arXiv subjects

Lucio Isa

Publications and source records attributed to Lucio Isa.

52 records · Page 3Linked to original sources

arXiv2019

Self-Templating Assembly of Soft Microparticles into Complex Tessellations

Self-assembled monolayers of microparticles encoding Archimedean and non-regular tessellations promise unprecedented structure-property relationships for a wide spectrum of applications in fields ranging from optoelectronics to surface technology. Yet, despite numerous computational studies predicting the emergence of exotic structures from simple interparticle interactions, the experimental realization of non-hexagonal patterns remains challenging. Not only kinetic limitations often hinder structural relaxation, but also programming the inteparticle interactions during assembly, and hence the target structure, remains an elusive task. Here, we demonstrate how a single type of soft polymeric microparticle (microgels) can be assembled into a wide array of complex structures as a result of simple pairwise interactions. We first let microgels self-assemble at a water-oil interface into a hexagonally packed monolayer, which we then compress to varying degrees and deposit onto a solid substrate. By repeating this process twice, we find that the resultant structure is not the mere stacking of two hexagonal patterns. The first monolayer retains its hexagonal structure and acts as a template into which the particles of the second monolayer rearrange to occupy interstitial positions. The frustration between the two lattices generates new symmetries. By simply varying the packing fraction of the two monolayers, we obtain not only low-coordination structures such as rectangular and honeycomb lattices, but also rhomboidal, hexagonal, and herringbone superlattices which display non-regular tessellations. Molecular dynamics simulations show that these structures are thermodynamically stable and develop from short-ranged repulsive interactions, making them easy to predict, and thus opening new avenues to the rational design of complex patterns.

cond-mat.soft↗

arXiv2019

Active Brownian motion with orientation-dependent motility: theory and experiments

Combining experiments on active colloids, whose propulsion velocity can be controlled via a feedback loop, and theory of active Brownian motion, we explore the dynamics of an overdamped active particle with a motility that depends explicitly on the particle orientation. In this case, the active particle moves faster when oriented along one direction and slower when oriented along another, leading to an anisotropic translational dynamics which is coupled to the particle's rotational diffusion. We propose a basic model of active Brownian motion for orientation-dependent motility. Based on this model, we obtain analytic results for the mean trajectories, averaged over the Brownian noise for various initial configurations, and for the mean-square displacements including their anisotropic non-Gaussian behavior. The theoretical results are found to be in good agreement with the experimental data. Our findings establish a methodology to engineer complex anisotropic motilities of active Brownian particles, with potential impact in the study of the swimming behavior of microorganisms subjected to anisotropic driving fields.

cond-mat.soft↗

arXiv2019

Microgels Adsorbed at Liquid-Liquid Interfaces: A Joint Numerical and Experimental Study

Soft particles display highly versatile properties with respect to hard colloids, even more so at fluid-fluid interfaces. In particular, microgels, consisting of a cross-linked polymer network, are able to deform and flatten upon adsorption at the interface due to the balance between surface tension and internal elasticity. Despite the existence of experimental results, a detailed theoretical understanding of this phenomenon is still lacking due to the absence of appropriate microscopic models. In this work, we propose an advanced modelling of microgels at a flat water/oil interface. The model builds on a realistic description of the internal polymeric architecture and single-particle properties of the microgel and is able to reproduce its experimentally observed shape at the interface. Complementing molecular dynamics simulations with in-situ cryo-electron microscopy experiments and atomic force microscopy imaging after Langmuir-Blodgett deposition, we compare the morphology of the microgels for different values of the cross-linking ratios. Our model allows for a systematic microscopic investigation of soft particles at fluid interfaces, which is essential to develop predictive power for the use of microgels in a broad range of applications, including the stabilization of smart emulsions and the versatile patterning of surfaces.

cond-mat.soft↗

arXiv2019

Tuning Interparticle Hydrogen Bonding in Shear-Jamming Suspensions: Kinetic Effects and Consequences for Tribology and Rheology

The shear-jamming of dense suspensions can be strongly affected by molecular-scale interactions between particles, e.g. by chemically controlling their propensity for hydrogen bonding. However, hydrogen bonding not only enhances interparticle friction, a critical parameter for shear jamming, but also introduces (reversible) adhesion, whose interplay with friction in shear-jamming systems has so far remained unclear. Here, we present atomic force microscopy studies to assess interparticle adhesion, its relationship to friction, and how these attributes are influenced by urea, a molecule that interferes with hydrogen bonding. We characterize the kinetics of this process with nuclear magnetic resonance, relating it to the time dependence of the macroscopic flow behavior with rheological measurements. We find that time-dependent urea sorption reduces friction and adhesion, causing a shift in the shear-jamming onset. These results extend our mechanistic understanding of chemical effects on the nature of shear jamming, promising new avenues for fundamental studies and applications alike.

cond-mat.soft↗

arXiv2018

Dynamics and wetting behavior of soft particles at a fluid-fluid interface

We investigate the conformation, position, and dynamics of core-shell nanoparticles (CSNPs) composed of a silica core encapsulated in a cross-linked poly-N-isopropylacrylamide shell at a water-oil interface for a systematic range of core sizes and shell thicknesses. We first present a free-energy model that we use to predict the CSNP wetting behavior at the interface as a function of its geometrical and compositional properties in the bulk phases, which gives good agreement with our experimental data. Remarkably, upon knowledge of the polymer shell deformability, the equilibrium particle position relative to the interface plane, an often elusive experimental quantity, can be extracted by measuring its radial dimensions after adsorption. For all the systems studied here, the interfacial dimensions are always larger than in bulk and the particle core resides in a configuration wherein it just touches the interface or is fully immersed in water. Moreover, the stretched shell induces a larger viscous drag at the interface, which appears to depend solely on the interfacial dimensions, irrespective of the portion of the CSNP surface exposed to the two fluids. Our findings indicate that tailoring the architecture of CSNPs can be used to control their properties at the interface, as of interest for applications including emulsion stabilization and nanopatterning.

cond-mat.soft↗

arXiv2018

Roughness-dependent tribology effects on discontinuous shear thickening

Surface roughness affects many properties of colloids, from depletion [1] and capillary interactions [2], to their dispersibility [3] and use as emulsion stabilizers [4]. It also impacts particle-particle frictional contacts, which have recently emerged as being responsible for the discontinuous shear thickening (DST) of dense suspensions [5-17]. Tribological properties of these contacts have been rarely experimentally accessed [6, 15, 17, 18], especially for non-spherical particles. Here, we systematically tackle the effect of nanoscale surface roughness by producing a library of all-silica, raspberry-like colloids [19] and linking their rheology to their tribology. Rougher surfaces lead to a significant anticipation of DST onset, both in terms of shear rate and solid loading. Strikingly, they also eliminate continuous thickening. DST is here due to the interlocking of asperities, which we have identified as "stick-slip" frictional contacts by measuring the sliding of the same particles via lateral force microscopy (LFM). Direct measurements of particle-particle friction therefore highlight the value of an engineering-tribology approach to tuning the thickening of suspensions.

cond-mat.soft↗

arXiv2017

Active Atoms and Interstitials in Two-dimensional Colloidal Crystals

We study experimentally and numerically the motion of a self-phoretic active particle in two-dimensional (2D) loosely-packed colloidal crystals at fluid interfaces. Two scenarios emerge depending on the interaction between the active particle and the lattice: the active particle either navigates throughout the crystal as an interstitial or is part of the lattice and behaves as an active atom. Active interstitials undergo a run-and-tumble motion, with the passive colloids of the crystal acting as tumbling sites. Instead, active atoms exhibit an intermittent motion, which stems from the interplay between the periodic potential landscape of the passive crystal and the particle's self-propulsion. Our results shed new light on the behaviour of dense active phases and constitute the first step towards the realization of non-close-packed crystalline phases with internal activity.

cond-mat.soft↗

arXiv2017

Rational design and fabrication of versatile active colloidal molecules

Active colloids, also known as artificial microswimmers, are self-propelled micro and nanoparticles that convert uniform sources of fuel (e.g. chemical) or uniform external driving fields (e.g. magnetic or electric) into directed motion by virtue of asymmetry in their shape or composition. These materials are currently attracting enormous scientific attention for two main end uses. First, active colloids are prototypical internally driven, out-of-equilibrium systems and their study has led to new emergent material properties, such as swarming and living crystallization. Secondly, they hold the promise to be used as micro- and nanoscale devices with tremendous potential from medical to environmental applications. However, the current fabrication of active colloids is limited in the programmability of materials, geometry, and modes of motion. Here, we use sequential capillarity- assisted particle assembly (sCAPA) to link microspheres of different materials into clusters of prescribed shapes ("colloidal molecules") that can actively translate, circulate and rotate powered by asymmetric electro-hydrodynamic flows. Further engineering of the geometry and composition provides active colloids that switch motion under external triggers or perform simple pick-up and transport tasks. Our fabrication strategy enables both physicists and engineers to design and create customized active colloids to explore novel fundamental phenomena in active matter and to investigate materials and propulsion schemes that are compatible with future applications.

cond-mat.soft↗

arXiv2015

Interfacial colloidal monolayers under steady shear: structure and flow profiles

We study the coupling between the structural dynamics and rheological response of charged colloidal monolayers at water/oil interfaces, driven into steady shear by a microdisk rotating at a controlled angular velocity. The flow causes particles to layer into rotating concentric rings linked to the local, position-dependent shear rate, which triggers two distinct dynamical regimes: particles move continuously "Flowing") close to the microdisk, or exhibit intermittent "Hopping" between local energy minima farther away. The shear-rate dependent surface viscosity of a monolayer can be extracted from an interfacial stress balance, giving "macroscopic" flow curves whose behavior corresponds to the distinct microscopic regimes of particle motion. Hopping Regions correspond to a surface yield stress $η\sim τ_S^Y \dotγ^{-1}$, whereas Flowing Regions exhibit surface viscosities with power-law shear-thinning characteristics.

cond-mat.soft↗

arXiv2015

Adsorption of soft particles at fluid interfaces

Soft particles can be better emulsifiers than hard particles because they stretch at fluid interfaces. This deformation can increase adsorption energies by orders of magnitude relative to rigid particles. The deformation of a particle at an interface is governed by a competition of bulk elasticity and surface tension. When particles are partially wet by the two liquids, deformation is localized within a material-dependent distance $L$ from the contact line. At the contact line, the particle morphology is given by a balance of surface tensions. When the particle radius $R \ll L$, the particle adopts a lenticular shape identical to that of an adsorbed fluid droplet. Particle deformations can be elastic or plastic, depending on the relative values of the Young modulus, $E$, and yield stress, $σ_p$. When surface tensions favour complete spreading of the particles at the interface, plastic deformation can lead to unusual fried-egg morphologies. When deformable particles have surface properties that are very similar to one liquid phase, adsorption can be extremely sensitive to small changes of their affinity for the other liquid phase. These findings have implications for the adsorption of microgel particles at fluid interfaces and the performance of stimuli-responsive Pickering emulsions.

cond-mat.soft↗

arXiv2014

Adsorption at Liquid Interfaces Induces Amyloid Fibril Bending and Ring Formation

Protein fibril accumulation at interfaces is an important step in many physiological processes and neurodegenerative diseases as well as in designing materials. Here we show, using $β$-lactoglobulin fibrils as a model, that semiflexible fibrils exposed to a surface do not possess the Gaussian distribution of curvatures characteristic for wormlike chains, but instead exhibit a spontaneous curvature, which can even lead to ring-like conformations. The long-lived presence of such rings is confirmed by atomic force microscopy, cryogenic scanning electron microscopy and passive probe particle tracking at air- and oil-water interfaces. We reason that this spontaneous curvature is governed by structural characteristics on the molecular level and is to be expected when a chiral and polar fibril is placed in an inhomogeneous environment such as an interface. By testing $β$-lactoglobulin fibrils with varying average thicknesses, we conclude that fibril thickness plays a determining role in the propensity to form rings.

q-bio.BM↗

arXiv2013

Microscopic mechanism for the shear-thickening of non-Brownian suspensions

We propose a simple model, supported by contact-dynamics simulations as well as rheology and friction measurements, that links the transition from continuous to discontinuous shear-thickening in dense granular pastes to distinct lubrication regimes in the particle contacts. We identify a local Sommerfeld number that determines the transition from Newtonian to shear-thickening flows, and then show that the suspension's volume fraction and the boundary lubrication friction coefficient control the nature of the shear-thickening transition, both in simulations and experiments.

cond-mat.soft↗

arXiv2009

Quantitative imaging of concentrated suspensions under flow

We review recent advances in imaging the flow of concentrated suspensions, focussing on the use of confocal microscopy to obtain time-resolved information on the single-particle level in these systems. After motivating the need for quantitative (confocal) imaging in suspension rheology, we briefly describe the particles, sample environments, microscopy tools and analysis algorithms needed to perform this kind of experiments. The second part of the review focusses on microscopic aspects of the flow of concentrated model hard-sphere-like suspensions, and the relation to non-linear rheological phenomena such as yielding, shear localization, wall slip and shear-induced ordering. Both Brownian and non-Brownian systems will be described. We show how quantitative imaging can improve our understanding of the connection between microscopic dynamics and bulk flow.

cond-mat.soft↗

arXiv2008

Quantitative imaging of colloidal flows

We present recent advances in the instrumentation and analysis methods for quantitative imaging of concentrated colloidal suspensions under flow. After a brief review of colloidal imaging, we describe various flow geometries for two and and three-dimensional (3D) imaging, including a `confocal rheoscope'. This latter combination of a confocal microscope and a rheometer permits simultaneous characterization of rheological response and 3D microstructural imaging. The main part of the paper discusses in detail how to identify and track particles from confocal images taken during flow. After analyzing the performance of the most commonly used colloid tracking algorithm by Crocker and Grier extended to flowing systems, we propose two new algorithms for reliable particle tracking in non-uniform flows to the level of accuracy already available for quiescent systems. We illustrate the methods by applying it to data collected from colloidal flows in three different geometries (channel flow, parallel plate shear and cone-plate rheometry).

cond-mat.soft↗

arXiv2008

Velocity oscillations in confined channel flows of concentrated colloidal suspensions

We study the pressure-driven flow of concentrated colloids confined in glass micro-channels at the single particle level using fast confocal microscopy. For channel to particle size ratios $a/\bar{D} \lesssim 30$, the flow rate of the suspended particles shows fluctuations. These turn into regular oscillations for higher confinements ($a/\bar{D} \simeq 20$). We present evidence to link these oscillations with the relative flow of solvent and particles (permeation) and the effect of confinement on shear thickening.

cond-mat.soft↗

arXiv2007

Shear zones and wall slip in the capillary flow of concentrated colloidal suspensions

We image the flow of a nearly random close packed, hard-sphere colloidal suspension (a `paste') in a square capillary using confocal microscopy. The flow consists of a `plug' in the center while shear occurs localized adjacent to the channel walls, reminiscent of yield-stress fluid behavior. However, the observed scaling of the velocity profiles with the flow rate strongly contrasts yield-stress fluid predictions. Instead, the velocity profiles can be captured by a theory of stress fluctuations originally developed for chute flow of dry granular media. We verified this behavior both for smooth and rough boundary conditions.

cond-mat.soft↗