JPS616200A - Process for doping crystal of gaas, inas, or the like with si - Google Patents

Process for doping crystal of gaas, inas, or the like with si

Info

Publication number
JPS616200A
JPS616200A JP12614984A JP12614984A JPS616200A JP S616200 A JPS616200 A JP S616200A JP 12614984 A JP12614984 A JP 12614984A JP 12614984 A JP12614984 A JP 12614984A JP S616200 A JPS616200 A JP S616200A
Authority
JP
Japan
Prior art keywords
gaas
crystal
sias
inas
amt
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.)
Pending
Application number
JP12614984A
Other languages
Japanese (ja)
Inventor
Ichiro Sudo
一郎 須藤
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.)
Furukawa Mining Co Ltd
Furukawa Kogyo Co Ltd
Original Assignee
Furukawa Mining Co Ltd
Furukawa Kogyo 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 Furukawa Mining Co Ltd, Furukawa Kogyo Co Ltd filed Critical Furukawa Mining Co Ltd
Priority to JP12614984A priority Critical patent/JPS616200A/en
Publication of JPS616200A publication Critical patent/JPS616200A/en
Pending legal-status Critical Current

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  • Crystals, And After-Treatments Of Crystals (AREA)

Abstract

PURPOSE:To obtain uniform crystal having only slight concn. difference in the crystal without entanglement of oxygen in the stage of synthesizing crystal of GaAs or InAs, or a crystal based thereon, or in the stage of growing single crystal by adding a necessary amt. of previously prepd. SiAs and regulating the degree of doping optionally. CONSTITUTION:For example, when GaAs is synthesized, Ga and As are charged in a crucible made of BN, etc., and B2O3 is placed thereon, and the synthesis is carried out by heating in the stream of N2, etc. under pressure. In this invention, calculated amt. of Si is added in the form of SiAs in addn. to Ga and As and heated. In this case, since the m.p. of SiAs is 11 deg.C which is lower than the m.p. of GaAs, i.e. 1,248 deg.C, SiAs becomes liquid and is easily reactive with GaAs, and is easily miscible and uniformized. Therefore, a regulated amt. of Si can be doped in the crystal of GaAs, InAs, etc.

Description

【発明の詳細な説明】 本発明はGaAs、 InAs又はそれらをベースとし
た結晶に規定量のSiをドーピングする方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for doping GaAs, InAs or crystals based thereon with a defined amount of Si.

GaAs、 InAsを従来石英ガラス製ボートで合成
されていた時は5i02とGa又はInが反応し、Si
O□が還元されてSlとなり、これが合成されたGaA
sやInAsに混入してSlをトープしたと同様に低抵
抗のGa1lsやInAsが合成された。しかしこの場
合Siの混入量が規定されるわけでなく、合成時間や温
度、ボートの表面状態等によりS】の混入量に大きな差
がある。又Siの他に同時に酸素も混入し、結晶中のS
i濃度も場所″によって異なり一定にならない欠点があ
った・ 本発明の目的は、Slのドープ量が任意に規定され、し
かも酸素の混入もなく、結晶中のSiの濃度差の少ない
均質な結晶を得る。GaAs、 !nAs等の結晶に3
1をドーピングする方法を櫂供することである。
When GaAs and InAs were conventionally synthesized in a quartz glass boat, 5i02 reacted with Ga or In, and Si
O□ is reduced to Sl, which is the synthesized GaA
Ga1ls and InAs with low resistance were synthesized in the same way as when Sl was mixed into S and InAs and S1 was doped. However, in this case, the amount of Si mixed in is not regulated, and the amount of S mixed in varies greatly depending on the synthesis time, temperature, surface condition of the boat, etc. In addition to Si, oxygen is also mixed in at the same time, causing S in the crystal to
The i concentration also varied depending on the location and was not constant. The purpose of the present invention is to create a homogeneous crystal in which the doping amount of Sl can be arbitrarily specified, there is no mixing of oxygen, and there is little difference in the concentration of Si in the crystal. 3 for crystals such as GaAs and !nAs.
1 is to provide a method of doping.

GaAsを合成する際、直接合成法によればGaとAs
をBNルツボ又は石英ルツボに入れ上部に8203を乗
せて窒素又はアルゴン気流加圧下で加熱合成する。本発
明の方法ではSlをSiAsの形で計算量加えて加熱す
る。この場合Siを単に加えた丈ではSlが融点140
0℃以上なので融解−Uず、しかもS】が比重2.3と
軽いのでGaの上に浮いてしまい一部しかGaAsに混
入しない。又混入量もSiの粒度や温度等条件によって
異なって(る。本発明の方法によれば、SiAsは融点
11’cで、GaAsの融点1248’cより低いから
、SiAsが液状となり、GaAsと反応し易く混合均
一化し易い。又GaAs、 1nAsも砒素化合物であ
り、親和性も良いので、添加したSiAsは全量混合さ
れると考えられ、酸素の混入も無い。依ってBNルツボ
を使う等容器からの混入がなければ本発明の方法により
GaAs、 1nAs等の結晶に現定量のSiをトービ
ンクすることか出来る。
When synthesizing GaAs, according to the direct synthesis method, Ga and As are
is placed in a BN crucible or quartz crucible, 8203 is placed on top, and the mixture is heated and synthesized under a pressurized nitrogen or argon stream. In the method of the invention, a calculated amount of Sl in the form of SiAs is added and heated. In this case, in the length where Si is simply added, the melting point of Sl is 140.
Since it is above 0°C, it melts, and since S] has a light specific gravity of 2.3, it floats on top of Ga and only a portion of it mixes with GaAs. The amount of mixture also varies depending on conditions such as Si particle size and temperature. According to the method of the present invention, since SiAs has a melting point of 11'c, which is lower than the melting point of GaAs of 1248'c, SiAs becomes liquid and is mixed with GaAs. It is easy to react and mix uniformly. GaAs and 1nAs are also arsenic compounds and have good affinity, so it is thought that all of the added SiAs will be mixed, and no oxygen will be mixed in. Therefore, if a container such as a BN crucible is used. If there is no contamination from Si, it is possible to ink the current amount of Si into crystals of GaAs, 1nAs, etc. by the method of the present invention.

実施例1 直接合成法のGaAs合成に於いて、Ga 1.000
g、As 1,096gにSiAs 1.5 gを加え
、B2o350gを加え、窒素80気圧の下にGaAs
を合成した。合成後窒素圧力を20気圧に落して単結晶
を引−ヒげ、L235gの1)結晶を得た。この単結晶
は抵抗率1.8 X1039cmであった。ウェハーの
測定からキャリヤー1度2X10”/ cd、 電子移
動度u−1、800cat / Vsecを得た。
Example 1 In GaAs synthesis by direct synthesis method, Ga 1.000
g, 1.5 g of SiAs was added to 1,096 g of As, 350 g of B2O was added, and the GaAs was heated under 80 atm of nitrogen.
was synthesized. After the synthesis, the nitrogen pressure was lowered to 20 atm and the single crystal was pulled off, yielding 235 g of 1) crystal. This single crystal had a resistivity of 1.8 x 1039 cm. From measurements of the wafer, carrier 1 degree 2X10''/cd, electron mobility u-1, 800cat/Vsec were obtained.

実施例2 ノンドープGaAs多結晶1.4kgにSiAs 1.
Ogを加え、820350gを加えて、4kg/cn+
の窒素雰囲気の下で融解した。融解後圧力を3kg/c
++lに下げて単結晶引上げを行い、径48〜52m/
mの単結晶658gを得た。この単結晶の比抵抗は1.
7103Ωcmであった。
Example 2 SiAs was added to 1.4 kg of non-doped GaAs polycrystal.
Add Og, add 820350g, 4kg/cn+
was melted under a nitrogen atmosphere. After melting, the pressure is 3kg/c.
++l and pulled the single crystal to a diameter of 48 to 52 m/
658 g of a single crystal of m was obtained. The specific resistance of this single crystal is 1.
It was 7103 Ωcm.

Claims (1)

【特許請求の範囲】[Claims] GaAs、InAs又はそれらをベースとした結晶を合
成又は単結晶を成長させる際に予め作成したSiAsを
必要量加えることを特徴とするGaAs、InAs等の
結晶へSiをドーピングする方法。
A method for doping Si into a crystal such as GaAs, InAs, etc., which comprises adding a necessary amount of previously prepared SiAs when synthesizing GaAs, InAs or a crystal based thereon or growing a single crystal thereof.
JP12614984A 1984-06-19 1984-06-19 Process for doping crystal of gaas, inas, or the like with si Pending JPS616200A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12614984A JPS616200A (en) 1984-06-19 1984-06-19 Process for doping crystal of gaas, inas, or the like with si

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12614984A JPS616200A (en) 1984-06-19 1984-06-19 Process for doping crystal of gaas, inas, or the like with si

Publications (1)

Publication Number Publication Date
JPS616200A true JPS616200A (en) 1986-01-11

Family

ID=14927885

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12614984A Pending JPS616200A (en) 1984-06-19 1984-06-19 Process for doping crystal of gaas, inas, or the like with si

Country Status (1)

Country Link
JP (1) JPS616200A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4929572A (en) * 1988-07-18 1990-05-29 Furukawa Co., Ltd. Dopant of arsenic, method for the preparation thereof and method for doping of semiconductor therewith

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4933036A (en) * 1972-08-07 1974-03-26
JPS5262200A (en) * 1975-11-17 1977-05-23 Sumitomo Electric Ind Ltd Single crystal of gallium arsenide without dislocation

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4933036A (en) * 1972-08-07 1974-03-26
JPS5262200A (en) * 1975-11-17 1977-05-23 Sumitomo Electric Ind Ltd Single crystal of gallium arsenide without dislocation

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4929572A (en) * 1988-07-18 1990-05-29 Furukawa Co., Ltd. Dopant of arsenic, method for the preparation thereof and method for doping of semiconductor therewith

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