Asymmetric Effects Underlying Dynamic Heterogeneity in Miscible Blends of Poly(methyl methacrylate) with Poly(ethylene oxide)

The emergence of spatially variable local dynamics, or dynamic heterogeneity, is common in multicomponent polymer systems. Although often attributed to differences in the intrinsic dynamics of each component, the molecular origin of their coupling and its dependencies remain unclear. Here, we use molecular dynamics simulations of poly-(ethylene oxide) (PEO)/poly-(methyl methacrylate) (PMMA) blends, across the full range of compositions and multiple thermal regimes, to characterize local fluctuations and subchain relaxations for both PEO and PMMA. By constructing probability distributions of local composition and computing entropic measures, we connect nanoscale heterogeneity to differences in mobility between PEO and PMMA, extending beyond mean-field treatments. While PMMA segmental fluctuations in blends broadly align with <i>T</i> _g-equivalent neat PMMA systems, PEO exhibits enhanced mobility correlated with increased free volume and broader, more diverse local compositions upon blending. Rouse-mode analysis, used to probe relaxation dynamics over different length scales, shows that PEO relaxation approaches neat-like behavior in PEO-rich domains, whereas PMMA relaxation accelerates uniformly across all mode numbers. Given the local mobility enhancement of PMMA by PEO, this uniform shift suggests a nanoscale facilitation process that extends PEO's influence beyond its immediate environment. These findings link the statistics of local compositional heterogeneity to dynamic asymmetry across length scales, provide physical insight into the behavior of this archetypal blend system, and establish a framework for analyzing dynamic coupling in others.