Quantitative relationship between nanotube length and anodizing current during constant current anodization
Creators
- 1. Shanghai Advanced Research Institute, China Academy of Sciences, Shanghai 201210 (China)
- 2. Key Laboratory of Soft Chemistry and Functional Materials of Education Ministry, Nanjing University of Science and Technology, Nanjing 210094 (China)
Description
Highlights: • Ti anodization was performed by constant current rather than constant voltage. • The nanotube length was controlled by ionic current rather than dissolution current. • Electronic current can be estimated by the nanotube length and the anodizing current. • Dissolution reaction hardly contributes electric current across the barrier layer. - Abstract: The growth kinetics of anodic TiO2 nanotubes (ATNTs) still remains unclear. ATNTs are generally fabricated under potentiostatic conditions rather than galvanostatic ones. The quantitative relationship between nanotube length and anodizing current (Jtotal) is difficult to determine, because the variable Jtotal includes ionic current (Jion) (also called oxide growth current Jgrow=Jion) and electronic current (Je), which cannot be separated from each other. One successful approach to achieve this objective is to use constant current anodization rather than constant voltage anodization, that is, through quantitative comparison between the nanotube length and the known Jtotal during constant current anodization, we can estimate the relative magnitudes of Jgrow and Je. The nanotubes with lengths of 1.24, 2.23, 3.51 and 4.70 μm, were formed under constant currents (Jtotal) of 15, 20, 25 and 30 mA, respectively. The relationship between nanotube length (y) and anodizing current (x =Jtotal=Jgrow+Je) can be expressed by a fitting equation: y=0.23(x-10.13), from which Jgrow (Jgrow = x -10.13) and Je (∼10.13 mA) could be inferred under the present conditions. Meanwhile, the same conclusion could also be deduced from the oxide volume data. These results indicate that the nanotube growth is attributed to the oxide growth current rather than the dissolution current.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.electacta.2015.08.098Additional details
Identifiers
- DOI
- 10.1016/j.electacta.2015.08.098;
- PII
- S0013-4686(15)30348-0;
Publishing Information
- Journal Title
- Electrochimica Acta
- Journal Volume
- 180
- Journal Page Range
- p. 147-154
- ISSN
- 0013-4686
- CODEN
- ELCAAV
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 48099367
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ANODES; ANODIZATION; DEPLETION LAYER; DISSOLUTION; ELECTRIC CURRENTS; ELECTRIC POTENTIAL; NANOTUBES; OXIDATION; TITANIUM OXIDES
- Descriptors DEC
- CHALCOGENIDES; CHEMICAL COATING; CHEMICAL REACTIONS; CORROSION PROTECTION; CURRENTS; DEPOSITION; ELECTROCHEMICAL COATING; ELECTRODES; ELECTROLYSIS; LAYERS; LYSIS; NANOSTRUCTURES; OXIDES; OXYGEN COMPOUNDS; SURFACE COATING; TITANIUM COMPOUNDS; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2015 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.