Effect of polydispersity on the crystallization kinetics of suspensions of colloidal hard spheres when approaching the glass transition

被引:74
作者
Schoepe, Hans Joachim
Bryant, Gary
van Megen, William
机构
[1] Johannes Gutenberg Univ Mainz, Inst Phys, D-552128 Mainz, Germany
[2] RMIT Univ, Dept Appl Phys, Melbourne, Vic 3001, Australia
关键词
D O I
10.1063/1.2760207
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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. (c) 2007 American Institute of Physics.
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页数:7
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