Selective Fluoride Transport in Subnanometer TiO2 Pores

Synthesizing nanopores which mimic the functionality of ion-selective biological channels has been a challenging yet promising approach to advance technologies for precise ion-ion separations. Inspired by the facilitated fluoride (F-) permeation in the biological fluoride channel, we designed a highly fluoride-selective TiO2 film using the atomic layer deposition (ALD) technique. The subnanometer voids within the fabricated TiO2 film (4 angstrom < d < 12 angstrom, with two distinct peaks at 5.5 and 6.5 angstrom), created by the hindered diffusion of ALD precursors (d = 7 angstrom), resulted in more than eight times faster permeation of sodium fluoride compared to other sodium halides. We show that the specific Ti-F interactions compensate for the energy penalty of F- dehydration during the partitioning of F- ions into the pore and allow for an intrapore accumulation of F- ions. Concomitantly, the accumulation of F- ions on the pore walls also enhances the transport of sodium (Na+) cations due to electrostatic interactions. Molecular dynamics simulations probing the ion concentration and mobility within the TiO2 pore further support our proposed mechanisms for the selective F- transport and enhanced Na+ permeation in the TiO2 film. Overall, our work provides insights toward the design of ion-selective nanopores using the ALD technique.

Automated summary

The study successfully designed a highly fluoride-selective TiO2 film using atomic layer deposition (ALD), which exhibited more than eight times faster permeation of sodium fluoride compared to other sodium halides. Specific Ti-F interactions, intrapore accumulation of F- ions, and enhanced transport of Na+ cations were identified as key mechanisms for the selective F- transport and enhanced Na+ permeation in the TiO2 film.