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The integration of photonic microstructure into organic microcavities represents an effective strategy for manipulating eigenstates of cavity or polariton modes. However, well-established fabrication processes for microstructured organic microcavities are still lacking. In this study, we propose a nanoimprint-bonding process as a novel fabrication method for microstructured organic microcavities. This process relies on a UV nanoimprint technique utilizing two different photopolymer resins, enabling the independent fabrication of highly reflective reflectors and photonic microstructures without compromising the accuracy of each. The resulting organic microcavities demonstrate spatially localized photonic modes within dot structures and their nonlinear responses on the pumping fluence. Furthermore, a highly precise photonic band is confirmed within a honeycomb lattice structure, which is owing to the high quality factor of the cavity achievable with the nanoimprint-bonding process. Additionally, a topological edge state is also observable within a zigzag lattice structure. These results highlight the significant potential of our fabrication method for advancing organic-based photonic devices, including lasers and polariton devices.

Spin-orbit coupling (SOC) of light plays a fundamental photophysics that is important for various fields such as materials science, optics, and quantum technology, contributing to the elucidation of new physical phenomena and the development of innovative applications. In this study, we investigate the impact of SOC in a microcavity system using the highly oriented molecular crystal. The unique molecular alignment of our crystal creates substantial optical anisotropy, enabling the observation of significant SOC effects within a microcavity form. Through angle-resolved photoluminescence measurements and theoretical calculations, the presence of Rashba-Dresselhaus (RD) SOC in the lower branch of polariton modes is revealed. We have observed for the first time polarization-coupled emission from polariton modes due to the RD-SOC effect in a microcavity with a medium having both strong light-matter coupling and strong optical anisotropy. Theoretical investigations further elucidate the intricate interplay between the RD-SOC effect and anisotropic light-matter coupling, leading to the emergence of both circularly and diagonally polarized mode splittings. This study not only advances our understanding of optical SOC in microcavities but also highlights the potential of highly oriented molecular crystals in manipulating SOC effects without external electric or magnetic fields. These findings offer greatly promising platforms for developing topological photonics and quantum technologies.

Disordered systems exhibit universal excitation, referred to as the boson peak, in the terahertz region. Meanwhile, the so-called fracton is expected to appear in the nanoscale region owing to the self-similar structure of monomers in polymeric glasses. We demonstrate that such excitations can be detected using terahertz spectroscopy. For the interaction between terahertz light and the vibrational density of states of the fractal structure, we formulate an infrared light-vibration coupling coefficient for the fracton region. Accordingly, we show that information concerning fractal and fracton dimensions appears in the exponent of the absorption coefficient. Finally, using terahertz time-domain spectroscopy and low-frequency Raman scattering, we experimentally observe these universal excitations in a protein lysozyme system that has an intrinsically disordered and self-similar nature in a single supramolecule. These findings are applicable to disordered and polymeric glasses in general and will be key to understanding universal dynamics of disordered systems by terahertz light.