JPH08213655A - Gallium nitride compound semiconductor light emitting device - Google Patents
Gallium nitride compound semiconductor light emitting deviceInfo
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- JPH08213655A JPH08213655A JP7291826A JP29182695A JPH08213655A JP H08213655 A JPH08213655 A JP H08213655A JP 7291826 A JP7291826 A JP 7291826A JP 29182695 A JP29182695 A JP 29182695A JP H08213655 A JPH08213655 A JP H08213655A
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- light emitting
- compound semiconductor
- gallium nitride
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Abstract
(57)【要約】
【目的】抵抗率を制御したN型のGaN 系の化合物半導体
発光素子の発光効率の改善
【構成】サファイア基板1上に500 ÅのAlN のバッファ
層2が形成され、その上に順に、膜厚約2.2 μm, シリ
コンドープされた電子濃度1.5 ×1018/cm3のGaNの高キ
ャリア濃度N+ 層3、膜厚約1.5 μm, 電子濃度 1×10
15/cm3以下のGaNの低キャリア濃度N層4、膜厚約0.2
μmのGaN から成るI層5が形成されている。I層5と
高キャリア濃度N+ 層3には、それぞれに接続する、ア
ルミニウムで形成された電極7と電極8とが形成されて
いる。
(57) [Abstract] [Purpose] Improving the luminous efficiency of N-type GaN-based compound semiconductor light-emitting devices with controlled resistivity [Constitution] A 500 Å AlN buffer layer 2 is formed on a sapphire substrate 1 and its In the order above, a film thickness of about 2.2 μm, a high carrier concentration N + layer 3 of GaN with an electron concentration of 1.5 × 10 18 / cm 3 doped with silicon, a film thickness of about 1.5 μm, an electron concentration of 1 × 10
GaN low carrier concentration N layer 4 of 15 / cm 3 or less, film thickness about 0.2
An I layer 5 of μm GaN is formed. Electrodes 7 and 8 made of aluminum are formed on the I layer 5 and the high carrier concentration N + layer 3, respectively.
Description
【0001】[0001]
【産業上の利用分野】本発明は、発光効率を改善した青
色発光の窒化ガリウム系化合物半導体発光素子に関す
る。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a blue light emitting gallium nitride compound semiconductor light emitting device having improved light emitting efficiency.
【0002】[0002]
【従来技術】従来、青色の発光ダイオードに、GaN 系の
化合物半導体が用いられている。そのGaN 系の化合物半
導体は直接遷移であることから発光効率が高いこと、光
の3原色の1つである青色を発光色とすること等から注
目されている。2. Description of the Related Art Conventionally, GaN-based compound semiconductors have been used for blue light emitting diodes. The GaN-based compound semiconductor is attracting attention because it has a high emission efficiency because it is a direct transition and because blue, which is one of the three primary colors of light, is the emission color.
【0003】このようなGaN 系の化合物半導体を用いた
発光ダイオードは、サファイア基板上に直接又は窒化ア
ルミニウムから成るバッファ層を介在させて、N型のGa
N 系の化合物半導体から成るN層を成長させ、そのN層
の上にP型不純物を添加してI型のGaN 系の化合物半導
体から成るI層を成長させた構造をとっている(特開昭
62-119196 号公報、特開昭63-188977 号公報) 。A light-emitting diode using such a GaN-based compound semiconductor has an N-type Ga directly on a sapphire substrate or with a buffer layer made of aluminum nitride interposed.
It has a structure in which an N layer made of an N 2 -based compound semiconductor is grown, and an I layer made of an I-type GaN-based compound semiconductor is grown by adding a P-type impurity on the N layer (Japanese Patent Application Laid-Open No. 2000-242242). Akira
62-119196, JP-A-63-188977).
【0004】[0004]
【発明が解決しようとする課題】上記構造の発光ダイオ
ードを製造する場合に、I層とN層との接合が用いられ
る。そして、GaN 系の化合物半導体を製造する場合に
は、通常、意図的に不純物をドーピングしなくても、そ
のGaN 系の化合物半導体はN導電型となり、逆に、シリ
コン等の半導体と異なり、I(Insulator)型の半導体を
得るには、亜鉛をドープしていた。又、N型のGaN を得
る場合には、その導電率の制御が困難であった。In manufacturing the light emitting diode having the above structure, the junction between the I layer and the N layer is used. When a GaN-based compound semiconductor is manufactured, the GaN-based compound semiconductor usually has an N conductivity type even if it is not intentionally doped with impurities, and conversely, unlike a semiconductor such as silicon, To obtain an (Insulator) type semiconductor, zinc was doped. Further, when obtaining N-type GaN, it was difficult to control the conductivity thereof.
【0005】しかしながら、本発明者は、上記のGaN 発
光ダイオードを製造する過程において、有機金属化合物
気相成長法によるGaN 半導体の気相成長技術を確立する
至り、高純度のGaN 気相成長膜を得ることができた。こ
の結果、従来、不純物のドーピングをしない場合には、
低抵抗率のN型GaN が得られたが、本発明者等の気相成
長技術の確立により、不純物のドーピングなしに高抵抗
率のGaN が得られた。However, in the process of manufacturing the above-mentioned GaN light emitting diode, the present inventor has established a vapor phase growth technique for a GaN semiconductor by a metalorganic vapor phase epitaxy method, and has developed a high purity GaN vapor phase growth film. I was able to get it. As a result, conventionally, when impurity doping is not performed,
Although N-type GaN with low resistivity was obtained, GaN with high resistivity was obtained without doping impurities by establishing vapor phase growth technology by the present inventors.
【0006】一方、今後、上記のGaN 発光ダイオードの
特性を向上させるためには、意図的に導電率の制御でき
るGaN 系化合物半導体の気相成長膜を得ることが必要と
なってきた。したがって、本発明の目的は、GaN 系化合
物半導体層を有する発光素子において、シリコンドープ
により抵抗率を制御可能することで、発光素子の発光効
率を向上させることである。On the other hand, in the future, in order to improve the characteristics of the above-mentioned GaN light emitting diode, it is necessary to obtain a vapor phase growth film of a GaN-based compound semiconductor whose conductivity can be controlled intentionally. Therefore, it is an object of the present invention to improve the luminous efficiency of a light emitting device having a GaN compound semiconductor layer by controlling the resistivity by silicon doping.
【0007】[0007]
【課題を解決するための手段】請求項1に記載の発明
は、窒化ガリウム系化合物半導体(AlXGa1-XN;X=0を含
む) を有する発光素子において、シリコンが添加された
窒化ガリウム系化合物半導体(AlXGa1-XN;X=0を含む) を
有することを特徴とする。According to a first aspect of the present invention, in a light emitting device having a gallium nitride-based compound semiconductor (including Al X Ga 1-X N; X = 0), silicon-doped nitriding is used. It is characterized by having a gallium compound semiconductor (including Al X Ga 1-X N; X = 0).
【0008】請求項2に記載の発明は、サファイア基板
上に形成された窒化ガリウム系化合物半導体(AlXGa
1-XN;X=0を含む) を有する発光素子において、シリコン
が添加された窒化ガリウム系化合物半導体(AlXGa1-XN;X
=0を含む) を有することを特徴とする。According to a second aspect of the present invention, there is provided a gallium nitride-based compound semiconductor (Al X Ga) formed on a sapphire substrate.
1-X N; including X = 0), a silicon-added gallium nitride-based compound semiconductor (Al X Ga 1-X N; X
(Including = 0).
【0009】請求項3に記載の発明は、サファイア基板
上に形成されたバッファ層上に形成された窒化ガリウム
系化合物半導体(AlXGa1-XN;X=0を含む) を有する発光素
子において、シリコンが添加された窒化ガリウム系化合
物半導体(AlXGa1-XN;X=0を含む) を有することを特徴と
する。According to a third aspect of the present invention, a light emitting device having a gallium nitride-based compound semiconductor (including Al X Ga 1 -X N; X = 0) formed on a buffer layer formed on a sapphire substrate. In gallium nitride-based compound semiconductor (including Al X Ga 1 -X N; X = 0) to which silicon is added.
【0010】請求項4に記載の発明は、シリコンが添加
された窒化ガリウム系化合物半導体(AlXGa1-XN;X=0を含
む) には取出電極が形成されていることを特徴とする。The invention according to claim 4 is characterized in that an extraction electrode is formed on a gallium nitride-based compound semiconductor (Al X Ga 1 -X N; including X = 0) to which silicon is added. To do.
【0011】請求項5に記載の発明は、シリコンが添加
された窒化ガリウム系化合物半導体(AlXGa1-XN;X=0を含
む) の抵抗率は3×10-1Ωcm−8×10-3Ωcmである
ことを特徴とする。According to a fifth aspect of the invention, the resistivity of the gallium nitride compound semiconductor (Al X Ga 1-X N; including X = 0) to which silicon is added has a resistivity of 3 × 10 -1 Ωcm-8 ×. It is characterized by being 10 −3 Ωcm.
【0012】[0012]
【発明の作用及び効果】本発明は、窒化ガリウム系化合
物半導体層(AlXGa1-XN;X=0を含む) を有する発光素子に
おいて、シリコンドープを可能として、その層の抵抗率
を制御可能とした結果、抵抗率の制御された窒化ガリウ
ム系化合物半導体層(AlXGa1-XN;X=0を含む) を精度良く
得ることができた。この結果、発光素子の発光効率を向
上させることができた。INDUSTRIAL APPLICABILITY The present invention makes it possible to dope silicon in a light emitting device having a gallium nitride-based compound semiconductor layer (including Al X Ga 1-X N; X = 0), and to improve the resistivity of the layer. As a result of making controllable, a gallium nitride-based compound semiconductor layer (including Al X Ga 1-X N; X = 0) with controlled resistivity could be obtained with high accuracy. As a result, the luminous efficiency of the light emitting element could be improved.
【0013】[0013]
【実施例】以下、本発明を具体的な実施例に基づいて説
明する。本発明の製造方法を用いて、図1に示す構造の
発光ダイオード10を製造した。EXAMPLES The present invention will be described below based on specific examples. The light emitting diode 10 having the structure shown in FIG. 1 was manufactured using the manufacturing method of the present invention.
【0014】図1において、発光ダイオード10はサフ
ァイア基板1を有しており、そのサファイア基板1に50
0 ÅのAlN のバッファ層2が形成されている。そのバッ
ファ層2の上には、順に、膜厚約 2.2μmのGaN から成
る高キャリア濃度N+ 層3と膜厚約 1.5μmのGaN から
成る低キャリア濃度N層4が形成されている。更に、低
キャリア濃度N層4の上に膜厚約 0.2μmのGaN から成
るI層5が形成されている。そして、I層5に接続する
アルミニウムで形成された電極7と高キャリア濃度N+
層3に接続するアルミニウムで形成された電極8とが形
成されている。In FIG. 1, the light emitting diode 10 has a sapphire substrate 1, and the sapphire substrate 1 has a sapphire substrate 1.
A buffer layer 2 of 0Å AlN is formed. On the buffer layer 2, a high carrier concentration N + layer 3 of GaN having a film thickness of about 2.2 μm and a low carrier concentration N layer 4 of GaN having a film thickness of about 1.5 μm are sequentially formed. Further, an I layer 5 made of GaN having a film thickness of about 0.2 μm is formed on the low carrier concentration N layer 4. Then, the electrode 7 formed of aluminum and connected to the I layer 5 and the high carrier concentration N +
An electrode 8 made of aluminum is formed which is connected to the layer 3.
【0015】次に、この構造の発光ダイオード10の製
造方法について説明する。上記発光ダイオード10は、
有機金属化合物気相成長法( 以下「M0VPE 」と記す) に
よる気相成長により製造された。用いられたガスは、NH
3 とキャリアガスH2とトリメチルガリウム(Ga(CH3)3)
(以下「TMG 」と記す) とトリメチルアルミニウム(Al
(CH3)3)(以下「TMA 」と記す) とシラン(SiH4)とジエ
チル亜鉛(以下「DEZ 」と記す) である。Next, a method of manufacturing the light emitting diode 10 having this structure will be described. The light emitting diode 10 is
It was manufactured by vapor phase growth by an organometallic compound vapor phase growth method (hereinafter referred to as “M0VPE”). The gas used was NH
3 and the carrier gas H 2 and trimethylgallium (Ga (CH 3) 3)
(Hereinafter referred to as "TMG") and trimethylaluminum (Al
(CH 3) 3) (a hereinafter referred to as "TMA") and silane (SiH 4) and diethyl zinc (hereinafter referred to as "DEZ").
【0016】まず、有機洗浄及び熱処理により洗浄した
a面を主面とする単結晶のサファイア基板1をM0VPE 装
置の反応室に載置されたサセプタに装着する。次に、H2
を流速 2 l/分で反応室に流しながら温度1200℃でサフ
ァイア基板1を10分間気相エッチングした。次に、温度
を 400℃まで低下させて、H2を流速20 l/分、NH3 を流
速10 l/分、15℃に保持したTMA をバブリングさせたH2
を50cc/ 分で供給してAlN のバッファ層2が約 500Åの
厚さに形成された。First, the single crystal sapphire substrate 1 whose main surface is the a-plane cleaned by organic cleaning and heat treatment is mounted on the susceptor placed in the reaction chamber of the M0VPE apparatus. Then H 2
Was flown into the reaction chamber at a flow rate of 2 l / min, and the sapphire substrate 1 was vapor-phase etched at a temperature of 1200 ° C. for 10 minutes. Next, the temperature was lowered to 400 ° C., H 2 was flown at 20 l / min, NH 3 was flown at 10 l / min, and TMA kept at 15 ° C. was bubbled into H 2
Was supplied at 50 cc / min to form an AlN buffer layer 2 having a thickness of about 500Å.
【0017】次に、TMA の供給を停止して、サファイア
基板1の温度を1150℃に保持し、H2を 20 l/分、他の
原料ガスとしてのNH3 を 10 l/分及び、-15 ℃に保持
したTMG をバブリングさせたH2を100 cc/ 分で流し、シ
リコンを含むガスとしてH2で0.86ppm まで希釈したシラ
ン(SiH4)を 200ml/ 分で30分流して、膜厚約 2.2μm、
キャリア濃度 1.5×1018/cm3のGaN から成る高キャリア
濃度N+ 層3を形成した。Next, the supply of TMA is stopped, the temperature of the sapphire substrate 1 is maintained at 1150 ° C., H 2 is 20 l / min, NH 3 as another source gas is 10 l / min, and − of H 2 which was bubbled TMG kept at 15 ℃ flowed at 100 cc / min, silane diluted with H 2 to 0.86ppm as a gas containing silicon (SiH 4) and 30 shunted 200ml / min, thickness About 2.2 μm,
To form a high carrier concentration N + layer 3 made of GaN having a carrier concentration 1.5 × 10 18 / cm 3.
【0018】続いて、サファイア基板1の温度を1150℃
に保持し、H2を 20 l/分、NH3 を10 l/分、-15 ℃
に保持したTMG をバブリングさせたH2を100 cc/ 分で20
分間流して、膜厚約 1.5μm、キャリア濃度 1×1015/c
m3以下のGaN から成る低キャリア濃度N層4を形成し
た。Then, the temperature of the sapphire substrate 1 is set to 1150 ° C.
, H 2 20 l / min, NH 3 10 l / min, -15 ℃
Of H 2 which was bubbled TMG held at 100 cc / min to 20
Flowing for 1 minute, film thickness about 1.5μm, carrier concentration 1 × 10 15 / c
A low carrier concentration N layer 4 made of GaN of m 3 or less was formed.
【0019】次に、サファイア基板1を 900℃にして、
H2 を20 l/分、NH3 を10 l/分、TMG を 1.7×10-4モ
ル/分、DEZ を 1.5×10-4モル/分の割合で供給して、
膜厚0.2μmのGaN から成るI層5を形成した。このよ
うにして、図2に示すような多層構造が得られた。次
に、図3に示すように、I層5の上に、スパッタリング
によりSiO2層11を2000Åの厚さに形成した。次に、そ
のSiO2層11上にフォトレジスト12を塗布して、フォ
トリソグラフにより、そのフォトレジスト12を高キャ
リア濃度N+層3に対する電極形成部位のフォトレジス
トを除去したパターンに形成した。Next, the sapphire substrate 1 is set to 900 ° C.,
H 2 at 20 l / min, NH 3 at 10 l / min, TMG at 1.7 × 10 −4 mol / min and DEZ at 1.5 × 10 −4 mol / min,
An I layer 5 made of GaN having a film thickness of 0.2 μm was formed. In this way, a multilayer structure as shown in FIG. 2 was obtained. Next, as shown in FIG. 3, a SiO 2 layer 11 having a thickness of 2000 Å was formed on the I layer 5 by sputtering. Next, a photoresist 12 was applied on the SiO 2 layer 11, and the photoresist 12 was formed by photolithography into a pattern in which the photoresist at the electrode formation site for the high carrier concentration N + layer 3 was removed.
【0020】次に、図4に示すように、フォトレジスト
12によって覆われていないSiO2層11をフッ酸系エッ
チング液で除去した。次に、図5に示すように、フォト
レジスト12及びSiO2層11によって覆われていない部
位のI層5とその下の低キャリア濃度N層4と高キャリ
ア濃度N+ 層3の上面一部を、真空度0.04Torr、高周波
電力0.44W/cm2 、CCl2F2ガスを10ml/分で供給しドライ
エッチングした後、Arでドライエッチングした。次に、
図6に示すように、I層5上に残っているSiO2層11を
フッ酸で除去した。Next, as shown in FIG. 4, the SiO 2 layer 11 not covered with the photoresist 12 was removed with a hydrofluoric acid-based etching solution. Next, as shown in FIG. 5, a part of the upper surface of the I layer 5 in a portion not covered by the photoresist 12 and the SiO 2 layer 11, the low carrier concentration N layer 4 and the high carrier concentration N + layer 3 thereunder. Was vacuum-dried at a rate of 0.04 Torr, high-frequency power of 0.44 W / cm 2 , and CCl 2 F 2 gas was supplied at 10 ml / min for dry etching, followed by dry etching with Ar. next,
As shown in FIG. 6, the SiO 2 layer 11 remaining on the I layer 5 was removed with hydrofluoric acid.
【0021】次に、図7に示すように、試料の上全面に
Al層13を蒸着により形成した。そして、そのAl層13
の上にフォトレジスト14を塗布して、フォトリソグラ
フにより、そのフォトレジスト14が高キャリア濃度N
+ 層3及びI層5に対する電極部が残るように、所定形
状にパターン形成した。次に、図7に示すようにそのフ
ォトレジスト14をマスクとして下層のAl層13の露出
部を硝酸系エッチング液でエッチングし、フォトレジス
ト14をアセトンで除去し、高キャリア濃度N+ 層3の
電極8、I層5の電極7を形成した。Next, as shown in FIG.
The Al layer 13 was formed by vapor deposition. And the Al layer 13
Photoresist 14 is applied on top of it, and the photoresist 14 has a high carrier concentration N by photolithography.
A pattern was formed in a predetermined shape so that the electrode portions for the + layer 3 and the I layer 5 remained. Next, as shown in FIG. 7, using the photoresist 14 as a mask, the exposed portion of the lower Al layer 13 is etched with a nitric acid-based etching solution, the photoresist 14 is removed with acetone, and the high carrier concentration N + layer 3 is removed. An electrode 8 and an electrode 7 of the I layer 5 were formed.
【0022】このようにして、図1に示す構造のMIS(Me
ta- l-Insulator-Semiconductor)構造の窒化ガリウム系
発光素を製造することができる。上記の製造過程におい
て、高キャリア濃度N+ 層3を気相成長させるとき、H2
を20 l/分、他の原料ガスとしてのNH3 を10 l/分及
び、-15 ℃に保持した TMGをバブリングさせたH2を100c
c/分で流し、シリコンを含むガスとしてH2で0.86ppm ま
で希釈したシラン(SiH4)を10cc/ 分〜300 cc/ 分の範囲
で制御することにより、高キャリア濃度N+ 層3のの抵
抗率は、図8に示すように、3 ×10-1Ωcmから 8×10-3
Ωcmまで変化させることができる。In this way, the MIS (Me with the structure shown in FIG.
It is possible to manufacture a gallium nitride-based luminescent element having a ta-l-Insulator-Semiconductor) structure. In the above manufacturing process, when the high carrier concentration N + layer 3 is vapor-phase grown, H 2
20 l / min, NH 3 as another source gas 10 l / min, and H 2 bubbling TMG held at -15 ℃
Flowing at c / min and controlling the silane (SiH 4 ) diluted with H 2 to 0.86 ppm as a gas containing silicon in the range of 10 cc / min to 300 cc / min, the high carrier concentration N + layer 3 As shown in Fig. 8, the resistivity is from 3 × 10 -1 Ωcm to 8 × 10 -3.
It can be changed up to Ωcm.
【0023】なお、上記方法では、シラン(SiH4)を制御
したが他の原料ガスの流量を制御しても良く、また、両
者の混合比率を制御して抵抗率を変化させても良い。ま
た、本実施例ではSiドーパント材料としてシランを使用
したが、Siを含む有機化合物例えばテトラエチルシラン
(Si(C2H5)4) などをH2でバブリングしたガスを用いても
良い。このようにして、高キャリア濃度N+ 層3と低キ
ャリ濃度N層4とを抵抗率の制御可能状態で形成するこ
とができた。In the above method, silane (SiH 4 ) was controlled, but the flow rates of other source gases may be controlled, and the mixture ratio of both may be controlled to change the resistivity. Although silane was used as the Si dopant material in this example, an organic compound containing Si such as tetraethylsilane is used.
A gas obtained by bubbling (Si (C 2 H 5 ) 4 ) or the like with H 2 may be used. In this way, the high carrier concentration N + layer 3 and the low carrier concentration N layer 4 could be formed in a state where the resistivity could be controlled.
【0024】この結果、上記の方法で製造された発光ダ
イオード10の発光強度は、0.2mcdであり、従来のI層
とN層とから成る発光ダイオードの発光強度の4倍に向
上した。又、発光面を観察した所、発光点の数が増加し
ていることも観察された。As a result, the light emitting intensity of the light emitting diode 10 manufactured by the above method is 0.2 mcd, which is four times as high as the light emitting intensity of the conventional light emitting diode including the I layer and the N layer. When the light emitting surface was observed, it was also observed that the number of light emitting points increased.
【図1】本発明の具体的な一実施例に係る発光ダイオー
ドの構成を示した構成図。FIG. 1 is a configuration diagram showing a configuration of a light emitting diode according to a specific embodiment of the present invention.
【図2】同実施例の発光ダイオードの製造工程を示した
断面図FIG. 2 is a cross-sectional view showing a manufacturing process of the light emitting diode of the same embodiment.
【図3】同実施例の発光ダイオードの製造工程を示した
断面図FIG. 3 is a cross-sectional view showing a manufacturing process of the light emitting diode of the same embodiment.
【図4】同実施例の発光ダイオードの製造工程を示した
断面図FIG. 4 is a sectional view showing a manufacturing process of the light emitting diode of the same embodiment.
【図5】同実施例の発光ダイオードの製造工程を示した
断面図FIG. 5 is a cross-sectional view showing a manufacturing process of the light emitting diode of the same embodiment.
【図6】同実施例の発光ダイオードの製造工程を示した
断面図FIG. 6 is a sectional view showing a manufacturing process of the light emitting diode of the embodiment.
【図7】同実施例の発光ダイオードの製造工程を示した
断面図FIG. 7 is a sectional view showing a manufacturing process of the light emitting diode of the same embodiment.
【図8】シランガスの流量と気相成長されたN層の電気
的特性との関係を示した測定図。FIG. 8 is a measurement diagram showing the relationship between the flow rate of silane gas and the electrical characteristics of a vapor-grown N layer.
10…発光ダイオード 1…サファイア基板 2…バッファ層 3…高キャリア濃度N+ 層 4…低キャリア濃度N層 5…I層 7,8…電極10 ... Light emitting diode 1 ... Sapphire substrate 2 ... Buffer layer 3 ... High carrier concentration N + layer 4 ... Low carrier concentration N layer 5 ... I layer 7, 8 ... Electrode
───────────────────────────────────────────────────── フロントページの続き (71)出願人 390014535 新技術事業団 埼玉県川口市本町4丁目1番8号 (72)発明者 佐々 道成 愛知県西春日井郡春日町大字落合字長畑1 番地 豊田合成株式会社内 (72)発明者 真部 勝英 愛知県西春日井郡春日町大字落合字長畑1 番地 豊田合成株式会社内 (72)発明者 馬淵 彰 愛知県西春日井郡春日町大字落合字長畑1 番地 豊田合成株式会社内 (72)発明者 加藤 久喜 愛知県西春日井郡春日町大字落合字長畑1 番地 豊田合成株式会社内 (72)発明者 橋本 雅文 愛知県愛知郡長久手町大字長湫字横道41番 地の1 (72)発明者 赤崎 勇 愛知県名古屋市千種区不老町(番地なし) 名古屋大学内 ─────────────────────────────────────────────────── ─── Continuation of the front page (71) Applicant 390014535 New Technology Corporation 4-8-8 Honmachi, Kawaguchi City, Saitama Prefecture (72) Inventor Sasa Dosei, Nagasaki, Kasuga Town, Nishikasugai District, Aichi Prefecture In-house (72) Inventor Masahide Masabe 1 Ochiai, Nagachi, Kasuga-cho, Nishikasugai-gun, Aichi Toyoda Gosei Co., Ltd. (72) Inventor Kuki, Kasuga-cho, Nishi-Kasugai-gun, Aichi 1 Ochiai, Nagahata 1 Toyoda Gosei Co., Ltd. Inventor Yu Akasaki Furo-cho, Chikusa-ku, Nagoya, Aichi Prefecture (no street number) Inside Nagoya University
Claims (5)
1-XN;X=0を含む) を有する発光素子において、 シリコンが添加された窒化ガリウム系化合物半導体(AlX
Ga1-XN;X=0を含む) を有することを特徴とする窒化ガリ
ウム系化合物半導体発光素子。1. A gallium nitride-based compound semiconductor (Al X Ga
1-X N; including X = 0), a silicon-doped gallium nitride-based compound semiconductor (Al X
Ga 1-X N; including X = 0).
ウム系化合物半導体(AlXGa1-XN;X=0を含む) を有する発
光素子において、 シリコンが添加された窒化ガリウム系化合物半導体(AlX
Ga1-XN;X=0を含む) を有することを特徴とする窒化ガリ
ウム系化合物半導体発光素子。2. A light emitting device having a gallium nitride-based compound semiconductor (including Al X Ga 1-X N; X = 0) formed on a sapphire substrate, wherein a gallium nitride-based compound semiconductor (Al X
Ga 1-X N; including X = 0).
層上に形成された窒化ガリウム系化合物半導体(AlXGa
1-XN;X=0を含む) を有する発光素子において、 シリコンが添加された窒化ガリウム系化合物半導体(AlX
Ga1-XN;X=0を含む) を有することを特徴とする窒化ガリ
ウム系化合物半導体発光素子。3. A gallium nitride based compound semiconductor (Al X Ga) formed on a buffer layer formed on a sapphire substrate.
1-X N; including X = 0), a silicon-doped gallium nitride-based compound semiconductor (Al X
Ga 1-X N; including X = 0).
系化合物半導体(AlXGa1-XN;X=0を含む) には取出電極が
形成されていることを特徴とする請求項3に記載の発光
素子。4. The extraction electrode is formed on the gallium nitride-based compound semiconductor (Al X Ga 1-X N; including X = 0) to which the silicon is added. Light emitting element.
系化合物半導体(AlXGa1-XN;X=0を含む) の抵抗率は3×
10-1Ωcm−8×10-3Ωcmであることを特徴とする請
求項1乃至請求項4に記載の発光素子。5. The resistivity of the gallium nitride-based compound semiconductor to which silicon is added (including Al X Ga 1-X N; X = 0) has a resistivity of 3 ×.
The light emitting device according to claim 1, wherein the light emitting device has a density of 10 -1 Ωcm-8 × 10 -3 Ωcm.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP29182695A JP3312715B2 (en) | 1995-10-13 | 1995-10-13 | Gallium nitride based compound semiconductor light emitting device |
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|---|---|---|---|
| JP29182695A JP3312715B2 (en) | 1995-10-13 | 1995-10-13 | Gallium nitride based compound semiconductor light emitting device |
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| JP5020990A Division JP2623466B2 (en) | 1990-02-28 | 1990-02-28 | Gallium nitride based compound semiconductor light emitting device |
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| JP11284752A Division JP2000091640A (en) | 1999-10-05 | 1999-10-05 | Method of manufacturing gallium nitride based compound semiconductor light emitting device |
| JP11284751A Division JP2000091633A (en) | 1999-10-05 | 1999-10-05 | Gallium nitride based compound semiconductor |
| JP2001237826A Division JP2002118283A (en) | 2001-08-06 | 2001-08-06 | Manufacturing method of gallium nitride semiconductor |
| JP2001238156A Division JP2002118286A (en) | 2001-08-06 | 2001-08-06 | Gallium nitride based compound semiconductor light emitting device |
| JP2001238206A Division JP2002118287A (en) | 2001-08-06 | 2001-08-06 | Gallium nitride based compound semiconductor |
| JP2001238061A Division JP2002118285A (en) | 2001-08-06 | 2001-08-06 | Manufacturing method of gallium nitride semiconductor |
| JP2001237927A Division JP2002118284A (en) | 2001-08-06 | 2001-08-06 | Manufacturing method of gallium nitride semiconductor |
| JP2001237997A Division JP2002057370A (en) | 2001-08-06 | 2001-08-06 | Manufacturing method of gallium nitride semiconductor |
| JP2001238119A Division JP3521201B2 (en) | 2001-08-06 | 2001-08-06 | Method of manufacturing gallium nitride compound semiconductor |
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| JPH08213655A true JPH08213655A (en) | 1996-08-20 |
| JP3312715B2 JP3312715B2 (en) | 2002-08-12 |
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Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH10261817A (en) * | 1998-02-12 | 1998-09-29 | Toyoda Gosei Co Ltd | Gallium nitride based compound semiconductor light emitting device |
| JP2000091633A (en) * | 1999-10-05 | 2000-03-31 | Toyoda Gosei Co Ltd | Gallium nitride based compound semiconductor |
| JP2000091640A (en) * | 1999-10-05 | 2000-03-31 | Toyoda Gosei Co Ltd | Method of manufacturing gallium nitride based compound semiconductor light emitting device |
| JP2001168048A (en) * | 2000-10-16 | 2001-06-22 | Toyoda Gosei Co Ltd | Manufacturing method of gallium nitride semiconductor |
| JP2001168389A (en) * | 2000-10-16 | 2001-06-22 | Toyoda Gosei Co Ltd | Method of manufacturing gallium nitride based compound semiconductor light emitting device |
| JP2001185499A (en) * | 2000-10-16 | 2001-07-06 | Toyoda Gosei Co Ltd | Method for manufacturing gallium nitride-based compound semiconductor |
| JP2002118286A (en) * | 2001-08-06 | 2002-04-19 | Toyoda Gosei Co Ltd | Gallium nitride based compound semiconductor light emitting device |
| JP2002118284A (en) * | 2001-08-06 | 2002-04-19 | Toyoda Gosei Co Ltd | Manufacturing method of gallium nitride semiconductor |
| JP2002118287A (en) * | 2001-08-06 | 2002-04-19 | Toyoda Gosei Co Ltd | Gallium nitride based compound semiconductor |
| JP2002118283A (en) * | 2001-08-06 | 2002-04-19 | Toyoda Gosei Co Ltd | Manufacturing method of gallium nitride semiconductor |
| JP2002118285A (en) * | 2001-08-06 | 2002-04-19 | Toyoda Gosei Co Ltd | Manufacturing method of gallium nitride semiconductor |
| US9130122B2 (en) | 2013-09-06 | 2015-09-08 | Industrial Technology Research Institute | Light emitting diode |
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|---|---|---|---|---|
| JPS59228776A (en) * | 1983-06-10 | 1984-12-22 | Nippon Telegr & Teleph Corp <Ntt> | Semiconductor hetero-junction element |
| JPH03252175A (en) * | 1990-02-28 | 1991-11-11 | Toyoda Gosei Co Ltd | Manufacture of gallium nitride compound semiconductor |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JPS59228776A (en) * | 1983-06-10 | 1984-12-22 | Nippon Telegr & Teleph Corp <Ntt> | Semiconductor hetero-junction element |
| JPH03252175A (en) * | 1990-02-28 | 1991-11-11 | Toyoda Gosei Co Ltd | Manufacture of gallium nitride compound semiconductor |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH10261817A (en) * | 1998-02-12 | 1998-09-29 | Toyoda Gosei Co Ltd | Gallium nitride based compound semiconductor light emitting device |
| JP2000091633A (en) * | 1999-10-05 | 2000-03-31 | Toyoda Gosei Co Ltd | Gallium nitride based compound semiconductor |
| JP2000091640A (en) * | 1999-10-05 | 2000-03-31 | Toyoda Gosei Co Ltd | Method of manufacturing gallium nitride based compound semiconductor light emitting device |
| JP2001168048A (en) * | 2000-10-16 | 2001-06-22 | Toyoda Gosei Co Ltd | Manufacturing method of gallium nitride semiconductor |
| JP2001168389A (en) * | 2000-10-16 | 2001-06-22 | Toyoda Gosei Co Ltd | Method of manufacturing gallium nitride based compound semiconductor light emitting device |
| JP2001185499A (en) * | 2000-10-16 | 2001-07-06 | Toyoda Gosei Co Ltd | Method for manufacturing gallium nitride-based compound semiconductor |
| JP2002118286A (en) * | 2001-08-06 | 2002-04-19 | Toyoda Gosei Co Ltd | Gallium nitride based compound semiconductor light emitting device |
| JP2002118284A (en) * | 2001-08-06 | 2002-04-19 | Toyoda Gosei Co Ltd | Manufacturing method of gallium nitride semiconductor |
| JP2002118287A (en) * | 2001-08-06 | 2002-04-19 | Toyoda Gosei Co Ltd | Gallium nitride based compound semiconductor |
| JP2002118283A (en) * | 2001-08-06 | 2002-04-19 | Toyoda Gosei Co Ltd | Manufacturing method of gallium nitride semiconductor |
| JP2002118285A (en) * | 2001-08-06 | 2002-04-19 | Toyoda Gosei Co Ltd | Manufacturing method of gallium nitride semiconductor |
| US9130122B2 (en) | 2013-09-06 | 2015-09-08 | Industrial Technology Research Institute | Light emitting diode |
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