JP2003017738A - Epitaxial wafer for light emitting element, its manufacturing method, and light emitting element using it - Google Patents
Epitaxial wafer for light emitting element, its manufacturing method, and light emitting element using itInfo
- Publication number
- JP2003017738A JP2003017738A JP2001198276A JP2001198276A JP2003017738A JP 2003017738 A JP2003017738 A JP 2003017738A JP 2001198276 A JP2001198276 A JP 2001198276A JP 2001198276 A JP2001198276 A JP 2001198276A JP 2003017738 A JP2003017738 A JP 2003017738A
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- Japan
- Prior art keywords
- type
- layer
- light emitting
- epitaxial wafer
- emitting device
- 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.)
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Links
- 238000004519 manufacturing process Methods 0.000 title claims description 19
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000001301 oxygen Substances 0.000 claims abstract description 16
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 16
- 239000012535 impurity Substances 0.000 claims abstract description 12
- 238000005253 cladding Methods 0.000 claims description 28
- 239000000758 substrate Substances 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 14
- 230000003287 optical effect Effects 0.000 claims description 9
- 239000007791 liquid phase Substances 0.000 claims description 8
- 125000005842 heteroatom Chemical group 0.000 claims description 4
- 238000000407 epitaxy Methods 0.000 claims 1
- 239000010410 layer Substances 0.000 description 144
- 235000012431 wafers Nutrition 0.000 description 41
- 229910001218 Gallium arsenide Inorganic materials 0.000 description 17
- 230000005540 biological transmission Effects 0.000 description 12
- 239000013078 crystal Substances 0.000 description 9
- 239000002019 doping agent Substances 0.000 description 9
- 229910021397 glassy carbon Inorganic materials 0.000 description 9
- 238000004891 communication Methods 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 8
- 239000004065 semiconductor Substances 0.000 description 7
- 238000010586 diagram Methods 0.000 description 6
- 230000003247 decreasing effect Effects 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 238000003860 storage Methods 0.000 description 5
- 230000007423 decrease Effects 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 239000007789 gas Substances 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- SWXQKHHHCFXQJF-UHFFFAOYSA-N azane;hydrogen peroxide Chemical compound [NH4+].[O-]O SWXQKHHHCFXQJF-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 238000005530 etching Methods 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 238000005204 segregation Methods 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 229910021642 ultra pure water Inorganic materials 0.000 description 2
- 239000012498 ultrapure water Substances 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000010583 slow cooling Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Crystals, And After-Treatments Of Crystals (AREA)
- Led Devices (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、発光素子、特に赤
外光を利用した光通信や空間伝送用に使用される高速・
高出力の半導体発光素子の作製に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a light emitting device, particularly a high speed / light source used for optical communication and space transmission utilizing infrared light.
The present invention relates to fabrication of a high-power semiconductor light emitting device.
【0002】[0002]
【従来の技術】Ga1-XAlXAs(以下、GaAlAs
と略す。)系化合物半導体を利用した発光素子(以下、
LEDと略す。)は、赤外から赤色用の光源として広く
用いられている。赤外LEDは光通信や空間伝送用に使
用されているが、伝送するデータの大容量化、伝送距離
の長距離化に伴い、高出力及び高速化への要求が高くな
っている。2. Description of the Related Art Ga 1-X Al X As (hereinafter referred to as GaAlAs
Abbreviated. ) A light-emitting device using a compound semiconductor (hereinafter,
Abbreviated as LED. ) Is widely used as a light source for infrared to red. Infrared LEDs are used for optical communication and space transmission, but as the capacity of data to be transmitted increases and the transmission distance increases, the demand for higher output and higher speed is increasing.
【0003】従来から知られているように、GaAlA
s系LEDにおいて、シングルへテロ構造よりもダブル
ヘテロ構造(以下、DH構造と略す。)の発光部を用い
た方が発光素子の出力が高く、また基板を除去すること
でさらなる高出力化が図られている。基板を除去したタ
イプのDH構造(以後、DDH構造と略す。)、即ち、
基板上にp型クラッド層、p型活性層およびn型クラッ
ド層の3層のみをエピタキシャル成長させた後基板を除
去した構造のエピタキシャルウェハでは、製品の厚さが
薄くなり、素子化の工程でのハンドリングが困難にな
る。また同時に、このエピタキシャルウェハから作製し
た発光素子の、底面からpn接合までの高さが低くな
り、素子を導体に接着するときのペーストが素子側面を
這い上がり、pn接合を短絡するという問題が発生す
る。As is known in the art, GaAlA
In the s-based LED, the output of the light emitting element is higher when the light emitting portion having the double hetero structure (hereinafter, abbreviated as DH structure) is used than the single hetero structure, and further higher output can be obtained by removing the substrate. Has been planned. The type of DH structure from which the substrate is removed (hereinafter abbreviated as DDH structure), that is,
In an epitaxial wafer having a structure in which only the p-type clad layer, the p-type active layer and the n-type clad layer are epitaxially grown on the substrate and then the substrate is removed, the product thickness is reduced and Handling becomes difficult. At the same time, the height from the bottom surface to the pn junction of the light emitting device manufactured from this epitaxial wafer becomes low, and the paste for adhering the device to the conductor crawls up the side surface of the device, causing a short circuit of the pn junction. To do.
【0004】これを防ぐために、基板除去後の仕上がり
の全厚と素子底面から接合までの距離を稼ぐための第4
のエピタキシャル層をDH構造に付加することが、DD
H構造では標準的な構成になっている。第4のエピタキ
シャル層はバンドギャップが活性層よりも広く、活性層
からの発光を吸収しないように設計される。In order to prevent this, the fourth method for increasing the total thickness of the finished product after removing the substrate and the distance from the element bottom surface to the junction.
Adding an epitaxial layer of
The H structure has a standard configuration. The fourth epitaxial layer has a bandgap wider than that of the active layer and is designed not to absorb light emitted from the active layer.
【0005】この第4のエピタキシャル層は、前記DH
構造のn型クラッド側に付加しても、p型クラッド側に
付加しても良い。さらに、この第4のエピタキシャル層
は単層である必要はなく、複数のエピタキシャル層を組
み合わせても良い。This fourth epitaxial layer is formed from the above-mentioned DH.
The structure may be added to the n-type clad side or the p-type clad side. Furthermore, the fourth epitaxial layer does not have to be a single layer, and a plurality of epitaxial layers may be combined.
【0006】[0006]
【発明が解決しようとする課題】光通信や空間伝送用途
の赤外LEDでは、電池駆動の携帯端末で使用されるこ
と、また、情報をより遠くへ送るために大きな電流を流
さなければならないことなどから、高出力・高速特性と
並んで、低い順方向電圧の要求も強くなっている。Infrared LEDs for optical communication and space transmission are used in battery-powered portable terminals, and a large current must be sent to send information farther. Therefore, along with high output and high speed characteristics, the demand for low forward voltage is increasing.
【0007】LEDの順方向電圧を決定する要素である
LEDの抵抗は、半導体結晶自身の抵抗と、半導体結晶
と電極との接触抵抗とに分けられる。GaAs−AlA
s系の半導体においては、結晶自身の抵抗は正孔よりも
電子の方が移動度が10倍以上高いため、キャリア濃度
とAl組成が同一であればn型層の方が抵抗が低く、p
型層の方が抵抗が高い。半導体結晶と電極との接触抵抗
は、電極と接する部分の結晶のAl組成やキャリア濃度
により左右される。LEDの順方向電圧を低くするため
には、特にp型層の抵抗を低くすることが必要である。The resistance of the LED, which is a factor that determines the forward voltage of the LED, is divided into the resistance of the semiconductor crystal itself and the contact resistance between the semiconductor crystal and the electrode. GaAs-AlA
In the s-based semiconductor, the resistance of the crystal itself is 10 times or more higher in the mobility of electrons than in the holes, so that if the carrier concentration and Al composition are the same, the resistance of the n-type layer is lower and p
The mold layer has higher resistance. The contact resistance between the semiconductor crystal and the electrode depends on the Al composition and carrier concentration of the crystal in the portion in contact with the electrode. In order to lower the forward voltage of the LED, it is necessary to lower the resistance of the p-type layer.
【0008】光通信や空間電送用途のLEDの一般的な
製造方法である液相エピタキシャル成長法では、GaA
lAsのp型のドーパントとしては通常Znが用いられ
ている。しかし、p型GaAlAs層の抵抗を下げるた
めにZnを高濃度にドープすると、GaAlAs層のキ
ャリア濃度が高くなり順方向電圧は低くなるが、高ドー
プによる発光の自己吸収が起こりLEDの出力が低下し
てしまう。さらに、p型クラッド層にZnを用いる場合
は、拡散エネルギーの低いZnが活性層を横切りn型層
に拡散し、pn接合位置が冶金学的界面からバンドギャ
ップの大きいn型クラッド層中にずれる。この現象はL
EDの低い順方向電圧を実現するためには不利である。
本発明は、主に光通信や空間電送用途の赤外LEDにお
いて、高出力・高速特性を維持しながら低い順方向電圧
の要求も満たすことができる新しい発光素子を作製する
ことを目的とする。In the liquid phase epitaxial growth method, which is a general method for manufacturing LEDs for optical communication and space transmission, GaA is used.
Zn is usually used as the p-type dopant of 1As. However, when Zn is heavily doped to reduce the resistance of the p-type GaAlAs layer, the carrier concentration of the GaAlAs layer increases and the forward voltage decreases, but self-absorption of light emission due to high doping occurs and the output of the LED decreases. Resulting in. Further, when Zn is used for the p-type clad layer, Zn having a low diffusion energy traverses the active layer and diffuses into the n-type layer, and the pn junction position shifts from the metallurgical interface into the n-type clad layer having a large band gap. . This phenomenon is L
It is disadvantageous for realizing a low forward voltage of ED.
It is an object of the present invention to produce a new light emitting element that can satisfy the requirement of low forward voltage while maintaining high output and high speed characteristics in infrared LEDs mainly used for optical communication and space transmission.
【0009】[0009]
【課題を解決するための手段】本発明者は、上述の赤外
LEDの順方向電圧の低減(低VF化)について鋭意努
力検討した。その結果、GaAlAs系化合物半導体を
利用した発光素子用エピタキシャルウェハでは、特にp
型GaAlAsクラッド層中の主たる不純物をMgと
し、かつそのキャリア濃度を制御することで、LEDの
出力を低下させずに低VF化を達成できること、また、
LEDの発光出力は、p型層厚、酸素原子の影響が大き
いことを見いだし、本発明を完成した。The inventor of the present invention diligently studied reduction of the forward voltage of the above-mentioned infrared LED (reduction of VF). As a result, especially in the epitaxial wafer for light emitting device using the GaAlAs compound semiconductor, p
By making Mg the main impurity in the type GaAlAs clad layer and controlling the carrier concentration thereof, it is possible to achieve a low VF without lowering the output of the LED.
The inventors have found that the p-type layer thickness and oxygen atoms have a great influence on the light emission output of the LED, and have completed the present invention.
【0010】即ち本発明は、
(1)n型Ga1-X1AlX1Asクラッド層(0<X1<
1)と、p型Ga1-X2AlX2As活性層(0<X2<
1)と、p型Ga1-X3AlX3Asクラッド層(0<X3
<1)とが順次積層されたダブルヘテロ構造の発光部を
具備する発光素子用エピタキシャルウェハにおいて、p
型Ga1-X3AlX3Asクラッド層の主たる不純物がMg
であり、且つ該p型Ga1-X3AlX3Asクラッド層の表
面キャリア濃度が1×1018〜6×1018/cm3の範
囲内であることを特徴とする発光素子用エピタキシャル
ウェハ。
(2)p型Ga1-X3AlX3Asクラッド層の表面キャリ
ア濃度が1×1018〜3×1018/cm3の範囲内であ
ることを特徴とする前記(1)に記載の発光素子用エピ
タキシャルウェハ。
(3)p型Ga1-X3AlX3Asクラッド層の層厚が5μ
m以上30μm以下であることを特徴とする前記(1)
または(2)に記載の発光素子用エピタキシャルウェ
ハ。
(4)p型Ga1-X3AlX3Asクラッド層中の酸素濃度
が3×1016/cm3以下であることを特徴とする前記
(1)乃至(3)に記載の発光素子用エピタキシャルウ
ェハ。
(5)n型Ga1-X1AlX1Asクラッド層のp型Ga
1-X2AlX2As活性層が積層された側と反対側の表面
に、1層以上のn型GaAlAs層が形成されているこ
とを特徴とする前記(1)乃至(4)に記載の発光素子
用エピタキシャルウェハ。である。That is, the present invention provides: (1) n-type Ga 1-X1 Al X1 As clad layer (0 <X1 <
1) and a p-type Ga 1-X2 Al X2 As active layer (0 <X2 <
1) and a p-type Ga 1-X3 Al X3 As clad layer (0 <X3
<1) is sequentially laminated, and a light emitting element epitaxial wafer having a double heterostructure light emitting portion is provided.
The main impurity of the Ga 1 -X3 Al X3 As clad layer is Mg.
And the surface carrier concentration of the p-type Ga 1-X 3 Al X3 As clad layer is within the range of 1 × 10 18 to 6 × 10 18 / cm 3 . (2) The light emitting device as described in (1) above, wherein the surface carrier concentration of the p-type Ga 1 -X 3 Al X3 As cladding layer is in the range of 1 × 10 18 to 3 × 10 18 / cm 3. Epitaxial wafer. (3) The p-type Ga 1-X3 Al X3 As clad layer has a thickness of 5 μm.
m or more and 30 μm or less, the above (1)
Alternatively, the epitaxial wafer for a light emitting device according to (2). (4) The epitaxial wafer for a light emitting device as described in (1) to (3) above, wherein the p-type Ga 1 -X3 Al X3 As cladding layer has an oxygen concentration of 3 × 10 16 / cm 3 or less. . (5) p-type Ga of n-type Ga 1-X1 Al X1 As clad layer
(1) to (4) above, wherein one or more n-type GaAlAs layers are formed on the surface opposite to the side where the 1-X2 Al X2 As active layers are laminated. Epitaxial wafer for devices. Is.
【0011】また、本発明は、
(6)p型Ga1-X3AlX3Asクラッド層の表面に接し
てp型電極が設けられていることを特徴とする前記
(1)乃至(4)の何れか1項に記載の発光素子用エピ
タキシャルウェハを用いて作製した発光素子。
(7)p型Ga1-X3AlX3Asクラッド層の表面に接し
てp型電極が設けられており、n型Ga1-X1AlX1As
クラッド層の表面に形成されたn型GaAlAs層の表
面に接してn型電極が設けられていることを特徴とする
前記(5)に記載の発光素子用エピタキシャルウェハを
用いて作製した発光素子。
(8)発光波長が850〜900nmの範囲内である前
記(6)または(7)に記載の発光素子。である。The present invention also provides (6) the p - type electrode provided in contact with the surface of the p-type Ga 1 -X3 Al X3 As clad layer. A light emitting device produced using the epitaxial wafer for a light emitting device according to any one of claims. (7) A p - type electrode is provided in contact with the surface of the p-type Ga 1-X3 Al X3 As clad layer, and n-type Ga 1-X1 Al X1 As is formed.
A light-emitting device produced using the epitaxial wafer for a light-emitting device according to (5) above, wherein an n-type electrode is provided in contact with the surface of the n-type GaAlAs layer formed on the surface of the clad layer. (8) The light emitting device according to (6) or (7), which has an emission wavelength in the range of 850 to 900 nm. Is.
【0012】さらに、本発明は、
(9)液相エピタキシャル成長方法により、GaAs基
板上に、n型Ga1-X1AlX1Asクラッド層(0<X1
<1)と、p型Ga1-X2AlX2As活性層(0<X2<
1)と、p型Ga1-X3AlX3Asクラッド層(0<X3
<1)を順次積層し、ダブルヘテロ構造の発光部を形成
する発光素子用エピタキシャルウェハの製造方法におい
て、p型Ga1-X3AlX3Asクラッド層の成長の際に不
純物としてMgを添加し、該p型Ga1-X3AlX3Asク
ラッド層の表面キャリア濃度を1×1018〜6×1018
/cm3の範囲内に制御することを特徴とする発光素子
用エピタキシャルウェハの製造方法。
(10)p型Ga1-X3AlX3Asクラッド層の表面キャ
リア濃度を1×1018〜3×1018/cm3の範囲内に
制御することを特徴とする前記(9)に記載の発光素子
用エピタキシャルウェハの製造方法。
(11)p型Ga1-X3AlX3Asクラッド層の層厚を5
μm以上30μm以下とすることを特徴とする前記
(9)または(10)に記載の発光素子用エピタキシャ
ルウェハの製造方法。
(12)p型Ga1-X3AlX3Asクラッド層中の酸素濃
度を3×1016/cm3以下とすることを特徴とする前
記(9)乃至(11)に記載の発光素子用エピタキシャ
ルウェハの製造方法。
である。Further, according to the present invention, (9) the n-type Ga 1 -X1 Al X1 As cladding layer (0 <X1 is formed on the GaAs substrate by the liquid phase epitaxial growth method.
<1) and a p-type Ga 1-X2 Al X2 As active layer (0 <X2 <
1) and a p-type Ga 1-X3 Al X3 As clad layer (0 <X3
In the method for manufacturing an epitaxial wafer for a light emitting device, in which <1) is sequentially laminated to form a light emitting portion having a double hetero structure, Mg is added as an impurity during the growth of the p-type Ga 1 -X3 Al X3 As clad layer, The surface carrier concentration of the p-type Ga 1-X3 Al X3 As clad layer is set to 1 × 10 18 to 6 × 10 18.
A method for manufacturing an epitaxial wafer for a light-emitting device, characterized by controlling within a range of / cm 3 . (10) Emission according to (9) above, wherein the surface carrier concentration of the p-type Ga 1-X 3 Al X3 As cladding layer is controlled within the range of 1 × 10 18 to 3 × 10 18 / cm 3. Manufacturing method of epitaxial wafer for device. (11) The thickness of the p-type Ga 1-X3 Al X3 As clad layer is 5
The method for producing an epitaxial wafer for a light emitting device according to (9) or (10) above, wherein the thickness is not less than 30 μm and not more than 30 μm. (12) The epitaxial wafer for a light-emitting device as described in (9) to (11) above, wherein the oxygen concentration in the p-type Ga 1-X3 Al X3 As clad layer is 3 × 10 16 / cm 3 or less. Manufacturing method. Is.
【0013】[0013]
【発明の実施の形態】以下、本発明の実施の形態につい
て説明する。図1に赤外発光LEDの作製に用いる本発
明の発光素子用エピタキシャルウェハの構造を模式的に
示す。図1に示す発光素子用エピタキシャルウェハにお
いて、各エピタキシャル層は、n型GaAs単結晶基板
1上に第1のn型GaAlAs層2、第2のn型GaA
lAs層3、n型Ga1-X1AlX1Asクラッド層4(0
<X1<1)、p型Ga1-X2Al X2As活性層5(0<
X2<1)、及びp型Ga1-X3AlX3Asクラッド層6
(0<X3<1)の順で積層されている。BEST MODE FOR CARRYING OUT THE INVENTION The embodiments of the present invention will be described below.
Explain. Fig. 1 shows the present invention used for manufacturing infrared emitting LEDs.
Schematic structure of the epitaxial wafer for light emitting device
Show. On the epitaxial wafer for light emitting device shown in FIG.
And each epitaxial layer is an n-type GaAs single crystal substrate
On the first n-type GaAlAs layer 2, second n-type GaA
lAs layer 3, n-type Ga1-X1AlX1As clad layer 4 (0
<X1 <1), p-type Ga1-X2Al X2As active layer 5 (0 <
X2 <1), and p-type Ga1-X3AlX3As clad layer 6
The layers are stacked in the order of (0 <X3 <1).
【0014】各エピタキシャル層のAl混晶比について
は、活性層5は発光波長が850〜900nmになるよ
うに選択され、第1のn型層2、第2のn型層3、n型
クラッド層4、p型クラッド層6は、活性層5からの発
光を吸収しないようバンドギャップが活性層5より広く
なるよう選択される。第1のn型層2、第2のn型層
3、n型クラッド層4のドーパントにはTe、p型活性
層5のドーパントにはGe、p型クラッド層6のドーパ
ントにはMgを用いる。ここで活性層へのGeのドープ
量については、発光素子の発光強度と応答速度が最適に
なるよう選択される。Regarding the Al mixed crystal ratio of each epitaxial layer, the active layer 5 is selected so that the emission wavelength is 850 to 900 nm, and the first n-type layer 2, the second n-type layer 3 and the n-type clad are formed. The layer 4 and the p-type cladding layer 6 are selected so that the bandgap is wider than that of the active layer 5 so as not to absorb the light emitted from the active layer 5. Te is used as the dopant for the first n-type layer 2, the second n-type layer 3, and the n-type cladding layer 4, Ge is used as the dopant for the p-type active layer 5, and Mg is used as the dopant for the p-type cladding layer 6. . Here, the amount of Ge doped into the active layer is selected so that the emission intensity and the response speed of the light emitting element are optimized.
【0015】本発明の発光素子用エピタキシャルウェハ
の作製は、液相エピタキシャル成長法により行うのが好
ましい。液相エピタキシャル成長には、例えば図2に示
すようなスライドボート型成長装置を使用することがで
きる。図2に示したスライドボート型成長装置の治具の
うち、スライダー9の基板収納溝8にn型GaAs基板
7をセットする。スライドボート本体10にはGaAs
基板7上に成長させる層の数に応じたルツボを配置し、
ルツボの中にはエピタキシャル層を成長するために好適
な配合のGaメタル、金属Al、及びGaAs多結晶と
それぞれのエピタキシャル層の導電型とキャリヤ濃度を
実現するために好適なドーパントを配合する。The epitaxial wafer for light emitting device of the present invention is preferably manufactured by a liquid phase epitaxial growth method. For the liquid phase epitaxial growth, for example, a slide boat type growth apparatus as shown in FIG. 2 can be used. In the jig of the slide boat type growth apparatus shown in FIG. 2, the n-type GaAs substrate 7 is set in the substrate storage groove 8 of the slider 9. GaAs is used for the slide boat body 10.
Arrange crucibles according to the number of layers to be grown on the substrate 7,
In the crucible, a Ga metal, a metal Al, and a GaAs polycrystal having a composition suitable for growing the epitaxial layer and a dopant suitable for realizing the conductivity type and the carrier concentration of each epitaxial layer are compounded.
【0016】また、図2に示したスライドボート治具の
うち、基板収納溝8の内側、及びルツボ11〜15の内
側をグラッシーカーボンでコートすること、また、Ga
溶液が直接接触する部分をグラッシーカーボンでコート
すること、さらに、ルツボ蓋16をグラッシーカーボン
製とすることが好ましい。(図2中、ハッチング部分
は、グラッシーカーボンでコートされた部分、あるいは
グラッシーカーボン製品を示す。)Further, in the slide boat jig shown in FIG. 2, the inside of the substrate storage groove 8 and the inside of the crucibles 11 to 15 are coated with glassy carbon.
It is preferable that the portion in direct contact with the solution is coated with glassy carbon, and that the crucible lid 16 is made of glassy carbon. (In FIG. 2, the hatched portion indicates a portion coated with glassy carbon or a glassy carbon product.)
【0017】本発明の発光素子の作製では、上記のごと
き構成の成長装置を用いて液相エピタキシャル成長法に
より、GaAs基板上に図1に示したような各GaAl
As層のエピタキシャル成長を行った後、エピタキシャ
ルウェハを取り出し、p型GaAlAsクラッド層表面
を耐酸シートで保護して、アンモニア−過酸化水素系エ
ッチャントでGaAs基板を選択的に除去する。その
後、エピタキシャルウェハのp型GaAlAsクラッド
層表面と第1のn型GaAlAs層表面の両面にそれぞ
れ金からなるp型電極およびn型電極を形成し、ダイシ
ングによりエピタキシャルウェハを素子形状に分離する
ことにより、p型GaAlAsクラッド層が表面側とな
るようにした赤外発光LEDを作製することができる。In the production of the light emitting device of the present invention, each GaAl as shown in FIG. 1 is formed on a GaAs substrate by the liquid phase epitaxial growth method using the growth apparatus having the above structure.
After epitaxially growing the As layer, the epitaxial wafer is taken out, the surface of the p-type GaAlAs cladding layer is protected by an acid resistant sheet, and the GaAs substrate is selectively removed by an ammonia-hydrogen peroxide-based etchant. Then, a p-type electrode and an n-type electrode made of gold are formed on both surfaces of the p-type GaAlAs clad layer surface and the first n-type GaAlAs layer surface of the epitaxial wafer, and the epitaxial wafer is separated into element shapes by dicing. It is possible to manufacture an infrared emitting LED in which the p-type GaAlAs clad layer is on the front surface side.
【0018】本発明によって得られた赤外LEDは、高
発光出力であるため、特に赤外線を利用した光通信機器
や空間伝送用機器に用いられる送信用発光素子に好適に
用いることができる。本発明の赤外LEDを組み込んだ
光通信機器、空間伝送機器は大容量データ転送、長距離
データ伝送に適している。Since the infrared LED obtained by the present invention has a high light emission output, it can be suitably used for a light emitting element for transmission used in an optical communication device or a space transmission device utilizing infrared rays. The optical communication device and the space transmission device incorporating the infrared LED of the present invention are suitable for large capacity data transfer and long distance data transfer.
【0019】[0019]
【実施例】以下、実施例により本発明を更に詳細に説明
するが、本発明はこれに限定されるものではない。The present invention will be described in more detail with reference to the following examples, but the present invention is not limited thereto.
【0020】(実施例1)本実施例1では、前に図1で
示した積層構造の発光素子用エピタキシャルウェハを作
製した。発光素子用エピタキシャルウェハの各GaAl
As層のエピタキシャル成長は、前記説明した基板収納
溝及びルツボの内部をグラッシーカーボンでコートし、
グラッシーカーボン製の蓋を用いた図2に示したスライ
ドボート型成長装置を用いて行った。Example 1 In Example 1, an epitaxial wafer for a light emitting device having the laminated structure shown in FIG. 1 was prepared. Each GaAl of epitaxial wafer for light emitting device
The epitaxial growth of the As layer is performed by coating the inside of the substrate storage groove and the crucible described above with glassy carbon,
The slide boat type growth apparatus shown in FIG. 2 using a lid made of glassy carbon was used.
【0021】発光素子用エピタキシャルウェハの作製
は、以下のように行った。スライドボート型成長装置の
基板収納溝にn型GaAs基板をセットし、エピタキシ
ャル成長を行う際の各ルツボには下表1に示すような配
合でGaメタル、GaAs多結晶、金属Al、及びドー
パントを入れた。The epitaxial wafer for light emitting device was manufactured as follows. An n-type GaAs substrate was set in the substrate storage groove of the slide boat growth apparatus, and Ga metal, GaAs polycrystal, metal Al, and a dopant were added to each crucible at the time of performing epitaxial growth in the composition shown in Table 1 below. It was
【0022】[0022]
【表1】 [Table 1]
【0023】これらの原料をセットしたスライドボート
型成長装置を、石英反応管(図示せず。)内にセット
し、水素気流中で950℃まで加温し、原料を溶解し
た。続いて雰囲気温度を915℃まで降温し、スライダ
ー9を右側に押し、n型GaAs基板7をルツボ11の
下まで移動して原料溶液(メルト)に接触させた。次に
雰囲気温度を0.5℃/分の速度で降温し、n型GaA
s基板上に図1に示した第1のn型GaAlAs層2を
成長させた。系の温度が870℃に達した後、スライダ
ー9を再び押して第1メルトから分離し第2メルトと接
触させた。以下、同様の手順で下表2に示した温度範囲
で、Al混晶比のそれぞれ異なる第2のGaAlAs層
3、n型GaAlAsクラッド層4、p型GaAlAs
活性層5、p型GaAlAsクラッド層6を順次成長さ
せた。A slide boat type growth apparatus in which these raw materials were set was set in a quartz reaction tube (not shown) and heated to 950 ° C. in a hydrogen stream to dissolve the raw materials. Subsequently, the ambient temperature was lowered to 915 ° C., the slider 9 was pushed to the right, the n-type GaAs substrate 7 was moved to below the crucible 11 and brought into contact with the raw material solution (melt). Next, the ambient temperature is lowered at a rate of 0.5 ° C./minute to make the n-type GaA
The first n-type GaAlAs layer 2 shown in FIG. 1 was grown on the s substrate. After the system temperature reached 870 ° C., the slider 9 was pushed again to separate it from the first melt and bring it into contact with the second melt. Hereinafter, in the same procedure as above, the second GaAlAs layer 3, the n-type GaAlAs cladding layer 4, and the p-type GaAlAs having different Al mixed crystal ratios were used in the temperature ranges shown in Table 2 below.
The active layer 5 and the p-type GaAlAs cladding layer 6 were sequentially grown.
【0024】[0024]
【表2】 [Table 2]
【0025】本実施例1において、p型GaAlAsク
ラッド層6のキャリア濃度の水準を振るために、Gaメ
タル1kg当たりに添加するMg量を0.03〜0.3
gに変化させ、その他の条件は上記記載の成長方法と同
じとして、エピタキシャルウェハの作製を繰り返し行っ
た。その結果、p型GaAlAsクラッド層の表面キャ
リア濃度が8×1017〜8×1018/cm3のエピタキ
シャルウェハを得た。In Example 1, in order to change the carrier concentration level of the p-type GaAlAs cladding layer 6, the amount of Mg added per kg of Ga metal was 0.03 to 0.3.
g was changed, and the other conditions were the same as the growth method described above, and the production of the epitaxial wafer was repeated. As a result, an epitaxial wafer was obtained in which the surface carrier concentration of the p-type GaAlAs cladding layer was 8 × 10 17 to 8 × 10 18 / cm 3 .
【0026】エピタキシャル成長終了後、エピタキシャ
ルウェハを取り出し、図1のp型GaAlAsクラッド
層6の表面を耐酸シートで保護して、アンモニア−過酸
化水素系エッチャントでn型GaAs基板1を選択的に
除去した。その後、エピタキシャルウェハのp型GaA
lAsクラッド層表面と第1のn型GaAlAs層表面
の両面にそれぞれ金からなるp型電極およびn型電極を
形成し、ダイシングによりエピタキシャルウェハを40
0μm角の素子形状に分離することにより、図3に示す
構造のLEDを作製した。図3で、17はn型電極、1
8は第1のn型GaAlAs層、19は第2のn型Ga
AlAs層、20はn型GaAlAsクラッド層、21
はp型GaAlAs活性層、22はp型GaAlAsク
ラッド層、23はp型電極である。After completion of the epitaxial growth, the epitaxial wafer was taken out, the surface of the p-type GaAlAs cladding layer 6 in FIG. 1 was protected with an acid resistant sheet, and the n-type GaAs substrate 1 was selectively removed with an ammonia-hydrogen peroxide based etchant. . Then, p-type GaAs of the epitaxial wafer
A p-type electrode and an n-type electrode made of gold are formed on both surfaces of the 1As clad layer surface and the first n-type GaAlAs layer surface, and an epitaxial wafer is formed into 40 by dicing.
An LED having a structure shown in FIG. 3 was produced by separating the element into a 0 μm square element shape. In FIG. 3, 17 is an n-type electrode, 1
8 is the first n-type GaAlAs layer, and 19 is the second n-type Ga
AlAs layer, 20 is n-type GaAlAs clad layer, 21
Is a p-type GaAlAs active layer, 22 is a p-type GaAlAs cladding layer, and 23 is a p-type electrode.
【0027】(比較例1)実施例1と同様の条件で発光
素子用エピタキシャルウェハの作製を行った。ただし、
本比較例1で作製したウェハでは、p型GaAlAsク
ラッド層の主たる不純物をZnとした。その後、作製し
たエピタキシャルウェハを用いて、実施例1と同様にし
て、LEDを作製した。Comparative Example 1 An epitaxial wafer for a light emitting device was manufactured under the same conditions as in Example 1. However,
In the wafer manufactured in Comparative Example 1, Zn was the main impurity in the p-type GaAlAs cladding layer. Then, using the produced epitaxial wafer, an LED was produced in the same manner as in Example 1.
【0028】図4に上記実施例1及び比較例1で得られ
たLEDのp型GaAlAsクラッド層の表面キャリア
濃度と発光出力の関係、また図5に上記実施例1及び比
較例1で得られたLEDのp型GaAlAsクラッド層
の表面キャリア濃度と順方向電圧(VF)の関係を示し
た。FIG. 4 shows the relationship between the surface carrier concentration of the p-type GaAlAs cladding layers of the LEDs obtained in Example 1 and Comparative Example 1 and the emission output, and FIG. 5 shows the relationship between Example 1 and Comparative Example 1. The relationship between the surface carrier concentration of the p-type GaAlAs clad layer of the LED and the forward voltage (VF) is shown.
【0029】図4から明らかなように、p型GaAlA
sクラッド層の主たる不純物がMgの場合、表面キャリ
ア濃度が8×1017〜3×1018/cm3の範囲におい
ては発光出力が一定であり、3×1018/cm3を越え
ると発光出力が低下し、6×1018/cm3を越えると
目標出力を下回った。一方VFについては、p型GaA
lAsクラッド層の主たる不純物がMgの場合、図5か
ら分かるように、表面キャリア濃度の増加に伴い低下し
た。図5中のVFの値は、チップサイズ400μm角の
LEDのVF(順方向電流が500mA時)を示してい
るが、標準的なチップサイズである400μm角のLE
Dでの実用性を勘案すると、VF(電流500mA時)
は2.2V以下とするのが好ましく、そのためp型Ga
AlAsクラッド層の表面キャリア濃度は1×1018/
cm3以上とするのが望ましい。As is apparent from FIG. 4, p-type GaAlA
If major impurities s clad layer is Mg, in the range surface carrier concentration of 8 × 10 17 ~3 × 10 18 / cm 3 is a light emitting output is constant, 3 × exceeding 10 18 / cm 3 and the light-emitting output Fell below the target output when it exceeded 6 × 10 18 / cm 3 . On the other hand, for VF, p-type GaA
When the main impurity of the 1As clad layer was Mg, it decreased as the surface carrier concentration increased, as can be seen from FIG. The VF value in FIG. 5 indicates the VF (at a forward current of 500 mA) of an LED with a chip size of 400 μm square, and the standard chip size of 400 μm square LE
Considering the practicality of D, VF (at a current of 500 mA)
Is preferably 2.2 V or less, and therefore p-type Ga
The surface carrier concentration of the AlAs clad layer is 1 × 10 18 /
It is desirable to set it to cm 3 or more.
【0030】一方、p型GaAlAsクラッド層の主た
る不純物をZnにした場合には、図4から明らかなよう
に、表面キャリア濃度が2×1018/cm3以上になる
と発光出力が低下した。またVFは、図5から分かるよ
うに表面キャリア濃度の増加に伴い低下した。On the other hand, when Zn was used as the main impurity of the p-type GaAlAs cladding layer, as is apparent from FIG. 4, the emission output decreased when the surface carrier concentration became 2 × 10 18 / cm 3 or more. Further, as can be seen from FIG. 5, VF decreased as the surface carrier concentration increased.
【0031】徐冷法の液相エピタキシャル成長法を用い
てGaAlAs層をエピタキシャル成長させた場合の層
内のキャリア濃度分布は、ドーパントとして用いる元素
により異なる。ドーパントがMgの場合は、成長温度が
下がるに従い偏析係数が大きくなるので、成長が進むに
従いキャリア濃度が高くなり、成長終了部分のキャリア
濃度が最も高くなる。実施例1で成長したp型GaAl
Asクラッド層の場合、成長開始部分となる活性層との
界面でのキャリア濃度が最も低く、電極を形成する表面
のキャリア濃度が高くなるので、電極との接触抵抗を下
げることができ、順方向電圧の低減につながる。When the GaAlAs layer is epitaxially grown using the liquid phase epitaxial growth method of the slow cooling method, the carrier concentration distribution in the layer differs depending on the element used as the dopant. When the dopant is Mg, the segregation coefficient increases as the growth temperature decreases, so that the carrier concentration increases as the growth proceeds, and the carrier concentration at the growth end portion becomes the highest. P-type GaAl grown in Example 1
In the case of the As clad layer, the carrier concentration at the interface with the active layer, which is the growth start portion, is the lowest, and the carrier concentration on the surface forming the electrode is high, so the contact resistance with the electrode can be lowered and the forward direction It leads to the reduction of voltage.
【0032】一方、ドーパントがZnの場合は、温度変
化に対する偏析係数の変化がほとんどないので、エピタ
キシャル層内でのキャリア濃度はほぼ一定となる。電極
と接触する部分のキャリア濃度を上げるために、p型G
aAlAsクラッド層に高濃度にZnをドープすると、
エピタキシャル層全体が高いキャリア濃度になってしま
い、高ドープによる出力の低下やn型クラッド層への拡
散が起こりやすくなり、順方向電圧の低下には不利とな
る。On the other hand, when the dopant is Zn, there is almost no change in the segregation coefficient with respect to temperature changes, so the carrier concentration in the epitaxial layer is almost constant. In order to increase the carrier concentration in the part that contacts the electrode, p-type G
When Zn is doped at high concentration in the aAlAs clad layer,
Since the entire epitaxial layer has a high carrier concentration, a decrease in output due to high doping and diffusion into the n-type cladding layer are likely to occur, which is disadvantageous in decreasing a forward voltage.
【0033】上記実施例1より、p型GaAlAsクラ
ッド層の主たる不純物をMgとし、表面キャリア濃度を
1×1018〜6×1018/cm3の範囲内、好ましくは
1×1018〜3×1018/cm3の範囲内にすることに
よりVFが低く、高出力のLEDが得られることが判明
した。From Example 1 above, the main impurity of the p-type GaAlAs cladding layer was Mg, and the surface carrier concentration was in the range of 1 × 10 18 to 6 × 10 18 / cm 3 , preferably 1 × 10 18 to 3 ×. It was found that a high output LED with a low VF can be obtained by setting it within the range of 10 18 / cm 3 .
【0034】(実施例2)さらに実施例1の結果を踏ま
えて、p型GaAlAsクラッド層の表面キャリア濃度
が3×1018/cm3となる条件で、p型GaAlAs
クラッド層の層厚を2〜41μmの範囲内で変化させ、
その他は実施例1と同様の条件で発光素子用エピタキシ
ャルウェハを成長させ、LEDの作製を繰り返し行っ
た。Example 2 Further, based on the results of Example 1, p-type GaAlAs is formed under the condition that the surface carrier concentration of the p-type GaAlAs cladding layer is 3 × 10 18 / cm 3.
By changing the layer thickness of the clad layer within a range of 2 to 41 μm,
Other than that, an epitaxial wafer for a light-emitting element was grown under the same conditions as in Example 1, and LED production was repeated.
【0035】図6に本実施例2で得られたLEDのp型
GaAlAsクラッド層の層厚と発光出力の関係を示
す。図6から明らかなように、p型GaAlAsクラッ
ド層の層厚が30μm以下になると発光出力が向上する
ことが分かった。更に、層厚が薄くなるに従い出力が向
上することが確認された。但し、層厚が5μm以下にな
ると出力が低下することも確認された。従って、p型G
aAlAsクラッド層の層厚を5μm以上30μm以下
の範囲内、好ましくは10〜20μmの範囲内とするこ
とにより、LEDは高出力となることが判明した。FIG. 6 shows the relationship between the layer thickness of the p-type GaAlAs clad layer of the LED obtained in Example 2 and the light emission output. As is clear from FIG. 6, it was found that the light emission output was improved when the layer thickness of the p-type GaAlAs cladding layer was 30 μm or less. Furthermore, it was confirmed that the output increased as the layer thickness became thinner. However, it was also confirmed that the output decreased when the layer thickness was 5 μm or less. Therefore, p-type G
It was found that the LED has a high output by setting the layer thickness of the aAlAs clad layer within the range of 5 μm or more and 30 μm or less, preferably within the range of 10 to 20 μm.
【0036】(実施例3)本発明では、p型GaAlA
sクラッド層中の酸素濃度を3×1016/cm3以下と
する必要があるが、p型GaAlAsクラッド層中の酸
素濃度を再現性よく3×1016/cm3以下に抑えるた
めに、以下に示す酸素濃度低減対策をとるのが好まし
い。すなわち、エピタキシャル成長に用いるGaAs単
結晶基板およびGaAs多結晶は、使用前にエッチング
処理を行い、その後、超純水による洗浄と乾燥を十分に
行う。また、エピタキシャル成長の雰囲気を形成する水
素ガス、アルゴンガスは、市販されている高純度ガスに
ついて更に精製装置を用いて純化処理し、反応炉に供給
する。黒鉛製のスライドボート型成長装置については、
原料と直接接触する部分をグラッシーカーボン製或いは
グラッシーカーボンコートとし、更に、900℃以上で
ベーキング処理を行い成長装置に付着している水分を十
分に除去する。Example 3 In the present invention, p-type GaAlA is used.
the oxygen concentration of the s cladding layer is required to be 3 × 10 16 / cm 3 or less, but in order to suppress the oxygen concentration in the p-type GaAlAs cladding layer reproducibly in 3 × 10 16 / cm 3 or less, It is preferable to take the oxygen concentration reduction measures shown in. That is, the GaAs single crystal substrate and the GaAs polycrystal used for epitaxial growth are subjected to etching treatment before use, and then sufficiently washed with ultrapure water and dried. Further, the hydrogen gas and the argon gas that form the atmosphere for epitaxial growth are purified by using a commercially available high-purity gas using a refining device, and then supplied to the reaction furnace. Regarding the slide boat type growth device made of graphite,
The portion that is in direct contact with the raw material is made of glassy carbon or is coated with glassy carbon, and a baking treatment is further performed at 900 ° C. or higher to sufficiently remove the moisture adhering to the growth apparatus.
【0037】本実施例3では、上記の酸素濃度低減対策
を行ったエピタキシャルウェハの作製を数回繰り返し
た。上記のごとき酸素濃度を低減させる方策を実施した
結果、得られたエピタキシャルウェハのp型GaAlA
sクラッド層の酸素濃度は、いずれも3×1016/cm
3以下であった。なお、本実施例3で作製したp型Ga
AlAsクラッド層の表面キャリア濃度は3×1018/
cm3、また層厚は15μmとした。In Example 3, the production of the epitaxial wafer having the above oxygen concentration reduction measures was repeated several times. As a result of implementing the measures for reducing the oxygen concentration as described above, the p-type GaAlA of the epitaxial wafer obtained was obtained.
The oxygen concentration of the s clad layer is 3 × 10 16 / cm
It was 3 or less. The p-type Ga produced in Example 3 was used.
The surface carrier concentration of the AlAs clad layer is 3 × 10 18 /
cm 3 , and the layer thickness was 15 μm.
【0038】(比較例2)本比較例2では、上記実施例
3に記載した酸素濃度を低減させるための方策、即ち、
GaAs多結晶の使用前のエッチング処理と超純水によ
る洗浄、乾燥処理や使用する雰囲気ガスの精製処理は行
わずにエピタキシャルウェハの作製を数回行った。その
結果、得られたエピタキシャルウェハのp型GaAlA
sクラッド層の酸素濃度は、すべて4×1016/cm3
以上であった。なお、本比較例2で作製したp型GaA
lAsクラッド層の表面キャリア濃度は3×1018/c
m3、また層厚は15μmとした。(Comparative Example 2) In Comparative Example 2, a measure for reducing the oxygen concentration described in Example 3 above, that is,
Epitaxial wafers were produced several times without performing the etching treatment before the use of GaAs polycrystal, the washing with ultrapure water, the drying treatment and the purification treatment of the atmosphere gas to be used. As a result, p-type GaAlA of the obtained epitaxial wafer
The oxygen concentration in the s clad layer is all 4 × 10 16 / cm 3
That was all. The p-type GaA produced in Comparative Example 2 was used.
The surface carrier concentration of the 1As clad layer is 3 × 10 18 / c
m 3 and the layer thickness was 15 μm.
【0039】図7に、上記実施例3および比較例2で作
製したLEDのp型GaAlAsクラッド層中の酸素濃
度と発光出力の関係を示す。この結果から、p型GaA
lAsクラッド層の酸素濃度を、3×1016/cm3以
下とすることにより、目標出力以上の発光出力が得られ
ることが明らかになった。FIG. 7 shows the relationship between the oxygen concentration in the p-type GaAlAs clad layer of the LEDs produced in Example 3 and Comparative Example 2 and the emission output. From this result, p-type GaA
It was clarified that a light emission output higher than the target output can be obtained by setting the oxygen concentration of the 1As clad layer to 3 × 10 16 / cm 3 or less.
【0040】[0040]
【発明の効果】以上説明したように、本発明によれば高
出力の赤外LEDを作製するためのエピタキシャルウェ
ハ、及びこのエピタキシャルウェハから作製された赤外
LEDを提供することができる。特に、p型GaAlA
sクラッド層の主たる不純物をMgとし、表面キャリア
濃度を1×1018〜6×1018/cm3の範囲内とする
ことにより発光出力の向上とVFの低減を実現すること
が可能となった。また、p型GaAlAsクラッド層の
層厚を5〜30μmの範囲内とすることでLEDの更な
る高出力化が可能となった。As described above, according to the present invention, it is possible to provide an epitaxial wafer for producing a high-power infrared LED, and an infrared LED produced from this epitaxial wafer. In particular, p-type GaAlA
By making Mg the main impurity of the s clad layer and setting the surface carrier concentration within the range of 1 × 10 18 to 6 × 10 18 / cm 3 , it has become possible to improve the light emission output and reduce the VF. . Further, by setting the layer thickness of the p-type GaAlAs clad layer within the range of 5 to 30 μm, it has become possible to further increase the output of the LED.
【0041】本発明の赤外LED用エピタキシャルウェ
ハによって、赤外LEDの高発光出力化が可能となり、
大容量データ伝送、長距離データ伝送に対応できるLE
Dを作製することが可能となった。特に本発明のLED
を光通信、空間伝送機器に組み込んだ場合、従来にない
高性能の機器を提供することが可能となった。The infrared LED epitaxial wafer of the present invention enables high emission output of the infrared LED,
LE capable of supporting large-capacity data transmission and long-distance data transmission
It became possible to fabricate D. Especially the LED of the present invention
When is incorporated into optical communication and space transmission equipment, it has become possible to provide high-performance equipment that has never existed before.
【図1】本発明の発光素子用エピタキシャルウェハの構
造を示す図。FIG. 1 is a diagram showing a structure of an epitaxial wafer for a light emitting device of the present invention.
【図2】液相エピタキシャル成長に使用するスライドボ
ート型成長装置を示す図。FIG. 2 is a view showing a slide boat type growth apparatus used for liquid phase epitaxial growth.
【図3】本発明の実施例1に係わるLEDの構造を示す
図。FIG. 3 is a diagram showing a structure of an LED according to the first embodiment of the present invention.
【図4】LEDのp型GaAlAsクラッド層の表面キ
ャリア濃度と発光出力の関係を示す図。FIG. 4 is a diagram showing a relationship between a surface carrier concentration of a p-type GaAlAs clad layer of an LED and a light emission output.
【図5】LEDのp型GaAlAsクラッド層の表面キ
ャリア濃度と順方向電圧(VF)の関係を示す図。FIG. 5 is a diagram showing a relationship between a surface carrier concentration of a p-type GaAlAs clad layer of an LED and a forward voltage (VF).
【図6】LEDのp型GaAlAsクラッド層の層厚と
発光出力の関係を示す図。FIG. 6 is a diagram showing a relationship between a layer thickness of a p-type GaAlAs clad layer of an LED and a light emission output.
【図7】LEDのp型GaAlAsクラッド層中の酸素
濃度と発光出力の関係を示す図。FIG. 7 is a diagram showing the relationship between the oxygen concentration in the p-type GaAlAs cladding layer of the LED and the light emission output.
1 n型GaAs基板 2 第1のn型GaAlAs層 3 第2のn型GaAlAs層 4 n型GaAlAsクラッド層 5 p型GaAlAs活性層 6 p型GaAlAsクラッド層 7 n型GaAs基板 8 基板収納溝 9 スライダー 10 スライドボート本体 11 ルツボ 12 ルツボ 13 ルツボ 14 ルツボ 15 ルツボ 16 ルツボ蓋 17 n型電極 18 第1のn型GaAlAs層 19 第2のn型GaAlAs層 20 n型GaAlAsクラッド層 21 p型GaAlAs活性層 22 p型GaAlAsクラッド層 23 p型電極 1 n-type GaAs substrate 2 First n-type GaAlAs layer 3 Second n-type GaAlAs layer 4 n-type GaAlAs clad layer 5 p-type GaAlAs active layer 6 p-type GaAlAs clad layer 7 n-type GaAs substrate 8 substrate storage groove 9 slider 10 Slide boat body 11 crucibles 12 crucibles 13 crucibles 14 crucibles 15 crucibles 16 crucible lid 17 n-type electrode 18 First n-type GaAlAs layer 19 Second n-type GaAlAs layer 20 n-type GaAlAs clad layer 21 p-type GaAlAs active layer 22 p-type GaAlAs clad layer 23 p-type electrode
Claims (12)
X1<1)と、p型Ga 1-X2AlX2As活性層(0<X
2<1)と、p型Ga1-X3AlX3Asクラッド層(0<
X3<1)とが順次積層されたダブルヘテロ構造の発光
部を具備する発光素子用エピタキシャルウェハにおい
て、p型Ga1-X3AlX3Asクラッド層の主たる不純物
がMgであり、且つ該p型Ga1-X3AlX3Asクラッド
層の表面キャリア濃度が1×1018〜6×1018/cm
3の範囲内であることを特徴とする発光素子用エピタキ
シャルウェハ。1. n-type Ga1-X1AlX1As clad layer (0 <
X1 <1) and p-type Ga 1-X2AlX2As active layer (0 <X
2 <1) and p-type Ga1-X3AlX3As clad layer (0 <
Double heterostructure light emission in which X3 <1) are sequentially stacked
Epitaxial wafer for light emitting device
And p-type Ga1-X3AlX3Main impurities of As clad layer
Is Mg and the p-type Ga is1-X3AlX3As clad
The surface carrier concentration of the layer is 1 × 1018~ 6 × 1018/ Cm
3Epitaxy for light-emitting devices characterized in that
Shull wafer.
キャリア濃度が1×10 18〜3×1018/cm3の範囲
内であることを特徴とする請求項1に記載の発光素子用
エピタキシャルウェハ。2. A p-type Ga1-X3AlX3Surface of As clad layer
Carrier concentration is 1 × 10 18~ 3 x 1018/ Cm3Range of
The light emitting element according to claim 1, wherein
Epitaxial wafer.
が5μm以上30μm以下であることを特徴とする請求
項1または2に記載の発光素子用エピタキシャルウェ
ハ。3. The epitaxial wafer for a light emitting device according to claim 1, wherein the p-type Ga 1 -X3 Al X3 As clad layer has a layer thickness of 5 μm or more and 30 μm or less.
素濃度が3×1016/cm3以下であることを特徴とす
る請求項1乃至3に記載の発光素子用エピタキシャルウ
ェハ。4. The epitaxial wafer for a light emitting device according to claim 1, wherein the p-type Ga 1 -X3 Al X3 As cladding layer has an oxygen concentration of 3 × 10 16 / cm 3 or less.
Ga1-X2AlX2As活性層が積層された側と反対側の表
面に、1層以上のn型GaAlAs層が形成されている
ことを特徴とする請求項1乃至4に記載の発光素子用エ
ピタキシャルウェハ。5. One or more n-type GaAlAs layers are formed on the surface of the n-type Ga 1-X1 Al X1 As cladding layer opposite to the side where the p-type Ga 1-X2 Al X2 As active layer is laminated. The epitaxial wafer for a light emitting device according to claim 1, wherein the epitaxial wafer is a light emitting device.
に接してp型電極が設けられていることを特徴とする請
求項1乃至4の何れか1項に記載の発光素子用エピタキ
シャルウェハを用いて作製した発光素子。6. The light emitting device according to claim 1, wherein a p-type electrode is provided in contact with the surface of the p-type Ga 1 -X3 Al X3 As clad layer. A light emitting device manufactured using an epitaxial wafer.
に接してp型電極が設けられており、n型Ga1-X1Al
X1Asクラッド層の表面に形成されたn型GaAlAs
層の表面に接してn型電極が設けられていることを特徴
とする請求項5に記載の発光素子用エピタキシャルウェ
ハを用いて作製した発光素子。7. A p-type electrode is provided in contact with the surface of the p-type Ga 1-X3 Al X3 As clad layer, and n-type Ga 1-X1 Al is provided.
N-type GaAlAs formed on the surface of the X1 As cladding layer
The light emitting device manufactured using the epitaxial wafer for a light emitting device according to claim 5, wherein an n-type electrode is provided in contact with the surface of the layer.
ある請求項6または7に記載の発光素子。8. The light emitting device according to claim 6, which has an emission wavelength in the range of 850 to 900 nm.
As基板上に、n型Ga 1-X1AlX1Asクラッド層(0
<X1<1)と、p型Ga1-X2AlX2As活性層(0<
X2<1)と、p型Ga1-X3AlX3Asクラッド層(0
<X3<1)を順次積層し、ダブルヘテロ構造の発光部
を形成する発光素子用エピタキシャルウェハの製造方法
において、p型Ga1-X3AlX3Asクラッド層の成長の
際に不純物としてMgを添加し、該p型Ga1-X3AlX3
Asクラッド層の表面キャリア濃度を1×1018〜6×
1018/cm3の範囲内に制御することを特徴とする発
光素子用エピタキシャルウェハの製造方法。9. A liquid phase epitaxial growth method is used to obtain Ga.
N-type Ga on As substrate 1-X1AlX1As clad layer (0
<X1 <1) and p-type Ga1-X2AlX2As active layer (0 <
X2 <1) and p-type Ga1-X3AlX3As clad layer (0
<X3 <1) are sequentially stacked to form a light emitting portion having a double hetero structure.
Method for manufacturing epitaxial wafer for light emitting device for forming light emitting element
In, p-type Ga1-X3AlX3Growth of As clad layer
At this time, Mg was added as an impurity, and the p-type Ga1-X3AlX3
The surface carrier concentration of the As clad layer is 1 × 1018~ 6x
1018/ Cm3Is characterized by controlling within the range of
Method for manufacturing epitaxial wafer for optical device.
面キャリア濃度を1×1018〜3×1018/cm3の範
囲内に制御することを特徴とする請求項9に記載の発光
素子用エピタキシャルウェハの製造方法。10. The surface carrier concentration of the p-type Ga 1 -X3 Al X3 As cladding layer is controlled within the range of 1 × 10 18 to 3 × 10 18 / cm 3 . Method for manufacturing epitaxial wafer for light emitting device.
厚を5μm以上30μm以下とすることを特徴とする請
求項9または10に記載の発光素子用エピタキシャルウ
ェハの製造方法。11. The method for producing an epitaxial wafer for a light emitting device according to claim 9, wherein the p-type Ga 1 -X3 Al X3 As clad layer has a layer thickness of 5 μm or more and 30 μm or less.
酸素濃度を3×1016/cm3以下とすることを特徴と
する請求項9乃至11に記載の発光素子用エピタキシャ
ルウェハの製造方法。12. The epitaxial wafer for a light emitting device according to claim 9, wherein the oxygen concentration in the p-type Ga 1 -X3 Al X3 As clad layer is 3 × 10 16 / cm 3 or less. Production method.
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Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH08288546A (en) * | 1995-04-14 | 1996-11-01 | Dowa Mining Co Ltd | Light-emitting diode |
| JPH10214993A (en) * | 1997-01-29 | 1998-08-11 | Hitachi Cable Ltd | Epitaxial wafer, method for manufacturing the same, and light emitting diode |
| JP2000082841A (en) * | 1998-06-22 | 2000-03-21 | Hitachi Cable Ltd | Epitaxial wafer and method for manufacturing the same |
| JP2001007383A (en) * | 1999-06-18 | 2001-01-12 | Showa Denko Kk | Epitaxial substrate for semiconductor light emitting element and light emitting element |
-
2001
- 2001-06-29 JP JP2001198276A patent/JP2003017738A/en active Pending
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH08288546A (en) * | 1995-04-14 | 1996-11-01 | Dowa Mining Co Ltd | Light-emitting diode |
| JPH10214993A (en) * | 1997-01-29 | 1998-08-11 | Hitachi Cable Ltd | Epitaxial wafer, method for manufacturing the same, and light emitting diode |
| JP2000082841A (en) * | 1998-06-22 | 2000-03-21 | Hitachi Cable Ltd | Epitaxial wafer and method for manufacturing the same |
| JP2001007383A (en) * | 1999-06-18 | 2001-01-12 | Showa Denko Kk | Epitaxial substrate for semiconductor light emitting element and light emitting element |
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