Static and dynamic correlation lengths in supercooled polymers

CRISTIAN BALBUENA; MELISA GIANETTI; EZEQUIEL R. SOULÉ

JOURNAL OF CHEMICAL PHYSICS

AMER INST PHYSICS

Lugar: New York; Año: 2019

0021-9606

A key point to understand the glass transition is the relationship between structural and dynamic behavior experienced by a glass former when it approaches Tg. In this work, the relaxation in a simple bead-spring polymer system in the supercooled regime near its glass transition temperature was investigated with Molecular Dynamic simulations. We develop a new manner to look at the dynamic length scales in a supercooled polymeric system, focusing on correlated motion of particles in an isoconfigurational ensemble (that is, associated with structure), as measured by the Pearson?s correlation coefficient. We found that, while the usual dynamic four-point correlation length deviates from the the structural (mosaic or point-to-set) length scale at low temperatures, Pearson?s length behaves similarly to the static length in the whole temperature range. The results lead to a consensus of similar scaling of structural and dynamical length scales, reinforcing the idea of the theories of Adam-Gibbs and Random First Order Transition.