Abstract
Developing a photocatalysis-based system is an effective strategy for removing antibiotics. Herein, La-doped NiAl-layered double hydroxides (LaNiAl-LDH) photocatalyst was synthesized using a chemical co-precipitation-hydrothermal method. The prepared samples were characterized by various advanced analyses and investigated for the photocatalytic degradation of tetracycline (TC). The crystalline phase and functional groups of the synthesized samples were successfully confirmed by XRD and FTIR analyses. By doping La into NiAl-LDH structure, the band gap was reduced from 3.01 eV to 2.57 eV, indicating higher photocatalytic activity of 1% LaNiAl-LDH. The surface morphology of the synthesized samples shows the formation of nanosheets in the structure of LDH. Under the optimum status ([TC]0 = 10 mg/L, [1% LaNiAl-LDH] = 0.2 g/L, and pH = 6), the photocatalytic activity of 1% LaNiAl-LDH (84.85%) was higher than NiAl-LDH (71.52%) within 90 min reaction. This difference can be attributed to the presence of La sites in 1% LaNiAl-LDH which act as electron-transfer mediators, leading to a significant improvement in the separation of photogenerated charge carriers. The effect of the addition of various scavengers was evaluated. Moreover, using the o-phenylenediamine (OPD), and photoluminescence (PL) analysis, the formation of •OH radicals was supported. The higher charge-transfer efficiency of 1% LaNiAl-LDH was confirmed by photoelectrochemical analysis. Furthermore, the reusability, stability, and degradation pathway of the as-synthesized nanocomposite were systematically examined. This work presents guidance for applying doped LDH-based materials in photocatalysis and promising applications in wastewater remediation.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.