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Fast and selective fluoride ion conduction in sub-1-nanometer metal-organic framework channels.


ABSTRACT: Biological fluoride ion channels are sub-1-nanometer protein pores with ultrahigh F- conductivity and selectivity over other halogen ions. Developing synthetic F- channels with biological-level selectivity is highly desirable for ion separations such as water defluoridation, but it remains a great challenge. Here we report synthetic F- channels fabricated from zirconium-based metal-organic frameworks (MOFs), UiO-66-X (X?=?H, NH2, and N+(CH3)3). These MOFs are comprised of nanometer-sized cavities connected by sub-1-nanometer-sized windows and have specific F- binding sites along the channels, sharing some features of biological F- channels. UiO-66-X channels consistently show ultrahigh F- conductivity up to ~10?S?m-1, and ultrahigh F-/Cl- selectivity, from ~13 to ~240. Molecular dynamics simulations reveal that the ultrahigh F- conductivity and selectivity can be ascribed mainly to the high F- concentration in the UiO-66 channels, arising from specific interactions between F- ions and F- binding sites in the MOF channels.

SUBMITTER: Li X 

PROVIDER: S-EPMC6560108 | biostudies-literature | 2019 Jun

REPOSITORIES: biostudies-literature

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Biological fluoride ion channels are sub-1-nanometer protein pores with ultrahigh F<sup>-</sup> conductivity and selectivity over other halogen ions. Developing synthetic F<sup>-</sup> channels with biological-level selectivity is highly desirable for ion separations such as water defluoridation, but it remains a great challenge. Here we report synthetic F<sup>-</sup> channels fabricated from zirconium-based metal-organic frameworks (MOFs), UiO-66-X (X = H, NH<sub>2</sub>, and N<sup>+</sup>(CH<s  ...[more]

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