The family of III-nitride materials has provided a platform for tremendous advances in efficient solid-state lighting sources such as light-emitting diodes and laser diodes. In particular, quantum dot (QD) lasers using the InGaN/GaN material system promise numerous benefits to enhance photonic performance in the blue wavelength regime. Nevertheless, issues of strained growth and difficulties in producing InGaN QDs with uniform composition and size pose daunting challenges in achieving an efficient blue laser. Through a review of two previous studies on InGaN/GaN QD microdisk lasers, we seek to provide a different perspective and approach in better understanding the potential of QD emitters. The lasers studied in this paper contain gain material where QDs are sparsely distributed, comprise a wide distribution of sizes, and are intermixed with “fragmented” quantum well (fQW) material. Despite these circumstances, the use of microdisk cavities, where a few distinct, high-quality modes overlap the gain region, not only produces ultralow lasing thresholds (∼6.2 μJ/cm²) but also allows us to analyze the dynamic competition between QDs and fQWs in determining the final lasing wavelength. These insights can facilitate “modal” optimization of QD lasing and ultimately help to broaden the use of III-nitride QDs in devices.

We introduce a microwave-assisted spectroscopy technique to determine the relative ratio of fluorescence emitted by nitrogen-vacancy (N-V) centers in diamond that are negatively charged (N−V−) and neutrally charged (N−V0) and present its application to studying spin-dependent ionization in N-V ensembles and enhancing N-V-magnetometer sensitivity. Our technique is based on selectively modulating the N−V− fluorescence with a spin-state-resonant microwave drive to isolate, in situ, the spectral shape of the N−V− and N−V0 contributions to an N-V-ensemble sample’s fluorescence. As well as serving as a reliable means to characterize the charge state, the method can be used as a tool to study spin-dependent ionization in N-V ensembles. As an example, we apply the microwave technique to a high-N-V-density diamond sample and find evidence for an additional spin-dependent ionization pathway, which we present here alongside a rate-equation model of the data. We further show that our method can be used to enhance the contrast of optically detected magnetic resonance (ODMR) on N-V ensembles and may lead to significant sensitivity gains in N-V magnetometers dominated by technical noise sources, especially where the N−V0 population is large. With the high-N-V-density diamond sample investigated here, we demonstrate an up to 4.8-fold enhancement in the ODMR contrast. We also propose a second postprocessing method of increasing the ODMR contrast in shot-noise-limited applications. The techniques presented here may also be applied to other solid-state defects, as long as their fluorescence can be selectively modulated by means of a microwave drive. We demonstrate this utility by applying our method to isolate room-temperature spectral signatures of the V2-type silicon vacancy from an ensemble of V1 and V2 silicon vacancies in 4H silicon carbide.

Silicon carbide has recently been developed as a platform for optically addressable spin defects. In particular, the neutral divacancy in the 4H polytype displays an optically addressable spin-1 ground state and near-infrared optical emission. Here, we present the Purcell enhancement of a single neutral divacancy coupled to a photonic crystal cavity. We utilize a combination of nanolithographic techniques and a dopant-selective photoelectrochemical etch to produce suspended cavities with quality factors exceeding 5000. Subsequent coupling to a single divacancy leads to a Purcell factor of ∼50, which manifests as increased photoluminescence into the zero-phonon line and a shortened excited-state lifetime. Additionally, we measure coherent control of the divacancy ground-state spin inside the cavity nanostructure and demonstrate extended coherence through dynamical decoupling. This spin-cavity system represents an advance toward scalable long-distance entanglement protocols using silicon carbide that require the interference of indistinguishable photons from spatially separated single qubits.

Titanium nitride (TiN) has been identified as a promising refractory material for high temperature plasmonic applications such as surface plasmon polaritons (SPPs) waveguides, lasers and light sources, and near field optics. Such SPPs are sensitive not only to the highly metallic nature of the TiN, but also to its low loss. We have formed highly metallic, low-loss TiN thin films on MgO substrates to create SPPs with resonances between 775-825 nm. Scanning near-field optical microscopy (SNOM) allowed imaging of the SPP fringes, the accurate determination of the effective wavelength of the SPP modes, and propagation lengths greater than 10 microns. Further, we show the engineering of the band structure of the plasmonic modes in TiN in the mid-IR regime and experimentally demonstrate, for the first time, the ability of TiN to support Spoof Surface Plasmon Polaritons in the mid-IR (6 microns wavelength).