High Intrinsic Activity Of The Oxygen Evolution Reaction In Low-Cost Nio Nanowall Electrocatalysts

Earth-abundant materials for electrochemical water splitting typically show a lower efficiency than noble and rare metal electrocatalysts. Nanostructuring and appropriate material design can largely improve the performances of low-cost electrocatalysts, opening the route towards profitable mass production. Here, we report on a quantitative investigation of the oxygen evolution reaction (OER) on Ni-based nanowall (NW) electrodes. The NiO and Ni(OH)(2) NW films (200 or 400 nm thick) are produced by chemical bath deposition followed by calcination at 350 degrees C. The morphology and the chemical arrangement of the NW were studied, before and after the OER, by scanning electron microscopy, energy dispersive X-ray analysis and X-ray photoelectron spectroscopy. The OER electrocatalytic activity was investigated by electrochemical measurements under alkaline conditions (1 M KOH), demonstrating a stable overpotential of 345 mV at 10 mA cm(-2), a Tafel slope of 48 mV dec(-1) and an O-2 turnover conversion frequency (TOF) of up to 0.18 s(-1). The quantitative measurement of active electrocatalysts, through cross-correlation of the experimental data, shows nearly 100% material utilization in the 200 nm NiO NW. In thicker NiO or Ni(OH)(2) NW films this fraction decreases below 60%, probably due to the decrease in the electric potential along the nanostructure, as revealed by numerical simulation. These data and discussion support the use of low-cost Ni-based nanostructures for high-efficiency and sustainable electrocatalysts.