arXiv subjects

Bilin Zhuang

Publications and source records attributed to Bilin Zhuang.

4 recordsLinked to original sources

arXiv2026

Stockmayer Fluid with a Shifted Dipole: Bulk Behavior

Shifting the point dipole from the center of a Stockmayer particle is a simple geometric modification that has been explored previously, yet its implications for liquid structure, dielectric response, and phase behavior remain incompletely understood. Here, we combine molecular dynamics simulations with analytical theory to provide a unified physical interpretation of how dipole displacement reshapes microscopic correlations and propagates to macroscopic thermodynamic properties. We show that dipole shifting breaks the fore-aft symmetry of the local electrostatic field, producing only modest changes in radial packing but strong alterations in angular structure within the first solvation shell. Enhanced alignment near the dipole head is accompanied by frustrated orientational correlations near the tail, leading to broader angular distributions and a shift away from axial configurations at strong coupling. These structural asymmetries weaken cooperative ordering and result in a systematic reduction of the dielectric constant, despite locally stronger interactions. For large shifts, the dielectric response approaches the Debye limit, indicating effective suppression of dipole-dipole correlations. The same geometric frustration governs vapor-liquid equilibria: while increasing dipole strength raises the critical temperature, even modest shifts disrupt the highly polarized liquid states that emerge at strong coupling and can suppress ferroelectric-like ordering. Predictions from a reparameterized COFFEE theory capture these trends within its domain of validity, highlighting the direct connection between local orientational structure and macroscopic observables. Overall, this work demonstrates that dipole location, not only magnitude, provides a powerful control parameter in dipolar fluids and offers a clear framework for understanding geometric frustration in electrostatic liquids.

cond-mat.soft↗

arXiv2025

Stockmayer Fluid with a Shifted Dipole: Interfacial Behavior

We investigate the properties of the liquid-vapor interface in the shifted Stockmayer fluid using molecular dynamics simulations in the canonical ensemble. We study the role of the dipole moment strength and the degree of asymmmetry on equilibrium interfacial characteristics, including density profiles, polar order, nematic order, interfacial polarization, electric field, and electrostatic potential. In addition, we compute angular distribution functions across the interface to gain insight into how the dipole shift affects the molecular orientation. We find that the shift significantly effects angular distribution functions by altering the polar order while leaving the nematic order relatively unaffected, in comparison to the reference symmetric Stockmayer fluid. We find that these results are consistently explained using an image-dipole construction that has been previously applied to symmetric Stockmayer fluids but has never been extended to the shifted model. We find remarkable agreement between the simple theory and the simulations in the qualitative shape of the distribution functions for both the liquid and vapor phases in proximity to the interface. Unexpectedly, the spontaneous polarization at the interface, and therefore the generated electric field, changes sign as the dipole moment strength increases. This also leads to an inversion of the sign of the potential difference across the interface.

cond-mat.soft↗

arXiv2024

The reentrant condensation of polyelectrolytes induced by diluted multivalent salts: A mean-field level revisiting

We study the reentrant condensation of polyelectrolytes in dilute solutions of small multivalent salts, whose phase-transition mechanism remains poorly understood. Motivated by recent full atomic simulation results reported by the Caltech group on phase behaviors of polyelectrolytes in presence of multivalent salts (DOIs: 10.1021/acs.macromol.3c02437 and 10.1021/acs.langmuir.3c03640), in this work we construct a simple but effective mean-field model which can rationalize the essential features of the reentrant condensation including the phase diagram of polyelectrolyte. The model unveils that the strong adsorption between the ionic monomers and multivalent ions can be at the origin of the peculiar phenomenon that rather low concentrations of multivalent salts trigger both collapse and re-entry transitions. For the first time, the analytical solution of the model indicates that a minimum of coupling energy due to sharing multivalent salt ions between ionic monomers is essential for a phase transition to occur, which can explain the enigmatic observation that polyelectrolytes can only show phase transition in a dilute solution of salts with selective multivalency. Our analytical calculations also show that the incompatibility of the uncharged moieties of the polyelectrolytes with water is critical to regulate phase behaviors of polyelectrolytes in aqueous solutions. This is in agreement with recent experimental investigations on solution properties of amphiphilic proteins. The obtained results will contribute to the understanding of liquid-liquid phase separation in biological systems where multivalent ions bound to bio-polyelectrolytes play an essential role.

cond-mat.soft↗

arXiv2011

Small-Network Approximations for Geometrically Frustrated Ising Systems

The study of frustrated spin systems often requires time-consuming numerical simulations. As the simplest approach, the classical Ising model is often used to investigate the thermodynamic behavior of such systems. Exploiting the small correlation lengths in frustrated Ising systems, we develop a method for obtaining a first approximation to the energetic properties of frustrated two-dimensional Ising systems using small networks of less than 30 spins. These small networks allow much faster numerical simulations, and more importantly, analytical calculation of the properties from the partition function is possible. We choose Ising systems on the triangular lattice, the Kagome lattice, and the triangular Kagome lattice as prototype systems and find small systems that can serve as good approximations to these prototype systems. We also develop criteria for constructing small networks to approximate general two-dimensional frustrated Ising systems. This method of using small networks provides a novel and efficient way to obtain a first approximation to the properties of frustrated spin systems.

cond-mat.stat-mech↗