A Visible Light-Driven α-MnO 2 /UiO-66-NH 2 S-Scheme Photocatalyst toward Ameliorated Oxy-TCH Degradation and H 2 Evolution.

Photocatalytic hydrogen production and pollutant degradation using a heterogeneous photocatalyst remains an alternative route for mitigating the impending pollution and energy crisis. Hence, the development of cost-effective and environmentally friendly semiconducting materials with high solar light captivation nature is imperative. To overcome this challenge, α-MnO 2 nanorod (NR)-modified MOF UiO-66-NH 2 (UNH) was prepared via a facile solvothermal method, which is efficient toward H 2 evolution and oxy-tetracycline hydrochloride (O-TCH) degradation. The field-emission scanning electron microscopy (FESEM) and high-resolution transmission electron microscopy (HR-TEM) results of the α-MnO 2 @UNH (MnU) hybrid reveals its nanorod embedded in MOF matrix, and the X-ray photoelectron spectroscopy (XPS) result confirms the interaction of UNH moiety with α-MnO 2 NRs. Additionally, the outstanding separation of photogenerated excitons and the charge-transfer efficacy are further validated by photoluminescence (PL), time-resolved photoluminescence (TRPL), electrochemical impedance spectroscopy (EIS), and transient photocurrent analysis, which are the key causes for photoactivity augmentation in the MnU composites. The MnU-2 composite shows a superior O-TCH degradation efficiency of 93.23% and an excellent H 2 production rate of about 410.6 μmol h -1 upon light irradiation. This study provides significant evidence in favor of the suggested mediator-free S-scheme-adapted charge migration path, and it effectively explains the enhanced exciton separation leading to extraordinary catalytic efficiency of the proposed composite.