*********************************
There is now a CONTENT FREEZE for Mercury while we switch to a new platform. It began on Friday, March 10 at 6pm and will end on Wednesday, March 15 at noon. No new content can be created during this time, but all material in the system as of the beginning of the freeze will be migrated to the new platform, including users and groups. Functionally the new site is identical to the old one. webteam@gatech.edu
*********************************
AACP seminar series - Prof. Hans Andersen, Stanford University
Scaling Analysis of Dynamic Heterogeneity in a Supercooled Lennard-Jones Liquid
Dynamic heterogeneity has been recognized as a significant feature of supercooled liquids. At any given time, there are some regions of such a material in which the molecules are more mobile and hence relaxation takes place at rates that are larger than the average relaxation rates in the material. Moreover, the correlation length that characterizes the sizes of these regions increases as the temperature is lowered. This behavior has been observed in computer simulations and inferred from experimental measurements on several kinds of materials. We have performed molecular dynamics computer simulations of a dense Lennard- Jones liquid mixture to study dynamic heterogeneity from normal liquid temperatures down to a supercooled temperature 15% above the previously identified mode coupling temperature Tc of the model. A susceptibility associated with the correlation function of mobility fluctuations was defined and calculated from simulation data as a function of wave vector and temperature. A correlation length for mobility fluctuations was obtained from the wave vector dependence for each temperature. The results were used to test two sets of scaling hypotheses for the liquid. The first set is based on the idea that the mobility correlation function obeys a scaling principle in which the only relevant length scale is the correlation length. The second set of hypotheses is based on the temperature dependence of singular functions predicted by mode coupling theory. The results are in close agreement with the inhomogeneous mode coupling theory of Biroli et al. [Phys. Rev. Lett. 97, 195701 (2006)] for both the α and β relaxation regimes. Comparison with results for kinetically constrained models suggest that the Lennard-Jones mixture studied is more similar to models for fragile liquids than models for strong liquids.
For more information contact Dr. Christine Payne (404-385-3125).
