JPH0478136B2 - - Google Patents
Info
- Publication number
- JPH0478136B2 JPH0478136B2 JP9466685A JP9466685A JPH0478136B2 JP H0478136 B2 JPH0478136 B2 JP H0478136B2 JP 9466685 A JP9466685 A JP 9466685A JP 9466685 A JP9466685 A JP 9466685A JP H0478136 B2 JPH0478136 B2 JP H0478136B2
- Authority
- JP
- Japan
- Prior art keywords
- light
- thin film
- observation
- plasma
- light introduction
- 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
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- 239000010409 thin film Substances 0.000 claims description 30
- 229910052751 metal Inorganic materials 0.000 claims description 18
- 239000002184 metal Substances 0.000 claims description 18
- 238000004804 winding Methods 0.000 claims description 6
- 239000000463 material Substances 0.000 description 18
- 239000010408 film Substances 0.000 description 10
- 239000002245 particle Substances 0.000 description 10
- 230000005284 excitation Effects 0.000 description 9
- 238000000034 method Methods 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 7
- 238000005259 measurement Methods 0.000 description 6
- 238000007740 vapor deposition Methods 0.000 description 5
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 238000004544 sputter deposition Methods 0.000 description 4
- 238000004020 luminiscence type Methods 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000007733 ion plating Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000001020 plasma etching Methods 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 238000002834 transmittance Methods 0.000 description 2
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 238000001755 magnetron sputter deposition Methods 0.000 description 1
- 230000010355 oscillation Effects 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/01—Arrangements or apparatus for facilitating the optical investigation
- G01N21/15—Preventing contamination of the components of the optical system or obstruction of the light path
Landscapes
- Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
- Optical Measuring Cells (AREA)
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、励起された元素からの発光を受光し
てその強度を測定する励起発光強度測定装置に関
するものである。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to an excitation emission intensity measurement device that receives light emission from an excited element and measures its intensity.
従来の技術
最近、真空装置の発達に伴なつて、薄膜形成は
ほとんど真空内で行なわれる。特にマグネトロン
スパツター法は、薄膜形成のスペードが著しく向
上したため、真空蒸着にとつてかわろうとしてい
る。一方、イオンプレーテング法は、蒸着物質を
一部イオン化し電界によつて加速することができ
るから、被蒸着物基板上に薄膜を強固に密着した
状態で形成することが可能となる。しかし、これ
等の方法で薄膜を形成する場合、薄膜及び薄膜形
成速度をどのように測定するかが問題である。特
に合金薄膜を一定の組成で形成する場合、薄膜形
成速度は非常に重要となる。従来、この等の量
は、水晶振動子を用い、この振動子上に薄膜形成
物質を付着させ、発振周波数の変化からこの量を
読み取つていた。しかしこの方法では、連続的に
多量の薄膜を計測することは不可能である。2. Description of the Related Art Recently, with the development of vacuum equipment, thin film formation is almost always carried out in a vacuum. In particular, magnetron sputtering has significantly improved its ability to form thin films and is now replacing vacuum evaporation. On the other hand, in the ion plating method, a part of the evaporation material can be ionized and accelerated by an electric field, so that it is possible to form a thin film firmly adhered to the substrate to be evaporated. However, when forming a thin film using these methods, the problem is how to measure the thin film and the rate of thin film formation. Particularly when forming an alloy thin film with a constant composition, the thin film formation rate is very important. Conventionally, these amounts have been determined by using a quartz crystal resonator, depositing a thin film-forming substance on the resonator, and reading the amount from changes in the oscillation frequency. However, with this method, it is impossible to continuously measure a large amount of thin films.
そこで最近では、プラズマによる元素励起発光
量から上記の膜形成速度等を計測することが試み
られている。例えばスパツター法によつて薄膜を
形成する場合やプラズマデポジシヨン法で薄膜を
形成する場合は、明瞭に発光が観察される。この
方法は、たえず発光材料が供給されるから、発光
現象が止まることはなく、有効な補正を行なうこ
とにより、連続的に精度良く多量の薄膜の薄膜形
成速度及び組成を制御することができる。 Therefore, recently, attempts have been made to measure the above-mentioned film formation rate, etc. from the amount of light emitted by elemental excitation by plasma. For example, when a thin film is formed by a sputtering method or a plasma deposition method, light emission is clearly observed. In this method, since the luminescent material is constantly supplied, the luminescence phenomenon does not stop, and by making effective corrections, it is possible to continuously and accurately control the thin film formation rate and composition of a large amount of thin films.
実際、すでにスパツター法では、ITOネサ膜形
成等で実用されている。また逆に、基板上に形成
されている薄膜をプラズマエツチングで剥離する
場合、発光モニターにより終了点を検出すること
が行なわれている。 In fact, the sputtering method has already been put to practical use, such as in the formation of ITO Nesa films. Conversely, when a thin film formed on a substrate is removed by plasma etching, the end point is detected using a light emission monitor.
一方、励起発光現象を伴なわない蒸着に対して
は、ホローカソードランプ等の発光源を用い、材
料元素がこの光源からの光を吸収して励起される
原子吸光現象を利用して、光の吸収量から材料元
素蒸気濃度を測定するという方法が取られる。 On the other hand, for vapor deposition that does not involve an excited luminescence phenomenon, a light emitting source such as a hollow cathode lamp is used, and the material element absorbs the light from the light source and is excited, making use of the atomic absorption phenomenon. A method is used to measure the material element vapor concentration from the absorbed amount.
発明が解決しようとする問題点
しかしながら、プラズマ発光強度から薄膜形成
速度等を測定しようとする場合、水晶振動子とは
逆の問題が起こる。すなわち、プラズマ中の材料
物質がプラズマによつて散乱され、プラズマ発光
強度の観測用光導入口に進入し、これにより観測
用窓が汚れるという問題があつた。第3図にこの
一例を示す。第3図において、1はプラズマ発光
体、2は観測用光導入口、3は集光用レンズ、4
は観測用光導入筒、5は観測用窓、6はベルジヤ
ー壁である。この例の場合、ベルジヤー壁6の一
部に観測用窓5が設置されている。この場合、プ
ラズマ発光体1で散乱された材料物質は、観測用
光導入口2を通過し、直接観測用窓5に付着す
る。このため、観測用窓5の光透過率が変化し、
このままでは精度良く長時間のプラズマ発光を観
測することは不可能であつた。Problems to be Solved by the Invention However, when attempting to measure the thin film formation rate, etc. from the plasma emission intensity, a problem opposite to that of a quartz crystal resonator occurs. That is, there is a problem in that material in the plasma is scattered by the plasma and enters the light inlet for observing the plasma emission intensity, thereby staining the observation window. An example of this is shown in FIG. In Figure 3, 1 is a plasma light emitter, 2 is an observation light inlet, 3 is a condensing lens, and 4
5 is an observation light introduction tube, 5 is an observation window, and 6 is a bell jar wall. In this example, an observation window 5 is installed in a part of the bell jar wall 6. In this case, the material scattered by the plasma emitter 1 passes through the observation light introduction port 2 and directly adheres to the observation window 5. Therefore, the light transmittance of the observation window 5 changes,
In this state, it was impossible to observe plasma emission with high precision over a long period of time.
これを解決するため、第4図のように、観測用
窓5の直前に光透過性を有するフイルム7を設置
し、これを除々に巻き上げて観測用窓5の汚れを
防止することが試みられていた。8はフイルムロ
ールである。しかしこの場合、光の透光性を利用
しているため、有機フイルムがほとんど大部分で
あるし、金属膜は使用できない。このため、観測
すべきプラズマ発光が350nmより長波長側にあ
れば問題はないが、大部分の材料物質の発光波長
は短波長側にある(例えばTe=200nm、pd=
250nm、p=250mm等)。このような発光波長を
含む場合、有機フイルムの透過特性は実質的に零
となり、もはや発光強度を測定することは不可能
となつてしまう。 To solve this problem, an attempt was made to install a light-transmitting film 7 just in front of the observation window 5 and gradually roll it up to prevent the observation window 5 from getting dirty, as shown in FIG. was. 8 is a film roll. However, in this case, since the translucency of light is utilized, most of the material is organic film, and metal films cannot be used. Therefore, there is no problem if the plasma emission to be observed is on the longer wavelength side than 350 nm, but the emission wavelength of most materials is on the short wavelength side (for example, Te = 200 nm, pd =
250nm, p=250mm, etc.). When such emission wavelengths are included, the transmission characteristics of the organic film become substantially zero, making it no longer possible to measure the emission intensity.
このため一部では、観測用窓までは観測用光導
入筒にミラーを設け、このミラーによつて発光光
を反射させると共に、このミラーにスパツターガ
スを吹き付けて物質粒子の付着を防ぐという方法
が取られている。しかしこの方法では、我々の実
験によると、一分間40c.c.以上のガスを吹き付けな
ければ付着を防ぐことができず、通常の排気系で
はかなりの負荷となり、実用的とは言えない。 For this reason, some methods have been adopted in which a mirror is installed in the observation light introduction tube up to the observation window, and the emitted light is reflected by this mirror, and sputter gas is sprayed onto this mirror to prevent the adhesion of material particles. It is being However, according to our experiments, with this method, adhesion cannot be prevented unless gas is blown at a rate of 40 c.c. or more per minute, which puts a considerable load on a normal exhaust system, making it impractical.
第5図に、蒸着の場合、ホロカソードランプ9
を用いた原子吸光方式を示す。この場合、観測用
窓5が2箇所あるので上気の汚れはよりいつそう
深刻な問題となる。なお10は蒸着蒸気である。 In the case of vapor deposition, a hollow cathode lamp 9 is shown in FIG.
This shows the atomic absorption method using . In this case, since there are two observation windows 5, contamination of the upper air becomes a more serious problem. Note that 10 is a vapor deposition vapor.
問題点を解決するための手段
上記問題点を解決するため、本発明の励起発光
強度措定装置は、略L字状の観測用光導入路を形
成する観測用光導入筒と、この観測用光導入筒内
の角部に配置されかつ励起元素の発光波長に対し
て良好な反射率を有する金属薄膜フイルムと、こ
の金属薄膜フイルムを所定速度で巻き上げる巻取
手段とを備えた構成としたものである。Means for Solving the Problems In order to solve the above problems, the excitation emission intensity measuring device of the present invention includes an observation light introduction tube forming a substantially L-shaped observation light introduction path, and an observation light introduction tube that forms a substantially L-shaped observation light introduction path. It has a structure that includes a metal thin film that is placed at a corner of the introduction tube and has a good reflectance for the emission wavelength of the excited element, and a winding means that winds up the metal thin film at a predetermined speed. be.
作 用
上記構成によれば、観測用光導入路に進入した
物質粒子は、金属薄膜フイルムに付着するので、
プラズマ発光中の物質粒子が観測用窓に付着して
光透過率が変動することにより測定誤差になると
いうことを防止できる。また金属薄膜フイルムを
巻取手段により所定速度で巻き上げるので、常に
物質粒子の付着の少ない金属薄膜フイルムで励起
光を反射でき、精度良く測定を行なえる。Effect According to the above configuration, the material particles that have entered the observation light introduction path adhere to the metal thin film, so that
It is possible to prevent measurement errors caused by fluctuations in light transmittance due to material particles during plasma emission adhering to the observation window. Furthermore, since the metal thin film is wound up at a predetermined speed by the winding means, the excitation light can always be reflected by the metal thin film to which less material particles are attached, making it possible to perform measurements with high precision.
実施例
以下、本発明の一実施例を図面に基づいて説明
する。Embodiment Hereinafter, an embodiment of the present invention will be described based on the drawings.
第1図は本発明の一実施例における励起発光強
度測定装置の要部の縦断面図、第2図は同要部の
横断面図で、第3図〜第5図に示す構成要素と同
一の構成要素には同一の符号を付してその説明を
省略する。第1図及び第2図において、11は金
属薄膜フイルム、12は巻き上げ用モータであ
る。L字状の一端がプラズマ発光体1の近くに位
置する中空の筒からなる観測用光導入筒4を設
け、この観測用光導入筒4の先に細い孔を形成し
て、これを観測用光導入口2としている。そして
観測用光導入筒4の角部には、観測用光導入口2
からの光が集光用レンズ3を通つて観測用窓5を
通過するように、所定の角度で金属薄膜フイルム
11が配置されている。 FIG. 1 is a longitudinal cross-sectional view of the main parts of an excitation emission intensity measuring device according to an embodiment of the present invention, and FIG. 2 is a cross-sectional view of the main parts, which are the same as the components shown in FIGS. 3 to 5. The same reference numerals are given to the constituent elements, and the explanation thereof will be omitted. In FIGS. 1 and 2, 11 is a metal thin film, and 12 is a winding motor. An observation light introduction tube 4 consisting of a hollow tube with one L-shaped end located near the plasma light emitting body 1 is provided, and a thin hole is formed at the tip of this observation light introduction tube 4 to be used for observation. This is the light introduction port 2. At the corner of the observation light introduction tube 4, there is an observation light introduction port 2.
The metal thin film 11 is arranged at a predetermined angle so that the light from the observation window 5 passes through the condensing lens 3 and the observation window 5.
次に動作を説明する。プラズマ発光体1により
散乱された物質粒子は、まず観測用光導入口2の
周囲の壁によつてかなりの部分が遮断される。し
かし一部の粒子は観測用光導入口2から観測用光
導入筒4内に進入する。一方、プラズマの発光光
は、反射用の金属薄膜フイルム11によつて反射
され、集光用レンズ3によつて集光された状態
で、観測用窓5から外部大気中へと導かれる。観
測用光導入筒4に進入した物質粒子は、金属薄膜
フイルム11に大部分付着する。したがつて物質
粒子はそれより先に進入することが出来ない。 Next, the operation will be explained. First, a considerable portion of the material particles scattered by the plasma light emitter 1 is blocked by the wall around the observation light introduction port 2 . However, some particles enter the observation light introduction tube 4 through the observation light introduction port 2. On the other hand, the emitted light of the plasma is reflected by the metal thin film 11 for reflection, and guided into the outside atmosphere through the observation window 5 while being focused by the focusing lens 3. Most of the material particles that have entered the observation light introduction cylinder 4 adhere to the metal thin film 11. Therefore, material particles cannot enter further.
なお、金属薄膜フイルム11としては、アルミ
ニウムを用いるのが好ましい。なぜなら、アルミ
ニウムは200nm〜1μmの波長にわたつて、反射
率は約95%以上になつているからである。またこ
の金属薄膜フイルム11は、全体が金属である必
要はない。すなわち、通常のフイルムベース上に
500Å以上のアルミコートを施しているものが最
も好ましい。 Note that it is preferable to use aluminum as the metal thin film 11. This is because aluminum has a reflectance of approximately 95% or more over a wavelength range of 200 nm to 1 μm. Further, the metal thin film 11 does not need to be entirely made of metal. i.e. on a regular film base
It is most preferable to use an aluminum coating with a thickness of 500 Å or more.
さて、このような金属薄膜フイルム11を少し
づつ勧めることにより、プラズマ発光光はたえず
物質粒子の付着していない新鮮な面によつて反射
されるので、材料物質の付着による反射率の低下
を防止することが可能となる。 Now, by introducing such a metal thin film 11 little by little, the plasma emitted light is constantly reflected by a fresh surface to which no material particles have adhered, thereby preventing a decrease in reflectance due to the adhesion of material substances. It becomes possible to do so.
以下、具体実施例について説明する。 Specific examples will be described below.
具体実施例
pd膜をスパツター方式で形成するとき、pdの
発光波長は250nmである。観測用光導入口をタ
ーゲツトのすぐ横に設置した。観測用光導入口の
直径を2mmとし、観測用光導入筒の直径を30mmと
した。金属薄膜フイルムとしては50μmのポリエ
ステルフイルムに1000Åのアルミニウムを蒸着し
たものを用い、毎分1cmの速さで巻き上げた。集
光用レンズはf=150のものを用いた。この方法
により、プラズマ発光強度を明瞭に測定すること
が可能となつた。Specific Example When a PD film is formed by a sputtering method, the emission wavelength of PD is 250 nm. The observation light inlet was installed right next to the target. The diameter of the observation light introduction port was 2 mm, and the diameter of the observation light introduction tube was 30 mm. The metal thin film used was a 50 μm polyester film with 1000 Å of aluminum vapor-deposited, and was wound at a speed of 1 cm per minute. A condensing lens with f=150 was used. This method made it possible to clearly measure plasma emission intensity.
具体実施例
pdを蒸着で付着させた。この場合、発光光源
として、pdのホロカソードランプを用いた。そ
して光源側にも第1図及び第2図に示す構造のも
のを用いた。このように発光側と受光側との双方
に上記構造の励起発光強度測定装置を用いること
により、観測用窓の汚れによる測定上の誤差は全
く無くなつた。Specific Example PD was deposited by vapor deposition. In this case, a PD hollow cathode lamp was used as the light source. The structure shown in FIGS. 1 and 2 was also used on the light source side. By using the excitation emission intensity measurement device having the above structure on both the light emitting side and the light receiving side, measurement errors due to dirt on the observation window were completely eliminated.
発明の効果
以上のべたごとく本発明によれば、物質粒子に
より観測用窓が汚れることがない。したがつて、
例えばスパツター装置、イオンプレーテイング装
置、プラズマエツチング装置、プラズマC、V、
D装置等において、プラズマからの発光を受光す
る場合、受光部に本発明にかかる励起発光強度測
定装置を設置することにより、安定に発光強度を
測定することが可能となる。また蒸着装置等、自
己発光がない場合、ホロカソードランプ等を用
い、本発明にかかる励起発光強度測定装置を発光
側及び受光側に設置することにより、安定に吸光
量を測定することが可能となる。Effects of the Invention As described above, according to the present invention, the observation window is not contaminated by material particles. Therefore,
For example, sputtering equipment, ion plating equipment, plasma etching equipment, plasma C, V,
When receiving light emitted from plasma in a device D or the like, it is possible to stably measure the emitted light intensity by installing the excitation emitted light intensity measuring device according to the present invention in the light receiving section. In addition, in cases where there is no self-luminescence, such as in a vapor deposition device, it is possible to stably measure the amount of light absorption by using a hollow cathode lamp or the like and installing the excitation emission intensity measuring device according to the present invention on the light emitting side and the light receiving side. Become.
第1図は本発明の一実施例における励起発光強
度測定装置の要部の縦断面図、第2図は同要部の
横断面図、第3図〜第5図は各々従来の励起発光
強度測定装置の要部の縦断面図である。
4……観測用光導入筒、8……フイルムロー
ル、11……金属薄膜フイルム、12……巻き上
げ用モーター。
FIG. 1 is a longitudinal cross-sectional view of a main part of an excitation emission intensity measurement device according to an embodiment of the present invention, FIG. 2 is a cross-sectional view of the same main part, and FIGS. FIG. 3 is a vertical cross-sectional view of the main parts of the measuring device. 4... Light introduction tube for observation, 8... Film roll, 11... Metal thin film, 12... Winding motor.
Claims (1)
光導入筒と、この観測用光導入筒内の角部に配置
されかつ励起元素の発光波長に対して良好な反射
率を有する金属薄膜フイルムと、この金属薄膜フ
イルムを所定速度で巻き上げる巻取手段とを備え
た励起発光強度測定装置。1. An observation light introduction tube that forms a substantially L-shaped observation light introduction path, and a metal that is arranged at a corner of the observation light introduction tube and has a good reflectance for the emission wavelength of the excited element. An excited emission intensity measuring device comprising a thin film and a winding means for winding up the metal thin film at a predetermined speed.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60094666A JPS61253444A (en) | 1985-05-01 | 1985-05-01 | Excitation emission intensity measuring device |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60094666A JPS61253444A (en) | 1985-05-01 | 1985-05-01 | Excitation emission intensity measuring device |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61253444A JPS61253444A (en) | 1986-11-11 |
| JPH0478136B2 true JPH0478136B2 (en) | 1992-12-10 |
Family
ID=14116569
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60094666A Granted JPS61253444A (en) | 1985-05-01 | 1985-05-01 | Excitation emission intensity measuring device |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61253444A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0426351U (en) * | 1990-06-25 | 1992-03-02 |
-
1985
- 1985-05-01 JP JP60094666A patent/JPS61253444A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61253444A (en) | 1986-11-11 |
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