The diffusive mass transport of individual redox molecules was probed experimentally in microfabricated nanogap electrodes. The residence times for molecules inside a well-defined detection volume were extracted and the resulting distribution was compared with quantitative analytical predictions from random-walk theory for the time of first passage. The results suggest that a small number of strongly adsorbing sites strongly influence mass transport at trace analyte levels.

Fluid and charge transport in micro-and nanoscale fluidic systems are intrinsically coupled via electrokinetic phenomena. While electroosmotic flows and streaming potentials are well understood for externally imposed stimuli, charge injection at electrodes localized inside fluidic systems via electrochemical processes remains to a large degree unexplored. Here, we employ ultramicroelectrodes and nanogap electrodes to study the subtle interplay between ohmic drops, streaming currents, and faradaic processes in miniaturized channels at low concentrations of supporting electrolyte. We show that electroosmosis can, under favorable circumstances, counteract the effect of ohmic losses and shift the apparent formal potential of redox reactions. This interplay can be described by simple circuit models, such that the results described here can be adapted to other micro-and nanofluidic electrochemical systems.

Bipolar electrodes provide a powerful and versatile means of coupling two or more spatially separated electrochemical reactions. While normally described in terms of macroscopic rate equations, the ongoing drive toward the miniaturization of bipolar electrodes means that new regimes are becoming accessible where stochasticity and the discreteness of the electronic charge become relevant or even dominant. Here we explore using both numerical simulations and analytical theory the behavior of bipolar electrodes with nanoscale dimensions. We focus in particular on the possibility of achieving single-molecule-level synchronization between the two poles of a bipolar electrode, which would dramatically extend the range of applicability of single-molecule electrochemistry. We conclude that, while possible, fundamental limits on the potential dependence of electron-transfer rates dictate that this will only be achieved in the smallest (less than 10 nm) bipolar nanoelectrodes.

Mass transport in fluidic channels under conditions of pressure-driven flow is controlled by a combination of convection and diffusion. For electrochemical measurements the height of a channel is typically of the same order of magnitude as the electrode dimensions, resulting in complex two-or threedimensional concentration distributions. Electrochemical nanofluidic devices, however, can have such a low height-to-length ratio that they can effectively be considered as one-dimensional. This greatly simplifies the modeling and quantitative interpretation of analytical measurements. Here we study mass transport in nanochannels using electrodes in a generator-collector configuration. The flux of redox molecules is monitored amperometrically. We observe the transition from diffusion-dominated to convection-dominated transport by varying both the flow velocity and the distance between the electrodes. These results are described quantitatively by the one-dimensional Nernst−Planck equation for mass transport over the full range of experimentally accessible parameters.

Electroactive materials and their applications are enjoying renewed attention, in no small part motivated by the advent of nanoscale tools for their preparation and study. While the fundamentals of charge and mass transport in electrolytes on this scale are by and large well understood, their interplay can have subtle manifestations in the more complex situations typical of, for example, integrated microfluidics-based applications. In particular, the role of faradaic processes is often overlooked or, at best, purposefully suppressed via experimental design. In this introductory article we discuss, using simple illustrations from our laboratories, some of the manifestations of electrochemistry in electroactive materials.