pH Dependence of Noble Metals Dissolution: Ruthenium

Abstract Ruthenium (Ru) or Ru‐based catalysts are widely used in various electrochemical applications such as biosensors, ammonia synthesis, CO2 reduction, electrolyzers, or fuel cells, operating at different conditions. While the activity of these catalysts is widely studied, works addressing stabi...

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Main Authors: Mária Minichová, Tatiana Priamushko, Matej Zlatar, Karl J. J. Mayrhofer, Serhiy Cherevko
Format: Article
Language:English
Published: Wiley-VCH 2025-05-01
Series:ChemElectroChem
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Online Access:https://doi.org/10.1002/celc.202400651
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author Mária Minichová
Tatiana Priamushko
Matej Zlatar
Karl J. J. Mayrhofer
Serhiy Cherevko
author_facet Mária Minichová
Tatiana Priamushko
Matej Zlatar
Karl J. J. Mayrhofer
Serhiy Cherevko
author_sort Mária Minichová
collection DOAJ
description Abstract Ruthenium (Ru) or Ru‐based catalysts are widely used in various electrochemical applications such as biosensors, ammonia synthesis, CO2 reduction, electrolyzers, or fuel cells, operating at different conditions. While the activity of these catalysts is widely studied, works addressing stability are less common, especially in neutral or alkaline environments. Therefore, we evaluate a real‐time potential‐dependent dissolution of polycrystalline Ru via scanning flow cell coupled to inductively coupled plasma mass spectrometry in acidic, alkaline, and phosphate buffer electrolytes using relevant potential ranges. On top of the fundamental understanding of Ru's dissolution, a particular focus lies on oxygen evolution reaction (OER) due to its importance in various electrochemical applications. We show that the dissolution behavior of Ru during dynamic operation is well in line with the thermodynamic predictions (except dissolution due to Ru2+ formation) and unique compared to other noble metals (Pt, Au, Ir). While the dissolution of polycrystalline Ru is the highest in alkaline pH at the onset of OER (1.4 VRHE), no stability issues are visible at potentials up to 0.85 VRHE at all pHs. This work establishes a stability baseline for researchers implementing Ru‐based catalysts.
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institution Kabale University
issn 2196-0216
language English
publishDate 2025-05-01
publisher Wiley-VCH
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series ChemElectroChem
spelling doaj-art-bba07edb279149c48e20072cd3d63d932025-08-20T03:52:32ZengWiley-VCHChemElectroChem2196-02162025-05-01129n/an/a10.1002/celc.202400651pH Dependence of Noble Metals Dissolution: RutheniumMária Minichová0Tatiana Priamushko1Matej Zlatar2Karl J. J. Mayrhofer3Serhiy Cherevko4Forschungszentrum Jülich GmbH Helmholtz Institute Erlangen-Nürnberg for Renewable Energy (IET-2) Cauerstr. 1 91058 Erlangen GermanyForschungszentrum Jülich GmbH Helmholtz Institute Erlangen-Nürnberg for Renewable Energy (IET-2) Cauerstr. 1 91058 Erlangen GermanyForschungszentrum Jülich GmbH Helmholtz Institute Erlangen-Nürnberg for Renewable Energy (IET-2) Cauerstr. 1 91058 Erlangen GermanyForschungszentrum Jülich GmbH Helmholtz Institute Erlangen-Nürnberg for Renewable Energy (IET-2) Cauerstr. 1 91058 Erlangen GermanyForschungszentrum Jülich GmbH Helmholtz Institute Erlangen-Nürnberg for Renewable Energy (IET-2) Cauerstr. 1 91058 Erlangen GermanyAbstract Ruthenium (Ru) or Ru‐based catalysts are widely used in various electrochemical applications such as biosensors, ammonia synthesis, CO2 reduction, electrolyzers, or fuel cells, operating at different conditions. While the activity of these catalysts is widely studied, works addressing stability are less common, especially in neutral or alkaline environments. Therefore, we evaluate a real‐time potential‐dependent dissolution of polycrystalline Ru via scanning flow cell coupled to inductively coupled plasma mass spectrometry in acidic, alkaline, and phosphate buffer electrolytes using relevant potential ranges. On top of the fundamental understanding of Ru's dissolution, a particular focus lies on oxygen evolution reaction (OER) due to its importance in various electrochemical applications. We show that the dissolution behavior of Ru during dynamic operation is well in line with the thermodynamic predictions (except dissolution due to Ru2+ formation) and unique compared to other noble metals (Pt, Au, Ir). While the dissolution of polycrystalline Ru is the highest in alkaline pH at the onset of OER (1.4 VRHE), no stability issues are visible at potentials up to 0.85 VRHE at all pHs. This work establishes a stability baseline for researchers implementing Ru‐based catalysts.https://doi.org/10.1002/celc.202400651DissolutionRutheniumpHElectrocatalysisStabilityICP-MS
spellingShingle Mária Minichová
Tatiana Priamushko
Matej Zlatar
Karl J. J. Mayrhofer
Serhiy Cherevko
pH Dependence of Noble Metals Dissolution: Ruthenium
ChemElectroChem
Dissolution
Ruthenium
pH
Electrocatalysis
Stability
ICP-MS
title pH Dependence of Noble Metals Dissolution: Ruthenium
title_full pH Dependence of Noble Metals Dissolution: Ruthenium
title_fullStr pH Dependence of Noble Metals Dissolution: Ruthenium
title_full_unstemmed pH Dependence of Noble Metals Dissolution: Ruthenium
title_short pH Dependence of Noble Metals Dissolution: Ruthenium
title_sort ph dependence of noble metals dissolution ruthenium
topic Dissolution
Ruthenium
pH
Electrocatalysis
Stability
ICP-MS
url https://doi.org/10.1002/celc.202400651
work_keys_str_mv AT mariaminichova phdependenceofnoblemetalsdissolutionruthenium
AT tatianapriamushko phdependenceofnoblemetalsdissolutionruthenium
AT matejzlatar phdependenceofnoblemetalsdissolutionruthenium
AT karljjmayrhofer phdependenceofnoblemetalsdissolutionruthenium
AT serhiycherevko phdependenceofnoblemetalsdissolutionruthenium