TY - JOUR
T1 - Benchmarking Electrocatalyst Stability for Acidic Oxygen Evolution Reaction
T2 - The Crucial Role of Dissolved Ion Concentration
AU - Wei, Chao
AU - Wang, Zhenbin
AU - Otani, Kanan
AU - Hochfilzer, Degenhart
AU - Zhang, Ke
AU - Nielsen, Rasmus
AU - Chorkendorff, Ib
AU - Kibsgaard, Jakob
N1 - Publisher Copyright:
© 2023 American Chemical Society.
PY - 2023
Y1 - 2023
N2 - Developing robust catalysts for the acidic oxygen evolution reaction (OER) is critical for large-scale implementation of proton exchange membrane (PEM) water electrolyzers. A promising strategy is to stabilize Ru-based catalysts by suppressing Ru dissolution, which requires knowledge of RuO2 stability. This work explores the influences on measuring the stability number of RuO2 and presents a comprehensive analysis and comparison of its stability with other electrocatalysts. We observe that RuO2 shows relatively higher stability in electrolytes with a confined working volume because of the Nernst shift caused by the concentration buildup of dissolved Ru. The stability number of RuO2 has a negligible dependence on the measurement duration, applied current density, Nafion content, and substrate materials. Furthermore, we analyze the effects of these factors on other typical OER catalysts and identify that the concentration of dissolved ions is key to understanding the stability number measured by different electrochemical cells and the claimed excellent stability of non-noble catalysts reported in the literature. In addition, the comparison of the stability number and intrinsic activity of RuO2, IrO2, and non-noble catalysts demonstrates that RuO2 is at least 2 orders of magnitude less stable but also 10-fold more active than IrO2 and that noble catalysts significantly outperform non-noble catalysts in terms of both stability and activity, posing a grand challenge in developing robust OER catalysts. This work establishes a baseline for enhancing the stability of Ru-based OER catalysts in acidic liquid cells and provides a valuable reference for PEM water electrolyzers.
AB - Developing robust catalysts for the acidic oxygen evolution reaction (OER) is critical for large-scale implementation of proton exchange membrane (PEM) water electrolyzers. A promising strategy is to stabilize Ru-based catalysts by suppressing Ru dissolution, which requires knowledge of RuO2 stability. This work explores the influences on measuring the stability number of RuO2 and presents a comprehensive analysis and comparison of its stability with other electrocatalysts. We observe that RuO2 shows relatively higher stability in electrolytes with a confined working volume because of the Nernst shift caused by the concentration buildup of dissolved Ru. The stability number of RuO2 has a negligible dependence on the measurement duration, applied current density, Nafion content, and substrate materials. Furthermore, we analyze the effects of these factors on other typical OER catalysts and identify that the concentration of dissolved ions is key to understanding the stability number measured by different electrochemical cells and the claimed excellent stability of non-noble catalysts reported in the literature. In addition, the comparison of the stability number and intrinsic activity of RuO2, IrO2, and non-noble catalysts demonstrates that RuO2 is at least 2 orders of magnitude less stable but also 10-fold more active than IrO2 and that noble catalysts significantly outperform non-noble catalysts in terms of both stability and activity, posing a grand challenge in developing robust OER catalysts. This work establishes a baseline for enhancing the stability of Ru-based OER catalysts in acidic liquid cells and provides a valuable reference for PEM water electrolyzers.
KW - Dissolved ion concentration
KW - Non-noble catalysts
KW - Oxygen evolution reaction
KW - Proton exchange membrane water electrolyzer
KW - RuO
KW - Stability number
U2 - 10.1021/acscatal.3c03257
DO - 10.1021/acscatal.3c03257
M3 - Journal article
AN - SCOPUS:85177489131
SN - 2155-5435
VL - 13
SP - 14058
EP - 14069
JO - ACS Catalysis
JF - ACS Catalysis
ER -