Photocatalytic characterization of TiO2 nanotubes with PD particles synthesized by photoreduction process

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Abstract

To decompose dye in aqueous solution, Pd nanoparticle-decorated TiO2 nanotube photocatalysts were fabricated through electrochemical anodization and photoreduction processes. Morphological and surface characterization of the TiO2/Pd heterojunction photocatalyst, as well as photoelectrochemical behaviors, were investigated by X-ray diffraction, UV/Vis diffuse reflectance and photocurrent response. It was found that the precipitated Pd particle size and distribution on TiO2 surface were affected by the photoreduction time. As the photoreduction time increased from 10 min to 180 min, the corresponding average diameter of the precipitated Pd particles on TiO2 photocatalyst increased from 4.35 nm to 9.29 nm. From the Aniline blue degradation results, the Pd decorated TiO2 catalysts enhanced photocatalytic activity compared to bare TiO2 catalyst, and the rate constant for dye degradation was dependent on the Pd particle size on the TiO2 surface. For an average Pd particle size lower than 7.80 nm, the particles were uniformly precipitated on the surface of the TiO2 nanotubes, and the dye degradation rate constants increased with increasing Pd particle size. However, for an average Pd particle size of more than 7.80 nm, the particles were agglomerated on the TiO2 surface, and the dye degradation rate constants gradually decreased. With an optimum Pd particle size of 7.80 nm, the TiO2/Pd photocatalyst showed higher photocatalytic activity and Aniline blue degradation rate, due to high photo absorbance response, and more efficient charge separation through electron transfer from the conduction band of the TiO2 to the Pd particles.

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Lee, J. H., Ahn, H. J., Youn, J. I., Kim, Y. J., Suh, S. J., & Oh, H. J. (2019). Photocatalytic characterization of TiO2 nanotubes with PD particles synthesized by photoreduction process. Journal of Korean Institute of Metals and Materials, 57(8), 510–520. https://doi.org/10.3365/KJMM.2019.57.8.510

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