Investigation of the stability of NiFe-(oxy)hydroxide anodes in alkaline water electrolysis under industrially relevant conditions
AuthorsEtzi Coller Pascuzzi, Marco
Man, Alex J.W.
Hofmann, Jan P.
Hensen, Emiel J.M.
Permanent link to this recordhttp://hdl.handle.net/10754/665863
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AbstractNiFe-(Oxy)hydroxide is one of the most active electrocatalysts for the oxygen evolution reaction (OER) in alkaline conditions. Herein we investigated the stability of NiFe-(oxy)hydroxide anodes at high current densities (100 mA cm-2) at different temperatures (25, 75 °C) and base concentrations (1, 5, 10 M KOH). While polarization led to minor structural and compositional changes under standard conditions (25 °C, 1 M KOH), the anodes were severely impacted at higher temperature (75 °C) and base concentrations (5, 10 M KOH). Overall leaching and preferential leaching of Fe (resulting in a lower Fe/Ni ratio) led to decreased OER performance and increased charge transfer resistance for the samples tested at industrially relevant conditions. A dramatic loss in the catalytic activity occurred for the sample polarized at 75 °C in 10 M KOH: besides extensive leaching, a transformation of Ni(OH)2 into NiO was noted in this case. For pure NiOxHy, incorporation of Fe impurities from the electrolyte during polarization at 75 °C in 5 M KOH led to an improvement in the catalytic activity and charge-transfer properties, approaching the performance of NiFeOxHy.
CitationEtzi Coller Pascuzzi, M., Man, A. J. W., Goryachev, A., Hofmann, J. P., & Hensen, E. J. M. (2020). Investigation of the stability of NiFe-(oxy)hydroxide anodes in alkaline water electrolysis under industrially relevant conditions. Catalysis Science & Technology, 10(16), 5593–5601. doi:10.1039/d0cy01179g
SponsorsThe authors thank Adelheid Elemans-Mehring for ICP-OES measurements. M. E. C. P. acknowledges funding by a Graduate School program from the Netherlands Organization for Scientific Research (NWO). A. G. and E. J. M. H. acknowledge funding from an NWO Vici grant.
PublisherRoyal Society of Chemistry (RSC)
JournalCatalysis Science and Technology
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