JPH03112128A - Vapor growth device for compound semiconductor - Google Patents

Vapor growth device for compound semiconductor

Info

Publication number
JPH03112128A
JPH03112128A JP1251486A JP25148689A JPH03112128A JP H03112128 A JPH03112128 A JP H03112128A JP 1251486 A JP1251486 A JP 1251486A JP 25148689 A JP25148689 A JP 25148689A JP H03112128 A JPH03112128 A JP H03112128A
Authority
JP
Japan
Prior art keywords
liner tube
susceptor
tube
substrate
gas
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
JP1251486A
Other languages
Japanese (ja)
Other versions
JP2849642B2 (en
Inventor
Katsuhide Manabe
勝英 真部
Masahiro Kotaki
正宏 小滝
Michinari Sasa
道成 佐々
Shiro Yamazaki
史郎 山崎
Isamu Akasaki
勇 赤崎
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.)
Nagoya University NUC
Japan Science and Technology Agency
Toyoda Gosei Co Ltd
Original Assignee
Nagoya University NUC
Research Development Corp of Japan
Toyoda Gosei 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 Nagoya University NUC, Research Development Corp of Japan, Toyoda Gosei Co Ltd filed Critical Nagoya University NUC
Priority to JP25148689A priority Critical patent/JP2849642B2/en
Publication of JPH03112128A publication Critical patent/JPH03112128A/en
Application granted granted Critical
Publication of JP2849642B2 publication Critical patent/JP2849642B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Led Devices (AREA)

Abstract

PURPOSE:To mix the reactive gas introduced into a liner tube in the upstream part of the liner tube, and also to throttle the gas flow above a substrate so as to obtain a uniform laminar flow by constituting a susceptor out of a liner tube in the shape of an inner tube when placing the substrate for crystal growth on the susceptor, and providing a minute gap at the side where the substrate is placed. CONSTITUTION:A conical liner tube 12, which is expanding in the direction of gas downstream, is provided in an inner chamber 11 surrounded by a quartz tube 10. That is, the cross section vertical to the axis of the liner tube 12 is constituted in a circle that the radius is large along the direction of an X axis being the gas flow direction. Moreover, on the side of the downstream of the liner tube 12, a conical susceptor 20 of barrel type is provided to cover it from upstream side. Moreover, the side of the susceptor 20 on which to place many sapphire substrates 50 is covered with the liner tube 12 small intervals apart. This way, the gap to the upper tube wall 24 of the liner tube 12 is 12mm at the upstream part of the substrate 50, and 4mm at the downstream part, and the reactive gas is made into a high speed and uniform laminar flow above the substrate 50.

Description

【発明の詳細な説明】[Detailed description of the invention] 【産業上の利用分野】[Industrial application field]

本発明は化合物半導体の気相成長装置に関する。 The present invention relates to a compound semiconductor vapor phase growth apparatus.

【従来技術】[Prior art]

従来、有機金属化合物気相成長法(以下rM。 VPEJと記す)を用いて、窒化ガリウム系化合物半導
体(A I X G a +−* N ; X=Oを含
む)薄膜をサファイア基板上に気相成長させることや、
その窒化ガリウム系化合物半導体薄膜を発光層とする発
光素子が研究されている。 窒化ガリウム系化合物半導体の単結晶ウェハーが容易に
得られないことから、窒化ガリウム系化合物半導体をそ
れと格子定数の近いサファイア基板上にエピタキシャル
成長させることが行われている。 そして、GaAsでは、円錐形状のバレル型のMOVP
E法による気相成長装置を用いて、−度に多数枚のウェ
ハの気相成長を行っている。
Conventionally, a thin film of a gallium nitride compound semiconductor (A I phase growth,
Light-emitting devices using the gallium nitride-based compound semiconductor thin film as a light-emitting layer are being researched. Since single-crystal wafers of gallium nitride-based compound semiconductors are not easily obtained, gallium nitride-based compound semiconductors are epitaxially grown on sapphire substrates having a lattice constant similar to that of gallium nitride-based compound semiconductors. In GaAs, a conical barrel-shaped MOVP
Using a vapor phase growth apparatus based on the E method, a large number of wafers are vapor phase grown at a time.

【発明が解決しようとする課題】[Problem to be solved by the invention]

ところが、窒化ガリウム系化合物半導体を異物質で格子
定数の異なるサファイア基板に結晶成長させる場合には
、結晶成長が回能であるため、反応ガスの微妙な乱れが
直ちに格子欠陥につながる。 又、窒化ガリウム系化合物半導体の気相成長の場合には
、成長温度が高いためV族元素の蒸気圧が高くなり、化
学量論数のバランスがくずれやすく、均質な大面積の結
晶膜を得ることが困難である。 従って、反応ガスの層流をくずさずに、流速を向上させ
ることが必要となる。 ところが、従来のバレル型の気相成長装置では、均一な
ガス流が得難く、化学量論数のバランスがくずれ易いG
aN等では、均質な大面積の結晶膜を得ることが困難で
あり、結晶にビットが発生し易く、表面モホロジーも悪
いという問題があった。 本発明は、上記の課題を解決するために成されたもので
あり、その目的とするところは、バレル型の気相成長装
置において、化合物半導体、特に、サファイア基板上に
窒化ガリウム系化合物半導体を結晶成長させる場合にお
いて、成長速度及び結晶の質に場所依存性の少ない結晶
成長を多量に行うための装置を提供することである。
However, when crystals of gallium nitride-based compound semiconductors are grown on a sapphire substrate that is a foreign material and has a different lattice constant, the crystal growth is circular, so subtle disturbances in the reaction gas immediately lead to lattice defects. In addition, in the case of vapor phase growth of gallium nitride-based compound semiconductors, the high growth temperature increases the vapor pressure of group V elements, which tends to upset the stoichiometric balance, making it difficult to obtain a homogeneous crystal film with a large area. It is difficult to do so. Therefore, it is necessary to increase the flow rate without disrupting the laminar flow of the reaction gas. However, with conventional barrel-type vapor phase growth equipment, it is difficult to obtain a uniform gas flow, and the stoichiometric balance is easily lost.
With aN and the like, there are problems in that it is difficult to obtain a homogeneous crystal film with a large area, bits are likely to occur in the crystal, and the surface morphology is poor. The present invention has been made to solve the above problems, and its purpose is to grow a compound semiconductor, particularly a gallium nitride compound semiconductor, on a sapphire substrate in a barrel-type vapor phase growth apparatus. An object of the present invention is to provide an apparatus for growing a large amount of crystals in which the growth rate and crystal quality are less dependent on location.

【課題を解決するための手段】[Means to solve the problem]

上記課題を解決するための発明の構成は、有機金属化合
物ガスを用いた化合物半導体薄膜を気相成長させる装置
において、 反応ガス流の上流側に向かって先鋭な円錐形状をし、化
合物半導体薄膜を成長させる基板を多数その側面に配設
するバレル型のサセプタと、前記サセプタの基板の配設
される側面部の上部を微小間隙を空けて覆うと共に前記
サセプタを前記反応ガスの上流側から覆うライナー管と
、前記ライナー管の内部に反応ガスを分離して導く複数
の導入管と、 を有することをである。
The structure of the invention for solving the above problem is that, in an apparatus for vapor phase growth of a compound semiconductor thin film using an organometallic compound gas, the compound semiconductor thin film is grown in a conical shape that is sharply pointed toward the upstream side of the reaction gas flow. a barrel-shaped susceptor on which a large number of substrates to be grown are disposed on its side; and a liner that covers the upper part of the side surface of the susceptor on which the substrates are disposed with a minute gap and also covers the susceptor from the upstream side of the reaction gas. A tube, and a plurality of introduction tubes for separating and guiding the reaction gas into the inside of the liner tube.

【作用】[Effect]

結晶成長の基板は円錐形状をしたバレル型のサセプタに
載置される。そのサセプタは円錐形状のライナー管によ
り、基板の載置される側面部で微小間隙を空けて覆われ
ている。従って、ライナー管に導入管で導かれた反応ガ
スは、ライナー管の上流部で混合されると共に、基板の
上部では、ガス流が絞られ円周方向及び径方向に均一な
高速の層流が得られる。 r発明の効果】 この結果、円錐形状のサセプタの側面部の位置によらず
均一な結晶の成長が可能となり、−度に多数枚の結晶成
長したウェハを得ることができる。
A substrate for crystal growth is placed on a barrel-shaped susceptor with a conical shape. The susceptor is covered with a conical liner tube with a minute gap left at the side surface on which the substrate is placed. Therefore, the reaction gas introduced into the liner tube through the introduction tube is mixed at the upstream portion of the liner tube, and at the top of the substrate, the gas flow is constricted to create a high-speed laminar flow that is uniform in the circumferential and radial directions. can get. [Effects of the Invention] As a result, uniform crystal growth is possible regardless of the position of the side surface of the conical susceptor, and a large number of crystal-grown wafers can be obtained at one time.

【実施例】【Example】

以下、本発明を具体的な実施例に基づいて説明する。 第1図において、石英管10はその上端で0リング15
でシールされてフランジ14に当接し、緩衝材38と固
定具39を用い、ポル)46.47とナツト48.49
等により数箇所にてフランジ14に固定されている。又
、石英管10の下端は0リング40でシールされてフラ
ンジ27に螺子締固定置41.42により固定されてい
る。 石英管10で囲われた内室11には、反応ガスを導くラ
イナー管12が配設されている。 ライナー管12はガスの下流方向に広がった円錐形状を
している。従って、そのライナー管12の軸に垂直な断
面は、第2図〜第5図に示すように、ガス流の方向であ
るX軸方向に沿って半径の大きくなる円形をしている。 又、ライナー管12は、その下流側において、円錐形状
をしたバレル型のサセプタ20を上流側から覆っている
。そして、多数のサファイア基板50が載置されるサセ
プタ20の側面部では、ライナー管12はサセプタ20
を微小間隙を隔てて覆っている。即ち、サファイア基板
50とそれに面するライナー管12の上部管壁24との
間隙は、サファイア基板50の上流部で12mm、下流
部で4ffII6に構成されている。このように、本実
施例では、微小間隙を下流側に沿って絞っている。この
ようにすることで、サファイア基板50上で反応ガスの
高速な均一な層流を得ることができる。 サセプタ20には操作棒26が接続されており、フラン
ジ27を取り外してその操作棒26により、サファイア
基板50を載置したサセプタ20をライナー管12の内
部に設置したり、結晶成長の終わった時に、ライナー管
12からサセプタ20を取り出せるようになっている。 又、ライナー管12の上流側には、第1ガス管28と第
2ガス管29とが配設されている。第1ガス管28は第
2ガス管29の内部にあり、それらの両管28.29は
同軸状に2重管構造をしている。第1ガス管28の第2
ガス管29で覆われていない部分の周辺部には多数の穴
3oが開けられており、第2ガス管29にも多数の穴3
oが開けられている。そして、第1ガス管28により導
入された反応ガスはライナー管12内へ吹出し、その場
所で、第2ガス管29により導入されたガスと初めて混
合される。 その第1ガス管28は第1マニホールド31に接続され
、第2ガス管29は第2マニホールド32に接続されて
いる。そして、第17二ホールド31にはキャリアガス
の供給系統Iとトリメチルガリウム(以下rTMG」と
記す)の供給系統Jとトリメチルアルミニウム(以下r
TMA」と記す)の供給系統にとジエチル亜鉛(以下r
DEZ」と記す)の供給系統りとが接続され、第27二
ホールド32にはNHsの供給系統Hとキャリアガスの
供給系統Iとが接続されている。 又、石英管10の外周部には冷却水を循環させる冷却管
33が形成され、その外周部には高周波電界を印加する
ための高周波コイル34が配設されている。 又、ライナー管12はフランジ14を介して外部管35
と接続されており、その外部管35がらはキャリアガス
が導入されるようになっている。 又、サセプタ20の側面部の試料載置面20aには、試
料の温度を測定する熱電対43が配設されてあり、その
熱電対43に接続された導線44゜45が操作棒26に
沿って、外部に延びており、それにより、試料の温度を
外部から測定できるように構成されている。 このような装置構成により、第1ガス管28で導かれた
TMGとTMAとDEZとH2との混合ガスと、第2ガ
ス管29で導かれたNH3とH2との混合ガスがそれら
の管の出口付近で混合され、その混合反応ガスはライナ
ー管12によりサセプタ20の側へ導かれ、サファイア
基板50とライナー管12の上部管壁24との間で形成
された間隙を通過する。この時、サファイア基板50上
の反応ガスの流れは、微小間隙により、円錐の円周方向
及び高さ方向に均一化された層流となる。この結果、基
板上での場所依存性の少ない良質な結晶が成長する。 尚、N型(DA I X G a l−X NH膜を形
成する場合には、DEZを停止させて第1ガス管28と
第2ガス管29から混合ガスを流出させれば良く、■型
のAJII Gat−x N薄膜を形成する場合には、
DEZを供給して第1ガス管28と第2ガス管29I!
:からそれぞれの混合ガスを流出させれば良い。 ■型のA I X G a l−X N薄膜を形成する
場合には、DEZはサファイア基板50に吹き付けられ
熱分解し、ドーパント元素は成長するAlzGa+−x
Nにドーピングされて、■型のAj2xGa+−xNが
得られる。 次に本装置を用いて、サファイア基板50上に次のよう
にして結晶成長をおこなった。 まず、有機洗浄及び熱処理により洗浄した(0001)
面を主面とする単結晶のサファイア基板50をサセプタ
20に装着する。次に、H2を31/分で、m1ガス管
28及び第2ガス管29及び外部管35を介してライナ
ー管12に流しながら、温度1100℃でサファイア基
板50を気相エツチングした。次に温度を400℃まで
低下させて、第1ガス管28からH3を101/分、1
5℃のTMA中をバブリングしたH3を50cc/分、
第2ガス管29からH2を1017分、NH,を101
/分で2分間供給した。 この成長工程で、第6図に示すように、AINのバッフ
ァ層51が約250Aの厚さに形成された。 次に、TMAの供給を停止して、試料温度を1150℃
に保持し、第1ガス管28からHlを101/分、−1
5℃のTMG中をバブリングしたH2を100 cc/
分、第2ガス管からH3を101/分、NH,を101
/分で60分間供給し、膜厚約7虜のN型のGaNから
成る8層52を成長させた。 この8層52のS8M像及びRHBBD像を測定した結
果、良好な結晶が得られていることが分かった。 又、サファイア基板500幅方向(ガス流に垂直な方向
)及び長さ方向くガス流に平行な方向)の膜厚を測定し
たが、均一な膜厚が得られた。
The present invention will be described below based on specific examples. In FIG. 1, the quartz tube 10 has an O-ring 15 at its upper end.
46.47 and nut 48.49 using the cushioning material 38 and fixture 39.
It is fixed to the flange 14 at several locations by, for example, The lower end of the quartz tube 10 is sealed with an O-ring 40 and fixed to the flange 27 with screw fixing devices 41 and 42. An inner chamber 11 surrounded by a quartz tube 10 is provided with a liner tube 12 for guiding a reaction gas. The liner pipe 12 has a conical shape that widens in the downstream direction of the gas. Therefore, the cross section perpendicular to the axis of the liner tube 12 has a circular shape whose radius increases along the X-axis direction, which is the direction of gas flow, as shown in FIGS. 2 to 5. Further, on the downstream side, the liner pipe 12 covers a conical barrel-shaped susceptor 20 from the upstream side. At the side surface of the susceptor 20 on which a large number of sapphire substrates 50 are placed, the liner tube 12 is connected to the susceptor 20.
covered with a tiny gap. That is, the gap between the sapphire substrate 50 and the upper tube wall 24 of the liner tube 12 facing it is 12 mm at the upstream portion of the sapphire substrate 50 and 4ffII6 at the downstream portion. In this way, in this embodiment, the minute gap is narrowed along the downstream side. By doing so, a high-speed, uniform laminar flow of the reaction gas can be obtained on the sapphire substrate 50. An operating rod 26 is connected to the susceptor 20, and by removing the flange 27 and using the operating rod 26, the susceptor 20 on which the sapphire substrate 50 is mounted can be installed inside the liner tube 12, or when crystal growth is finished. , the susceptor 20 can be taken out from the liner pipe 12. Further, on the upstream side of the liner pipe 12, a first gas pipe 28 and a second gas pipe 29 are arranged. The first gas pipe 28 is located inside the second gas pipe 29, and both pipes 28 and 29 are coaxial and have a double pipe structure. The second of the first gas pipe 28
A large number of holes 3o are made in the periphery of the part not covered by the gas pipe 29, and a large number of holes 3o are made in the second gas pipe 29 as well.
o is opened. Then, the reaction gas introduced through the first gas pipe 28 is blown into the liner pipe 12, where it is first mixed with the gas introduced through the second gas pipe 29. The first gas pipe 28 is connected to a first manifold 31 and the second gas pipe 29 is connected to a second manifold 32. The 17th second hold 31 includes a carrier gas supply system I, a trimethyl gallium (hereinafter referred to as "rTMG") supply system J, and a trimethyl aluminum (hereinafter referred to as "rTMG") supply system I.
diethylzinc (hereinafter referred to as r) in the supply system of
The 27th second hold 32 is connected to an NHs supply system H and a carrier gas supply system I. A cooling pipe 33 for circulating cooling water is formed on the outer periphery of the quartz tube 10, and a high frequency coil 34 for applying a high frequency electric field is disposed on the outer periphery of the cooling pipe 33. Further, the liner pipe 12 is connected to the outer pipe 35 via the flange 14.
The carrier gas is introduced into the external pipe 35. Further, a thermocouple 43 for measuring the temperature of the sample is arranged on the sample mounting surface 20a on the side surface of the susceptor 20, and a conductive wire 44°45 connected to the thermocouple 43 runs along the operating rod 26. and extends to the outside, so that the temperature of the sample can be measured from the outside. With this device configuration, the mixed gas of TMG, TMA, DEZ, and H2 led through the first gas pipe 28 and the mixed gas of NH3 and H2 led through the second gas pipe 29 are The mixed reaction gases are mixed near the outlet and are guided to the susceptor 20 side by the liner tube 12 and pass through the gap formed between the sapphire substrate 50 and the upper tube wall 24 of the liner tube 12. At this time, the flow of the reaction gas on the sapphire substrate 50 becomes a uniform laminar flow in the circumferential direction and height direction of the cone due to the minute gaps. As a result, high-quality crystals with less location dependence on the substrate grow. In addition, when forming an N-type (DA I When forming an AJII Gat-x N thin film,
DEZ is supplied to the first gas pipe 28 and the second gas pipe 29I!
: All you have to do is let the respective mixed gases flow out. When forming a type A I
By doping with N, type Aj2xGa+-xN is obtained. Next, using this apparatus, crystal growth was performed on the sapphire substrate 50 in the following manner. First, it was cleaned by organic cleaning and heat treatment (0001)
A single-crystal sapphire substrate 50 having a main surface is attached to the susceptor 20. Next, the sapphire substrate 50 was vapor-phase etched at a temperature of 1100° C. while flowing H2 into the liner tube 12 through the m1 gas pipe 28, the second gas pipe 29, and the external pipe 35 at a rate of 31/min. Next, the temperature is lowered to 400°C, and H3 is supplied from the first gas pipe 28 at 101/min.
50 cc/min of H3 bubbled in TMA at 5°C;
H2 from the second gas pipe 29 for 1017 minutes, NH, for 101 minutes
/min for 2 minutes. In this growth step, the AIN buffer layer 51 was formed to a thickness of about 250 Å, as shown in FIG. Next, stop the supply of TMA and raise the sample temperature to 1150°C.
Hl is supplied from the first gas pipe 28 at 101/min, -1
100 cc/H2 bubbled in TMG at 5°C
min, H3 from the second gas pipe 101/min, NH, 101/min
/min for 60 minutes to grow eight layers 52 made of N-type GaN with a film thickness of about 7 mm. As a result of measuring the S8M image and the RHBBD image of this eight layer 52, it was found that good crystals were obtained. Further, the film thickness of the sapphire substrate 500 in the width direction (direction perpendicular to the gas flow) and length direction (direction parallel to the gas flow) was measured, and a uniform film thickness was obtained.

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

第1図は本発明の具体的な一実施例に係る気相成長装置
の構成図、第2図、第3図、第4図、第5図はX軸に垂
直なライナー管及びその内部の断面図、第6図はサファ
イア基板に成長する薄膜の構造を示した断面図である。 10・・・−石英管 12°・・ライナー管20・・サ
セプタ 28・・第1ガス管 29・−第2ガス管50・・・・
サファイア基板 51・・AINバッファ層 52・・N層 H・・−NH,の供給系統 ■・・・・キャリアガスの供給系統 J−・・−TMGの供給系統 K・・・・TMAの供給
系統L・・・DEZの供給系統
FIG. 1 is a block diagram of a vapor phase growth apparatus according to a specific embodiment of the present invention, and FIGS. 2, 3, 4, and 5 show a liner tube perpendicular to the Cross-sectional view, FIG. 6 is a cross-sectional view showing the structure of a thin film grown on a sapphire substrate. 10...-Quartz tube 12°...Liner tube 20...Susceptor 28...First gas pipe 29...-Second gas pipe 50...
Sapphire substrate 51...AIN buffer layer 52...N layer H...-NH, supply system ■...Carrier gas supply system J-...-TMG supply system K...TMA supply system L...DEZ supply system

Claims (1)

【特許請求の範囲】 有機金属化合物ガスを用いた化合物半導体薄膜を気相成
長させる装置において、 反応ガス流の上流側に向かって先鋭な円錐形状をし、化
合物半導体薄膜を成長させる基板を多数その側面に配設
するバレル型のサセプタと、前記サセプタの基板の配設
される側面部の上部を微小間隙を空けて覆うと共に前記
サセプタを前記反応ガスの上流側から覆うライナー管と
、前記ライナー管の内部に反応ガスを分離して導く複数
の導入管と、 を有することを特徴とする化合物半導体の気相成長装置
[Claims] In an apparatus for vapor phase growth of a compound semiconductor thin film using an organometallic compound gas, a large number of substrates having a conical shape with a sharp point toward the upstream side of a reaction gas flow and on which a compound semiconductor thin film is grown are formed. a barrel-shaped susceptor disposed on a side surface; a liner tube that covers the upper part of the side surface portion of the susceptor on which the substrate is disposed with a minute gap and also covers the susceptor from the upstream side of the reaction gas; and the liner tube. A compound semiconductor vapor phase growth apparatus comprising: a plurality of introduction pipes for separating and guiding a reaction gas into the interior of the apparatus;
JP25148689A 1989-09-26 1989-09-26 Compound semiconductor vapor deposition equipment Expired - Lifetime JP2849642B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP25148689A JP2849642B2 (en) 1989-09-26 1989-09-26 Compound semiconductor vapor deposition equipment

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP25148689A JP2849642B2 (en) 1989-09-26 1989-09-26 Compound semiconductor vapor deposition equipment

Publications (2)

Publication Number Publication Date
JPH03112128A true JPH03112128A (en) 1991-05-13
JP2849642B2 JP2849642B2 (en) 1999-01-20

Family

ID=17223522

Family Applications (1)

Application Number Title Priority Date Filing Date
JP25148689A Expired - Lifetime JP2849642B2 (en) 1989-09-26 1989-09-26 Compound semiconductor vapor deposition equipment

Country Status (1)

Country Link
JP (1) JP2849642B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5707066A (en) * 1994-12-02 1998-01-13 Nok Corporation Boot assembly with adapter
WO2005096356A1 (en) 2004-03-31 2005-10-13 Toyo Tanso Co., Ltd. Susceptor
US9622635B2 (en) 2001-01-24 2017-04-18 Irobot Corporation Autonomous floor-cleaning robot

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6996150B1 (en) 1994-09-14 2006-02-07 Rohm Co., Ltd. Semiconductor light emitting device and manufacturing method therefor

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5707066A (en) * 1994-12-02 1998-01-13 Nok Corporation Boot assembly with adapter
US9622635B2 (en) 2001-01-24 2017-04-18 Irobot Corporation Autonomous floor-cleaning robot
WO2005096356A1 (en) 2004-03-31 2005-10-13 Toyo Tanso Co., Ltd. Susceptor
JP2005294508A (en) * 2004-03-31 2005-10-20 Toyo Tanso Kk Susceptor

Also Published As

Publication number Publication date
JP2849642B2 (en) 1999-01-20

Similar Documents

Publication Publication Date Title
JP3026087B2 (en) Gas phase growth method of gallium nitride based compound semiconductor
US6271104B1 (en) Fabrication of defect free III-nitride materials
KR102489127B1 (en) Hydride vapor phase epitaxy apparatus for growth of Gallium Nitride single crystalline
JP2002316892A (en) Vapor phase growth equipment
CN1988109A (en) Process for producing a free-standing III-N layer, and free-standing III-N substrate
JP2733518B2 (en) Compound semiconductor film vapor phase growth system
JP2849642B2 (en) Compound semiconductor vapor deposition equipment
JP2818776B2 (en) Gallium nitride based compound semiconductor vapor phase growth equipment
KR102536978B1 (en) Hydride vapor phase epitaxy apparatus for growth of Gallium Nitride single crystalline
KR102489015B1 (en) Hydride vapor phase epitaxy apparatus for growth of Gallium Nitride single crystalline
JP2631286B2 (en) Gas phase growth method of gallium nitride based compound semiconductor
JPH03112129A (en) Vapor growth device for compound semiconductor
JPH0380198A (en) Method for growing single crystal film of nitrogen compound semiconductor
JP3112445B2 (en) Gallium nitride based compound semiconductor vapor phase growth equipment
JP3534252B2 (en) Vapor phase growth method
JPH02291112A (en) Vapor growth apparatus for compound semiconductor
JPH02291111A (en) Vapor growth apparatus for compound semiconductor
JPH11340153A (en) Vapor-phase growth system for compound semiconductor
JPH04338636A (en) Semiconductor vapor growth device
KR20030071098A (en) Apparatus for manufacturing GaN substrate
JPH01286997A (en) Production of silicon carbide single crystal
JP3418384B2 (en) Vapor growth method
JPH0773099B2 (en) Semiconductor vapor deposition equipment
JPH11121801A (en) Gallium nitride based compound semiconductor light emitting device
JPH01173708A (en) Semiconductor device

Legal Events

Date Code Title Description
S111 Request for change of ownership or part of ownership

Free format text: JAPANESE INTERMEDIATE CODE: R313115

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20071113

Year of fee payment: 9

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20081113

Year of fee payment: 10

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20081113

Year of fee payment: 10

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20091113

Year of fee payment: 11

EXPY Cancellation because of completion of term