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While the concept of high entropy has gained prominence in materials design, disentangling specific impacts of entropy on material properties from the enthalpy of mixing remains elusive. It is demonstrated that the role of entropy can be distinguished from the dynamics of glass-forming liquids through micro-alloying. Based on experiment analysis of 79 compositions, liquid fragility is found to consistently decreases under two conditions: i) when the alloying content x is minimal, irrespective of the elements used; or ii) when increasing the diversity of alloying elements at a constant x, namely the high-entropy micro-alloying. These observations are consistent with thermodynamic principles that favor an entropy-dominated regime over enthalpy. These findings elucidate the subtle impact of mixing entropy on material properties and provide evidence of the entropy nature of glass transition.
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http://dx.doi.org/10.1002/advs.202502568 | DOI Listing |
J Phys Chem B
September 2025
School of Materials Science & Engineering, Shandong University of Technology, Zibo 255000, China.
The glass transition is dynamically heterogeneous with non-Arrhenius, nonexponential, and nonlinear features, and those parameters are mutually correlated in most cases. This study systematically investigates these interrelated features through thermodynamic analysis of polyvinylpyrrolidone (PVP)/salt complexes, employing enthalpy relaxation parameters, specifically the heat capacity jump (Δ) at and enthalpy hysteresis (Δ). Notably, the introduction of ionic interactions induces simultaneous reductions in dynamic fragility (), nonexponential parameter (β), and nonlinear parameter (), thereby disrupting their previously established empirical correlations.
View Article and Find Full Text PDFJ Chem Phys
August 2025
Polymer Science and Engineering Division, CSIR-National Chemical Laboratory, Pune 411008, India.
Understanding the connection between thermodynamics and dynamics in glass-forming liquids remains a central challenge in condensed matter physics. In this study, we investigate a novel model system that enables a continuous crossover from a standard three dimensional liquid to a fully connected mean field like system by introducing pseudo neighbors. These pseudo neighbors enhance the effective connectivity of the system without altering its local structure.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
January 2026
Amala Cancer, Research Center, Thrissur, Kerala 680 555, India.
Rationale: Procaine HCl (PrHCl), a protic ionic liquid (PIL), exhibits intricate relaxation due to ionic and neutral species interactions. However, its glass-forming ability is limited. To overcome these limitations, this study explores the synthesis of a novel PIL, PrHIb, by replacing Cl with the bulky, asymmetric ibuprofen anion.
View Article and Find Full Text PDFPhys Rev Lett
June 2025
University of Illinois, Department of Materials Science, Urbana, Illinois 61801, USA.
A successful microscopic theory of activated relaxation in metastable supercooled liquids is extended to the equilibrated deep glass regime. Surprisingly, the predicted power-law scaling connections of the dynamic barrier with diverse scalar order parameters (medium-range order correlation length, dimensionless compressibility, shear modulus) remain unchanged up to astronomically long timescales, despite a fundamental crossover of equilibrium thermodynamics and structure near the laboratory kinetic vitrification point. Quantitative tests against experiments on aged to equilibrium glass-forming liquids up to nearly 20 decades in time scale reveal good agreement.
View Article and Find Full Text PDFJ Chem Phys
July 2025
Center for Theoretical Biological Physics, Rice University, Houston, Texas 77005, USA.
The Random First Order Transition (RFOT) theory of glasses provides a unified framework for explaining the observed correlations of the kinetic and thermodynamic behaviors of glass-forming liquids having a wide variety of chemical compositions and interactions. The theory also provides a solid starting point for calculating glassy dynamics starting from the microscopic forces. Network liquids, which interact via long-lived, geometrically constraining interactions, such as covalent bonding, have competing energy scales for bond breaking events and for collective particle rearrangement events.
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