arXiv subjects

Bethany E. Matthews

Publications and source records attributed to Bethany E. Matthews.

12 recordsLinked to original sources

arXiv2026

Voltage-tunable Josephson Junctions on Germanium Quantum Wells with in-situ Aluminum Contacts

Voltage-tunable Josephson junctions (VT-JJs) are an emerging element in superconducting quantum electronics with potential to expand the functionality of conventional designs. While VT-JJs are largely compatible with wafer-scale semiconductor processing, their integration into quantum circuits remains a challenge due to unmitigated semiconductor microwave loss. Here, a deep mesa etch process, wherein the epitaxial material is removed except the VT-JJ device, will facilitate the integration of VT-JJs with low-microwave-loss circuit elements by allowing these circuit elements to be placed directly on a low-loss substrate. A Germanium quantum well is grown by Molecular Beam Epitaxy (MBE) on a float zone silicon substrate with in-situ deposited aluminum contacts. This combination allows the formation of an oxide-free superconductor-semiconductor interface. The deep mesa etch process is optimized to produce a sidewall taper sufficient for continuous metal deposition from the substrate to the top of the mesa for electrostatic gate electrodes and interconnects. The fabricated Josephson junctions demonstrate gate-tunable supercurrents with a maximum critical current over 100 nA and critical-current normal-resistance product of $8.63~μV$. These results demonstrate a pathway toward improved integration of voltage-tunable superconducting circuit elements with quantum electronic building blocks such as couplers and qubits.

cond-mat.mes-hall↗

arXiv2026

Multimode magnon-phonon cavity driven by symmetry-locked strain fields

Hybrid magnon-phonon cavities with precise control knobs are highly sought after for coherent energy and signal transduction in solid-state platforms. While strain offers a powerful means to tune magnonic characteristics, extending strain engineering into magnon-phonon hybridization has remained elusive. Moreover, implementing controllable strain at the meso- or nanoscale poses a formidable challenge, as spatial inhomogeneity of strain fields often leads to enhanced damping and reduced coherence, thereby hindering device integration and scalability. Here, we present an epitaxial La0.7Sr0.3MnO3/SrTiO3 (LSMO/STO) heterostructure that exhibits strong coupling between the Kittel magnon and acoustic phonon. Leveraging the emergence of structural domains when STO undergoes a cubic-to-tetragonal phase transition, we create anisotropic local strains at the interface. Remarkably, the anisotropic local strain of less than 0.1 % drives the pronounced splitting of the magnon into three branches. Each branch independently hybridizes with acoustic phonons, forming a matrix of magnon-phonon avoided crossings that underpins multimode transduction and programmable networks in frequency and magnetic field space. An analytical model reveals that the split magnon branches are deterministically locked to the three main crystalline axes, enabling robust, orientation-selective control of the hybridized magnon-phonon spectrum against spatial inhomogeneity. Our results establish designed local strain as an exceptionally sensitive trigger for multimode magnon-phonon hybridization in magnetoelastic oxide heterostructures, and highlight local strain engineering as a viable strategy for designing tunable hybrid magnonic and phononic devices.

cond-mat.mtrl-sci↗

arXiv2026

Sub-nanosecond control for spin-defect quantum memories with a low-cost, compact FPGA platform

Dynamical decoupling techniques are widely used to characterize and control the environments of solid-state quantum defects, enabling solid-state quantum memories and nanoscale quantum sensors. However, resolution is often limited by the timing granularity of control hardware, which can undersample narrow spectral features and distort extracted parameters. Here, we demonstrate sub-nanosecond timing control on an inexpensive FPGA-based platform by extending the open-source QICK (Quantum Instrumentation Control Kit) framework using a waveform-offset method. This approach achieves an effective timing resolution of 200~ps on an RF system-on-chip device without modification to the underlying hardware. We apply this capability to dynamical decoupling spectroscopy of nitrogen-vacancy centers in diamond, enabling precise extraction of hyperfine couplings of individual $^{13}\mathrm{C}$ nuclear spins and resolving spectral features that are otherwise undersampled. These results demonstrate that high-resolution, device-level characterization of spin-based quantum memories can be achieved using flexible, inexpensive control hardware, providing a scalable alternative to commercial arbitrary waveform generators.

quant-ph↗

arXiv2025

Selective Oxidation and Cr Segregation in High-Entropy Oxide Thin Films

High-entropy oxides (HEOs) offer exceptional compositional flexibility and structural stability, making them promising materials for energy and catalytic applications. Here, we investigate Sr doping effects on B-site cation oxidation states, local composition, and structure in epitaxial La1-xSrx(Cr0.2Mn0.2Fe0.2Co0.2Ni0.2)O3 thin films. X-ray spectroscopies reveal that Sr doping preferentially promotes Cr oxidation from Cr3+ to Cr6+, partially oxidizes Co and Ni, while leaving Mn4+ and Fe3+ unchanged. Atomic-resolution scanning transmission electron microscopy with energy-dispersive X-ray spectroscopy shows pronounced Cr segregation, with Cr exhibiting depletion at the film-substrate interface and enrichment at the film surface, along with the formation of a partially amorphous phase in heavily Sr-doped samples. This segregation is likely driven by oxidation-induced migration of smaller, high-valence Cr cations during the growth. These findings underscore the critical interplay between charge transfer, local strain, and compositional fluctuations, providing strategies to control surface composition and electronic structure in HEOs for more robust electrocatalyst design.

cond-mat.mtrl-sci↗

arXiv2024

Revealing the Evolution of Order in Materials Microstructures Using Multi-Modal Computer Vision

The development of high-performance materials for microelectronics, energy storage, and extreme environments depends on our ability to describe and direct property-defining microstructural order. Our present understanding is typically derived from laborious manual analysis of imaging and spectroscopy data, which is difficult to scale, challenging to reproduce, and lacks the ability to reveal latent associations needed for mechanistic models. Here, we demonstrate a multi-modal machine learning (ML) approach to describe order from electron microscopy analysis of the complex oxide La$_{1-x}$Sr$_x$FeO$_3$. We construct a hybrid pipeline based on fully and semi-supervised classification, allowing us to evaluate both the characteristics of each data modality and the value each modality adds to the ensemble. We observe distinct differences in the performance of uni- and multi-modal models, from which we draw general lessons in describing crystal order using computer vision.

cond-mat.mtrl-sci↗

arXiv2024

Isolation of Single Donors in ZnO

The shallow donor in zinc oxide (ZnO) is a promising semiconductor spin qubit with optical access. Single indium donors are isolated in a commercial ZnO substrate using plasma focused ion beam (PFIB) milling. Quantum emitters are identified optically by spatial and frequency filtering. The indium donor assignment is based on the optical bound exciton transition energy and magnetic dependence. The single donor emission is intensity and frequency stable with a transition linewidth less than twice the lifetime limit. The isolation of optically stable single donors post-FIB fabrication is promising for optical device integration required for scalable quantum technologies based on single donors in direct band gap semiconductors.

cond-mat.mes-hall↗

arXiv2023

Creation of color centers in diamond by recoil implantation through dielectric films

The need of near-surface color centers in diamond for quantum technologies motivates the controlled doping of specific extrinsic impurities into the crystal lattice. Recent experiments have shown that this can be achieved by momentum transfer from a surface precursor via ion implantation, an approach known as ``recoil implantation.'' Here, we extend this technique to incorporate dielectric precursors for creating nitrogen-vacancy (NV) and silicon-vacancy (SiV) centers in diamond. Specifically, we demonstrate that gallium focused-ion-beam exposure to a thin layer of silicon nitride or silicon dioxide on the diamond surface results in the introduction of both extrinsic impurities and carbon vacancies. These defects subsequently give rise to near-surface NV and SiV centers with desirable optical properties after annealing.

quant-ph↗

arXiv2023

Silicon-lattice-matched boron-doped gallium phosphide: A scalable acousto-optic platform

The compact size, scalability, and strongly confined fields in integrated photonic devices enable new functionalities in photonic networking and information processing, both classical and quantum. Gallium phosphide (GaP) is a promising material for active integrated photonics due to its high refractive index, wide band gap, strong nonlinear properties, and large acousto-optic figure of merit. In this work we demonstrate that silicon-lattice-matched boron-doped GaP (BGaP), grown at the 12-inch wafer scale, provides similar functionalities as GaP. BGaP optical resonators exhibit intrinsic quality factors exceeding 25,000 and 200,000 at visible and telecom wavelengths respectively. We further demonstrate the electromechanical generation of low-loss acoustic waves and an integrated acousto-optic (AO) modulator. High-resolution spatial and compositional mapping, combined with ab initio calculations indicate two candidates for the excess optical loss in the visible band: the silicon-GaP interface and boron dimers. These results demonstrate the promise of the BGaP material platform for the development of scalable AO technologies at telecom and provide potential pathways toward higher performance at shorter wavelengths.

physics.optics↗

arXiv2022

Jahn-Teller-driven Phase Segregation in Mn$_{x}$Co$_{3-x}$O$_{4}$ Spinel Thin Films

Transition metal spinel oxides comprised of Earth-abundant Mn and Co have long been explored for their use in catalytic reactions and energy storage. However, understanding of functional properties can be challenging due to differences in sample preparation and the ultimate structural properties of the materials. Epitaxial thin film synthesis provides a novel means of producing precisely-controlled materials to explore the variations reported in the literature. In this work, Mn$_{x}$Co$_{3-x}$O$_{4}$ samples from x = 0 to x = 1.28 were synthesized through molecular beam epitaxy and characterized to develop a material properties map as a function of stoichiometry. Films were characterized via in situ X-ray photoelectron spectroscopy, X-ray diffraction, scanning transmission electron microscopy, and polarized K-edge X-ray absorption spectroscopy. Mn cations within this range were found to be octahedrally coordinated, in line with an inverse spinel structure. Samples largely show mixed Mn$^{3+}$ and Mn$^{4+}$ character with evidence of phase segregation tendencies with increasing Mn content and increasing Mn$^{3+}$ formal charge. Phase segregation may occur due to structural incompatibility between cubic and tetragonal crystal structures associated with Mn$^{4+}$ and Jahn-Teller active Mn$^{3+}$ octahedra, respectively. Our results help to explain the reported differences across samples in these promising materials for renewable energy technologies.

cond-mat.mtrl-sci↗

arXiv2022

Resolving diverse oxygen transport pathways across Sr-doped lanthanum ferrite and metal-perovskite heterostructures

Perovskite structured transition metal oxides are important technological materials for catalysis and solid oxide fuel cell applications. Their functionality often depends on oxygen diffusivity and mobility through complex oxide heterostructures, which can be significantly impacted by structural and chemical modifications, such as doping. Further, when utilized within electrochemical cells, interfacial reactions with other components (e.g. Ni- and Cr-based alloy electrodes and interconnects) can influence the perovskite's reactivity and ion transport, leading to complex dependencies that are difficult to control in real-world environments. Here we use isotopic tracers and atom probe tomography to directly visualize oxygen diffusion and transport pathways across perovskite and metal-perovskite heterostructures, i.e. (Ni-Cr coated) Sr-doped lanthanum ferrite (LSFO). Annealing in 18O2(g) results in elemental and isotopic redistributions through oxygen exchange (OE) in the LSFO while Ni-Cr undergoes oxidation via multiple mechanisms and transport pathways. Complementary density functional theory (DFT) calculations at experimental conditions provide rationale for OE reaction mechanisms and reveal a complex interplay of different thermodynamic and kinetic drivers. Our results shed light on the fundamental coupling of defects and oxygen transport in an important class of catalytic materials.

cond-mat.mtrl-sci↗

arXiv2022

Free-Standing Epitaxial SrTiO$_3$ Nanomembranes via Remote Epitaxy using Hybrid Molecular Beam Epitaxy

The epitaxial growth of functional materials using a substrate with a graphene layer is a highly desirable method for improving structural quality and obtaining free-standing epitaxial nano-membranes for scientific study, applications, and economical reuse of substrates. However, the aggressive oxidizing conditions typically employed to grow epitaxial perovskite oxides can damage graphene. Here, we demonstrate a technique based on hybrid molecular beam epitaxy that does not require an independent oxygen source to achieve epitaxial growth of complex oxides without damaging the underlying graphene. The technique produces films with self-regulating cation stoichiometry control and epitaxial orientation to the oxide substrate. Furthermore, the films can be exfoliated and transferred to foreign substrates while leaving the graphene on the original substrate. These results open the door to future studies of previously unattainable free-standing nano-membranes grown in an adsorption-controlled manner by hybrid molecular beam epitaxy, and has potentially important implications for the commercial application of perovskite oxides in flexible electronics.

cond-mat.mtrl-sci↗

arXiv2022

Hybrid Molecular Beam Epitaxy of Ge-based Oxides

Germanium-based oxides such as rutile GeO2 are garnering attention owing to their wide band gaps and the prospects for ambipolar doping for application in high-power devices. Here, we present the use of germanium tetraisopropoxide (GTIP) (an organometallic chemical precursor) as a source of Ge for the demonstration of hybrid molecular beam epitaxy (MBE) for Ge-containing compounds. We use Sn1-xGexO2 and SrSn1-xGexO3 as model systems to demonstrate this new synthesis method. A combination of high-resolution X-ray diffraction, scanning transmission electron microscopy, and X-ray photoelectron spectroscopy confirms the successful growth of epitaxial rutile Sn1-xGexO2 on TiO2(001) substrates up to x = 0.54 and coherent perovskite SrSn1-xGexO3 on GdScO3(110) substrates up to x = 0.16. Characterization and first-principles calculations corroborate that Ge preferentially occupies the Sn site, as opposed to the Sr site. These findings confirm the viability of the GTIP precursor for the growth of germanium-containing oxides by hybrid MBE, and thus open the door to high-quality perovskite germanate films.

cond-mat.mtrl-sci↗