Abstract
We report a novel cost-effective scaling process for the synthesis of the quinary IrPdPtRhRu high-entropy alloy nanoparticles (HEA-NPs). The process is based on the plasma ionic liquid reduction strategy. A combination of PXRD, HRTEM, XPS, and EDX analyses confirms that the application of the developed wet plasma reduction method yields the IrPdPtRhRu HEA-NPs. HEA-NPs ≈5 nm in size are synthesized under a mild temperature condition at atmospheric pressure and without support assistance. All elements constituting the as-prepared IrPdPtRhRu HEA-NPs are uniformly distributed in the FCC single-phase nanostructure. The valence band emission suggests the hybridization of the metal orbitals in the IrPdPtRhRu HEA-NPs. The work function (WF) of 4.63 eV for the HEA is determined by ultraviolet photoelectron spectroscopy. The WF value is lower than those of the metals constituting the HEA, suggesting higher catalytic activity. The IrPdPtRhRu/C electrocatalyst shows excellent catalytic performance toward hydrogen evolution reaction (HER) with an overpotential of 60 mV at a current density of 10 mA cm−2. A Tafel slope of 42 mV dec−1 is recorded in the alkaline electrolyte. The HEA electrocatalyst exhibits good long-term stability for 6 h without significant decay under a high constant current density of 100 mA cm−2. The findings in this study contribute to our basic scientific understanding of catalysts and provide a platform for the further development of HEA-NPs electrocatalysts for large-scale applications.
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