JPS5856323A - Manufacture of semiconductor substrate - Google Patents
Manufacture of semiconductor substrateInfo
- Publication number
- JPS5856323A JPS5856323A JP15437881A JP15437881A JPS5856323A JP S5856323 A JPS5856323 A JP S5856323A JP 15437881 A JP15437881 A JP 15437881A JP 15437881 A JP15437881 A JP 15437881A JP S5856323 A JPS5856323 A JP S5856323A
- Authority
- JP
- Japan
- Prior art keywords
- substrate
- growth
- epitaxial
- sio2 film
- single crystal
- 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
Links
- 239000000758 substrate Substances 0.000 title claims abstract description 31
- 239000004065 semiconductor Substances 0.000 title claims abstract description 8
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- 239000013078 crystal Substances 0.000 claims abstract description 23
- 238000000034 method Methods 0.000 claims abstract description 19
- 238000001312 dry etching Methods 0.000 abstract description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 8
- 229910052681 coesite Inorganic materials 0.000 abstract 4
- 229910052906 cristobalite Inorganic materials 0.000 abstract 4
- 239000000377 silicon dioxide Substances 0.000 abstract 4
- 235000012239 silicon dioxide Nutrition 0.000 abstract 4
- 229910052682 stishovite Inorganic materials 0.000 abstract 4
- 229910052905 tridymite Inorganic materials 0.000 abstract 4
- 229910052581 Si3N4 Inorganic materials 0.000 abstract 3
- 230000002349 favourable effect Effects 0.000 abstract 2
- 238000001459 lithography Methods 0.000 abstract 1
- 238000005516 engineering process Methods 0.000 description 11
- 230000007547 defect Effects 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 101100434016 Caenorhabditis elegans gar-2 gene Proteins 0.000 description 1
- 241000238557 Decapoda Species 0.000 description 1
- 241001092070 Eriobotrya Species 0.000 description 1
- 235000009008 Eriobotrya japonica Nutrition 0.000 description 1
- 241001461123 Matrona Species 0.000 description 1
- 208000032825 Ring chromosome 2 syndrome Diseases 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 230000003071 parasitic effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 238000003325 tomography Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02365—Forming inorganic semiconducting materials on a substrate
- H01L21/02367—Substrates
- H01L21/0237—Materials
- H01L21/02373—Group 14 semiconducting materials
- H01L21/02381—Silicon, silicon germanium, germanium
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02365—Forming inorganic semiconducting materials on a substrate
- H01L21/02518—Deposited layers
- H01L21/02521—Materials
- H01L21/02524—Group 14 semiconducting materials
- H01L21/02532—Silicon, silicon germanium, germanium
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02365—Forming inorganic semiconducting materials on a substrate
- H01L21/02612—Formation types
- H01L21/02617—Deposition types
- H01L21/0262—Reduction or decomposition of gaseous compounds, e.g. CVD
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02365—Forming inorganic semiconducting materials on a substrate
- H01L21/02612—Formation types
- H01L21/02617—Deposition types
- H01L21/02636—Selective deposition, e.g. simultaneous growth of mono- and non-monocrystalline semiconductor materials
- H01L21/02639—Preparation of substrate for selective deposition
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L29/00—Semiconductor devices specially adapted for rectifying, amplifying, oscillating or switching and having potential barriers; Capacitors or resistors having potential barriers, e.g. a PN-junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof ; Multistep manufacturing processes therefor
- H01L29/02—Semiconductor bodies ; Multistep manufacturing processes therefor
- H01L29/06—Semiconductor bodies ; Multistep manufacturing processes therefor characterised by their shape; characterised by the shapes, relative sizes, or dispositions of the semiconductor regions ; characterised by the concentration or distribution of impurities within semiconductor regions
- H01L29/0603—Semiconductor bodies ; Multistep manufacturing processes therefor characterised by their shape; characterised by the shapes, relative sizes, or dispositions of the semiconductor regions ; characterised by the concentration or distribution of impurities within semiconductor regions characterised by particular constructional design considerations, e.g. for preventing surface leakage, for controlling electric field concentration or for internal isolations regions
- H01L29/0642—Isolation within the component, i.e. internal isolation
- H01L29/0649—Dielectric regions, e.g. SiO2 regions, air gaps
- H01L29/0653—Dielectric regions, e.g. SiO2 regions, air gaps adjoining the input or output region of a field-effect device, e.g. the source or drain region
Landscapes
- Engineering & Computer Science (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Computer Hardware Design (AREA)
- Manufacturing & Machinery (AREA)
- Ceramic Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は絶縁@餉域をもり単iti墨基碩上Kltな高
品質のSムエビタキシャル層をJlSl沢的に成長によ
多形成する゛半導体基板の#!遣方法に関するものであ
る。DETAILED DESCRIPTION OF THE INVENTION The present invention is directed to forming a high-quality S-layer with an insulating layer by growing it in large quantities on a semiconductor substrate. It is related to the method of sending.
通常、MOSデバイスにお^て社Sムエビタ中シャル層
は用いられておらず、tt、&板そのものにイオンイン
クラテーシ曹ン法や不純拡散法を用いて所望の伝導11
(P型又はN11)の層が形成され、それぞれ能動領域
1分離領域などが形成されている0分離領域形成の一方
法として部分酸化法(Local 0xidat io
n of 8i1icon −・−L O008法)が
良く由いられてbる。Normally, a MOS layer is not used in MOS devices, and the desired conduction 11 is achieved by using the ion increment method or impurity diffusion method on the tt, & board itself.
A partial oxidation method (Local Oxidatio
n of 8i1icon -・-LO008 method) is often used.
最近では、mLslデバイス指向の微細加工技術の研究
開発か進み、サブミクロンの加工がUV篇元、越子ビー
ム、X@等を用めたリング2フイ技術とドライエツチン
グ技術の進歩によ)容易にできるようになってbる。し
かしながら部分酸化法を用いたMOSデバイスでは、種
々の不都合が生じてきて^る。すなわち微細加工技術が
先行し部分酸化法の制鉤技術が問題となりつつある。そ
れは基板を酸化する場合にはb”jA換をマスクとして
単結晶領域が熱酸化される。しかしその酸化されたM[
ffiは半楕円形となル所要の能動領域にはみ出し、又
隣接する能動領域との間隔も大きくなることとな)、デ
バイスの高密度化、高速化及び設計上も問題となる。Recently, research and development of microfabrication technology for mLsl devices has progressed, and submicron machining has become easier due to advancements in ring-2-fi technology and dry etching technology using UV beams, Etsuko beams, X@, etc. I am now able to do this. However, MOS devices using the partial oxidation method have various disadvantages. In other words, microfabrication technology has taken the lead, and partial oxidation technology is becoming a problem. When oxidizing the substrate, the single crystal region is thermally oxidized using the b''jA conversion as a mask.However, the oxidized M[
The ffi has a semi-elliptical shape and protrudes into the required active area, and the distance between adjacent active areas also increases), which poses problems in terms of higher density, higher speed, and design of the device.
他の問題としては、鍔えばC−MO8デバイスにおいて
1通常の基板を部分鍾化し分m領域を形成し、それぞれ
PチャンネルとNチャンネルトランジスタを形成した場
合に、デバイスの動作中に大きな外米雑音感圧が、入力
又は出力端子から内部回路に入ると%電源端子から接地
端子へ赦(HAから数十mムもの14常電流が流れる現
象(ラフ、チアラグ)が起る、等の問題がある。Another problem is that in a C-MO8 device, when a normal substrate is partially plated to form m regions and P-channel and N-channel transistors are formed respectively, a large amount of external noise occurs during device operation. If pressure sensing enters the internal circuit from the input or output terminal, there are problems such as a phenomenon (rough, cheer lag) in which a normal current of several tens of mm flows from the HA to the ground terminal. .
以上のように従来技術でのML)8デバイス構造では高
vli寂化への障害があII、このことL寄生容量を増
大させ、デバイスOa速化の障害と1なる。As described above, in the conventional ML)8 device structure, there is an obstacle to high vli, which increases the L parasitic capacitance and becomes an obstacle to increasing the device Oa speed.
さらに先に述べたように構造上^當電流が處れる等の欠
点を有して−る。Furthermore, as mentioned earlier, it has structural disadvantages such as the electric current being damaged.
本発面の目的は半導体基板その鳴のKl!allii@
域を形成することなく、絶縁Jig(f8j鳩又は8ム
洩)をマスクとして%旧エビメキシャル成長層を選択的
に半導体基板上に形成し、従来接輪0欠点をおぎないデ
バイスI?#性の向上をねらおうとすゐものである。The purpose of this discovery is the sound of semiconductor substrates! allii@
By selectively forming an old evimexial growth layer on a semiconductor substrate using an insulating Jig (F8J dove or 8M leak) as a mask without forming an area, a device I? #It is something that aims to improve sexuality.
その構成要件としては81単結晶基11に杷鑞纒を形成
し、リングラフィ技術とドライエツチング技mt−用い
サブミクロンの微細加工を施す。この基板を減圧エピタ
キシャル成長炉にセットし、19j鳩Cl 、−1〜系
を用i減圧下で成長し、半導体基板上又は絶縁基板上に
もわた9選択的に単結晶膜を形成しようとするものであ
る。Its constituent elements include forming a loquat on the 81 single crystal base 11, and subjecting it to submicron microfabrication using phosphorography technology and dry etching technology mt-. This substrate is set in a reduced pressure epitaxial growth furnace, and 19j Cl, -1~ system is grown under reduced pressure to selectively form a single crystal film over a semiconductor substrate or an insulating substrate. It is.
btu晶の選択成長技術の公知列としては1)ジャーナ
ル・オブ・エレクトロケミカル ンサイテ4 (J−h
lectrochem−8oc−、VoL、120.M
L5 、P−664゜1973)及び2)ジャーナル・
オプ・エレクトロケミカル ソサイテ4 (J伊kle
ctrochan−8ac−。Publicly known columns on selective growth techniques for btu crystals include 1) Journal of Electrochemical Research 4 (J-h
lectrochem-8oc-, VoL, 120. M
L5, P-664゜1973) and 2) Journal
Op Electrochemical Society 4 (JIkle
ctrochan-8ac-.
VOL、122.醜12.l’−1666,1975)
があ)、杓σ者では5il14−)ICI−)1.系に
! D I 150℃テBtus @4f マスクとし
て、別基板の(111)、(110)、(115)と(
100)面t−選び成長したとζろ、エピタキシャル表
面の平滑性は(−110)面が最も艮<s (11t
)血と(115)面を用いた場合Klま良くなり0さら
に(115)面t−用いた場合のエピタキシャル層では
下地パターンとエピタキシャル層のパターンがずれるパ
ターン変形が大きく、問題でおることが記載されている
。後者では基板に巾10〜20^mで深さが〜1100
aの溝を形成し、基板上に何ら絶縁膜を形成することな
しに%溝部だけに選択的に81単結晶を棚込み成長しよ
うとするもので、Siソー ス(!: L テ8i K
、8iHC1s 、5iH1cl、 ト8 i C1
4K加えて1(Clガスを導入して行うものである。選
択成長のポイントはC3/8iの滴縦比が重曹であるこ
とが記載されてbる。又8iにcl、 −)1Q 1−
H,系では基板方位t” (110)面に選び1080
℃で試みたが、平滑な表面が得られなりことが述べであ
る。VOL, 122. Ugly 12. l'-1666, 1975)
Yes), 5il14-)ICI-)1. To the system! D I 150℃Te Btus @4f As a mask, (111), (110), (115) and (
When grown selectively on the 100) plane t-plane, the smoothness of the epitaxial surface is the highest on the (-110) plane.
) It is stated that when the (115) plane is used, the Kl is better. Furthermore, when the (115) plane is used, the epitaxial layer has a large pattern deformation in which the underlying pattern and the pattern of the epitaxial layer are misaligned, which is a problem. has been done. In the latter case, the substrate has a width of 10 to 20 m and a depth of ~1100 m.
This method aims to form a groove of 81 and selectively grow the 81 single crystal only in the groove without forming any insulating film on the substrate.
, 8iHC1s, 5iH1cl, 8 i C1
4K plus 1 (This is done by introducing Cl gas. It is stated that the point of selective growth is that the droplet aspect ratio of C3/8i is baking soda.Also, 8i has Cl, -) 1Q 1-
In the H, system, the substrate orientation is t” (110), and 1080
Although I tried it at ℃, I was unable to obtain a smooth surface.
又BiaN、I!をマスクとした選択的な81エビタキ
クヤル成長技術の公知ガとして3)ザ・エレクトロケミ
カル・ノサイティ・ホールミーティング。BiaN, I! 3) The Electrochemical Nocy Hall Meeting as a known method of selective 81 Ettakikuyaru growth technology using a mask.
10月、1969.アブストラクト81181.476
頁(T、he El ectrochem@8oc−に
’a1 トMeet ing、Oct 。October, 1969. Abstract 81181.476
Page (T, he El electrochem @ 8oc-Meeting, Oct.
1969、ムbs、ML181.P−476)b 4)
ジャバフ−ジャーナル・アプライド・フイズイクス・ポ
リ、ラム10,19フ1年、 1675頁(Japan
−J、Appl。1969, MUBS, ML181. P-476) b 4)
Javaf-Journal Applied Physics Poly, Ram 10, 19f 1, p. 1675 (Japan
-J, Appl.
Phy s −10(1971) e PI375 )
とあるが、 Sj単結晶基板上に加工された8isべ展
は熱的、化学的に強いが、l:li、N、自体が真性応
力をもつために熱グnセスを経れば8!基板又は選択8
iエピタキシヤル領域に、Hえば転位等の結晶欠陥を導
入し易いことはよく知られて−るところである。Phys-10 (1971) e PI375)
However, the 8is base fabricated on the Sj single crystal substrate is thermally and chemically strong, but since l:li and N themselves have intrinsic stress, if they undergo thermal stress, they will become 8! Substrate or selection 8
It is well known that crystal defects such as dislocations are easily introduced into the i-epitaxial region.
又S&基板上には通常S1嶋−と8i、N、験の二層構
造が用いられておプ、歪補償を行う厚さが1)9欠陥が
発生しな一工夫もされてbる。In addition, a two-layer structure of S1, N, and N is usually used on the S& substrate, and the thickness for strain compensation has been devised to prevent the occurrence of defects.
以上のように8i結晶の選択区長の公知例では(111
)面を用いても結晶表面の千′P#直が悪く。As mentioned above, in the known example of the selection section length of 8i crystal (111
) plane, the crystal surface has poor alignment.
81鳩Cl、−)ICI−鶴系を用iても結晶性が良く
ない等の問題かある。又絶縁膜として* Sin′N4
−のみを用いると、熱プロセスで結晶欠陥を導入し易い
等の不利な点がある。Even if 81 HatoCl, -) ICI-Tsuru series is used, there are problems such as poor crystallinity. Also, as an insulating film *Sin'N4
If only - is used, there are disadvantages such as easy introduction of crystal defects during thermal process.
本発明で社従来の選択成長技術の不備な点を改良できる
もので、そのキーポイントはbi基板上の開口したS
i (J* 11M面に84.N、を形成し、 8i)
4CI冨−に系で、減圧下で選択成長を行うことである
。The present invention can improve the deficiencies of the conventional selective growth technology, and the key point is that the open S
i (84.N is formed on the J* 11M plane, 8i)
Selective growth is carried out under reduced pressure in a 4CI-rich system.
減圧下で81エビ!キシヤル成長を行うとその表面が平
滑になる理由社、減圧エビタキ7ヤル法の特徴である/
’メタン形が起らない仁とと関連し成長のメカニズムが
異なるものと考えられる。しかし明確な理由は今のとこ
ろ分ってhない。81 shrimp under reduced pressure! The reason why the surface becomes smooth when the surface is grown
'It is thought that the growth mechanism is different from that of kernels in which methane formation does not occur. However, the exact reason is not known at this time.
次に本発明を説明するための実mガについて述べる。Next, a real model will be described for explaining the present invention.
実施同一1
3#φの8i基板の面方位がガえは(111)面を迦び
%8i0.l[を〜5000A堆積し、リングラフィ技
術とドライエツチング技術を用いて、その線巾をα5〜
3.0μmとなる微細加工を施す、これらの基板をシリ
ンダ薯エピタキシャル成長炉にセットする。Same implementation 1 The plane orientation of the 8i substrate with 3#φ is (111) plane and %8i0. Deposit ~5000A of l[, and use phosphorography and dry etching techniques to increase the line width to α5~
These substrates, which are microfabricated to 3.0 μm, are set in a cylinder epitaxial growth furnace.
基板温度を〜120G℃としプレベーキングを15分行
う、さらに基板温度を1080℃として、lも〜1、0
017分、 8i)4101 @ : 500 c c
/分、成長圧カニ80’i”o r rの条件で2.0
分成長すると〜1.0μmの81結晶−が成長する。The substrate temperature was set to ~120G°C, pre-baking was performed for 15 minutes, and the substrate temperature was set to 1080°C, and l was also ~1,0.
017 minutes, 8i) 4101 @: 500 cc
/min, growth pressure crab 2.0 under the condition of 80'i"o r r
81 crystals of ~1.0 μm grow.
Rrfi状態は金属干渉顕微鏡(ノマルスキー)でその
断面は走査mat子顕微@(8EM)で観証できる。こ
の場合のJエピタキシャル成長lTh0l膚面の模式図
をaK1因に示す。The Rrfi state can be observed using a metal interference microscope (Nomarski), and its cross section can be observed using a scanning matron microscope @ (8EM). A schematic diagram of the J epitaxial growth lTh0l skin surface in this case is shown in aK1.
8i*結晶基板1、k絶縁i12を形成し、この上に3
の8i映が形成される。高温成長のため、溝底部の3i
q−側面がSi結晶に食われていることが分った。これ
は8i0,1111が#細なため、熱プロセスを経るに
つれ、映が剥離する等のデバイス作製上間亀となる。こ
れt−縞1図の4,4′に示す。8i*crystal substrate 1, k insulation i12 are formed, and 3
An 8i image is formed. 3i at the bottom of the groove due to high temperature growth.
It was found that the q-side was eaten by the Si crystal. This is because 8i0 and 1111 are thin, so as the film undergoes a thermal process, the film peels off, resulting in problems during device fabrication. This is shown at 4 and 4' in Figure 1 of the t-stripe.
実施ガー2
3″−のδi暴板の面方位が囲えば(111)面を選び
h ”!LJtll14t〜5000A堆積し、リン
グラフィ技術とドライエツチング技術を用いてその線巾
をα5〜3.0μmとなる微細加工を施す、さらに開口
された!iiCJm IilliOlillmK 8i
sNa ’IIIktj41idkfb1m下td実施
内−1と同じ条件1080℃、BQTorr、2.0分
成長で1.0ttrn cD 8i結晶映が成長する。If the plane orientation of the δi plate of Implementation Gar 2 3″- is enclosed, select the (111) plane and h ”! LJtll14t ~ 5000A was deposited, and microfabricated using phosphorography technology and dry etching technology to make the line width α5 ~ 3.0 μm, and further opened! iiCJm IilliOlillmK 8i
A 1.0ttrn cD 8i crystal was grown under the same conditions as sNa 'IIIktj41idkfb1m lower td implementation-1 at 1080°C, BQTorr, and 2.0 minutes of growth.
81工ピタキシヤル成長層の表面状態は金属干渉顕微−
で、その断面は走査型−子顕微鏡で観察できる。この場
合のSiエピタキシャル成長層の断面の模式図tM2図
に示す。The surface condition of the 81st pitaxial growth layer was observed using a metal interference microscope.
Its cross section can be observed using a scanning microscope. A schematic cross-sectional view of the Si epitaxial growth layer in this case is shown in Figure tM2.
8轟θ黛w面に熱的に強い8isNall14があるた
めに111図に見られるような8i結晶にSi(%眼が
食われる現象は見られず、溝部の形状はエピタキシャル
成長前と変らず、シャープであった。Because there is a thermally strong 8isNall14 on the 8i crystal on the 8i crystal, as seen in Figure 111, the phenomenon of Si(%) being eaten away is not observed, and the shape of the groove remains unchanged and sharp as before epitaxial growth. Met.
絽2図の1は8i単結晶基板、 2Fi別O雪瞑、3は
エピタキシャル膜で、5.5’は840*lK上の岨エ
ピタキシャル層で、6はsi、N、験である。In Fig. 2, 1 is an 8i single crystal substrate, 2 is an epitaxial film, 3 is an epitaxial film, 5.5' is an epitaxial layer on 840*1K, and 6 is a Si, N, and E.
以上のように81基板の面方位を岡えば(111)に・
選び、4碁板上の開口した8iへm側面を81゜Na
mで保藤しb1鵬C5,−鳩系を用い減圧下で成長を行
えば、その表面が平滑で良好な結晶性を有する選択81
工ピタキシヤル層が形成てきるものである。As mentioned above, if the plane orientation of the 81 substrate is changed, it becomes (111).
Select and move the m side to the open 8i on the 4 Go board at 81°Na.
If growth is performed under reduced pressure using Yato and B1PengC5, - Hato systems, the surface will be smooth and have good crystallinity.81
This is due to the formation of a pitaxial layer.
本発明の夾總−による第2図の5.5′のようKll!
!縁基板上にも成長することは、この領域にソース、ド
レインを形成することができ%異常*aの発生(ラッチ
アップをも防止できる。又部分に化法による一密夏化の
不利な点をカバーし、シャープなジャンクシ璽ン形成が
できるため、高田度で、4速なM(JS又はC−MU8
デバイスを形成できるものである。さらにこの選択成長
技術の利点としては、多層配線のためのコンタクトネー
ルの埋込み成長技術としても応用でき、配線の平滑化を
可能ならしめデバイスの信頼性を向上させることもでき
る0本発明ではMO8デノ(イスにつ匹テ述べたが、パ
イボーラデノ(イスにも応用できることは−うまでもな
い。According to the combination of the present invention, as shown in 5.5' in FIG. 2, Kll!
! By growing on the edge substrate, the source and drain can be formed in this region, and the occurrence of % abnormality *a (latch-up) can also be prevented.Also, there is a disadvantage of dense summerization due to the partial chemical method. , and can form a sharp junction.
A device can be formed. Furthermore, the advantage of this selective growth technique is that it can be applied as a buried growth technique for contact nails for multilayer wiring, and it can also smooth the wiring and improve device reliability. I mentioned this about chairs, but it goes without saying that it can also be applied to chairs.
第1図は減圧エピタキシャル法で8LO@@をマスクと
して成長した場合の成長層断層の模式図。
謳2図は本発明によるfiI&面方位t−(111)面
とじ81ヘ−の開口部−面を5iaj’% kで保験し
減圧下でエピタキシャル成長した場合の成長階断面の模
式図。
1・・・81本結晶基板
2・・、8i(J、瞑
3・・・Siエピタキシャル成長層
4.4′・・・8iO1−の侵蝕部
5.5′−・絶縁膜上の81工ピタキシヤル層6.6′
・−5isべ暎FIG. 1 is a schematic diagram of the tomography of a grown layer when grown by the reduced pressure epitaxial method using 8LO@@ as a mask. Figure 2 is a schematic diagram of a growth step cross section when epitaxial growth is performed under reduced pressure while maintaining the fiI & plane orientation t-(111) plane binding 81 plane at 5iaj'% k according to the present invention. 1...81 crystal substrate 2..., 8i (J, medi 3...Si epitaxial growth layer 4.4'...8iO1- erosion part 5.5'--81 crystal epitaxial layer on insulating film 6.6′
・-5isbeyo
Claims (1)
、且つ開口された8i0.@の側壁に組−4[を堆積し
この膜をマスクとして単結晶基板上に別)iICl、ン
ースを用い、減圧下でその成長圧力が20〜200To
rrの範囲で成長することを特徴とする8ム単結晶−の
選択成長によシ形成することを特徴とする半導体基板の
製造方法。An 8i0. Deposit Group-4 on the sidewalls of @, and use this film as a mask on a single crystal substrate.
1. A method for manufacturing a semiconductor substrate, characterized in that the semiconductor substrate is formed by selective growth of an 8-μm single crystal, which is characterized by growth in the range of rr.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15437881A JPS5856323A (en) | 1981-09-29 | 1981-09-29 | Manufacture of semiconductor substrate |
US06/395,110 US4637127A (en) | 1981-07-07 | 1982-07-06 | Method for manufacturing a semiconductor device |
DE19823225398 DE3225398A1 (en) | 1981-07-07 | 1982-07-07 | SEMICONDUCTOR DEVICE AND METHOD FOR THEIR PRODUCTION |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15437881A JPS5856323A (en) | 1981-09-29 | 1981-09-29 | Manufacture of semiconductor substrate |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5856323A true JPS5856323A (en) | 1983-04-04 |
Family
ID=15582837
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP15437881A Pending JPS5856323A (en) | 1981-07-07 | 1981-09-29 | Manufacture of semiconductor substrate |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5856323A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6318668A (en) * | 1986-07-11 | 1988-01-26 | Canon Inc | Photoelectric transducer device |
JPS6376367A (en) * | 1986-09-18 | 1988-04-06 | Canon Inc | Photoelectric conversion device |
JPS63133615A (en) * | 1986-11-26 | 1988-06-06 | Fujitsu Ltd | Vapor growth method |
JPH01189914A (en) * | 1988-01-25 | 1989-07-31 | Sony Corp | Manufacture of semiconductor device |
US6503799B2 (en) * | 2001-03-08 | 2003-01-07 | Mitsubishi Denki Kabushiki Kaisha | Method of manufacturing semiconductor device |
-
1981
- 1981-09-29 JP JP15437881A patent/JPS5856323A/en active Pending
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6318668A (en) * | 1986-07-11 | 1988-01-26 | Canon Inc | Photoelectric transducer device |
JPS6376367A (en) * | 1986-09-18 | 1988-04-06 | Canon Inc | Photoelectric conversion device |
JPS63133615A (en) * | 1986-11-26 | 1988-06-06 | Fujitsu Ltd | Vapor growth method |
JPH01189914A (en) * | 1988-01-25 | 1989-07-31 | Sony Corp | Manufacture of semiconductor device |
US6503799B2 (en) * | 2001-03-08 | 2003-01-07 | Mitsubishi Denki Kabushiki Kaisha | Method of manufacturing semiconductor device |
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