The full UV-visible dielectric tensor and the corresponding directions of the principal axes of triclinic tetracene crystals are reported as deduced either by polarized absorption and ellipsometry measurements or by calculations based on the molecular and crystallographic data. The results allow the attribution of the polarized bands observed in both absorption and photoluminescence emission spectra. In particular, the spectral line shape and polarization of the emission are found to depend on the sample thickness, and the effect is attributed to the modification of the state of polarization of the emitted light during its propagation inside the crystal. Indeed, the directions of polarization of the lowest optical transitions and the directions of the principal axes of the dielectric tensor are demonstrated not to coincide, in contrast to the assumptions typically made in the literature, thus causing the mixed transverse/longitudinal character of light propagation.

International audienceThe optical response of rubrene crystals is described by providing the full UV-VIS dielectric tensor. Consistently with the molecular and crystal symmetries, the lowest crystal transition originates from an Au molecular transition, it is polarized along the c axis (normal to the larger crystal face), and it is the origin of the emission, which is self-guided towards the edge where the corresponding polarization and intensity angular distribution are detected. By contrast, the Bu molecular transitions give rise to Davydov states described by the other two components of the diagonal dielectric tens

Polarized superradiant emission and exciton delocalization in tetracene single crystals are reported. Polarization-, time-, and temperature-resolved spectroscopy evidence the complete polarization of the zero-phonon line of the intrinsic tetracene emission from both the lower (F state) and the upper (thermally activated) Davydov excitons. The superradiance of the F emission is substantiated by a nearly linear decrease of the radiative lifetime with temperature, being fifteen times shorter at 30 K compared to the isolated molecule, with an exciton delocalization of about 40 molecules.

A new approach for microfluidics-based production of polymeric particles, namely two-photon continuous flow lithography, is reported. This technique takes advantage of two-photon lithography to create objects with sub-micrometer and 3D features, and overcomes the traditional process limitations of two-photon lithography by using multiple beam production under continuous flow. Polymeric fibers, helical and bow-tie particles with sub-diffraction resolution and surface roughness as low as 10 nm are demonstrated.