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Integrated diffraction gratings offer a compact route to magneto-optical traps (MOTs) for atom cooling and trapping, thus preparing MOTs for future scalable quantum systems. While segmented tri-gratings ensure axial radiation pressure balance, they are limited in optical trapping volume. Planar 2D gratings, though offer larger trapping regions, suffer from low diffraction efficiency and the resulting axial pressure imbalance, necessitating the use of a neutral density (ND) filter to achieve this balance. We present a numerically optimized 2D diffraction grating design that overcomes these limitations and satisfies the required optical conditions for laser cooling, namely, radiation pressure balance, specular reflection cancellation, and circular polarization handedness reversal upon diffraction, thus achieving an optical molasses – a necessary condition in MOT. Using Rigorous Coupled Wave Analysis (RCWA) and a Genetic Algorithm (GA), we design a grating for (_ ^87)Rb grating MOT (GMOT) that achieves a 24% first-order diffraction efficiency, of which 99.7% have the correct circular handedness. These properties enable efficient atom cooling without an ND filter when used with a flat-top beam inside the vacuum chamber. Our design simplifies optical alignment, reduces system footprint, and advances the integration of GMOTs into compact quantum devices. 

When you start a Ph.D. program, you may be thrilled to be studying a fancy topic that you love—and you should be! But don’t let that prevent you from carefully considering the impact that your Ph.D. supervisor has on your educational experience and career. To set yourself up for success, it’s worth taking the time to select someone who aligns well with your professional goals, work style and personality. 

Abstract Dielectric metasurfaces, composed of planar arrays of subwavelength dielectric structures that collectively mimic the operation of conventional bulk optical elements, have revolutionized the field of optics by their potential in constructing high-efficiency and multi-functional optoelectronic systems on chip. The performance of a dielectric metasurface is largely determined by its constituent material, which is highly desired to have a high refractive index, low optical loss and wide bandgap, and at the same time, be fabrication friendly. Here, we present a new material platform based on tantalum pentoxide (Ta₂O₅) for implementing high-performance dielectric metasurface optics over the ultraviolet and visible spectral region. This wide-bandgap dielectric, exhibiting a high refractive index exceeding 2.1 and negligible extinction coefficient across a broad spectrum, can be easily deposited over large areas with good quality using straightforward physical vapor deposition, and patterned into high-aspect-ratio subwavelength nanostructures through commonly-available fluorine-gas-based reactive ion etching. We implement a series of high-efficiency ultraviolet and visible metasurfaces with representative light-field modulation functionalities including polarization-independent high-numerical-aperture lensing, spin-selective hologram projection, and vivid structural color generation, and the devices exhibit operational efficiencies up to 80%. Our work overcomes limitations faced by scalability of commonly-employed metasurface dielectrics and their operation into the visible and ultraviolet spectral range, and provides a novel route towards realization of high-performance, robust and foundry-manufacturable metasurface optics. 

In the continuously evolving realm of nonlinear optics, epsilon near zero (ENZ) materials have captured significant scientific interest, becoming a compelling focal point over the past decade. During this time, researchers have shown extraordinary demonstrations of nonlinear processes such as unity order index change via intensity dependent refractive index, enhanced second harmonic generation, saturable absorption in ultra-thin films and more recently, frequency shifting via time modulation of permittivity. More recently, remarkable strides have also been made in uncovering the intricacies of ENZ materials' nonlinear optical behavior. This review provides a comprehensive overview of the various types of nonlinearities commonly observed in these systems, with a focus on Drude based homogenous materials. By categorizing the enhancement into intrinsic and extrinsic factors, it provides a framework to compare the nonlinearity of ENZ media with other nonlinear media. The review emphasizes that while ENZ materials may not significantly surpass the nonlinear capabilities of traditional materials, either in terms of fast or slow nonlinearity, they do offer distinct advantages. These advantages encompass an optimal response time, inherent enhancement of slow light effects, and a broadband characteristic, all encapsulated in a thin film that can be purchased off-the shelf. The review further builds upon this framework and not only identifies key properties of transparent conducting oxides that have so far made them ideal test beds for ENZ nonlinearities, but also brings to light alternate material systems, such as perovskite oxides, that could potentially outperform them. We conclude by reviewing the upcoming concepts of time varying physics with ENZ media and outline key points the research community is working toward. 

Abstract The commercialization of atomic technologies requires replacing laboratory-scale laser setups with compact and manufacturable optical platforms. Complex arrangements of free-space beams can be generated on chip through a combination of integrated photonics and metasurface optics. In this work, we combine these two technologies using flip-chip bonding and demonstrate an integrated optical architecture for realizing a compact strontium atomic clock. Our planar design includes twelve beams in two co-aligned magneto-optical traps. These beams are directed above the chip to intersect at a central location with diameters as large as 1 cm. Our design also includes two co-propagating beams at lattice and clock wavelengths. These beams emit collinearly and vertically to probe the center of the magneto-optical trap, where they will have diameters of ≈100 µm. With these devices we demonstrate that our integrated photonic platform is scalable to an arbitrary number of beams, each with different wavelengths, geometries, and polarizations. 

Metallic nanostructures supporting surface plasmon modes can concentrate optical fields, and enhance luminescence processes from the metal surface at plasmonic hotspots. Such nanoplasmonic metal luminescence contributes to the spectral background in surface-enhanced Raman spectroscopy (SERS) measurements and is helpful in bioimaging, nano-thermometry, and chemical reaction monitoring applications. Despite increasing interest in nanoplasmonic metal luminescence, little attention has been paid to investigating its dependence on voltage modulation. Also, the hyphenated electrochemical surface-enhanced Raman spectroscopy (EC-SERS) technique typically ignores voltage-dependent spectral background information associated with nanoplasmonic metal luminescence due to limited mechanistic understanding and poor measurement reproducibility. Here, we report a combined experiment and theory study on dynamic voltage-modulated nanoplasmonic metal luminescence from hotspots at the electrode-electrolyte interface using multiresonant nanolaminate nano-optoelectrode arrays. Our EC-SERS measurements under 785 nm laser excitation demonstrate that short-wavenumber nanoplasmonic metal luminescence associated with plasmon-enhanced electronic Raman scattering (PE-ERS) exhibits a negative voltage modulation slope (up to ≈30 % V-1) in physiological ionic solutions. Furthermore, we have developed a phenomenological model to intuitively capture plasmonic, electronic, and ionic characteristics at the metal-electrolyte interface to understand the observed dependence of the PE-ERS voltage modulation slope on voltage polarization and ionic strength. The current work represents a critical step toward the general application of nanoplasmonic metal luminescence signals in optical voltage biosensing, hybrid optical-electrical signal transduction, and interfacial electrochemical monitoring. 

Abstract In situ monitoring of short‐lived transition states (TSs) is crucial for understanding electrochemical reaction mechanisms but remains challenging. Conventional electrochemical surface‐enhanced Raman spectroscopy (EC‐SERS) primarily provides vibrational information, with limitations in hotspot reproducibility and often overlooking electronic information associated with TSs. This study introduces a dual‐channel EC‐SERS strategy using nanolaminate nano‐optoelectrode (NLNOE) devices, integrating plasmon‐enhanced vibrational Raman scattering (PE‐VRS) and plasmon‐enhanced electronic Raman scattering (PE‐ERS) to concurrently probe TS dynamics within electrically connected plasmonic nanocavities. Using theAgCl(s) +e⁻⇌Ag(s) +Cl⁻(aq) redox system, this approach distinct PE‐VRS and PE‐ERS signatures of the (AgCl)^*TS. Notably, a significant increase in PE‐ERS signals concurrent with (AgCl)^*TS emergence, characterized by filled bonding and unoccupied antibonding orbitals with negligible energy gaps. This enhanced PE‐ERS signal correlates with increased (AgCl)^*TS polarizability, leading to amplified PE‐VRS signals due to enhanced electron cloud distortion. By modulating Cl⁻ ion concentrations via electrolyte composition (1× PBS and 1× PBS‐equivalent KH₂PO₄) while maintaining constant total ion concentration, the competition between Ag/AgCl and Ag/AgH₂PO₄ redox reactions within Ag nanolayers is influenced. These results demonstrate the capability of dual‐channel EC‐SERS to distinguish interfacial redox reactions based on distinct electronic and vibrational signatures associated with covalent and ionic bond characteristics. 

We present results on trapping ensembles of cold atoms with metasurface optics for portable atomic clock application, and progress towards single atom trapping and detection in high-NA optical tweezers with dielectric metalenses.