Nonlinear relaxation phenomena in three different systems of condensed matter are investigated. (i) First, the phase dynamics in Josephson junctions is analyzed. Specifically, a superconductor-graphene-superconductor (SGS) system exhibits quantum metastable states, and the average escape time from these metastable states in the presence of Gaussian and correlated fluctuations is calculated, accounting for variations in the the noise source intensity and the bias frequency. Moreover, the transient dynamics of a long-overlap Josephson junction (JJ) subject to thermal fluctuations and non-Gaussian noise sources is investigated. Noise induced phenomena are observed, such as the noise enhanced stability and the stochastic resonant activation. (ii) Second, the electron spin relaxation process in a n-type GaAs bulk driven by a fluctuating electric field is investigated. In particular, by using a Monte Carlo approach, we study the influence of a random telegraph noise on the spin polarized transport. Our findings show the possibility to raise the spin relaxation length by increasing the amplitude of the external fluctuations. Moreover, we find that, crucially, depending on the value of the external field strength, the electron spin depolarization length versus the noise correlation time increases up to a plateau. (iii) Finally, the stabilization of quantum metastable states by dissipation is presented. Normally, quantum fluctuations enhance the escape from metastable states in the presence of dissipation. We show that dissipation can enhance the stability of a quantum metastable system, consisting of a particle moving in a strongly asymmetric double well potential, interacting with a thermal bath. We find that the escape time from the metastable region has a nonmonotonic behavior versus the system- bath coupling and the temperature, producing a stabilizing effect.

The translocation of molecules across cellular membranes or through synthetic nanopores is strongly affected by thermal fluctuations. In this work we study how the dynamics of a polymer in a noisy environment changes when the translocation process is driven by an oscillating electric field. An improved version of the Rouse model for a flexible polymer has been adopted to mimic the molecular dynamics, by taking into account the harmonic interactions between adjacent monomers and the excluded-volume effect by introducing a Lennard-Jones potential between all beads. A bending recoil torque has also been included in our model. The polymer dynamics is simulated in a two-dimensional domain by numerically solving the Langevin equations of motion. Thermal fluctuations are taken into account by introducing a Gaussian uncorrelated noise. The mean first translocation time of the polymer centre of inertia shows a minimum as a function of the frequency of the oscillating forcing field. This finding represents the first evidence of the resonant activation behaviour in the dynamics of polymer translocation.

This paper addresses the efficacy of an open-inquiry approach that allows students to build on traditionally received knowledge. A sample of thirty engineering undergraduates, having already attended traditional university physics instruction, was selected for this study. The students were involved in a six-week long learning experience of open-inquiry research activities within the highly motivating context of developing a thermodynamically efficient space base on Mars. They designed and carried out their own scientific investigations, which involved gathering information, collecting and analyzing data, providing explanations, and sharing results. A questionnaire containing fifteen open-ended real-world problems in thermal science was administered to the students both prior to and after all activities, with the aim of investigating the nature of their difficulties in problem solving. Students' answers were classified into three epistemological profiles and a prepost instruction comparison was carried out, using methods of statistical implicative analysis. The students obtained significant benefits from their open-inquiry experiences, in terms of the strengthening of their practical and reasoning abilities, by proficiently applying the learned concepts to face and solve real-world problem situations.

The temperature tunability of complex dielectric constants of vanadium dioxide (VO2) makes it a promising phase-change material for use in active, dynamic, tunable photonics applications. Specifically, the semiconductor-to-metal phase transition in VO2 enables reversible, broadband, and large complex refractive index variation and paves the way for a plethora of applications. Although the critical temperature for phase-transition is 68 °C for VO2 films, its transition temperature can be reduced to room temperature by tungsten-doping of vanadium dioxide. Such a degree of freedom in controlling the critical temperature through tungsten doping provides further tunability of the thermochromic behavior. In this work, we investigate a variety of W-doped VO2 thin films deposited by laser ablation of targets with increasing W doping content and report detailed infrared characterization together with numerical simulations. Our experimental results indicate that the perfect absorption can be achieved at different temperatures, within the VO2 insulator-to-metal phase transition process, as a function of W doping content. Tunable subwavelength layers allow perfect absorption under different temperature conditions around λ = 12 µm. We show that a high dynamic range of reflectivity can be achieved when the temperature is increased above the phase transition temperature. Furthermore, we observe perfect absorption at 11.8 µm at room temperature for a W content of 0.75%. We believe that W-doped VO2 thin films with tunable and controllable perfect absorption will open the way for a class of promising thermo-optical devices including thermos-photovoltaics, infrared filters, radiative cooling devices, and thermal emitters.