JPH0281483A - Gallium nitride-based compound semiconductor light-emitting element - Google Patents
Gallium nitride-based compound semiconductor light-emitting elementInfo
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- JPH0281483A JPH0281483A JP63232886A JP23288688A JPH0281483A JP H0281483 A JPH0281483 A JP H0281483A JP 63232886 A JP63232886 A JP 63232886A JP 23288688 A JP23288688 A JP 23288688A JP H0281483 A JPH0281483 A JP H0281483A
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- layer
- compound semiconductor
- gallium nitride
- sapphire substrate
- light emitting
- Prior art date
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Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
本発明は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。The present invention relates to a gallium nitride 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1導電型のGaN系の化合物半導体から成る1層を成
長させた構造をとっている。Conventionally, blue light emitting diodes using GaN-based compound semiconductors are known. The GaN-based compound semiconductor is attracting attention because it has high luminous efficiency due to direct transition, and because it emits blue light, which is one of the three primary colors of light. A light emitting diode using such a GaN-based compound semiconductor is produced by growing an N layer made of an N-conductivity type GaN-based compound semiconductor on a sapphire substrate directly or with a buffer layer made of aluminum nitride interposed therebetween. It has a structure in which one layer made of a GaN-based compound semiconductor of one conductivity type is grown on the N layer.
ところで、上記の発光ダイオードの発光輝度を向上させ
るためには、発光に寄与するキャリア数を多くするため
に、NFJの厚さはできるだけ厚い方が望ましい。又、
良質な1層の結晶を得るためにもN層の厚さは厚い方が
望ましい。
一方、動作電圧を均一にするためには、1層の膜厚は薄
く均一に精度良く制御される必要がある。
ところが、従来のMOVPE法だけで結晶成長させると
、結晶成長速度が遅く、厚いN層を形成するのに時間が
かかるという問題がある。
一方、サファイア基板上に順次N型GaN、1型GaN
をハライド気相成長法で成長させるという方法もあるが
、ハライド気相成長法では成長速度が速く1層の膜厚を
薄く均一にすることが困難であった。
本発明者らはGaNの結晶成長について研究を重ねてき
た結果、ハライド気相成長法で大部分のN層を成長させ
た後、上層部を薄<MOVPE法で成長させることによ
り、その上にMOVPE法により結晶性の良い1層を成
長させることができることを見出した。
本発明は、係る結論に基づいてなされたものであり、そ
の目的は、発光素子の製造速度及び発光特性を向上させ
ることである。Incidentally, in order to improve the luminance of the light emitting diode described above, it is desirable that the thickness of the NFJ be as thick as possible in order to increase the number of carriers contributing to light emission. or,
In order to obtain a high-quality single-layer crystal, it is desirable that the N layer be thick. On the other hand, in order to make the operating voltage uniform, the thickness of one layer needs to be thin, uniform, and precisely controlled. However, when crystal growth is performed only by the conventional MOVPE method, there is a problem that the crystal growth rate is slow and it takes time to form a thick N layer. On the other hand, N-type GaN and 1-type GaN are sequentially deposited on the sapphire substrate.
There is also a method of growing by halide vapor phase epitaxy, but with halide vapor phase epitaxy, the growth rate is fast and it is difficult to make the thickness of one layer thin and uniform. As a result of repeated research on GaN crystal growth, the present inventors have found that after growing most of the N layer using halide vapor phase epitaxy, the upper layer is grown using thin <MOVPE. It has been found that a single layer with good crystallinity can be grown by the MOVPE method. The present invention was made based on such a conclusion, and its purpose is to improve the manufacturing speed and light emitting characteristics of a light emitting device.
上記課題を解決するための発明の構成は、サファイア基
板と、サファイア基板上に直接的又は間接的に成長した
N型の窒化ガリウム系化合物半導体(A I2X G
a =−N : X=Oを含む)からなるN層と、N層
上に成長した■型の窒化ガリウム系化合物半導体(Al
xGa1 +−x N ;x=oを含む)からなる1層
とを有し、
N層はハライド気相成長法により成長させた膜厚の厚い
第1N層と、その第1N層の上に有機金屑化合物気相成
長法(MOVPE)で成長させた膜厚の薄い第2N層と
を有し、
1層は有機金属化合物気相成長法(MOVPE)で成長
させたことを特徴とする。The structure of the invention for solving the above problems consists of a sapphire substrate and an N-type gallium nitride compound semiconductor (A I2X G) grown directly or indirectly on the sapphire substrate.
a = -N: N layer consisting of X=O) and ■ type gallium nitride compound semiconductor (Al
xGa1 + - x N ; x = o), and the N layer is a thick first N layer grown by halide vapor phase epitaxy, and an organic layer is formed on the first N layer. It has a thin second N layer grown by gold scrap compound vapor phase epitaxy (MOVPE), and the first layer is grown by organometallic compound vapor phase epitaxy (MOVPE).
N層の大部分はハライド気相成長法により成長されるた
め、厚いNF31が高速度で得られるので、発光素子の
製造速度が向上した。又、N層の上層部の第2N層はM
OVPE法で形成し、その上に1層をMOVPE法で成
長したので、1層は結晶性が良く且つその層厚が均一に
制御された。その結果、発光特性が向上した。Since most of the N layer is grown by halide vapor phase epitaxy, thick NF31 can be obtained at high speed, and the manufacturing speed of the light emitting device has been improved. Moreover, the second N layer in the upper layer part of the N layer is M
Since it was formed by the OVPE method and one layer was grown thereon by the MOVPE method, the first layer had good crystallinity and its layer thickness was controlled to be uniform. As a result, the light emission characteristics were improved.
以下、本発明を具体的な実施例に基づいて説明する。
第1実施例
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1の構成を示した断面図である。
主面を0面((0001)面)とするサファイア基板2
を硝酸で洗浄した後、更にアセトンで洗浄した。
そして、洗浄後、窒素ガスを吹き付けて軟岩させた後、
そのサファイア基板2をハライド気相成長装置のサセプ
タに取り付けた。その後、反応室の温度を900℃とし
て、ガス流の上流側に載置された金属GaにHC1ガス
を流し、両者の反応生成物として得られたGaCj’と
、NH,と、キャリアガスN、を1000℃に加熱され
たサファイア基板2に向かって流した。流速はGaCl
1が10m1/分、NH,が1.OA/分、N、が2.
0117分とした。
サファイア基板2上に成長したN型のGaNから成る第
1N層4の厚さは20即であり、その成長速度は約1虜
/分であった。
次に、第1N層4が成長したサファイア基板2をハライ
ド気相成長装置から取り出し、MOVPE装置の反応室
のサセプタに載置した。そして、そして、サファイア基
板2を1000t′に加熱して、キャリアガスとしてH
7を2.5jl!/分、N H、を、1.5j!/分、
トリメチルガリウム(TMG)を20rnl/分の割合
で12分間供給し、膜厚約2虜のN型のG a Nから
成る第2N層8を形成した。
次に、サファイア基板2を900℃にして、H2を2.
51.7分、N H、を1.511/分、TMGを15
ntl/分、ジエチル亜鉛(DEZ)を5XIO−’モ
ル/分の割合で5分間供給して、■型のGaNから戊る
1層5を膜厚1.0μsに形成した。
次に、第1N層4及び第2N層8の側壁と1層5の上面
にアルミニウム電極6.7を蒸着して、発光ダイオード
を形成した。
このようにして得られた発光ダイオード1の第1N層4
.第2N層8及び1層5の断面の顕微鏡写真、高エネル
ギー電子線による反射回折法(RIIIEED)により
、それぞれ、良好な結晶性が得られていることが分かっ
た。
特に、第1N層4をハライド気相成長法で高速に成長さ
せ、その上にMOVPE法で精密に成長させた第2N層
8を形成したので、1層5の結晶性は、N層をハライド
気相成長法だけで成長させたものに比べて良くなった。
又、この発光ダイオード1の発光ピークのスペクトルは
480nmであり、発光強度(・軸上輝度)は10mc
dであった。
第2実施例
第2図は第2実施例に係る発光ダイオード10の構成を
示した断面図である。第1実施例と同様にして、主面を
0面((0001)面)とするサファイア基板2を硝酸
で洗浄した後、更にアセトンで洗浄した。そして、洗浄
後、窒素ガスを吹き付けて乾燥させた後、そのサファイ
ア基板2をMOVPE装置のサセプタに取り付けた。そ
の後、サファイア基板2を600℃に加熱して、キャリ
アガスとしてHりを212/分、NH,を1.51/分
、トリメチルアルミニウム(TMA)を15−/分の割
合で6分間供給し、AINから成るバッファ層3を厚さ
約0.1μsに形成した。その後、第1実施例と同様な
手順にて、第1N層4.第2N層8.1層5を順次形成
して、発光ダイオード10を作成した。
このように作成された発光ダイオード10の第1NFJ
4.第2N層8及び1層5の断面の顕微鏡写真、高エネ
ルギー電子線による反射回折法(R11(!BD)によ
り、それぞれ、良好な結晶性が得られていることが分か
った。
又、この発光ダイオード1の発光ピークのスペクトルは
480nmであり、発光強度(軸上輝りは10mcdで
あった。
第3実施例
本実施例は、第2実施例において、第2図のバッファ層
3を分子線エピタキシー法(MBE)により作成したも
のである。
第2実施例と同様にして、主面を0面((0001)面
)とするサファイア基板2を洗浄した後、そのサファイ
ア基板2をMBE装置のサセプタに取り付けた。その後
、サファイア基板2を500℃に加熱して、窒素ガスプ
ラズマ中で、アルミニウムを蒸発させて、サファイア基
板2の主面上に窒化アルミニウム(AIN)から成るバ
ッファ層3を約500人の厚さに形成した。
その後の第1N層4.第2N層8.1層5.電極6.7
の作成方法は、第1実施例と同様である。
このようにして得られた発光ダイオードの第1N層4.
第2N層8及び1層5の断面の顕微鏡写真、高エネルギ
ー電子線による反射回折法(RIIEHD)により、良
好な結晶性が得られていることが分かった。
又、この発光ダイオード1の発光ピークのスペクトルは
480nn+であり、発光強度(軸上輝度)は10mc
’dであった。
尚、本発明者らの考察によれば、MBEで形成されたバ
ッファ層3では、m1NFjF4のGaNの成長の核が
、バッファ層3をMOVPEで成長させたものと比べて
、均一に分散し、そのために、第1N層4、第2N層8
及び1層5の単結晶性が良くなったと考えられる。
又、バッファ層3は、サファイア基板2を500℃にし
てMBEで形成したので、多結晶であった。
又、本発明者らは、バッファ層3は多結晶で成長させた
方が単結晶で成長させた方よりも、第1N層4、第2N
層8及び1層5の単結晶性が良いことも見出した。
このためにもMBEでバッファ層3を成長させることは
効果があり、多結晶さする成長′a度は、室温〜−50
0℃が望ましい。
又、第1N層4、第2N層8及び1層5の単結晶性を良
くするためには、バッファ層3の厚さは100〜100
0人が望ましい。
尚、上記実施例では、第1N層4、第2N層8及び1層
5をGaNで形成したが、AIXGaNで形成しても良
い。The present invention will be described below based on specific examples. First Embodiment FIG. 1 is a sectional view showing the structure of a light emitting diode 1 according to a specific embodiment of the present invention. Sapphire substrate 2 whose main surface is the 0 plane ((0001) plane)
was washed with nitric acid and then further washed with acetone. After cleaning and blowing nitrogen gas to soften the rock,
The sapphire substrate 2 was attached to a susceptor of a halide vapor phase growth apparatus. Thereafter, the temperature of the reaction chamber was set to 900°C, and HC1 gas was flowed over the metal Ga placed on the upstream side of the gas flow, and the reaction products of both were GaCj', NH, and carrier gas N, was flowed toward the sapphire substrate 2 heated to 1000°C. The flow rate is GaCl
1 is 10 m1/min, NH, is 1. OA/min, N, is 2.
0117 minutes. The thickness of the first N layer 4 made of N-type GaN grown on the sapphire substrate 2 was 20 mm, and the growth rate was about 1 layer/min. Next, the sapphire substrate 2 on which the first N layer 4 had been grown was taken out from the halide vapor phase epitaxy apparatus and placed on a susceptor in the reaction chamber of the MOVPE apparatus. Then, the sapphire substrate 2 is heated to 1000 t' and H is used as a carrier gas.
7 for 2.5jl! /min, N H, 1.5j! / minute,
Trimethyl gallium (TMG) was supplied at a rate of 20 rnl/min for 12 minutes to form a second N layer 8 made of N-type GaN with a film thickness of about 2 mm. Next, the sapphire substrate 2 is heated to 900°C, and H2 is heated to 2.
51.7 min, NH, 1.511/min, TMG 15
ntl/min, and diethyl zinc (DEZ) was supplied at a rate of 5XIO-' mol/min for 5 minutes to form one layer 5 made of ■-type GaN to a thickness of 1.0 μs. Next, aluminum electrodes 6.7 were deposited on the side walls of the first N layer 4 and the second N layer 8 and on the top surface of the first layer 5 to form a light emitting diode. The first N layer 4 of the light emitting diode 1 thus obtained
.. Microscopic photographs of the cross sections of the second N layer 8 and the first layer 5 and reflection diffraction method using a high-energy electron beam (RIIIEED) revealed that good crystallinity was obtained, respectively. In particular, the first N layer 4 was grown at high speed by halide vapor phase epitaxy, and the second N layer 8 was formed on top of it by precisely growing by MOVPE. The results were better than those grown using only the vapor phase growth method. Furthermore, the emission peak spectrum of this light emitting diode 1 is 480 nm, and the emission intensity (on-axis brightness) is 10 mc.
It was d. Second Embodiment FIG. 2 is a sectional view showing the structure of a light emitting diode 10 according to a second embodiment. In the same manner as in the first embodiment, a sapphire substrate 2 having a 0 principal surface ((0001) plane) was cleaned with nitric acid and then further cleaned with acetone. After cleaning and drying by blowing nitrogen gas, the sapphire substrate 2 was attached to a susceptor of a MOVPE apparatus. Thereafter, the sapphire substrate 2 is heated to 600° C., and H2 is supplied as carrier gas at a rate of 212/min, NH, at a rate of 1.51/min, and trimethylaluminum (TMA) at a rate of 15/min for 6 minutes. A buffer layer 3 made of AIN was formed to a thickness of about 0.1 μs. Thereafter, the first N layer 4. A light emitting diode 10 was created by sequentially forming the second N layer 8.1 layer 5. The first NFJ of the light emitting diode 10 created in this way
4. Microscopic photographs of the cross sections of the second N layer 8 and the first layer 5 and reflection diffraction method (R11 (!BD)) using high-energy electron beams revealed that good crystallinity was obtained in each. The emission peak spectrum of the diode 1 was 480 nm, and the emission intensity (on-axis brightness was 10 mcd). Third Embodiment In this embodiment, the buffer layer 3 of FIG. It was created by the epitaxy method (MBE). After cleaning the sapphire substrate 2 whose main surface is the 0 plane ((0001) plane) in the same manner as in the second embodiment, the sapphire substrate 2 was placed in the MBE apparatus. After that, the sapphire substrate 2 was heated to 500° C. and aluminum was evaporated in nitrogen gas plasma to form a buffer layer 3 made of aluminum nitride (AIN) on the main surface of the sapphire substrate 2. It was formed to a thickness of 500. After that, the first N layer 4. The second N layer 8.1 layer 5. The electrode 6.7
The method for creating is the same as in the first embodiment. The first N layer 4 of the light emitting diode thus obtained.
A microscopic photograph of the cross section of the second N layer 8 and the first layer 5 and a reflection diffraction method using a high-energy electron beam (RIIEHD) revealed that good crystallinity was obtained. Furthermore, the spectrum of the emission peak of this light emitting diode 1 is 480nn+, and the emission intensity (on-axis brightness) is 10mc.
It was 'd. According to the inventors' considerations, in the buffer layer 3 formed by MBE, the growth nuclei of GaN of m1NFjF4 are more uniformly dispersed than in the buffer layer 3 grown by MOVPE. For this purpose, the first N layer 4, the second N layer 8
It is considered that the single crystallinity of the first layer 5 was improved. Further, the buffer layer 3 was polycrystalline because it was formed by MBE at 500° C. on the sapphire substrate 2. In addition, the present inventors have found that when the buffer layer 3 is grown as a polycrystalline layer, the first N layer 4 and the second N layer 3 are
It was also found that layer 8 and layer 1 5 had good single crystallinity. For this reason, it is effective to grow the buffer layer 3 by MBE, and the degree of growth of polycrystalline crystals is from room temperature to -50°C.
0°C is desirable. Further, in order to improve the single crystallinity of the first N layer 4, the second N layer 8, and the first layer 5, the thickness of the buffer layer 3 should be 100 to 100 nm.
0 people is desirable. In the above embodiment, the first N layer 4, the second N layer 8, and the first layer 5 are made of GaN, but they may be made of AIX GaN.
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である。第2図は他の実施例に
係る発光ダイオードの構成を示した構成図である。
1゜
10 ・発光ダイオード 2 ・サファイア基板バッフ
ァ層 4 第1N層 8 第2N層■層
特許出願人 豊田合戊株式会社
同 名古屋大学長
同 新技術開発事業団
代 理 人 藤 谷
修第1FIG. 1 is a block diagram showing the structure of a light emitting diode according to a specific embodiment of the present invention. FIG. 2 is a block diagram showing the structure of a light emitting diode according to another embodiment. 1゜10 ・Light-emitting diode 2 ・Sapphire substrate buffer layer 4 1st N layer 8 2nd N layer ■ layer Patent applicant: Toyota Gosho Co., Ltd., Nagoya University President, New Technology Development Corporation Representative, Fujitani
Shu 1st
Claims (1)
型の窒化ガリウム系化合物半導体(Al_xGa_1_
−_xN;X=0を含む)からなるN層と、前記N層上
に成長したI型の窒化ガリウム系化合物半導体(Al_
xGa_1_−_xN;X=0を含む)からなるI層と
を有し、 前記N層はハライド気相成長法により成長させた膜厚の
厚い第1N層と、その第1N層の上に有機金属化合物気
相成長法(MOVPE)で成長させた膜厚の薄い第2N
層とを有し、 前記I層は有機金属化合物気相成長法(MOVPE)で
成長させた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。[Claims] A sapphire substrate; and N grown directly or indirectly on the sapphire substrate.
type of gallium nitride-based compound semiconductor (Al_xGa_1_
−_xN; including X=0), and an I-type gallium nitride compound semiconductor (Al_
xGa_1_-_xN; A thin second N film grown by compound vapor phase epitaxy (MOVPE)
A gallium nitride-based compound semiconductor light emitting device, comprising: a gallium nitride compound semiconductor light emitting device, wherein the I layer is grown by metal organic compound vapor phase epitaxy (MOVPE).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP23288688A JP3140751B2 (en) | 1988-09-16 | 1988-09-16 | Gallium nitride based compound semiconductor light emitting device |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP23288688A JP3140751B2 (en) | 1988-09-16 | 1988-09-16 | Gallium nitride based compound semiconductor light emitting device |
Related Child Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11203573A Division JP2000040842A (en) | 1999-07-16 | 1999-07-16 | Gallium nitride based compound semiconductor light emitting device |
| JP11203574A Division JP2000040843A (en) | 1999-07-16 | 1999-07-16 | Gallium nitride based compound semiconductor light emitting device |
| JP20357299A Division JP3402460B2 (en) | 1999-07-16 | 1999-07-16 | Gallium nitride based compound semiconductor growth method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0281483A true JPH0281483A (en) | 1990-03-22 |
| JP3140751B2 JP3140751B2 (en) | 2001-03-05 |
Family
ID=16946381
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP23288688A Expired - Lifetime JP3140751B2 (en) | 1988-09-16 | 1988-09-16 | Gallium nitride based compound semiconductor light emitting device |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3140751B2 (en) |
Cited By (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5278433A (en) * | 1990-02-28 | 1994-01-11 | Toyoda Gosei Co., Ltd. | Light-emitting semiconductor device using gallium nitride group compound with double layer structures for the n-layer and/or the i-layer |
| US5290393A (en) * | 1991-01-31 | 1994-03-01 | Nichia Kagaku Kogyo K.K. | Crystal growth method for gallium nitride-based compound semiconductor |
| US5408120A (en) * | 1992-07-23 | 1995-04-18 | Toyoda Gosei Co., Ltd. | Light-emitting device of gallium nitride compound semiconductor |
| US5633192A (en) * | 1991-03-18 | 1997-05-27 | Boston University | Method for epitaxially growing gallium nitride layers |
| US5686738A (en) * | 1991-03-18 | 1997-11-11 | Trustees Of Boston University | Highly insulating monocrystalline gallium nitride thin films |
| US5734182A (en) * | 1992-11-20 | 1998-03-31 | Nichia Chemical Industries Ltd. | Light-emitting gallium nitride-based compound semiconducor device |
| US5733796A (en) * | 1990-02-28 | 1998-03-31 | Toyoda Gosei Co., Ltd. | Light-emitting semiconductor device using gallium nitride group compound |
| US6081399A (en) * | 1995-08-01 | 2000-06-27 | Samsung Electronics Co., Ltd. | Disk drive having double heads and method for controlling head switching |
| WO2001015241A1 (en) * | 1999-08-21 | 2001-03-01 | Mat Science Tech Co., Ltd. | Ultraviolet-ray detecting device |
| US6362017B1 (en) | 1990-02-28 | 2002-03-26 | Toyoda Gosei Co., Ltd. | Light-emitting semiconductor device using gallium nitride group compound |
| US6830992B1 (en) | 1990-02-28 | 2004-12-14 | Toyoda Gosei Co., Ltd. | Method for manufacturing a gallium nitride group compound semiconductor |
| JP2006073578A (en) * | 2004-08-31 | 2006-03-16 | Nokodai Tlo Kk | Vapor phase growth method and vapor phase growth apparatus for AlGaN |
| KR100595177B1 (en) * | 2000-02-10 | 2006-07-03 | 엘지전자 주식회사 | Nitride Light Emitting Device Manufacturing Method |
| JP2008063221A (en) * | 2007-09-25 | 2008-03-21 | Sony Corp | Nitride III-V compound layer and substrate using the same |
| JP2013028533A (en) * | 2012-10-26 | 2013-02-07 | Nokodai Tlo Kk | VAPOR DEPOSITION METHOD OF AlGaN AND THICK FILM SUBSTRATE OF AlGaN CRYSTAL PRODUCED BY THE METHOD |
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| JPS60207332A (en) * | 1984-03-30 | 1985-10-18 | Matsushita Electric Ind Co Ltd | Growth of gallium nitride |
| JPS63188977A (en) * | 1987-01-31 | 1988-08-04 | Toyoda Gosei Co Ltd | Light emitting element of gallium nitride compound semiconductor |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JPS60207332A (en) * | 1984-03-30 | 1985-10-18 | Matsushita Electric Ind Co Ltd | Growth of gallium nitride |
| JPS63188977A (en) * | 1987-01-31 | 1988-08-04 | Toyoda Gosei Co Ltd | Light emitting element of gallium nitride compound semiconductor |
Cited By (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6249012B1 (en) | 1990-02-28 | 2001-06-19 | Toyoda Gosei Co., Ltd. | Light emitting semiconductor device using gallium nitride group compound |
| US6984536B2 (en) | 1990-02-28 | 2006-01-10 | Toyoda Gosei Co., Ltd. | Method for manufacturing a gallium nitride group compound semiconductor |
| US6830992B1 (en) | 1990-02-28 | 2004-12-14 | Toyoda Gosei Co., Ltd. | Method for manufacturing a gallium nitride group compound semiconductor |
| US6607595B1 (en) | 1990-02-28 | 2003-08-19 | Toyoda Gosei Co., Ltd. | Method for producing a light-emitting semiconductor device |
| US5278433A (en) * | 1990-02-28 | 1994-01-11 | Toyoda Gosei Co., Ltd. | Light-emitting semiconductor device using gallium nitride group compound with double layer structures for the n-layer and/or the i-layer |
| US6593599B1 (en) | 1990-02-28 | 2003-07-15 | Japan Science And Technology Corporation | Light-emitting semiconductor device using gallium nitride group compound |
| US5733796A (en) * | 1990-02-28 | 1998-03-31 | Toyoda Gosei Co., Ltd. | Light-emitting semiconductor device using gallium nitride group compound |
| US6472690B1 (en) | 1990-02-28 | 2002-10-29 | Toyoda Gosei Co., Ltd. | Gallium nitride group compound semiconductor |
| US6472689B1 (en) | 1990-02-28 | 2002-10-29 | Toyoda Gosei Co., Ltd. | Light emitting device |
| US6362017B1 (en) | 1990-02-28 | 2002-03-26 | Toyoda Gosei Co., Ltd. | Light-emitting semiconductor device using gallium nitride group compound |
| US5290393A (en) * | 1991-01-31 | 1994-03-01 | Nichia Kagaku Kogyo K.K. | Crystal growth method for gallium nitride-based compound semiconductor |
| US5725674A (en) * | 1991-03-18 | 1998-03-10 | Trustees Of Boston University | Device and method for epitaxially growing gallium nitride layers |
| US5686738A (en) * | 1991-03-18 | 1997-11-11 | Trustees Of Boston University | Highly insulating monocrystalline gallium nitride thin films |
| US5633192A (en) * | 1991-03-18 | 1997-05-27 | Boston University | Method for epitaxially growing gallium nitride layers |
| USRE36747E (en) * | 1992-07-23 | 2000-06-27 | Toyoda Gosei Co., Ltd | Light-emitting device of gallium nitride compound semiconductor |
| US5408120A (en) * | 1992-07-23 | 1995-04-18 | Toyoda Gosei Co., Ltd. | Light-emitting device of gallium nitride compound semiconductor |
| US5734182A (en) * | 1992-11-20 | 1998-03-31 | Nichia Chemical Industries Ltd. | Light-emitting gallium nitride-based compound semiconducor device |
| US6081399A (en) * | 1995-08-01 | 2000-06-27 | Samsung Electronics Co., Ltd. | Disk drive having double heads and method for controlling head switching |
| WO2001015241A1 (en) * | 1999-08-21 | 2001-03-01 | Mat Science Tech Co., Ltd. | Ultraviolet-ray detecting device |
| KR100595177B1 (en) * | 2000-02-10 | 2006-07-03 | 엘지전자 주식회사 | Nitride Light Emitting Device Manufacturing Method |
| JP2006073578A (en) * | 2004-08-31 | 2006-03-16 | Nokodai Tlo Kk | Vapor phase growth method and vapor phase growth apparatus for AlGaN |
| JP2008063221A (en) * | 2007-09-25 | 2008-03-21 | Sony Corp | Nitride III-V compound layer and substrate using the same |
| JP2013028533A (en) * | 2012-10-26 | 2013-02-07 | Nokodai Tlo Kk | VAPOR DEPOSITION METHOD OF AlGaN AND THICK FILM SUBSTRATE OF AlGaN CRYSTAL PRODUCED BY THE METHOD |
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