Controlling colloidal phase transitions with critical Casimir forces

The critical Casimir effect provides a thermodynamic analogue of the well-known quantum mechanical Casimir effect. It acts between two surfaces immersed in a critical binary liquid mixture, and results from the confinement of concentration fluctuations of the solvent. Unlike the quantum mechanical effect, the magnitude and range of this attraction can be adjusted with temperature via the solvent correlation length, thus offering new opportunities for the assembly of nano and micron-scale structures. Here, we demonstrate the active assembly control of equilibrium phases using critical Casimir forces. We guide colloidal particles into analogues of molecular liquid and solid phases via exquisite control over their interactions. By measuring the critical Casimir particle pair potential directly from density fluctuations in the colloidal gas, we obtain insight into liquefaction at small scales: We apply the Van der Waals model of molecular liquefaction and show that the colloidal gas-liquid condensation is accurately described by the Van der Waals theory, even on the scale of a few particles. These results open up new possibilities in the active assembly control of micro and nanostructures

Long-range strain correlations in sheared colloidal glasses

Glasses behave as solids on experimental time scales due to their slow relaxation. Growing dynamic length scales due to cooperative motion of particles are believed to be central to this slow response. For quiescent glasses, however, the size of the cooperatively rearranging regions has never been observed to exceed a few particle diameters, and the observation of long-range correlations that are signatures of an elastic solid has remained elusive. Here, we provide direct experimental evidence of long-range correlations during the deformation of a dense colloidal glass. By imposing an external stress, we force structural rearrangements that make the glass flow, and we identify long-range correlations in the fluctuations of microscopic strain, and elucidate their scaling and spatial symmetry. The applied shear induces a transition from homogeneous to inhomogeneous flow at a critical shear rate, and we investigate the role of strain correlations in this transition.Comment: 11 pages, 3 figures. Accepted for publication in PR

Experimental observation of the intricate free-energy landscape for a soft glassy system

In the free energy landscape picture of glassy systems, the slow dynamics characteristic of these systems is believed to be due to the existence of a complicated free-energy landscape with many local minima. We show here that for a colloidal glassy material multiple paths can be taken through the free energy landscape, that can even lead to different 'final' non-ergodic states at the late stages of aging. We provide clear experimental evidence for the distinction of gel and glassy states in the system and show that for a range of colloid concentrations, the transition to non-ergodicity can occur in either direction (gel or glass), and may be accompanied by 'hesitations' between the two directions. This shows that colloidal gels and glasses are merely global free-energy minima in the same free energy landscape, and that the paths leading to these minima can indeed be complicated.Comment: 5 pages, 5 figure

Dynamics of colloidal aggregation in microgravity by critical Casimir forces

Using the critical Casimir force, we study the attractive-strength dependence of diffusion-limited colloidal aggregation in microgravity. By means of near field scattering we measure both the static and dynamic structure factor of the aggregates as the aggregation process evolves. The simultaneous measurement of both the static and dynamic structure factor under ideal microgravity conditions allows us to uniquely determine the ratio of the hydrodynamic and gyration radius as a function of the fractal dimension of the aggregate, enabling us to elucidate the internal structure of the aggregates as a function of the interaction potential. We find that the mass is evenly distributed in all objects with fractal dimension ranging from 2.55 for a shallow to 1.75 for the deepest potential.Comment: 5 pages, 4 figure

Fluctuation-dissipation theorem in an aging colloidal glass

We provide a direct experimental test of the Stokes-Einstein relation as a special case of the fluctuation-dissipation theorem (FDT) in an aging colloidal glass. The use of combined active and passive microrheology allows us to independently measure both the correlation and response functions in this non-equilibrium situation. Contrary to previous reports, we find no deviations from the FDT over several decades in frequency (1 Hz-10 kHz) and for all aging times. In addition, we find two distinct viscoelastic contributions in the aging glass, including a nearly elastic response at low frequencies that grows during aging. This is the clearest change in material properties of the system with aging.Comment: 5 pages,4 figure

Revealing Driving Forces in Quantum Dot Supercrystal Assembly

The assembly of semiconductor nanoparticles, quantum dots (QDs), into dense crystalline nanostructures holds great promise for future optoelectronic devices. However, knowledge of the sub-nanometer scale driving forces underlying the kinetic processes of nucleation, growth, and final densification during QD assembly remains poor. Emulsion-templated assembly has recently been shown to provide good control over the bulk condensation of QDs into highly ordered 3D supercrystals. Here, emulsion-templated assembly is combined with in situ small-angle X-ray scattering to obtain direct insight into the nanoscale interactions underlying the nucleation, growth, and densification of QD supercrystals. At the point of supercrystal nucleation, nanoparticles undergo a hard-sphere-like crystallization into a hexagonal-close-packed lattice, slowly transforming into a face-centered-cubic lattice. The ligands play a crucial role in balancing steric repulsion against attractive van der Waals forces to mediate the initial equilibrium assembly, but cause the QDs to be progressively destabilized upon densification. The rich detail of this kinetic study elucidates the assembly and thermodynamic properties that define QD supercrystal fabrication approaching single-crystal quality, paving the way toward their use in optoelectronic devices.</p

Colloidal aggregation in microgravity by critical Casimir forces

By using the critical Casimir force, we study the attractive strength dependent aggregation of colloids with and without gravity by means of Near Field scattering. Significant differences were seen between microgravity and ground experiments, both in the structure of the formed fractal aggregates as well as the kinetics of growth. Ground measurements are severely affected by sedimentation resulting in reaction limited behavior. In microgravity, a purely diffusive behavior is seen reflected both in the measured fractal dimensions for the aggregates as well as the power law behavior in the rate of growth. Formed aggregates become more open as the attractive strength increases.Comment: 4 pages, 3 figure