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Tunable structure-property engineering and visible-light photocatalytic performance of ZnO:TiO2 nanocomposites
Saliou Baïlo Diallo1, N Khlifi2, Modou Fall1
1Laboratory of Organic Physical Chemistry and Environmental Analyses, Department of Chemistry, Faculty of Sciences and Techniques, Cheikh Anta Diop University Dakar Senegal.
Abstract:
This study investigates the synthesis and characterization of (1 - x)ZnO:(x)TiO2 nanocomposites (x = 0.01 to 0.15) using the solid-state method. The structural properties are analyzed using X-ray diffraction (XRD). The XRD analysis reveals changes in phase composition, indicating TiO2-dependent structural modifications. At low content (x ≤ 0.05), Ti4+ ions dissolve substitutionally in the ZnO hexagonal structure. Beyond this threshold, the system reaches Ti saturation in ZnO and instead forms discrete Zn2TiO4 crystallites as a secondary phase. The crystallite size, estimated via the Debye-Scherrer model, decreases significantly from 50.8 nm to 44.5 nm with increasing TiO2 content, and reaches 22.2 nm for 3% TiO2 addition. Fourier transform infrared (FTIR) analysis likely confirms the Ti-doping of ZnO through the presence of Zn-O and Ti-O bonding. The band-gap energy was calculated using Tauc's model based on optical Reflectance data in the UV-Vis wavelength range. The direct band-gap transition exhibits a red-shift from 3.224 to 3.185 eV, while the indirect band-gap transition shows a more noticeable red-shift from 3.121 to 3.021 eV. The red-shift suggests band-gap narrowing, possibly due to defect states introduced by the Ti4+ cation. Furthermore, photocatalytic tests reveal that Ti-doping improves the methylene blue (MB) degradation efficiency under visible light. Notably, the ZnTi10% and ZnTi15% samples exhibit the highest degradation rates, reaching 87% with an apparent rate constant K app = 1.19 × 10-2 min-1, while pure ZnO and TiO2 remain more active under visible light. This can be related to defects or interfacial states induced by Ti-doping, which act as electron-hole recombination centers.
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