6533b851fe1ef96bd12a9729

RESEARCH PRODUCT

Polymer-specific effects of bulk relaxation and stringlike correlated motion in the dynamics of a supercooled polymer melt

Francis W. StarrFrancis W. StarrSharon C. GlotzerY. GebremichaelY. GebremichaelJörg BaschnagelM AicheleM Aichele

subject

chemistry.chemical_classificationQuantitative Biology::BiomoleculesMaterials scienceScatteringGeneral Physics and Astronomy02 engineering and technologyPolymer021001 nanoscience & nanotechnology01 natural sciencesExponential functionCondensed Matter::Soft Condensed MatterCrystallographychemistry.chemical_compoundMonomerchemistryChain (algebraic topology)Chemical physics0103 physical sciencesRelaxation (physics)Physical and Theoretical Chemistry010306 general physics0210 nano-technologySupercoolingGlass transition

description

We analyze dynamical heterogeneities in a simulated “bead-spring” model of a nonentangled, supercooled polymer melt. We explore the importance of chain connectivity on the spatially heterogeneous motion of the monomers. We find that when monomers move, they tend to follow each other in one-dimensional paths, forming strings as previously reported in atomic liquids and colloidal suspensions. The mean string length is largest at a time close to the peak time of the mean cluster size of mobile monomers. This maximum string length increases, roughly in an exponential fashion, on cooling toward the critical temperature TMCT of the mode-coupling theory, but generally remains small, although large strings involving ten or more monomers are observed. An important contribution to this replacement comes from directly bonded neighbors in the chain. However, mobility is not concentrated along the backbone of the chains. Thus, a relaxation mechanism in which neighboring mobile monomers along the chain move predominant...

https://doi.org/10.1063/1.1597473