TY - JOUR
T1 - (Ni1-xFex)OOH Binary Nanoparticles in as-Prepared and Purified KOH Electrolyte Solutions for Water Splitting
AU - Wang, Baiyu
AU - Schlegel, Nicolas
AU - Aalling-Frederiksen, Olivia
AU - Berner, Etienne
AU - Zhang, Damin
AU - Pittkowski, Rebecca K.
AU - Jensen, Kirsten M.Ø.
AU - Arenz, Matthias
N1 - Funding Information:
We acknowledge support from the Swiss National Science Foundation (SNSF) project No. 200021_184742 and the Danish National Research Foundation Center for High Entropy Alloy Catalysis (DNRF 149). We are grateful to the Villum Foundation for the financial support through a Villum Young Investigator grant (No. 0015416). We furthermore thank DANSCATT (supported by the Danish Agency for Science and Higher Education) for the support. Funding from the Danish Ministry of Higher Education and Science through the SMART Lighthouse is gratefully acknowledged. We acknowledge DESY (Hamburg, Germany), a member of the Helmholtz Association HGF, for the provision of experimental facilities. Parts of this research were carried out at PETRA III, and we would like to thank Henrik Jeppesen for assistance in using the beamline P02.1. Beamtime was allocated by an In-House contingent. The authors acknowledge access to the Microscopy Imaging Center (MIC) facilities of the University of Bern.
Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024
Y1 - 2024
N2 - Replacing critical raw materials employed in water electrolysis applications as electrocatalysts with earth-abundant materials is paramount for future upscaling to industrial dimensions. In that regard, Ni and Ni-based multimetallic hydroxides, above all NiFe hydroxides, have shown promising performance toward the oxygen evolution reaction (OER) in alkaline conditions. However, it has been shown that the extraordinary performance of these materials is largely due to Fe impurities found in commercial KOH from which electrolyte solutions are prepared. The mechanism of action of these impurities is still not fully understood and, therefore, at the heart of ongoing discussions. In this study, we investigate the OER activity of different nanostructured (Ni1-xFex)OOH samples and find their activities to be influenced differently by the presence of Fe impurities in the electrolyte. From the gathered data, we conclude that the presence of Fe impurities impacts the structure sensitivity of the OER. In purified electrolyte solutions, the OER appears to be a structure-sensitive reaction, while in the presence of Fe impurities, the interaction of the catalyst with these impurities and thus the catalyst surface area becomes paramount.
AB - Replacing critical raw materials employed in water electrolysis applications as electrocatalysts with earth-abundant materials is paramount for future upscaling to industrial dimensions. In that regard, Ni and Ni-based multimetallic hydroxides, above all NiFe hydroxides, have shown promising performance toward the oxygen evolution reaction (OER) in alkaline conditions. However, it has been shown that the extraordinary performance of these materials is largely due to Fe impurities found in commercial KOH from which electrolyte solutions are prepared. The mechanism of action of these impurities is still not fully understood and, therefore, at the heart of ongoing discussions. In this study, we investigate the OER activity of different nanostructured (Ni1-xFex)OOH samples and find their activities to be influenced differently by the presence of Fe impurities in the electrolyte. From the gathered data, we conclude that the presence of Fe impurities impacts the structure sensitivity of the OER. In purified electrolyte solutions, the OER appears to be a structure-sensitive reaction, while in the presence of Fe impurities, the interaction of the catalyst with these impurities and thus the catalyst surface area becomes paramount.
KW - alkaline OER
KW - KOH purification
KW - nanoparticle catalyst
KW - NiFe-LDH
KW - structure sensitivity
U2 - 10.1021/acsanm.3c05983
DO - 10.1021/acsanm.3c05983
M3 - Journal article
AN - SCOPUS:85195028615
VL - 7
SP - 12345−12355
JO - ACS Applied Nano Materials
JF - ACS Applied Nano Materials
SN - 2574-0970
IS - 11
ER -