Contribution of the oxygen reduction reaction to the electrochemical cathodic partial reaction for Mg-Al-Ca solid solutions

The electrochemical corrosion rate of magnesium depends on the stability of the surface layer formed. Based on the Mg substrate, the oxide structure comprises a dense MgO/Mg(OH)2 mixture underneath a porous plate-like Mg(OH)2 layer. While the kinetics of the anodic partial reaction have been mainly...

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Main Authors: Markus Felten, Siyuan Zhang, Rasa Changizi, Christina Scheu, Mark Bruns, Michael Strebl, Sannakaisa Virtanen, Daniela Zander
Format: Article
Language:English
Published: Elsevier 2023-08-01
Series:Electrochemistry Communications
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1388248123001030
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author Markus Felten
Siyuan Zhang
Rasa Changizi
Christina Scheu
Mark Bruns
Michael Strebl
Sannakaisa Virtanen
Daniela Zander
author_facet Markus Felten
Siyuan Zhang
Rasa Changizi
Christina Scheu
Mark Bruns
Michael Strebl
Sannakaisa Virtanen
Daniela Zander
author_sort Markus Felten
collection DOAJ
description The electrochemical corrosion rate of magnesium depends on the stability of the surface layer formed. Based on the Mg substrate, the oxide structure comprises a dense MgO/Mg(OH)2 mixture underneath a porous plate-like Mg(OH)2 layer. While the kinetics of the anodic partial reaction have been mainly attributed to MgO, recent studies have showed an effect of the Mg(OH)2 layer thickness on the cathodic partial reaction. A thinner Mg(OH)2 layer has been associated with higher kinetics of the oxygen reduction reaction. In the present study, the mechanism has been further investigated via in situ respirometric measurements using Mg-Al-Ca solid solution in electrolytes with different pH values (pH = 8.0–13.0). The results indicate an additional effect based on the structure of the surface layer for Mg-Al-Ca alloys in the passive state. Furthermore, two different Al-enriched interfaces were observed and discussed in terms of their thermodynamic stability under alkaline immersion conditions.
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spelling doaj.art-70d85b8f906e4caba30140b7f7431f522023-08-05T05:15:37ZengElsevierElectrochemistry Communications1388-24812023-08-01153107529Contribution of the oxygen reduction reaction to the electrochemical cathodic partial reaction for Mg-Al-Ca solid solutionsMarkus Felten0Siyuan Zhang1Rasa Changizi2Christina Scheu3Mark Bruns4Michael Strebl5Sannakaisa Virtanen6Daniela Zander7Chair of Corrosion and Corrosion Protection, Division of Materials Science and Engineering, Foundry Institute Aachen, RWTH Aachen University, Aachen GermanyMax-Planck-Institut für Eisenforschung, Düsseldorf GermanyMax-Planck-Institut für Eisenforschung, Düsseldorf GermanyMax-Planck-Institut für Eisenforschung, Düsseldorf GermanyDepartment of Materials Science, Institute for Surface Science and Corrosion, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen GermanyDepartment of Materials Science, Institute for Surface Science and Corrosion, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen GermanyDepartment of Materials Science, Institute for Surface Science and Corrosion, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen GermanyChair of Corrosion and Corrosion Protection, Division of Materials Science and Engineering, Foundry Institute Aachen, RWTH Aachen University, Aachen Germany; Corresponding author.The electrochemical corrosion rate of magnesium depends on the stability of the surface layer formed. Based on the Mg substrate, the oxide structure comprises a dense MgO/Mg(OH)2 mixture underneath a porous plate-like Mg(OH)2 layer. While the kinetics of the anodic partial reaction have been mainly attributed to MgO, recent studies have showed an effect of the Mg(OH)2 layer thickness on the cathodic partial reaction. A thinner Mg(OH)2 layer has been associated with higher kinetics of the oxygen reduction reaction. In the present study, the mechanism has been further investigated via in situ respirometric measurements using Mg-Al-Ca solid solution in electrolytes with different pH values (pH = 8.0–13.0). The results indicate an additional effect based on the structure of the surface layer for Mg-Al-Ca alloys in the passive state. Furthermore, two different Al-enriched interfaces were observed and discussed in terms of their thermodynamic stability under alkaline immersion conditions.http://www.sciencedirect.com/science/article/pii/S1388248123001030MagnesiumCorrosionInterfacesTEMORR
spellingShingle Markus Felten
Siyuan Zhang
Rasa Changizi
Christina Scheu
Mark Bruns
Michael Strebl
Sannakaisa Virtanen
Daniela Zander
Contribution of the oxygen reduction reaction to the electrochemical cathodic partial reaction for Mg-Al-Ca solid solutions
Electrochemistry Communications
Magnesium
Corrosion
Interfaces
TEM
ORR
title Contribution of the oxygen reduction reaction to the electrochemical cathodic partial reaction for Mg-Al-Ca solid solutions
title_full Contribution of the oxygen reduction reaction to the electrochemical cathodic partial reaction for Mg-Al-Ca solid solutions
title_fullStr Contribution of the oxygen reduction reaction to the electrochemical cathodic partial reaction for Mg-Al-Ca solid solutions
title_full_unstemmed Contribution of the oxygen reduction reaction to the electrochemical cathodic partial reaction for Mg-Al-Ca solid solutions
title_short Contribution of the oxygen reduction reaction to the electrochemical cathodic partial reaction for Mg-Al-Ca solid solutions
title_sort contribution of the oxygen reduction reaction to the electrochemical cathodic partial reaction for mg al ca solid solutions
topic Magnesium
Corrosion
Interfaces
TEM
ORR
url http://www.sciencedirect.com/science/article/pii/S1388248123001030
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