arXiv subjects

Thomas Salez

Publications and source records attributed to Thomas Salez.

120 records · Page 7Linked to original sources

arXiv2014

Approach to universal self-similar attractor for the levelling of thin liquid films

We compare the capillary levelling of a random surface perturbation on a thin polystyrene film with a theoretical study on the two-dimensional capillary-driven thin film equation. Using atomic force microscopy, we follow the time evolution of samples prepared with different initial perturbations of the free surface. In particular, we show that the surface profiles present long term self-similarity, and furthermore, that they converge to a universal self-similar attractor that only depends on the volume of the perturbation, consistent with the theory. Finally, we look at the convergence time for the different samples and find very good agreement with the analytical predictions.

cond-mat.soft↗

arXiv2014

Viscoelastic effects and anomalous transient levelling exponents in thin films

We study theoretically the profile evolution of a thin viscoelastic film supported onto a no-slip flat substrate. Due to the nonconstant initial curvature at the free surface, there is a flow driven by Laplace pressure and mediated by viscoelasticity. In the framework of lubrication theory, we derive a thin film equation that contains local viscoelastic stress through the Maxwell model. Then, considering a sufficiently regular small perturbation of the free surface, we linearise the equation and derive its general solution. We analyse and discuss in details the behaviour of this function. We then use it to study the viscoelastic evolution of a Gaussian initial perturbation through its transient levelling exponent. For initial widths of the profile that are smaller than a characteristic length scale involving both the film thickness and the elastocapillary length, this exponent is shown to reach anomalously high values at the elastic-to-viscous transition. This prediction should in particular be observed at sufficiently short times in experiments on thin polymer films.

cond-mat.soft↗

arXiv2014

Capillary levelling of a cylindrical hole in a viscous film

The capillary levelling of cylindrical holes in viscous polystyrene films was studied using atomic force microscopy as well as quantitative analytical scaling arguments based on thin film theory and self-similarity. The relaxation of the holes was shown to consist of two different time regimes: an early regime where opposing sides of the hole do not interact, and a late regime where the hole is filling up. For the latter, the self-similar asymptotic profile was derived analytically and shown to be in excellent agreement with experimental data. Finally, a binary system of two holes in close proximity was investigated where the individual holes fill up at early times and coalesce at longer times.

cond-mat.soft↗

arXiv2013

Relaxation and Intermediate Asymptotics of a Rectangular Trench in a Viscous Film

The surface of a thin liquid film with nonconstant curvature flattens as a result of capillary forces. While this leveling is driven by local curvature gradients, the global boundary conditions greatly influence the dynamics. Here, we study the evolution of rectangular trenches in a polystyrene nanofilm. Initially, when the two sides of a trench are well separated, the asymmetric boundary condition given by the step height controls the dynamics. In this case, the evolution results from the leveling of two noninteracting steps. As the steps broaden further and start to interact, the global symmetric boundary condition alters the leveling dynamics. We report on full agreement between theory and experiments for: the capillary-driven flow and resulting time dependent height profiles; a crossover in the power-law dependence of the viscous energy dissipation as a function of time as the trench evolution transitions from two noninteracting to interacting steps; and the convergence of the profiles to a universal self-similar attractor that is given by the Green's function of the linear operator describing the dimensionless linearized thin film equation.

cond-mat.soft↗

arXiv2013

From adhesion to wetting of a soft particle

Using a thermodynamical approach, we calculate the deformation of a spherical elastic particle placed on a rigid substrate, under zero external load, and including an ingredient of importance in soft matter: the interfacial tension of the cap. In a first part, we limit the study to small deformation. In contrast with previous works, we obtain an expression for the energy that precisely contains the JKR and Young-Dupré asymptotic regimes, and which establishes a continuous bridge between them. In a second part, we consider the large deformation case, which is relevant for future comparison with numerical simulations and experiments on very soft materials. Using a fruitful analogy with fracture mechanics, we derive the exact energy of the problem and thus obtain the equilibrium state for any given choice of physical parameters.

cond-mat.soft↗

arXiv2013

Numerical solutions of thin film equations for polymer flows

We report on the numerical implementation of thin film equations that describe the capillary-driven evolution of viscous films, in two-dimensional configurations. After recalling the general forms and features of these equations, we focus on two particular cases inspired by experiments: the leveling of a step at the free surface of a polymer film, and the leveling of a polymer droplet over an identical film. In each case, we first discuss the long-term self-similar regime reached by the numerical solution before comparing it to the experimental profile. The agreement between theory and experiment is excellent, thus providing a versatile probe for nanorheology of viscous liquids in thin film geometries.

cond-mat.soft↗

arXiv2013

Capillary leveling of stepped films with inhomogeneous molecular mobility

A homogeneous thin polymer film with a stepped height profile levels due to the presence of Laplace pressure gradients. Here we report on studies of polymeric samples with precisely controlled, spatially inhomogeneous molecular weight distributions. The viscosity of a polymer melt strongly depends on the chain length distribution; thus, we learn about thin-film hydrodynamics with viscosity gradients. These gradients are achieved by stacking two films with different molecular weights atop one another. After a sufficient time these samples can be well described as having one dimensional viscosity gradients in the plane of the film, with a uniform viscosity normal to the film. We develop a hydrodynamic model that accurately predicts the shape of the experimentally observed self-similar profiles. The model allows for the extraction of a capillary velocity, the ratio of the surface tension and the viscosity, in the system. The results are in excellent agreement with capillary velocity measurements of uniform mono- and bi-disperse stepped films and are consistent with bulk polymer rheology.

cond-mat.soft↗

arXiv2012

Capillary-driven flow induced by a stepped perturbation atop a viscous film

Thin viscous liquid films driven by capillarity are well described in the lubrication theory through the thin film equation. In this article, we present an analytical solution of this equation for a particular initial profile: a stepped perturbation. This initial condition allows a linearization of the problem making it amenable to Fourier analysis. The solution is obtained and characterized. As for a temperature step in the heat equation, self-similarity of the first kind of the full evolution is demonstrated and a long-term expression for the excess free energy is derived. In addition, hydrodynamical fields are described. The solution is then compared to experimental profiles from a model system: a polystyrene nanostep above the glass transition temperature which flows due to capillarity. The excellent agreement enables a precise measurement of the capillary velocity for this polymeric liquid, without involving any numerical simulation. More generally, as these results hold for any viscous system driven by capillarity, the present solution may provide a useful tool in hydrodynamics of thin viscous films.

cond-mat.soft↗

arXiv2012

Beyond Tanner's Law: Crossover between Spreading Regimes of a Viscous Droplet on an Identical Film

We present results on the leveling of polymer microdroplets on thin films prepared from the same material. In particular, we explore the crossover from a droplet spreading on an infinitesimally thin film (Tanner's law regime) to that of a droplet leveling on a film thicker than the droplet itself. In both regimes, the droplet's excess surface area decreases towards the equilibrium configuration of a flat liquid film, but with a different power law in time. Additionally, the characteristic leveling time depends on molecular properties, the size of the droplet, and the thickness of the underlying film. Flow within the film makes this system fundamentally different from a droplet spreading on a solid surface. We thus develop a theoretical model based on thin film hydrodynamics that quantitatively describes the observed crossover between the two leveling regimes.

cond-mat.soft↗

arXiv2012

Self-Similarity and Energy Dissipation in Stepped Polymer Films

The surface of a thin liquid film with nonconstant curvature is unstable, as the Laplace pressure drives a flow mediated by viscosity. We present the results of experiments on one of the simplest variable curvature surfaces: a stepped polymer film. Height profiles are measured as a function of time for a variety of molecular weights. The evolution of the profiles is shown to be self-similar. This self-similarity offers a precise measurement of the capillary velocity by comparison with numerical solutions of the thin film equation. We also derive a master expression for the time dependence of the excess free energy as a function of the material properties and film geometry. The experiment and theory are in excellent agreement and indicate the effectiveness of stepped polymer films to elucidate nanoscale rheological properties.

cond-mat.soft↗

arXiv2011

Photoassociative creation of ultracold heteronuclear 6Li40K* molecules

We investigate the formation of weakly bound, electronically excited, heteronuclear 6Li40K* molecules by single-photon photoassociation in a magneto-optical trap. We performed trap loss spectroscopy within a range of 325 GHz below the Li(2S_(1/2))+K(4P_(3/2)) and Li(2S_(1/2))+K(4P_(1/2)) asymptotic states and observed more than 60 resonances, which we identify as rovibrational levels of 7 of 8 attractive long-range molecular potentials. The long-range dispersion coefficients and rotational constants are derived. We find large molecule formation rates of up to ~3.5x10^7s^(-1), which are shown to be comparable to those for homonuclear 40K_2*. Using a theoretical model we infer decay rates to the deeply bound electronic ground-state vibrational level X^1Σ^+(v'=3) of ~5x10^4s^(-1). Our results pave the way for the production of ultracold bosonic ground-state 6Li40K molecules which exhibit a large intrinsic permanent electric dipole moment.

physics.atom-ph↗

arXiv2011

Large atom number dual-species magneto-optical trap for fermionic 6Li and 40K atoms

We present the design, implementation and characterization of a dual-species magneto-optical trap (MOT) for fermionic 6Li and 40K atoms with large atom numbers. The MOT simultaneously contains 5.2x10^9 6Li-atoms and 8.0x10^9 40K-atoms, which are continuously loaded by a Zeeman slower for 6Li and a 2D-MOT for 40K. The atom sources induce capture rates of 1.2x10^9 6Li-atoms/s and 1.4x10^9 40K-atoms/s. Trap losses due to light-induced interspecies collisions of ~65% were observed and could be minimized to ~10% by using low magnetic field gradients and low light powers in the repumping light of both atomic species. The described system represents the starting point for the production of a large-atom number quantum degenerate Fermi-Fermi mixture.

cond-mat.quant-gas↗