4.8 Article

Nanoscale Visualization of Electrochemical Activity at Indium Tin Oxide Electrodes

Journal

ANALYTICAL CHEMISTRY
Volume 94, Issue 11, Pages 4729-4736

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.1c05168

Keywords

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Funding

  1. University of Warwick Chancellor's International Scholarship
  2. Australian Research Council (ARC) Discovery Early Career Researcher Award (DECRA) [DE220101105]
  3. Engineering and Physical Sciences Research Council (EPSRC)
  4. EPSRC [EP/V047981/1]
  5. Royal Society
  6. Australian Government
  7. Bio-Electrical Engineering Innovation Hub, University of Warwick
  8. UK's Biological and Biotechnological Sciences [BB/S506783/1]
  9. Australian Research Council [DE220101105] Funding Source: Australian Research Council

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This study investigates nanoscale electrochemistry at indium tin oxide (ITO) electrodes using high-resolution scanning electrochemical cell microscopy (SECCM). The research reveals the spatially heterogeneous charge transfer activity of ITO surfaces and measures a significantly higher charge transfer rate at the nanoscale compared to the macroscale.
Indium tin oxide (ITO) is a popular electrode choice, with diverse applications in (photo)electrocatalysis, organic photovoltaics, spectroelectrochemistry and sensing, and as a support for cell biology studies. Although ITO surfaces exhibit heterogeneous local electrical conductivity, little is known as to how this translates to electrochemistry at the same scale. This work investigates nanoscale electrochemistry at ITO electrodes using high-resolution scanning electrochemical cell microscopy (SECCM). The nominally fast outer-sphere one-electron oxidation of 1,1'-ferrocenedimethanol (FcDM) is used as an electron transfer (ET) kinetic marker to reveal the charge transfer properties of the ITO/electrolyte interface. SECCM measures spatially resolved linear sweep voltammetry at an array of points across the ITO surface, with the topography measured synchronously. Presentation of SECCM data as current maps as a function of potential reveals that, while the entire surface of ITO is electroactive, the ET activity is highly spatially heterogeneous. Kinetic parameters (standard rate constant, k(0), and transfer coefficient, alpha) for FcDM(0/+) are assigned from 7200 measurements at sites across the ITO surface using finite element method modeling. Differences of 3 orders of magnitude in k(0) are revealed, and the average k(0) is about 20 times larger than that measured at the macroscale. This is attributed to macroscale ET being largely limited by lateral conductivity of the ITO electrode under electrochemical operation, rather than ET kinetics at the ITO/electrolyte interface, as measured by SECCM. This study further demonstrates the considerable power of SECCM for direct nanoscale characterization of electrochemical processes at complex electrode surfaces.

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