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JPS6159656B2 - - Google Patents
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JPS6159656B2 - - Google Patents

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Publication number
JPS6159656B2
JPS6159656B2 JP54020431A JP2043179A JPS6159656B2 JP S6159656 B2 JPS6159656 B2 JP S6159656B2 JP 54020431 A JP54020431 A JP 54020431A JP 2043179 A JP2043179 A JP 2043179A JP S6159656 B2 JPS6159656 B2 JP S6159656B2
Authority
JP
Japan
Prior art keywords
metal film
electrode
inp
alloy
heat treatment
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
Application number
JP54020431A
Other languages
Japanese (ja)
Other versions
JPS55113369A (en
Inventor
Masaki Ogawa
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.)
NEC Corp
Original Assignee
Nippon Electric 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 Nippon Electric Co Ltd filed Critical Nippon Electric Co Ltd
Priority to JP2043179A priority Critical patent/JPS55113369A/en
Publication of JPS55113369A publication Critical patent/JPS55113369A/en
Publication of JPS6159656B2 publication Critical patent/JPS6159656B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は族元素としてインジウム(In)、V
族元素として燐(P)あるいは砒素(As)を含
む−化合物半導体に対するオーム性電極の構
造と製造方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention uses indium (In) and V as group elements.
The present invention relates to the structure and manufacturing method of an ohmic electrode for a compound semiconductor containing phosphorus (P) or arsenic (As) as a group element.

前記化合物半導体に対するオーム性電極は、従
来金(Au)あるいは銀(Ag)あるいはインジウ
ム(In)を含む金属層(この発明においては反応
層や合金も含めて金属膜あるいは金属層と称して
いる。)を前記化合物半導体表面に被着し、非酸
化性雰囲気中で、熱処理を行うことにより、前記
金属膜と前記化合物半導体との合金化反応をおこ
す方法によつて形成されていた。例えば前記−
化合物半導体としてP型のインジウム燐
(InP)に対しては金−亜鉛(Au−Zn)合金が電
極材料としてよく用いられている。InPに対して
低接触抵抗を得るために、415℃〜440℃の温度範
囲で、水素雰囲気中で約1分間熱処理が行われて
いる。この熱処理が行われた電極部の断面を第1
図aに示す。基板InP11の上には、Au−In合金
層12が形成される。基板InP11とAu−In合金
層12の間にはごく薄いZnドープ層が形成され
ている。
The ohmic electrode for the compound semiconductor has conventionally been a metal layer containing gold (Au), silver (Ag), or indium (In) (in this invention, a reaction layer and an alloy are also referred to as a metal film or metal layer). ) is deposited on the surface of the compound semiconductor and heat-treated in a non-oxidizing atmosphere to cause an alloying reaction between the metal film and the compound semiconductor. For example, the above-
Gold-zinc (Au-Zn) alloy is often used as an electrode material for P-type indium phosphide (InP) as a compound semiconductor. In order to obtain low contact resistance for InP, heat treatment is performed in a hydrogen atmosphere for about 1 minute at a temperature range of 415°C to 440°C. The cross section of the electrode part that has been subjected to this heat treatment is
Shown in Figure a. An Au-In alloy layer 12 is formed on the substrate InP11. A very thin Zn-doped layer is formed between the substrate InP 11 and the Au-In alloy layer 12.

熱処理温度を450℃以上に選ぶと、Au−In合金
は凝集して第1図bに示すごとく凝集物13が局
部的に形成され、同時に凝集物13があらわれる
部分以外の表面はInPが露出する。このため、
450℃以上の熱処理を行うと良好なオーム性電極
は製造できずこの理由により熱処理温度を415℃
〜440℃の範囲にとどめる必要があつた。しかし
このような温度範囲で熱処理したものは、InPと
電極材料との反応が完了していないため、電極形
成後の諸昇温過程で反応がさらに進みオーム性電
極特性が変化するという欠点があつた。このよう
なInPと電極材料との反応の進行は、InとPとの
結合エネルギーが小さいためにPが解離して蒸発
しやすいことが原因となつていることが、発明者
によつて明らかとなつた。オーム性電極特性の変
化を抑えるためには電極形成時の熱処理温度を
450℃以上の高温で行うかあるいは、電極形成後
の諸昇温過程でのPの解離と蒸発を防ぐことが必
要である。したがつて本発明の第1の目的は高温
での熱処理によつても基板半導体との反応生成物
の凝集がない電極構造を提供することにあり、第
2の目的は、電極形成後の諸昇温過程でのPの解
離と蒸発を防ぐオーム性電極の製造方法を提供す
ることにある。本発明では、解離温度の高いリン
化合物を形成する第2金属膜を、AuあるいはAg
あるいはInを主成分とする第1の電極金属層上に
形成することによつて、解離されたPが前記第2
の金属膜中にとらえられ、電極中のPの圧力が高
まりInPの分解を防ぐ現象が利用されている。以
下本発明の実施例を半導体基板としてInP第1の
電極金属材料としてAu−Zn合金を用いたものに
ついて詳述する。
When the heat treatment temperature is selected to be 450°C or higher, the Au-In alloy aggregates and aggregates 13 are locally formed as shown in Figure 1b, and at the same time, InP is exposed on the surface other than the area where the aggregates 13 appear. . For this reason,
If heat treatment is performed at a temperature higher than 450℃, a good ohmic electrode cannot be produced.For this reason, the heat treatment temperature was changed to 415℃.
It was necessary to keep the temperature within the range of ~440℃. However, products heat-treated in such a temperature range have the disadvantage that the reaction between InP and the electrode material is not completed, and the reaction progresses further during various temperature raising processes after electrode formation, resulting in changes in the ohmic electrode characteristics. Ta. The inventor has clarified that the progress of the reaction between InP and the electrode material is caused by the fact that P dissociates and evaporates easily because the bond energy between In and P is small. Summer. In order to suppress changes in ohmic electrode characteristics, the heat treatment temperature during electrode formation must be adjusted.
It is necessary to carry out the process at a high temperature of 450° C. or higher, or to prevent dissociation and evaporation of P during various temperature raising processes after electrode formation. Therefore, the first object of the present invention is to provide an electrode structure in which reaction products with the substrate semiconductor do not agglomerate even during heat treatment at high temperatures, and the second object is to provide an electrode structure that does not cause aggregation of reaction products with the substrate semiconductor even after heat treatment at high temperatures. The object of the present invention is to provide a method for manufacturing an ohmic electrode that prevents dissociation and evaporation of P during the temperature raising process. In the present invention, the second metal film forming a phosphorus compound with a high dissociation temperature is made of Au or Ag.
Alternatively, by forming the first electrode metal layer containing In as a main component, the dissociated P can be transferred to the second electrode metal layer.
InP is trapped in the metal film, increasing the pressure of P in the electrode and preventing the decomposition of InP. Hereinafter, an embodiment of the present invention will be described in detail using an Au--Zn alloy as a semiconductor substrate and an InP first electrode metal material.

第2図aはInP基板21上に厚さ0.15μmでZn
を3重量%含むAu−Zn合金からなる第1の電極
金属層22被着する。被着源として前記組成の
Au−Zn合金を用い真空蒸着法で被着した場合に
は、AuとZnの蒸気圧の違いによつて第1の電極
金属層22中の組成は一様ではなく、InP基板2
1と接する部分ではZnが主体の組成となり、InP
基板21から離れた部分ではAuが主体の組成を
示すが、InPとの電極の合金化反応に対してはこ
のような組成の非一様性は、問題とはならない。
次に本発明による改善の効果をもたらす第2の金
属膜23を0.15μmの厚さで第1の金属層22上
に被着する(第2図a)。第2の金属膜23とし
ては、タングステンW、モリブデンMo、タンタ
ルTa、ハフニウムHfからなる金属群のうち1種
類以上の元素を含む材料から構成される。第2図
aを水素雰囲気中、490℃で1分間熱処理して第
2図bに示されるようなオーム性電極の構造が得
られる。第1図bと異つて、第2図bでは反応生
成物24は凝集することがなく、InP基板21と
一様に反応する。第3図は第2図bの熱処理され
た試料の表面から深さ方向の元素分布をオージエ
電子分光法により測定した結果である。この試料
では第2の金属膜23の材料としてタングステン
を用いてある。熱処理された電極は、InP基板と
接してAu−In合金部分、Au−In合金部分上にP
を含むW部分とに分離した2つの部分からなる構
造を示していることがわかる。すなわち、第1の
金属膜(Au−Zn)22上に第2の金属膜W23
を被着した場合には、Au−Zn22とInP21が反
応して解離されたPはW中に捕えられている。
Figure 2 a shows Zn deposited on an InP substrate 21 with a thickness of 0.15 μm.
A first electrode metal layer 22 made of an Au--Zn alloy containing 3% by weight of is deposited. of the above composition as a deposition source.
When depositing by vacuum evaporation using an Au-Zn alloy, the composition in the first electrode metal layer 22 is not uniform due to the difference in vapor pressure between Au and Zn, and the InP substrate 2
In the part in contact with 1, the composition is mainly Zn, and InP
Although the portion away from the substrate 21 shows a composition mainly composed of Au, such compositional non-uniformity does not pose a problem for the alloying reaction of the electrode with InP.
Next, a second metal film 23, which provides the improved effect of the invention, is deposited on the first metal layer 22 to a thickness of 0.15 μm (FIG. 2a). The second metal film 23 is made of a material containing one or more elements from the metal group consisting of tungsten W, molybdenum Mo, tantalum Ta, and hafnium Hf. The structure of the ohmic electrode shown in FIG. 2b is obtained by heat-treating FIG. 2a at 490 DEG C. for 1 minute in a hydrogen atmosphere. Unlike FIG. 1b, the reaction product 24 in FIG. 2b does not aggregate and reacts uniformly with the InP substrate 21. In FIG. FIG. 3 shows the results of measuring the elemental distribution in the depth direction from the surface of the heat-treated sample shown in FIG. 2b using Auger electron spectroscopy. In this sample, tungsten is used as the material for the second metal film 23. The heat-treated electrode has an Au-In alloy part in contact with the InP substrate, and P on the Au-In alloy part.
It can be seen that it shows a structure consisting of two parts separated into a W part containing . That is, the second metal film W23 is formed on the first metal film (Au-Zn) 22.
When Au-Zn 22 and InP 21 react and dissociate, P is captured in W.

このため、反応生成物24中のPの圧力が高ま
り、InP21の著しい分解が抑えられている。一
方W膜を被着しない場合には、InP基板と反応し
て形成されたAu−In合金が融体化し、融体化し
たAu−In液体は、熱処理雰囲気に直接さらされ
るため、Pが蒸発しやすくInPの分解が促進され
る。実際、第1図bの凝集物14中にはPは検出
されなかつた。このため、InP基板は著しく分解
され、融体化したInPは凝集して第1図bに示す
ような電極構造を呈する。第3図では第2の金属
膜材料としてWを用いてあるが、Pと解離しにく
い化合物をつくる金属元素であれば有効であり、
W以外の他の元素としてはMo,Ta,Hfが有効で
あつた。第2の金属膜の被着膜厚は第1の金属膜
厚の0.5倍から2倍の厚さが適当であつた。すな
わち第2の金属膜が薄すぎると第1の金属膜と半
導体基板との反応生成物が凝固する際に波うつて
しまい、第2の金属膜が厚すぎると熱処理後の電
極中の機械的ひずみが大きくなつて、電極がもろ
くなつた。本発明の一実施例であるタングステン
を第2の金属膜として用いたInPへのオーム性電
極は、450℃以上での熱処理が可能であるため、
従来の構造のものと異つて、電極形成後の諸昇温
過程においても、熱的に安定であり、素子特性の
変化が認められなかつた。
Therefore, the pressure of P in the reaction product 24 increases, and significant decomposition of InP 21 is suppressed. On the other hand, when the W film is not deposited, the Au-In alloy formed by reaction with the InP substrate is molten, and the molten Au-In liquid is directly exposed to the heat treatment atmosphere, so that P evaporates. This facilitates the decomposition of InP. In fact, no P was detected in the aggregate 14 of FIG. 1b. As a result, the InP substrate is significantly decomposed, and the molten InP aggregates to form an electrode structure as shown in FIG. 1b. In Figure 3, W is used as the second metal film material, but any metal element that forms a compound that is difficult to dissociate with P is effective.
Mo, Ta, and Hf were effective as elements other than W. The appropriate thickness of the second metal film was 0.5 to 2 times the thickness of the first metal film. In other words, if the second metal film is too thin, the reaction product between the first metal film and the semiconductor substrate will wave when it solidifies, and if the second metal film is too thick, it will cause mechanical damage in the electrode after heat treatment. As the strain increased, the electrodes became brittle. The ohmic electrode for InP using tungsten as the second metal film, which is an embodiment of the present invention, can be heat-treated at 450°C or higher.
Unlike the conventional structure, it was thermally stable and no change in device characteristics was observed even during various temperature raising processes after electrode formation.

上に述べたような熱的安定性を増す効果は、第
1の金属膜を被して半導体基板と熱処理を行い、
半導体基板と第1の金属膜との合金化反応させた
後に第2の金属膜を被着しても得られる。第4図
はInP基板41上にZnを3重量%含むAu−Zn合
金を0.15μmの厚さに被着した後非酸化性雰囲気
中で430℃で1分間熱処理して形成されたInPと
の反応層42上にタングステン膜43を0.15μm
の厚さに被着したものである。
The effect of increasing thermal stability as described above can be obtained by covering the first metal film and performing heat treatment on the semiconductor substrate.
It can also be obtained by depositing the second metal film after an alloying reaction between the semiconductor substrate and the first metal film. Figure 4 shows the relationship between InP and InP, which was formed by depositing an Au-Zn alloy containing 3% by weight of Zn on an InP substrate 41 to a thickness of 0.15 μm and then heat-treating it at 430°C for 1 minute in a non-oxidizing atmosphere. A tungsten film 43 with a thickness of 0.15 μm is formed on the reaction layer 42.
It is coated to a thickness of .

このようにして製造された電極も、電極形成後
の昇温過程においても熱的安定性が高く、素子特
性の変化が少なかつた。この原因は、タングステ
ン被膜が昇温過程中に発生するリンを捕えるた
め、InPの分解を抑え、電極反応の促進を妨げる
ためである。
The electrode manufactured in this way also had high thermal stability even during the temperature rising process after electrode formation, and there were few changes in device characteristics. The reason for this is that the tungsten film captures phosphorus generated during the temperature rising process, suppressing the decomposition of InP and preventing the promotion of electrode reactions.

以上、本発明の実施例として半導体基板にInP
を用いてきたが、V族元素の解離しやすい他の半
導体材料例えば、InGaAsP混晶,InAs等にも適
用可能である。本発明で述べた第2の金属膜材料
群(W,Mo,Ta,Hf)は砒素(As)とも解離
しにくい化合物を形成するので、V族元素として
砒素(As)を含む化合物半導体に対しても有効
である。また第1の金属膜材料として金−ゲルマ
ニウム合金、金−スズ合金などの金を含む材料の
他に、インジウム、インジウム−テルル合金、イ
ンジウム−スズ合金のようにインジウムを含む材
料、および、銀−スズ合金、インジウム−スズ−
銀合金のように銀を含む材料に対しても、第2の
金属膜を被着することによる本発明で述べた効果
があらわれる。
As described above, as an example of the present invention, InP is applied to a semiconductor substrate.
However, it is also applicable to other semiconductor materials in which group V elements are easily dissociated, such as InGaAsP mixed crystal, InAs, etc. The second metal film material group (W, Mo, Ta, Hf) described in the present invention forms a compound that is difficult to dissociate with arsenic (As), so it is not suitable for compound semiconductors containing arsenic (As) as a group V element. It is also effective. In addition to materials containing gold such as gold-germanium alloy and gold-tin alloy, materials containing indium such as indium, indium-tellurium alloy, and indium-tin alloy can be used as the first metal film material, and silver- Tin alloy, indium-tin
The effects described in the present invention can also be obtained by depositing the second metal film on a material containing silver such as a silver alloy.

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

第1図は従来のオーム性電極の構造を示す断面
図であり、第1図aは415℃〜440℃で非酸化性雰
囲気で熱処理された電極の構造を、第1図bは
450℃以上で熱処理された電極の構造を示す。図
中11はInP基板、12は415℃〜440℃熱処理で
形成されたAu−Inからなる反応層、13は450℃
以上の熱処理で形成された反応物を示す。第2図
は本発明の製造方法により得られた電極の構造を
示す断面図で第2図aは被着直後の電極構造、第
2図bは、490℃で熱処理した電極の構造を示
す。図中、21はInP基板、22はAu−Zn合金か
らなる第1の金属膜、23はWからなる第2の金
属膜、24は490℃熱処理によつて形成された反
応層を示す。第3図は、第2図bの電極中の元素
の深さ方向分布をオージエ電子分光法により測定
した結果を示す。第4図は本発明の一実施例によ
るオーム性電極の構造を示す断面図で、図中41
はInP基板、42はAu−Zn合金からなる第1の金
属膜とInPとの反応層を、43はタングステン膜
を示す。
Fig. 1 is a cross-sectional view showing the structure of a conventional ohmic electrode, Fig. 1a shows the structure of an electrode heat-treated at 415°C to 440°C in a non-oxidizing atmosphere, and Fig. 1b shows the structure of the electrode.
The structure of an electrode heat-treated at 450°C or higher is shown. In the figure, 11 is an InP substrate, 12 is a reaction layer made of Au-In formed by heat treatment at 415°C to 440°C, and 13 is at 450°C.
The reactants formed by the above heat treatment are shown. FIG. 2 is a sectional view showing the structure of an electrode obtained by the manufacturing method of the present invention. FIG. 2a shows the electrode structure immediately after deposition, and FIG. 2b shows the structure of the electrode after heat treatment at 490°C. In the figure, 21 is an InP substrate, 22 is a first metal film made of an Au-Zn alloy, 23 is a second metal film made of W, and 24 is a reaction layer formed by heat treatment at 490°C. FIG. 3 shows the results of measuring the depth distribution of elements in the electrode of FIG. 2b by Auger electron spectroscopy. FIG. 4 is a cross-sectional view showing the structure of an ohmic electrode according to an embodiment of the present invention.
4 is an InP substrate, 42 is a reaction layer of InP and a first metal film made of an Au-Zn alloy, and 43 is a tungsten film.

Claims (1)

【特許請求の範囲】[Claims] 1 族元素としてインジウム、V族元素として
燐あるいは砒素を含む−族化合物半導体の表
面に、金あるいは銀あるいはインジウムを主成分
とする第1の金属膜を被着し、さらに前記第1の
金属膜上にタングステン、モリブデン、タンタ
ル、ハフニウムからなる元素群から選ばれた1種
類以上の元素を含み、かつ第1の金属膜の0.5な
いし2倍の膜厚の有する第2の金属膜を被着した
後、450℃以上の温度で熱処理を行うことを特徴
とするオーム性電極の製造方法。
A first metal film containing gold, silver, or indium as a main component is deposited on the surface of a - group compound semiconductor containing indium as a group 1 element and phosphorus or arsenic as a group V element, and further comprising: depositing a first metal film mainly composed of gold, silver, or indium; A second metal film containing one or more elements selected from the element group consisting of tungsten, molybdenum, tantalum, and hafnium and having a thickness of 0.5 to 2 times that of the first metal film is deposited thereon. A method for producing an ohmic electrode, which is then subjected to heat treatment at a temperature of 450°C or higher.
JP2043179A 1979-02-22 1979-02-22 Ohmic electrode and its manufacture Granted JPS55113369A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2043179A JPS55113369A (en) 1979-02-22 1979-02-22 Ohmic electrode and its manufacture

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2043179A JPS55113369A (en) 1979-02-22 1979-02-22 Ohmic electrode and its manufacture

Publications (2)

Publication Number Publication Date
JPS55113369A JPS55113369A (en) 1980-09-01
JPS6159656B2 true JPS6159656B2 (en) 1986-12-17

Family

ID=12026845

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2043179A Granted JPS55113369A (en) 1979-02-22 1979-02-22 Ohmic electrode and its manufacture

Country Status (1)

Country Link
JP (1) JPS55113369A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0658954B2 (en) * 1986-01-21 1994-08-03 インタ−ナショナル ビジネス マシ−ンズ コ−ポレ−ション III-Group V compound semiconductor device and method for forming the same
JP7653078B2 (en) * 2021-07-06 2025-03-28 ウシオ電機株式会社 Infrared LED element

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51146180A (en) * 1975-06-11 1976-12-15 Mitsubishi Electric Corp Iii-v family compound semi-conductor electric pole formation

Also Published As

Publication number Publication date
JPS55113369A (en) 1980-09-01

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