1. Introduction
Near-infrared light-emitting diodes (NIR-LEDs) were recently used as emitters for optical sensors in wearable devices, small vehicles, time-of-flight (T.O.F) sensors, and flying drones [
1,
2]. To meet the demands of these applications, small NIR-LEDs that can deliver higher power outputs at large injection currents are required. For several years, multiple quantum wells (MQWs), distributed Bragg reflector (DBR), omni-directional reflector (ODR), and current spreading layers have been used to improve the output powers in NIR-LEDs [
3,
4,
5,
6]. However, the abrupt decrease in the surface-emitting area of these devices, due to a reduction in the chip size, was not investigated in prior research efforts [
7,
8,
9,
10].
Based on previous studies, it could be assumed that the use of ODR by the wafer bonding process is an effective approach for the remarkable improvement of the light efficiency of LEDs [
11,
12,
13,
14]. Most light photons, which are emitted from the active region to the absorbing substrate, are effectively reflected in either the upper surface or sidewalls by the reflective function of ODR. It is known that the reflectivity of the reflector is essentially influenced by the metal and structural frame of the reflective structure used as ODR. Therefore, reflective structures used for the ODR are very important for effective improvements of the output power of NIR-LEDs. Reflective structures typically consist of both reflectors and insulators. Herein, an insulator has an important role in sustaining the reflectivity of the reflector. This insulator, which is inserted between the Si substrate and the LED, clearly increases the series resistance in the reflective LED. Therefore, the insulator has been universally patterned for use in reflective LEDs. The conductive characteristic of ohmic materials on patterned insulators should be studied to reduce the series resistance of reflective LEDs.
In addition, the top layer of the IR-LED (in contact with the ohmic material) should also be considered to improve ohmic contact and reflectivity. Previously, the GaP top layer was mainly used because of the existent Au/Be ohmic alloy material and non-absorption surface. However, the GaP, which causes a lattice mismatch (3.57 %) to (Al)GaAs, is no more useful for reflective (Al)GaAs based IR-LEDs owing to the use of the insulators for reflective structures [
15]. A lattice mismatch between Al
xGa
1−xAs (x = 0) and Al
xGa
1−xAs(x = 1) is known as approximately under 0.5 % [
16].
In this manuscript, we would like to use the p-AlGaAs contact layer to obtain 850 nm IR-LED with higher power due to the p-GaP contact layer, which is one of the absorbing factors on lights emitted from the active region. The GaP (5.45 Å) is lattice-mismatched with Al
xGa
1−xAs(~5.62 Å) mainly used for 850 nm IR-LEDs [
17]. Therefore, there are a lot of lattice defects between GaP and AlGaAs materials. Light in the LED structure was absorbed and reduced by lattice defects.
In this study, we investigated the Al/Au alloyed material in an effort to effectively improve the characteristics of ohmic contacts in reflective IR-LEDs made with a p-AlGaAs top layer. The Al/Au alloyed material with a 10% Al composition was the favorite for improving the light efficiency and series resistance of reflective NIR-LEDs.
2. Materials and Methods
The AlxGa1−xAs layers used were grown on an n-type GaAs (111) substrate at a 10 tilt toward [0−1-1], using a metal organic chemical vapor deposition (MOCVD) system. The GaAs substrate used was lattice-matched with AlxGa1−xAs. Trimethylgallium (TMGa), trimethyl-aluminum (TMAl), and trimethyl-indium (TMIn) were used as group III sources, and arsine (AsH3), and phosphine (PH3) were used as group V sources. Disilane (Si2H6) gas and cyclopentadienyl magnesium (Cp2Mg) were used as the n and p-dopant sources, respectively. Hydrogen (H2) gas was used as the source carrier.
Generally, various multiple quantum well (MQW) (active region) structures of different wavelengths are located between the
n and
p confinement layers. Four pairs of MQWs, each with 5 nm-thick GaAs wells and 12 nm-thick Al
0.05Ga
0.95As barriers, were used as the active region. The active region was located between the
n- and
p-type confinement layers, which are
n- and
p-doped Al
0.3Ga
0.7As materials, respectively. The photonic excitations of the MQWs were measured using a photoluminescence (P.L.) system with laser sources of 660 nm. The MQW structure of 850 nm was measured with a laser source of 660 nm. Normally, the epitaxial layer (active region) was analyzed through using the TEM system.
Figure 1 shows the TEM image and PL data for the developed 850 nm MQW (active region).
For the wafer bond process, n-GaInP and 5 µm-thick n-Al0.2Ga0.8As layers, grown sequentially on the GaAs substrate, were employed as the current-spreading effect and etching-stop layer (ESL), respectively. Developed reflective structures with different optical thicknesses and repeated 10 µm-hole patterns were fabricated on the n-Al0.3Ga0.7As layer.
A 110 nm-thick Si3N4 (n = 2.0 @ 850 nm) film was deposited on the p-doped Al0.3Ga0.7As layer to maintain reflectivity of the Ag reflector. The Si3N4 film on epitaxial wafer was coated and patterned by a photo-lithography process. The Si3N4 with photo-resistance hole patterns was selectively etched by plasma etching through using an RIE etcher with CF4 gas. The epitaxial wafer with patterned PR/Si3N4 film was dipped in BOE solution for 5 s. It was loaded on evaporation to deposit the Al0.1Au0.9 alloy. After the lift-off process, the Al0.1Au0.9 alloy was filled selectively into the vacant area (p-doped Al0.3Ga0.7As layer) of Si3N4 film.
Developed reflective structures, which have different optical thicknesses and repeated 10 μm hole patterns, were fabricated on the Si
3N
4 (
n = 2.0 @ 850 nm). Approximately 80 patterns exist with a diameter of 10 μm in one fabricated 14 mil NIR-LED chip. For bonding wafer to wafer, a 400 nm-thick Ag material and 5000 nm-thick Ti/Au/In/Ti (titanium/gold/indium/titanium) structures were used as the reflector and eutectic structures, respectively. After the wafer bonding process, the absorbing GaAs substrate was selectively removed in the H
2O
2:NH
3 solution until the appearance of the GaInP layer. The GaInP ESL was eliminated in a HCl solution for 10 s. Bonded IR-LED wafers were sequentially cleaned with acetone and methanol to remove organic contamination, which was followed by removing the surface oxidation of the n-Al
0.2Ga
0.8As top window (front surface) and p-Si substrate (back surface) in a HF: DI (10:1) solution. After cleaning, the bonding pads were placed on the anterior and posterior surfaces using a combination of photolithography and selective etching. It is noteworthy that Au/AuGeNi (1000 nm/100 nm) on the anterior surface was deposited using an electron beam evaporator, and Au/Au/Be (500 nm/100 nm) was deposited on the posterior surface using a thermal evaporator.
Figure 2 shows the structural schematic and compositional information of the reflective 850 nm IR-LED chip made with the Al/Au contact metal.
3. Results and Discussion
The reflective structures for high-power IR-LEDs were fabricated by combining the Si
3N
4 insulator and Ag reflector because the reflectivity of the Ag reflector was effectively sustained by the Si
3N
4 insulator. The Si
3N
4 insulator used is one of the important factors responsible for the increase of the series resistance in reflective IR-LEDs. To overcome this increased series resistance issue, the Si
3N
4 insulator was patterned to specific sizes and was filled with ohmic contact metal.
Figure 3a shows the Si
3N
4 insulator patterned by ohmic contact metal and
Figure 3b shows the corresponding optical microscopy images of patterned Si
3N
4 layer in the reflective IR-LEDs. In
Figure 3a, the Si
3N
4 film was deposited on the top layer of the LED; it was then patterned periodically to form circular patterns using the lithographic and etching processes. The ohmic contact metal filled the patterns to an approximate thickness of 110 nm because of the thickness (110 nm) of the Si
3N
4 film. The Ag reflector and eutectic materials were sequentially deposited on the patterned Si
3N
4 film with ohmic contact metal. Herein, it was observed that circles with an approximate diameter of 10 μm were patterned every 20 μm in the Si
3N
4 insulator, as shown in the IR permeation image in
Figure 3c.
Figure 3d showed scanning electron microscopy images for the Ag reflector, eutectic structure, and patterned Si
3N
4/Al/Au in 850 nm IR-LED fabricated by wafer bonding process. Here, both eutectic structure and insulator in
Figure 3d could easily be measured by the FIB-SEM system.
As mentioned earlier, the ohmic contact metal is a critical factor for the electric characteristics of the developed reflective IR-LEDs. Generally, Au/Be alloyed materials have been extensively used for reflective LEDs because use of the p-GaP top layer for reflective IR-LEDs. However, p-GaP is lattice-mismatched for AlGaAs materials used mainly for reflective 850 nm IR-LEDs. Furthermore, Be in Au/Be is not useful for AlGaAs-based quantum wells due to its high likelihood to be diffused to the active region [
18,
19].
On the other hand, here, the p-AlGaAs top layer was used for developed reflective IR-LEDs. Therefore, approximately 100 Al/Au patterns were inserted in one IR-LED chip (355 μm × 355 μm). The total area of patterns occupied almost 6% of the IR-LED chip.
Figure 4 shows the measurement scheme for patterned contact metal and current-voltage characteristics of patterned Au/Be for the p-GaP layer and those of the patterned Au/Be for the p-AlGaAs layer. The current-voltage characteristics of the patterned contact metals were systematically measured by a dual probe tip.
Figure 4b shows the current-voltage characteristic for p-GaP/Au/Be and p-AlGaAs/Au/Be structures annealed at 550 °C. The current-voltage curve of the p-GaP/Au/Be structure demonstrates an excellent ohmic property. In the current-voltage curve of the p-GaP/Au/Be structure, the injection current was 100 mA, and the voltage was 5.75 V. Conversely, in the current-voltage curve of p-AlGaAs/Au/Be, at the same current conditions, the voltage was 3.44 V. Furthermore, p-AlGaAs/Au/Be yielded an abnormal curve compared with that of p-GaP/Au/Be. Given the fact that p-AlGaAs is the top layer of the IR-LED epi-wafer, Au/Be was not suitable for the development of reflective IR-LEDs.
To identify an optimum ohmic contact condition for the p-AlGaAs top layer, we investigated Al and the contained Au ohmic metal. The Al composition in the AlxAu1−x alloy was controlled to 5%, 10%, and 20%.
Figure 5a shows the current-voltage curves for the pattern of Al
0.05Au
0.95, Al
0.1Au
0.9, Al
0.2Au
0.8, and conventional Au/Be for p-AlGaAs. For a current of 100 mA, the voltage was finely increased as the Al composition increased. The voltages of Al
0.05Au
0.95 and Al
0.1Au
0.9 were 3.59 V and 3.96 V, respectively, compared with that of the Au/Be (3.44 V). However, the voltage of Al
0.2Au
0.8 decreased to 3.13 V. The current-voltage curves show that the Al
xAu
1−x (x = 0.05, 0.1) alloy has better ohmic characteristics than those of the Au/Be alloy for the p-AlGaAs layer. Furthermore, the current-voltage characteristics of Al
xAu
1−x were obtained without any prior thermal treatments. The best ohmic characteristics were obtained by the patterned Al
0.1Au
0.9 alloy. From the current-voltage results of
Figure 5a, it was found that the Al
0.1Au
0.9 is more suitable for the p-AlGaAs layer because it showed the highest voltage value when compared with the others at 100 mA. Based on the current-voltage results, the Al
0.5Au
0.95 and Al
0.2Au
0.9 alloyed materials have worse current-voltage characteristics than the Al
0.1Au
0.9 for p-AlGaAs layer.
Therefore, we tested different thermal conditions for p-AlGaAs/Al0.1Au0.9 structures. The injected thermal temperature was limited to 600 °C owing to the epitaxial growth temperature of 580 °C. It was found that the current-voltage characteristics increased as a function of thermal temperature. At a current of 100 mA, remarkable improved voltage outputs (5.8–6.0 V) were observed from 500 °C and 600 °C. The current-voltage characteristic (6.0 V) of the p-AlGaAs/Al0.1Au0.9 structure obtained at 500 °C yielded a higher voltage than that (5.75 V) of p-GaP/Au/Be at 550 °C. Therefore, it was demonstrated that the p-AlGaAs/Al0.1Au0.9 structure is essential to achieve excellent current-voltage characteristics and lower thermal conditions for reflective IR-LEDs.
For more detailed information, the component of the Al
xAu
1−x alloyed material was investigated. To measure the composition ratio in the Al
0.1Au
0.9 alloyed materials, the Al
0.1Au
0.9 was melted and evaporated on the GaAs wafer. The Al
0.1Au
0.9 alloyed materials were measured by an energy dispersive spectrometer (EDS). It was found that deposited Al
0.1Au
0.9 film has significant smooth and clean surface.
Figure 6b showed surface and EDS data of Al
0.1Au
0.9 alloyed materials. The result of EDS clearly presents that there is 9.8% Al and 90.2% Au deposited in Al
0.1Au
0.9 alloyed materials. We believed that appropriate ratio of Al
0.1Au
0.9 with a clean surface is very useful in improving ohmic characteristics for p-AlGaAs of reflective 850 nm IR-LEDs.
To obtain detailed information, the light power-current-voltage curve characteristics of the 850 nm reflective IR-LED chip which contained p-GaP/Au/Be, p-AlGaAs/Au/Be, and p-AlGaAs/Al0.1Au0.9 structures were also investigated. Herein, Au/Be-based and Al0.1Au0.9-based structures used for reflective IR-LED chips were thermally treated by post-annealing processes at 550 °C and 500 °C, respectively. Here, Au/Be and Al0.1Au0.9 have the same thickness because alloys are filled with a 110 nm-thick pattern hole of Si3N4 film. Normally, I–V property was not dependent on metal thickness, but rather the composition of either Be in the Au/Be alloy or Al in the Al/Au alloy.
Based on the current–voltage curves of
Figure 7, the considerably increased forward voltage clearly proves that the AlGaAs/Au/Be structure was not suitable for the development of reflective IR-LEDs. Conversely, reflective IR-LED chips with p-AlGaAs/Al/Au structures yielded lower forward voltages compared with the reflective IR-LEDs with conventional p-GaP/Au/Be structures. This is owing to the reduction of series resistivity of the IR-LED chips caused by alloying aluminum (Al) and gold (Au). These results exhibited almost similar trends to those of the current-voltage characteristics in
Figure 5.
From the light power-current curves at the injection current of 200 mA, it was found that the reflective IR-LED chip with the p-AlGaAs/Al0.1Au0.9 structure yielded the highest output power (182 mW), compared with the other reflective IR-LED chips. The output power of the IR-LED chip with the p-AlGaAs/Al0.1Au0.9 structure was approximately 65% higher than the output power (110 mW) of the IR-LED chip with the p-AlGaAs/Au/Be structure. An increase in the output power of the conventional reflective IR-LED with the p-GaP/Au/Be structure of 13.5% was observed in one p-AlGaAs/Al0.1Au0.9 structure. These results demonstrate that the electrical and optical characteristics of the reflective IR-LED could be improved effectively by using the alloyed metal Al0.1Au0.9.
Table 1 presents summarized data for light power-current-voltage characteristics of reflective IR-LED chips with different ohmic contact layers. From the current-voltage data in
Table 1, it was found that the IR-LED chip with the p-AlGaAs/Al
0.1Au
0.9 structure showed lower forward voltage and higher output power when compared with the others under various current densities. In comparison with normal IR-LED chips with p-GaP/Au/Be especially, approximately 12.5% low forward voltage and 13% high output power were observed from one alloyed material with the p-AlGaAs/Al
0.1Au
0.9 structure. From the results of
Table 1, it was demonstrated that Al
0.1Au
0.9 alloyed materials are essential to improve optical efficiency of reflective 850 nm IR-LEDs with a p-AlGaAs top layer.
At an injection current of 20 mA, the emission intensities of developed LED chips are compared in
Figure 8. It can be seen that the emission intensity of the 850 nm IR-LED chip with the p-AlGaAs/Al
0.1Au
0.9 structure is approximately 1.23 times that of the conventional 850 nm IR-LED chip with p-GaP/Au/Be, which is equivalent to a 23 % increase. This could be attributed to the increase in the effective photon emission area, which is caused by the improvement of the ohmic characteristic of the p-AlGaAs/Al
0.1Au
0.9 structure. This indicates that the use of the Al
0.1Au
0.9 alloyed materials for the reflective 850 nm IR-LED with the p-AlGaAs top layer would significantly increase the optical efficiency of the device.
On the basis of these results, we can assume that using the patterned AlxAuy alloy effectively improves the series resistance of reflective IR-LEDs at lower thermal temperatures. It was verified that the I–V characteristics of the p-AlGaAs/Al0.1Au0.9 structure were more attractive than those of the p-GaP/Au/Be structure for reflective IR-LEDs at relatively low temperatures. As an extension of our results, we posit that the Al0.1Au0.9 alloy should be highly useful for application in reflective NIR or mid-infrared (MIR) LED at higher output powers.