Search Results (18)

Using the Bridgman technique, GaSe single crystals were obtained which were mechanically split into plane-parallel plates with a wide range of thicknesses. By heat treatment in air at 820 °C and 900 °C, for 30 min and 6 h, micro- and nanocomposite layers of Ga₂Se₃–Ga₂O₃ and β–Ga₂O₃ (native oxide) with surfaces made of nanowires/nanoribbons were obtained. The obtained composite Ga₂Se₃–Ga₂O₃ and nanostructured β–Ga₂O₃ are semiconductor materials with band gaps of 2.21 eV and 4.60 eV (gallium oxide) and photosensitivity bands in the green–red and ultraviolet-C regions that peaked at 590 nm and 262 nm. For an applied voltage of 50 V, the dark current in the photodetector based on the nanostructured β–Ga₂O₃ layer was of 8.0 × 10⁻¹³ A and increased to 9.5 × 10⁻⁸ A upon 200 s excitation with 254 nm-wavelength radiation with a power density of 15 mW/cm². The increase and decrease in the photocurrent are described by an exponential function with time constants of τ_1r = 0.92 s, τ_2r = 14.0 s, τ_1d = 2.18 s, τ_2d = 24 s, τ_1r = 0.88 s, τ_2r = 12.2 s, τ_1d = 1.69 s, and τ_2d = 16.3 s, respectively, for the photodetector based on the Ga₂Se₃–Ga₂S₃–GaSe composite. Photoresistors based on the obtained Ga₂Se₃–Ga₂O₃ composite and nanostructured β–Ga₂O₃ layers show photosensitivity bands in the spectral range of electronic absorption bands of ozone in the same green–red and ultraviolet-C regions, and can serve as ozone sensors (detectors). Full article

Gallium oxide (Ga₂O₃), an ultrawide bandgap semiconductor, is an ideal material for solar-blind photodetectors, but challenges such as low responsivity and response speed persist. In this paper, one-dimensional (1D) Ga₂O₃ nanorods were designed to achieve high photodetection performance due to their effective light absorption and light field confinement. Through modulating source concentration, pH value, temperature, and reaction time, 1D β-Ga₂O₃ nanorods were controllably fabricated using a cost-effective hydrothermal method, followed by post-annealing. The nanorods had a diameter of ~500 nm, length from 0.5 to 3 μm, and structure from nanorods to spindles, indicating that different β-Ga₂O₃ nanorods can be utilized controllably through tuning reaction parameters. The 1D β-Ga₂O₃ nanorods with a high length-to-diameter ratio were chosen to construct metal-semiconductor-metal type photodetectors. These devices exhibited a high responsivity of 8.0 × 10⁻⁴ A/W and detectivity of 4.58 × 10⁹ Jones under 254 nm light irradiation. The findings highlighted the potential of 1D Ga₂O₃ nanostructures for high-performance solar-blind ultraviolet photodetectors, paving the way for future integrable deep ultraviolet optoelectronic devices. Full article

In this study, chemical deposition was used to synthesize structures of Ga₂O₃ -NW/SiO₂/Si (NW—nanowire) at 348 K and SnO₂-NW/SiO₂/Si at 323 K in track templates SiO₂/Si (either n- or p-type). The resulting crystalline nanowires were δ-Ga₂O₃ and orthorhombic SnO₂. Computer modeling of the delta phase of gallium oxide yielded a lattice parameter of a = 9.287 Å, which closely matched the experimental range of 9.83–10.03 Å. The bandgap is indirect with an Eg = 5.5 eV. The photoluminescence spectra of both nanostructures exhibited a complex band when excited by light with λ = 5.16 eV, dominated by luminescence from vacancy-type defects. The current–voltage characteristics of δ-Ga₂O₃ NW/SiO₂/Si-p showed one-way conductivity. This structure could be advantageous in devices where a reverse current is undesirable. The p-n junction with a complex structure was formed. This junction consists of a polycrystalline nanowire base exhibiting n-type conductivity and a monocrystalline Si substrate with p-type conductivity. The I–V characteristics of SnO₂-NW/SiO₂/Si suggested near-metallic conductivity due to the presence of metallic tin. Full article

Metal oxide core–shell fibrous nanostructures are promising gas-sensitive materials for the detection of a wide variety of both reducing and oxidizing gases. In these structures, two dissimilar materials with different work functions are brought into contact to form a coaxial heterojunction. The influence of the shell material on the transportation of the electric charge carriers along these structures is still not very well understood. This is due to homo-, hetero- and metal/semiconductor junctions, which make it difficult to investigate the electric charge transfer using direct current methods. However, in order to improve the gas-sensing properties of these complex structures, it is necessary to first establish a good understanding of the electric charge transfer in ambient air. In this article, we present an impedance spectroscopy study of networked SnO₂/Ga₂O₃ core–shell nanobelts in ambient air. Tin dioxide nanobelts were grown directly on interdigitated gold electrodes, using the thermal sublimation method, via the vapor–liquid–solid (VLS) mechanism. Two forms of a gallium oxide shell of varying thickness were prepared via halide vapor-phase epitaxy (HVPE), and the impedance spectra were measured at 189–768 °C. The bulk resistance of the core–shell nanobelts was found to be reduced due to the formation of an electron accumulation layer in the SnO₂ core. At temperatures above 530 °C, the thermal reduction of SnO₂ and the associated decrease in its work function caused electrons to flow from the accumulation layer into the Ga₂O₃ shell, which resulted in an increase in bulk resistance. The junction resistance of said core–shell nanostructures was comparable to that of SnO₂ nanobelts, as both structures are likely connected through existing SnO₂/SnO₂ homojunctions comprising thin amorphous layers. Full article

Gallium oxide (Ga₂O₃) is a promising material for high-power semiconductor applications due to its wide band gap and high breakdown voltage. However, the current methods for fabricating Ga₂O₃ nanostructures have several disadvantages, including their complex manufacturing processes and high costs. In this study, we report a novel approach for synthesizing β-Ga₂O₃ nanostructures on gallium phosphide (GaP) using ultra-short laser pulses for in situ nanostructure generation (ULPING). We varied the process parameters to optimize the nanostructure formation, finding that the ULPING method produces high-quality β-Ga₂O₃ nanostructures with a simpler and more cost-effective process when compared with existing methods. Scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDX) were used to characterize the samples, which indicated the presence of phosphorous. X-ray photoelectron spectroscopy (XPS) confirmed the formation of gallium oxide, along with a minor amount of phosphorus-containing compounds. Structural analysis using X-ray diffraction (XRD) revealed the formation of a monoclinic β-polymorph of Ga₂O₃. We also measured the band gap of the materials using reflection electron energy loss spectroscopy (REELS), and found that the band gap increased with higher nanostructure formation, reaching 6.2 eV for the optimized sample. Furthermore, we observed a change in the heterojunction alignment, which we attribute to the change in the oxidation of the samples. Our results demonstrate the potential of ULPING as a novel, simple, and cost-effective method for fabricating Ga₂O₃ nanostructures with tunable optical properties. The ULPING method offers a green alternative to existing fabrication methods, making it a promising technology for future research in the field of Ga₂O₃ nanostructure fabrication. Full article

The scientific field of two-dimensional (2D) nanostructures has witnessed tremendous development during the last decade. To date, different synthesis approaches have been developed; therefore, various exceptional properties of this family of advanced materials have been discovered. It has recently been found that the natural surface oxide films of room-temperature liquid metals is an emerging platform for the synthesis of novel types of 2D nanostructures with numerous functional applications. However, most of the developed synthesis techniques for these materials are based on the direct mechanical exfoliation of 2D materials as research targets. This paper reports a facile and functional sonochemical-assisted approach for the synthesis of 2D hybrid and complex multilayered nanostructures with tunable characteristics. In this method, the intense interaction of acoustic waves with microfluidic gallium-based room-temperature liquid galinstan alloy provides the activation energy for synthesis of hybrid 2D nanostructures. The microstructural characterizations reveal the impact of sonochemical synthesis parameters, including the processing time and composition of the ionic synthesis environment, on the growth of Ga_xO_y/Se 2D hybrid structures and InGa_xO_y/Se multilayered crystalline structures with tunable photonic characteristics. This technique shows promising potential for synthesis of various types of 2D and layered semiconductor nanostructures with tunable photonic characteristics. Full article

Plasmonic nanostructures ensure the reception and harvesting of visible lights for novel photonic applications. In this area, plasmonic crystalline nanodomains decorated on the surface of two-dimensional (2D) semiconductor materials represent a new class of hybrid nanostructures. These plasmonic nanodomains activate supplementary mechanisms at material heterointerfaces, enabling the transfer of photogenerated charge carriers from plasmonic antennae into adjacent 2D semiconductors and therefore activate a wide range of visible-light assisted applications. Here, the controlled growth of crystalline plasmonic nanodomains on 2D Ga₂O₃ nanosheets was achieved by sonochemical-assisted synthesis. In this technique, Ag and Se nanodomains grew on 2D surface oxide films of gallium-based alloy. The multiple contribution of plasmonic nanodomains enabled the visible-light-assisted hot-electron generation at 2D plasmonic hybrid interfaces, and therefore considerably altered the photonic properties of the 2D Ga₂O₃ nanosheets. Specifically, the multiple contribution of semiconductor–plasmonic hybrid 2D heterointerfaces enabled efficient CO₂ conversion through combined photocatalysis and triboelectric-activated catalysis. The solar-powered acoustic-activated conversion approach of the present study enabled us to achieve the CO₂ conversion efficiency of more than 94% in the reaction chambers containing 2D Ga₂O₃-Ag nanosheets. Full article

In this study, we report enhancement of terahertz (THz) radiation with indium-tin-oxide (ITO) thin-film deposited on semi-insulating gallium arsenide substrate (SI-GaAs). The amplitude of THz emission from both ITO/SI-GaAs and bare SI-GaAs substrate as a function of optical pump (i) incident angle, (ii) polarization angle, and (iii) power were investigated. The enhancement of peak amplitude of a THz pulse transmitted through the ITO/SI-GaAs sample in comparison to bare SI-GaAs substrate varied from 100% to 0% when the pump incidence angle changed from 0° to 50°. The maximum enhancement ratio of peak amplitude for a coated sample relative to the bare substrate is approximately up to 2.5 times at the minimum pump intensity of 3.6 TW/m² and gradually decreased to one at the maximum pump intensity of 20 TW/m². From outcomes of these studies, together with data on surface and material characterization of the samples, we show that THz emission originates from the ITO/GaAs interfaces. Further, both interface-field-induced transient current and field-induced optical rectification contribute to the observed THz signal. Observed enhancement was tentatively attributed to surface-plasmon-induced local field enhancement, coupled with constructive interference of forward and retro-reflected backward THz emission from the ITO/GaAs interfaces. The polarity-flip reported previously for very thin Au-coated GaAs was not observed. This was explained by the wide-bandgap, transparency and lower free carriers of ITO. For best results, the incident angle should be in the range of 0 to 30° and the incident polarization should be 0 to 45°. We further predict that the ITO thin film of suitable thickness or with engineered nanostructures, post-annealed under optimum conditions may lead to further enhancement of THz radiation from ITO-coated semiconductor surfaces. Full article

β-Ga₂O₃ nanostructures, including nanowires (NWs), nanosheets (NSHs), and nanorods (NRs), were synthesized using thermally dewetted Au nanoparticles as catalyst in a chemical vapor deposition process. The morphology of the as-grown β-Ga₂O₃ nanostructures depends strongly on the growth temperature and time. Successful growth of β-Ga₂O₃ NWs with lengths of 7–25 μm, NSHs, and NRs was achieved. It has been demonstrated that the vapor–liquid–solid mechanism governs the NW growth, and the vapor–solid mechanism occurs in the growth of NSHs and NRs. The X-ray diffraction analysis showed that the as-grown nanostructures were highly pure single-phase β-Ga₂O₃. The bandgap of the β-Ga₂O₃ nanostructures was determined to lie in the range of 4.68–4.74 eV. Characteristic Raman peaks were observed with a small blue and red shift, both of 1–3 cm⁻¹, as compared with those from the bulk, indicating the presence of internal strain and defects in the as-grown β-Ga₂O₃ nanostructures. Strong photoluminescence emission in the UV-blue spectral region was obtained in the β-Ga₂O₃ nanostructures, regardless of their morphology. The UV (374–377 nm) emission is due to the intrinsic radiative recombination of self-trapped excitons present at the band edge. The strong blue (404–490 nm) emissions, consisting of five bands, are attributed to the presence of the complex defect states in the donor (V_O) and acceptor (V_Ga or V_Ga–O). These β-Ga₂O₃ nanostructures are expected to have potential applications in optoelectronic devices such as tunable UV–Vis photodetectors. Full article

Gallium oxide, as an emerging semiconductor, has attracted a lot of attention among researchers due to its high band gap (4.8 eV) and a high critical field with the value of 8 MV/cm. This paper presents a review on different chemical and physical techniques for synthesis of nanostructured β-gallium oxide, as well as its properties and applications. The polymorphs of Ga₂O₃ are highlighted and discussed along with their transformation state to β-Ga₂O₃. Different processes of synthesis of thin films, nanostructures and bulk gallium oxide are reviewed. The electrical and optical properties of β-gallium oxide are also highlighted, based on the synthesis methods, and the techniques for tuning its optical and electrical properties compared. Based on this information, the current, and the possible future, applications for β-Ga₂O₃ nanostructures are discussed. Full article

Interest in the synthesis and fabrication of gallium oxide (Ga₂O₃) nanostructures as wide bandgap semiconductor-based ultraviolet (UV) photodetectors has recently increased due to their importance in cases of deep-UV photodetectors operating in high power/temperature conditions. Due to their unique properties, i.e., higher surface-to-volume ratio and quantum effects, these nanostructures can significantly enhance the sensitivity of detection. In this work, two Ga₂O₃ nanostructured films with different nanowire densities and sizes obtained by thermal oxidation of Ga on quartz, in the presence and absence of Ag catalyst, were investigated. The electrical properties influenced by the density of Ga₂O₃ nanowires (NWs) were analyzed to define the configuration of UV detection. The electrical measurements were performed on two different electric contacts and were located at distances of 1 and 3 mm. Factors affecting the detection performance of Ga₂O₃ NWs film, such as the distance between metal contacts (1 and 3 mm apart), voltages (5–20 V) and transient photocurrents were discussed in relation to the composition and nanostructure of the Ga₂O₃ NWs film. Full article

The importance of Ga₂O₃-based material for harsh environmental applications has attracted the interest of researchers in exploring various fabrication and growth techniques of Ga₂O₃-based nanomaterials using effective and low-cost processes. Herein, a demonstration to improve the wettability of liquid gallium on a rough silicon surface is presented. To control the roughness process, the silicon surface was patterned and groove-shape structures on the silicon were created using a photoelectrochemical (PEC) etching technique. Gallium oxide nanostructures were grown by thermal oxidation from liquid Ga in the presence and the absence of a silver thin film used as a catalyst. Scanning Electron Microscopy (SEM) was used to observe the morphology of the nanostructures grown on the roughed surface of the silicon substrate. The conformal deposition of Ga₂O₃ nanostructures inside the grooves of the PEC etched silicon surface was observed. The presence of Ag catalyst was found to completely change the morphology of Ga₂O₃. This method is recommended for the sustainable and low-cost synthesis of nanostructured gallium oxide for applications, including gas sensing. Full article

Silica nanosprings (NS) were coated with gallium nitride (GaN) by high-temperature atomic layer deposition. The deposition temperature was 800 °C using trimethylgallium (TMG) as the Ga source and ammonia (NH₃) as the reactive nitrogen source. The growth of GaN on silica nanosprings was compared with deposition of GaN thin films to elucidate the growth properties. The effects of buffer layers of aluminum nitride (AlN) and aluminum oxide (Al₂O₃) on the stoichiometry, chemical bonding, and morphology of GaN thin films were determined with X-ray photoelectron spectroscopy (XPS), high-resolution x-ray diffraction (HRXRD), and atomic force microscopy (AFM). Scanning and transmission electron microscopy of coated silica nanosprings were compared with corresponding data for the GaN thin films. As grown, GaN on NS is conformal and amorphous. Upon introducing buffer layers of Al₂O₃ or AlN or combinations thereof, GaN is nanocrystalline with an average crystallite size of 11.5 ± 0.5 nm. The electrical properties of the GaN coated NS depends on whether or not a buffer layer is present and the choice of the buffer layer. In addition, the IV curves of GaN coated NS and the thin films (TF) with corresponding buffer layers, or lack thereof, show similar characteristic features, which supports the conclusion that atomic layer deposition (ALD) of GaN thin films with and without buffer layers translates to 1D nanostructures. Full article

Gallium oxide (Ga₂O₃) is a new wide bandgap semiconductor with remarkable properties that offers strong potential for applications in power electronics, optoelectronics, and devices for extreme conditions. In this work, we explore the morphology of Ga₂O₃ nanostructures on different substrates and temperatures. We used silver catalysts to enhance the growth of Ga₂O₃ nanowires on substrates such as p-Si substrate doped with boron, 250 nm SiO₂ on n-Si, 250 nm Si₃N₄ on p-Si, quartz, and n-Si substrates by using a thermal oxidation technique at high temperatures (~1000 °C) in the presence of liquid silver paste that served as a catalyst layer. We present the results of the morphological, structural, and elemental characterization of the Ga₂O₃ nanostructures. This work offers in-depth explanation of the dense, thin, and long Ga₂O₃ nanowire growth directly on the surfaces of various types of substrates using silver catalysts. Full article

Gallium oxide (Ga₂O₃) thin films were fabricated on glass substrates using a combination of chemical bath deposition and post-annealing process. From the field-emission scanning electron microscopy and x-ray diffraction results, the GaOOH nanorods precursors with better crystallinity can be achieved under higher concentrations (≥0.05 M) of gallium nitrate (Ga(NO₃)₃). It was found that the GaOOH synthesized from lower Ga(NO₃)₃ concentration did not transform into α-Ga₂O₃ among the annealing temperatures used (400–600 °C). Under higher Ga(NO₃)₃ concentrations (≥0.05 M) with higher annealing temperatures (≥500 °C), the GaOOH can be transformed into the Ga₂O₃ film successfully. An α-Ga₂O₃ sample synthesized in a mixed solution of 0.075 M Ga(NO₃)₃ and 0.5 M hexamethylenetetramine exhibited optimum crystallinity after annealing at 500 °C, where the α-Ga₂O₃ nanostructure film showed the highest aspect ratio of 5.23. As a result, the photodegeneration efficiencies of the α-Ga₂O₃ film for the methylene blue aqueous solution can reach 90%. Full article