Comparative Analysis of Anodized TiO[sub.2] Nanotubes and Hydrothermally Synthesized TiO[sub.2] Nanotubes: Morphological, Structural, and Photoelectrochemical Properties
This study presents a comparative analysis of anodization and hydrothermal techniques for synthesizing TiO[sub.2] nanotubes directly on titanium foil. It emphasizes its advantages as a substrate due to its superior conductivity and efficient charge transfer. Optimized synthesis conditions enable a t...
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Veröffentlicht in: | Materials 2024-11, Vol.17 (21) |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | This study presents a comparative analysis of anodization and hydrothermal techniques for synthesizing TiO[sub.2] nanotubes directly on titanium foil. It emphasizes its advantages as a substrate due to its superior conductivity and efficient charge transfer. Optimized synthesis conditions enable a thorough evaluation of the resulting nanotubes’ morphology, structure, and optical properties, ultimately assessing their photoelectrochemical and photocatalytic performances. Scanning electron microscopy (SEM) reveals differences in tube diameter and organization. An X-ray diffraction (XRD) analysis shows a dominant anatase (101) crystal phase in both methods, with the hydrothermally synthesized nanotubes exhibiting a biphase structure after annealing at 500 °C. UV–Vis and photoluminescence analyses indicate slight variations in band gaps (around 0.02 eV) and recombination rates. The anodized TiO[sub.2] nanotubes, exhibiting superior hydrophilicity and order, demonstrate significantly enhanced photocatalytic degradation of a model pollutant, amido black (80 vs. 78%), and achieve a 0.1% higher photoconversion efficiency compared to the hydrothermally synthesized tubes. This study underscores the potential advantages of the anodization method for photocatalytic applications, particularly by demonstrating the efficacy of direct TiO[sub.2] nanotube growth on titanium foil for efficient photocatalysis. |
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ISSN: | 1996-1944 1996-1944 |
DOI: | 10.3390/ma17215182 |