| Autor: |
Wahab OJ; Department of Chemistry, University of Warwick, Coventry CV4 7AL, United Kingdom., Kang M; Department of Chemistry, University of Warwick, Coventry CV4 7AL, United Kingdom.; Institute for Frontier Materials Deakin University, Burwood, Victoria 3125, Australia., Meloni GN; Department of Chemistry, University of Warwick, Coventry CV4 7AL, United Kingdom., Daviddi E; Department of Chemistry, University of Warwick, Coventry CV4 7AL, United Kingdom., Unwin PR; Department of Chemistry, University of Warwick, Coventry CV4 7AL, United Kingdom. |
| Jazyk: |
angličtina |
| Zdroj: |
Analytical chemistry [Anal Chem] 2022 Mar 22; Vol. 94 (11), pp. 4729-4736. Date of Electronic Publication: 2022 Mar 07. |
| DOI: |
10.1021/acs.analchem.1c05168 |
| Abstrakt: |
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, α) 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. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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