Effect of polydispersity on the crystallization kinetics of suspensions of colloidal hard spheres when approaching the glass transition
Author(s) -
Hans Joachim Schöpe,
Gary Bryant,
W. van Megen
Publication year - 2007
Publication title -
the journal of chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.071
H-Index - 357
eISSN - 1089-7690
pISSN - 0021-9606
DOI - 10.1063/1.2760207
Subject(s) - nucleation , dispersity , crystallization , volume fraction , hard spheres , glass transition , colloid , volume (thermodynamics) , fractionation , ostwald ripening , materials science , crystal (programming language) , atomic packing factor , induction period , chemical engineering , kinetics , chemical physics , chemistry , thermodynamics , crystallography , polymer chemistry , nanotechnology , chromatography , organic chemistry , composite material , polymer , catalysis , computational chemistry , physics , quantum mechanics , computer science , engineering , programming language
We present a comprehensive study of the solidification scenario in suspensions of colloidal hard spheres for three polydispersities between 4.8% and 5.8%, over a range of volume fractions from near freezing to near the glass transition. From these results, we identify four stages in the crystallization process: (i) an induction stage where large numbers of precursor structures are observed, (ii) a conversion stage as precursors are converted to close packed structures, (iii) a nucleation stage, and (iv) a ripening stage. It is found that the behavior is qualitatively different for volume fractions below or above the melting volume fraction. The main effect of increasing polydispersity is to increase the duration of the induction stage, due to the requirement for local fractionation of particles of larger or smaller than average size. Near the glass transition, the nucleation process is entirely frustrated, and the sample is locked into a compressed crystal precursor structure. Interestingly, neither polydispersity nor volume fraction significantly influences the precursor stage, suggesting that the crystal precursors are present in all solidifying samples. We speculate that these precursors are related to the dynamical heterogeneities observed in a number of dynamical studies.
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