Literature DB >> 18355084

Scanning electrochemical microscopy. 60. Quantitative calibration of the SECM substrate generation/tip collection mode and its use for the study of the oxygen reduction mechanism.

Carlos M Sánchez-Sánchez1, Joaquín Rodríguez-López, Allen J Bard.   

Abstract

The substrate generation/tip collection (SG/TC) mode of scanning electrochemical microscopy (SECM) coupled with linear voltammetry is proposed as a way to quantify reaction intermediates generated in the solution at small substrates (100 mum diameter). The collection efficiency (CE) for SG/TC mode depends on the collector tip radius (a), the tip/substrate distance (d), and the size of the insulating glass sheath surrounding the collector tip (RG). In this work, we present experimental and simulated calibration CE values for different SG/TC geometries. Results of digital simulations in axial 2-D symmetry with the tip approaching a planar substrate are shown and fit experimental results obtained using ferrocenemethanol as a redox mediator very well. This model assumes that the mediator reacts under stationary-state conditions and undergoes diffusion-controlled electron transfer without any heterogeneous or homogeneous kinetic complications. Empirical equations for all SG/TC geometries reported here are provided as a convenient way to predict the maximum CE value for any given distance within the calibration range. Hydrogen peroxide quantification during the oxygen reduction reaction (ORR) at a Hg on Au electrode in acid pH was carried out using the SG/TC mode of SECM to demonstrate the utility of this technique in determining the number of electrons transferred (n) in the ORR. The results (n = 2.12-2.19) clearly point out the predominance of the two-electron pathway over the four-electron pathway when ORR takes place at this electrode material. Therefore, this work presents a powerful alternative to the rotating ring-disk electrode (RRDE) as means of obtaining mechanistic information by calculating the number of electrons transferred during an electrochemical reaction.

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Year:  2008        PMID: 18355084     DOI: 10.1021/ac702453n

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  5 in total

1.  Ultramicroelectrode Studies of Self-Terminated Nickel Electrodeposition and Nickel Hydroxide Formation upon Water Reduction.

Authors:  Nicole L Ritzert; Thomas P Moffat
Journal:  J Phys Chem C Nanomater Interfaces       Date:  2016-11-14       Impact factor: 4.126

2.  Quasi-steady-state voltammetry of rapid electron transfer reactions at the macroscopic substrate of the scanning electrochemical microscope.

Authors:  Nikoloz Nioradze; Jiyeon Kim; Shigeru Amemiya
Journal:  Anal Chem       Date:  2010-12-22       Impact factor: 6.986

3.  Real-Time Detection of Hydroxyl Radical Generated at Operating Electrodes via Redox-Active Adduct Formation Using Scanning Electrochemical Microscopy.

Authors:  Jaxiry S Barroso-Martínez; Adolfo I B Romo; Sanja Pudar; Seth T Putnam; Erika Bustos; Joaquín Rodríguez-López
Journal:  J Am Chem Soc       Date:  2022-10-10       Impact factor: 16.383

4.  Insight into the PEC and interfacial charge transfer kinetics at the Mo doped BiVO4 photoanodes.

Authors:  Sriram Kumar; Satyaprakash Ahirwar; Ashis Kumar Satpati
Journal:  RSC Adv       Date:  2019-12-16       Impact factor: 4.036

5.  Co-axial heterostructures integrating palladium/titanium dioxide with carbon nanotubes for efficient electrocatalytic hydrogen evolution.

Authors:  Giovanni Valenti; Alessandro Boni; Michele Melchionna; Matteo Cargnello; Lucia Nasi; Giovanni Bertoni; Raymond J Gorte; Massimo Marcaccio; Stefania Rapino; Marcella Bonchio; Paolo Fornasiero; Maurizio Prato; Francesco Paolucci
Journal:  Nat Commun       Date:  2016-12-12       Impact factor: 14.919

  5 in total

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