arXiv subjects

Jennifer A. Dionne

Publications and source records attributed to Jennifer A. Dionne.

At least 19 recordsLinked to original sources

arXiv2026

In situ Gas-Cell Electron Microscopy Reveals Pressure-Selected Restructuring Pathways in AuRu Ammonia Catalysts

Bimetallic catalysts provide new routes toward sustainable ammonia synthesis, but the nanoscale structural dynamics under reaction-relevant conditions remain poorly understood. Here, we combine in situ gas-cell and multimodal electron microscopy to determine how temperature, gas pressure, and chemistry select among distinct restructuring pathways in AuRu nanocrystal catalysts. Initially, the AuRu nanocrystals form polycrystalline face-centered cubic (FCC) alloys with Au/Ru intermixing. Elevated temperature ($\geq 350~^\circ$C) induces intraparticle phase segregation into distinct Au-rich (FCC) and Ru-rich hexagonal close-packed (HCP) domains that exhibit localized plasmonic modes. Atmospheric-pressure 3:1 H$_2$:N$_2$ gas unlocks a distinct restructuring regime absent at lower pressures, characterized by pronounced faceting and nanovoid formation. Systematic gas variation identifies hydrogen as the dominant driver. Density functional theory-trained machine-learning interatomic potentials and grand-canonical Monte Carlo simulations reveal that H-Ru interactions enhance the Au/Ru diffusivity mismatch, promoting vacancy accumulation and nanovoid formation. Together, these results show that, rather than simply accelerating the thermally driven phase segregation observed at lower pressures, atmospheric-pressure H$_2$:N$_2$ gas redirects restructuring toward faceting and nanovoid formation through a gas-mediated Kirkendall-type mechanism.

cond-mat.mtrl-sci↗

arXiv2026

Unsupervised segmentation and clustering workflow for efficient processing of 4D-STEM and 5D-STEM data

Four-dimensional scanning transmission electron microscopy (4D-STEM) enables mapping of diffraction information with nanometer-scale spatial resolution, offering detailed insight into local structure, orientation, and strain. However, as data dimensionality and sampling density increase, particularly for in situ scanning diffraction experiments (5D-STEM), robust segmentation of structurally consistent behavior across sequential measurements becomes essential for efficient and physically meaningful analysis. Here, we introduce a clustering framework that identifies crystallographically distinct domains from 4D-STEM datasets. By using local diffraction-pattern similarity as a metric, the method extracts closed contours delineating spatially contiguous regions. This approach produces cluster-averaged diffraction patterns that improve signal quality while reducing data volume by orders of magnitude, enabling rapid and accurate orientation, phase, and strain mapping. We demonstrate the applicability of this approach to in situ liquid-cell 4D-STEM data of gold nanoparticle growth. Our method provides a scalable and generalizable route for spatially coherent segmentation, data compression, and quantitative structure-strain mapping across diverse 4D-STEM modalities. The full analysis code and example workflows are publicly available to support reproducibility and reuse.

cond-mat.mtrl-sci↗

arXiv2026

Plasmonic Photocatalysis Enables Selective Oxidative Coupling of Methane with Nitrous Oxide under Ambient Conditions

Methane (CH4) and nitrous oxide (N2O) are potent greenhouse gases that represent substantial chemical energy. Conversion of these abundant waste gases to high-value chemicals typically requires high temperatures up to 1000 C, producing substantial CO2 emissions and limited selectivity toward desirable multi-carbon products. Here we demonstrate a plasmonic photocatalyst that enables CH4 and N2O conversion under ambient conditions to form C2 and C3 hydrocarbons. By systematically tuning AuPd alloys on TiO2, we identify an optimal composition (AuPd0.05) where Au enhances light harvesting and Pd enables selective C-H activation and C-C coupling. Under visible-light illumination, this catalyst produces C2H4, C2H6, C3H6, and C3H8 with ~80% selectivity while suppressing CO2 formation. In-situ spectroscopy and hot-carrier calculations show that plasmon-generated carriers redistribute interfacial hydroxyl intermediates, shifting the hydrophilic center to suppress overoxidation. Ab-initio calculations further reveal the reduction in C-C coupling barriers from 2.7 eV to 0.7 eV under illumination. Our work illustrates how engineering interfacial electronic and adsorbate dynamics enables selective multicarbon formation.

cond-mat.mtrl-sci↗

arXiv2026

Alkaline-Earth Rare-Earth Fluoride Nanoparticle Superlattices for Ultrafast, Radiation Stable Scintillators

Radioluminescent nanostructures provide a pathway to the fabrication of next-generation scintillators with tunability in composition, size, and morphology, and spectral and temporal properties, as well as scalable processing. Here we create a 3D millimeter-scale solid-state scintillators from SrLuF Ce3+, Pr3+ (SrLuF) core-shell nanostructures, integrating nanoscale building blocks into self-assembled macroscopic crystals. These scintillators exhibit single-digit nanosecond decay times, linear response, resistance to radiation-induced degradation, and optical emission yields within an order of magnitude of YAG Ce3+. We select a SrLuF host lattice owing to its high effective atomic number, wide band gap, and low phonon energy, which together support efficient 4f-5d radiative transitions from Ce3+ and Pr3+ activators while suppressing afterglow. We create a library of core-shell nanoscintillators with undoped SrLuF shells and cores spanning compositions from undoped SrLuF to fully doped SrCeF or SrPrF. Time-resolved and steady-state X-ray excited optical luminescence (XEOL) reveal broadband emission at 310 nm (Ce3+) and 335 nm (Pr3+) with biexponential decays in the sub-nanosecond (100-500 ps) and sub-15 ns (4-13 ns) regimes, demonstrating tunable radiative efficiency and ultrafast dynamics. Ensemble performance of the mm-scale superlattices is characterized under both continuous-wave and femtosecond high-intensity excitation, revealing high light yield, linear response, and radiation hardness under extreme irradiation of ultrafast 50fs X-ray pulses up to 5mJ per mm2 corresponding to a peak intensity of 1013 W per cm2. Together, these results establish a design framework for stable, bright, and tunable scintillation platforms with applications in precision health, space exploration and hard X-ray imaging at next-generation free-electron laser facilities.

cond-mat.mtrl-sci↗

arXiv2026

$Q$ Factors Exceeding $10^{4}$ in Wavelength-to-Subwavelength-Scale Free-Space Resonators

Free-space-addressable optical resonators that combine long photon lifetimes (high $Q$ factors) with strong spatial localization of optical fields (small mode volumes, $V_m$) enhance light-matter interactions with facile far-field excitation. The Purcell factor governing spontaneous emission enhancement scales as $Q\,V_m^{-1}$. Periodically asymmetric resonators, in which perturbations convert bound modes into radiating modes, offer a route to free-space resonances, with the radiative $Q$ factor tuned by the geometric and optical strength of the asymmetry-inducing perturbations. However, free-space resonators that simultaneously achieve high $Q$ and small $V_m$ have remained rare. This limitation arises in part because existing designs do not tailor geometric and optical asymmetries concurrently, thus limiting access to high-$Q$ regimes. Here, we show that jointly tuning geometric and optical asymmetries unlocks a biaxial radiative landscape with iso-$Q$ contours that connect disparate perturbations with equivalent $Q$ factors. We demonstrate this framework with very-large-scale-integrated single-crystalline Si nanoantenna pixels (VINPix) with out-of-plane perturbations of 35-150 nm amorphous Si, SiN$_x$, and SiO$_2$. We experimentally establish biaxial $Q$ factor control in air and achieve $Q$ factors up to $76,000$ at wavelength-scale mode volumes ($V_m \sim 1.7\,λ_0^3\,n_{\mathrm{eff}}^{-3}$) in simultaneously imaged arrays of $>80$ resonators in water. Furthermore, we computationally demonstrate 50-nm-wide slotted VINPix that reach $Q$ factors of $10^6$ at subwavelength mode volumes ($V_m \sim 0.2\,λ_0^3\,n_{\mathrm{eff}}^{-3}$) with 20 nm SiO$_2$ perturbations, yielding Purcell factors as high as $5 \times 10^5$ in an all-dielectric free-space resonator.

physics.optics↗

arXiv2026

Enhanced enantiomer discrimination with chiral surface plasmons

Strong light-matter coupling in chiral cavities has been proposed as an effective way to selectively interact with an enantiomer that shares the same handedness as the cavity's chiral mode. We show that surface plasmons supported by a two-dimensional interface with both electric and chiral conductivities discriminate enantiomers more efficiently than chiral optical cavities. A quantum-electrodynamic treatment is developed to incorporate the molecule's electric and magnetic dipole moments. We show that the discrimination factor for a chiral plasmon can exceed that of the best chiral-mirror cavity by almost an order of magnitude due to stronger field confinement. In addition, surface plasmons couple to a dipole's projection onto an entire plane, whereas cavity (or free-space) modes couple only to a single polarization axis. This geometric difference produces a $\sqrt{2}$ orientation-averaged boost in chiral discrimination for chiral surface platforms. A handedness-preserving reflector further amplifies the enhancement, opening a practical route towards chiral sensing using twisted-layer platforms.

physics.optics↗

arXiv2026

Spin dissymmetry in optical cavities

We introduce the spin dissymmetry factor, a measure of the spin-selectivity in the optical transition rate of quantum particles. This spin dissymmetry factor is valid locally, including at material interfaces and within optical cavities. We design and numerically demonstrate a metasurface optical cavity with three-fold rotational symmetry that maximizes spin dissymmetry, thereby maximizing the spin-selective radiative coupling of a cavity-coupled emitter. We also show the near-field and far-field response of spin and chiral dipoles to these cavities that preferentially enhance either spin or chirality. Our approach emphasizes the difference between spin and chirality in the near-field and reveals a compact parameter for designing more efficient quantum optical devices.

physics.app-ph↗

arXiv2025

Channel-last gate-all-around nanosheet oxide semiconductor transistors

As we move beyond the era of transistor miniaturization, back-end-of-line-compatible transistors that can be stacked monolithically in the third dimension promise improved performance for low-power electronics. In advanced transistor architectures, such as gate-all-around nanosheets, the conventional channel-first process involves depositing dielectrics directly onto the channel. Atomic layer deposition of gate dielectrics on back-end-of-line compatible channel materials, such as amorphous oxide semiconductors, can induce defects or cause structural modifications that degrade electrical performance. While post-deposition annealing can partially repair this damage, it often degrades other device metrics. We report a novel channel-last concept that prevents such damage. Channel-last gate-all-around self-aligned transistors with amorphous oxide-semiconductor channels exhibit high on-state current ($>$ 1 mA/$μ$m) and low subthreshold swing (minimum of 63 mV/dec) without the need for post-deposition processing. This approach offers a general, scalable pathway for transistors with atomic layer deposited channel materials, enabling the future of low-power three-dimensional electronics.

cond-mat.mtrl-sci↗

arXiv2025

Room-temperature valley-selective emission in Si-MoSe2 heterostructures enabled by high-quality-factor chiroptical cavities

Transition metal dichalcogenides possess valley pseudospin, enabling coupling between photon spin and electron spin for classical and quantum information processing. However, rapid valley-dephasing processes have impeded the development of scalable, high-performance valleytronic devices operating at room temperature. Here we demonstrate that a chiral resonant metasurface can enable room-temperature valley-selective emission in MoSe2 monolayers independent of excitation polarization. This platform provides circular eigen-polarization states with a high quality factor (Q-factor) and strong chiral near-field enhancement. The fabricated Si chiral metasurfaces exhibit chiroptical resonances with Q-factors up to 450 at visible wavelengths. We reveal degrees of circular polarization (DOP) reaching a record high of 0.5 at room temperature. Our measurements show that the high DOP can be attributed to the significantly increased chiroptical local density of states, which enhances valley-specific radiative transition rates by a factor of ~13. Our work could facilitate the development of ultracompact chiral classical and quantum light sources.

physics.optics↗

arXiv2025

Mechanosensitive polymer matrices of biologically-relevant compliance based on upconverting nanoparticles

Upconverting nanoparticles (UCNPs) are promising optical biomechanical force sensors due to their near infrared excitation, low toxicity, photostability, and linear colorimetric sensitivity to micronewtons of force. Recently, a composite force sensor based on UCNPs embedded in a polystyrene microbead enabled the first real time measurement of feeding forces in living nematodes. However, the comparatively large stiffness of polystyrene only makes it relevant to biomedical application in a small subset of biological tissue. To facilitate deployment of UCNPs into biological tissues with a range of mechanical properties, we expand upon polymer UCNP composite systems by embedding UCNPs in three polymer matrices with varying stiffnesses (epoxy resin, polydimethylsiloxane, and alginate hydrogels). Furthermore, to enhance these composites mechanosensitivity, we methodically investigate using two different core-shell architectures of SrLuF based UCNPs doped with ytterbium, erbium, and varying manganese concentrations. We calibrate polymer UCNP composite optical force sensitivity with colocalized atomic force and confocal microscopy. Using the red to green emission ratio (Delta Percent IRed:IGreen) as the force read-out, we determine that SrLuF:Yb0.28Er0.025Mn0.013 with SrYF inert shell dispersed in epoxy resin exhibits the greatest emission color change (12 Delta Percent IRed:IGreen per microNewton). Finally, we map forces in the epoxy UCNP composite on the macroscale between the joint of a chicken wing bone using a commercially available wide field microscope, thereby demonstrating its ability to optically measure pressures in situ. This work establishes the utility and modularity of the UCNP polymer composite system for force sensing in geometrically and mechanically diverse biological systems.

physics.app-ph↗

arXiv2025

Upconverting microgauges reveal intraluminal force dynamics in vivo

The forces generated by action potentials in muscle cells shuttle blood, food and waste products throughout the luminal structures of the body. Although non-invasive electrophysiological techniques exist, most mechanosensors cannot access luminal structures non-invasively. Here we introduce non-toxic ingestible mechanosensors to enable the quantitative study of luminal forces and apply them to study feeding in living Caenorhabditis elegans roundworms. These optical 'microgauges' comprise NaY0.8Yb0.18Er0.02F4@NaYF4 upconverting nanoparticles embedded in polystyrene microspheres. Combining optical microscopy and atomic force microscopy to study microgauges in vitro, we show that force evokes a linear and hysteresis-free change in the ratio of emitted red to green light. With fluorescence imaging and non-invasive electrophysiology, we show that adult C. elegans generate bite forces during feeding on the order of 10 micronewtons and that the temporal pattern of force generation is aligned with muscle activity in the feeding organ. Moreover, the bite force we measure corresponds to Hertzian contact stresses in the pressure range used to lyse the bacterial food of the worm. Microgauges have the potential to enable quantitative studies that investigate how neuromuscular stresses are affected by aging, genetic mutations and drug treatments in this organ and other luminal organs.

q-bio.TO↗

arXiv2025

GHz-speed wavefront shaping metasurface modulators enabled by resonant electro-optic nanoantennas

Electrically tunable metasurfaces that control the amplitude and phase of light through biasing of nanoscale antennas present a route to compact, sub-micron thick modulator devices. However, most platforms face limitations in bandwidth, absolute optical efficiency, and tuning response. Here, we present electro-optically tunable metasurfaces capable of both GHz amplitude modulation and transmissive wavefront shaping in the telecom range. Our resonant electro-optic nanoantenna design consists of a silicon nanobar atop thin-film lithium niobate, with gold electrodes. The silicon nanobar is a periodically perturbed optical waveguide that supports high quality factor (Q $>$ 1000) guided mode resonances excited with free space light. Applying a voltage bias to the lithium niobate tunes its refractive index, modulating the resonant behavior of the silicon nanobar through evanescent mode overlap. We demonstrate an absolute transmittance modulation of 7.1% with $\pm$5 V applied voltage, and show the dependence of this modulation behavior on the resonance quality factor. We additionally study the electrode limitations on modulation bandwidth, demonstrating bandwidths exceeding 800 MHz. Finally, we show how this resonant antenna platform can be used to design wavefront shaping metasurfaces. We demonstrate a beamsplitting metasurface device, whose diffraction efficiency can be modulated with a bandwidth of 1.03 GHz. The high-speed modulation and wavefront control capabilities of this platform provide a foundation for compact, high bandwidth free space communications and sensing devices.

physics.optics↗

arXiv2024

High-throughput antibody screening with high-quality factor nanophotonics and bioprinting

Empirical investigation of the quintillion-scale, functionally diverse antibody repertoires that can be generated synthetically or naturally is critical for identifying potential biotherapeutic leads, yet remains burdensome. We present high-throughput nanophotonics- and bioprinter-enabled screening (HT-NaBS), a multiplexed assay for large-scale, sample-efficient, and rapid characterization of antibody libraries. Our platform is built upon independently addressable pixelated nanoantennas exhibiting wavelength-scale mode volumes, high-quality factors (high-Q) exceeding 5000, and pattern densities exceeding one million sensors per square centimeter. Our custom-built acoustic bioprinter enables individual sensor functionalization via the deposition of picoliter droplets from a library of capture antigens at rates up to 25,000 droplets per second. We detect subtle differentiation in the target binding signature through spatially-resolved spectral imaging of hundreds of resonators simultaneously, elucidating antigen-antibody binding kinetic rates, affinity constant, and specificity. We demonstrate HT-NaBS on a panel of antibodies targeting SARS-CoV-2, Influenza A, and Influenza B antigens, with a sub-picomolar limit of detection within 30 minutes. Furthermore, through epitope binning analysis, we demonstrate the competence and diversity of a library of native antibodies targeting functional epitopes on a priority pathogen (H5N1 bird flu) and on glycosylated therapeutic Cetuximab antibodies against epidermal growth factor receptor. With a roadmap to image tens of thousands of sensors simultaneously, this high-throughput, resource-efficient, and label-free platform can rapidly screen for high-affinity and broad epitope coverage, accelerating biotherapeutic discovery and de novo protein design.

physics.optics↗

arXiv2024

Atmospheric Pressure Ammonia Synthesis on AuRu Catalysts Enabled by Plasmon-Controlled Hydrogenation and Nitrogen-species Desorption

Ammonia is a key component of fertilizer and a potential clean fuel and hydrogen carrier. The Haber-Bosch process for ammonia synthesis consumes more than half of industrial hydrogen and contributes up to ~3% of global greenhouse gas emissions. Light-driven reactions via surface plasmon resonances offer a less energy-intensive pathway for ammonia production by altering reaction intermediates. Here, we report gold-ruthenium plasmonic bimetallic alloys for ammonia synthesis at room temperature and pressure, driven by visible light. We use colloidal synthesis to create AuRu$_x$ alloys (x=0.1, 0.2, 0.3) and disperse these nanoparticles on MgO supports for gas-phase ammonia synthesis. We observe a ~60 $μ$mol/g/h reactivity and ~0.12% external quantum efficiency on a AuRu$_0$$_.$$_2$ sample under 100 mW/cm$^2$ visible light. In-situ diffuse reflective infrared Fourier transform spectroscopic measurements show that hydrogenation of nitrogen adsorbates is accelerated under light compared to thermocatalysis. Combining wavelength-dependent reactivity and spectroscopic findings with semi-classical electromagnetic modeling, we show plasmonic bimetallic alloys expedite ammonia synthesis by aiding hydrogenation of adsorbed nitrogen species via plasmon-mediated hot electrons. Quantum mechanical calculations reveal hydrogen-assisted N$_2$ splitting in the excited state is key to activating the reaction under ambient conditions. Therefore, light or H$_2$ alone cannot dissociate N$_2$ -- the key bottleneck to breaking N$_2$'s triple bond. Our findings are consistent with recent hypotheses on how nitrogenase enzymes catalyze ammonia production at mild conditions and provide insights for sustainable photochemical transformations.

physics.chem-ph↗

arXiv2024

Rapid, antibiotic incubation-free determination of tuberculosis drug resistance using machine learning and Raman spectroscopy

Tuberculosis (TB) is the world's deadliest infectious disease, with over 1.5 million deaths annually and 10 million new cases reported each year. The causative organism, Mycobacterium tuberculosis (Mtb) can take nearly 40 days to culture, a required step to determine the pathogen's antibiotic susceptibility. Both rapid identification of Mtb and rapid antibiotic susceptibility testing (AST) are essential for effective patient treatment and combating antimicrobial resistance. Here, we demonstrate a rapid, culture-free, and antibiotic incubation-free drug susceptibility test for TB using Raman spectroscopy and machine learning. We collect few-to-single-cell Raman spectra from over 25,000 cells of the MtB complex strain Bacillus Calmette Guerin (BCG) resistant to one of the four mainstay anti-TB drugs, isoniazid, rifampicin, moxifloxacin and amikacin, as well as a pan susceptible wildtype strain. By training a neural network on this data, we classify the antibiotic resistance profile of each strain, both on dried samples and in patient sputum samples. On dried samples, we achieve >98% resistant versus susceptible classification accuracy across all 5 BCG strains. In patient sputum samples, we achieve ~79% average classification accuracy. We develop a feature recognition algorithm in order to verify that our machine learning model is using biologically relevant spectral features to assess the resistance profiles of our mycobacterial strains. Finally, we demonstrate how this approach can be deployed in resource-limited settings by developing a low-cost, portable Raman microscope that costs <$5000. We show how this instrument and our machine learning model enables combined microscopy and spectroscopy for accurate few-to-single-cell drug susceptibility testing of BCG.

physics.bio-ph↗

arXiv2024

Very-Large-Scale-Integrated High-$Q$ Nanoantenna Pixels (VINPix)

Metasurfaces provide a versatile and compact approach to free-space optical manipulation and wavefront shaping. Comprised of arrays of judiciously-arranged dipolar resonators, metasurfaces precisely control the amplitude, polarization, and phase of light, with applications spanning imaging, sensing, modulation, and computing. Three crucial performance metrics of metasurfaces and their constituent resonators are the quality factor ($Q$-factor), mode-volume ($V_m$), and the ability to control far-field radiation. Often, resonators face a trade-off between these parameters: a reduction in $V_m$ leads to an equivalent reduction in $Q$, albeit with more control over radiation. Here, we demonstrate that this perceived compromise is not inevitable $-$ high-$Q$, subwavelength $V_m$, and controlled dipole-like radiation can be achieved, simultaneously. We design high-$Q$, very-large-scale integrated silicon nanoantenna pixels $-$ VINPix $-$ that combine guided mode resonance waveguides with photonic crystal cavities. With optimized nanoantennas, we achieve $Q$-factors exceeding 1500 with $V_m$ less than 0.1 $(λ/n_{\text{air}})^3$. Each nanoantenna is individually addressable by free-space light, and exhibits dipole-like scattering to the far-field. Resonator densities exceeding a million nanoantennas per $\text{cm}^2$ can be achieved, as demonstrated by our fabrication of an 8 mm x 8 mm VINPix array. As a proof-of-concept application, we demonstrate spectrometer-free, spatially localized, refractive-index sensing utilizing a VINPix array. Our platform provides a foundation for compact, densely multiplexed devices such as spatial light modulators, computational spectrometers, and in-situ environmental sensors.

physics.optics↗

arXiv2024

Highly confined epsilon-near-zero- and surface-phonon polaritons in SrTiO3 membranes

Recent theoretical studies have suggested that transition metal perovskite oxide membranes can enable surface phonon polaritons in the infrared range with low loss and much stronger subwavelength confinement than bulk crystals. Such modes, however, have not been experimentally observed so far. Here, using a combination of far-field Fourier-transform infrared (FTIR) spectroscopy and near-field synchrotron infrared nanospectroscopy (SINS) imaging, we study the phonon-polaritons in a 100 nm thick freestanding crystalline membrane of SrTiO3 transferred on metallic and dielectric substrates. We observe a symmetric-antisymmetric mode splitting giving rise to epsilon-near-zero and Berreman modes as well as highly confined (by a factor of 10) propagating phonon polaritons, both of which result from the deep-subwavelength thickness of the membranes. Theoretical modeling based on the analytical finite-dipole model and numerical finite-difference methods fully corroborate the experimental results. Our work reveals the potential of oxide membranes as a promising platform for infrared photonics and polaritonics.

cond-mat.mtrl-sci↗

arXiv2023

Millimeter-scale exfoliation of hBN with tunable flake thickness

As a two-dimensional (2D) dielectric material, hexagonal boron nitride (hBN) is in high demand for applications in photonics, nonlinear optics, and nanoelectronics. Unfortunately, the high-throughput preparation of macroscopic-scale, high-quality hBN flakes with controlled thickness is an ongoing challenge, limiting device fabrication and technological integration. Here, we present a metal thin-film exfoliation method to prepare hBN flakes with millimeter-scale dimension, near-unity yields, and tunable flake thickness distribution from 1-7 layers, a substantial improvement over scotch tape exfoliation. The single crystallinity and high quality of the exfoliated hBN are demonstrated with optical microscopy, atomic force microscopy, Raman spectroscopy, and second harmonic generation. We further explore a possible mechanism for the effectiveness and selectivity based on thin-film residual stress measurements, density functional theory calculations, and transmission electron microscopy imaging of the deposited metal films. We find that the magnitude of the residual tensile stress induced by thin film deposition plays a key role in determining exfoliated flake thickness in a manner which closely resembles 3D semiconductor spalling. Lastly, we demonstrate that our exfoliated, large-area hBN flakes can be readily incorporated as encapsulating layers for other 2D monolayers. Altogether, this method brings us one step closer to the high throughput, mass production of hBN-based 2D photonic, optoelectronic, and quantum devices.

cond-mat.mtrl-sci↗