Multispeckle x-ray photon correlation spectroscopy was employed to characterize the slow dynamics of a suspension of highly charged, nanometer-sized disks. At wave vectors q corresponding to interparticle length scales, the dynamic structure factor follows a form f(q,t) approximately exp([-(t/tau)(beta)], where beta approximately 1.5. The relaxation time tau increases with the sample age t(a) approximately as tau approximately t(1.8)(a) and decreases with q as tau approximately q(-1). Such behavior is consistent with models that describe the dynamics in disordered elastic media in terms of strain from random, local structural rearrangements. The measured amplitude of f(q,t) varies with q in a manner that implies caged particle motion. The decrease in the range of this motion and an increase in suspension conductivity with increasing t(a) indicate a growth in interparticle repulsion as the mechanism for internal stress development implied by these models.

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X-ray photon correlation spectroscopy is employed to investigate the motion of dilute suspensions of gold nanoparticles in low-molecular-weight polystyrene melts. At high temperatures, the observed motion is diffusive, with a rate that follows a Vogel-Fulcher temperature dependence. Closer to the glass transition temperature Tg, diffusion is superseded by a hyperdiffusive process that first becomes observable near a crossover temperature Tc approximately 1.1Tg and is identified with heterogeneous strain in the melts. Following rapid cooling to temperatures sufficiently below Tc, but still above Tg, the hyperdiffusive dynamics displays a time dependence similar to aging in polymer glasses.

We describe x-ray photon correlation spectroscopy (XPCS) experiments tracking the motion of gold nanoparticles within solutions of high-molecular-weight polystyrene. Over displacements from nanometers to tens of nanometers, the particles undergo subdiffusive motion that is dictated by the temporal evolution of the entangled polymer mesh in the immediate vicinity of the particles. The results thus provide a novel microscopic dynamical characterization of this key structural property of polymers and more broadly demonstrate the capability of XPCS-based microrheology to interrogate heterogeneous mechanical environments in nanostructured soft materials.