TY - JOUR
T1 - Investigation of the stability of NiFe-(oxy)hydroxide anodes in alkaline water electrolysis under industrially relevant conditions
AU - Etzi Coller Pascuzzi, Marco
AU - Man, Alex J.W.
AU - Goryachev, Andrey
AU - Hofmann, Jan P.
AU - Hensen, Emiel J.M.
N1 - KAUST Repository Item: Exported on 2020-11-10
Acknowledgements: The 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.
PY - 2020/7/17
Y1 - 2020/7/17
N2 - NiFe-(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.
AB - NiFe-(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.
UR - http://hdl.handle.net/10754/665863
UR - http://xlink.rsc.org/?DOI=D0CY01179G
UR - http://www.scopus.com/inward/record.url?scp=85094965938&partnerID=8YFLogxK
U2 - 10.1039/d0cy01179g
DO - 10.1039/d0cy01179g
M3 - Article
SN - 2044-4761
VL - 10
SP - 5593
EP - 5601
JO - Catalysis Science and Technology
JF - Catalysis Science and Technology
IS - 16
ER -