TY - JOUR
T1 - 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
AU - Sánchez-Sánchez, Carlos M.
AU - Rodríguez-López, Joaquín
AU - Bard, Allen J.
PY - 2008/5/1
Y1 - 2008/5/1
N2 - 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 μm 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.
AB - 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 μm 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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U2 - 10.1021/ac702453n
DO - 10.1021/ac702453n
M3 - Article
C2 - 18355084
AN - SCOPUS:42949177059
SN - 0003-2700
VL - 80
SP - 3254
EP - 3260
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 9
ER -