4.7 Article

Carbon-based heterostructure from multi-photo-active nanobuilding blocks SrTiO3@NiFe2O4@Fe0@Ni0@CNTs with derived nanoreaction metallic clusters for enhanced solar light-driven photodegradation of harmful antibiotics

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APPLIED SURFACE SCIENCE
卷 622, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.apsusc.2023.156987

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Carbon nanotubes; Chemical vapor deposition; SrTiO3; Synchrotron XAS Zero-valent metals

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We reported the development of a high-operative photocatalyst with improved charge trapping characteristics for enhanced solar light-driven photocatalytic degradation. The synthesized samples were investigated using various characterization techniques to understand their structural, morphological, optical, and electronic properties. The fibrous photocatalyst achieved a high-to-total degradation of tetracycline antibiotic under visible light irradiation, demonstrating its potential for efficient pollutant removal.
We reported on the sequential development of a high-operative photocatalyst with penta-component inorganic bulk heterojunction for improved charge trapping characteristics at particle-particle interfaces for enhanced solar light-driven photocatalytic degradation of active tetracycline antibiotic. Structural, morphological, optical, and electronic properties of the synthesized samples were investigated using a series of complementary char-acterization techniques, such as XRD, FE-SEM, HR-TEM, XPS, as well as hard and soft XAS in both total electron yield (TEY) and fluorescence yield (TFY). For the case of the carbon composite material, SrTiO3@NiFe2O4@-Fe0@Ni0@CNTs, a reduced crystallinity when compared to the starting support material was noticed, although this translated into a significant improvement of the morphology and the photocatalytic performance. The SrTiO3@NiFe2O4@Fe0@Ni0@CNTs fibrous photocatalyst can efficiently achieve a high-to-total degradation of tetracycline antibiotic under visible light irradiation in less than two hours, following a non-linear PFO kinetic model with an apparent reaction rate of about 0.0606 min-1 and an 98% photodegradation activity. The XPS and XAS analysis demonstrated unequivocally the appearance of nanoscale zero-valent iron (Fe0) and zero-valent nickel (Ni0) on the photocatalyst surface, which facilitates the separation of photogenerated e+ and h+ pairs, and the appearance of more active sites.

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