Ultrafast rectifying counter-directional transport of proton and metal ions in metal-organic framework-based nanochannels

Bioinspired control of ion transport at the subnanoscale has become a major focus in the fields of nanofluidics and membrane separation. It is fundamentally important to achieve rectifying ion-specific transport in artificial ion channels, but it remains a challenge. Here, we report a previously unidentified metal-organic framework nanochannel (MOF NC) nanofluidic system to achieve unidirectional ultrafast counter-directional transport of alkaline metal ions and proton. This highly effective ion-specific rectifying transport behavior is attributed to two distinct mechanisms for metal ions and proton, elucidated by theoretical simulations. Notably, the MOF NC exhibits ultrafast proton conduction stemming from ultrahigh proton mobility, i.e., 11.3 x 10(-7) m(2) /V.s, and low energy barrier of 0.075 eV in MIL-53-COOH subnanochannels. Furthermore, the MOF NC shows excellent osmotic power-harvesting performance in reverse electrodialysis. This work expects to inspire further research into multifunctional biomimetic ion channels for advanced nanofluidics, biomimetics, and separation applications.

Automated summary

This study presents a metal-organic framework nanochannel system that achieves unidirectional ultrafast counter-directional transport of alkaline metal ions and proton. The ion-specific rectifying transport behavior is attributed to distinct mechanisms for metal ions and proton, which were elucidated through theoretical simulations. The nanochannel system exhibits ultrafast proton conduction and osmotic power-harvesting performance.