Vapor nucleation paths in lyophobic nanopores

Abstract.: In recent years, technologies revolving around the use of lyophobic nanopores gained considerable attention in both fundamental and applied research. Owing to the enormous internal surface area, heterogeneous lyophobic systems (HLS), constituted by a nanoporous lyophobic material and a non-wetting liquid, are promising candidates for the efficient storage or dissipation of mechanical energy. These diverse applications both rely on the forced intrusion and extrusion of the non-wetting liquid inside the pores; the behavior of HLS for storage or dissipation depends on the hysteresis between these two processes, which, in turn, are determined by the microscopic details of the system. It is easy to understand that molecular simulations provide an unmatched tool for understanding phenomena at these scales. In this contribution we use advanced atomistic simulation techniques in order to study the nucleation of vapor bubbles inside lyophobic mesopores. The use of the string method in collective variables allows us to overcome the computational challenges associated with the activated nature of the phenomenon, rendering a detailed picture of nucleation in confinement. In particular, this rare event method efficiently searches for the most probable nucleation path(s) in otherwise intractable, high-dimensional free-energy landscapes. Results reveal the existence of several independent nucleation paths associated with different free-energy barriers. In particular, there is a family of asymmetric transition paths, in which a bubble forms at one of the walls; the other family involves the formation of axisymmetric bubbles with an annulus shape. The computed free-energy profiles reveal that the asymmetric path is significantly more probable than the symmetric one, while the exact position where the asymmetric bubble forms is less relevant for the free energetics of the process. A comparison of the atomistic results with continuum models is also presented, showing how, for simple liquids in mesoporous materials of characteristic size of ca. 4nm, the nanoscale effects reported for smaller pores have a minor role. The atomistic estimates for the nucleation free-energy barrier are in qualitative accord with those that can be obtained using a macroscopic, capillary-based nucleation theory. Graphical abstract: [Figure not available: see fulltext.]

Shock formation in the collapse of a vapor nano-bubble

In this paper a diffuse-interface model featuring phase change, transition to supercritical conditions, thermal conduction, compressibility effects and shock wave propagation is exploited to deal with the dynamics of a cavitation bubble. At variance with previous descriptions, the model is uniformly valid for all phases (liquid, vapor and supercritical) and phase transitions involved, allowing to describe the non-equilibrium processes ongoing during the collapse. As consequence of this unitary description, rather unexpectedly for pure vapor bubbles, the numerical experiments show that the collapse is accompanied by the emission of a strong shock wave in the liquid and by the oscillation of the bubble that periodically disappears and reappears, due to transition to super/sub critical conditions. The mechanism of shock wave formation is strongly related to the transition of the vapor to supercritical state, with a progressive steepening of the compression wave to form the shock which is eventually reflected as an outward propagating wave in the liquid

Diffuse interface modeling of a radial vapor bubble collapse

A diffuse interface model is exploited to study in details the dynamics of a cavitation vapor bubble, by including phase change, transition to supercritical conditions, shock wave propagation and thermal conduction. The numerical experiments show that the actual dynamic is a sequence of collapses and rebounds demonstrating the importance of nonequilibrium phase changes. In particular the transition to supercritical conditions avoids the full condensation and leads to shockwave emission after the collapse and to successive bubble rebound

Thermally activated vapor bubble nucleation: the Landau-Lifshitz/Van der Waals approach

Vapor bubbles are formed in liquids by two mechanisms: evaporation (temperature above the boiling threshold) and cavitation (pressure below the vapor pressure). The liquid resists in these metastable (overheating and tensile, respectively) states for a long time since bubble nucleation is an activated process that needs to surmount the free energy barrier separating the liquid and the vapor states. The bubble nucleation rate is difficult to assess and, typically, only for extremely small systems treated at atomistic level of detail. In this work a powerful approach, based on a continuum diffuse interface modeling of the two-phase fluid embedded with thermal fluctuations (Fluctuating Hydrodynamics) is exploited to study the nucleation process in homogeneous conditions, evaluating the bubble nucleation rates and following the long term dynamics of the metastable system, up to the bubble coalescence and expansion stages. In comparison with more classical approaches, this methodology allows on the one hand to deal with much larger systems observed for a much longer times than possible with even the most advanced atomistic models. On the other it extends contin- uum formulations to thermally activated processes, impossible to deal with in a purely determinist setting

Collapse of superhydrophobicity on nanopillared surfaces

The mechanism of the collapse of the superhydrophobic state is elucidated for submerged nanoscale textures forming a three-dimensional interconnected vapor domain. This key issue for the design of nanotextures poses significant simulation challenges as it is characterized by diverse time and length scales. State-of-the-art atomistic rare events simulations are applied for overcoming the long time scales connected with the large free energy barriers. In such interconnected surface cavities wetting starts with the formation of a liquid finger between two pillars. This break of symmetry induces a more gentle bend in the rest of the liquid-vapor interface, which triggers the wetting of the neighboring pillars. This collective mechanism, involving the wetting of several pillars at the same time, could not be captured by previous atomistic simulations using surface models comprising a small number of pillars (often just one). Atomistic results are interpreted in terms of a sharp-interface continuum model which suggests that line tension, condensation, and other nanoscale phenomena play a minor role in the simulated conditions

Anisotropic fluctuations in turbulent sheared flows

An experimental analysis of small-scales anisotropic turbulent fluctuations has been performed in two different flows. We analyzed anisotropic properties of an homogeneous shear flows and of a turbulent boundary layer by means of two cross-wire probes to obtain multi-point multi-component measurements. Data are analyzed at changing inter-probe separation without the use of Taylor hypothesis. The results are consistent with the ``exponent-only'' scenario for universality, i.e. all experimental data can be fit by fixing the same set of anisotropic scaling exponents at changing only prefactors, for different shear intensities and boundary conditions.Comment: 11 pages, 8 figure

Dynamics of a vapor nanobubble collapsing near a solid boundary

In the present paper a diffuse interface approach is used to address the collapse of a sub-micron vapor bubble near solid boundaries. This formulation enables an unprecedented description of interfacial flows that naturally takes into account topology modification and phase changes (both vapor/liquid and vapor/supercritical fluid transformations). Results from numerical simulations are exploited to discuss the complex sequence of events associated with the bubble collapse near a wall, encompassing shock-wave emissions in the liquid and reflections from the wall, their successive interaction with the expanding bubble, the ensuing asymmetry of the bubble and the eventual jetting phase

Intrusion and extrusion of water in hydrophobic nanopores

Heterogeneous systems composed of hydrophobic nanoporous materials and water are capable, depending on their characteristics, of efficiently dissipating (dampers) or storing ("molecular springs") energy. However, it is difficult to predict their properties based on macroscopic theories-classical capillarity for intrusion and classical nucleation theory (CNT) for extrusion-because of the peculiar behavior of water in extreme confinement. Here we use advanced molecular dynamics techniques to shed light on these nonclassical effects, which are often difficult to investigate directly via experiments, owing to the reduced dimensions of the pores. The string method in collective variables is used to simulate, without artifacts, the microscopic mechanism of water intrusion and extrusion in the pores, which are thermally activated, rare events. Simulations reveal three important nonclassical effects: the nucleation free-energy barriers are reduced eightfold compared with CNT, the intrusion pressure is increased due to nanoscale confinement, and the intrusion/extrusion hysteresis is practically suppressed for pores with diameters below 1.2 nm. The frequency and size dependence of hysteresis exposed by the present simulations explains several experimental results on nanoporous materials. Understanding physical phenomena peculiar to nanoconfined water paves the way for a better design of nanoporous materials for energy applications; for instance, by decreasing the size of the nanopores alone, it is possible to change their behavior from dampers to molecular springs

Unraveling the Salvinia paradox: design principles for submerged superhydrophobicity

The complex structure of the Salvinia molesta is investigated via rare event molecular dynamics simulations. Results show that a hydrophilic/hydrophobic patterning together with a re-entrant geometry control the free energy barriers for bubble nucleation and for the Cassie-Wenzel transition. This natural paradigm is translated into simple macroscopic design criteria for engineering robust superhydrophobicity in submerged applications