Synthesis of Co2-xNixO2 (0 < x < 1.0) hexagonal nanostructures as efficient bifunctional electrocatalysts for overall water splitting.

Designing low-cost and high-performance bifunctional electrocatalysts towards hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is vitally important for water splitting. Herein, we synthesize Co2-xNixO2 (0 < x < 1.0) hexagonal nanosheets with different Co/Ni molar ratios via a facile coprecipitation process followed by calcination under an Ar atmosphere. Changing the Co/Ni molar ratios of the Co2-xNixO2 products is found to have a momentous influence on the microstructures, specific surface areas and electrocatalytic performances. At a Co/Ni molar ratio of 0.6, the Co1.4Ni0.6O2 nanosheet exhibits the largest specific surface area of 60.63 m2 g-1, the best OER with an onset overpotential of 278.5 mV, and HER of 72.8 mV as a bifunctional electrocatalyst. Meanwhile, the minimum Tafel slope is 113.6 mV dec-1 for OER and 77.4 mV dec-1 for HER. The Co1.4Ni0.6O2 nanosheet has excellent OER and HER activity at 0.1 mg cm-2 trace loading. Moreover, we construct an overall water splitting cell using the Co1.4Ni0.6O2 bifunctional electrocatalyst in a two-electrode system to further demonstrate the practical application, which needs a cell voltage of 1.75 V at a current density of 10 mA cm-2 and exhibits great long-term stability. These results provide an efficient strategy for the rational design of Co-based oxides towards bifunctional overall water electrocatalysts.

Effective Oxygen Reduction Reaction Performance of FeCo Alloys In Situ Anchored on Nitrogen-Doped Carbon by the Microwave-Assistant Carbon Bath Method and Subsequent Plasma Etching.

Electrocatalysts with strong stability and high electrocatalytic activity have received increasing interest for oxygen reduction reactions (ORRs) in the cathodes of energy storage and conversion devices, such as fuel cells and metal-air batteries. However, there are still several bottleneck problems concerning stability, efficiency, and cost, which prevent the development of ORR catalysts. Herein, we prepared bimetal FeCo alloy nanoparticles wrapped in Nitrogen (N)-doped graphitic carbon, using Co-Fe Prussian blue analogs (Co3[Fe(CN)6]2, Co-Fe PBA) by the microwave-assisted carbon bath method (MW-CBM) as a precursor, followed by dielectric barrier discharge (DBD) plasma treatment. This novel preparation strategy not only possessed a fast synthesis rate by MW-CBM, but also caused an increase in defect sites by DBD plasma treatment. It is believed that the co-existence of Fe/Co-N sites, rich active sites, core-shell structure, and FeCo alloys could jointly enhance the catalytic activity of ORRs. The obtained catalyst exhibited a positive half-wave potential of 0.88 V vs. reversible hydrogen electrode (RHE) and an onset potential of 0.95 V vs. RHE for ORRs. The catalyst showed a higher selectivity and long-term stability than Pt/C towards ORR in alkaline media.