Synthesis of diverse titanium dioxide (TiO2) nanostructures for enhanced photocatalytic degradation and supercapacitor performance

In this investigation, we employed a straightforward hydrothermal method to synthesize various TiO 2 nanostructures, including titanium nanoparticles (TNPs), titanium nanorods (TNRs), and titanium nanotubes (TNTs). Generally, TiO 2 is a widely studied chemical compound in the materials research fiel...

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Veröffentlicht in:Journal of solid state electrochemistry 2024-07, Vol.28 (7), p.2035-2045
Hauptverfasser: Arla, Sai Kumar, Godlaveeti, Sreenivasa Kumar, Sana, Siva Sankar, Jwuiyad, Ahmad, Konidena, Naga Sathya Sai, Boya, Vijaya Kumar Naidu
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Sprache:eng
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Zusammenfassung:In this investigation, we employed a straightforward hydrothermal method to synthesize various TiO 2 nanostructures, including titanium nanoparticles (TNPs), titanium nanorods (TNRs), and titanium nanotubes (TNTs). Generally, TiO 2 is a widely studied chemical compound in the materials research field, which finds applications in diverse areas such as photocatalysis and energy storage systems. Furthermore, these nanostructures hold immense potential for applications in dye degradation and supercapacitors. To characterize the synthesized photocatalysts, we employed techniques such as XRD, DLS, UV–Vis spectra, SEM, TEM, and electrochemical workstation. The as-synthesized photocatalysts demonstrated remarkable efficiency in degrading different concentrations of rhodamine B (RhB) and methyl orange (MO) dyes under direct sunlight while also exhibiting excellent electrochemical properties. For comparison, we included bulk TiO 2 anatase powder in our study. In the case of supercapacitor application, TNRs exhibited the highest specific capacitance of 122 F g −1 at a current density of 0.5 A g −1 , outperforming the 0-dimensional (0D) nanostructures and bulk TiO 2 powder (TBP). Our results indicate that the 1-dimensional (1D) TiO 2 nanostructures offer superior performance under optimal experimental conditions compared to the other forms of TiO 2 .
ISSN:1432-8488
1433-0768
DOI:10.1007/s10008-023-05720-6