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JPS627266B2 - - Google Patents
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JPS627266B2 - - Google Patents

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Publication number
JPS627266B2
JPS627266B2 JP1895878A JP1895878A JPS627266B2 JP S627266 B2 JPS627266 B2 JP S627266B2 JP 1895878 A JP1895878 A JP 1895878A JP 1895878 A JP1895878 A JP 1895878A JP S627266 B2 JPS627266 B2 JP S627266B2
Authority
JP
Japan
Prior art keywords
wavelength
value
spectral
thin film
film thickness
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
JP1895878A
Other languages
Japanese (ja)
Other versions
JPS54110938A (en
Inventor
Eiichiro Tanaka
Shinji Fujiwara
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP1895878A priority Critical patent/JPS54110938A/en
Publication of JPS54110938A publication Critical patent/JPS54110938A/en
Publication of JPS627266B2 publication Critical patent/JPS627266B2/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
    • C23C14/54Controlling or regulating the coating process
    • C23C14/542Controlling the film thickness or evaporation rate
    • C23C14/545Controlling the film thickness or evaporation rate using measurement on deposited material
    • C23C14/547Controlling the film thickness or evaporation rate using measurement on deposited material using optical methods

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Physical Vapour Deposition (AREA)
  • Inorganic Insulating Materials (AREA)
  • Length Measuring Devices By Optical Means (AREA)
  • Optical Filters (AREA)

Description

【発明の詳細な説明】 本発明は、例えば基板上に薄膜を蒸着する際に
その膜厚を制御する光電式の膜厚蒸着方法に関す
る。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a photoelectric film thickness deposition method for controlling the thickness of a thin film when depositing it on a substrate, for example.

現在、光電式の膜厚制御方法には大別して次の
4つの方法が考えられている。単色測光法、2色
測光法、波長走査法、偏光解析法である。単色測
光法は、必要膜厚での分光反射率又は分光透過率
をあらかじめ計算しておき、その最大値又は最小
値を有する波長での検出信号を最大又は最小とな
るまで、薄膜を形成する方法で、装置自体は小型
で取り扱いも簡単で最も多く用いられているが、
検出信号のピーク値が検出し難く、制御精度は十
分とは言えない。2色測光法は装置自体も小型で
取り扱いも比較的簡単で測定精度もよいが、一般
に2枚の狭帯域干渉フイルタを必要とし、所望の
波長に対する狭帯域フイルタが入取し難く、制御
膜厚が任意に選べない欠点がある。波長走査法は
測定精度は非常によいが装置自体は大がかりで、
薄膜形成前の分光感度の設定が複雑で安定性に欠
ける欠点がある。偏光解析法は、感度が良すぎて
下地基板の影響を受け安く、又不均質な膜に対し
て制御が難しく、又多層膜に対しては解析が非常
に困難である。
Currently, the following four methods are being considered as photoelectric film thickness control methods. These are monochromatic photometry, two-color photometry, wavelength scanning method, and ellipsometry. Monochromatic photometry is a method in which the spectral reflectance or spectral transmittance at the required film thickness is calculated in advance, and a thin film is formed until the detection signal at the wavelength that has the maximum or minimum value reaches the maximum or minimum. The device itself is small and easy to handle, so it is the most commonly used device.
It is difficult to detect the peak value of the detection signal, and the control accuracy cannot be said to be sufficient. In the two-color photometry method, the device itself is small and relatively easy to handle, and the measurement accuracy is good, but it generally requires two narrowband interference filters, and it is difficult to obtain a narrowband filter for the desired wavelength, and it is difficult to control the film thickness. It has the disadvantage that it cannot be chosen arbitrarily. The wavelength scanning method has very good measurement accuracy, but the equipment itself is large-scale.
The drawback is that setting the spectral sensitivity before forming the thin film is complicated and lacks stability. Ellipsometry is too sensitive and is easily influenced by the underlying substrate, is difficult to control for non-uniform films, and is extremely difficult to analyze for multilayer films.

本発明は、以上の様な欠点を持つ光電式の膜厚
制御方法と異なり、安定性のよい、高精度な光電
式の膜厚制御方法を提供するものである。
The present invention provides a photoelectric film thickness control method with good stability and high accuracy, unlike the photoelectric film thickness control method which has the above-mentioned drawbacks.

以下その詳細を誘電体薄膜の真空蒸着の際の制
御を例にとつて図面と共に説明する。
The details will be explained below with reference to the drawings, taking as an example the control during vacuum deposition of a dielectric thin film.

第1図は本発明の一実施例を示す構成図であ
る。金属ベルジヤ11内に設けられた蒸着基板1
3はベースプレート12に固定された基板ホルダ
ーに設置され、信号光Aの光軸ずれを防いでい
る。信号光Aは、ハロゲンランプ光源31よりチ
ヨツパ32により3KHzに変調され、レンズ33
により平行光として間欠的に入射する。一方参照
光Bは信号光Aとは180゜位相の異なつた3KHz
の変調光として、チヨツパ32により信号光Aと
交互にレンズ34から取り出される。基板13に
よつて反射された信号光Aは参照ガラス20を通
り、又参照光Bは参照ガラス20により反射され
交互に高速走査分光器40に入射する。本実施例
ではTeO2高速分光素子41を用いた。分光され
た変調光は光電子増信管42によつて電気信号に
変換される。変換された電気信号は帯域増幅器、
アナログデータプロセツサ、多接点ポテンシヨメ
ーター、除算器、A/D変換器よりなるアナログ
信号処理装置51により、デイジタル信号に変換
される。変換された信号は、デイジタル信号処理
装置60に入力される。デイジタル信号処理装置
60は、デイジタルデータプロセツサ、記憶回
路、制御回路、同期回路等より成り、検出された
信号値その波長値を電子計算機70に入力し、解
析命令を発する。電子計算機70ではN点比較法
により極値を有する波長を求め、必要な膜厚に達
した時蒸着停止命令を制御装置80に送り蒸着を
停止する。なお上記N点比較法は、分光透過特性
のような連続関数のある範囲[x1、xo]のN点
でのf(x)を用い極値を求める方法で、範囲内
に例えば極大値が存在するならば両端のf
(x1)、f(xo)の大きい方を基準とし残りのf
(x)とを比較してゆくと、例えばf(x1)>f
(xo)とすれば、f(x1)より大きな値を持つf
(xo-n)とf(x1)より小さいf(xo-n+1)が連
続して存在する。この時、(xo-n+x1)/2と
(xo-n+1+x1)/2の間に極大値が存在する。両
方のf(xo-n)、f(xo-n+1)とf(x1)を用い
て最後に補間法を用いて極大値を有するxの値を
数値計算する方法である。また、極小値を求める
場合は上記とは逆に小さい値を求めることで得ら
れる。
FIG. 1 is a block diagram showing an embodiment of the present invention. Vapor deposition substrate 1 provided in metal bell gear 11
3 is installed on a substrate holder fixed to the base plate 12 to prevent the optical axis of the signal light A from shifting. Signal light A is modulated at 3KHz by a chopper 32 from a halogen lamp light source 31, and is then modulated by a lens 33.
The light is intermittently incident as parallel light. On the other hand, reference light B is 3KHz with a 180° phase difference from signal light A.
A chopper 32 extracts the modulated light from the lens 34 alternately with the signal light A. The signal light A reflected by the substrate 13 passes through the reference glass 20, and the reference light B is reflected by the reference glass 20 and alternately enters the high-speed scanning spectrometer 40. In this example, a TeO 2 high-speed spectroscopic element 41 was used. The separated modulated light is converted into an electrical signal by a photomultiplier tube 42. The converted electrical signal is passed through a bandpass amplifier,
The signal is converted into a digital signal by an analog signal processing device 51 consisting of an analog data processor, a multi-contact potentiometer, a divider, and an A/D converter. The converted signal is input to digital signal processing device 60. The digital signal processing device 60 consists of a digital data processor, a storage circuit, a control circuit, a synchronization circuit, etc., inputs the detected signal value and its wavelength value to the electronic computer 70, and issues an analysis command. The electronic computer 70 determines the wavelength having the extreme value using the N-point comparison method, and when the required film thickness is reached, sends a vapor deposition stop command to the control device 80 to stop the vapor deposition. Note that the N-point comparison method described above is a method of finding the extreme value using f(x) at N points in a certain range [x 1 , x o ] of a continuous function such as spectral transmission characteristics. exists, then f at both ends
(x 1 ) and f(x o ), and the remaining f
(x), for example, f(x 1 )>f
(x o ), then f has a value larger than f(x 1 )
(x on ) and f(x o-n+1 ) smaller than f(x 1 ) continuously exist. At this time, a maximum value exists between (x on +x 1 )/2 and (x o-n+1 +x 1 )/2. This method uses both f(x on ), f(x o-n+1 ), and f(x 1 ) and finally uses an interpolation method to numerically calculate the value of x having the maximum value. Moreover, when finding the minimum value, it can be obtained by finding a small value in the opposite way to the above.

TeO2高速分光素子41による高速分光器40
は400〜700nmの可視波長領域を100〜47MHzの
高周波発振器52の周波数走査で分光が可能で、
この際約10nm間隔で31波長の分光が可能である
が、スイツチングによりこの内9点を選択し分光
反射率を測定できる。1回の走査に約0.25秒を要
し1点につき約100回の信号を加算平均しS/N
比を向上させている。そして電子計算機による9
点の比較法により極値及びその波長を演算する
が、この間要する時間は約0.7秒であつた。つま
り、約1回/秒の割合で分光反射率の極値及びそ
の波長が算出できる。
High-speed spectrometer 40 using TeO 2 high-speed spectroscopic element 41
It is possible to perform spectroscopy in the visible wavelength region of 400 to 700 nm by scanning the frequency of the high frequency oscillator 52 of 100 to 47 MHz.
At this time, it is possible to perform spectroscopy at 31 wavelengths at intervals of about 10 nm, and by switching, it is possible to select 9 of these points and measure the spectral reflectance. It takes about 0.25 seconds for one scan, and the signal is averaged about 100 times per point, and the S/N is
improving the ratio. and 9 by electronic computer.
The point comparison method was used to calculate the extreme values and their wavelengths, and the time required for this was approximately 0.7 seconds. In other words, the extreme value of the spectral reflectance and its wavelength can be calculated at a rate of about 1 time/second.

この様にして得られる制御は、電子計算機のN
点比較法を利用するものであるため精度は高く、
又安定性も良い。
The control obtained in this way is
The accuracy is high because it uses the point comparison method.
It also has good stability.

TiO2−SiO2−TiO2の3層構造の670nmに反射
ピークを持つ第2図示の赤増反射フイルタの製作
において、600nm〜680nmの9点の測定によ
り、薄膜形成後の吸湿を考慮して基板温度390℃
で反射ピーク640nmで蒸着を行なうと、空気中
への取り出し後約30nm反射ピークが吸湿により
シフトし、670nmで反射ピークが得られた。
In manufacturing the red-enhanced reflection filter shown in Figure 2, which has a three-layer structure of TiO 2 -SiO 2 -TiO 2 and has a reflection peak at 670 nm, measurements were taken at nine points from 600 nm to 680 nm, taking into account moisture absorption after the thin film was formed. Substrate temperature 390℃
When vapor deposition was performed with a reflection peak of 640 nm, the reflection peak was shifted by about 30 nm after being taken out into the air due to moisture absorption, and a reflection peak was obtained at 670 nm.

第2図の曲線は蒸着後の分光特性を、曲線
は空気中取り出し後の分光特性を示す。
The curve in FIG. 2 shows the spectral characteristics after vapor deposition, and the curve shows the spectral characteristics after being taken out into the air.

この際の精度は25nm以下の誤差範囲内で蒸着
可能であつた。
The accuracy at this time was that vapor deposition was possible within an error range of 25 nm or less.

ところで、本発明によれば、分光特性全体の評
価をしながらの蒸着も可能である。
By the way, according to the present invention, it is also possible to perform vapor deposition while evaluating the entire spectral characteristics.

例えば第3図におけるTiO2−SiO2による12層
構造のシアンフイルタにおいて、曲線A及び同B
のTiO2−SiO22層及び5層構造等のように短波長
に生じるリツプルの極値を同時モニタすることも
可能で、31点の測定を極値を持つ波長域を区別
し、各々の極値及びその波長を算出する事もでき
る。したがつてリツプルの極値の大きな変化を利
用して膜厚の制御が容易となる。また曲線Cの最
終層(12層目)の蒸着の際には、400〜560nmの
波長域の測定値を加算し加算値が最小となるまで
蒸着を行なう事により、リツプルの少ない、しか
も半値波長の安定したフイルタが得られる。
For example, in a cyan filter with a 12-layer structure made of TiO 2 -SiO 2 in Fig. 3, curves A and B
It is also possible to simultaneously monitor the extreme values of ripples that occur at short wavelengths, such as in TiO 2 -SiO 2 two-layer and five-layer structures, etc. It is possible to simultaneously monitor the extreme values of ripples that occur at short wavelengths, such as in TiO 2 -SiO 2 two-layer and five-layer structures. It is also possible to calculate extreme values and their wavelengths. Therefore, the film thickness can be easily controlled by utilizing the large change in the ripple extreme value. In addition, when depositing the final layer (12th layer) of curve C, by adding the measured values in the wavelength range of 400 to 560 nm and performing deposition until the added value becomes the minimum, it is possible to achieve a method with less ripple and a half-value wavelength. A stable filter can be obtained.

第3図は651.6nmの反射ピークとして、基板温
度390℃で蒸着を行ない、空気中取り出しによる
波長シフト後の反射ピークが680nmの波長の半
値波長602nmのものが得られた。なお1〜11層
目はnd=λ/4、12層目はnd=λ/8λ=
651.6nmである。
FIG. 3 shows the reflection peak at 651.6 nm, which was obtained by vapor deposition at a substrate temperature of 390° C., and after the wavelength shift by taking it out in the air, the reflection peak was 602 nm at half the wavelength of 680 nm. Note that nd=λ/4 for the 1st to 11th layers, nd=λ/8λ= for the 12th layer
It is 651.6nm.

以上説明したように本発明によれば、基板の分
光透過率又は分光反射率を少なくとも3点以上の
波長で測定し、その極値とそれを有する波長を演
算処理して求め、これによつて膜厚を制御するも
のであるため、高精度な安定性のよい制御が行え
る。
As explained above, according to the present invention, the spectral transmittance or spectral reflectance of the substrate is measured at at least three wavelengths, and the extreme value and the wavelength having the extreme value are calculated and determined. Since the film thickness is controlled, highly accurate and stable control can be performed.

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

第1図は本発明の一実施例を示す構成図、第2
図および第3図は本発明によつて作製したフイル
タの分光特性を示す図である。 11……金属ベルジヤ、12……ベースプレー
ト、13……蒸着基板、20……参照ガラス、3
1……光源、32……チヨツパ、33,34……
レンズ、40……高速走査分光器、41……
TeO2高速分光素子、42……光電子増信管、5
1……アナログ信号処理装置、52……高周波発
振器、60……デイジタル信号処理装置、70…
…電子計算機、80……制御装置。
FIG. 1 is a configuration diagram showing one embodiment of the present invention, and FIG.
3 and 3 are diagrams showing the spectral characteristics of the filter produced according to the present invention. DESCRIPTION OF SYMBOLS 11... Metal bell gear, 12... Base plate, 13... Evaporation substrate, 20... Reference glass, 3
1... Light source, 32... Chiyotsupa, 33, 34...
Lens, 40... High-speed scanning spectrometer, 41...
TeO 2 high-speed spectroscopic element, 42...Photoelectron intensifier, 5
1... Analog signal processing device, 52... High frequency oscillator, 60... Digital signal processing device, 70...
...Electronic computer, 80...Control device.

Claims (1)

【特許請求の範囲】[Claims] 1 薄膜形成用基板上に形成される薄膜の分光透
過率または分光反射率を間欠的な3個以上の波長
で検出し、前記検出した透過率または反射率の値
を用いて分光透過率または分光反射率の極大値あ
るいは極小値を有する波長を計算し、前記薄膜の
厚さを検知する手段を有する膜厚制御方法におい
て、前記検出波長域を前記極大値あるいは極小値
を有する波長を内在する波長域とすることを特徴
とする膜厚制御方法。
1 Detect the spectral transmittance or spectral reflectance of the thin film formed on the thin film forming substrate at three or more wavelengths intermittently, and use the detected transmittance or reflectance value to determine the spectral transmittance or spectral reflectance. In a film thickness control method comprising means for calculating the wavelength having the maximum value or minimum value of reflectance and detecting the thickness of the thin film, the detection wavelength range is set to a wavelength including the wavelength having the maximum value or the minimum value. A film thickness control method characterized by:
JP1895878A 1978-02-20 1978-02-20 Method and apparatus for controlling film thickness Granted JPS54110938A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1895878A JPS54110938A (en) 1978-02-20 1978-02-20 Method and apparatus for controlling film thickness

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1895878A JPS54110938A (en) 1978-02-20 1978-02-20 Method and apparatus for controlling film thickness

Publications (2)

Publication Number Publication Date
JPS54110938A JPS54110938A (en) 1979-08-30
JPS627266B2 true JPS627266B2 (en) 1987-02-16

Family

ID=11986145

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1895878A Granted JPS54110938A (en) 1978-02-20 1978-02-20 Method and apparatus for controlling film thickness

Country Status (1)

Country Link
JP (1) JPS54110938A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH026989U (en) * 1988-06-27 1990-01-17

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2538005B1 (en) * 1982-12-17 1987-06-12 Solvay CATHODE FOR THE ELECTROLYTIC PRODUCTION OF HYDROGEN AND ITS USE
RU2006136761A (en) * 2006-10-18 2008-04-27 ФГОУ ВПО Российский государственный университет имени Иммануила Канта (РГУ им. И. Канта) (RU) METHOD FOR FILM THICKNESS CONTROL DURING ITS APPLICATION BY DEPOSITION IN A VACUUM CAMERA

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH026989U (en) * 1988-06-27 1990-01-17

Also Published As

Publication number Publication date
JPS54110938A (en) 1979-08-30

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