Searcharxiv⌕ Search

arXiv · 2610.37581

Water at the molecular frontier

Abstract

Much of the water that matters most - flowing through biological cells and membranes, percolating through soils and rocks, or processed by filtration and desalination technologies - is not bulk water. It is water in nano- and molecular-scale confinement or at interfaces. Nanoscale water is therefore central to many challenges of our time, from the global water crisis and the water-energy nexus to catalysis, electrochemistry, and health. Beyond its applications, nanoscale water has emerged as a rich scientific field in its own right: discoveries are accumulating rapidly, revealing that confinement and interfacial forces produce a range of behaviours absent in the bulk. Sometimes this amounts to a renormalization of bulk properties; in other cases, new and non-intuitive phenomena emerge - exotic phases, anomalous transport, and dielectric responses that defy continuum expectations. A convergence of atomically precise nanofluidic devices, novel spectroscopies and microscopy approaches, and machine-learning-accelerated simulations is now exposing the molecular mechanisms behind these behaviours. This Perspective argues that the recent findings should not be viewed as isolated nanoscale anomalies, but as evidence for a molecular regime of water in which continuum descriptions must be rethought and molecular-level understanding becomes essential. Recognising and exploring this regime should have consequences ranging from fundamental physics to the rational design of future technologies that rely on water and dissolved ions.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Mischa Bonn, Marie-Laure Bocquet, Andre Geim, Laura Fumagalli, Angelos Michaelides, Lyderic Bocquet. 2026-10-27. Water at the molecular frontier. https://arxiv.org/abs/2610.37581

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Active tissue mechanics drives a diversity of collective flows in uniaxially compressed 3D spheroids

Compression can enhance or suppress cell motion and induce coherent rotation in tissue spheroids, but the physical factors governing these responses remain unclear. Using a minimal three-dimensional active vertex model, we examine how tissue mechanics, active driving, and directional alignment shape the response to uniaxial compression. Without alignment, compression enhances transverse motion in solid-like spheroids throughout the tested activity range, whereas fluid-like spheroids switch from acceleration at low activity to slowing at high activity. Changes in contact persistence connect these responses to neighbor exchange. Passive five-cell calculations show that compression reshapes local rearrangement barriers depending on geometry and loading direction; a high-strain increase in the fluid-like mean coexists with many low-barrier paths. With strong alignment, compression induces coherent rotation in solid-like spheroids, while fluid-like spheroids show no comparable rotation. Rotating solids retain more persistent cell contacts than fluids and develop tangential organization of peripheral cells. Controlled perturbations reveal that compression softens a differential-twist mode and activity slows its relaxation. Together, these results link activity-dependent reversal of the speed response and compression-induced coherent rotation to contact dynamics, local rearrangement costs, and active driving. Our findings demonstrate that one minimal model, with parameters representing effective mechanical and active tissue properties, captures diverse collective responses to compression and provides a framework for predicting how different tissues respond to mechanical loading.

cond-mat.soft↗

Tribocharging of Granular Materials Dictated by Geometric and Thermoelectric Effects

Tribocharging of granular materials is a widespread phenomenon ranging from volcanic eruptions and dust storms to pharmaceutical processing, yet its underlying mechanism remains elusive. Recent thermoelectric models have provided a quantitative framework for triboelectric charge transfer, but they have difficulty accounting for charging between identical materials. In this Letter, we propose a theory of granular tribocharging based on the interplay between particle geometry and thermoelectric response. Collision-induced frictional heating produces a size-dependent temperature asymmetry between particles, generating a thermoelectric voltage that drives charge transfer. The sign of the Seebeck coefficient determines the charging polarity, while particle size and thermal properties set its magnitude. Our multi-collision theory explains the experimentally observed size- and material-dependent reversal of charging polarity, as in quartz and nylon.

cond-mat.soft↗

Mixed symmetries in active non-reciprocal systems

Active materials are driven out of equilibrium at the microscopic scale and display diverse phenomenology; non-reciprocity is a subclass of activity in which action-reaction symmetry is also broken. These models are often grouped by the order of symmetry of their components, such as polar bird flocks or hexatic cellular tissues. However, many biological examples exist in which the components appear to have two or more symmetries simultaneously. To study this effect we introduce two independently controllable symmetries to the non-reciprocal XY model. This lattice model demonstrates wide ranging behavior dictated by the chosen symmetries. We derive a full hydrodynamic description of our lattice model that highlights the mechanisms driving its behavior. Each combination of symmetries can lead to a different hydrodynamic model with one or two simultaneous order parameters with different levels of orientational order that can appear active or not.

cond-mat.soft↗