JPH01181561A - Manufacture of semiconductor device - Google Patents

Manufacture of semiconductor device

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Publication number
JPH01181561A
JPH01181561A JP63003240A JP324088A JPH01181561A JP H01181561 A JPH01181561 A JP H01181561A JP 63003240 A JP63003240 A JP 63003240A JP 324088 A JP324088 A JP 324088A JP H01181561 A JPH01181561 A JP H01181561A
Authority
JP
Japan
Prior art keywords
silicon
conductivity type
oxygen
doped
amorphous
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
JP63003240A
Other languages
Japanese (ja)
Inventor
Toshihiko Hamazaki
浜崎 利彦
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.)
Toshiba Corp
Original Assignee
Toshiba Corp
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 Toshiba Corp filed Critical Toshiba Corp
Priority to JP63003240A priority Critical patent/JPH01181561A/en
Publication of JPH01181561A publication Critical patent/JPH01181561A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To facilitate forming of an oxygen-doped silicon single crystal layer with excellent property of a single crystal by a method wherein, after polycrystalline silicon containing oxygen is deposited on a silicon substrate, silicon ions are implanted so that the substrate surface and the polycrystalline silicon film is made to be amorphous, and then the substrate surface and the amorphous silicon film are subjected to a thermal treatment for single- crystallization. CONSTITUTION:The required part of the main surface of a first conductivity type silicon single crystal substrate 1 is doped with an impurity to form a second conductivity type region 2. Then a silicone film 3 doped with oxygen and a first conductivity type impurity is formed on the second conductivity type region 2 and a silicon film 4 doped with a first conductivity type impurity is built up. Then silicon ions (Si<+>) are implanted so as to reach the silicon substrate 1 surface and the silicon films 3 and 4 and the silicon substrate 1 surface are made to be amorphous 3a and 4a. Further, a thermal treatment is carried out to change the amorphous regions into single-crystallized regions 3 and 4 by solid phase epitaxial growth. With this constitution, an emitter-base hetero-junction with excellent property of a single crystal can be obtained easily.

Description

【発明の詳細な説明】 (産業上の利用分f) 本発明は、半導体Hrltの製造rJ法、とく昏こシリ
コンヘテc1@合バイポーラトランジスタの裂a方法に
関する。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Application) The present invention relates to a method for manufacturing a semiconductor Hrlt, and in particular to a method for manufacturing a bipolar transistor made of silicon.

(従来の技術) シリコンバイポーラトランジスタをさらに飛躍的に高速
化するためには、従来用いてきたシリコンエミッタにか
わってシリコンよりバンドキャップの広い、いわゆるワ
イドギャップエミッ゛りのへテロ接合材料を用いること
が必要となる。
(Conventional technology) In order to dramatically increase the speed of silicon bipolar transistors, it is necessary to replace the conventionally used silicon emitter with a so-called wide-gap emitter heterojunction material, which has a wider band gap than silicon. Is required.

ワイドギャップエミッタを作製するにあたり。When making a wide gap emitter.

酸素をシリコンに添加する事Cζよって作製する事が行
なわれる。例えば1通常のCVD暎、ffiを用いるS
 I POS (SSem1−1nsulatin p
olycrystallinesilicon)である
が、こn+こより形成されたエミッタは結晶性が悪く抵
抗頃が高い、また、牟結晶化さまた列として& Sl高
真空蒸着(、St MBg)を用いたOXS EF (
OX)’ger−Doped Si Epitaxia
l Filma)があるが、MBEffl置は量産性が
低いという問題があり、MBEを用いる製法は現在の所
実用的ではない、また、これまでの報告列ではプロセス
上エミッタ抵抗に酸素添加シリコンを用いているため、
エミッタ抵抗を増大させてしまうという問題があった。
Fabrication is performed by adding oxygen to silicon (Cζ). For example, 1 normal CVD method, S using ffi
I POS (SSem1-1nsulatin p
However, the emitter formed from this n+ has poor crystallinity and high resistance, and OXS EF (
OX)'ger-Doped Si Epitaxia
However, the MBEffl device has the problem of low mass productivity, and the manufacturing method using MBE is currently not practical.Also, in previous reports, oxygen-doped silicon was used for the emitter resistor due to the process. Because
There is a problem in that the emitter resistance increases.

理想的には、ワイドギャップはエミッタとペース接合界
面付近で必要なのであり、エミッタ全体がワイドギャッ
プである必要はない。
Ideally, a wide gap is needed near the emitter-paste junction interface, and the entire emitter does not need to be wide-gap.

(発明が解決しようとする課題) 本発明は上記事情を考慮してなされたもので。(Problem to be solved by the invention) The present invention has been made in consideration of the above circumstances.

その目的とするところは、シリコンへテロ接合バイポー
ラトランジスタを形成するに際し、単結晶性の優れた酸
素添加シリコン単結晶層を簡便に形成し、少りエミッタ
抵抗を低減して素子性能を大幅に向上せしめることので
きる半導体装置の製造5法を提供することにある。
The purpose of this is to easily form an oxygen-doped silicon single crystal layer with excellent single crystallinity when forming a silicon heterojunction bipolar transistor, reduce emitter resistance slightly, and significantly improve device performance. It is an object of the present invention to provide five methods for manufacturing semiconductor devices that can be used to produce semiconductor devices.

〔発明の構成〕[Structure of the invention]

(!II@を解決するための手段) 我々は、鋭意検討を重ねた結果、シリコン基板上にLP
CVD法を用いて酸素を10%〜50′4含む多結晶シ
リコンを堆積した後、前記多結晶シリコン膜にシリコン
イオンを打ち込み、前記シリコン基板表面及び多結晶シ
リコン膜を非晶質化した後、650℃〜700℃で熱処
理したところ、前記いずれの範囲の酸素濃度でも前記非
晶質化シリコンが単結晶化している事を見い出した。
(Means to solve !II@) As a result of intensive study, we have decided to use LP on a silicon substrate.
After depositing polycrystalline silicon containing 10% to 50'4 of oxygen using the CVD method, implanting silicon ions into the polycrystalline silicon film to make the silicon substrate surface and the polycrystalline silicon film amorphous, When heat-treated at 650° C. to 700° C., it was found that the amorphous silicon became single crystallized at any oxygen concentration within the above range.

一方、多結晶シリコンIllに含まれる酸素濃度を堆積
過程において増減さすた。すなわち、100Aの堆積時
に最大50俤の酸素濃度とし、さらに200A堆積した
後、酸素の供給を停止し、さらに多結晶シリコン模を6
0OA堆積させた麦、上記と同様にシリコンのイオン注
入、熱処理を行ったところ非晶質化されたシリコンは表
面まで革結晶化している事を見い出した。
On the other hand, the oxygen concentration contained in polycrystalline silicon Ill was increased or decreased during the deposition process. In other words, the oxygen concentration was set to a maximum of 50 t during deposition of 100 A, and after further 200 A was deposited, the supply of oxygen was stopped, and the polycrystalline silicon pattern was
When 0OA-deposited wheat was subjected to silicon ion implantation and heat treatment in the same manner as described above, it was found that the amorphous silicon was crystallized to the surface.

以上の知見に基づいた本発明の概要を第1図を用いて説
明する。
An outline of the present invention based on the above knowledge will be explained using FIG. 1.

すなわら、まず第1図ta)に示すように第1導電型シ
リコン手結晶基板(1)の主面の所望部分に不純物をa
 /70し、第2導環型碩域(2)を形成する。15)
はシリコン酸化膜である。
That is, first, as shown in FIG.
/70 to form a second ring type subregion (2). 15)
is a silicon oxide film.

ここで、前記不純物の添加方法はイオン注入でも不純物
をiむガス雰囲気からの拡散でも、不純物を富む薄膜か
らの拡散でもよい。
Here, the method for adding the impurity may be ion implantation, diffusion from a gas atmosphere containing impurities, or diffusion from a thin film rich in impurities.

次に、第1図1b)fこ示すように少なくとも第2導V
t型領域(2)の上に酸素及び第1導1型不純物添加シ
リコン膜(3)を形成し、続いて第1導市型不純物添加
シリコン膜4)を堆積する。
Next, as shown in FIG. 1b), at least the second conductor V
An oxygen and first type impurity doped silicon film (3) is formed on the t-type region (2), and then a first type impurity doped silicon film 4) is deposited.

続いて第1図+clに示すようにシリコンイオン(Sl
”)をシリコン檻板表面迄到達するように注入し、シリ
コン模13) 、 +4)及びシリコン基板表面を非晶
質化(3a)、(4a)させる。
Next, silicon ions (Sl
") is injected so as to reach the surface of the silicon cage plate, and the silicon pattern 13), +4) and the silicon substrate surface are made amorphous (3a), (4a).

さらに、第1図(d)に示すように熱処理を行ない前記
非晶質化した領域を固相エピタキシャル成長により手詰
晶化した領域(3b)、(4b)として形成する。
Furthermore, as shown in FIG. 1(d), heat treatment is performed to form the amorphous regions into hand-crystallized regions (3b) and (4b) by solid phase epitaxial growth.

(作用) 上記工程によりシリコンへテロ接片バイポーラトランジ
スタを作製すれば、簡便に単結晶性の優れたエミッター
ペースへテロ接合を得る事ができ。
(Function) If a silicon heterojunction bipolar transistor is manufactured by the above process, an emitter-paste heterojunction with excellent single crystallinity can be easily obtained.

しかもエミッタ抵抗を低くする事が可能となる為素子性
を大幅に向上させる事が可能となる。
Furthermore, since it is possible to lower the emitter resistance, it is possible to significantly improve device properties.

(実施列) 以下2本発明による実施列を図面を参照して詳細に説明
する。第2図は、その製造工程断面図である。
(Implementation row) Two implementation rows according to the present invention will be described in detail below with reference to the drawings. FIG. 2 is a sectional view of the manufacturing process.

まず、第2図1a)に示すようにpを添り口したn型シ
リコン基板161 O表面にシリコン酸化膜を図に示す
ように(力の領域で厚さ5ooX、(7a)の領域でマ
スク+8) i用いてB(ボロン)等の不純物イオンを
棚連電圧20 kV、打ち込み量3 X 1()”cm
−雪で打ち込み、p型半導体領域(外部ベース)(9)
を形成した。
First, as shown in FIG. 2 (1a), a silicon oxide film is deposited on the surface of an n-type silicon substrate 161 with a p-type silicon substrate (with a thickness of 500× in the region of 50×, and masked in the region of (7a) as shown in the figure). +8) Impurity ions such as B (boron) were introduced using i at a voltage of 20 kV and an implantation amount of 3 x 1()”cm.
- Driven with snow, p-type semiconductor region (external base) (9)
was formed.

次いで、第2図(b)に示すようGこレジストマスク(
8)を除去したffl、 Bイオンを全面にv口達電圧
15kV、打ち込み量I X 10”cm−鵞で打ち造
本pを手導体須域(ベース) (10)を形成した。
Next, as shown in FIG. 2(b), a G resist mask (
8) was removed, and B ions were applied to the entire surface at a voltage of 15 kV and an implantation amount of I x 10" cm to form a hand conductor base (10).

ここで、ボロンイオンの打ち込みの深さは第1図(a)
でのボロンの打ち込み深さよりも浅くてよい。
Here, the implantation depth of boron ions is shown in Figure 1 (a).
It may be shallower than the boron implant depth in .

更に嬉2図(clに示すよりにレジストマスクを用いた
弗酸処理等多こよりシリコン酸化@1ηに幅1.5μm
の開孔部(11)を形成した。
Furthermore, as shown in Figure 2 (cl), silicon oxidation @ 1η with a width of 1.5 μm was obtained by hydrofluoric acid treatment using a resist mask.
An opening (11) was formed.

続いて、第2図(d)に示すようf(As(砒素)を2
.0 X 10!Ocm−”、 O(酸素)を1.0 
X 10 ”cm−”添jJDした多結晶シリコンg 
(12)をLPCVD法により100A堆積させた後、
さらにAsを1×10冨■cm−”  添加した多結晶
シリコン「漢(」3)をLPCVD法(こより70OA
堆積させた。
Next, as shown in Figure 2(d), f(As (arsenic)) was
.. 0 x 10! Ocm-”, O (oxygen) 1.0
X 10 "cm-" added JJD polycrystalline silicon g
After depositing (12) at 100A by LPCVD method,
In addition, polycrystalline silicon "Kan" 3) doped with As to 1x10 cm-" was processed using the LPCVD method
deposited.

その浸、第2図(e)#こ示すようにシリコンイオン(
St  )ヲttoi電EE40kV 、 打チ込*i
l lX15g1cm″″1 で打ち込む事により、前
記多結晶シリコン模(12) 、 (13)と1孔部(
11)のシリコン基板(6)表面を非晶質化(14) 
(14a)させた。
The immersion in silicon ions (Fig. 2(e)
St) Wottoi electric EE40kV, driving*i
The polycrystalline silicon patterns (12), (13) and 1 hole (
11) Making the surface of the silicon substrate (6) amorphous (14)
(14a) Let it happen.

しかる後、第2図げ)に示すように1列えば1150℃
、15秒Dランプ熱処理を行ない、固相エピタキシャル
成長により前記開口部(11)上の非晶質化された多結
晶シリコン膜を単結晶シリコン1漠(15)として形成
した。
After that, as shown in the second figure, one row will be heated to 1150℃.
, D-lamp heat treatment was performed for 15 seconds, and an amorphous polycrystalline silicon film on the opening (11) was formed as a monocrystalline silicon film (15) by solid phase epitaxial growth.

ここで、酸化膜(71、(7a)上のシリコン層(16
)は多結晶になった。
Here, the silicon layer (16) on the oxide film (71, (7a)
) became polycrystalline.

さらに、第2図智)に示すようにレジストマスクを用い
た反応性イオンエツチング等により単結晶シリコン層(
15)を残してシリコン層(16)を除去した。この単
結晶シリコン層(15)がエミッタ領域となる。さらに
また第2図色)に示すようにシリコン酸化膜(17)を
CVD法により3000A堆積したのち、レジストマス
クを用いた反応性イオンエツチング等により開孔部(1
B) 、 (19)を設けた後、電極用アルミニウム層
(20)、(21)を形成した。
Furthermore, as shown in Figure 2, a single crystal silicon layer (
The silicon layer (16) was removed leaving 15). This single crystal silicon layer (15) becomes an emitter region. Furthermore, as shown in Figure 2 (color), a silicon oxide film (17) of 3000A was deposited by the CVD method, and then the openings (17) were etched by reactive ion etching using a resist mask.
B) After providing (19), electrode aluminum layers (20) and (21) were formed.

上記工程により形成されたNPN トランジスタの直流
増幅率−,は400であり、多結晶シリコン(t2)の
堆積時において、0(酸素)をa 730しないで作製
したNPN)ランジスタの環流増幅率が80であるのC
ζ比べて大きく改善された。
The DC amplification factor of the NPN transistor formed by the above process is 400, and the circulation amplification factor of the NPN transistor fabricated without adding 0 (oxygen) during the deposition of polycrystalline silicon (t2) is 80. is C
Great improvement compared to ζ.

次に多結晶シリコン層(12)(200Δ)の酸素6f
keJLをシリコン基板表面から100Aの位置で50
易としてその上下では[機内に10%まで減少させた以
外は上記工程と同様の方法によってNPN)ランジスタ
を作製した。上記工程により単結晶化Cたシリコン層の
単結晶性は、前記した@1の実施例に比べて改善されて
いる事がラザーフォード後方散乱測定蛋こよって明らか
Cどなった。すなわち、この発#!Alこおいて貸票密
度は10幅〜50憾に設定するのがよい。
Next, the oxygen 6f of the polycrystalline silicon layer (12) (200Δ)
keJL at 50A at a position of 100A from the silicon substrate surface.
For simplicity, NPN transistors were fabricated above and below in the same manner as the above process except that the amount inside the machine was reduced to 10%. It is clear from Rutherford backscattering measurements that the single crystallinity of the silicon layer monocrystallized by the above process is improved compared to the example @1 described above. In other words, this release #! In Al, the bill lending density is preferably set to 10 to 50.

また、この場合結晶欠陥の減少により電流l!1@率h
F)i、は、600に改善された。
In addition, in this case, due to the reduction of crystal defects, the current l! 1@rate h
F) i was improved to 600.

なお1本発明は上述した実寓例方法に限定されるもので
はない。例えば、エミッタ領域の不純物としてAs(砒
素)、コレクタ領域の不純物としてP (I)ン)を用
いたが、それぞれの領域の不、袖物がAs、Pいずれで
あってもその効果が得られることは明らかである。また
、固相エピタキシャル成長させる際の熱処理方法として
不純物拡散の少ないランプクロ熱性を用いたが1通常の
横型炉でもよく、そのd度・時間第こ・ついても不馴物
拡散が所望の範囲内でおさえられる限り、固相エピタキ
シャル成長及び不純物の活性化がなされる条件でよい。
Note that the present invention is not limited to the illustrative method described above. For example, As (arsenic) was used as the impurity in the emitter region, and P (I) was used as the impurity in the collector region, but the effect can be obtained even if the impurity in each region is As or P. That is clear. In addition, as a heat treatment method for solid-phase epitaxial growth, we used lamp chromatography, which causes less diffusion of impurities, but a normal horizontal furnace may also be used, and the diffusion of foreign substances can be kept within the desired range regardless of the temperature and time. As long as conditions are possible, conditions that allow solid phase epitaxial growth and activation of impurities may be used.

その他1本光明はその要旨を逸脱しない範囲で、櫨々変
形して実施する事ができる。
In addition, this Komei can be modified and implemented without departing from its gist.

〔発明の@果〕[@Results of invention]

以上詳述したよう1(、本発明によればバンドギャップ
がStよりも拡い酸素添加シリコン単結晶層をエミッタ
ペース界面に容易に形成する事ができ& hF’Eの高
いシリコンへテロ接合バイポーラトランジスタを形成す
ることが可能となった。
As detailed above, 1 (According to the present invention, an oxygen-doped silicon single crystal layer with a band gap wider than that of St can be easily formed at the emitter paste interface & a silicon heterojunction bipolar layer with high hF'E). It became possible to form transistors.

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

第11は本発明方法の概要を説明するための工程断Ij
rI図、第2図は本発明による一実施例を説明するため
の工程断面図である。 1・・・第1導電型シリコン基板、2川第2導成を手詰
、lil領域、3・・・第1導電型不純物及び酸素添7
111多結晶シリコン、4・・・第1導電梨多結晶シリ
コン。 5・・・シリコン酸化膜、6・・・@1導電型シリコン
基板、7e7a・・・シリコン酸化膜、8・・・レジス
トマスク、9・・・外部ベースelii*、1’o・・
・内部ヘース領域、11・・・開孔部、12・・・@1
4i1C型不純物及びtvi素添加多結晶シリコン模、
13・・・第1導電型不純物添加多結晶シリコン模、1
4・・・非晶質化された第1等電駿不純物添すロシリコ
ン膜、14a・・・非晶質化された@1導′IC型不純
物及び酸素添加多結晶シリコン膜、15・・・固相エピ
タキシャル成長したvlL結晶シリコン領域、16・・
・多結晶化したシリコン領域、17・・・シリコン酸化
膜、18.19・・・開孔部、20・・・エミッタ電極
、21・・・ベース電極。 代理人 弁理士  則 近 憲 佑 同        孤  山  光  之第1図 Φ                    呻−一ノ
                       −ノ
O′1=
The eleventh is a process cut-off Ij for explaining the outline of the method of the present invention.
RI diagram and FIG. 2 are process cross-sectional views for explaining an embodiment according to the present invention. 1... First conductivity type silicon substrate, 2nd conductivity, lil region, 3... First conductivity type impurity and oxygen addition 7
111 polycrystalline silicon, 4... first conductive pear polycrystalline silicon. 5...Silicon oxide film, 6...@1 conductivity type silicon substrate, 7e7a...Silicon oxide film, 8...Resist mask, 9...External base elii*, 1'o...
・Internal heath area, 11...Opening part, 12...@1
4i1C type impurity and tvi element doped polycrystalline silicon model,
13... First conductivity type impurity doped polycrystalline silicon model, 1
4... Amorphous first isoelectrically impurity-added polysilicon film, 14a... Amorphous @1 conductive IC type impurity and oxygen-added polycrystalline silicon film, 15... Solid phase epitaxially grown vlL crystalline silicon region, 16...
- Polycrystalline silicon region, 17... silicon oxide film, 18.19... opening portion, 20... emitter electrode, 21... base electrode. Agent Patent Attorney Nori Ken Ken Yudo Ko Yama Hikaru 1st Diagram Φ Oan-ichino -noO'1=

Claims (2)

【特許請求の範囲】[Claims] (1)第1導電型シリコン基板の主面の一部に不純物を
添加して第2導電型領域を形成する工程と、少なくとも
前記第2導電型領域上に薄い酸素及び第1導電型不純物
添加シリコン膜を形成する工程と、前記酸素及び第1導
電型不純物添加シリコン膜上に第1導電型シリコン模を
形成する工程と、シリコンイオンを前記基板の主面上か
ら、少なくとも上記酸素添加シリコン膜に到達するよう
に注入する工程と、その後熱処理によって前記シリコン
酸化膜と上記第1導電型シリコン膜を単結晶化する工程
を含むことを特徴とする半導体装置の製造方法。
(1) A step of adding an impurity to a part of the main surface of a first conductivity type silicon substrate to form a second conductivity type region, and adding a thin layer of oxygen and a first conductivity type impurity onto at least the second conductivity type region. forming a silicon film; forming a first conductivity type silicon pattern on the silicon film doped with oxygen and a first conductivity type; 1. A method for manufacturing a semiconductor device, comprising the steps of: implanting the silicon oxide film and the first conductivity type silicon film into a single crystal by heat treatment.
(2)前記酸素及び第1導電型不純物添加シリコン膜の
酸素濃度は、膜内で50%以下である1つの所望の最大
値を有し、上下両方向に向かって減少せしめるように形
成したものであることを特徴とする請求項1記載の半導
体装置の製造方法。
(2) The oxygen concentration of the silicon film doped with oxygen and first conductivity type impurities has a desired maximum value of 50% or less within the film, and is formed so as to decrease in both upward and downward directions. 2. The method of manufacturing a semiconductor device according to claim 1, further comprising the following steps.
JP63003240A 1988-01-12 1988-01-12 Manufacture of semiconductor device Pending JPH01181561A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63003240A JPH01181561A (en) 1988-01-12 1988-01-12 Manufacture of semiconductor device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63003240A JPH01181561A (en) 1988-01-12 1988-01-12 Manufacture of semiconductor device

Publications (1)

Publication Number Publication Date
JPH01181561A true JPH01181561A (en) 1989-07-19

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
JP63003240A Pending JPH01181561A (en) 1988-01-12 1988-01-12 Manufacture of semiconductor device

Country Status (1)

Country Link
JP (1) JPH01181561A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5296388A (en) * 1990-07-13 1994-03-22 Matsushita Electric Industrial Co., Ltd. Fabrication method for semiconductor devices

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5296388A (en) * 1990-07-13 1994-03-22 Matsushita Electric Industrial Co., Ltd. Fabrication method for semiconductor devices

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