Facile aqueous synthesis and comparative evaluation of TiO2-semiconductor and TiO2-metal nanohybrid photocatalysts in antibiotics degradation under visible light

简便的水相合成及 TiO2-半导体和 TiO2-金属纳米杂化光催化剂在可见光下降解抗生素的比较评价

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作者:Yuping Zhang, Shijie Ju, Gregori Casals, Jie Tang, Yichao Lin, Xiaofang Li, Lihua Liang, Zhiyu Jia, Muling Zeng, Eudald Casals

Abstract

Advanced oxidation processes using TiO2-based nanomaterials are sustainable technologies that hold great promise for the degradation of many types of pollutants including pharmaceutical residues. A wide variety of heterostructures coupling TiO2 with visible-light active nanomaterials have been explored to shift its photocatalytic properties to harness sun irradiation but a systematic comparison between them is lacking in the current literature. Furthermore, the high number of proposed nanostructures with different size, morphology, and surface area, and the often complex synthesis processes hamper the transition of these materials into commercial and effective solutions for environmental remediation. Herein, we have designed a facile and cost-effective method to synthesize two heterostructured photocatalysts representative of two main families of novel structures proposed, hybrids of TiO2 with metal (Au) and semiconductor (CeO2) nanomaterials. The photocatalysts have been extensively characterized to ensure a good comparability in terms of co-catalyst doping characteristics, morphology and surface area. The photocatalytic degradation of ciprofloxacin and sulfamethoxazole as target pollutants, two antibiotics of high concern polluting water sources, has been evaluated and CeO2/TiO2 exhibited the highest activity, achieving complete antibiotic degradation at very low photocatalyst concentrations. Our study provides new insights into the development of inexpensive heterostructured photocatalysts and suggests that the non-stoichiometry and characteristic d and f electronic orbital configuration of CeO2 have a significantly improved role in the enhancement of the photocatalytic reaction.

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