We propose a novel physical mechanism for the creation of long-lived macroscopic exciton-photon qubits in semiconductor microcavities with embedded quantum wells in the strong coupling regime. The polariton qubit is a superposition of lower branch and upper branch exciton-polariton states. We argue that the coherence time of Rabi oscillations can be dramatically enhanced due to their stimulated pumping from a permanent thermal reservoir of polaritons. We discuss applications of such qubits for quantum information processing, cloning, and storage purposes.
The problem of photonic phase transition for the system of a two-level atomic ensemble interacting with a quantized single-mode electromagnetic field in the presence of optical collisions (OC) is considered. We have shown that for large and negative atom-field detuning a photonic field exhibits high temperature second order phase transition to superradiant state under thermalization condition for coupled atom-light states. Such a transition can be connected with superfluid (coherent) properties of photon-like low branch (LB) polaritons. We discuss the application of metallic cylindrical waveguide for observing predicted effects.
We stabilize monoatomic carbon chains in water by attaching them to gold nanoparticles (NPs) by means of the laser ablation process. Resulting nanoobjects represent pairs of NPs connected by multiple straight carbon chains of several nanometer lengths. If NPs at the opposite ends of a chain differ in size, the structure acquires a dipole moment due to the difference in work functions of the two NPs. We take advantage of the dipole polarisation of carbon chains for ordering them by the external electric field. We deposit them on a glass substrate by the sputtering method in the presence of static electric fields of magnitudes up to 105 V/m. The formation of one-dimensional carbyne quasi-crystals deposited on a substrate is evidenced by high-resolution TEM and X-ray diffraction measurements. The original kinetic model describing the dynamics of ballistically flowing nano-dipoles reproduces the experimental diagram of orientation of the deposited chains.
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