Abstract
Organic exciton-photon polariton lasers are promising candidates for the efficient generation of coherent light at room temperature. While their thresholds are now comparable with those of conventional organic photon lasers, tuning of molecular conformation and orientation as a means to control fundamental properties of their emission and thus further enhance performance remains largely unexplored. Here, a two-fold reduction in the threshold of a microcavity polariton laser based on an active layer of poly(9,9-dioctylfluorene) (PFO) is achieved when 15% beta-phase conformation is introduced. In addtion, taking advantage of the liquid crystalline properties of PFO, a thin photoalignment layer is used to induce nematic alignment of the polymer chains. The resulting transition dipole moment orientation increases the Rabi energy, bringing the system into the ultra-strong coupling regime and facilitating anisotropic polariton lasing with an eight-fold reduction in absorbed threshold, down to 1.14 pJ (0.36 mu J cm(-2)) for the direction parallel to the orientation, with no emission along the orthogonal direction. This represents the first demonstration of anisotropic polariton lasing in conjugated polymer microcavities and a lower threshold than current organic vertical cavity surface-emitting photon and polariton lasers. Dipole orientation offers new opportunities for switchable, more efficient polaritonic devices, and observation of fundamental effects at low polariton numbers.