08-18
US3963594A (en) * 1975-06-03 1976-06-15 Aluminum Company Of America Electrochemical treatment of aluminum surfaces with an aqueous solution of hydrochloric acid and gluconic acid
DE3217552A1 (en) * 1982-05-10 1983-11-10 Hoechst Ag, 6230 Frankfurt METHOD FOR ELECTROCHEMICALLY Roughening ALUMINUM FOR PRINTING PLATE CARRIERS
JPS59227494A (en) * 1983-06-09 1984-12-20 Fuji Photo Film Co Ltd Manufacture of support for lithographic plate
JPS6227192A (en) * 1985-07-26 1987-02-05 Fuji Photo Film Co Ltd Production of base for planographic plate
DE3533532A1 (en) * 1985-09-20 1987-04-02 Hoechst Ag METHOD FOR ELECTROCHEMICALLY Roughening ALUMINUM FOR PRINTING PLATE CARRIERS
JPH07119152B2 (en) * 1987-12-18 1995-12-20 富士写真フイルム株式会社 Method for electrolytically roughening aluminum support for lithographic printing plate
DE3934683A1 (en) * 1989-10-18 1991-04-25 Kurt Hausmann METHOD AND DEVICE FOR ELECTROCHEMICALLY Roughening A METAL SURFACE
GB9112211D0 (en) * 1991-06-06 1991-07-24 Alcan Int Ltd Treating a1 sheet
US5186795A (en) * 1991-07-22 1993-02-16 Eastman Kodak Company Two-stage process for electrolytic graining of aluminum
KR100348378B1 (en) * 1993-09-21 2002-11-29 알칸 인터내셔널 리미티드 Rolled aluminum sheet, flat plate support comprising the same, and a method of manufacturing thereof, and flat plate containing the above flat plate support
GB9326150D0 (en) * 1993-12-22 1994-02-23 Alcan Int Ltd Electrochemical roughening method
US5728503A (en) * 1995-12-04 1998-03-17 Bayer Corporation Lithographic printing plates having specific grained and anodized aluminum substrate
US6120640A (en) * 1996-12-19 2000-09-19 Applied Materials, Inc. Boron carbide parts and coatings in a plasma reactor
JP3160229B2 (en) * 1997-06-06 2001-04-25 日本エー・エス・エム株式会社 Susceptor for plasma CVD apparatus and method for manufacturing the same
JP3591701B2 (en) * 1998-12-14 2004-11-24 三菱製紙株式会社 Lithographic printing plate
US20030047464A1 (en) * 2001-07-27 2003-03-13 Applied Materials, Inc. Electrochemically roughened aluminum semiconductor processing apparatus surfaces

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4468295A (en) * 1982-05-10 1984-08-28 Hoechst Aktiengesellschaft Process for electrochemically roughening aluminum for printing plate supports
US5275691A (en) * 1991-02-28 1994-01-04 Fuji Photo Film Co., Ltd. Method for treating a surface of an aluminum substrate for a printing plate
US5565058A (en) * 1992-08-27 1996-10-15 Applied Materials, Inc. Lid and door for a vacuum chamber and pretreatment therefor
US5755887A (en) * 1995-04-06 1998-05-26 Nihon Sinku Gijutsu Kabusiki Components of apparatus for film making and method for manufacturing the same
US5916454A (en) * 1996-08-30 1999-06-29 Lam Research Corporation Methods and apparatus for reducing byproduct particle generation in a plasma processing chamber
US6007673A (en) * 1996-10-02 1999-12-28 Matsushita Electronics Corporation Apparatus and method of producing an electronic device
US6444304B1 (en) * 1998-10-09 2002-09-03 Kabushiki Kaisha Kobe Seiko Sho (Kobe Steel, Ltd.) Anodic oxide layer and ceramic coating for aluminum alloy excellent in resistance to gas and plasma corrosion

Cited By (113)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6793835B2 (en) 1999-12-28 2004-09-21 Lee Luo System level in-situ integrated dielectric etch process particularly useful for copper dual damascene
US20030057179A1 (en) * 1999-12-28 2003-03-27 Applied Materials, Inc. System level in-situ integrated dielectric etch process particularly useful for copper dual damascene
US20040224171A1 (en) * 2001-07-27 2004-11-11 Sun Jennifer Y. Electrochemically roughened aluminum semiconductor chamber surfaces
US6933508B2 (en) 2002-03-13 2005-08-23 Applied Materials, Inc. Method of surface texturizing
US20030173526A1 (en) * 2002-03-13 2003-09-18 Applied Materials, Inc. Method of surface texturizing
US20040056211A1 (en) * 2002-03-13 2004-03-25 Applied Materials, Inc. Method of surface texturizing
US6812471B2 (en) 2002-03-13 2004-11-02 Applied Materials, Inc. Method of surface texturizing
US20060264259A1 (en) * 2002-07-27 2006-11-23 Zalewski Gary M System for tracking user manipulations within an environment
US10086282B2 (en) 2002-07-27 2018-10-02 Sony Interactive Entertainment Inc. Tracking device for use in obtaining information for controlling game program execution
US20110086708A1 (en) * 2002-07-27 2011-04-14 Sony Computer Entertainment America Llc System for tracking user manipulations within an environment
US8675915B2 (en) 2002-07-27 2014-03-18 Sony Computer Entertainment America Llc System for tracking user manipulations within an environment
US20070021208A1 (en) * 2002-07-27 2007-01-25 Xiadong Mao Obtaining input for controlling execution of a game program
US20060287085A1 (en) * 2002-07-27 2006-12-21 Xiadong Mao Inertially trackable hand-held controller
US20060287084A1 (en) * 2002-07-27 2006-12-21 Xiadong Mao System, method, and apparatus for three-dimensional input control
US20060274032A1 (en) * 2002-07-27 2006-12-07 Xiadong Mao Tracking device for use in obtaining information for controlling game program execution
US20060274911A1 (en) * 2002-07-27 2006-12-07 Xiadong Mao Tracking device with sound emitter for use in obtaining information for controlling game program execution
US20060264258A1 (en) * 2002-07-27 2006-11-23 Zalewski Gary M Multi-input game control mixer
US7964085B1 (en) 2002-11-25 2011-06-21 Applied Materials, Inc. Electrochemical removal of tantalum-containing materials
US9068273B2 (en) 2002-11-25 2015-06-30 Quantum Global Technologies LLC Electrochemical removal of tantalum-containing materials
US6902627B2 (en) 2002-11-25 2005-06-07 Applied Materials, Inc. Cleaning chamber surfaces to recover metal-containing compounds
US20060032586A1 (en) * 2003-05-09 2006-02-16 Applied Materials, Inc. Reducing electrostatic charge by roughening the susceptor
US20060185795A1 (en) * 2003-05-09 2006-08-24 Applied Materials, Inc. Anodized substrate support
US7732010B2 (en) 2003-05-09 2010-06-08 Applied Materials, Inc. Method for supporting a glass substrate to improve uniform deposition thickness
US8947347B2 (en) 2003-08-27 2015-02-03 Sony Computer Entertainment Inc. Controlling actions in a video game unit
US20070025562A1 (en) * 2003-08-27 2007-02-01 Sony Computer Entertainment Inc. Methods and apparatus for targeted sound detection
US20060239471A1 (en) * 2003-08-27 2006-10-26 Sony Computer Entertainment Inc. Methods and apparatus for targeted sound detection and characterization
US7874917B2 (en) 2003-09-15 2011-01-25 Sony Computer Entertainment Inc. Methods and systems for enabling depth and direction detection when interfacing with a computer program
US20110034244A1 (en) * 2003-09-15 2011-02-10 Sony Computer Entertainment Inc. Methods and systems for enabling depth and direction detection when interfacing with a computer program
US20070060336A1 (en) * 2003-09-15 2007-03-15 Sony Computer Entertainment Inc. Methods and systems for enabling depth and direction detection when interfacing with a computer program
US7910218B2 (en) 2003-10-22 2011-03-22 Applied Materials, Inc. Cleaning and refurbishing chamber components having metal coatings
KR101223154B1 (en) * 2003-12-19 2013-01-17 퀀텀 글로벌 테크놀로지스, 엘엘씨 Cleaning tantalium-containing deposits from process chamber components
WO2005068681A2 (en) * 2003-12-19 2005-07-28 Applied Materials, Inc. Cleaning tantalum-containing deposits from process chamber components
WO2005068681A3 (en) * 2003-12-19 2005-09-15 Applied Materials Inc Cleaning tantalum-containing deposits from process chamber components
US20050271984A1 (en) * 2004-06-07 2005-12-08 Applied Materials, Inc. Textured chamber surface
US7618769B2 (en) 2004-06-07 2009-11-17 Applied Materials, Inc. Textured chamber surface
US20100059366A1 (en) * 2004-06-07 2010-03-11 Applied Materials, Inc. Textured chamber surface
US8142989B2 (en) 2004-06-07 2012-03-27 Quantum Global Technologies LLC Textured chamber surface
US7670436B2 (en) 2004-11-03 2010-03-02 Applied Materials, Inc. Support ring assembly
US20060105182A1 (en) * 2004-11-16 2006-05-18 Applied Materials, Inc. Erosion resistant textured chamber surface
US8021743B2 (en) 2004-11-24 2011-09-20 Applied Materials, Inc. Process chamber component with layered coating and method
US7579067B2 (en) 2004-11-24 2009-08-25 Applied Materials, Inc. Process chamber component with layered coating and method
US20100086805A1 (en) * 2004-11-24 2010-04-08 Applied Materials, Inc. Process chamber component with layered coating and method
US20060110620A1 (en) * 2004-11-24 2006-05-25 Applied Materials, Inc. Process chamber component with layered coating and method
JP2006241589A (en) * 2005-01-18 2006-09-14 Applied Materials Inc Corrosion-resistant aluminum component having multi-layer coating
US20060159940A1 (en) * 2005-01-18 2006-07-20 Applied Materials, Inc. Corrosion-resistant aluminum component having multi-layer coating
US7732056B2 (en) * 2005-01-18 2010-06-08 Applied Materials, Inc. Corrosion-resistant aluminum component having multi-layer coating
US20060292310A1 (en) * 2005-06-27 2006-12-28 Applied Materials, Inc. Process kit design to reduce particle generation
US8617672B2 (en) 2005-07-13 2013-12-31 Applied Materials, Inc. Localized surface annealing of components for substrate processing chambers
US9481608B2 (en) 2005-07-13 2016-11-01 Applied Materials, Inc. Surface annealing of components for substrate processing chambers
US20070059460A1 (en) * 2005-09-09 2007-03-15 Applied Materials, Inc. Flow-formed chamber component having a textured surface
US7762114B2 (en) 2005-09-09 2010-07-27 Applied Materials, Inc. Flow-formed chamber component having a textured surface
US11658016B2 (en) 2005-10-31 2023-05-23 Applied Materials, Inc. Shield for a substrate processing chamber
US20070102286A1 (en) * 2005-10-31 2007-05-10 Applied Materials, Inc. Process kit and target for substrate processing chamber
US10347475B2 (en) 2005-10-31 2019-07-09 Applied Materials, Inc. Holding assembly for substrate processing chamber
US9127362B2 (en) 2005-10-31 2015-09-08 Applied Materials, Inc. Process kit and target for substrate processing chamber
US20070113783A1 (en) * 2005-11-19 2007-05-24 Applied Materials, Inc. Band shield for substrate processing chamber
US20070173059A1 (en) * 2005-11-25 2007-07-26 Applied Materials, Inc. Process kit components for titanium sputtering chamber
US8790499B2 (en) 2005-11-25 2014-07-29 Applied Materials, Inc. Process kit components for titanium sputtering chamber
US8173228B2 (en) 2006-01-27 2012-05-08 Applied Materials, Inc. Particle reduction on surfaces of chemical vapor deposition processing apparatus
US20070178810A1 (en) * 2006-01-27 2007-08-02 Applied Materials, Inc. Particle reduction on surfaces of chemical vapor deposition processing apparatus
US20070274535A1 (en) * 2006-05-04 2007-11-29 Sony Computer Entertainment Inc. Echo and noise cancellation
US20070260340A1 (en) * 2006-05-04 2007-11-08 Sony Computer Entertainment Inc. Ultra small microphone array
US20110014981A1 (en) * 2006-05-08 2011-01-20 Sony Computer Entertainment Inc. Tracking device with sound emitter for use in obtaining information for controlling game program execution
US20070283884A1 (en) * 2006-05-30 2007-12-13 Applied Materials, Inc. Ring assembly for substrate processing chamber
US20100065216A1 (en) * 2006-05-30 2010-03-18 Applied Materials, Inc. Ring assembly for substrate processing chamber
US7981262B2 (en) 2007-01-29 2011-07-19 Applied Materials, Inc. Process kit for substrate processing chamber
US20080178801A1 (en) * 2007-01-29 2008-07-31 Applied Materials, Inc. Process kit for substrate processing chamber
US8980045B2 (en) 2007-05-30 2015-03-17 Applied Materials, Inc. Substrate cleaning chamber and components
US20080295872A1 (en) * 2007-05-30 2008-12-04 Applied Materials, Inc. Substrate cleaning chamber and components
US7942969B2 (en) 2007-05-30 2011-05-17 Applied Materials, Inc. Substrate cleaning chamber and components
US20090084317A1 (en) * 2007-09-28 2009-04-02 Applied Materials, Inc. Atomic layer deposition chamber and components
US20090194414A1 (en) * 2008-01-31 2009-08-06 Nolander Ira G Modified sputtering target and deposition components, methods of production and uses thereof
US10336656B2 (en) 2012-02-21 2019-07-02 Applied Materials, Inc. Ceramic article with reduced surface defect density
US11279661B2 (en) 2012-02-22 2022-03-22 Applied Materials, Inc. Heat treated ceramic substrate having ceramic coating
US10364197B2 (en) 2012-02-22 2019-07-30 Applied Materials, Inc. Heat treated ceramic substrate having ceramic coating
US10774436B2 (en) 2013-03-14 2020-09-15 Applied Materials, Inc. High purity aluminum top coat on substrate
US9850591B2 (en) 2013-03-14 2017-12-26 Applied Materials, Inc. High purity aluminum top coat on substrate
US9850568B2 (en) 2013-06-20 2017-12-26 Applied Materials, Inc. Plasma erosion resistant rare-earth oxide based thin film coatings
US10119188B2 (en) 2013-06-20 2018-11-06 Applied Materials, Inc. Plasma erosion resistant rare-earth oxide based thin film coatings
US11680308B2 (en) 2013-06-20 2023-06-20 Applied Materials, Inc. Plasma erosion resistant rare-earth oxide based thin film coatings
US11053581B2 (en) 2013-06-20 2021-07-06 Applied Materials, Inc. Plasma erosion resistant rare-earth oxide based thin film coatings
US10501843B2 (en) 2013-06-20 2019-12-10 Applied Materials, Inc. Plasma erosion resistant rare-earth oxide based thin film coatings
US9711334B2 (en) 2013-07-19 2017-07-18 Applied Materials, Inc. Ion assisted deposition for rare-earth oxide based thin film coatings on process rings
US10796888B2 (en) 2013-07-19 2020-10-06 Applied Materials, Inc. Ion assisted deposition for rare-earth oxide based thin film coatings on process rings
US9583369B2 (en) 2013-07-20 2017-02-28 Applied Materials, Inc. Ion assisted deposition for rare-earth oxide based coatings on lids and nozzles
US11424136B2 (en) 2013-07-20 2022-08-23 Applied Materials, Inc. Rare-earth oxide based coatings based on ion assisted deposition
US9812341B2 (en) 2013-07-20 2017-11-07 Applied Materials, Inc. Rare-earth oxide based coatings based on ion assisted deposition
US10930526B2 (en) 2013-07-20 2021-02-23 Applied Materials, Inc. Rare-earth oxide based coatings based on ion assisted deposition
US9869012B2 (en) 2013-07-20 2018-01-16 Applied Materials, Inc. Ion assisted deposition for rare-earth oxide based coatings
US20150064450A1 (en) * 2013-08-29 2015-03-05 Applied Materials, Inc. Anodization architecture for electro-plate adhesion
US9624593B2 (en) * 2013-08-29 2017-04-18 Applied Materials, Inc. Anodization architecture for electro-plate adhesion
US9101954B2 (en) 2013-09-17 2015-08-11 Applied Materials, Inc. Geometries and patterns for surface texturing to increase deposition retention
US9663870B2 (en) 2013-11-13 2017-05-30 Applied Materials, Inc. High purity metallic top coat for semiconductor manufacturing components
US9879348B2 (en) 2013-11-13 2018-01-30 Applied Materials, Inc. High purity metallic top coat for semiconductor manufacturing components
US10260160B2 (en) 2013-11-13 2019-04-16 Applied Materials, Inc. High purity metallic top coat for semiconductor manufacturing components
US11566319B2 (en) 2013-12-06 2023-01-31 Applied Materials, Inc. Ion beam sputtering with ion assisted deposition for coatings on chamber components
US11566317B2 (en) 2013-12-06 2023-01-31 Applied Materials, Inc. Ion beam sputtering with ion assisted deposition for coatings on chamber components
US11566318B2 (en) 2013-12-06 2023-01-31 Applied Materials, Inc. Ion beam sputtering with ion assisted deposition for coatings on chamber components
US9725799B2 (en) 2013-12-06 2017-08-08 Applied Materials, Inc. Ion beam sputtering with ion assisted deposition for coatings on chamber components
US9797037B2 (en) 2013-12-06 2017-10-24 Applied Materials, Inc. Ion beam sputtering with ion assisted deposition for coatings on chamber components
US10563297B2 (en) 2014-04-25 2020-02-18 Applied Materials, Inc. Ion assisted deposition top coat of rare-earth oxide
US11773479B2 (en) 2014-04-25 2023-10-03 Applied Materials, Inc. Plasma erosion resistant thin film coating for high temperature application
US10544500B2 (en) 2014-04-25 2020-01-28 Applied Materials, Inc. Ion assisted deposition top coat of rare-earth oxide
US10815562B2 (en) 2014-04-25 2020-10-27 Applied Materials, Inc. Plasma erosion resistant thin film coating for high temperature application
US9869013B2 (en) 2014-04-25 2018-01-16 Applied Materials, Inc. Ion assisted deposition top coat of rare-earth oxide
US9970095B2 (en) 2014-04-25 2018-05-15 Applied Materials, Inc. Ion assisted deposition top coat of rare-earth oxide
US10730798B2 (en) 2014-05-07 2020-08-04 Applied Materials, Inc. Slurry plasma spray of plasma resistant ceramic coating
US10196728B2 (en) 2014-05-16 2019-02-05 Applied Materials, Inc. Plasma spray coating design using phase and stress control
US10604831B2 (en) 2014-05-16 2020-03-31 Applied Materials, Inc. Plasma spray coating design using phase and stress control
US11578398B2 (en) 2014-05-16 2023-02-14 Applied Materials, Inc. Plasma spray coating design using phase and stress control
US9460898B2 (en) 2014-08-08 2016-10-04 Applied Materials, Inc. Plasma generation chamber with smooth plasma resistant coating
JP2018502223A (en) * 2014-12-15 2018-01-25 アプライド マテリアルズ インコーポレイテッドApplied Materials,Incorporated Method for texturing a chamber component and chamber component having a textured surface
US20210225616A1 (en) * 2018-01-08 2021-07-22 Lam Research Corporation Components and Processes for Managing Plasma Process Byproduct Materials

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US20040224171A1 (en) 2004-11-11
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