Directional amplification, in which signals are selectively amplified depending on their propagation direction, has attracted much attention as key resource for applications, including quantum information processing. Recently, several, physically very different, directional amplifiers have been proposed and realized in the lab. In this work, we present a unifying framework based on topology to understand non-reciprocity and directional amplification in driven-dissipative cavity arrays. Specifically, we unveil a one-to-one correspondence between a non-zero topological invariant defined on the spectrum of the dynamic matrix and regimes of directional amplification, in which the end-to-end gain grows exponentially with the number of cavities. We compute analytically the scattering matrix, the gain and reverse gain, showing their explicit dependence on the value of the topological invariant. Parameter regimes achieving directional amplification can be elegantly obtained from a topological ‘phase diagram’, which provides a guiding principle for the design of both phase-preserving and phase-sensitive multimode directional amplifiers.

A general theory is developed for the evolution of the cell order (CO) distribution in planar granular systems. Dynamic equations are constructed and solved in closed form for several examples: systems under compression; dilation of very dense systems; and the general approach to steady state. We find that all the steady states are stable and that they satisfy a detailed balance-like condition when the CO$$\,\le 6$$ ≤ 6 . Illustrative numerical solutions of the evolution are shown. Our theoretical results are validated against an extensive simulation of a sheared system. The formalism can be readily extended to other structural characteristics, paving the way to a general theory of structural organisation of granular systems. Graphic abstract

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We have performed fully atomistic molecular dynamics simulations of the intracellular domain of a model of the GABA A receptor with and without the GABA receptor associated protein (GABARAP) bound. We have also calculated the electrostatic potential due to the receptor, in the absence and presence of GABARAP. We find that GABARAP binding changes the electrostatic properties around the GABA A receptor and could lead to increased conductivity of chloride ions through the receptor. We also find that ion motions that would result in conducting currents are observed nearly twice as often when GABARAP binds. These results are consistent with data from electrophysiological experiments.