JP3605907B2 - Semiconductor device having contact resistance reduction layer - Google Patents
Semiconductor device having contact resistance reduction layer Download PDFInfo
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- JP3605907B2 JP3605907B2 JP28195995A JP28195995A JP3605907B2 JP 3605907 B2 JP3605907 B2 JP 3605907B2 JP 28195995 A JP28195995 A JP 28195995A JP 28195995 A JP28195995 A JP 28195995A JP 3605907 B2 JP3605907 B2 JP 3605907B2
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- 239000004065 semiconductor Substances 0.000 title claims description 22
- 239000010409 thin film Substances 0.000 claims description 10
- 239000010408 film Substances 0.000 claims description 8
- 239000010410 layer Substances 0.000 description 29
- 239000000758 substrate Substances 0.000 description 14
- 229910002601 GaN Inorganic materials 0.000 description 12
- JMASRVWKEDWRBT-UHFFFAOYSA-N Gallium nitride Chemical compound [Ga]#N JMASRVWKEDWRBT-UHFFFAOYSA-N 0.000 description 12
- 238000010586 diagram Methods 0.000 description 6
- 239000002994 raw material Substances 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- 238000002488 metal-organic chemical vapour deposition Methods 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000005036 potential barrier Methods 0.000 description 3
- XCZXGTMEAKBVPV-UHFFFAOYSA-N trimethylgallium Chemical compound C[Ga](C)C XCZXGTMEAKBVPV-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 239000012159 carrier gas Substances 0.000 description 2
- 238000005253 cladding Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000002019 doping agent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000005284 excitation Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229910052594 sapphire Inorganic materials 0.000 description 2
- 239000010980 sapphire Substances 0.000 description 2
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical compound C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 description 2
- IBEFSUTVZWZJEL-UHFFFAOYSA-N trimethylindium Chemical compound C[In](C)C IBEFSUTVZWZJEL-UHFFFAOYSA-N 0.000 description 2
- RHUYHJGZWVXEHW-UHFFFAOYSA-N 1,1-Dimethyhydrazine Chemical compound CN(C)N RHUYHJGZWVXEHW-UHFFFAOYSA-N 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- UCSVJZQSZZAKLD-UHFFFAOYSA-N ethyl azide Chemical compound CCN=[N+]=[N-] UCSVJZQSZZAKLD-UHFFFAOYSA-N 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000002052 molecular layer Substances 0.000 description 1
- 238000005121 nitriding Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
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- Led Devices (AREA)
Description
【0001】
【産業上の利用分野】
本発明は半導体装置に関し、特に窒化ガリウム系材料を使用した青色〜緑色発光ダイオード、青色〜緑色レーザーダイオード等の発光素子に関し、特に接触抵抗を大きく低減した半導体装置に関する。
【0002】
【従来の技術】
最近の青色及び緑色の発光ダイオード(LED)の高輝度化の進展には目ざましいものがあり、材料として、ZnSSe系やAlGaInN系が用いられている。現在、サファイア、SiCなどの基板上への高品質な窒化ガリウム(GaN)系化合物半導体膜の成長とGaN系への高濃度p型ドーピングが可能となったことにより、高輝度の青色発光ダイオードが実現されており、図2に示すようなダブルヘテロ構造が用いられている。
【0003】
【発明が解決しようとする課題】
しかしながら、表面コンタクト層にワイドバンドギャップのGaN(Eg=3.39eV)を用いているために、電極との電位障壁が大きくなりやすく、このことが動作電圧の増加を招いてしまう(図3、n型の場合、ECは伝導帯の底のエネルギー、EFはフェルミ準位、EVは価電子帯の底のエネルギー、qφBは電位障壁)。このようなワイドバンドギャップ半導体で、接触抵抗を下げるには、まず、ヘビードープした層を電極直下に挿入する、すなわちmetal−n+−n、metal−p+−pなる構造を形成する手法がある(図4、ただし、n型の場合)。n型GaNではホール濃度が1019台という高濃度までドーピングが可能であるが、一方p型GaNドーピングでは、現状では1017台レベルまでしか入らない。このために、特にp型AlGaInNからなる層とは、充分低い接触抵抗の実現は困難である。この動作電圧の増加は、素子の発熱につながり、寿命の点で大きな問題となる。
【0004】
【課題を解決するための手段】
我々は、MOCVDやMBE法でAlGaInN系LEDを作製するにあたり、InAlGaN系からなる層を電極との間に薄膜のGaPxN1−x(x≧0.9)層と薄膜のGaPyN1−y(y≦0.1)層を交互に積層した多層膜を挿入すること、より好ましくは1周期当りの厚層が10分子層以下である前記GaPxN1−x(x≧0.9)層及びGaPxN1−x(x≦0.1)層を挿入することにより、上記の課題を解決するに至った。
【0005】
GaPN混晶はGaNからP組成を増加させても、またGaPからN組成を増加させてもバンドギャップが減少し、中間組成でバンドギャップがゼロになってしまうという特殊なバンド構造を有している。しかし、中間組成の混晶は、ミッシビリティギャップの存在のため、成長が困難とされている。そこで、GaPリッチの薄膜とGaNリッチの薄膜からなる超格子を積層することにより、GaPNバルクと同様なバンド構造を実現することができる。そこで、ワイドバンドギャップ半導体で、接触抵抗を下げるために、非常にバンドギャップが小さいもしくはゼロである、薄膜のGaPxN1−x(x≧0.9)層と薄膜のGaPyN1−y(y≦0.1)層を交互に積層した多層膜を挿入することにより、キャリア濃度を非常に高くすることができなくても、電極と表面層との間で形成される電位障壁が大幅に低減され、オーミックコンタクトを非常に取り易くなる(図5、ただし、n型の場合)。
【0006】
この場合の多層膜の層の数は、2(1周期)以上であれば特に限定されないが、好ましくは5周期以上である。又、多い分には特に抵抗等の問題を生じない範囲で、任意に設定すればよい。
尚、本明細書においてAlGaInN系からなる層とは、Al又はInの組成が0のものを含むものとする。
【0007】
以下、本発明を実施例を用いてより詳細に説明するが、本発明はその要旨を超えない限り、実施例に限定されるものではない。
(実施例)
本発明の成長に使用した装置の構成は図6に示すように中央に基板搬送室を設け、基板交換室1室と減圧MOCVD装置3台を設置してある。成長室1は通常のMOCVD装置であり、AlGaInN系化合物半導体の成長に用いる。成長室2も通常のMOCVD装置であるがAlGaInN系以外のIII−V族化合物半導体の成長に用いる。成長室3は、原料をマイクロ波励起によりラジカル分解することができ、基板表面の窒化及びAlGaInN系化合物の成長に用いる。図1に示すような構造のエピタキシャルウエハを成長手順を示す。
【0008】
まずサファイア基板を成長室3に導入し、加熱昇温する。500゜Cにおいて、成長前に窒素ガス(N2)を原料として、マイクロ波励起によりラジカル窒素を基板表面に供給し、表面の酸素(O)原子をN原子と置換させる工程、すなわち窒化を行う。この表面上に、GaNバッファ層20nmを成長させる。この後、基板を冷却し、搬送室を経て成長室1へ基板を移動させる。成長温度1000゜Cで加熱し、前記エピタキシャル膜成長基板上に、n型GaNバッファ層4μm、n型Al0.2Ga0.8Nクラッド層1μm、ZnドープIn0.1Ga0.9N活性層0.1μm、p型Al0.2Ga0.8Nクラッド層1μm、p型GaNコンタクト層1μmを順次成長させる。このとき、キャリアガスに水素を用いて、III族原料ガスに、トリメチルガリウム(TMG)、トリメチルアルミニウム(TMA)、トリメチルインジウム(TMI)を用いた。V族原料には、一般的にはアンモニア(NH3)が用いられるが、成長温度の低減のために、低温での分解効率のよいジメチルヒドラジンやアジ化エチルなどの有機金属を用いてもよい。n型ドーパントには、SiまたはGeを、p型ドーパントには、MgまたはZnを用いた。必要に応じて、成長後に引き続いて成長室内で熱処理を行い、キャリアを活性化させる。この後、基板を冷却し、搬送室を経て成長室2へ基板を移動させる。基板を700゜Cに加熱し、前記エピタキシャル膜成長基板上に厚み1分子層のGaPと厚み3分子層のGaNを交互に10周期積層した超格子を接触抵抗低減層として成長させる。このとき、キャリアガスに水素を用いて、III族原料ガスに、TMGをV族原料には、NH3及びホスフィン(PH3)を使用した。前記GaP0.2 5N0. 75接触抵抗低減層は、余り厚くすると発光した光の吸収を大きくしてしまうが、上記実施例のように、光吸収の影響のない非常に薄い薄膜でも接触抵抗の低減に、非常に有効である。また、この接触抵抗低減層は、抵抗率が非常に小さいために、表面で電流を広げる役割も果たしてくれる。
【0009】
このようにして成長したエピタキシャルウエハを表面側に電極を形成し、チップに加工した。このチップを発光ダイオードとして組み立てて発光させたところ、順方向電流20mAにおいて、発光波長420nm、発光出力800μWと非常に良好な値が得られた。このとき動作電圧は3.4Vであり、比較のために作製したp−GaN表面上に電極を形成した従来の発光ダイオードでは動作電圧が4.0Vであった。この動作電圧の低減は、素子自体の発熱の低下を意味し、素子の寿命を大きく改善できた。
【0010】
上記実施例は、発光ダイオードについてであったが、半導体レーザにも同様な効果があることはもちろん、他の半導体装置においても同様の特性の向上が得られることは言うまでもない。
【0011】
【発明の効果】
本発明により、AlGaInN系半導体層と電極の間の抵抗を低減した半導体装置が得られ、これを発光装置として用いた場合には、動作電圧を大きく低減することができ、紫外〜赤色のAlGaInN系発光素子の特性及び素子の寿命も大幅に改善できる。
【図面の簡単な説明】
【図1】図1は、本発明の半導体装置の一例を示す説明図である。
【図2】図2は従来の半導体装置の一例を示す説明図である。
【図3】図3は、従来のAlGaInN系半導体層の上に直接電極を設置した場合のエネルギーバンドの説明図である。
【図4】図4は、従来のAlGaInN系半導体層の上にヘビードープ層を設けその上に電極を設置した場合のエネルギーバンドの説明図である。
【図5】図5は、本発明のAlGaInN系半導体層の上に薄膜のGaPxN1−x(x≧0.9)層と薄膜のGaPyN1−y(y≦0.1)層を交互に積層した多層膜を挿入して電極を設置した場合のエネルギーバンドの説明図である。
【図6】図6は、実施例1で用いた製造装置の説明図である。[0001]
[Industrial applications]
The present invention relates to a semiconductor device, and more particularly, to a light emitting element using a gallium nitride-based material, such as a blue to green light emitting diode and a blue to green laser diode, and more particularly to a semiconductor device having significantly reduced contact resistance.
[0002]
[Prior art]
Recent progress in increasing the brightness of blue and green light-emitting diodes (LEDs) is remarkable, and ZnSSe-based and AlGaInN-based materials are used as materials. At present, it is possible to grow a high-quality gallium nitride (GaN) -based compound semiconductor film on a substrate such as sapphire or SiC and to perform a high-concentration p-type doping on a GaN-based semiconductor, so that a high-intensity blue light emitting diode can be manufactured. It has been realized, and a double hetero structure as shown in FIG. 2 is used.
[0003]
[Problems to be solved by the invention]
However, since GaN (Eg = 3.39 eV) having a wide band gap is used for the surface contact layer, a potential barrier between the electrode and the electrode tends to be large, which causes an increase in operating voltage (FIG. 3, FIG. 3). for n-type, E C is the bottom energy of the conduction band, E F is the Fermi level, E V is the bottom of the valence band energy, qφ B potential barrier). In order to reduce the contact resistance of such a wide band gap semiconductor, first, there is a method of inserting a heavy-doped layer immediately below an electrode, that is, forming a structure of metal-n + -n and metal-p + -p (FIG. 4, but for n-type). the hole concentration in n-type GaN is possible doped to a concentration as high as 10 19 units, while in the p-type GaN doping can get only up to 10 17 units level at present. For this reason, it is difficult to realize a sufficiently low contact resistance especially with a layer made of p-type AlGaInN. This increase in operating voltage leads to heat generation of the element, which is a major problem in terms of life.
[0004]
[Means for Solving the Problems]
When fabricating an AlGaInN-based LED by MOCVD or MBE, we use a thin-film GaP x N 1-x (x ≧ 0.9) layer and a thin-film GaP y N 1 between an InAlGaN-based layer and an electrode. -Y (y ≦ 0.1) by inserting a multilayer film in which layers are alternately laminated, more preferably the GaP x N 1-x (x ≧ 0. 9) The above problem has been solved by inserting a layer and a GaP x N 1-x (x ≦ 0.1) layer.
[0005]
The GaPN mixed crystal has a special band structure in which the band gap decreases even if the P composition is increased from GaN or the N composition is increased from GaP, and the band gap becomes zero at the intermediate composition. I have. However, it is considered that the growth of a mixed crystal having an intermediate composition is difficult due to the existence of a missibility gap. Therefore, by stacking a superlattice composed of a GaP-rich thin film and a GaN-rich thin film, a band structure similar to that of a GaPN bulk can be realized. Therefore, in order to reduce the contact resistance, a thin band GaP x N 1-x (x ≧ 0.9) layer and a thin film GaP y N 1− of a wide band gap semiconductor having a very small or zero band gap to reduce contact resistance. By inserting a multilayer film in which y (y ≦ 0.1) layers are alternately stacked, a potential barrier formed between the electrode and the surface layer can be formed even if the carrier concentration cannot be extremely increased. It is greatly reduced, and it becomes very easy to obtain an ohmic contact (FIG. 5, in the case of n-type).
[0006]
In this case, the number of layers of the multilayer film is not particularly limited as long as it is 2 (one cycle) or more, but is preferably 5 cycles or more. In addition, the amount may be arbitrarily set within a range that does not particularly cause a problem such as resistance.
In this specification, an AlGaInN-based layer includes one in which the composition of Al or In is zero.
[0007]
Hereinafter, the present invention will be described in more detail with reference to examples, but the present invention is not limited to the examples unless it exceeds the gist.
(Example)
As shown in FIG. 6, the apparatus used for the growth of the present invention is provided with a substrate transfer chamber at the center, one substrate exchange chamber and three reduced pressure MOCVD apparatuses. The growth chamber 1 is a normal MOCVD apparatus and is used for growing an AlGaInN-based compound semiconductor. The growth chamber 2 is also a normal MOCVD apparatus, but is used for growing a group III-V compound semiconductor other than AlGaInN. The growth chamber 3 can radically decompose the raw material by microwave excitation, and is used for nitriding the substrate surface and growing an AlGaInN-based compound. A procedure for growing an epitaxial wafer having a structure as shown in FIG. 1 will be described.
[0008]
First, a sapphire substrate is introduced into the growth chamber 3 and heated and heated. At 500 ° C., before the growth, using nitrogen gas (N 2 ) as a raw material, radical nitrogen is supplied to the substrate surface by microwave excitation to replace oxygen (O) atoms on the surface with N atoms, that is, nitridation is performed. . On this surface, a GaN buffer layer of 20 nm is grown. Thereafter, the substrate is cooled, and the substrate is moved to the growth chamber 1 via the transfer chamber. The substrate was heated at a growth temperature of 1000 ° C., and an n-type GaN buffer layer of 4 μm, an n-type Al 0.2 Ga 0.8 N cladding layer of 1 μm, and Zn-doped In 0.1 Ga 0.9 N were formed on the epitaxial film growth substrate. An active layer of 0.1 μm, a p-type Al 0.2 Ga 0.8 N cladding layer of 1 μm, and a p-type GaN contact layer of 1 μm are sequentially grown. At this time, hydrogen was used as a carrier gas, and trimethylgallium (TMG), trimethylaluminum (TMA), and trimethylindium (TMI) were used as group III source gases. Ammonia (NH 3 ) is generally used as the group V raw material, but an organic metal such as dimethylhydrazine or ethyl azide, which has high decomposition efficiency at low temperatures, may be used to reduce the growth temperature. . Si or Ge was used for the n-type dopant, and Mg or Zn was used for the p-type dopant. If necessary, after the growth, a heat treatment is performed subsequently in the growth chamber to activate the carriers. Thereafter, the substrate is cooled, and the substrate is moved to the growth chamber 2 via the transfer chamber. The substrate is heated to 700 ° C., and a superlattice in which one molecular layer of GaP and three molecular layers of GaN are alternately stacked on the epitaxial film growth substrate for ten periods is grown as a contact resistance reducing layer. At this time, hydrogen was used as a carrier gas, TMG was used as a group III raw material gas, and NH 3 and phosphine (PH 3 ) were used as a group V raw material. The GaP 0.2 5 N 0. When the contact resistance reducing layer 75 is too thick, it increases the absorption of emitted light. However, as in the above embodiment, even a very thin thin film having no influence of light absorption is very effective in reducing the contact resistance. is there. In addition, the contact resistance reducing layer has a very low resistivity, and thus plays a role of spreading the current on the surface.
[0009]
An electrode was formed on the surface side of the epitaxial wafer grown in this manner, and processed into chips. When this chip was assembled as a light emitting diode and emitted light, a very good value of an emission wavelength of 420 nm and an emission output of 800 μW was obtained at a forward current of 20 mA. At this time, the operating voltage was 3.4 V, and the operating voltage was 4.0 V in the conventional light emitting diode having an electrode formed on the p-GaN surface manufactured for comparison. This reduction in the operating voltage means that the heat generated by the element itself is reduced, and the life of the element can be greatly improved.
[0010]
In the above embodiment, the light emitting diode is used. However, it is needless to say that a semiconductor laser has the same effect, and that the same characteristics can be improved in other semiconductor devices.
[0011]
【The invention's effect】
According to the present invention, a semiconductor device in which the resistance between an AlGaInN-based semiconductor layer and an electrode is reduced can be obtained. When this semiconductor device is used as a light-emitting device, the operating voltage can be greatly reduced, and the ultraviolet to red AlGaInN-based The characteristics of the light emitting element and the life of the element can be significantly improved.
[Brief description of the drawings]
FIG. 1 is an explanatory diagram illustrating an example of a semiconductor device of the present invention.
FIG. 2 is an explanatory diagram illustrating an example of a conventional semiconductor device.
FIG. 3 is an explanatory diagram of an energy band when an electrode is directly provided on a conventional AlGaInN-based semiconductor layer.
FIG. 4 is an explanatory diagram of an energy band when a heavy dope layer is provided on a conventional AlGaInN-based semiconductor layer and an electrode is provided thereon.
FIG. 5 is a diagram showing a thin-film GaP x N 1-x (x ≧ 0.9) layer and a thin-film GaP y N 1-y (y ≦ 0.1) on the AlGaInN-based semiconductor layer of the present invention. It is explanatory drawing of the energy band at the time of installing an electrode by inserting the multilayer film which laminated | stacked the layer by turns.
FIG. 6 is an explanatory diagram of the manufacturing apparatus used in the first embodiment.
Claims (3)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP28195995A JP3605907B2 (en) | 1994-10-28 | 1995-10-30 | Semiconductor device having contact resistance reduction layer |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6-265499 | 1994-10-28 | ||
| JP26549994 | 1994-10-28 | ||
| JP28195995A JP3605907B2 (en) | 1994-10-28 | 1995-10-30 | Semiconductor device having contact resistance reduction layer |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH08213651A JPH08213651A (en) | 1996-08-20 |
| JP3605907B2 true JP3605907B2 (en) | 2004-12-22 |
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| JP28195995A Expired - Fee Related JP3605907B2 (en) | 1994-10-28 | 1995-10-30 | Semiconductor device having contact resistance reduction layer |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6677619B1 (en) | 1997-01-09 | 2004-01-13 | Nichia Chemical Industries, Ltd. | Nitride semiconductor device |
| US6100586A (en) * | 1997-05-23 | 2000-08-08 | Agilent Technologies, Inc. | Low voltage-drop electrical contact for gallium (aluminum, indium) nitride |
| EP1014455B1 (en) | 1997-07-25 | 2006-07-12 | Nichia Corporation | Nitride semiconductor device |
| US20010042866A1 (en) * | 1999-02-05 | 2001-11-22 | Carrie Carter Coman | Inxalygazn optical emitters fabricated via substrate removal |
| JP2002094110A (en) * | 2000-09-12 | 2002-03-29 | ▲さん▼圓光電股▲ふん▼有限公司 | Structure of light emitting diode |
| KR100662191B1 (en) | 2004-12-23 | 2006-12-27 | 엘지이노텍 주식회사 | Nitride semiconductor light emitting device and manufacturing method |
-
1995
- 1995-10-30 JP JP28195995A patent/JP3605907B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH08213651A (en) | 1996-08-20 |
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