Principal Investigator

James L. McGrath, Ph.D. University of Rochester work Box 270168 Rochester NY 14627-0168 office: Goergen Hall 306 p (585) 273-5489 f (585) 273-4746

Ion-Selective Permeability of UltrathinNanopore silicon Membrane as Studied Using Nanofabricated Micropipet Probes

Project Collaborator:

(a) Scheme of ion transport across ultrathin nanopore silicon membrane as induced by a micropipet-supported liquid/liquid interface as an SECM probe. (b) TEM image of the membrane with pores (bright circles) and diffracting nanocrystals (dark spots).

We report on the application of scanning electrochemical microscopy (SECM) to the measurement of the ion-selective permeability of porous nanocrystalline silicon membrane as a new type of nanoporous material with potential applications in analytical, biomedical, and biotechnology device development. The reliable measurement of high permeability in the molecularly thin nanoporous membrane to various ions is important for greater understanding of its structure-permeability relationship and also for its successful applications. In this work, this challenging measurement is enabled by introducing two novel features into amperometric SECM tips based on the micropipet-supported interface between two immiscible electrolyte solutions (ITIES) to reveal the important ion-transport properties of the ultrathin nanopore membrane.

Permeability v. Pore Size

The tip of a conventional heat-pulled micropipet is milled using the focused ion beam (FIB) technique to be smoother, better aligned, and subsequently, approach closer to the membrane surface, which allows for more precise and accurate permeability measurement. The high membrane permeability to small monovalent ions is determined using FIB-milled micropipet tips to establish a theoretical formula for the membrane permeability that is controlled by free ion diffusion across water-filled nanopores. Moreover, the ITIES tips are rendered selective for larger polyions with biomedical importance, i.e., polyanionic pentasaccharide Arixtra and polycationic peptide protamine, to yield the membrane permeability that is lower than the corresponding diffusion-limited permeability. The hindered transport of the respective polyions is unequivocally ascribed to electrostatic and steric repulsions from the wall of the nanopores, i.e., the charge and size effects.

Shigeru Amemiya's laboratory at the University of Pittsburgh used a highly senstitive electrochemical probe to measure small ion diffusion through pnc-Si without interference from stagnant layers. The paper demonstrates that pnc-Si membranes have a permeability to small monovalent ions (< 1/10th of pore size) that is predictable from membrane geometry alone. By contrast, multivalent and/or large (>30% of pore size) ions experience hindrance from steric and electrostatic effects.


Ishimatsu et al. (September, 2010). Ion-selective permeability of an ultrathin nanoporous silicon membrane as probed by scanning electrochemical microscopy using micropipet-supported ITIES tips. Anal Chem 82:7127-34.

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