Search arXiv⌕ Search

arXiv · 2610.09705

Interfacial Water Responds Linearly to Charge yet Is Charge-Asymmetric

Abstract

The organization of interfacial water shapes the electric double layer behavior in aqueous electrolytes. Asymmetries upon charge reversal are commonly attributed to specific ion adsorption or surface chemistry. Yet it is unresolved whether interfacial water is net oriented at zero charge, and whether such orientation alone makes its response charge-asymmetric. Here, using electrochemical heterodyne-detected sum-frequency generation spectroscopy and constant-potential molecular dynamics simulations, we resolve the absolute orientation of water at a weakly interacting graphene electrode. We show that interfacial water retains a net H-down orientation, with hydrogens pointing toward the bulk, at zero net surface charge. Superimposed on this offset, the field-induced reorientation is linear and symmetric upon charge reversal, independent of how the charge is introduced or distributed. The zero-charge offset therefore shifts the potential of zero water orientation negatively relative to the potential of zero charge, making the interfacial water response intrinsically charge-asymmetric. These results establish an electrostatic baseline against which extrinsic contributions at electrified interfaces can be isolated.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Yair Litman, Yongkang Wang, Stephen Cox, Mischa Bonn. 2026-10-07. Interfacial Water Responds Linearly to Charge yet Is Charge-Asymmetric. https://arxiv.org/abs/2610.09705

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

KEEP EXPLORING

Related papers

Putting PASPT2 on a Firmer Basis

The recently proposed partial-active-space (PAS) multi-state second-order perturbation theory (PASPT2) [Precis. Chem. 4, 997 (2026)] features connected amplitudes and a connected, closed intermediate Hamiltonian. Despite these hallmarks, PASPT2 (denoted as PASPT2H from now on) is not strictly size-extensive, as originally thought (and numerically confirmed), albeit strictly size-consistent. Nevertheless, PASPT2 is near-extensive for the states with major projections on the chosen PAS $\mathcal{M}_0$. This becomes more transparent upon introducing PASPT2X, a strictly size-extensive variant. Compared with the intruder-prone PASPT2X, the intruder-free PASPT2H merely neglects the second-order corrections that are important only for those states with major projections on the orthogonal complement $\mathcal{R}_X$ of $\mathcal{M}_0$ within the closed space $\mathcal{M}_X$ ($=\mathcal{M}_0\oplus\mathcal{R}_X$); however, such states are not supported by the chosen finite one-particle basis set. The weak violation of size-extensivity is therefore numerically insignificant for the target states supported by $\mathcal{M}_0$, reinforcing the theoretical basis of PASPT2H.

physics.chem-ph↗

Isotope Effects at Classical Cost through Mass-Differentiable Machine Learning

Isotope effects govern fractionation and modulate reactivity, with applications from hydrogen energy to environmental science and catalysis, yet predicting them requires resolving small isotope-dependent free-energy differences that remain very challenging for conventional path-integral simulations in complex systems. Here we introduce iso-EPIGS, a path-integral coarse-graining framework built on a mass-differentiable neural network that reconstructs the mass- and temperature-dependent path integral centroid free-energy surface. Classical molecular dynamics on the learned surface yields rigorous isotope-resolved thermodynamics without explicit path-integral sampling. Benchmarks spanning gas, liquid, and crystalline phases, including liquid water and oxalic acid crystal, reproduce reference path-integral isotope free-energy differences, enthalpies, and lattice parameters at near classical computational cost. Crucially, iso-EPIGS trained solely on all-H and all-D isotopologues retains high accuracy for unseen partially deuterated isotopologues, demonstrating robust transferability across nuclear masses. Iso-EPIGS makes accurate isotope-effect simulations feasible for complex systems and lays the groundwork for foundation models of isotope effects across chemical space.

physics.chem-ph↗

Non-Perturbative Vibrational Excitation by Arbitrary Electric Fields from Classical Phase-Space Dynamics

We present a non-perturbative framework for the quantum treatment of vibrational excitation in molecular systems driven by electric fields with arbitrary time dependence. For harmonic potentials with linear dipole coupling, the field-induced dynamics is exactly described by a displaced coherent state, whose evolution is completely determined by a complex phase-space coordinate. Closed-form expressions for this coordinate reveal a clear distinction between resonant and non-resonant regimes. The resulting vibrational populations follow a Poisson distribution determined by a dimensionless time-dependent phase-space displacement, for both resonant and non-resonant driving. Resonant driving results in an enhanced phase-space displacement, whereas finite detuning between the driving and vibrational frequencies leads to an exponential suppression of the phase-space displacement and vibrational excitation. While the approach reduces to the standard time-dependent perturbation theory in the weak-field limit, it remains valid in the strong-field regime, where perturbative treatments fail. Our results provide a transparent phase-space picture of vibrational control and enable non-perturbative state preparation in ultrafast spectroscopy.

physics.chem-ph↗