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JPS6411116B2 - - Google Patents
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JPS6411116B2 - - Google Patents

Info

Publication number
JPS6411116B2
JPS6411116B2 JP20473782A JP20473782A JPS6411116B2 JP S6411116 B2 JPS6411116 B2 JP S6411116B2 JP 20473782 A JP20473782 A JP 20473782A JP 20473782 A JP20473782 A JP 20473782A JP S6411116 B2 JPS6411116 B2 JP S6411116B2
Authority
JP
Japan
Prior art keywords
processed
ionization electrode
electrode
vacuum chamber
ionization
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
JP20473782A
Other languages
Japanese (ja)
Other versions
JPS5996261A (en
Inventor
Saburo Tabata
Yoshuki Sato
Hideo Hayashi
Yasushi Kawashita
Masami Nakasone
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.)
National Institute of Advanced Industrial Science and Technology AIST
Shinko Seiki Co Ltd
Original Assignee
Agency of Industrial Science and Technology
Shinko Seiki Co Ltd
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 Agency of Industrial Science and Technology, Shinko Seiki Co Ltd filed Critical Agency of Industrial Science and Technology
Priority to JP20473782A priority Critical patent/JPS5996261A/en
Publication of JPS5996261A publication Critical patent/JPS5996261A/en
Publication of JPS6411116B2 publication Critical patent/JPS6411116B2/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
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/22Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
    • C23C14/24Vacuum evaporation
    • C23C14/32Vacuum evaporation by explosion; by evaporation and subsequent ionisation of the vapours, e.g. ion-plating

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Chemical Vapour Deposition (AREA)

Description

【発明の詳細な説明】 この発明は、被処理物の表面に薄膜を作成する
装置に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an apparatus for forming a thin film on the surface of a workpiece.

従来、上記のような装置としては反応性スパツ
タリング、CVD、プラズマCVD、イオンプレー
テイング等に基づくものがある。反応性スパツタ
リングによるものは、ターゲツト材が固形物であ
り、グロー放電によつて生じたイオンでターゲツ
ト材を叩き出し、グロー放電を生じているガスと
反応させるものであるが、ターゲツト材から叩き
出された粒子のイオン化がほとんど行なわれず、
グロー放電を起こしているガスのイオン化率も
0.1%以下と低いので良質の膜を得るには、被処
理物の温度を高くする必要があつた。例えばSiC
を作製する場合、ターゲツト材としてSi、反応ガ
スとしてC2H2,Arを用いた場合、被処理物の温
度は600℃以上にする必要がある。またCVDは反
応ガスを被処理物上で反応させるため1000℃以上
必要であるし、薄膜の堆積速度が初期、中期、後
期では異なるため膜厚制御が困難である。さらに
プラズマCVDは反応ガスをイオン化させるため
にCVDに比べて低温で処理できるが、反応ガス
のイオン化率が低いため、良質な膜を得るために
は被処理物の温度を500℃以上にしなければなら
ない。またイオンプレーテイングの場合、蒸発源
が固体で有限なので10μm以上の膜を連続的に作
成するには無理があつた。
Conventionally, such devices as described above are based on reactive sputtering, CVD, plasma CVD, ion plating, and the like. In reactive sputtering, the target material is a solid substance, and the ions generated by glow discharge are used to knock out the target material and cause it to react with the gas that is generating the glow discharge. The ionized particles are hardly ionized,
The ionization rate of the gas causing the glow discharge is also
Since the content is as low as 0.1% or less, it was necessary to raise the temperature of the object to be treated in order to obtain a good quality film. For example, SiC
When producing a target material using Si as a target material and using C 2 H 2 or Ar as a reaction gas, the temperature of the object to be processed needs to be 600°C or higher. In addition, CVD requires a temperature of 1000°C or higher in order to cause the reaction gas to react on the object to be processed, and the deposition rate of the thin film differs in the initial, middle, and late stages, making it difficult to control the film thickness. Furthermore, plasma CVD can process at a lower temperature than CVD in order to ionize the reactive gas, but because the ionization rate of the reactive gas is low, the temperature of the processed material must be raised to 500°C or higher in order to obtain a high-quality film. No. In addition, in the case of ion plating, since the evaporation source is solid and limited, it is impossible to continuously create films with a thickness of 10 μm or more.

この発明は、上記の問題を解決したもので、イ
オン化率を高めて低い被処理物温度でも良質な薄
膜を連続的に作成できる装置を提供することを目
的とする。
The present invention solves the above-mentioned problems, and aims to provide an apparatus that can increase the ionization rate and continuously form high-quality thin films even at low temperatures of the object to be processed.

以下、この発明を図示の1実施例に基づいて説
明する。図において、2は真空槽、4は、この真
空槽2用の真空ポンプである。この真空槽2内の
下部には電子銃6が設けられ、その上面にはアー
ス電位とされた被処理物、例えば硬質カーボン8
が配置されている。電子銃6はこれが生成する電
子ビーム10によつて被処理物8を加熱するため
のものである。
The present invention will be explained below based on one embodiment shown in the drawings. In the figure, 2 is a vacuum tank, and 4 is a vacuum pump for this vacuum tank 2. An electron gun 6 is provided in the lower part of the vacuum chamber 2, and an object to be processed, such as hard carbon 8, is placed on the upper surface of the vacuum chamber 2.
is located. The electron gun 6 is for heating the object to be processed 8 with the electron beam 10 it generates.

被処理物の一方の縁部付近から上方に向つて30
乃至100mm(この実施例では50mm)の距離l1を
隔ててイオン化電極12が配置されている。この
イオン化電極12は幅3cm、長さ7cmの矩形状に
形成されており、正の500乃至10V(この実施例で
は80V)の直流電圧が印加されている。14がそ
の直流電源である。
30 upwards from near one edge of the object to be processed
Ionization electrodes 12 are arranged at a distance l1 of 100 mm to 100 mm (50 mm in this embodiment). This ionization electrode 12 is formed in a rectangular shape with a width of 3 cm and a length of 7 cm, and a positive DC voltage of 500 to 10 V (80 V in this embodiment) is applied. 14 is its DC power supply.

このイオン化電極12から下方に向つて5〜50
mmの距離l2を隔てて熱電子放射電極16が配置
されている。18はその交流電源である。
5 to 50 points downward from this ionization electrode 12.
Thermionic emission electrodes 16 are arranged at a distance l2 of mm. 18 is its AC power supply.

このイオン化電極12と熱電子放射電極16と
の間には、イオン化電極から下方に向つて10乃至
20mmの距離l3を隔てて、かつイオン化電極12
から真空槽2の側壁側に10〜20mmの距離l4を隔
てて供給口が位置するように反応ガス導入パイプ
20が配置されている。このパイプ20を介して
真空槽2内に反応ガス(例えばC2H2、SiH4及び
Arを適当な割合に混合したもの)が真空槽2の
外部から供給される。22は反応ガスの流量制御
弁、24は同停止弁である。
Between the ionization electrode 12 and the thermionic emission electrode 16, there are
At a distance l3 of 20 mm, and an ionization electrode 12
A reactant gas introduction pipe 20 is arranged so that the supply port is located at a distance l4 of 10 to 20 mm from the side wall of the vacuum chamber 2. A reaction gas (for example, C 2 H 2 , SiH 4 and
(mixed with Ar in an appropriate ratio) is supplied from outside the vacuum chamber 2. 22 is a flow rate control valve for the reaction gas, and 24 is a stop valve thereof.

電子銃6の側方には例えば永久磁石からなる磁
界発生体26が配置されており、同図に点線で囲
んだ範囲27内に同図の表裏方向に向う磁界を発
生する。この磁界は30〜500ガウスであり、イオ
ン化電極12から被処理物に向う(同図における
上下方向)電界に対して直交するものである。磁
界が30ガウス以下であると、後述するように電子
にらせん運動をさせることができず、500ガウス
以上では電子ビーム10が影響を受けるからであ
る。
A magnetic field generator 26 made of, for example, a permanent magnet is arranged on the side of the electron gun 6, and generates a magnetic field directed in the front and back directions in the figure within an area 27 surrounded by a dotted line in the figure. This magnetic field is 30 to 500 Gauss, and is perpendicular to the electric field directed from the ionization electrode 12 toward the object to be processed (in the vertical direction in the figure). This is because if the magnetic field is less than 30 Gauss, the electrons cannot be caused to have a spiral motion, as will be described later, and if the magnetic field is more than 500 Gauss, the electron beam 10 will be affected.

被処理物8の中央部から上方に向つて150乃至
300mmの距離l5を隔ててイオン銃28が配置さ
れている。これはビーム形状が60mmφで、加速電
圧3KVでビーム出力が20mAのものである。また
真空槽2の側壁には相対向するように覗窓29,
30が形成されており、覗窓29には光学膜厚測
定器の発光部31が、覗窓30には光学膜厚測定
器の受光部32がそれぞれ設けられている。33
は温度測定器で、被処理物の温度を測定するため
のものである。
150 to upward from the center of the workpiece 8
An ion gun 28 is placed at a distance l5 of 300 mm. This has a beam shape of 60mmφ, an acceleration voltage of 3KV, and a beam output of 20mA. In addition, a viewing window 29 is provided on the side wall of the vacuum chamber 2 so as to face each other.
30 is formed, the viewing window 29 is provided with a light emitting part 31 of an optical film thickness measuring device, and the viewing window 30 is provided with a light receiving part 32 of the optical film thickness measuring device. 33
is a temperature measuring device, which is used to measure the temperature of the object to be processed.

このように構成した薄膜作成装置では、まず真
空槽2内を例えば10-6Torr程度の真空度に真空
ポンプ4によつて排気する。そして、電子銃6に
よつて被処理物を例えば300℃に加熱し、熱電子
放射電極16から0.1〜1mAの熱電子を放射させ
る。さらに、反応ガス停止弁24、反応ガス流量
制御弁22を調整して、反応ガス導入パイプ20
を介して真空槽2内の圧力が3×10-4 Tprrになる
ように反応ガスを供給する。
In the thin film forming apparatus configured as described above, the inside of the vacuum chamber 2 is first evacuated to a degree of vacuum of, for example, about 10 -6 Torr using the vacuum pump 4. Then, the object to be processed is heated to, for example, 300° C. by the electron gun 6, and thermionic electrons of 0.1 to 1 mA are emitted from the thermionic emission electrode 16. Furthermore, by adjusting the reaction gas stop valve 24 and the reaction gas flow rate control valve 22, the reaction gas introduction pipe 20
A reaction gas is supplied through the vacuum chamber 2 so that the pressure within the vacuum chamber 2 becomes 3×10 −4 Tprr .

この状態では、熱電子放射電極16から放射さ
れた熱電子はイオン化電極12に向うが、イオン
化電極12による電界に対して磁界発生体26に
よる磁界を直交するように印加しているので、熱
電子はらせん軌道を描いてイオン化電極12に向
う。そのため、イオン化電極12と熱電子放射電
極16との間に供給されている反応ガスと衝突し
て反応ガスをイオン化する確率が単に電界のみを
印加した場合よりも高くなる。また反応ガスをイ
オン化したことにより発生した電子も同様にらせ
ん軌道を描いてイオン化電極に向うので、益々反
応ガスのイオン化率が高くなる。このようにして
イオン化された反応ガスはイオン化電極12と被
処理物8との間に生成された電界によつて被処理
物8に向い、被処理物8上にSiCの薄膜を作成す
る。
In this state, the thermionic electrons emitted from the thermionic emission electrode 16 head toward the ionization electrode 12, but since the magnetic field by the magnetic field generator 26 is applied orthogonally to the electric field by the ionization electrode 12, the thermionic electrons The particles move toward the ionization electrode 12 in a spiral trajectory. Therefore, the probability of colliding with the reactive gas supplied between the ionization electrode 12 and thermionic emission electrode 16 and ionizing the reactive gas is higher than when only an electric field is applied. Further, since the electrons generated by ionizing the reactive gas similarly move toward the ionization electrode in a spiral trajectory, the ionization rate of the reactive gas becomes higher. The reaction gas ionized in this manner is directed toward the object to be processed 8 by the electric field generated between the ionization electrode 12 and the object to be processed 8, and forms a thin film of SiC on the object to be processed 8.

この際にイオン銃28より被処理物8に向つて
イオン化した反応ガスを放射すると、より一層安
定した薄膜を作成できる。
At this time, if ionized reaction gas is emitted from the ion gun 28 toward the object 8, a more stable thin film can be created.

なお、真空槽2内の圧力が1×10-3 Tprrになる
ように反応ガスを供給すると、電子銃6からの電
子ビーム10が反応ガスと衝突し、さらに反応ガ
スのイオン化が促進される。また真空槽2内の圧
力が3×10-4 Tprrまたは1×10-3 Tprrに維持される
ように反応ガスの供給と真空槽2内の排気とは並
行して行なわれる。さらに、光学用薄膜を作成す
る場合には、光学薄膜測定器の発光部31から光
を被処理物8に照射し、その反射光を光学薄膜測
定器の受光部32で受けて、被処理物8上の薄膜
の屈折率及び吸収係数を間欠的に測定することに
よつて所望の光学薄膜を得ることができる。
Note that when the reactive gas is supplied so that the pressure inside the vacuum chamber 2 becomes 1×10 -3 Tprr , the electron beam 10 from the electron gun 6 collides with the reactive gas, further promoting ionization of the reactive gas. Furthermore, the supply of the reaction gas and the evacuation of the vacuum chamber 2 are carried out in parallel so that the pressure within the vacuum chamber 2 is maintained at 3×10 −4 Tprr or 1×10 −3 Tprr . Furthermore, when creating an optical thin film, the workpiece 8 is irradiated with light from the light emitting part 31 of the optical thin film measuring instrument, and the reflected light is received by the light receiving part 32 of the optical thin film measuring instrument. By intermittently measuring the refractive index and absorption coefficient of the thin film on 8, a desired optical thin film can be obtained.

以上述べたように、この発明による薄膜作成装
置では、イオン化電極12と被処理物8とは、比
較的接近しており、しかも、このイオン化電極1
2と被処理物8との間に、熱電子放射電極16が
設けられ、この熱電子放射電極16とイオン化電
極12との間に反応ガス供給パイプ20が開口し
ている。従つて、熱電子放射電極16から放射さ
れた熱電子が、イオン化電極12に向う際に、熱
電子放射電極16とイオン化電極12との間に供
給されている反応ガスと衝突して、反応ガスを効
率的にイオン化する。従つて、イオン化された反
応ガスの密度が高くなる。そして、イオン化され
た反応ガスは、イオン化電極12と被処理物8と
の間の電界によつて、被処理物8に向うので被処
理物8上に効率的に成膜される。例えば、イオン
化が、イオン化電極12と被処理物8との間では
なく、イオン化電極とこれを挟んで被処理物とは
反対側との間で行なわれた場合、被処理物を相当
に高温に加熱するか、被処理物に高い負の電圧を
印加しない限り、充分に成膜させることができな
いが、この発明によれば、被処理物は比較的低温
に加熱するだけでよく、また基準電位に接続する
だけで充分に成膜させることができる。しかも、
イオンプレーテイングでは、蒸発源として固体で
ある金属を用いているので有限であり、蒸発源が
枯渇すると、真空槽2内の蒸発源の取換をしなけ
ればならず、イオンプレーテイング作業が中断さ
れ、連続的に10μm以上の厚さの薄膜を作成する
ことができなかつたが、この装置では、反応ガス
源は真空槽2の外部に設けてあるので、真空槽2
内の取換作業が不要で、連続的に10μm以上の厚
さの薄膜を作成することができる。
As described above, in the thin film forming apparatus according to the present invention, the ionization electrode 12 and the object to be processed 8 are relatively close to each other, and the ionization electrode 1
A thermionic emission electrode 16 is provided between the thermoelectron emission electrode 16 and the object to be processed 8 , and a reaction gas supply pipe 20 is opened between the thermionic emission electrode 16 and the ionization electrode 12 . Therefore, when the thermoelectrons emitted from the thermionic emission electrode 16 head towards the ionization electrode 12, they collide with the reaction gas supplied between the thermionic emission electrode 16 and the ionization electrode 12, and the reaction gas efficiently ionizes. Therefore, the density of the ionized reaction gas increases. The ionized reaction gas is directed toward the object to be processed 8 by the electric field between the ionization electrode 12 and the object to be processed 8, so that a film is efficiently formed on the object to be processed 8. For example, if ionization is performed not between the ionization electrode 12 and the workpiece 8, but between the ionization electrode and the opposite side of the workpiece, the workpiece may be heated to a considerably high temperature. A sufficient film cannot be formed unless the object is heated or a high negative voltage is applied to the object, but according to this invention, the object only needs to be heated to a relatively low temperature, and the reference potential A sufficient film can be formed just by connecting to the . Moreover,
In ion plating, solid metal is used as the evaporation source, so the evaporation source is limited, and when the evaporation source is exhausted, the evaporation source in the vacuum chamber 2 must be replaced, and the ion plating work is interrupted. However, in this device, the reactant gas source is provided outside the vacuum chamber 2, so it was not possible to continuously create a thin film with a thickness of 10 μm or more.
There is no need for internal replacement work, and thin films with a thickness of 10 μm or more can be created continuously.

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

図はこの発明による薄膜作成装置の概略構成図
である。 2…真空槽、6…電子銃(加熱源)、8…被処
理物、12…イオン化電極、16…熱電子放射電
極、20…反応ガス供給パイプ(反応ガス供給通
路)、26…磁界発生体。
The figure is a schematic configuration diagram of a thin film forming apparatus according to the present invention. 2... Vacuum chamber, 6... Electron gun (heating source), 8... Processing object, 12... Ionization electrode, 16... Thermionic emission electrode, 20... Reactive gas supply pipe (reactive gas supply passage), 26... Magnetic field generator .

Claims (1)

【特許請求の範囲】[Claims] 1 真空槽と、この真空槽内に配置されており基
準電位とされた被処理物と、この被処理物に接近
して配置されており正の電圧が印加され上記被処
理物との間に電界を形成しているイオン化電極
と、このイオン化電極と上記被処理物との間に配
置された熱電子放射電極と、この熱電子放射電極
と上記イオン化電極との間に供給口が配置されて
おり上記イオン化電極によつてイオン化される反
応ガスを上記真空槽内にその外部から供給する反
応ガス供給通路と、上記被処理物を加熱する加熱
源と、上記イオン化電極と上記被処理物との間の
電界に対して直交する磁界を上記イオン化電極と
上記被処理物との間に発生する磁界発生体とを、
具備する薄膜作成装置。
1. Between a vacuum chamber, a workpiece placed in the vacuum chamber and set to a reference potential, and a workpiece placed close to the workpiece and to which a positive voltage is applied. An ionization electrode forming an electric field, a thermionic emission electrode disposed between the ionization electrode and the object to be treated, and a supply port disposed between the thermionic emission electrode and the ionization electrode. a reaction gas supply passage for supplying a reaction gas to be ionized by the ionization electrode into the vacuum chamber from the outside; a heat source for heating the object to be processed; and a connection between the ionization electrode and the object to be processed. a magnetic field generator that generates a magnetic field orthogonal to the electric field between the ionization electrode and the object to be processed;
Equipped with a thin film forming device.
JP20473782A 1982-11-22 1982-11-22 Thin film forming device Granted JPS5996261A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20473782A JPS5996261A (en) 1982-11-22 1982-11-22 Thin film forming device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20473782A JPS5996261A (en) 1982-11-22 1982-11-22 Thin film forming device

Publications (2)

Publication Number Publication Date
JPS5996261A JPS5996261A (en) 1984-06-02
JPS6411116B2 true JPS6411116B2 (en) 1989-02-23

Family

ID=16495473

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20473782A Granted JPS5996261A (en) 1982-11-22 1982-11-22 Thin film forming device

Country Status (1)

Country Link
JP (1) JPS5996261A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6328873A (en) * 1986-07-22 1988-02-06 Ulvac Corp Plasma cvd device

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS589156B2 (en) * 1975-03-28 1983-02-19 松下電器産業株式会社 Ionization plating device
JPS5420973A (en) * 1977-07-18 1979-02-16 Nippon Telegr & Teleph Corp <Ntt> Inorganic compound thin film forming device
JPS585985B2 (en) * 1977-09-12 1983-02-02 光音電気株式会社 Ionization method
JPS5452685A (en) * 1978-05-12 1979-04-25 Canon Inc Vacuum ionization plating method
JPS594045Y2 (en) * 1979-05-23 1984-02-04 神港精機株式会社 Ionization device for thin film production

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JPS5996261A (en) 1984-06-02

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