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Exploring the non-Hermitian properties of semiconductor materials for optical applications is at the forefront of photonic research. However, the selection of appropriate systems to implement such photonic devices remains a topic of debate. In this work, we demonstrate that a perovskite crystal, characterized by its easy and low-cost manufacturing, when placed between two distributed Bragg reflectors with an air gap, can form a natural double microcavity. This construction shows promising properties for the realisation of novel, tunable non-Hermitian photonic devices through strong light-matter coupling. We reveal that such a system exhibits double-coupled polariton modes with dispersion including multiple inflection points. Owing to its non-Hermiticity, our system exhibits nonreciprocal properties and allows for the observation of exceptional points. Our experimental studies are in agreement with the theoretical analysis based on coupled mode theory and calculations based on transfer matrix method., Comment: Accepted manuscript (AM)

The tunability of individual coupling amplitudes in photonic lattices is highly desirable for photonic Hamiltonian engineering and for studying topological transitions in situ. In this work, we demonstrate the tunneling control between individual lattice sites patterned inside an optical microcavity. The tuning is achieved by applying a voltage to a liquid crystal microcavity possessing photonic Rashba-Dresselhaus spin-orbit coupling. This type of spin-orbit coupling emerges due to the high birefringence of the liquid crystal material and constitutes an artificial gauge field for photons. The proposed technique can be combined with strong-light matter coupling and non-Hermitian physics already established in liquid crystal microcavities.

We create a one-dimensional photonic crystal with strong polarization dependence and tunable by an applied electric field. We accomplish this in a planar microcavity by embedding a cholesteric liquid crystal (LC), which spontaneously forms a uniform lying helix (ULH). The applied voltage controls the orientation of the LC molecules and, consequently, the strength of a polarization-dependent periodic potential. It leads to opening or closing of photonic band gaps in the dispersion of the massive photons in the microcavity. In addition, when the ULH structure possesses a molecular tilt, it induces a spin-orbit coupling between the lattice bands of different parity. This interband spin-orbit coupling (ISOC) is analogous to optical activity and can be treated as a synthetic non-Abelian gauge potential. Finally, we show that doping the LC with dyes allows us to achieve lasing that inherits all the above-mentioned tunable properties of LC microcavity, including dual and circularly-polarized lasing.

In Bose-Einstein condensates, spin-orbit coupling produces supersolidity. It is a peculiar state of matter, which, in addition to the superfluid behaviour of weakly interacting Bose condensates, shows a periodic modulation of its density typical for crystals and called stripe phase. Here, we report the fabrication of a new type of samples allowing to achieve room-temperature supersolidity for a quantum fluid of light. The structure is an optical microcavity filled with a nematic liquid crystal (LC) sandwiched between two layers of the organic polymer MeLPPP. We demonstrate the formation of cavity exciton-polaritons in the presence of Rashba-Dresselhaus spin-orbit coupling (RDSOC), which is tuned by external voltage controlling the LC birefringence. In the RDSOC regime, we demonstrate exciton-polariton condensation in the two distinct degenerate minima of the dispersion. The condensate real space distribution shows both polarization and density stripes, which stem from the interference between phase-coherent condensate components characterized by different wavevectors and polarizations. The possibilities offered by this platform to tune the particle dispersion and to perform full state tomography, including time-resolved, open wide perspectives for detailed future studies of the static and dynamical behaviour of supersolids and of quantum fluids in presence of SOC and topologically non-trivial bands.

In the presence of Rashba-Dresselhaus coupling, strong spin-orbit interactions in liquid crystal optical cavities result in a distinctive spin-split entangled dispersion. Spin coherence between such modes give rise to an optical persistent-spin-helix. In this letter, we introduce optical gain in such a system, by dispersing a molecular dye in a liquid-crystal microcavity. We demonstrate both lasing in the Rashba-Dresselhaus regime and the emergence of an optical persistent spin helix.

Spin-orbit interactions which couple spin of a particle with its momentum degrees of freedom lie at the center of spintronic applications. Of special interest in semiconductor physics are Rashba and Dresselhaus spin-orbit coupling (SOC). When equal in strength, the Rashba and Dresselhaus fields result in SU(2) spin rotation symmetry and emergence of the persistent spin helix (PSH) only investigated for charge carriers in semiconductor quantum wells. Recently, a synthetic Rashba-Dresselhaus Hamiltonian was shown to describe cavity photons confined in a microcavity filled with optically anisotropic liquid crystal. In this work, we present a purely optical realisation of two types of spin patterns corresponding to PSH and the Stern-Gerlach experiment in such a cavity. We show how the symmetry of the Hamiltonian results in spatial oscillations of the spin orientation of photons travelling in the plane of the cavity.

We demonstrate an application of retardation-modulation polarimetry in studies of nanocomposite materials. Molecular ordering is explored on both nonchiral and chiral liquid crystals (LCs) in the bulk state and embedded into parallel-arrays of cylindrical channels of alumina or silica membranes of different channel sizes (12-42 nm). Two arms polarimetry serves for simultaneous measurements of the birefringence retardation and optical activity characterizing, respectively, orientational molecular ordering and chiral structuring inside nanochannels., Comment: Conference article, 5 pages, 5 figures

The orientational and translational order of a thermotropic ferroelectric liquid crystal (2MBOCBC) imbibed in self-organized, parallel, cylindrical pores with radii of 10, 15, or 20 nm in anodic aluminium oxide monoliths (AAO) are explored by high-resolution linear and circular optical birefringence as well as neutron diffraction texture analysis. The results are compared to experiments on the bulk system. The native oxidic pore walls do not provide a stable smectogen wall anchoring. By contrast, a polymeric wall grafting enforcing planar molecular anchoring results in a thermal-history independent formation of smectic C* helices and a reversible chevron-like layer buckling. An enhancement of the optical rotatory power by up to one order of magnitude of the confined compared to the bulk liquid crystal is traced to the pretransitional formation of helical structures at the smectic-A*-to-smectic-C* transformation. A linear electro-optical birefringence effect evidences collective fluctuations in the molecular tilt vector direction along the confined helical superstructures, i.e. the Goldstone phason excitations typical of the para-to-ferroelectric transition. Their relaxation frequencies increase with the square of the inverse pore radii as characteristic of plane-wave excitations and are two orders of magnitude larger than in the bulk, evidencing an exceptionally fast electro-optical functionality of the liquid-crystalline-AAO nanohybrids., Comment: 14 pages, 13 figures, 2 ancillary files, as submitted, Nanoscale (in press)