Enhanced hydrogen production via urea electrolysis over Ni-NiO electrodeposited on Ti mesh.

The sluggish kinetics of anodic oxygen evolution reaction (OER) is regarded as the main bottleneck for ineffective hydrogen production efficiency, limiting the industrial application of electrochemical water splitting. Substituting the OER by urea electrooxidation reaction (UOR) and simultaneously developing highly active and economical bifunctional electrocatalyst for UOR and hydrogen evolution reaction (HER) is a promising method to realize energy-saving hydrogen production and urea-rich wastewater abatement. Herein, self-supporting Ni-NiO film grown on Ti mesh (Ni-NiO/TM) was successfully prepared by a facile cathodic electrodeposition method with using nickel acetate as the only raw material. Electrodeposition process was optimized by modulating the electrodeposition time and potential. x-ray diffraction, scanning electron microscopy, transmission electron microscopy, x-ray photoelectron spectroscopy and Raman characterization revealed the optimized Ni-NiO/TM was comprised of crystalline Ni and amorphous NiO and its morphology exhibited nanosphere structure, assembled by nanosheets. Ni-NiO/TM sample prepared under the potential of -1.5 V and deposition time of 10 min illustrated the lowest UOR potential of 1.34 V at 50 mA cmand robust stability, superior to the recently reported literatures. Furthermore, the HER potential was only -0.235 V to drive the current density of 50 mA cm. The cell voltage of urea-assisted electrolysis for hydrogen production in Ni-NiO/TM||Ni-NiO/TM two-electrode system only required 1.56 V to deliver 50 mA cm, obviously lower than that (>1.72 V) for overall water splitting. This work demonstrated the potential of Ni-based material as bifunctional electrocatalyst for energy-saving Hproduction by urea-rich wastewater electrolysis.