arXiv subjects

Nikita Kavokine

Publications and source records attributed to Nikita Kavokine.

At least 19 recordsLinked to original sources

arXiv2026

Fluctuation-induced ionic friction at solid-electrolyte interfaces

In this article, we explore how transport at a solid--electrolyte interface is affected by the internal fluctuations of the solid and quantify the role of solid excitations on ionic friction. Combining molecular dynamics simulations with theoretical modeling, we show that the presence of ions enhances the dynamical response of the electrolyte compared to pure water. This leads to an ionic contribution to the fluctuation-induced interfacial friction. We show that collective ionic modes dominate the dissipation, such that ionic friction arises from many-body effects rather than from individual drag forces. Furthermore, high-frequency molecular modes are found to be ion-specific, suggesting possible routes toward spectral separation of ions, with implications for desalination, filtration, and energy conversion.

cond-mat.soft↗

arXiv2026

Fluctuation-induced and quantum effects in nanofluidic transport

The hydrodynamic wall has traditionally been considered a featureless object, whose only role is to provide a boundary for fluid flow. Yet, there is now ample evidence that at nanometer scales, liquid flows are sensitive to the wall's internal -- in particular, electronic -- degrees of freedom. Here, after reviewing the experimental evidence for nanoscale liquid-electron couplings, we present the theoretical advances that have allowed for their quantitative understanding. We discuss how a quantum description of the liquid-solid interface reveals the influence of electron dynamics on classical fluid transport, in the form of the fluctuation-induced quantum friction effect. Quantum friction is at the root of liquid-electron coupled transport phenomena, that may be combined into a hydro-electronic transport matrix. We present analytical formulas for the hydro-electronic transport coefficients, that allow for their quantitative estimation in practical cases; we further outline the potential consequences of coupled liquid-electron transport for the water-energy nexus. Fluctuation-induced and quantum effects at liquid-solid interfaces represent an emerging interface between fluid dynamics and condensed-matter physics, and a largely uncharted territory for both theory and experiment.

physics.flu-dyn↗

arXiv2026

Electrostatic Screening in Nanotubes: A Tubular Response Function Framework

The structure and transport of electrolytes in nanoscale channels are known to be affected by the electronic properties of the confining walls. This influence is particularly pronounced in quasi-one-dimensional nanotubes, where the high surface-to-volume ratio makes the wall the dominant source of electrostatic screening. For instance, ideal metallic tubes suppress long-range Coulomb interactions between ions exponentially. Yet, there exists no generic framework for evaluating electrostatic interactions in tubular confinement. Here, we introduce tubular response functions - a generalisation of surface response functions that captures how nanotubes with arbitrary electronic properties screen Coulomb interactions. Using this framework, we evaluate the interaction potential of ions confined in a metallic carbon nanotube, treating its long-range electronic properties exactly within a Luttinger liquid model. We demonstrate that the screening characteristic of metallic armchair carbon nanotubes is almost identical to that of an ideal metal, regardless of electron density. We trace the origin of such strong screening to the quantum confinement of electrons around the tube circumference and to the suppression of Friedel oscillations. Our framework opens the way for quantitative descriptions of ionic correlations and charge storage in nanotube-based electrodes, and can be further extended to address confined ion dynamics.

cond-mat.mes-hall↗

arXiv2026

Electron-electrolyte coupling in AC transport through nanofluidic channels

The transport properties of nanofluidic channels are usually studied under constant (DC) voltage or pressure driving. However, the frequency response under sinusoidal (AC) drivings offers rich insights into the time-dependent transport mechanisms. Inspired by recent electrochemical approaches, we investigate the couplings between ionic and electronic transport under AC driving. We show that conduction electrons of the channel walls participate in ionic current via capacitive electrochemical coupling, defining a critical frequency and length scale where electron-dominated conductivity emerges. We further analyze how electron-ion coupling modifies electro-osmotic flows, and demonstrate that fluctuation-induced momentum transfer between the electrolyte and wall electrons produces distinct AC transport signatures depending on the charge carrier polarity. Altogether, we establish a frequency-dependent transport matrix that couples ionic, electronic and hydrodynamic flows. These findings establish AC nanofluidic transport as a powerful probe of interfacial phenomena under confinement, and suggest new directions for engineering nanofluidic functionalities through electron-electrolyte coupling.

cond-mat.mes-hall↗

arXiv2025

Hydrodynamic permeability of fluctuating porous membranes

In this paper we examine how porosity fluctuations affect the hydrodynamic permeability of a porous matrix or membrane. We introduce a fluctuating Darcy model, which couples the Navier-Stokes equation to the space- and time-dependent porosity fluctuations via a Darcy friction term. Using a perturbative approach, a Dyson equation for hydrodynamic fluctuations is derived and solved to express the permeability in terms of the matrix fluctuation spectrum. Surprisingly, the model reveals strong modifications of the fluid permeability in fluctuating matrices compared to static ones. Applications to various matrix excitation models - breathing matrix, phonons, active forcing - highlight the significant influence of matrix fluctuations on fluid transport, offering insights for optimizing membrane design for separation applications.

cond-mat.soft↗

arXiv2025

Momentum tunnelling between nanoscale liquid flows

The world of nanoscales in fluidics is the frontier where the continuum of fluid mechanics meets the atomic, and even quantum, nature of matter. While water dynamics remains largely classical under extreme confinement, several experiments have recently reported coupling between water transport and the electronic degrees of freedom of the confining materials. This avenue prompts us to reconsider nanoscale hydrodynamic flows under the perspective of interacting excitations, akin to condensed matter frameworks. Here we show, using a combination of many-body theory and molecular simulations, that the flow of a liquid can induce the flow of another liquid behind a separating wall, at odds with the prediction of continuum hydrodynamics. We further show that the range of this 'flow tunnelling' can be tuned through the solid's electronic excitations, with a maximum occurring when these are at resonance with the liquid's charge density fluctuations. Flow tunnelling is expected to play a role in global transport across nanoscale fluidic networks, such as lamellar graphene oxide or MXene membranes. It further suggests exploiting the electronic properties of the confining walls for manipulating liquids via their dielectric spectra, beyond the nature and characteristics of individual molecules.

cond-mat.mes-hall↗

arXiv2024

Hydroelectric energy conversion of waste flows through hydroelectronic drag

Hydraulic energy is a key component of the global energy mix, yet there exists no practical way of harvesting it at small scales, from flows at low Reynolds number. This has triggered the search for alternative hydroelectric conversion methodologies, leading to unconventional proposals based on droplet triboelectricity, water evaporation, osmotic energy or flow-induced ionic Coulomb drag. Yet, these approaches systematically rely on ions as intermediate charge carriers, limiting the achievable power density. Here, we predict that the kinetic energy of small-scale "waste" flows can be directly and efficiently converted into electricity thanks to the hydro-electronic drag effect, by which an ion-free liquid induces an electronic current in the solid wall along which it flows. This effect originates in the fluctuation-induced coupling between fluid motion and electron transport. We develop a non-equilibrium thermodynamic formalism to assess the efficiency of such hydroelectric energy conversion, dubbed hydronic energy. We find that hydronic energy conversion is analogous to thermoelectricity, with the efficiency being controlled by a dimensionless figure of merit. However, in contrast to its thermoelectric analogue, this figure of merit combines independently tunable parameters of the solid and the liquid, and can thus significantly exceed unity. Our findings suggest new strategies for blue energy harvesting without electrochemistry, and for waste flow mitigation in membrane-based filtration processes.

physics.flu-dyn↗

arXiv2024

Exact numerical solution of the fully-connected classical and quantum Heisenberg spin glass

We present the mean field solution of the quantum and classical Heisenberg spin glasses, using the combination of a high precision numerical solution of the Parisi full replica symmetry breaking equations and a continuous time Quantum Monte Carlo. We characterize the spin glass order and its low-energy excitations down to zero temperature. The Heisenberg spin glass has a rougher energy landscape than its Ising analogue, and exhibits a very slow temperature evolution of its dynamical properties. We extend our analysis to the doped, metallic Heisenberg spin glass, which displays an unexpectedly slow spin dynamics reflecting the proximity to the melting quantum critical point and its associated Sachdev-Ye-Kitaev Planckian dynamics.

cond-mat.dis-nn↗

arXiv2023

Collective modes and quantum effects in two-dimensional nanofluidic channels

Nanoscale fluid transport is typically pictured in terms of atomic-scale dynamics, as is natural in the real-space framework of molecular simulations. An alternative Fourier-space picture, that involves the collective charge fluctuation modes of both the liquid and the confining wall, has recently been successful at predicting new nanofluidic phenomena such as quantum friction and near-field heat transfer, that rely on the coupling of those fluctuations. Here, we study the charge fluctuation modes of a two-dimensional (planar) nanofluidic channel. Introducing confined response functions that generalize the notion of surface response function, we show that the channel walls exhibit coupled plasmon modes as soon as the confinement is comparable to the plasmon wavelength. Conversely, the water fluctuations remain remarkably bulk-like, with significant confinement effects arising only when the wall spacing is reduced to 7 A. We apply the confined response formalism to predict the dependence of the solid-water quantum friction and thermal boundary conductance on channel width for model channel wall materials. Our results provide a general framework for Coulomb interactions of fluctuating matter in nanoscale confinement.

cond-mat.mes-hall↗

arXiv2023

Electron cooling in graphene enhanced by plasmon-hydron resonance

Evidence is accumulating for the crucial role of a solid's free electrons in the dynamics of solid-liquid interfaces. Liquids induce electronic polarization and drive electric currents as they flow; electronic excitations, in turn, participate in hydrodynamic friction. Yet, the underlying solid-liquid interactions have been lacking a direct experimental probe. Here, we study the energy transfer across liquid-graphene interfaces using ultrafast spectroscopy. The graphene electrons are heated up quasi-instantaneously by a visible excitation pulse, and the time evolution of the electronic temperature is then monitored with a terahertz pulse. We observe that water accelerates the cooling of the graphene electrons, whereas other polar liquids leave the cooling dynamics largely unaffected. A quantum theory of solid-liquid heat transfer accounts for the water-specific cooling enhancement through a resonance between the graphene surface plasmon mode and the so-called hydrons -- water charge fluctuations --, particularly the water libration modes, that allows for efficient energy transfer. Our results provide direct experimental evidence of a solid-liquid interaction mediated by collective modes and support the theoretically proposed mechanism for quantum friction. They further reveal a particularly large thermal boundary conductance for the water-graphene interface and suggest strategies for enhancing the thermal conductivity in graphene-based nanostructures.

cond-mat.mes-hall↗

arXiv2023

Quantum feedback at the solid-liquid interface: flow-induced electronic current and its negative contribution to friction

An electronic current driven through a conductor can induce a current in another conductor through the famous Coulomb drag effect. Similar phenomena have been reported at the interface between a moving fluid and a conductor, but their interpretation has remained elusive. Here, we develop a quantum-mechanical theory of the intertwined fluid and electronic flows, taking advantage of the non-equilibrium Keldysh framework. We predict that a globally neutral liquid can generate an electronic current in the solid wall along which it flows. This hydrodynamic Coulomb drag originates from both the Coulomb interactions between the liquid's charge fluctuations and the solid's charge carriers, and the liquid-electron interaction mediated by the solid's phonons. We derive explicitly the Coulomb drag current in terms of the solid's electronic and phononic properties, as well as the liquid's dielectric response, a result which quantitatively agrees with recent experiments at the liquid-graphene interface. Furthermore, we show that the current generation counteracts momentum transfer from the liquid to the solid, leading to a reduction of the hydrodynamic friction coefficient through a quantum feedback mechanism. Our results provide a roadmap for controlling nanoscale liquid flows at the quantum level, and suggest strategies for designing materials with low hydrodynamic friction.

cond-mat.mes-hall↗

arXiv2023

Strong electronic winds blowing under liquid flows on carbon surfaces

The interface between a liquid and a solid is the location of plethora of intrincate mechanisms at the nanoscale, at the root of their specific emerging properties in natural processes or technological applications. However, while the structural properties and chemistry of interfaces have been intensively explored, the effect of the solid-state electronic transport at the fluid interface has been broadly overlooked up to now. It has been reported that water flowing against carbon-based nanomaterials, such as carbon nanotubes or graphene sheets, does induce electronic currents, but the mechanism at stake remains controversial. Here, we unveil the molecular mechanisms underlying the hydro-electronic couplings by investigating the electronic conversion under flow at the nanoscale. We use a tuning fork-Atomic Force Microscope (AFM) to deposit and displace a micrometric droplet of both ionic and non-ionic liquids on a multilayer graphene sample, while recording the electrical current across the carbon flake. We report measurements of an oscillation-induced current which is several orders of magnitude larger than previously reported for water on carbon , and further boosted by the presence of surface wrinkles on the carbon layer. Our results point to a peculiar momentum transfer mechanism between fluid molecules and charge carriers in the carbon walls mediated by phonon excitations in the solid. Our findings pave the way for active control of fluid transfer at the nanoscale by harnessing the complex interplay between collective excitations in the solid and the molecules in the fluid.

cond-mat.mes-hall↗

arXiv2023

Ion filling of a one-dimensional nanofluidic channel in the interaction confinement regime

Ion transport measurements are widely used as an indirect probe for various properties of confined electrolytes. It is generally assumed that the ion concentration in a nanoscale channel is equal to the ion concentration in the macroscopic reservoirs it connects to, with deviations arising only in the presence of surface charges on the channel walls. Here, we show that this assumption may break down even in a neutral channel, due to electrostatic correlations between the ions arising in the regime of interaction confinement, where Coulomb interactions are reinforced due to the presence of the channel walls. We focus on a one-dimensional channel geometry, where an exact evaluation of the electrolyte's partition function is possible with a transfer operator approach. Our exact solution reveals that in nanometre-scale channels, the ion concentration is generally lower than in the reservoirs, and depends continuously on the bulk salt concentration, in contrast to conventional mean-field theory that predicts an abrupt filling transition. We develop a modified mean-field theory taking into account the presence of ion pairs that agrees quantitatively with the exact solution and provides predictions for experimentally-relevant observables such as the ionic conductivity. Our results will guide the interpretation of nanoscale ion transport measurements.

cond-mat.soft↗

arXiv2022

Interaction confinement and electronic screening in two-dimensional nanofluidic channels

The transport of fluids at the nanoscale is fundamental to manifold biological and industrial processes, ranging from neurotransmission to ultrafiltration. Yet, it is only recently that well-controlled channels with cross-sections as small as a few molecular diameters became an experimental reality. When aqueous electrolytes are confined within such channels, the Coulomb interactions between the dissolved ions are reinforced due to dielectric contrast at the channel walls: we dub this effect `interaction confinement'. Yet, no systematic way of computing these confined interactions has been proposed beyond the limiting cases of perfectly metallic or perfectly insulating channel walls. Here, we introduce a new formalism, based on the so-called surface response functions, that expresses the effective Coulomb interactions within a two-dimensional channel in terms of the wall's electronic structure, described to any desired level of precision. We use it to demonstrate that in few-nanometer-wide channels, the ionic interactions can be tuned by the wall material's screening length. We illustrate this approach by implementing these interactions in brownian dynamics simulations of a strongly confined electrolyte, and show that the resulting ionic conduction can be adjusted between Ohm's law and a Wien effect behavior. Our results provide a quantitative approach to tuning nanoscale ion transport through the electronic properties of the channel wall material.

cond-mat.mes-hall↗

arXiv2021

Fluctuation-induced quantum friction in nanoscale water flows

The flow of water in carbon nanochannels has defied understanding thus far, with accumulating experimental evidence for ultra-low friction, exceptionally high water flow rates, and curvature-dependent hydrodynamic slippage. These unique properties have raised considerable interest in carbon-based membranes for desalination, molecular sieving and energy harvesting. However, the mechanism of water-carbon friction remains unknown, with neither current theories, nor classical or ab initio molecular dynamics simulations providing satisfactory rationalisation for its singular behaviour. Here, we develop a quantum theory of the solid-liquid interface, which reveals a new contribution to friction, due to the coupling of charge fluctuations in the liquid to electronic excitations in the solid. We expect that this quantum friction, which is absent in Born-Oppenheimer molecular dynamics, is the dominant friction mechanism for water on carbon-based materials. As a key result, we demonstrate a dramatic difference in quantum friction between the water-graphene and water-graphite interface, due to the coupling of water Debye collective modes with a thermally excited plasmon specific to graphite. This suggests an explanation for the radius-dependent slippage of water in carbon nanotubes, in terms of the nanotubes' electronic excitations. Our findings open the way to quantum engineering of hydrodynamic flows through the confining wall electronic properties.

cond-mat.mes-hall↗

arXiv2021

Modeling of emergent memory and voltage spiking in ionic transport through angström-scale slits

Recent advances in nanofluidics have enabled the confinement of water down to a single molecular layer. Such monolayer electrolytes show promise in achieving bio-inspired functionalities through molecular control of ion transport. However, the understanding of ion dynamics in these systems is still scarce. Here, we develop an analytical theory, backed up by molecular dynamics simulations, predicting strongly nonlinear effects in ion transport across quasi-two-dimensional slits. We show that under an electric field, ions assemble into elongated clusters, whose slow dynamics result in hysteretic conduction. This phenomenon, known as memristor effect, can be harnessed to build an elementary neuron. As a proof-of-concept, we carry out molecular simulations of two nanofluidic slits reproducing the Hodgkin-Huxley model, and observe spontaneous emission of voltage spikes characteristic of neuromorphic activity.

cond-mat.soft↗

arXiv2021

Ultrafast photomechanical transduction through thermophoretic implosion

Since the historical experiments of Crookes, the direct manipulation of matter by light has been both a challenge and a source of scientific debate. Here we show that laser illumination allows to displace a vial of nanoparticle solution over centimetre-scale distances. Cantilever-based force measurements show that the movement is due to millisecond long force spikes, which are synchronised with a sound emission. We observe that the nanoparticles undergo negative thermophoresis, while ultrafast imaging reveals that the force spikes are followed by the explosive growth of a bubble in the solution. We propose a mechanism accounting for the propulsion based on a thermophoretic instability of the nanoparticle cloud, analogous to the Jeans instability that occurs in gravitational systems. Our experiments demonstrate a new type of laser propulsion, and a remarkably violent actuation of soft matter, reminiscent of the strategy used by certain plants to propel their spores.

cond-mat.soft↗

arXiv2020

Fluids at the Nanoscale: from continuum to sub-continuum transport

Nanofluidics has firmly established itself as a new field in fluid mechanics, as novel properties have been shown to emerge in fluids at the nanometric scale. Thanks to recent developments in fabrication technology, artificial nanofluidic systems are now being designed at the scale of biological nanopores. This ultimate step in scale reduction has pushed the development of new experimental techniques and new theoretical tools, bridging fluid mechanics, statistical mechanics and condensed matter physics. This review is intended as a toolbox for fluids at the nanometre scale. After presenting the basic equations that govern fluid behaviour in the continuum limit, we will show how these equations break down and new properties emerge in molecular scale confinement.

physics.flu-dyn↗