Belami, Debora, Lindley, Matthew, Jonnalagadda, Umesh S ORCID: https://orcid.org/0000-0002-4715-4993, Goncalves Bullock, Annie Mae, Fan, Qianwenhao ORCID: https://orcid.org/0000-0002-0591-1669, Liu, Wen ORCID: https://orcid.org/0000-0002-1107-131X, Haigh, Sarah J ORCID: https://orcid.org/0000-0001-5509-6706, Kwan, James, Regmi, Yagya N ORCID: https://orcid.org/0000-0001-6588-7683 and King, Laurie A ORCID: https://orcid.org/0000-0002-0772-2378 (2024) Active and highly durable supported catalysts for proton exchange membrane electrolysers. EES Catalysis, 2 (5). pp. 1139-1151. ISSN 2753-801X
|
Published Version
Available under License Creative Commons Attribution. Download (1MB) | Preview |
Abstract
The design and development of supported catalysts for the oxygen evolution reaction (OER) is a promising pathway to reducing iridium loading in proton exchange membrane water electrolysers. However, supported catalysts often suffer from poor activity and durability, particularly when deployed in membrane electrode assemblies. In this work, we deploy iridium coated hollow titanium dioxide particles as OER catalysts to achieve higher Ir mass activities than the leading commercial catalysts. Critically, we demonstrate state-of-the-art durabilities for supported iridium catalysts when compared against the previously reported values for analogous device architectures, operating conditions and accelerated stress test profiles. Through extensive materials characterisations alongside rotating disk electrode measurements, we investigate the role of conductivity, morphology, oxidation state and crystallinity on the OER electrochemical performance. Our work highlights a new supported catalyst design that unlocks high-performance OER activity and durability in commercially relevant testing configurations.
Impact and Reach
Statistics
Additional statistics for this dataset are available via IRStats2.