Andrew Meyertholen, Massimiliano Di Ventra
Ionic transport in nanopores or nanochannels is key to many cellular processes and is now being explored as a method for DNA/polymer sequencing and detection. Although apparently simple in its scope, the study of ionic dynamics in confined geometries has revealed interesting new phenomena that have an almost one-to-one correspondence with the quantum regime. The picture that emerges is that ions can form two `quasi-particle' states, one in which they surround themselves with other ions of opposite charge - ionic atmosphere - and one in which semi-bound water molecules form layers at different distances from the ions - hydration layers. The second state gives rise to two additional effects. In the first, which is a single quasi-particle effect, the ionic conductance through a nanopore is predicted to be `quantized' as a function of pore radius, with the corresponding `quantization units' not related to universal constants - like the Plank constant and the elementary charge - but rather to the radii of the hydration layers. The second effect instead involves the many-body interaction among ionic quasi-particles of the same sign, and occurs when the pore has a finite capacitance to accommodate ions so that there is a threshold concentration beyond which ions of the same sign are not energetically allowed to enter the pore. Similar to the electron transport case, the ionic counterpart appears only in the `quantum' regime, when the hydration layers forming the ionic quasi-particles need to break in order to pass through the pore. Here, we review all these phenomena, and discuss the conditions under which they may be detected making the analogy with the electronic transport case. Since nanopores are being considered for a host of technological applications in DNA sequencing and detection, we expect these phenomena will become very relevant and their understanding paramount to progress.
View original:
http://arxiv.org/abs/1305.7450
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