Microscopic ergodicity breaking governs the emergence and evolution of elasticity in glass-forming nanoclay suspensions
Microscopic ergodicity breaking governs the emergence and evolution of elasticity in glass-forming nanoclay suspensions
复制标题
微观遍历性破坏控制玻璃形成纳米粘土悬浮液中弹性的出现和演变
DOI:
10.1103/physreve.102.042619
复制
发表时间:
2020
影响因子:
2.4
通讯作者:
Leheny, Robert L.
中科院分区:
文献类型:
--
作者:
Chen, Yihao;Rogers, Simon A.;Narayanan, Suresh;Harden, James L.;Leheny, Robert L.
We report a study combining x-ray photon correlation spectroscopy (XPCS) within siturheology to investigate the microscopic dynamics and mechanical properties of aqueous suspensions of the synthetic hectorite clay Laponite, which is composed of charged, nanometer-scale, disk-shaped particles. The suspensions, with particle concentrations ranging from 3.25 to 3.75 wt %, evolve over time from a fluid to a soft glass that displays aging behavior. The XPCS measurements characterize the localization of the particles during the formation and aging of the soft-glass state. The fraction of localized particles,, increases rapidly during the early formation stage and grows more slowly during subsequent aging, while the characteristic localization lengthsteadily decreases. Despite the strongly varying rates of aging at different concentrations, bothandscale with the elastic shear modulusin a manner independent of concentration. During the later aging stage, the scaling betweenandagrees quantitatively with a prediction of naive mode coupling theory. Breakdown of agreement with the theory during the early formation stage indicates the prevalence of dynamic heterogeneity, suggesting the soft solid forms through precursors of dynamically localized clusters.