Theory of Spatial Gradients of Relaxation, Vitrification Temperature and Fragility of Glass-Forming Polymer Liquids near Solid Substrates

We employ a new force-level statistical mechanical theory to predict spatial gradients of the structural relaxation time and T_g of polymer liquids near microscopically rough and smooth hard surfaces and contrast the results with vapor interface systems. Repulsive rough (smooth) surfaces induce large slowing down (modest speeding up) of the relaxation time compared to the bulk. Nevertheless, a remarkable degree of universality of distinctive dynamical behaviors is predicted for different polymer chemistries and all interfaces, including a double exponential form of the alpha time gradient, power law decoupling of the relaxation time from its bulk value with exponential spatial variation of the exponent, exponential spatial gradient of T_g, weak dependence of normalized T_g gradients on vitrification criterion, and near linear growth with cooling of the slowed down layer thickness near a rough hard interface. The results appear consistent with simulations and experiments, and multiple testable predictions are made.