Improving the water
oxidation performance of abundantly available
materials, such as stainless steel (SS), with notable intrinsic electrocatalytic
oxygen evolution reaction (OER) activity due to the presence of Ni
and Fe is highly anticipated in water splitting. A new method for
promoting the corrosion of stainless steel (304) was found which assisted
the uniform formation of oxygen evolution reaction (OER) enhancing
NiO incorporated Fe2O3 nanocrystals with the
simultaneous reduction in the surface distribution of OER inactive
Cr. An equimolar combination of KOH and hypochlorite was used as the
corroding agent at 180 °C. The effect of corrosion time on the
OER activity was studied and found that better water oxidation performance
was observed when the corrosion time was 12 h (SS-12). The SS-12 showed
an abnormal enhancement in OER activity compared to the untreated
SS and other optimized versions of the same by requiring very low
overpotentials of 260, 302, and 340 mV at the current densities of
10, 100, and 500 mA cm–2 along with a very low Tafel
slope in the range of 35.6 to 43.5 mV dec–1. These
numbers have certainly shown the high-performance electrocatalytic
water oxidizing ability of SS-12. The comparative study revealed that
the state-of-the-art IrO2 had failed to compete with our
performance improved catalytic water oxidation anode “the SS-12”.
This fruitful finding indicates that the SS-12 has the potential to
be an alternate anode material to precious IrO2/RuO2 for alkaline water electrolyzers in future.