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Superconducting circuits constitute a promising platform for future implementation of quantum processors and simulators. Arrays of capacitively coupled transmon qubits naturally implement the Bose-Hubbard model with attractive on-site interaction. The spectrum of such many-body systems is characterised by low-energy localised states defining the lattice analog of bright solitons. Here, we demonstrate that these bright solitons can be pinned in the system, and we find that a soliton moves while maintaining its shape. Its velocity obeys a scaling law in terms of the combined interaction and number of constituent bosons. In contrast, the source-to-drain transport of photons through the array occurs through extended states that have higher energy compared to the bright soliton. For weak coupling between the source/drain and the array, the populations of the source and drain oscillate in time, with the chain remaining nearly unpopulated at all times. Such a phenomenon is found to be parity dependent. Implications of our results for the actual experimental realisations are discussed.

A self-propelled artificial microswimmer is often modeled as a ballistic Brownian particle moving with constant speed aligned along one of its axis, but changing direction due to random collisions with the environment. Similarly to thermal noise, its angular randomization is described as a memoryless stochastic process. Here, we speculate that finite-time correlations in the orientational dynamics can affect the swimmer's diffusivity. To this purpose we propose and solve two alternative models. In the first one we simply assume that the environmental fluctuations governing the swimmer's propulsion are exponentially correlated in time, whereas in the second one we account for possible damped fluctuations of the propulsion velocity around the swimmer's axis. The corresponding swimmer's diffusion constants are predicted to get, respectively, enhanced or suppressed upon increasing the model memory time. Possible consequences of this effect on the interpretation of the experimental data are discussed., Comment: accepted by J. Chem. Phys