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Hunter D. Ellis

Publications and source records attributed to Hunter D. Ellis.

12 recordsLinked to original sources

Crystallinity Evolution of MOCVD-Grown $β$-Ga$_2$O$_3$ Films Probed by In Situ HT-XRD under Different Reactor Heights

The crystallinity of $β$-Ga$_2$O$_3$ thin films grown by metal-organic chemical vapor deposition (MOCVD) is strongly influenced by reactor design and the resulting growth environment. In this work, we investigate the role of reactor height on the crystallinity evolution of MOCVD-grown $β$-Ga$_2$O$_3$ films by directly comparing long- and short-chamber showerhead configurations. Structural evolution was probed by in situ high-temperature X-ray diffraction (HT-XRD) as the MOCVD-grown films were heated from 25~$^\circ$C to 1100~$^\circ$C. Temperature-dependent XRD reveals a consistent redshift of the $β$-Ga$_2$O$_3$~($-201$) reflection after HT-XRD heating and subsequent cooling to room temperature for both reactor geometries, indicating a similar thermally driven strain response. Quantitative rocking-curve analysis shows a non-monotonic temperature dependence of the ($-201$) full width at half maximum (FWHM), with minimum values of approximately 2.03$^\circ$ and 2.72$^\circ$ for the short- and long-chamber films, respectively, reflecting differences in mosaic alignment established during growth. Atomic force microscopy further shows that short-chamber-grown films exhibit smoother surfaces, with root-mean-square roughness values of approximately 7.7~nm before and 7.3~nm after HT-XRD heating, compared to 19.3~nm and 12.3~nm, respectively, for long-chamber-grown films. Overall, these results indicate that reactor height influences the initial crystalline and morphological templates of $β$-Ga$_2$O$_3$ films and modulates their elevated-temperature structural response, providing practical insights for optimizing MOCVD reactor design for high-quality $β$-Ga$_2$O$_3$ growth.

cond-mat.mtrl-sci

Dosimetry for Proton Therapy Using a β-Ga$_2$O$_3$ Metal-Semiconductor-Metal Detector with Low-Noise Amplification

Intensity-modulated proton therapy (IMPT) employs proton radiation rather than conventional X-rays to treat cancerous tumors. This approach offers significant advantages by minimizing the radiation exposure of surrounding healthy tissue, leading to improved patient outcomes and reduced side effects compared to traditional X-ray therapy. To ensure patient safety, each treatment plan must be experimentally validated before clinical implementation. However, current dosimetry devices face limitations in performing angled beam measurements and obtaining multi-depth assessments, both of which are essential for verifying IMPT treatment plans. In this study, the performance of a β-Ga$_2$O$_3$-based metal-semiconductor-metal (MSM) detector with a low-noise amplifier is studied and evaluated under various proton radiation doses and energy levels delivered by a MEVION S250i proton accelerator. The detector performance is also compared with that of an ionization chamber. The β-Ga$_2$O$_3$ detector exhibits a linear response with proton dose for single-spot irradiations, and its response to varying proton energies closely matches both the ion chamber data and simulated dose distributions. These findings highlight the potential of β-Ga$_2$O$_3$-based detectors as robust dosimetry devices for IMPT applications.

physics.med-ph

High thermal conductivity of rutile-GeO$_2$ films grown by MOCVD: $52.9~\mathrm{W\,m^{-1}\,K^{-1}}$

Rutile germanium dioxide (r-GeO2) has recently emerged as a promising ultrawide-bandgap (UWBG) semiconductor owing to its wide bandgap (~4.4-5.1 eV), ambipolar doping potential, and high theoretical thermal conductivity. However, experimental data on the thermal conductivity of r-GeO2 epitaxial layers have not been reported, primarily due to challenges in phase control and surface roughness. Here, we report a high thermal conductivity of 52.9 +/- 6.6 W m^-1 K^-1 for high-quality (002) r-GeO2 films grown by metal-organic chemical vapor deposition (MOCVD) and characterized using time-domain thermoreflectance (TDTR). The phase control was achieved through a seed-driven stepwise crystallization (SDSC) approach, and the surface roughness was significantly reduced from 76 nm to 16 nm (locally as low as 1 A) via chemical mechanical polishing (CMP). These results highlight the promise of r-GeO2 as a UWBG oxide platform for power electronics applications.

cond-mat.mtrl-sci

$β$-Ga$_2$O$_3$--Based Radiation Detector for Proton Therapy

Intensity modulated proton therapy (IMPT) is an advanced cancer treatment modality that offers significant advantages over conventional X-ray therapies, particularly in its ability to minimize radiation dose beyond the tumor target. This reduction in unnecessary irradiation exposure significantly lowers the risk to surrounding healthy tissue and reduces side effects compared to conventional X-ray treatments. However, due to the high complexity of IMPT plans, each plan must be independently validated to ensure the safety and efficacy of the radiation exposure to the patient. While ion chambers are currently used for this purpose, their limitations-particularly in angled-beam measurements and multi-depth assessments-hinder their effectiveness. Silicon-based detectors, commonly used in X-ray therapy, are unsuitable for IMPT due to their rapid degradation under proton irradiation. In this study, a $β$-Ga$_2$O$_3$-based metal-semiconductor-metal (MSM) detector was evaluated and compared with a commercial ion chamber using a MEVION S250i proton accelerator. The $β$-Ga$_2$O$_3$ detector demonstrated reliable detection of single-pulse proton doses as low as 0.26 MU and exhibited a linear charge-to-dose relationship across a wide range of irradiation conditions. Furthermore, its measurement variability was comparable to that of the ion chamber, with improved sensitivity observed at higher bias voltages. These results highlight the strong potential of $β$-Ga$_2$O$_3$ as a radiation-hard detector material for accurate dose verification in IMPT.

physics.med-ph

Study of Optical Properties of MOCVD-Grown Rutile GeO2 Films

Rutile germanium dioxide (r-GeO$_2$) is a promising ultra-wide bandgap (UWBG) semiconductor, offering a high theoretical Baliga figure of merit, potential for p-type doping, and favorable thermal and electrical properties. In this work, we present a comprehensive optical investigation of crystalline r-GeO$_2$ thin films grown on r-TiO$_2$ (001) substrates via metal-organic chemical vapor deposition (MOCVD). Cathodoluminescence (CL) spectroscopy reveals broad visible emissions with distinct peaks near 470~nm and 520~nm. CL mapping indicates enhanced emission intensity in regions with larger crystalline domains, highlighting the correlation between domain size and optical quality. X-ray photoelectron spectroscopy (XPS) confirms the presence of Ge$^{4+}$ oxidation state and provides a bandgap estimation of $\sim$4.75~eV based on valence band and secondary electron cutoff analysis. UV--Vis transmittance measurements show a sharp absorption edge near 250--260~nm, corresponding to an optical bandgap in the range of 4.81--5.0~eV. These findings offer valuable insights into the defect-related emission behavior and band-edge characteristics of r-GeO$_2$, reinforcing its potential for future applications in power electronics and deep-ultraviolet optoelectronic devices.

cond-mat.mtrl-sci

Phase Competition and Rutile Phase Stabilization of Growing GeO2 Films by MOCVD

Rutile germanium dioxide (r-GeO2) is an ultra-wide bandgap semiconductor with potential for ambipolar doping, making it a promising candidate for next-generation power electronics and optoelectronics. Growth of phase-pure r-GeO2 films by vapor phase techniques like metalorganic chemical vapor deposition (MOCVD) is challenging because of polymorphic competition from amorphous and quartz GeO2. Here, we introduce seed-driven stepwise crystallization (SDSC) as a segmented growth strategy for obtaining r-GeO2 films on r-TiO2 (001) substrate. SDSC divides the growth into repeated cycles of film deposition and cooling-heating ramps, which suppress the non-rutile phases. We discuss the underlying mechanisms of phase selection during SDSC growth. We demonstrate continuous, phase-pure, partially epitaxial r-GeO2 (001) films exhibiting x-ray rocking curves with a FWHM of 597 arcsec. SDSC-based growth provides a generalizable pathway for selective vapor-phase growth of metastable or unstable phases, offering new opportunities for phase-selective thin-film engineering.

cond-mat.mtrl-sci

Seed-Driven Stepwise Crystallization (SDSC) for Growing Rutile GeO2 Films via MOCVD

Germanium dioxide (r-GeO2) is an emerging new ultrawide bandgap (UWBG) semiconductor with significant potential for power electronics, thanks to its large-size substrate compatibility and ambipolar doping capability. However, phase segregation during metal-organic chemical vapor deposition (MOCVD) on substrates like r-TiO2 has posed a significant barrier to achieving high-quality films. Conventional optimization of growth parameters has been found so far not very insufficient in film coverage and film quality. To address this, a seed-driven stepwise crystallization (SDSC) growth approach was employed in this study, featuring multiple sequential deposition steps on a pre-templated substrate enriched with r-GeO2 seeds. The process began with an initial 180-minute deposition to establish r-GeO2 nucleation seeds, followed by a sequence of shorter deposition steps (90, 60, 60, 60, 60, and 60 minutes). This stepwise growth strategy progressively increased the crystalline coverage to 57.4%, 77.49%, 79.73%, 93.27%, 99.17%, and ultimately 100%. Concurrently, the crystalline quality improved substantially, evidenced by a ~30% reduction in the Full Width at Half Maximum (FWHM) of X-ray diffraction rocking curves. These findings demonstrate the potential of the SDSC approach for overcoming phase segregation and achieving high-quality, large-area r-GeO2 films.

cond-mat.mtrl-sci

Carbon-Nanotube/$β$-Ga$_2$O$_3$ Heterojunction PIN Diodes

$β$-Ga$_2$O$_3$ is gaining attention as a promising semiconductor for next-generation high-power, high-efficiency, and high-temperature electronic devices, thanks to its exceptional material properties. However, challenges such as the lack of viable p-type doping have hindered its full potential, particularly in the development of ambipolar devices. This work introduces a novel heterojunction diode (HD) that combines p-type carbon nanotubes (CNTs) with i/n-type $β$-Ga$_2$O$_3$ to overcome these limitations. For the first time, a CNT/$β$-Ga$_2$O$_3$ hetero-p-n-junction diode is fabricated. Compared to a traditional Schottky barrier diode (SBD) with the same $β$-Ga$_2$O$_3$ epilayer, the CNT/$β$-Ga$_2$O$_3$ HD demonstrates significant improvements, including a higher rectifying ratio ($1.2 \times 10^{11}$), a larger turn-on voltage (1.96 V), a drastically reduced leakage current at temperatures up to 300 °C, and a 26.7% increase in breakdown voltage. Notably, the CNT/$β$-Ga$_2$O$_3$ HD exhibits a low ideality factor of 1.02, signifying an ideal interface between the materials. These results underline the potential of CNT/$β$-Ga$_2$O$_3$ heterojunctions for electronic applications, offering a promising solution to current limitations in $β$-Ga$_2$O$_3$-based devices.

physics.app-ph

A TEM Study of MOCVD-Grown Rutile GeO2 Films

Ultrawide bandgap (UWBG) semiconductors are promising for next-generation power electronics, largely attributed to their substantial bandgap and exceptional breakdown electric field. Rutile GeO2 (r-GeO2) emerges as a promising alternative, particularly because of its ambipolar dopability. However, research on r-GeO2 is still in its infancy, and further investigation into its structural properties is essential for enhancing epilayer quality. In our previous work, we identified distinct surface morphologies; square-patterned and smooth regions of epitaxial r-GeO2 films grown on r-TiO2 (001) substrates using metal-organic chemical vapor deposition (MOCVD).This research employs transmission electron microscopy (TEM) to investigate the structural characteristics of the material. The findings indicate that the square-patterned regions are crystalline, whereas the smooth regions exhibit amorphous properties. The measured lattice spacing in the (110) plane is 0.324 nm, slightly exceeding the theoretical value of 0.312 nm. This discrepancy suggests the presence of tensile strain in the r-GeO2 film, resulting from lattice mismatch or thermal expansion differences with the substrate. We also observed a threading dislocation density of 1.83*10^9 cm-2, consisting of 11.76% screw-type, 29.41% edge-type, 55.89% mixed-type dislocations, and 2.94% planar defects. These findings offer valuable insights into the growth mechanisms and defect characteristics of r-GeO2.

cond-mat.mtrl-sci

Epitaxial Growth of Rutile GeO$_2$ via MOCVD

Rutile Germanium Dioxide (r-GeO$_2$) has been identified as an ultrawide bandgap (UWBG) semiconductor recently, featuring a bandgap of 4.68 eV, comparable to Ga$_2$O$_3$ but offering bipolar dopability, higher electron mobility, higher thermal conductivity, and higher Baliga's figure of merit (BFOM).These superior properties position GeO$_2$ as a promising material for various semiconductor applications. However, the epitaxial growth of r-GeO$_2$, particularly in its most advantageous rutile polymorph, is still at an early stage. This work explores the growth of r-GeO$_2$ using metal-organic chemical vapor deposition (MOCVD) on an r-TiO$_2$ (001) substrate, utilizing tetraethyl germane (TEGe) as the precursor. Our investigations reveal that higher growth temperatures significantly enhance crystalline quality, achieving a full width at half maximum (FWHM) of 0.181 degree at 925 degree C, compared to 0.54 degree at 840 degree C and amorphous structures at 725 degree C. Additionally, we found that longer growth durations increase surface roughness due to the formation of faceted crystals. Meanwhile, adjusting the susceptor rotation speed from 300 RPM to 170 RPM plays a crucial role in optimizing crystalline quality, effectively reducing surface roughness by approximately 15 times. This study offers a foundational guide for optimizing MOCVD growth conditions of r-GeO$_2$ films, emphasizing the crucial need for precise control over deposition temperature and rotation speed to enhance adatom mobility and effectively minimize the boundary layer thickness.

physics.app-ph

Growth of GeO2 on R-plane and C-plane Sapphires by MOCVD

Rutile Germanium Dioxide (GeO2) has been recently theoretically identified as an ultrawide bandgap (UWBG) semiconductor with bandgap 4.68 eV similar to Ga2O3 but having bipolar dopability and ~2x higher electron mobility, Baliga figure of merit (BFOM) and thermal conductivity than Ga2O3. Bulk crystal growth is rapidly moving towards making large sized native substrates available. These outstanding material properties position GeO2 as a highly attractive UWBG semiconductor for various applications. However, the epitaxial growth in the most advantageous polymorph (rutile), ensuring controlled phase, pristine surface/interface quality, precise microstructure, and optimal functional properties, is still in its infancy. In this work, we explored growth of GeO2 by metal-organic chemical vapor deposition (MOCVD) on both C- and R-plane sapphire. Utilizing tetramethylgermane (TMGe) as a precursor, we have investigated the influences of different parameters on the film properties, including growth temperature, chamber pressure, TMGe flow rate, oxygen flow rate, shroud gas flow rate, and rotation speed. The total pressure emerged as a crucial parameter while growth attempts at low total pressure resulted in no films for a wide range of temperatures, precursor flow rate, argon flow rates, and susceptor rotation rate. A phase diagram, derived from our experimental findings, delineates the growth windows for GeO2 films on sapphire substrates. This study serves as a pioneering guide for the MOCVD growth of GeO2 films.

cond-mat.mtrl-sci

Robust Diamond/\b{eta}-Ga2O3 Hetero-p-n-junction Via Mechanically Integrating Their Building Blocks

We report a novel approach for crafting robust diamond/\b{eta}-Ga2O3 hetero-p-n-junctions through the mechanical integration of their bulk materials. This resulting heterojunction, with a turn-on voltage of ~2.7 V at room temperature, exhibits resilient electrical performance across a temperature spectrum up to 125°C, displaying minimal hysteresis-measuring as low as 0.2 V at room temperature and below 0.7 V at 125°C. Remarkably, the ideality factor achieves a record low value of 1.28, setting a new benchmark for diamond/ \b{eta}-Ga2O3 heterojunctions. The rectification ratio reaches over 10^8 at different temperatures. This effortlessly fabricated and remarkably resilient diamond/Ga2O3 hetero-p-n-junction pioneers a novel pathway for the exploration and fabrication of heterojunctions for ultra-wide bandgap semiconductors with substantial lattice mismatch and different thermal expansion coefficients.

cond-mat.mtrl-sci