arXiv subjects

Ryan W. Spangler

Publications and source records attributed to Ryan W. Spangler.

4 recordsLinked to original sources

arXiv2026

Deterministic control over launching efficiency of higher-order hyperbolic phonon polaritons

Hyperbolic materials, which exhibit an extreme form of birefringence enabling the volume confinement and frequency-dependent propagation of deeply sub-diffractional optical modes, offer the opportunity for extreme confinement via the stimulation polaritonic modes, with substantially higher confinement obtained through the efficient excitation of of the higher-order (shorter wavelength) hyperbolic polaritonic modes, which they can support. However, while these higher-order hyperbolic polaritons (HO-HPhPs) form high-momentum ray-like propagation within the bulk, efficient excitation of these modes, especially in contrast to the long-wavelength lower-momentum surface polariton propagating modes, has remained a challenge. Critically, the large momentum mismatch between these modes and free-space light, alongside the spatial mismatch between the sub-diffractional scatterer and the distinct modal distribution of HO-HPhPs, lead to a suppressed launching efficiency of these higher-order modes, limiting their use in nanophotonic applications. Here, we report the experimental observation of a 10-fold enhancement in the excitation efficiency of HO-HPhPs through the use of subsurface scatterers over traditional surface scattering (e.g. a flake edge or gold launcher) within single-crystalline {\alpha}-MoO3 slabs. We employ full-wave numerical simulations to investigate the role of the spatial overlap between HO-HPhP modal distributions and the scatterer placement upon excitation efficiency. Furthermore, we develop a generalized process using transfer matrix method to selectively design modal HO-HPhP excitation, which advances the capabilities of HPhP multiplexing for on-chip applications.

physics.optics↗

arXiv2026

Multi-resonant non-dispersive infrared gas sensing: breaking the selectivity and sensitivity tradeoff

In applications such as atmospheric monitoring of greenhouse gases and pollutants, the detection and identification of trace concentrations of harmful gases is commonly achieved using non-dispersive infrared (NDIR) sensors. These devices employ a broadband infrared emitter, thermopile detector, and a spectrally selective bandpass filter tuned to the vibrational resonance of the target analyte. However, the fabrication of these filters is costly and limited to a single frequency. This limitation introduces a fundamental tradeoff, as broadening the optical passband width enhances sensitivity but compromises selectivity, whereas narrowing improves selectivity at the expense of sensitivity. In this work, we validate a filterless NDIR approach using a multi-peak thermal emitter developed through inverse design. This emitter enhances detection sensitivity by targeting multiple absorption bands, demonstrated through the creation of a sensor designed for the C-H vibrational modes of propane. Additionally, a set of single-peak emitters were developed to showcase the capability of designing highly selective sensors operating within close spectral proximity. These emitters, targeting the stretching modes of carbon monoxide and carbon dioxide, exhibit Q-factors above 50 and minimal crosstalk, enabling accurate detection of the target gas without interference from gases with spectrally adjacent absorption bands. This is enabled by the implementation of an aperiodic distributed Bragg reflectors, which allows for higher Q-factors with fewer layers than a periodic Bragg reflector using the same materials and number of layers, thereby reducing fabrication complexity and cost. Experimental results validate that this approach breaks the tradeoff between sensitivity and selectivity. This work highlights the potential of optimized thermal emitters for more efficient and compact gas sensing applications.

cond-mat.mes-hall↗

arXiv2026

Tailoring phonon-driven responses in α-MoO3 through isotopic enrichment

The implementation of polaritonic materials into nanoscale devices requires selective tuning of parameters to realize desired spectral or thermal responses. One robust material is α-MoO3, which as an orthorhombic crystal boasts three distinct phonon dispersions, providing three polaritonic dispersions of hyperbolic phonon polaritons (HPhPs) across the mid-infrared (MIR). Here, the tunability of both optical and thermal responses in isotopically enriched α-MoO3 (98MoO3, Mo18O3 and 98Mo18O3) are explored. A uniform ~5 % spectral redshift from 18O enrichment is observed in both Raman- and IR-active TO phonons. Both the in- and out-of-plane thermal conductivities for the isotopic variations are reported. Ab initio calculations both replicate experimental findings and analyze the select-mode three-phonon scattering contributions. The HPhPs from each isotopic variation are probed with s-SNOM and their Q- factors are reported. A Q-factor maxima increase of ~50 % along the [100] in the RB2 and ~100 % along the [001] in the RB3 are reported for HPhPs supported in 98Mo18O3. Observations in both real and Fourier space of higher-order HPhP modes propagating in single slabs of isotopically enriched α-MoO3 without the use of a subdiffractional surface scatterer are presented here. This work illustrates the tunability of α-MoO3 for thermal and nanophotonic applications.

cond-mat.mtrl-sci↗

arXiv2025

Rapid synthesis of dual-element isotope-enriched alpha-MoO3 crystals by reactive vapor transport

In this work, we develop a rapid reactive vapor transport technique to efficiently utilize limited isotopically pure precursors, particularly gaseous 18O2, and synthesize mm-scale, high-quality crystals within few-minute growth durations. We unlock this capability by using metallic molybdenum precursors with high source temperatures (900 C) and total pressures (1 atm) to maximize precursor efficiency and yield. Subsequently, we grow MoO3 single crystals with high and uniform enrichment levels of 98Mo and 18O isotopes in several different permutations. As probed by Raman spectroscopy, modest and significant phonon energy redshifts occur following 98Mo and 18O enrichment, respectively. By demonstrating control over both molybdenum and oxygen isotopic fractions, we establish a powerful tool to advance nanophotonics and thermal management goals using MoO3. This work is motivated by the possibility to enhance and engineer lattice vibrational mode phenomena including thermal conduction and hyperbolic phonon polariton (HPhP) dispersion, with particular interest in comparing the effects of light and heavy element enrichment.

cond-mat.mtrl-sci↗