Solvation

Nanotechnology

Organic chemistry

Membrane

Nanofluidics

Ion transporter

Solvation shell

Engineering

Chemical physics

Ionic bonding

Inorganic chemistry

Chemistry

Materials science

In situ

Molecule

Chemical engineering

Permeation

Biochemistry

Journal of the American Chemical Society

The transport of hydrated ions across nanochannels is central to biological systems and membrane-based applications, yet little is known about their hydrated structure during transport due to the absence of in situ characterization techniques. Herein, we report experimentally resolved ion dehydration during transmembrane transport using modified in situ liquid ToF-SIMS in combination with MD simulations for a mechanistic reasoning. Notably, complete dehydration was not necessary for transport to occur across membranes with sub-nanometer pores. Partial shedding of water molecules from ion solvation shells, observed as a decrease in the average hydration number, allowed the alkali-metal ions studied here (lithium, sodium, and potassium) to permeate membranes with pores smaller than their solvated size. We find that ions generally cannot hold more than two water molecules during this sterically limited transport. In nanopores larger than the size of the solvation shell, we show that ionic mobility governs the ion hydration number distribution. Viscous effects, such as interactions with carboxyl groups inside the membrane, preferentially hinder the transport of the mono- and dihydrates. Our novel technique for studying ion solvation in situ represents a significant technological leap for the nanofluidics field and may enable important advances in ion separation, biosensing, and battery applications.

<i>In Situ</i> Characterization of Dehydration during Ion Transport in Polymeric Nanochannels

In Situ Characterization of Dehydration during Ion Transport in Polymeric Nanochannels