摘要
Oxygen evolution reaction (OER) is a key step for electrochemical water splitting and understanding the surface reconstruction of OER pre-catalysts is of vital importance. Herein, hybrid Ni 5 P 4 @FeP nanosheet arrays were evaluated as promising OER pre-catalysts. The dynamic surface evolution was probed by in situ Raman spectroscopy, which revealed that Ni 5 P 4 @FeP was rapidly reconstructed to NiFe 2 O 4 during the anodic scan. The structural instability of amorphous NiFe 2 O 4 led to partial reconstitution to Ni/FeOOH at high oxidation potentials. As-formed Ni/FeOOH@NiFe 2 O 4 hybrid with high structural reversibility was established as a truly active species, which exhibited excellent alkaline OER performance with a low overpotential of 205 and 242 mV under current densities of 10 and 100 mA cm −2 , respectively. This work provides a facile strategy to in situ construct an amorphous spinel/oxyhydroxide hybrid structure using electrochemical activation that holds strong promise for potential application in electrochemical water splitting and related energy devices.
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