JPS636873A - Semiconductor device - Google Patents
Semiconductor deviceInfo
- Publication number
- JPS636873A JPS636873A JP14828686A JP14828686A JPS636873A JP S636873 A JPS636873 A JP S636873A JP 14828686 A JP14828686 A JP 14828686A JP 14828686 A JP14828686 A JP 14828686A JP S636873 A JPS636873 A JP S636873A
- Authority
- JP
- Japan
- Prior art keywords
- film
- gate electrode
- gate
- piled
- added
- 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
Links
- 239000004065 semiconductor Substances 0.000 title claims description 10
- 229910052785 arsenic Inorganic materials 0.000 claims abstract description 18
- 229910052733 gallium Inorganic materials 0.000 claims abstract description 18
- 239000000463 material Substances 0.000 claims abstract description 14
- 239000000758 substrate Substances 0.000 claims abstract description 8
- 229910052721 tungsten Inorganic materials 0.000 claims abstract description 8
- 229910001218 Gallium arsenide Inorganic materials 0.000 claims abstract description 6
- 229910052751 metal Inorganic materials 0.000 claims description 18
- 239000002184 metal Substances 0.000 claims description 18
- 238000002844 melting Methods 0.000 claims description 10
- 150000002739 metals Chemical class 0.000 claims description 10
- 230000008018 melting Effects 0.000 claims description 8
- JBRZTFJDHDCESZ-UHFFFAOYSA-N AsGa Chemical compound [As]#[Ga] JBRZTFJDHDCESZ-UHFFFAOYSA-N 0.000 claims description 7
- 229910045601 alloy Inorganic materials 0.000 claims description 7
- 239000000956 alloy Substances 0.000 claims description 7
- 229910021332 silicide Inorganic materials 0.000 claims description 6
- 239000010937 tungsten Substances 0.000 claims description 6
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 5
- 229910052715 tantalum Inorganic materials 0.000 claims description 4
- 239000010936 titanium Substances 0.000 claims description 4
- 229910052750 molybdenum Inorganic materials 0.000 claims description 3
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 claims description 3
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 2
- 239000011733 molybdenum Substances 0.000 claims description 2
- 229910052702 rhenium Inorganic materials 0.000 claims description 2
- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 claims description 2
- FVBUAEGBCNSCDD-UHFFFAOYSA-N silicide(4-) Chemical compound [Si-4] FVBUAEGBCNSCDD-UHFFFAOYSA-N 0.000 claims description 2
- 229910052719 titanium Inorganic materials 0.000 claims description 2
- FTWRSWRBSVXQPI-UHFFFAOYSA-N alumanylidynearsane;gallanylidynearsane Chemical compound [As]#[Al].[As]#[Ga] FTWRSWRBSVXQPI-UHFFFAOYSA-N 0.000 claims 1
- 239000007772 electrode material Substances 0.000 abstract description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 8
- 238000004519 manufacturing process Methods 0.000 abstract description 7
- 238000004544 sputter deposition Methods 0.000 abstract description 5
- 229910021342 tungsten silicide Inorganic materials 0.000 abstract description 5
- 238000000137 annealing Methods 0.000 abstract description 4
- 229910052681 coesite Inorganic materials 0.000 abstract description 4
- 229910052906 cristobalite Inorganic materials 0.000 abstract description 4
- 238000010438 heat treatment Methods 0.000 abstract description 4
- 150000002500 ions Chemical class 0.000 abstract description 4
- 238000000034 method Methods 0.000 abstract description 4
- 239000000377 silicon dioxide Substances 0.000 abstract description 4
- 235000012239 silicon dioxide Nutrition 0.000 abstract description 4
- 229910052682 stishovite Inorganic materials 0.000 abstract description 4
- 229910052905 tridymite Inorganic materials 0.000 abstract description 4
- WQJQOUPTWCFRMM-UHFFFAOYSA-N tungsten disilicide Chemical compound [Si]#[W]#[Si] WQJQOUPTWCFRMM-UHFFFAOYSA-N 0.000 abstract description 3
- 238000009792 diffusion process Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 3
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 150000004767 nitrides Chemical class 0.000 description 2
- 229910002601 GaN Inorganic materials 0.000 description 1
- JMASRVWKEDWRBT-UHFFFAOYSA-N Gallium nitride Chemical compound [Ga]#N JMASRVWKEDWRBT-UHFFFAOYSA-N 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- GPBUGPUPKAGMDK-UHFFFAOYSA-N azanylidynemolybdenum Chemical compound [Mo]#N GPBUGPUPKAGMDK-UHFFFAOYSA-N 0.000 description 1
- YXTPWUNVHCYOSP-UHFFFAOYSA-N bis($l^{2}-silanylidene)molybdenum Chemical compound [Si]=[Mo]=[Si] YXTPWUNVHCYOSP-UHFFFAOYSA-N 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000005468 ion implantation Methods 0.000 description 1
- 229910021344 molybdenum silicide Inorganic materials 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- XGZGDYQRJKMWNM-UHFFFAOYSA-N tantalum tungsten Chemical compound [Ta][W][Ta] XGZGDYQRJKMWNM-UHFFFAOYSA-N 0.000 description 1
- 229910021341 titanium silicide Inorganic materials 0.000 description 1
- MAKDTFFYCIMFQP-UHFFFAOYSA-N titanium tungsten Chemical compound [Ti].[W] MAKDTFFYCIMFQP-UHFFFAOYSA-N 0.000 description 1
- -1 tungsten nitride Chemical class 0.000 description 1
- 230000005533 two-dimensional electron gas Effects 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
Landscapes
- Electrodes Of Semiconductors (AREA)
- Junction Field-Effect Transistors (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は化合物半導体を用いて半導体装置に関するもの
で、特にそのショットキー電極部に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a semiconductor device using a compound semiconductor, and particularly to a Schottky electrode portion thereof.
高融点金属をゲート材料に使用し、自己整合法によって
作製されるヒ化ガリウム(GaAs) M E 5FE
Tには、該ゲート材料としてこれまで各種の高融点材料
が試みられてきた。−例として高融点金属シリサイドを
使用することにより比較的良好な特性が得られることが
知られている(たとえば特開昭57−113289参照
)。Gallium arsenide (GaAs) M E 5FE manufactured by self-alignment method using high melting point metal as gate material
Various high melting point materials have been tried as the gate material for T. - For example, it is known that relatively good properties can be obtained by using high-melting point metal silicides (see, for example, JP-A-57-113289).
従来は各種金属酸いは金属シリサイドを用いたゲート電
極中の微量の不純物は特に問題とされていない。即ち、
高温(約800°C)加熱工程での微量のガリウム(G
a)或いはヒ素(A s )のゲート電極中への拡散は
無視されている。しかしながら、ゲート電極下に形成さ
れるnチャネル層の厚さが〜100n’m以下と薄くな
った場合、Ga或いはAsのゲート電極中への拡散に伴
なうしきい電圧の変動等の素子特性への悪影響が無視で
きなくなって来た。Conventionally, trace amounts of impurities in gate electrodes using various metal acids or metal silicides have not been considered a particular problem. That is,
A trace amount of gallium (G
a) Or the diffusion of arsenic (A s ) into the gate electrode is ignored. However, when the thickness of the n-channel layer formed under the gate electrode is reduced to ~100 nm or less, device characteristics such as fluctuations in threshold voltage due to diffusion of Ga or As into the gate electrode may be affected. The negative effects of this have become impossible to ignore.
本発明の目的は化合物半導体装置の製造工程中、高温熱
処理を経ても、当該装置の特性に大きな影響をおよぼさ
ないために有効なゲート電極の構成を提供するものであ
る。An object of the present invention is to provide an effective gate electrode structure that does not significantly affect the characteristics of a compound semiconductor device even after undergoing high-temperature heat treatment during the manufacturing process of the device.
ゲート電極用の材料としては(1)タングステン(W)
、モリブデン(Mo)、タンタル(Ta)。Materials for gate electrodes include (1) tungsten (W);
, molybdenum (Mo), tantalum (Ta).
チタン(Ti)、レニウム(Re)等の耐熱性金属、(
2)前記金属の合金、(3)前記金属酸いは前記金属の
合金の各シリサイド、(4)前記金HI或いは前記金属
の合金の各窒化物、等の高融点材料が好適である。Heat-resistant metals such as titanium (Ti) and rhenium (Re), (
High melting point materials are suitable, such as 2) alloys of the metals, (3) silicides of the metal acids or alloys of the metals, and (4) nitrides of the gold HI or alloys of the metals.
上記ゲート電極用材料へのガリウム(Ga)。Gallium (Ga) as the gate electrode material.
ヒ素(As)、或いはこれらの両者を添加する場合、添
加量は材料の種類、膜質等に依存するが。When adding arsenic (As) or both, the amount added depends on the type of material, film quality, etc.
各材料に対するGa、Asの溶解度程度以上が好適であ
る。溶解度以上に添加された場合、余分のGaやAsは
結晶粒界などの欠陥に析出し、該欠陥を経路とする拡散
を抑制する。ゲート電極として用いる目的から原子数%
で0.1%程度が限界である。It is preferable that the solubility of Ga and As in each material be equal to or higher. When added in excess of the solubility, excess Ga or As precipitates at defects such as grain boundaries, suppressing diffusion through the defects. Atomic % due to the purpose of using it as a gate electrode
The limit is about 0.1%.
上述した高融点材料とした場合の製造方法は通常、スパ
ッタ堆積法を用いる。この場合、GaやAsをあらかじ
め母体となる材料に添加しておく。In the case of using the above-mentioned high melting point material, a sputter deposition method is usually used as a manufacturing method. In this case, Ga or As is added to the base material in advance.
またGaやAsの添加は、ヒ化ガリウム(GaAs)、
窒化ガリウム(G a N )等のターゲットを使用し
、他の材料と同時或いは交互スパッタ堆積を行ってもよ
い。その他、真空蒸着法等をも用いることが出来る。こ
の場合、QaやAsをゲート材料蒸着時に、同時に蒸着
すればよい。この方法は、GaやAsの添加量を制御し
易い利点がある。In addition, the addition of Ga and As can be applied to gallium arsenide (GaAs),
A target such as gallium nitride (G a N ) may be used for simultaneous or alternating sputter deposition with other materials. In addition, a vacuum evaporation method or the like can also be used. In this case, Qa or As may be deposited at the same time as the gate material is deposited. This method has the advantage that the amounts of Ga and As added can be easily controlled.
本発明の前提となる問題点として述べたGa或いはAs
のゲート電極材料への拡散は、半導体基板と当該ゲート
電極材料中のGa或いはAsの化学ポテンシャルの差が
駆動力として発生する。本発明はゲート電極材料中にG
a、Asをあらかじめ添加しておき、前述の駆動力を低
減せしめることにより、GaやAsの拡散を抑ff1l
f L/得る。Ga or As mentioned as the problem which is the premise of the present invention
Diffusion into the gate electrode material is caused by the difference in chemical potential between Ga or As in the semiconductor substrate and the gate electrode material as a driving force. The present invention provides G in the gate electrode material.
By adding a, As in advance and reducing the above-mentioned driving force, diffusion of Ga and As can be suppressedff1l
f L/obtain.
実施例1゜
第1図をもとに本発明の第1の実施例を説明する。半絶
縁性GaAs基板lに膜厚50nmのSiO2膜を全面
に堆積し、しかる後にこの8102膜を通して加速電圧
75kVでSiイオンを所定個所に5 X 1012c
m−”の濃度で注入することにより、第1図(a)に示
すように能動居2を形成する。次いで該5102膜を除
去した後に第1図(b)に示すようにゲート電極材料3
′を堆積する。ここではGa、Asの添加されたWター
ゲットとSiターゲットを使用し、スパッタ法により同
時或いは交互スパッタし、にa、Asの添加されたタン
グステンシリサイドを堆積する。Embodiment 1 A first embodiment of the present invention will be described based on FIG. A SiO2 film with a thickness of 50 nm is deposited on the entire surface of a semi-insulating GaAs substrate l, and then Si ions are deposited at predetermined locations through this 8102 film at an accelerating voltage of 75 kV.
By implanting at a concentration of 5102, an active region 2 is formed as shown in FIG.
′ is deposited. Here, a W target doped with Ga and As and a Si target are used, and tungsten silicide doped with A and As is deposited by sputtering simultaneously or alternately.
Wターゲット中のGa、Asの濃度は、数lOppmか
ら致方ppmとする。また膜厚は約300nmとする。The concentration of Ga and As in the W target is from several lOppm to several ppm. Further, the film thickness is approximately 300 nm.
次いで該ゲート電極材料を所定のパターン3に加工し、
更に該ゲート電極3をマスクにしてSiイオンを打込み
、第1図(e)に示すようにオーミック電極用低抵抗層
4を形成する。Next, the gate electrode material is processed into a predetermined pattern 3,
Furthermore, using the gate electrode 3 as a mask, Si ions are implanted to form a low resistance layer 4 for an ohmic electrode as shown in FIG. 1(e).
次いで第1図(d)のようにアニール用キャップ膜とし
て膜厚約200nmのSi○2膜5を被着し、800℃
、20分のアニールによって打込まれたStの活性化を
行なった後、第1図(a)のようにオーミック電極6を
形成する。こうしてGaAsM E S F E Tが
完成する。Next, as shown in FIG. 1(d), a Si○2 film 5 with a thickness of about 200 nm was deposited as a cap film for annealing, and the film was heated at 800°C.
After activating the implanted St by annealing for 20 minutes, an ohmic electrode 6 is formed as shown in FIG. 1(a). In this way, GaAsMESFET is completed.
ゲート電極にG a或いはAsの添加を行なわなかった
場合、FETのに値(Conduct、ance定数)
は1.2 (ゲート長1μm)にとどまったのに対し、
本実施例によるFETでは、K値は1.4に向上した。When Ga or As is not added to the gate electrode, the conductivity value (conduct, ance constant) of the FET
was only 1.2 (gate length 1 μm), whereas
In the FET according to this example, the K value was improved to 1.4.
また、ここでは、ゲート電極材料にタングステンシリサ
イドおよびタングステンを使用した場合について説明し
たが、このほか、前述した耐熱性金属をはじめチタンシ
リサイド、タンタルシリサイド、モリブデンシリサイド
、さらに、Ti。In addition, although the case where tungsten silicide and tungsten are used as gate electrode materials has been described here, in addition to the above-mentioned heat-resistant metals, titanium silicide, tantalum silicide, molybdenum silicide, and Ti may also be used.
T a 、 W、 M oの合金のシリサイド、たとえ
ば。Silicides of alloys of Ta, W, Mo, e.g.
チタン−タングステン シリサイド、タンタル−タング
ステン シリサイド等を使用した場合、さらには前記高
融点金属や合金の窒化物(たとえばタングステン・ナイ
トライド、モリブデン・ナイトライド)を使用した場合
にも同様の効果が得られる。Similar effects can be obtained when using titanium-tungsten silicide, tantalum-tungsten silicide, etc., or when using nitrides of the above-mentioned high-melting point metals and alloys (e.g., tungsten nitride, molybdenum nitride). .
実M1例2゜
先の実施例中のゲート電極材料としてGaを添加したタ
ングステンを使用する。Gaの添加は、Wターゲット中
にあらかじめGaをドープしておき、該ターゲットを使
用しスパッタ堆積することにより容易に達成される。W
中のGaの濃度は約0.1%とする。Actual M1 Example 2° Tungsten doped with Ga is used as the gate electrode material in the previous example. Addition of Ga can be easily achieved by doping Ga into a W target in advance and performing sputter deposition using the target. W
The concentration of Ga therein is approximately 0.1%.
Gaを添加しなかった場合、FETは所望の動作をしな
かったのに対し、本実施例によれば、K値1.1 (ゲ
ート長1μm)で動作した。When Ga was not added, the FET did not operate as desired, but according to this example, it operated with a K value of 1.1 (gate length 1 μm).
また以上の例では、半絶縁性基板にイオン打込みにより
能動層を形成するGaAsM E S F E Tにつ
いて説明したが、エピタキシャル成長により能動層を形
成した周知のMESFETの場合も全く同様の効果が得
られる。さらに、2次元電子ガス層を利用したいわゆる
ヘテロ接合利用のFETの場合も、ゲート電極にGa、
Asを添加することにより、ゲートのショットキー特性
の加熱工程での安定性を向上することができる。Although the above example describes a GaAs MESFET in which the active layer is formed by ion implantation into a semi-insulating substrate, exactly the same effect can be obtained in the case of a well-known MESFET in which the active layer is formed by epitaxial growth. . Furthermore, in the case of a so-called heterojunction FET that uses a two-dimensional electron gas layer, Ga is used in the gate electrode.
By adding As, the stability of the Schottky characteristic of the gate during the heating process can be improved.
本発明によれば、G a A sまたはAΩGaAs上
にショットキー電極を有する半導体装置において。According to the present invention, in a semiconductor device having a Schottky electrode on GaAs or AΩGaAs.
製造工程で受ける加熱工程での装置の特性の劣化のない
装置を再現性良く製造することができる。It is possible to manufacture a device with good reproducibility without deterioration of the characteristics of the device during the heating process during the manufacturing process.
特に、従来単体の高融点金属は界面の熱的安定性が不十
分とされてきたが、本発明によれば、タングステン等の
単体金属の使用を可能にする。In particular, although it has been conventionally believed that single high melting point metals have insufficient thermal stability at the interface, the present invention enables the use of single metals such as tungsten.
第1図は、化合物半導体を基板に用い
MESFETを製造する製造工程を示す。
1・・・半絶縁性GaAs基板、2・・・能動層、3・
・・高融点金属層、4・・・オーミック電極用低抵抗層
、5・・・アニール用キャップ膜、6・・・オーミック
電極。
特許出願人 飯J’3ミ幸三
工業技術院長 1 。FIG. 1 shows a manufacturing process for manufacturing a MESFET using a compound semiconductor as a substrate. DESCRIPTION OF SYMBOLS 1... Semi-insulating GaAs substrate, 2... Active layer, 3...
... High melting point metal layer, 4... Low resistance layer for ohmic electrode, 5... Cap film for annealing, 6... Ohmic electrode. Patent applicant Kozo Ii J'3, Director of the Institute of Industrial Technology 1.
Claims (1)
する高融点材料より成るショットキー電極がヒ化ガリウ
ム基板またはヒ化アルミニウム・ガリウム基板上に設け
られていることを特徴とする半導体装置。 2、前記高融点材料は、タングステン、モリブデン、タ
ンタル、チタンおよびレニウムの群からなる耐熱性金属
、および前記耐熱性金属間の合金、および前記耐熱性金
属又はこれら耐熱性金属間の合金のシリサイドより成る
群より選ばれた一者なることを特徴とする特許請求の範
囲第1項記載の半導体装置。[Claims] 1. A Schottky electrode made of a high melting point material containing at least one member of the group consisting of Ga and As is provided on a gallium arsenide substrate or an aluminum gallium arsenide substrate. semiconductor device. 2. The high melting point material is made of a heat-resistant metal from the group of tungsten, molybdenum, tantalum, titanium, and rhenium, an alloy of the heat-resistant metals, and a silicide of the heat-resistant metal or an alloy of these heat-resistant metals. The semiconductor device according to claim 1, wherein the semiconductor device is one selected from the group consisting of:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14828686A JPS636873A (en) | 1986-06-26 | 1986-06-26 | Semiconductor device |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14828686A JPS636873A (en) | 1986-06-26 | 1986-06-26 | Semiconductor device |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS636873A true JPS636873A (en) | 1988-01-12 |
| JPH0581068B2 JPH0581068B2 (en) | 1993-11-11 |
Family
ID=15449371
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP14828686A Granted JPS636873A (en) | 1986-06-26 | 1986-06-26 | Semiconductor device |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS636873A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63148679A (en) * | 1986-12-12 | 1988-06-21 | Nec Corp | Electrode |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6081860A (en) * | 1983-10-11 | 1985-05-09 | Matsushita Electric Ind Co Ltd | Schottky barrier semiconductor device |
-
1986
- 1986-06-26 JP JP14828686A patent/JPS636873A/en active Granted
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6081860A (en) * | 1983-10-11 | 1985-05-09 | Matsushita Electric Ind Co Ltd | Schottky barrier semiconductor device |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63148679A (en) * | 1986-12-12 | 1988-06-21 | Nec Corp | Electrode |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0581068B2 (en) | 1993-11-11 |
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