Interference Colors of TiO2 Nanotube Arrays Grown by Anodic Oxidation

2014 ◽  
Vol 875-877 ◽  
pp. 370-374 ◽  
Author(s):  
Jong Yun Moon ◽  
Marianna Kemell ◽  
Risto Punkkinen ◽  
Hannu Pekka Hedman ◽  
Byungki Park ◽  
...  

The study describes the interference color of anodic TiO2 nanotube arrays on titanium foil. TiO2 nanotube arrays are prepared by oxidizing titanium foil in an aqueous electrolyte solution of hydrofluoric acid (HF, 0.5 wt.%). The morphologies of the oxide film are characterized by FESEM. The empirical color properties are obtained using the L*a*b* system. The different interference colors of oxidized Ti samples are obtained depending on the anodization time. The anodization time clearly indicates a strong effect on the reflectance at the visible wavelength region, thus confirming the observed color differences. Consequently, the interference colors can be controlled by the anodization time. By observing the coloration of Ti during the anodization, the interference colors can be utilized to identify the thickness of oxide layer and the formation of nanotubes on Ti sheet.

2001 ◽  
Vol 16 (12) ◽  
pp. 3331-3334 ◽  
Author(s):  
Dawei Gong ◽  
Craig A. Grimes ◽  
Oomman K. Varghese ◽  
Wenchong Hu ◽  
R. S. Singh ◽  
...  

Titanium oxide nanotubes were fabricated by anodic oxidation of a pure titanium sheet in an aqueous solution containing 0.5 to 3.5 wt% hydrofluoric acid. These tubes are well aligned and organized into high-density uniform arrays. While the tops of the tubes are open, the bottoms of the tubes are closed, forming a barrier layer structure similar to that of porous alumina. The average tube diameter, ranging in size from 25 to 65 nm, was found to increase with increasing anodizing voltage, while the length of the tube was found independent of anodization time. A possible growth mechanism is presented.


2010 ◽  
Vol 148-149 ◽  
pp. 873-876
Author(s):  
Jian Ling Zhao ◽  
Ying Ru Kang ◽  
Xi Xin Wang ◽  
Cheng Chun Tang

Titania nanotube arrays were synthesized via anodic oxidization of titanium foil in dimethyl sulfoxide (DMSO) solution containing 2 wt% HF and 3 wt% H2O at 40 V. The microstructure of the arrays was characterized with scanning electron microscopy (SEM). The results show that morphology of titania nanotube arrays is evidently influenced by the anodization time, and with the extension of oxidation time, the better morphology could be obtained. The possible formation mechanism of titania nanotube arrays has been discussed.


2021 ◽  
Vol 21 (1) ◽  
pp. 32-48
Author(s):  
Svetlana S. Popova ◽  
◽  
Hussein Ali Hussein ◽  
Lyubov’ N. Olshanskaya ◽  
Sergei V. Arzamastsev ◽  
...  

It was established that at the cathodic treatment of titanium in aqueous dimethyl sulfoxide solutions of sodium molybdate, containing phosphoric acid, at the potential of the cathodic incorporation of sodium (Ec = −2.6 V) in the potentiostatic mode, the composition formed on the electrode surface layer depended not only on the composition of the solution, but also on the volume ratio of the aqueous electrolyte solution and the organic solvent (dimethyl sulfoxide).


2016 ◽  
Vol 860 ◽  
pp. 7-11 ◽  
Author(s):  
Somkuan Photharin ◽  
Buagun Samran ◽  
Rinnatha Vongwatthaporn ◽  
Narongsak Kodtharin ◽  
Ramida Chaiyarat ◽  
...  

In this work, we present the effect of preparation temperature of electrolytes for fabricating undoped and silver (Ag) doped titanium dioxide (TiO2) nanotubes by the electrochemical anodic oxidation of pure titanium sheets in electrolytes, mixtures of ethylene glycol (EG), ammonium fluoride (NH4F) and deionized water, that contain with different of silver ions. Heat treatment of electrolytes was carried out at 100 °C during preparation process. The morphology and structure of prepared nanotubes were characterized by X-ray diffraction (XRD) and scanning electron microscope (SEM). The structures of TiO2 nanotubes obtained from heat treatment and non-heat treatment of electrolyte solutions and adding silver ions in electrolyte solution are similar. The nanotubes appear in arrays and the diameters of nanotubes were about 92 nm for non-heat treatment electrolyte solution and undoped TiO2 and about 102 nm for heat treatment electrolyte solution and all Ag-doped TiO2 nanotube arrays. When the concentration of silver nitrate (AgNO3) increases, the TiO2 nanotube arrays cracked and are not well arranged.


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