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In this review, we describe measurements and applications of interest to the analytical community that makes use of simple nanopipettes. Fabricated by applying heat during the separation of a glass capillary, nanopipettes provide a route for nanoscale studies of ion transport and for development of chemical and biochemical sensors. When mounted on a translation stage, nanopipettes also enable unique modes of imaging and material deposition. These facets of nanopipette research, as well as some of the unique properties of nanopipettes, will be discussed.

Nafion has found utility in a wide variety of applications, particularly as the most commonly used electrolyte membrane in fuel cell technology. Despite decades of characterization by X-ray Photoelectron Spectroscopy (XPS), a dispute exists within literature over the proper assignment of oxygen binding energies from the ether and sulfonate functional groups present in Nafion. Here, we have employed highly oriented pyrolytic graphite (HOPG) as an internal standard to calibrate all XPS spectra and are able to correlate binding energies from C1s, O1s, F1s and S2p to the Nafion structure. Further, microscale heterogeneities inherent to this formulation of Nafion membranes are revealed through two-dimensional XPS mapping of membrane cross-sections as well as surface ablation via Ar + ion sputtering. Results clearly show Nafion membranes are comprised of two chemically distinct layers: a surface layer several microns thick that is comprised of sulfonate groups and an inner layer that shields the more non-polar perfluoroether moieties.

Synthetic hydrogels were utilized to explore influence of both charge and phenylalanine-glycine (FG) repeat concentration on translocation of select proteins. Hydrogels studied represent a biomimetic platform of the nuclear pore complex (NPC) found in eukaryotic cells. Polyacrylamide/phenylalanine-serine-phenylalanine-glycine (FSFG) peptide copolymers have previously demonstrated similar selectivity to native NPCs. Entry of a nuclear transport receptor (Impβ) into hydrogels was monitored with fluorescence microscopy and observed to be greater within gels that contained larger concentrations of FG peptide. Low-resolution structural studies of gels demonstrated changes in morphology and porous network dimensions as FG-repeat concentration was varied. Copolymerization of charged acrylates within the polyacrylamide/FSFG matrix was performed to produce charged hydrogels. Enhanced entry of Impβ, which is negatively charged, was observed in positively charged hydrogels, whereas entry was greatly diminished in negatively charged gels. Synthetic NPC mimics provide a useful testbed for further investigation of nucleocytoplasmic transport and may illuminate new routes for biomimetic separations.

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