JPH042553B2 - - Google Patents
Info
- Publication number
- JPH042553B2 JPH042553B2 JP59243790A JP24379084A JPH042553B2 JP H042553 B2 JPH042553 B2 JP H042553B2 JP 59243790 A JP59243790 A JP 59243790A JP 24379084 A JP24379084 A JP 24379084A JP H042553 B2 JPH042553 B2 JP H042553B2
- Authority
- JP
- Japan
- Prior art keywords
- substrate
- atomic layer
- evaporation source
- growth
- molecular beam
- 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 - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B23/00—Single-crystal growth by condensing evaporated or sublimed materials
- C30B23/02—Epitaxial-layer growth
- C30B23/08—Epitaxial-layer growth by condensing ionised vapours
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Crystallography & Structural Chemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
- Physical Deposition Of Substances That Are Components Of Semiconductor Devices (AREA)
Description
【発明の詳細な説明】
(産業上の利用分野)
この発明は、化合物半導体の結晶成長を制御す
る分子線エピタキシヤル成長方法に関する。DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a molecular beam epitaxial growth method for controlling crystal growth of compound semiconductors.
(従来の技術)
従来から知られている分子線エピタキシヤル成
長方法は、その分子線の強度を測定し、その強度
が一定になるように加熱温度や蒸発源収納容器の
開口時間等を調整して、膜厚や一原子層成長を制
御するようにしていた。(Prior art) The conventionally known molecular beam epitaxial growth method measures the intensity of the molecular beam and adjusts the heating temperature, opening time of the evaporation source storage container, etc. so that the intensity remains constant. Therefore, the film thickness and single atomic layer growth were controlled.
また、当該蒸発源収納容器の開口時間や開口径
を、経験的要素を基準にして制御することも実際
には行なわれている。 Furthermore, the opening time and opening diameter of the evaporation source storage container are actually controlled based on empirical factors.
さらに、一原子層成長を制御する方法として、
当該成長層に電子を飛ばしてそれを反射させ、そ
の反射電子によつて原子層の成長状況を把握する
反射型高速電子線回折を利用することも従来から
知られている。 Furthermore, as a method to control single atomic layer growth,
It has also been known to utilize reflection-type high-speed electron diffraction, in which electrons are ejected into the growth layer and reflected, and the growth status of the atomic layer is determined by the reflected electrons.
(本発明が解決しようとする問題点)
上記のように分子線の強度を測定する従来の方
法では、当該基板に形成される結晶成長を直接制
御するのではなく、分子線の強度という間接的な
要素を基にした制御なので、どうしてもその正確
性に欠けるという問題があつた。(Problems to be Solved by the Present Invention) As described above, the conventional method of measuring the intensity of molecular beams does not directly control the growth of crystals formed on the substrate, but indirectly measures the intensity of molecular beams. Since the control is based on various elements, there was a problem that it lacked accuracy.
また、蒸発源収納容器の開口径や開口時間を制
御する方法も、当該基板の表面の直接的な情報に
基づいた制御ではなく、正確性という点で分子線
強度を測定する場合と同様の問題があつた。 In addition, the method of controlling the opening diameter and opening time of the evaporation source storage container is not based on direct information about the surface of the substrate, and has the same accuracy problem as measuring molecular beam intensity. It was hot.
さらに、反射型高速電子線回折を利用した場合
には、電子を基板に照射したとき、真空中に残留
している微量の炭素化合物を分解して、その基板
上に炭素を付着させるので、当該原子層の純度を
損ない、その原子層中に格子欠陥を発生させる原
因となる等、品質管理に問題を残すことが多かつ
た。 Furthermore, when reflection-type high-speed electron diffraction is used, when the substrate is irradiated with electrons, trace amounts of carbon compounds remaining in the vacuum are decomposed and carbon is deposited on the substrate. This often left problems in quality control, such as impairing the purity of the atomic layer and causing lattice defects to occur in the atomic layer.
この発明は、当該基板上の条件を直接検出し
て、より正確な制御を可能にした分子線エピタキ
シヤル成長方法の提供を目的にする。 An object of the present invention is to provide a molecular beam epitaxial growth method that enables more accurate control by directly detecting the conditions on the substrate.
(課題を解決するための手段)
この発明は、超高真空室に基板を設置するとと
もに、この基板の表面に成長させる原子層の蒸発
源を収納する蒸発源収納容器を設け、この容器内
の物質を蒸発させて基板に単原子層を成長させる
分子線エピタキシヤル成長方法を前提にするもの
である。(Means for Solving the Problems) In the present invention, a substrate is installed in an ultra-high vacuum chamber, and an evaporation source storage container is provided to store an evaporation source for an atomic layer to be grown on the surface of the substrate. This method is based on the molecular beam epitaxial growth method, in which a monoatomic layer is grown on a substrate by evaporating a substance.
上記の方法を前提にしつつ、この発明は、基板
表面から放射される赤外線エネルギー量の変動を
赤外線放射温度計で検出し、この検出エネルギー
の変化に応じて蒸発源収納容器の開口径、開口時
間あるいは加熱温度等を調整して結晶成長を制御
する点に特徴を有する。 Based on the above-mentioned method, the present invention detects variations in the amount of infrared energy emitted from the substrate surface using an infrared radiation thermometer, and adjusts the opening diameter and opening time of the evaporation source storage container according to the changes in the detected energy. Another feature is that the crystal growth is controlled by adjusting the heating temperature and the like.
(作用)
この発明は、上記のように構成したので、基板
の最外原子層からの赤外線放射エネルギー量の変
動を、赤外線放射温度計で検出する。そして、そ
の検出したエネルギーの変化に応じて蒸発源収納
容器の開口径、開口時間あるいは加熱温度等を調
整する。(Function) Since the present invention is configured as described above, a variation in the amount of infrared radiation energy from the outermost atomic layer of the substrate is detected by an infrared radiation thermometer. Then, the opening diameter, opening time, heating temperature, etc. of the evaporation source storage container are adjusted in accordance with the detected energy change.
(発明の効果)
この発明の分子線エピタキシヤル成長方法によ
れば、基板の状態変化を直接検出して結晶成長を
制御できるので、それだけ正確性が増すととも
に、従来のように炭素が付着したりすることもな
くなる。(Effects of the Invention) According to the molecular beam epitaxial growth method of the present invention, crystal growth can be controlled by directly detecting changes in the state of the substrate. There will be nothing to do.
また、赤外線エネルギー量の変動を赤外線放射
温度計で検出するようにしたので、例えば、特開
昭59−92998号公報に記載されたもののように、
原子層の屈折率の差から生じる赤外線の干渉効果
を測定するものに比べて、高精度な原子層の成長
制御が可能になる。 In addition, since changes in the amount of infrared energy are detected using an infrared radiation thermometer, for example, as described in Japanese Patent Application Laid-open No. 59-92998,
Compared to methods that measure the interference effect of infrared rays caused by differences in the refractive index of atomic layers, it is possible to control the growth of atomic layers with higher precision.
(本発明の実施例)
超高真空室1内には、GaAs基板2を加熱する
ための温度制御器3を設けるとともに、GaAs基
板2の下方に蒸発源収納容器4,5を設けてい
る。(Embodiment of the present invention) Inside the ultra-high vacuum chamber 1, a temperature controller 3 for heating the GaAs substrate 2 is provided, and evaporation source storage containers 4 and 5 are provided below the GaAs substrate 2.
そして、一方の容器4にはガリウムGaを収納
し、他方の容器5にはヒ素Asを収納している。
さらに、この容器は図示していないヒータによつ
て加熱し、蒸発源であるガリウムGa、ヒ素Asを
蒸発させ、GaAs基板2の表面に結晶成長させ
る。 One container 4 stores gallium Ga, and the other container 5 stores arsenic As.
Further, this container is heated by a heater (not shown) to evaporate gallium Ga and arsenic As, which are evaporation sources, and grow crystals on the surface of the GaAs substrate 2.
上記のように蒸発源を収納した容器4,5の上
方には、その開口部を開閉するシヤツター6,7
を設けているが、このシヤツター6,7は、当該
容器4,5の開口時間を調整するとともに、その
開口径も調整しうるようにしている。 As mentioned above, above the containers 4 and 5 containing the evaporation sources, there are shutters 6 and 7 that open and close the openings of the containers 4 and 5.
The shutters 6 and 7 are arranged so that the opening time of the containers 4 and 5 can be adjusted, and the opening diameter thereof can also be adjusted.
さらに、超高真空室1には、ビユーイングポー
ト8を設けるとともに、このビユーイングポート
8の外方には赤外線放射温度計9を設けている。
この赤外線放射温度計9は、GaAs基板2の表面
から放射される赤外線エネルギーを検出するため
のものである。 Further, the ultra-high vacuum chamber 1 is provided with a viewing port 8, and an infrared radiation thermometer 9 is provided outside the viewing port 8.
This infrared radiation thermometer 9 is for detecting infrared energy radiated from the surface of the GaAs substrate 2.
すなわち、どのような物質でも、絶対温度零度
以上であれば、自らの温度に対応した赤外線を放
射している。したがつて、上記基板2の表面に所
定の原子層が成長すれば、その原子層に応じた赤
外線を放射することになる。その赤外線放射エネ
ルギー(W)は、絶対温度(T°K)の関数で、W
=εσT4(εは放射率、σはステフアンボルツマン
定数)で表わされる。 In other words, any substance, if its temperature is above absolute zero, emits infrared rays corresponding to its own temperature. Therefore, if a predetermined atomic layer grows on the surface of the substrate 2, infrared rays corresponding to the atomic layer will be emitted. Its infrared radiation energy (W) is a function of absolute temperature (T°K), W
= εσT 4 (ε is emissivity, σ is Stephan-Boltzmann constant).
この原子層に応じた赤外線の温度を検出して、
当該原子層の成長状況を判断するのがこの上記赤
外線放射温度計9である。 By detecting the temperature of the infrared rays according to this atomic layer,
It is this infrared radiation thermometer 9 that determines the growth status of the atomic layer.
そこで、上記基板2に結晶成長させるために
は、先ず、GaAs基板2を温度制御器3で600℃
程度に加熱して、基板表面の酸化層を除去する。
このように酸化層を除去すると、基板2のヒ素が
飛散するので、それを補充するために十分なヒ素
を照射する。 Therefore, in order to grow crystals on the substrate 2, first, the GaAs substrate 2 is heated to 600°C using a temperature controller 3.
The oxide layer on the surface of the substrate is removed by heating to a certain degree.
When the oxide layer is removed in this way, the arsenic on the substrate 2 is scattered, so sufficient arsenic is irradiated to replenish it.
このようにして酸化層が除去された基板2の表
面の最外原子層は、第2図aで示すように、ヒ素
原子層10となる。 The outermost atomic layer on the surface of the substrate 2 from which the oxide layer has been removed in this manner becomes an arsenic atomic layer 10, as shown in FIG. 2a.
次に、蒸発源収納容器4のシヤツター6を開い
てGaAs成長を開始する。この場合にGa原子は、
成長前の基板2表面における最外原子層であるヒ
素原子層10上に飛来し、ガリウム原子層11を
形成する。 Next, the shutter 6 of the evaporation source container 4 is opened to start GaAs growth. In this case, the Ga atom is
It flies onto the arsenic atomic layer 10, which is the outermost atomic layer on the surface of the substrate 2 before growth, to form a gallium atomic layer 11.
また、ガリウム原子層11が存在する場所にし
かAs原子が付着しないので、上記シヤツター6,
7を交互に開閉することによつて、第2図a〜c
に示すように、ヒ素原子層10及びガリウム原子
層11が交互に成長することになる。 Furthermore, since As atoms are attached only to the locations where the gallium atomic layer 11 is present, the above-mentioned shutter 6,
By alternately opening and closing 7, Fig. 2 a to c
As shown in FIG. 2, arsenic atomic layers 10 and gallium atomic layers 11 grow alternately.
そして、上記の成長過程において、基板2の加
熱温度は温度制御器3で一定に保たれている。し
かし、その表面の原子層が、ヒ素原子層10ある
いはガリウム原子層11のいずれであるかによつ
て、その表面からの赤外線放射率が異なる。 During the above growth process, the heating temperature of the substrate 2 is kept constant by the temperature controller 3. However, the infrared emissivity from the surface differs depending on whether the atomic layer on the surface is the arsenic atomic layer 10 or the gallium atomic layer 11.
したがつて、この赤外線エネルギーを赤外線放
射温度計9で検出すれば、当該原子層の成長状況
を把握することができる。このようにして検出し
た原子層の成長状況を勘案して、上記シヤツター
6,7の開口径、開口時間あるいは当該蒸発物質
の加熱温度等を制御してその原子成長を制御でき
る。 Therefore, by detecting this infrared energy with the infrared radiation thermometer 9, it is possible to grasp the growth status of the atomic layer. The atomic growth can be controlled by controlling the aperture diameter and opening time of the shutters 6 and 7 or the heating temperature of the evaporated substance, taking into account the growth situation of the atomic layer detected in this way.
第3図は、実際の測定結果を示すもので、赤外
線放射温度計9の出力の変動周期が明らかにされ
ている。この変動周期の数から、成長した原子層
の層数を把握できる。 FIG. 3 shows actual measurement results, and the fluctuation period of the output of the infrared radiation thermometer 9 is clarified. The number of atomic layers grown can be determined from the number of fluctuation cycles.
なお、上記実施例では、GaAs基板に原子層を
成長させる場合であるが、ZnSe、InPなどの全て
の化合物半導体についても、また異種金属につい
ても上記方法が適用できること当然である。 In the above embodiments, an atomic layer is grown on a GaAs substrate, but it goes without saying that the above method can be applied to all compound semiconductors such as ZnSe and InP, as well as to different metals.
図面はこの発明の実施例を示すもので、第1図
は分子線エピタキシヤル装置の概略図、第2図a
〜cは原子層が成長した基板の断面図、第3図は
成長層の赤外線放射エネルギーの強度変化を示す
グラフである。
1……超高真空室、2……基板、4,5……蒸
発源収納容器、10,11……原子層。
The drawings show an embodiment of the present invention, and FIG. 1 is a schematic diagram of a molecular beam epitaxial apparatus, and FIG.
-c is a cross-sectional view of a substrate on which an atomic layer has been grown, and FIG. 3 is a graph showing changes in the intensity of infrared radiation energy of the grown layer. 1... Ultra-high vacuum chamber, 2... Substrate, 4, 5... Evaporation source storage container, 10, 11... Atomic layer.
Claims (1)
基板の表面に成長させる原子層の蒸発源を収納す
る蒸発源収納容器を設け、この容器内の物質を蒸
発させて基板に単原子層を成長させる分子線エピ
タキシヤル成長方法において、上記基板表面から
放射される赤外線エネルギー量の変動を赤外線放
射温度計で検出し、この検出エネルギーの変化に
応じて蒸発源収納容器の開口径、開口時間あるい
は加熱温度等を調整して結晶成長を制御する分子
線エピタキシヤル成長方法。1 A substrate is placed in an ultra-high vacuum chamber, and an evaporation source storage container is provided to store an evaporation source for the atomic layer to be grown on the surface of the substrate, and the substance in this container is evaporated to grow a monoatomic layer on the substrate. In the molecular beam epitaxial growth method, changes in the amount of infrared energy emitted from the substrate surface are detected with an infrared radiation thermometer, and the opening diameter, opening time, or heating of the evaporation source storage container is adjusted according to the changes in the detected energy. A molecular beam epitaxial growth method that controls crystal growth by adjusting temperature, etc.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP24379084A JPS61122193A (en) | 1984-11-19 | 1984-11-19 | Epitaxial growth with molecular beam |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP24379084A JPS61122193A (en) | 1984-11-19 | 1984-11-19 | Epitaxial growth with molecular beam |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61122193A JPS61122193A (en) | 1986-06-10 |
| JPH042553B2 true JPH042553B2 (en) | 1992-01-20 |
Family
ID=17108994
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP24379084A Granted JPS61122193A (en) | 1984-11-19 | 1984-11-19 | Epitaxial growth with molecular beam |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61122193A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5296701A (en) * | 1993-04-19 | 1994-03-22 | Owens-Brockway Glass Container Inc. | Apparatus for inspecting containers having a dual optical transmission means, a dual light sensing means and a rotating head |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5948786B2 (en) * | 1982-11-19 | 1984-11-28 | 工業技術院長 | Molecular beam crystal growth method |
-
1984
- 1984-11-19 JP JP24379084A patent/JPS61122193A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61122193A (en) | 1986-06-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Mao et al. | The structure and crystallization characteristics of phase change optical disk material Ge1Sb2Te4 | |
| JPH05139882A (en) | Molecular beam source | |
| US6342265B1 (en) | Apparatus and method for in-situ thickness and stoichiometry measurement of thin films | |
| US4640720A (en) | Method of manufacturing a semiconductor device | |
| JPH042553B2 (en) | ||
| Gillet et al. | Stranski-Krastanov growth mode of Au ON Mo (llO) surface: Investigation by Auger electron spectroscopy | |
| JPS5992998A (en) | Method for growing crystal using molecular beam | |
| JP2818124B2 (en) | Semiconductor device manufacturing method | |
| Strite et al. | Reliable substrate temperature measurements for high temperature AlGaAs molecular‐beam epitaxy growth | |
| JP2688365B2 (en) | Board holder | |
| JPS61220414A (en) | Apparatus for generating molecular beam | |
| JPS59223293A (en) | Molecular beam epitaxial growth device | |
| JPH0437908Y2 (en) | ||
| JPS63937B2 (en) | ||
| JPH03142921A (en) | Manufacturing device for iii-v compound semiconductor thin film | |
| JPS6142125A (en) | Mbe substrate and method for measuring temperature thereof | |
| JP3216950B2 (en) | Substrate temperature controller | |
| JPS61176131A (en) | Measurement of substrate temperature | |
| JPS60240119A (en) | Molecular beam crystal growth | |
| JPS61127695A (en) | Molecular beam crystal growth device | |
| JPS62290122A (en) | Device for measuring substrate temperature of molecular beam epitaxial device | |
| JPS62211379A (en) | Vapor deposition method | |
| JP2759298B2 (en) | Thin film formation method | |
| JPS61263212A (en) | Molecular beam epitaxy substrate holder | |
| JP2007162042A (en) | Film forming apparatus and film forming method |