Z-scheme heterojunction Cu2O/CuO/C with broad-spectrum light absorption as efficient photocatalytst for hydrogen evolution
摘要
Photocatalytic water splitting has emerged as a pivotal strategy to tackle global energy crises and environmental degradation by producing clean hydrogen. In this study, a novel Cu2O/CuO/C composite photocatalyst was prepared from cupric nitrate trihydrate and 1,3,5-benzenetricarboxylic acid via the two-step solvothermal-calcination method as the photocatalyst for hydrogen evolution. Advanced characterization techniques, including X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), ultraviolet–visible diffuse reflectance spectroscopy (UV–Vis DRS), transient photocurrent responses, electrochemical impedance spectroscopy (EIS), linear sweep voltammetry (LSV), and Mott-Schottky test, confirmed the composite's excellent visible and near-infrared light absorption and Z-scheme heterojunction architecture. Its remarkable performance originates from the effective p-n heterojunction formed between Cu2O and CuO. Upon a 300 W xenon lamp (350 < λ < 780 nm) illumination, photogenerated electrons and holes are produced in Cu2O and CuO, respectively. Electrons from the conduction band (CB) of CuO migrate to the valence band (VB) of Cu2O, recombining with holes. This mechanism not only enhances charge separation and extends carrier lifetime but also preserves the strong reducing capability of Cu2O, significantly boosting photocatalytic activity. The composite achieved a hydrogen production rate of 511.07 μmol/(g h). Notably, it retained stable performance over three consecutive cycles without significant activity loss, demonstrating robust durability. These findings highlight the potential of Cu2O/CuO/C Z-scheme heterojunctions as efficient, stable photocatalysts for sustainable hydrogen evolution.