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Register a new userDetermination of polariton condensates critical temperature
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We investigate the thermal robustness of traveling polariton condensates. We create remote condensates that have never been in contact, and study their interference in momentum space, when they travel with the same velocity, by means of time-resolved photoluminescence. We determine the condensed to thermal, uncondensed polariton fraction, which shows a gradual decay with increasing temperature, and obtain the critical temperature for the Bose-Einstein-like condensate (BEC) phase transition. We tentatively compare our experimental findings with theoretical models, developed for atomic condensates, to describe the condensates coherence fading with temperature.
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The strong light-matter coupling of a microcavity mode to tightly bound Frenkel excitons in organic materials emerged as a versatile, room-temperature compatible platform to study nonlinear many-particle physics and bosonic condensation. However, various aspects of the optical response of Frenkel excitons in this regime remained largely unexplored. Here, we utilize a hemispheric optical cavity filled with the fluorescent protein mCherry to address two important questions in the field of room-temperature polariton condensates. First, combining the high quality factor of the microcavity with a well-defined mode structure allows us to provide a definite answer whether temporal coherence in such systems can become competitive with their low-temperature counterparts. We observe highly monochromatic and coherent light beams emitted from the condensate, characterized by a coherence time greater than 150$,$ps, which exceeds the polariton lifetime by two orders of magnitude. Second, the high quality of our device allows to sensibly trace the emission energy of the condensate, and thus to establish a fundamental picture which quantitatively explains the core nonlinear processes yielding the characteristic density-dependent blueshift. We find that the energy shift of Frenkel exciton-polaritons is largely dominated by the reduction of the Rabi-splitting due to phase space filling effects, which is influenced by the redistribution of polaritons in the system. While our finding of highly coherent condensation at ambient conditions addresses the suitability of organic polaritonics regarding their utilization as highly coherent room temperature polariton lasers, shedding light on the non-linearity is of great benefit towards implementing non-linear devices, optical switches, and lattices based on exciton-polaritons at room temperature.
We examine the photoluminescence of highly-excited exciton-polariton condensates in semiconductor microcavities. Under strong pumping, exciton-polariton condensates have been observed to undergo a lasing transition where strong coupling between the excitons and photons is lost. We discuss an alternative high-density scenario, where the strong coupling is maintained. We find that the photoluminescence smoothly transitions between the lower polariton energy to the cavity photon energy. An intuitive understanding of the change in spectral characteristics is given, as well as differences to the photoluminescence characteristics of the lasing case.
Open-dissipative systems obeying parity-time ($mathcal{PT}$) symmetry are capable of demonstrating oscillatory dynamics akin to the conservative systems. In contrast to limit cycle solutions characteristic of nonlinear systems, the $mathcal{PT}$-symmetric oscillations form a continuum of non-isolated orbits. However, precise sculpturing of the real potential and the gain-loss spatial profiles required for establishing of the $mathcal{PT}$-symmetry is practically challenging. The optical devices, such as lasers, exhibit relaxation dynamics and do not operate as the $mathcal{PT}$-symmetric systems. Here we demonstrate how these constraints can be overcome. We predict that a pair of optically trapped polariton condensates (a polariton dimer) can be excited and operated in the oscillating regime typical of the isolated systems. This regime can be realized in the presence of both dissipative and conservative coupling between the condensates and can be maintained at an arbitrary external pump intensity. Every orbit is characterised by a frequency comb appearing in the spectrum of a dimer in the presence of the conservative nonlinearity. Our results pave the way for the creation of the optical computing devices operating under the constant-wave external pumping.
The phase and the frequency of an exciton polariton condensate excited by a nonresonant pump can be efficiently manipulated by an external coherent light. Being tuned close to the resonance with the condensate eigenfrequency, the external laser light imposes its frequency to the condensate and locks its phase, thereby manifesting a synchronization effect. The conditions of formation of the phase synchronized regime are determined. The synchronization of a couple of closely spaced polariton condensates by a spatially uniform coherent light is examined. At the moderate strength of the coherent driving the synchronization is accompanied by the appearance of symmetry-breaking states of the polariton dyad, while these states are superseded by the symmetric state at the high-intensity driving. By employing a zero-dimensional model of coupled dissipative oscillators with both dissipative and conservative coupling, we study the bifurcation scenario of the symmetry-breaking state formation.
We report on the origin of energy-shifts in organic polariton condensates. The localised nature of Frenkel excitons in molecular semiconductors precludes interparticle Coulomb exchange interactions -the latter being the dominant mechanism for blueshifts in inorganic semiconductor microcavities that bear Wannier-Mott excitons. We examine the contribution of optically induced change of the intracavity non-linear refractive index, gain induced frequency-pulling and quenching of the Rabi splitting, as well as the role of polariton-exciton and polariton-polariton scattering in the energy-shift of the polariton mode at condensation threshold in strongly coupled molecular dye microcavities. We conclude that blueshifts in organic polariton condensates arise from the interplay of the saturation of molecular optical transitions and intermolecular energy migration. Our model predicts the commonly observed step-wise increase of both the emission energy and degree of linear polarisation at polariton condensation threshold.
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