Competitive Adsorption and Interplay between Methanol and Water during Electro-Oxidation on Pd-Based Electrocatalyst

The methanol oxidation reaction on palladium-based materials at different concentrations is studied theoretically and experimentally through its electrochemical response. Using a well-established reaction mechanism for the methanol oxidation reaction under alkaline conditions, we analyze the role of...

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Bibliographic Details
Main Authors: Hernández, S.I (Author), Ledesma-Durán, A. (Author), Maya-Cornejo, J. (Author), Santamaría-Holek, I. (Author)
Format: Article
Language:English
Published: IOP Publishing Ltd 2022
Subjects:
Online Access:View Fulltext in Publisher
LEADER 02823nam a2200421Ia 4500
001 10.1149-1945-7111-ac6321
008 220510s2022 CNT 000 0 und d
020 |a 00134651 (ISSN) 
245 1 0 |a Competitive Adsorption and Interplay between Methanol and Water during Electro-Oxidation on Pd-Based Electrocatalyst 
260 0 |b IOP Publishing Ltd  |c 2022 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1149/1945-7111/ac6321 
520 3 |a The methanol oxidation reaction on palladium-based materials at different concentrations is studied theoretically and experimentally through its electrochemical response. Using a well-established reaction mechanism for the methanol oxidation reaction under alkaline conditions, we analyze the role of methanol, water adsorption and oxidation steps on the total electrochemical current obtained from linear voltammetry experiments. Solving the kinetic equations numerically, we fit the data obtained from experiments performed with a commercial catalyst at different methanol concentrations. Comparison of the numerical calculations with analytical expressions deduced following Laviron s theoretical approach leads to discerning the adsorption contributions from methanol and water to the overall shape of the oxidation current from the nonlinear contribution associated with carbon-dioxide production. This identification allows, in turn, to use the peak current of the adsorption-related processes as a tool to characterize the overall catalyst's performance. © 2022 The Author(s). Published on behalf of The Electrochemical Society by IOP Publishing Limited. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License (CC BY, http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse of the work in any medium, provided the original work is properly cited. [DOI: 10.1149/1945-7111/ac6321]. 
650 0 4 |a Adsorption 
650 0 4 |a Alkaline conditions 
650 0 4 |a Carbon dioxide 
650 0 4 |a Competitive adsorption 
650 0 4 |a Electrocatalysis 
650 0 4 |a Electrocatalysis 
650 0 4 |a Electrocatalysts 
650 0 4 |a Electrochemical response 
650 0 4 |a Electrode kinetics 
650 0 4 |a Electrode Kinetics 
650 0 4 |a Electrooxidation 
650 0 4 |a Electrooxidations 
650 0 4 |a Fuel cells 
650 0 4 |a Fuel Cells 
650 0 4 |a Integral equations 
650 0 4 |a Methanol 
650 0 4 |a Methanol oxidation reactions 
650 0 4 |a Methanol-water 
650 0 4 |a Pd-based electrocatalysts 
650 0 4 |a Reaction mechanism 
650 0 4 |a Reaction under 
700 1 |a Hernández, S.I.  |e author 
700 1 |a Ledesma-Durán, A.  |e author 
700 1 |a Maya-Cornejo, J.  |e author 
700 1 |a Santamaría-Holek, I.  |e author 
773 |t Journal of the Electrochemical Society