Abstract

Titanium oxide nanotube (TiO2 nanotube) arrays were produced by anodizing titanium foils in two different electrolytes. The first electrolyte consisted of ethylene glycol containing 0.5 wt% NH4F and 4 vol% of distilled water to produce pure TiO2 nanotube arrays and the second consisted of HF aqueous solution (0.5 wt%) containing 0.5% polyvinylalcohol to produce carbon doped TiO2 nanotube arrays. The fabricated TiO2 nanotube arrays were subsequently annealed in the atmosphere of nitrogen. The morphology and crystal structure of fabricated arrays were characterized by means of scanning electron microscopy and X-ray diffraction. The electrical conductivity and capacitance of TiO2 nanotube arrays were investigated by electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). Water contact angle and biocompatibility of fabricated nanotube arrays were investigated. The results showed that carbon doped TiO2 nanotube arrays annealed in the atmosphere of nitrogen have higher conductivity and capacitance than those of pure arrays annealed in the same atmosphere. Doping with carbon enhances the biocompatibility and wettability of TiO2 nanotube arrays. It has also noted that electrical conductivity and capacitance of TiO2 nanotube arrays were directly proportional to the tube wall thickness.

Highlights

  • Considerable attention has been paid to T iO2 nanotube arrays as they can provide a direct way for charge transport and provide a large surface area

  • To obtain C-doped T iO2 nanotube arrays with morphologies close to those of pure nanotubes, three other samples were anodized in electrolyte B at 15 V, 20 V and 25 V

  • It can be seen that T iO2 nanotube films have main peaks that match with the anatase phase of titanium dioxide at 2θ values of (25.31), (37.57 ), (47.91 ), (53.75) and (55.08)

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Summary

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This content has been downloaded from IOPscience. Please scroll down to see the full text. Ser. 829 012010 (http://iopscience.iop.org/1742-6596/829/1/012010) View the table of contents for this issue, or go to the journal homepage for more. Download details: IP Address: 139.216.216.252 This content was downloaded on 26/06/2017 at 13:23. Please note that terms and conditions apply.

Introduction
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Conclusions

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