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We use field emission scanning electron microscope (FE-SEM) to investigate the growth of palladium colloids over the surface of thin films of WO3/glass. The film is prepared by Pulsed Laser Deposition (PLD) at different temperatures. A PdCl2 (aq) droplet is injected on the surface and in the presence of steam hydrogen the droplet is dried through a reduction reaction process. Two distinct aggregation regimes of palladium colloids are observed over the substrates. We argue that the change in aggregation dynamics emerges when the measured water drop Contact Angel (CA) for the WO3/glass thin films passes a certain threshold value, namely CA = 46 degrees, where a crossover in kinetic aggregation of palladium colloids occurs. Our results suggest that the mass fractal dimension of palladium aggregates follows a power-law behavior. The fractal dimension (Df) in the fast aggregation regime, where the measured CA values vary from 27 up to 46 degrees, according to different substrate deposition temperatures, is Df = 1.75 (0.02). This value of Df is in excellent agreement with kinetic aggregation of other colloidal systems in fast aggregation regime. Whereas for the slow aggregation regime, with CA = 58 degrees, the fractal dimension changes abruptly to Df=1.92 (0.03). We have also used a modified Box-Counting method to calculate fractal dimension of gray-level images and observe that the crossover at around CA = 46 degrees remains unchanged.
A theoretical study of the structure formation observed very recently [Phys. Rev. Lett. 90, 128303 (2003)] in binary colloids is presented. In our model solely the dipole-dipole interaction of the particles is considered, electrohidrodynamic effects
Despite the omnipresence of colloidal suspensions, little is known about the influence of shape on phase transformations, especially in nonequilibrium. To date, real-space imaging results are limited to systems composed of spherical colloids. In most
The far-from-equilibrium dynamics of glassy systems share important phenomenological traits. A transition is generally observed from a time-homogeneous dynamical regime to an aging regime where physical changes occur intermittently and, on average, a
We report experiments that show rapid crystallization of colloids tethered to an oil-water interface in response to laser illumination. This light-induced transition is due to a combination of long-ranged thermophoretic pumping and local optical bind
We construct a theoretical model for the dynamics of a microscale colloidal particle, modeled as an interval, moving horizontally on a DNA-coated surface, modelled as a line coated with springs that can stick to the interval. Averaging over the fast