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Updated: May 8, 2026

A Complete Method for Evaluating the Performance of Photocatalysts for the Degradation of Antibiotics in Environmental Remediation
Published on: October 6, 2022
Designing 3D-Printed TiO2/BiFeO3-Hybrid Materials for Enhanced Photocatalytic Degradation of Acyclovir via Visible
Roshanak Mohammadi Siahboomi1, Stephane Kenmoe2, Dick H Douma3
1Organic Chemistry and Center for Nanointegration Duisburg-Essen (CENIDE), University of Duisburg-Essen, Essen 45141, Germany.
Abstract:
3D-printed porous TiO2/BiFeO3 nanocomposite monoliths with surface areas of up to 65 m2 g-1 were fabricated via two ways employing 3D printing. In method A, BiFeO3 nanoparticles were directly embedded into a TiO2-based hybrid ink for the direct ink writing (DIW) technique, while in method B, BiFeO3 nanoparticles were deposited as a surface coating onto a 3D-printed TiO2 scaffold. The obtained materials were comprehensively characterized by X-ray diffraction (XRD), electron microscopy (SEM, TEM), nitrogen adsorption-desorption, UV-vis spectroscopy, photoluminescence spectroscopy, and X-ray photoelectron spectroscopy (XPS). The photocatalytic performance of the materials was evaluated for the degradation of acyclovir under three different irradiation conditions: a medium-pressure Hg lamp (emission mostly in the UV region, 150 W) and blue LED sources at 420 nm (6 W) and 440 nm (40 W). The sample prepared by method A, including 1 wt % BiFeO3 inside a TiO2 matrix, showed the best performance under all irradiation conditions, which could be attributed to the combination of high surface area and the improved charge separation across the heterojunction interface. Additionally, Density Functional Theory (DFT) calculations were performed to confirm the formation of type-II heterojunctions between BiFeO3 embedded in TiO2 materials, consistent with the experimentally observed enhancement. These 3D-printed materials represent a significant advancement toward the development of photocatalytic water treatment under visible light conditions.

