US20110101412A1

US20110101412A1 - Light-emitting semiconductor device using group III nitrogen compound

Info

Publication number: US20110101412A1
Application number: US12/929,231
Authority: US
Inventors: Katsuhide Manabe; Hisaki Kato; Michinari Sassa; Shiro Yamazaki; Makoto Asai; Naoki Shibata; Masayoshi Koike
Original assignee: Toyoda Gosei Co Ltd
Current assignee: Toyoda Gosei Co Ltd
Priority date: 1994-03-22
Filing date: 2011-01-10
Publication date: 2011-05-05
Also published as: US6265726B1; US20060118821A1; US20010019849A1; US7001790B2; US20050224834A1; US7332366B2; US7138286B2; US7867800B2; US20080173880A1; US6005258A; US20140239313A1; US20120217510A1

Abstract

A method of producing a light-emitting semiconductor device of a group III nitride compound includes forming an N-layer of an N-type conduction, the N-layer comprising gallium nitride, forming a high carrier concentration N⁺-layer satisfying the formula (Al_x3Ga_1-x3)_y3In_1-y3N, wherein 0≦x3≦1, 0≦y3≦1 and 0≦x3+y3≦1, on the N-layer, forming an emission layer of a group III nitride compound semiconductor satisfying the formula, Al_x1Ga_y1In_1-x1-y1N, where 0≦x1≦1, 0≦y1≦1 and 0≦x1+y1≦1 on the high carrier concentration layer N⁺layer, doping Si and Zn into the emission layer, forming a P-layer of a P-type conduction, on the emission layer, the P-layer including aluminum gallium nitride satisfying the formula Al_x2Ga_1-x2N, wherein 0≦x2≦1, and forming a contact layer of a P-type conduction, on the P-type layer, the contact layer including gallium nitride.

Description

The present Applicant is a Divisional Application of U.S. patent application Ser. No. 12/003,173 filed on Dec. 20, 2007, which is a Divisional Application of U.S. patent application Ser. No. 11/328,079 filed on Jan. 10, 2006, now U.S. Pat. No. 7,332,366, which is a Divisional Application of U.S. patent application Ser. No. 11/143,664 filed on Jun. 3, 2005, now U.S. Pat. No. 7,138,286, which in turn is a Divisional Application of U.S. patent application Ser. No. 09/783,035 filed on Feb. 15, 2001, now U.S. Pat. No. 7,001,790, which in turn is a Divisional Application of U.S. patent application Ser. No. 09/379,621 filed on Aug. 24, 1999, now U.S. Pat. No. 6,256,726, which in turn is a Divisional Application of U.S. patent application Ser. No. 08/806,646 filed on Feb. 26, 1997, now U.S. Pat. No. 6,005,258, which in turn is a Continuation Application of U.S. patent application Ser. No. 08/408,164 filed Mar. 21, 1995.

BACKGROUND OF THE INVENTION

1. Field of the Invention
The present invention relates to a light-emitting semiconductor device that emits blue light and uses a group III nitrogen compound.
2. Description of the Prior Art
It has been known that an aluminum gallium indium nitride (AlGaInN) compound semiconductor may be used to obtain a light-emitting diode (LED) which emits blue light. This semiconductor device is useful because of its high luminous efficiency resulting from direct electron transition and because of its ability to emit blue light, which is one of the three primary colors.
Irradiating an electron beam into an i-layer to which magnesium (Mg) is doped and heat treatment is carried out enables the i-layer to have a p-type layer of the AlGaInN semiconductor device. As a result, a LED with a double hetero p-n junction structure includes an aluminum gallium nitride (AlGaN) p-layer, a zinc (Zn) doped indium gallium nitride (InGaN) emission layer and an AlGaN n-layer, becomes useful instead of conventional LED of metal insulator semiconductor (MIS) structure which includes an n-layer and a semi-insulating i-layer.
The conventional LED with a double hetero p-n junction structure is doped with Zn as an emission center. Luminous intensity of this type of LED has been improved fairly. Still, there exists a problem in luminous efficiency and further improvement is necessary.
The emission mechanism of a LED with an emission layer doped with only Zn, or only an acceptor impurity, as the emission center is electron transition between conduction band and acceptor energy levels. However, a large difference of their energy levels makes recombination of electrons through deep levels dominant which deep level recombination does not contribute to emission. This results in lower luminous intensity. Further, the wavelength of light from the conventional LED is about 380 to 440 nm, or shorter than that of pure blue light.
Further, the emission layer doped with Zn as the emission center exhibits semi-insulative characteristics. Its emission mechanism is explained by recombination of an electron through acceptor level injected from an n-layer and a hole injected from a p-layer. However, the diffusion length of the hole is shorter than that of the electron. It results in high ratio of holes disappearing in a non-emission process before recombination of the hole and electron occurs in the emission layer. This phenomenon impedes higher luminous intensity.

SUMMARY OF THE INVENTION

It is an object of the present invention to solve the above problem and improve the luminous intensity of the LED of AlGaInN semiconductor, or.obtain enough spectrum to emit a purer blue light.
According to the first aspect.of the invention, there is provided a light-emitting. semiconductor device comprising:
an n-layer with n-type conduction of group III nitride compound semiconductor satisfying the formula Al_x3Ga_y3In_1-x3-y3N, inclusive of x3=0, y3=0 and x3=y3=0,
a p-layer with p-type conduction of group III nitride compound semiconductor satisfying the formula Al_x1Ga_y1In_1-x1-y1N, inclusive of x1=0, y1=0 and x1=y1=0,
an emission layer of group III nitride compound semiconductor satisfying the formula Al_x2Ga_y2In_1-x2-y2N, inclusive of x2=0, y2=0 and x2=y2=0;
the junction layer of the n-layer, the p-layer, and the emission layer being any one of a homo-junction structure, a single hetero-junction structure, and a double hetero-junction structure; and
wherein the emission layer is formed between the n-layer and the p-layer, and doped with both a donor and an acceptor impurity.
It is preferable that the donor impurity is one of the group IV elements and that the acceptor impurity is one of the group II elements.
Preferable combinations of a donor and an acceptor impurity include silicon (Si) and cadmium (Cd), silicon (Si) and zinc (Zn), and silicon (Si) and magnesium (Mg), respectively.
The emission layer can.be controlled to exhibit any one of n-type conduction, semi-insulative, and p-type conduction depending on the concentration ratio of a donor impurity and an acceptor impurity doped thereto.
Further, the donor impurity can be one of the group VI elements.
Further, it is desirable to design the composition ratio of Al, Ga, and In in the n-layer, p-layer, and emission layer to meet each of the lattice constants of the three layers to an n⁺-layer of high carrier concentration on which the three layers are formed.
Further, a double hetero-structure sandwiching of the emission layer of p-type conduction by the n-layer and p-layer improves luminous efficiency. Making the concentration of acceptor impurity larger than that of the donor impurity and processing by electron irradiation or heat treatment changes the emission layer to exhibit p-type conduction. Magnesium, an acceptor impurity, is especially efficient for obtaining p-type conduction.
Further, doping any combinations of the described acceptor and donor impurity to an emission layer of p-type conduction also improves luminous efficiency. The luminous mechanism doped with acceptor and donor impurities is due to recombination of an electron at donor level and a hole at the acceptor. level. This recombination occurs within the emission layer, so that luminous intensity is improved.
Further, a double hetero-junction structure of a triple-layer sandwiching the emission layer having a narrower bad gap by the n-layer and p-layer having a wider band gap improves luminous intensity. Since the emission layer and the p-layer exhibit p-type conduction, valence bands of those layers are successive even without applying external voltage. Consequently, holes readily highly exist within the emission layer. In contrast, conduction bands of the n-layer and the emission layer are not successive without applying an external voltage. Applying a voltage enables the conduction bands to be successive and electrons to be injected deeper into the emission layer. Consequently, the number of injected electrons into the emission layer increases ensuring recombination with holes and a consequent improvement in luminous intensity.
Other objects, features, and characteristics of the present invention will become apparent upon consideration of the following description in the appended claims with reference to the accompanying drawings, all of which form a part of the specification, and wherein referenced numerals designate corresponding parts in the various figures.

BRIEF DESCRIPTION OF THE DRAWING

In the accompanying drawings:

FIG. 1 is a diagram showing the structure of the LED embodied in Example 1;

FIGS. 2 through 7 are sectional views illustrating successive steps of producing the LED embodied in Example 1;

FIG. 8 is a diagram showing the structure of the LED embodied in Example 2;

FIG. 9 is a diagram showing the structure of the LED embodied in Example 3;

FIG. 10 is a diagram showing the structure of the LED embodied in Example 4;

FIG. 11 is a diagram showing the structure of the LED embodied in Example 5;

FIGS. 12 and 13 are diagrams showing the structure of the LED embodied in Example 6;

FIG. 14 is a diagram showing the structure of the LED embodied in Example 7; and

FIGS. 15 and 16 are diagrams showing the structure of the LED embodied in Example 8.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

The invention will be more fully understood by reference to the following examples.

Example 1

FIG. 1 shows a LED 10 embodied in Example 1. It has a sapphire (Al₂O₃) substrate 1 upon which the following five layers are consecutively formed: an AlN buffer layer 2; a silicon (Si) doped GaN n⁺-layer 3 of high carrier (n-type) concentration; a Si-doped (Al_x2Ga_1-x2)_y2In_1-y2N n⁺-layer 4 of high carrier (n-type) concentration; a cadmium (Cd) and Si-doped (Al_x1Ga_1-x1)_y1In_1-y1 N emission layer 5; and a Mg-doped (Al_x2Ga_1-x2)_y2In_1-y2N p-layer 6. The AlN layer 2 has 500 Å thickness. The GaN n⁺-layer 3 is about 2.0 μm in thickness and has a 2×10¹⁸/cm³electron concentration. The n⁺-layer 4 is about 2.0 μm in thickness and has a 2×10¹⁸/cm³electron concentration. The emission layer 5 is about 0.5 μm in thickness. The i-layer 6 is about 1.0 μm in thickness and has a 2×10¹⁷/cm³hole concentration. Nickel electrodes 7 and 8 are connected to the p-layer 6 and the n⁺-layer 4, respectively. They are electrically insulated by a groove 9.
The LED 10 is produced by gaseous phase growth, called metal organic vapor phase epitaxy referred to as MOVPE hereinafter.
The gases employed in this process are ammonia (NH₃), a carrier gas (H₂or N₂), trimethyl gallium (Ga(CH₃)₃) (TMG hereinafter), trimethyl aluminum (Al(CH₃)₃) (TMA hereinafter), trimethyl indium (In(CH₃)₃) (TMI hereinafter), dimethylcadmium ((Cd(CH₃)₂) (DMCd hereinafter), silane (SiH₄), diethylzinc ((C₂H₅)₂Zn) (DEZ hereinafter) and biscyclopentadienyl magnesium (Mg(C₅H₅)₂) (CP₂Mg hereinafter).
The single crystalline sapphire substrate 1, whose main surface ‘a’ was cleaned by an organic washing solvent and heat treatment, was placed on a susceptor in a reaction chamber for the MOVPE treatment. Then the sapphire substrate 1 was etched at 1100° C. by a vapor of H₂fed into the chamber at a flow rate of 2 liter/min. under normal pressure for a period of 5 min.
On the etched sapphire substrate 1, a 500 Å thick AlN buffer layer 2 was epitaxially formed on the surface ‘a’ under conditions of lowering the temperature in the chamber to 400° C., keeping the temperature constant, and supplying H₂, NH₃and TMA for a period of about 90 sec. at a flow rate of 20 liter/min., 10 liter/min., and 1.8×10⁻⁵mol/min., respectively. On the buffer layer 2, about a 2.2 μm thick Si-doped GaN n⁺-layer 3 of high carrier concentration with an electron concentration of about 2×10¹⁸/cm³was formed under conditions of keeping the temperature of the sapphire substrate 1 at 1150° C. and supplying H₂, NH₃, TMG, and diluted silane to 0.86 ppm by H₂for thirty minutes at a flow rate of 20 liter/min., 10 liter/min., 1.7×10⁻⁴mol/min. and 200 ml/min., respectively.
The following manufacturing process provides for an emission layer 5 as an active layer, an n⁺-layer 4 of high carrier concentration, and a p-layer 6 as a clad layer; the LED 10 is designed to emit at a 450 nm wavelength peak in the luminous spectrum and have luminous centers of Cd and Si.
On the n⁺-layer 3, about a 0.5 μm thick Si-doped (Al_0.47Ga_0.53)_0.9In_0.1N n⁺-layer 4 of high carrier concentration with an electron concentration of 1×10¹⁸/cm³was formed under conditions of keeping the temperature of the sapphire substrate 1 at 850° C. and supplying N₂or H₂, NH₃, TMG, TMA, TMI, and diluted silane to 0.86 ppm by H₂for 60 min. at a flow rate of 10 liter/min., 10 liter/min., 1.12×10⁻⁴mol/min., 0.47×10⁻⁴mol/min., 0.1×10⁻⁴mol/min. and 10×10⁻⁹mol/min., respectively.
On the n⁺-layer 4, about a 0.5 μm thick Cd and Si-doped (Al_0.3Ga_0.7)_0.94In_0.06 N emission layer 5 was formed under conditions of keeping the temperature of the sapphire substrate 1 at 850° C. and supplying N₂or H₂, NH₃, TMG, TMA, TMI, DMCd, and diluted silane to 0.86 ppm by H₂for 60 min. at a flow rate of 20 liter/min., 10 liter/min., 1.53×10⁻⁴mol/min., 0.47×10⁻⁴mol/min., 0.02×10⁻⁴mol/min., 2×10⁻⁷mol/min. and 10×10⁻⁹mol/min., respectively. At this stage, the layer 5 exhibited high resistivity. The impurity concentrations of the Cd and the Si doped to the emission layer 5 were 5×10¹⁸/cm³and 1×10¹⁸/cm³, respectively.
On the emission layer 5, about a 1.0 μm thick Mg-doped (Al_0.47Ga_0.53)_0.9In_0.1N p-layer 6 was formed under conditions of keeping the temperature of the sapphire substrate 1 at 1000° C. and supplying N₂or H₂, NH₃, TMG, TMA, TMI, and CP₂Mg for 120 min. at a flow rate of 20 liter/min., 10 liter/min., 1.12×10⁻⁴mol/min., 0.47×10⁻⁴mol/min., 0.1×10⁻⁴mol/min. and 2×10⁻⁴mol/min., respectively. Resistivity of the p-layer 6 was 10⁸Ω·cm or more exhibiting insulative characteristics. The impurity concentration of the Mg-doped into the p-layer 6 was 1×10²⁰/cm³.
Then, electron rays were uniformly irradiated into the p-layer 6 using a reflective electron beam diffraction device. The irradiation conditions were set at 10 KV for the accelerating voltage. 1 μA for the sample current, 0.2 mm/sec. for the speed of the beam scanning, 60 μmφ for the beam aperture, and at 5.0×10⁻⁵Torr vacuum. This irradiation changed the insulative p-layer 6 into a p-type conductive semiconductor with a hole concentration of 2×10¹⁷/cm³and a resistivity of 2 Ω·cm. Thereby, a wafer with multi-structural layers was obtained as shown in FIG. 2.
The following FIGS. 3 to 7 show sectional views of an individual element on the wafer. In actual practice and in accordance with industry custom, a wafer with a large number of elements thereon is treated by the following process and divided or diced into individual elements.
A 2000 Å thick SiO₂layer 11 was formed on the p-layer 6 by sputtering. Then, the layer 11 was coated with a photoresist layer 12. Two selected parts or areas of the photoresist layer 12, named A and B, were removed by photolithography as shown in FIG. 3. The part or area A is an electrode forming part which corresponds to a place where a hole 15, shown in FIG. 5, is formed extending to and into the n⁻-layer 4 of high carrier concentration. The part or area B corresponds to a place where a groove 9 shown in FIGS. 5 and 6 is formed for insulating or electrically insulating the part or area A from an electrode in contact with the p-layer 5.
As shown in FIG. 4, two parts of the SiO₂layer 11 which were not covered with the photoresist layer 12 were etched off by an etching liquid such as hydrofluoric acid. Then, the exposed part.of the following successive three layers from the surface of the device, the p-layer 6, the emission layer 5, and the upper part of the n⁺-layer 4 of high carrier concentration, were removed by dry etching, or supplying a high-frequency power density of 0.44 W/cm²and BCl₃gas of 10 ml/min. at a vacuum degree of 0.04 Torr as shown in FIG. 5. After that, dry etching with argon (Ar) was carried out on the device. Consequently, a hole 15 for forming an electrode reaching the n⁺-layer 4 of high carrier concentration and a groove 9 for insulation are formed.
The SiO₂layer 11 remaining on the p-layer 6 was removed by hydrofluoric acid as shown in FIG. 6. A nickel (Ni) layer 13 was laminated on the entire surface of the device by vapor deposition. Thus, the so-formed Ni layer 13 in the hole 15 is in electrical contact with the n⁺-layer 4 of high carrier concentration. A photoresist 14 was deposited on the Ni layer 13 and, then, was selectively etched off by photolithography as shown in FIG. 7 leaving patterns of configuration for electrodes connected to the n⁺-layer 4 of high carrier concentration and the p-layer 6, respectively.
Using the photoresist 14 as a mask, the exposed part or area of the Ni layer 13 from the photoresist 14 was etched off by an etching liquid such as nitric acid. At this tine, the nickel layer 13 laminated in the groove 9 was also removed completely. Then, the photoresist layer 14 was removed by a photoresist removal liquid such as acetone. There were formed two electrodes, the electrode 8 for the n⁺-layer 4 of high carrier concentration and the electrode 7 for the p-layer 6. A wafer treated with the above-mentioned process was divided or diced, into each element which shows a gallium nitride light-emitting diode with a p-n junction structure as shown in FIG. 1.
The obtained LED 10 was found to have a luminous intensity of 100 mcd and a wavelength of 450 nm by driving current of 20 mA.
The emission layer 5 preferably contains impurity concentrations of Cd and Si within a range of 1×10¹⁷/cm³to 1×10²⁰/cm³, respectively, in order to improve luminous intensity. It is further desirable that the concentration of Si is smaller than that of Cd by ten to fifty percent.
In order to make the band gap of the emission layer 5 smaller than those of its respective adjacent two layers, i.e., the p-layer 6 and the n⁺-layer 4 of high carrier concentration, a double hetero-junction structure was utilized for the LED 10 in this embodiment. Alternatively, a single hetero-junction structure can be utilized.
Further, it is preferable that the composition ratio of Al, Ga, and In in the respective three layers 4, 5, and 6 is selectively designed to meet the lattice constants of their layers 4, 5, and 6 with the lattice constant of GaN in the n⁺-layer 3 of high carrier concentration as precisely as possible.

Example 2

FIG. 8 shows a LED 10 utilized in Example 2. The emission layer 5 in Example 1 was doped with Cd and Si. In this Example 2, an emission layer 5 is doped with Zn and Si.
A manufacturing process of a sapphire substrate 1, the formation of the AlN buffer layer 2 and the n⁺-layers 3 was similar to that discussed in the previous example.
About a 0.5 μm thick Si-doped (Al_0.3Ga_0.7)_0.94In_0.06N n⁺-layer 4 of high carrier concentration with an electron concentration of 2×10¹⁹/cm³was formed on the n⁺-layer 3 under conditions of lowering the temperature in the chamber to 800° C., keeping the temperature constant, and supplying N₂, NH₃, TMG, TMA, TMI, and diluted silane to 0.86 ppm by H₂for 120 min. at a flow rate of 20 liter/min., 10 liter/min., 1.12×10⁻⁴mol/min., 0.47×10⁻⁴mol/min., 0.1×10⁻⁴mol/min., and 10×10⁻⁹mol/min., respectively.
About a 0.5 μm thick Si- and Zn-doped (Al_0.09Ga_0.91)_0.99In_0.01 N emission layer 5 was formed on the n⁺-layer 4 under conditions of lowering the temperature in the chamber to 1150° C., keeping it constant, and supplying N₂, NH₃, TMG, TMA, TMI, diluted silane to 0.86 ppm by H₂, and DEZ for 7 min. at a flow rate of 20 liter/min., 10 liter/min., 1.53×10⁻⁴mol/min., 0.47×10⁻⁴mol/min., 0.02×10⁻⁴mol/min. and 10×10⁻⁹mol/min., and 2×10⁻⁴mol/min., respectively. The impurity concentration of the Zn- and Si-doped into the emission layer 5 was 2×10¹⁸/cm³and 1×10¹⁸/cm³, respectively.
About a 1.0 μm thick Mg-doped (Al_0.3Ga_0.7)_0.94In_0.06N p-layer 6 was formed on the emission layer 5 under conditions of lowering the temperature in the chamber to 1100° C., keeping the temperature constant, and supplying N₂, NH₃, TMG, TMA, TMI, and CP₂Mg at a flow rate of 20 liter/min., 10 liter/min., 1.12×10⁻⁴mol/min., 0.47×10⁻⁴mol/min., 0.1×10⁻⁴mol/min., and 2×10⁻⁴mol/min., respectively. The impurity concentration of Mg doped into the p-layer 6 was 1×10²⁰/cm³. At this stage, the p-layer 6 remained insulative with a resistivity of 10⁸Ω·cm or more.
Then, the p-layer 6 was processed to have p-type conduction by electron beam irradiation under the same conditions described in Example 1. The subsequent process steps of forming the electrodes are the same as that described in the previous example. The so-obtained LED 10 was found to have a luminous intensity of 1000 mcd and a wavelength of 450 nm by driving current of 20 mA.

Example 3

FIG. 9 shows a structural view of a LED 10 embodied in Example 3. The LED 10 in Example 3 was manufactured by additionally doping Mg to the emission layer 5 of the LED in Example 2. Other layers and electrodes were manufactured in the same way as those in Example 2.
CP₂Mg was fed at a flow rate of 2×10⁻⁴mol/min. into a chamber in addition to the gasses employed in Example 2 in order to manufacture the emission layer 5 in Example 3. The emission layer 5 was about 0.5 μm thick comprising Mg, Zn, and Si-doped (Al_0.09Ga_0.9)_0.99In_0.01N. Its resistivity was 10⁸Ω·cm remaining insulative. Impurity concentration of Mg, Zn, and Si was 1×10¹⁹/cm³, 2×10¹⁸/cm³, and 1×10¹⁸/cm³, respectively.
Then, both of the emission layer 5 and a p-layer 6 were subject to electron beam irradiation with the electron beam diffraction device under as same conditions as in Example 1. Thus, the emission layer 5 and the p-layer 6 turned into layers exhibiting p-type conduction with a hole concentration of 2×10¹⁷/cm³and resistivity of 2 Ω·cm.

Example 4

FIG. 10 shows a structural view of a LED 10 embodied in Example 4. In this example, an emission layer 5 includes GaN and had a single hetero-junction structure. Namely, one junction comprises a heavily Si-doped n⁺-layer 4 of high carrier concentration and a Zn- and Si-doped GaN emission layer 5, and another junction includes the GaN emission layer 5 and a Mg-doped Al_0.1Ga_0.9N p-layer 61 with p-type conduction. In this example, the Mg-doped GaN p-layer 62 as a contact layer is formed on the p-layer 61. An insulation groove 9 is formed through the contact layer 62, the p-layer 61 and the emission layer 5.
The LED 10 in this example has a sapphire substrate 1 upon which the following five layers are consecutively formed: an A1N buffer layer 2; a Si-doped GaN n⁺-layer 4 of high carrier (n-type) concentration; a Zn and Si-doped GaN emission layer 5, Mg-doped Al_0.1Ga_0.9N p-layer 61, and Mg-doped GaN contact layer 62. The AN layer 2 has a 500 Å thickness. The GaN n⁺-layer 4 has about a 4.0 μm thickness and a 2×10¹⁸/cm³electron concentration. The emission layer 5 has about a 0.5 μm thickness. The p-layer 61 has about a 0.5 μm _thickness and a 2×10¹⁷/cm³hole concentration. The contact layer 62 has about a 0.5 μm thickness and a 2×10¹⁷/cm³hole concentration. Nickel electrodes 7 and 8 are formed to connect to the contact layer 62 and the n⁺-layer 4 of high carrier concentration, respectively. The two electrodes are electrically insulated by a groove 9.
Here is explained a manufacturing process of the LED 10. The sapphire substrate 1 and the AlN buffer layer 2 were prepared by the same process described in detail in Example 1. On the AlN buffer layer 2, about a 4.0 μm thick Si-doped GaN n⁺-layer 4 of high carrier concentration with an electron concentration of 2×10¹⁸/cm³was formed under conditions of lowering the temperature in the chamber to 1150° C., keeping the temperature constant and supplying N₂, NH₃, TMG, and diluted silane to 0.86 ppm by H₂for 60 min. at a flow rate of 20 liter/min., 10 liter/min., 1.7×10⁻⁴mol/min., 0.47×10⁻⁴mol/min., 0.1×10⁻⁴mol/min., and 10×10⁻⁹mol/min., respectively.
The following manufacturing process and composition ratio provide for the three layers, the emission layer 5 as an active layer, the p-layer 62 as a clad layer, and the contact layer 62. The LED is designed to have 430 nm wavelength at peak in the luminous spectrum and have luminous centers of Zn and Si.
About a 0.5 μm thick Zn- and Si-doped GaN emission layer 5 was formed on the n⁺-layer 4 under conditions of lowering the temperature in the chamber to 1000° C., keeping it constant and supplying N₂or H₂, NH₃, TMG, DMZ, and diluted silane to 0.86 ppm by H₂for 8 min. at a flow rate of 20 liter/min., 10 liter/min., 1.53×10⁻⁴mol/min., 2×10⁻⁷mol/min., and 10×10⁻⁹mol/min., respectively.
About a 0.5 μm thick Mg-doped Al_0.1Ga_0.9N p-layer 61 was formed on the emission layer 5 under conditions of lowering the temperature in the chamber to 1000° C., keeping the temperature constant and supplying N₂or H₂, NH₃, TMG, TMA, and CP₂Mg for 7 min. at a flow rate of 20 liter/min., 10 liter/min., 1.12×10⁻⁴mol/min., 0.47×10⁻⁴mol/min., and 2×10⁻⁷mol/min., respectively. At this stage, the p-layer 61 remained insulative with a resistivity of 10⁸Ω·cm or more. The impurity concentration of the Mg-doped into the p-layer 61 was 1×10¹⁹/cm³.
Then, about a 0.5 μm thick Mg-doped GaN contact layer 62 was formed on the p-layer 61 under conditions of lowering the temperature in the chamber to 1000° C., keeping the temperature constant and supplying N₂or H₂, NH₃, TMG, and CP₂Mg for 10 min. at a flow rate of 20 liter/min., 10 liter/min., 1.12×10⁻⁴mol/min., and 2×10⁻⁴mol/min., respectively. At this stage, the Mg-doped contact layer 62 remained insulative with a resistivity of 10⁸Ω·cm or more. The impurity concentration of the Mg-doped into the contact layer 62 was 1×10²⁰/cm³.
Then, the p-layer 61 and contact layer 62 were uniformly irradiated by an electron beam under the same conditions as described in Example 1. Consequently, the p-layer 61 and contact layer 62 are processed to exhibit p-type conduction with a 2×10¹⁷/cm³hole concentration and 2 Ω·cm or more resistivity. The subsequent process steps of forming the electrodes is the same as that described in the previous example. As a result, the LED 10 having a single hetero-junction structure is obtained whose emission layer is doped with Zn as an acceptor and Si as a donor impurity. Alternatively, doping Mg and irradiating electrons into the emission layer 5 can be used to obtain an emission layer 5 with p-type conduction.

Example 5

FIG. 11 shows a LED 10 embodied in this example. Three layers, a p-layer 61, an emission layer 5, and an n⁺-layer 4, are unique to Example 5. The p-layer 61 is formed of Mg-doped Al_x1Ga_1-x1N. The emission layer 5 is Zn- and Si-doped Al_x2Ga_1-x2N. The n³⁰-layer 4 of high carrier concentration is Si-doped Al_x3Ga_1-x3N. Other layers and electrodes are formed the same as those described in Example 4. The composition ratio of x1, x2 and x3 in each layer is designed to make the band gap of the emission layer 5 smaller than those of the n⁺-layer 4 and p-layer 61 forming a double hetero-junction structure or a single hetero-junction structure. Thanks to this structure, carriers are confined in the emission layer 5 contributing to higher luminous intensity. The emission layer 5 can exhibit any one of semi-insulative, p-type conductivity, or n-type conductivity.

Example 6

FIG. 12 shows a LED 10 embodied in this example. Three layers, a p-layer 61, an emission layer 5, and an n⁺-layer 4, are unique to Example 6. The p-layer 61 formed of Mg-doped Al_x1Ga_1-x1N. The emission layer 5 is formed of Zn- and Si-doped Ga_yIn_1-yN. The n⁺-layer 4 of high carrier concentration is formed of Si-doped Al_x2Ga_1-x2N. Other layers and electrodes are formed the same as those described in Example 4. The composition ratio of x1, x2, and x3 in each layer is designed to make the.band gap of the emission layer 5 smaller than those of the n⁺-layer 4 and p-layer 61 forming a double hetero-junction structure or a single hetero-junction structure. Thanks to this structure, carriers are confined in the emission layer 5 contributing to higher luminous intensity. The emission layer 5 can exhibit any one of semi-insulative, p-type conductivity, or n-type conductivity.
The LED 10 in this example has a sapphire substrate 1 which has the following five layers are consecutively formed thereon: an AlN buffer layer 2; a Si-doped Al_x2Ga_1-x2N n⁺-layer 4 of high carrier (n-type) concentration; a Zn- and Si-doped Ga_0.94In_0.06 N emission layer 5, Mg-doped Al_0.1Ga_0.9N p-layer 61 of p-type, and an Mg-doped GaN contact layer 62 of p-type. The AlN layer 2 has a 500 Å thickness. The Al_x2Ga_1-x2N n⁺-layer 4 has about a 4.0 μm thickness and a 2×10¹⁸/cm³electron concentration. The emission layer 5 has about 0.5 μm thickness. The p-layer 61 has about a 0.5 μm thickness and a 2×10¹⁷/cm³hole concentration. The contact layer 62 has about a 0.5 μm thickness and a 2×10¹⁷/cm³hole concentration. Nickel electrodes 7 and 8 are formed to connect to the contact layer 62 and n⁺-layer 4 of high carrier concentration, respectively. The two electrodes are electrically insulated by a groove 9.
A manufacturing process for the LED 10 of FIG. 12 is as follows. The sapphire substrate 1 and the AlN buffer layer 2 were prepared by the same process described in detail in Example 1. On the AlN buffer layer 2, about a 4.0 μm thick Si-doped Al_x2Ga_1-x2N n⁺-layer 4 of high carrier concentration with an electron concentration of 2×10¹⁸/cm³was formed under conditions of lowering the temperature in the chamber to 1150° C., keeping it constant, and supplying N₂, NH₃, TMG, TMA, and diluted silane to 0.86 ppm by H₂for 60 min. at a flow rate of 20 liter/min., 10 liter/min., 1.12×10⁻⁴mol/min., 0.47×10⁻⁴mol/min., and 10×10⁻⁹mol/min., respectively.
Following manufacturing process and composition ratio for the three layers, the emission layer 5 as an active layer, the p-layer 61 as a clad layer, and the contact layer 62, show an example where the LED 10 is designed to have 450 nm wavelength at peak in luminous spectrum and have luminous centers of Zn and Si.
About a 0.5 μm thick Zn- and Si-doped Ga_0.94 1n_0.06 N emission layer 5 was formed on the n⁺-layer 4 under conditions of raising the temperature in the chamber to 850° C., keeping it constant, and supplying N₂or H₂, NH₃, TMG, TMI, DMZ and, silane for 60 min. at a flow rate of 20 liter/min., 10 liter/min., 1.53×10⁻⁴mol/min., 0.02×10⁻⁴mol/min., 2×10⁻⁷mol/min., and 10×10⁻⁹mol/min., respectively.
About a 0.5 μm thick Mg-doped Al_0.1Ga_0.9N p-layer 61 was formed on the emission layer 5 under conditions of raising the temperature in the chamber to 1000° C., keeping the temperature constant and supplying N₂or H₂, NH₃, TMG, TMA, and CP₂Mg for 7 min. at a flow rate of 20 liter/min., 10 liter/min., 1.12×10⁻⁴mol/min., 0.47×10⁻⁴mol/min., and 2×10⁻⁷mol/min., respectively. At this stage, the p-layer 61 remained insulative with a resistivity of 10⁸Ω·cm or more. The impurity concentration of the Mg doped into the p-layer 61 was 1×10¹⁹/cm³.
Then, about a 0.5 μm thick Mg-doped GaN contact layer 62 was formed on the p-layer 61 under conditions of keeping the temperature in the chamber at 1000° C. and supplying N₂or H₂, NH₃, TMG, and CP₂Mg for 10 min. at a flow rate of 20 liter/min., 10 liter/min., 1.12×10⁻⁴mol/min., and 2×10⁻⁴mol/min., respectively. At this stage, the Mg-doped contact layer 62 remained insulative with a resistivity of 10 ⁸Ω·cm or more. The impurity concentration of the Mg doped into the contact layer 62 was 1×10²⁰/cm³.
Then, the p-layer 61 and contact layer 62 were uniformly irradiated by an electron beam with the same conditions described in Example 1. Consequently, the p-layer 61 and contact layer 62 are processed to exhibit p-type conduction with a 2×10¹⁷/cm³hole concentration and a 2 Ω·cm resistivity. The subsequent process steps of forming the electrodes is the same as that described in the previous example.
In Examples 1 to 6, the emission layer 5 can exhibit any one of semi-insulation, p-type conductivity, or n-type conductivity. When the concentration of the Zn-doped to the emission layer 5 is higher than that of the Si, the layer 5 exhibits semi-insulative characteristics. When the concentration of the Zn is smaller than that of the Si, the emission layer 5 exhibits n-type conduction.
In order to improve the luminous intensity, the impurity concentration of Zn and Si doped to the emission layer 5 is preferably in the 1×10¹⁷/cm³to 1×10²⁰/cm³range, respectively. The concentration is more preferably in the 1×10¹⁸/cm³to 1×10¹⁹/cm³range. It is not preferable that the impurity concentration be lower than 1×10¹⁸/cm³, because the luminous intensity of the LED decreases as a result. It is not desirable that the impurity concentration is higher than 1×10¹⁹/cm³, because poor crystallinity occurs. It is preferable that the concentration of Si is ten to one-tenth as that of Zn. The most preferable concentration of Si is in the one to one-tenth range or closer to one-tenth to Zn.
In Examples 1 to 6, Cd, Zn, and Mg were employed as acceptor impurities and Si as a donor impurity. Alternatively, beryllium (Be) and mercury (Hg) can be used as an acceptor impurity. Alternatively, carbon (C), germanium (Ge), tin (Sn), lead (Pb), sulfur (S), selenium (Se), and tellurium (Te) can be used as a donor impurity.
Electron irradiation was used in Examples 1 to 6 in order to process an emission layer 5 to exhibit p-type conduction. Alternatively, annealing, heat processing in the atmosphere of N₂plasma gas and laser irradiation can be used.

Example 7

FIG. 14 shows a structural view of a LED 10 embodied in Example 7. The LED 10 in this example was manufactured by additionally doping Mg to the emission layer 5 of the LED 10 in Example 1. Other layers and electrodes were manufactured the same way as those described in Example 1.
CP₂Mg was fed at a flow rate of 2×10⁻⁷mol/min. into a chamber in addition to gasses employed in Example 1 in order to manufacture the emission layer 5 in Example 7. The emission layer 5 was about a 0.5 thick including Mg-, Cd-, and Si-doped) (Al_0.99Ga_0.91)_0.99In_0.01N remaining high insulative. Impurity concentration of the Mg, Cd and Si was 1×10²⁰/cm³, 5×10¹⁸/cm³, and 1×10¹⁸/cm³, respectively.
Then, electron beam was uniformly irradiated on both of the emission layer 5 and p-layer 6 with an electron diffraction device under the same conditions as in Example 1. The emission layer 5 and p-layer 6 came to exhibit p-type conduction with a hole concentration of 2×10¹⁷/cm³and a resistivity of 2 Ω·cm.

Example 8

FIGS. 15 and 16 show structural views of a LED 10 embodied in Example 8. The LED 10 in this example was manufactured by additionally doping Mg and irradiating electrons into the emission layer 5 of the LED 10 in Example 6. The emission layer 5 of Example 8 includes Mg-, Zn-, and Si-doped Ga_yIn_1-yN exhibiting p-type conduction. Other layers and electrodes were manufactured the same way as those described in Example 1.
FIG. 16 shows an example where the LED 10 is designed to have a 450 nm wavelength at peak in the luminous intensity. The manufacturing process and composition equation of the three layers, the emission layer 5 as an active layer, the p-layer 61 as a clad layer and the contact layer 62 are described hereinafter.
The CP₂Mg was fed at a flow rate of 2×10⁻⁴mol/min. into a chamber in addition to gasses employed in Example 6 in order to manufacture the emission layer 5 in Example 8. The emission layer 5 was about a 0.5 μm thick including Mg-, Zn-, and Si-doped Ga_0.94In_0.06N remaining highly insulative.
Then, the emission layer 5, p-layer 61 and contact layer 61 were uniformly irradiated by an electron diffraction device under the same conditions as those described in Example 1. This irradiation changed the emission layer 5, p-layer 61, and contact layer 62 into layers exhibiting p-type conduction with a hole concentration of 2×10¹⁷/cm³and a resistivity of 2 Ω·cm.
In Examples 7 and 8, the impurity concentration of Zn and Si doped into the emission layer 5 are preferably in the 1×10¹⁷/cm³to 1×20²⁰/cm³range, respectively. The concentration is more preferably in the 1×10¹⁸/cm³to 1×10¹⁹/cm³range. It is not preferable that the impurity concentration be lower than 1×10¹⁸/cm³, because luminous intensity of the LED decreases as a result. It is not desirable that the impurity concentration be higher than 1×10¹⁹/cm³, because poor crystallinity occurs. It is further preferable that the concentration of Si be ten to one-tenth as same as that of Zn. The most preferable concentration of Si is in the two to one-tenth range.
In Examples 7 and 8, Cd, Zn and Mg were employed as acceptor impurities and Si as a donor impurity. Alternatively, beryllium (Be) and mercury (Hg) can be used as an acceptor impurity. Alternatively, carbon (C), germanium (Ge), tin (Sn), lead (Pb), sulfur (S), selenium (Se) and tellurium (Te) can be used as a donor impurity.
Electron irradiation was used in Examples 7 and 8 in order to change layers to have p-type conduction. Alternatively, annealing, heat process in the atmosphere of N₂plasma gas, laser irradiation and any combination thereof can be used.
While the invention has been described in connection with what are presently considered to be the most practical and preferred embodiments, it is to be understood that the invention is not to be limited to the disclosed embodiments, but on the contrary, is intended to cover various modifications and equivalent arrangements included within the spirit and scope of the appended claims.

Claims

1. A method of producing a light-emitting semiconductor device of a group III nitride compound, comprising:

forming an N-layer of an N-type conduction, said N-layer comprising gallium nitride;

forming a high carrier concentration N⁺-layer satisfying the formula (Al_x3Ga_1-x3)_y3In_1-y3N, wherein 0≦x3≦1 and 0≦y3≦1 and 0≦x3+y3≦1, on said N-layer;

forming an emission layer of a group III nitride compound semiconductor satisfying the formula, Al_x1Ga_y1In_1-x1-y1N, where 0≦x1≦1, 0≦y1≦1 and 0≦x1+y1≦1 on said high carrier concentration layer N⁺-layer;

doping Si and Zn into said emission layer;

forming a P-layer of a P-type conduction, on said emission layer, said P-layer comprising aluminum gallium nitride satisfying the formula Al_x2Ga_1-x2N, wherein 0≦x2≦1; and

forming a contact layer of a P-type conduction, on said P-type layer, said contact layer comprising gallium nitride.

2. The method according to claim 1, wherein said high carrier concentration N⁺-layer has an electron concentration of 10⁸/cm³order.

3. The method according to claim 1, wherein the contact layer of P-type conduction has a Mg concentration of 10²⁰/cm³order.

4. The method according to claim 1, wherein an electron concentration of said N⁺-layer is larger than an electron concentration of said N-layer.

5. The method according to claim 1, wherein said high carrier concentration N⁺-layer comprises a quaternary compound.

6. The method according to claim 1, wherein the high carrier concentration N⁺-layer has a thickness of 2 μm-4 μm.

7. A semiconductor light emitting device comprising:

an n-type clad layer consisting of a gallium nitride base compound semiconductor;

an active layer consisting of a gallium nitride based compound semiconductor, said active layer being made from a material having a band gap energy smaller than that of said n-type clad layer; and

a p-type clad layer consisting of a gallium nitride based compound semiconductor, said p-type clad layer being made from a material having a band gap energy greater than that of said active layer, and sandwiching said active layer accompanying with said n-type clad layer,

wherein said materials of said n-type clad layer and said p-type clad layer are selected as to make a band gap energy of said n-type clad layer smaller than the band gap energy of said p-type clad layer.

8. A semiconductor light emitting device comprising:

a substrate; and

GaN-type compound semiconductor layers stacked on the substrate, the GaN-type layers including:

at least one active layer;

at least one n-type layer; and

at least one p-type layer,

wherein a band gap energy of the one n-type layer is smaller than a band gap energy of the one p-type layer.