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The breakdown of the Stokes-Einstein relation in supercooled liquids, which is the increase in the ratio ττ between the two macroscopic times for structural relaxation and diffusion on decreasing the temperature, is commonly ascribed to dynamic heterogeneities, but a clear-cut microscopic interpretation is still lacking. Here, we tackle this issue exploiting the single-particle cage-jump framework to analyze molecular dynamics simulations of soft disk assemblies and supercooled water. We find that ττ∝⟨t⟩⟨t⟩, where ⟨t⟩ and ⟨t⟩ are the cage-jump times characterizing slow and fast particles, respectively. We further clarify that this scaling does not arise from a simple term-by-term proportionality; rather, the relations τ∝⟨t⟩⟨Δr ⟩ and τ∝⟨t⟩⟨Δr ⟩ effectively connect the macroscopic and microscopic timescales, with the mean square jump length ⟨Δr ⟩ shrinking on cooling. Our work provides a microscopic perspective on the Stokes-Einstein breakdown and generalizes previous results on lattice models to the case of more realistic glass-formers.
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http://dx.doi.org/10.1063/5.0059622 | DOI Listing |
Phys Rev E
July 2025
Emory University, Department of Physics, Atlanta, Georgia 30322, USA.
Observations of glassy dynamics in dense cellular tissues have inspired a wealth of research modeling their collective behavior. Initial studies of the physical properties of several geometric cell models have highlighted anomalous sub-Arrhenius, or "ultrastrong," scaling of the dynamics with temperature. Here we show that the dynamics in this sub-Arrhenius regime deviate even further from the standard glassforming paradigm, displaying unusual scaling of the viscosity with temperature, a lack of breakdown of the Stokes-Einstein-Sutherland relation, and strongly suppressed dynamical heterogeneities.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
July 2025
Kuang Yaming Honors School, Nanjing University, Nanjing 210023, China.
Understanding the dynamics of macromolecules adsorbed from extracellular fluids onto cell membranes is crucial for elucidating basic cellular processes and advancing applications in biotechnology, such as biosensing, therapeutics, and synthetic biology. However, this is complicated by the interplay between membrane heterogeneity, macromolecule conformation, and fluid hydrodynamics. We investigate the dynamics of linear polymers on binary lipid membranes using hydrodynamics simulations and single-molecule tracking experiments.
View Article and Find Full Text PDFPhys Rev E
March 2025
Tata Institute of Fundamental Research, 36/P, Gopanpally Village, Serilingampally Mandal, Ranga Reddy District, Hyderabad, Telangana 500046, India.
The Stokes-Einstein (SE) relation, which relates diffusion constants with the viscosity of a liquid at high temperatures in equilibrium, is violated in the supercooled temperature regime. Whether this relation is obeyed in nonequilibrium active liquids is a question of significant current interest to the statistical physics community trying to develop the theoretical framework of nonequilibrium statistical mechanics. Via extensive computer simulations of model active glass-forming liquids in three dimensions, we show that SE is obeyed at a high temperature similar to the equilibrium behavior, and it gets violated in the supercooled temperature regimes.
View Article and Find Full Text PDFJ Chem Phys
April 2025
Department of Physics, Indian Institute of Technology Palakkad, Nila Campus, Kanjikode, Palakkad, Kerala 678623, India.
We investigate the dynamical properties of liquid and supercooled liquid silicon, modeled using the Stillinger-Weber potential, to examine the validity of the Stokes-Einstein (SE) relation. Toward this end, we examine the relationship among various dynamical quantities, including (i) the macroscopic transport coefficients-self-diffusion coefficient D and viscosity η, (ii) relaxation time τα, and (iii) lengthscale dependent relaxation times τα(q) over a broad range of temperature T, pressure P, and density ρ covering both equilibrium and metastable liquid state points in the phase diagram. Our study shows a weak breakdown in the SE relation involving D and η, and the loci of the breakdown of the SE relation (SEB) are found in the high T liquid phase.
View Article and Find Full Text PDFJ Phys Chem B
December 2024
August Chełkowski Institute of Physics, University of Silesia, 75 Pulku Piechoty 1, 41-500 Chorzow, Poland.
The fundamental Debye-Stokes-Einstein (DSE) relation between rotational relaxation times and shear viscosity attracts longstanding research interest as one of the most important characteristics of many glass-forming liquids. Here, we provide strong evidence, missing so far, for the relevance of anisotropy for DSE-related behavior. Dielectric spectroscopy and shear viscosity measurements were employed to get insight into the decoupling between reorientation relaxation times and viscosity for anisotropic glass-formers with dipole moments oriented parallel or perpendicular to the long molecular axis.
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