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A Unique NiOOH@FeOOH Heteroarchitecture for Enhanced Oxygen Evolution in Saline Water

机译:A Unique NiOOH@FeOOH Heteroarchitecture for Enhanced Oxygen Evolution in Saline Water

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摘要

The development of highly efficient non-precious metal electrocatalysts forthe oxygen evolution reaction (OER) in low-grade or saline water is currentlyof great importance for the large-scale production of hydrogen. In this study,by using an electrochemical activation pretreatment, metal oxy(hydroxide)nanosheet structures derived from self-supported nickel–iron phosphide andnitride nanoarrays grown on Ni foam are successfully fabricated for OER catalysisin saline water. It is demonstrated that the different NiOOH and NiOOH@FeOOH (NiOOH grown on FeOOH) structures are generated from nickel–ironnitride and phosphide, respectively, after electrochemical activation. In particular,the NiOOH@FeOOH heteroarchitecture shows outstanding electrocatalyticperformance with an ultralow overpotential of 292 mV to drive the currentdensity of 500 mA cm~(?2). An unconventional dual-sites mechanism (UDSM) isproposed to address the OER process on NiOOH@FeOOH and show that theFeOOH underlayer plays a critical role regarding the enhanced OER activity ofNiOOH. The new possible UDSM involving two reaction sites presents a differentunderstanding of the OER process on multi-OH layer complexes, whichis expected to guide the design of heteroarchitecture electrocatalysts.

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