Phosphide-Based Electrocatalysts for Urea Electrolysis: Recent Trends and Progress.

Electrolysis is a trend in producing hydrogen as a fuel for renewable energy development, and urea electrolysis is considered as one of the advanced electrolysis processes, where efficient materials still need to be explored. Notably, urea electrolysis came into existence to counter-part the electrode reactions in water electrolysis, which has hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). Among those reactions, OER is sluggish and limits water splitting. Hence, urea electrolysis emerged with urea oxidation reaction (UOR) and HER as their reactions to tackle the water electrolysis. Among the explored materials, noble-metal catalysts are efficient, but their cost and scarcity limit the scaling-up of the Urea electrolysis. Hence, current challenges must be addressed, and novel efficient electrocatalysts are to be implemented to commercialize urea electrolysis technology. Phosphides, as an efficient UOR electrocatalyst, have gained huge attention due to their exceptional lattice structure geometry. The phosphide group benefits the water molecule adsorption and water dissociation, and facilitates the oxyhydrate of the metal site. This review summarizes recent trends in phosphide-based electrocatalysts for urea electrolysis, discusses synthesis strategies and crystal structure relationship with catalytic activity, and presents the challenges of phosphide electrocatalysts in urea electrolysis.

Anchoring Polydopamine on ZnCo2 O4 Nanowire To Facilitate Urea Water Electrolysis.

To overcome the sluggishness of the oxygen evolution reaction (OER), the urea oxidation reaction was developed. In the case of OER application studies ZnCo2 O4 is an excellent electrocatalyst, towards the UOR has been performed with surface-grown polydopamine (PDA) with surface-grown polydopamine (PDA). ZnCo2 O4 @PDA is produced over the surface of nickel foam by a hydrothermal method followed by self-polymerization of dopamine hydrochloride. Dopamine hydrochloride was varied in solution to study the optimal growth of PDA necessary to enhance the electrochemical activity. Prepared ZnCo2 O4 @PDA was characterized by X-ray diffraction, electronic structural, and morphology/microstructure studies. With successful confirmation, the developed electrode material was applied to UOR and ZnCo2 O4 @PDA-1.5, delivering an excellent low overpotential of 80 mV at 20 mA cm-2 in the electrolyte mixture of 1 M potassium hydroxide+0.33 M urea. To support the excellent UOR activity, other electrochemical properties such as the Tafel slope, electrochemical surface active sites, and electrochemical impedance spectroscopy were also studied. Furthermore, a schematic illustration explaining the UOR mechanism is shown to allow a clear understanding of the obtained electrochemical activity. Finally, urea water electrolysis was carried out in a two-electrode symmetrical cell and compared with water electrolysis. This clearly showed the potential of the developed material for efficient electrochemical hydrogen production.