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Carlos A. Silvera Batista

Publications and source records attributed to Carlos A. Silvera Batista.

2 recordsLinked to original sources

The "Intensity" Countoscope: Measuring particle dynamics in real space from microscopy images

Advances in intensity-based microscopy techniques have improved our ability to quantify particle motion at microscopic scales, enabling insight into diffusion and collective dynamics. Building on this foundation, we introduce a novel real-space approach that analyses intensity fluctuations within virtual observation boxes of variable size on microscopy images. By correlating these signals, we uncover distinct temporal regimes in the mean square changes of intensity, $\langle ΔI^2(t) \rangle$, which are strongly dependent on the box size compared to the particle width. For small boxes or short timescales, $\langle ΔI^2(t) \rangle$ scales with the mean-square displacement, while for longer timescales and larger boxes, it scales with its square root. We develop a general theoretical framework that captures these regimes and explicitly apply it to a dilute colloidal suspension imaged with confocal microscopy as an experimental model system. This allows for a robust extraction of diffusion coefficients and physical insights into particle dynamics. Our method complements intensity-based and real-space analysis, offering a tool for studying individual and potentially collective behaviour directly from image intensities, even in systems where individual particles cannot be resolved.

cond-mat.soft↗

Artificial Chemotaxis under Electrodiffusiophoresis

Diffusiophoretic motion induced by gradients of dissolved species has enabled the manipulation of colloids over large distances, spanning hundreds of microns. Nonetheless, studies have primarily focused on simple geometries that feature 1D gradients of solutes generated by reactions or selective dissolution. Thus, our understanding of 3D diffusiophoresis remains elusive despite its importance in wide-ranging scenarios, such as cellular transport and nanofluidics. Herein, we present a strategy to generate 3D chemical gradients under electric fields. In this approach, faradaic reactions at electrodes induce global pH gradients that drive long-range transport through electrodiffusiophoresis. Simultaneously, the electric field induces local pH gradients by driving the particle's double layer far from equilibrium. As a result, while global pH gradients lead to 2D focusing away from electrodes, local pH gradients induce aggregation in the third dimension. Resulting interparticle interactions display a strong dependence on surface chemistry, and particle size. Furthermore, pH gradients can be readily tuned by adjusting the voltage and frequency of the electric field. For large Péclet numbers, we observed a chemotactic-like collapse. Remarkably, such collapse occurs without reactions at a particle's surface. By mixing particles with different sizes, we also demonstrate the emergence of non-reciprocal interactions through experiments and Brownian dynamics simulations. These findings suggest a wide array of possibilities for the dynamic assembly of materials and the design of responsive matter.

cond-mat.soft↗