On the Synthesis and Characterizations of TiO2 Nanotubes

被引:9
作者
Dubey, P. K. [1 ]
Mishra, P. R. [1 ]
Sinha, A. S. K. [2 ]
Srivastava, O. N. [1 ]
机构
[1] Banaras Hindu Univ, Dept Phys, Varanasi 221005, Uttar Pradesh, India
[2] Banaras Hindu Univ, Dept Chem Engn, Inst Technol, Varanasi 221005, Uttar Pradesh, India
关键词
Anodic Oxidation; TiO2; Nanotubes; UV-Visible Spectroscopy; SENSITIZED SOLAR-CELLS; TITANIA NANOTUBES; OXIDE-FILMS; FABRICATION; HYDROGEN; ARRAYS; WATER; ANODIZATION; ALUMINUM; ELECTROLYTE;
D O I
10.1166/jnn.2009.1115
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the present work, aligned TiO2 nanotubes have been synthesized by a simple method of electrochemical anodization of high purity, well cleaned, etched and ultrasonicated Ti-sheet (Purity similar to 99.99%) in a fluoride mediated electrolytic media consisting of a solution of 0.14 M NaF and a solution of 0.5 M/1.0 M H3PO4. Studies on the effects of anodization voltage, time and electrolyte concentration on the formation of TiO2 nanotubes have been carried out. The TiO2 nanotube arrays have been synthesized at applied anodization voltages of similar to 10 V and similar to 20 V. The anodization was carried out for 1 hour and 2 hours at each applied voltage. Structural/microstructural characterizations of TiO2 nanotubes have been carried out through scanning electron microscopy (SEM) and transmission electron microscopy (TEM). SEM images of TiO2 nanotubes showed interesting features relating to morphology, the pore size (diameter of the tubes) and the lengths of the tube. TEM investigations revealed that the as synthesized nanotubes are amorphous in nature and on electron beam annealing, these transformed to crystalline phases (rutile and brookite). The optical characterizations through UV-Visible spectroscopy exhibited that the band gap are similar to 3.03 eV and similar to 2.87 eV for tubes synthesized at applied anodization voltages of similar to 10 V and similar to 20 V respectively. A tentative mechanism for the growth of TiO2 nanotube has been put forward.
引用
收藏
页码:5507 / 5514
页数:8
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