Self-magnetic-attracted NixFe(1−x)@NixFe(1−x)O nanoparticles on nickel foam as highly active and stable electrocatalysts towards alkaline oxygen evolution reaction

A facile self-magnetic-attracted approach was developed for highly active and stable Ni x Fe (1− x ) @Ni x Fe (1− x ) O/NF electrocatalysts towards alkaline oxygen evolution reaction. Firstly, a low-cost and scalable synthesis method was developed to synthesis 4–5 nm hydrophilic Ni x Fe (1− x ) @Ni...

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Veröffentlicht in:Nano research 2020-02, Vol.13 (2), p.461-466
Hauptverfasser: Yang, Zuobo, Liang, Xin
Format: Artikel
Sprache:eng
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Zusammenfassung:A facile self-magnetic-attracted approach was developed for highly active and stable Ni x Fe (1− x ) @Ni x Fe (1− x ) O/NF electrocatalysts towards alkaline oxygen evolution reaction. Firstly, a low-cost and scalable synthesis method was developed to synthesis 4–5 nm hydrophilic Ni x Fe (1− x ) @Ni x Fe (1− x ) O core–shell nanocrystals with superparamagnetism. Then, these Ni x Fe (1− x ) @Ni x Fe (1− x ) O nanoparticles (NPs) could be easily supported on nickel foam without any binders or additives. Optimized by the composition effect, the Ni 0.7 Fe 0.3 @Ni 0.7 Fe 0.3 O/NF exhibits excellent activity for oxygen evolution reaction (OER), requires only 215 mV at 10 mA·cm −2 and 260 mV at 100 mA·cm −2 , with a Tafel slope of 47.4 mV·dec −1 in 1.0 M KOH. Moreover, the underlying mechanism was carefully studied by X-ray diffraction (XRD), Raman, X-ray photoelectron spectroscopy (XPS) and X-ray absorption near-edge spectra (XANES) analysis and density functional theory (DFT) calculations. Due to the self-magnetic attraction, the catalyst shows outstanding stability throughout the electrocatalysis, surpassing than most self-supported catalysts. This work provides a new strategy for the construction of highly active and stable OER electrocatalysts, the nearly monodisperse magnetic Ni x Fe (1− x ) @Ni x Fe (1− x ) O NPs also serve an ideal building block for fundamental research of nickel-iron based catalyst.
ISSN:1998-0124
1998-0000
DOI:10.1007/s12274-020-2630-2