Preparation of Well-Ordered TiO2 Nanotube Arrays by Electrochemical Anodization of Titanium Foil in Neutral Electrolytes

2011 ◽  
Vol 233-235 ◽  
pp. 2047-2050
Author(s):  
Chao Wang ◽  
Da Chen ◽  
Shu Liu ◽  
Xia Ni Huang ◽  
Yue Xiang Huang ◽  
...  

To obtain high performance TiO2nanotube arrays (TNAs)-based material is interesting because of its wide applications in photocatalysis field such as solar energy conversion, photocatalysis and sensors. In the present work, the well-ordered TNAs were prepared by electrochemical anodization of titanium foil in the SO42−/F−based electrolyte under 20 V for 2 h during which the Ti foil and Pt wire were used as anode and cathode, respectively. The FESEM results showed that the as-obtained TNAs were well-aligned on Ti substrate with ~ 1.5 μm in length and ~ 100 nm pore in diameter. The XRD results indicated that the as-formed TNAs was in the form of amorphous and could be transformed into crystalline anatase phase under the heat treatment at 450 °C. Meanwhile, the UV-vis diffuse reflectance spectra demonstrated that the band-gap of the obtained TNAs was narrower than the commercial TiO2nanoparticles, indicating a better photocatalytic activity of the as-prepared TNAs over the commercial TiO2nanoparticles.

2020 ◽  
Vol 10 (4) ◽  
pp. 537-542
Author(s):  
Fei Tian ◽  
Gen Zhu ◽  
Kexin Shen ◽  
Chunju Li ◽  
Haitao Li ◽  
...  

Organic pollutants pose a serious threat to human health, and so their control by photocatalytic techniques has become an important field. There is an urgent need to devise convenient syntheses of effective photocatalysts for the degradation of contaminants. Here, high-performance anatase TiO2 nanowires have been obtained through a hydrothermal method followed by calcination at different temperatures in Ar. The products have been characterized by SEM, XRD, FTIR, and UV/Vis DRS measurements. The photocatalytic performances of the as-prepared catalysts in the degradation of rhodamine 6G (R6G) have been evaluated. The experimental results revealed that as-prepared TiO2 nanowires calcined at 600 °C (TNWs-600) exhibited the highest degree of R6G degradation (96%) under simulated solar irradiation. This could be attributed to their stable anatase phase with good photocatalytic activity, the excellent light absorption ability of which favors excitation. Overall, the fabricated TNWs-600 constitute a promising candidate material for photocatalytic applications in the removal of environmental pollutants.


Materials ◽  
2019 ◽  
Vol 12 (15) ◽  
pp. 2434 ◽  
Author(s):  
Tho Chau Minh Vinh Do ◽  
Duy Quoc Nguyen ◽  
Kien Trung Nguyen ◽  
Phuoc Huu Le

Antibiotic residues in aquaculture wastewater are considered as an emerging environmental problem, as they are not efficiently removed in wastewater treatment plants. To address this issue, we fabricated TiO2 nanotube arrays (TNAs), TiO2 nanowires on nanotube arrays (TNWs/TNAs), Au nanoparticle (NP)-decorated-TNAs, and TNWs/TNAs, which were applied for assessing the photocatalytic degradation of eight antibiotics, simultaneously. The TNAs and TNWs/TNAs were synthesized by anodization using an aqueous NH4F/ethylene glycol solution. Au NPs were synthesized by chemical reduction method, and used to decorate on TNAs and TNWs/TNAs. All the TiO2 nanostructures exhibited anatase phase and well-defined morphology. The photocatalytic performance of TNAs, TNWs/TNAs, Au-TNAs and Au-TNWs/TNAs was studied by monitoring the degradation of amoxicillin, ampicillin, doxycycline, oxytetracycline, lincomycin, vancomycin, sulfamethazine, and sulfamethoxazole under ultraviolet (UV)-visible (VIS), or VIS illumination by LC-MS/MS method. All the four kinds of nanomaterials degraded the antibiotics effectively and rapidly, in which most antibiotics were removed completely after 20 min treatment. The Au-TNWs/TNAs exhibited the highest photocatalytic activity in degradation of the eight antibiotics. For example, reaction rate constants of Au-TNWs/TNAs for degradation of lincomycin reached 0.26 min−1 and 0.096 min−1 under UV-VIS and VIS irradiation, respectively; and they were even higher for the other antibiotics. The excellent photocatalytic activity of Au-TNWs/TNAs was attributed to the synergistic effects of: (1) The larger surface area of TNWs/TNAs as compared to TNAs, and (2) surface plasmonic effect in Au NPs to enhance the visible light harvesting.


2015 ◽  
Vol 2015 ◽  
pp. 1-12 ◽  
Author(s):  
Gabriela Byzynski ◽  
Caue Ribeiro ◽  
Elson Longo

The defects caused by doping are important for understanding the increased photocatalytic activities of TiO2:N in organic reactions and in the evaluation of OH radical production after doping. TiO2:N was therefore synthesized using a modified polymeric method and N doping was performed by calcination with urea. The resulting powders were characterized using field emission scanning electron microscopy, X-ray diffraction, diffuse reflectance spectroscopy, Raman spectroscopy, Fourier transformation infrared spectroscopy, and photoluminescence emission spectroscopy (PL). N doping did not alter the morphology of the nanoparticles, and the anatase phase predominated, with the retention of the rutile phase. The band gap values, superficial areas, and crystallite sizes of the powders decreased after doping. The PL results showed an additional energy level in the TiO2:N band gap structure as a result of TiO2lattice defects caused by doping. At low N contents, the powders showed continuous emissions from the blue region to the yellow region and a high N content shifted the PL emissions to the red region. These results suggest that the use of these powders could increase the efficiencies of solar cells and water-splitting processes. The photocatalytic activity of the powders under UVC illumination was confirmed for different organic dye molecules. The OH radical production did not change extensively after doping, as shown by experiments with terephthalic acid, and higher photocatalytic efficiencies in Rhodamine-B degradation under UVC illumination were achieved using the doped samples.


2013 ◽  
Vol 860-863 ◽  
pp. 907-910
Author(s):  
Xiao Xia Lin ◽  
Jia Liu ◽  
De Gang Fu

B-doped TiO2nanotube arrays (B-TNTs) were synthesized by anodization method combined with dip-calcination technique. The physicochemical properties and surface morphology were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and UV-Vis diffuse reflectance spectrum (DRS). Methyl blue (MB) solution was utilized as the degradation model to evaluate the photocatalytic activity of B-TNTs under visible light irradiation. The results show B-TNTs shifts the absorption edge of TiO2nanotube arrays to the visible light region and B-TNTs displays higher photocatalytic activity compared with undoped TNTs.


2011 ◽  
Vol 364 ◽  
pp. 377-381 ◽  
Author(s):  
Syazwani Mohd Zaki ◽  
Srimala Sreekantan

This paper described the preparation of Cu loaded TiO₂ nanotube arrays. Firstly, TiO₂ nanotube arrays were formed by anodization. Afterwards, the formed nanotube arrays were incorporated with Cu by wet impregnation method. The soaking time and concentration were varied to obtain an optimum set of parameter for Cu incorporation in TiO₂ nanotubes. After anodization, all samples were annealed at 400°C for 4 hours to obtain anatase phase. The nanotube arrays were characterized by field emission scanning electron microscopy (FESEM), x-ray diffraction (XRD) and x-ray photoelectron spectra (XPS). An average diameter 63.02 nm and length 12.15µm were obtained for TiO₂ nanotubes. The photocatalytic activity of these nanotubes were investigated with methyl orange (MO) and the TiO₂ nanotube prepared in 0.01M of Cu (NO₃)₂ solution within 3 hours demonstrates the highest photocatalytic activity with 83.6% degradation of methyl orange. Keywords: copper doping, wet impregnation, photocatalytic activity


2013 ◽  
Vol 2013 ◽  
pp. 1-9 ◽  
Author(s):  
Min Zhang ◽  
Dandan Lu ◽  
Guotian Yan ◽  
Juan Wu ◽  
Jianjun Yang

Mo,N-codoped TiO2nanotube arrays (TNAs) were fabricated by a two-step method consisting of electrochemical anodization and subsequent magnetron sputtering of Mo. The samples were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and ultraviolet-visible diffuse reflectance spectroscopy (UV-Vis DRS). The results showed that the Mo,N-codoped TiO2nanotube arrays exhibited higher visible light absorbance and remarkably enhanced photocurrent density and photocatalytic activity compared with single N-doped TiO2. The highly efficient photoelectrochemical and photocatalytic activity is associated with the codoping effect between Mo and N, which plays a key role in producing new states, narrowing the bandgap, and reducing the recombination thereby effectively improving the visible light absorption and photocatalytic activity of TNAs.


2011 ◽  
Vol 181-182 ◽  
pp. 702-706
Author(s):  
Yu Cheng Wu ◽  
Yan Wang ◽  
Jie Wu Cui ◽  
Guang Qing Xu ◽  
Xin Yi Zhang

In this paper, highly-ordered TiO2 nanotube arrays (TNAs) were firstly fabricated by electrochemical anodization. Secondly, the as-prepared TNAs were used as precursors for hydrothermal treatment and large percentage of nanoparticles with special shape were achieved. Their photocatalytic activity was evaluated based upon the removal of methylene blue (MB) dye in the aqueous solution. In order to enhance the photocatalytic properties, we added a certain amount of AgNO3 solution (0.1M) in the hydrothermal treatment process and the experiment demonstrated that the addition of AgNO3 solution displayed an excellent improvement for the photocatalytic activity. Under sunlight irradiation, the methylene blue pollutant of 1×10−5M was almostly completely degraded by Ag -TiO2 nanoparticles within 300 min.


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