Electrochemically addressed FET-like nanofluidic channels with dynamic ion-transport regimes

LAUCIRICA, GREGORIO; TOUM TERRONES, YAMILI; WAGNER, MICHAEL F. P.; CAYÓN, VANINA M.; CORTEZ, MARÍA LORENA; TOIMIL-MOLARES, MARIA EUGENIA; TRAUTMANN, CHRISTINA; MARMISOLLÉ, WALDEMAR; AZZARONI, OMAR

Nanoscale

Royal Society of Chemistry

Año: 2023 vol. 15 p. 1782 - 1793

2040-3364

Nanofluidic channels in which the ionic transport can be modulated by the application of an external voltage to the nanochannel walls have been described as nanofluidic field effect transistors (nFETs) because of their analogy with electrolyte-gated field effect transistors. The creation of nFETs is attracting increasing attention due to the possibility of controlling ion transport by using an external voltage as a non-invasive stimulus. In this work, we show that it is possible to extend the actuation range of nFETs by using the supporting electrolyte as a “chemical effector”. For this aim, a gold-coated poly(ethylene terephthalate) (PET) membrane was modified with electroactive poly-o-aminophenol. By exploiting the interaction between the electroactive poly-o-aminophenol and the ions in the electrolyte solution, the magnitude and surface charge of the nanochannels were fine-tuned. In this way, by setting the electrolyte nature it has been possible to set different ion transport regimes, i.e.: cation-selective or anion-selective ion transport, whereas the rectification efficiency of the ionic transport was controlled by the gate voltage applied to the electroactive polymer layer. Remarkably, under both regimes, the platform displays a reversible and rapid response. We believe that this strategy to preset the actuation range of nFETs by using the supporting electrolyte as a chemical effector can be extended to other devices, thus offering new opportunities for the development of stimulus-responsive solid-state nanochannels.