arXiv subjects

A. Maitra

Publications and source records attributed to A. Maitra.

4 recordsLinked to original sources

arXiv2019

Far-from-equilibrium noise heating and laser cooling dynamics in radio-frequency Paul traps

We study the stochastic dynamics of a particle in a periodically driven potential. For atomic ions trapped in radio-frequency Paul traps, noise heating and laser cooling typically act slowly in comparison with the unperturbed motion. These stochastic processes can be accounted for in terms of a probability distribution defined over the action variables, which would otherwise be conserved within the regular regions of the Hamiltonian phase space. We present a semiclassical theory of low-saturation laser cooling applicable from the limit of low-amplitude motion to large-amplitude motion, accounting fully for the time-dependent and anharmonic trap. We employ our approach to a detailed study of the stochastic dynamics of a single ion, drawing general conclusions regarding the nonequilibrium dynamics of laser-cooled trapped ions. We predict a regime of anharmonic motion in which laser cooling becomes diffusive (i.e., it is equally likely to cool the ion as it is to heat it), and can also turn into effective heating. This implies that a high-energy ion could be easily lost from the trap despite being laser cooled; however, we find that this loss can be counteracted using a laser detuning much larger than Doppler detuning.

physics.atom-ph↗

arXiv2019

Can a periodically driven particle resist laser cooling and noise?

Studying a single atomic ion confined in a time-dependent periodic anharmonic potential, we find large amplitude trajectories stable for millions of oscillation periods in the presence of stochastic laser cooling. The competition between energy gain from the time-dependent drive and damping leads to the stabilization of such stochastic limit cycles. Instead of converging to the global minimum of the averaged potential, the steady-state phase-space distribution develops multiple peaks in the regions of phase space where the frequency of the motion is close to a multiple of the periodic drive. Such distinct nonequilibrium behaviour can be observed in realistic radio-frequency traps with laser-cooled ions, suggesting that Paul traps offer a well-controlled test-bed for studying transport and dynamics of microscopically driven systems.

physics.atom-ph↗

arXiv2015

Active Viscoelastic Matter: from Bacterial Drag Reduction to Turbulent Solids

A paradigm for internally driven matter is the active nematic liquid crystal, whereby the equations of a conventional nematic are supplemented by a minimal active stress that violates time reversal symmetry. In practice, active fluids may have not only liquid crystalline but also viscoelastic polymer degrees of freedom. Here we explore the resulting interplay by coupling an active nematic to a minimal model of polymer rheology. We find that adding polymer can greatly increase the complexity of spontaneous flow, but can also have calming effects, thereby increasing the net throughput of spontaneous flow along a pipe (a 'drag-reduction' effect). Remarkably, active turbulence can also arise after switching on activity in a sufficiently soft elastomeric solid.

cond-mat.soft↗

arXiv2007

Cation Transport in Polymer Electrolytes: A Microscopic Approach

A microscopic theory for cation diffusion in polymer electrolytes is presented. Based on a thorough analysis of molecular dynamics simulations on PEO with LiBF$_4$ the mechanisms of cation dynamics are characterised. Cation jumps between polymer chains can be identified as renewal processes. This allows us to obtain an explicit expression for the lithium ion diffusion constant D_{Li} by invoking polymer specific properties such as the Rouse dynamics. This extends previous phenomenological and numerical approaches. In particular, the chain length dependence of D_{Li} can be predicted and compared with experimental data. This dependence can be fully understood without referring to entanglement effects.

cond-mat.soft↗