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Teun W. J. Verouden

Publications and source records attributed to Teun W. J. Verouden.

2 recordsLinked to original sources

Effect of a Cone Shape on the Motion of Active Janus Colloids

The propulsion of active colloids is governed by their symmetry and shape, yet a systematic investigation of how small geometric effects influence the locomotion of anisotropic active colloids is lacking. In this paper, we study the effect of a cone shape by combining high-resolution two-photon polymerization 3D printing with AC electric field experiments to study anisotropic Janus micro swimmers. We fabricate a series of Janus colloids with different shapes, ranging from a sphere to a hemisphere with a cone-protrusion, but containing similar hemispherical gold-coatings. Under an applied alternating current (AC) electric field, all particles exhibit active, ballistic motion. We find a shape and size dependence on the propulsion velocity, with the spherical Janus particle moving fastest, followed by a small cone and a large cone protrusion, while surprisingly a printed sphere with a flat side moves slowest. In addition, a reversal in the direction of motion for all shapes was triggered, a phenomenon governed by a transition from induced-charge electrophoresis (ICEP) at low frequencies to self-dielectrophoresis (sDEP) at high frequencies. We reveal a distinct shape influence, with the large cone-protrusion increasing their velocity in the sDEP regime. Our results provide insight into the link between active particle geometry and their propulsion velocity that are important for understanding biological micro swimmers and designing optimized microrobots.

cond-mat.soft↗

Unraveling and controlling the self-assembly pathways of cubic colloids

The self-assembly of anisotropic building blocks into complex spatial architectures is an important design strategy in material science but the mechanisms by which the anisotropic interactions influence the early-stage growth and formation of disordered (non-)equilibrium structures remain poorly understood. Here, we experimentally demonstrate that tuning the strength of shape-induced directional bonds changes the self-assembly pathways of cubic colloids. By tracking the growth kinetics and internal reorganizations of small clusters at increasing attraction strength, we identify three self-assembly regimes: (i) nucleation and growth regime: slow reorganization-dominated growth of crystalline clusters, (ii) dynamic regime: diffusion-limited growth with dynamic cube reorganizations leading to disordered crystalline clusters and (iii) static regime: diffusion-limited growth of kinetically arrested clusters unable to reorganize due to directional bonding constraints. We further show that transitions between these regimes are reversible and allow pathway engineering to control the structure and disorder. Our results reveal how directional bonding governs pathway selection, providing important insights for the rational design of reconfigurable colloidal, nano-, and biomaterials.

cond-mat.soft↗