Real-space Hopfield diagonalization of inhomogeneous dispersive media

We introduce a real-space technique able to extend the standard Hopfield approach commonly used in quantum polaritonics to the case of inhomogeneous lossless materials interacting with the electromagnetic field. We derive the creation and annihilation polaritonic operators for the system normal modes as linear, space-dependent superpositions of the microscopic light and matter fields, and we invert the Hopfield transformation expressing the microscopic fields as functions of the polaritonic operators. As an example, we apply our approach to the case of a planar interface between vacuum and a polar dielectric, showing how we can consistently treat both propagative and surface modes, and express their nonlinear interactions, arising from phonon anharmonicity, as polaritonic scattering terms. We also show that our theory can be naturally extended to the case of dissipative materials

Theoretical Investigation of Phonon Polaritons in SiC Micropillar Resonators

Of late there has been a surge of interest in localised phonon polariton resonators which allow for sub-diffraction confinement of light in the mid-infrared spectral region by coupling to optical phonons at the surface of polar dielectrics. Resonators are generally etched on deep substrates which support propagative surface phonon polariton resonances. Recent experimental work has shown that understanding the coupling between localised and propagative surface phonon polaritons in these systems is vital to correctly describe the system resonances. In this paper we comprehensively investigate resonators composed of arrays of cylindrical SiC resonators on SiC substrates. Our bottom-up approach, starting from the resonances of single, free standing cylinders and isolated substrates, and exploiting both numerical and analytical techniques, allows us to develop a consistent understanding of the parameter space of those resonators, putting on firmer ground this blossoming technology.Comment: 10 Pages, 8 Figure

Excitonic spectral features in strongly-coupled organic polaritons

Starting from a microscopic model, we investigate the optical spectra of molecules in strongly-coupled organic microcavities examining how they might self-consistently adapt their coupling to light. We consider both rotational and vibrational degrees of freedom, focusing on features which can be seen in the peak in the center of the spectrum at the bare excitonic frequency. In both cases we find that the matter-light coupling can lead to a self-consistent change of the molecular states, with consequent temperature-dependent signatures in the absorption spectrum. However, for typical parameters, these effects are much too weak to explain recent measurements. We show that another mechanism which naturally arises from our model of vibrationally dressed polaritons has the right magnitude and temperature dependence to be at the origin of the observed data.Comment: 14 pages, 6 figur

Observing the evolution of a quantum system that does not evolve

This article deals with the problem of gathering information on the time evolution of a single metastable quantum system whose evolution is impeded by the quantum Zeno effect. It has been found it is in principle possible to obtain some information on the time evolution and, depending on the specific system, even to measure its average decay rate, even if the system does not undergo any evolution at all.Comment: Two over three PRA referees didn't like the old title... And no more quantum circuits in the new versio

Accurate Determination of Conformational Transitions in Oligomeric Membrane Proteins

The structural dynamics governing collective motions in oligomeric membrane proteins play key roles in vital biomolecular processes at cellular membranes. In this study, we present a structural refinement approach that combines solid-state NMR experiments and molecular simulations to accurately describe concerted conformational transitions identifying the overall structural, dynamical, and topological states of oligomeric membrane proteins. The accuracy of the structural ensembles generated with this method is shown to reach the statistical error limit, and is further demonstrated by correctly reproducing orthogonal NMR data. We demonstrate the accuracy of this approach by characterising the pentameric state of phospholamban, a key player in the regulation of calcium uptake in the sarcoplasmic reticulum, and by probing its dynamical activation upon phosphorylation. Our results underline the importance of using an ensemble approach to characterise the conformational transitions that are often responsible for the biological function of oligomeric membrane protein states