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Confocal Imaging of Confined Quiescent and Flowing Colloid-polymer Mixtures
Published on: May 20, 2014
Structure-dynamics decoupling in soft-colloid suspensions
Adrián Arenas-Gullo1,2, Joaquím Clara-Rahola3, Phil N Segré4
1Department of Condensed Matter Physics, University of Barcelona, Barcelona, Spain.
Abstract:
The accepted paradigm in materials science is that the internal structure of a material determines its macroscopic properties. This connection is reflected in the particle dynamics, which are known to become slower at length scales comparable to the mean interparticle distance. This implies that the q-dependent relaxation time, with q the magnitude of the scattering wave vector, correlates with the structure factor of the material. This is known as de Gennes narrowing in simple atomic liquids, and is a behavior also seen in colloidal suspensions, where the quantities at play are more easily accessible experimentally. We here find that this familiar correlation can breakdown for soft-colloid suspensions. In both experiments and simulations, we find that the q-dependent relaxation time of the suspension does not follow the structure factor, but that instead, it remains unchanged relative to the length scale at which it is measured. We justify this unusual behavior by alluding to single-particle elasticity and how this aspect allows additional relaxation pathways for the characteristic time of the suspension to remain unaffected by the suspension structure. Our findings challenge the prevailing wisdom that the structure of a material unequivocally determines its properties.
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A solution is a homogeneous mixture composed of a solvent, the major component, and a solute, the minor component. The physical state of a solution—solid, liquid, or gas—is typically the same as that of the solvent. Solute concentrations are often described with qualitative terms such as dilute (of relatively low concentration) and concentrated (of relatively high concentration).
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