Volume 210, 2018

Nanoscale electrochemical kinetics & dynamics: the challenges and opportunities of single-entity measurements

Abstract

The development of nanoscale electrochemistry since the mid-1980s has been predominately coupled with steady-state voltammetric (iE) methods. This research has been driven by the desire to understand the mechanisms of very fast electrochemical reactions, by electroanalytical measurements in small volumes and unusual media, including in vivo measurements, and by research on correlating electrocatalytic activity, e.g., O2 reduction reaction, with nanoparticle size and structure. Exploration of the behavior of nanoelectrochemical structures (nanoelectrodes, nanoparticles, nanogap cells, etc.) of a characteristic dimension λ using steady-state iE methods generally relies on the well-known relationship, λ2Dt, which relates diffusional lengths to time, t, through the coefficient, D. Decreasing λ, by performing measurements at a nanometric length scales, results in a decrease in the effective timescale of the measurement, and provides a direct means to probe the kinetics of steps associated with very rapid electrochemical reactions. For instance, steady-state voltammetry using a nanogap twin-electrode cell of characteristic width, λ ∼ 10 nm, allows investigations of events occurring at timescales on the order of ∼100 ns. Among many other advantages, decreasing λ also increases spatial resolution in electrochemical imaging, e.g., in scanning electrochemical microscopy, and allows probing of the electric double layer. This Introductory Lecture traces the evolution and driving forces behind the “λ2Dt” steady-state approach to nanoscale electrochemistry, beginning in the late 1950s with the introduction of the rotating ring-disk electrode and twin-electrode thin-layer cells, and evolving to current-day investigations using nanoelectrodes, scanning nanocells for imaging, nanopores, and nanoparticles. The recent focus on so-called “single-entity” electrochemistry, in which individual and very short redox events are probed, is a significant departure from the steady-state approach, but provides new opportunities to probe reaction dynamics. The stochastic nature of very fast single-entity events challenges current electrochemical methods and modern electronics, as illustrated using recent experiments from the authors’ laboratory.

Graphical abstract: Nanoscale electrochemical kinetics & dynamics: the challenges and opportunities of single-entity measurements

Article information

Article type
Paper
Submitted
14 Sep 2018
Accepted
19 Sep 2018
First published
19 Sep 2018

Faraday Discuss., 2018,210, 9-28

Author version available

Nanoscale electrochemical kinetics & dynamics: the challenges and opportunities of single-entity measurements

M. A. Edwards, D. A. Robinson, H. Ren, C. G. Cheyne, C. S. Tan and H. S. White, Faraday Discuss., 2018, 210, 9 DOI: 10.1039/C8FD00134K

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements