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Radiative recombination processes can occur in solid-state systems through the pairing of donor and acceptor defects of the lattice. Recently, donor-acceptor pairs (DAP) have been proposed as promising candidates for quantum applications, and their signature has been observed in emerging low-dimensional materials. Therefore, the identification of such processes is gaining interest and requires methods to efficiently and reliably characterize them. Here, we introduce a general algorithm to identify DAP processes starting from the experimental photoluminescence (PL) emission spectrum and basic material parameters, including the lattice structure and dielectric constant. The algorithm recognizes possible DAP transitions from the emission pattern in the spectrum and returns the characteristic energy of the DAP transition and the separation between the donor and acceptor sites. By testing the algorithm on the photoluminescence spectrum of hexagonal boron nitride (hBN), we show that our method is robust against experimental errors and adds new capabilities to the investigation toolbox of semiconductors and their optical properties. 

Single-photon emitters serve as building blocks for many emerging concepts in quantum photonics. The recent identification of bright, tunable and stable emitters in hexagonal boron nitride (hBN) has opened the door to quantum platforms operating across the infrared to ultraviolet spectrum. Although it is widely acknowledged that defects are responsible for single-photon emitters in hBN, crucial details regarding their origin, electronic levels and orbital involvement remain unknown. Here we employ a combination of resonant inelastic X-ray scattering and photoluminescence spectroscopy in defective hBN, unveiling an elementary excitation at 285 meV that gives rise to a plethora of harmonics correlated with single-photon emitters. We discuss the importance of N π* anti-bonding orbitals in shaping the electronic states of the emitters. The discovery of elementary excitations in hBN provides fundamental insights into quantum emission in low-dimensional materials, paving the way for future investigations in other platforms. 

Due to the enhanced nature of the interactions of light with quantum excitations, topological polaritonic (TP) systems form a unique platform that offers on‐chip control over half‐light, half‐matter excitations via synthetic degrees of freedom. Among other polaritonic platforms, van der Waals materials (vdW) have recently attracted significant interest due to the relative simplicity of their integration into topological photonic structures. Several TP insulators based on vdW materials have been demonstrated; however, they rely on hybrid structures with nanopatterned dielectric substrates, which limit the strength of light‐matter interactions. Here, a monolithic all‐vdW TP insulator based on bulk crystals of transition metal dichalcogenide WS₂is designed and experimentally realized. Due to their high refractive index and the presence of exciton modes, these nanomaterials prove to be excellent platforms for TPs, offering both excellent confinement and strong light‐matter interactions in monolithic structures. The emergence of TP boundary modes is confirmed by Fourier and real‐space imaging, and a dramatic reduction in dissipation is observed at cryogenic temperatures. The proposed monolithic all‐vdW topological insulators, which are characterized by extreme confinement of optical fields and moderate losses, can serve as an alternative to silicon photonics‐based systems in the quest for the development of polaritonic quantum technologies. 

Abstract The growing field of quantum information technology requires propagation of information over long distances with efficient readout mechanisms. Excitonic quantum fluids have emerged as a powerful platform for this task due to their straightforward electro-optical conversion. In two-dimensional transition metal dichalcogenides, the coupling between spin and valley provides exciting opportunities for harnessing, manipulating, and storing bits of information. However, the large inhomogeneity of single layers cannot be overcome by the properties of bright excitons, hindering spin-valley transport. Nonetheless, the rich band structure supports dark excitonic states with strong binding energy and longer lifetime, ideally suited for long-range transport. Here we show that dark excitons can diffuse over several micrometers and prove that this repulsion-driven propagation is robust across non-uniform samples. The long-range propagation of dark states with an optical readout mediated by chiral phonons provides a new concept of excitonic devices for applications in both classical and quantum information technology. 

Abstract The topological features of optical vortices have been opening opportunities for free-space and on-chip photonic technologies, e.g., for multiplexed optical communications and robust information transport. In a parallel but disjoint effort, polar anisotropic van der Waals nanomaterials supporting hyperbolic phonon polaritons (HP 2 s) have been leveraged to drastically boost light-matter interactions. So far HP 2 studies have been mainly focusing on the control of their amplitude and scale features. Here we report the generation and observation of mid-infrared hyperbolic polariton vortices (HP 2 Vs) associated with reconfigurable topological charges. Spiral-shaped gold disks coated with a flake of hexagonal boron nitride are exploited to tailor spin–orbit interactions and realise deeply subwavelength HP 2 Vs. The complex interplay between excitation spin, spiral geometry and HP 2 dispersion enables robust reconfigurability of the associated topological charges. Our results reveal unique opportunities to extend the application of HP 2 s into topological photonics, quantum information processing by integrating these phenomena with single-photon emitters, robust on-chip optical applications, sensing and nanoparticle manipulation.