JPH0116378B2 - - Google Patents
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- Publication number
- JPH0116378B2 JPH0116378B2 JP9392182A JP9392182A JPH0116378B2 JP H0116378 B2 JPH0116378 B2 JP H0116378B2 JP 9392182 A JP9392182 A JP 9392182A JP 9392182 A JP9392182 A JP 9392182A JP H0116378 B2 JPH0116378 B2 JP H0116378B2
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- Prior art keywords
- crystal
- raman
- phonon
- plane
- peak intensity
- Prior art date
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- 239000013078 crystal Substances 0.000 claims description 29
- 238000001069 Raman spectroscopy Methods 0.000 claims description 27
- 238000001228 spectrum Methods 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 6
- 230000001678 irradiating effect Effects 0.000 claims 1
- 238000000691 measurement method Methods 0.000 claims 1
- 239000000758 substrate Substances 0.000 description 14
- 238000005259 measurement Methods 0.000 description 5
- JBRZTFJDHDCESZ-UHFFFAOYSA-N AsGa Chemical compound [As]#[Ga] JBRZTFJDHDCESZ-UHFFFAOYSA-N 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 239000004065 semiconductor Substances 0.000 description 4
- 229910001218 Gallium arsenide Inorganic materials 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 238000002441 X-ray diffraction Methods 0.000 description 2
- 238000003776 cleavage reaction Methods 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 230000010287 polarization Effects 0.000 description 2
- 230000007017 scission Effects 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 1
- 238000012790 confirmation Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- HZXMRANICFIONG-UHFFFAOYSA-N gallium phosphide Chemical compound [Ga]#P HZXMRANICFIONG-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- WGPCGCOKHWGKJJ-UHFFFAOYSA-N sulfanylidenezinc Chemical group [Zn]=S WGPCGCOKHWGKJJ-UHFFFAOYSA-N 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
- G01N21/62—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
- G01N21/63—Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
- G01N21/65—Raman scattering
Landscapes
- Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Physics & Mathematics (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)
Description
【発明の詳細な説明】
本発明はレーザラマン分光法を用いた結晶の面
方位測定方法及び装置に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method and apparatus for measuring crystal plane orientation using laser Raman spectroscopy.
ヒ化ガリウム(GaAs)、リン化ガリウム
(GaP)等の半導体バルク結晶は、各種半導体デ
バイス用の基板としてウエハ状に切り出され、市
販されている。これらの結晶の面方位の決定に
は、現在主にX線回折法が用いられているが、X
線を扱うため安全対策等も含めて装置が大がかり
になつてしまう、面方位を精度良く測定するため
に必要な測定系の設定には高い精度を要し、高度
な技術と時間が必要である等の大きな問題点があ
つた。 Semiconductor bulk crystals such as gallium arsenide (GaAs) and gallium phosphide (GaP) are cut into wafer shapes and commercially available as substrates for various semiconductor devices. Currently, X-ray diffraction is mainly used to determine the plane orientation of these crystals;
Because it handles wires, the equipment becomes large-scale, including safety measures, and setting up the measurement system necessary to accurately measure surface orientation requires high precision, advanced technology, and time. There were major problems such as:
本発明は、X線回折法を用いることに起因する
これらの問題点を、レーザラマン分光法を用いる
ことにより解決するものであり、(a)結晶体表面に
レーザ光を照射し、それによつて生じるラマン光
を分光光度計に導入し、該ラマン光のスペクトル
中のTOフオノンに対応するラマンバンドのピー
ク強度とLOフオノンに対応するラマンバンドの
ピーク強度の比を求め、(b)上記結晶体を該結晶体
のレーザ光が入射する面が存在する面内で180゜回
転させて前記(a)を行いピーク強度の比を求め、上
記(a)、(b)で求めた2つの比の値から結晶の面方位
を求めることを特徴としている。 The present invention solves these problems caused by using X-ray diffraction by using laser Raman spectroscopy. Raman light is introduced into a spectrophotometer, and the ratio of the peak intensity of the Raman band corresponding to the TO phonon and the peak intensity of the Raman band corresponding to the LO phonon in the spectrum of the Raman light is determined. Rotate the crystal body by 180° in the plane where the laser beam is incident, perform the above (a), and calculate the ratio of the peak intensities, and calculate the value of the two ratios obtained in the above (a) and (b). It is characterized by finding the plane orientation of the crystal from.
以下、閃亜鉛鉱構造の結晶(Zincblend型結晶)
を例にとつて本発明を詳説する。Zincblend型結
晶を後方散乱法で測定すると、選択則により
(100)面からはLOフオノンによるスペクトルが、
(110)面からはTOフオノンによるスペクトルが
夫々現れる。そして、結晶表面の面方位が(100)
面からずれていると、第1図に示すようにLO、
TOフオノンによる両方のスペクトルが現れる。 Below, crystals with zinc blende structure (Zincblend type crystals)
The present invention will be explained in detail by taking this as an example. When a Zincblend crystal is measured using the backscattering method, due to the selection rule, the spectrum due to LO phonons from the (100) plane is
Spectra due to TO phonons appear from the (110) plane. And the plane orientation of the crystal surface is (100)
If it is out of plane, as shown in Figure 1, LO,
Both spectra due to TO phonones appear.
この時のLO、TOフオノン強度の面方位依存
性は、一次ラマン散乱のラマンテンソルから計算
できる。今、結晶の主軸をX、Y、Zとし、実際
の結晶面(X′−Y′)が(100)から(110)方向
へφ゜傾いているとすれば、その結晶面へレーザ光
を入射させたとき、結晶の主軸X、Y、Zと結晶
内をレーザ光が進む方向Kiとの位置関係は、第
2図に示すa,b,c,の3種類が考えられる。
図中Ksへ散乱光が進む方向で、Z′軸と一致する
よう配置される。また、qはフオノンが進む方
向、θはKiとZ軸が成す角である。第2図にお
いてa,bはY軸とY′軸が一致しており、aと
bはZ′軸を中心として結晶面(X′−Y′面)を180゜
回転させた関係にある。又cはX軸とX′軸が一
致しており、φはcの斜視図である第2図dから
わかるようにY−Z平面上での回転ずれとして表
わされる。 The surface orientation dependence of the LO and TO phonon intensities at this time can be calculated from the Raman tensor of first-order Raman scattering. Now, let us assume that the main axes of the crystal are X, Y, and Z, and that the actual crystal plane (X'-Y') is tilted by φ° from the (100) to (110) direction. When the laser beam is incident, there are three possible positional relationships between the main axes X, Y, and Z of the crystal and the direction Ki in which the laser beam travels within the crystal: a, b, and c shown in FIG. 2.
It is arranged so that it coincides with the Z′ axis in the direction in which the scattered light travels toward Ks in the figure. Further, q is the direction in which the phonon moves, and θ is the angle between Ki and the Z axis. In FIG. 2, a and b have the Y-axis and Y' axis coincident, and a and b have a relationship in which the crystal plane (X'-Y' plane) is rotated 180° about the Z' axis. In addition, the X axis and the X' axis of c coincide with each other, and φ is expressed as a rotational deviation on the Y-Z plane, as can be seen from FIG. 2d, which is a perspective view of c.
ここで第2図aの配置をA+、bの配置をA-と
すれば、LO、TOフオノン強度ILO、ITOは次式で
与えられる。 Here, if the arrangement in Figure 2 a is A + and the arrangement in b is A - , the LO and TO phonon intensities I LO and I TO are given by the following equations.
ILO HV=AHdL 2cos2(3θ/2±2φ) …(1)
ITO HV=AHdT 2sin2(3θ/2±2φ) …(2)
ILO HH=0 …(3)
ITO HH=AHdT 2sin2(θ±2φ) …(4)
上式において±はA+とA-に対応し、添字Hは
偏光が入射面に平行(P偏光)、Vは偏光が入射
面に垂直(S偏光)であることを夫々示す。そし
てHVは入射光がP偏光、散乱光がS偏光であ
り、HHは入射光も散乱光もP偏光であることを
示す。dL、dTはLO及びTOフオノンの散乱効率、
AHはP偏光入射時の定数である。 I LO HV =A H d L 2 cos 2 (3θ/2±2φ) …(1) I TO HV =A H d T 2 sin 2 (3θ/2±2φ) …(2) I LO HH =0 … (3) I TO HH = A H d T 2 sin 2 (θ±2φ) …(4) In the above equation, ± corresponds to A + and A - , and the subscript H indicates that the polarized light is parallel to the incident plane (P polarized light) , V indicate that the polarization is perpendicular to the plane of incidence (S polarization), respectively. HV indicates that the incident light is P-polarized light and the scattered light is S-polarized light, and HH indicates that both the incident light and the scattered light are P-polarized light. d L and d T are the scattering efficiency of LO and TO phonons,
A H is a constant when P-polarized light is incident.
上式からA+とA-の夫々についてのLOフオノ
ン強度とTOフオノン強度の比をr+、r-とすれば、
r+、r-は
r±=ITO HV/ILO HV
=(dT/dL)2tan2(3θ/2±2φ) …(5)
となる。次にr+とr-の比を求めると、
r-/r+=tan2(3θ/2−2φ)/
tan2(3θ/2+2φ) …(6)
となる。(6)式においてθは結晶面への入射角θi及
び屈折率nがわかれば、スネルの法則からsinθ=
(sinθi)/nと求めることができ、従つてr+とr-
を測定により求めれば、(6)式からφを求めること
ができる。 From the above equation, if the ratio of the LO phonon intensity and TO phonon intensity for A + and A - , respectively, is r + and r - , then
r + and r - are r±=I TO HV /I LO HV = (d T /d L ) 2 tan 2 (3θ/2±2φ)...(5). Next, finding the ratio of r + and r - , we get r - /r + = tan 2 (3θ/2-2φ)/tan 2 (3θ/2+2φ)...(6). In equation (6), θ is defined as sinθ=
(sinθi)/n, and therefore r + and r -
If is determined by measurement, φ can be determined from equation (6).
第3図は上述の如き考え方に基づく本発明を実
施するための装置の一例を示す。図中1は試料と
なる半導体基板で、回転可能なホルダ2上に保持
されており、該基板1の表面にはレーザ発振器3
において生成されたレーザ光4が照射される。照
射に伴なつて発生したラマン散乱光5は、P偏
光、S偏光を選択的に通過させるアナライザ6を
介してレーザラマン分光光度計7へ導入される。
8はアナライザ6を切換えるための切換機構、9
は上記ホルダ2を軸10を中心として回転させる
ためのパルスモータ等の駆動機構、11は該駆動
機構9へ電流を供給するための駆動電源である。
12は分光光度計7からの測定データに基づいて
演算処理を行うと共に、前記切換機構8、駆動電
源11及び分光光度計7へ測定手順に従つて制御
信号を送る中央制御装置である。 FIG. 3 shows an example of an apparatus for implementing the present invention based on the above-mentioned concept. In the figure, 1 is a semiconductor substrate serving as a sample, which is held on a rotatable holder 2, and a laser oscillator 3 is mounted on the surface of the substrate 1.
The laser beam 4 generated in is irradiated. Raman scattered light 5 generated during irradiation is introduced into a laser Raman spectrophotometer 7 via an analyzer 6 that selectively passes P-polarized light and S-polarized light.
8 is a switching mechanism for switching the analyzer 6; 9
1 is a drive mechanism such as a pulse motor for rotating the holder 2 about the shaft 10, and 11 is a drive power source for supplying current to the drive mechanism 9.
A central control device 12 performs arithmetic processing based on measurement data from the spectrophotometer 7, and sends control signals to the switching mechanism 8, drive power source 11, and spectrophotometer 7 according to measurement procedures.
ここで、(100)から(110)方向へφ゜傾いた面
方位を持つ半絶縁性GaAs基板について、上述し
た装置を用いて測定した例を示す。ホルダ2上に
保持された基板1に対し第3図及び第4図に示す
ようにX′、Y′、Z′軸が設定される。測定すべき
基板面はX′−Y′面内にあり、第4図に示す様に
基板のへきかいした断面とY′軸が45゜の傾きを持
つように設定される。レーザ光4はP偏光で、
X′−Z′面に沿つて基板面に垂直な方向からθi゜傾
いた角度で入射し、それにより発生したラマン光
のうちZ′軸方向のものが分光光度計7へ導入され
る。 Here, an example will be shown in which a semi-insulating GaAs substrate having a plane orientation tilted by φ° from the (100) to (110) direction was measured using the above-mentioned apparatus. X', Y', and Z' axes are set for the substrate 1 held on the holder 2, as shown in FIGS. 3 and 4. The substrate surface to be measured lies within the X'-Y' plane, and is set so that the cut section of the substrate and the Y' axis have an inclination of 45 degrees, as shown in FIG. Laser light 4 is P-polarized light,
The Raman light is incident along the X'-Z' plane at an angle inclined by θi° from the direction perpendicular to the substrate surface, and among the Raman light generated thereby, that in the Z'-axis direction is introduced into the spectrophotometer 7.
先ず最初に、制御装置12はアナライザ6から
P偏光のラマン散乱光を取り出すように切換機構
8を設定すると共に、第1図に示されるスペクト
ルのうちLOフオノンによりピークを検出するよ
うに分光光度計7をセツトする。この時分光光度
計7から得られるスペクトル強度はILO HHであり、
前記(3)式からILO HHは0となることがわかる。そし
てこのことから、へきかい面とY′軸のなす角が
45゜であることが確認できる。 First, the control device 12 sets the switching mechanism 8 to extract the P-polarized Raman scattered light from the analyzer 6, and also sets the spectrophotometer to detect the peak of the spectrum shown in FIG. 1 by the LO phonon. Set 7. At this time, the spectral intensity obtained from the spectrophotometer 7 is I LO HH ,
It can be seen from the above equation (3) that I LO HH is 0. And from this, the angle between the cleavage plane and the Y′ axis is
It can be confirmed that the angle is 45°.
確認後、制御装置12はアナライザ6を切換え
てラマン散乱光のうちS偏光のものが分光光度計
へ到達するようにする。この状態で制御装置12
はLOフオノンによるピーク強度ILO HV及びTOフオ
ノンによるピーク強度ITO HVを測定するように分光
光度計7に指令を与える。この時の状態を第2図
におけるA+とすれば、ここで測定した2つのピ
ーク強度の比を求めることにより(5)式におけるr+
を得ることができる。 After confirmation, the control device 12 switches the analyzer 6 so that the S-polarized light among the Raman scattered light reaches the spectrophotometer. In this state, the control device 12
commands the spectrophotometer 7 to measure the peak intensity I LO HV due to the LO phonon and the peak intensity I TO HV due to the TO phonon. If the state at this time is A + in Figure 2, then by finding the ratio of the two peak intensities measured here, r + in equation (5) is calculated.
can be obtained.
次に制御装置12は駆動電源11へ指令を送
り、ホルダ2を軸10を中心として180゜回転させ
る。それにより基板1も基板表面を含む面上で
180゜回転することになる。そしてその状態で制御
装置12は再びLOフオノンによるピーク強度ILO HV
及びTOフオノンによるピーク強度ITO HVを測定する
ように分光光度計7に指令を与える。この時の状
態は第2図におけるA-に対応することは言うま
でもなく、ここで測定した2つのピーク強度の比
を求めれば、(5)式におけるr-を得ることができ
る。 Next, the control device 12 sends a command to the drive power source 11 to rotate the holder 2 by 180 degrees about the shaft 10. As a result, the substrate 1 also has a surface including the substrate surface.
It will rotate 180°. In this state, the control device 12 again controls the peak intensity I LO HV due to the LO phonon.
and spectrophotometer 7 to measure the peak intensity I TO HV due to TO phonon. It goes without saying that the state at this time corresponds to A - in FIG. 2, and by finding the ratio of the two peak intensities measured here, r - in equation (5) can be obtained.
このようにしてr+及びr-が得られた後、制御装
置12は(6)式に基づいてφを求める。尚、その演
算に先立つてオペレータがレーザ光4の基板面へ
の入射角θiとGaAsの屈折率n(レーザ光としてア
ルゴンレーザの5145Å線を用いた場合n=4.25)
を制御装置12へ入力しておけば、先に述べたよ
うにθはスネルの法則から即座に計算できるの
で、(6)式からφを求めることができる。 After r + and r - are obtained in this way, the control device 12 calculates φ based on equation (6). In addition, prior to the calculation, the operator calculates the incident angle θi of the laser beam 4 on the substrate surface and the refractive index n of GaAs (n=4.25 when using the 5145 Å line of an argon laser as the laser beam).
If θ is input to the control device 12, θ can be immediately calculated from Snell's law as described above, so φ can be obtained from equation (6).
面方位が(100)から(110)方向へ0゜(±0.5゜)、
2゜(±0.5゜)傾いた市販の半絶縁性GaAs基板2種
について上述の如き手順で測定した結果、夫々φ
=0.043゜、1.86゜の測定値が得られ、誤差範囲内に
収まつていることが確認できた。又、同じく5゜
(±0.5゜)傾いた基板についても測定したところ、
φ=6.5゜の測定値が得られた。この場合誤差が大
きい原因として、A-の配置で得られるTOフオノ
ンによるピーク強度が分光光度計の検出限界
(2.5pulse/sec)以下となる点が考えられ、装置
の検出限界の改良によつて、この試料の場合でも
誤差範囲内に収めることができるであろうことは
容易に推察できる。 The surface orientation is 0° (±0.5°) from (100) to (110),
As a result of measuring two types of commercially available semi-insulating GaAs substrates tilted by 2° (±0.5°) using the procedure described above, each φ
Measured values of = 0.043° and 1.86° were obtained, confirming that they were within the error range. In addition, we also measured the board tilted by 5° (±0.5°).
A measured value of φ=6.5° was obtained. In this case, the reason for the large error may be that the peak intensity due to TO phonon obtained with the A - configuration is below the detection limit of the spectrophotometer (2.5 pulse/sec), and it is possible that the detection limit of the device could be improved. , it can be easily inferred that even in the case of this sample, it would be possible to keep it within the error range.
以上詳述した如く本発明によれば、レーザラマ
ン分光法を用いて面方位を決定できるため、X線
を用いる従来のような被爆の危険性なしに正確な
測定を簡単に行うことができる。 As described in detail above, according to the present invention, since the surface orientation can be determined using laser Raman spectroscopy, accurate measurement can be easily performed without the risk of exposure unlike the conventional method using X-rays.
尚、上記は一例であり幾多の変形が可能であ
る。たとえばZincblend形結晶だけではなく他の
結晶系でも全く同様に適用できる。 Note that the above is an example, and many modifications are possible. For example, it can be applied not only to Zincblend crystals but also to other crystal systems in exactly the same way.
第1図はLO、TOフオノンによるスペクトル
を示す図、第2図は結晶面へレーザ光を入射させ
た時、結晶の主軸X、Y、Zとレーザ光が進む方
向Kiとの関係を示す図、第3図は本発明にかか
る方法を実施するための装置の一例を示す図、第
4図は基板のへきかい面とY′軸との傾きを示す
図である。
1:半導体基板、2:ホルダ、3:レーザ発振
器、4:レーザ光、5:ラマン散乱光、6:アナ
ライザ、7:レーザラマン分光光度計、8:切換
機構、9:駆動機構、12:中央制御装置。
Figure 1 is a diagram showing spectra due to LO and TO phonons, and Figure 2 is a diagram showing the relationship between the main axes X, Y, and Z of the crystal and the direction Ki in which the laser beam travels when the laser beam is incident on the crystal plane. , FIG. 3 is a diagram showing an example of an apparatus for carrying out the method according to the present invention, and FIG. 4 is a diagram showing the inclination between the cleavage surface of the substrate and the Y' axis. 1: Semiconductor substrate, 2: Holder, 3: Laser oscillator, 4: Laser light, 5: Raman scattered light, 6: Analyzer, 7: Laser Raman spectrophotometer, 8: Switching mechanism, 9: Drive mechanism, 12: Central control Device.
Claims (1)
よつて生じるラマン光を分光光度計に導入し、
該ラマン光のスペクトル中のTOフオノンに対
応するラマンバンドのピーク強度とLOフオノ
ンに対応するラマンバンドのピーク強度の比を
求めること、 (b) 上記結晶体を該結晶体のレーザ光が入射する
面が存在する面内で180゜回転させて前記(a)を行
いピーク強度の比を求めること、 (c) 上記(a)、(b)で求めた2つの比の値から結晶の
面方位を求めること、 より成る結晶の面方位測定法。 2 結晶体表面に照射するレーザ光を発生するた
めのレーザ発振器と、結晶体表面から生じるラマ
ン光のスペクトル中のTOフオノンに対応するラ
マンバンドのピーク強度とLOフオノンに対応す
るラマンバンドのピーク強度を検出するためのラ
マン分光光度計と、前記結晶体を該結晶体のレー
ザ光が入射する面が存在する面内で180゜回転させ
るための回転機構と、該回転機構によつて180回
転させる前後において前記分光光度計により検出
されたTOフオノンに対応するラマンバンドのピ
ーク強度とLOフオノンに対応するラマンバンド
のピーク強度から結晶の面方位を求めるための演
算手段から成る特許請求の範囲第1項記載の方法
を実施するための装置。[Claims] 1 (a) Irradiating the surface of the crystal with a laser beam and introducing the Raman light generated thereby into a spectrophotometer,
determining the ratio of the peak intensity of the Raman band corresponding to the TO phonon and the peak intensity of the Raman band corresponding to the LO phonon in the spectrum of the Raman light; (b) the laser beam of the crystal is incident on the crystal; (c) Determine the plane orientation of the crystal from the two ratio values obtained in (a) and (b) above by rotating the plane by 180° within the plane in which it exists and performing (a) above. A crystal plane orientation measurement method consisting of: 2 Laser oscillator for generating laser light to irradiate the crystal surface and the peak intensity of the Raman band corresponding to TO phonon and the Raman band corresponding to LO phonon in the spectrum of Raman light generated from the crystal surface. a Raman spectrophotometer for detecting; a rotation mechanism for rotating the crystal body by 180 degrees within a plane on which the laser beam enters the crystal body; and a rotation mechanism for rotating the crystal body by 180 degrees by the rotation mechanism. Claim 1 comprising calculation means for determining the plane orientation of the crystal from the peak intensity of the Raman band corresponding to the TO phonon and the peak intensity of the Raman band corresponding to the LO phonon detected by the spectrophotometer before and after. Apparatus for carrying out the method described in Section 1.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9392182A JPS58210546A (en) | 1982-06-01 | 1982-06-01 | Method and apparatus for measuring plane orientation of crystal |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9392182A JPS58210546A (en) | 1982-06-01 | 1982-06-01 | Method and apparatus for measuring plane orientation of crystal |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58210546A JPS58210546A (en) | 1983-12-07 |
| JPH0116378B2 true JPH0116378B2 (en) | 1989-03-24 |
Family
ID=14095913
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9392182A Granted JPS58210546A (en) | 1982-06-01 | 1982-06-01 | Method and apparatus for measuring plane orientation of crystal |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58210546A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005024391A1 (en) * | 2003-09-05 | 2005-03-17 | National Institute Of Advanced Industrial Science And Technology | Optical measurement method and device |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4747684A (en) * | 1986-09-30 | 1988-05-31 | The United States Of America As Represented By The Secretary Of The Army | Method of and apparatus for real-time crystallographic axis orientation determination |
-
1982
- 1982-06-01 JP JP9392182A patent/JPS58210546A/en active Granted
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005024391A1 (en) * | 2003-09-05 | 2005-03-17 | National Institute Of Advanced Industrial Science And Technology | Optical measurement method and device |
| US7408635B2 (en) | 2003-09-05 | 2008-08-05 | National Institute Of Advanced Industrial Science And Technology | Optical measurement method and device |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58210546A (en) | 1983-12-07 |
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