Optical Experiments on a Crystallizing Hard Sphere - Polymer Mixture at Coexistence

Details Optical Experiments on a Crystallizing Hard Sphere - Polymer Mixture at Coexistence Optical Experiments on a Crystallizing Hard Sphere - Polymer Mixture at Coexistence

2009-10-15

arxiv.org/abs/0910.2813v1

Physical Review E 81, 051401 (2010)

Physics

Condensed Matter

Soft Condensed Matter

33 pages, 11 figures

Scientific paper

10.1103/PhysRevE.81.051401

We report on the crystallization kinetics in an entropically attractive colloidal system using a combination of time resolved scattering methods and microscopy. Hard sphere particles are polystyrene microgels swollen in a good solvent (radius a=380nm, starting volume fraction 0.534) with the short ranged attractions induced by the presence of short polymer chains (radius of gyration rg = 3nm, starting volume fraction 0.0224). After crystallization, stacking faulted face centred cubic crystals coexist with about 5% of melt remaining in the grain boundaries. From the Bragg scattering signal we infer the amount of crystalline material, the average crystallite size and the number density of crystals as a function of time. This allows to discriminate an early stage of conversion, followed by an extended coarsening stage. The small angle scattering (SALS) appears only long after completed conversion and exhibits Furukawa scaling for all times. Additional microscopic experiments reveal that the grain boundaries have a reduced Bragg scattering power but possess an increased refractive index. Fits of the Furukawa function indicate that the dimensionality of the scatterers decreases from 2.25 at short times to 1.65 at late times and the characteristic length scale is slightly larger than the average crystallite size. Together this suggests the SALS signal is due scattering from a foam like grain boundary network as a whole.

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