WO2010119430A1 - Reaction chamber of an epitaxial reactor and reactor that uses said chamber - Google Patents

Reaction chamber of an epitaxial reactor and reactor that uses said chamber Download PDF

Info

Publication number
WO2010119430A1
WO2010119430A1 PCT/IB2010/051666 IB2010051666W WO2010119430A1 WO 2010119430 A1 WO2010119430 A1 WO 2010119430A1 IB 2010051666 W IB2010051666 W IB 2010051666W WO 2010119430 A1 WO2010119430 A1 WO 2010119430A1
Authority
WO
WIPO (PCT)
Prior art keywords
quartz
reaction chamber
walls
chamber according
component
Prior art date
Application number
PCT/IB2010/051666
Other languages
French (fr)
Inventor
Srinivas Yarlagadda
Natale Speciale
Franco Preti
Mario Preti
Original Assignee
Lpe S.P.A.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=41226172&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2010119430(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Lpe S.P.A. filed Critical Lpe S.P.A.
Priority to EP10727855.8A priority Critical patent/EP2419552B1/en
Priority to US13/259,818 priority patent/US9382642B2/en
Priority to JP2012505290A priority patent/JP6116900B2/en
Priority to CN201080016602.6A priority patent/CN102395714B/en
Publication of WO2010119430A1 publication Critical patent/WO2010119430A1/en

Links

Classifications

    • 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
    • C30B25/08Reaction chambers; Selection of materials therefor
    • 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
    • C23C16/46Chemical 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 heating the substrate
    • 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
    • C30B25/10Heating of the reaction chamber or the substrate
    • 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
    • C30B29/00Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
    • C30B29/02Elements
    • C30B29/06Silicon
    • 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
    • C30B29/00Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
    • C30B29/02Elements
    • C30B29/08Germanium
    • 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
    • C30B29/00Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
    • C30B29/10Inorganic compounds or compositions
    • C30B29/36Carbides
    • 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
    • C30B29/00Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
    • C30B29/10Inorganic compounds or compositions
    • C30B29/40AIIIBV compounds wherein A is B, Al, Ga, In or Tl and B is N, P, As, Sb or Bi
    • C30B29/403AIII-nitrides
    • 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
    • C30B29/00Single crystals or homogeneous polycrystalline material with defined structure characterised by the material or by their shape
    • C30B29/10Inorganic compounds or compositions
    • C30B29/40AIIIBV compounds wherein A is B, Al, Ga, In or Tl and B is N, P, As, Sb or Bi
    • C30B29/403AIII-nitrides
    • C30B29/406Gallium nitride
    • 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
    • C30B35/00Apparatus not otherwise provided for, specially adapted for the growth, production or after-treatment of single crystals or of a homogeneous polycrystalline material with defined structure

Definitions

  • the present invention relates to a reaction chamber of an epitaxial reactor and to a reactor that uses said chamber.
  • Epitaxial reactors are machines used to deposit smooth and uniform monocrystalline or polycrystalline layers of materials on substrates; the substrates thus treated are used to produce electric devices (such as solar cells), electronic devices (such as MOSFETs and LEDs) and microelectronic devices (such as integrated circuits). Therefore, the quality of the layer deposited, in terms of defectiveness, uniform thickness and uniform resistivity, is extremely important and subject to increasingly strict requirements.
  • the materials deposited are typically conductor and semiconductor materials, such as silicon [Si], silicon carbide [SiC], germanium [Ge], gallium arsenide
  • GaAs aluminium nitride [AIN], gallium nitride [GaN].
  • the layer deposited and the substrate below can be made of the same material or of different materials.
  • the thickness of the layer deposited can be in a wide interval from a few nanometres to several millimetres; when the thickness of the layer deposited is greater than 1 mm, the deposition process is generally called "bulk growth".
  • Known epitaxial reactors comprise a reaction chamber consisting in general essentially of a quartz piece; the quartz piece comprises a quartz piece portion having the shape of a cylinder, prism, cone, pyramid or parallelepiped and provided with at least one internal cavity defined by walls; this cavity comprises a reaction and deposition zone of the epitaxial reactor; this zone is adapted to house at least one susceptor to be heated therein; the susceptor serves to support and often also to heat the substrates.
  • the chamber can be arranged vertically or horizontally (rarely obliquely); depending on the type, the susceptor can have the shape of a disk, prism, cylinder, pyramid, cone and can be solid or hollow; depending on the type, the susceptor can be heated by means of resistors, inductors, lamps (rarely internal burners); depending on the type, the reactors can be "cold wall” or “hot wall) (these terms refer to the walls defining the space inside which the reaction and deposition takes place).
  • the processes of epitaxial reactors are performed at high temperatures, i.e.
  • deposition of polycrystalline silicon is performed at temperatures typically between 45O 0 C and 800°C
  • deposition of monocrystalline silicon on silicon substrates is performed at temperatures typically between 850 0 C and 1 '25O 0 C
  • deposition of monocrystalline silicon carbide on silicon substrates is performed at temperatures typically between 1 '200°C and 1'400°C
  • deposition of monocrystalline silicon carbide on silicon carbide substrates is performed at temperatures typically between 1 '500 0 C and 1 '700 0 C for "epitaxial growth” and at temperatures typically between 1 '900 0 C and 2'400 0 C for "bulk growth", and use a great deal of energy (tens of kW) for heating.
  • an important requirement is that the substrates are heated uniformly during the deposition process to obtain high uniformity of thickness and resistivity.
  • a drawback of the solution with gold layer is that, after a certain time (i.e. a few months), the gold layer becomes detached from the quartz surface of the reaction chamber - the hotter the quartz surface is, the faster the gold layer detaches, also due to the fact that thermal expansion of gold is higher than that of quartz; this phenomenon occurs even more rapidly if the reaction chamber is cooled by means of a gaseous flow (which is relatively common), also due to the mechanical action of the gaseous flow on the layer; moreover, this phenomenon is increased by traces of acids, deriving from previous wash cycles of the reaction chamber, on the surface of the reaction chamber.
  • Detachment of the gold layer results in an increase in consumption of electrical power of the epitaxial reactor, as part of the infrared radiation emitted by the susceptor is released into the environment. Moreover, as detachment of the gold layer is not smooth and uniform, this also results in a reduction in the quality of the substrates grown. Therefore, when detachment occurs, it is necessary to disassemble the reaction chamber from the epitaxial reactor, completely remove the gold layer (already partly detached), re-apply the gold layer and re-assemble the reaction chamber in the epitaxial reactor; these operations take time, are costly and can only be performed a limited number of times.
  • the general object of the present invention is to overcome the aforesaid drawbacks and satisfy the aforesaid requirements. This and other objects are achieved through the reaction chamber having the features set out in the appended claims, which form an integral part of the present description.
  • the idea underlying the present invention is that of providing a quartz component arranged close to the walls of the cavity of the reaction chamber in such a manner as to form a counterwall and to be a wall of the reaction and deposition zone.
  • A excellent uniformity of thickness and resistivity of the layers deposited
  • B low defectiveness of the layers deposited
  • C reduction in consumption of electricity to heat the reaction and deposition zone
  • D improved utilization of the precursor gases injected into the reaction and deposition zone and therefore greater deposition velocity
  • E a reduction of parasitic depositions on the walls of the cavity of the chamber and therefore fewer stray particles in the reaction and deposition zone and less need to "wash" the chamber
  • the reaction chamber of an epitaxial reactor essentially consists of a quartz piece; said quartz piece comprises a quartz piece portion having at least one internal cavity defined, at least partly, by walls; said cavity comprises a reaction and deposition zone of the epitaxial reactor; said zone is adapted to house at least one susceptor to be heated therein; the reaction chamber also comprises a quartz component arranged close to one or more of said walls in such a manner as to form a counterwall and to be a wall of said zone.
  • said quartz component can be arranged in such a manner as to form a counterwall for two or three or four of said walls, preferably for three of said walls.
  • said quartz component can rest on one or two of said walls, preferably on only one of said walls.
  • said quartz component can essentially consist of a straight or shaped quartz slab, preferably a shaped quartz slab, more preferably a U-shaped quartz slab.
  • said quartz slab can have a uniform or variable thickness.
  • At least one interspace is typically defined between said quartz component and said walls.
  • Said interspace can be isolated from said reaction and deposition zone, in particular hermetically isolated.
  • said interspace can have a uniform or variable width.
  • two or three or four interspaces preferably three interspaces, can be defined between said quartz component and said walls, the widths of said interspaces being preferably uniform and equal to one another.
  • the quartz of said quartz component can be transparent, opaque or reflective.
  • said quartz component can be coated with a reflective layer on either the interior side or the exterior side, preferably on the side which is closer to said walls.
  • Said reflective layer is typically adapted to reflect back the infrared radiation emitted by said susceptor in the wavelength interval from 1'000 nm to 10'0OO nm, preferably from 1'500 nm to 3'00O nm.
  • Said reflective layer is preferably made of a quartz-based material. Said reflective layer can completely or partly coat said quartz component.
  • Said reflective layer can be completely or partly coated by a layer of vitrified quartz.
  • said quartz piece portion can have the shape of a cylinder or prism or pyramid cone, preferably substantially of a parallelepiped, and has an axial through hole forming said cavity.
  • the reaction chamber according to the present invention can comprise flanges at the ends of said quartz piece.
  • at least one interspace is typically defined between said quartz component and said walls; means can therefore be provided, associated with the chamber, adapted to carry at least one fluid flow, preferably gaseous, within said interspace.
  • Said means can be adapted to carry at least two fluid flows, preferably gaseous, within said interspace, the direction of flow of said flows preferably forming an angle of around
  • the direction of flow of one or each of said flows can change before and/or during and/or after a growth process.
  • the velocity and/or flow rate of one or each of said fluid flows can change before and/or during and/or after a growth process.
  • the fluid of one or each of said flows can comprise hydrogen and/or helium and/or argon.
  • composition of one or each of said flows can change before and/or during and/or after a growth process.
  • One or each of said flows can be adapted to cool said quartz component.
  • One or each of said flows can be adapted to control or determine thermal exchange between said quartz component and at least one of said walls, in particular the thermal exchange coefficient of said at least one interspace.
  • One or each of said flows can be such as to maintain substantially the same pressure on two sides of said quartz component before and/or during and/or after a growth process.
  • the present invention also relates to an epitaxial reactor comprising a reaction chamber having one or more of the features set out above.
  • Fig.1 shows a reaction chamber according to prior art in three different views (Fig. 1 A is a side view, Fig. 1 B is a top view, Fig. 1 C is a front view),
  • Fig.2 shows an example of embodiment of the reaction chamber according to the present invention in three different sectional views (Fig. 2A is a side view, Fig. 2B is a top view, Fig. 2C is a front view) - the chamber of Fig. 2 corresponds to the chamber of Fig. 1 to which technical characteristics according to the present invention have been added, and
  • Fig.3 shows a second example of embodiment of the reaction chamber according to the present invention in a sectional side view - the chamber of Fig. 3 is very similar to the chamber of Fig. 2.
  • Fig.1 shows a reaction chamber of an epitaxial reactor essentially consisting of a hollow quartz piece; this hollow quartz piece comprises a quartz piece portion 1 having the shape of a parallelepiped (with rounded longitudinal edges) and an axial through hole 2 produced in the portion 1 ; the portion 1 is adapted to define according to two of three directions (i.e.
  • a reaction and deposition zone 3 (not shown in Fig.1 ) and to house at least one susceptor (not shown in Fig.1 ) to be heated within the hole 2;
  • the hole 2 has a rectangular section (with rounded corners) corresponding in shape to the section of the portion 1 and, in this manner, the portion 1 forms a tube with walls having a substantially constant section;
  • 1 A indicates the internal surface of the lower wall, 1 B the internal surface of the first lateral wall, 1 C the internal surface of the upper wall and 1 D the internal surface of the second lateral wall.
  • the chamber of Fig.1 is adapted to be arranged horizontally, to house a disk- shaped susceptor, to be associated with induction heating means, and to be used in a "cold wall” reactor (i.e. the temperature of the portion 1 of the hollow quartz piece does not exceed 400-600 0 C during epitaxial growth processes and is therefore much lower with respect to that of the susceptor).
  • the chamber of Fig.1 also comprises two flanges 7 at the ends of the hollow quartz piece, in particular of the portion 1.
  • the portion 1 is made of transparent quartz, in particular transparent to visible light, but also to infrared light.
  • the flanges 7 are made of opaque quartz, in particular opaque (i.e. which blocks the passage and therefore partly reflects and partly absorbs) to visible light, but also to infrared light.
  • Fig.2 shows a disk-shaped susceptor 4, mounted on a vertical shaft 8 to support it and make it rotate; the susceptor 4 has slight recesses (in particular five recesses) on the upper face thereof adapted to house substrates on which to perform epitaxial growth; the shaft 8 passes through a circular hole produced in the lower wall of the chamber (retaining means, not shown in this figure, are provided); moreover, this figure shows the reaction and deposition zone 3; finally, it is noted that neither the susceptor 4 nor the shaft 8 is part of the chamber.
  • the chamber of Fig.2 differs from that of Fig.1 essentially due to the fact that it comprises a quartz component 5 arranged close to one or more of the walls of the cavity 2 in such a manner as to form a counterwall and to be a wall of the zone 3; in particular, this is a U-shaped slab, arranged overturned and resting only on the lower wall, specifically on the internal surface 1A of this wall; all this is clearly visible in Fig.2C; the slab 5 has uniform thickness.
  • This shaped slab can be produced by joining three straight slabs: one adapted to be arranged horizontally and two adapted to be arranged vertically.
  • the component 2 extends for the complete length of the chamber, in particular to the edge of the flanges 7; alternatively, it could, for example, extend only for the complete length of the portion 1.
  • the component 5 is arranged in such a manner as to produce a counterwall for three walls of the cavity 2, in particular for the two lateral walls and for the upper wall.
  • An interspace 6 is defined between the component 5 and the walls of the cavity 2, which is divided into three portions 6B, 6C, 6D, which are in turn interspaces; the interspace 6B is located between the component 5 and the internal surface 1 B of the first lateral wall, the interspace 6C is located between the component 5 and the internal surface 1C of the upper wall, the interspace 6D is located between the component 5 and the internal surface 1 D of the second lateral wall; the interspace 6 (and therefore its portions 6B, 6C, 6D) is isolated more or less hermetically from the reaction and deposition zone 3; the widths of the three interspaces 6B, 6C and 6D are substantially (there are slight differences at the edges) uniform and equal to one another, as can be clearly seen in Fig.2C; these widths are typically in the interval from 1 mm to 10 mm
  • the quartz of the component 5 can be transparent, opaque or reflective.
  • the component 5 can be coated with a reflective layer either on the interior side or on the exterior side thereof; the coating can be total or partial.
  • the component 5 is made of transparent quartz and coated with a reflective layer on the side closer to the walls of the cavity 2, i.e. close to the surfaces 6B, 6C, 6D.
  • This reflective layer is typically adapted to reflect back the infrared radiation emitted by the susceptor 4 in the wavelength interval from 1'000 nm to 10'0OO nm, preferably from 1'500 nm to 3'00O nm.
  • the reflective layer is preferably made of a quartz-based material; in this manner, the material of the layer is compatible from a chemical point of view (equal or similar chemical properties, i.e. resistance), from a mechanical point of view (equal or similar mechanical properties) and from a thermal point of view (equal or similar thermal properties, i.e. CTE [Coefficient of Thermal Expansion]) with the material of the component.
  • a chemical point of view equal or similar chemical properties, i.e. resistance
  • mechanical point of view equal or similar mechanical properties
  • thermal point of view i.e. CTE [Coefficient of Thermal Expansion]
  • the thickness of the reflective layer is typically in the interval from 0.5 mm to 1.5 mm and is preferably around 1 mm.
  • the reflective layer can be obtained according to the following process: applying a semi-liquid slurry with a high content (i.e. greater than 80% and lower than 95%) of amorphous quartz particles in dispersion (the dispersion liquid can be water or, for example, alcohol) to the transparent quartz reaction chamber, then - drying the slurry applied, then sintering the dried slurry.
  • the reflective layer can be completely or partly coated by a layer of vitrified quartz; this vitrified layer can have a thickness typically in the interval from 0.5 mm to 1.5 mm.
  • the reflective quartz layer and the superimposed vitrified quartz layer can be obtained with the following single process: applying a semi-liquid slurry with a high content (i.e.
  • the dispersion liquid can be water or, for example, alcohol
  • the dispersion liquid can be water or, for example, alcohol
  • the vitrified layer allows the reflective layer below to be protected both from a chemical and from a mechanical point of view; if a vitrified layer of excellent quality is produced, it is also possible to place the reflective layer on the interior of the component (i.e. directly adjacent to the zone 3), which further reduces the thermal energy released into the environment.
  • Fig. 3 The example of embodiment of Fig. 3 is very similar to that of Fig.2 (the similarity between Fig.2A and Fig.3 are noted); for this reason, corresponding elements are indicated with the same references.
  • the susceptor 4 is housed in a recess 10 of the lower wall having the shape of a cylinder and that the shaft 8 is housed in a tube 18 that projects vertically starting from the lower wall of the cavity 2;
  • the hole 2 has an inlet 21 (at the left flange) and an outlet 22 (at the right flange); the precursor gases enter through the inlet 21 , pass into the zone 3 where chemical reactions and deposition take place, and the depleted gases exit through the outlet 22;
  • the lower wall has a raised area 11 upstream of the susceptor 4 whose internal surface is aligned with the upper surface of the susceptor 4, and a lowered zone downstream of the susceptor 4; an edge 12 is positioned between the susceptor and the lowered zone;
  • the slab forming the component 5 has constant thickness; the width of the interspace 6C varies gradually, in particular increases gradually from the inlet 21 to the outlet 22 (in this manner the "depletion" effect of the precursor gases can be compensated along the path in the chamber
  • At least one interspace is typically defined between the quartz component and the walls; therefore, means associated with the chamber can be provided, adapted to carry at least one fluid flow, preferably gaseous, within the interspace.
  • This is schematized in Fig.3, where the component is indicated with 5, the interspace is indicated with 6C and is located between the component 6C and the internal surface 1 C of the upper wall, and the arrows AA and BA represent the directions of two possible gas flows.
  • the characteristics of the gas flow or flows can vary greatly; the direction of flow of one or each of said flows can change before and/or during and/or after a growth process; the velocity and/or flow rate of one or each of said flows can change before and/or during and/or after a growth process; the fluid of one or each of said flows can comprise hydrogen and/or helium and/or argon; the composition of one or each of said flows can change before and/or during and/or after a growth process.
  • the gas flow or flows can be used for various purposes.
  • One or each of said flows can be adapted to cool the quartz component (indicated in the figures with 5).
  • One or each of said flows can be adapted to control or determine the thermal exchange between the quartz component (indicated in the figures with 5) and at least one of the walls of the cavity (indicated in the figures with 2), in particular the thermal exchange coefficient of the relative interspace (indicated in the figures with 6).
  • One or each of said flows can be such as to maintain substantially the same pressure on the two sides of said quartz component (indicated in the figures with 5) before and/or during and/or after a growth process.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Mechanical Engineering (AREA)
  • Chemical Vapour Deposition (AREA)
  • Crystals, And After-Treatments Of Crystals (AREA)

Abstract

The present invention relates to a reaction chamber of an epitaxial reactor that essentially consists of a quartz piece; the quartz piece comprises a quartz piece portion (1 ) having an internal cavity (2) defined by walls (1A, 1B, 1C, 1 D); the cavity (2) comprises a reaction and deposition zone (3) of the epitaxial reactor; the zone (3) is adapted to house a susceptor (4) to be heated therein; the reaction chamber also comprises a quartz component (5) arranged close to said walls (1A, 1 B, 1 C, 1 D) in such a manner as to form a counterwall and to be a wall of said zone (3).

Description

REACTION CHAMBER OF AN EPITAXIAL REACTOR AND REACTOR THAT USES SAID CHAMBER FIELD OF THE INVENTION
The present invention relates to a reaction chamber of an epitaxial reactor and to a reactor that uses said chamber.
BACKGROUND ART
Epitaxial reactors are machines used to deposit smooth and uniform monocrystalline or polycrystalline layers of materials on substrates; the substrates thus treated are used to produce electric devices (such as solar cells), electronic devices (such as MOSFETs and LEDs) and microelectronic devices (such as integrated circuits). Therefore, the quality of the layer deposited, in terms of defectiveness, uniform thickness and uniform resistivity, is extremely important and subject to increasingly strict requirements.
Substrates are very thin disks (typically in the interval from 100 μm to 1 '500 μm) and with greatly variable diameter (typically in the interval from 1"=25mm to
18"=450mm), and can be made, for example, of silicon [Sl], silicon carbide [SiC], germanium [Ge], gallium arsenide [GaAs], aluminium oxide or "sapphire" [AI2O3], gallium nitridefGaN].
The materials deposited are typically conductor and semiconductor materials, such as silicon [Si], silicon carbide [SiC], germanium [Ge], gallium arsenide
[GaAs], aluminium nitride [AIN], gallium nitride [GaN].
The layer deposited and the substrate below can be made of the same material or of different materials.
The thickness of the layer deposited can be in a wide interval from a few nanometres to several millimetres; when the thickness of the layer deposited is greater than 1 mm, the deposition process is generally called "bulk growth".
Known epitaxial reactors comprise a reaction chamber consisting in general essentially of a quartz piece; the quartz piece comprises a quartz piece portion having the shape of a cylinder, prism, cone, pyramid or parallelepiped and provided with at least one internal cavity defined by walls; this cavity comprises a reaction and deposition zone of the epitaxial reactor; this zone is adapted to house at least one susceptor to be heated therein; the susceptor serves to support and often also to heat the substrates.
There are reactors of many types; depending on the type, the chamber can be arranged vertically or horizontally (rarely obliquely); depending on the type, the susceptor can have the shape of a disk, prism, cylinder, pyramid, cone and can be solid or hollow; depending on the type, the susceptor can be heated by means of resistors, inductors, lamps (rarely internal burners); depending on the type, the reactors can be "cold wall" or "hot wall) (these terms refer to the walls defining the space inside which the reaction and deposition takes place). The processes of epitaxial reactors are performed at high temperatures, i.e. from several hundreds of degrees Celsius to a few thousands of degrees Celsius (for example, deposition of polycrystalline silicon is performed at temperatures typically between 45O0C and 800°C, deposition of monocrystalline silicon on silicon substrates is performed at temperatures typically between 8500C and 1 '25O0C, deposition of monocrystalline silicon carbide on silicon substrates is performed at temperatures typically between 1 '200°C and 1'400°C, deposition of monocrystalline silicon carbide on silicon carbide substrates is performed at temperatures typically between 1 '5000C and 1 '7000C for "epitaxial growth" and at temperatures typically between 1 '9000C and 2'4000C for "bulk growth", and use a great deal of energy (tens of kW) for heating.
Therefore, an important requirement is to prevent the thermal energy generated from being released into the environment.
For this purpose, for many tens of years it has been common practice to apply a thin layer (less than 100μm) of gold-based material to the outer surface of the reaction chamber of epitaxial reactors; this gold layer is produced by means of a certain number of painting and drying cycles (it is not easy to obtain a smooth, uniform and non-porous layer) and reflects the infrared radiation emitted by the susceptor well. In epitaxial reactors where the susceptor is the main element that heats the substrates (for example, in epitaxial reactors with induction heating), appropriate reflection advantageously results in a reduction in the difference in temperature between the front and the back of the substrates during the growth processes. In general, an important requirement is that the substrates are heated uniformly during the deposition process to obtain high uniformity of thickness and resistivity. A drawback of the solution with gold layer is that, after a certain time (i.e. a few months), the gold layer becomes detached from the quartz surface of the reaction chamber - the hotter the quartz surface is, the faster the gold layer detaches, also due to the fact that thermal expansion of gold is higher than that of quartz; this phenomenon occurs even more rapidly if the reaction chamber is cooled by means of a gaseous flow (which is relatively common), also due to the mechanical action of the gaseous flow on the layer; moreover, this phenomenon is increased by traces of acids, deriving from previous wash cycles of the reaction chamber, on the surface of the reaction chamber.
Detachment of the gold layer results in an increase in consumption of electrical power of the epitaxial reactor, as part of the infrared radiation emitted by the susceptor is released into the environment. Moreover, as detachment of the gold layer is not smooth and uniform, this also results in a reduction in the quality of the substrates grown. Therefore, when detachment occurs, it is necessary to disassemble the reaction chamber from the epitaxial reactor, completely remove the gold layer (already partly detached), re-apply the gold layer and re-assemble the reaction chamber in the epitaxial reactor; these operations take time, are costly and can only be performed a limited number of times.
As already mentioned, the processes of the epitaxial reactors are performed in a cavity of a reaction chamber at high temperatures; therefore, it is necessary to cool the reaction chamber. However, this cooling of chamber can cause excessive and/or non-uniform cooling of the walls that define the space in which the reaction and deposition take place; this results in a reduction in the quality of the substrates grown. SUMMARY OF THE INVENTION The general object of the present invention is to overcome the aforesaid drawbacks and satisfy the aforesaid requirements. This and other objects are achieved through the reaction chamber having the features set out in the appended claims, which form an integral part of the present description.
The idea underlying the present invention is that of providing a quartz component arranged close to the walls of the cavity of the reaction chamber in such a manner as to form a counterwall and to be a wall of the reaction and deposition zone. Experiments were conducted implementing this idea and results well beyond those expected were achieved: (A) excellent uniformity of thickness and resistivity of the layers deposited, (B) low defectiveness of the layers deposited, (C) reduction in consumption of electricity to heat the reaction and deposition zone, (D) improved utilization of the precursor gases injected into the reaction and deposition zone and therefore greater deposition velocity, (E) a reduction of parasitic depositions on the walls of the cavity of the chamber and therefore fewer stray particles in the reaction and deposition zone and less need to "wash" the chamber, (F) less capture of dopant by the walls of the cavity of the chamber and therefore possibility of producing adjacent deposition layers with more marked or less gradual transition of the level and of the type of doping.
In general, the reaction chamber of an epitaxial reactor, according to the present invention, essentially consists of a quartz piece; said quartz piece comprises a quartz piece portion having at least one internal cavity defined, at least partly, by walls; said cavity comprises a reaction and deposition zone of the epitaxial reactor; said zone is adapted to house at least one susceptor to be heated therein; the reaction chamber also comprises a quartz component arranged close to one or more of said walls in such a manner as to form a counterwall and to be a wall of said zone.
In the reaction chamber according to the present invention, said quartz component can be arranged in such a manner as to form a counterwall for two or three or four of said walls, preferably for three of said walls. In the reaction chamber according to the present invention, said quartz component can rest on one or two of said walls, preferably on only one of said walls. In the reaction chamber according to the present invention, said quartz component can essentially consist of a straight or shaped quartz slab, preferably a shaped quartz slab, more preferably a U-shaped quartz slab. In the reaction chamber according to the present invention, said quartz slab can have a uniform or variable thickness.
In the reaction chamber according to the present invention, at least one interspace is typically defined between said quartz component and said walls. Said interspace can be isolated from said reaction and deposition zone, in particular hermetically isolated. In the reaction chamber according to the present invention, said interspace can have a uniform or variable width.
In the reaction chamber according to the present invention, two or three or four interspaces, preferably three interspaces, can be defined between said quartz component and said walls, the widths of said interspaces being preferably uniform and equal to one another.
In the reaction chamber according to the present invention, the quartz of said quartz component can be transparent, opaque or reflective. In the reaction chamber according to the present invention, said quartz component can be coated with a reflective layer on either the interior side or the exterior side, preferably on the side which is closer to said walls.
Said reflective layer is typically adapted to reflect back the infrared radiation emitted by said susceptor in the wavelength interval from 1'000 nm to 10'0OO nm, preferably from 1'500 nm to 3'00O nm. Said reflective layer is preferably made of a quartz-based material. Said reflective layer can completely or partly coat said quartz component.
Said reflective layer can be completely or partly coated by a layer of vitrified quartz.
In the reaction chamber according to the present invention, said quartz piece portion can have the shape of a cylinder or prism or pyramid cone, preferably substantially of a parallelepiped, and has an axial through hole forming said cavity. The reaction chamber according to the present invention can comprise flanges at the ends of said quartz piece. In the reaction chamber according to the present invention, at least one interspace is typically defined between said quartz component and said walls; means can therefore be provided, associated with the chamber, adapted to carry at least one fluid flow, preferably gaseous, within said interspace. Said means can be adapted to carry at least two fluid flows, preferably gaseous, within said interspace, the direction of flow of said flows preferably forming an angle of around
180° between them.
The direction of flow of one or each of said flows can change before and/or during and/or after a growth process. The velocity and/or flow rate of one or each of said fluid flows can change before and/or during and/or after a growth process.
The fluid of one or each of said flows can comprise hydrogen and/or helium and/or argon.
The composition of one or each of said flows can change before and/or during and/or after a growth process.
One or each of said flows can be adapted to cool said quartz component.
One or each of said flows can be adapted to control or determine thermal exchange between said quartz component and at least one of said walls, in particular the thermal exchange coefficient of said at least one interspace. One or each of said flows can be such as to maintain substantially the same pressure on two sides of said quartz component before and/or during and/or after a growth process.
According to a further aspect, the present invention also relates to an epitaxial reactor comprising a reaction chamber having one or more of the features set out above.
BRIEF DESCRIPTION OF THE FIGURES
The present invention will be described in detail below, together with the accompanying drawings, wherein:
Fig.1 shows a reaction chamber according to prior art in three different views (Fig. 1 A is a side view, Fig. 1 B is a top view, Fig. 1 C is a front view),
Fig.2 shows an example of embodiment of the reaction chamber according to the present invention in three different sectional views (Fig. 2A is a side view, Fig. 2B is a top view, Fig. 2C is a front view) - the chamber of Fig. 2 corresponds to the chamber of Fig. 1 to which technical characteristics according to the present invention have been added, and
Fig.3 shows a second example of embodiment of the reaction chamber according to the present invention in a sectional side view - the chamber of Fig. 3 is very similar to the chamber of Fig. 2. Detailed Description of the Invention
This description and these drawings are provided by way of non-limiting examples; moreover, they are schematic and simplified. Fig.1 shows a reaction chamber of an epitaxial reactor essentially consisting of a hollow quartz piece; this hollow quartz piece comprises a quartz piece portion 1 having the shape of a parallelepiped (with rounded longitudinal edges) and an axial through hole 2 produced in the portion 1 ; the portion 1 is adapted to define according to two of three directions (i.e. width and height - see Fig.1 C) a reaction and deposition zone 3 (not shown in Fig.1 ) and to house at least one susceptor (not shown in Fig.1 ) to be heated within the hole 2; the hole 2 has a rectangular section (with rounded corners) corresponding in shape to the section of the portion 1 and, in this manner, the portion 1 forms a tube with walls having a substantially constant section; 1 A indicates the internal surface of the lower wall, 1 B the internal surface of the first lateral wall, 1 C the internal surface of the upper wall and 1 D the internal surface of the second lateral wall. The chamber of Fig.1 is adapted to be arranged horizontally, to house a disk- shaped susceptor, to be associated with induction heating means, and to be used in a "cold wall" reactor (i.e. the temperature of the portion 1 of the hollow quartz piece does not exceed 400-6000C during epitaxial growth processes and is therefore much lower with respect to that of the susceptor). The chamber of Fig.1 also comprises two flanges 7 at the ends of the hollow quartz piece, in particular of the portion 1.
The portion 1 is made of transparent quartz, in particular transparent to visible light, but also to infrared light. The flanges 7 are made of opaque quartz, in particular opaque (i.e. which blocks the passage and therefore partly reflects and partly absorbs) to visible light, but also to infrared light.
Fig.2 shows a disk-shaped susceptor 4, mounted on a vertical shaft 8 to support it and make it rotate; the susceptor 4 has slight recesses (in particular five recesses) on the upper face thereof adapted to house substrates on which to perform epitaxial growth; the shaft 8 passes through a circular hole produced in the lower wall of the chamber (retaining means, not shown in this figure, are provided); moreover, this figure shows the reaction and deposition zone 3; finally, it is noted that neither the susceptor 4 nor the shaft 8 is part of the chamber.
The chamber of Fig.2 differs from that of Fig.1 essentially due to the fact that it comprises a quartz component 5 arranged close to one or more of the walls of the cavity 2 in such a manner as to form a counterwall and to be a wall of the zone 3; in particular, this is a U-shaped slab, arranged overturned and resting only on the lower wall, specifically on the internal surface 1A of this wall; all this is clearly visible in Fig.2C; the slab 5 has uniform thickness. This shaped slab can be produced by joining three straight slabs: one adapted to be arranged horizontally and two adapted to be arranged vertically. The component 2 extends for the complete length of the chamber, in particular to the edge of the flanges 7; alternatively, it could, for example, extend only for the complete length of the portion 1.
In the example of Fig.2, the component 5 is arranged in such a manner as to produce a counterwall for three walls of the cavity 2, in particular for the two lateral walls and for the upper wall. An interspace 6 is defined between the component 5 and the walls of the cavity 2, which is divided into three portions 6B, 6C, 6D, which are in turn interspaces; the interspace 6B is located between the component 5 and the internal surface 1 B of the first lateral wall, the interspace 6C is located between the component 5 and the internal surface 1C of the upper wall, the interspace 6D is located between the component 5 and the internal surface 1 D of the second lateral wall; the interspace 6 (and therefore its portions 6B, 6C, 6D) is isolated more or less hermetically from the reaction and deposition zone 3; the widths of the three interspaces 6B, 6C and 6D are substantially (there are slight differences at the edges) uniform and equal to one another, as can be clearly seen in Fig.2C; these widths are typically in the interval from 1 mm to 10 mm.
The quartz of the component 5 can be transparent, opaque or reflective.
The component 5 can be coated with a reflective layer either on the interior side or on the exterior side thereof; the coating can be total or partial.
According to the most typical embodiment, the component 5 is made of transparent quartz and coated with a reflective layer on the side closer to the walls of the cavity 2, i.e. close to the surfaces 6B, 6C, 6D.
This reflective layer is typically adapted to reflect back the infrared radiation emitted by the susceptor 4 in the wavelength interval from 1'000 nm to 10'0OO nm, preferably from 1'500 nm to 3'00O nm.
The reflective layer is preferably made of a quartz-based material; in this manner, the material of the layer is compatible from a chemical point of view (equal or similar chemical properties, i.e. resistance), from a mechanical point of view (equal or similar mechanical properties) and from a thermal point of view (equal or similar thermal properties, i.e. CTE [Coefficient of Thermal Expansion]) with the material of the component.
The thickness of the reflective layer is typically in the interval from 0.5 mm to 1.5 mm and is preferably around 1 mm. The reflective layer can be obtained according to the following process: applying a semi-liquid slurry with a high content (i.e. greater than 80% and lower than 95%) of amorphous quartz particles in dispersion (the dispersion liquid can be water or, for example, alcohol) to the transparent quartz reaction chamber, then - drying the slurry applied, then sintering the dried slurry.
In this manner, a layer can be obtained capable of reflecting on average over 80-
90% of the infrared radiation (in the aforesaid wavelength intervals) that strikes the layer. The reflective layer can be completely or partly coated by a layer of vitrified quartz; this vitrified layer can have a thickness typically in the interval from 0.5 mm to 1.5 mm. The reflective quartz layer and the superimposed vitrified quartz layer can be obtained with the following single process: applying a semi-liquid slurry with a high content (i.e. greater than 80% and lower than 95%) of amorphous quartz particles in dispersion (the dispersion liquid can be water or, for example, alcohol) to the transparent quartz reaction chamber, then drying the slurry applied, then sintering the dried slurry, then vitrifying the surface of the sintered slurry only to a predetermined depth, for example by means of a flame or a laser; naturally, sufficient slurry must be applied to produce both the reflective quartz layer and the vitrified quartz layer.
The vitrified layer allows the reflective layer below to be protected both from a chemical and from a mechanical point of view; if a vitrified layer of excellent quality is produced, it is also possible to place the reflective layer on the interior of the component (i.e. directly adjacent to the zone 3), which further reduces the thermal energy released into the environment.
The example of embodiment of Fig. 3 is very similar to that of Fig.2 (the similarity between Fig.2A and Fig.3 are noted); for this reason, corresponding elements are indicated with the same references.
In Fig.3 it is noted that the susceptor 4 is housed in a recess 10 of the lower wall having the shape of a cylinder and that the shaft 8 is housed in a tube 18 that projects vertically starting from the lower wall of the cavity 2; the hole 2 has an inlet 21 (at the left flange) and an outlet 22 (at the right flange); the precursor gases enter through the inlet 21 , pass into the zone 3 where chemical reactions and deposition take place, and the depleted gases exit through the outlet 22; the lower wall has a raised area 11 upstream of the susceptor 4 whose internal surface is aligned with the upper surface of the susceptor 4, and a lowered zone downstream of the susceptor 4; an edge 12 is positioned between the susceptor and the lowered zone; the slab forming the component 5 has constant thickness; the width of the interspace 6C varies gradually, in particular increases gradually from the inlet 21 to the outlet 22 (in this manner the "depletion" effect of the precursor gases can be compensated along the path in the chamber even with a chamber with lower and upper wall perfectly parallel to each other). As already mentioned, in the reaction chamber according to the present invention, at least one interspace is typically defined between the quartz component and the walls; therefore, means associated with the chamber can be provided, adapted to carry at least one fluid flow, preferably gaseous, within the interspace. This is schematized in Fig.3, where the component is indicated with 5, the interspace is indicated with 6C and is located between the component 6C and the internal surface 1 C of the upper wall, and the arrows AA and BA represent the directions of two possible gas flows.
It is possible to provide only one gas flow according to the direction indicated by the arrow AA, only one gas flow according to the direction indicated by the arrow BA, or both these two gas flows; in this latter case, the flows forming an angle of around 180° between them. The characteristics of the gas flow or flows can vary greatly; the direction of flow of one or each of said flows can change before and/or during and/or after a growth process; the velocity and/or flow rate of one or each of said flows can change before and/or during and/or after a growth process; the fluid of one or each of said flows can comprise hydrogen and/or helium and/or argon; the composition of one or each of said flows can change before and/or during and/or after a growth process. The gas flow or flows can be used for various purposes.
One or each of said flows can be adapted to cool the quartz component (indicated in the figures with 5). One or each of said flows can be adapted to control or determine the thermal exchange between the quartz component (indicated in the figures with 5) and at least one of the walls of the cavity (indicated in the figures with 2), in particular the thermal exchange coefficient of the relative interspace (indicated in the figures with 6). One or each of said flows can be such as to maintain substantially the same pressure on the two sides of said quartz component (indicated in the figures with 5) before and/or during and/or after a growth process. From what has been stated, it is understood that, according to the preferred embodiment of the present invention, moving from the reaction and deposition zone (indicated with 3 in the figures) toward the outside of the reaction chamber, first the counterwall (indicated with 5 in the figures), then an interspace (indicated with 6 in the figures) and finally a wall (indicated with 1 in the figures) are encountered; a fluid (preferably gaseous) can flow in the interspace; a fluid (preferably liquid) can flow on the exterior side of the wall . Therefore, there are many parameters (geometric, chemical, thermodynamic and fluid-dynamic) that can be appropriately chosen to control the temperature of the internal surface of the counterwall and the heat that flows from the reaction and deposition zone toward the outside.

Claims

1. Reaction chamber of an epitaxial reactor, essentially consisting of a quartz piece, wherein said quartz piece comprises a quartz piece portion (1 ) having an internal cavity (2) defined by walls (1A, 1 B, 1 C, 1 D), wherein said cavity (2) comprises a reaction and deposition zone (3) of the epitaxial reactor, wherein said zone (3) is adapted to house a susceptor (4) to be heated therein, characterized by comprising a quartz component (5) arranged close to said walls (1A, 1 B, 1 C, 1 D) in such a manner as to form a counterwall and to be a wall of said zone (3).
2. Reaction chamber according to claim 1 , wherein said quartz component (5) is arranged in such a manner as to form a counterwall for two or three or four of said walls, preferably for three (1 B, 1 C, 1 D) of said walls.
3. Reaction chamber according to claim 1 or 2, wherein said quartz component (5) rests on one or two of said walls, preferably on only one (1A) of said walls.
4. Reaction chamber according to claim 1 or 2 or 3, wherein said quartz component (5) essentially consists of a straight or shaped quartz slab, preferably a profiled quartz slab, more preferably a U-shaped quartz slab.
5. Reaction chamber according to any of the preceding claims, wherein at least one interspace (6) having a uniform or variable width is defined between said quartz component (5) and said walls (1 A, 1 B, 1C, 1 D).
6. Reaction chamber according to claim 5, wherein two or three or four interspaces, preferably three interspaces (6B, 6C, 6D) are defined between said quartz component (5) and said walls (1A, 1 B, 1 C, 1 D), the widths of said interspaces being preferably uniform and equal to one another.
7. Reaction chamber according to any of the preceding claims, wherein said quartz component (5) is coated with a reflective layer on either the interior side or the exterior side, preferably on the side which is closer to said walls (1 B, 1 C, 1 D).
8. Reaction chamber according to any of the preceding claims, wherein at least one interspace (6) is defined between said quartz component (5) and said walls (1A, 1 B, 1 C, 1 D), characterized in that said chamber is associated with means adapted to carry at least one fluid flow, preferably a gaseous fluid flow, within said interspace (6).
9. Reaction chamber according to claim 8, wherein the velocity and/or flow rate and/or direction and/or composition of said at least one fluid flow changes before and/or during and/or after a growth process.
10. Epitaxial reactor characterized by comprising at least one reaction chamber according to any of the preceding claims 1 to 9.
PCT/IB2010/051666 2009-04-17 2010-04-16 Reaction chamber of an epitaxial reactor and reactor that uses said chamber WO2010119430A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
EP10727855.8A EP2419552B1 (en) 2009-04-17 2010-04-16 Reaction chamber of an epitaxial reactor and reactor using the chamber
US13/259,818 US9382642B2 (en) 2009-04-17 2010-04-16 Reaction chamber of an epitaxial reactor and reactor that uses said chamber
JP2012505290A JP6116900B2 (en) 2009-04-17 2010-04-16 Reaction chamber of epitaxial reactor and reactor using said reaction chamber
CN201080016602.6A CN102395714B (en) 2009-04-17 2010-04-16 Reaction chamber of an epitaxial reactor and reactor that uses said chamber

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
ITMI2009A000629A IT1393695B1 (en) 2009-04-17 2009-04-17 REACTION CHAMBER OF AN EPITAXIAL REACTOR AND REACTOR THAT USES IT
ITMI2009A000629 2009-04-17

Publications (1)

Publication Number Publication Date
WO2010119430A1 true WO2010119430A1 (en) 2010-10-21

Family

ID=41226172

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IB2010/051666 WO2010119430A1 (en) 2009-04-17 2010-04-16 Reaction chamber of an epitaxial reactor and reactor that uses said chamber

Country Status (6)

Country Link
US (1) US9382642B2 (en)
EP (1) EP2419552B1 (en)
JP (1) JP6116900B2 (en)
CN (1) CN102395714B (en)
IT (1) IT1393695B1 (en)
WO (1) WO2010119430A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT202100014984A1 (en) 2021-06-09 2022-12-09 Lpe Spa REACTION CHAMBER WITH COATING SYSTEM AND EPITAXILE REACTOR

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103266307A (en) * 2013-05-22 2013-08-28 光垒光电科技(上海)有限公司 Reaction cavity
KR102372893B1 (en) * 2014-12-04 2022-03-10 삼성전자주식회사 Chemical vapor deposition apparatus for fabricating light emitting diode(LED)
CN105350073B (en) * 2015-10-30 2018-09-25 中国电子科技集团公司第四十八研究所 A kind of the graphite plate rotary sealing appts and automatic loading and unloading system of silicon epitaxy equipment
CN107723790B (en) * 2016-08-12 2020-07-07 上海新昇半导体科技有限公司 Epitaxial equipment, equipment manufacturing method and epitaxial method
CN106282967B (en) * 2016-08-23 2019-03-26 深圳市国创新能源研究院 A kind of equipment preparing SiO/C composite material
RU2638575C1 (en) * 2016-11-08 2017-12-14 Общество с ограниченной ответственностью "МеГа Эпитех" Method of producing semiconductor structures by liquid phase epitaxy with high uniformity on thickness of epitaxial layers
CA3066089C (en) 2017-06-09 2022-09-13 Prc-Desoto International, Inc. Dual cure sealants
US10597565B2 (en) 2017-07-07 2020-03-24 Prc-Desoto International, Inc. Hydraulic fluid and fuel resistant sealants
US10351674B2 (en) 2017-10-17 2019-07-16 Prc-Desoto International, Inc. Sulfur-containing polymeric particles and compositions
US11098222B2 (en) 2018-07-03 2021-08-24 Prc-Desoto International, Inc. Sprayable polythioether coatings and sealants
US10843180B2 (en) 2018-10-02 2020-11-24 Prc-Desoto International, Inc. Delayed cure micro-encapsulated catalysts
CN113677504B (en) 2019-02-11 2023-09-15 Ppg工业俄亥俄公司 3D printing of sealing caps
US20220097299A1 (en) 2019-02-11 2022-03-31 Ppg Industries Ohio, Inc. Methods of making chemically resistant sealing components
CA3129262C (en) 2019-02-11 2024-01-09 Ppg Industries Ohio, Inc. Multilayer systems and methods of making multilayer systems
US11015097B2 (en) 2019-03-06 2021-05-25 Prc-Desoto International, Inc. Chemically resistant sealant compositions and uses thereof
US11015057B2 (en) 2019-04-03 2021-05-25 Prc-Desoto International, Inc. Dual-cure compositions
US11173692B2 (en) 2019-12-19 2021-11-16 Prc-Desoto International, Inc. Free radical polymerizable adhesion-promoting interlayer compositions and methods of use
US11466125B2 (en) 2019-12-19 2022-10-11 Prc-Desoto International, Inc. Low nucleation temperature polythioether prepolymers and uses thereof
US11608458B2 (en) 2019-12-19 2023-03-21 Prc-Desoto International, Inc. Adhesion-promoting interlayer compositions containing organic titanates/zirconates and methods of use
US11600470B2 (en) * 2019-12-27 2023-03-07 Applied Materials, Inc. Targeted heat control systems
US11624007B2 (en) 2020-01-29 2023-04-11 Prc-Desoto International, Inc. Photocurable adhesion-promoting compositions and methods of use
US11214666B2 (en) 2020-04-15 2022-01-04 Prc-Desoto International, Inc. Controlling cure rate with wetted filler
US20240132752A1 (en) 2021-02-16 2024-04-25 Prc-Desoto International, Inc. Compositions containing a free radical polymerization initiator
EP4140589A4 (en) * 2021-03-12 2023-05-10 BOE Technology Group Co., Ltd. Microfluidic substrate, and microfluidic chip and manufacturing method therefor
AU2022252479A1 (en) 2021-03-29 2023-10-12 Prc-Desoto International, Inc. Hybrid dual cure compositions
WO2022232730A1 (en) 2021-04-27 2022-11-03 Ppg Industries Ohio, Inc. Multiple cure coreactive compositions for additive manufacturing and uses thereof
CA3228686A1 (en) 2021-09-02 2023-03-09 Shane Xiufeng Peng Applicators for high viscosity materials
AU2022388723A1 (en) 2021-11-10 2024-05-30 Ppg Industries Ohio, Inc. Linear sealing components and methods and compositions for additively manufacturing thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0147967A2 (en) * 1983-12-09 1985-07-10 Applied Materials, Inc. Induction heated reactor system for chemical vapor deposition
US4991540A (en) * 1987-06-30 1991-02-12 Aixtron Gmbh Quartz-glass reactor for MOCVD systems

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2734197B2 (en) * 1990-11-21 1998-03-30 富士電機株式会社 Vapor phase growth equipment
US5256060A (en) * 1992-01-28 1993-10-26 Digital Equipment Corporation Reducing gas recirculation in thermal processing furnace
US5221356A (en) * 1992-10-08 1993-06-22 Northern Telecom Limited Apparatus for manufacturing semiconductor wafers
US5441570A (en) * 1993-06-22 1995-08-15 Jein Technics Co., Ltd. Apparatus for low pressure chemical vapor deposition
IT1271233B (en) 1994-09-30 1997-05-27 Lpe EPITAXIAL REACTOR EQUIPPED WITH FLAT DISCOID SUSCEPECTOR AND HAVING GAS FLOW PARALLEL TO THE SUBSTRATES
US6093252A (en) 1995-08-03 2000-07-25 Asm America, Inc. Process chamber with inner support
US6259062B1 (en) * 1999-12-03 2001-07-10 Asm America, Inc. Process chamber cooling
US6331212B1 (en) 2000-04-17 2001-12-18 Avansys, Llc Methods and apparatus for thermally processing wafers
JP2002110558A (en) * 2000-09-29 2002-04-12 Hitachi Kokusai Electric Inc Substrate processor and processing method therefor
DE10209763A1 (en) * 2002-03-05 2003-10-02 Bosch Gmbh Robert Device and method for anisotropic plasma etching of a substrate, in particular a silicon body
JP2006284077A (en) * 2005-03-31 2006-10-19 Kumamoto Technology & Industry Foundation Heat radiation reflecting furnace
JP2007149774A (en) * 2005-11-24 2007-06-14 Sharp Corp Vapor phase deposition apparatus
US8497587B2 (en) * 2009-12-30 2013-07-30 Stmicroelectronics Pte Ltd. Thermally enhanced expanded wafer level package ball grid array structure and method of making the same

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0147967A2 (en) * 1983-12-09 1985-07-10 Applied Materials, Inc. Induction heated reactor system for chemical vapor deposition
US4991540A (en) * 1987-06-30 1991-02-12 Aixtron Gmbh Quartz-glass reactor for MOCVD systems

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT202100014984A1 (en) 2021-06-09 2022-12-09 Lpe Spa REACTION CHAMBER WITH COATING SYSTEM AND EPITAXILE REACTOR
WO2022259137A1 (en) * 2021-06-09 2022-12-15 Lpe S.P.A. Reaction chamber with covering system and epitaxial reactor

Also Published As

Publication number Publication date
EP2419552A1 (en) 2012-02-22
ITMI20090629A1 (en) 2010-10-18
IT1393695B1 (en) 2012-05-08
CN102395714A (en) 2012-03-28
EP2419552B1 (en) 2016-07-06
JP6116900B2 (en) 2017-04-19
US9382642B2 (en) 2016-07-05
US20120027646A1 (en) 2012-02-02
CN102395714B (en) 2014-07-09
JP2012524013A (en) 2012-10-11

Similar Documents

Publication Publication Date Title
US9382642B2 (en) Reaction chamber of an epitaxial reactor and reactor that uses said chamber
US20150083046A1 (en) Carbon fiber ring susceptor
CN106537566A (en) Light pipe arrays for thermal chamber applications and thermal processes
US20130323420A1 (en) Apparatus and method for atomic layer deposition on a surface
CN100468631C (en) Susceptor
AU2009200196A1 (en) Methods and apparatus for manufacturing semiconductor wafers
CN109207962B (en) Chemical vapor growth device
US20090208725A1 (en) Layer transfer for large area inorganic foils
JP2002265296A (en) Diamond thin film and manufacturing method therefor
US6243534B1 (en) Method and apparatus to compensate for non-uniform film growth during chemical vapor deposition
TW201216368A (en) Heater assembly and wafer processing apparatus using the same
RU2644216C2 (en) Microwave plasma reactor for obtaining a homogeneous nanocrystalline diamond film
KR100375335B1 (en) A Method for Depositing Diamond Films Without Fracture by a Control of Substrate Temperatures Using Powders
EP2367964B1 (en) Reaction chamber of an epitaxial reactor
CN100567565C (en) The formation method of silicon-containing film and the method that reduces granule amount
JP6058491B2 (en) Vapor growth reactor
US6331260B1 (en) VD process and apparatus for producing stand-alone thin films
TWI807253B (en) Semiconductor reaction device and method
JPS60192326A (en) Formation of diamond film
JPS63291894A (en) Reactor for vapor surface treatment
EP2088617A1 (en) Methods and apparatus for manufacturing semiconductor wafers
KR20110101556A (en) Apparatus for depositing epitaxial layer on wafer

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 201080016602.6

Country of ref document: CN

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 10727855

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 13259818

Country of ref document: US

WWE Wipo information: entry into national phase

Ref document number: 2012505290

Country of ref document: JP

NENP Non-entry into the national phase

Ref country code: DE

REEP Request for entry into the european phase

Ref document number: 2010727855

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 2010727855

Country of ref document: EP