Search arXivSearch

arXiv · 2601.01135

Ion Clustering Regulated by Extreme Nanoconfinement Enables Mechanosensitive Nanochannels

Abstract

Mechanosensitive ion nanochannels regulate transport by undergoing conformational changes within nanopores. However, achieving precise control over these conformational states remains a major challenge for both artificial soft or solid pores. Here, we propose an alternative mechanism that modulates the charge carrier density inside nanopores, inspired by transistors in solid-state electronics. This strategy leverages a novel phenomenon of confinement-regulated ion clustering in two-dimensional extremely confined nanochannels, revealed by extensive $μ$s-scale enhanced-sampling molecular simulations based on an \emph{ab initio}-refined force field and nucleation theory. The resulting \emph{force-ion transistor} enables mechanically gated control of ion transport and provides a conceptual foundation for designing ionic mechanical logic gates. Our findings offer new insights into piezochannel mechanosensing and electromechanical coupling in biosystems beyond conformational signaling, opening pathways to integrate artificial ion channels with neuromorphic devices for processing mechanical stimuli.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Ke Zhou. 2026-01-03. Ion Clustering Regulated by Extreme Nanoconfinement Enables Mechanosensitive Nanochannels. https://arxiv.org/abs/2601.01135

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

KEEP EXPLORING

Related papers

Intrinsic Matching Frustration in Fluctuating Finite Systems

We formulate intrinsic matching frustration (IMF), a fluctuation-induced, kinetics-independent reduction in the mean capacity permitted by a prescribed matching rule. For complementary one-to-one matching, the instantaneous capacity is set by the minority population, so fluctuations produce a nonzero mean deficit even when the two populations are balanced on average. At finite size, this deficit depends on the full distribution of the population difference and is determined by its variance alone only in the Gaussian limit. Compartmentalization hides matching capacity by preventing cancellation between local imbalances of opposite sign. Fusion releases this hidden capacity monotonically under coarse graining, producing a measurable recovery of product yield following local reaction to completion.

physics.chem-ph

Phonon chirality as an additive control of CISS: a symmetry-protected law

Chirality-induced spin selectivity (CISS) is usually associated with molecular handedness. The possible contribution of chiral phonons is less established. We study a helical tight-binding model in which local phonon angular momentum modulates spin-dependent nearest-neighbor hopping. Fewest-switches surface hopping calculations give the transmitted spin polarization $\mathrm{SP}=aC+b\mathrm{PH}$. Here $C$ is the molecular chirality and $\mathrm{PH}$ is the phonon chirality. A mirror symmetry reverses $C$, $\mathrm{PH}$, and $\mathrm{SP}$ simultaneously. This symmetry excludes both a chirality-independent offset and a $C\cdot\mathrm{PH}$ term. The phonon contribution can therefore enhance, cancel, or reverse the molecular CISS signal.

physics.chem-ph

A fast physics-based matrix model for the impedance of a PEM fuel cell: Incorporating functionally graded catalyst layer and channel impedances

We extend a recent physics-based matrix model for calculating PEM fuel cell impedance (doi:10.1149/2754-2734/ad6ce8) to cases of low air flow stoichiometry and functionally graded cathode catalyst layers (CCLs). We demonstrate that the matrix model produces accurate spectra and is almost three orders of magnitude faster than a model based on the standard boundary-value problem solver. The physics-based matrix model can compete with equivalent circuit models for fitting experimental EIS spectra, particularly those measured from cells with functionally graded CCL.

physics.chem-ph