Anodic Fabrication of Ti-Nb-Zr-O Nanotube Arrays

Liu, Qiang; Ding, Dongyan; Ning, Congqin

doi:https://doi.org/10.1155/2014/240346

Journal of Nanomaterials

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Nanoceramics: Synthesis, Characterization, and Applications

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Research Article | Open Access

Volume 2014 | Article ID 240346 | https://doi.org/10.1155/2014/240346

Anodic Fabrication of Ti-Nb-Zr-O Nanotube Arrays

Qiang Liu,¹Dongyan Ding,¹and Congqin Ning²

Academic Editor: Amirkianoosh Kiani

Received14 Dec 2013

Revised01 Mar 2014

Accepted01 Mar 2014

Published27 Mar 2014

Abstract

Highly ordered Ti-Nb-Zr-O nanotube arrays were fabricated through pulse anodic oxidation of Ti-Nb-Zr alloy in 1 M NaH₂PO₄ containing 0.5 wt% HF electrolytes. The effect of anodization parameters and Zr content on the microstructure and composition of Ti-Nb-Zr-O nanotubes was investigated using a scanning electron microscope equipped with energy dispersive X-ray analysis. It was found that length of the Ti-Nb-Zr-O nanotubes increased with increase of Zr contents. The diameter and the length of Ti-Nb-Zr-O nanotubes could be controlled by pulse voltage. XRD analysis of Ti-Nb-Zr-O samples annealed at 500°C in air indicated that the (101) diffraction peaks shifted from 25.78° to 25.05° for annealed Ti-Nb-Zr-O samples with different Zr contents because of larger lattice parameter of Ti-Nb-Zr-O compared to that of undoped TiO₂.

1. Introduction

Nanostructures of different metals or semiconductors have received much attention due to the wide application of these materials in photocatalysts, solar energy conversion, gas sensing, and biomedical applications [1–4]. TiO₂ nanotubes have been widely investigated due to their excellent biomedical application and photocatalytic effect since 1972 [5]. However, TiO₂ can be only excited by UV light which only occupies 5% of the solar spectrum because of its wide band gap (3.2 eV). Therefore, many approaches were used to extend the spectral response of the titanium dioxide to the visible light region and impurity doping is one of the typical and effective approaches. Many metal elements (Fe, Mo, Cr, Nb, etc.) and nonmetal elements (B, C, N, S, and F) have been used to dope TiO₂ to broaden its application fields [6–8]. Zr and Nb doping could affect the optical absorption ability of TiO₂ oxide. Hirano et al. reported that the onset of absorption of TiO₂ shifted to longer wavelengths by Zr and Nb doping [9, 10].

One-dimensional nanostructures have advantages over films and powder because the former can provide large surface-to-volume ratio and unidirectional electrical channel. Several research groups have reported the anodic formation of oxide nanostructures on the surfaces of titanium alloys to achieve good photocatalysts, solar energy conversion, gas sensing, and biomedical applications. Numerous methods have been reported for fabricating TiO₂ nanotubes including template-assisted process [11], hydrothermal reaction [12], seed growth [13], and anodization methods [14].

Anodic oxidation technique is relatively a simple method to fabricate one-dimensional nanotubes in comparison with other methods. Allam et al. reported the fabrication of Ti-Pd mixed oxynitride nanotube arrays through anodization of Ti-Pd alloy [15]. Berger et al. reported on the fabrication of Ti-Al-O nanotubes through anodization of Ti-Al alloys [16]. Nb- and Zr-doped TiO₂ nanotubes were also investigated recently. Liu et al. fabricated Ti-Nb-O nanotubes on Ti35Nb alloy and found that Nb-doped TiO₂ nanostructures had excellent hydrogen sensing capability [17]. Allam et al. fabricated Ti-Nb-Zr-O nanotubes through anodization of Ti35Nb5Zr alloy for enhanced hydrogen generation by water photoelectrolysis [18]. Li et al. found that the Nb- and Zr-doped TiO₂ nanostructures showed good biological properties [19].

To date, rare work has been reported on the effect of Zr content on the formation of Ti-Nb-Zr-O nanotubes. In the present work, we fabricated highly ordered Ti-Nb-Zr-O nanotube arrays on Ti-Nb-Zr alloy substrate with different Zr contents by pulse anodic oxidation. The effect of Zr content and anodization parameters on the microstructures of Ti-Nb-Zr-O oxides was investigated.

2. Experiment Section

2.1. Synthesis of Ti-Nb-Zr-O Nanotubes

Prior to anodization, all of the Ti-Nb-Zr alloy samples (Ti35Nb5Zr, Ti35Nb10Zr, Ti35Nb15Zr) were ground and polished with number 2000 SiC emery papers and then ultrasonically cleaned with absolute alcohol. Finally, they were rinsed with deionized water and dried in N₂ stream. Electrochemical anodization was carried out with a pulse voltage stabilizer. Anodic samples were fabricated with pulse voltages of 20 V, 30 V, and 40 V with a constant frequency of 4000 Hz and duty cycle of 20% for 90 minutes in electrolytes of 1 M NaH₂PO₄ containing 0.5 wt% HF. The pulse frequency varied from 2000 Hz to 4000 Hz. The effects of anodization voltage and pulse frequency on the microstructures and composition of Ti-Nb-Zr-O samples with different Zr contents were investigated.

2.2. Microstructural Characterization

The structure morphology and composition of Ti-Nb-Zr-O samples were investigated using a scanning electron microscope (SEM; FEI SIRION 200, USA) equipped with energy dispersive X-ray analysis (EDXA; OXFORD INCA, USA). The as-anodized Ti-Nb-Zr-O samples grown on different Ti-Nb-Zr alloy substrates were annealed at 500°C in air. Phase structures of the as-annealed Ti-Nb-Zr-O samples were characterized with X-ray diffraction (XRD, D/max 2550 V). For reference, undoped TiO₂ nanotubes were also fabricated through anodization of pure Ti substrate.

3. Results and Discussion

Figure 1 shows top and cross-section views of Ti-Nb-Zr-O nanotubes grown on Ti35Nb5Zr alloy substrate at different voltages. The oxide sample prepared at 20 V showed a web-like structure rather than a nanotubular array morphology. When the anodization voltage increased to 30 V, the nanotube arrays could form. The average diameter and length of the nanotubes were 170 nm and 4.75 μm, respectively. When the anodization voltage increased to 40 V, the average diameter and length of the nanotubes were 220 nm and 4.8 μm, respectively. The slight increase in length from about 4.75 μm to 4.8μm was attributed to a competition between an electrochemical oxide formation and chemical dissolution of oxide by fluoride ions. The formation rate of the nanotube bottom and the dissolution rate of the nanotube top at an anodization voltage of 30 V were almost equivalent. Therefore, the length of the nanotubes almost remained unchanged when the anodization voltage increased to 40 V.

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Figure 2 shows top and cross-section views of Ti-Nb-Zr-O nanotubes grown on Ti35Nb10Zr alloy substrate at different voltages. When the anodization voltage was 20 V, the as-grown Ti-Nb-Zr-O nanotube arrays had a clear nanotubular morphology. When the anodization voltage increased to 30 V, the average diameter and length were 150 nm and 5.25 μm, respectively. At 40 V, Ti-Nb-Zr-O nanotube arrays grown on the Ti35Nb10Zr alloy substrate had an average diameter of 206 nm and average length of 6.12 μm. The diameter was slightly smaller than that of the nanotubes grown on Ti35Nb5Zr alloy substrate.

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Figure 3 shows top and cross-section views of Ti-Nb-Zr-O nanotubes grown on Ti35Nb15Zr alloy substrate at different voltages. The average length of the Ti-Nb-Zr-O nanotubes was 8.13 μm when the anodic voltage was 40 V. Summary of the nanotube length and diameter of the three kinds of nanotubes is shown in Table 1.

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During the anodization process, many factors such as oxidation electrolyte, anodization voltage, and time could affect the formation of Ti-Nb-Zr-O nanotubes. There is a competition between the electrochemical oxide formation and chemical dissolution of oxide by fluoride ions. The nanotube growth could reach a steady state in which the formation rate at the bottom and dissolution rate at the top are equal [20]. The growth of Ti-Nb-Zr-O nanotubes remarkably depended on local electric field and solution diffusion rate and took place preferentially at some locations on the Ti-Nb-Zr alloy substrate. The anodic formation mechanism of the Ti-Nb-Zr-O nanotubes can be represented as follows [21, 22]:

At first, oxidized metal species react with O²⁻ ions (from H₂O) to form an oxide layer growth on the metal surface. In contrast, due to the presence of F⁻ ions, dissolution and breakdown of oxide layer occur along random path through this layer and form disordered wormlike structure. The oxide layer will be finally removed by chemical dissolution and water-soluble [XF₆]²⁻ or [NbF₇]²⁻ formed, making the underneath highly ordered tube structure observable from the top. Meanwhile, oxidized metal species could react with O²⁻ ions to form a new oxide layer. When the formation rate of the nanotube bottom and the dissolution rate of the nanotube top are equivalent, the length of nanotube remains unchanged. For the Ti-Nb-Zr alloy an increase in anodization voltage could increase the nanotube length since the driving force for ionic transport through the barrier layer at the pore bottom could be enhanced, which will result in faster migration of cations and/or anions and thus movement of the Ti-Nb-Zr/Ti-Nb-Zr-O interface into the Ti-Nb-Zr alloy.

Our experimental results revealed that Zr content in the Ti-Nb-Zr alloy played an important role in formation of Ti-Nb-Zr-O nanotubes because of different electrochemical properties of Ti and Zr elements. The solubility of the fluoride complex for [ZrF₆]²⁻ is larger than that for [TiF₆]²⁻. This could result in a larger anodic current for the Ti-Nb-Zr alloy with higher Zr content than that with lower Zr content at the same potential [21, 23]. The dissolution rate of the as-formed oxide layers by fluoride ion should be another factor in determining the length of the Ti-Nb-Zr-O nanotubes [24]. As shown above, the formation of Ti-Nb-Zr-O nanotubes with a high Zr content was easier than that with a low Zr content.

EDS analyses of the as-anodized Ti-Nb-Zr-O samples with different Zr contents were carried out to investigate the composition of the Ti-Nb-Zr-O samples. As shown in Table 2, each sample was mainly composed of Ti, Nb, Zr, and O elements. With the increase of Zr content of original alloys, contents of the Ti and Zr elements in the Ti-Nb-Zr-O oxide layer also changed correspondingly. The contents of Nb and Zr elements in the Ti-Nb-Zr-O samples were smaller than those of the original alloys. This phenomenon may be explained by considering the difference in the dissolution rate for different oxide systems since previous reports have shown that the nanotube formation on different pure metals had different chemical dissolution rates in the dilute HF electrolytes [25].

The effect of pulse frequency on the formation of Ti-Nb-Zr-O nanotubes was also investigated. Figure 4 shows SEM images of the Ti-Nb-Zr-O samples fabricated at 40 V with a constant frequency of 2000 Hz and duty cycle of 20% for 90 minutes on different Ti-Nb-Zr alloy substrates. As shown in Figure 4(a), the top surface of the oxide layer had a lot of irregular nanoporous structures and high aligned nanotube arrays did not form due to a low electrical field. However, the nanotube structure grown on Ti35Nb10Zr alloy substrate became denser and more vertically oriented at the same condition. Furthermore, the nanotubes grown on Ti35Nb15Zr alloy substrate presented a much more regular, well-aligned nanotube array architecture. This proved that the Ti35Nb15Zr system was easier for nanotube growth than the Ti35Nb5Zr system did.

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(b)

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XRD analyses were conducted to characterize the crystal structure of the as-annealed Ti-Nb-Zr-O oxides with different Zr contents. As shown in Figure 5, diffraction peaks corresponding to the anatase TiO₂ phase in the as-annealed Ti-Nb-Zr-O samples could be found. The (101) diffraction peak of undoped TiO₂ appeared at 2 value of 25.78°. However, after Nb- and Zr-doping the (101) diffraction peaks of the Ti-Nb-Zr-O samples gradually shifted from 25.78° to 25.05°with increase of the Zr content. This performance should be mainly attributed to the change of TiO₂ lattice parameter because of the larger radius of Zr⁴⁺ (0.72 Å) compared to that of Ti⁴⁺ (0.61 Å) [26].

4. Conclusions

In summary, anodic Ti-Nb-Zr-O nanotube arrays were grown on Ti-Nb-Zr alloy substrates in 1 M NaH₂PO₄ containing 0.5 wt% HF electrolytes. The average length of the Ti-Nb-Zr-O nanotubes increased with increase of the Zr content. The anodic current for the Ti-Nb-Zr alloy with higher Zr content was larger than that with lower Zr content at the same anodization voltage. XRD analysis indicated that the Ti-Nb-Zr-O oxides annealed at 500°Cwere anatase phase. The diffraction peaks shifted to lower 2θ values with increase of the Zr content because of the larger radius of Zr⁴⁺ compared to that of Ti⁴⁺. The formation of Ti-Nb-Zr-O nanotubes for the system with a higher Zr content was relatively easier.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

This work was supported by Shanghai Pujiang Program (no. 07pj14047). The authors thank the contribution from SEM Lab at Instrumental Analysis Center of SJTU.

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Copyright © 2014 Qiang Liu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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