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Ionic selectivity and filtration from fragmented dehydration in multilayer graphene nanopores



Subin Sahu, Michael P. Zwolak


Selective ion transport is a hallmark of biological ion channel behavior but is a major challenge to engineer into artificial membranes. Here, we demonstrate, with all-atom molecular dynamics, that bare graphene nanopores yield measurable ion selectivity that varies over one to two orders of magnitude simply by changing the pore radius and number of graphene layers. Monolayer graphene does not display dehydration-induced selectivity until the pore radius is small enough to exclude the first hydration layer from inside the pore. Bi- and tri-layer graphene, though, display such selectivity already for a pore size that barely encroaches on the first hydration layer, which is due to the more significant water loss from the second hydration layer. Measurement of selectivity and activation barriers from both first and second hydration layer barriers will help elucidate the behavior of biological ion channels. Moreover, the energy barriers responsible for selectivity -- while small on the scale of hydration energies -- are already relatively large, i.e. several $\kt$. For separation of ions from water, therefore, one can exchange longer, larger radius pores for shorter, smaller radius pores, giving a practical method for maintaining exclusion efficiency while enhancing other properties (e.g., water throughput).


ion transport, nanopores, desalination


Sahu, S. and Zwolak, M. (2017), Ionic selectivity and filtration from fragmented dehydration in multilayer graphene nanopores, Nanoscale, [online], (Accessed May 28, 2024)


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Created July 25, 2017, Updated November 10, 2018