arXiv subjects

Hai-Bin Yu

Publications and source records attributed to Hai-Bin Yu.

9 recordsLinked to original sources

arXiv2026

Percolation-driven $\beta$ -relaxation enables resonant acceleration of crystallization in amorphous phase-change materials

Amorphous phase-change materials enable fast and reversible switching in optical and electronic devices, yet crystallization kinetics are still controlled primarily through empirical thermal protocols. Here we identify a microscopic picture governing crystallization in the prototypical phase-change material Ge2Sb2Te5, in which crystallization pathways are organized by the percolation of mobile atomic networks associated with $\beta$-relaxation. We show that this percolation transition distinguishes the dominance of diffusion-driven and diffusionless nucleation and growth during crystallization processes. We further demonstrate that frequency-selected ultrasonic excitation, applied in conjunction with heating, accelerates crystallization by enhancing percolation-mediated atomic dynamics. This acceleration is maximized near the $\beta$-relaxation frequency, consistent with resonant excitation of mobile atoms. Our results establish a direct link between glassy relaxation, atomic-scale percolation, and crystallization, and introduce a new route to modulating phase-change kinetics through targeted excitation of fundamental glassy dynamics.

cond-mat.mtrl-sci↗

arXiv2025

A Non-Equilibrium Dissipation Parameter and the Ideal Glass

Glass materials, as quintessential non-equilibrium systems, exhibit properties such as energy dissipation that are highly sensitive to their preparation histories. A key challenge has been identifying a unified order parameter to rationalize these properties. Here, we demonstrate that a configurational distance metric can effectively collapse energy dissipation data across diverse preparation histories and testing protocols, including varying cooling rates, aging processes, probing times, and the amplitudes of mechanical excitation, as long as the temperature remains above the so-called ideal glass transition (where the extrapolated structural relaxation time diverges). Our results provide a unified description for the non-equilibrium dissipation and suggest that the putative concept of the ideal glass transition is imprinted in material characteristics

cond-mat.dis-nn↗

arXiv2024

Unified percolation scenario for the $\alpha$ and $\beta$ processes in simple glass formers

Given the vast differences in interaction details, describing the dynamics of structurally disordered materials in a unified theoretical framework presents a fundamental challenge to condensed-matter physics and materials science. Here, we numerically investigate a double-percolation scenario for the two most important relaxation processes of supercooled liquids and glasses, the so-called alpha and beta relaxations. For several simple glass formers, we find that when monitoring the dynamic shear modulus as temperature is lowered from the liquid state, percolation of immobile particles takes place at the temperature locating the alpha process. Mirroring this, upon continued cooling into the glass state, the mobile-particle percolation transition pinpoints a beta process whenever the latter is well separated from the main (alpha) process. For two-dimensional systems under the same conditions, percolation of mobile and immobile particles occurs nearly simultaneously and no beta relaxation can be identified. Our findings suggest that a general description of glassy dynamics should be based on a percolation perspective.

cond-mat.soft↗

arXiv2024

Universal Origin of Glassy Relaxation as Recognized by Configuration Pattern-matching

Relaxation processes are crucial in understanding the structural rearrangements of liquids and amorphous materials. However, the overarching principle that governs these processes across vastly different materials remains an open question. Substantial analysis has been carried out based on the motions of individual particles. Here, alternatively, we propose viewing the global configuration as a single entity. We introduce a global order parameter, namely the inherent structure minimal displacement (IS Dmin), to quantify the variability of configurations by a pattern-matching technique. Through atomic simulations of seven model glass-forming liquids, we unify the influences of temperature, pressure, and perturbation time on the relaxation dissipation, via a scaling law between the mechanical damping factor and IS Dmin. Fundamentally, this scaling reflects the curvature of the local potential energy landscape. Our findings uncover a universal origin of glassy relaxation and offer an alternative approach to studying disordered systems.

cond-mat.dis-nn↗

arXiv2023

Approach to Hyperuniformity in a Metallic Glass-Forming Material Exhibiting a Fragile to Strong Glass Transition

We investigate a metallic glass-forming (GF) material (Al90Sm10) exhibiting a fragile-strong (FS) glass-formation by molecular dynamics simulation to better understand this highly distinctive pattern of glass-formation in which many of the usual phenomenological relations describing relaxation times and diffusion of OGF liquids no longer apply, and where instead genuine thermodynamic features are observed in response functions and little thermodynamic signature is exhibited at the glass transition temperature, Tg. Given the many unexpected similarities between the thermodynamics and dynamics of this metallic GF material with water, we first focus on the anomalous static scattering in this liquid, following recent studies on water, silicon and other FS GF liquids. In particular, we quantify the 'hyperuniformity index' H of our liquid which provides a quantitative measure of molecular 'jamming'. To gain insight into the T-dependence and magnitude of H, we also estimated another more familiar measure of particle localization, the Debye-Waller parameter $ $ describing the mean-square particle displacement on a timescale on the order of the fast relaxation time, and we also calculate H and $ $ for heated crystalline Cu. This comparative analysis between H and $ $ for crystalline and metallic glass materials allows us to understand the critical value of H on the order of $10^{-3}$ as being analogous to the Lindemann criterion for both the melting of crystals and the 'softening' of glasses. We further interpret the emergence of FS GF and liquid-liquid phase separation in this class of liquids to arise from a cooperative assembly process in the GF liquid.

cond-mat.soft↗

arXiv2022

Elastic properties of a Sc-Zr-Nb-Ta-Rh-Pd high-entropy alloy superconductor

We report a comprehensive study on the elastic properties of a hexanary high-entropy alloy superconductor (ScZrNbTa)$_{0.685}$[RhPd]$_{0.315}$ at room and cryogenic temperatures, by Resonant Ultrasound Spectroscopy experiments. The derived elastic constants are bulk modulus $K=132.7$ GPa, Young's modulus $E=121.0$ GPa, shear modulus $G=44.9$ GPa, and Poisson's ratio $ν$=0.348 for room temperature. The Young's and shear moduli are $\sim 10\%$ larger than those in NbTi superconductor with similar $T_c$, while the ductility is comparable. Moreover, the mechanical performance is further enhanced at cryogenic temperature. Our work confirms the advantageous mechanical properties of high-entropy alloy superconductors and suggests the application prospects.

cond-mat.supr-con↗

arXiv2021

Dynamic Heterogeneity, Cooperative Motion, and Johari-Goldstein $β$-Relaxation in a Metallic Glass-Forming Material Exhibiting a Fragile to Strong Transition

We investigate the Johari-Goldstein (JG) $β$-relaxation process in a model metallic glass-forming (GF) material (Al90Sm10), previously studied extensively by both frequency-dependent mechanical measurements and simulation studies devoted to equilibrium properties, by molecular dynamics simulations based on validated and optimized interatomic potentials with the primary aim of better understanding the nature of this universal relaxation process from a dynamic heterogeneity (DH) perspective. The present relatively low temperature and long-time simulations reveal a direct correspondence between the JG $β$-relaxation time $τ_{JG}$ and the lifetime of the mobile particle clusters $τ_M$, defined as in previous DH studies, a relationship dual to the corresponding previously observed relationship between the $α$-relaxation time $τ_α$ and the lifetime of immobile particle clusters $τ_{IM}$. Moreover, we find that the average diffusion coefficient D nearly coincides with D$_{Al}$, of the smaller atomic species (Al), and that the hopping time associated with D coincides with $τ_{JG}$ to within numerical uncertainty, both trends being in accord with experimental studies. This indicates that the JG $α$-relaxation is dominated by the smaller atomic species and the observation of a direct relation between this relaxation process and rate of molecular diffusion in GF materials at low temperatures where the JG $β$-relaxation becomes the prevalent mode of structural relaxation. As an unanticipated aspect of our study, we find that Al90Sm10 exhibits fragile-to-strong (FS) glass-formation, as found in many other metallic GF liquids, but this fact does not greatly alter the geometrical nature of DH in this material and the relation of DH to dynamical properties.

cond-mat.mtrl-sci↗

arXiv2021

Fast Dynamics in a Model Metallic Glass-forming Material

We investigate the fast $β$- and Johari-Goldstein (JG) $β$-relaxation processes, along with the elastic scattering response of glass-forming (GF) liquids and the Boson peak, in a simulated Al-Sm GF material exhibiting a fragile-strong (FS) transition. These dynamical processes are universal in 'ordinary' GF fluids and collectively describe their 'fast dynamics', and we find these relaxation processes also arise in a GF liquid exhibiting a fragile-strong transition. String-like particle motion, having both an irreversible and reversible nature ('stringlets') component, occurs in the fast-dynamics regime, corresponding to a ps timescale. String-like collective motion associated with localized unstable modes facilitate irreversible and intermittent particle 'jumping' events at long times associated with the JG $β$-relaxation process, while stringlets associated with localized stable modes and corresponding perfectly reversible atomic motion give rise to the Boson peak. To further clarify the origin of the Boson peak, we calculate the density of states for both the stringlet particles and the 'normal' particles and find that the stringlet particles give rise to a Boson peak while the normal atoms do not. The growth of stringlets upon heating ultimately also leads to the 'softening' of these excitations, and the Boson peak frequency and shear modulus drop in concert with this softening. The growth of string-like collective motion upon heating in the fast-dynamics regime is further shown to be responsible for the growth in the intensity of the fast relaxation process. Relaxation in cooled liquids clearly involves a hierarchy of relaxation processes acting on rather different time and spatial scales.

cond-mat.mtrl-sci↗

arXiv2019

Predicting Complex Relaxation Processes in Metallic Glass

Relaxation processes significantly influence the properties of glass materials. However, understanding their specific origins is difficult, even more challenging is to forecast them theoretically. In this study, using microseconds molecular dynamics simulations together with an accurate many-body interaction potential, we predict that an Al$_{\text{90}}$Sm$_{\text{10}}$ metallic glass would have complex relaxation behaviors: In addition to the main ($α$) relaxation, the glass (i) shows a pronounced secondary ($β$) relaxation at cryogenic temperatures and (ii) exhibits an anomalous relaxation process ($α_2$) accompanying $α$ relaxation. Both of the predictions are verified by experiments. Computational simulations reveal the microscopic origins of relaxation processes: while the pronounced $β$ relaxation is attributed to the abundance of string-like cooperative atomic rearrangements, the anomalous $α_2$ process is found to correlate with the decoupling of the faster motions of Al with slower Sm atoms. The combination of simulations and experiments represents a first glimpse of what may become a predictive routine and integral step for glass physics.

cond-mat.mtrl-sci↗