JPS6338430B2 - - Google Patents

Info

Publication number
JPS6338430B2
JPS6338430B2 JP59201230A JP20123084A JPS6338430B2 JP S6338430 B2 JPS6338430 B2 JP S6338430B2 JP 59201230 A JP59201230 A JP 59201230A JP 20123084 A JP20123084 A JP 20123084A JP S6338430 B2 JPS6338430 B2 JP S6338430B2
Authority
JP
Japan
Prior art keywords
gas
reaction
supply nozzle
reaction gas
gas supply
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
JP59201230A
Other languages
Japanese (ja)
Other versions
JPS6179771A (en
Inventor
Kazuo Maeda
Toku Tokumasu
Toshihiko Fukuyama
Tsuguaki Hirata
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Applied Materials Japan Inc
Original Assignee
Applied Materials Japan Inc
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
Application filed by Applied Materials Japan Inc filed Critical Applied Materials Japan Inc
Priority to JP20123084A priority Critical patent/JPS6179771A/en
Priority to US06/780,205 priority patent/US4731255A/en
Publication of JPS6179771A publication Critical patent/JPS6179771A/en
Publication of JPS6338430B2 publication Critical patent/JPS6338430B2/ja
Granted legal-status Critical Current

Links

Classifications

    • 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D1/00Processes for applying liquids or other fluent materials
    • B05D1/60Deposition of organic layers from vapour phase
    • 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
    • C23C16/48Chemical 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 by irradiation, e.g. photolysis, radiolysis, particle radiation
    • C23C16/482Chemical 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 by irradiation, e.g. photolysis, radiolysis, particle radiation using incoherent light, UV to IR, e.g. lamps
    • 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
    • C23C16/48Chemical 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 by irradiation, e.g. photolysis, radiolysis, particle radiation
    • C23C16/487Chemical 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 by irradiation, e.g. photolysis, radiolysis, particle radiation using electron radiation
    • 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
    • C23C16/48Chemical 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 by irradiation, e.g. photolysis, radiolysis, particle radiation
    • C23C16/488Protection of windows for introduction of radiation into the coating chamber
    • 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
    • C30B25/105Heating of the reaction chamber or the substrate by irradiation or electric discharge
    • 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D3/00Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
    • B05D3/06Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by exposure to radiation
    • B05D3/061Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by exposure to radiation using U.V.

Landscapes

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

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は気相成長装置に関し、一層詳細には、
クローズドチヤンバーを用いずに、不活性ガスの
高速カーテン流により外界と内部反応領域を区切
る開放チヤンバーにすることによつて、パーテイ
クルの発生をほぼ完全になくすことができる気相
成長装置に関するものである。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Field of Application) The present invention relates to a vapor phase growth apparatus, and more specifically,
This relates to a vapor phase growth device that can almost completely eliminate the generation of particles by using an open chamber that separates the outside world from the internal reaction area using a high-speed curtain flow of inert gas, without using a closed chamber. be.

(従来の技術) 従来の気相成長装置は、例えば特開昭53―
54181号公報に開示されているように、加熱支持
台上に載置した被処理物に対面して2重管構造の
ノズルを配置し、該ノズルの内管から反応ガスと
キヤリアガスを、外管から窒素ガス等のカーテン
ガスを被処理物に向けて噴出するようになつてい
る装置が知られている。
(Prior art) A conventional vapor phase growth apparatus is, for example,
As disclosed in Publication No. 54181, a nozzle with a double tube structure is arranged facing the workpiece placed on a heating support, and a reaction gas and a carrier gas are supplied from the inner tube of the nozzle to the outer tube. An apparatus is known in which a curtain gas such as nitrogen gas is ejected from a chamber toward an object to be treated.

この装置によれば反応管を必要とすることな
く、大気中でスプレー式に反応生成物を被着せし
めることが可能となる。
According to this device, it is possible to apply a reaction product by spraying in the atmosphere without requiring a reaction tube.

また、特開昭57―187033号公報に開示されてい
るように、被処理物の支持壁と外部から照射され
る紫外線を透過する石英窓との間の空間に、反応
ガス供給ノズルにより被処理物表面に反応ガスを
層流にて供給し、キヤリアガス供給ノズルにより
石英窓に沿つてキヤリアガスを層流にて供給する
気相成長装置が知られている。
Furthermore, as disclosed in Japanese Patent Application Laid-Open No. 57-187033, a reactant gas supply nozzle is used to fill the space between the support wall of the object to be treated and a quartz window that transmits ultraviolet rays irradiated from the outside. 2. Description of the Related Art A vapor phase growth apparatus is known in which a reactant gas is supplied to the surface of an object in a laminar flow, and a carrier gas is supplied in a laminar flow along a quartz window using a carrier gas supply nozzle.

(発明が解決しようとする問題点) しかしながら上記従来の気相成長装置には次の
ような問題点がある。
(Problems to be Solved by the Invention) However, the conventional vapor phase growth apparatus described above has the following problems.

すなわち前者の装置においては、反応ガスおよ
びカーテンガスが被処理物に向けて噴出されるも
のであるため、被処理物表面で反応ガスおよびカ
ーテンガスの乱流が生じ、反応ガス中で生成した
気相反応生成物が、反応ガスの吹き上げによつ
て、被処理物表面に成長した皮膜上に落下して付
着する、いわゆるパーテイクルの発生が生じ易い
という問題点がある。
In other words, in the former device, the reaction gas and curtain gas are ejected toward the object to be treated, so a turbulent flow of the reaction gas and curtain gas occurs on the surface of the object, and the gas generated in the reaction gas is There is a problem in that phase reaction products tend to fall and adhere to the film grown on the surface of the object to be treated due to the blow-up of the reaction gas, which tends to cause so-called particles.

一方、後者の装置においては、反応ガス中で生
成した気相反応生成物は反応ガス流に乗つて比較
的排出され易いものではあるが、石英窓等の器壁
に付着した反応生成物が落下して被処理物上の皮
膜に再付着するおそれがある。特に被処理物を加
熱する場合には、被処理物付近で急に反応ガスや
キヤリアガスが加熱されて両ガス間に乱流状態が
生じ易いという問題点がある。
On the other hand, in the latter device, the gas phase reaction products generated in the reaction gas are relatively easily discharged along with the reaction gas flow, but the reaction products attached to the vessel walls such as quartz windows fall out. There is a risk that it will re-adhere to the film on the object to be treated. Particularly when heating the object to be processed, there is a problem in that the reactant gas and the carrier gas are suddenly heated near the object to be processed, which tends to cause turbulent flow between the two gases.

そこで本発明は上記種々の問題点を解決すべく
なされたものであり、その目的とするところは、
パーテイクルの発生がほぼ完全なまでに抑制され
るのみならず、装置の簡略化をも図ることができ
る気相成長装置を提供するにある。
Therefore, the present invention has been made to solve the various problems mentioned above, and its purpose is to:
It is an object of the present invention to provide a vapor phase growth apparatus in which not only the generation of particles is almost completely suppressed, but also the apparatus can be simplified.

(問題点を解決するための手段) 上記目的による本発明では、被処理物表面に反
応ガスを流通させて被処理物表面に皮膜を成長さ
せる気相成長装置において、被処理物を載置し、
該被処理物を反応温度にまで加熱するホツトプレ
ートを備え、該ホツトプレート周辺が開放されて
いる開放チヤンバーと、反応ガスを被処理物表面
に沿つて被処理物表面と平行な方向に流す反応ガ
ス供給ノズルと、この反応ガス流の少なくとも反
被処理物側を覆つて不活性ガスカーテンを形成す
るように不活性ガスを供給する不活性ガス供給ノ
ズルと、反応ガス流と不活性ガス流とが層流をな
すように、前記各ガス供給ノズルから流される反
応ガスと不活性ガスとをあらかじめほぼ等しい温
度にまで加熱する加熱手段とを具備することを特
徴としている。
(Means for Solving the Problems) In the present invention according to the above object, the object to be treated is placed in a vapor phase growth apparatus that grows a film on the surface of the object by flowing a reactive gas over the surface of the object. ,
A reaction system that includes a hot plate that heats the object to be processed to a reaction temperature, an open chamber that is open around the hot plate, and a reaction gas that flows along the surface of the object to be processed in a direction parallel to the surface of the object. a gas supply nozzle; an inert gas supply nozzle for supplying an inert gas so as to form an inert gas curtain covering at least a side opposite to the object to be processed of the reaction gas flow; and a reaction gas flow and an inert gas flow. The present invention is characterized in that it includes a heating means for preheating the reaction gas and inert gas flowing from each gas supply nozzle to approximately the same temperature so that the gas forms a laminar flow.

(作 用) 作用について述べる。(effect) Let's talk about the action.

反応ガスをあらかじめ加熱して、反応ガス供給
ノズル24から、ウエハー22表面に沿つて帯状
に流し、N2ガスをあらかじめ加熱してN2ガス供
給ノズル38から反応ガス上を覆つて帯状に流し
て、ウエハー22表面上に所望の皮膜を形成させ
ることができる。この場合に両ガスがあらかじめ
同温度付近にまで加熱されているから、両ガス間
で上昇気流等による乱流が生じることがなく、従
つて層流状態で供給されるから、反応ガス気相中
で生成した反応生成物がウエハー22表面上に落
下して、パーテイクルが発生する等の事態が生じ
ない。
The reaction gas is heated in advance and flows in a band shape from the reaction gas supply nozzle 24 along the surface of the wafer 22, and the N 2 gas is heated in advance and is flowed in a band shape from the N 2 gas supply nozzle 38 over the reaction gas. , a desired film can be formed on the surface of the wafer 22. In this case, since both gases have been heated to around the same temperature in advance, turbulent flow due to upward air currents etc. does not occur between the two gases, and therefore they are supplied in a laminar flow state. This prevents the reaction products generated from falling onto the surface of the wafer 22 and causing particles.

(実施例) 以下、本発明の好適な実施例を添付図面に基づ
いて詳細に説明する。
(Embodiments) Hereinafter, preferred embodiments of the present invention will be described in detail based on the accompanying drawings.

第1図は本発明装置の概略を示す説明図であ
る。
FIG. 1 is an explanatory diagram showing an outline of the apparatus of the present invention.

20はホツトプレートであり、その上面にウエ
ハー22を載置する。ホツトプレート20はウエ
ハー22を反応温度付近にまで加熱する。
20 is a hot plate, and a wafer 22 is placed on the top surface thereof. The hot plate 20 heats the wafer 22 to near the reaction temperature.

ホツトプレート20は適宜な支持体(図示せ
ず)により支持されることはもちろんであるが、
ホツトプレート20の周辺は開放されており、本
発明においては、このホツトプレート22を含む
反応部を開放チヤンバーとよぶ。
Of course, the hot plate 20 is supported by a suitable support (not shown),
The periphery of the hot plate 20 is open, and in the present invention, the reaction section including the hot plate 22 is called an open chamber.

24は反応ガス供給ノズルであり、ホツトプレ
ート20側方に配置され、反応ガスをウエハー2
2表面に沿つてウエハー22表面と平行に流す。
反応ガス供給ノズル24は、中空状のガス留め2
6を有し、このガス留め26に連通する多数のス
リツト状あるいは小孔状をなすガス噴出口28を
有するノズル本体30にガス供給管32が連結さ
れてなる(第1図、第2図)。ノズル本体30か
らはノズル本体30前方に厚さ数mmの帯状の反応
ガス流がウエハー22表面に沿つて流せるように
なつている。
Reference numeral 24 denotes a reaction gas supply nozzle, which is arranged on the side of the hot plate 20 and supplies the reaction gas to the wafer 2.
2 surface parallel to the wafer 22 surface.
The reaction gas supply nozzle 24 is connected to a hollow gas stopper 2.
6, and a gas supply pipe 32 is connected to a nozzle body 30 having a large number of slit-shaped or small hole-shaped gas jet ports 28 communicating with the gas stop 26 (FIGS. 1 and 2). . From the nozzle body 30, a band-shaped reactive gas flow having a thickness of several mm can flow along the surface of the wafer 22 in front of the nozzle body 30.

34は反応ガス加熱用コイルであり、ガス供給
管32の適所に巻回され、反応ガスをあらかじめ
ウエハー22表面温度付近にまで加熱してウエハ
ー22表面上を通過させるものである。
Reference numeral 34 denotes a reactant gas heating coil, which is wound around the gas supply pipe 32 at an appropriate position, and is used to heat the reactant gas in advance to near the surface temperature of the wafer 22 and pass it over the wafer 22 surface.

36はウエハー22を挾んで反応ガス供給ノズ
ル24と対向して配置された排出管であり、未反
応ガス、気相中の反応生成物を排出する。
Reference numeral 36 denotes a discharge pipe disposed opposite to the reaction gas supply nozzle 24 with the wafer 22 in between, and discharges unreacted gas and reaction products in the gas phase.

38は不活性ガス供給ノズルたるN2ガス供給
ノズルであり、反応ガス供給ノズル24とほぼ同
様に構成され、反応ガス供給ノズル24の上方に
配置されて、反応ガス供給ノズル24から流出す
る反応ガス流の上方を覆つてN2ガスを帯状に流
すものである。このN2ガスも、N2ガス供給管4
0に巻回された加熱用コイル42によつて、反応
ガスとほぼ同温度にまで加熱されて供給される。
Reference numeral 38 denotes an N 2 gas supply nozzle, which is an inert gas supply nozzle, and is configured in substantially the same manner as the reaction gas supply nozzle 24, and is arranged above the reaction gas supply nozzle 24 to control the reaction gas flowing out from the reaction gas supply nozzle 24. This involves flowing N 2 gas in a band over the top of the flow. This N2 gas is also N2 gas supply pipe 4
The heating coil 42, which is wound around zero, heats the reactant gas to approximately the same temperature as the reactant gas and supplies the reactant gas.

44は上記のN2ガスを排出するN2ガス排出管
である。
44 is an N 2 gas discharge pipe for discharging the above N 2 gas.

本実施例は上記のように構成される。 This embodiment is configured as described above.

しかして反応ガスをあらかじめ加熱して、反応
ガス供給ノズル24から、ウエハー22表面に沿
つて帯状に流し、N2ガスをあらかじめ加熱して
N2ガス供給ノズル38から反応ガス上方を覆つ
て帯状に流して、ウエハー22表面上に所望の皮
膜を形成させることができる。この場合に両ガス
があらかじめ同温度付近にまで加熱されているか
ら、両ガス間で上昇気流等による乱流が生じるこ
とがなく、したがつて層流状態で供給されるか
ら、反応ガス気相中で生成した反応生成物がウエ
ハー22表面上に落下して、パーテイクルが発生
する等の事態が生じない。
In this way, the reaction gas is heated in advance and flows in a band shape from the reaction gas supply nozzle 24 along the surface of the wafer 22, and the N 2 gas is heated in advance.
A desired film can be formed on the surface of the wafer 22 by flowing the reaction gas in a band form from the N 2 gas supply nozzle 38 over the upper part of the reaction gas. In this case, since both gases have been heated to around the same temperature in advance, turbulent flow due to upward air currents etc. does not occur between the two gases, and therefore they are supplied in a laminar flow state, so the reactant gas vapor phase Reaction products generated therein will not fall onto the surface of the wafer 22 and particles will not be generated.

反応ガス系はSiH4―O2系、SiH4―PH3―O2
のような無機シラン系による、SiO2膜、PSG膜
の形成が可能である。
The reaction gas system is an inorganic silane system such as SiH 4 --O 2 system or SiH 4 --PH 3 --O 2 system, and it is possible to form a SiO 2 film or a PSG film.

なお上記の場合、例えばSiH4―O2系において、
加熱用コイル34によつて反応ガスをあらかじめ
約400℃の反応温度にまで加熱してしまうと、例
えば反応ガス供給ノズル24内で反応してしまう
ことが考えられるから、加熱用コイル34によつ
ては、反応が起こらない温度、例えば約200℃程
度に加熱(N2ガスも200℃程度に加熱する)して
供給し、ウエハー22近傍で他の適宜な加熱源に
よつて反応温度にまで加熱するのが望ましい。
In the above case, for example, in the SiH 4 -O 2 system,
If the reaction gas is preheated to a reaction temperature of approximately 400°C by the heating coil 34, it is conceivable that it will react within the reaction gas supply nozzle 24, for example. is heated to a temperature at which no reaction occurs, for example, about 200°C (N 2 gas is also heated to about 200°C), and then heated to the reaction temperature near the wafer 22 by another suitable heating source. It is desirable to do so.

実施例 1 SiH4を200℃、400c.c./分、O2を200℃、600
c.c./分、N2ガスを200℃、2500c.c./分で供給し、
反応温度400℃で反応させたところ、SiO2皮膜が
1200Å/分で得られた。
Example 1 SiH 4 at 200℃, 400 c.c./min, O 2 at 200℃, 600
cc/min, N2 gas was supplied at 200℃, 2500c.c./min,
When the reaction was carried out at a reaction temperature of 400℃, a SiO 2 film was formed.
Obtained at 1200 Å/min.

パーテイクルの発生は見られなかつた。 No particle formation was observed.

なお装置は第1図乃至第3図に概略的に示した
装置を用いた。ウエハーは50mm径のものを12枚第
3図に示すように並べた。各ガス供給ノズル2
4,38と各ガス排出管36,44との間隔は約
150mmにセツトした。また各ガス供給ノズル24,
38の噴出口は、大きさ0.3mmの小孔を0.5mm間隔
に一列に約400mmの長さに亘つて配列した小孔群
とした。これにより各ガスは厚さ数mmの状態で層
流となつて供給された。
Note that the apparatus used was the apparatus schematically shown in FIGS. 1 to 3. Twelve 50 mm diameter wafers were arranged as shown in Figure 3. Each gas supply nozzle 2
The distance between 4, 38 and each gas exhaust pipe 36, 44 is approximately
I set it to 150mm. In addition, each gas supply nozzle 24,
The 38 jet ports were formed into a group of small holes each having a size of 0.3 mm and arranged in a row at intervals of 0.5 mm over a length of approximately 400 mm. As a result, each gas was supplied in a laminar flow with a thickness of several mm.

第4図はさらに他の実施例を示す。 FIG. 4 shows yet another embodiment.

本実施例は紫外線照射ランプを設けた他は前記
実施例を同じである。
This embodiment is the same as the previous embodiment except that an ultraviolet irradiation lamp is provided.

紫外線照射ランプ50(Hgランプ)はN2ガス
流のさらに上方に位置するように設けられ、ホツ
トプレート20上に載置されるウエハー22上面
に紫外線を照射するものである。52は反射板で
ある。
The ultraviolet irradiation lamp 50 (Hg lamp) is provided above the N 2 gas flow and irradiates the upper surface of the wafer 22 placed on the hot plate 20 with ultraviolet rays. 52 is a reflecting plate.

54は上記紫外線照射ランプ50を収納するボ
ツクスであり、ボツクス54内にはN2ガスが流
通される。ポツクス54内にN2ガスを流通させ
るのは、O2が存在するとO2ガスによつて紫外線
が吸収されるからである。
Reference numeral 54 denotes a box that houses the ultraviolet irradiation lamp 50, and N2 gas is passed through the box 54. The reason why N 2 gas is passed through the pocket 54 is that if O 2 exists, ultraviolet rays will be absorbed by the O 2 gas.

56は石英ガラス製のカバーであり、該カバー
56の周縁部には紫外線を透過しない例えばクロ
ム蒸着皮膜が形成され、中央透過部から紫外線を
ウエハー22表面上に照射するようになつてい
る。
Reference numeral 56 denotes a cover made of quartz glass, and a chromium vapor-deposited film, for example, which does not transmit ultraviolet rays is formed on the peripheral edge of the cover 56, so that ultraviolet rays are irradiated onto the surface of the wafer 22 from a central transmitting portion.

本実施例においては、紫外線照射によつて励起
される反応ガス系が好適に用いられる。
In this embodiment, a reactive gas system excited by ultraviolet irradiation is preferably used.

例えば、有機シラン(テトラエトキシシラン)
+O2系、有機シラン+PH3(あるいは有機リン)
+O2系等の反応ガス系が有用である。
For example, organic silane (tetraethoxysilane)
+O 2 system, organic silane + PH 3 (or organic phosphorus)
Reactive gas systems such as +O 2 systems are useful.

このような有機シラン系は一般的に700℃以上
の高温条件でなければ反応しない。しかしながら
発明者は、このような有機シラン系においても、
紫外線を照射することによつて400℃程度の低温
条件でも充分に反応が進行することを見出した。
Such organic silane systems generally do not react unless the temperature is 700°C or higher. However, the inventors believe that even in such organic silane systems,
It was discovered that by irradiating with ultraviolet rays, the reaction proceeded satisfactorily even at low temperatures of around 400°C.

本実施例においては上記事実は極めて有用であ
る。すなわち反応ガス、N2ガスを上記の400℃程
度にまで予熱して供給できる。この温度では反応
ガス系は反応せず、紫外線ランプ50の紫外線照
射領域において初めて、必要な反応を起こし、ウ
エハー22上に皮膜を生成するからである。この
ように反応ガスおよびN2ガスを、反応ガスの後
に起こる反応の反応温度にまであらかじめ予熱し
て供給しうるから、他の加熱源は全く不要である
とともに、反応ガス流とN2ガスとは層流状態で
流れ、前記実施例と同様に、パーテイクルの発生
を抑止することができる。
The above fact is extremely useful in this embodiment. That is, the reaction gas and N 2 gas can be preheated to about 400° C. and then supplied. This is because the reactive gas system does not react at this temperature, and the necessary reaction occurs only in the ultraviolet irradiation region of the ultraviolet lamp 50 to form a film on the wafer 22. In this way, the reaction gas and the N 2 gas can be preheated and supplied to the reaction temperature of the reaction that occurs after the reaction gas, so no other heating source is required, and the reaction gas flow and the N 2 gas can be flows in a laminar flow state, and the generation of particles can be suppressed as in the previous embodiment.

また上記有機シラン系に紫外線を照射して起こ
る反応は、被処理物の表面で起こる表面反応であ
る。このため反応においては、凹部にも凸部と変
わりなく皮膜が生成し、いわゆるステツプカバリ
ツジ(均一被着性)にすぐれる。
The reaction that occurs when the organic silane system is irradiated with ultraviolet light is a surface reaction that occurs on the surface of the object to be treated. Therefore, during the reaction, a film is formed on the concave portions as well as on the convex portions, resulting in excellent so-called step coverage (uniform adhesion).

さらにこの実施例においては、ウエハー22の
若干上方に、適宜なマスク(図示せず)をおくこ
とによつて、マスクのパターン通りに皮膜をウエ
ハー22上に成長させることも可能である。マス
クは石英ガラス等の紫外線を透過する素材のもの
を用い、前記のカバー56と同様にクロム蒸着等
によつて紫外線非透過部を形成して用いる。
Furthermore, in this embodiment, by placing an appropriate mask (not shown) slightly above the wafer 22, it is possible to grow a film on the wafer 22 according to the pattern of the mask. The mask is made of a material that transmits ultraviolet rays, such as quartz glass, and similarly to the cover 56, a portion that does not transmit ultraviolet rays is formed by chromium deposition or the like.

実施例 2 テトラエトキシシランを200℃、600c.c./分、
O2ガスを200℃、600c.c./分、N2ガスを200℃、
0.8/分で供給し、Hgランプ(波長184.9nm、
254.0nm)でウエハー上を照射し、反応温度400
℃で反応させたところ、SiO2皮膜が1000Å/分
で得られた。
Example 2 Tetraethoxysilane at 200℃, 600c.c./min,
O 2 gas at 200℃, 600c.c./min, N 2 gas at 200℃,
Hg lamp (wavelength 184.9nm,
254.0nm) onto the wafer, and the reaction temperature was 400°C.
When the reaction was carried out at ℃, a SiO 2 film was obtained at a rate of 1000 Å/min.

装置は前記実施例1で用いた装置に、第4図に
示す紫外線照射ランプを取り付けて用いた。この
紫外線照射ランプとホツトプレートとの間隔は30
mmに設定した。
The apparatus used was the same as that used in Example 1, with the ultraviolet irradiation lamp shown in FIG. 4 attached. The distance between this ultraviolet irradiation lamp and the hot plate is 30
It was set to mm.

パーテイクルの発生はみられず、ステツプカバ
リツジも良好であつた。
No particles were observed, and step coverage was good.

またウエハー表面から若干離してマスクをお
き、マスクを通して紫外線を照射したところ、マ
スクのパターン通りに皮膜をウエハー上に選択成
長させることができた。
Furthermore, when a mask was placed slightly away from the wafer surface and ultraviolet rays were irradiated through the mask, a film could be selectively grown on the wafer according to the pattern of the mask.

なお、反応系は上記の他に、SiH4―O2系、(紫
外線照射によつて常温で反応する)、SiH4
N2O、CO2、NO2、NO、NH3系(紫外線照射に
よつて約400℃で反応する)、有機シラン―NO2
CO2、N2O、NO、NH3系(同約400℃で反応)
を用いたところ同様の効果が得られた。
In addition to the above, reaction systems include SiH 4 -O 2 system (reacts at room temperature when exposed to ultraviolet rays), SiH 4 -
N 2 O, CO 2 , NO 2 , NO, NH 3 system (reacts at about 400°C with ultraviolet irradiation), organic silane - NO 2 ,
CO 2 , N 2 O, NO, NH 3 system (reacts at about 400℃)
A similar effect was obtained using .

なお以上の各実施例においては、N2ガスカー
テンを形成する例を示したが、これに限られず、
アルゴンその他の不活性ガスを用いることができ
ることはもちろんである。
In each of the above embodiments, an example of forming an N 2 gas curtain was shown, but the invention is not limited to this.
Of course, argon or other inert gas can be used.

(発明の効果) 以上のように本発明によれば次の特有な作用効
果を奏する。
(Effects of the Invention) As described above, the present invention provides the following unique effects.

すなわち、 反応ガスと不活性ガスとをあらかじめほぼ等
しい温度に加熱する加熱手段を設けているの
で、被処理物表面で急に加熱されるのと異な
り、両ガスに上昇気流等の乱流を生じさせず、
したがつてチヤツバーをクローズドでなく開放
チヤンバーに設けても確実に反応ガスと不活性
ガスとの層流を得ることができる。
In other words, since a heating means is provided to heat the reaction gas and the inert gas to approximately the same temperature in advance, unlike sudden heating on the surface of the object to be treated, turbulent flow such as an upward current is generated in both gases. Don't let it happen,
Therefore, even if the chamber is provided as an open chamber instead of a closed chamber, a laminar flow of the reactant gas and the inert gas can be reliably obtained.

チヤンバーが開放チヤンバーであるから、装
置全体の小型化とそのコストの低減化が図れる
ばかりか、チヤンバー内壁に付着した反応生成
物が落下して皮膜上に再付着するというパーテ
イクルの発生を完全に防止できる。
Since the chamber is an open chamber, not only can the entire device be made smaller and its cost reduced, but it also completely prevents the generation of particles, where reaction products adhering to the inner wall of the chamber fall and re-adhere to the film. can.

被処理物表面に流れる反応ガスと不活性ガス
とが、両者が層流状態をなすように流れるか
ら、気相中での反応生成物は反応ガス流と共に
排出される。したがつてこの点でもパーテイク
ルの発生が抑止される。
Since the reaction gas and the inert gas flow on the surface of the object to be treated in a laminar flow state, the reaction products in the gas phase are discharged together with the flow of the reaction gas. Therefore, the generation of particles is also suppressed in this respect.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明装置の概要を示す説明図、第3
図はその平面図、第2図は反応ガス供給ノズルの
説明図、第4図は本発明装置の他の実施例を示す
説明図である。 20……ホツトプレート、22……ウエハー、
24……反応ガス供給ノズル、26……ガス留
め、28……ガス噴出口、30……ノズル本体、
32……ガス供給管、34……反応ガス加熱用コ
イル、36……排出管、38……N2ガス供給ノ
ズル、40……N2ガス供給管、42……加熱用
コイル、44……N2ガス排出管、50……紫外
線照射ランプ、52……反射板、54……ボツク
ス、56……カバー。
Fig. 1 is an explanatory diagram showing the outline of the device of the present invention;
The figure is a plan view thereof, FIG. 2 is an explanatory diagram of a reaction gas supply nozzle, and FIG. 4 is an explanatory diagram showing another embodiment of the apparatus of the present invention. 20... hot plate, 22... wafer,
24... Reaction gas supply nozzle, 26... Gas stopper, 28... Gas spout, 30... Nozzle body,
32...Gas supply pipe, 34...Reaction gas heating coil, 36...Discharge pipe, 38... N2 gas supply nozzle, 40... N2 gas supply pipe, 42...Heating coil, 44... N2 gas exhaust pipe, 50...ultraviolet irradiation lamp, 52...reflector, 54...box, 56...cover.

Claims (1)

【特許請求の範囲】 1 被処理物表面に反応ガスを流通させて被処理
物表面に皮膜を成長させる気相成長装置におい
て、 被処理物を載置し、該被処理物を反応温度にま
で加熱するホツトプレートを備え、該ホツトプレ
ート周辺が開放されている開放チヤンバーと、 反応ガスを被処理物表面に沿つて被処理物表面
と平行な方向に流す反応ガス供給ノズルと、 この反応ガス流の少なくとも反被処理物側を覆
つて不活性ガスカーテンを形成するように不活性
ガスを供給する不活性ガス供給ノズルと、 反応ガス流と不活性ガス流とが層流をなすよう
に、前記各ガス供給ノズルから流される反応ガス
と不活性ガスとをあらかじめほぼ等しい温度にま
で加熱する加熱手段と を具備することを特徴とする気相成長装置。
[Scope of Claims] 1. In a vapor phase growth apparatus for growing a film on the surface of a workpiece by flowing a reaction gas over the surface of the workpiece, the workpiece is placed on the workpiece, and the workpiece is heated to a reaction temperature. an open chamber equipped with a hot plate to be heated and open around the hot plate; a reaction gas supply nozzle that flows a reaction gas along the surface of the object to be processed in a direction parallel to the surface of the object to be processed; and a flow of the reaction gas. an inert gas supply nozzle for supplying an inert gas so as to form an inert gas curtain covering at least the side opposite to the object to be treated; A vapor phase growth apparatus characterized by comprising heating means for heating a reaction gas and an inert gas flowing from each gas supply nozzle to approximately the same temperature in advance.
JP20123084A 1984-09-26 1984-09-26 Method and device for vapor growth Granted JPS6179771A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP20123084A JPS6179771A (en) 1984-09-26 1984-09-26 Method and device for vapor growth
US06/780,205 US4731255A (en) 1984-09-26 1985-09-26 Gas-phase growth process and an apparatus for the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20123084A JPS6179771A (en) 1984-09-26 1984-09-26 Method and device for vapor growth

Publications (2)

Publication Number Publication Date
JPS6179771A JPS6179771A (en) 1986-04-23
JPS6338430B2 true JPS6338430B2 (en) 1988-07-29

Family

ID=16437488

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20123084A Granted JPS6179771A (en) 1984-09-26 1984-09-26 Method and device for vapor growth

Country Status (1)

Country Link
JP (1) JPS6179771A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6326369A (en) * 1986-07-19 1988-02-03 Ulvac Corp Cvd method
JPS6326368A (en) * 1986-07-19 1988-02-03 Ulvac Corp Cvd method
JP3498255B2 (en) * 1996-06-17 2004-02-16 東芝機械株式会社 Single wafer decompression CVD system

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5354181A (en) * 1976-10-28 1978-05-17 Fujitsu Ltd Chemical evaporation apparatus
JPS57187033A (en) * 1981-05-12 1982-11-17 Seiko Epson Corp Vapor phase chemical growth device

Also Published As

Publication number Publication date
JPS6179771A (en) 1986-04-23

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