The present invention relates to a semiconductor device. More particularly, the present invention relates to a semiconductor device having high brightness and a method of fabricating the same.
Nitride-based semiconductors are mainly used for optical semiconductor devices, such as light emitting diodes or laser diodes. III-nitride-based semiconductors are direct-type compound semiconductor materials having widest band gaps used in optical semiconductor fields. Such III-nitride-based semiconductors are used to fabricate high efficient light emitting devices capable of emitting light having wide wavelength bands in a range between a yellow band and an ultraviolet band. However, although various endeavors have performed for several years in various industrial fields to provide the light emitting device having the large area, high capacity, and high brightness, such endeavors have ended in a failure due to the following basic difficulties related to materials and technologies.
First, a difficulty of providing a substrate adapted to grow a nitride-based semiconductor having a high quality.
Second, a difficulty of growing an InGaN layer and an AlGaN layer including a great amount of indium (In) or aluminum (Al).
Third, a difficulty of growing a p-nitride-based semiconductor having a higher hole carrier density.
Fourth, a difficulty of forming a high-quality ohmic contact electrode (=ohmic contact layer) suitable for an n-nitride-based semiconductor and a p-nitride-based semiconductor.
Nevertheless of the above difficulties derived from materials and technologies, in late 1993, Nichia chemicals (Japanese Company) has developed a blue light emitting device by using a nitride-based semiconductor for the first time in the world. In these days, a white light emitting device including a high brightness blue/green light emitting device coupled with a phosphor has been developed. Such a white light emitting device is practically used in various illumination industrial fields.
In order to realize a next-generation light emitting device having high efficiency, large area and high capacity, such as a light emitting diode (LED) or a laser diode (LD) employing a high-quality nitride-based semiconductor, a low EQE (extraction quantum efficiency) and heat dissipation must be improved.
Nitride-based LEDs are classified into two types based on the shape of a light emitting device and the emission direction of light generated from a nitride-based active layer. The shape of the light emitting device relates to the electric characteristics of a substrate. Thus, in accordance with the shape of the light emitting device, the nitride-based LEDs are classified into a MESA-structured nitride-based LED, in which a nitride-based light emitting structure is grown on an upper portion of an insulating substrate and N type and P type ohmic electrode layers are aligned in parallel to the nitride-based light emitting structure, and a vertical-structured nitride-based LED which is grown on an upper portion of a conductive substrate including silicon (Si) or silicon carbide (SiC).
In view of light intensity, heat elimination, and device reliability, the vertical-structured nitride-based LED is advantageous than the MESA-structured nitride-based LED because the vertical-structured nitride-based LED is grown on the conductive substrate having superior electric and thermal properties. In addition, the nitride-based LEDs are classified into a top-emission type LED and a flip-chip type LED according to the emission direction of light generated from an active layer of a nitride-based light emitting device. In the case of the top-emission type LED, the light generated from the nitride-based active layer is emitted to an exterior through a p-ohmic contact layer. In contrast, in the case of the flip-chip type LED, light generated from the nitride-based light emitting structure using a high-reflective p-ohmic contact layer is emitted to an exterior through a transparent (sapphire) substrate.
In the case of the MESA-structured nitride-based LED, which has been widely used, light generated from the nitride-based active layer is emitted to an exterior through a p-ohmic electrode layer that directly makes contact with a p-nitride-based cladding layer. Therefore, a high-quality p-ohmic contact layer is necessary in order to obtain the top-emission type MESA-structured nitride-based LED having a high quality. Such a high-quality p-ohmic contact layer must have a higher light transmittance of 90% or more, and a specific contact ohmic resistance value as low as possible.
In other words, in order to fabricate a next-generation nitride-based top emission type LED having the high capacity, large area, and high brightness, electric characteristics, such as low specific contact ohmic resistance and sheet resistance, are essentially necessary to simultaneously perform the current spreading in the lateral direction and the current injecting in the vertical direction of the p-electrode layer such that a high sheet-resistance value of a p-nitride-based cladding layer caused by a low hole density can be compensated. In addition, a p-ohmic contact electrode having higher light transmittance and sheet-resistance must be provided in order to minimize light absorption when the light generated from the nitride-based active layer is output to the exterior through the p-type ohmic electrode layer.
The MESA-structured top-emission type LED employing the nitride-based semiconductor, which is generally known in the art, uses a p-ohmic electrode layer that can be obtained by stacking a dual layer of thin nickel (Ni) gold (Au) or a thick transparent conducting layer, such as indium tin oxide (ITO), on a p-nitride-based cladding layer and then annealing the p-nitride-based cladding layer in the oxygen (O2) atmosphere or in the nitrogen (N2) atmosphere. In particular, when the ohmic electrode layer including semi-transparent nickel-gold (Ni—Au) and having a low specific contact resistance value of about 10−3 cm2 to 10−4 cm2 is subject to the annealing process at the temperature of about 500° C., nickel oxide (NiO), which is p-semiconductor oxide, is distributed in the form of an island on the interfacial surface between the p-nitride-based cladding layer and the nickel-gold ohmic electrode layer. In addition, gold (Au) particles having superior conductivity are embedded into the island-shaped nickel oxide (NiO), thereby forming a micro structure.
Such a micro structure may reduce the height and width of the schottky barrier formed between the p-nitride-based cladding layer and the nickel-gold ohmic electrode layer, provide hole carriers to the n-nitride-based cladding layer, and distribute gold (Au) having superior conductivity, thereby achieving superior current spreading performance. However, since the nitride-based top emission type LED employing the p-ohmic electrode layer consisting of nickel-gold (Ni—Au) includes gold (Au) that reduces the light transmittance, the nitride-based top emission type LED represents a low EQE (external quantum efficiency), so the nitride-based top emission type LED is not suitable for the next-generation LED having the high capacity, large area and high brightness.
For this reason, another method of providing a p-ohmic contact layer without using the semi-transparent Ni—Au layer has been suggested. According to this method, the p-ohmic contact layer is obtained by directly depositing a transparent conducting oxide layer including a thick transparent conducting material, such as indium (In), tin (Sn) or zinc (Zn) which is generally known in the art as a material for a high transparent ohmic contact electrode, and a transparent conducting nitride layer including transition metal, such as titanium (Ti) or tantalum (Ta), on a p-nitride-based cladding layer. However, although the p-ohmic electrode layer fabricated through the above method can improve the light transmittance, the interfacial characteristic between the p-ohmic electrode layer and the p-nitride-based cladding layer is deteriorated, so the p-ohmic electrode layer is not suitable for the MESA-structured top emission type nitride-based LED.
Various documents (for example, IEEE PTL, Y. C. Lin, etc. Vol. 14, 1668 and IEEE PTL, Shyi-Ming Pan, etc. Vol. 15, 646) disclose a nitride-based top emission type LED having superior electrical and thermal stability and representing the great EQE by employing a p-ohmic electrode layer, which is obtained by combining a transparent conducting oxide layer having superior electrical conductivity with a metal, such as nickel (Ni) or ruthenium (Ru), without using a noble metal, such as gold (Au) or a platinum (Pt) in such a manner that the p-ohmic electrode layer has light transmittance higher than that of the conventional p-ohmic electrode layer of a nickel-gold (Ni—Au) electrode.
Recently, Semicond. Sci. Technol. discloses a document related to a nitride-based top emission type LED, which employs an indium tin oxide (ITO) transparent layer as a p-ohmic electrode layer and represents an output power higher than that of a conventional LED employing the conventional nickel-gold (Ni—Au) ohmic electrode.
However, although the p-ohmic electrode layer employing the ITO transparent layer can maximize the EQE of the LED, a great amount of heat may be generated when the nitride-based LED is operated because the p-ohmic electrode layer has a relatively high specific contact ohmic resistance value, so the above p-ohmic electrode layer is not suitable for the nitride-based LED having the large area, high capacity, and high brightness.
In order to improve the electrical characteristics of the LED, which may be degraded due to the p-ohmic electrode layer including transparent conductive oxide (TCO) or transparent conductive nitride (TCN), LumiLeds Lighting Company (U.S.) has developed an LED having higher light transmittance and superior electrical characteristics by combining indium tin oxide (ITO) with thin nickel-gold (Ni—Au) or thin nickel-silver (Ni—Ag) (U.S. Pat. No. 6,287,947 issued to Michael J. Ludowise etc.). However, the LED disclosed in the above patent requires a complicated process to form a p-ohmic contact layer and employs gold (Au) or silver (Ag), so this LED is not suitable for the nitride-based LED having the high capacity, large area and high brightness.
Recently, a new MESA-structured nitride-based top emission type LED provided with a high-quality p-ohmic electrode layer has been developed by Samsung Electronics. According to the above MESA-structured nitride-based top emission type LED, new spherical transparent nano particles having sizes of 100 nano meter or less are provided onto an interfacial surface between a p-nitride-based cladding layer and a transparent conducing oxide electrode, such as an ITO electrode or a ZnO electrode, so as to reduce the high ohmic contact resistance value therebetween.
In addition, various patent documents and publications disclose technologies related to the fabrication of the MESA-structured top-emission type nitride-based LED. For instance, in order to directly use a highly transparent conducting layer (ITO layer or TiN layer) as a p-ohmic electrode layer, the transparent conducting layer (ITO layer or TiN layer) is deposited onto a super lattice structure including +-InGaN/n-GaN, n+-GaN/n-InGaN, or n+-InGaN/n-InGaN after repeatedly growing the super lattice structure on an upper surface of a p-nitride-based cladding layer. Then, a high-quality n-ohmic contact is formed through an annealing process, and a tunneling junction process is performed, thereby obtaining the MESA-structured top-emission type nitride-based LED having the high quality.
In these days, many companies recognize that the MESA-structured top-emission type nitride-based LED including the transparent p-ohmic electrode layer combined with a nitride-based light emitting structure grown on a sapphire substrate may not be suitable for the next-generation LED having the high capacity, large area and high brightness because of great amount of heat generated from an active layer and various interfacial layers during the operation of a light emitting device.
LumiLeds Lighting Company (U.S.) and Toyoda Gosei Company (JP) have developed another advanced nitride-based light emitting device for a next-generation light source having high brightness by stacking a nitride-based light emitting structure on a sapphire substrate having an insulating property. According to the above nitride-based light emitting device, silver (Ag) and rhodium (Rh) materials, which are high-reflective thin metals, are combined with the p-ohmic electrode layer to provide the MESA-structured nitride-based flip-chip LED, which is an LED chip having the high capacity and the large area of 1 square millimeter scale. However, such a MESA-structured nitride-based flip-chip LED may degrade the product yield due to complicated processes. In addition, since the p-ohmic electrode layer including the high-reflective thin metals (Ag and Rh) is thermally unstable and represents low light reflectance at a wavelength band of 400 nm or less, so the p-ohmic electrode layer is not suitable for a (near) ultraviolet light emitting diode that emits light having a short wavelength.
Recently, the vertical-structured nitride-based LED has been spotlighted as a next-generation white light source having the large area, high brightness and high capacity. The vertical-structured nitride-based LED can be obtained by stacking a nitride-based light emitting structure on the conductive silicon carbide (SiC) substrate representing electrical and thermal stability, or can be obtained through the steps of stacking a nitride-based light emitting structure on the sapphire substrate having insulating properties, removing the sapphire substrate through a laser lift-off (LLO) scheme using a strong laser beam, and bonding the structure onto a heat sink having the superior heat emission function and including high-reflective ohmic electrode materials, such as Ag or Rh, copper (Cu) or a copper-related alloy. Since the above vertical-structured nitride-based LED employs the heat sink having superior thermal conductivity, the vertical-structured nitride-based LED can easily emit heat during the operation of the LED having the large area and high capacity.
However, the above vertical-structured nitride-based LED requires a p-type high reflective ohmic electrode layer having thermal stability and represents total internal reflection/absorption of light, thereby causing the low EQE and low product yield and resulting in low productivity and high costs. Thus, the vertical-structured nitride-based LED must be more advanced so as to be used as a next generation white light source having high-brightness. In particular, although the light emitting device stacked on the silicon carbide (SiC) substrate represents superior heat dissipation, there are technical difficulties and high costs in fabrication of the SiC substrate. In addition, Since the vertical-structured nitride-based LED exhibits the low EQE due to the high light absorption, the nitride-based LED employing the SiC substrate may not be extensively used.
The vertical-structured nitride-based LED employing the LLO scheme, which is recently spotlighted as a next generation white light source having high brightness, is classified into a p-side down vertical-structured nitride-based LED and an n-side down vertical-structured nitride-based LED according to the emission direction of light generated from the active layer.
In general, the p-side down vertical-structured nitride-based LED, which emits light through an n-nitride-based cladding layer, represents superior optical and electrical properties and is simply manufactured as compared with the n-side vertical-structured nitride-based LED, which emits light generated from the active layer through a p-nitride-based cladding layer.
The difference of optical and electrical properties between the p-side down vertical-structured nitride-based LED and the n-side down vertical-structured nitride-based LED is caused by the characteristic difference of reflective and transparent ohmic electrode layers used to manufacture the p-side down vertical-structured nitride-based LED and the n-side down vertical-structured nitride-based LED. In the case of the p-side down vertical-structured nitride-based LED, as disclosed in various documents, the p-ohmic electrode layer includes high reflective metals, such as silver (Ag) or rhodium (Rh), and the n-nitride-based cladding layer having low sheet resistance is positioned at the uppermost portion of the p-side down vertical-structured nitride-based LED, so the p-side down vertical-structured nitride-based LED can directly emit light to the exterior through the n-nitride-based cladding layer without using an additional high transparent n-ohmic electrode layer. Accordingly, the p-side down vertical-structured nitride-based LED has superior LED characteristics.
However, as mentioned above, the p-side down vertical-structured nitride-based LED may significantly degrade various characteristics because the high reflective p-ohmic electrode layer causes a problem in the light emitting structure that emits light having a wavelength band of 400 nm or less. Different from the p-side down vertical-structured nitride-based LED, the n-side down vertical-structured nitride-based LED can use the high reflective metals, such as silver (Ag) or rhodium (Rh), as materials for the n type high reflective ohmic electrode layer. In addition, aluminum (Al) having superior reflectance can be used as a material for the n type high reflective ohmic electrode layer in a short wavelength band of 400 nm or less. However, since the p-nitride-based cladding layer having high sheet resistance is positioned at the uppermost portion of the n-side down vertical-structured nitride-based LED, the high transparent conductive p-ohmic electrode layer is additionally required. However, as described above, there is difficulty in fabrication of the high transparent conductive p-ohmic electrode layer due to bad electric characteristics of the p-nitride-based cladding layer.
Various companies in the world famous for the nitride-based light emitting devices, such as OSRAM in Germany, sell the LED having the large area, high capacity and high brightness by fabricating the LED using the LLO technique. However, when the nitride-based LED having the large area, high capacity and high brightness is fabricated by using the LLO technique, the product yield of the nitride-based LED is about 50% or less, so low productivity and high costs may result.
In order to realize the semiconductor devices, that is, in order to provide optical devices using GaN-based semiconductors, such as RF transistors having high capacity and being used in the extremely low or high temperature condition, various electronic devices, LEDs, LDs, photo-detectors, or solar cells, a substrate capable of growing an epitaxial stack structure including GaN-based semiconductors having high quality must be fabricated.
In order to obtain such a substrate, materials having similar lattice constant and thermal expansion coefficient must be selected. To this end, preparation of a homo-substrate, that is, preparation of a growth substrate including III-nitride-based material is necessarily required.
Conventionally, in order to grow the GaN-based semiconductor epitaxial stack structure suitable for high-performance electronic and optoelectronic devices, hetero-substrates including sapphire, silicon carbide, silicon or gallium arsenide have been developed and used.
Among other things, sapphire (Al2O3) and silicon carbide (SiC) substrates have recently been used extensively to grow the GaN-based semiconductor epitaxial stack structure. However, the sapphire and silicon carbide substrates represent fatal problems to obtain the high-performance electronic and optoelectronic devices using the GaN-based semiconductor epitaxial stack structure.
First, according to the GaN-based semiconductor epitaxial stack structure formed on the upper portion of the sapphire substrate, high-density crystalline defects, such as dislocation and stacking fault, may occur in the GaN-based semiconductor epitaxial stack structure due to the difference of the lattice constant and thermal expansion coefficient between the GaN-based semiconductor epitaxial stack structure and the sapphire substrate, thereby degrading the reliability of the device and making it difficult to fabricate or operate the GaN-based electronic and optoelectronic devices.
In addition, since the sapphire substrate has inferior thermal conductivity, the optoelectronic devices employing the GaN-based semiconductor epitaxial stack structure formed on the upper portion of the sapphire substrate do not easily emit heat to the exterior during the operation thereof, so that the life span of the devices may be shortened and the reliability of the devices may be degraded.
In addition to the above problems, due to the electrical insulating characteristic of the sapphire substrate, vertical-structured optoelectronic devices, which have been regarded as ideal optoelectronic devices, may not be achieved. For this reason, the MESA-structured optoelectronic devices causing the high cost and low performance must be fabricated by performing the dry etching and photolithography processes.
Although the SiC substrate is advantageous than the sapphire substrate having the electrical insulating property, the SiC substrate also represents several technical and economical disadvantages.
In particular, high costs may be incurred to fabricate single-crystalline silicon carbide, which is necessary to realize the electronic and optoelectronic devices employing the high-performance GaN-based semiconductor. In addition, since light generated from the active layer of the LED is mostly absorbed in the SiC substrate, the SiC substrate is not suitable for the next-generation LED having high efficiency.
To solve the above technical and economical problems derived from the hetero-substrates, various study groups have suggested methods of fabricating homo-substrates including GaN and AlN using the HVPE (hydride vapor phase epitaxy) method (see, phys. stat. sol. (c) No 6, 16271650, 2003).
In addition, a method of fabricating a thick III-nitride-based epitaxial substrate has been suggested. According to this method, a thick III-nitride-based epitaxial layer having a thickness of about 300 □ is formed on the upper portion of the sapphire substrate through the HVPE method, and a strong laser beam is irradiated to remove the sapphire substrate through the LLO scheme. Then, the post-treatment process is performed to obtain the thick III-nitride-based epitaxial substrate (see, phys. Stat. sol. (c) No 7, 1985-1988, 2003).
Besides the above conventional methods, another method of fabricating a thick III-nitride-based epitaxial substrate has been suggested to provide a GaN-based semiconductor epitaxial stack structure. According to this method, zinc oxide (ZnO), which has superior electric conductivity, represents similar lattice constant and thermal expansion coefficient, and is easily soluble through wet etching, is introduced into an original growth substrate or onto a sapphire substrate as a sacrificial layer when growing the GaN-based semiconductor epitaxial stack structure to form the high-quality GaN-based semiconductor epitaxial stack structure. Then, the sapphire substrate is removed through wet etching.
However, the above-described methods and technologies used for the III-nitride-based epitaxial growth substrate represent the technical difficulty, high cost, low quality, and low product yield, so the future prospect of the high-performance electronic and optoelectronic devices employing the nitride-based semiconductor epitaxial stack structure is unclear.
The present invention provides a semiconductor device having high brightness.
The present invention also provides a method of manufacturing such a semiconductor device.
In one aspect of the present invention, a semiconductor device includes: a growth substrate having an insulating property; a nucleation layer formed on the growth substrate; an undoped buffering nitride-based layer formed on the nucleation layer while serving as a buffering layer; a first type nitride-based cladding layer formed on the undoped buffering nitride-based layer; a multi quantum well nitride-based active layer formed on the first type nitride-based cladding layer; a second type nitride-based cladding layer formed on the multi quantum well nitride-based active layer, the second type being different from the first type; and a tunnel junction layer formed between the undoped buffering nitride-based layer and the first type nitride-based cladding layer or formed on the second type nitride-based cladding layer or formed both between the undoped buffering nitride-based layer and the first type nitride-based cladding layer and formed on the second type nitride-based cladding layer.
In another aspect of the present invention, a semiconductor device includes a growth substrate having an insulating property; a nitride-based semiconductor thin film layer formed on the growth substrate; a supporting substrate layer formed on the nitride-based semiconductor thin film layer; and a light emitting structure formed on the supporting substrate layer.
The supporting substrate layer includes an AlN-based material layer prepared as a single layer or a multi-layer.
The supporting substrate layer includes metal, nitride, oxide, boride, carbide, silicide, oxy-nitride, and carbon nitride prepared as a single layer or a multi-layer.
The supporting substrate layer is prepared in a form of a single layer, or a multi-layer including an AlaObNc (a, b and c are integers) and a GaxOy (x and y are integers).
The supporting substrate layer is prepared in a form of a single layer, or a multi-layer including SiaAlbNcCd-based material (a, b, c and d are integers).
In still another aspect of the present invention, a semiconductor device includes a thick film layer; a first epitaxial layer formed on the thick film layer, in which a top surface of the first epitaxial layer is surface-treated; and second epitaxial layer formed on the first epitaxial layer and having a multi-layer including nitride-based semiconductors for electronic and optoelectronic devices, wherein each of the first and second epitaxial layer is prepared in a form of a single layer or a multi-layer including at least one compound expressed as InxAlyGazN (x, y and z are integers) or SixCyNz (x, y and z are integers).
In still yet another aspect of the present invention, a method for manufacturing a semiconductor device comprising: forming a first epitaxial layer on a growth substrate having an insulating property; depositing a thick film layer having a thickness of 30 □ or more on the first epitaxial layer; removing the growth substrate by using a laser beam; and treating a surface of the first epitaxial layer, which is exposed as the growth substrate is removed.
The semiconductor device according to the present invention exhibits high-quality, large area, high brightness, and high capacity. In addition, the layers or the light emitting structure provided in the semiconductor device of the present invention cannot be thermally or mechanically deformed or dissolved. Further, the semiconductor device according to the present invention may employ a high-performance semiconductor epitaxial layer.
Hereinafter, exemplary embodiments of the present invention will be described with reference to accompanying drawings.
As shown in
Different from the vertical-structured nitride-based LED as it can be fabricated through the laser lift-off (LLO) scheme, the above nitride-based light emitting structure includes the first tunnel junction layer 440a formed on the undoped nitride-based layer 430a.
The p-down vertical-structured nitride-based LED fabricated by using the nitride-based light emitting structure shown in
Referring to
The supporting substrate 410b, which serves as a heat sink to protect the light emitting structure and to emit heat when the thin nitride-based light emitting structure is removed from the sapphire substrate through the LLO scheme, preferably includes metals, alloys or solid solution having superior electric and thermal conductivity. For example, instead of using a silicon substrate, the supporting substrate 410b includes silicide that is an intermetallic compound, aluminum (Al), Al-related alloy or solid solution, copper (Cu), Cu-related alloy or solid solution, silver (Ag), or Ag-related alloy or solid solution. Such a supporting substrate 410b can be fabricated through mechanical, electrochemical, physical or chemical deposition.
The present invention adopts the LLO scheme so as to remove the nitride-based light emitting structure from the sapphire substrate. Although the LLO scheme is conventionally performed under the normal temperature and normal pressure, according to the present invention, the LLO scheme is performed in a state in which the sapphire substrate is immersed in acid solution such as HCl or base solution having the temperature of 40° C. or more, in order to improve the product yield which may be lowered if crack of the nitride-based light emitting structure occurs during the process.
The bonding material layer 420b preferably includes metals having higher cohesion properties and low melting points, such as indium (In), tin (Sn), zinc (Zn), silver (Ag), palladium (Pd), or gold (Au), and alloys or solid solution of the above metals.
The p-reflective ohmic contact layer 430b may include a thick layer of Ag and Rh without using Al and Al-related alloy or solid solution, which is a high reflective material that represents low specific contact resistance and high light reflectance on the p-nitride-based cladding layer. In addition, the p-reflective ohmic contact layer 430b may include a dual reflective layer or a triple reflective layer including the high reflective metal combined with nickel (Ni), palladium (Pd), platinum (Pt), zinc (Zn), magnesium (Mg), or gold (Au). Further, the p-reflective ohmic contact layer 430b may include a combination of transparent conductive oxide (TCO), transitional metal-based transparent conductive nitride, and the high reflective metal. Aluminum, Al-related alloy and Al-related solid solution are more prefer than other high reflective metals, alloys, and solid solution thereof.
Each of the p-type nitride-based cladding layer 440b, the multi-quantum well nitride-based active layer 450b, and the n-type nitride-based cladding layer 460b basically includes one selected from compounds expressed as AlxInyGazN (x, y, and z are integers) which is a general formula of III-nitride-based compound. Dopants are added to the p-type nitride-based cladding layer 440b and the n-type nitride-based cladding layer 460b.
In addition, the nitride-based active layer 450b can be prepared in the form of a single layer or a multi-quantum well (MQW) structure.
For instance, if GaN-based compound is employed, the n-type nitride-based cladding layer 460b includes GaN and n-type dopants added to GaN, such as Si, Ge, Se, Te, etc., and the nitride-based active layer 450b has an InGaN/GaN MQW structure or an AlGaN/GaN MQW structure. In addition, the p-type nitride-based cladding layer 440b includes GaN and p-type dopants added to GaN, such as Mg, Zn, Ca, Sr, Ba, Be, etc.
The first tunnel junction layer 470b basically includes one selected from compounds expressed as AlaInbGacNxPyAsz (a, b, c, x, y and z are integers) consisting of III-V group elements. The first tunnel junction layer 470b can be prepared in the form of a single layer having a thickness of 50 nm or less. Preferably, the first tunnel junction layer 470b is prepared in the form of a bi-layer, a tri-layer or a multi-layer.
Preferably, the first tunnel junction layer 470b has a super-lattice structure. For instance, 30 or less pairs of elements can be repeatedly stacked in the form of a thin stack structure by using III-V group elements, such as InGaN/GaN, AlGaN/GaN, AlInN/GaN, AlGaN/InGaN, AlInN/InGaN, AlN/GaN, or AlGaAs/InGaAs.
More preferably, the first tunnel junction layer 470b may include an single-crystal layer, a poly-crystal layer or an amorphous layer having III-group elements (Mg, Be, Zn) or IV-group elements (Si, Ge) added thereto. In order to improve electrical and optical characteristics of the nitride-based light emitting device by providing a photonic crystal effect or by adjusting a roughness of an upper surface or a lower surface of the first tunnel junction layer 470b, a dot, a hole, a pyramid, a nano-rod, or a nano-columnar having a size of 10 nm or less can be provided through an interferometry scheme using interference of the laser beam and photo-reactive polymer or through an etching technology.
Another method of improving the electrical and optical characteristics of the nitride-based light emitting device through the surface roughness adjustment and photonic crystal effect has been suggested. This method is performed for 10 seconds to 1 hour at the temperature in a range of the normal temperature to 800° C. under oxygen (O2), nitrogen (N2), argon (Ar), or hydrogen (H2) atmosphere.
The n-electrode pad 480b may have a stack structure including refractory metals, such as titanium (Ti), aluminum (Al), gold (Au) and tungsten (W) which are sequentially stacked.
As shown in
Preferably, the high transparent conductive thin film layer formed on the first tunnel junction layer 570b, that is, the n-type ohmic current spreading layer 580b includes transparent conducive oxide (TCO) or transitional metal-based transparent conductive nitride (TCN). Here, TCO is transparent conductive compound including oxygen (O) combined with at least one selected from the group consisting of indium (In), tin (Sn), zinc (Zn), gallium (Ga), cadmium (Cd), magnesium (Mg), beryllium (Be), silver (Ag), molybdenum (Mo), vanadium (V), copper (Cu), iridium (Ir), rhodium (Rh), ruthenium (Ru), tungsten (W), titanium (Ti), tantalum (Ta), cobalt (Co), nickel (Ni), manganese (Mn), platinum (Pt), palladium (Pd), aluminum (Al), and lanthanum (La).
In addition, TCN is transparent conductive compound obtained by combining nitrogen (N) with titanium (Ti), tungsten (W), tantalum (Ta), vanadium (V), chrome (Cr), zirconium (Zr), niobium (Nb), hafnium (Hf), rhenium (Re) or molybdenum (Mo).
More preferably, the current spreading layers stacked on the n-type and p-type nitride-based cladding layers may be combined with metallic components that form new transparent conductive thin layers when the heat treatment process is performed in the nitrogen (N2) or oxygen (O2) atmosphere.
In order to improve the quality of the n-type ohmic current spreading layer 580b, the sputtering deposition process using plasma including oxygen (O2), nitrogen (N2), argon (Ar) or hydrogen (H2), and the pulsed laser deposition (PLD) process using storing laser beam are primarily utilized. Besides these, electron-beam or thermal evaporation, atomic layer deposition (ALD), chemical vapor deposition (CVD), electroplating, or electrochemical deposition can be used. In particular, in the vertical-structured nitride-based light emitting devices obtained through the LLO scheme, ions having strong energy may exert bad influence upon the surface of the nitride-based cladding layer when the n-type or p-type ohmic current spreading layer is deposited on the nitride-based cladding layer. In order to avoid this problem, evaporator using the electron-beam or thermal resistance is preferably used.
In order to improve the electrical and optical characteristics of the nitride-based light emitting device by providing photonic crystal effect or by adjusting the surface roughness of the n-type or p-type ohmic contact layer or n-type or p-type ohmic current spreading layer, the above deposition is performed for 10 seconds to 1 hour at the temperature in a range of the normal temperature to 800° C. under oxygen (O2), nitrogen (N2), argon (Ar), or hydrogen (H2) atmosphere.
Hereinafter, the third to eleventh embodiments of the present invention will be described. In the third to eleventh embodiments, some elements are identical to those of the first and second embodiments. Thus, the similar reference numerals are designated to the similar elements throughout the
As shown in
The p-down vertical-structured nitride-based LED fabricated by using the nitride-based light emitting structure shown in
Referring to
The second tunnel junction layer 640b basically includes one selected from compounds expressed as AlaInbGacNxPyAsz (a, b, c, x, y and z are integers) consisting of III-V group elements. The second tunnel junction layer 640b can be prepared in the form of a single layer having a thickness of 50 nm or less. Preferably, the second tunnel junction layer 640b is prepared in the form of a bi-layer, a tri-layer or a multi-layer.
Preferably, the second tunnel junction layer 640b has a super-lattice structure. For instance, 30 or less pairs of elements can be repeatedly stacked in the form of a thin stack structure by using III-V group elements, such as InGaN/GaN, AlGaN/GaN, AlInN/GaN, AlGaN/InGaN, AlInN/InGaN, AlN/GaN, or AlGaAs/InGaAs.
More preferably, the second tunnel junction layer 640b may include a single crystal layer, a poly-crystal layer or an amorphous layer having III-group elements (Mg, Be, Zn) or IV-group elements (Si, Ge) added thereto.
Each of the p-type nitride-based cladding layer 650b, the multi-quantum well nitride-based active layer 660b, and the n-type nitride-based cladding layer 670b basically includes one selected from compounds expressed as AlxInyGazN (x, y, and z are integers) which is a general formula of III-nitride-based compound. Dopants are added to the p-type nitride-based cladding layer 650b and the n-type nitride-based cladding layer 670b.
In addition, the nitride-based active layer 660b can be prepared in the form of a single layer or a multi-quantum well (MQW) structure.
For instance, if GaN-based compound is employed, the n-type nitride-based cladding layer 670b includes GaN and n-type dopants added to GaN, such as Si, Ge, Se, Te, etc., and the nitride-based active layer 660b has an InGaN/GaN MQW structure or an AlGaN/GaN MQW structure. In addition, the p-type nitride-based cladding layer 650b includes GaN and p-type dopants added to GaN, such as Mg, Zn, Ca, Sr, Ba, Be, etc.
In order to improve electrical and optical characteristics of the nitride-based light emitting device by providing a photonic crystal effect or by adjusting a roughness of an upper surface of the n-type nitride-based cladding layer 670b, a dot, a hole, a pyramid, a nano-rod, or a nano-columnar having a size of 10 nm or less can be provided through an interferometry scheme using interference of the laser beam and photo-reactive polymer or through an etching technology.
Another method of improving the electrical and optical characteristics of the nitride-based light emitting device through the surface roughness adjustment and photonic crystal effect has been suggested. This method is performed for 10 seconds to 1 hour at the temperature in a range of the normal temperature to 800° C. under oxygen (O2), nitrogen (N2), argon (Ar), or hydrogen (H2) atmosphere.
The n-electrode pad 680b may have a stack structure including refractory metals, such as titanium (Ti), aluminum (Al), gold (Au) and tungsten (W) which are sequentially stacked.
As shown in
As shown in
Different from the vertical-structured nitride-based LED, which is fabricated through the laser lift-off (LLO) scheme, the above nitride-based light emitting structure includes the first and second tunnel junction layers 840a and 880a formed on the undoped nitride-based layer 830a and the p-type nitride-based cladding layer 880a, respectively.
The p-down vertical-structured nitride-based LED fabricated by using the nitride-based light emitting structure shown in
Referring to
Each of the p-type nitride-based cladding layer 850b, the multi-quantum well nitride-based active layer 860b, and the n-type nitride-based cladding layer 870b basically includes one selected from compounds expressed as AlxInyGazN (x, y, and z are integers), which is a general formula of III-nitride-based compound. Dopants are added to the p-type nitride-based cladding layer 850b and the n-type nitride-based cladding layer 870b. In addition, the nitride-based active layer 860b can be prepared in the form of a single layer or a multi-quantum well (MQW) structure.
The n-electrode pad 890b may have a stack structure including refractory metals, such as titanium (Ti), aluminum (Al), gold (Au) and tungsten (W) which are sequentially stacked.
As shown in
As shown in
Different from the vertical-structured nitride-based LED as it can be fabricated through the laser lift-off (LLO) scheme, the above nitride-based light emitting structure includes the first tunnel junction layer 1040a formed on the undoped nitride-based layer 1030a.
The n-down vertical-structured nitride-based LED fabricated by using the nitride-based light emitting structure shown in
Referring to
The n-reflective ohmic contact layer 1030b may include a thick layer of Ag, Rh or Al, which is a high reflective metal that represents low specific contact resistance and high light reflectance. The n-reflective ohmic contact layer 1030b may include alloys or solid solution based on the high reflective metals. In addition, the n-reflective ohmic contact layer 1030b may include a dual reflective layer or a triple reflective layer including the high reflective metal combined with nickel (Ni), palladium (Pd), platinum (Pt), zinc (Zn), magnesium (Mg), or gold (Au). Further, the n-reflective ohmic contact layer 1030b may include a combination of transparent conductive oxide (TCO), transitional metal-based transparent conductive nitride, and the high reflective metal.
Each of the n-type nitride-based cladding layer 1050b, the multi-quantum well nitride-based active layer 1060b, and the p-type nitride-based cladding layer 1070b basically includes one selected from compounds expressed as AlxInyGazN (x, y, and z are integers) which is a general formula of III-nitride-based compound. Dopants are added to the n-type nitride-based cladding layer 1050b and the p-type nitride-based cladding layer 1070b.
In addition, the nitride-based active layer 1060b can be prepared in the form of a single layer or a multi-quantum well (MQW) structure.
For instance, if GaN-based compound is employed, the n-type nitride-based cladding layer 1050b includes GaN and n-type dopants added to GaN, such as Si, Ge, Se, Te, etc., and the nitride-based active layer 1060b has an InGaN/GaN MQW structure or an AlGaN/GaN MQW structure. In addition, the p-type nitride-based cladding layer 1070b includes GaN and p-type dopants added to GaN, such as Mg, Zn, Ca, Sr, Ba, Be, etc.
The high transparent conductive thin layer, that is, the p-type ohmic current spreading layer 1080b formed on the p-type nitride-based cladding layer 1070b is identical to that of the second embodiment.
As shown in
The n-down vertical-structured nitride-based LED fabricated by using the nitride-based light emitting structure shown in
Referring to
As shown in
As shown in
The n-down vertical-structured nitride-based LED fabricated by using the nitride-based light emitting structure shown in
Referring to
As shown in
Hereinafter, embodiments of the present invention having supporting substrates capable of preventing the thin film layer or the light emitting structure from being thermally or mechanically deformed or decomposed will be described. In the following description, the same elements, such as the ohmic contact layer and the tunnel junction layer that have been described in the previous embodiments, may have the same function and structure if there are no special comments for them.
Referring to
Referring to
The supporting substrate layer 130 is prepared in the form of a single layer, a bi-layer or a tri-layer including SiaAlbNcCd (a, b, c and d are integers). An epitaxial layer, a poly-crystal layer or an amorphous material layer including SiC or SiCN, or having a chemical formula of SiCAIN is primarily applied to the supporting substrate layer 130.
In addition, preferably, the supporting substrate layer 130 is deposited at a thickness of 10 or less micrometers by means of chemical vapor deposition (CVD), such as metal organic chemical vapor deposition (MOCVD), sputtering deposition using gas ions having high energy, or physical vapor deposition (PVD), such as pulsed laser deposition (PLD) using a laser energy source.
Meanwhile, the supporting substrate layer 130 is prepared in the form of a single layer, a bi-layer or a tri-layer, such as AlaObNc (a, b and c are integers) or GaxOy (x and y are integers). Preferably, a single crystal layer having a hexagonal system, a poly-crystal layer, or an amorphous material layer having the chemical formula of Al2O3 or Ga2O3, is applied to the supporting substrate layer 130.
In this case, the supporting substrate layer 130 having insulating properties is deposited at a thickness of 10 or less by means of chemical vapor deposition (CVD) such as metal organic chemical vapor deposition (MOCVD), or physical vapor deposition (PVD) such as sputtering deposition using gas ions having high energy or pulsed laser deposition (PLD) using a laser energy source.
Meanwhile, the supporting substrate layer 130 may have a high melting point. In this case, the supporting substrate layer 130 having the high melting point is prepared in the form of a single layer, a bi-layer or a tri-layer regardless of the stacking order thereof. Preferably, a single crystal layer having a hexagonal system or a cubic system, a poly-crystal layer, or an amorphous material layer is primarily applied to the supporting substrate layer 130.
More preferably, supporting substrate layer 130 may include materials having reduction-resistant properties under a hydrogen atmosphere and or an ion atmospheres at the temperature of 1000° C. or above. Such materials include metal, nitride, oxide, boride, carbide, silicide, oxy-nitride, and carbon nitride.
In detail, the metal is selected from the group consisting of Ta, Ti, Zr, Cr, Sc, Si, Ge, W, Mo, Nb, and Al, the nitride is selected from the group consisting of Ti, V, Cr, Be, B, Hf, Mo, Nb, V, Zr, Nb, Ta, Hf, Al, B, Si, In, Ga, Sc, W, and rare-earth metal-based nitride, the oxide is selected from the group consisting of Ti, Ta, Li, Al, Ga, In, Be, Nb, Zn, Zr, Y, W, V, Mg, Si, Cr, La and rare-earth metal-based oxide, the boride is selected from the group consisting of Ti, Ta, Li, Al, Be, Mo, Hf, W, Ga, In, Zn, Zr, V, Y, Mg, Si, Cr, La and rare-earth metal-based boride, the carbide is selected from the group consisting of Ti, Ta, Li, B, Hf, Mo, Nb, W, V, Al, Ga, In, Zn, Zr, Y, Mg, Si, Cr, La and rare-earth metal-based carbide, the silicide is selected from the group consisting of Cr, Hf, Mo, Nb, Ta, Th, Ti, W, V, Zr and rare-earth metal-based silicide, the oxy-nitride includes Al—O—N and the carbon nitride includes Si—C—N.
In addition, preferably, the supporting substrate layer 130 having the high melting point is deposited at a thickness of 10 or less by means of chemical vapor deposition (CVD) such as metal organic chemical vapor deposition (MOCVD), or physical vapor deposition (PVD) such as sputtering deposition using gas ions having high energy and pulsed laser deposition (PLD) using a laser energy source.
Referring to
In particular, different from
The nitride-based light emitting structure is primarily used for the LED and the LD.
In detail, similar to
In particular, the nitride-based light emitting devices shown in
In detail, similar to
In particular, the nitride-based light emitting device shown in
In detail, similar to
In particular, the nitride-based light emitting devices shown in
In detail, similar to
In particular, the nitride-based light emitting devices shown in
As mentioned above, the supporting substrate 80, which serves as a heat sink to protect the light emitting structure used for the nitride-based light emitting device of the present invention and to emit heat, preferably includes metals, alloys or solid solution having superior electric and thermal conductivity. For example, instead of using a silicon substrate, the supporting substrate 80 includes silicide that is an intermetallic compound, aluminum (Al), Al-related alloy or solid solution, copper (Cu), Cu-related alloy or solid solution, silver (Ag), or Ag-related alloy or solid solution. Such a supporting substrate 80 can be fabricated through mechanical, electrochemical, physical or chemical deposition.
The present invention adopts the LLO scheme so as to remove the nitride-based light emitting structure from the insulating sapphire substrate 100. The LLO scheme is not performed under the normal temperature and normal pressure. According to the present invention, the LLO scheme is performed in a state in which the sapphire substrate is immersed in acid solution such as HCI or base solution having the temperature of 40 or more, in order to improve the product yield which may be lowered if crack of the nitride-based light emitting structure occurs during the process.
The bonding material layer 90 preferably includes metals having higher cohesion properties and low melting points, such as indium (In), tin (Sn), zinc (Zn), silver (Ag), palladium (Pd), or gold (Au), and alloys or solid solution of the above metals.
The p-reflective ohmic contact layer 140 may include a thick layer of Ag and Rh without using Al and Al-related alloy or solid solution, which is a high reflective material that represents low specific contact resistance and high light reflectance on the p-nitride-based cladding layer. In addition, the p-reflective ohmic contact layer 140 may include a dual reflective layer or a triple reflective layer including the high reflective metal combined with nickel (Ni), palladium (Pd), platinum (Pt), zinc (Zn), magnesium (Mg), or gold (Au). Further, the p-reflective ohmic contact layer 430b may include a combination of transparent conductive oxide (TCO), transitional metal-based transparent conductive nitride, and the high reflective metal.
Each of the p-type nitride-based cladding layer 50, the multi-quantum well nitride-based active layer 40, and the n-type nitride-based cladding layer 30 basically includes one selected from compounds expressed as AlxInyGazN (x, y, and z are integers) which is a general formula of III-nitride-based compound. Dopants are added to the p-type nitride-based cladding layer 50 and the n-type nitride-based cladding layer 30.
In addition, the nitride-based active layer 40 can be prepared in the form of a single layer or a multi-quantum well (MQW) structure.
For instance, if GaN-based compound is employed, the n-type nitride-based cladding layer 30 includes GaN and n-type dopants added to GaN, such as Si, Ge, Se, Te, etc., and the nitride-based active layer 40 has an InGaN/GaN MQW structure or an AlGaN/GaN MQW structure. In addition, the p-type nitride-based cladding layer 50 includes GaN and p-type dopants added to GaN, such as Mg, Zn, Ca, Sr, Ba, Be, etc.
The first and second tunnel junction layers 60 and 70 basically include one selected from compounds expressed as AlaInbGacNxPyAsz (a, b, c, x, y and z are integers) consisting of III-V group elements. The first and second tunnel junction layers 60 and 70 can be prepared in the form of a single layer having a thickness of 50 nm or less. Preferably, the first and second tunnel junction layers 60 and 70 are prepared in the form of a bi-layer, a tri-layer or a multi-layer.
Preferably, the first and second tunnel junction layers 60 and 70 have super-lattice structures. For instance, 30 or less pairs of elements can be repeatedly stacked in the form of a thin stack structure by using III-V group elements, such as InGaN/GaN, AlGaN/GaN, AlInN/GaN, AlGaN/InGaN, AlInN/InGaN, AlN/GaN, or AlGaAs/InGaAs.
More preferably, the first and second tunnel junction layers 60 and 70 may include an epitaxial layer, a poly-crystal layer or an amorphous layer having III-group elements (Mg, Be Zn) or IV-group elements (Si, Ge) added thereto.
In order to improve electrical and optical characteristics of the nitride-based light emitting device by providing a photonic crystal effect or by adjusting a roughness of an upper surface or a lower surface of the first tunnel junction layer 470b, a dot, a hole, a pyramid, a nano-rod, or a nano-columnar having a size of 10 nm or less can be provided through an interferometry scheme using interference of the laser beam and photo-reactive polymer or through an etching technology.
Another method of improving the electrical and optical characteristics of the nitride-based light emitting device through the surface roughness adjustment and photonic crystal effect has been suggested. This method is performed for 10 seconds to 1 hour at the temperature in a range of the normal temperature to 800° C. under oxygen (O2), nitrogen (N2), argon (Ar), or hydrogen (H2) atmosphere.
The n-electrode pad 170 may have a stack structure including refractory metals, such as titanium (Ti), aluminum (Al), gold (Au) and tungsten (W) which are sequentially stacked.
The p-electrode pad 160 may have a stack structure including refractory metals, such as titanium (Ti), aluminum (Al), gold (Au) and tungsten (W) which are sequentially stacked.
In detail, referring to
The sacrificial layer 20′ formed under the low temperature condition absorbs laser beams having strong energy irradiated through a rear surface of the sapphire substrate 10′ and facilitates the release of the sapphire growth substrate using heat obtained from the laser beam. When the sapphire substrate 10′ is separated by means of the laser beam, the supporting substrate layer 30′ including the AlN-based materials prevents the nitride-based thick film layer formed on the supporting substrate layer 30′ or the thin film layer of the light emitting structure from being thermally and mechanically deformed or decomposed.
The supporting substrate layer 30′ including the AlN-based materials has chemical formula of AlxGa1-xN (x is 50% or more), and is prepared in the form of a single layer or a bi-layer. Preferably, the supporting substrate layer 30′ includes a thick AlN single layer.
The supporting substrate layer 30′ including the AlN-based materials is preferably deposited through the MOCVD or hybrid vapor phase epitaxy (HVPE) to improve quality of the thin film layer. However, the supporting substrate layer 30′ can also be deposited through ALD, PLD, sputtering using plasma having a strong energy source, or physical and chemical deposition.
In detail,
The thick film layer 50′ may provide a high-quality nitride-based substrate required for optoelectronic devices, such as high-quality LEDs and LDs, and various transistors. To this end, the HVPE method or the MOCVD method exhibiting a relatively high growth rate is primarily applied when forming the thick film layer 50′. However, the PLD method or the sputtering method can also be used.
In detail,
The initial sapphire substrate is removed from the template shown in
In detail, the LED stack structure including II-nitride-based semiconductors formed on the AlN-based supporting substrate layer 30′ basically includes four layers of an undoped buffering nitride-based layer 70′ serving as a buffer layer, an n-type nitride-based cladding layer 80′, a multi-quantum well nitride-based active layer 90′, and a p-type nitride-based cladding layer 100′. A nucleation layer 60′ formed under the temperature less than 800° C. can be interposed between the AlN-based supporting substrate layer 30′ and the undoped buffering nitride-based layer 70′, or not.
In more detail, each of the undoped buffering nitride-based layer 70′ serving as a buffer layer, the n-type nitride-based cladding layer 80′, the multi-quantum well nitride-based active layer 90′, and the p-type nitride-based cladding layer 100′ basically includes one selected from compounds expressed as AlxInyGazN (x, y, and z are integers) which is a general formula of III-nitride-based compound. Dopants are added to the n-type nitride-based cladding layer 80′ and the p-type nitride-based cladding layer 100′.
In addition, the nitride-based active layer 90′ can be prepared in the form of a single layer, a multi-quantum well (MQW) structure, or multi-quantum dots or wires.
For instance, if GaN-based compound is employed, the n-type nitride-based cladding layer 80′ includes GaN and n-type dopants added to GaN, such as Si, Ge, Se, Te, etc., and the nitride-based active layer 90′ has an InGaN/GaN MQW structure or an AlGaN/GaN MQW structure. In addition, the p-type nitride-based cladding layer 100 includes GaN and p-type dopants such as Mg, Zn, Ca, Sr, Ba, Be, etc. added to GaN.
In detail,
The first tunnel junction layer 110a′ basically includes one selected from compounds expressed as AlaInbGacNxPyAsz (a, b, c, x, y and z are integers) consisting of III-V group elements. The first tunnel junction layer 110a′ can be prepared in the form of a single layer having a thickness of 50 nm or less. Preferably, the first tunnel junction layer 110a′ is prepared in the form of a bi-layer, a tri-layer or a multi-layer.
Preferably, the first tunnel junction layer 110a′ has a super-lattice structure. For instance, 30 or less pairs of elements can be repeatedly stacked in the form of a thin stack structure by using III-V group elements, such as InGaN/GaN, AlGaN/GaN, AlInN/GaN, AlGaN/InGaN, AlInN/InGaN, AlN/GaN, or AlGaAs/InGaAs.
More preferably, the first tunnel junction layer 110a′ may include an epitaxial layer, a poly-crystal layer or an amorphous layer having II-group elements (Mg, Be, Zn) or IV-group elements (Si, Ge) added thereto.
In detail,
The second tunnel junction layer 110b′ basically includes one selected from compounds expressed as AlaInbGacNxPyAsz (a, b, c, x, y and z are integers) consisting of III-V group elements. The second tunnel junction layer 110b′ can be prepared in the form of a single layer having a thickness of 50 nm or less. Preferably, the second tunnel junction layer 110b′ is prepared in the form of a bi-layer, a tri-layer or a multi-layer.
Preferably, the second tunnel junction layer 110b′ has a super-lattice structure. For instance, 30 or less pairs of elements can be repeatedly stacked in the form of a thin stack structure by using III-V group elements, such as InGaN/GaN, AlGaN/GaN, AlInN/GaN, AlGaN/InGaN, AlInN/InGaN, AlN/GaN, or AlGaAs/InGaAs.
More preferably, the second tunnel junction layer 110b′ may include an epitaxial layer, a poly-crystal layer or an amorphous layer having III-group elements (Mg, Be, Zn) or IV-group elements (Si, Ge) added thereto.
In detail,
The first and second tunnel junction layers 110a′ and 110b′ basically include one selected from compounds expressed as AlaInbGacNxPyAsz (a, b, c, x, y and z are integers) consisting of III-V group elements. The first and second tunnel junction layers 110a′ and 110b′ can be prepared in the form of a single layer having a thickness of 50 nm or less. Preferably, the first and second tunnel junction layers 110a′ and 110b′ are prepared in the form of a bi-layer, a tri-layer or a multi-layer.
Preferably, the first and second tunnel junction layers 110a′ and 110b′ have a super-lattice structure. For instance, 30 or less pairs of elements can be repeatedly stacked in the form of a thin stack structure by using III-V group elements, such as InGaN/GaN, AlGaN/GaN, AlInN/GaN, AlGaN/InGaN, AlInN/InGaN, AlN/GaN, or AlGaAs/InGaAs.
More preferably, the first tunnel junction layer 110a′ may include an epitaxial layer, a poly-crystal layer or an amorphous layer having II-group elements (Mg, Be, Zn) or IV-group elements (Si, Ge) added thereto.
In detail,
In order to minimize dislocation density and cracks, which are generated in the process of growing the nitride-based light emitting structure, the surface treatment, the dry etching, or the lateral epitaxial overgrowth (LEO) scheme using amorphous silicon oxide SiO or amorphous nitride SiNx can be performed before the layers from the undoped buffering nitride-based layer 70′ serving as a buffer layer to the p-type nitride-based cladding layer 100′ have been deposited. Then, after growing the high-quality nitride-based light emitting structure, the p-type highly reflective ohmic electrode is formed (step {circle around (2)}).
Before the p-type highly reflective ohmic electrode is formed, the litho-process, the patterning process, the etching process, and the surface roughening process can be performed relative to the upper surface of the p-type nitride cladding layer or the second tunnel junction layer. In particular, if the tunnel junction layer is stacked on the p-type nitride cladding layer, an Al-related high reflective metal can be directly used for the highly-reflective p-type ohmic electrode. After forming the highly-reflective p-type ohmic electrode, a thick film for a heat sink is formed through the typical bonding transfer and electroplating processes (step {circle around (3)}).
Then, the laser beam having strong energy is irradiated through a rear surface of the transparent sapphire substrate 10, so that the sacrificial layer 20′ including III-nitride-based semiconductors and being formed on the sapphire substrate 10 absorbs the laser beam while generating heat having the temperature about 1000° C. Thus, the nitride-based semiconductor materials are thermo-chemically decomposed, thereby removing the sapphire substrate, which is the initial insulating growth substrate (step {circle around (4)}).
After that, the lithography and etching processes are performed to completely remove the supporting substrate layer including the AlN-based materials, which are semi-insulating or insulating materials (step {circle around (5)}). Then, the highly-transparent n-type ohmic contact layer and the n-type electrode pad are formed (step {circle around (6)}). Before the highly-transparent n-type ohmic contact layer is formed, the surface roughening process and the surface patterning process can be performed in order to discharge the light generated from the active layer to the exterior as much as possible.
In detail, if the bonding transfer process is employed, a bonding layer 130′ is necessary to bond the heat sink plate to a highly reflective p-type ohmic electrode layer 120′. The bonding material layer 130′ preferably includes metals having higher cohesion properties and low melting points, such as indium (In), tin (Sn), zinc (Zn), silver (Ag), palladium (Pd), or gold (Au), and alloys or solid solution of the above metals. However, if the electroplating process is employed, such a bonding layer 130′ is not necessary. According to the present invention, the electroplating process, which is an electrochemical process, is primarily applied instead of the bonding transfer process.
In general, the n-type nitride-based cladding layer has low sheet resistance, so the highly transparent n-type ohmic electrode layer is not necessary. However, in order to fabricate the high-quality light emitting device having higher reliability, the highly transparent n-type ohmic electrode layer is necessary. Accordingly, the highly transparent n-type ohmic electrode layer is primarily formed. At the same time, the surface roughening process and the patterning process can be employed in order to maximize the external quantum efficiency.
In detail, the LED according to the twenty-ninth embodiment of the present invention is similar to that of the twenty-eighth embodiment of the present invention, but the first tunnel junction layer 110a′ is introduced onto the n-type nitride-based cladding layer 80′.
In detail, the LED according to the thirteenth embodiment of the present invention is similar to that of the twenty-eighth embodiment of the present invention, but the second tunnel junction layer 110b′ is introduced at a lower portion of the p-type nitride-based cladding layer 100′.
In detail, the LED according to the thirtieth-first embodiment of the present invention is similar to that of the twenty-eighth embodiment of the present invention, but the first and second tunnel junction layers 110a′ and 110b′ are introduced at an upper portion of the n-type nitride-based cladding layer 80′ and at a lower portion of the p-type nitride-based cladding layer 100′, respectively.
In detail,
In order to minimize dislocation density and cracks, which are generated in the process of growing the nitride-based light emitting structure, the surface treatment, the dry etching, or the lateral epitaxial overgrowth (LEO) scheme using amorphous silicon oxide SiO2 or amorphous nitride SiNx can be performed before the layers from the undoped buffering nitride-based layer 70′ serving as a buffer layer to the p-type nitride-based cladding layer 100′ have been deposited. Then, after growing the high-quality nitride-based light emitting structure, a Si-substrate, a GaAs-substrate, a sapphire substrate or a temporal substrate is bonded to an upper portion of the p-type nitride-based cladding or the second tunnel junction layer by using bonding materials, such as wax which is an organic bonding material. Prior to the above procedure, the surface roughening and patterning processes can be performed relative to the upper portion of the p-type nitride-based cladding or the second tunnel junction layer. In addition, the temporal substrate can be attached to the upper portion of the p-type nitride-based cladding or the second tunnel junction layer after forming the highly transparent p-type ohmic electrode (step {circle around (2)}).
Then, the laser beam having strong energy is irradiated through a rear surface of the transparent sapphire substrate 10′, so that the sacrificial layer 20′ including III-nitride-based semiconductors and being formed on the sapphire substrate 10 absorbs the laser beam while generating heat having the temperature about 1000° C. Thus, the nitride-based semiconductor materials are thermo-chemically decomposed, thereby removing the sapphire substrate, which is the initial insulating growth substrate (step {circle around (3)}).
In addition, after removing the insulating sapphire substrate through the LLO scheme, the supporting substrate layer including the AlN-based materials, which are semi-insulating or insulating materials, is completed removed (step {circle around (4)}). Then, the highly-transparent n-type ohmic electrode is formed on the n-type nitride cladding layer or the first tunnel junction layer.
Before the highly-transparent n-type ohmic electrode is formed, the litho-process, the patterning process, the etching process, and the surface roughening process can be performed relative to the upper surface of the n-type nitride cladding layer or the first tunnel junction layer (step {circle around (5)}).
In particular, if the tunnel junction layer is stacked on the n-type nitride cladding layer, an Al-related high reflective metal can be directly used for the highly-reflective n-type ohmic electrode. After forming the highly-reflective n-type ohmic electrode, a thick film for a heat sink is formed through the typical bonding transfer and electroplating processes (step {circle around (6)}).
Then, the highly transparent p-type ohmic electrode and the p-type electrode pad are formed (step {circle around (7)}). Before the highly transparent p-type ohmic electrode, the surface roughening process, and the surface patterning process can be performed in order to discharge the light generated from the active layer to the exterior as much as possible. If the highly transparent p-type ohmic electrode has already been formed in step, the p-type electrode pad 180′ is only formed in step.
Different from the p-side down LED, the p-type nitride-based cladding layer located at the uppermost portion of the LED has high sheet resistance, so the highly transparent ohmic electrode layer 170′ having high transmittance and capable of facilitating the lateral current spreading and the vertical current injecting must be formed on the p-type nitride-based cladding layer.
In detail, the LED according to the thirteen-fourth embodiment of the present invention is similar to that of the thirtieth-third embodiment of the present invention, but the first tunnel junction layer 110a′ is introduced at a lower portion of the n-type nitride-based cladding layer 80′.
In detail, the LED according to the thirtieth-fifth embodiment of the present invention is similar to that of the thirtieth-third embodiment of the present invention, but the second tunnel junction layer 110b′ is introduced on the p-type nitride-based cladding layer 100′.
In detail, the LED according to the thirtieth-sixth embodiment of the present invention is similar to that of the thirtieth-third embodiment of the present invention, but the first and second tunnel junction layers 110a′ and 110b′ are introduced at lower and upper portions of the n-type and p-type nitride-based cladding layer 80′ and 100′, respectively.
In detail,
In order to minimize dislocation density and cracks, which are generated in the process of growing the nitride-based light emitting structure, the surface treatment, the dry etching, or the lateral epitaxial overgrowth (LEO) scheme using amorphous silicon oxide SiO2 or amorphous nitride SiNx can be performed before the layers from the undoped buffering nitride-based layer 70′ serving as a buffer layer to the p-type nitride-based cladding layer 100′ have been deposited. Then, after growing the high-quality nitride-based light emitting structure, a Si-substrate, a GaAs-substrate, a sapphire substrate or a temporal substrate is bonded to an upper portion of the p-type nitride-based cladding or the second tunnel junction layer by using bonding materials, such as wax which is an organic bonding material. Prior to the above procedure, the surface roughening and patterning processes can be performed relative to the upper portion of the p-type nitride-based cladding or the second tunnel junction layer. In addition, the temporal substrate can be attached to the upper portion of the p-type nitride-based cladding or the second tunnel junction layer after forming the highly transparent p-type ohmic electrode (step {circle around (2)}).
Then, the laser beam having strong energy is irradiated through a rear surface of the transparent sapphire substrate 10′, so that the sacrificial layer 20′ including III-nitride-based semiconductors and being formed on the sapphire substrate 10 absorbs the laser beam while generating heat having the temperature about 1000° C. Thus, the nitride-based semiconductor materials are thermo-chemically decomposed, thereby removing the sapphire substrate, which is the initial insulating growth substrate (step {circle around (3)}).
In addition, after removing the insulating sapphire substrate through the LLO scheme, the supporting substrate layer including the AlN-based materials, which are semi-insulating or insulating materials, is partially removed through the lithography and etching processes (step {circle around (4)}). Then, the highly-reflective n-type ohmic electrode is formed on the n-type nitride cladding layer or the first tunnel junction layer. Before the highly-reflective n-type ohmic electrode is formed, the litho-process, the patterning process, the etching process, and the surface roughening process can be performed relative to the upper surface of the n-type nitride cladding layer or the first tunnel junction layer (step {circle around (5)}).
In particular, if the tunnel junction layer is stacked on the n-type nitride cladding layer, an Al-related high reflective metal can be directly used for the highly-reflective n-type ohmic electrode. After forming the highly-reflective n-type ohmic electrode, a thick film for a heat sink is formed through the typical bonding transfer and electroplating processes (step {circle around (6)}).
Then, the highly transparent p-type ohmic electrode and the p-type electrode pad are formed (step {circle around (7)}). Before the highly transparent p-type ohmic electrode, the surface roughening process, and the surface patterning process can be performed in order to discharge the light generated from the active layer to the exterior as much as possible. If the highly transparent p-type ohmic electrode has already been formed in step {circle around (2)}, the p-type electrode pad 180′ is only formed.
In addition,
Different from the p-side down LED, the p-type nitride-based cladding layer located at the uppermost portion of the LED has high sheet resistance, so the highly transparent ohmic electrode layer 170′ having high transmittance and capable of facilitating the lateral current spreading and the vertical current injecting must be formed on the p-type nitride-based cladding layer.
In detail, different from the thirtieth-third embodiment of the present invention, the supporting substrate layer 30′ including the AlN-base materials is not completely removed, but still supports the nitride-based light emitting structure at a predetermined interval, so the high quality nitride-based LED has structural stability. In addition, since the p-type ohmic electrode layer 120′ directly makes contact with the n-type nitride-based cladding layer 80′ through the supporting substrate layer 30′ including the AlN-base materials, the p-type ohmic electrode layer 120′ may serve as an electrode layer having superior current injecting and light reflecting characteristics.
In addition,
In detail, the LED according to the fortieth-first embodiment of the present invention is similar to that of the thirtieth-eighth and thirtieth-ninth embodiments of the present invention, but the first tunnel junction layer 110a′ is introduced at a lower portion of the n-type nitride-based cladding layer 80′.
In addition,
In detail, the LED according to the fortieth-third embodiment of the present invention is similar to that of the thirtieth-eighth and thirtieth-ninth embodiments of the present invention, but the second tunnel junction layer 110b′ is introduced on the p-type nitride-based cladding layer 100′.
In addition,
In detail, the LED according to the fortieth-fifth embodiment of the present invention is similar to that of the thirtieth-eighth and thirtieth-ninth embodiments of the present invention, but the first and second tunnel junction layers 110a′ and 110b′ are introduced on lower and upper portions of the n-type and p-type nitride-based cladding layers 80′ and 100′.
The subject matter of the present invention can be summarized as follows.
The supporting substrate layer 30′ including AlN-based materials is stacked/grown on the semiconductor thin layer. The semiconductor thin layer consists of the nitride-based flattening layer 20′ or the nitride-based flattening layer 20′ and the sacrificial layer 20′ including III-nitride-based semiconductors, and is formed on the insulating sapphire substrate 10′. Such a supporting substrate layer 30′ including the AlN-based materials attenuate stress derived from thermal and mechanical deformation when removing the sapphire substrate 10′ through the LLO scheme, thereby preventing the nitride-based thin film layer or the light emitting structure grown on the supporting substrate layer 30′ from being thermally and mechanically deformed or decomposed. The supporting substrate layer 30′ including the AlN-based materials is prepared in the form of a single layer or a bi-layer. Preferably, an single crystal material layer having a hexagonal system or a cubic system is primarily employed.
Meanwhile, before the supporting substrate layer 30′ including the AlN-based materials is stacked/grown on the flattening layer 20′ including III-nitride-based semiconductors, if amorphous silicon oxide SiO2 or amorphous nitride SiNx is formed on the flattening layer 20′ in the shape of an island through the patterning and etching processes, the nitride-based light emitting structure having a low dislocation density can be grown on the supporting substrate layer 30′.
In addition, preferably, the supporting substrate layer 30′ including the AlN-based materials is deposited at a thickness of 10 or less by means of chemical vapor deposition (CVD), such as metal organic chemical vapor deposition (MOCVD), hybrid vapor phase epitaxy deposition (HVPED), or atomic layer deposition (ALD), sputtering deposition using gas ions having high energy, or physical vapor deposition (PVD), such as pulsed laser deposition (PLD) using a laser energy source.
As mentioned above, the heat sink, which emits heat and protects the light emitting structure for the nitride-based light emitting device of the present invention, preferably includes metals, alloys or solid solution having superior electric and thermal conductivity. More preferably, instead of using silicon (Si) or a silicon substrate, the heat sink includes silicide that is an intermetallic compound, aluminum (Al), Al-related alloy or solid solution, copper (Cu), Cu-related alloy or solid solution, silver (Ag), Ag-related alloy or solid solution, tungsten (W), W-related alloy or solid solution, nickel (Ni), or Ni-related alloy or solid solution.
The present invention adopts the LLO scheme so as to remove the nitride-based light emitting structure from the insulating sapphire substrate 100. According to the present invention, the LLO scheme is not performed under the normal temperature and normal pressure and is performed in a state in which the sapphire substrate is immersed in acid solution such as HCl or base solution having the temperature of 40 or more degrees, in order to improve the product yield which may be lowered if crack of the nitride-based light emitting structure occurs during the process.
The bonding material layer 130′ preferably includes metals having higher cohesion properties and low melting points, such as indium (In), tin (Sn), zinc (Zn), silver (Ag), palladium (Pd), or gold (Au), and alloys or solid solution of the above metals.
The highly reflective p-type ohmic contact layer 120′ may include a thick layer of Ag and Rh without using Al and Al-related alloy or solid solution, which is a high reflective material that represents low specific contact resistance and high light reflectance on the p-nitride-based cladding layer 100′ or the second tunnel junction layer 110b′. In addition, the p-reflective ohmic contact layer 120′ may include a dual reflective layer or a triple reflective layer including the high reflective metal combined with nickel (Ni), palladium (Pd), platinum (Pt), zinc (Zn), magnesium (Mg), or gold (Au). Further, the p-reflective ohmic contact layer 430b may include a combination of transparent conductive oxide (TCO), transitional metal-based transparent conductive nitride, and the high reflective metal.
Each of the undoped buffering nitride-based layer 70′ serving as a buffer layer, the n-type nitride-based cladding layer 80′, the multi-quantum well nitride-based active layer 90′, and the p-type nitride-based cladding layer 100′ basically includes one selected from compounds expressed as AlxInyGazN (x, y, and z are integers) which is a general formula of III-nitride-based compound. Dopants are added to the n-type nitride-based cladding layer 80′ and the p-type nitride-based cladding layer 100′.
In addition, the n-type nitride-based active layer 90′ can be prepared in the form of a single layer, a multi-quantum well (MQW) structure, or multi-quantum dots or wires.
For instance, if GaN-based compound is employed, the n-type nitride-based cladding layer 80′ includes GaN and n-type dopants added to GaN, such as Si, Ge, Se, Te, etc., and the nitride-based active layer 90′ has an InGaN/GaN MQW structure or an AlGaN/GaN MQW structure. In addition, the p-type nitride-based cladding layer 100′ includes GaN and p-type dopants added to GaN, such as Mg, Zn, Ca, Sr, Ba, Be, etc.
The first and second tunnel junction layers 110a′ and 110b′ basically include one selected from compounds expressed as AlaInbGacNxPyAsz (a, b, c, x, y and z are integers) consisting of III-V group elements. The first and second tunnel junction layers 110a′ and 110b′ can be prepared in the form of a single layer having a thickness of 50 nm or less. Preferably, the first and second tunnel junction layers 110a′ and 110b′ are prepared in the form of a bi-layer, a tri-layer or a multi-layer.
Preferably, the first and second tunnel junction layers 110a′ and 110b′ have super-lattice structures. For instance, 30 or less pairs of elements can be repeatedly stacked in the form of a thin stack structure by using III-V group elements, such as InGaN/GaN, AlGaN/GaN, AlInN/GaN, AlGaN/InGaN, AlInN/InGaN, AlN/GaN, or AlGaAs/InGaAs.
More preferably, the first and second tunnel junction layers 110a′ and 110b′ may include a single-crystal layer, a poly-crystal layer or an amorphous layer having II-group elements (Mg, Be, Zn) or IV-group elements (Si, Ge) added thereto.
The high transparent ohmic electrode layers 150′ and 170′ stacked on the n-type and p-type nitride-based cladding layers 80′ and 100′ include oxide or transitional metal-based nitride. In particular, transparent conducive oxide (TCO) includes oxygen (O) combined with at least one selected from the group consisting of indium (In), tin (Sn), zinc (Zn), gallium (Ga), cadmium (Cd), magnesium (Mg), beryllium (Be), silver (Ag), molybdenum (Mo), vanadium (V), copper (Cu), iridium (Ir), rhodium (Rh), ruthenium (Ru), tungsten (W), titanium (Ti), tantalum (Ta), cobalt (Co), nickel (Ni), manganese (Mn), platinum (Pt), palladium (Pd), aluminum (Al), and lanthanoids (La).
In addition, transitional metal-based nitride includes nitrogen (N) combined with titanium (Ti), tungsten (W), tantalum (Ta), vanadium (V), chrome (Cr), zirconium (Zr), niobium (Nb), hafnium (Hf), rhenium (Re) or molybdenum (Mo).
The high transparent ohmic electrode layers 150′ and 170′ stacked on the n-type and p-type nitride-based cladding layers 80′ and 100′ include metal components that may form a new transparent conductive thin film in combination with the n-type and p-type nitride-based cladding layers 80′ and 100′ when it is subject to the heat treatment process at the oxygen atmosphere.
Preferably, the highly reflective n-type and p-type ohmic electrode layers 120′ formed on the bonding layer 130′ may include high reflective metals, such as aluminum (Al), silver (Ag), rhodium (Rh), nickel (Ni), palladium (Pd), and gold (Au), or alloys or solid solution of the above metals. In particular, according to the present invention, aluminum (Al) or Al-related alloy or solid solution is primarily used as a material for the highly reflective n-type and p-type ohmic electrode layers 120′ because aluminum (Al) represent thermal stability and superior reflectance at the wavelength band of 400 nm or less.
More preferably, the highly reflective n-type and p-type ohmic electrode layers 120′ may include the combination of the TCO, TCN and the high reflective metals.
In order to improve electrical and optical characteristics of the nitride-based light emitting device by providing a photonic crystal effect or by adjusting a roughness of an upper surface or a lower surface of the tunnel junction layers 110a′ and 110b′, a dot, a hole, a pyramid, a nano-rod, or a nano-columnar having a size of 10 nm or less can be provided through an interferometry scheme using interference of the laser beam and photo-reactive polymer or through an etching technology.
Another method of improving the electrical and optical characteristics of the nitride-based light emitting device through the surface roughness adjustment and photonic crystal effect has been suggested. This method is performed for 10 seconds to 1 hour at the temperature in a range of the normal temperature to 800° C. under oxygen (O2), nitrogen (N2), argon (Ar), or hydrogen (H2) atmosphere.
The n-type and p-type electrode pads 160′ and 180′ may have a stack structure including refractory metals, such as titanium (Ti), aluminum (Al), gold (Au) and tungsten (W) which are sequentially stacked.
Hereinafter, a method of growing a high quality epitaxial layer to fabricate a semiconductor device according to embodiments of the present invention will be described. In the following description, the same elements that have been described in the previous embodiments may have the same function and structure if there are no special comments for them.
Referring to
The first epitaxial layer 2 includes materials having a single crystalline structure, such as GaN, AlN, InN, AlGaN, InGaN, AlInN, InAlGaN, SiC, or SiCN, which is expressed as chemical formula InxAlyGazN (x, y and z are integers) or SixCyNz (x, y and z are integers). In addition, the first epitaxial layer 2 is deposited in the form of a single layer having a thickness of 30 nm or more. Preferably, the first epitaxial layer 2 is prepared in the form of a bi-layer or a multi-layer.
The first epitaxial layer 2 formed on the growth substrate 1 may have a multi-structure corresponding to InxAlyGazN (x, y and z are integers) or SixCyNz (x, y and z are integers).
IV-elements (Si, Ge, Te, Se), which are n-type dopant, and III-elements (Mg, Zn, Be), which are p-type dopant, can be added to the first epitaxial layer 2 according to the type of the electronic and optoelectronic devices.
The first epitaxial layer 2 is preferably deposited through chemical vapor deposition (CVD), such as MOCVD, HVPE or ALD (atomic level deposition), or through physical vapor deposition, such as PLD (pulsed laser deposition) using a strong energy source, or MBE (molecular beam epitaxy).
Then, as shown in
The thick film layer 3 can be formed by using materials having electrical conductivity or electrical insulating property. At this time, the thick film layer 3 is formed through electrochemical deposition, such as electroplating or electroless plating representing higher deposition rate, physical and chemical vapor deposition, such as LPCVD (low pressure CVD) or PECVD (plasma enhanced CVD), sputtering, PLD, screen printing, or fusion bonding using a metal foil.
The material of the thick film layer 3 having the thickness of 30 nm or more must have superior electrical and thermal conductivity without causing oxidation and reduction reaction under hydrogen (H) and ammonia (NH3) atmosphere and the high temperature condition of 1000° C. or more.
In detail, the thick film layer includes at least one selected from the group consisting of Si, Ge, SiGe, GaAs, GaN, AlN, AlGaN, InGaN, BN, BP, BAs, BSb, AlP, AlAs, Alsb, GaSb, InP, InAs, InSb, GaP, InP, InAs, InSb, In2S3, PbS, CdTe, CdSe, CdlxZnxTe, In2Se3, CuInSe2, Hgl-xCdxTe, Cu2S, ZnSe, ZnTe, ZnO, W, Mo, Ni, Nb, Ta, Pt, Cu, Al, Ag, Au, ZrB2, WB, MoB, MoC, WC, ZrC, Pd, Ru, Rh, Ir, Cr, Ti, Co, V, Re, Fe, Mn, RuO, IrO2, BeO, MgO, SiO2, SiN, TiN, ZrN, HfN, VN, NbN, TaN, MoN, ReN, CuI, Diamond, DLC (diamond like carbon), SiC, WC, TiW, TiC, CuW, or SiCN.
In addition, a single crystalline stack structure, a poly-crystalline stack structure, or an amorphous stack structure is prepared in the form of a single layer, a bi-layer or a tri-layer by using the material for the thick film layer 3. As a material for the thick film layer 3 having the thickness of 30 nm or more, alloys or solid solution of the above metals can be utilized.
Next, as shown in
If the laser beam having strong energy is irradiated through the rear surface of the sapphire substrate, which is the growth substrate 1, the laser beam is absorbed into the boundary surface between the first epitaxial layer and the sapphire substrate 1, so that GaN and AlN is thermally decomposed into Ga, Al and N. Thus, the sapphire substrate is removed.
Then, as shown in
That is, before forming the stack structure of a second epitaxial layer 4 including materials expressed as chemical formula InxAlyGazN (x, y and z are integers) or SixCyNz (x, y and z are integers), in order to improve the thermal stability of the thick film layer 3 and the first epitaxial layer 2 formed on the thick film layer 3, the heat treatment process is performed for 30 seconds to 24 hours under the oxygen, nitrogen, argon, vacuum, air, hydrogen or ammonia atmosphere at the temperature of 800° C. or above.
In particular, the high-quality epitaxial substrate for the electronic and optoelectronic devices can be fabricated at high efficiency and low cost through the processes shown in
Next, as shown in
At this time, the second epitaxial layer 4 is prepared in the form of a multi-layer by using materials expressed as chemical formula InxAlyGazN (x, y and z are integers) or SixCyNz (x, y and z are integers).
In addition, IV-elements (Si, Ge, Te, Se), which are n-type dopant, and III-elements (Mg, Zn, Be), which are p-type dopant, can be added to the second epitaxial layer 4 according to the type of the electronic and optoelectronic devices.
Referring to
The first epitaxial layer 2 formed on the growth substrate 1 may have a multi-structure corresponding to InxAlyGazN (x, y and z are integers) or SixCyNz (x, y and z are integers).
IV-elements (Si, Ge, Te, Se), which are n-type dopant, and III-elements (Mg, Zn, Be), which are p-type dopant, can be added to the first epitaxial layer 2 according to the type of the electronic and optoelectronic devices.
The first epitaxial layer 2 is preferably deposited through chemical vapor deposition (CVD), such as MOCVD, HVPE or ALD (atomic level deposition), or through physical vapor deposition, such as PLD (pulsed laser deposition) using a strong energy source, or MBE (molecular beam epitaxy).
Then, as shown in
The thick film layer 3 can be formed by using materials having electrical conductivity or electrical insulating property. At this time, the thick film layer 3 is formed through electrochemical deposition, such as electroplating or electroless plating representing higher deposition rate, physical and chemical vapor deposition, such as LPCVD (low pressure CVD) or PECVD (plasma enhanced CVD), sputtering, PLD, screen printing, or fusion bonding using a metal foil.
The material of the thick film layer 3 having the thickness of 30 nm or more must have superior electrical and thermal conductivity without causing oxidation and reduction reaction under hydrogen (H2) and ammonia (NH3) atmosphere and the high temperature condition of 1000° C. or more.
In detail, the thick film layer includes at least one selected from the group consisting of Si, Ge, SiGe, GaAs, GaN, AlN, AlGaN, InGaN, BN, BP, BAs, BSb, AlP, AlAs, Alsb, GaSb, InP, InAs, InSb, GaP, InP, InAs, InSb, In2S3, PbS, CdTe, CdSe, CdlxZnxTe, In2Se3, CuInSe2, Hgl-xCdxTe, Cu2S, ZnSe, ZnTe, ZnO, W, Mo, Ni, Nb, Ta, Pt, Cu, Al, Ag, Au, ZrB2, WB, MoB, MoC, WC, ZrC, Pd, Ru, Rh, Ir, Cr, Ti, Co, V, Re, Fe, Mn, RuO, IrO2, BeO, MgO, SiO2, SiN, TiN, ZrN, HfN, VN, NbN, TaN, MoN, ReN, CuI, Diamond, DLC (diamond like carbon), SiC, WC, TiW, TiC, CuW, or SiCN.
In addition, a single crystalline stack structure, a poly-crystalline stack structure, or an amorphous stack structure is prepared in the form of a single layer, a bi-layer or a tri-layer by using the material for the thick film layer 3.
As a material for the thick film layer 3 having the thickness of 30 nm or more, alloys or solid solution of the above metals can be utilized.
Next, as shown in
If the laser beam having strong energy is irradiated through the rear surface of the sapphire substrate, which is the growth substrate 1, the laser beam is absorbed into the boundary surface between the first epitaxial layer and the sapphire substrate 1, so that GaN and AlN is thermally decomposed into Ga, Al and N. Thus, the sapphire substrate is removed.
Then, as shown in
That is, before forming the stack structure of a second epitaxial layer 4 including materials expressed as chemical formula InxAlyGazN (x, y and z are integers) or SixCyNz (x, y and z are integers), in order to improve the thermal stability of the thick film layer 3 and the first epitaxial layer 2 formed on the thick film layer 3, the heat treatment process is performed for 30 seconds to 24 hours under the oxygen, nitrogen, argon, vacuum, air, hydrogen or ammonia atmosphere at the temperature of 800° C. or above.
Then, as shown in
Next, as shown in
At this time, the second epitaxial layer 4 is prepared in the form of a multi-layer by using materials expressed as chemical formula InxAlyGazN (x, y and z are integers) or SixCyNz (x, y and z are integers).
In addition, IV-elements (Si, Ge, Te, Se), which are n-type dopant, and III-elements (Mg, Zn, Be), which are p-type dopant, can be added to the second epitaxial layer 4 according to the type of the electronic and optoelectronic devices.
Referring to
Referring to
As described above, when growing the light emitting structure including nitride-based semiconductors on the sapphire growth substrate, the first tunnel junction layer is introduced between the undoped nitride-based layer serving as a buffering layer and the n-type nitride-based cladding layer, or the second tunnel junction layer is formed on the p-type nitride-based cladding layer. In addition, the sapphire substrate is removed through the LLO scheme, thereby fabricating the nitride-based light emitting device having high brightness, large area, and high capacity.
In addition, electrical and optical characteristics of the n-type and p-type highly transparent or highly reflective nitride-based ohmic electrode layers formed on the n-type and p-type nitride-based cladding layers can be improved, so that the nitride-based light emitting device has superior current-voltage and high brightness characteristics. In addition, the surface roughness process and the photonic crystal effect are applied to upper and lower portions of the nitride-based cladding layer and the ohmic electrode layer, so that the external quantum efficiency (EQE) is improved and the nitride-based light emitting device having high brightness, large area, and high capacity can be fabricated as a next-generation white light source.
Furthermore, before the nitride-based light emitting structure including the nitride-based semiconductors is grown on the sapphire substrate, the nitride-based sacrificial layer, the nitride-based flattening layer and the supporting substrate layer are sequentially stacked on the sapphire substrate. In this state, the nitride-based light emitting structure including the nitride-based semiconductors is continuously grown on the sapphire substrate. When growing the nitride-based light emitting structure, the first tunnel junction layer is introduced between the undoped nitride-based layer serving as a buffering layer and the n-type nitride-based cladding layer, or the second tunnel junction layer is formed on the p-type nitride-based cladding layer. In addition, the sapphire substrate is removed through the LLO scheme, thereby fabricating the nitride-based light emitting device having high brightness, large area, and high capacity.
Accordingly, when the laser beam having strong energy is irradiated, the nitride-based semiconductor layer can be prevented from being thermally and mechanically deformed or decomposed. In addition, electrical and optical characteristics of the n-type and p-type highly transparent or highly reflective nitride-based ohmic electrode layers formed on the n-type and p-type nitride-based cladding layers can be improved, so that the nitride-based light emitting device has superior current-voltage and high brightness characteristics.
In addition, since the high-quality nitride-based semiconductor epitaxial layer is grown, the semiconductor device may have superior electrical, optical and thermal characteristics.
Number | Date | Country | Kind |
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10-2005-0102645 | Oct 2005 | KR | national |
10-2005-0108408 | Nov 2005 | KR | national |
10-2005-0130217 | Dec 2005 | KR | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/KR2006/004425 | 10/27/2006 | WO | 00 | 4/29/2008 |