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JPS6262076B2 - - Google Patents
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JPS6262076B2 - - Google Patents

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Publication number
JPS6262076B2
JPS6262076B2 JP53064289A JP6428978A JPS6262076B2 JP S6262076 B2 JPS6262076 B2 JP S6262076B2 JP 53064289 A JP53064289 A JP 53064289A JP 6428978 A JP6428978 A JP 6428978A JP S6262076 B2 JPS6262076 B2 JP S6262076B2
Authority
JP
Japan
Prior art keywords
layer
gap
forming
type
electrode
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
JP53064289A
Other languages
Japanese (ja)
Other versions
JPS54156493A (en
Inventor
Norio Ozawa
Masako Nakabashi
Yasuhisa Oana
Noburo Yasuda
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
Tokyo Shibaura 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 Tokyo Shibaura Electric Co Ltd filed Critical Tokyo Shibaura Electric Co Ltd
Priority to JP6428978A priority Critical patent/JPS54156493A/en
Publication of JPS54156493A publication Critical patent/JPS54156493A/en
Publication of JPS6262076B2 publication Critical patent/JPS6262076B2/ja
Granted legal-status Critical Current

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  • Led Devices (AREA)

Description

【発明の詳細な説明】 本発明は隣化ガリウム(GaP)の化合物半導体
発光素子用電極の形成方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for forming a gallium chloride (GaP) compound semiconductor electrode for a light emitting device.

一般に化合物半導体発光素子としては、GaP、
GaAs或いはGaAs等の結晶が用いられている。そ
してこれらの素子は、第1図に示すように例えば
GaP結晶を用いた場合、n型GaP結晶基板11上
に液相エピタキシヤル成長によりn型GaP層11
a及びP型GaP層12を順次形成してp−n接合
13を構成し素子本体を得る。そしてこの本体の
P型層に電極として価の金属例えばベリリウム
(Be)または亜鉛(Zn)皮膜14を、n型GaP結
晶基板11に電極として例えばAu−SiまたはAu
−Ge合金皮膜15を夫々形成する。この後熱処
理を施して電極の構成元素をGaP結晶中に拡散せ
しめ、オーミツクコンタクトを取る。
Generally, compound semiconductor light emitting devices include GaP,
A crystal such as GaAs or GaAs is used. These elements are, for example, as shown in Figure 1.
When a GaP crystal is used, an n-type GaP layer 11 is formed on the n-type GaP crystal substrate 11 by liquid phase epitaxial growth.
A and P-type GaP layers 12 are sequentially formed to form a p-n junction 13 to obtain an element body. A film 14 of a valent metal such as beryllium (Be) or zinc (Zn) is coated as an electrode on the P-type layer of this main body, and a film 14 of a valent metal such as beryllium (Be) or zinc (Zn) is coated as an electrode on the n-type GaP crystal substrate 11 as an electrode such as Au-Si or Au.
-Ge alloy films 15 are formed respectively. After this, heat treatment is performed to diffuse the constituent elements of the electrode into the GaP crystal and establish ohmic contact.

さらに上記夫々の電極皮膜上に通常Au層14
a,15aを付着し、そしてP型層側のAu層1
4aにリード線14bをボンデングしている。
Furthermore, a normal Au layer 14 is formed on each of the above electrode films.
a, 15a, and Au layer 1 on the P-type layer side.
A lead wire 14b is bonded to 4a.

ところでP型層12の電極として用いる価の
金属特にZnは蒸気圧が高い為に容易に蒸発する
が蒸発源として使用する量に比べGaP結晶面に沈
積する量が少なく、蒸発後熱処理を行つてもGaP
結晶中に充分なZn量が拡散していかずオーミツ
クコンタクトが取れないという問題があつた。ま
たZnはGaP結晶との密着性が悪いため、GaP結晶
との界面において剥離が生じ、後の処理工程にお
いて非常な困難を伴う。
Incidentally, the valent metal used as the electrode of the P-type layer 12, especially Zn, easily evaporates due to its high vapor pressure, but the amount deposited on the GaP crystal plane is small compared to the amount used as an evaporation source, so heat treatment is performed after evaporation. Also GaP
There was a problem that a sufficient amount of Zn was not diffused into the crystal, making it impossible to establish ohmic contact. Furthermore, since Zn has poor adhesion to the GaP crystal, peeling occurs at the interface with the GaP crystal, making subsequent processing steps extremely difficult.

以上説明した理由から、GaPの発光素子のP型
層の電極としてZnまたはZn合金を用いて信頼性
良く且つ安定したオーミツクコンタクトを得るこ
とは非常に困難なことであつた。
For the reasons explained above, it has been extremely difficult to obtain reliable and stable ohmic contact using Zn or Zn alloy as the electrode of the P-type layer of a GaP light emitting device.

本発明は上記した点に鑑みなされたものでGaP
結晶の化合物半導体結晶のP型層とオーミツクコ
ンタクトが信頼性よく得られ、更には優れたボン
デイング性を有し、且つ強固に接続可能に形成で
きるようにした化合物半導体発光素子用電極の形
成方法を提供するものである。
The present invention has been made in view of the above-mentioned points.
A method for forming an electrode for a compound semiconductor light-emitting device, which allows reliable ohmic contact with a P-type layer of a compound semiconductor crystal, has excellent bonding properties, and can be formed to form a strong connection. It provides:

即ち本発明は、p−n接合を形成するP型層の
電極として、例えば第2図に示す如く、まず化合
物半導体結晶のP型層12上に金薄層24を形成
し、しかるのちこの金薄層24上に、膜厚2.5μ
mあたり亜鉛を20〜260μg/cm2を含む金−亜鉛合
金層24aを沈積せしめこれらを一体としてアル
ゴン(Ar)または窒素(N2)雰囲気中460℃〜550
℃の温度領域で熱処理を施こし安定したオーミツ
クコンタクトと優れたボンデング性を有する化合
物半導体発光素子の形成方法でである。
That is, in the present invention, as an electrode for a P-type layer forming a p-n junction, for example, as shown in FIG. 2, a thin gold layer 24 is first formed on a P-type layer 12 of a compound semiconductor crystal, and then this gold Film thickness 2.5μ on thin layer 24
A gold-zinc alloy layer 24a containing 20 to 260 μg/cm 2 of zinc per m is deposited, and the layers are heated together in an argon (Ar) or nitrogen (N 2 ) atmosphere at 460°C to 550°C.
This is a method for forming a compound semiconductor light emitting device which is heat-treated in the temperature range of 0.degree. C. and has stable ohmic contact and excellent bonding properties.

以下図面を参照して本発明に実施例を説明す
る。この実施例において化合物半導体発光素子は
GaP結晶を用いた場合で従来と同様第2図に示す
ようにn型GaP結晶基板11上に液相エピキシヤ
ル成長によりn型GaP層11a及びP型GaP層1
2を順次形成してp−n接合13を構成して素子
本体を得たものである。そこで上述のようにして
得られた素子本体上に、P型層12側に金薄層2
4を600Å程度蒸着し、この上にAu−Zn合金層2
4aを2.5μm程度蒸着して、このAu−Zn形成層
内にZnが130μg/cm2程度含有するようにする。
なお従来と同様にn型GaP結晶板11側にはAu
−Si合金層15及びAu層15aを形成してい
る。この後に500℃程度のArなどの不活性雰囲気
中で5〜20分間熱処理を施して上記夫々の合金層
を合金化せしめてオーミツクコンタクトを得る。
Embodiments of the present invention will be described below with reference to the drawings. In this example, the compound semiconductor light emitting device is
When GaP crystal is used, an n-type GaP layer 11a and a p-type GaP layer 1 are grown on an n-type GaP crystal substrate 11 by liquid phase epitaxy as shown in FIG.
2 are sequentially formed to form a pn junction 13 to obtain an element body. Therefore, on the element body obtained as described above, a thin gold layer 2 is placed on the P-type layer 12 side.
4 is deposited to a thickness of about 600 Å, and on top of this, an Au-Zn alloy layer 2 is deposited.
4a is deposited to a thickness of about 2.5 μm so that Zn is contained in the Au-Zn forming layer at a concentration of about 130 μg/cm 2 .
Note that as in the past, Au is placed on the n-type GaP crystal plate 11 side.
-Si alloy layer 15 and Au layer 15a are formed. Thereafter, heat treatment is performed for 5 to 20 minutes in an inert atmosphere such as Ar at about 500 DEG C. to alloy the above-mentioned respective alloy layers and obtain an ohmic contact.

このようにして得られたGaP発光素子のP型層
側の電極24,24aは、接触抵抗Rsが30Ω以
下という良好なオーミツクコンタクトが得られて
おり、しかもリード線14bのボンデング性も安
定であつた。なお当然ながらn型基板側の電極も
良好なオーミツクコンタクトが取られていた。
The electrodes 24, 24a on the P-type layer side of the GaP light emitting device thus obtained have good ohmic contact with a contact resistance Rs of 30Ω or less, and the bonding properties of the lead wire 14b are also stable. It was hot. Of course, good ohmic contact was also made with the electrode on the n-type substrate side.

ところで上記実施例に用いる金薄層24は、非
常に薄くても有効であり、例えば、P型GaP層に
100Å程度の厚さで付着していても効果は充分発
揮できる。即ち、P型GaP面に金が薄く付着する
ことにより、金とGaPが直ちに反応して、一部
Au−Ga合金が生成する。このためGaP結晶格子
中のGaの格子点に空孔が生成する。この後、Au
−Znが積層され、さらに熱処理を行うことによ
り、ZnとAuがGaP中に拡散するが、この際空孔
があるため拡散が容易となる。さらに空孔にZn
が位置することにより、オーミツク性が得られ
る。一方、ZnはAuと非常に合金化しやすく薄膜
においては、常温でも反応する。したがつてGaP
面にAuを先に付着しておくことにより、蒸着源
より飛来したZnは、Au面に到着するや直ちに合
金を生成する。この際一部Gaも合金化に寄与し
Au−Zn−Gaの三元合金を生成する。このため剥
離などは生じない。
By the way, the thin gold layer 24 used in the above embodiment is effective even if it is very thin.
Even if it is attached to a thickness of about 100 Å, the effect can be fully demonstrated. In other words, when a thin layer of gold adheres to the P-type GaP surface, the gold and GaP immediately react, causing some
Au-Ga alloy is formed. For this reason, vacancies are generated at Ga lattice points in the GaP crystal lattice. After this, Au
- When Zn is layered and further heat treated, Zn and Au diffuse into GaP, but at this time, the presence of vacancies facilitates the diffusion. Furthermore, Zn in the pores
By locating , ohmic properties can be obtained. On the other hand, Zn is very easy to alloy with Au and reacts even at room temperature in a thin film. Therefore GaP
By attaching Au to the surface first, the Zn that comes from the evaporation source forms an alloy as soon as it reaches the Au surface. At this time, some Ga also contributes to alloying.
A ternary alloy of Au-Zn-Ga is produced. Therefore, no peeling occurs.

また上記実施例に用いた金−亜鉛合金層24a
は、膜内にZnが130μg/cm2含有する層であつた
が20〜260μg/cm2含有する層であつてもよい。即
ち第3図の一点鎖線で示す如く膜内のZn濃度が
20〜260μg/cm2の領域であれば熱処理温度を460
〜550℃の範囲で選定することにより安定したオ
ーミツクコンタクトが得られる。又第3図の一点
鎖線に示すように20μg/cm2以下では熱処理温度
を変えてもオーミツクコンタクトが得られにく
く、さらにZn濃度が260μg/cm2以上となるとオ
ーミツクコンタクトが得られるが、第3図点線に
示すように熱処理温度を下げてもボンデング性が
悪くなる。なおAu−Zn合金層の膜厚が一定の
時、熱処理温度を上げるとオーミツクコンタクト
が得られやすく、逆に熱処理温度が高くなるとボ
ンデング性は低下する傾向にある。
Moreover, the gold-zinc alloy layer 24a used in the above example
Although the film contained 130 μg/cm 2 of Zn, it may contain 20 to 260 μg/cm 2 of Zn. That is, as shown by the dashed line in Fig. 3, the Zn concentration in the film is
If the range is 20 to 260μg/cm2, the heat treatment temperature should be set to 460μg/ cm2 .
A stable ohmic contact can be obtained by selecting a temperature within the range of ~550°C. Furthermore, as shown by the dashed line in Fig. 3, if the Zn concentration is less than 20 μg/cm 2 , it is difficult to obtain ohmic contact even if the heat treatment temperature is changed, and if the Zn concentration is 260 μg/cm 2 or more, ohmic contact cannot be obtained. As shown by the dotted line in FIG. 3, even if the heat treatment temperature is lowered, the bonding properties deteriorate. Note that when the thickness of the Au-Zn alloy layer is constant, ohmic contact tends to be obtained when the heat treatment temperature is increased, and conversely, when the heat treatment temperature is increased, bonding properties tend to decrease.

以上説明したように膜膜が2.5μmにおいて第
3図から明らかなようにオーミツク性とボンデン
グ性とも満足するような領域の交差する一点鎖線
と点線の範囲内になるようなZn量処理温度を選
定する。即ちZn量が20〜260μg/cm2の範囲で熱
処理温度460〜550℃の組合せによりオーミツク性
とボンデング性が得られる。特に良好なオーミツ
ク接触及びボンデング性を示す部分は、第3図中
実線で囲まれた斜線領域の範囲内の時である。
As explained above, the Zn amount treatment temperature was selected so that the film was within the range between the dashed line and the dotted line, which intersect the region that satisfies both ohmic properties and bonding properties as shown in Figure 3 when the film is 2.5 μm thick. do. That is, ohmic properties and bonding properties can be obtained by combining a Zn content in the range of 20 to 260 μg/cm 2 and a heat treatment temperature of 460 to 550°C. Particularly good ohmic contact and bonding properties are exhibited within the shaded area surrounded by solid lines in FIG.

またボンデング性に関しては、熱処理に際し
Au層においてAu−Zn−Gaの三元合金化がすすみ
熱処理時にGaが電極表面に折出するのを阻止
し、また同時にZnもGaによつて一部トラツプさ
れる。
Regarding bonding properties, during heat treatment,
A ternary alloy of Au-Zn-Ga progresses in the Au layer, preventing Ga from depositing on the electrode surface during heat treatment, and at the same time, a portion of Zn is also trapped by Ga.

このためAuのリード線をボンデングした場
合、Au層がない場合に比べ著しく改善されほと
んど金属Au層にボンデングしたもの同程度のボ
ンデング性およびボンデング強度が得られる。
Therefore, when an Au lead wire is bonded, the bonding performance and bonding strength are significantly improved compared to the case where there is no Au layer, and almost the same level of bonding performance and bonding strength as those bonded to a metal Au layer can be obtained.

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

第1図は、従来のGaP発光素子用電極の形成方
法を説明するための構成断面図、第2図は本発明
の一実施例のGaP発光素子用電極の形成方法を説
明するための構成断面図、第3図は、本発明の作
用効果であるオーミツク性とボンデング性を説明
する曲線図である。 第2図において、11はn型GaP結晶基板、1
1aはn型GaP層、12はp型GaP層、13はp
−n接合、24は金薄層、24aはAu−Zn合金
層、14bはリード線、15はAu−Si合金層、
15aはAu層である。
FIG. 1 is a cross-sectional view of the structure for explaining a conventional method of forming an electrode for a GaP light-emitting device, and FIG. 2 is a cross-sectional view of the structure for explaining a method of forming an electrode for a GaP light-emitting device according to an embodiment of the present invention. 3 are curve diagrams illustrating ohmic properties and bonding properties, which are the effects of the present invention. In Fig. 2, 11 is an n-type GaP crystal substrate;
1a is an n-type GaP layer, 12 is a p-type GaP layer, and 13 is a p-type GaP layer.
-n junction, 24 is a gold thin layer, 24a is an Au-Zn alloy layer, 14b is a lead wire, 15 is an Au-Si alloy layer,
15a is an Au layer.

Claims (1)

【特許請求の範囲】[Claims] 1 n型GaP層上にP型GaP層を形成して発光素
子本体を形成する工程と、前記P型GaP層上に金
薄層を形成する工程と、該工程により形成された
金薄層上に、膜厚が2.5μmあたり亜鉛を20〜260
μg/cm2含む金−亜鉛合金を形成した後にアルゴ
ンまたは窒素雰囲気中で460〜550℃の温度領域で
熱処理を施してオーミツク接触と該形成層にリー
ド線ボンデイングする工程とを具備したことを特
徴とするGaP発光素子用電極の形成方法。
1 A step of forming a P-type GaP layer on the n-type GaP layer to form a light emitting device body, a step of forming a thin gold layer on the P-type GaP layer, and a step of forming a thin gold layer on the thin gold layer formed by the step. Add 20 to 260 zinc per film thickness of 2.5μm.
The method is characterized by comprising a step of forming a gold-zinc alloy containing μg/cm 2 and then performing heat treatment in an argon or nitrogen atmosphere in a temperature range of 460 to 550°C to make ohmic contact and bond lead wires to the formed layer. A method for forming an electrode for a GaP light emitting device.
JP6428978A 1978-05-31 1978-05-31 Forming method of compound semiconductor light emitting element electrode Granted JPS54156493A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6428978A JPS54156493A (en) 1978-05-31 1978-05-31 Forming method of compound semiconductor light emitting element electrode

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6428978A JPS54156493A (en) 1978-05-31 1978-05-31 Forming method of compound semiconductor light emitting element electrode

Publications (2)

Publication Number Publication Date
JPS54156493A JPS54156493A (en) 1979-12-10
JPS6262076B2 true JPS6262076B2 (en) 1987-12-24

Family

ID=13253916

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6428978A Granted JPS54156493A (en) 1978-05-31 1978-05-31 Forming method of compound semiconductor light emitting element electrode

Country Status (1)

Country Link
JP (1) JPS54156493A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022268599A1 (en) 2021-06-24 2022-12-29 Alfa Laval Corporate Ab An arrangement handling purged alcohol-based fuel and a method therefor

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS531468A (en) * 1976-06-25 1978-01-09 Sharp Corp Formation of semiconductor electrode

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022268599A1 (en) 2021-06-24 2022-12-29 Alfa Laval Corporate Ab An arrangement handling purged alcohol-based fuel and a method therefor

Also Published As

Publication number Publication date
JPS54156493A (en) 1979-12-10

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