Abstract

To overcome the global challenges of energy crises and environmental threats, urea oxidation is a hopeful route to utilize urea-rich wastewater as an energy source for hydrogen production. Herein, we report an inorganic/organic type of nano-heterostructure (NHs–Ni-TiO2/p-NDIHBT) as a photoanode with excellent urea oxidation efficiency driven by visible light. This heterostructured photoanode consists of nickel (Ni)-doped TiO2 nanorods (NRs) arrays as an inorganic part and a D-A-D type organic polymer i.e p-NDIHBT as an organic part. The as-prepared photoanode was characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). The morphological studies of TEM confirm the coating of p-NDIHBT on Ni–TiO2 NPs (∼1 μm). The consequence of heterostructure formation on optical and photoelectrochemical (PEC) properties of photoanode were explored through photoelectrochemical responses under visible light irradiation. The photoelectrochemical activity of Ni–TiO2 and Ni–TiO2/p-NDIHBT photoanode from linear sweep voltammetry (LSV) shows the ultrahigh photocurrent density of 0.36 mA/cm2 and 2.21 mA/cm2, respectively measured at 1.965 VRHE. Electrochemical impedance spectroscopy (EIS) of both photoanodes shows a highly sensitive nature toward the urea oxidation reaction. The hybrid photoanode also exhibits high photostability, good solar-to-hydrogen conversion efficiency, and high faradaic efficiency for urea oxidation.

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