JPH06276049A - Surface acoustic wave element and its manufacture - Google Patents

Surface acoustic wave element and its manufacture

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Publication number
JPH06276049A
JPH06276049A JP8570793A JP8570793A JPH06276049A JP H06276049 A JPH06276049 A JP H06276049A JP 8570793 A JP8570793 A JP 8570793A JP 8570793 A JP8570793 A JP 8570793A JP H06276049 A JPH06276049 A JP H06276049A
Authority
JP
Japan
Prior art keywords
film
acoustic wave
surface acoustic
crystal grain
grain size
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.)
Granted
Application number
JP8570793A
Other languages
Japanese (ja)
Other versions
JP3233489B2 (en
Inventor
Hideaki Yokota
英明 横田
Hisao Morooka
久雄 師岡
Katsuo Sato
勝男 佐藤
Katsuto Nagano
克人 長野
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.)
TDK Corp
Original Assignee
TDK Corp
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Filing date
Publication date
Application filed by TDK Corp filed Critical TDK Corp
Priority to JP08570793A priority Critical patent/JP3233489B2/en
Publication of JPH06276049A publication Critical patent/JPH06276049A/en
Application granted granted Critical
Publication of JP3233489B2 publication Critical patent/JP3233489B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Surface Acoustic Wave Elements And Circuit Networks Thereof (AREA)

Abstract

PURPOSE:To obtain the surface acoustic wave element which is fast in the propagation velocity of a surface acoustic wave and high in its propagation speed and has excellent characteristics by forming a carbon film containing diamond of less than specific size as a surface wave propagation film. CONSTITUTION:The surface acoustic wave element 11 has the surface surface propagation film 14 and a piezoelectric film 15 on a substrate 12 in this order and also has an electrode 16 for applying an electric field to the piezoelectric film 15; and the surface wave propagation film 14 is the carbon film containing diamond of <=100nm mean crystal grain size. The film which is small in crystal grain size like this behaviors as a medium which is isotropic to a surface acoustic wave with short wavelength, so the phase of the surface acoustic wave is hardly disordered and excellent element characteristics are obtained. Further, the surface acoustic wave is not scattered by crystal grain borders since the extremely small crystal grain size, so the propagation loss becomes small. The effect can not be obtained when the mean crystal grain size of the diamond exceeds the range. The lower limit of the mean crystal grain size of the diamond is not specially determined, but the sound velocity tends to decreases remarkably when the mean crystal grain size is <=5nm.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、弾性表面波素子とその
製造方法とに関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a surface acoustic wave device and a method for manufacturing the same.

【0002】[0002]

【従来の技術】ダイヤモンド薄膜は、弾性表面波(SA
W)素子の表面波伝搬膜として注目を浴びている。弾性
表面波素子は、表面波伝搬膜と圧電膜とが積層された構
成となっており、圧電膜にクシ型電極により電界を印加
して振動させることにより、表面波伝搬膜に表面波を励
振するものである。弾性表面波素子は、フィルタを始め
として通信分野で広く利用されているが、簡単な構造で
良好な特性が得られることから、移動通信等の分野への
適用が期待されている。移動通信では、通常、UHF帯
を用いるため、動作周波数が極めて高くなる。弾性表面
波素子の動作周波数を高くするためには、例えば、クシ
型電極の周期を小さくしたり、音速の速い表面波伝搬膜
を用いたりする。クシ型電極は、通常、フォトリソグラ
フィーにより形成されるため、電極周期を小さくするに
は限界がある。一方、ダイヤモンド中での音速は極めて
速いため、表面波伝搬膜としてダイヤモンド薄膜を用い
ればギガヘルツ(GHz)帯に対応できる弾性表面波素
子が実現する可能性がでてくる。
2. Description of the Related Art A diamond thin film is a surface acoustic wave (SA
W) Has attracted attention as a surface wave propagation film for devices. The surface acoustic wave element has a structure in which a surface wave propagating film and a piezoelectric film are laminated, and a surface wave is excited in the surface wave propagating film by applying an electric field to the piezoelectric film by a comb-shaped electrode to vibrate the film. To do. The surface acoustic wave element is widely used in the field of communication including filters, but since it has good characteristics with a simple structure, it is expected to be applied to fields such as mobile communication. In mobile communication, since the UHF band is usually used, the operating frequency becomes extremely high. In order to increase the operating frequency of the surface acoustic wave element, for example, the period of the comb-shaped electrode is shortened or a surface acoustic wave propagation film having a high sound velocity is used. Since the comb-shaped electrode is usually formed by photolithography, there is a limit in reducing the electrode period. On the other hand, since the sound velocity in diamond is extremely high, using a diamond thin film as the surface wave propagation film may lead to the realization of a surface acoustic wave device capable of supporting the gigahertz (GHz) band.

【0003】ダイヤモンド薄膜の形成には、バルクダイ
ヤモンドに近い結晶構造が得られることからCVD法が
好ましく用いられている。しかし、表面波伝搬膜に必要
な厚さは約10μm 以上であり、このような厚さのダイ
ヤモンド膜を通常のCVD法で形成した場合には結晶粒
径が1μm 程度の多結晶膜となってしまう。ダイヤモン
ドは音速に異方性があるので、このような多結晶膜を用
いると膜を伝搬する音波の位相にばらつきが生じ、良好
な特性が得られない。また、結晶粒径が弾性表面波の波
長と同程度以上となると、結晶粒界による散乱のために
伝搬損失が大きくなるという問題がある。また、このよ
うな多結晶ダイヤモンド薄膜は、弾性表面波の波長と比
較して表面の凹凸が激しいので、表面波が散乱して伝搬
ロスを生じる。伝搬される際に表面波が侵入する深さは
極めて浅く、ほぼその波長程度の深さとなるので、使用
波長が短くなるほど膜表面の凹凸による伝搬ロスの割合
は大きくなる。これを防ぐために膜形成後に表面を研磨
しなければならず、低コスト化が困難である。
The CVD method is preferably used for forming a diamond thin film because a crystal structure close to that of bulk diamond can be obtained. However, the thickness required for the surface wave propagation film is about 10 μm or more, and when a diamond film having such a thickness is formed by a normal CVD method, it becomes a polycrystalline film having a crystal grain size of about 1 μm. I will end up. Since diamond has anisotropy in sound velocity, when such a polycrystalline film is used, the phase of a sound wave propagating through the film varies, and good characteristics cannot be obtained. Further, when the crystal grain size is equal to or larger than the wavelength of the surface acoustic wave, there is a problem that the propagation loss becomes large due to scattering by the crystal grain boundaries. In addition, since such a polycrystalline diamond thin film has severe surface irregularities as compared with the wavelength of the surface acoustic wave, the surface wave is scattered and a propagation loss occurs. The depth at which the surface wave penetrates when propagating is extremely shallow and is about the wavelength thereof. Therefore, the shorter the wavelength used, the larger the proportion of the propagation loss due to the unevenness of the film surface. In order to prevent this, the surface must be polished after the film is formed, and it is difficult to reduce the cost.

【0004】一方、結晶粒をもたない非晶質炭素膜(通
常、ダイヤモンド状炭素膜と呼ばれる)を表面波伝搬膜
として使うこともある。非晶質炭素膜は、音速に異方性
はないがダイヤモンド膜よりも音速が遅い。したがっ
て、電極周期をより小さくしなければならず、高周波へ
の対応が難しい。
On the other hand, an amorphous carbon film having no crystal grains (usually called a diamond-like carbon film) may be used as a surface wave propagation film. The sound velocity of the amorphous carbon film has no anisotropy, but the sound velocity is slower than that of the diamond film. Therefore, the electrode period must be made smaller, and it is difficult to cope with high frequencies.

【0005】[0005]

【発明が解決しようとする課題】本発明は、弾性表面波
の伝搬速度が高速でその伝搬効率が高く、特性の良好な
弾性表面波素子を提供することを目的とする。
SUMMARY OF THE INVENTION It is an object of the present invention to provide a surface acoustic wave device having a high propagation speed of surface acoustic waves, a high propagation efficiency thereof, and excellent characteristics.

【0006】[0006]

【課題を解決するための手段】これらの目的は、下記
(1)〜(8)の本発明によって達成される。 (1)基板上に表面波伝搬膜および圧電膜をこの順で有
し、圧電膜に電界を印加する電極を有する弾性表面波素
子であって、前記表面波伝搬膜が、平均結晶粒径100
nm以下のダイヤモンドを含む炭素膜であることを特徴と
する弾性表面波素子。 (2)前記ダイヤモンドの平均結晶粒径が5nm以上であ
る上記(1)の弾性表面波素子。 (3)前記表面波伝搬膜中の音速が5700m/s 以上で
ある上記(1)または(2)の弾性表面波素子。 (4)上記(1)ないし(3)のいずれかの弾性表面波
素子を製造する方法であって、1×10-5〜5×10-3
Torrの圧力中でプラズマCVD法により前記表面波伝搬
膜を形成することを特徴とする弾性表面波素子の製造方
法。 (5)原料中性粒子ガスを加熱体に衝突させてガスの粒
子速度を増加させた後、前記ガスの分子を電離、解離し
てプラズマCVDを行なう上記(4)の弾性表面波素子
の製造方法。 (6)前記加熱体が加熱管であり、この加熱管内壁に前
記ガスを衝突させる上記(5)の弾性表面波素子の製造
方法。 (7)前記加熱体が700K以上の温度に加熱されてい
る上記(5)または(6)の弾性表面波素子の製造方
法。 (8)前記分子の電離・解離を有磁場マイクロ波プラズ
マによって行なう上記(5)ないし(7)のいずれかの
弾性表面波素子の製造方法。
These objects are achieved by the present invention described in (1) to (8) below. (1) A surface acoustic wave element having a surface wave propagating film and a piezoelectric film in this order on a substrate, and an electrode for applying an electric field to the piezoelectric film, wherein the surface wave propagating film has an average crystal grain size of 100.
A surface acoustic wave device characterized by being a carbon film containing diamond of not more than nm. (2) The surface acoustic wave device according to the above (1), wherein the diamond has an average crystal grain size of 5 nm or more. (3) The surface acoustic wave device according to (1) or (2), wherein the speed of sound in the surface wave propagation film is 5700 m / s or more. (4) A method for manufacturing the surface acoustic wave device according to any one of (1) to (3) above, which comprises 1 × 10 −5 to 5 × 10 −3.
A method of manufacturing a surface acoustic wave device, characterized in that the surface acoustic wave propagation film is formed by a plasma CVD method under a pressure of Torr. (5) Manufacture of the surface acoustic wave device according to (4), wherein the raw material neutral particle gas is caused to collide with a heating body to increase the particle velocity of the gas, and then the molecules of the gas are ionized and dissociated to perform plasma CVD. Method. (6) The method for manufacturing a surface acoustic wave element according to (5), wherein the heating body is a heating tube, and the gas collides with the inner wall of the heating tube. (7) The method for manufacturing a surface acoustic wave device according to the above (5) or (6), wherein the heating body is heated to a temperature of 700 K or higher. (8) The method for manufacturing a surface acoustic wave device according to any one of (5) to (7) above, wherein the molecules are ionized and dissociated by microwave plasma with magnetic field.

【0007】[0007]

【作用および効果】本発明の弾性表面波素子は、平均結
晶粒径100nm以下のダイヤモンドを含む炭素膜を表面
波伝搬膜として用いる。このように結晶粒径が小さい膜
は、短波長の弾性表面波に対しても等方的な媒質として
振る舞うので、弾性表面波の位相の乱れは殆ど生じず、
良好な素子特性が得られる。また、結晶粒径が極めて小
さいために結晶粒界による弾性表面波の散乱が殆ど生じ
ないので、伝搬損失が極めて小さくなる。したがって、
本発明では極めて短波長の弾性表面波を使用することが
でき、しかも、前記表面波伝搬膜は非晶質炭素膜に比べ
音速が速いので、ギガヘルツ帯に対応する弾性表面波素
子が容易に実現する。
In the surface acoustic wave device of the present invention, a carbon film containing diamond having an average crystal grain size of 100 nm or less is used as the surface wave propagation film. Since a film having a small crystal grain size behaves as an isotropic medium even for surface acoustic waves of short wavelength, there is almost no disturbance of the phase of the surface acoustic waves.
Good device characteristics can be obtained. Moreover, since the crystal grain size is extremely small, the surface acoustic waves are hardly scattered by the crystal grain boundaries, so that the propagation loss is extremely small. Therefore,
In the present invention, a surface acoustic wave having an extremely short wavelength can be used, and since the surface wave propagating film has a higher sound velocity than the amorphous carbon film, a surface acoustic wave device corresponding to the GHz band can be easily realized. To do.

【0008】また、本発明では表面伝搬膜表面の凹凸が
極めて小さくなるので、素子化する際に膜表面の研磨が
不要である。
Further, in the present invention, since the unevenness on the surface of the surface propagation film becomes extremely small, it is not necessary to polish the surface of the film when forming the device.

【0009】[0009]

【具体的構成】以下、本発明の具体的構成について詳細
に説明する。
Specific Structure The specific structure of the present invention will be described in detail below.

【0010】本発明の弾性表面波素子の構成例を、図1
に示す。同図において、弾性表面波素子11は、基板1
2上に、表面波伝搬膜14および圧電膜15をこの順で
有し、圧電膜に電界を印加するためのクシ型の電極16
が表面波伝搬膜14上に設けられている。
An example of the structure of the surface acoustic wave device of the present invention is shown in FIG.
Shown in. In the figure, the surface acoustic wave element 11 is a substrate 1
2 has a surface wave propagation film 14 and a piezoelectric film 15 in this order, and a comb-shaped electrode 16 for applying an electric field to the piezoelectric film.
Are provided on the surface wave propagation film 14.

【0011】表面波伝搬膜は、平均結晶粒径100nm以
下のダイヤモンドを含む炭素膜である。前記ダイヤモン
ドの平均結晶粒径が前記範囲を超えると上記した本発明
の効果が得られなくなる。前記ダイヤモンドの平均結晶
粒径の下限は特にないが、平均結晶粒径が5nm未満とな
ると音速が低下する傾向が顕著になる。なお、ダイヤモ
ンドのより好ましい平均結晶粒径は20〜100nmであ
る。膜中に多結晶ダイヤモンドが含まれていることはX
線回折により確認することができ、ダイヤモンドの平均
結晶粒径は透過型電子顕微鏡などにより測定することが
できる。また、表面波伝搬膜表面が平坦で自形面が現わ
れていないことは、走査型電子顕微鏡等により確認する
ことができる。
The surface wave propagation film is a carbon film containing diamond having an average crystal grain size of 100 nm or less. If the average crystal grain size of the diamond exceeds the above range, the effects of the present invention described above cannot be obtained. There is no particular lower limit to the average crystal grain size of the diamond, but when the average crystal grain size is less than 5 nm, the tendency for the sound velocity to decrease becomes remarkable. The more preferable average crystal grain size of diamond is 20 to 100 nm. The fact that polycrystalline diamond is contained in the film is X
It can be confirmed by line diffraction, and the average crystal grain size of diamond can be measured by a transmission electron microscope or the like. Further, it can be confirmed by a scanning electron microscope or the like that the surface of the surface wave propagating film is flat and no free-form surface appears.

【0012】表面波伝搬膜の好ましい厚さは、動作周波
数帯域等の各種条件によっても異なるが、通常、10〜
20μm 程度である。
The preferable thickness of the surface wave propagating film varies depending on various conditions such as an operating frequency band, but is usually 10 to 10.
It is about 20 μm.

【0013】表面伝搬膜中の音速は圧電膜の構成によっ
ても異なるが、通常、5700m/s以上、特に8000m
/s 以上と高速である。
The speed of sound in the surface propagation film varies depending on the structure of the piezoelectric film, but is usually 5700 m / s or more, especially 8000 m.
It is faster than / s.

【0014】表面波伝搬膜は、CVD法により形成され
ることが好ましい。CVD法としては、各種プラズマC
VD法または各種熱CVD法から選択することが好まし
く、特にプラズマCVD法を用いることが好ましい。
The surface wave propagation film is preferably formed by the CVD method. As the CVD method, various plasma C
It is preferable to select from the VD method and various thermal CVD methods, and it is particularly preferable to use the plasma CVD method.

【0015】本発明では、好ましくは1×10-5〜5×
10-3Torr、より好ましくは1×10-4〜5×10-3To
rrの圧力中でプラズマCVD法により表面波伝搬膜を形
成する。膜形成時の雰囲気圧力が前記範囲を超えている
と、結晶粒径の小さい膜が得られにくい。また、雰囲気
圧力が前記範囲未満であると、膜形成が難しくなる。
In the present invention, preferably 1 × 10 -5 to 5 ×
10 −3 Torr, more preferably 1 × 10 −4 to 5 × 10 −3 To
A surface wave propagation film is formed by a plasma CVD method under a pressure of rr. If the atmospheric pressure during film formation exceeds the above range, it is difficult to obtain a film having a small crystal grain size. Further, if the atmospheric pressure is less than the above range, film formation becomes difficult.

【0016】プラズマCVD法におけるプラズマ発生源
としては、例えば特開昭64−65843号公報に開示
されているようなエレクトロン・サイクロトロン・レゾ
ナンス(ECR)を利用したプラズマ生成手段や高周波
誘導加熱を利用したプラズマ生成手段等が挙げられる。
これらのうち、高密度の電子が得られて処理速度が高い
ことから、ECRを用いるものが好ましい。
As a plasma generating source in the plasma CVD method, for example, a plasma generating means utilizing electron cyclotron resonance (ECR) as disclosed in Japanese Patent Laid-Open No. 64-65843 or high frequency induction heating is used. Examples include plasma generating means.
Among these, the one using ECR is preferable because high-density electrons are obtained and the processing speed is high.

【0017】ECR型プラズマCVD装置では、電界と
磁界との相互作用により共鳴的に電子を加速し、この電
子の衝突によりガスをプラズマ化して、プラズマ中のイ
オン、ラジカル等を基板上に堆積させることにより成膜
を行なう。また、このプラズマから電子を引き出し、引
き出された電子を原料ガスに衝突させてプラズマ化し、
発生したイオン、ラジカル等を基板上に堆積させること
もできる。
In the ECR type plasma CVD apparatus, electrons are resonantly accelerated by the interaction between an electric field and a magnetic field, and the collision of these electrons turns the gas into plasma, so that the ions and radicals in the plasma are deposited on the substrate. By doing so, film formation is performed. Also, electrons are extracted from this plasma, and the extracted electrons are collided with the raw material gas to form plasma,
The generated ions, radicals, etc. can be deposited on the substrate.

【0018】本発明における表面波伝搬膜の形成に好適
なプラズマCVD装置を、図2および図3に示す。
A plasma CVD apparatus suitable for forming the surface wave propagation film in the present invention is shown in FIGS. 2 and 3.

【0019】図2および図3に示されるプラズマ処理装
置1は、真空系8内にプラズマ生成室7を有し、このプ
ラズマ生成室7に連通して原料ガス導入管2が設けられ
ている。プラズマ生成室7には、マイクロ波電源(図示
せず)と接続された導波管9がマイクロ波導入窓を介し
て設けられており、また、プラズマ生成室7の外周には
磁石としてヘルムホルツ型の電磁石4が設けられてお
り、これらがECR型等の有磁場マイクロ波プラズマ生
成手段を構成している。また、真空系8内には真空排気
口が設けられ、所定の動作圧力とすることができるとと
もに、基板ホルダ6が移動可能に設けられており、基板
を所定の温度に加熱した状態で、プラズマ生成室7内の
所定の位置に載置できるようにされている。
The plasma processing apparatus 1 shown in FIGS. 2 and 3 has a plasma generating chamber 7 in a vacuum system 8, and a source gas introducing pipe 2 is provided in communication with the plasma generating chamber 7. A waveguide 9 connected to a microwave power source (not shown) is provided in the plasma generation chamber 7 through a microwave introduction window, and a Helmholtz type magnet as a magnet is provided around the plasma generation chamber 7. The electromagnet 4 is provided, and these constitute ECR type magnetic field microwave plasma generation means. Further, a vacuum exhaust port is provided in the vacuum system 8 so that a predetermined operating pressure can be achieved, and a substrate holder 6 is provided so as to be movable so that the plasma can be generated while the substrate is heated to a predetermined temperature. It can be placed at a predetermined position in the generation chamber 7.

【0020】原料ガス導入管2の先端開口には、加熱体
として加熱管3が接続されており、導入された原料中性
粒子ガスが加熱管3の内壁に衝突するように構成されて
いる。加熱管3の内壁は700K以上、特に1600〜
2000Kの温度とされており、ガス粒子はこの内壁に
実質的に弾性衝突して、粒子速度(運動エネルギー)が
増大する。加速手段としての加熱管の構造やガスの衝突
のさせ方等について特に制限はなく、Ta、Mo、W等
の管に発熱体をらせん状に巻いたり、ハニカム型ヒータ
を用いたりする等が可能であるが、加速効率を高めるた
めには図4に示されるような加熱管3を用いることが好
ましい。図示例では、例えばW、Ta等の内径0.7〜
1.4mm、肉厚0.1〜0.2mm、長さ15〜40mmの
管体31の両端に、一対の電極35を接続し、印加電圧
を変化させながら直接通電加熱を行ない、所定の温度と
する構造とされている。この他、加熱手段としては、抵
抗加熱、誘導加熱等いずれであってもよく、管体31の
材質についても特に制限はない。
A heating tube 3 as a heating element is connected to the tip end opening of the raw material gas introduction tube 2 so that the introduced raw material neutral particle gas collides with the inner wall of the heating tube 3. The inner wall of the heating pipe 3 is 700K or more, especially 1600 to
The temperature is set to 2000 K, and the gas particles substantially elastically collide with the inner wall to increase the particle velocity (kinetic energy). There is no particular limitation on the structure of the heating tube as the accelerating means and how to collide the gas, and it is possible to spirally heat the heating element around the tube of Ta, Mo, W, etc. or use a honeycomb heater. However, in order to improve the acceleration efficiency, it is preferable to use the heating tube 3 as shown in FIG. In the illustrated example, for example, the inner diameter of W, Ta or the like is 0.7 to
A pair of electrodes 35 are connected to both ends of a tubular body 31 having a thickness of 1.4 mm, a thickness of 0.1 to 0.2 mm, and a length of 15 to 40 mm, and direct current heating is performed while changing an applied voltage to a predetermined temperature. It is said to be a structure. In addition, the heating means may be resistance heating, induction heating, or the like, and the material of the tubular body 31 is not particularly limited.

【0021】原料ガス導入管2からこの加熱管3を介し
てプラズマ生成室7内に原料中性粒子ガスを導入し、粒
子速度を増大させる。このとき、原料中性粒子ガスは、
通常、約0.025eVの運動エネルギーと約630m/se
c の粒子速度をもって導入されるが、加熱管により原料
中性粒子ガスは0.06eV以上、特に0.11〜0.2
1eVの運動エネルギーと1300〜1780m/sec (1
300〜2400K)の粒子速度を与えられる。
Raw material neutral particle gas is introduced into the plasma generation chamber 7 from the raw material gas introduction pipe 2 through the heating pipe 3 to increase the particle velocity. At this time, the raw material neutral particle gas is
Usually about 0.025 eV kinetic energy and about 630 m / se
It is introduced with a particle velocity of c, but the raw material neutral particle gas is 0.06 eV or more, especially 0.11 to 0.2 due to the heating tube.
Kinetic energy of 1 eV and 1300 to 1780 m / sec (1
Particle velocities of 300-2400 K) are provided.

【0022】プラズマ生成室7では、マイクロ波導入窓
からマイクロ波が導入されており、同時に、プラズマ生
成室内部には電磁石4により、好ましくはECR条件を
満たす磁界が付与されている。このため、プラズマ生成
室7内の電子は、この磁界とマイクロ波の電界とにより
加速されて加速ガス粒子に衝突し、プラズマが生成す
る。そして、前述したような低い動作圧力でのプラズマ
CVDが可能となり、3インチ平方以上、特に4〜6イ
ンチ平方の大面積での処理が可能である。また基板温度
も通常より低温化することが可能となる。
In the plasma generation chamber 7, microwaves are introduced through the microwave introduction window, and at the same time, a magnetic field preferably satisfying the ECR condition is applied to the inside of the plasma generation chamber by the electromagnet 4. Therefore, the electrons in the plasma generation chamber 7 are accelerated by the magnetic field and the electric field of the microwave and collide with the accelerated gas particles to generate plasma. Then, plasma CVD can be performed at a low operating pressure as described above, and processing in a large area of 3 inches square or more, particularly 4 to 6 inches square is possible. Also, the substrate temperature can be lowered than usual.

【0023】加熱管3等の加熱体は、基板5の好ましく
は垂直上方に設けることが好ましく、加速粒子は基板面
にほぼ垂直に差し向けられ、その間プラズマ中にて電離
・解離を行なうことが好ましい。これにより処理効率が
向上する。
The heating body such as the heating tube 3 is preferably provided vertically above the substrate 5, and the accelerated particles are directed almost vertically to the substrate surface, during which ionization / dissociation may be performed in the plasma. preferable. This improves the processing efficiency.

【0024】なお、以上では、プラズマ生成室7内で処
理を行なう例について述べてきたが、ECRキャビティ
等のプラズマ生成室と連通する系内でプラズマ処理を行
なったり、イオン引き出し電極等を用いたりして、生成
室7外でプラズマ処理を行なうことも可能である。
In the above, an example in which the processing is performed in the plasma generation chamber 7 has been described. However, the plasma processing is performed in a system communicating with the plasma generation chamber such as the ECR cavity, or an ion extraction electrode or the like is used. Then, it is also possible to perform plasma processing outside the generation chamber 7.

【0025】なお、本発明では、このようなプラズマC
VD装置の他、特願平4−355784号に開示されて
いるプラズマCVD装置、すなわち、ECR型のプラズ
マ生成手段と被処理体ホルダとが設けられたプラズマ室
を有し、プラズマ生成手段により形成されたプラズマ高
密度領域と被処理体ホルダとの間に遮蔽部材が設けられ
た構成のプラズマCVD装置、あるいは、プラズマ生成
室と処理室とが設けられたプラズマ室を有し、プラズマ
生成室にプラズマ生成手段が設けられ、処理室に被処理
体ホルダが設けられ、プラズマ生成室で生成したプラズ
マから電子を処理室に引き出すための電子引き出し電極
がプラズマ生成室と処理室との間に設けられ、電子引き
出し電極と被処理体ホルダとの間に遮蔽部材が設けられ
た構成のプラズマCVD装置も好ましく用いることがで
きる。
In the present invention, such plasma C
In addition to the VD apparatus, a plasma CVD apparatus disclosed in Japanese Patent Application No. 4-355784, that is, a plasma chamber provided with an ECR type plasma generating means and a target object holder, and formed by the plasma generating means A plasma CVD apparatus having a configuration in which a shielding member is provided between the processed plasma high-density region and the object holder, or a plasma chamber in which a plasma generation chamber and a processing chamber are provided. A plasma generating unit is provided, a processing object holder is provided in the processing chamber, and an electron extraction electrode for extracting electrons from the plasma generated in the plasma generation chamber to the processing chamber is provided between the plasma generation chamber and the processing chamber. A plasma CVD apparatus having a structure in which a shielding member is provided between the electron extraction electrode and the object holder can also be preferably used.

【0026】CVD法における原料ガスとしてはCH4
やC24 等の各種炭素化合物などを用いればよい。ま
た、これらに加えてCO2 を用いれば、膜の結晶性が向
上する。キャリアガスとしてH2 ガスを用いることが好
ましい。H2 ガスは膜中の不純物を排除する作用を有す
る。原料ガス流量とキャリアガス流量との合計に対し、
キャリアガス流量は80%以上、特に85〜99%とす
ることが好ましい。キャリアガス流量をこのような範囲
とすることにより、極めて純度の高い膜を形成すること
ができる。
CH 4 is used as a source gas in the CVD method.
And various carbon compounds such as C 2 H 4 may be used. If CO 2 is used in addition to these, the crystallinity of the film is improved. It is preferable to use H 2 gas as the carrier gas. The H 2 gas has a function of eliminating impurities in the film. For the total of the source gas flow rate and the carrier gas flow rate,
The carrier gas flow rate is preferably 80% or more, and more preferably 85 to 99%. By setting the carrier gas flow rate within such a range, a film with extremely high purity can be formed.

【0027】膜形成の際の基板温度は、400〜700
℃とすることが好ましい。
The substrate temperature during film formation is 400 to 700.
The temperature is preferably set to ° C.

【0028】基板12の材質に特に制限はなく、各種金
属、合金およびセラミックスから適宜選択すればよく、
例えば、Si、W、Mo、Cu、Ta、AlおよびTi
から選択される1種以上の元素を含有する金属または合
金、あるいはAl23 、ZrO2 、MgO等のセラミ
ックス等を好ましく用いることができる。また、基板の
寸法も特に限定されない。
The material of the substrate 12 is not particularly limited and may be appropriately selected from various metals, alloys and ceramics.
For example, Si, W, Mo, Cu, Ta, Al and Ti
A metal or alloy containing one or more elements selected from the above, ceramics such as Al 2 O 3 , ZrO 2 and MgO can be preferably used. Moreover, the size of the substrate is not particularly limited.

【0029】圧電膜15の材質は、LiNbO3 やZn
O、AlN等の各種圧電体から選択すればよく、通常、
スパッタ法等により成膜される。圧電膜の厚さは、通
常、0.1〜4μm 程度とする。一般に、圧電膜が厚い
ほど弾性表面波への変換効率は高くなるが、音速は遅く
なる。
The material of the piezoelectric film 15 is LiNbO 3 or Zn.
It may be selected from various piezoelectric materials such as O and AlN.
The film is formed by a sputtering method or the like. The thickness of the piezoelectric film is usually about 0.1 to 4 μm. Generally, the thicker the piezoelectric film, the higher the conversion efficiency into surface acoustic waves, but the slower the speed of sound.

【0030】電極16は、通常、真空蒸着法等により形
成され、各種のエッチングによりクシ型形状とされる。
電極周期は、動作周波数、表面波伝搬膜の音速、圧電膜
の音速およびその厚さなどに応じて適宜設定すればよ
い。図1に示される構成例では、クシ型の電極16は表
面波伝搬膜14上に形成され、その上から圧電膜15が
形成されているが、本発明ではこの態様に限らず、例え
ば、圧電膜上に電極を形成するなど、弾性表面波素子と
して利用できる電極構成であればどのようなものであっ
てもよい。
The electrode 16 is usually formed by a vacuum vapor deposition method or the like, and formed into a comb shape by various etchings.
The electrode period may be appropriately set according to the operating frequency, the speed of sound of the surface wave propagation film, the speed of sound of the piezoelectric film, the thickness thereof, and the like. In the configuration example shown in FIG. 1, the comb-shaped electrode 16 is formed on the surface wave propagation film 14, and the piezoelectric film 15 is formed on the surface wave propagation film 14. However, the present invention is not limited to this mode. Any electrode configuration may be used as long as it can be used as a surface acoustic wave element, such as forming an electrode on a film.

【0031】基板12と表面波伝搬膜14との間には、
必要に応じて下地膜を設けてもよい。下地膜は、通常、
表面波伝搬膜の接着性を向上させるために設けられる
が、その場合、基板構成元素と炭素とを含む組成、例え
ばSiCやWC等とすることが好ましい。
Between the substrate 12 and the surface wave propagation film 14,
A base film may be provided if necessary. The base film is usually
It is provided in order to improve the adhesiveness of the surface wave propagation film, and in that case, it is preferable to use a composition containing a substrate constituent element and carbon, such as SiC or WC.

【0032】[0032]

【実施例】以下、具体的実施例を挙げ、本発明をさらに
詳細に説明する。
EXAMPLES The present invention will be described in more detail with reference to specific examples.

【0033】図2に示される構成を有するプラズマCV
D装置の基板ホルダ上にSi(100)基板を載置し、
系内を1×10-5Torrに排気して、基板温度を600℃
に上昇させ、さらに排気を行なった。
Plasma CV having the configuration shown in FIG.
Place the Si (100) substrate on the substrate holder of the D device,
The system was evacuated to 1 × 10 -5 Torr and the substrate temperature was 600 ° C.
And exhausted.

【0034】次いで、中性粒子の加速源である加熱管3
を通電加熱した。放射温度計で温度をモニタしたとこ
ろ、2000Kであった。加熱管3のサイズは内径0.
7mm、肉厚0.1mm、長さ40mmとした。CH4 の平均
速度Vave=(8kT/πmCH41/ 2 は1625m/sec と推
定される。
Next, the heating tube 3 which is an acceleration source of neutral particles
Was electrically heated. When the temperature was monitored with a radiation thermometer, it was 2000K. The heating tube 3 has an inner diameter of 0.
The thickness was 7 mm, the wall thickness was 0.1 mm, and the length was 40 mm. Average speed Vave = (8kT / πmCH 4) 1/2 of CH 4 is estimated to be 1625m / sec.

【0035】この後、原料ガスを導入した。原料ガスは
流量比でCH4 :CO2 :H2 =5:10:85とし
た。次いでマイクロ波および電磁石の電源を入れ、プラ
ズマを生成させた。プラズマはキャビティのプラズマ生
成室7内に一様に広がっていることが確認された。さら
に、2.45GHz 、500W のマイクロ波を投入し、印
加磁界875G、基板温度600℃、1×10-3Torrの
動作圧力で厚さ15μmの表面波伝搬膜を形成した。こ
の際、加熱管3は基板5の垂直上方50nmの位置に基板
面に開口して配置した。
After that, a source gas was introduced. The raw material gas was set to have a flow rate ratio of CH 4 : CO 2 : H 2 = 5: 10: 85. Then the microwave and electromagnet were turned on to generate plasma. It was confirmed that the plasma uniformly spreads in the plasma generation chamber 7 of the cavity. Further, a microwave of 2.45 GHz and 500 W was applied to form a surface wave propagation film having a thickness of 15 μm under an applied magnetic field of 875 G, a substrate temperature of 600 ° C. and an operating pressure of 1 × 10 −3 Torr. At this time, the heating tube 3 was placed at a position 50 nm vertically above the substrate 5 with an opening on the substrate surface.

【0036】なお、動作圧力を0.5Torrとした以外は
上記と同様にして、比較例の表面波伝搬膜も形成した。
A surface acoustic wave propagation film of a comparative example was also formed in the same manner as above except that the operating pressure was 0.5 Torr.

【0037】成膜終了後、冷却して基板を取り出し、こ
れらの表面波伝搬膜に対してX線回折を行なったとこ
ろ、ダイヤモンドが含まれていることが確認された。そ
して、50000倍の走査型電子顕微鏡により観察した
ところ、比較例では膜表面に自形面がみられたが、本発
明例では自形面は観察されず、平坦な表面であった。ま
た、ダイヤモンドの平均結晶粒径を測定した結果、比較
例では2μm であったが本発明例では95nmと極めて小
さかった。結晶粒径は、比較例では走査型電子顕微鏡に
より、本発明例では透過型電子顕微鏡により測定した。
After the completion of film formation, the substrate was cooled and taken out, and X-ray diffraction was performed on these surface wave propagation films. As a result, it was confirmed that diamond was contained. When observed with a scanning electron microscope at 50000 times, a self-shaped surface was observed on the film surface in the comparative example, but no self-shaped surface was observed in the example of the present invention, and it was a flat surface. As a result of measuring the average crystal grain size of diamond, it was 2 μm in the comparative example, but it was extremely small as 95 nm in the example of the present invention. The crystal grain size was measured by a scanning electron microscope in the comparative example and by a transmission electron microscope in the example of the present invention.

【0038】次に、表面波伝搬膜上に、電子ビーム蒸着
によりAl膜を形成し、フォトリソグラフィーによりエ
ッチングして、クシ型電極とした。電極周期は8μm と
した。なお、比較例のものでは、Al膜蒸着前に表面波
伝搬膜の表面をバフ研磨して平滑化した。
Next, an Al film was formed on the surface wave propagating film by electron beam vapor deposition and etched by photolithography to form a comb-shaped electrode. The electrode period was 8 μm. In the comparative example, the surface of the surface wave propagation film was buffed and smoothed before the Al film was deposited.

【0039】さらに、この上に、スパッタ法により厚さ
2μm のZnO膜を形成し、圧電膜とした。
Further, a ZnO film having a thickness of 2 μm was formed thereon by a sputtering method to form a piezoelectric film.

【0040】このようにして作製された本発明例および
比較例の弾性表面波素子を用いて、伝送特性を測定し
た。本発明の素子の結果を図5に、比較例の素子の結果
を図6に示す。本発明の素子は比較例の素子に比べ共振
周波数での振幅が大きい、すなわち挿入損失が小さい。
このことから、本発明の素子は比較例の素子に比べ伝搬
損失が小さいことがわかる。また、本発明の素子は比較
例の素子よりも零点での振幅が小さくなっており、弾性
表面波の位相のばらつきが小さいことがわかる。
The transmission characteristics were measured using the surface acoustic wave devices of the present invention and the comparative example thus manufactured. The results of the device of the present invention are shown in FIG. 5, and the results of the device of the comparative example are shown in FIG. The element of the present invention has a larger amplitude at the resonance frequency than the element of the comparative example, that is, the insertion loss is smaller.
From this, it is understood that the device of the present invention has a smaller propagation loss than the device of the comparative example. Further, the element of the present invention has a smaller amplitude at the zero point than the element of the comparative example, and it can be seen that the phase variation of the surface acoustic wave is small.

【0041】上記した本発明の素子の他に、表面波伝搬
膜の平均結晶粒径の異なる素子を作製した。表面波伝搬
膜形成の際の圧力は、上記本発明の素子のときよりも低
くした。これらについて弾性表面波伝搬速度を測定し
た。それぞれの素子の表面波伝搬膜における平均結晶粒
径と音速とは、以下の通りであった。
In addition to the above-mentioned device of the present invention, devices having different average crystal grain sizes of the surface wave propagation film were prepared. The pressure at the time of forming the surface wave propagation film was set lower than that at the time of the element of the present invention. Surface acoustic wave propagation velocities were measured for these. The average crystal grain size and the sound velocity in the surface wave propagation film of each element were as follows.

【0042】 [0042]

【0043】以上の結果から本発明の効果が明らかであ
る。
From the above results, the effect of the present invention is clear.

【図面の簡単な説明】[Brief description of drawings]

【図1】本発明の弾性表面波素子の構成例を示す部分断
面図である。
FIG. 1 is a partial cross-sectional view showing a configuration example of a surface acoustic wave device of the present invention.

【図2】表面波伝搬膜の形成に好適なプラズマCVD装
置の構成図である。
FIG. 2 is a configuration diagram of a plasma CVD apparatus suitable for forming a surface wave propagation film.

【図3】表面波伝搬膜の形成に好適なプラズマCVD装
置の構成図である。
FIG. 3 is a configuration diagram of a plasma CVD apparatus suitable for forming a surface wave propagation film.

【図4】加熱管の斜視図である。FIG. 4 is a perspective view of a heating tube.

【図5】本発明の弾性表面波素子の伝送特性を示すグラ
フである。
FIG. 5 is a graph showing the transmission characteristics of the surface acoustic wave device of the present invention.

【図6】従来の弾性表面波素子の伝送特性を示すグラフ
である。
FIG. 6 is a graph showing the transmission characteristics of a conventional surface acoustic wave device.

【符号の説明】[Explanation of symbols]

1 プラズマ処理装置 2 原料ガス導入管 3 加熱管 31 管体 35 電極 4 電磁石 5 基板 6 基板ホルダ 7 プラズマ生成室 8 真空系 9 マイクロ波導波管 11 弾性表面波素子 12 基板 14 表面波伝搬膜 15 圧電膜 16 電極 DESCRIPTION OF SYMBOLS 1 Plasma processing apparatus 2 Raw material gas introduction pipe 3 Heating pipe 31 Tubular body 35 Electrode 4 Electromagnet 5 Substrate 6 Substrate holder 7 Plasma generation chamber 8 Vacuum system 9 Microwave waveguide 11 Surface acoustic wave element 12 Substrate 14 Surface wave propagation film 15 Piezoelectric Membrane 16 electrodes

───────────────────────────────────────────────────── フロントページの続き (72)発明者 長野 克人 東京都中央区日本橋一丁目13番1号 ティ ーディーケイ株式会社内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Katsuto Nagano 1-13-1 Nihonbashi, Chuo-ku, Tokyo Inside TDC Corporation

Claims (8)

【特許請求の範囲】[Claims] 【請求項1】 基板上に表面波伝搬膜および圧電膜をこ
の順で有し、圧電膜に電界を印加する電極を有する弾性
表面波素子であって、 前記表面波伝搬膜が、平均結晶粒径100nm以下のダイ
ヤモンドを含む炭素膜であることを特徴とする弾性表面
波素子。
1. A surface acoustic wave device having a surface wave propagation film and a piezoelectric film in this order on a substrate, and an electrode for applying an electric field to the piezoelectric film, wherein the surface wave propagation film is an average crystal grain. A surface acoustic wave device comprising a carbon film containing diamond having a diameter of 100 nm or less.
【請求項2】 前記ダイヤモンドの平均結晶粒径が5nm
以上である請求項1の弾性表面波素子。
2. The average crystal grain size of the diamond is 5 nm
The surface acoustic wave device according to claim 1, which is as described above.
【請求項3】 前記表面波伝搬膜中の音速が5700m/
s 以上である請求項1または2の弾性表面波素子。
3. The speed of sound in the surface wave propagation film is 5700 m /
The surface acoustic wave device according to claim 1 or 2, which is s or more.
【請求項4】 請求項1ないし3のいずれかの弾性表面
波素子を製造する方法であって、 1×10-5〜5×10-3Torrの圧力中でプラズマCVD
法により前記表面波伝搬膜を形成することを特徴とする
弾性表面波素子の製造方法。
4. A method of manufacturing a surface acoustic wave device according to claim 1, wherein the plasma CVD is performed at a pressure of 1 × 10 −5 to 5 × 10 −3 Torr.
A method of manufacturing a surface acoustic wave element, characterized in that the surface wave propagation film is formed by a method.
【請求項5】 原料中性粒子ガスを加熱体に衝突させて
ガスの粒子速度を増加させた後、前記ガスの分子を電
離、解離してプラズマCVDを行なう請求項4の弾性表
面波素子の製造方法。
5. The surface acoustic wave device according to claim 4, wherein the raw material neutral particle gas is collided with a heating body to increase the particle velocity of the gas, and then the molecules of the gas are ionized and dissociated to perform plasma CVD. Production method.
【請求項6】 前記加熱体が加熱管であり、この加熱管
内壁に前記ガスを衝突させる請求項5の弾性表面波素子
の製造方法。
6. The method of manufacturing a surface acoustic wave device according to claim 5, wherein the heating body is a heating tube, and the gas collides with the inner wall of the heating tube.
【請求項7】 前記加熱体が700K以上の温度に加熱
されている請求項5または6の弾性表面波素子の製造方
法。
7. The method of manufacturing a surface acoustic wave device according to claim 5, wherein the heating element is heated to a temperature of 700 K or higher.
【請求項8】 前記分子の電離・解離を有磁場マイクロ
波プラズマによって行なう請求項5ないし7のいずれか
の弾性表面波素子の製造方法。
8. The method of manufacturing a surface acoustic wave device according to claim 5, wherein the ionization / dissociation of the molecules is performed by microwave plasma with magnetic field.
JP08570793A 1993-03-19 1993-03-19 Surface acoustic wave device and method of manufacturing the same Expired - Fee Related JP3233489B2 (en)

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US7812395B2 (en) 2003-04-22 2010-10-12 Chien-Min Sung Semiconductor-on-diamond devices and methods of forming
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US7095157B2 (en) * 2000-10-13 2006-08-22 Chien-Min Sung Cast diamond tools and formation thereof by chemical vapor deposition
US6858969B2 (en) * 2002-01-25 2005-02-22 Board Of Trustees Of Michigan State University Surface acoustic wave devices based on unpolished nanocrystalline diamond
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JP2015030646A (en) * 2013-08-05 2015-02-16 住友電気工業株式会社 Nano-polycrystalline diamond and industrial tool including the same

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