Multiple glass transitions in star polymer mixtures: Insights from theory and simulations

Abstract

The glass transition in binary mixtures of star polymers is studied by mode coupling theory and extensive molecular dynamics computer simulations. In particular, we have explored vitrification in the parameter space of size asymmetry $\delta$ and concentration ${\rho }_2$ of the small star polymers at fixed concentration of the large ones. Depending on the choice of parameters, three different glassy states are identified: a single glass of big polymers at low $\delta$ and low ${\rho }_2$, a double glass at high $\delta$ and low ${\rho }_2$, and a novel double glass at high ${\rho }_2$ and high $\delta$ which is characterized by a strong localization of the small particles. At low $\delta$ and high ${\rho }_2$ there is a competition between vitrification and phase separation. Centered in the $(\delta ,{\rho }_2)$-plane, a liquid lake shows up revealing reentrant glass formation. We compare the behavior of the dynamical density correlators with the predictions of the theory and find remarkable agreement between the two.

15 figures, to be published in Macromolecules

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• Slow dynamics coupled with cluster formation in ultrasoft-potential glasses
• Effective potentials induced by mixtures of patchy and hard co-solutes
• Decoupling of single-particle and collective dynamics in arrested phase-separating glassy mixtures