In this study, we are reporting for the first time the utilization of Solanum tuberosum tuber-driven, starch-mediated, green-hydrothermally synthesized cerium oxide nanoparticles (G-CeO NPs) for the antibacterial activity and photodegradation of cationic (methylene blue, MB) and anionic (methyl orange, MO) dyes separately and in combination, aimed at environmental remediation. The XRD analysis confirms the fluorite structure of G-CeO NPs, displaying an average crystallite size of 9.6 nm. Further, XPS confirms the existence of 24% of Ce oxidation states within G-CeO NPs. Morphological studies through FE-SEM and TEM reveal that starch-driven OH ion production leads to a high percentage of active crystal facets, favoring the formation of Ce-rich CeO NPs. Photocatalytic experiments conducted under UV-A illumination demonstrate the superior degradation performance of G-CeO NPs, with MB degradation reaching 93.4% and MO degradation at 77.2% within 90 min. This outstanding catalytic activity is attributed to the mesoporous structure (pore diameter of 5.63 nm) with a narrow band gap, a large surface area (103.38 mg), and reduced charge recombination, as validated by BET, UV-visible, and electrochemical investigations. The identification of photogenerated intermediates is achieved through LCMS, while the mineralization is monitored via total organic carbon analysis. Moreover, the scavenging experiments point towards the involvement of reactive oxygen species in organic oxidation, demonstrating efficiency over five consecutive trials. Additionally, G-CeO NPs exhibit potent antibacterial activity against both gram-positive and gram-negative bacteria. This study presents an innovative, and efficient approach to environmental remediation, shedding light on the potential of G-CeO NPs in addressing environmental pollution challenges.
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http://dx.doi.org/10.1016/j.chemosphere.2024.141418 | DOI Listing |
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