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Solid-state platforms provide exceptional opportunities for advancing on-chip quantum technologies by enhancing interaction strengths through coupling, scalability, and robustness. Cuprous oxide ($\text{Cu}_{2}\text{O}$) has recently emerged as a promising medium for scalable quantum technology due to its high-lying Rydberg excitonic states, akin to those in hydrogen atoms. To harness these nonlinearities for quantum applications, the confinement dimensions must match the Rydberg blockade size, which can reach several microns in $\text{Cu}_{2}\text{O}$. Using a CMOS-compatible growth technique, this study demonstrates the bottom-up fabrication of site-selective arrays of $\text{Cu}_{2}\text{O}$ microparticles. We observed Rydberg excitons up to the principal quantum number $n$=5 within these $\text{Cu}_{2}\text{O}$ arrays on a quartz substrate and analyzed the spatial variation of their spectrum across the array, showing robustness and reproducibility on a large chip. These results lay the groundwork for the deterministic growth of $\text{Cu}_{2}\text{O}$ around photonic structures, enabling substantial light-matter interaction on integrated photonic platforms and paving the way for scalable, on-chip quantum devices., Comment: 14 pages, 9 figures

In this work a hybrid nanoplasmonic-Weyl Semimetal (WSM) structure is realized for the first time utilizing silver nanopatch antennas and WSM Tantalum Arsenide (TaAs). The studied hybrid WSM-nanoplasmonic structure demonstrated a substantial, over x4.5 enhancement of the second harmonic generation (SHG) process compared to a bare TaAs film. To realize the hybrid structure while preserving TaAs properties, a scalable, non-destructive manufacturing approach was developed that involves the fabrication of TaAs flakes from single crystalline TaAs, overgrowth of a silicon nitride overlayer, and drop-casting of silver nanopatch antennas. The strong polarization response of both the bare flakes, along with the hybrid-nanoplasmonic cavities demonstrates that this approach uniquely preserves the TaAs crystal structure and its optical response while providing significant enhancement of the nonlinear properties. The developed method allows leveraging the capabilities of plasmonics to control and enhance light-matter interactions at the nanometer scale to access and engineer WSM response. This work is the first step towards high-performance nanophotonic devices utilizing WSM topological properties.

A robust process for fabricating intrinsic single-photon emitters in silicon nitride has been recently established. These emitters show promise for quantum applications due to room-temperature operation and monolithic integration with the technologically mature silicon nitride photonics platform. Here, the fundamental photophysical properties of these emitters are probed through measurements of optical transition wavelengths, linewidths, and photon antibunching as a function of temperature from 4.2K to 300K. Important insight into the potential for lifetime-limited linewidths is provided through measurements of inhomogeneous and temperature-dependent homogeneous broadening of the zero-phonon lines. At 4.2K, spectral diffusion was found to be the main broadening mechanism, while time-resolved spectroscopy measurements revealed homogeneously broadened zero-phonon lines with instrument-limited linewidths., Comment: 21 pages, 10 figures

All optical switches offer advanced control over the properties of light at ultrafast timescales using optical pulses as both the signal and the control. Limited only by material response times, these switches can operate at terahertz speeds, essential for technology-driven applications such as all-optical signal processing and ultrafast imaging, as well as for fundamental studies such as frequency translation and novel optical media concepts such as photonic time crystals. In conventional systems, the switching time is determined by the relaxation response of a single active material, which is challenging to adjust dynamically. This work demonstrates that the zero-to-zero response time of an all-optical switch can instead be varied through the combination of so-called fast and slow materials in a single device. When probed in the epsilon-near-zero operational regime of a material with a slow response time, namely, plasmonic titanium nitride, the switch exhibits a relatively slow, nanosecond response time. The response time then decreases reaching the picosecond time scale in the ENZ regime of the faster material, namely, aluminum-doped zinc oxide. Overall, the response time of the switch is shown to vary by two orders of magnitude in a single device and can be selectively controlled through the interaction of the probe signal with the constituent materials. The ability to adjust the switching speed by controlling the light-matter interaction in a multi-material structure provides an additional degree of freedom in all-optical switch design. Moreover, the proposed approach utilizes slower materials that are very robust and allow to enhance the field intensities while faster materials ensure an ultrafast dynamic response. The proposed control of the switching time could lead to new functionalities within key applications in multiband transmission, optical computing, and nonlinear optics.

Two-dimensional hexagonal boron nitride (hBN) has been known to host a variety of quantum emitters with properties suitable for a broad range of quantum photonic applications. Among them, the negatively charged boron vacancy (VB-) defect with optically addressable spin states has emerged recently due to its potential use in quantum sensing. Compared to spin defects in bulk crystals, VB- preserves its spin coherence properties when placed at nanometer-scale distances from the hBN surface, enabling nanometer-scale quantum sensing. On the other hand, the low quantum efficiency of VB- has hindered its use in practical applications. Several studies have reported improving the overall quantum efficiency of VB- defects using plasmonic effects; however, the overall enhancements of up to 17 times reported to date are relatively modest. In this study, we explore and demonstrate much higher emission enhancements of VB- with ultralow-loss nano-patch antenna (NPA) structures. An overall intensity enhancement of up to 250 times is observed for NPA-coupled VB- defects. Since the laser spot exceeds the area of the NPA, where the enhancement occurs, the actual enhancement provided by the NPA is calculated to be ~1685 times, representing a significant increase over the previously reported results. Importantly, the optically detected magnetic resonance (ODMR) contrast is preserved at such exceptionally strong enhancement. Our results not only establish NPA-coupled VB- defects as high-resolution magnetic field sensors operating at weak laser powers, but also provide a promising approach to obtaining single VB- defects., Comment: 17 pages, 4 figures

The recent discovery of room temperature intrinsic single-photon emitters in silicon nitride (SiN) provides the unique opportunity for seamless monolithic integration of quantum light sources with the well-established SiN photonic platform. In this work, we develop a novel approach to realize planar waveguides made of low-autofluorescing SiN with intrinsic quantum emitters and demonstrate the single-photon emission coupling into the waveguide mode. The observed emission coupling from these emitters is found to be in line with numerical simulations. The coupling of the single-photon emission to a waveguide mode is confirmed by second-order autocorrelation measurements of light outcoupled off the photonic chip by grating couplers. Fitting the second-order autocorrelation histogram yields $g^{(2)}(0)=0.35\pm0.12$ without spectral filtering or background correction with an outcoupled photon rate of $10^4$ counts per second. This demonstrates the first successful coupling of photons from intrinsic single-photon emitters in SiN to monolithically integrated waveguides made of the same material. The results of our work pave the way toward the realization of scalable, technology-ready quantum photonic integrated circuitry efficiently interfaced with solid-state quantum emitters., Comment: 10 pages, 5 figures

We present an approach for adapting the Gaussian dispersion analysis (GDA) of optical materials to time-domain simulations. Within a GDA model, the imaginary part of a measured dielectric function is presented as a sum of Gaussian absorption terms. Such a simple model is valid for materials where inhomogeneous broadening is substantially larger than the homogeneous linewidth. The GDA model is the essential broadband approximation for the dielectric function of many glasses, polymers, and other natural and artificial materials with disorder. However, efficient implementation of this model in time-domain full-wave electromagnetic solvers has never been fully achieved. We start with a causal form of an isolated oscillator with Gaussian-type absorption - Causal Dawson-Gauss oscillator. Then, we derive explicit analytical formulas to implement the Gaussian oscillator in a finite-difference time-domain (FDTD) solver with minimal use of memory and floating point operations. The derivation and FDTD implementation employ our generalized dispersive material (GDM) model - a universal, modular approach to describing optical dispersion with Pad\'e approximants. We share the FDTD prototype codes that include automated generation of the approximants and a universal FDTD dispersion implementation that employs various second-order accurate numerical schemes. The codes can be used with non-commercial solvers and commercial software for time-domain simulations of light propagation in dispersive media, which are experimentally characterized with GDA models., Comment: 72 Pages, 13 Figures, Code can be found on Code Ocean as package MADIS

Single-photon emitters are essential for enabling several emerging applications in quantum information technology, quantum sensing and quantum communication. Scalable photonic platforms capable of hosting intrinsic or directly embedded sources of single-photon emission are of particular interest for the realization of integrated quantum photonic circuits. Here, we report on the first-time observation of room-temperature single-photon emitters in silicon nitride (SiN) films grown on silicon dioxide substrates. As SiN has recently emerged as one of the most promising materials for integrated quantum photonics, the proposed platform is suitable for scalable fabrication of quantum on-chip devices. Photophysical analysis reveals bright (>$10^5$ counts/s), stable, linearly polarized, and pure quantum emitters in SiN films with the value of the second-order autocorrelation function at zero time delay $g^{(2)}(0)$ below 0.2 at room temperatures. The emission is suggested to originate from a specific defect center in silicon nitride due to the narrow wavelength distribution of the observed luminescence peak. Single-photon emitters in silicon nitride have the potential to enable direct, scalable and low-loss integration of quantum light sources with the well-established photonic on-chip platform., Comment: 15 pages, 4 figures, and Supplementary Information