Multimodal In Situ Characterization Uncovers Unexpected Stability of a Cobalt Electrocatalyst for Acidic Sustainable Energy Technologies

An accelerated development of durable and affordable sustainable energy technologies is often hindered by a limited understanding of how nonprecious materials within these systems degrade. In acidic proton exchange membrane fuel cells and water electrolyzers, metallic cobalt (Co) is considered an unstable component that is often combined with precious metals or other stabilizers. To understand the mechanisms behind Co instability, we employ an experimental platform that quantifies dissolution with on-line inductively coupled plasma mass spectrometry and product formation with electrochemical mass spectrometry during electrochemical testing, along with ex situ characterization. Under varied conditions (electrocatalysis, time, gas-type saturation, and ion concentration), windows of Co stability are observed that are different than predicted with classical chemical thermodynamics, suggesting new stabilization and degradation mechanisms than previously understood. Notably, Co is active for the hydrogen evolution reaction (HER), with prolonged stability that is ∼300 mV greater than thermodynamically projected. Additionally, in an oxygenated environment, Co concurrently performs the HER and the oxygen reduction reaction (ORR) yet undergoes different morphology changes and dissolution mechanisms. Interestingly, at open-circuit voltage, there is a 22× decrease in dissolution in an oxygen-free environment, proposing a route to decrease Co losses during device shutdown protocols. Lastly, under more extreme operating conditions, Co becomes stable after a substantial amount of dissolution, suggesting that high concentrations of Co<sup>2+</sup> ions in the microenvironment induce the formation of a stable CoHO<sub>2</sub> surface. Altogether, these results can be leveraged to improve the design and development of more robust and cost-effective sustainable energy technologies, as well as promote strategic strategies for prolonged material utilization.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-03-13
DOI
https://doi.org/10.1021/jacs.4c16707
Citations
12
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
4.36

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article

Multimodal In Situ Characterization Uncovers Unexpected Stability of a Cobalt Electrocatalyst for Acidic Sustainable Energy Technologies

Michaela Burke Stevens, Aniket S. Mule, Gaurav A. Kamat, Adam C. Nielander et al.
12 citations
Journal of the American Chemical Society
Electrocatalysts for Energy Conversion
4.36
article

Multimodal In Situ Characterization Uncovers Unexpected Stability of a Cobalt Electrocatalyst for Acidic Sustainable Energy Technologies

Michaela Burke Stevens, Aniket S. Mule, Gaurav A. Kamat, Adam C. Nielander, Ashton M. Aleman, Colin Flynn Crago, Jaime E. Avilés Acosta, Thomas Francisco Jaramillo, Ryan T. Hannagan, Jesse E. Matthews, Nathaniel Keyes
article en
12 citations

Abstract

An accelerated development of durable and affordable sustainable energy technologies is often hindered by a limited understanding of how nonprecious materials within these systems degrade. In acidic proton exchange membrane fuel cells and water electrolyzers, metallic cobalt (Co) is considered an unstable component that is often combined with precious metals or other stabilizers. To understand the mechanisms behind Co instability, we employ an experimental platform that quantifies dissolution with on-line inductively coupled plasma mass spectrometry and product formation with electrochemical mass spectrometry during electrochemical testing, along with ex situ characterization. Under varied conditions (electrocatalysis, time, gas-type saturation, and ion concentration), windows of Co stability are observed that are different than predicted with classical chemical thermodynamics, suggesting new stabilization and degradation mechanisms than previously understood. Notably, Co is active for the hydrogen evolution reaction (HER), with prolonged stability that is ∼300 mV greater than thermodynamically projected. Additionally, in an oxygenated environment, Co concurrently performs the HER and the oxygen reduction reaction (ORR) yet undergoes different morphology changes and dissolution mechanisms. Interestingly, at open-circuit voltage, there is a 22× decrease in dissolution in an oxygen-free environment, proposing a route to decrease Co losses during device shutdown protocols. Lastly, under more extreme operating conditions, Co becomes stable after a substantial amount of dissolution, suggesting that high concentrations of Co<sup>2+</sup> ions in the microenvironment induce the formation of a stable CoHO<sub>2</sub> surface. Altogether, these results can be leveraged to improve the design and development of more robust and cost-effective sustainable energy technologies, as well as promote strategic strategies for prolonged material utilization.

Journal of the American Chemical SocietyVol. 147(12)
SLAC National Accelerator Laboratory (US), Interface (United States) (US), Stanford University (US)
Toyota Research Institute, Stanford Precourt Institute for Energy, Division of Electrical, Communications and Cyber Systems, Basic Energy Sciences, Chemical Sciences, Geosciences, and Biosciences Division
Responsible consumption and production
Openalex Percentile: Top 5%
Electrocatalysts for Energy Conversion
4.36
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