The role of Fe incorporation into Ni-MOF-74 derived oxygen evolution electrocatalysts for anion exchange membrane water electrolysis

Abstract

The performance of Ni-based oxygen evolution reaction (OER) electrocatalysts is enhanced upon Fe incorporation into the structure during the synthesis process or electrochemical Fe uptake from the electrolyte. In light of the promising potential of metal–organic framework (MOF) electrocatalysts for water splitting, Ni-MOF-74 is used as a model catalyst to study the effect of Fe incorporation from KOH electrolyte on the electrocatalyst's OER activity and stability. The insights obtained from X-ray diffraction and operando X-ray absorption spectroscopy characterization of Ni-MOF-74 and an amorphous Ni metal organic compound (Ni-MOC*) reveal that Fe uptake enhances OER by two processes: higher Ni oxidation states and enhanced flexibility of both, the electronic state and the local structure, when cycling the potential below and above the OER onset. To demonstrate the impressive OER activity and stability in Fe containing KOH, an Ni-MOC* anode was implemented in an anion exchange membrane water electrolyzer (AEM-WE) with 3 ppm Fe containing 1 M KOH electrolyte resulting in an outstanding cell voltage of 1.7 V (at an anode potential of 1.51 V) at 60 °C and 0.5 A cm−2 exceeding 130 h of stable continuous operation.

Graphical abstract: The role of Fe incorporation into Ni-MOF-74 derived oxygen evolution electrocatalysts for anion exchange membrane water electrolysis

Supplementary files

Article information

Article type
Paper
Submitted
15 Nov 2024
Accepted
24 Jan 2025
First published
04 Feb 2025
This article is Open Access
Creative Commons BY license

EES. Catal., 2025, Advance Article

The role of Fe incorporation into Ni-MOF-74 derived oxygen evolution electrocatalysts for anion exchange membrane water electrolysis

J. Linke, T. Rohrbach, A. H. Clark, C. Borca, T. Huthwelker, F. L. Buchauer, M. R. Kraglund, C. Chatzichristodoulou, E. Meade, J. Guehl, M. Wojtas, M. Ranocchiari, T. J. Schmidt and E. Fabbri, EES. Catal., 2025, Advance Article , DOI: 10.1039/D4EY00250D

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