US20010003271A1 - Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film - Google Patents

Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film Download PDF

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US20010003271A1
US20010003271A1 US09731722 US73172200A US20010003271A1 US 20010003271 A1 US20010003271 A1 US 20010003271A1 US 09731722 US09731722 US 09731722 US 73172200 A US73172200 A US 73172200A US 20010003271 A1 US20010003271 A1 US 20010003271A1
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gas
chamber
film
apparatus
upper
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Hayashi Otsuki
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Tokyo Electron Ltd
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Tokyo Electron Ltd
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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
    • C23C16/455Chemical 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 characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
    • C23C16/45563Gas nozzles
    • C23C16/45565Shower nozzles
    • 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
    • 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
    • C23C16/455Chemical 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 characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
    • C23C16/45514Mixing in close vicinity to the substrate
    • 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
    • C23C16/455Chemical 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 characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
    • C23C16/45561Gas plumbing upstream of the reaction chamber
    • 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
    • C23C16/455Chemical 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 characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
    • C23C16/45563Gas nozzles
    • C23C16/45574Nozzles for more than one gas
    • 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
    • C23C16/455Chemical 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 characterised by the method used for introducing gases into reaction chamber or for modifying gas flows in reaction chamber
    • C23C16/45563Gas nozzles
    • C23C16/4558Perforated rings
    • 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
    • C23C16/50Chemical 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 using electric discharges
    • C23C16/505Chemical 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 using electric discharges using radio frequency discharges
    • C23C16/507Chemical 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 using electric discharges using radio frequency discharges using external electrodes, e.g. in tunnel type reactors
    • 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
    • C23C4/00Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge
    • C23C4/04Coating by spraying the coating material in the molten state, e.g. by flame, plasma or electric discharge characterised by the coating material
    • C23C4/10Oxides, borides, carbides, nitrides or silicides; Mixtures thereof
    • C23C4/11Oxides
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J37/00Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
    • H01J37/32Gas-filled discharge tubes, e.g. for surface treatment of objects such as coating, plating, etching, sterilising or bringing about chemical reactions
    • H01J37/32009Arrangements for generation of plasma specially adapted for examination or treatment of objects, e.g. plasma sources
    • H01J37/32082Radio frequency generated discharge
    • H01J37/321Radio frequency generated discharge the radio frequency energy being inductively coupled to the plasma
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J37/00Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
    • H01J37/32Gas-filled discharge tubes, e.g. for surface treatment of objects such as coating, plating, etching, sterilising or bringing about chemical reactions
    • H01J37/32431Constructional details of the reactor
    • H01J37/32458Vessel
    • H01J37/32477Vessel characterised by the means for protecting vessels or internal parts, e.g. coatings
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01JELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
    • H01J37/00Discharge tubes with provision for introducing objects or material to be exposed to the discharge, e.g. for the purpose of examination or processing thereof
    • H01J37/32Gas-filled discharge tubes, e.g. for surface treatment of objects such as coating, plating, etching, sterilising or bringing about chemical reactions
    • H01J37/32431Constructional details of the reactor
    • H01J37/32458Vessel
    • H01J37/32477Vessel characterised by the means for protecting vessels or internal parts, e.g. coatings
    • H01J37/32495Means for protecting the vessel against plasma
    • 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

Abstract

A processing apparatus of the present invention has a mounted chamber holding a semiconductor wafer and having members for work-processing the substrate under any of heating, plasma and process gas or a combination of them, in which a film of Al2O3 and Y2O3 is formed on an inner wall surface of the chamber and on those exposed surface of the members within the chamber and has a high-corrosion resistance and insulating property and, when the process gas is introduced onto a processing surface of a semiconductor wafer and diffused into it, any product is less liable to be deposited on a plasma generation area and on those members held within the chamber.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • [0001]
    This application is based upon and claims the benefit of priority from the prior Japanese Patent Application No. 11-352018, filed Dec. 10, 1999, the entire contents of which are incorporated herein by reference.
  • BACKGROUND OF THE INVENTION
  • [0002]
    A present invention relates to a processing chamber having a mounted chamber having a high-corrosion-resistant film and applied to a film forming apparatus, heat processing apparatus and etching apparatus as used in a CVD (Chemical Vapor Deposition), etc.
  • [0003]
    In response to a recent demand for a high density and high integration unit, a semiconductor device is progressed from a two-dimensional connection structure toward a three-dimensional multi-connection structure. For this reason, the burying technique for electrical interlayer connection using a contact hole for connection between an underlying circuit element and an overlying connection layer and a via hole for connection between an underlying connection layer and an overlying connection layer, and so on, is becoming important. For the burying of the contact hole and via hole, use is made of Al (aluminum), W (tungsten) or an alloy including these as a main component.
  • [0004]
    At the burying step using aluminum or aluminum alloy, a heating step and so on are involved during a manufacture. If the aluminum connection line and underlying silicon (Si) substrate are directly contacted with each other, there is a risk that there will occur a “Si-sucking-up” effect of aluminum, etc., at its boundary area and an alloy will be newly formed there. The alloy thus formed is greater in the value of a resistance and is not desirable from the standpoint of a power saving and high-speed operation demanded of a resultant device. Further, when tungsten or tungsten alloy is used as a burying layer in the contact hole, WF6 gas intrudes into the silicon substrate, thus offering a possibility of deteriorating the electrical characteristic, etc., of the device. This is, therefore, not preferable.
  • [0005]
    In order to prevent the occurrence of such a problem, a barrier layer is formed on the bottom and inner wall of the hole before forming a buried layer in the contact hole or via hole and then such a buried layer is formed. Generally, a TiN film is known as a barrier layer.
  • [0006]
    With a trend toward the high-density integration, on the other hand, a high dielectric constant material such as Ta2O5 is used as a capacitor gate material to obtain a higher capacitance without changing its scale. However, such a higher dielectric constant material is not stabler in characteristic than SiO2 conventionally used as the capacitor gate material. If a poly-Si is used on the overlying electrode, it is oxidized due to the chemical reaction after the formation of the capacitance, thus failing to manufacture a device element of stable characteristics. It is, therefore, necessary that a less-oxidized TiN film be used as an overlying electrode.
  • [0007]
    The TiN film has been formed by using a physical vapor deposition (PVD) technique and a demand has been made for a finer and higher integration device in particular. In addition, the design rules are particularly stringent. Hence, in PVD that can hardly achieve high coverage. Therefore, a chemical vapor deposition (CVD) technique is used by which it is possible to form a TiN film of a better quality. Stated in more detail, a thermal CVD is used, in which TiCl4 and NH3 (ammonia) or MMH (monomethylhydrazine) is applied, as a reaction gas, to a heated substrate. In the case where the TiN film is formed by such a thermal CVD, chlorine is liable to be retained in a formed film, thus presenting a problem. The retaining of such chlorine results in a higher specific resistance and it is not possible to obtain a proper characteristic if the film is applied to an electrode overlying a capacitor.
  • [0008]
    Further, the TiN film, being a columnar crystal, is liable to be boundary-diffused and involves a lower barrier characteristic. The lower barrier characteristic presents a problem in the case where the TiN film is used as a barrier layer for a Cu connection line or an oxygen diffusion barrier for Ta2O5 connection line of an electrode overlying the capacitor. That is, a problem occurs due to the corrosion of the Cu connection line by the residual chlorine or a lowering of a capacitance of Ta2O5 by the diffusion of oxygen.
  • [0009]
    An amount of Cl in the formed film can be indeed reduced by making a film formation temperature higher. However, a high temperature process is not preferable due to a problem, such as thermal resistance and the corrosion, of a connection line material such as Cu and Al.
  • [0010]
    As one technique of plasma CVD, there is an ICP (Inductively Coupled Plasma)—CVD according to which an antenna member such as a coil is provided around a bell jar (chamber). By applying a high frequency power to it, an inductive electromagnetic field is created to provide plasma. In the case where the TiN film is formed using this technique, the formed TiN film becomes low-resistance and low in chlorine, and even a film formed at a relatively low temperature is made low in an amount of residual chlorine.
  • [0011]
    Although a chamber made of quartz or alumina is used in the formation of the TiN film by the ICP-CVD, it is not good in a plasma-resistant characteristic and a corrosion resistance to an etching gas such as ClF3 used for cleaning the interior of the apparatus after the formation of the TiN film is not better, thus presenting a problem.
  • [0012]
    Further, in this type of CVD film formation apparatus, a deposit is formed on the inner wall of the chamber due to the introduction of a process gas from above the chamber and a foreign deposit is liable to be formed. In the case of forming the TiN film, the plasma created is attenuated due to the deposit of a conductive film on the inner wall of the upper chamber, thus making it difficult to form a film.
  • BRIEF SUMMARY OF THE INVENTION
  • [0013]
    An object of the present invention is to provide a processing apparatus having a chamber applied to a film forming apparatus, heat processing apparatus and etching apparatus and having a high-corrosion-resistant property and less liable to deposit a product by a process gas or a product, such as an etching product, on its inner wall thereof.
  • [0014]
    The thus constructed processing apparatus has a mounted chamber holding a to-be-processed substrate and having members for work-processing the substrate by any of heating, plasma, process gas or a combination thereof, in which a film of Al2O3 and Y2O3 is formed on the inner wall surface of the chamber and on the exposed surfaces of the members within the chamber, the Al2O3/Y2O3 weight ratio being above 0.5. The Al2O3/Y2O3 weight ratio is in a range above 0.5 but below 4. The thickness of the formed film is above 50 μm.
  • [0015]
    Additional objects and advantages of the invention will be set forth in the description which follows, and in part will be obvious from the description, or may be learned by practice of the invention. The objects and advantages of the invention may be realized and obtained by means of the instrumentalities and combinations particularly pointed out hereinafter.
  • BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWING
  • [0016]
    The accompanying drawings, which are incorporated in and constitute a part of the specification, illustrate presently preferred embodiments of the invention, and together with the general description given above and the detailed description of the preferred embodiments given below, serve to explain the principles of the invention.
  • [0017]
    [0017]FIG. 1 is a view showing a practical structure of a plasma CVD apparatus according to a first embodiment of the present invention;
  • [0018]
    [0018]FIGS. 2A and 2B are views showing a sample of a test by etching and evaluation standard;
  • [0019]
    [0019]FIG. 3 is a view showing a relation of members in an etching time to an etched amount;
  • [0020]
    [0020]FIG. 4 is a view showing an X-ray diffraction pattern of a sprayed film when an Al2O3/Y2O3 weight ratio=0.43;
  • [0021]
    [0021]FIG. 5 is a view showing an X-ray diffraction pattern of a sprayed film when an Al2O3/Y2O3 weight ratio=0.66;
  • [0022]
    [0022]FIG. 6 is a view showing an X-ray diffraction pattern of a sprayed film when an Al2O3/Y2O3 weight ratio=1.50;
  • [0023]
    [0023]FIG. 7 is a view showing a rate of a composite oxide when the Al2O3/Y2O3 weight ratio of a sprayed film varies;
  • [0024]
    [0024]FIG. 8 is a view showing a relation of an Al2O3/Y2O3 weight ratio of a sprayed film to an etched amount;
  • [0025]
    [0025]FIG. 9 is a view showing an X-ray diffraction pattern of a sprayed film when sprayed is made using a YAG;
  • [0026]
    [0026]FIG. 10 is a view showing a practical form of a plasma CVD apparatus according to a second embodiment;
  • [0027]
    [0027]FIG. 11 is a view showing a practical form of a plasma CVD apparatus according to a third embodiment;
  • [0028]
    [0028]FIG. 12 is a view showing a practical structure of a plasma CVD apparatus according to a fourth embodiment;
  • [0029]
    [0029]FIGS. 13A and 13B show a practical structure of a shower head in the fourth embodiment;
  • [0030]
    [0030]FIGS. 14A and 14B are a view showing a modified structure of the shower head in the fourth embodiment;
  • [0031]
    [0031]FIG. 15 is a view showing practical structures of head section;
  • [0032]
    [0032]FIG. 16 is a perspective view showing a first modified structure of a gas discharge member;
  • [0033]
    [0033]FIG. 17 is a perspective view showing a second modified structure of a gas discharge member;
  • [0034]
    [0034]FIG. 18 is a view showing one form of a lower-height thin type chamber;
  • [0035]
    [0035]FIG. 19 is a view showing one form of a semi-spherical type chamber;
  • [0036]
    [0036]FIG. 20 is a view showing one form of a dome-type chamber;
  • [0037]
    [0037]FIG. 21 is a view showing a practical structure of a heat processing apparatus;
  • [0038]
    [0038]FIG. 22 is a view showing a practical structure of an ashing apparatus;
  • [0039]
    [0039]FIG. 23 is a view showing a practical structure of an etching apparatus; and
  • [0040]
    [0040]FIG. 24 is a view showing a relation of a breakdown voltage to the thickness of the sprayed film in the respective embodiment of the present invention.
  • DETAILED DESCRIPTION OF THE INVENTION
  • [0041]
    The embodiments of the present invention will be described below with reference to the accompanying drawings.
  • [0042]
    [0042]FIG. 1 is a cross-sectional view showing a practical example applied to a CVD film forming apparatus as a first embodiment of the present invention in a processing apparatus having a mounted chamber having a high corrosion-resistant thermal sprayed film.
  • [0043]
    The film forming apparatus of the present invention is directed to forming, for example, a TiN thin film. The film forming apparatus 10 includes a chamber 11 having a lower chamber 11 a and upper chamber 11 formed as an integral unit in a hermetically sealable way. The upper chamber 11 b is made smaller in diameter than the lower chamber 11 a. The lower chamber 11 a is comprised of an electric conductor 12, such as aluminum, whose surface is anadigation processed for example. The upper chamber 11 b comprises a base material 13 of, for example, a ceramic material and a sprayed film 14. The film 14 may contain oxide of Y, Sc, La, Ce, Eu, Dy or the like, or fluoride of one of these metals. The film 14 may be made of a compound of a III-a element of the periodic table, such as Y2O3. Needless to say, the film 14 may be made of such a compound and any other material. In the present invention, the film 14 containing a compound of a III-a element is a sprayed film that substantially comprises Al2O3 and Y2O3. As the material of the chamber use can be made of ceramic (Al2O3, SiO2, AlN etc.,), aluminum or stainless steel, metal or metal alloy.
  • [0044]
    A weight ratio of Al2O3/Y2O3 of the sprayed film 14 is preferably 0.5 to 4. It is to be noted that FIG. 8 simply shows data of the weight ratio of up to 1.5. In the formation of the sprayed film 14 it may be possible to spray an Al2O3 and Y2O3 compound or to spray, for example, yttrium-aluminum-garnet (YAG) in a composite oxide state of the above-mentioned composition range. The thickness of the sprayed film is based on the insulation withstand characteristic for plasma generation and, from the standpoint of the breakdown voltage characteristic shown in, for example, FIG. 2, may be of the order of at least 50 μm and preferably of the order of 50 μm but not above 300 μm from the standpoint of a manufacturing process and cost.
  • [0045]
    The ceramics of the base material 13 may be Al2O3, SiO2, such as silica glass and quartz, AlN, alternatively, rigid plastic may be used, and, here, the sprayed film as set out above is not formed on the inner wall of the upper chamber 11 b but it may be formed there.
  • [0046]
    On the inner bottom of the lower chamber 11 a an insulating plate 15 of ceramic, etc., and support base 16 are provided and a substantially cylindrical susceptor 17 is provided on the support base 16 to place a semiconductor wafer (hereinafter referred to as a wafer) as a to-be-processed object on it.
  • [0047]
    A coolant chamber 18 is provided in the interior of the support base 16 to receive the coolant via a coolant introducing tube 19. The coolant is discharged out of a discharge tube 20. Through such a circulation, a cold is conducted through the susceptor 17 to the wafer W. A heating element 21 is buried in the susceptor 17 to heat the wafer W to a predetermined temperature by supplying power from a power source 22. To the power source 22, a controller 23 is connected. And the temperature of the wafer W is controlled by a cold of the coolant and heat of the heating element.
  • [0048]
    At the susceptor 17, an electrostatic chuck 24 is provided which is substantially the same in configuration as the wafer W. The electrostatic chuck 24 is so formed as to have an electrode 26 buried in an insulating material 25. The wafer W is electrostatically attracted by a Coulomb force, etc., generated by applying a DC voltage from a DC power source 27 to the electrode 26. At the outer peripheral portion of an upper surface of the electrostatic chuck 24 an area for achieving the uniformity of a film formation, for example, a focusing ring 28 is provided to surround the wafer W. The above-mentioned sprayed film 14 is formed on those exposed surfaces of the support base 16, susceptor 17, electrostatic chuck 24 and focusing ring 28 within the chamber.
  • [0049]
    A shower head member 30 is provided above the chamber 11 b. In the shower head member 30, many gas discharge holes 30 a (Ar, ClF3), 30 b (Ar, TiCl4) and 30 c (NH3) are alternately formed to discharge gases in a down direction within the chamber. The pipes of a gas supply system 40 are connected to the shower head member 30. That is, as will be set out below, a pipe 55 for supplying a gas (Ar, ClF3) is connected to the gas discharge holes 30 a, a pipe 56 for supplying a gas (Ar, TiCl4) is connected to the gas discharge holes 30 b and a pipe 57 for supplying a gas (NH3) is connected to the gas discharge holes 30 c. By doing so, the respective gases are introduced through the shower head member 30 into the upper chamber 11 b.
  • [0050]
    The shower head member 30 is comprised of, for example, a three-layers-stacked structure of three gas dispersion plate and has discharge plate having the gas discharge holes. The respective gas discharge plate has a groove and holes for allowing one kind of gas to be dispersed evenness to a whole gas discharge surface area in the head. In particular, the discharge holes of the gas dispersion plate are so formed as not be overlapped with the discharge holes of the other gas dispersion plate. Though being not illustrated in the Figure, the gas discharge holes are arranged in a matrix array upon viewing the gas discharge hole surface side from below. And a post-mixing system is adopted according to which TiCl4 gas and NH3 gas are discharged from the alternately formed different discharge holes and these gases are mixed as a process gas after being discharged.
  • [0051]
    The gas supply system 40 has a ClF3 supply source 41 for supplying ClF3 as a cleaning gas, Ar supply sources 42 and 43 for supplying Ar, a TiCl4 supply source 44 for supplying TiCl4 as a process gas and an NH3 supply source 45 for supplying NH3 as a process gas. A gas line 46 is connected to the ClF3 supply source 41, gas lines 47 and 48 are connected to the Ar supply sources 42 and 43, respectively, a gas line 49 is connected to the TiCl4 supply source 44 and a gas line 50 is connected to the NH3 supply source 45. A valve 51 (51 a, 51 b) and mass flow controller 52 are provided at these gas lines.
  • [0052]
    Into the gas line 47 extending from the Ar supply source 42, the gas line 46 extending from the ClF3 supply source 41 is joined and the gas line 46 extending form the ClF3 supply source 41 is joined. The gas line 46 extending form the ClF3 supply source 41 is joined into a gas line 53. By opening the valve 51 provided on the gas line 46, ClF3 serving as a cleaning gas is passed through the gas line 46 and pipe 53 and reaches the shower head 30 to allow it to be introduced via the gas discharge holes 30 a into the upper chamber 11 b. Needless to say, there is the case where Ar alone is supplied from the Ar supply source 42.
  • [0053]
    Into the gas line 48 extending from the Ar supply source 43, the gas line 49 extending from the TiCl4 supply source 44 is joined. TiCl4 gas passed through the gas line 49 and pipe 54 is carried by the argon gas and reaches the shower head 30. The TiCl4 gas is introduced from the gas discharge holes 30 b into the chamber 11.
  • [0054]
    Further, the NH3 gas is supplied from the NH3 supply source 45 past the gas line 50 and pipe 55 to the shower head 30 and introduced from the gas discharge holes 30 c into the upper chamber 11 b. It is to be noted that, in place of NH3, monomethylhydrazine (MMH) may be used.
  • [0055]
    At the bottom wall of the lower chamber 11 a the exhaust tube 61 is provided which is connected to an exhaust apparatus 62 including a vacuum pump. By operating the exhaust apparatus 62 it is possible to reduce pressure in the chamber 11 to a predetermined vacuum level. A gate valve 63 is provided at the sidewall of the lower chamber 11 a and, in its open state, allows the wafer W to be passed into and out of an outside, for example, an adjacent load lock chamber, not shown.
  • [0056]
    A coil 65 as an antenna member is wound around the upper chamber 11 b and a high frequency power source 66 is connected to the coil 65. The high frequency power source 66 has a frequency of, for example, 13.65 MHz. By supplying a high frequency power from the high frequency power source 66 to the coil 65 an inductive electromagnetic field is created within the upper chamber 11 b. Further, a cooling mechanism 67 using a cooling medium such as a coolant and a cooling source 68 for driving this are provided.
  • [0057]
    With this apparatus, the gate valve 63 is opened and, in its open state, a wafer W is loaded into the chamber 11 and placed onto the electrostatic chuck 24. The wafer W is attracted to the electrostatic chuck 24 by applying a voltage to the electrode 26. Thereafter, the gate valve 63 is closed, and the interior of the chamber 11 is evacuated by the exhaust system 62 to a predetermined vacuum level. Then, while introducing an Ar gas from the Ar supply source 42 into the chamber 11, a high frequency power is supplied from the high frequency power source 66 to the coil 65 to create an inductive electromagnetic field within the upper chamber 11 b. Plasma is generated under this high frequency electric field.
  • [0058]
    Then, a predetermined amount of NH2 gas and TiCl4 gas are introduced into the upper chamber 11 b from the NH3 supply source 45 and TiCl4 supply source 44 to generate plasma and are brought to the lower chamber 11 a side. By this plasma, a TiN thin film is formed onto the wafer W. At this time, the formation of the TiN thin film is effected at a temperature of about 300 to 450° C. by controlling an output to the heating element 21 and an amount of flow of a coolant. After the film formation, the wafer W is unloaded out of the chamber 11 and the ClF3 gas serving as a cleaning gas is introduced into the chamber 11 to clean the interior of the chamber.
  • [0059]
    In the above-mentioned processing, the inner wall of the upper chamber 11 b is attacked by the plasma generated in the upper chamber 11 b and exposed to the ClF3 gas (etching gas) at a cleaning time. Under such an environment, no adequate corrosion resistance was not obtained in a conventional chamber made of quartz and Al2O3 with the resultant disadvantage of a short life. According to the present invention, however, use is made mainly of Al2O3 and Y2O3 and a high-corrosion-resistant sprayed film 14 having Al2O3/Y2O3 weight ratio of above 0.5 is formed on the inner wall of the upper chamber 11 b. Hence, even if being contacted with plasma and cleaning gas, the inner wall of the chamber is less likely to be etched and ensures a longer service life.
  • [0060]
    The sprayed film 14 has insulating property because it contains 6 a III-a group element of the periodic table. Use can be made of, as the basic material, various kinds of materials such as ceramic herein used, aluminum, stainless steel, rigid plastic (engineering plastic) etc. Further, the sprayed film 14 is lower in cost than a sintered product and has a greater merit of forming a film for a short period of time. It is to be noted that such sprayed film may be formed on the inner wall of the lower chamber 11 a and can enhance a corrosion resistance of the lower chamber 11 a.
  • [0061]
    An explanation will be made below about the results of experiments by which the corrosion resistance of the sprayed film is confirmed. Here, a parallel flat type plasma etching apparatus was used by way of example. A strayed film was irradiated, with plasma, at an intra-chamber pressure of 133.3 Pa (1000m Torrs) and a gas flow rate of CF4: Ar:O2=95: 950:10 (a total flow rate of 0.0633 m3/sec (1055 sccm)) for 20 hours through the application of a high frequency power of 13.56 MHz at 1300 W.
  • [0062]
    Eight types of samples were used, each comprised a 20×20×2 mm aluminum base, a 200 μm-thick first sprayed film made of Al2O3 and Y2O3 and formed on the aluminum base, and a 200 μm-thick second sprayed film formed on the first sprayed film. The first sprayed film is made of Y2O3 in the first type sample, Sc2O3 in the second type sample, Sc2F3 in the third type sample, YF3 in the fourth type sample, La2O3 in the fifth fifty type sample, CeO2 in the sixth type sample, Eu2O3 in the seventh type sample, and DyO3 in the eighth type sample. Stated in more detail, use was made of a sprayed film having a weight ratio of Al2O3/Y2O3=0.5 and a film sprayed with a 99.9%-purity YAG (Y3Al5O12 a weight ratio of Al2O3/Y2O3=0.75). As shown in FIG. 2A, the sample was, while leaving a central area of 10 mm square, masked at its outer peripheral area with a polyimide film and irradiated with plasma. And a plasma-resistant property was evaluated with an etched amount. The etched amount was evaluated with its depth, as shown in FIG. 2B, with the use of a surface roughness meter. For comparison, samples of other materials were also evaluated in terms of the corrosion-resistant property. The result of evaluation is as shown in FIG. 3. Here, the etched amount is shown with the etched amount of alumina standardized as “1”.
  • [0063]
    It was confirmed that, as shown in FIG. 3, the films containing a III-a element of the periodic table had higher corrosion resistance to plasma than the other materials. Of these films, the sprayed film made of Al2O3 and Y2O3 exhibited a particularly high corrosion resistance since it was of YAG composition.
  • [0064]
    Then, with an Al2O3/Y2O3 weight ratio set to 0.43, 0.66, and 1.5, these mixed powders were sprayed onto an aluminum basic material to form a sprayed film. FIGS. 4, 5 and 6 show and X-ray diffraction pattern each. As shown in these figures, for any of the sprayed films, diffraction peaks corresponding to the Al2O3 and Y2O3 crystals are dominant but the diffraction peaks of composite oxides, such as YAlO3 and Y4Al2O9 were also confirmed. It is found that the producing rate of these composite oxides is increased with an increase in the weight ratio of Al2O3/Y2O3 as shown in FIG. 7.
  • [0065]
    In the same way as set out above, these samples were tested for corrosion resistance to plasma. The evaluation of the etched amount was made by measuring its depth at a central portion of the above-mentioned 10 mm square portion except the edge portion. The result is as shown in FIG. 8. From this Figure it is found that, with an Al2O3/Y2O3 weight ratio of above 0.5, the corrosion resistance is better. Since, as set out above, with an increase in the weight ratio of Al2O3/Y2O3, the production rate of the composite oxide is increased, there is a possibility that the composite oxide contributes to the corrosion resistance.
  • [0066]
    On the other hand, the YAG sprayed film evaluated for the corrosion resistance at the first test was substantially amorphous as shown in FIG. 9.
  • [0067]
    From this it may be considered that the corrosion resistance is improved by making the sprayed film amorphous.
  • [0068]
    A second embodiment of the present invention will be explained below.
  • [0069]
    [0069]FIG. 10 is a cross-sectional view showing a CVD apparatus according to the second embodiment. In this embodiment, a chamber, shower head and gas supply system are different in structure from those of the first embodiment. In this Figure, the same reference numerals are employed to designate parts or elements corresponding in structure to those shown in FIG. 1 and any further explanation is, therefore, omitted.
  • [0070]
    In this apparatus, an upper chamber 11 c is provided above a lower chamber 11 a and it is made of a ceramic material, such as Al2O3, SiO2 and AlN. At a shower head member 70 of pipe type provided at the top of the upper chamber 11 c, gas discharge holes 70 a, 70 b and 70 c are alternately formed to discharge gases toward a lower zone within the chamber. A gas supply system 40 a comprises gas supply sources and valves 51 and mass flow controllers 52 as in the case of the gas supply system 40 as set out above. This embodiment is different from the first embodiment with respect to a pipe array from the gas supply system 40 to the shower head member 70.
  • [0071]
    That is, the pipes of the gas supply system 40 are connected to the shower head member 70. As will be set out below, a pipe 81 for supplying an Ar gas and ClF2 gas is connected to the gas discharge holes 70 a, a pipe 82 for supplying a TiCl4 gas and Ar gas is connected to the gas discharge holes 70 b, and a pipe 83 for supplying an NH3 gas is connected to the gas discharge holes 70 c. Pipe-like gas discharge members 71 and 72 extending from the upper chamber 11 c toward the upper zone of the lower chamber 11 a are connected to the gas discharge holes 70 b and 70 c. A gas discharge hole 71 a is formed in the gas discharge member 71 and a gas discharge hole 72 a is formed in the gas discharge member 72.
  • [0072]
    A gas line 47 extending from an Ar supply source 42 and gas line 46 extending from a ClF3 supply source 41 are connected to the pipe 81. The Ar gas and ClF3 gas are introduced from the pipe 81 into the upper chamber 11 c via the gas discharge hole 70 a, noting that the Ar gas alone is sometimes supplied there.
  • [0073]
    A gas line 49 extending from a TiCl4 supply source 44 and gas line 48 extending from an Ar supply source 43 are connected to the pipe 82. The TiCl4 gas using an Ar gas as a carrier gas is introduced from the pipe 82 through the gas discharge hole 70 b and gas discharge hole 71 a in the gas discharge member 71 into the upper zone of the lower chamber 11 a. A gas line 50 extending from an NH3 supply source 43 is connected to the pipe 83 and the NH3 gas is introduced from the pipe 83 through a gas discharge hole 70 c and gas discharge hole 72 a in the gas discharge member 72 into the upper zone of the lower chamber 11 a.
  • [0074]
    Thus, the TiCl4 gas and NH3 gas are supplied directly into the upper zone of the lower chamber 11 a without passing through the upper chamber 11 c. After so discharged, these gases are mixed within the lower chamber 11 a. The gas line 46 extending from the ClF3 supply source 41 is joined into the gas line 81 and, by opening a valve 51 on the gas line 46, the ClF3 as a cleaning gas is supplied past the gas line 46 and then the pipe 81 to the shower head 70 to allow the ClF3 gas to be introduced via the discharge hole 70 a into the upper chamber 11 c.
  • [0075]
    In the thus structured CVD apparatus, a wafer W is loaded into the chamber 11 and the Ar gas as a plasma generation gas is introduced via the gas discharge holes 70 a in the shower head into the upper chamber 11 c. By supplying a high frequency power from a high frequency power source 66 to a coil 65, an inductive electromagnetic field is created within the upper chamber 11 c to generate a plasma of the Ar gas.
  • [0076]
    On the other hand, the TiCl4 gas and NH3 gas serving as a process gas are directly introduced into the upper zone of the lower chamber 11 a via the discharge members 71 and 72 and these gases are excited by the plasma of the Ar gas diffused from the upper chamber 11 c into the lower chamber 11 a. By doing so, the gases generate a plasma at the upper zone of the lower chamber 11 a, so that a reaction occurs on the surface of the wafer W to form a TiN thin film on the wafer.
  • [0077]
    Even in this embodiment, the film-formed semiconductor wafer is externally unloaded out of the chamber 11 and a ClF3 gas serving as a cleaning gas is introduced into the chamber 11 to clean the inner wall of the chamber.
  • [0078]
    In this embodiment, as set out above, the Ar gas alone for plasma generation is supplied into the upper chamber 11 c and the TiCl4 gas and NH3 gas, serving as a process gas, are supplied directly into the lower chamber 11 a via the gas discharge members 71 and 72, so that the process gas almost never reaches the inner wall of the upper chamber 11 c. As a result, almost no deposit resulting from the process gas is formed on the inner wall of the upper chamber 11 c.
  • [0079]
    Thus, unlike the prior art technique, a conductive film is not deposited, by the process gas, on the inner wall of the chamber and it is never difficult to form a film under the attenuation of plasma involved.
  • [0080]
    A third embodiment of the present invention will be described below.
  • [0081]
    [0081]FIG. 11 is a cross-sectional view showing a CVD apparatus according to a third embodiment of the present invention.
  • [0082]
    This embodiment constitutes a combined structure of a lower chamber 11 a similar to that in the first embodiment shown in FIG. 1 and an upper chamber 11 c similar to that of the second embodiment shown in FIG. 10. A sprayed film 14 of mainly Al2O3 and Y2O3 having an insulating property and high corrosion resistance as set out above is formed on the inner wall of the upper chamber 11 b. In this embodiment, the same reference numerals are employed to designate parts or elements corresponding in structure to those shown in FIGS. 1 and 10 and any further explanation is, therefore, omitted.
  • [0083]
    In the third embodiment, a high-corrosion-resistant sprayed film 14 is formed on the inner wall of the upper chamber 11 c and, even if plasma and cleaning gas are contacted with the inner wall, is hard to be etched to provide a longer service life to the chamber. In addition, almost no deposit resulting from the process gas is formed on the upper chamber 11 b. As a result, unlike the prior art technique, there is no inconvenience of the plasma being attenuated by a conductive film deposited on the inner wall of the chamber and hence no difficulty is encountered in the formation of a film.
  • [0084]
    It is to be noted that, even in the second and third embodiments, a sprayed film may be formed on the inner wall of the lower chamber 11 a and, by forming such a sprayed film, it is possible to improve a high corrosion resistance to the lower chamber 11 a.
  • [0085]
    A fourth embodiment of the present invention will be explained below.
  • [0086]
    [0086]FIG. 12 is a cross-sectional view showing a CVD apparatus according to the fourth embodiment of the present invention.
  • [0087]
    The apparatus structure of this embodiment comprises a combination of a lower chamber 11 a similar to that of the above-mentioned first embodiment and an upper chamber lid different in gas supply position above the lower chamber 11 a. In this embodiment, the same reference numerals are employed to designate parts or elements corresponding in structure to those shown in FIG. 1 and any further explanation is, therefore, omitted.
  • [0088]
    In this film forming apparatus, a shower head 81 for supplying a process gas into a chamber 11 is formed in an annular shape between the upper chamber 11 d and the lower chamber 11 a. A high corrosion-resistant and insulating sprayed film 14 is formed on the whole inner surface of the upper chamber 11 d. A gas supply system 40 is similar in structure to that of the first embodiment but a ClF3 gas serving as a cleaning gas and Ar gas can be introduced from the top side and sidewall side of the upper chamber 11 d by a switching operation of the valves 82 and 83.
  • [0089]
    By this structure, a gas supplied from the gas supply system 40 is discharged and directed toward a central area at the upper zone of the lower chamber 11 a and diffused onto a wafer W. In this embodiment, it is possible to obtain an effect similar to that of the above-mentioned embodiments. And a deposit resulting from a process gas is almost hardly formed on the inner wall of the upper chamber 11 d. Further, a sprayed film 14 is formed on the inner wall of the upper chamber and, even if plasma and cleaning gas are contacted with the inner wall, etching is less liable to occur and it is possible to extend the service life of the chamber.
  • [0090]
    [0090]FIGS. 13A and 13B each shows a practical structure of a shower head 81 in this embodiment.
  • [0091]
    The shower head 81 is comprised of a ring-type three-layered structure and so designed as to collect gases in the respective outer head sections into a middle-layer head section. That is, ring-like diffusion channels 84 a, 85 a and 86 a are provided in the head sections 84, 85 and 86 to allow the process gas to be introduced into the chamber. A plurality of discharge holes 84 b (NH3 gas), discharge holes 85 b (Ar gas) and discharge holes 86 b (TiCl4 gas or ClF3 gas) leading to the diffusion channels 84 a, 85 a and 86 a are provided in a middle layer of the head section 85 in one array to allow a corresponding gas to be discharged in a horizontal direction. For example, these discharge holes are so arranged as to allow different kinds of process gases to be sequentially discharged with an argon gas in between.
  • [0092]
    In the practical example shown in FIG. 13B, as a first combination the discharge holes 85 b, 86 b, 85 b, 84 b, 85 b, 86 b, . . . , that is, an Ar gas, TiCl4 gas or ClF3 gas, Ar gas, NH3 gas, Ar gas, TiCl4 gas or ClF3 gas, . . . are used. As a second combination, the discharge holes 85 b, 86 b, 84 b, 85 b, 85 b, 86 b, 84 b, 85 b, , that is, the Ar gas, TiCl4 gas or ClF3, NH3 gas, Ar gas, Ar gas, TiCl4 gas or ClF3 gas, NH3 gas, Ar gas, . . . are used. It is needless to say that these combinations may be properly set depending upon the chamber configuration and process condition, etc. Further, to the TiCl4 gas and ClF3 gas, respective independent discharge holes may be provided.
  • [0093]
    [0093]FIGS. 14A and 14B show a modified structure of the above-mentioned shower head 81. Although, in the above-mentioned shower head 81, the gases from the respective head sections are collected into the middle layer head section, this modified structure is of such a type that a plurality of discharge holes are formed in the respective head sections in a not-overlapped fashion in a stacked direction.
  • [0094]
    This shower head 90 is of a ring-type three-layered structure such that ring-like diffusion channels 91 a, 92 a and 93 a are provided in the corresponding head sections 91, 92 and 93 to allow a process gas to be introduced into the chamber. A plurality of discharge holes 91 b (NH3 gas), discharge holes 92 b (Ar gas) and discharge holes 93 b (TiCl4 gas or ClF3 gas) leading to the diffusion channels 91 a, 92 a and 93 a are formed in the corresponding head sections to allow these gases to be discharged in a horizontal direction.
  • [0095]
    Various practical structures as shown in FIG. 15 are realized depending upon the order in which these head sections are stacked. In these structures, six cases are shown in FIG. 15. It is to be noted that the TiCl4 gas and ClF3 gas are switchingly used at a film forming time and cleaning time but that independent corresponding discharge holes may be provided for these gases.
  • [0096]
    Even in these embodiments it is possible to obtain the same advantage as set out in connection with the above-mentioned embodiment.
  • [0097]
    The shower heads for introducing the gases into the chamber can be variously changed or modified in the embodiment of the present invention.
  • [0098]
    Although, in the above-mentioned embodiment, a plurality of members are used to introduced the process gas into the chamber 11, as shown in FIG. 16, for example, a shower head is so configured as to have one gas introducing member 95 for allowing a process gas to be supplied from the top side of an upper bell jar onto a wafer W within a lower chamber and a gas discharge section 96 connected to the lower end of the gas introducing member 95 and having a plurality of discharge holes to allow a gas to be spirally supplied down toward the wafer W.
  • [0099]
    As shown in FIG. 17, a shower head comprises one gas introducing member 97 similar to the gas introducing member 95 and a plurality of gas discharge sections 98 connected to the lower end of the gas introducing member 97, provided in an outwardly branched fashion and having a plurality of discharge holes so provided as to allow a gas to be discharged down onto a wafer W. Further, although two kinds of process gases are separately individually introduced into the chamber, these gases may be introduced together.
  • [0100]
    Although, in the above-mentioned respective embodiment, the formation of the TiN thin film has been explained, the present invention is not restricted thereto and other films may be formed. In the case where a film is formed using a Ti-containing material or Si-containing material, a Cl-containing gas is used as a feed gas and the present invention is effective to the formation of a film using these materials. As such materials, use is made of, for example, TiN, Ti, TiSiN, SiN, Ta, TaN, Ta2O5, PZT, BST, RuO and ZrO; a LOWK material, such as SiOF recently used as an insulating interlayer of a low dielectric constant; and Ta, TaN used as a barrier of Cu and SiN used as a etching stop.
  • [0101]
    Although, in the above-mentioned embodiment, use is made of the ICP-CVD apparatus using a coil as an antenna, if the plasma CVD apparatus uses a chamber and bell jar, it can use a TCP (Transformer Coupled Plasma) using a spiral type antenna and it is also possible to use a helicon wave plasma processing apparatus using a helicon wave.
  • [0102]
    Those applied forms of chambers provided in the processing apparatus according to the above-mentioned embodiments will be explained below with reference to FIGS. 18, 19 and 20. As a lower chamber of the processing apparatus as will be explained below the lower chamber 11 a shown in FIG. 1 is taken as an example and, as a gas supply system, a gas supply system for supplying a gas from the sidewall of the chamber shown in FIG. 12 is taken as an example. Here, only the featuring aspect is explained with the same reference numerals employed to designate corresponding parts or elements shown. And an explanation thereof is, therefore, omitted.
  • [0103]
    [0103]FIG. 18 is one example of a lower-height thin type chamber. This thin type chamber 11 e is thin and has a height (depth) H of, for example, about 0.65 to 10 cm and, preferably, 0.65 to 5 cm. And the distance from the inner top surface of the chamber to a wafer W is about 3.8 to 30 cm and, preferably, 3.8 to 20 cm. Since, in this way, the chamber has a lower-volume shape, an exposed area within the chamber is smaller and hence the apparatus is smaller and ensures an easier maintenance. It is, therefore, possible to alleviate an evacuation load on the system 62.
  • [0104]
    An upper chamber 11 f shown in FIG. 19 is of a semi-spherical type, that is, a bell jar type and an upper chamber 11 g shown in FIG. 20 is of a dome-shaped type. According to these upper chambers, the distribution of an electric field by an antenna relative to the wafer W is made uniform compared with that of a box-type chamber and hence the thickness profile of a formed film, etching, etc., are made uniform.
  • [0105]
    [0105]FIG. 21 is a view showing a practical structure applied to a heat processing apparatus as a fifth embodiment in a processing apparatus with a mounted chamber having a high-corrosion-resistant sprayed film according to the present invention.
  • [0106]
    The heat processing apparatus 101 can perform an anneal process for promoting recrystallization of a formed film and a thermal oxidation process.
  • [0107]
    This heat processing apparatus 101 has a susceptor 103 located within a chamber 102 to support a wafer W, a wafer lifting mechanism 105 provided below the susceptor 103 to allow the wafer W to be lifted up by a plurality of lift pins 104 at a transfer of the wafer W, a heater 106 provided in the susceptor 103 and a gas flow chamber 107 for hermetically supplying a gas such as an Ar gas and oxygen gas onto the wafer W. A sprayed film 14 of Al2O3/Y2O3 is formed on the inner surface of the gas flow chamber 107 and on the surface of a guide section 108 provided on the susceptor 103 to guide a wafer mounting position and, by doing so, it is possible to obtain the same effect as in the above-mentioned respective embodiments.
  • [0108]
    [0108]FIG. 22 is a view showing a practical structure applied to an ashing apparatus as a sixth embodiment in a processing apparatus with a mounted chamber having a high-corrosion-resistant sprayed film according to the present invention.
  • [0109]
    The ashing apparatus comprises a hermetically sealable chamber 111 having a lower chamber 111 a and upper chamber 111 b, a susceptor 112 on which a wafer W is placed, a heater 113 provided in the susceptor 112 to heat the wafer W, a gas supply system, not shown, for supplying a process gas such as oxygen, and an evacuation apparatus for evacuating the interior of the chamber 111.
  • [0110]
    In this ashing apparatus, a high-corrosion-resistant sprayed film is formed on the whole inner surface of the upper chamber 111 band on the sidewall of the lower chamber 111 a except the inner bottom surface and, by doing so, it is possible to obtain the same effect as in the above-mentioned respective embodiment.
  • [0111]
    [0111]FIG. 23 is a view showing a practical structure applied to an etching apparatus as a seventh embodiment in a processing apparatus with a mounted chamber having a high-corrosion-resistant sprayed film according to the present invention.
  • [0112]
    This etching apparatus comprises a hermetically sealable chamber 121, a process gas supplying shower head provided within the chamber 121 and functioning as an upper electrode for plasma generation, a susceptor 123 allowing a wafer W to be placed and functioning as an upper electrode for plasma generation, a process gas supply system 126 having a plurality of valves 124 and a plurality of process gas sources 125, a high frequency power source 127 for applying a high frequency power to the shower head 122, a shield ring 128 provided around the shower head 122, an electrostatic chuck system 129 provided on the top surface of the susceptor 123, a focusing ring 130 provided at an outer peripheral portion of the electrostatic chuck 129 to surround the wafer W, a gate valve 131 provided on the sidewall of the chamber 121 to allow the wafer to be loaded and unloaded into and out of the chamber 121, and a deposition shield 132 provided on the inner side surface of the chamber 121.
  • [0113]
    A sprayed film 14 is formed, as the above-mentioned case, on exposed surfaces of the susceptor 123, focusing ring 130, shower head 122 and shield ring 128 within the chamber and further on the inner upper surface and inner bottom surface of the chamber 121.
  • [0114]
    It is to be noted that the sprayed film formed in the above-mentioned respective embodiments need only have a thickness of above 50 μm. In the case where the thickness of the sprayed film is less than 50 μm, the insulating resistance and withstand voltage are lower. This is based on our empirically obtained data showing a relation of a breakdown voltage to the film thickness shown in FIG. 24. According to FIG. 24, out of the film thickness range of 50 to 300 μm is preferable.
  • [0115]
    Even in this embodiment, the same effect as set out in connection with the above-mentioned embodiment can be obtained by forming the sprayed film.
  • [0116]
    Although, in the above-mentioned respective embodiments, the semiconductor wafer as a substrate has been explained by way of example, the present invention is not restricted thereto and it may also be applied to the formation of a glass substrate for a liquid crystal display device (LCD).
  • [0117]
    According to the above-mentioned respective embodiments, a sprayed film of substantially Al2O3/Y2O3 whose weight ratio is above 0.5 is formed on the inner wall of the chamber and, by doing so, the chamber is less liable to be etched under a plasma and cleaning gas due to the presence of the high-corrosion resistant sprayed film. Thus the present invention can be preferably applied to the film formation, etching, ashing and heat treatment on a less-etching thermal sprayed film of the chamber.
  • [0118]
    Further, since the gas supply system supplies a process gas near the upper zone of a wafer within the chamber, the gas hardly reaches the inner wall of the chamber and almost no product is deposited on the wall. As a material for the chamber, use can be made of a ceramic (Al2O3, SiO2, AlN, etc.), aluminum, stainless steel, metal or alloy.
  • [0119]
    Additional advantages and modifications will readily occur to those skilled in the art. Therefore, the invention in its broader aspects is not limited to the specific details and representative embodiments shown and described herein. Accordingly, various modifications may be made without departing from the spirit or scope of the general inventive concept as defined by the appended claims and their equivalents.

Claims (27)

    What is claimed is:
  1. 1. A processing apparatus comprising:
    a chamber for holding a substrate that is to be processed;
    a sprayed film formed on an inner surface of the chamber and containing a compound of a III-a element of the periodic table; and
    a processing mechanism for processing a substrate held in the chamber.
  2. 2. The processing apparatus according to
    claim 1
    , wherein the sprayed film contains Al2O3.
  3. 3. The processing apparatus according to
    claim 1
    , wherein the sprayed film comprises Al2O3 and Y2O3.
  4. 4. The processing apparatus according to
    claim 1
    , wherein the weight ratio of Al2O3 to Y2O3 is 0.5 or more in the sprayed film.
  5. 5. The processing apparatus according to
    claim 1
    , wherein a sprayed film containing a III-a element of the periodic table is formed on a part of the processing mechanism, which is exposed to the chamber.
  6. 6. The processing apparatus according to
    claim 1
    , wherein the sprayed film is made of Y2O3, Sc2O3, Sc2F3, YF3, La2O3, CeO2, Eu2O3, or DyO3.
  7. 7. The processing apparatus according to
    claim 4
    , wherein the sprayed film is made of Y2O3, Sc2O3, Sc2F3, YF3, La2O3, CeO2, Eu2O3, or DyO3.
  8. 8. The processing apparatus according to
    claim 1
    , wherein the processing mechanism performs plasma process on the substrate.
  9. 9. The processing apparatus according to
    claim 1
    , wherein the processing mechanism processes the substrate, while applying a corrosive gas into the chamber.
  10. 10. The processing apparatus according to
    claim 1
    , wherein the processing mechanism performs a heating process on the substrate.
  11. 11. A processing apparatus comprising:
    a lower chamber containing a susceptor for holding a substrate that is to be processed;
    an upper chamber provided above the lower chamber;
    antenna means arranged around the upper chamber, for generating an induction magnetic field in the upper chamber and on the substrate;
    high-frequency wave applying means for applying high-frequency power to the antenna means;
    gas-supplying means for supplying a plurality of process gases onto the substrate in the lower chamber;
    gas-exhausting means for exhausting the process gases from the upper and lower chambers; and
    a film formed by sprayed on an inner surface of the upper chamber and containing a compound of a III-a element of the periodic table, for preventing corrosion from taking place while the substrate is being processed,
    wherein an induction electromagnetic field is generated in the upper and lower chambers, generating a plasma, and the plasma is applied to the substrate, thereby to process the substrate.
  12. 12. A processing apparatus comprising:
    a lower chamber containing a susceptor for holding a substrate that is to be processed;
    an upper chamber provided above the lower chamber;
    antenna means arranged around the upper chamber, for generating an induction magnetic field in the upper chamber and on the substrate;
    high-frequency wave applying means for applying high-frequency power to the antenna means;
    a gas-supplying means for shaped like a ring, surrounding an upper part of the lower chamber, and supplies the process gases and a plasma-generating gas into the lower chamber so that the gases may mix at a position above the substrate held on the susceptor; and
    gas-exhausting means for exhausting the process gases from the upper and lower chambers,
    wherein an induction electromagnetic field is generated in the upper chamber, generating a plasma, and the plasma is applied to the substrate, thereby to process the substrate.
  13. 13. The processing apparatus according to
    claim 9
    , wherein the gas-supplying means comprises a plurality of annular layers mounted one upon another, each having a gas-inlet port in the outer circumfrential surface and an inner passage connected to the gas-inlet port, one of the annular layers has a row of gas-outlet ports in the inner circumferential surface, every other gas-outlet port is connected to the inner passage of said one of the annular layers, and the remaining gas-outlet port are connected to the inner passages of the other annular layers alternately.
  14. 14. The processing apparatus according to
    claim 9
    , wherein the gas-supplying means comprises a plurality of annular layers mounted one upon another, each having a gas-inlet port made in the outer circumfrential surface, an inner passage connected to the gas-inlet port, and a plurality of gas-outlet holes made in the inner circumferntial surface and connected to the inner passage, and the gas-outlet holes are arranged in staggered fashion in the inner circumferential surface of the gas-supplying means.
  15. 15. The processing apparatus according to
    claim 8
    , wherein the sprayed film comprises an Al2O3 film and a Y2O3 film.
  16. 16. The processing apparatus according to
    claim 8
    , wherein the weight ratio of the Al2O3 film to the Y2O3 film is 0.5 or more in the sprayed film.
  17. 17. The processing apparatus according to
    claim 2
    , wherein the weight ratio of the Al2O3 film to the Y2O3 film is 0.5 or more in the sprayed film.
  18. 18. The processing apparatus according to
    claim 6
    , wherein the weight ratio of the Al2O3 film to the Y2O3 film is 0.5 or more in the sprayed film.
  19. 19. The processing apparatus according to
    claim 8
    , wherein the upper chamber has a base made of material selected from the group consisting of ceramic, metal, alloy containing the metal and hard plastic.
  20. 20. The processing apparatus according to
    claim 19
    , wherein the ceramic is one selected from the group consisting of Al2O3, SiO2 and AlN.
  21. 21. The processing apparatus according to
    claim 8
    , wherein the sprayed film has a thickness of 50 μm or more.
  22. 22. The processing apparatus according to
    claim 8
    , which further comprises a coolant source for decreasing a temperature in the upper chamber, and in which the lower chamber and the upper chamber are connected in airtight fashion, the induction electromagnetic field generates a plasma above the susceptor, the gas-supplying means supplies process gases to the plasma, thereby forming a film on the substrate.
  23. 23. The process apparatus according to
    claim 8
    , which further comprises a power supply for applying a high-frequency voltage between the lower and upper chambers, and in which the induction electromagnetic filed generates a plasma above the susceptor, the gas-supplying means supplies the process gases, and the high-frequency voltage is applied between the lower and upper chambers, thereby etching a surface of the substrate.
  24. 24. The process apparatus according to
    claim 8
    , wherein the upper chamber is a semi-spherical one, a dome-shaped one, or a thin-type one shorter in height than a plasma-generating area.
  25. 25. The process apparatus according to
    claim 12
    , wherein a weight ratio between Al2O3 to Y2O3 is 5:3 in the sprayed film.
  26. 26. The process apparatus according to
    claim 21
    , wherein the film containing Y2O3 is YAG.
  27. 27. The process apparatus according to
    claim 8
    , wherein the lower chamber is connected to the upper chamber and used as a heating chamber for performing heat processing on the substrate, an ashing chamber for removing a resist mask from the substrate or an etching chamber for etching the substrate.
US09731722 1999-12-10 2000-12-08 Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film Abandoned US20010003271A1 (en)

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US10444957 US7846291B2 (en) 1999-12-10 2003-05-27 Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film
US11980596 US7879179B2 (en) 1999-12-10 2007-10-31 Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film
US11980570 US20080069966A1 (en) 1999-12-10 2007-10-31 Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film

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US10444957 Active US7846291B2 (en) 1999-12-10 2003-05-27 Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film
US11980596 Active US7879179B2 (en) 1999-12-10 2007-10-31 Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film
US11980570 Abandoned US20080069966A1 (en) 1999-12-10 2007-10-31 Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film

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US11980596 Active US7879179B2 (en) 1999-12-10 2007-10-31 Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film
US11980570 Abandoned US20080069966A1 (en) 1999-12-10 2007-10-31 Processing apparatus with a chamber having therein a high-corrosion-resistant sprayed film

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