Scalable and robust beam shaping using apodized fish-bone grating couplers.

Efficient power coupling between on-chip guided and free-space optical modes requires precision spatial mode matching with apodized grating couplers. Yet, grating apodizations are often limited by the minimum feature size of the fabrication approach. This is especially challenging when small feature sizes are required to fabricate gratings at short wavelengths or to achieve weakly scattered light for large-area gratings. Here, we demonstrate a fish-bone grating coupler for precision beam shaping and the generation of millimeter-scale beams at 461 nm wavelength. Our design decouples the minimum feature size from the minimum achievable optical scattering strength, allowing smooth turn-on and continuous control of the emission. Our approach is compatible with commercial foundry photolithography and has reduced sensitivity to both the resolution and the variability of the fabrication approach compared to subwavelength meta-gratings, which often require electron beam lithography.

Integrating planar photonics for multi-beam generation and atomic clock packaging on chip.

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.

Meta-grating outcouplers for optimized beam shaping in the visible.

Accurate coupling between optical modes at the interface between photonic chips and free space is required for the development of many on-chip devices. This control is critical in quantum technologies where large-diameter beams with designed mode profiles are required. Yet, these designs are often difficult to achieve at shorter wavelengths where fabrication limits the resolution of designed devices. In this work we demonstrate optimized outcoupling of free-space beams at 461 nm using a meta-grating approach that achieves a 16 dB improvement in the apodized outcoupling strength. We design and fabricate devices, demonstrating accurate reproduction of beams with widths greater than 100 µm.

Nonlinear Optics at Excited States of Exciton Polaritons in Two-Dimensional Atomic Crystals.

Exciton polaritons (EPs) are partial-light partial-matter quasiparticles in semiconductors demonstrating striking quantum phenomena such as Bose-Einstein condensation and single-photon nonlinearity. In these phenomena, the governing process is the EP relaxation into the ground states upon excitation, where various mechanisms are extensively investigated with thermodynamic limits. However, the relaxation process becomes drastically different and could significantly advance the understanding of EP dynamics for these quantum phenomena, when excited states of EPs are involved. Here, for the first time, we observe nonlinear optical responses at the EP excited states in a monolayer tungsten disulfide (WS2) microcavity, including dark excited states and dynamically metastable upper polariton bands. The nonlinear optics leads to unique emissions of ground states with prominent valley degree of freedom (DOF) via an anomalous relaxation process, which is applicable to a wide range of semiconductors from monolayer transition metal dichalcogenides (TMDs) to emerging halide perovskites. This work promises possible approaches to challenging experiments such as valley polariton condensation. Moreover, it also constructs a valley-dependent solid-state three-level system for terahertz photonics and stimulated Raman adiabatic passage.

Magnetically Aligned Nanorods in Alginate Capsules (MANiACs): Soft Matter Tumbling Robots for Manipulation and Drug Delivery.

Soft, untethered microrobots composed of biocompatible materials for completing micromanipulation and drug delivery tasks in lab-on-a-chip and medical scenarios are currently being developed. Alginate holds significant potential in medical microrobotics due to its biocompatibility, biodegradability, and drug encapsulation capabilities. Here, we describe the synthesis of MANiACs-Magnetically Aligned Nanorods in Alginate Capsules-for use as untethered microrobotic surface tumblers, demonstrating magnetically guided lateral tumbling via rotating magnetic fields. MANiAC translation is demonstrated on tissue surfaces as well as inclined slopes. These alginate microrobots are capable of manipulating objects over millimeter-scale distances. Finally, we demonstrate payload release capabilities of MANiACs during translational tumbling motion.

Electropermanent magnets for variable-field NMR.

In this work, a dynamically tunable B0 field is used to perform variable-field NMR. The system consists of an array of electropermanent AlNiCo-5 magnets whose magnetizations are individually programmed using pulse-power control. This design allows the field strength to be varied for field-dispersion measurements. An ultra-broadband front-end is utilized that maintains efficient power transmission over a broad range of frequencies for robust operation without probe tuning. We perform T1-T2 correlation measurements at various B0 field strengths (0.5-2 MHz) and demonstrate discrimination of different dairy products. We observe variation in the frequency dependence of the proton spin-lattice relaxation for the different products as a function of the degree of protein hydration. This variable-field technique provides a low-cost alternative to fast field-cycling NMR and could open possibilities for novel contrast measurements and spatial encoding in magnetic resonance imaging.

Control of Coherently Coupled Exciton Polaritons in Monolayer Tungsten Disulphide.

Monolayer transition metal dichalcogenides (TMD) with confined 2D Wannier-Mott excitons are intriguing for the fundamental study of strong light-matter interactions and the exploration of exciton polaritons at high temperatures. However, the research of 2D exciton polaritons has been hindered because the polaritons in these atomically thin semiconductors discovered so far can hardly support strong nonlinear interactions and quantum coherence due to uncontrollable polariton dynamics and weakened coherent coupling. In this work, we demonstrate, for the first time, a precisely controlled hybrid composition with angular dependence and dispersion-correlated polariton emission by tuning the polariton dispersion in TMD over a broad temperature range of 110-230 K in a single cavity. This tamed polariton emission is achieved by the realization of robust coherent exciton-photon coupling in monolayer tungsten disulphide (WS_{2}) with large splitting-to-linewidth ratios (>3.3). The unprecedented ability to manipulate the dispersion and correlated properties of TMD exciton polaritons at will offers new possibilities to explore important quantum phenomena such as inversionless lasing, Bose-Einstein condensation, and superfluidity.

Emergence of an enslaved phononic bandgap in a non-equilibrium pseudo-crystal.

Material systems that reside far from thermodynamic equilibrium have the potential to exhibit dynamic properties and behaviours resembling those of living organisms. Here we realize a non-equilibrium material characterized by a bandgap whose edge is enslaved to the wavelength of an external coherent drive. The structure dynamically self-assembles into an unconventional pseudo-crystal geometry that equally distributes momentum across elements. The emergent bandgap is bestowed with lifelike properties, such as the ability to self-heal to perturbations and adapt to sudden changes in the drive. We derive an exact analytical solution for both the spatial organization and the bandgap features, revealing the mechanism for enslavement. This work presents a framework for conceiving lifelike non-equilibrium materials and emphasizes the potential for the dynamic imprinting of material properties through external degrees of freedom.

Nanostructure-Induced Distortion in Single-Emitter Microscopy.

Single-emitter microscopy has emerged as a promising method of imaging nanostructures with nanoscale resolution. This technique uses the centroid position of an emitter's far-field radiation pattern to infer its position to a precision that is far below the diffraction limit. However, nanostructures composed of high-dielectric materials such as noble metals can distort the far-field radiation pattern. Previous work has shown that these distortions can significantly degrade the imaging of the local density of states in metallic nanowires using polarization-resolved imaging. But unlike nanowires, nanoparticles do not have a well-defined axis of symmetry, which makes polarization-resolved imaging difficult to apply. Nanoparticles also exhibit a more complex range of distortions, because in addition to introducing a high dielectric surface, they also act as efficient scatterers. Thus, the distortion effects of nanoparticles in single-emitter microscopy remains poorly understood. Here we demonstrate that metallic nanoparticles can significantly distort the accuracy of single-emitter imaging at distances exceeding 300 nm. We use a single quantum dot to probe both the magnitude and the direction of the metallic nanoparticle-induced imaging distortion and show that the diffraction spot of the quantum dot can shift by more than 35 nm. The centroid position of the emitter generally shifts away from the nanoparticle position, which is in contradiction to the conventional wisdom that the nanoparticle is a scattering object that will pull in the diffraction spot of the emitter toward its center. These results suggest that dielectric distortion of the emission pattern dominates over scattering. We also show that by monitoring the distortion of the quantum dot diffraction spot we can obtain high-resolution spatial images of the nanoparticle, providing a new method for performing highly precise, subdiffraction spatial imaging. These results provide a better understanding of the complex near-field coupling between emitters and nanostructures and open up new opportunities to perform super-resolution microscopy with higher accuracy.

Nanoscale probing of image-dipole interactions in a metallic nanostructure.

An emitter near a surface induces an image dipole that can modify the observed emission intensity and radiation pattern. These image-dipole effects are generally not taken into account in single-emitter tracking and super-resolved imaging applications. Here we show that the interference between an emitter and its image dipole induces a strong polarization anisotropy and a large spatial displacement of the observed emission pattern. We demonstrate these effects by tracking the emission of a single quantum dot along two orthogonal polarizations as it is deterministically positioned near a silver nanowire. The two orthogonally polarized diffraction spots can be displaced by up to 50 nm, which arises from a Young's interference effect between the quantum dot and its induced image dipole. We show that the observed spatially varying interference fringe provides a useful measure for correcting image-dipole-induced distortions. These results provide a pathway towards probing and correcting image-dipole effects in near-field imaging applications.

Scanning localized magnetic fields in a microfluidic device with a single nitrogen vacancy center.

Nitrogen vacancy (NV) color centers in diamond enable local magnetic field sensing with high sensitivity by optical detection of electron spin resonance (ESR). The integration of this capability with microfluidic technology has a broad range of applications in chemical and biological sensing. We demonstrate a method to perform localized magnetometry in a microfluidic device with a 48 nm spatial precision. The device manipulates individual magnetic particles in three dimensions using a combination of flow control and magnetic actuation. We map out the local field distribution of the magnetic particle by manipulating it in the vicinity of a single NV center and optically detecting the induced Zeeman shift with a magnetic field sensitivity of 17.5 µT Hz(-1/2). Our results enable accurate nanoscale mapping of the magnetic field distribution of a broad range of target objects in a microfluidic device.

Fabrication of nanoassemblies using flow control.

Synthetic nanostructures, such as nanoparticles and nanowires, can serve as modular building blocks for integrated nanoscale systems. We demonstrate a microfluidic approach for positioning, orienting, and assembling such nanostructures into nanoassemblies. We use flow control combined with a cross-linking photoresist to position and immobilize nanostructures in desired positions and orientations. Immobilized nanostructures can serve as pivots, barriers, and guides for precise placement of subsequent nanostructures.

Nanoscale imaging and spontaneous emission control with a single nano-positioned quantum dot.

Plasmonic nanostructures confine light on the nanoscale, enabling ultra-compact optical devices that exhibit strong light-matter interactions. Quantum dots are ideal for probing plasmonic devices because of their nanoscopic size and desirable emission properties. However, probing with single quantum dots has remained challenging because their small size also makes them difficult to manipulate. Here we demonstrate the use of quantum dots as on-demand probes for imaging plasmonic nanostructures, as well as for realizing spontaneous emission control at the single emitter level with nanoscale spatial accuracy. A single quantum dot is positioned with microfluidic flow control to probe the local density of optical states of a silver nanowire, achieving 12 nm imaging accuracy. The high spatial accuracy of this scanning technique enables a new method for spontaneous emission control where interference of counter-propagating surface plasmon polaritons results in spatial oscillations of the quantum dot lifetime as it is positioned along the wire axis.

Positioning and immobilization of individual quantum dots with nanoscale precision.

We demonstrate a technique for the precise immobilization of nanoscale objects at accurate positions on two-dimensional surfaces. We have developed a water-based photoresist that causes nanostructures such as colloidal quantum dots to segregate to a thin layer at surfaces. By combining this material with electroosmotic feedback control, we demonstrate the ability to position selected, individual quantum dots at specific locations and to immobilize them with 130 nm precision via localized UV exposure.

Manipulating quantum dots to nanometer precision by control of flow.

We present a method for manipulating preselected quantum dots (QDs) with nanometer precision by flow control. The accuracy of this approach scales more favorably with particle size than optical trapping, enabling more precise positioning of nanoscopic particles. We demonstrate the ability to position a single QD in a 100 microm working region to 45 nm accuracy for holding times exceeding one hour and the ability to take active quantum measurements on the dynamically manipulated QD.