arXiv subjects

Javier Oller-Iscar

Publications and source records attributed to Javier Oller-Iscar.

3 recordsLinked to original sources

arXiv2026

Effect of substrate mismatch, orientation, and flexibility on heterogeneous ice nucleation

Heterogeneous nucleation is the main path to ice formation on Earth. The ice nucleating ability of a certain substrate is mainly determined by both molecular interactions and the structural mismatch between the ice and the substrate lattices. We focus on the latter factor using molecular simulations of the mW model. Quantifying the effect of structural mismatch alone is challenging due to its coupling with molecular interactions. To disentangle both factors, we use a substrate composed of water molecules in such a way that any variation on the nucleation temperature can be exclusively ascribed to the structural mismatch. We find that a one per cent increase of structural mismatch leads to a decrease of approximately 4 K in the nucleation temperature. We also analyse the effect of the orientation of the substrate with respect to the liquid. The three main ice orientations (basal, primary prism and secondary prism) have a similar ice nucleating ability. We finally asses the effect of lattice flexibility by comparing substrates where molecules are immobile with others where a certain freedom to fluctuate around the lattice positions is allowed. Interestingly, we find that the latter type of substrate is more efficient in nucleating ice because it can adapt its structure to that of ice.

cond-mat.mtrl-sci↗

arXiv2026

Heterogeneous ice nucleation on model substrates

Ice nucleation is greatly important in areas as diverse as climate change, cryobiology, geology or food industry. Predicting the ability of a substrate to induce the nucleation of ice from supercooled water is a difficult problem. Here, we use molecular simulations to analyse how the ice nucleating ability is affected by the substrate lattice structure and orientation. We focus on different model lattices: simple cubic, body centred cubic and face centred cubic, and assess their ability to induce ice nucleation by calculating nucleation rates. Several orientations are studied for the case of the face centred cubic lattice. Curiously, a hexagonal symmetry does not guarantee a better ice nucleating ability. By comparing the body centred cubic and the cubic lattices we determined that there is a significant role of the underlying crystal plane(s) on ice nucleation. The structure of the liquid layer adjacent to the substrate reveals that more efficient nucleants induce a more structured liquid. The most efficient substrates present a strong sensitivity of their ice nucleating ability to the lattice parameters. Introducing a novel methodological approach, we use Classical Nucleation Theory to estimate the contact angle of the ice nucleus on the studied substrates from the calculated nucleation rates. The method also provides the nucleation free energy barrier height, the kinetic pre-factor and the critical cluster size. The latter is in agreement with the nucleus size obtained through a microscopic analysis of the nucleation trajectories, which supports the validity of Classical Nucleation Theory down to small critical clusters.

cond-mat.mtrl-sci↗

arXiv2024

Computational study of active polar polymer melts: from active reptation to activity induced local alignment

This work investigates the effects of tangent polar activity on the conformational and dynamic properties of entangled polymer melts through Langevin molecular dynamics simulations. We examine systems composed of all self-propelled, monodisperse linear chains, so that constraint release is considered. The range of activities explored here includes values where the active reptation theory is applicable, as well as higher activities that challenge the validity of the theory. Chain conformations exhibit a moderate increase in coil size increase, which becomes more pronounced at higher activity levels. Under these conditions, a local bond alignment along the chain contour appears together with a non-homogeneous segmental stretching, and orientation and stretching of the tube. Dynamically, polar activity induces a molecular-weight-independent diffusion coefficient, a transient superdiffusive behavior, and an end-to-end relaxation time inversely proportional to the molecular weight. Finally, our results are summarized in a diagram that classifies the various regimes of behavior observed in the simulations. Overall, these findings provide valuable insights into the complex interplay between activity and entanglements, advancing our understanding of active polymer systems and their potential applications across various fields.

cond-mat.soft↗