Dehydration and ionic conductance quantization in nanopores
arXiv:1005.2550 · doi:10.1088/0953-8984/22/45/454126
Abstract
There has been tremendous experimental progress in the last decade in identifying the structure and function of biological pores (ion channels) and fabricating synthetic pores. Despite this progress, many questions still remain about the mechanisms and universal features of ionic transport in these systems. In this paper, we examine the use of nanopores to probe ion transport and to construct functional nanoscale devices. Specifically, we focus on the newly predicted phenomenon of quantized ionic conductance in nanopores as a function of the effective pore radius - a prediction that yields a particularly transparent way to probe the contribution of dehydration to ionic transport. We study the role of ionic species in the formation of hydration layers inside and outside of pores. We find that the ion type plays only a minor role in the radial positions of the predicted steps in the ion conductance. However, ions with higher valency form stronger hydration shells, and thus, provide even more pronounced, and therefore, more easily detected, drops in the ionic current. Measuring this phenomenon directly, or from the resulting noise, with synthetic nanopores would provide evidence of the deviation from macroscopic (continuum) dielectric behavior due to microscopic features at the nanoscale and may shed light on the behavior of ions in more complex biological channels.
13 pages, 10 figures
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- Colloquium: Ionic phenomena in nanoscale pores through 2D materials
- Ionic selectivity and filtration from fragmented dehydration in multilayer graphene nanopores
- Maxwell-Hall access resistance in graphene nanopores
- Golden aspect ratio for ion transport simulation in nanopores
- Diffusion Limitations and Translocation Barriers in Atomically Thin Biomimetic Pores