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We determine the zero temeperature phase diagram of excitons in the symmetric transition-metal dichalcogenide tri-layer heterosctructure WSe2/MoSe2/WSe2. First principle calculations reveal two distinct types of interlayer excitonic states, a lower energy symmetric quadrupole and a higher energy asymmetric dipole. While interaction between quadrupolar excitons is always repulsive, anti-parallel dipolar excitons attract at large distances. We find quantum phase transitions between a repulsive quadrupole lattice phase and a staggered (anti-parallel) dipolar lattice phase, driven by the competition between the exciton-exciton interactions and the single exciton energies. Remarkably, the intrinsic nature of each interlayer exciton is completely different in each phase. This is a striking example for the possible rich quantum physics in a system where the single particle properties and the many-body state are dynamically coupled through the particle interactions.

The interaction between aligned dipoles is long-ranged and highly anisotropic: it changes from repulsive to attractive depending on the relative positions of the dipoles. We report on the observation of the attractive component of the dipolar coupling between excitonic dipoles in stacked semiconductor bilayers. We show that the presence of a dipolar exciton fluid in one bilayer modifies the spatial distribution and increases the binding energy of excitonic dipoles in a vertically remote layer. The binding energy changes are explained by a many-body polaron model describing the deformation of the exciton cloud due to its interaction with a remote dipolar exciton. The results open the way for the observation of theoretically predicted new and exotic collective phases, the realization of interacting dipolar lattices in semiconductor systems as well as for engineering and sensing their collective excitations., Comment: 11 Pages, 9 Figures

The formation of a dense Bose-Einstein condensate in dark spin states of two-dimensional dipolar excitons is shown to be driven by a dynamical transition to the long-lived dark states. The condensate is stabilized by strong dipole-dipole interactions up to densities high enough for a dark quantum liquid to form. The persistence of dark condensation was observed in recent experiments. A model describing the non-equilibrium dynamics of externally driven coupled dark and bright condensates reproduces the step-like dependence of the exciton density on the pump power or on temperature. This unique condensate dynamics demonstrates the possibility of observing new unexpected collective phenomena in coupled condensed Bose systems, where the particle number is not conserved.

Exciton-polaritons are mutually interacting quantum hybridizations of confined photons and electronic excitations. Here we demonstrate a system of optically guided, electrically polarized exciton-polaritons ('dipolaritons') that displays up to 200-fold enhancement of the polariton-polariton interaction strength compared to unpolarized polaritons. The magnitude of the dipolar interaction enhancement can be turned on and off and be easily tuned over a very wide range by varying the applied polarizing electric-field. The very large interaction strengths and the very long propagation distances of these fully-guided dipolaritons open up new opportunities for realizing complex quantum circuitry and quantum simulators, as well as topological states based on exciton-polaritons, for which the interactions between polaritons need to be large and spatially or temporally controlled. The results also raise fundamental questions on the origin of such large enhancements.

Recently we reported on the condensation of cold, electrostatically trapped dipolar excitons in GaAs bilayer heterostructure into a new, dense and dark collective phase. Here we analyze and discuss in detail the experimental findings and the emerging evident properties of this collective liquid-like phase. We show that the phase transition is characterized by a sharp increase of the number of non-emitting dipoles, by a clear contraction of the fluid spatial extent into the bottom of the parabolic-like trap, and by spectral narrowing. We extract the total density of the condensed phase which we find to be consistent with the expected density regime of a quantum liquid. We show that there are clear critical temperature and excitation power onsets for the phase transition and that as the power further increases above the critical power, the strong darkening is reduced down until no clear darkening is observed. At this point another transition appears which we interpret as a transition to a strongly repulsive yet correlated $e$-$h$ plasma. Based on the experimental findings, we suggest that the physical mechanism that may be responsible for the transition is a dynamical final-state stimulation of the dipolar excitons to their dark spin states, which have a long lifetime and thus support the observed sharp increase in density. Further experiments and modeling will hopefully be able to unambiguously identify the physical mechanism behind these recent observations.

Spatially indirect excitons in semiconducting double quantum wells have been shown to exhibit rich collective many-body behavior that result from the nature of the extended dipole-dipole interactions between particles. For many spectroscopic studies of the emission from a system of such indirect excitons, it is crucial to separate the single particle properties of the excitons from the many-body effects arising from their mutual interactions. In particular, knowledge of the relation between the emission energy of indirect excitons and their radiative lifetime could be highly beneficial for control, manipulation, and analysis of such systems. Here we study a simple analytic approximate relation between the radiative lifetime of indirect excitons and their emission energy. We show, both numerically and experimentally, the validity and the limits of this approximate relation. This relation between the emission energy and the lifetime of indirect excitons can be used to tune and determine their lifetime and their resulting dynamics without the need of directly measuring it, and as a tool for design of indirect exciton based devices., Comment: * Added references. * Corrected the Al content mentioned as the sample's and used in Sec. II