AI Article Synopsis

  • The Oxygen evolution reaction (OER) is the slowest step in water electrolysis, making it hard to find efficient catalysts for both acidic and alkaline environments.
  • Researchers developed NiIr nanowire assemblies (NAs) using a simple hydrothermal method, which showed exceptional OER performance in both 0.1 M HClO and 1.0 M KOH.
  • DFT calculations indicated that the combination of nickel and iridium enhances bonding with oxygen, leading to superior catalytic abilities in the NiIr NAs.

Article Abstract

Oxygen evolution reaction (OER) is the rate-limiting step in water electrolysis due to its sluggish kinetic, and it is challenging to develop an OER catalyst that could work efficiently in both acid and alkaline environment. Herein, NiIr nanowire assembles (NAs) with unique nanoflower morphology were prepared by a facile hydrothermal method. As a result, the NiIr NAs exhibited superior OER activity in both acid and alkaline media. Specifically, in 0.1 M HClO, NiIr NAs presented a superior electrocatalytic performance with a low overpotential of merely 242 mV at 10 mA cm and a Tafel slope of only 58.1 mV dec, surpassing that of commercial IrO and pure Ir NAs. And it achieved a significantly higher mass activity of 148.40 A/g at -1.5 V versus RHE. In 1.0 M KOH, NiIr NAs has an overpotential of 291 mV at 10 mA cm and a Tafel slope of 42.1 mV dec. Such remarkable activity makes the NiIr NAs among the best of recently reported representative Ir-based OER electrocatalysts. Density functional theory (DFT) calculations confirmed alloying effect promotes surface bonding of NiIr with oxygen-containing reactants, resulting in excellent catalytic properties.

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Source
http://dx.doi.org/10.1002/asia.202400851DOI Listing

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