JP3193981B2 - Gallium nitride based compound semiconductor light emitting device - Google Patents
Gallium nitride based compound semiconductor light emitting deviceInfo
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- JP3193981B2 JP3193981B2 JP5021190A JP5021190A JP3193981B2 JP 3193981 B2 JP3193981 B2 JP 3193981B2 JP 5021190 A JP5021190 A JP 5021190A JP 5021190 A JP5021190 A JP 5021190A JP 3193981 B2 JP3193981 B2 JP 3193981B2
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Description
本発明は青色発光の窒素ガリウム系化合物半導体発光
素子に関する。The present invention relates to a nitrogen-gallium-based compound semiconductor light-emitting device that emits blue light.
従来、青色の発光ダイオードとしてGaN系の化合物半
導体を用いたものが知られている。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。 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型導電型のGaN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)。Conventionally, a blue light emitting diode using a GaN-based compound semiconductor has been known. Since the GaN-based compound semiconductor is a direct transition, the luminous efficiency is high,
Attention has been paid to making blue, one of the three primary colors of light, the emission color. A light emitting diode using such a GaN-based compound semiconductor grows an N-layer made of an N-type conductive GaN-based compound semiconductor on a sapphire substrate directly or with a buffer layer made of aluminum nitride interposed therebetween. A structure in which a P-type impurity is added to the N-layer to grow an I-layer made of an I-type GaN-based compound semiconductor (Japanese Patent Laid-Open No. Sho 62-62).
119196, JP-A-63-188977).
【発明が解決しようとする課題】 しかし、上記構造の発光ダイオードの発光強度は未だ
十分ではなく、改良が望まれている。 そこで、本発明の目的は、GaN系の化合物半導体の発
光ダイオードの青色の発光強度を向上させることであ
る。However, the light emission intensity of the light emitting diode having the above structure is not yet sufficient, and improvement is desired. Therefore, an object of the present invention is to improve the blue light emission intensity of a GaN-based compound semiconductor light emitting diode.
本発明は、N型の窒素ガリウム系化合物半導体(AlXG
a1-XN;X=0を含む)からなるN層と、P型不純物を添
加したI型の窒素ガリウム系化合物半導体(AlXGa1-XN;
X=0を含む)からなるI層を有する窒素ガリウム系化
合物半導体発光素子において、 N層をI層と接合する側から順に、低キャリア濃度N
層と高キャリア濃度N+層との二重層構造とし、I層をN
層と接合する側から順に、P型不純物が比較的低濃度の
低不純物濃度IL層とP型の不純物が比較的高濃度の高不
純物濃度IH層との二重層構造としたことを特徴とする。 尚、上記低キャリア濃度N層のキャリア濃度は1×10
14〜1×1017/cm3で膜厚は0.5〜2μmが望ましい。キ
ャリア濃度が1×1017/cm3以上となると発光強度が低下
するので望ましくなく、1×1014/cm3以下となると発光
素子の直列抵抗が高くなりすぎ電流を流すと発熱するの
で望ましくない。又、膜厚が2μm以上となると発光素
子の直列抵抗が高くなりすぎ電流を流すと発熱するので
望ましくなく、膜厚が0.5μm以下になると発光強度が
低下するので望ましくない。 更に、高キャリア濃度N+層のキャリア濃度は1×1017
〜1×1019/cm3で膜厚は1〜10μmが望ましい。キャリ
ア濃度が1×1019/cm3以上となると結晶性が悪化するの
で望ましくなく、1×1017/cm3以下となると高抵抗とな
るので望ましくない。又、膜厚が10μm以上となると基
板が湾曲するので望ましくなく、膜厚が1μm以下とな
ると高抵抗となるので望ましくない。 又、上記低不純物濃度IL層のP型不純物濃度は1×10
16〜5×1019/cm3で膜厚は0.01〜1μmが望ましい。P
型不純物濃度が5×1019/cm3以上となると発光ダイオー
ドの直列抵抗が増大したり立上がり電圧が上昇するので
望ましくなく、1×1016/cm3以下となるとN導電型とな
るので望ましくない。又、膜厚が1μm以上となると発
光ダイオードの直列抵抗が増大したり立上がり電圧が上
昇するので望ましくなく、膜厚が0.01μm以下となると
従来構造と等しくなるので望ましくない。更に、高不純
物濃度IH層の不純物濃度は1×1019〜5×1020/cm3で膜
厚は0.02〜0.3μmが望ましい。不純物濃度が5×1020/
cm3以上となると結晶性が悪化するので望ましくなく、
1×1019/cm3以下となると発光強度が低下するので望ま
しくない。又、膜厚が0.3μm以上となると高抵抗とな
るので望ましくなく、膜厚が0.02μm以下となるとI層
が破壊されるので望ましくない。The present invention provides an N-type gallium-based compound semiconductor (Al X G
a 1-X N; including X = 0) and an I-type nitrogen-gallium-based compound semiconductor (Al X Ga 1-X N;
X = 0 (including X = 0) in the nitrogen-gallium-based compound semiconductor light-emitting device having an I layer.
Layer and a high carrier concentration N + layer.
It has a double-layer structure consisting of a low-impurity-concentration IL layer with a relatively low concentration of P-type impurities and a high-impurity-concentration IH layer with a relatively high concentration of P-type impurities, in order from the side that joins the layers And The carrier concentration of the low carrier concentration N layer is 1 × 10
The thickness is preferably 14 to 1 × 10 17 / cm 3 and the thickness is 0.5 to 2 μm. When the carrier concentration is 1 × 10 17 / cm 3 or more, the emission intensity is decreased. Undesirably, when the carrier concentration is 1 × 10 14 / cm 3 or less, the series resistance of the light-emitting element becomes too high and heat is generated when a current is applied. . On the other hand, when the film thickness is 2 μm or more, the series resistance of the light emitting element becomes excessively high, and heat is generated when an electric current is applied. Further, the carrier concentration of the high carrier concentration N + layer is 1 × 10 17
It is preferable that the thickness is 1 to 10 μm at 1 × 10 19 / cm 3 . If the carrier concentration is 1 × 10 19 / cm 3 or more, the crystallinity is deteriorated, and if it is 1 × 10 17 / cm 3 or less, the resistance becomes high, which is not desirable. On the other hand, when the film thickness is 10 μm or more, the substrate is undesirably curved, and when the film thickness is 1 μm or less, high resistance is undesirably obtained. The P-type impurity concentration of the low impurity concentration IL layer is 1 × 10
The thickness is preferably 16 to 5 × 10 19 / cm 3 and the thickness is preferably 0.01 to 1 μm. P
Since type impurity concentration is rising voltage or series resistance increases the light emitting diode becomes 5 × 10 19 / cm 3 or more is increased undesirably, undesirable since 1 × 10 16 / cm 3 or less when it comes to the N conductivity type . On the other hand, if the film thickness is 1 μm or more, the series resistance of the light-emitting diode increases and the rise voltage rises, which is not desirable. Further, the film thickness impurity concentration at 1 × 10 19 ~5 × 10 20 / cm 3 of high impurity concentration I H layer 0.02~0.3μm is desirable. The impurity concentration is 5 × 10 20 /
If it is more than cm 3 , crystallinity deteriorates, which is not desirable,
When the density is less than 1 × 10 19 / cm 3 , the emission intensity is undesirably reduced. On the other hand, when the film thickness is 0.3 μm or more, the resistance becomes high, which is not desirable. When the film thickness is 0.02 μm or less, the I layer is destroyed, which is not desirable.
本発明は、N層をI層と接合する側から順に、低キャ
リア濃度N層と高キャリア濃度N+層との二重層構造と
し、I層をN層と接合する側から順に、P型不純物が比
較的低濃度の低不純物濃度IL層とP型不純物が比較的高
濃度の高不純物濃度IH層との二重層構造としたことで、
発光ダイオードの青色の発光強度を増加させることがで
きた。 即ち、高キャリア濃度N+層によりN層全体の電気抵抗
を小さくでき、I層と低キャリア濃度N層との接合に有
効に電圧を印加することができる。又、I層に接合する
N層は低キャリア濃度とすることで、I層にN層の非発
光不純物原子が拡散または混入するのが防止される。
又、N層からI層に電子が注入されるとき、N層に接合
するI層を低不純物濃度IL層とすることで、電子はその
低不純物濃度IL層でトラップされることなく、次の高不
純物濃度IH層に注入される。このため、電子は発光効率
の悪いN層に接合した低不純物濃度IL層を通過して、高
不純物濃度IH層に至り、その層で高効率で発光すること
になる。 この結果、発光効率が従来の単純なI−N接合に比べ
て、飛躍的に向上した。The present invention provides a double layer structure of a low carrier concentration N layer and a high carrier concentration N + layer in order from the side where the N layer is joined to the I layer, and a P-type impurity in order from the side where the I layer is joined to the N layer. Has a double-layered structure of a relatively low-concentration low-impurity-concentration IL layer and a relatively high-concentration high-impurity-concentration IH layer having a relatively high concentration of P-type impurities.
The blue light emission intensity of the light emitting diode could be increased. That is, the electric resistance of the entire N layer can be reduced by the high carrier concentration N + layer, and a voltage can be effectively applied to the junction between the I layer and the low carrier concentration N layer. Further, by making the N layer bonded to the I layer have a low carrier concentration, diffusion or mixing of non-emitting impurity atoms of the N layer into the I layer can be prevented.
Further, when electrons are injected from the N layer to the I layer, the I layer joined to the N layer is formed as the low impurity concentration IL layer, so that the electrons are not trapped in the low impurity concentration IL layer. It is implanted into the next high impurity concentration I H layer. For this reason, the electrons pass through the low impurity concentration I L layer joined to the N layer having poor luminous efficiency, reach the high impurity concentration I H layer, and emit light with high efficiency in that layer. As a result, the luminous efficiency was dramatically improved as compared with the conventional simple IN junction.
以下、本発明を具体的な実施例に基づいて説明する。 第1図において、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500Å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、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、膜厚約1.5μ
m、キャリア濃度1×1015/cm3のGaNから成る低キャリ
ア濃度N層4、Zn濃度5×1019/cm3の低不純物濃度IL層
5及びZn濃度2×1020/cm3の高不純物濃度IH層6とが形
成されている。そして、高不純物濃度IH層6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。 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「MOVPE」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、NH3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。 まず、有機洗浄及び熱処理により洗浄したc面を主面
とする単結晶のサファイア基板1をMOVPE装置の反応室
に載置されたサセプタに装着する。 次に、常圧でH2を2/分で反応室に流しながら温度
1100℃でサファイア基板1を気相エッチングした。 次に、温度を400℃まで低下させて、H2を20/分、N
H3を10/分、TMAを1.8×10-5モル/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。 次に、サファイア基板1の温度を1150℃に保持し、H2
を20/分、NH3を10/分、TMGを1.7×10-4モル/
分、H2で0.86ppmまで希釈したシラン(SiH4)を200ml/
分の割合で30分間供給し、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。 続いて、サファイア基板1の温度を1150℃に保持し、
H2を20/分、NH3を10/分、TMGを1.7×10-4モル/
分、の割合で20分間供給し、膜厚約1.5μm、キャリア
濃度1×1015/cm3のGaNから成る低キャリア濃度N層4
を形成した。 次に、サファイア基板1を1000℃にして、H2を20/
分、NH3を10/分、TMGを1.7×10-4モル/分、DEZを1.
5×10-4モル/分の割合で2分間供給して、膜厚0.2μ
m、GaNから成るZn濃度5×1019/cm3の低不純物濃度IL
層5を形成した。 続いて、サファイア基板1を900にして、H2を20/
分、NH3を10/分、TMGを1.7×10-4モル/分、DEZを1.
5×10-4モル/分の割合で2分間供給して、膜厚0.2μ
m、GaNから成るZn濃度2×1020/cm3の高不純物濃度IH
層6を形成した。 このようにして、第2図に示すような多層構造が得ら
れた。 次に、第3図に示すように、高不純物濃度IH層6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。 次に、第4図に示すように、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、第5図に示すように、フォトレジスト12及びSi
O2層11によって覆われていない部位の高不純物濃度IH層
6とその下の低不純物濃度IL層5と低キャリア濃度N層
4と高キャリア濃度N+層3の上面一部を、真空度44Tor
r、高周波電力0.44W/cm3、CCl2F2ガスを10cc/分でドラ
イエッチングした後、Arでドライエッチングした。 次に、第6図に示すように、IH層6上に残っているSi
O2層11をフッ酸で除去した。 次に、第7図に示すように、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及び高不純
物濃度IH層6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、第7図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、高不純物濃度IH層
6の電極7を形成した。 このようにして、第1図に示すようにMIS(Metal−In
sulator−Semiconductor)構造の窒素ガリウム系発光素
を製造することができる。 このようにして製造された発光ダイオード10の発光強
度を測定したところ、0.2mcdであった。これは、単純に
キャリア濃度2×1020/cm3、厚さ0.2μmのI層とキャ
リア濃度5×1017/cm3、厚さ4μmのN層とを接続した
従来の発光ダイオードに比べて、発光強度が8倍に向上
した。 又、発光面を観察した所、発光点の数が飛躍的に増加
していることも観察された。 尚、低キャリア濃度N層4のキャリア濃度を各種変化
させた上記試料を製造して、発光強度及び発光スペクト
ラムを測定した。その結果を、第8図に示す。 キャリア濃度が増加するに連れて、発光強度が減少
し、且つ、発光波長が赤色側に変位することが分かる。 又、高不純物濃度IH層6の不純物濃度を各種変化させ
た上記構造の試料を製造して、不純物濃度と発光強度及
び発光スペクトラムとの関係を測定した。その結果を、
第9図に示す。 不純物濃度が増加するに連れて、発光強度が増加す
る。しかし、発光波長は幾分、赤色側に変位するが約48
50Åで安定することが分かる。Hereinafter, the present invention will be described based on specific examples. In FIG. 1, a light emitting diode 10 has a sapphire substrate 1, and the sapphire substrate 1
Buffer layer 2 is formed. On the buffer layer 2, a film thickness of about 2.2 μm and a carrier concentration of 1.5 × 10 18
/ cm 3 GaN high carrier concentration N + layer 3, about 1.5μ thick
m, a low carrier concentration N layer 4 made of GaN having a carrier concentration of 1 × 10 15 / cm 3 , a low impurity concentration IL layer 5 having a Zn concentration of 5 × 10 19 / cm 3 and a Zn concentration of 2 × 10 20 / cm 3 . A high impurity concentration IH layer 6 is formed. Then, an electrode 7 made of aluminum connected to the high impurity concentration I H layer 6 and an electrode 8 made of aluminum connected to the high carrier concentration N + layer 3 are formed. Next, a method for manufacturing the light emitting diode 10 having this structure will be described. The light emitting diode 10 was manufactured by vapor phase growth using a metal organic compound vapor phase epitaxy method (hereinafter referred to as “MOVPE”). The gases used were NH 3 , carrier gas H 2 , trimethylgallium (Ga (CH 3 ) 3 ) (hereinafter referred to as “TMG”), and trimethylaluminum (Al (CH 3 ) 3 ) (hereinafter referred to as “TMA”). ), Silane (SiH 4 ) and diethylzinc (hereinafter “DEZ”)
Is written). First, a single-crystal sapphire substrate 1 whose main surface is a c-plane cleaned by organic cleaning and heat treatment is mounted on a susceptor placed in a reaction chamber of a MOVPE apparatus. Next, while flowing H 2 at a normal pressure into the reaction chamber at a rate of 2 / minute,
The sapphire substrate 1 was subjected to gas phase etching at 1100 ° C. Then, by lowering the temperature to 400 ° C., the H 2 20 / min, N
H 3 10 / min, AlN supplied at 1.8 × 10 -5 mol / min TMA
Was formed to a thickness of about 500 °. Then, maintaining the temperature of the sapphire substrate 1 to 1150 ° C., H 2
20 / min, NH 3 10 / min, TMG 1.7 × 10 −4 mol /
Silane (SiH 4 ) diluted to 0.86 ppm with H 2
And a carrier concentration of 1.5 × 10 18 / cm 3 , to form a high carrier concentration N + layer 3 of GaN having a thickness of about 2.2 μm and a carrier concentration of 1.5 × 10 18 / cm 3 . Subsequently, the temperature of the sapphire substrate 1 is maintained at 1150 ° C.
H 2 at 20 / min, NH 3 at 10 / min, TMG at 1.7 × 10 −4 mol /
And a low carrier concentration N layer 4 made of GaN having a film thickness of about 1.5 μm and a carrier concentration of 1 × 10 15 / cm 3.
Was formed. Then the sapphire substrate 1 to 1000 ° C., H 2 20 /
Min, the NH 3 10 / min, 1.7 × 10 -4 mol / min TMG, the DEZ 1.
It is supplied at a rate of 5 × 10 -4 mol / min for 2 minutes to give a film thickness of 0.2 μm.
Low impurity concentration I L with Zn concentration of 5 × 10 19 / cm 3 consisting of m and GaN
Layer 5 was formed. Subsequently, the sapphire substrate 1 was set to 900, and H 2 was changed to 20 /
Min, the NH 3 10 / min, 1.7 × 10 -4 mol / min TMG, the DEZ 1.
It is supplied at a rate of 5 × 10 -4 mol / min for 2 minutes to give a film thickness of 0.2 μm.
High impurity concentration I H with Zn concentration of 2 × 10 20 / cm 3 consisting of m and GaN
Layer 6 was formed. Thus, a multilayer structure as shown in FIG. 2 was obtained. Next, as shown in FIG. 3, an SiO 2 layer 11 was formed on the high impurity concentration I H layer 6 to a thickness of 2000 ° by sputtering. Next, a photoresist 12 is applied on the SiO 2 layer 11, and the photoresist is applied by photolithography.
12 was formed in a pattern in which the photoresist at the electrode formation site for the high carrier concentration N + layer 3 was removed. Next, as shown in FIG. 4, the SiO 2 layer 11 not covered with the photoresist 12 was removed with a hydrofluoric acid-based etchant. Next, as shown in FIG.
A portion of the upper surface of the high impurity concentration I H layer 6 at a portion not covered by the O 2 layer 11, the low impurity concentration IL layer 5, the low carrier concentration N layer 4, and the high carrier concentration N + layer 3 Vacuum 44Tor
r, dry etching was performed with a high frequency power of 0.44 W / cm 3 and CCl 2 F 2 gas at a rate of 10 cc / min, followed by dry etching with Ar. Next, as shown in FIG. 6, Si remaining on I H layer 6
The O 2 layer 11 was removed with hydrofluoric acid. Next, as shown in FIG. 7, an Al layer 13
Was formed by vapor deposition. Then, a photoresist 14 is applied on the Al layer 13 and a predetermined photolithography is performed so that the photoresist 14 has an electrode portion for the high carrier concentration N + layer 3 and the high impurity concentration I H layer 6. A pattern was formed into a shape. 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 etchant, the photoresist 14 is removed with acetone, and the high carrier concentration N + layer 3 is removed. And the electrode 7 of the high impurity concentration IH layer 6 were formed. In this manner, as shown in FIG. 1, the MIS (Metal-In
A gallium-based luminous element having a (sulator-semiconductor) structure can be manufactured. The light emission intensity of the light-emitting diode 10 manufactured as described above was 0.2 mcd. This is compared with a conventional light emitting diode in which an I layer having a carrier concentration of 2 × 10 20 / cm 3 and a thickness of 0.2 μm is simply connected to an N layer having a carrier concentration of 5 × 10 17 / cm 3 and a thickness of 4 μm. The luminous intensity was improved eight times. Further, when the light emitting surface was observed, it was also observed that the number of light emitting points increased dramatically. In addition, the above-mentioned sample in which the carrier concentration of the low carrier concentration N layer 4 was variously changed was manufactured, and the light emission intensity and the light emission spectrum were measured. The results are shown in FIG. It can be seen that the emission intensity decreases and the emission wavelength shifts to the red side as the carrier concentration increases. In addition, samples having the above-described structure in which the impurity concentration of the high impurity concentration IH layer 6 was varied in various ways were manufactured, and the relationship between the impurity concentration, the light emission intensity, and the light emission spectrum was measured. The result is
As shown in FIG. The emission intensity increases as the impurity concentration increases. However, the emission wavelength slightly shifted to the red side, but about 48
It turns out that it stabilizes at 50Å.
第1図は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、第2図乃至第7図は同実施例
の発光ダイオードの製造工程を示した断面図、第8図は
低キャリア濃度N層のキャリア濃度と発光強度及び発光
波長との関係を示した測定図、第9図は高不純物濃度IH
層の不純物濃度と発光強度及び発光波長との関係を示し
た測定図である。 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……低不純物濃度IL層 6……高不純物濃度IH層、7,8……電極FIG. 1 is a configuration diagram showing a configuration of a light emitting diode according to a specific embodiment of the present invention, FIGS. 2 to 7 are cross-sectional views showing manufacturing steps of the light emitting diode of the embodiment, FIG. FIG measurement diagram showing the relationship between the carrier concentration of the low carrier concentration N layer and the emission intensity and emission wavelength, FIG. 9 is a high impurity concentration I H
FIG. 4 is a measurement diagram showing a relationship between an impurity concentration of a layer, an emission intensity, and an emission wavelength. 10 light emitting diode, 1 sapphire substrate 2 buffer layer 3 high carrier concentration N + layer 4 low carrier concentration N layer 5 low impurity concentration I L layer 6 high impurity concentration I H layer, 7,8 …… Electrode
───────────────────────────────────────────────────── フロントページの続き (73)特許権者 999999999 科学技術振興事業団 埼玉県川口市本町4丁目1番8号 (72)発明者 真部 勝英 愛知県西春日井郡春日村大字落合字長畑 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村大字落合字長畑 1番地 豊田合成株式会社内 (72)発明者 山崎 史郎 愛知県西春日井郡春日村大字落合字長畑 1番地 豊田合成株式会社内 (72)発明者 小出 典克 愛知県西春日井郡春日村大字落合字長畑 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 株式会社豊田中央研究所内 (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 (56)参考文献 特開 昭53−34486(JP,A) 特開 昭59−228776(JP,A) 特開 昭63−188977(JP,A) 特開 昭62−119196(JP,A) 実開 昭64−17484(JP,U) (58)調査した分野(Int.Cl.7,DB名) H01L 33/00 H01L 21/205 ──────────────────────────────────────────────────続 き Continuing on the front page (73) Patent holder 999999999 Japan Science and Technology Corporation 4-1-8, Honcho, Kawaguchi-shi, Saitama (72) Inventor Katsuhide Mabe 1 Ochiai-Ochiagai, Nagasahata Within Toyoda Gosei Co., Ltd. Inside (72) Inventor Norikatsu Koide 1 Ochiai Nagahata, Kasuga-mura, Nishi-Kasugai-gun, Aichi Prefecture Inside Toyoda Gosei Co., Ltd. Inside Toyota Central Research Laboratory Co., Ltd. (72) Inventor Isamu Isamachi, Chikusa-ku, Nagoya, Aichi On-campus (56) References JP-A-53-34486 (JP, A) JP-A-59-228776 (JP, A) JP-A-63-188977 (JP, A) JP-A-62-119196 (JP, A) Actual Opening Sho 64-17484 (JP, U) (58) Fields investigated (Int. Cl. 7 , DB name) H01L 33/00 H01L 21/205
Claims (1)
a1-XN;X=0を含む)からなるN層と、P型不純物を添
加したI型の窒素ガリウム系化合物半導体(AlXGa1-XN;
X=0を含む)からなるI層とを有する窒素ガリウム系
化合物半導体発光素子において、 前記N層を前記I層と接合する側から順に、低キャリア
濃度N層と高キャリア濃度N+層との二重層構造とし、 前記I層を前記N層と接合する側から順に、前記P型不
純物が比較的低濃度の低不純物濃度IL層と前記P型不純
物が比較的高濃度の高不純物濃度IH層との二重層構造と
したことを特徴とする発光素子。1. An N-type nitrogen gallium-based compound semiconductor (Al X G
a 1-X N; including X = 0) and an I-type nitrogen-gallium-based compound semiconductor (Al X Ga 1-X N;
X = 0 (including X = 0), and a nitrogen-gallium-based compound semiconductor light-emitting device having an I layer composed of a low carrier concentration N layer and a high carrier concentration N + layer in order from the side where the N layer is joined to the I layer. A double-layer structure, in which, from the side where the I layer is joined to the N layer, the P-type impurity has a relatively low concentration of a low impurity concentration I L layer and the P-type impurity has a relatively high concentration of a high impurity concentration I L A light-emitting element having a double-layer structure with an H layer.
Priority Applications (14)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5021190A JP3193981B2 (en) | 1990-02-28 | 1990-02-28 | Gallium nitride based compound semiconductor light emitting device |
| CA002037198A CA2037198C (en) | 1990-02-28 | 1991-02-27 | Light-emitting semiconductor device using gallium nitride group compound |
| EP91102921A EP0444630B1 (en) | 1990-02-28 | 1991-02-27 | Light-emitting semiconductor device using gallium nitride group compound |
| DE69126152T DE69126152T2 (en) | 1990-02-28 | 1991-02-27 | Gallium nitride compound semiconductor light emitting device |
| US07/926,022 US5278433A (en) | 1990-02-28 | 1992-08-07 | Light-emitting semiconductor device using gallium nitride group compound with double layer structures for the n-layer and/or the i-layer |
| US08/556,232 US5733796A (en) | 1990-02-28 | 1995-11-09 | Light-emitting semiconductor device using gallium nitride group compound |
| US08/956,950 US6249012B1 (en) | 1990-02-28 | 1997-10-23 | Light emitting semiconductor device using gallium nitride group compound |
| US09/417,778 US6593599B1 (en) | 1990-02-28 | 1999-10-14 | Light-emitting semiconductor device using gallium nitride group compound |
| US09/586,607 US6362017B1 (en) | 1990-02-28 | 2000-06-02 | Light-emitting semiconductor device using gallium nitride group compound |
| US09/677,787 US6472689B1 (en) | 1990-02-28 | 2000-10-02 | Light emitting device |
| US09/677,788 US6607595B1 (en) | 1990-02-28 | 2000-10-02 | Method for producing a light-emitting semiconductor device |
| US09/677,789 US6472690B1 (en) | 1990-02-28 | 2000-10-02 | Gallium nitride group compound semiconductor |
| US09/677,781 US6830992B1 (en) | 1990-02-28 | 2000-10-02 | Method for manufacturing a gallium nitride group compound semiconductor |
| US10/052,347 US6984536B2 (en) | 1990-02-28 | 2002-01-23 | Method for manufacturing a gallium nitride group compound semiconductor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP5021190A JP3193981B2 (en) | 1990-02-28 | 1990-02-28 | Gallium nitride based compound semiconductor light emitting device |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH03252177A JPH03252177A (en) | 1991-11-11 |
| JP3193981B2 true JP3193981B2 (en) | 2001-07-30 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP5021190A Expired - Fee Related JP3193981B2 (en) | 1990-02-28 | 1990-02-28 | Gallium nitride based compound semiconductor light emitting device |
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| JP (1) | JP3193981B2 (en) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05308154A (en) * | 1992-04-28 | 1993-11-19 | Toyoda Gosei Co Ltd | Gallium nitride compound semiconductor light emitting element |
| JP2681733B2 (en) * | 1992-10-29 | 1997-11-26 | 豊田合成株式会社 | Nitrogen-3 group element compound semiconductor light emitting device |
| JP2626431B2 (en) * | 1992-10-29 | 1997-07-02 | 豊田合成株式会社 | Nitrogen-3 group element compound semiconductor light emitting device |
| JP2778405B2 (en) † | 1993-03-12 | 1998-07-23 | 日亜化学工業株式会社 | Gallium nitride based compound semiconductor light emitting device |
| US6996150B1 (en) | 1994-09-14 | 2006-02-07 | Rohm Co., Ltd. | Semiconductor light emitting device and manufacturing method therefor |
| JP3726252B2 (en) | 2000-02-23 | 2005-12-14 | 独立行政法人理化学研究所 | Ultraviolet light emitting device and method for producing InAlGaN light emitting layer |
| US6881983B2 (en) | 2002-02-25 | 2005-04-19 | Kopin Corporation | Efficient light emitting diodes and lasers |
| US6911079B2 (en) | 2002-04-19 | 2005-06-28 | Kopin Corporation | Method for reducing the resistivity of p-type II-VI and III-V semiconductors |
| US6847052B2 (en) | 2002-06-17 | 2005-01-25 | Kopin Corporation | Light-emitting diode device geometry |
| US6734091B2 (en) | 2002-06-28 | 2004-05-11 | Kopin Corporation | Electrode for p-type gallium nitride-based semiconductors |
| US7002180B2 (en) | 2002-06-28 | 2006-02-21 | Kopin Corporation | Bonding pad for gallium nitride-based light-emitting device |
| US6955985B2 (en) | 2002-06-28 | 2005-10-18 | Kopin Corporation | Domain epitaxy for thin film growth |
| US7122841B2 (en) | 2003-06-04 | 2006-10-17 | Kopin Corporation | Bonding pad for gallium nitride-based light-emitting devices |
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1990
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| JPH03252177A (en) | 1991-11-11 |
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