Optical and Electrical Properties of TiO2 Nanotubes Grown by Titanium Anodization

2009 ◽  
Vol 1178 ◽  
Author(s):  
Yahya Alivov ◽  
Vladimir Kuryatkov ◽  
Mahesh Pandikunta ◽  
Gautam Rajanna ◽  
Daniel Johnstone ◽  
...  

AbstractIn this work we investigated the structural, electrical, and optical properties of titanium dioxide (TiO2) nanotubes (NTs) formed by electrochemical anodization of Ti metal sheets in NH4F+glycerol electrolyte at different anodization voltages (Va) and acid concentrations. Our results revealed that TiO2 NTs can be grown in a wide range of anodization voltages from 10 V to 240 V. The maximum NH4F acid concentration, at which NTs can be formed, decreases with the anodization voltage, which is 0.7% for Va<60V, and decreases to 0.1% at Va =240 V. Glancing angle X-ray diffraction (GAXRD) experiments show that as-grown amorphous TiO2 transforms to anatase phase after annealing at 400 oC, and further transforms to rutile phase at annealing temperatures above 500 oC. Samples grown in 30-120 voltage range have higher crystal quality as seen from anatase (101) peak intensity and reduced linewidth. The electrical resistivity of the NTs varies with Va concentration and increases by eight orders of magnitude when Va increases from 10 V to 240 V. This is consistent with cathodoluminescense studies which showed improved optical properties for samples grown in this voltage range. Optical properties of samples were also studied by low temperature photoluminescence. Temperature dependent I-V and photo-induced current transient spectroscopy were employed to analyze electrical properties and defect structure on NT samples.

Nanomaterials ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 128 ◽  
Author(s):  
Nurul Tasnim Sahrin ◽  
Rab Nawaz ◽  
Chong Fai Kait ◽  
Siew Ling Lee ◽  
Mohd Dzul Hakim Wirzal

In this study, a series of TiO2 nanotubes (NTs) were synthesized employing electrochemical anodization of titanium foil in an ionic liquid solution containing a mixture of glycerol and choline chloride, acting as electrolyte. The as-synthesized TiO2 NTs were calcined at 350, 450, or 550 °C for a 2 h duration to investigate the influence of calcination temperature on NTs formation, morphology, surface properties, crystallinity, and subsequent photocatalytic activity for visible light photodegradation of gaseous formaldehyde (HCHO). Results showed that the calcination temperature has a significant effect on the structure and coverage of TiO2 NTs on the surface. Freshly synthesized TiO2 NTs showed better-ordered structure compared to calcined samples. There was significant pore rupture with increasing calcination temperature. The transformation from anatase to rutile phase appeared after calcination at 450 °C and the weight fraction of the rutile phase increased from 19% to 36% upon increasing the calcination temperature to 550 °C. The band gaps of the TiO2 NTs were in the range from 2.80 to 2.74 eV, shifting the active region of the materials to visible light. The presence of mixed anatase–rutile TiO2 phases in the sample calcined at 450 °C showed enhanced photoactivity, which was confirmed by the 21.56 mg∙L−1∙g−1 removal of gaseous formaldehyde under 120 min of visible light irradiation and displayed enhanced quantum yield, ∅HCHO of 17%.


Molecules ◽  
2020 ◽  
Vol 25 (9) ◽  
pp. 2121
Author(s):  
Vinsensia Ade Sugiawati ◽  
Florence Vacandio ◽  
Thierry Djenizian

All-solid-state batteries were fabricated by assembling a layer of self-organized TiO2 nanotubes grown on as anode, a thin-film of polymer as an electrolyte and separator, and a layer of composite LiFePO4 as a cathode. The synthesis of self-organized TiO2 NTs from Ti-6Al-4V alloy was carried out via one-step electrochemical anodization in a fluoride ethylene glycol containing electrolytes. The electrodeposition of the polymer electrolyte onto anatase TiO2 NTs was performed by cyclic voltammetry. The anodized Ti-6Al-4V alloys were characterized by scanning electron microscopy and X-ray diffraction. The electrochemical properties of the anodized Ti-6Al-4V alloys were investigated by cyclic voltammetry and chronopotentiometry techniques. The full-cell shows a high first-cycle Coulombic efficiency of 96.8% with a capacity retention of 97.4% after 50 cycles and delivers a stable discharge capacity of 63 μAh cm−2 μm−1 (119 mAh g−1) at a kinetic rate of C/10.


Materials ◽  
2019 ◽  
Vol 12 (4) ◽  
pp. 626 ◽  
Author(s):  
Metka Benčina ◽  
Ita Junkar ◽  
Rok Zaplotnik ◽  
Matjaz Valant ◽  
Aleš Iglič ◽  
...  

Facile crystallization of titanium oxide (TiO2) nanotubes (NTs), synthesized by electrochemical anodization, with low pressure non-thermal oxygen plasma is reported. The influence of plasma processing conditions on TiO2 NTs crystal structure and morphology was examined by X-ray diffraction (XRD) and scanning electron microscopy (SEM). For the first time we report the transition of amorphous TiO2 NTs to anatase and rutile crystal structures upon treatment with highly reactive oxygen plasma. This crystallization process has a strong advantage over the conventional heat treatments as it enables rapid crystallization of the surface. Thus the crystalline structure of NTs is obtained in a few seconds of treatment and it does not disrupt the NTs’ morphology. Such a crystallization approach is especially suitable for medical applications in which stable crystallized nanotubular morphology is desired. The last part of the study thus deals with in vitro biological response of whole blood to the TiO2 NTs. The results indicate that application of such surfaces for blood connecting devices is prospective, as practically no platelet adhesion or activation on crystallized TiO2 NTs surfaces was observed.


2020 ◽  
Vol 2020 ◽  
pp. 1-11
Author(s):  
O. Zakir ◽  
R. Idouhli ◽  
M. Elyaagoubi ◽  
M. Khadiri ◽  
A. Aityoub ◽  
...  

In this study, a self-organized nanotubular titanium dioxide (TiO2) array was successfully produced by anodizing pure titanium in a mixture of glycerol, distilled water (8% vol.), and ammonium fluoride using a dual electrode system. The size control and distribution of the nanopores were performed in a DC voltage range varying from 30 V to 60 V. The diameter of TiO2 nanopores varies from 59 to 128 nm depending on the anodizing voltage. Energy-dispersive X-ray spectroscopy (EDX) analysis reveals that the as-prepared films are essentially composed of TiO2. According to the X-ray diffraction (XRD) and Raman spectroscopy analysis, the nanotubular arrays of TiO2 annealed at 600°C for 2 hours are composed of a phase mixture of anatase and rutile. Mott-Schottky analysis showed that the TiO2 nanotubes are consistent with an n-type semiconductor with a donor density of about 1017 cm-3. Preliminary results on the photocatalytic degradation of a pharmaceutical pollutant showed that the TiO2 nanotubes can be used as a promising material for application in wastewater treatment.


Open Physics ◽  
2011 ◽  
Vol 9 (2) ◽  
Author(s):  
Robert Evarestov ◽  
Yuri Zhukovskii ◽  
Andrei Bandura ◽  
Sergei Piskunov

AbstractThe formalism of line symmetry groups for one-periodic (1D) nanostructures with rotohelical symmetry has been applied for symmetry analysis of single-walled titania nanotubes (SW TiO2 NTs) formed by rolling up the stoichiometric two-periodic (2D) slabs of anatase structure. Either six- or twelve-layer (101) slabs have been cut from TiO2 crystal in a stable anatase phase. After structural optimization, the latter keeps the centered rectangular symmetry of initial slab slightly compressed along a direction coincided with large sides of elemental rectangles. We have considered two sets of SW TiO2 NTs with optimized six- and twelve-layer structures, which possess chiralities (−n, n) and (n, n) of anatase nanotubes. To analyze the structural and electronic properties of titania slabs and nanotubes, we have performed their ab initio LCAO calculations, using the hybrid Hartree-Fock/Kohn-Sham exchange-correlation functional PBE0. The band gaps (Δɛ gap) and strain energies (E strain) of six-layer nanotubes have been computed and analyzed as functions of NT diameter (D NT). As to models of 12-layer SW TiO2 NTs of both chiralities, their optimization results in structural exfoliation, i.e., the multi-walled structure should be rather formed in nanotubes with such a number of atomic layers.


1996 ◽  
Vol 442 ◽  
Author(s):  
A. Castaldini ◽  
A. Cavallini ◽  
P. Fernandez ◽  
B. Fraboni ◽  
J. Piqueras

AbstractDeep levels in II-VI compounds have been investigated to understand their role in the compensation mechanism and their influence on the material electrical and optical properties. The electrical properties have been studied by current and capacitance transient spectroscopy, while the optical properties have been studied by cathodoluminescence. We have focused our attention on the traps involved in the compensation process, such as centre A and the deep levels located near midgap.


2013 ◽  
Vol 686 ◽  
pp. 71-76
Author(s):  
Nur Aimi Jani ◽  
Mohd Faizal Achoi ◽  
Mohd Muzamir Mahat ◽  
Saifollah Abdullah ◽  
Zainovia Lockman ◽  
...  

An electrochemical anodization is a simple and low cost technique, to electrochemically synthesize self-organized titanium dioxide (TiO2) nanotubes (NTs) from 1M Na2SO4 electrolyte with anodization of Ti foil. The FESEM results showed that the average diameter size and length of TiO2 NTs was found between 50 to 60 nm and 2.5 μm, respectively. The surface morphology of arrays TiO2 NTs is uniformly deposited on Ti substrate. While, the cross-sectional of TiO2 NTs revealed that, the TiO2 NTs is arrays alignment and close each other deposited. From current-anodisation time analysis (I-t) indicates that TiO2 nanotubes were start formed at anodisation time 429.03 sec with current flows is 51.69 mA in electrochemical system.


2015 ◽  
Vol 93 (1) ◽  
pp. 106-112 ◽  
Author(s):  
Lijia Liu ◽  
Jun Li ◽  
Tsun-Kong Sham

Freestanding TiO2 nanograss–nanotube hierarchical membranes are synthesized from a Ti metal foil by electrochemical anodization. It is found that the two nanostructures exhibit different luminescence properties, which are also affected by the crystal phases upon phase transformation. An unusual near-UV luminescence is observed from the amorphous nanograss, which is found to be excitation element specific. The amorphous nanotube shows no luminescence. Upon calcination, both nanograss and nanotubes are crystalized into the anatase phase with some rutile phase present, and both structures emit visible green luminescence at slightly different energies. The luminescence mechanism is explored using UV–vis spectroscopy, X-ray absorption near-edge structures (XANES), and X-ray excited optical luminescence (XEOL), and its implications are presented.


2018 ◽  
Vol 9 (1) ◽  
pp. 121-127 ◽  
Author(s):  
Henia Fraoucene ◽  
Djedjiga Hatem ◽  
Florence Vacandio ◽  
Marcel Pasquinelli

Background: A nano-tubular structure of Titanium dioxide (TiO2) was obtained using an electrochemical process based on the anodization of titanium foil in an organic electrolyte prepared with ethylene glycol (HOCH2CH2OH) containing Ammonium fluorides (NH4F) and ultrapure water under different anodization voltage. The morphological characteristics showed the formation of TiO2 nanotubes with different geometrical parameters. The electronic properties of the TiO2 NTs films were measured by the Mott-Schottky (MS) plots, indicating a positive slope for all graphs implying the n-type semiconductor nature of the TiO2 nanotubes (TiO2 NTs). The donor density (Nd) and the flat band potential (Efb) increases slightly with increase the anodization voltage. Methods: Prior the anodization, the titanium (Ti) foils were cut into square shape (2.25 cm2) with a selected work area of 0.6 cm2. The samples were subjected to a final polishing using a rotating felt pad (01 &µm) impregnated with alumina until a metallic mirror surface was obtained. The Ti foils were degreased by sonication in acetone, methanol and 2-Propanol for 10 minutes respectively, rinsed with ultrapure water and dried in a stream of compressed air. To form a TiO2 NTs, electrochemical anodization process was carried out at room temperature in Ethylene Glycol (EG) solution containing 0.3 wt% Ammonium fluorides (NH4F) and 2wt % ultrapure water for three (03) hours at different anodization voltage (20, 40 and 60V). A two-electrode cell was used for all the anodization measurements, with a platinum plate as the counter electrode, separated from the working electrode (titanium foil) by 1.5 cm. Immediately after anodization, the samples were soaked in ultrapure water to remove residual electrolyte for 10 minutes and then dried in an oven at 50 °C for 10 minutes. Results: TiO2 NTs grown from anodization of Ti foil in fluoride EG solution for 3h by varying the anodization voltage. The micrographic analysis shows a strong influence of the anodizing voltage on the morphology and geometrical parameters of the TiO2 NTs. Non homogenous NTs morphology was observed at 20 V with the presence of corrugations along the walls of the tubes. A perfect and regular nanotublar structure with smooth’s walls tubes was obtained at an anodization voltage of 60V. Moreover, the increase of anodization voltage leads to an increase in both the diameter and the length of tubes. In fact, the inner diameter and the length of the tubes (Di and L) values increase with increasing potential, being around (39 nm and 2 &µm) respectively at 20 V and (106 nm and 16,1 &µm) at 60 V. The measured electronic properties of TiO2 NTs indicating the n type semiconducting nature. It is remarkable that the donor density Nd increases toward higher values by increasing the anodizing voltage until 40V. However, for an anodization at 60V, the Nd has a small decrease value (7, 03 * 1019 cm-3) indicating a diminution of defects present in the material. Also, by increasing the anodizing voltage, Efb takes increasingly more positive values. In fact, the Efb values are – 0.12, 0.05 and 0.15 V for films prepared at 20, 40 and 60 V respectively. Therefore, this behavior can be attributed to a displacement of the Fermi level toward the conduction band edge which leads to a larger band bending at the interface. Conclusion: By varying the anodization voltage, titanium dioxide nanotubes (TiO2 NTs) were grown using electrochemical anodization of titanium foil in fluoride ethylene glycol solution for 3 hours. The morphology of the TiO2 NTs obtained was considerably affected; the anodizing potential determines the migration of ions in electrolyte during anodization process and simultaneously the tube diameter. An average small a nanotube diameter around 39 nm was obtained for 20V corresponding to 106 nm average diameter for TiO2 NTs structure synthesized at 60V. Furthermore, the semiconductor properties of the TiO2 NTs films have also been modified with increased values while increasing the anodization voltage. This behavior was attributed that the TiO2 NTs structure is more disordered, having much more defects provide abundant local donor energy levels which increases conductivity and decrease the probability of recombination of electrons and holes in these films, that can be integrated as active layer in the solar cells, in particular the Gratzel cells.


1995 ◽  
Vol 411 ◽  
Author(s):  
A. Castaldini ◽  
A. Cavallini ◽  
P. Fernandez ◽  
B. Fraboni ◽  
J. Piqueras ◽  
...  

ABSTRACTDeep levels in II-VI compounds were investigated by complementary junction and optical spectroscopy methods to assess the characteristics of the traps as well as the limits and the reliability of the techniques applied. The electrical properties have been investigated by current and capacitance transient spectroscopy, while the optical properties have been studied by cathodoluminescence. A critical and comparative analysis of the results obtained with the various methods allowed the determination of the parameters and the nature (majority or minority carrier trap) of most of the detected levels.


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