On a flow of transformations of a Wiener space

In this paper, we define, via Fourier transform, an ergodic flow of transformations of a Wiener space which preserves the law of the Ornstein-Uhlenbeck process and which interpolates the iterations of a transformation previously defined by Jeulin and Yor. Then, we give a more explicit expression for this flow, and we construct from it a continuous gaussian process indexed by R^2, such that all its restriction obtained by fixing the first coordinate are Ornstein-Uhlenbeck processes

Capillarity-Driven Flows at the Continuum Limit

We experimentally investigate the dynamics of capillary-driven flows at the nanoscale, using an original platform that combines nanoscale pores and microfluidic features. Our results show a coherent picture across multiple experiments including imbibition, poroelastic transient flows, and a drying-based method that we introduce. In particular, we exploit extreme drying stresses - up to 100 MPa of tension - to drive nanoflows and provide quantitative tests of continuum theories of fluid mechanics and thermodynamics (e.g. Kelvin-Laplace equation) across an unprecedented range. We isolate the breakdown of continuum as a negative slip length of molecular dimension.Comment: 5 pages; 4 figure

A stochastic derivation of the geodesic rule

We argue that the geodesic rule, for global defects, is a consequence of the randomness of the values of the Goldstone field $\phi$ in each causally connected volume. As these volumes collide and coalescence, $\phi$ evolves by performing a random walk on the vacuum manifold $\mathcal{M}$. We derive a Fokker-Planck equation that describes the continuum limit of this process. Its fundamental solution is the heat kernel on $\mathcal{M}$, whose leading asymptotic behavior establishes the geodesic rule.Comment: 12 pages, No figures. To be published in Int. Jour. Mod. Phys.

How a "pinch of salt" can tune chaotic mixing of colloidal suspensions

Efficient mixing of colloids, particles or molecules is a central issue in many processes. It results from the complex interplay between flow deformations and molecular diffusion, which is generally assumed to control the homogenization processes. In this work we demonstrate on the contrary that despite fixed flow and self-diffusion conditions, the chaotic mixing of colloidal suspensions can be either boosted or inhibited by the sole addition of trace amount of salt as a co-mixing species. Indeed, this shows that local saline gradients can trigger a chemically-driven transport phenomenon, diffusiophoresis, which controls the rate and direction of molecular transport far more efficiently than usual Brownian diffusion. A simple model combining the elementary ingredients of chaotic mixing with diffusiophoretic transport of the colloids allows to rationalize our observations and highlights how small-scale out-of-equilibrium transport bridges to mixing at much larger scales in a very effective way. Considering chaotic mixing as a prototypal building block for turbulent mixing, this suggests that these phenomena, occurring whenever the chemical environment is inhomogeneous, might bring interesting perspective from micro-systems up to large-scale situations, with examples ranging from ecosystems to industrial contexts.Comment: Submitte

Three-dimensional flows in slowly-varying planar geometries

We consider laminar flow in channels constrained geometrically to remain between two parallel planes; this geometry is typical of microchannels obtained with a single step by current microfabrication techniques. For pressure-driven Stokes flow in this geometry and assuming that the channel dimensions change slowly in the streamwise direction, we show that the velocity component perpendicular to the constraint plane cannot be zero unless the channel has both constant curvature and constant cross-sectional width. This result implies that it is, in principle, possible to design "planar mixers", i.e. passive mixers for channels that are constrained to lie in a flat layer using only streamwise variations of their in-plane dimensions. Numerical results are presented for the case of a channel with sinusoidally varying width

Derivation of quantum work equalities using quantum Feynman-Kac formula

On the basis of a quantum mechanical analogue of the famous Feynman-Kac formula and the Kolmogorov picture, we present a novel method to derive nonequilibrium work equalities for isolated quantum systems, which include the Jarzynski equality and Bochkov-Kuzovlev equality. Compared with previous methods in the literature, our method shows higher similarity in form to that deriving the classical fluctuation relations, which would give important insight when exploring new quantum fluctuation relations.Comment: 5 page

Quantum Diffusion and Delocalization for Band Matrices with General Distribution

We consider Hermitian and symmetric random band matrices $H$ in $d \geq 1$ dimensions. The matrix elements $H_{xy}$, indexed by $x,y \in \Lambda \subset \Z^d$, are independent and their variances satisfy \sigma_{xy}^2:=\E \abs{H_{xy}}^2 = W^{-d} f((x - y)/W) for some probability density $f$. We assume that the law of each matrix element $H_{xy}$ is symmetric and exhibits subexponential decay. We prove that the time evolution of a quantum particle subject to the Hamiltonian $H$ is diffusive on time scales $t\ll W^{d/3}$. We also show that the localization length of the eigenvectors of $H$ is larger than a factor $W^{d/6}$ times the band width $W$. All results are uniform in the size \abs{\Lambda} of the matrix. This extends our recent result \cite{erdosknowles} to general band matrices. As another consequence of our proof we show that, for a larger class of random matrices satisfying $\sum_x\sigma_{xy}^2=1$ for all $y$, the largest eigenvalue of $H$ is bounded with high probability by $2 + M^{-2/3 + \epsilon}$ for any $\epsilon > 0$, where M \deq 1 / (\max_{x,y} \sigma_{xy}^2).Comment: Corrected typos and some inaccuracies in appendix

Macroscopic quantum jumps and entangled state preparation

Recently we predicted a random blinking, i.e. macroscopic quantum jumps, in the fluorescence of a laser-driven atom-cavity system [Metz et al., Phys. Rev. Lett. 97, 040503 (2006)]. Here we analyse the dynamics underlying this effect in detail and show its robustness against parameter fluctuations. Whenever the fluorescence of the system stops, a macroscopic dark period occurs and the atoms are shelved in a maximally entangled ground state. The described setup can therefore be used for the controlled generation of entanglement. Finite photon detector efficiencies do not affect the success rate of the state preparation, which is triggered upon the observation of a macroscopic fluorescence signal. High fidelities can be achieved even in the vicinity of the bad cavity limit due to the inherent role of dissipation in the jump process.Comment: 14 pages, 12 figures, proof of the robustness of the state preparation against parameter fluctuations added, figure replace