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JPH0315333B2 - - Google Patents
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JPH0315333B2 - - Google Patents

Info

Publication number
JPH0315333B2
JPH0315333B2 JP57070991A JP7099182A JPH0315333B2 JP H0315333 B2 JPH0315333 B2 JP H0315333B2 JP 57070991 A JP57070991 A JP 57070991A JP 7099182 A JP7099182 A JP 7099182A JP H0315333 B2 JPH0315333 B2 JP H0315333B2
Authority
JP
Japan
Prior art keywords
molecular beam
wafer
substrate
crystal
ejection
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
Application number
JP57070991A
Other languages
Japanese (ja)
Other versions
JPS58188128A (en
Inventor
Toshio Fujii
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.)
Fujitsu Ltd
Original Assignee
Fujitsu 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 Fujitsu Ltd filed Critical Fujitsu Ltd
Priority to JP57070991A priority Critical patent/JPS58188128A/en
Publication of JPS58188128A publication Critical patent/JPS58188128A/en
Publication of JPH0315333B2 publication Critical patent/JPH0315333B2/ja
Granted legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10PGENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
    • H10P14/00Formation of materials, e.g. in the shape of layers or pillars
    • H10P14/20Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials
    • H10P14/29Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials characterised by the substrates
    • H10P14/2901Materials
    • H10P14/2907Materials being Group IIIA-VA materials
    • H10P14/2911Arsenides
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10PGENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
    • H10P14/00Formation of materials, e.g. in the shape of layers or pillars
    • H10P14/20Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials
    • H10P14/22Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials using physical deposition, e.g. vacuum deposition or sputtering
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10PGENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
    • H10P14/00Formation of materials, e.g. in the shape of layers or pillars
    • H10P14/20Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials
    • H10P14/29Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials characterised by the substrates
    • H10P14/2924Structures
    • H10P14/2925Surface structures
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10PGENERIC PROCESSES OR APPARATUS FOR THE MANUFACTURE OR TREATMENT OF DEVICES COVERED BY CLASS H10
    • H10P14/00Formation of materials, e.g. in the shape of layers or pillars
    • H10P14/20Formation of materials, e.g. in the shape of layers or pillars of semiconductor materials
    • H10P14/34Deposited materials, e.g. layers
    • H10P14/3402Deposited materials, e.g. layers characterised by the chemical composition
    • H10P14/3414Deposited materials, e.g. layers characterised by the chemical composition being group IIIA-VIA materials
    • H10P14/3421Arsenides

Landscapes

  • Junction Field-Effect Transistors (AREA)
  • Physical Deposition Of Substances That Are Components Of Semiconductor Devices (AREA)
  • Crystals, And After-Treatments Of Crystals (AREA)

Description

【発明の詳細な説明】 (a) 発明の技術分野 本発明は凹凸のある基板上に、均一な不純物濃
度分布をもつ半導体結晶を形成する分子線結晶成
長方法に関する。
DETAILED DESCRIPTION OF THE INVENTION (a) Technical Field of the Invention The present invention relates to a molecular beam crystal growth method for forming a semiconductor crystal having a uniform impurity concentration distribution on an uneven substrate.

(b) 技術の背景 分子線結晶成長法(分子線エピタキシー)は単
結晶基板に対し結晶の構成元素からなる分子の流
れすなわち分子線を噴出セルより蒸発せしめ基板
面に衝突させることにより化学吸着させて結晶軸
の揃つた結晶をエピタキシヤル成長させる方法で
ある。
(b) Background of the technology Molecular beam crystal growth (molecular beam epitaxy) is a method of chemically adsorbing a single crystal substrate by evaporating a flow of molecules consisting of the constituent elements of the crystal, or molecular beams, from an ejection cell and colliding with the substrate surface. This is a method of epitaxially growing crystals with aligned crystal axes.

第1図は分子線結晶成長装置の基本的な構成を
示すもので真空蒸着装置と異るところは超高真空
を必要とすること、基板上に最高の効率でエピタ
キシヤル成長が行われるように基板温度が選ばれ
ること、結晶を構成する各の成分元素を蒸発する
ための分子線源を備え、その蒸発速度分布がコン
トロールされていることなどである。
Figure 1 shows the basic configuration of a molecular beam crystal growth system.It differs from a vacuum evaporation system in that it requires an ultra-high vacuum and is designed to perform epitaxial growth on the substrate with the highest efficiency. The substrate temperature is selected, a molecular beam source is provided to evaporate each component element that makes up the crystal, and the evaporation rate distribution is controlled.

すなわち第1図においてチヤンバ1内の真空度
は10-10torr程度の超高真空度に保持されて蒸発
分子の平均自由行程を充分に大きくし分子相互の
衝突の影響を無視できるようになつている。
In other words, in Figure 1, the degree of vacuum in chamber 1 is maintained at an ultra-high degree of vacuum of about 10 -10 torr, so that the mean free path of the evaporated molecules is made sufficiently large so that the effects of collisions between molecules can be ignored. There is.

次に分子線源を構成する複数の噴出セル2,3
(この図の場合2個)から成分元素の分子を適当
な比率で蒸発させこれをウエハ4の表面に付着さ
せることにより薄膜結晶をエピタキシヤル成長せ
しめる。
Next, a plurality of ejection cells 2 and 3 that constitute the molecular beam source
Molecules of component elements (two in this figure) are evaporated at an appropriate ratio and attached to the surface of the wafer 4, thereby growing a thin film crystal epitaxially.

例えばガリウム砒素(GaAs)を成長させる例
について云えばガリウム分子(Ga)を蒸発させ
る噴出セル2と砒素分子(As,As2,As4)を蒸
発させる噴出セル3の加熱温度を前者については
1000〜1050℃後者については300〜330℃とGaAs
の組成成分比に合わせて蒸気圧を調節し一方
GaAsからなるウエハ4の温度をこの例の場合
600〜650℃に維持して単結晶が効率良く成長でき
るようにしている。
For example, in the case of growing gallium arsenide (GaAs), the heating temperature of the ejection cell 2 that evaporates gallium molecules (Ga) and the ejection cell 3 that evaporates arsenic molecules (As, As 2 , As 4 ) is
1000-1050℃ for the latter 300-330℃ and GaAs
While adjusting the vapor pressure according to the composition ratio of
In this example, the temperature of wafer 4 made of GaAs is
The temperature is maintained at 600-650°C to allow efficient growth of single crystals.

すなわち噴出セル2,3より蒸発飛来してくる
各元素の分子線はウエハ4に衝突するがこの際成
分元素によつて附着効率が違い効率の高いものも
あれば極めて低いものもある。それで成分元素が
必要な組成比で付着しまた安定した格子位置に収
まるように必要なエネルギーを与えてある。
That is, the molecular beams of each element that evaporate and fly from the ejection cells 2 and 3 collide with the wafer 4, but at this time, the deposition efficiency differs depending on the component element, and some have high efficiency while others have very low efficiency. Therefore, the necessary energy is applied so that the component elements adhere in the required composition ratio and are settled in stable lattice positions.

本発明はかゝる分子線結晶成長方法を用いて凹
凸のある基板面上に均一な不純物濃度分布をもつ
結晶をエピタキシヤル成長させる方法に関するも
のである。
The present invention relates to a method of epitaxially growing a crystal having a uniform impurity concentration distribution on an uneven substrate surface using such a molecular beam crystal growth method.

(c) 従来技術と問題点 分子線結晶成長方法により結晶成長を行う場
合、構成元素数に等しい噴出セルを用意し、これ
より分子線を基板に投射しているがこの理由は先
に記したように各成分元素の蒸気圧を調節して目
的の組成比をもつ単結晶を成長させるためであ
る。
(c) Prior art and problems When crystal growth is performed using the molecular beam crystal growth method, ejection cells equal in number to the number of constituent elements are prepared, and molecular beams are emitted from these cells onto the substrate.The reason for this is described above. This is to grow a single crystal having a desired composition ratio by adjusting the vapor pressure of each component element.

さてGaAsのような化合物半導体に不純物元素
をドーパントとして含有させて電子電導型(N
型)或は正孔電導型(P型)半導体を分子線結晶
成長法によりエピタキシヤル成長させる場合、従
来は第2図に示すように結晶成分元素の噴出セル
2,3に隣接してドーパント用の噴出セル5が設
けられこれにより各元素の分子線6をウエハ4に
照射して行つていた。
Now, by incorporating an impurity element as a dopant into a compound semiconductor such as GaAs, an electronically conductive type (N
When epitaxially growing a hole-conducting type (type) or hole-conducting type (P-type) semiconductor by molecular beam crystal growth, conventionally, as shown in FIG. An ejection cell 5 was provided to irradiate the wafer 4 with molecular beams 6 of each element.

こゝで噴出セル2,3,5はグラフアイト或は
窒化硼素(BN)からなりタンタル(Ta)或は
タングステン(W)からなるヒータを用いて抵抗
加熱することにより中に充填した各元素を噴出孔
(オリフイス)7より分子線として噴出せしめる。
Here, the ejection cells 2, 3, and 5 are made of graphite or boron nitride (BN), and each element filled therein is heated by resistance heating using a heater made of tantalum (Ta) or tungsten (W). The molecular beam is ejected from the ejection hole (orifice) 7.

こゝでエピタキシヤル成長を行わせるウエハ4
は分子線6に対し低速回転するような構成がとら
れ分子線6がウエハ4に一様に投射されるように
配慮されているが、ウエハ4の固定位置が第2図
に示すように母体結晶構成元素の噴出セル2,3
に近くドーパント元素の噴出セル5より離れて設
けられている場合がある。
Wafer 4 on which epitaxial growth is performed
is configured to rotate at a low speed with respect to the molecular beam 6, so that the molecular beam 6 is uniformly projected onto the wafer 4, but the fixed position of the wafer 4 is fixed to the base body as shown in Ejection cells 2 and 3 of crystal constituent elements
In some cases, the dopant element ejection cell 5 is provided close to the dopant element ejection cell 5 .

かゝる場合ウエハ4の表面が平坦な場合は問題
はないがデバイス形成のためエツチングなどの加
工により凹凸のある表面が作られており、この上
に分子線結晶を成長させる場合は凹凸のために影
になる部分を生ずし、総べての分子線が均一にウ
エハ表面に達しない。
In such a case, there would be no problem if the surface of the wafer 4 was flat, but an uneven surface is created by processing such as etching for device formation, and when a molecular beam crystal is grown on this surface, the uneven surface may cause problems. This results in shadowed areas on the surface of the wafer, and all molecular beams do not reach the wafer surface uniformly.

こゝでドーパント元素が到達しない部分は、そ
の存在量が少いため高抵抗となりそのため半導体
デバイスの歩留り低下の原因となつていた。
The portions where the dopant elements do not reach have high resistance due to the small amount of dopant elements present, which causes a decrease in the yield of semiconductor devices.

(d) 発明の目的 本発明はたとえ半導体ウエハの表面に凹凸があ
る場合でも均一な不純物分布をもつ半導体結晶を
成長させることが可能な分子線結晶成長法を提供
するにある。
(d) Object of the Invention The object of the present invention is to provide a molecular beam crystal growth method capable of growing a semiconductor crystal with a uniform impurity distribution even if the surface of a semiconductor wafer is uneven.

(e) 発明の構成 本発明の目的は、分子線材料に不純物を添加
し、該分子線材料を蒸発させて得た分子線を基板
上に照射することにより、該基板上に所定の量の
不純物を含有してなる成長膜を形成することで達
成できる。
(e) Structure of the Invention An object of the present invention is to add impurities to a molecular beam material, evaporate the molecular beam material, irradiate the substrate with the molecular beam, and thereby apply a predetermined amount of the molecular beam onto the substrate. This can be achieved by forming a grown film containing impurities.

(f) 発明の実施例 第3図および第4図はヘテロ接合構造をもつウ
エハをメサエツチしGaAsとN−AlGaAsとの界
面が露出している状態のものにオーミツクコンタ
クト用のN+−GaAsを分子線結晶成長法を用いて
形成する場合の実施例である。
(f) Embodiments of the Invention Figures 3 and 4 show wafers with a heterojunction structure that are mesa-etched to expose the interface between GaAs and N - AlGaAs. This is an example in which the crystal structure is formed using a molecular beam crystal growth method.

図において高抵抗GaAsウエハ8の上にはN型
のAlGaAs9がエピタキシヤル成長されて接合し
ているが、両者の禁止帯幅が異るため、この界面
10の近傍には2次元電子ガス11が存在してい
る。
In the figure, N-type AlGaAs 9 is epitaxially grown and bonded onto a high-resistance GaAs wafer 8, but since the forbidden band widths of the two are different, a two-dimensional electron gas 11 is generated near this interface 10. Existing.

かゝるウエハをメサエツチしこの界面10の露
出している部分からオーミツクコンタクトをとる
ために低抵抗N+−GaAs層12を分子線を用いて
形成する必要がある。この場合、均一な特性をも
つN+−GaAs層をメサエツチされたデバイス形成
位置に成長させることが必要である。
It is necessary to mesa-etch such a wafer and form a low-resistance N + -GaAs layer 12 using molecular beams in order to establish ohmic contact from the exposed portion of this interface 10. In this case, it is necessary to grow an N + -GaAs layer with uniform properties at the mesa-etched device formation locations.

然し乍ら第2図に示すようにドーパント用噴出
セル5が他の噴出セル2,3より離れて存在し、
またメサエツチされたウエハ8の傾斜が大きな場
合は分子線の到達し難い影の部分を生ずる。第3
図はこれを誇張して示すものでGaおよびAsの分
子線13とドーパントである錫(Sn)の分子線
14の照射角度および方向が異るためウエハ8が
回転していてもN+−GaAs層12で影となつてい
た部分16はSnの濃度分布が不均一で部分的に
高抵抗な層となる。
However, as shown in FIG. 2, the dopant ejection cell 5 is located apart from the other ejection cells 2 and 3,
Furthermore, if the slope of the mesa-etched wafer 8 is large, a shadowed area is created that is difficult for the molecular beam to reach. Third
The figure shows this in an exaggerated manner. Because the irradiation angles and directions of the Ga and As molecular beams 13 and the dopant tin (Sn) molecular beams 14 are different, even if the wafer 8 is rotating, N + -GaAs The shaded portion 16 of the layer 12 has a non-uniform Sn concentration distribution and is partially high in resistance.

本発明はGaの噴出セルの中にドーパントを一
定の比率に混和するものでN+−GaAsを得んとす
る本実施例の場合Gaに対しSnを105:1のモル比
になるようにに混合した。
In the present invention, a dopant is mixed at a certain ratio in a Ga ejection cell, and in this example where N + -GaAs is to be obtained, the molar ratio of Sn to Ga is 10 5 :1. mixed with.

こゝでGa噴出セルは1050℃でまたAs噴出セル
は330℃に加熱してそれぞれの分子線を発生させ
毎時1μmの速さでN+−GaAs層を形成させた。
Here, the Ga ejection cell was heated to 1050°C and the As ejection cell was heated to 330°C to generate respective molecular beams and form an N + -GaAs layer at a rate of 1 μm/hour.

なおこの場合GaAsウエハ8は560℃に加熱す
ると共に5γpmの速度で回転させた。
In this case, the GaAs wafer 8 was heated to 560° C. and rotated at a speed of 5γpm.

第4図はGa,AsおよびSnを含んだ分子線15
の照射状態を示している。
Figure 4 shows molecular beam 15 containing Ga, As and Sn.
shows the irradiation status.

以上のように本発明を実施する場合は母体結晶
用分子線とドーパント用分子線が同じ位置から発
生するためウエハ表面に劇しい凹凸が存在して分
子線の到達し難い影が生ずる場合でも不純物分布
の均一な結晶膜を得ることができる。
As described above, when carrying out the present invention, the molecular beam for the host crystal and the molecular beam for the dopant are generated from the same position, so even if the wafer surface has significant unevenness and a shadow is created that is difficult for the molecular beam to reach, impurities can be detected. A crystal film with uniform distribution can be obtained.

(g) 発明の効果 本発明の実施によりメサエツチなどの加工によ
り凹凸のあるウエハ上にも分子線結晶法を用いド
ーパントの分布が一様なエピタキシヤル成長が可
能となり、これにより製造歩留りを向上すること
ができる。
(g) Effects of the invention By carrying out the present invention, it becomes possible to perform epitaxial growth with uniform dopant distribution using the molecular beam crystallization method even on wafers that have irregularities due to processing such as mesa etching, thereby improving manufacturing yield. be able to.

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

第1図は分子線結晶成長装置の構成図、第2図
は噴出セルとウエハとの位置関係の説明図、第3
図および第4図はメサエツチ面に対する分子線結
晶の成長状態説明図である。 図において、2,3,5は噴出セル、4はウエ
ハ、6,13,14,15は分子線、8はGaAs
ウエハ、12はN+−GaAs層。
Figure 1 is a configuration diagram of the molecular beam crystal growth apparatus, Figure 2 is an explanatory diagram of the positional relationship between the ejection cell and the wafer, and Figure 3 is an illustration of the positional relationship between the ejection cell and the wafer.
This figure and FIG. 4 are explanatory views of the growth state of molecular beam crystals on the mesa etched plane. In the figure, 2, 3, and 5 are ejection cells, 4 is a wafer, 6, 13, 14, and 15 are molecular beams, and 8 is GaAs.
Wafer 12 is an N + -GaAs layer.

Claims (1)

【特許請求の範囲】 1 結晶成分元素を含む分子線材料を噴出セル内
に導入し、該分子線材料を蒸発させて得た分子線
を該基板上に照射することにより該基板上に結晶
成長を行う分子線結晶成長方法において、 前記分子線材料に不純物を添加し、 該不純物を添加した分子線材料を蒸発させて得
た分子線を前記基板上に照射することにより、該
基板上に所定の量の不純物を含有してなる成長膜
を形成することを特徴とする分子線結晶成長方
法。
[Scope of Claims] 1. A molecular beam material containing a crystal component element is introduced into an ejection cell, and the molecular beam obtained by evaporating the molecular beam material is irradiated onto the substrate to cause crystal growth on the substrate. In the molecular beam crystal growth method, impurities are added to the molecular beam material, and the substrate is irradiated with a molecular beam obtained by evaporating the impurity-added molecular beam material, thereby forming a predetermined pattern on the substrate. A molecular beam crystal growth method characterized by forming a grown film containing an amount of impurities.
JP57070991A 1982-04-27 1982-04-27 Method for growth of molecular beam crystallization Granted JPS58188128A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57070991A JPS58188128A (en) 1982-04-27 1982-04-27 Method for growth of molecular beam crystallization

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57070991A JPS58188128A (en) 1982-04-27 1982-04-27 Method for growth of molecular beam crystallization

Publications (2)

Publication Number Publication Date
JPS58188128A JPS58188128A (en) 1983-11-02
JPH0315333B2 true JPH0315333B2 (en) 1991-02-28

Family

ID=13447513

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57070991A Granted JPS58188128A (en) 1982-04-27 1982-04-27 Method for growth of molecular beam crystallization

Country Status (1)

Country Link
JP (1) JPS58188128A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20010052323A1 (en) * 1999-02-17 2001-12-20 Ellie Yieh Method and apparatus for forming material layers from atomic gasses

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4898775A (en) * 1972-03-28 1973-12-14
GB1574525A (en) * 1977-04-13 1980-09-10 Philips Electronic Associated Method of manufacturing semiconductor devices and semiconductor devices manufactured by the method
JPS5443351A (en) * 1977-09-13 1979-04-05 Mitsubishi Electric Corp Hot water apparatus
JPS5635409A (en) * 1979-08-29 1981-04-08 Nec Corp Method of doping impurity into compound semiconductor
JPS57115821A (en) * 1981-01-09 1982-07-19 Matsushita Electric Ind Co Ltd Manufacture of semiconductor device

Also Published As

Publication number Publication date
JPS58188128A (en) 1983-11-02

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