arXiv subjects

Łukasz Baran

Publications and source records attributed to Łukasz Baran.

7 recordsLinked to original sources

arXiv2025

Impact of the sodium and calcium chlorides uptake on the interfacial behavior of ice: premelting, structure, and dynamics

Hypothesis: Seawater ice and frozen aqueous solutions in contact with air can exhibit a thin quasi-brine surface layer intruding between ice and vapor, but a detailed characterization of surface properties and its relation to three phase coexistence has been lacking. Using thermodynamic arguments we show how it is possible to characterize the surface layers by comparison to the three phase ice-brine-air bulk phase diagram, despite the difficulty to control or monitor all of the relevant thermodynamic fields of the two component system. Simulations: We performed computer simulations of surface briny layers of sodium and calcium chloride adsorbed on ice. Using suitable order parameters and a rigorous geometrical dividing surface, we are able to characterize the layer's thermodynamic state, measure its properties and relate them to the corresponding properties of the bulk solution. Results: Our results confirm that undersaturated briny surface layers can form down to the eutectic point, with a maximum concentration that is bound by the liquidus line of the ice-brine phase diagram. Such layers are distinct from finite size realizations of three phase coexistence, and can be regarded as genuine surface states, but their salt content can increase the premelting layer thickness by a factor of two or more. Owing to this significant thickness, these layers can be related to bulk electrolyte solutions of similar concentration, both as regards the structural organization of ions and the dynamical properties of the quasi-liquid film.

cond-mat.soft↗

arXiv2025

How important is the dielectric constant in water modeling? Evaluation of the performance of the TIP4P/$\varepsilon$ force field and its compatibility with the Joung-Cheatham NaCl model

Efficient large-scale computer simulations of aqueous solutions require the use of accurate but simple empirical force fields for water. However, the complexity of these systems evidences the difficulties in describing solution properties without due account of polarization. Different strategies to remedy this problem are parametrizing water force fields to the dielectric constant or charge scaling of solvated ions. In this work, we compare results from TIP4P/$\varepsilon$ and OPC models, which are parametrized to predict the dielectric constant, with results from TIP4P/2005, which is closer in spirit to the charge scaling strategy. The performance of the models is rated according to the Vega-Abascal benchmark. Our results show that TIP4P/$\varepsilon$ and TIP4P/2005 perform equally well, with the OPC model lying significantly behind. TIP4P/$\varepsilon$ can predict bulk phase properties (transport properties, thermal expansion coefficients, densities) of both liquid water and ice polymorphs, but also surface tensions, with an accuracy very similar to TIP4P/2005, while performing very well for dielectric constants over a wide range of pressures and temperatures. On the other hand, TIP4P/2005 provides a better description of phase boundaries, including liquid-vapor and freezing transitions. However, the accurate prediction of dielectric constants allows TIP4P/$\varepsilon$ to describe densities of NaCl solutions for models parametrized to their crystal and melt properties only. This is achieved without the need to rescale charges, modify the Lorentz-Berthelot rule or tune the ion's Lennard-Jones parameters. Our findings hinge on the significance of dielectric constants as a target property and show that a robust parametrization can be achieved without invoking the concept of charge scaling.

cond-mat.soft↗

arXiv2025

Self-assembly of chromatic patchy particles with tetrahedrally arranged patches

The achievement of selectivity in the formation of cubic diamond is challenging due to the emergence of competing phases such as its hexagonal polymorph or clathrates possessing similar free energy. Although both polymorphs exhibit a complete photonic bandgap, the cubic diamond exhibits it at lower frequencies than the hexagonal counterpart, positioning him as a promising candidate for photonic applications.Herein, we demonstrate that the 1:1 mixture of identical patchy particles cannot selectively form the cubic diamond polymorph due to the frustrations present in the system that are manifested in the primary adsorption layer and propagate as the film grows. We provide a plausible} explanation why the binary system under confinement, resembling interactions between the complementary DNA bases cannot yield the selectivity in the formation of cubic diamond crystals which is based on the similarities to the antiferromagnetic systems. We always observe the mixture of both hexagonal and cubic diamonds, however, the formation of such stacking hybrids is observed for a wider range of patch sizes compared to the one-component system.

cond-mat.soft↗

arXiv2024

Understanding Interfacial Ice Premelting: Structure, Adhesion and Nucleation

In this work, we perform a systematic computer simulation study of ice premelting, and explore the thickness and structure of quasi-liquid layers formed at the interface of ice with substrates of different hydrophilicity. Our study shows that interfacial premelting occurs on neutral substrates of whatever hydrophilicity, forming films of limited thickness for substrates with contact angles larger than ca. 50$^\circ$ but exhibiting complete interfacial premelting at smaller contact angles. Contrary to most experimental studies, we focus not only on the premelting behavior with temperature, but also with pressure, which is a matter of relevance in important situations such as ice friction. Our study is guided within a rigorous framework of surface thermodynamics, demonstrating that the premelting film structure is a function of a single thermodynamic variable. By this token we are able to relate properties measured along an isobar, with premelting films at arbitrary temperature and pressure. We also find that adhesion strength in atomically smooth surfaces is one to two orders of magnitude larger than those found in experiments, and conjecture that the reason is substrate roughness and the presence of organic adsorbents. Our theoretical framework also allows us to exploit our results on interfacial premelting in order to gain insight into heterogeneous ice nucleation. We show that apolar smooth substrates of whatever hydrophilicity are unlikely nucleators, and that too large hydrophilicity conspires also against ice nucleation. Furthermore, we exploit statistical-thermodynamic framework to shed light into the nature of the surface intermolecular forces promoting interfacial premelting, and provide a model to predict quasi-liquid layer thickness as a function of the substrate's hydrophilicity with great potential applications in fields ranging from earth sciences to aircraft engineering.

cond-mat.soft↗

arXiv2024

On the selective formation of cubic tetrastack crystals from tetravalent patchy particles

Achieving the formation of target open crystalline lattices from colloidal particles is of paramount importance for their potential application in photonics. Examples of such desired structures are the diamond, tetrastack, and pyrochlore lattices. Here, we demonstrate that the self-assembly of tetravalent patchy particles results in the selective formation of cubic tetrastack crystals, both in the bulk and in the systems subjected to external fields exerted by the solid substrate. It is demonstrated that the presence of an external field allows for the formation of well-defined single crystals with a low density of defects. Moreover, depending on the strength of the applied external field, the mechanism of epitaxial growth changes. For weakly attractive external fields, the crystallization occurs in a similar manner as in the bulk, since the fluid does not wet the substrate. Nonetheless, the formed crystal is considerably better ordered than the crystals formed in bulk, since the surface induces the ordering in the first layer. On the other hand, it is demonstrated that the formation of well-ordered cubic tetrastack crystals is considerably enhanced by the increase in external field strength, and the formation of the thick crystalline film occurs via a series of layering transitions.

cond-mat.soft↗

arXiv2024

Pursuing colloidal diamond

The endeavor to selectively fabricate a cubic diamond is challenging due to the formation of competing phases such as its hexagonal polymorph or others possessing similar free energy. The necessity to achieve this is of paramount importance since the cubic diamond is the only polymorph exhibiting a complete photonic bandgap, making it a promising candidate in view of photonic applications. Herein, we demonstrate that due to the presence of an external field and delicate manipulation of its strength we can attain selectivity in the formation of a cubic diamond in a one-component system comprised of designer tetrahedral patchy particles. The driving force of such a phenomenon is the structure of the first adlayer which is commensurate with the (110) face of the cubic diamond. Moreover, after a successful nucleation event, once the external field is turned off, the structure remains stable, paving an avenue for further post-synthetic treatment.

physics.chem-ph↗

arXiv2022

Self-diffusion and shear viscosity for the TIP4P/Ice water model

With an ever-increasing interest in water properties, many intermolecular force fields have been proposed to describe the behavior of water. Unfortunately, good models for liquid water usually cannot provide simultaneously an accurate melting point for ice. For this reason, the TIP4P/Ice model was developed at targeting the melting point, and has become the preferred choice for simulating ice at coexistence. Unfortunately, available data for its dynamic properties in the liquid state are scarce. Therefore, we demonstrate a series of simulations aimed at the calculation of transport coefficients for the TIP4P/Ice model over a large range of thermodynamic conditions, ranging from $T=245$ K to $T=350$ K for the temperature and from $p=0$ to $p=500$ MPa for the pressure. We have found that the self-diffusion (shear viscosity) exhibits smaller (increased) values than TIP4P/2005 and experiments. However, rescaling the temperature with respect to the triple point temperature as in a corresponding states plot we find TIP4P/Ice compares very well with TIP4P/2005 and to experiment. Such observations allow us to infer that despite the different original purposes of these two models examined here, one can benefit from a vast number of reports regarding the behavior of transport coefficients for the TIP4P/2005 model and utilize them following the routine described in this paper.

physics.chem-ph↗