GB2181460A - Apparatus and method for chemical vapor deposition using an axially symmetric gas flow - Google Patents

Apparatus and method for chemical vapor deposition using an axially symmetric gas flow Download PDF

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Publication number
GB2181460A
GB2181460A GB08623978A GB8623978A GB2181460A GB 2181460 A GB2181460 A GB 2181460A GB 08623978 A GB08623978 A GB 08623978A GB 8623978 A GB8623978 A GB 8623978A GB 2181460 A GB2181460 A GB 2181460A
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substrate
gas
chemical vapor
vapor deposition
deposition
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GB2181460B (en
GB8623978D0 (en
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Wiebe B Deboer
Klavs F Jensen
Wayne L Johnson
Mcdonald Robinson
Gary W Read
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Epsilon LP
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Epsilon LP
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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
    • C23C16/45502Flow conditions in reaction chamber
    • C23C16/45504Laminar flow
    • 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
    • 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
    • C23C16/45502Flow conditions in reaction chamber
    • C23C16/45508Radial flow
    • 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
    • C23C16/45587Mechanical means for changing the gas flow
    • C23C16/45591Fixed means, e.g. wings, baffles
    • 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
    • C23C16/54Apparatus specially adapted for continuous coating
    • CCHEMISTRY; METALLURGY
    • C30CRYSTAL GROWTH
    • C30BSINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
    • C30B25/00Single-crystal growth by chemical reaction of reactive gases, e.g. chemical vapour-deposition growth
    • C30B25/02Epitaxial-layer growth
    • C30B25/14Feed and outlet means for the gases; Modifying the flow of the reactive gases

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  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Fluid Mechanics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Chemical Vapour Deposition (AREA)

Abstract

In a chemical vapor deposition chamber, an improved technique for providing deposition materials to the growth surface is described in which the gas carrying deposition materials is constrained to have axial symmetry thereby proving a uniform deposition of materials on the substrate. As illustrated in Fig. 4 the gas can be initially directed toward the substrate (10) with a generally uniform perpendicular velocity. The gas can be introduced into the deposition chamber through a multiplicity of apertures (74) and is extracted from the vicinity of the substrate (10) in a manner to preserve the axial symmetry. The apparatus permits convenient control of the deposition process by varying the distance between apparatus introducing the gas carrying the deposition materials and the substrate. The flow of gas minimizes the problems arising from autodoping of the growth layer of material. The flow of gas and generally small size of the deposition chamber minimize particulate contamination of the growing film. <IMAGE>

Description

SPECIFICATION Apparatus and method for chemical vapor deposition using an axially symmetric gas flow This invention relates generally to the chemical vapor deposition of material onto a substrate and, more particularly, to the use of an axially symmetric gas flow for improving the deposition onto a substrate of a material carried by the gas.
It is known in the related art of chemical deposition of a material onto a substrate, to provide a susceptor in an enclosed container, the susceptor typically supporting a plurality of substrates. A carrier gas, containing gaseous forms of the atoms to be deposited on the substrate, is introduced into the container in the vicinity of the susceptor. The flow of the gas, determined by the geometry of the container and the susceptor, is generally constrained to flow parallel to the substrates. By a combination of transport and chemical reaction, the atoms of the deposition materials adhere at high temperature to the substrate surfaces, forming the desired deposition layer.
This deposition technique has proved satisfactory in the past, however as higher volumes of material have been required and higher quality materials needed, limits of this technique are being reached. The deposition technique has four problems. The first problem is that, as the gas flows over the surfaces of the substrates and the susceptor, deposition of the material onto the surface changes the concentration of the deposition materials in the carrier gas. Consequently, over the length of the susceptor, and indeed over the length of each substrate, a different rate of growth of the layer of material is found. A second problem is that, as the deposition material is depleted in the region of deposition, new deposition material must be transported across relatively long distances in the large reaction containers used for deposit.This transport controlled deposition limits the rate at which deposition can occur, and therefore, is related to the cost of the manufacture of the materials such as in the epitaxial process. A third problem is generally referred to as autodoping.
In the autopoding process, impurity atoms from the highly doped substrate can be detached from the substrate surface and can be incorporated via the gas phase into the more lightly doped layer of material being deposited.
In the related art, special steps must be taken to minimise autodoping, such as deposition of an extra coating onto the back of the substrate. A final problem is particulate contamination. As chemical vapor deposition chambers have become larger, the wall area of the chamber has increased. Unwanted deposits that form upon these walls are sources for particulates that can be inadvertently incorporated into the deposition material.
A need has therefore been felt for a technique of vapor deposition in which the growth rate of the deposited material onto a substrate is highly uniform over the entire area of the substrate, in which the growth rate of the deposited material can be increased, in which autodoping of the deposited material can be prevented without additional process steps, and in which particulate contamination can be minimized.
It is therefore an object of the present invention to provide method and apparatus for improved chemical vapor deposition of a material onto a substrate.
It is a further object of the present invention to provide a method and apparatus for providing improved chemical vapor deposition of material, wherein the concentration of the deposition materials in the carrier gas is generally constant over the entire area of the substrate.
It is yet another object of the present invention to provide for chemical vapor deposition of a material onto a substrate wherein the substrate and the flow of the carrier gas have axial symmetry.
It is yet another object of the present invention to provide for chemical vapor deposition of a material onto a substrate using stagnation point flow of the carrier gas.
It is still a further object of the present invention to provide for a uniform flow of vapor directly toward a substrate for purposes of chemical vapor deposition of materials carried by the vapor.
It is yet another object of the present invention to provide, in a chemical vapor growth reaction chamber, a uniform axially symmetric flow of gas toward a circular substrate by having a plurality of apertures through which the carrier gas with the deposition material can pass.
It is still a further object of the present invention to provide for uniform growth of material in a chemical vapor reaction chamber by applying an axially symmetric gas flow onto a substrate, and by rotating the substrate.
It is yet another object of the present invention to provide, in a chemical vapor deposition reaction chamber, for the uniform removal of the gaseous products following deposition.
It is still a further object of the present invention to provide, in a chemical vapor deposition reaction chamber, a convenient technique for controlling the rate of deposition of the deposition material on a substrate.
According to the present invention apparatus for chemical vapor deposition of material on a substrate comprises: a circular substrate; and apparatus for directing a flow of gas carrying the deposition material perpendicular to the circular substrate, said flow of gas generally having an axial symmetry with respect to a centre of said substrate.
In a preferred embodiment a chemical vapor reaction chamber is which a gas, introduced at a preselected distance from a- circular substrate, has an initial uniform velocity toward the substrate. As the gas approaches the substrate, the gas is redirected radially outward in an axially symmetric flow. The gas is withdrawn from the chamber by a multiplicity of apertures, by a series of baffles, or by other means that generally preserve the axial symmetry of the gas flow. The circular substrate can be rotated to provide increased deposition uniformity by averaging irregularities in the gas flow. The distance from the substrate to the apparatus introducing the gas can be varied.
In addition, the axial symmetry of the flow of gas reduces the autodoping of the deposited material. The radial flow of gas and the small wall area of the deposition chamber combine to minimize particulate contamination of the growing film.
The invention is further described by means of example and not in any limitative sense, with reference to the accompanying drawings, of which: Figure 7a, Figure ib and Figure ic are diagrammatic views showing the flow of the gas containing the deposition material over substrates according to typical configurations of the prior art.
Figure 2 is a schematic diagram, in which the flow of gas is initially directed uniformly toward a circular substrate, according to the present invention.
Figure 3 is a cross-section diagram of the flow of gas carrying deposition material to the substrate according to the present invention.
Figure 4 is a schematic diagram of an apparatus for providing the initial conditions for the flow of gas in Fig. 3.
Figure 5a is a top cross-sectional view of the apparatus showing the position of baffles for maintaining axial symmetry of the flow of gas according to the present invention.
Figure 5b is a horizontal cross-section view of a portion of the apparatus showing the position of the baffles of Fig. 5a as related to the semiconductor substrate for providing a uniform flow of gas.
Referring now to Fig. 1a, a plurality of substrate materials 10 are located on a susceptor material 15. A gaseous substance 11 traverses the substrate material and deposits preselected components to the vapor onto the substrate. Fig. 1 b shows a susceptor geometry in which a plurality of surfaces 13 can each support a plurality of substrates 10 for exposure to gas 11 flowing over the surfaces.
Fig. 1c shows a geometry in which a susceptor 15 support a plurality of substrates 10.
The gas carrying the deposition material is introduced through an aperture 14 in the centre of the susceptor.
Referring next to Fig. 2, a schematic diagram of the instant invention illustrates that gas 11, carrying the vapor deposition material(s), is directed onto a generally circular substrate 10 supported by a susceptor 15.
The gas flows first toward the surface, and then in a radially outward direction, away from the axis of the susceptor-substrate combination.
Referring next to Fig. 3, a cross-sectional view in a plane containing the axis of symmetry of the flow of the gas 11 as it approaches the substrate 10 is shown. The gas 11 initially has a generally uniform velocity directed perpendicular- to the entire surface of substrate 10. The solid substrate, as the gas 11 approaches the substrate, causes the velocity vector to become parallel to the surface of substrate .20 and flow away from the axis of symmetry. At one point 21 on the axis of symmetry, generally referred to as the stagnation point, there is theoretically no flow of gas. The axially symmetric gas flow resulting from uniform gas flow toward a surface is generally referred to as stagnation point flow.
Referring next to Fig. 4, an implementation of the actual arrangement for providing the initial conditions of a gas with velocity vector with uniform magnitude directed towards the substrate is shown. A surface 71, either a surface of an enclosure or one of two generally parallel plates, has the gas 11 introduced into the region above surface 71. The gas 11 is forced through the apertures 74 in the surface 71 towards the semiconductor substrate 10. Thus, the initial vector of the velocity is directed toward the substrate. Because of the relatively small size of the apertures 74, the magnitude of the gas velocity will generally be uniform among all of the apertures 74 as the gas passes through toward the plane of substrate 10.To reduce the effects of any granularity that can result from the use of discrete apertures, and to smooth out any irregularities in distribution of the gas, the substrate 10 can be rotated during the period of gas flow. It has been found that a generally uniform flow can be obtained when the apertures 74 are located at the apexes of equilateral triangles, and are distributed uniformly over the region of surface 71 approximately the same size as substrate 10 and axially symmetrical therewith.
Referring next to Fig. 5a, a top view of the procedure for removing the gas from the chamber without altering the axial symmetry in the vicinity of the substrate 10 is shown. In one embodiment, a plurality of relatively large apertures 53 are located generally equidistant from the axis of symmetry of the gas flow and the gas is removed therethrough. However, this configuration, without additional structure, can cause a large amount of structure in the gas flow in the vicinity of the substrate 10. To reduce this structure, baffles 51 and 52 can be interposed between the sub strates and the apertures 53. This structure, in redirecting the flow of the gas, causes a smoothing and, therefore, enhances the axial symmetry of the gas flow.It will be clear that when a multiplicity of apertures 53 extending around the semiconductor substrate can be used, and if the number of these apertures is sufficiently large, the actual departure from axial symmetry in the vicinity of substrate 10 can be minimized even without baffles 51 and 52. Fig. 5b generally is a horizontal partial cross-section view showing the relationship of baffles 52 and 51 and apertures 53 to substrate 10 and susceptor 15.
The chemical vapor deposition of material on the semiconductor substrate is the result of a flow of gas along the surface of the semiconductor substrate 10, the flow of gas being generally constrainted to have axial symmetry. This flow configuration is generally known as stagnation point flow. The density of deposition material carried by the gas and deposited onto the substrate is generally uniform across the entire surface under these conditions. This result is known from the study of this flow configuration in other applications, and these results have been confirmed by computer simulation studies performed by inventors under the conditions determined by the parameters of the deposition reactor.In essence, because of the expanding area present in departing from the axis of symmetry, gas containing the original density of deposition materials can come in contract with the surface as a result of both convection and diffusion phenomena. It is further known from studies in other physical areas, and confirmed by computer simulation studies, that the temperature profile of the impinging gas is generally uniform radially. That is, the isotherms over the substrate are a constant distance from the substrate surface. Similarly, for chemical reactions occuring in the gas, the mole fraction of gas components will be generally radially uniform at a given distance from the substrate surface.
Because it is necessary, as a practical matter, to introduce the gas through a series of apertures to establish the required initial conditions, and because of the difficulty in precise centering of the circular semiconductor substrate relative to the entering and departing vapor, the substrate can be rotated to reduce non-uniformity structure in the carrier gas as seen by the substrate.
While the discussion has been directed on the particular gas flow with respect to the substrate, it will be clear that certain other features are significant. For example, if the substrate is to be heated, and particularly if the substrate is to be heated by optical radiation, the apparatus containing the apertures through which the gas is introduced will generally be made of a suitable transparent material, for example, fused quartz. It will also be clear that although the apparatus is shown as having the semiconductor substrate in the horizontal plane with the vapor impinging from above, that this orientation can be varied without altering the operation of the preferred embodiment.
One important aspect of the instant invention is the ability to control the distance as shown in Fig. 4 between the apparatus introducing the gas and the substrate. The ability to determine this distance provides an important tool in controlling the growth of the deposited materials on the substrate 10. The axially symmetric flow of gas (away from the axis) has the important benefit of reducing autodoping by creating a flow of gas in a direction, relative to the substrate, that is opposite from the flow of materials producing the autodoping. This effect can be enhanced and autodoping further reduced, by applying a purge gas to the bottom of the substrate.
This technique of chemical vapor deposition is particularly useful for epitaxial deposition and especially for deposition of epitaxial silicon on a substrate.
The above description is included to illustrate the operation of the preferred embodiment and is not meant to limit the scope of the invention. The scope of the invention is to be limited only by the following claims. Many variations will be apparent to those skilled in the art that would yet be encompassed by the scope of the present invention.

Claims (20)

1. Apparatus for chemical vapor deposition of material on a substrate comprising: a circular substrate; and apparatus for directing a flow of gas carrying the deposition material perpendicular to the circular substrate, said flow of gas generally having an axial symmetry with respect to a centre of said substrate.
2. The chemical vapor deposition apparatus of claim 1, wherein a distance between said apparatus and said substrate can be varied.
3. The chemical vapor deposition apparatus of claim 1 wherein said substrate can be rotated.
4. The chemical vapor deposition apparatus of claim 1, wherein said apparatus is used for epitaxial deposition.
5. The chemical vapor deposition apparatus of claim 4, wherein said apparatus is used for deposition of epitaxial silicon onto said substrate.
6. The apparatus for chemical vapor deposition of claim 1, further including apparatus for introducing a purge gas on a reverse side of said substrate.
7. The method of chemical vapor deposition of material on a substrate comprising the step of: applying a gas including deposition materials to the substrate wherein said substrate and the flow of said gas generally have axial symmetry.
8. The method of chemical vapor deposition of claim 7, further comprising the step of controlling the rate of said deposition by varying a distance between said substrate and apparatus applying said gas.
9. The method of material deposition of claim 7, further comprising the step of rotating said substrate.
10. The method of material deposition of claim 7 further comprising the step of maintaining a stagnation point flow of said gas.
11. Apparatus for chemical vapor deposition of materials on a substrate comprising: a generally circular substrate; and gas flow means for producing a flow of gas having axial symmetry across said circular substrate.
12. The apparatus for chemical vapor deposition of claim 11, wherein said gas flow means introduces said gas with a generally uniform magnitude of velocity perpendicular to said substrate.
13. The apparatus for chemical vapor de-position of claim 12, wherein said gas flow means includes means for varying a distance between said substrate and a region where said gas is directed toward said substrate.
14. The apparatus for chemical vapor deposition of material of claim 13, further including means for rotating said substrate.
15. The apparatus for chemical vapor deposition of claim 13 wherein said gas flow means includes a plurality of apertures for extracting said gas without significantly altering said axial symmetry.
16. The apparatus for chemical vapor deposition of claim 15 further comprising a plurality of baffles between substrate and said extracting apertures.
17. The apparatus for chemical vapor deposition of claim 11, further including means for reducing autodoping of said substrate.
18. The apparatus for chemical vapor deposition of claim 17 wherein said gas flow means includes means for maintaining a stagnation point flow of said gas.
19. Apparatus for chemical vapor deposition of material on a substrate substantially as hereinbefore described with reference to Figs.
2 to 5 of the accompanying drawings.
20. A method of chemical vapor deposition of material on a substrate substantially as hereinbefore described with reference to Figs.
2 to 5 of the accompanying drawings.
GB8623978A 1985-10-07 1986-10-06 Apparatus and method for chemical vapor deposition using an axially symmetric gas flow Expired GB2181460B (en)

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US78473885A 1985-10-07 1985-10-07

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GB2181460A true GB2181460A (en) 1987-04-23
GB2181460B GB2181460B (en) 1989-10-04

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Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2194966A (en) * 1986-08-20 1988-03-23 Gen Electric Plc Deposition of films
EP0272140A2 (en) * 1986-12-19 1988-06-22 Applied Materials, Inc. TEOS based plasma enhanced chemical vapor deposition process for deposition of silicon dioxide films.
GB2220679A (en) * 1987-09-09 1990-01-17 Edward William Johnson Apparatus for thin film deposition of aerosol particles by thermolytic decomposition
US4997677A (en) * 1987-08-31 1991-03-05 Massachusetts Institute Of Technology Vapor phase reactor for making multilayer structures
EP0415191A1 (en) * 1989-08-31 1991-03-06 Lpe Spa System for controlling epitaxial grow rate in vertical provided with a frustum pyramid susceptor
US5052339A (en) * 1990-10-16 1991-10-01 Air Products And Chemicals, Inc. Radio frequency plasma enhanced chemical vapor deposition process and reactor
WO1993025723A1 (en) * 1992-06-15 1993-12-23 Materials Research Corporation Rotating susceptor semiconductor wafer processing cluster tool module useful for tungsten cvd
WO1993025724A1 (en) * 1992-06-15 1993-12-23 Materials Research Corporation Semiconductor wafer processing cvd reactor cleaning method and apparatus
US5755886A (en) * 1986-12-19 1998-05-26 Applied Materials, Inc. Apparatus for preventing deposition gases from contacting a selected region of a substrate during deposition processing
WO2001086035A1 (en) * 2000-05-08 2001-11-15 Memc Electronic Materials, Inc. Epitaxial silicon wafer free from autodoping and backside halo
US6444027B1 (en) 2000-05-08 2002-09-03 Memc Electronic Materials, Inc. Modified susceptor for use in chemical vapor deposition process
CN1312326C (en) * 2000-05-08 2007-04-25 Memc电子材料有限公司 Epitaxial silicon wafer free from autodoping and backside halo
AT513190A1 (en) * 2012-08-08 2014-02-15 Berndorf Hueck Band Und Pressblechtechnik Gmbh Apparatus and method for plasma coating a substrate, in particular a press plate

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GB1056430A (en) * 1962-11-13 1967-01-25 Texas Instruments Inc Epitaxial process and apparatus for semiconductors
GB1124329A (en) * 1964-12-29 1968-08-21 Siemens Ag Improvements in or relating to the epitaxial deposition of crystalline layers
US3874900A (en) * 1973-08-13 1975-04-01 Materials Technology Corp Article coated with titanium carbide and titanium nitride
US3894164A (en) * 1973-03-15 1975-07-08 Rca Corp Chemical vapor deposition of luminescent films
GB2141386A (en) * 1983-05-11 1984-12-19 Semiconductor Res Found Fabricating semiconductor devices

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US3854443A (en) * 1973-12-19 1974-12-17 Intel Corp Gas reactor for depositing thin films
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GB1056430A (en) * 1962-11-13 1967-01-25 Texas Instruments Inc Epitaxial process and apparatus for semiconductors
GB1124329A (en) * 1964-12-29 1968-08-21 Siemens Ag Improvements in or relating to the epitaxial deposition of crystalline layers
US3894164A (en) * 1973-03-15 1975-07-08 Rca Corp Chemical vapor deposition of luminescent films
US3874900A (en) * 1973-08-13 1975-04-01 Materials Technology Corp Article coated with titanium carbide and titanium nitride
GB2141386A (en) * 1983-05-11 1984-12-19 Semiconductor Res Found Fabricating semiconductor devices

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Cited By (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2194966A (en) * 1986-08-20 1988-03-23 Gen Electric Plc Deposition of films
US5755886A (en) * 1986-12-19 1998-05-26 Applied Materials, Inc. Apparatus for preventing deposition gases from contacting a selected region of a substrate during deposition processing
EP0272140A2 (en) * 1986-12-19 1988-06-22 Applied Materials, Inc. TEOS based plasma enhanced chemical vapor deposition process for deposition of silicon dioxide films.
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Also Published As

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JPH07100861B2 (en) 1995-11-01
NL8602357A (en) 1987-05-04
GB2181460B (en) 1989-10-04
DE3634130A1 (en) 1987-05-07
GB8623978D0 (en) 1986-11-12
JPS6289870A (en) 1987-04-24

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