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Harishwar Raman

Publications and source records attributed to Harishwar Raman.

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Clustering Dynamics of SiO2-Pt Active Janus Colloids

Active colloid clustering is central to understanding non-equilibrium self-organization, with implications for programmable active materials and synthetic or biological assemblies. While most prior studies have focused on dimers or small aggregates, the dynamics of larger clusters remain relatively unexplored. Here, we experimentally investigate chemically active, monodisperse SiO2-Pt Janus colloid (JC) clusters as large as n=9 in a dynamic clustering regime, where clusters continuously form, dissolve, and merge as swimmer density increases. We show that clusters move in circular trajectories, and that both their translational and rotational dynamics can be predicted directly from the orientations of constituent JCs. Furthermore, we identify that their formation undergoes a mechanistic transition: while small clusters are mediated by chemical interactions, larger clusters are predominantly formed by steric effects. This transition arises from a mismatch of motilities between incoming JCs and clusters, combined with increased Pt-surface exposure. Our results extend prior dimer-focused studies to larger aggregates and establish a predictive description that bridges individual swimmer behavior with collective dynamics.

cond-mat.soft

Pair-Interactions of Self-Propelled SiO2-Pt Janus Colloids: Chemically Mediated Interactions

Driven by the necessity to achieve a thorough comprehension of the bottom-up fabrication process of functional materials, this experimental study investigates the pair-wise interactions or collisions between chemically active SiO2-Pt Janus Colloids. These collisions are categorized based on the Janus colloids orientations before and after they make physical contact. In addition to the hydrodynamic interactions, the Janus colloids are also known to affect each others chemical field, resulting in chemophoretic interactions, which depend on the degree of surface anisotropy in reactivity and solute-surface interaction. These interactions lead to a noticeable decrease in particle speed and changes in orientation that correlate with the contact duration and yield different collision types. Our findings reveal distinct configurations of contact during collisions, whose mechanisms and likelihood is found to be dependent primarily on the chemical interactions. Such estimates of collision and their characterization in dilute suspensions shall have key impact in determining the arrangement and time scales of dynamical structures and assemblies of denser suspensions, and potentially the functional materials of the future.

cond-mat.soft