<p>The development
of electrocatalysts for the oxygen evolution reaction (OER) is one of the principal
challenges in the area of renewable energy research. Within this context,
mixed-metal oxides have recently emerged as the highest performing OER
catalysts. Their structural and compositional modification to further boost
their activity is crucial to the wide-spread use of electrolysis technologies.
In this work, we investigated a series of mixed-metal F-containing materials as
OER catalysts to probe possible benefits of the high electronegativity of
fluoride ions. We found that crystalline
hydrated fluorides, CoFe<sub>2</sub>F<sub>8</sub>(H<sub>2</sub>O)<sub>2</sub>,
NiFe<sub>2</sub>F<sub>8</sub>(H<sub>2</sub>O)<sub>2, </sub>and amorphous
oxyfluorides, NiFe<sub>2</sub>F<sub>4.4</sub>O<sub>1.8 </sub>and CoFe<sub>2</sub>F<sub>6.6</sub>O<sub>0.7,
</sub>feature excellent activity and stability for the OER in alkaline
electrolyte. Subsequent electroanalytical and spectroscopic characterization
hinted that the electronic structure modulation conferred by the fluoride
ions aided their
reactivity. Finally, the best catalyst of the set, NiFe<sub>2</sub>F<sub>4.4</sub>O<sub>1.8</sub>,
was applied as anode in an electrolyzer comprised solely of earth-abundant
materials.</p>