Heterogeneous electrocatalyst of nanoscale Fe-based medium-entropy alloy and sulfide for oxygen evolution reaction
Heterojunctions of Fe-based medium entropy alloy and FeS2 in composites generate the good synergistic effect on OER electrocatalytic activity. [Display omitted] The construction of heterojunctions between non-noble-metal based compounds affords a scheme for accelerating the reaction kinetics of oxyg...
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Veröffentlicht in: | Journal of colloid and interface science 2025-02, Vol.680 (Pt A), p.742-752 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Heterojunctions of Fe-based medium entropy alloy and FeS2 in composites generate the good synergistic effect on OER electrocatalytic activity.
[Display omitted]
The construction of heterojunctions between non-noble-metal based compounds affords a scheme for accelerating the reaction kinetics of oxygen evolution reaction (OER) without using precious mental materials, which is extremely important but remains challenging. Herein, the heterogeneous structure between Fe60Co10Ni10Cr10Mn10 medium-entropy alloy (MEA) and FeS2 is developed by a mechanical alloying approach. The resulting MEA-30 wt%FeS2 delivers a high OER activity with a low overpotential of 261.6 mV at 10 mA/cm2, along with Tafel slope of 52.7 mV/dec in 1.0 mol/L KOH solution, superior to the commercial RuO2. The combination of detailed characterization techniques and density functional theory (DFT) calculation reveals that the heterojunctions between Fe-based MEA and FeS2 generates the synergistic effect on the activation and formation steps of OOH*, thus promoting the OER reaction kinetics. Furthermore, the abundant active sites provided by the reconstructions of MEA-30 wt%FeS2 during OER process also contributes to the catalytic performance. This work greatly expands the application scope of medium-entropy materials and provides a new method for the fabrication of novel heterogeneous electrocatalyst of Fe-based MEA and FeS2. |
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ISSN: | 0021-9797 1095-7103 1095-7103 |
DOI: | 10.1016/j.jcis.2024.11.034 |