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ZnCo2O4/g-C3N4/Cu nanocomposite as a new efficient and recyclable heterogeneous photocatalyst with enhanced photocatalytic activity towards the metronidazole degradation under the solar light irradiation

光催化 降级(电信) 纳米复合材料 材料科学 X射线光电子能谱 激进的 猝灭(荧光) 可见光谱 辐照 化学工程 带隙 光化学 核化学
作者
Roya Jahanshahi,Alieh Mohammadi,Mohammadreza Doosti,Sara Sobhani,José Miguel Sansano
出处
期刊:Environmental Science and Pollution Research [Springer Nature]
标识
DOI:10.1007/s11356-022-19969-3
摘要

In this study, ZnCo2O4/g-C3N4/Cu is synthesized as a new and highly effectual solar light-driven heterogeneous photocatalyst. The prepared photocatalyst is characterized using FT-IR, XRD, XPS, DRS, FESEM, TEM, EDS, and elemental mapping techniques. The performance of ZnCo2O4/g-C3N4/Cu is studied towards the metronidazole (MNZ) degradation under solar light irradiation. The kinetics of MNZ degradation and efficacy of the operational parameters comprising the initial MNZ amount (10-30 mg L-1), photocatalyst dosage (0.005-0.05 g L-1), pH (3-11), and contact time (5-30 min) on the MNZ degradation process are investigated. Surprisingly, the ZnCo2O4/g-C3N4/Cu nanocomposite presents a privileged photocatalytic performance towards the MNZ degradation under solar light irradiation. The enhanced photocatalytic activity of this photocatalyst can be ascribed to the synergistic optical effects of ZnCo2O4, g-C3N4, and Cu. The value of band gap energy for ZnCo2O4/g-C3N4/Cu is estimated to be 2.3 eV based on the Tauc plot of (αhν)2 vs. hν. The radical quenching experiments confirm that the superoxide radicals and holes are the principal active species in the photocatalytic degradation of MNZ, whereas the hydroxyl radicals have no major role in such degradation. The as-prepared photocatalyst is simply isolated and recycled for at least eight runs without noticeable loss of the efficiency. Using the natural sunlight source, applying a very low amount of the photocatalyst, neutrality of the reaction medium, short reaction time, high efficiency of the degradation procedure, utilizing air as the oxidant, low operational costs, and easy to recover and reuse of the photocatalyst are the significant highlights of the present method. It is supposed that the current investigation can be a step forward in the representation of an efficacious photocatalytic system in the treatment of a wide range of contaminated aquatic environments.
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