In-situ preparation of multi-layer TiO2 nanotube array thin films by anodic oxidation method
Source abstract
Abstract
Abstract The multi-layer TiO2 nanotube array thin films have been formed by anodic oxidation method via adjusting the outer voltage during oxidation process in glycerol electrolyte containing 0.3% NH4HF2. The diameter of the nanotube array increases with the outer voltage, and the length of nanotube in every layer increases with the anodic oxidation time. These multi-layers bring new possibilities to tailor the properties of the TiO2 nanotube array thin films formed via anodic oxidation method. Further, such multi-layer structure provide a new approach to evaluate the growth rate of TiO2 nanotube, which will help us to understand more deeply the formation mechanism of the TiO2 nanotubes. The growth rate of TiO2 nanotube array is respectively 1.2 and 3.6 μm/h under the anodic voltage of 30 V and 60 V. These multi-layer TiO2 nanotube array thin films may exhibit lots of potential applications in photoelectrochemical fields.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: TiO2 Photocatalysis and Solar Cells · Anodic Oxide Films and Nanostructures · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (22)
Show source-provided references
1. Zwilling · Electrochim Acta · 1999 · 45 · 92110.1016/S0013-4686(99)00283-2 ↗
2. Gong · Mater Res · 2001 · 16 · 333110.1557/JMR.2001.0457 ↗
3. Ruan · J Phys Chem B · 2005 · 109 · 1575410.1021/jp052736u ↗
4. Paulose · J Phys Chem B · 2006 · 110 · 617910.1021/jp064020k ↗
5. Feng · Nano Lett · 2008 · 8 · 378110.1021/nl802096a ↗
6. Macak J.M., Tsuchiya H., Schmuki P. Angew. Chem. Int. Ed. 005, 44: 2100–2102.10.1002/anie.200462459 ↗
7. Macak · Electrochem Solid-State Lett · 2007 · 10 · K2810.1149/1.2737544 ↗
8. Li · Electrochem Solid-State Lett · 2006 · 9 · B2810.1149/1.2180534 ↗
9. Shankar · Nanotechnology · 2007 · 18 · 110.1088/0957-4484/18/6/065707 ↗
10. Paulose · J Phys Chem C · 2007 · 111 · 1499210.1021/jp075258r ↗
11. Habazaki · Electrochim Acta · 2010 · 5510.1016/j.electacta.2010.02.036 ↗
12. Li · Rare Met Mater Eng · 2007 · 36 · 1257
13. Mor · Nano Lette · 2009 · 9 · 425010.1021/nl9024853 ↗
14. Liu · J Phys D Appl Phys · 2010 · 43 · 20510310.1088/0022-3727/43/20/205103 ↗
15. Xu · Appl Surf Sci · 2010 · 256 · 439710.1016/j.apsusc.2010.02.037 ↗
16. Macak J.M., Zlamal M., Krysa J., Schmuki P. Small 007, 3: 300–304.10.1002/smll.200600426 ↗
17. Li · J Electrochem Soc · 2007 · 154 · C63110.1149/1.2777104 ↗
18. Varghese O.K., Gong D.W., Paulose M., Ong K.G., Grimes C.A. Sens. Actu. B-Chem.l2003, 93: 338–44.10.1016/S0925-4005(03)00222-3 ↗
19. Joo · J Electrochem Soc. · 2010 · 157 · J22110.1149/1.3374643 ↗
20. Wang · Mater Lett · 2010 · 64 · 16410.1016/j.matlet.2009.10.033 ↗
21. Yang X.Z., Yang N.W. Chemical Industry Press, Beijing, 1975, p. 227.
22. Macak · Electroanalyt. Chem. · 2008 · 621 · 25410.1016/j.jelechem.2008.01.005 ↗