arXiv subjects

Michal Duška

Publications and source records attributed to Michal Duška.

3 recordsLinked to original sources

arXiv2021

Communication: Two-structure thermodynamics unifying all scenarios for water anomalies

Anomalous behavior of water in superooled region (namely decrease of density and sharp increase of response functions at atmospheric pressure) are manly associated with either existence of liquid-liquid criticality or re-entering vapor-liquid spinodal into positive pressure. Despite different origin both scenarios introduce divergence of the response functions. We articulate in the communication that the criticality is behind water anomalies, water has normal vapor-liquid spinodal and that the re-entering feature was predicted because of curved density surface as a consequence of existence of critical point. We can proof this by new two structure equation of state with criticality resulting from non-ideal mixing of two states and a background state being modeled by exactly the same equation of state which was deployed for predicting of vapor-liquid spinodal while formulating the re-entering scenario.

physics.chem-ph↗

arXiv2020

Water above spinodal

The liquid spinodal, which is the bedrock of water thermodynamics, has long been discussed alongside the elusive liquid-liquid critical point hidden behind the limit of homogeneous nucleation. This has inspired numerous scenarios that attempt to explain water anomalies. Despite recent breakthrough experiments eliminating several of thous scenarios, we lacked a tool to localize the spinodal and the liquid-liquid critical point. We constructed a unique equation of state combining the famous Speedy's equation and the liquid-liquid critical point to remove that deficit and to review these explanations. For the first time, the proposed equation of state independently depicts the spinodal in the presence of the liquid-liquid critical point and demonstrates that the explanation for water anomalies based on the reentrance of the spinodal is not valid; this feature (reentering the spinodal) was solely predicted based on the curved density surface caused by the existence of the second critical point. However, the critical point alone is not sufficient to explain the shape of the density surface of water. In the new equation, hydrogen bond cooperativity is important to force the critical point to exist outside of zero temperature. Together with mounting evidence for the existence of a compressibility maximum behind the homogeneous nucleation limit at positive pressure, the findings practically exclude all explanations for water anomalies except for the existence of the liquid-liquid critical point at positive pressure. Finally, an extensive study of heat capacity demonstrated profound disagreement between the two major experimental heat capacity datasets and identified the more accurate dataset.

physics.chem-ph↗

arXiv2017

Thermodynamics of Fluid Polyamorphism

"Fluid polyamorphism" is the existence of different condensed amorphous states in a single-component fluid. It is either found or predicted, usually at extreme conditions, for a broad group of very different substances, including helium, carbon, silicon, phosphorous, sulfur,tellurium, cerium, hydrogen and tin tetraiodide. This phenomenon is also hypothesized for metastable and deeply supercooled water, presumably located a few degrees below the experimental limit of homogeneous ice formation. We present a generic phenomenological approach to describe polyamorphism in a single-component fluid, which is completely independent of the molecular origin of the phenomenon. We show that fluid polyamorphism may occur either in the presence or the absence of fluid phase separation depending on the symmetry of the order parameter. In the latter case, it is associated with a second-order transition, such as in liquid helium or liquid sulfur. To specify the phenomenology, we consider a fluid with thermodynamic equilibrium between two distinct interconvertible states or molecular structures. A fundamental signature of this concept is the identification of the equilibrium fraction of molecules involved in each of these alternative states. However, the existence of the alternative structures may result in polyamorphic fluid phase separation only if mixing of these structures is not ideal. The two-state thermodynamics unifies all the debated scenarios of fluid polyamorphism in different areas of condensed-matter physics, with or without phase separation, and even goes beyond the phenomenon of polyamorphism by generically describing the anomalous properties of fluids exhibiting interconversion of alternative molecular states.

cond-mat.stat-mech↗