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Volume 2020 |Article ID 8984697 | https://doi.org/10.1155/2020/8984697

Lester D. Bernardino, Gil Nonato C. Santos, "Synthesis and Characterization of Gallium Oxide/Tin Oxide Nanostructures via Horizontal Vapor Phase Growth Technique for Potential Power Electronics Application", Advances in Materials Science and Engineering, vol. 2020, Article ID 8984697, 14 pages, 2020. https://doi.org/10.1155/2020/8984697

Synthesis and Characterization of Gallium Oxide/Tin Oxide Nanostructures via Horizontal Vapor Phase Growth Technique for Potential Power Electronics Application

Academic Editor: Guian Qian
Received26 Jun 2020
Revised17 Sep 2020
Accepted05 Nov 2020
Published23 Nov 2020

Abstract

The monoclinic β-gallium oxide (Ga2O3) was viewed as a potential candidate for power electronics due to its excellent material properties. However, its undoped form makes it highly resistive. The Ga2O3/SnO2 nanostructures were synthesized effectively via the horizontal vapor phase growth (HVPG) technique without the use of a magnetic field. Different concentrations of Ga2O3 and SnO2 were varied to analyze and describe the surface morphology and elemental composition of the samples using the scanning electron microscopy (SEM) and energy-dispersive X-ray (EDX) spectroscopy, respectively. Meanwhile, the polytype of the Ga2O3 was confirmed through the Fourier transform infrared (FTIR) spectroscopy. The current-voltage (I–V) characteristics were established using a Keithley 2450 source meter. The resistivity was determined using the van der Pauw technique. The mobility and carrier concentration was done through the Hall effect measurements at room temperature using a 0.30-Tesla magnet. It was observed that there was an increase in the size of the nanostructures, and more globules appeared after the concentration of SnO2 was increased. It was proven that the drop in the resistivity of Ga2O3 was due to the presence of SnO2. The data gathered were supported by the Raman peak located at 662 cm−1, attributed to the high conductivity of β-Ga2O3. However, the ε-polytype was verified to appear as a result of adding SnO2. All the samples were considered as n-type semiconductors. High mobility, low power loss, and low specific on-resistance were attained by the highest concentration of SnO2. Hence, it was clinched as the optimal n-type Ga2O3/SnO2 concentration and recommended to be a potential substrate for power electronics application.

1. Introduction

Silicon-based technology has been the mainstream in power electronics [1]. However, its power devices are approaching their physical limitation [2] when operating at extreme voltage, current, power, and temperature environments, allowing other semiconductor materials to dominate large market sectors untouched by Si-based devices [3]. Consequently, research and development on wide bandgap materials [4] are carried out in the past years so that the volume and weight of power electronic devices can be improved for more extensive applications [5].

Recently, gallium oxide (Ga2O3) gained significant attention as a material for power electronics applications [6] because of its extremely large bandgap [7] in the range of 4.6 eV to 4.9 eV, depending on the specific crystal orientation and measurement method [8].

Among the five phases of Ga2O3, the most studied is the ground state [9] because of its availability and outstanding properties [10, 11]. Its potential applications range from transparent conducting electrodes to power electronics [12]. The breakdown voltage of Ga2O3 is 8 MV/cm, which is higher than that of Si, SiC, and GaN, which makes it suitable for high voltage and high-temperature applications [1]. However, the undoped β-Ga2O3 is highly resistive because of its wide bandgap. Electrical property measurements of Ga2O3 nanowires and nanoribbons have revealed n-type semiconductor behavior [13], which has been attributed to oxygen vacancies (Vo) or Ga interstitials [3, 14]. As reported by Varley et al. [15], Vo acts as a deep donor and does not contribute to its conductivity. Hence, doping with elements acting as shallow donors is necessary to enhance its electrical conductivity [16].

Sn was found to be a shallow donor when incorporated into the Ga site [15, 1719]. The mixing of Ga with Sn inevitably causes the replacement of Ga+3 ions with Sn+4 ions [20]. The tetravalent Sn ion is most often chosen as donor dopant [18] since it is also an n-type that enhances the natural conductivity of β-Ga2O3 [21, 22] and their ionic radii are close with each other [18, 21].

In the past years, a high amount of work was devoted to the growth of the undoped semiconductor nanowires by several approaches. Up to this date, a cost-efficient synthesis technique of manufacturing nanostructure is still a grand challenge [1]. The fabrication of one-dimensional structures gained interests due to their importance in understanding the dependence of properties on the size and dimensionality of materials, and their potential applications as functional building blocks for electrical, optical, and magnetic devices [14]. Although there are several synthesis methodologies, the thermal evaporation using a metal catalyst is a successful route to fabricate semiconducting oxide nanostructure from single nanowires or nanorods to hierarchical nanostructures [23]. Nevertheless, few papers have been reported for the conductivity control of β-Ga2O3 by doping [24]. Experimentally determined results for free charge carrier concentrations and mobility parameters are currently scarce for β-Ga2O3 [25].

The horizontal vapor phase growth (HVPG) is a home-developed [26] and low-cost synthesis technique which proved to produce various one-dimensional nanostructures using different starting materials such as SnO2 [27, 28], Fe2O3 [26], and In2O3 [29]. Recently, undoped nanowires were successfully fabricated by the presence of a magnetic field via HVPG for high-concentration ethanol vapor detection [30]. In this regard, SnO2 was chosen as dopant since there were studies already conducted using HVPG and its small amount was known to increase the electrical conductivity of Ga2O3 [21].

This pursuit was an initial investigation on the synthesis of Ga2O3/SnO2 via the horizontal vapor phase growth (HVPG) technique without the application of the magnetic field. The concentration of SnO2 was varied to determine its effect on the surface morphology and electrical attributes of Ga2O3 for potential power electronic applications. The characterizations were performed using SEM and EDX, while the polytypes were affirmed through the known peaks of Raman. The I–V curves were uncovered using a two-point probe test and the van der Pauw technique for the electrical resistivity. The Hall effect measurements revealed the carrier concentration and mobility. Additionally, the specific on-resistance and power loss were studied for potential power electronics applications.

2. Experimental Setup

2.1. Synthesis of Ga2O3/SnO2 Nanostructures

This study employed the horizontal vapor phase growth (HVPG) technique patented by Santos et al. [28] for the synthesis of Ga2O3/SnO2 nanostructures. The HVPG is a deposition method that follows a spontaneous growth or vapor-solid (VS) process, which employs the evaporation-condensation process at a very low pressure of 10−6 Torr. The annealing process requires metal oxide material to evaporate at a very high temperature. Subsequently, the vapor nucleates into particles and transports to the substrate. The source material then condenses and deposits on the substrate’s surface because of the temperature difference along the silica quartz tube, resulting in the formation of distinct nanomaterials.

Fifty milligrams of Ga2O3 powder was mixed with or without SnO2 powder purchased from Sigma-Aldrich. The variation of Ga2O3 and SnO2 was based on the weight percent (wt.%) ratio of 98 : 2 used in relation to [31]. Consequently, the mass loadings were named as sample A (100 : 0 wt.%) or the as-grown, sample B (99 : 2 wt.%), sample C (98 : 2 wt.%), and sample D (90 : 10 wt.%). The samples were poured in fused-silica quartz tubes and sealed under a high-vacuum system, while the pressure was maintained at 10−6 Torr. Afterward, the sealed tubes were injected midway through a Thermolyne horizontal tube furnace and then annealed at 1,200°C with a ramp time of 40 minutes for 8 hours as shown in Figure 1(a). Regions of interest were assigned according to their position in the furnace during the annealing process. Figure 1(b) shows that zone 1 contained the powder which was positioned inside the furnace. Meanwhile, the middle portion of the tube was designated as zone 2. The last part of the tube that was completely outside the furnace was designated as zone 3 [27].

As affirmed by [27], the temperature in zone 1 was 1200°C, 353°C to 800°C in zone 2, and 63°C to 352°C in zone 3. After the tubes cooled down, they were removed from the furnace and then ruptured to collect the nanomaterials for characterization. The Ga2O3/SnO2 was compared to the initially prepared as-grown specimen.

2.2. Characterization of Ga2O3/SnO2 Nanostructures

JEOL JFC-1200 fine coater was used to gold (Au) sputter every sample at 50 mA for 90 seconds to become conductive.

Then, the Au coated samples were subjected to Phenom XL Scanning Electron Microscope equipped with energy-dispersive X-ray spectroscopy for surface morphology and elemental composition of the nanostructures. Point analyses were performed to know and to verify the elemental contents of the nanostructures and globules. The traditional manual image analysis using ImageJ was utilized to determine the size of the nanostructures.

The zone where the nanostructures were found was subjected to polytype analysis. The Fourier transform infrared (FTIR) spectroscopy confirmed the occurrence of β-Ga2O3, which was reported by Higashiwaki et al. [1] to be suitable for power electronics applications. Furthermore, FTIR was utilized to know the other Ga2O3 phases present in the specimens based on their known peaks [32].

A two-point probe using Keithley 2450 source meter was operated to establish the current-voltage (I–V) characteristics of the samples. The voltage sweep was set to 200 points, while the voltage was varied from −5.0 V to +5.0 V. The resulting current was recorded automatically and plotted by the source meter.

On the other hand, Hall effect and electrical resistivity measurements were carried at room temperature (RT) using the van der Pauw method. The sense terminals of Keithley 2450 Source Meter were used to measure the voltage of the sample under test (SUT), while the force terminals sourced current to SUT. For Hall effect measurement, the method used by Matsumura and Sato [33] was followed where a magnetic field of 0.30 T was applied in the direction of the sample’s thickness, and the change in voltage between the point contacts placed at diagonally opposite corners was measured. Consequently, mobility and carrier concentrations were calculated based on the resistivity and Hall coefficients of each sample.

Both power loss and specific on-resistance were likewise computed based on the applied current and the established value of the electrical resistivity for potential power electronics applications.

3. Results and Discussion

3.1. Surface Morphology and Elemental Composition Analyses

The nanostructures presented in Figure 2(a) were excellently viewed at 6,500x magnification showing a pile of bulk and rigid nanostructures. Their size ranged from 4.46 μm to 11.357 μm and an average of 3.177 μm. Figure 2(b) shows that Ga and O had 32.30% and 31.20% compositions, respectively, leading to the ratio of 1 : 1. It can be seen that Au appeared in the EDX since all the zones were sputtered to make them conductive for surface morphology and elemental analysis. It was noticed that the samples charged up when sputtering was done less than 90 seconds. However, the concentration of Au became more apparent than those of Ga and O. Similar observations were noticed across all the zones and prepared specimens. No other impurities appeared besides Au.

It was perceived in Figure 3(a) that combinations of straight, crossing, and twisted nanowires were in good agreement with the literature [34]. A manual assessment revealed that their diameter ranged from 52.287 nm to 167.401 nm and a mean diameter of 90.976 nm. No nanobelts nor nanorods were observed in this zone. Thicker yields were noticed compared to [3436]. On the other hand, thinner nanowires were seen compared to [30] using the same deposition technique with an applied magnetic field. Figure 3(b) shows Ga to O ratio of approximately 2 : 3.

The deposits found in Figure 2(a) were very similar to those in Figure 4(a) but much smaller considering the fact that they were viewed at the same magnification. Their size ranged from 0.156 μm to 2.971 μm and a mean size of 0.837 μm. The ratio of Ga to O was not proportionate with Ga2O3 due to few Ga atoms. No other impurities appeared in the analysis as seen in Figure 4(b), besides Au.

Figure 5(a) shows the same SEM image taken in relation to [30]. The assessed size of the nanostructures ranged from 233.836 nm to 998.948 nm and a mean size of 575.231 nm. A similar ratio was assessed with zone 3 of sample A based on Figure 5(b).

The nanostructures had smoother and straighter morphology but much thicker compared to the as-grown sample. The appearance of globules was evident in all SEM images in Figure 6, which were not seen in the as-grown sample. They were not only attached to the tip of the nanostructures but likewise on its lateral surface [32]. It was likewise examined that the globules fit the nanostructures and none of which fell off onto the substrate due to their sufficient amount. Few globules were seen in the image due to a very small concentration of SnO2. More globules attached to the nanostructures were considered as salient and novel information of this study. The size of the nanostructures ranged from 30.864 nm to 277.055 nm with an average of 98.781 nm and was considered as 1D nanomaterials, specifically nanowires. On the other hand, the size of the globules ranged from 0.575 μm, while the largest was 6.086 μm with an average of 2.336 μm.

Based on Figure 7(a), the ratio of Ga to O of the nanostructure was approximately 2 : 7, which was due to the presence of the dopant, while the globule was 1 : 6. According to Jessen et al. [37], the chemical composition of the droplet was purely Sn through the EDS and EDX analyses; however, this study revealed that the globule was mixed of Sn and Ga atoms. Consequently, both the nanostructures and globules were comprised of Ga, Sn, and O atoms as shown in Figures 7(b) and 7(c).

A similar image is noticed in Figure 8(a) and the as-grown sample, which matches the bulk Ga2O3 powder, with size ranging from 190 nm to 1,937 nm and mean size of 662.265 nm. Zone 3 was found to be Ga deficient due to a very small concentration as seen in Figure 8(b).

Small and large pieces of crystalline nanoblocks are spotted in Figure 9(a) signifying that the Ga2O3 powder was not melted totally during the deposition. The size of the nanostructures ranged from 248 nm to 2,364 nm and an average size of 804.615 nm. As assessed in Figure 9(b), Ga to O ratio was verified to be approximately 2 : 3.

It was observed that more globules of different sizes and twisted nanostructures were present in this concentration compared to sample B. Furthermore, smaller globules positioned at the tip and lateral surface of the nanostructures are noticed in Figures 10(a)10(c). The size of the nanostructures ranged from 52.305 nm to 157.893 nm and an average diameter of 107.274 nm. On the other hand, the assessed diameter of the globules ranged from 0.169 μm to 9.782 μm and a mean diameter of 2.042 μm. The quantity of the globules depends on the increase in the concentration of SnO2 to Ga2O3.

Figure 11(a) reveals that the nanostructures were composed of combined O, Sn, and Ga atoms with 34.40%, 6.73%, and 6.34%, respectively. Ga to O ratio was found to be 2 : 11 as contributed by SnO2. Compared with sample B, the nanostructures’ main content was Ga; however, Sn in this concentration was seen in Figure 11(b). Consistently, the main component of the globule was Sn with 14.44 atm% as shown in Figure 11(c).

Since few nanoparticles were found, Figures 12(a) and 12(b) prove that Ga has the least share of 1.54% compared with Au, O, and Si with 62.31%, 24.13%, and 12.02%, respectively. Consequently, Ga to O ratio was found to be 2 : 12.

Figure 13(a) shows bulk and small nanomaterials with a rigid structure. However, Figure 13(b) proves that this zone was made up of 7.50% Ga and 37.98% O, leading to Ga to O ratio of 2 : 8. No other impurities were found in this zone besides 47.18% Au and 7.34% Si.

A similar image is observed in Figure 14(a) and supported by Ga to O ratio of 5 : 2 based on EDX analysis in Figure 14(b).

More globules but larger in diameter were produced in this concentration compared with samples B and C. Figure 15(a) shows an excellent view of a melting nanostructure with a globule attached on its end, while a globule was attached permanently on two nanostructures in Figure 15(b). Meanwhile, it was observed that the nanostructures were not sufficient to hold all the globules permanently in Figure 15(c). It was further noticed that there were many globules compared to nanostructures causing them to fall onto the substrate. Only a small amount of Sn has been shown to incorporate successfully without segregation effectively [22]. The size of the nanostructure ranged from 65.788 nm to 526.316 nm and an average diameter of 247.341 nm. On the contrary, the globules’ size ranged from 0.521 μm to 18.872 μm and a mean diameter of 2.725 μm. The presence of nanorods was significant since the globules were attached to its surface. A huge globule cannot be supported by a single nanostructure. Thus, if the nanostructures were neither aggregated nor thicker, the huge globules just fell off onto the substrate. Due to this reason, the concentration was not further increased.

SEM image shown in Figure 16(a), supported by Figure 16(b), proved that the nanostructures’ main composition was Ga with 13.06 atm% and a lesser concentration of Sn of 1.74%. O had a 21.10% share, which led to a Ga to O ratio of 2 : 3. Conversely, the major component of the globules was Sn with 24.89% as supported by its higher EDX peak in Figure 16(c) compared with Ga and O. Ga and O compositions had 4.79% and 22.11% shares, respectively, leading to Ga to O ratio of 2 : 9.

3.2. Polytype Analysis

According to [17], 142 cm−1 and 179.69 cm−1 low modes were attributed to the vibration and translation of doubly connected straight chains of GaO6 octahedra. The Raman modes at 449.87 cm−1 and 477.68 cm−1 according to [22, 38], respectively, were related to the deformation of GaO6 octahedra. The group of Raman modes located at 632.31 cm−1 and 650.67 cm−1 represents the stretching and bending of GaO4. The spectrum of SiO2 at 521.81 cm−1 appeared in Figure 17.

As noticed in Figure 18, only 1 low peak of β phase was observed, particularly at 160.73 cm−1, in agreement with [39]. However, the peaks of the deformation of GaO6 octahedra dominated this sample located at 349.02 cm−1, 419.52 cm−1, and 470.89 cm−1. On the other hand, 2 high spectra were located at 627.86 cm−1 and 661.81 cm−1 resulting in the distortion of Ga2O3 caused by the presence of Sn. Nonetheless, 1 peak of ε-Ga2O3 was observed at 714.93 cm−1 as a result of adding SnO2 to Ga2O3. The peak of SnO2 was not observed in this concentration due to its small concentration [22].

Figure 19 reveals 3 mid peaks at 302.04 cm−1, 317.60 cm−1, and 348.62 cm−1 and 2 high peaks at 662.61 cm−1 and 759.87 cm−1. According to [22], the Raman peak located at 662.61 cm−1 indicates that the majority of the nanostructures grew in [010] direction, which exhibits the highest electrical conductivity for β-Ga2O3 nanowires. Similar to sample B, 1 peak of ε-Ga2O3 was noticed at 211.25 cm−1 as reported in the previous study [40]. Conversely, 2 peaks of rutile SnO2 were analyzed at 473.25 cm−1 and 486.42 cm−1. The 473.25 cm−1 peaks confirmed the rutile-type SnO2 single crystal, while 486.42 cm−1 was attributed to lower wavenumbers as the nanoparticle’s size decreased.

Sample D showed 1 peak of β-Ga2O3 for the low and mid modes, particularly at 159.60 cm−1 and 415.88 cm−1, respectively, as spotted in Figure 20. Raman peak located at 662.62 cm−1 was likewise observed. No other peaks of the Ga2O3 phases were detected in this concentration. On the other hand, 2 peaks of SnO2 were seen specifically: 493.84 cm−1, which appeared as the consequence of disorder activation in its rutile structure, and 638.73 cm−1, which corresponds to the classical vibration modes as shown in [41].

3.3. Electrical Properties for Potential Power Electronics Application

The I–V curves shown in Figures 21(a) and 21(b) were almost straight and similar to the graph of a resistor and the as-grown Ga2O3, which is in good agreement with the previous research [42]. On the other hand, Figure 21(c) shows resemblance to the I–V curve of a diode and a single Sn-doped Ga2O3 in relation to [42].

The shifting of the I–V graph of specimen C implied that there was an enormous increase in its conductivity. This was consistent with other works on Ga2O3 nanowires in which a strong enhancement of the electrical conductivity was observed due to the incorporation of Sn [42]. Nevertheless, the measured currents for sample D, shown in Figure 21(d), ranged from −1.888 × 103 nA to 1.827 × 103 nA and were found to have the greatest correlation among the other specimens. This sample was expected to have the greatest increase in electrical conductivity since it has the greatest concentration of Sn. However, the length of the contacts attached to this during the 2-point probe test might affect the result.

As can be gleaned in Table 1, the resistivity of sample A was higher compared to the reported value of 1.43 × 10−1 Ω·cm in [24]. Conversely, the resistivity of sample B was found to be 2.01757 × 10−1 Ω·cm. There was a slight decrease in the resistivity since a very small amount of SnO2 was added to Ga2O3. An increase of 1.15328 S/cm was still observed, which proved that the incorporation of SnO2 increases the conductivity of the resistive Ga2O3. Smaller resistivity of 1.67619 Ω·cm was observed in sample C compared to that of A and B. The conductivity increased by approximately 2.162714 S/cm and 1.0094 S/cm for samples A and B, respectively. As discussed in the previous research, when Sn+4 substitutes Ga3+ on the octahedral site, it donates an electron to the Ga2O3 lattice which increases the carrier concentration and thus conductivity [43]. The data obtained in sample C was clear evidence that the chosen dopant increased the conductivity of Ga2O3. Another sample proved this information since there was a drastic increase in conductivity in sample D. It was analyzed that the increase resulted in 10.596741 S/cm for sample A, 9.443455 S/cm for sample B, and 8.434027 S/cm for sample C. The mentioned resistivities of Ga2O3/SnO2 specimens fell on the range of 10−3 to 1012 Ω cm with changing doping concentration, which was in good agreement with [11]. The conductivity of the specimens might be affected by the Au sputtering; however, its effect was assumed to be the same throughout the specimens.


SampleCarrier typeResistivity ρ (Ω·cm)Carrier concentration n (cm−3)Mobility μ (cm2/V·s)

An2.62938 × 10−11.1053 × 101821.4752
Bn2.01757 × 10−12.5791 × 101811.9946
Cn1.67619 × 10−11.9344 × 101819.2499
Dn6.94449 × 10−21.2896 × 101869.6956

The as-grown β-Ga2O3 has n-type with a carrier concentration of 1.1053 × 1018 cm−3 and mobility of 21.4752 cm2/V·s at RT. Greater carrier concentration was analyzed in sample B compared with sample A with 2.5791 × 1018 cm−3, while its bulk mobility was compensated with the lowest value of 11.9946 cm2/V·s among the Ga2O3/SnO2 samples. As per Table 1, sample D has the greatest mobility of 69.6956 cm2/V·s among the other synthesized Ga2O3/SnO2 specimens. The carrier density increases to the order of 100 times as the Sn-concentration increases, implying that the electrical resistivity and the carrier concentration of β-Ga2O3 can be controlled by Sn doping in the range of 1016 to 1018 cm−3 [24].

As per Table 2, sample D showed the smallest power loss with 4.3403 × 10−6 W compared with samples B and C with 1.2610 × 10−5 W and 1.0476 × 10−5 W, respectively. Sample A had the greatest power loss compared to the three samples with SnO2. Sample D had the least conduction loss due to its low specific on-resistance among the Ga2O3/SnO2 specimens.


SamplePower loss Ploss (W)Specific on-resistance RON,sp (Ω·cm2)

A1.3147 × 10−54.2070 × 10−1
B1.2610 × 10−51.5132 × 10−1
C1.0476 × 10−54.6095 × 10−1
D4.3403 × 10−68.6806 × 10−2

4. Conclusions

The result of this study highlighted that the HVPG technique was effective in the production of different nanostructures. The as-grown Ga2O3 nanowires were produced with an average diameter of 90.976 nm. When SnO2 was mixed up, the appearance of globules was apparent indicating the presence of Sn in the samples.

There was a direct correspondence on the size of nanostructures and globules to the concentration of Ga2O3 and SnO2 as observed in the SEM images. When the concentration of SnO2 was increased, the size of the nanostructures likewise increased and the appearance of the globules became more apparent. A large amount of SnO2 produced more globules, which led to an increase in the size of the nanostructures but decreased on its quantity. Consequently, the globules fell off onto the substrate since the number of nanostructures was not enough to hold them permanently.

EDX findings revealed that both globules and nanostructures were composed of mixed Ga, Sn, and O atoms. The major composition of nanostructures was Ga, while the globules were Sn. Nevertheless, the long exposure of the samples to Au sputtering affected the EDX results.

All Ga2O3/SnO2 samples were dominated by Raman peak located at 662 cm−1 and grew at [010] direction, which exhibits the highest electrical conductivity for β-Ga2O3. Doping of SnO2 was proven to unfold the ε polytype of Ga2O3. The rutile peaks of SnO2 and peaks due to its disorder activation were identified in the Ga2O3/SnO2 samples.

The I–V curves of the samples showed similarity to the literature. Furthermore, the incorporation of Sn was proven to lower the resistivity of the undoped sample. The decrease in resistivity was attributed to the presence of Sn+4. When some of the Ga+3 ions in the lattice were replaced by Sn+4 or some of the Sn ions as interstitial atoms were located in the lattice, conduction electrons were produced as supported by the presented Raman data and previous research works. It was likewise clinched that Ga2O3/SnO2 has the potential to meet the criteria for the selection of semiconductor substrate suitable for the fabrication of power electronics devices. On the other hand, there was an indirect correspondence between mobility and carrier concentration since the former increased and the latter decreased when the concentration of SnO2 was augmented. For the application, it was concluded that the highest concentration of SnO2 exhibited the lowest power loss and specific on-resistance. It was ascertained that it has the potential to be used for power electronics applications. Future research shall be geared towards the analysis of the mechanical behavior of the Ga2O3/SnO2 nanostructures. Also, exploring the p-type and ohmic contacts suitable for Ga2O3/SnO2 shall be investigated to realize its full potential for the fabrication of power electronic devices such as the Schottky barrier diode and metal oxide semiconductor field-effect transistor.

Data Availability

All data used in this manuscript are cited within the article.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this paper.

Acknowledgments

The authors would like to express their appreciation to the iNano Lab graduate students, Staffs of the Surface Physics Laboratory, the DLSU College of Science, and Jumar Cadondon for the FTIR micrographs. The publication expenses of this study were funded by the DOST PCIEERD, Commission on Higher Education, DLSU Science Foundation, and iNano.

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Copyright © 2020 Lester D. Bernardino and Gil Nonato C. Santos. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


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