Catalyst-Specific Accelerated Stress Tests in Proton Exchange Membrane Low-Temperature Electrolysis for Intermittent Operation

Shaun M. Alia, Kimberly S. Reeves, Haoran Yu, Jae Hyung Park, Nancy N. Kariuki, A. Jeremy Kropf, Deborah J. Myers, David A. Cullen

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Device-level stress tests are developed that focus on anode catalyst layer degradation and future anticipated operating conditions, including intermittent load and reduced platinum group metal content. Square-wave cycles with an upper load limit of 2.5 A cm‒2 are utilized to screen commercial iridium (Ir) materials. Performance losses are primarily due to decreasing kinetics and are accompanied by catalyst migration into the membrane, worsening catalyst/ionomer integration, and weakening of the catalyst/membrane interface. For ruthenium-containing catalysts, the in situ performances are higher but durabilities lower than Ir baselines, and any performance advantage is lost within the test. Increased loss is likely due to the higher dissolution rate; microscopy confirmed greater degrees of ruthenium migration. For Ir metal or mixed oxides, ex situ activity improvements generally did not translate to in situ performance. The durability, however, is significantly lower and the loss rate increased from 3 (oxide) to 9 (metal) μV cycle‒1. These results are consistent with historical findings in literature, rationalize the continued use of iridium oxide as a baseline catalyst, and demonstrate that traditional catalyst development approaches may not improve device-level durability when focused on low-cost applications. A shift in focus may therefore be more effective at improving catalyst utilization and lessening load requirements.

Original languageEnglish
Article number024505
JournalJournal of the Electrochemical Society
Volume171
Issue number2
DOIs
StatePublished - Feb 1 2024

Funding

This work was authored by the National Renewable Energy Laboratory, operated by Alliance for Sustainable Energy, LLC, for the U.S. Department of Energy (DOE) under Contract No. DE-AC36-08GO28308. The submitted manuscript has been created in part by UChicago Argonne, LLC, Operator of Argonne National Laboratory (“Argonne”). Argonne, a U.S. Department of Energy Office of Science laboratory, is operated under Contract No. DEAC02-06CH11357. Funding was provided by U.S. Department of Energy Office of Energy Efficiency and Renewable Energy, Hydrogen and Fuel Cell Technologies Office through H2@Scale and the H2NEW Consortium. Electron microscopy was conducted at the Center for Nanophase Materials Sciences, which is a DOE Office of Science User Facility. The X-ray absorption (MRCAT, 10-BM and 10-ID) and scattering (XSD, 9-ID-C) experiments were performed at the Advanced Photon Source (APS), a DOE Office of Science User Facility operated for the DOE Office of Science by Argonne under Contract No. DE-AC02-06CH11357. The operation of MRCAT at the APS is supported by the Department of Energy and the MRCAT member institutions. The authors would like to thank Jan Ilavsky and Ivan Kuzmenko of the APS 9-ID-C. This work was authored by the National Renewable Energy Laboratory, operated by Alliance for Sustainable Energy, LLC, for the U.S. Department of Energy (DOE) under Contract No. DE-AC36–08GO28308. The submitted manuscript has been created in part by UChicago Argonne, LLC, Operator of Argonne National Laboratory (“Argonne”). Argonne, a U.S. Department of Energy Office of Science laboratory, is operated under Contract No. DEAC02–06CH11357. Funding was provided by U.S. Department of Energy Office of Energy Efficiency and Renewable Energy, Hydrogen and Fuel Cell Technologies Office through H2@Scale and the H2NEW Consortium. Electron microscopy was conducted at the Center for Nanophase Materials Sciences, which is a DOE Office of Science User Facility. The X-ray absorption (MRCAT, 10-BM and 10-ID) and scattering (XSD, 9-ID-C) experiments were performed at the Advanced Photon Source (APS), a DOE Office of Science User Facility operated for the DOE Office of Science by Argonne under Contract No. DE-AC02–06CH11357. The operation of MRCAT at the APS is supported by the Department of Energy and the MRCAT member institutions. The authors would like to thank Jan Ilavsky and Ivan Kuzmenko of the APS 9-ID-C.

FundersFunder number
U.S. Department of EnergyDE-AC36–08GO28308
Office of Science10-BM, 10-ID
Argonne National LaboratoryDE-AC02–06CH11357
Hydrogen and Fuel Cell Technologies Office

    Keywords

    • degradation
    • energy conversion
    • low temperature electrolysis

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