Publications by authors named "D A Matoz-Fernandez"

Surfactant-stabilized oil-in-water and water-in-oil emulsions, encompassing a wide range of chemical compositions, exhibit remarkable temperature-controlled sphere-to-icosahedron droplet shape transformations. These transformations are controlled by the elasticity and closed-surface topology of a self-assembled interfacial crystalline monolayer. Since many practical emulsions are synergistically costabilized by both surfactants and colloidal particles, we explore the influence of surface-adsorbed hydrophobic and hydrophilic colloidal particles on these shape transformations.

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We examine the influence of density on the transition between chain and spiral structures in planar assemblies of active semiflexible filaments, utilizing detailed numerical simulations. We focus on how increased density, and higher Péclet numbers, affect the activity-induced transition spiral state in a semiflexible, self-avoiding active chain. Our findings show that increasing the density causes the spiral state to break up, reverting to a motile chain-like shape.

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Many motile microorganisms communicate with each other and their environments chemical signaling which leads to long-range interactions mediated by self-generated chemical gradients. However, consequences of the interplay between crowding and chemotactic interactions on their collective behavior remain poorly understood. In this work, we use Brownian dynamics simulations to investigate the effect of packing fraction on the formation of non-equilibrium structures in a monolayer of diffusiophoretic self-propelled colloids as a model for chemically active particles.

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Self-organized shells are fundamental in biological compartmentalization. They protect genomic material or enclose enzymes to aid the metabolic process. Studies of crystalline shells have shown the importance of the mechanical properties of building units in the shell morphology.

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Patterns and morphology develop in living systems such as embryos in response to chemical signals. To understand and exploit the interplay of chemical reactions with mechanical transformations, chemomechanical polymer systems have been synthesized by attaching chemicals into hydrogels. In this work, we design autonomous responsive elastic shells that undergo morphological changes induced by chemical reactions.

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