Electrodeposited Pd/TiO2 Nanotube Arrays with Size-Controlled Pd for High-Performance UV and Visible-Light Photocatalytic Water Remediation

Environmental contamination by persistent industrial dyes such as Amido Black demands highly efficient photocatalysts for advanced water treatment. Structural, chemical, and optical strategies based on TiO2 nanotube engineering are widely explored for this purpose. In this work, highly ordered TiO2 nanotube arrays were fabricated by electrochemical anodization and subsequently decorated with Pd nanoparticles via potentiostatic electrodeposition (10–300 s), enabling precise control of Pd nanoparticle size and loading. The resulting materials were systematically characterized by SEM, TEM, XRD, XPS, UV–vis DRS, and PL spectroscopy, and their properties were correlated with the photocatalytic degradation of Amido Black under both UV and visible light irradiation. The study reveals a clear size-dependent duality in the role of Pd. For intermediate Pd nanoparticles (≈9 nm, 20 s), Pd behaves predominantly as an electron sink, forming an efficient Schottky junction with anatase TiO2 that markedly suppresses charge carrier recombination. This configuration yields ≈ 97% Amido Black removal after 120 min of UV irradiation, with an apparent rate constant about three times higher than that of bare TiO2 nanotubes. In contrast, for ultra-small Pd nanoparticles (≈6 nm, 10 s), interfacial defect states sensitize TiO2 to visible light, enabling ≈ 65% degradation after 270 min and a rate constant roughly four times higher than that of undecorated nanotubes under visible illumination. At long deposition times (≥150 s), Pd agglomeration leads to enhanced photoluminescence and markedly reduced photocatalytic activity, indicating increased recombination and less effective utilization of photogenerated charges. This provides a practical design rule to rationally tailor Pd–TiO2 nanotube photocatalysts for targeted UV or visible light applications in dye removal and broader environmental remediation scenarios

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Publication Details

Journal
Catalysts
Published
2026-04-14
DOI
https://doi.org/10.3390/catal16040350
Primary Topic
TiO2 Photocatalysis and Solar Cells
Type
article
Field-Weighted Citation Impact
0.00

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article

Electrodeposited Pd/TiO2 Nanotube Arrays with Size-Controlled Pd for High-Performance UV and Visible-Light Photocatalytic Water Remediation

Syrine Sassi, Amal Bouich, Bernabé Marí Soucase, Hafedh Dhiflaoui et al.
Catalysts
TiO2 Photocatalysis and Solar Cells
article

Electrodeposited Pd/TiO2 Nanotube Arrays with Size-Controlled Pd for High-Performance UV and Visible-Light Photocatalytic Water Remediation

Syrine Sassi, Amal Bouich, Bernabé Marí Soucase, Hafedh Dhiflaoui, Farid Fadhillah, R. Benabderrahmane Zaghouani, Jie Zhang, Amine Aymen Assadi, Ayda Mehdaoui, Anouar Hajjaji, Lofti Khezami
article en

Abstract

Environmental contamination by persistent industrial dyes such as Amido Black demands highly efficient photocatalysts for advanced water treatment. Structural, chemical, and optical strategies based on TiO2 nanotube engineering are widely explored for this purpose. In this work, highly ordered TiO2 nanotube arrays were fabricated by electrochemical anodization and subsequently decorated with Pd nanoparticles via potentiostatic electrodeposition (10–300 s), enabling precise control of Pd nanoparticle size and loading. The resulting materials were systematically characterized by SEM, TEM, XRD, XPS, UV–vis DRS, and PL spectroscopy, and their properties were correlated with the photocatalytic degradation of Amido Black under both UV and visible light irradiation. The study reveals a clear size-dependent duality in the role of Pd. For intermediate Pd nanoparticles (≈9 nm, 20 s), Pd behaves predominantly as an electron sink, forming an efficient Schottky junction with anatase TiO2 that markedly suppresses charge carrier recombination. This configuration yields ≈ 97% Amido Black removal after 120 min of UV irradiation, with an apparent rate constant about three times higher than that of bare TiO2 nanotubes. In contrast, for ultra-small Pd nanoparticles (≈6 nm, 10 s), interfacial defect states sensitize TiO2 to visible light, enabling ≈ 65% degradation after 270 min and a rate constant roughly four times higher than that of undecorated nanotubes under visible illumination. At long deposition times (≥150 s), Pd agglomeration leads to enhanced photoluminescence and markedly reduced photocatalytic activity, indicating increased recombination and less effective utilization of photogenerated charges. This provides a practical design rule to rationally tailor Pd–TiO2 nanotube photocatalysts for targeted UV or visible light applications in dye removal and broader environmental remediation scenarios

CatalystsVol. 16(4)
Tunis University (TN), Imam Mohammad ibn Saud Islamic University (SA), Université Ibn-Tofail (MA), Research and Technology Center of Energy (TN), Universitat Politècnica de València (ES), Tunis El Manar University (TN), Newcastle University (GB)
Al-Imam Muhammad Ibn Saud Islamic University
Clean water and sanitation
Openalex Percentile: Top 25%
TiO2 Photocatalysis and Solar Cells
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