MoSe2 modified TiO2 nanotube arrays with superior photoelectrochemical performance

Science.gov (United States)

Zhang, Yaping; Zhu, Haifeng; Yu, Lianqing; He, Jiandong; Huang, Chengxing

2018-04-01

TiO2 nanotube arrays (TNTs) are first prepared by anodization Ti foils in ethylene glycol electrolyte. Then, MoSe2 deposites electrochemically on TNTs. The as-synthesized MoSe2/TiO2 composite has a much higher photocurrent density of 1.07 mA cm‑2 at 0 V than pure TNTs of 0.38 mA cm‑2, which suggests that the MoSe2/TiO2 composite film has optimum photoelectrocatalysis properties. The electron transport resistances of the MoSe2/TiO2 decreases to half of pure TiO2, at 295.6 ohm/cm2. Both photocurrent-time and Mott-Schottky plots indicate MoSe2 a p-type semiconductor characteristics. MoSe2/TiO2 composite can achieve a maximum 5 orders of magnitude enhancement in carrier density (4.650 × 1027 cm‑3) than that of pure TiO2 arrays. It can be attributed to p-n heterojunction formed between MoSe2 and TiO2, and the composite can be potentially applied in photoelectrochemical, photocatalysis fields.

Photocatalytic performance of pure anatase nanocrystallite TiO2 synthesized under low temperature hydrothermal conditions

International Nuclear Information System (INIS)

Sayilkan, Funda; Erdemoglu, Sema; Asiltuerk, Meltem; Akarsu, Murat; Sener, Sadiye; Sayilkan, Hikmet; Erdemoglu, Murat; Arpac, Ertugrul

2006-01-01

Photocatalytic performance of a hydrothermally synthesized pure anatase TiO 2 with 8 nm average crystallite size for decomposition of Reactive Red 141 was examined by investigating the effects of UV-light irradiation time, irradiation power, amount of TiO 2 and initial dye concentration. Change in the UV absorbance of the dye during irradiation was monitored. One wt.% TiO 2 in 30 mg/l Reactive Red 141 aqueous solution was found adequate for complete decolorization in 70 min at 770 W/m 2 irradiation power. It was realized that, compared to Degussa P-25, the synthesized nano-TiO 2 can be repeatedly used as a new catalyst. The results also proved that Reactive Red 141 is decomposed catalytically due to the pseudo first-order reaction kinetics

XAFS Study on TiO2 Photocatalyst Loaded on Zeolite Synthesized from Steel Slag

International Nuclear Information System (INIS)

Kuwahara, Yasutaka; Ohmichi, Tetsutaro; Mori, Kosuke; Katayama, Iwao; Yamashita, Hiromi

2007-01-01

The convenient route for the synthesis of Y-zeolites by utilizing steel slag as a material source was developed. Through hydrothermal treatment, well-crystallized Y-zeolite was obtained. We also synthesized TiO2-loaded Y-zeolites by an impregnation method. The structure of titanium oxide species highly dispersed on the zeolite, which couldn't be detected by XRD patterns, was investigated by XAFS analysis. Photocatalytic activity for decomposition of 2-propanol in liquid phase was found to be enhanced by the hydrophobic surface property of zeolite. It has been demonstrated that the zeolite synthesized from steel slag would be applicable as a promising support of TiO2 photocatalyst

Synthesis of TiO2 by electrochemical method from TiCl4 solution as anode material for lithium-ion batteries

International Nuclear Information System (INIS)

Nur, Adrian; Purwanto, Agus; Jumari, Arif; Dyartanti, Endah R.; Sari, Sifa Dian Permata; Hanifah, Ita Nur

2016-01-01

Metal oxide combined with graphite becomes interesting composition. TiO 2 is a good candidate for Li ion battery anode because of cost, availability of sufficient materials, and environmentally friendly. TiO 2 gravimetric capacity varied within a fairly wide range. TiO 2 crystals form highly depends on the synthesis method used. The electrochemical method is beginning to emerge as a valuable option for preparing TiO 2 powders. Using the electrochemical method, the particle can easily be controlled by simply adjusting the imposed current or potential to the system. In this work, the effects of some key parameters of the electrosynthesis on the formation of TiO 2 have been investigated. The combination of graphite and TiO 2 particle has also been studied for lithium-ion batteries. The homogeneous solution for the electrosynthesis of TiO 2 powders was TiCl 4 in ethanol solution. The electrolysis was carried out in an electrochemical cell consisting of two carbon electrodes with dimensions of (5 × 2) cm. The electrodes were set parallel with a distance of 2.6 cm between the electrodes and immersed in the electrolytic solution at a depth of 2 cm. The electrodes were connected to the positive and negative terminals of a DC power supply. The electrosynthesis was performed galvanostatically at 0.5 to 2.5 hours and voltages were varied from 8 to 12 V under constant stirring at room temperature. The resulted suspension was aged at 48 hrs, filtered, dried directly in an oven at 150°C for 2 hrs, washed 2 times, and dried again 60 °C for 6 hrs. The particle product has been used to lithium-ion battery as anode. Synthesis of TiO 2 particle by electrochemical method at 10 V for 1 to 2.5 hrs resulted anatase and rutile phase

An Experimental Study on the Shape Changes of TiO2 Nanocrystals Synthesized by Microemulsion-Solvothermal Method

Directory of Open Access Journals (Sweden)

Wei Kong

2011-01-01

Full Text Available Titanium dioxide (TiO2 nanocrystals of different shape were successfully synthesized in a new microemulsion system through a solvothermal process. The TiO2 nanocrystals were prepared from the reaction of tetrabutyl titanate (TBT, H2O, and oleic acid (OA, which were used as solvent and surfactant at 300∘C and 240∘C in a stainless steel autoclave. The sphere, polygon, and rhombus-shaped nanocrystals have been prepared at 300∘C and the dot- and- rod shaped nanocrystals have been synthesized at 240∘C. The effect of the reaction time on the shape and size of TiO2 nanocrystals in this method was studied in the present paper. The size distribution of TiO2 nanocrystals prepared at 300∘C for different hours is also studied. In addition, an attempt to describe the mechanism of shape change of TiO2 nanocrystals was presented in this paper.

Electrochemical Characterization of TiO 2 Blocking Layers for Dye-Sensitized Solar Cells

KAUST Repository

Kavan, Ladislav; Té treault, Nicolas; Moehl, Thomas; Grä tzel, Michael

2014-01-01

Thin compact layers of TiO2 are grown by thermal oxidation of Ti, by spray pyrolysis, by electrochemical deposition, and by atomic layer deposition. These layers are used in dye-sensitized solar cells to prevent recombination of electrons from

Electrochemical synthesis of self-organized TiO2 crystalline nanotubes without annealing

Science.gov (United States)

Giorgi, Leonardo; Dikonimos, Theodoros; Giorgi, Rossella; Buonocore, Francesco; Faggio, Giuliana; Messina, Giacomo; Lisi, Nicola

2018-03-01

This work demonstrates that upon anodic polarization in an aqueous fluoride-containing electrolyte, TiO2 nanotube array films can be formed with a well-defined crystalline phase, rather than an amorphous one. The crystalline phase was obtained avoiding any high temperature annealing. We studied the formation of nanotubes in an HF/H2O medium and the development of crystalline grains on the nanotube wall, and we found a facile way to achieve crystalline TiO2 nanotube arrays through a one-step anodization. The crystallinity of the film was influenced by the synthesis parameters, and the optimization of the electrolyte composition and anodization conditions (applied voltage and time) were carried out. For comparison purposes, crystalline anatase TiO2 nanotubes were also prepared by thermal treatment of amorphous nanotubes grown in an organic bath (ethylene glycol/NH4F/H2O). The morphology and the crystallinity of the nanotubes were studied by field emission gun-scanning electron microscopy (FEG-SEM) and Raman spectroscopy, whereas the electrochemical and semiconducting properties were analyzed by means of linear sweep voltammetry, impedance spectroscopy, and Mott-Schottky plots. X-ray photoelectron spectroscopy (XPS) and ultraviolet photoelectron spectroscopy (UPS) allowed us to determine the surface composition and the electronic structure of the samples and to correlate them with the electrochemical data. The optimal conditions to achieve a crystalline phase with high donor concentration are defined.

Raman spectra of TiO2 thin films deposited electrochemically and by spray pyrolysis

International Nuclear Information System (INIS)

Shishiyanu, S.; Vartic, V.; Shishiyanu, T.; Stratan, Gh.; Rusu, E.; Zarrelli, M.; Giordano, M.

2013-01-01

In this paper we present our experimental results concerning the fabrication of TiO 2 thin films by spray pyrolysis and electrochemical deposition method onto different substrates - Corning glass, Si and optical fibers. The surface morphology of the TiO 2 thin films have been investigated by Atomic Force Microscopy. Raman shift spectra measurements have been done for the optical characterization of the fabricated titania thin films. The post-growth rapid photothermal processing (RPP) at temperatures of 100-800 degrees Celsius for 1-3 min have been applied. Our experimental results prove that by the application of post-growth RPP is possible to essentially improve the crystallinity of the deposited TiO 2 films. (authors)

Gold and TiO2 Nanostructure Surfaces for Assembling of Electrochemical Biosensors

International Nuclear Information System (INIS)

Curulli, A.; Zane, D.

2008-01-01

Devices based on nano materials are emerging as a powerful and general class of ultrasensitive sensors for the direct detection of biological and chemical species. In this work, we report the preparation and the full characterization of nano materials such as gold nano wires and TiO 2 nano structured films to be used for assembling of electrochemical biosensors. Gold nano wires were prepared by electroless deposition within the pores of polycarbonate particle track-etched membranes (PMS). Glucose oxidase was deposited onto the nano wires using self-assembling monolayer as an anchor layer for the enzyme molecules. Finally, cyclic voltammetry was performed for different enzymes to test the applicability of gold nano wires as biosensors. Considering another interesting nano material, the realization of functionalized TiO 2 thin films on Si substrates for the immobilization of enzymes is reported. Glucose oxidase and horseradish peroxidase immobilized onto TiO 2 -based nano structured surfaces exhibited a pair of well-defined and quasi reversible voltammetric peaks. The electron exchange between the enzyme and the electrodes was greatly enhanced in the TiO 2 nano structured environment. The electrocatalytic activity of HRP and GOD embedded in TiO 2 electrodes toward H 2 O 2 and glucose, respectively, may have a potential perspective in the fabrication of third-generation biosensors based on direct electrochemistry of enzymes.

High-Quality Fe-doped TiO2 films with Superior Visible-Light Performance

DEFF Research Database (Denmark)

Su, Ren; Bechstein, Ralf; Kibsgaard, Jakob

2012-01-01

We report on high-quality polycrystalline Fe-doped TiO2 (Fe–TiO2) porous films synthesized via one-step electrochemical oxidation. We demonstrate that delicate properties such as the impurity concentration and the microstructure that strongly influence the performance of the material for photovol...

Photocatalytic degradation of methyl orange with W-doped TiO2 synthesized by a hydrothermal method

International Nuclear Information System (INIS)

Tian Hua; Ma Junfeng; Li Kang; Li Jinjun

2008-01-01

Nanosized W-doped TiO 2 photocatalysts were synthesized by a simple hydrothermal method, and characterized by energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), transmission electron microscopy (TEM) and BET surface area analyzer. The photocatalytic activity of undoped TiO 2 and W-doped TiO 2 photocatalysts was evaluated by the photocatalytic oxidation degradation of methyl orange in aqueous solution. The results show that the photocatalytic activity of the W-doped TiO 2 photocatalyst is much higher than that of undoped TiO 2 , and the optimum percentage of W doped is 2.0 mol%. The enhanced photocatalytic activity of the doped photocatalyst may be attributed to the increase in the charge separation efficiency and the presence of surface acidity

Chemically synthesized TiO2 and PANI/TiO2 thin films for ethanol sensing applications

Science.gov (United States)

Gawri, Isha; Ridhi, R.; Singh, K. P.; Tripathi, S. K.

2018-02-01

Ethanol sensing properties of chemically synthesized titanium dioxide (TiO2) and polyaniline/titanium dioxide nanocomposites (PANI/TiO2) had been performed at room temperature. In-situ oxidative polymerization process had been employed with aniline as a monomer in presence of anatase titanium dioxide nanoparticles. The prepared samples were structurally and morphologically characterized by x-ray diffraction, fourier transform infrared spectra, high resolution-transmission electron microscopy and field emission-scanning electron microscopy. The crystallinity of PANI/TiO2 nanocomposite was revealed by XRD and FTIR spectra confirmed the presence of chemical bonding between the polymer chains and metal oxide nanoparticles. HR-TEM micrographs depicted that TiO2 particles were embedded in polymer matrix, which provides an advantage over pure TiO2 nanoparticles in efficient adsorption of vapours. These images also revealed that the TiO2 nanoparticles were irregular in shape with size around 17 nm. FE-SEM studies revealed that in the porous structure of PANI/TiO2 film, the intercalation of TiO2 in PANI chains provides an advantage over pure TiO2 film for uniform interaction with ethanol vapors. The sensitivity values of prepared samples were examined towards ethanol vapours at room temperature. The PANI/TiO2 nanocomposite exhibited better sensing response and faster response-recovery examined at different ethanol concentrations ranging from 5 ppm to 20 ppm in comparison to pure TiO2 nanoparticles. The increase in vapour sensing of PANI/TiO2 sensing film as compared to pure TiO2 film had been explained in detail with the help of gas sensing mechanism of TiO2 and PANI/TiO2. This provides strong evidence that gas sensing properties of TiO2 had been considerably improved and enhanced with the addition of polymer matrix.

Black TiO2 synthesized via magnesiothermic reduction for enhanced photocatalytic activity

Science.gov (United States)

Wang, Xiangdong; Fu, Rong; Yin, Qianqian; Wu, Han; Guo, Xiaoling; Xu, Ruohan; Zhong, Qianyun

2018-04-01

Utilizing solar energy for hydrogen evolution is a great challenge for its insufficient visible-light power conversion. In this paper, we report a facile magnesiothermic reduction of commercial TiO2 nanoparticles under Ar atmosphere and at 550 °C followed by acid treatment to synthesize reduced black TiO2 powders, which possesses a unique crystalline core-amorphous shell structure composed of disordered surface and oxygen vacancies and shows significantly improved optical absorption in the visible region. The unique core-shell structure and high absorption enable the reduced black TiO2 powders to exhibit enhanced photocatalytic activity, including splitting of water in the presence of Pt as a cocatalyst and degradation of methyl blue (MB) under visible light irradiation. Photocatalytic evaluations indicate that the oxygen vacancies play key roles in the catalytic process. The maximum hydrogen production rates are 16.1 and 163 μmol h-1 g-1 under the full solar wavelength range of light and visible light, respectively. This facile and versatile method could be potentially used for large scale production of colored TiO2 with remarkable enhancement in the visible light absorption and solar-driven hydrogen production.

Microporous TiO2-WO3/TiO2 films with visible-light photocatalytic activity synthesized by micro arc oxidation and DC magnetron sputtering

International Nuclear Information System (INIS)

Wu, Kee-Rong; Hung, Chung-Hsuang; Yeh, Chung-Wei; Wu, Jiing-Kae

2012-01-01

Highlights: ► A simple MAO is used to prepare porous WO 3 /TiO 2 layer on Ti sheet as a visible-light enabled catalyst. ► The photocatalytic activity of the WO 3 /TiO 2 is enhanced by sputtering over an N,C-TiO 2 layer. ► This is ascribed to the synergetic effect of hybrid sample prepared by two-step method. - Abstract: This study reports the preparation of microporous TiO 2 -WO 3 /TiO 2 films with a high surface area using a two-step approach. A porous WO 3 /TiO 2 template was synthesized by oxidizing a titanium sheet using a micro arc oxidation (MAO) process. This sheet was subsequently overlaid with a visible light (Vis)-enabled TiO 2 (N,C-TiO 2 ) film, which was deposited by codoping nitrogen (N) and carbon (C) ions into a TiO 2 lattice using direct current magnetron sputtering. The resulting microporous TiO 2 -WO 3 /TiO 2 film with a 0.38-μm-thick N,C-TiO 2 top-layer exhibited high photocatalytic activity in methylene blue (MB) degradation among samples under ultraviolet (UV) and Vis irradiation. This is attributable to the synergetic effect of two-step preparation method, which provides a highly porous microstructure and the well-crystallized N,C-TiO 2 top-layer. This is because a higher surface area with high crystallinity favors the adsorption of more MB molecules and more photocatalytic active areas. Thus, the microporous TiO 2 -WO 3 /TiO 2 film has promising applications in the photocatalytic degradation of dye solution under UV and Vis irradiation. These results imply that the microporous WO 3 /TiO 2 can be used as a template of hybrid electrode because it enables rapid fabrication.

Electrochemical Characterization of TiO 2 Blocking Layers for Dye-Sensitized Solar Cells

KAUST Repository

Kavan, Ladislav

2014-07-31

Thin compact layers of TiO2 are grown by thermal oxidation of Ti, by spray pyrolysis, by electrochemical deposition, and by atomic layer deposition. These layers are used in dye-sensitized solar cells to prevent recombination of electrons from the substrate (FTO or Ti) with the hole-conducting medium at this interface. The quality of blocking is evaluated electrochemically by methylviologen, ferro/ferricyanide, and spiro-OMeTAD as the model redox probes. Two types of pinholes in the blocking layers are classified, and their effective area is quantified. Frequency-independent Mott-Schottky plots are fitted from electrochemical impedance spectroscopy. Certain films of the thicknesses of several nanometers allow distinguishing the depletion layer formation both in the TiO2 film and in the FTO substrate underneath the titania film. The excellent blocking function of thermally oxidized Ti, electrodeposited film (60 nm), and atomic-layer-deposited films (>6 nm) is documented by the relative pinhole area of less than 1%. However, the blocking behavior of electrodeposited and atomic-layer-deposited films is strongly reduced upon calcination at 500 °C. The blocking function of spray-pyrolyzed films is less good but also less sensitive to calcination. The thermally oxidized Ti is well blocking and insensitive to calcination. © 2014 American Chemical Society.

TiO2 coated Si nanowire electrodes for electrochemical double layer capacitors in room temperature ionic liquid

International Nuclear Information System (INIS)

Konstantinou, F; Shougee, A; Albrecht, T; Fobelets, K

2017-01-01

Three TiO 2 deposition processes are used to coat the surface of Si nanowire array electrodes for electrochemical double layer capacitors in room temperature ionic liquid [Bmim][NTF 2 ]. The fabrication processes are based on wet chemistry only and temperature treatments are kept below 450 °C. Successful TiO 2 coatings are found to be those that are carried out at low pressure and with low TiO 2 coverage to avoid nanowires breakage. The best TiO 2 coated Si nanowire array electrode in [Bmim][NTF 2 ] showed energy densities of 0.9 Wh·kg −1 and power densities of 2.2 kW·kg −1 with a nanowire length of ∼10 µ m. (paper)

The electrochemical behavior of Co(TPTZ)2 complex on different carbon based electrodes modified with TiO2 nanoparticles

International Nuclear Information System (INIS)

Ortaboy, Sinem; Atun, Gülten

2015-01-01

Electrochemical behavior of cobalt (II) complex with the N-donor ligand 2,2′-bipyridyl-1,3,5-tripyridyl-s-triazine (TPTZ) was investigated to elucidate the electron-proton transfer mechanisms. The electrochemical response of the complex was studied using square-wave voltammetry (SWV) and electrochemical impedance spectroscopy (EIS) techniques. A conventional three-electrode system, consisting of glassy carbon (GCE), TiO 2 modified glassy carbon (T/GCE), carbon paste (CPE) and TiO 2 modified carbon paste (T/CPE) working electrodes were employed. The ligand/metal ratio and stability constant of the complex as well as the mechanisms of the electrode processes were elucidated by examining the effects of pH, ligand concentration and frequency on the voltammograms. The EIS results indicated that the samples modified with TiO 2 had the higher charge transfer resistance than that of the bare electrodes and also suggested that the electroactivity of the electrode surfaces increased in the following order, T/CPE > CPE > T/GCE > GCE. The surface morphology of the working electrodes was also characterized by atomic force microscopy (AFM). The values of surface roughness parameters were found to be consistent with the results obtained by EIS experiments. - Graphical abstract: Schematic illustration of the experimental process. - Highlights: • Electrochemical behavior of Co(TPTZ) 2 complex studied by SWV and EIS techniques. • GCE, CPE T/GCE and T/CPE were used as working electrodes for comparative studies. • The surface morphologies of the electrodes were characterized by AFM. • Mechanisms were proposed from the effects of pH, ligand concentration and frequency. • EIS and morphologic relationships of the surfaces were established successfully

Adsorption of methyl orange by synthesized and functionalized-CNTs with 3-aminopropyltriethoxysilane loaded TiO2 nanocomposites.

Science.gov (United States)

Ahmad, Amirah; Razali, Mohd Hasmizam; Mamat, Mazidah; Mehamod, Faizatul Shimal Binti; Anuar Mat Amin, Khairul

2017-02-01

This study aims to develop a highly efficient adsorbent material. CNTs are prepared using a chemical vapor deposition method with acetylene and synthesized mesoporous Ni-MCM41 as the carbon source and catalyst, respectively, and are then functionalized using 3-aminopropyltriethoxysilane (APTES) through the co-condensation method and loaded with commercial TiO 2 . Results of X-ray powder diffraction (XRD), Raman spectra, and Fourier transform infrared spectroscopy (FTIR) confirm that the synthesized CNTs grown are multi-walled carbon nanotubes (MWNTs). Transmission electron microscopy shows good dispersion of TiO 2 nanoparticles onto functionalized-CNTs loaded TiO 2 , with the diameter of a hair-like structure measuring between 3 and 8 nm. The functionalized-CNTs loaded TiO 2 are tested as an adsorbent for removal of methyl orange (MO) in aqueous solution, and results show that 94% of MO is removed after 10 min of reaction, and 100% after 30 min. The adsorption kinetic model of functionalized-CNTs loaded TiO 2 follows a pseudo-second order with a maximum adsorption capacity of 42.85 mg/g. This study shows that functionalized-CNTs loaded TiO 2 has considerable potential as an adsorbent material due to the short adsorption time required to achieve equilibrium. Copyright © 2016 Elsevier Ltd. All rights reserved.

The Effect of Deposition on Electrochemical Impedance Properties of TiO2/FTO Photoanodes.

Czech Academy of Sciences Publication Activity Database

Balkan, T.; Guler, Z.; Morozová, Magdalena; Dytrych, Pavel; Šolcová, Olga; Sarac, A.S.

2016-01-01

Roč. 36, 1-4 (2016), s. 102-111 ISSN 1385-3449 Grant - others:STRC(TR) TBAG 111T051 Institutional support: RVO:67985858 Keywords : nanofiber * titanium dioxide (TiO2) * electrochemical impedance spectroscopy Subject RIV: CI - Industrial Chemistry, Chemical Engineering Impact factor: 1.238, year: 2016

Optical properties of TiO2 nanotube arrays fabricated by the electrochemical anodization method

International Nuclear Information System (INIS)

Ly, Ngoc Tai; Nguyen, Van Chien; Dao, Thi Hoa; Hoang To, Le Hong; Pham, Duy Long; Do, Hung Manh; Vu, Dinh Lam; Le, Van Hong

2014-01-01

Perpendicularly self-aligned TiO 2 nanotube samples of size of 3 × 5 cm 2 were fabricated by the electrochemical anodization method using a solution containing NH 4 F. Influences of the technological conditions such as NH 4 F concentration and anodization voltage were studied. It was found that NH 4 F concentration in the solution and anodization voltage significantly affect the diameter and length of a TiO 2 nanotube. The diameter and the length of a TiO 2 nanotube were observed and estimated by using scanning electron microscopy. It has shown that the largest diameter and the longest length of about 80 nm and 20 μm, respectively, were obtained for the sample anodized in a solution containing 0.4% of NH 4 F, under a voltage of 48 V. Photoluminescence spectra excited by laser lights having wavelengths of 325 and 442 nm (having energies higher and lower than the band gap energy of TiO 2 ) was recorded at room temperature for the TiO 2 nanotube arrays. An abnormal luminescence result was observed. It is experimental evidence that the manufactured TiO 2 nanotube array is an expected material for hydrogen splitting from water by photochemical effect under sunlight as well as for the nano solar cells. (paper)

Anodic Materials for Lithium-ion Batteries: TiO2-rGO Composites for High Power Applications

International Nuclear Information System (INIS)

Minella, M.; Versaci, D.; Casino, S.; Di Lupo, F.; Minero, C.; Battiato, A.; Penazzi, N.; Bodoardo, S.

2017-01-01

Titanium dioxide/reduced graphene oxide (TiO 2 -rGO) composites were synthesized at different loadings of carbonaceous phase, characterized and used as anode materials in Lithium-ion cells, focusing not only on the high rate capability but also on the simplicity and low cost of the electrode production. It was therefore chosen to use commercial TiO 2 , GO was synthesized from graphite, adsorbed onto TiO 2 and reduced to rGO following a chemical, a photocatalytic and an in situ photocatalytic procedure. The synthesized materials were in-depth characterized with a multi-technique approach and the electrochemical performances were correlated i) to an effective reduction of the GO oxidized moieties and ii) to the maintenance of the 2D geometry of the final graphenic structure observed. TiO 2 -rGO obtained with the first two procedures showed good cycle stability, high capacity and impressive rate capability particularly at 10% GO loading. The photocatalytic reduction applied in situ on preassembled electrodes showed similarly good results reaching the goal of a further simplification of the anode production.

Study on preparation of SnO2-TiO2/Nano-graphite composite anode and electro-catalytic degradation of ceftriaxone sodium.

Science.gov (United States)

Guo, Xiaolei; Wan, Jiafeng; Yu, Xiujuan; Lin, Yuhui

2016-12-01

In order to improve the electro-catalytic activity and catalytic reaction rate of graphite-like material, Tin dioxide-Titanium dioxide/Nano-graphite (SnO 2 -TiO 2 /Nano-G) composite was synthesized by a sol-gel method and SnO 2 -TiO 2 /Nano-G electrode was prepared in hot-press approach. The composite was characterized by X-ray photoelectron spectroscopy, fourier transform infrared, Raman, N 2 adsorption-desorption, scanning electrons microscopy, transmission electron microscopy and X-ray diffraction. The electrochemical performance of the SnO 2 -TiO 2 /Nano-G anode electrode was investigated via cyclic voltammetry and electrochemical impedance spectroscopy. The electro-catalytic performance was evaluated by the degradation of ceftriaxone sodium and the yield of ·OH radicals in the reaction system. The results demonstrated that TiO 2 , SnO 2 and Nano-G were composited successfully, and TiO 2 and SnO 2 particles dispersed on the surface and interlamination of the Nano-G uniformly. The specific surface area of SnO 2 modified anode was higher than that of TiO 2 /Nano-G anode and the degradation rate of ceftriaxone sodium within 120 min on SnO 2 -TiO 2 /Nano-G electrode was 98.7% at applied bias of 2.0 V. The highly efficient electro-chemical property of SnO 2 -TiO 2 /Nano-G electrode was attributed to the admirable conductive property of the Nano-G and SnO 2 -TiO 2 /Nano-G electrode. Moreover, the contribution of reactive species ·OH was detected, indicating the considerable electro-catalytic activity of SnO 2 -TiO 2 /Nano-G electrode. Copyright © 2016 Elsevier Ltd. All rights reserved.

Au Nanoparticles Decorated TiO2 Nanotube Arrays as a Recyclable Sensor for Photoenhanced Electrochemical Detection of Bisphenol A.

Science.gov (United States)

Hu, Liangsheng; Fong, Chi-Chun; Zhang, Xuming; Chan, Leo Lai; Lam, Paul K S; Chu, Paul K; Wong, Kwok-Yin; Yang, Mengsu

2016-04-19

A photorefreshable and photoenhanced electrochemical sensing platform for bisphenol A (BPA) detection based on Au nanoparticles (NPs) decorated carbon doped TiO2 nanotube arrays (TiO2/Au NTAs) is described. The TiO2/Au NTAs were prepared by quick annealing of anodized nanotubes in argon, followed by controllable electrodeposition of Au NPs. The decoration of Au NPs not only improved photoelectrochemical behavior but also enhanced electrocatalytic activities of the resulted hybrid NTAs. Meanwhile, the high photocatalytic activity of the NTAs allowed the electrode to be readily renewed without damaging the microstructures and surface states after a short UV treatment. The electrochemical detection of BPA on TiO2/Au NTAs electrode was significantly improved under UV irradiation as the electrode could provide fresh reaction surface continuously and the further increased photocurrent resulting from the improved separation efficiency of the photogenerated electron-hole pairs derived from the consumption of holes by BPA. The results showed that the refreshable TiO2/Au NTAs electrode is a promising sensor for long-term BPA monitoring with the detection limit (S/N = 3) of 6.2 nM and the sensitivity of 2.8 μA·μM(-1)·cm(-2).

The comparison of photocatalytic activity of synthesized TiO2 and ZrO2 nanosize onto wool fibers

International Nuclear Information System (INIS)

Moafi, Hadi Fallah; Shojaie, Abdollah Fallah; Zanjanchi, Mohammad Ali

2010-01-01

TiO 2 and ZrO 2 nanocrystals were successfully synthesized and deposited onto wool fibers using the sol-gel technique at low temperature. The photocatalytic activities of TiO 2 -coated and ZrO 2 -coated wool fibers were measured by studying photodegradation of methylene blue and eosin yellowish dyes. The initial and the treated samples were characterized by several techniques such as scanning electron microscopy (SEM), transmission electron microscopy (TEM), diffuse reflectance spectroscopy (DRS) and X-ray diffraction. The TEM study shows dispersed particles with 10-30 nm in size for TiO 2 -coated and 20-40 nm in size for ZrO 2 -coated samples on the fiber surface. Comparison of the photocatalytic activity of the coated samples reveals superiority of TiO 2 modified sample with respect to that of ZrO 2 for degradation of both dyes. Our observations indicate that by applying this technique to the fabrics, self-cleaning materials could be designed for practical application.

Enhancing the electrochemical performance of commercial TiO2 by eliminating sulfate radicals and coating carbon

International Nuclear Information System (INIS)

Wang, Li-Ying; Wu, Yan; Han, Jian-Ping; Zhang, Bo; Bai, Xue; Qi, Yong-Xin; Lun, Ning; Cao, Yu-Mei; Bai, Yu-Jun

2017-01-01

Highlights: •Commercial TiO 2 (c-TiO 2 ) exhibits poor electrochemical performance. •The performance of c-TiO 2 is improved by coating carbon at temperatures above 750 °C. •The removal of SO 4 2− and formation of carbon coating are responsible for the enhanced performance. -- Abstract: Despite the low price of commercial TiO 2 (c-TiO 2 ), the poor electrochemical performance restricts its practical application in Li-ion batteries, so clarifying the reasons and taking appropriate measures to improve the performance are of great significance. Herein, c-TiO 2 was coated with carbon at 600 and 750 °C using glucose as the carbon source. The product obtained at 750 °C exhibits markedly enhanced reversible capacities and outstanding rate performance compared to that obtained at 600 °C. In terms of the comparative experiments and detailed characterizations by several techniques, the SO 4 2− remained in the c-TiO 2 is the dominant impurity affecting the electrochemical performance mostly. The thorough decomposition of SO 4 2− at 750 °C and the formation of carbon coating give rise to the enhanced electronic and ionic conductivities of the c-TiO 2 , and thus are responsible for the significant improvement in the electrochemical performance. The easy fabrication and the low cost of the raw materials enable the carbon-coated c-TiO 2 to industrially apply in the LIBs.

Photo-electrochemical properties of graphene wrapped hierarchically branched nanostructures obtained through hydrothermally transformed TiO2 nanotubes

Science.gov (United States)

Rambabu, Y.; Jaiswal, Manu; Roy, Somnath C.

2017-10-01

Hierarchically structured nanomaterials play an important role in both light absorption and separation of photo-generated charges. In the present study, hierarchically branched TiO2 nanostructures (HB-MLNTs) are obtained through hydrothermal transformation of electrochemically anodized TiO2 multi-leg nanotubes (MLNT) arrays. Photo-anodes based on HB-MLNTs demonstrated 5 fold increase in applied bias to photo-conversion efficiency (%ABPE) over that of TiO2 MLNTs without branches. Further, such nanostructures are wrapped with reduced graphene oxide (rGO) films to enhance the charge separation, which resulted in ∼6.5 times enhancement in %ABPE over that of bare MLNTs. We estimated charge transport (η tr) and charge transfer (η ct) efficiencies by analyzing the photo-current data. The ultra-fine nano branches grown on the MLNTs are effective in increasing light absorption through multiple scattering and improving charge transport/transfer efficiencies by enlarging semiconductor/electrolyte interface area. The charge transfer resistance, interfacial capacitance and electron decay time have been estimated through electrochemical impedance measurements which correlate with the results obtained from photocurrent measurements.

Microstructure and antibacterial property of in situ TiO(2) nanotube layers/titanium biocomposites.

Science.gov (United States)

Cui, C X; Gao, X; Qi, Y M; Liu, S J; Sun, J B

2012-04-01

The TiO(2) nanotube layer was in situ synthesized on the surface of pure titanium by the electrochemical anodic oxidation. The diameter of nano- TiO(2) nanotubes was about 70~100 nm. The surface morphology and phase compositions of TiO(2) nanotube layers were observed and analyzed using the scanning electron microscope (SEM). The important processing parameters, including anodizing voltage, reaction time, concentration of electrolyte, were optimized in more detail. The photocatalytic activity of the nano- TiO(2) nanotube layers prepared with optimal conditions was evaluated via the photodegradation of methylthionine in aqueous solution. The antibacterial property of TiO(2) nanotube layers prepared with optimal conditions was evaluated by inoculating Streptococcus mutans on the TiO(2) nanotube layers in vitro. The results showed that TiO(2) nanotube layers/Ti biocomposites had very good antibacterial activity to resist Streptococcus mutans. As a dental implant biomaterial, in situ TiO(2) nanotube layer/Ti biocomposite has better and wider application prospects. Copyright © 2012 Elsevier Ltd. All rights reserved.

Influences of Mg Doping on the Electrochemical Performance of TiO2 Nanodots Based Biosensor Electrodes

Directory of Open Access Journals (Sweden)

M. S. H. Al-Furjan

2014-01-01

Full Text Available Electrochemical biosensors are essential for health monitors to help in diagnosis and detection of diseases. Enzyme adsorptions on biosensor electrodes and direct electron transfer between them have been recognized as key factors to affect biosensor performance. TiO2 has a good protein adsorption ability and facilitates having more enzyme adsorption and better electron transfer. In this work, Mg ions are introduced into TiO2 nanodots in order to further improve electrode performance because Mg ions are considered to have good affinity with proteins or enzymes. Mg doped TiO2 nanodots on Ti substrates were prepared by spin-coating and calcining. The effects of Mg doping on the nanodots morphology and performance of the electrodes were investigated. The density and size of TiO2 nanodots were obviously changed with Mg doping. The sensitivity of 2% Mg doped TiO2 nanodots based biosensor electrode increased to 1377.64 from 897.8 µA mM−1 cm−2 and its KMapp decreases to 0.83 from 1.27 mM, implying that the enzyme achieves higher catalytic efficiency due to better affinity of the enzyme with the Mg doped TiO2. The present work could provide an alternative to improve biosensor performances.

Structural, optical, and magnetic properties of polycrystalline Co-doped TiO2 synthesized by solid-state method

International Nuclear Information System (INIS)

Bouaine, Abdelhamid; Schmerber, G.; Ihiawakrim, D.; Derory, A.

2012-01-01

Highlights: ► Influence of Co doping on the TiO 2 tetragonal structure. ► Decrease of the energy band gap after doping with Co atoms. ► Appearance of ferromagnetism in Co-doped TiO 2 diluted magnetic semiconductors. - Abstract: We have used a solid-state method to synthesize polycrystalline Co-doped TiO 2 diluted magnetic semiconductors (DMSs) with Co concentrations of 0, and 0.5 at.%. X-ray diffraction patterns reveal that Co doped TiO 2 crystallizes in the rutile tetragonal structure with no additional peaks. Transmission electron microscopy (TEM) did not indicate the presence of magnetic parasitic phases and confirmed that Co ions are uniformly distributed inside the samples. Optical absorbance measurements showed an energy band gap which decreases after doping with the Co atoms into the TiO 2 matrix. Magnetization measurements revealed a paramagnetic behavior for the as-prepared Co-doped TiO 2 and a ferromagnetic behavior for the same samples after annealed under a mixture of H 2 /N 2 atmosphere.

Mesoporous TiO2 nanosheets anchored on graphene for ultra long life Na-ion batteries

Science.gov (United States)

Zhang, Ruifang; Wang, Yuankun; Zhou, Han; Lang, Jinxin; Xu, Jingjing; Xiang, Yang; Ding, Shujiang

2018-06-01

Sodium-ion batteries, which have a similar electrochemical reaction mechanism to lithium-ion batteries, have been considered as one of the most potential lithium-ion battery alternatives due to the rich reserves of sodium. However, it is very hard to find appropriate electrode materials imputing the large radius of sodium-ion. TiO2 is particularly interesting as anodes for sodium-ion batteries due to their reasonable operation voltage, cost, and nontoxicity. To obtain a better electrochemical property, mesoporous TiO2 nanosheets (NSs)/reduced graphene oxide (rGO) composites have been synthesized via a scalable hydrothermal-solvothermal method with a subsequent calcination process. Benefitting from unique structure design, TiO2 NSs@rGO exhibits a superior cycle stability (90 mAh g‑1 after 10 000 cycles at a high current rate of 20 C) and satisfactory rate performance (97.3 mAh g‑1 at 25 C). To our knowledge, such ultra long cycle life has not previously been reported.

Chemical and electrochemical synthesis of nano-sized TiO2 anatase for large-area photon conversion

International Nuclear Information System (INIS)

Babasaheb, Raghunath Sankapal; Shrikrishna, Dattatraya Sartale; Lux-Steiner, M.Ch.; Ennaoui, A.

2006-01-01

We report on the synthesis of nanocrystalline titanium dioxide thin films and powders by chemical and electrochemical deposition methods. Both methods are simple, inexpensive and suitable for large-scale production. Air-annealing of the films and powders at T = 500 C leads to densely packed nanometer sized anatase TiO 2 particles. The obtained layers are characterized by different methods such as: X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM). Titanium dioxide TiO 2 (anatase) phase with (101) preferred orientation has been obtained for the films deposited on glass; indium doped tin oxide (ITO) and quartz substrates. The powder obtained as the byproduct consists of TiO 2 with anatase-phase as well. (authors)

Room temperature alcohol sensing by oxygen vacancy controlled TiO2 nanotube array

International Nuclear Information System (INIS)

Hazra, A.; Dutta, K.; Bhowmik, B.; Bhattacharyya, P.; Chattopadhyay, P. P.

2014-01-01

Oxygen vacancy (OV) controlled TiO 2 nanotubes, having diameters of 50–70 nm and lengths of 200–250 nm, were synthesized by electrochemical anodization in the mixed electrolyte comprising NH 4 F and ethylene glycol with selective H 2 O content. The structural evolution of TiO 2 nanoforms has been studied by field emission scanning electron microscopy. Variation in the formation of OVs with the variation of the structure of TiO 2 nanoforms has been evaluated by photoluminescence and X-ray photoelectron spectroscopy. The sensor characteristics were correlated to the variation of the amount of induced OVs in the nanotubes. The efficient room temperature sensing achieved by the control of OVs of TiO 2 nanotube array has paved the way for developing fast responding alcohol sensor with corresponding response magnitude of 60.2%, 45.3%, and 36.5% towards methanol, ethanol, and 2-propanol, respectively.

Quantum dot sensitized solar cell based on TiO2/CdS/Ag2S heterostructure

Science.gov (United States)

Pawar, Sachin A.; Patil, Dipali S.; Kim, Jin Hyeok; Patil, Pramod S.; Shin, Jae Cheol

2017-04-01

Quantum dot sensitized solar cell (QDSSC) is fabricated based on a stepwise band structure of TiO2/CdS/Ag2S to improve the photoconversion efficiency of TiO2/CdS system by incorporating a low band gap Ag2S QDs. Vertically aligned TiO2 nanorods assembly is prepared by a simple hydrothermal technique. The formation of CdS and Ag2S QDs over TiO2 nanorods assembly as a photoanode is carried out by successive ionic layer adsorption and reaction (SILAR) technique. The synthesized electrode materials are characterized by XRD, XPS, field emission scanning electron microscopy (FE-SEM), Optical, solar cell and electrochemical performances. The results designate that the QDs of CdS and Ag2S have efficiently covered exterior surfaces of TiO2 nanorods assembly. A cautious evaluation between TiO2/CdS and TiO2/CdS/Ag2S sensitized cells tells that CdS and Ag2S synergetically helps to enhance the light harvesting ability. Under AM 1.5G illumination, the photoanodes show an improved power conversion efficiency of 1.87%, in an aqueous polysulfide electrolyte with short-circuit photocurrent density of 7.03 mA cm-2 which is four fold higher than that of a TiO2/CdS system.

Optical and Morphological Properties of ZnO- and TiO2-Derived Nanostructures Synthesized via a Microwave-Assisted Hydrothermal Method

Directory of Open Access Journals (Sweden)

Nosipho Moloto

2012-01-01

Full Text Available A microwave-assisted hydrothermal method was used to synthesize ZnO and TiO2 nanostructures. The experimental results show that the method resulted in crystalline monodispersed ZnO nanorods that have pointed tips with hexagonal crystal phase. TiO2 nanotubes were also formed with minimum bundles. The mechanism for the formation of the tubes was validated by HRTEM results. The optical properties of both ZnO and TiO2 nanostructures showed characteristics of strong quantum confinement regime. The photoluminescence spectrum of TiO2 nanotubes shows good improvement from previously reported data.

Photocatalytical Properties and Theoretical Analysis of N, Cd-Codoped TiO2 Synthesized by Thermal Decomposition Method

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Hongtao Gao

2012-01-01

Full Text Available N, Cd-codoped TiO2 have been synthesized by thermal decomposition method. The products were characterized by X-ray diffraction (XRD, scanning electron microscope (SEM, UV-visible diffuse reflectance spectra (DRS, X-ray photoelectron spectroscopy (XPS, and Brunauer-Emmett-Teller (BET specific surface area analysis, respectively. The products represented good performance in photocatalytic degradation of methyl orange. The effect of the incorporation of N and Cd on electronic structure and optical properties of TiO2 was studied by first-principle calculations on the basis of density functional theory (DFT. The impurity states, introduced by N 2p or Cd 5d, lied between the valence band and the conduction band. Due to dopants, the band gap of N, Cd-codoped TiO2 became narrow. The electronic transition from the valence band to conduction band became easy, which could account for the observed photocatalytic performance of N, Cd-codoped TiO2. The theoretical analysis might provide a probable reference for the experimentally element-doped TiO2 synthesis.

The influence of TiO2 and aeration on the kinetics of electrochemical oxidation of phenol in packed bed reactor

International Nuclear Information System (INIS)

Wang Lizhang; Zhao Yuemin; Fu Jianfeng

2008-01-01

The electrochemical oxidation of phenolic wastewater in a lab-scale reactor, packed into granular activated carbon (GAC) with Ti/SnO 2 anodes and stainless steel cathodes, was interpreted in this study. GAC saturated rapidly if it was only used as sorbent, but application of suitable electric energy for the system simultaneously could recover the adsorption ability of GAC and maintain the continuous running effectively. The titanium dioxide (TiO 2 ) as catalyst and airflow were also applied to the electrochemical reactor to examine the enhancement for phenol oxidation process. Results revealed that the electrochemical degradation of phenol could be reasonably described by first-order kinetics. In addition, it was illustrated that acid region, increased voltage, more dosage of TiO 2 and higher aeration intensity were all beneficial parameters for phenol oxidation rates. By inspecting the relationship between the rate constants (k) and influencing factors, respectively, an overall kinetic model for phenol oxidation was proposed. The kinetics obtained from the experiments under corresponding electrochemical conditions could provide an accurate estimation of phenol concentration effluent and better design of the packed bed reactor

Comparison of TiO2 photocatalysis, electrochemically assisted Fenton reaction and direct electrochemistry for simulation of phase I metabolism reactions of drugs.

Science.gov (United States)

Ruokolainen, Miina; Gul, Turan; Permentier, Hjalmar; Sikanen, Tiina; Kostiainen, Risto; Kotiaho, Tapio

2016-02-15

The feasibility of titanium dioxide (TiO2) photocatalysis, electrochemically assisted Fenton reaction (EC-Fenton) and direct electrochemical oxidation (EC) for simulation of phase I metabolism of drugs was studied by comparing the reaction products of buspirone, promazine, testosterone and 7-ethoxycoumarin with phase I metabolites of the same compounds produced in vitro by human liver microsomes (HLM). Reaction products were analysed by UHPLC-MS. TiO2 photocatalysis simulated the in vitro phase I metabolism in HLM more comprehensively than did EC-Fenton or EC. Even though TiO2 photocatalysis, EC-Fenton and EC do not allow comprehensive prediction of phase I metabolism, all three methods produce several important metabolites without the need for demanding purification steps to remove the biological matrix. Importantly, TiO2 photocatalysis produces aliphatic and aromatic hydroxylation products where direct EC fails. Furthermore, TiO2 photocatalysis is an extremely rapid, simple and inexpensive way to generate oxidation products in a clean matrix and the reaction can be simply initiated and quenched by switching the UV lamp on/off. Copyright © 2015 Elsevier B.V. All rights reserved.

A Facile Method for Synthesizing TiO2 Sea-Urchin-Like Structures and Their Applications in Solar Energy Harvesting

International Nuclear Information System (INIS)

Wang Wen-Hui; Xu Hong-Xing; Wang Wen-Zhong

2011-01-01

We present a new method to prepare TiO 2 sea-urchin-like structures, which involves the initial formation of tubular nanostructures and subsequent self-assembly of the nanotubes into micrometer-scale sea-urchin-like structures. We also investigate the important role of alkali aqueous conditions in the preparation of TiO 2 sea-urchin-like structures. This facile and cost-effective approach provides a new route for the preparation of self-assembled TiO 2 structures. In addition, the performance of the as-synthesized TiO 2 sea-urchin-like structures as the active layer of an efficient solar energy harvester is also studied and discussed. (cross-disciplinary physics and related areas of science and technology)

Flower-like hydrogenated TiO2(B) nanostructures as anode materials for high-performance lithium ion batteries

Science.gov (United States)

Zhang, Zhonghua; Zhou, Zhenfang; Nie, Sen; Wang, Honghu; Peng, Hongrui; Li, Guicun; Chen, Kezheng

2014-12-01

Flower-like hydrogenated TiO2(B) nanostructures have been synthesized via a facile solvothermal approach combined with hydrogenation treatment. The obtained TiO2(B) nanostructures show uniform and hierarchical flower-like morphology with a diameter of 124 ± 5 nm, which are further constructed by primary nanosheets with a thickness of 10 ± 1.2 nm. The Ti3+ species and/or oxygen vacancies are well introduced into the structures of TiO2(B) after hydrogen reduction, resulting in an enhancement in the electronic conductivity (up to 2.79 × 10-3 S cm-1) and the modified surface electrochemical activity. When evaluated for lithium storage capacity, the hydrogenated TiO2(B) nanostructures exhibit enhanced electrochemical energy storage performances compared to the pristine TiO2(B) nanostructures, including high capacity (292.3 mA h g-1 at 0.5C), excellent rate capability (179.6 mA h g-1 at 10C), and good cyclic stability (98.4% capacity retention after 200 cycles at 10C). The reasons for these improvements are explored in terms of the increased electronic conductivity and the facilitation of lithium ion transport arising from the introduction of oxygen vacancies and the unique flower-like morphologies.

Photoelectrocatalytic properties of Ag nanoparticles loaded TiO2 nanotube arrays prepared by pulse current deposition

International Nuclear Information System (INIS)

Xie Kunpeng; Sun Lan; Wang Chenglin; Lai Yuekun; Wang Mengye; Chen Hongbo; Lin Changjian

2010-01-01

A pulse current deposition technique was adopted to construct highly dispersed Ag nanoparticles on TiO 2 nanotube arrays which were prepared by the electrochemical anodization. The morphology, crystallinity, elemental composition, and UV-vis absorption of Ag/TiO 2 nanotube arrays were characterized by scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and diffuse reflectance spectra (DRS). In particular, the photoelectrochemical properties and photoelectrocatalytic activity under UV light irradiation and the photocatalytic activity under visible light irradiation for newly synthesized Ag/TiO 2 nanotube arrays were investigated. The maximum incident photon to charge carrier efficiency (IPCE) value of Ag/TiO 2 nanotube arrays was 51%, much higher than that of pure TiO 2 nanotube arrays. Ag/TiO 2 nanotube arrays exhibited higher photocatalytic activities than the pure TiO 2 nanotube arrays under both UV and visible light irradiation. The photoelectrocatalytic activity of Ag/TiO 2 nanotube arrays under UV light irradiation was 1.6-fold enhancement compared with pure TiO 2 nanotube arrays. This approach can be used in synthesizing various metal-loaded nanotube arrays materials.

Chalcogenide Sensitized Carbon Based TiO2 Nanomaterial For Solar Driven Applications

Science.gov (United States)

Pathak, Pawan

The demand for renewable energy is growing because fossils fuels are depleting at a rapid pace. Solar energy an abundant green energy resource. Utilizing this resource in a smart manner can resolve energy-crisis related issues. Sun light can be efficiently harvested using semiconductor based materials by utilizing photo-generated charges for numerous beneficial applications. The main goal of this thesis is to synthesize different nanostructures of TiO2, develop a novel method of coupling and synthesizing chalcogenide nanocrystals with TiO2 and to study the charge transportation effects of the various carbon allotropes in the chalcogenide nanocrystal sensitized TiO2 nanostructure. We have fabricated different nanostructures of TiO2 as solar energy harvesting materials. Effects of the different phases of TiO2 have also been studied. The anatase phase of TiO2 is more photoactive than the rutile phase of TiO2, and the higher dimension of the TiO2 can increase the surface area of the material which can produce higher photocurrent. Since TiO2 only absorbs in the UV range; to increase the absorbance TiO2 should be coupled to visible light absorbing materials. This dissertation presents a simple approach to synthesize and couple chalcogenide nanocrystals with TiO2 nanostructure to form a heterostructured composite. An atmospheric pressure based, single precursor, one-pot approach has been developed and tested to assemble chalcogenide nanocrystal on the TiO2 surface. Surface characterization using microscopy, X-ray diffraction, and elemental analysis indicates the formation of nanocrystals along the nanotube walls and inter-tubular spacing. Optical measurements indicate that the chalcogenide nanocrystals absorb in the visible region and demonstrate an increase in photocurrent in comparison to bare TiO2 nanostructure. The CdS synthesized TiO2 nanostructure produced the highest photocurrent as measured in the three electrode system. We have also assembled the PbS nanocrystal

Comparison of TiO2 photocatalysis, electrochemically assisted Fenton reaction and direct electrochemistry for simulation of phase I metabolism reactions of drugs

NARCIS (Netherlands)

Ruokolainen, Miina; Gül, Turan; Permentier, Hjalmar; Sikanen, Tiina; Kostiainen, Risto; Kotiaho, Tapio

2016-01-01

The feasibility of titanium dioxide (TiO2) photocatalysis, electrochemically assisted Fenton reaction (EC-Fenton) and direct electrochemical oxidation (EC) for simulation of phase I metabolism of drugs was studied by comparing the reaction products of buspirone, promazine, testosterone and

Electrochemical & osteoblast adhesion study of engineered TiO2 nanotubular surfaces on titanium alloys

International Nuclear Information System (INIS)

Rahman, Zia Ur; Haider, Waseem; Pompa, Luis; Deen, K.M.

2016-01-01

TiO 2 nanotubes were grafted on the surface of cpTi, Ti6Al4V and Ti6Al4V-ELI with the aim to provide a new podium for human pre-osteoblast cell (MC3T3) adhesion and proliferation. The surface morphology and chemistry of these alloys were examined with scanning electron microscopy and energy dispersive x-ray spectroscopy. TiO 2 nanotubes were further characterized by cyclic potentiodynamic polarization tests and electrochemical impedance spectroscopy. The vertically aligned nanotubes were subjected to pre-osteoblast cell proliferation in order to better understand cell–material interaction. The study demonstrated that these cells interact differently with nanotubes of different titanium alloys. The significant acceleration in the growth rate of pre-osteoblast cell adhesion and proliferation is also witnessed. Additionally, the cytotoxicity of the leached metal ions was evaluated by using a tetrazolium-based bio-assay, MTS. Each group of data was operated for p < 0.05, concluded one way ANOVA to investigate the significance difference. - Highlights: • TiO 2 nanotubes were grafted on cpTi, Ti6Al4V and Ti6Al4V-ELI via anodization. • MC3T3 cells interact differently with nanotubes of different titanium alloys. • TiO 2 nanotubes have a positive impact on the osteoblast cell viability.

Plasma-induced synthesis of Pt nanoparticles supported on TiO2 nanotubes for enhanced methanol electro-oxidation

Science.gov (United States)

Su, Nan; Hu, Xiulan; Zhang, Jianbo; Huang, Huihong; Cheng, Jiexu; Yu, Jinchen; Ge, Chao

2017-03-01

A Pt/C/TiO2 nanotube composite catalyst was successfully prepared for enhanced methanol electro-oxidation. Pt nanoparticles with a particle size of 2 nm were synthesized by plasma sputtering in water, and anatase TiO2 nanotubes with an inner diameter of approximately 100 nm were prepared by a simple two-step anodization method and annealing process. Field-emission scanning electron microscopy images indicated that the different morphologies of TiO2 synthesized on the surface of Ti foils were dependent on the different anodization parameters. The electrochemical performance of Pt/C/TiO2 catalysts for methanol oxidation showed that TiO2 nanotubes were more suitable for use as Pt nanoparticle support materials than irregular TiO2 short nanorods due to their tubular morphology and better electronic conductivity. X-ray photoelectron spectroscopy characterization showed that the binding energies of the Pt 4f of the Pt/C/TiO2 nanotubes exhibited a slightly positive shift caused by the relatively strong interaction between Pt and the TiO2 nanotubes, which could mitigate the poisoning of the Pt catalyst by COads, and further enhance the electrocatalytic performance. Thus, the as-obtained Pt/C/TiO2 nanotubes composites may become a promising catalyst for methanol electro-oxidation.

Study of the electrochemical behavior at low temperatures of green anodes for Lithium ion batteries prepared with anatase TiO2 and water soluble sodium carboxymethyl cellulose binder

International Nuclear Information System (INIS)

Mancini, M.; Nobili, F.; Tossici, R.; Marassi, R.

2012-01-01

Highlights: ► Water soluble CMC and PVDF binders are used to prepare anatase TiO 2 electrodes. ► The electrochemical behavior of the different electrodes is studied between 20 and −30 °C. ► CMC/TiO 2 anodes show lower ICL, lower polarization and higher low-temperature capacity at high rates than PVDF/TiO 2 anodes. ► Electrochemical Impedance Spectroscopy results show better kinetics for CMC/TiO 2 electrodes. - Abstract: The electrochemical behavior at low temperatures of anatase TiO 2 electrodes for Lithium ion batteries have been evaluated by galvanostatic cycles in the temperature range 20 to −30 °C. Two different manufacturing processes have been used to prepare anatase anodes containing water soluble sodium carboxymethyl cellulose (CMC) or poly(vinilydene fluoride) (PVDF) as binder. The low temperature performances at different charge/discharge rates of TiO 2 /CMC and TiO 2 /PVDF electrodes are compared and discussed in terms of irreversible capacity loss (ICL) at the first cycle, capacity retention and reversible capacity. The kinetics of the electrodes containing CMC or PVDF is evaluated by Electrochemical Impedance Spectroscopy.

Enhancement in photo-electrochemical efficiency by reducing recombination rate in branched TiO2 nanotube array on functionalizing with ZnO micro crystals

Science.gov (United States)

Boda, Muzaffar Ahmad; Ashraf Shah, Mohammad

2018-06-01

In this study, branched TiO2 nanotube array were fabricated through electrochemical anodization process at constant voltage using third generation electrolyte. On account of morphological advantage, these nanotubes shows significant enhancement in photo-electrochemical property than compact or conventional titania nanotube array. However, their photo-electrochemical efficiency intensifies on coating with ZnO micro-crystals. ZnO coated branched TiO2 nanotube array shows a photocurrent density of 27.8 mA cm‑2 which is 1.55 times the photocurrent density (17.2 mA cm‑2) shown by bare branched titania nanotubes. The significant enhancement in photocurrent density shown by the resulting ZnO/TiO2 hybrid structure is attributed to suppression in electron–hole recombination phenomenon by offering smooth pathway to photo generated excitons on account of staggered band edge positions in individual semiconductors.

Exchange of TiO2 nanoparticles between streams and streambeds.

Science.gov (United States)

Boncagni, Natalia Ticiana; Otaegui, Justo Manuel; Warner, Evelyn; Curran, Trisha; Ren, Jianhong; de Cortalezzi, Maria Marta Fidalgo

2009-10-15

The expanding use of manufactured nanoparticles has increased the potential for their release into the natural environment. Particularly, TiO2 nanoparticles pose significant exposure risk to humans and other living species due to their extensive use in a wide range of fields. To better understand the environmental and health risks associated with the release of TiO2 nanoparticles, knowledge on their fate and transport is needed. This study evaluates the transport of two different TiO2 nanoparticles: one commercially available (P25 TiO2 and the other synthesized at a lab scale (synthesized TiO2). Laboratory flume, column, and batch experiments were conducted to investigate the processes dominating the transport of TiO2 nanoparticles between streams and streambeds and to characterize the properties of these nanoparticles under different physicochemical conditions. Results show that the synthesized TiO2 was more stable compared to the P25 TiO2, which underwent significant aggregation under the same experimental conditions. As a result, P25 TiO2 deposited at a faster rate than the synthesized TiO2 in the streambed. Both types of TiO2 nanoparticles deposited in the streambed were easily released when the stream velocity was increased. The aggregation and deposition of P25 TiO2 were highly dependent on pH. A process-based colloid exchange model was applied to interpret the observed transport behavior of the TiO2 nanoparticles.

Amine functionalized TiO2-carbon nanotube composite: synthesis, characterization and application to glucose biosensing

Science.gov (United States)

Tasviri, Mahboubeh; Rafiee-Pour, Hossain-Ali; Ghourchian, Hedayatollah; Gholami, Mohammad Reza

2011-12-01

The synthesis of amine functionalized TiO2-coated multiwalled carbon nanotubes (NH2-TiO2-CNTs) using sol-gel method was investigated. The synthesized nanocomposite was characterized with XRD, FTIR spectroscopy, BET test and SEM imaging. The results demonstrated a unique nanostructure with no destruction of the CNTs' shape. In addition, the presence of amine groups on the composite surface was confirmed by FTIR. This nanocomposite was used for one-step immobilization of glucose oxidase (GOx) to sense glucose. The result of cyclic voltammetry showed a pair of well-defined and quasi-reversible peaks for direct electron transfer of GOx in the absence of glucose. Also, the result of electrochemical impedance spectroscopy indicated that GOx was successfully immobilized on the surface of NH2-TiO2-CNTs. Furthermore, good amperometric response showed that immobilized GOx on the NH2-TiO2-CNTs exhibits exceptional bioelectrocatalytic activity toward glucose oxidation.

Photoelectrochemical oxidation of ibuprofen via Cu_2O-doped TiO_2 nanotube arrays

International Nuclear Information System (INIS)

Sun, Qiannan; Peng, Yen-Ping; Chen, Hanlin; Chang, Ken-Lin; Qiu, Yang-Neng; Lai, Shiau-Wu

2016-01-01

Highlights: • A p–n junction material was synthesized to enhance photocatalytic ability. • Cu_2O-doped TiO_2 nanotube arrays works as a photoanode in a PEC system. • Recombination of photo-generated holes and electrons were greatly reduced. • Synergetic effect was quantified in PEC degradation. • Recombination of photogenerated holes and electrons was greatly enhanced. - Abstract: A p–n junction based Cu_2O-doped TiO_2 nanotube arrays (Cu_2O-TNAs) were synthesized and used as a working anode in a photoelectrochemical (PEC) system. The results revealed that the Cu_2O-TNAs were dominated by the anatase phase and responded significantly to visible light. XPS analyses indicated that with an amount of 24.79% Cu doping into the structure, the band gap of Cu_2O-TNAs was greatly reduced. SEM images revealed that the supported TiO_2 nanotubes had diameters of approximately 80 nm and lengths of about 2.63 μm. Upon doping with Cu_2O, the TiO_2 nanotubes maintained their structural integrity, exhibiting no significant morphological change, favoring PEC applications. Under illumination, the photocurrent from Cu_2O/TNAs was 2.4 times larger than that from TNAs, implying that doping with Cu_2O significantly improved electron mobility by reducing the rate of recombination of electron-hole pairs. The EIS and Bode plot revealed that the estimated electron lifetimes, τ_e_l, of TNAs and Cu_2O/TNAs were 6.91 and 26.26 ms, respectively. The efficiencies of degradation of Ibuprofen by photoelectrochemical, photocatalytic (PC), electrochemical (EC) and photolytic (P) methods were measured.

Effect of ambient pressure on the crystalline phase of nano TiO2 particles synthesized by a dc thermal plasma reactor

International Nuclear Information System (INIS)

Banerjee, I.; Karmakar, Soumen; Kulkarni, Naveen V.; Nawale, Ashok B.; Mathe, V. L.; Das, A. K.; Bhoraskar, S. V.

2010-01-01

The synthesis of nanoparticles of titanium dioxide (TiO 2 ) with varying percentages of anatase and rutile phases is reported. This was achieved by controlling the operating pressure in a transferred-arc, direct current thermal plasma reactor in which titanium vapors are evaporated, and then exposed to ambient oxygen. The average particle size remained around 15 nm in each case. The crystalline structure of the as-synthesized nanoparticles of TiO 2 was studied with X-ray diffraction analysis; whereas the particle morphology was investigated with the help of transmission electron microscopy. The precursor species responsible for the growth of these nanoparticles was studied with the help of optical emission spectroscopy. As inferred from the X-ray diffraction analysis, the relative abundance of anatase TiO 2 was found to be dominant when synthesized at 760 Torr, and the same showed a decreasing trend with decreasing chamber pressure. The study also reveals that anatase TiO 2 is a more effective photocatalytic agent in degrading methylene blue by comparison to its rutile phase.

Simple fabrication of TiO2/C nanocomposite with enhanced electrochemical performance for lithium-ion batteries

International Nuclear Information System (INIS)

Bai, Xue; Li, Tao; Qi, Yong-Xin; Gao, Xue-Ping; Yin, Long-Wei; Li, Hui; Zhu, Hui-Ling; Lun, Ning; Bai, Yu-Jun

2015-01-01

TiO 2 /C nanocomposites were fabricated by simple hydrolysis of tetrabutyl titanate to yield TiO 2 nanoparticles followed by carbonizing the mixture of glucose and TiO 2 at 600 °C. By merely varying the weight ratio of glucose:TiO 2 , the electrochemical performance of the composites could be optimized significantly. At a ratio of 0.8, the composite exhibits a high reversible capacity of 283.7 mA h g −1 after cycling 100 times at a current density of 100 mA g −1 , as well as the capacities of 245.1, 213.6, 179.9 and 136.6 mA h g −1 at the corresponding densities of 200, 400, 800 and 1600 mA g −1 . After cycling 1000 times at 500 mA g −1 , a capacity of 122.8 mA h g −1 was retained for the composite with a ratio of 0.8, and even a capacity of 149.1 mA h g −1 for the composite with a ratio of 0.7. The enhanced performance is ascribed to the carbon-coated TiO 2 nanoparticles uniformly embedding in the carbon matrix with appropriate carbon content

Inverted organic solar cells with solvothermal synthesized vanadium-doped TiO2 thin films as efficient electron transport layer

Institute of Scientific and Technical Information of China (English)

Mehdi Ahmadi; Sajjad Rashidi Dafeh; Samaneh Ghazanfarpour; Mohammad Khanzadeh

2017-01-01

We investigated the effects of using different thicknesses of pure and vanadium-doped thin films of TiO2 as the electron transport layer in the inverted configuration of organic photovoltaic cells based on poly (3-hexylthiophene) P3HT:[6-6] phenyl-(6) butyric acid methyl ester (PCBM).1％ vanadium-doped TiO2 nanoparticles were synthesized via the solvothermal method.Crystalline structure,morphology,and optical properties of pure and vanadium-doped TiO2 thin films were studied by different techniques such as x-ray diffraction,scanning electron microscopy,transmittance electron microscopy,and UV-visible transmission spectrum.The doctor blade method which is compatible with roll-2-roll printing was used for deposition of pure and vanadium-doped TiO2 thin films with thicknesses of 30 nm and 60 nm.The final results revealed that the best thickness of TiO2 thin films for our fabricated cells was 30 nm.The cell with vanadium-doped TiO2 thin film showed slightly higher power conversion efficiency and great Jsc of 10.7 mA/cm2 compared with its pure counterpart.In the cells using 60 nm pure and vanadium-doped TiO2 layers,the cell using the doped layer showed much higher efficiency.It is remarkable that the extemal quantum efficiency of vanadium-doped TiO2 thin film was better in all wavelengths.

An innovative approach to synthesize highly-ordered TiO2 nanotubes.

Science.gov (United States)

Isimjan, Tayirjan T; Yang, D Q; Rohani, Sohrab; Ray, Ajay K

2011-02-01

An innovative route to prepare highly-ordered and dimensionally controlled TiO2 nanotubes has been proposed using a mild sonication method. The nanotube arrays were prepared by the anodization of titanium in an electrolyte containing 3% NH4F and 5% H2O in glycerol. It is demonstrated that the TiO2 nanostructures has two layers: the top layer is TiO2 nanowire and underneath is well-ordered TiO2 nanotubes. The top layer can easily fall off and form nanowires bundles by implementing a mild sonication after a short annealing time. We found that the dimensions of the TiO2 nanotubes were only dependent on the anodizing condition. The proposed technique may be extended to fabricate reproducible well-ordered TiO2 nanotubes with large area on other metals.

Sol-gel synthesis of TiO2 nanoparticles and photocatalytic degradation of methyl orange in aqueous TiO2 suspensions

International Nuclear Information System (INIS)

Yang Huaming; Zhang Ke; Shi Rongrong; Li Xianwei; Dong Xiaodan; Yu Yongmei

2006-01-01

Anatase TiO 2 nanoparticles of about 16 nm in crystal size have been successfully synthesized via a sol-gel method. Thermal treatment of the precursor at 500-600 deg. C results in the formation of different TiO 2 phase compositions. The samples were characterized by means of X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM). Effects of the pH value of the solution, H 2 O 2 addition, TiO 2 phase composition and recycled TiO 2 on the photocatalytic degradation of methyl orange (MeO) in TiO 2 suspensions under ultraviolet (UV) illumination were primarily investigated. The results indicate that a low pH value, proper amount of H 2 O 2 and pure anatase TiO 2 will facilitate the photocatalytic oxidation of the MeO solution. The photodegradation degree decreases with increasing the pH value of the solution and varies with different amounts of H 2 O 2 . Pure anatase TiO 2 shows better photocatalytic activity for MeO decolorization than biphase TiO 2 . The photocatalytic mechanism of the as-synthesized TiO 2 nanoparticles was discussed

Characterization and Comparison of Photocatalytic Activity Silver Ion doped on TiO2(TiO2/Ag+) and Silver Ion doped on Black TiO2(Black TiO2/Ag+)

Science.gov (United States)

Kim, Jin Yi; Sim, Ho Hyung; Song, Sinae; Noh, Yeoung Ah; Lee, Hong Woon; Taik Kim, Hee

2018-03-01

Titanium dioxide (TiO2) is one of the representative ceramic materials containing photocatalyst, optic and antibacterial activity. The hydroxyl radical in TiO2 applies to the intensive oxidizing agent, hence TiO2 is suitable to use photocatalytic materials. Black TiO2was prepared through reduction of amorphous TiO2 conducting under H2 which leads to color changes. Its black color is proven that absorbs 100% light across the whole-visible light, drawing enhancement of photocatalytic property. In this study, we aimed to compare the photocatalytic activity of silver ion doped on TiO2(TiO2/Ag+) and silver ion doped on black TiO2(black TiO2/Ag+) under visible light range. TiO2/Ag+ was fabricated following steps. 1) TiO2 was synthesized by a sol-gel method from Titanium tetraisopropoxide (TTIP). 2) Then AgNO3 was added during an aging process step for silver ion doping on the surface of TiO2. Moreover, Black TiO2/Ag+ was obtained same as TiO2/Ag+ except for calcination under H2. The samples were characterized X-ray diffraction (XRD), UV-visible reflectance (UV-vis DRS), and Methylene Blue degradation test. XRD analysis confirmed morphology of TiO2. The band gap of black TiO2/Ag+ was confirmed (2.6 eV) through UV-vis DRS, which was lower than TiO2/Ag+ (2.9 eV). The photocatalytic effect was conducted by methylene blue degradation test. It demonstrated that black TiO2/Ag+ had a photocatalytic effect under UV light also visible light.

The Effect of Normal Force on Tribocorrosion Behaviour of Ti-10Zr Alloy and Porous TiO2-ZrO2 Thin Film Electrochemical Formed

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Dănăilă, E.; Benea, L.

2017-06-01

The tribocorrosion behaviour of Ti-10Zr alloy and porous TiO2-ZrO2 thin film electrochemical formed on Ti-10Zr alloy was evaluated in Fusayama-Mayer artificial saliva solution. Tribocorrosion experiments were performed using a unidirectional pin-on-disc experimental set-up which was mechanically and electrochemically instrumented, under various solicitation conditions. The effect of applied normal force on tribocorrosion performance of the tested materials was determined. Open circuit potential (OCP) measurements performed before, during and after sliding tests were applied in order to determine the tribocorrosion degradation. The applied normal force was found to greatly affect the potential during tribocorrosion experiments, an increase in the normal force inducing a decrease in potential accelerating the depassivation of the materials studied. The results show a decrease in friction coefficient with gradually increasing the normal load. It was proved that the porous TiO2-ZrO2 thin film electrochemical formed on Ti-10Zr alloy lead to an improvement of tribocorrosion resistance compared to non-anodized Ti-10Zr alloy intended for biomedical applications.

THERMALLY STABLE NANOCRYSTALLINE TIO2 PHOTOCATALYSTS SYNTHESIZED VIA SOL-GEL METHODS MODIFIED WITH IONIC LIQUID AND SURFACTANT MOLECULES

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Recently, sol-gel methods employing ionic liquids (ILs) have shown significant implications for the synthesis of well-defined nanostructured inorganic materials. Herein, we synthesized nanocrystalline TiO2 particles via an alkoxide sol-gel method employing a water-immi...

Well-defined copolymers synthesized by RAFT polymerization as effective modifiers to enhance the photocatalytic performance of TiO_2

International Nuclear Information System (INIS)

Vasilaki, E.; Kaliva, M.; Katsarakis, N.; Vamvakaki, M.

2017-01-01

Highlights: • Well-defined, random functional copolymers were synthesized by RAFT polymerization. • Novel TiO_2 particles in-situ modified with copolymers were synthesized. • The hybrid catalysts exhibited reduced aggregation and particle size. • The photocatalytic removal of methylene blue was higher for the hybrid catalysts. - Αbstract: The enhancement of the photocatalytic performance of anatase TiO_2 nanoparticles is demonstrated by a facile route, involving their in-situ surface modification with preformed polymer chains. Random copolymers of poly(ethylene glycol) methyl ether acrylate-co-methacrylic acid (PEGA-co-MAA) or poly(ethylene glycol) methyl ether acrylate-co-dopamine methacrylamide (PEGA-co-DMA) were synthesized by reversible addition−fragmentation chain-transfer (RAFT) polymerization and were bound onto the surface of anatase titania nanoparticles via the “grafting to” method. The hybrid nanocatalysts were characterized by fourier transform infrared spectroscopy, zeta-potential measurements, X-ray powder diffraction, thermogravimetric analysis and transmission electron microscopy. Their photocatalytic performance was evaluated by the decoloration of methylene blue (MB) dye in aqueous media under UV–vis light irradiation. The enhanced photoactivity and reusability of the polymer modified photocatalysts compared to that of bare TiO_2 nanoparticles was attributed to their improved dispersability and colloidal stability, the smaller particle size that leads to a larger surface area and the increased adsorption capacity of the dye onto the polymer modified nanoparticles.

Interaction of NO during cathodic polarization in alkaline conditions at the interface of Pt-nanostructures supported on C and TiO2-C

International Nuclear Information System (INIS)

Estudillo-Wong, L.A.; Arce-Estrada, E.M.; Manzo-Robledo, A.

2014-01-01

The electroreduction of nitric oxide (NO) in alkaline media was carried out on Pt nanoparticles (5 wt.% Pt), which were synthesized by the carbonyl route. The as-prepared materials were supported on Carbon Black (XC-72R, C) and TiO 2 -C composite (10 wt.% TiO 2 ) and deposited on glassy carbon (GC) electrode. X-ray Diffraction (XRD), CO-stripping and hydrogen adsorption-desorption (H upd ) analysis were employed to characterize the structure and electrochemical properties. According to XRD patterns, the particle size increases from 3.95 to 8.98 nm due to the interaction of Pt with TiO 2 in the carbon matrix. This modification promotes a better performance during CO-oxidation and proton adsorption-desorption. As a consequence, the performance toward NO-reduction was more important in TiO 2 -C composite, linked with the electrochemical active-surface area and chemical surface area relationship (ECSA/CSA). It was found that the mechanism for the reduction of nitric oxide toward nitrogen is a bi-functional process with coupled chemical and electrochemical interfacial-reactions with NH 2 specie as intermediate, as demonstrated by the induced reduction reaction of NO 2 − and NO 2 − + NO, and UV-vis spectrometry

Scalable Synthesis of Triple-Core-Shell Nanostructures of TiO2 @MnO2 @C for High Performance Supercapacitors Using Structure-Guided Combustion Waves.

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Shin, Dongjoon; Shin, Jungho; Yeo, Taehan; Hwang, Hayoung; Park, Seonghyun; Choi, Wonjoon

2018-03-01

Core-shell nanostructures of metal oxides and carbon-based materials have emerged as outstanding electrode materials for supercapacitors and batteries. However, their synthesis requires complex procedures that incur high costs and long processing times. Herein, a new route is proposed for synthesizing triple-core-shell nanoparticles of TiO 2 @MnO 2 @C using structure-guided combustion waves (SGCWs), which originate from incomplete combustion inside chemical-fuel-wrapped nanostructures, and their application in supercapacitor electrodes. SGCWs transform TiO 2 to TiO 2 @C and TiO 2 @MnO 2 to TiO 2 @MnO 2 @C via the incompletely combusted carbonaceous fuels under an open-air atmosphere, in seconds. The synthesized carbon layers act as templates for MnO 2 shells in TiO 2 @C and organic shells of TiO 2 @MnO 2 @C. The TiO 2 @MnO 2 @C-based electrodes exhibit a greater specific capacitance (488 F g -1 at 5 mV s -1 ) and capacitance retention (97.4% after 10 000 cycles at 1.0 V s -1 ), while the absence of MnO 2 and carbon shells reveals a severe degradation in the specific capacitance and capacitance retention. Because the core-TiO 2 nanoparticles and carbon shell prevent the deformation of the inner and outer sides of the MnO 2 shell, the nanostructures of the TiO 2 @MnO 2 @C are preserved despite the long-term cycling, giving the superior performance. This SGCW-driven fabrication enables the scalable synthesis of multiple-core-shell structures applicable to diverse electrochemical applications. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Eco-friendly synthesis of TiO2, Au and Pt doped TiO2 nanoparticles for dye sensitized solar cell applications and evaluation of toxicity

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Gopinath, K.; Kumaraguru, S.; Bhakyaraj, K.; Thirumal, S.; Arumugam, A.

2016-04-01

Driven by the demand of pure TiO2, Au and Pt doped TiO2 NPs were successfully synthesized using Terminalia arjuna bark extract. The eco-friendly synthesized NPs were characterized by UV-Vis-DRS, ATR-FT-IR, PL, XRD, Raman, SEM with EDX and TEM analysis. The synthesized NPs were investigation for dye sensitized solar cell applications. UV-Vis-Diffused Reflectance Spectra clearly showed that the expected TiO2 inter band absorption below 306 nm, incorporation of gold shows surface plasma resonant (SPR) near 555 nm and platinum incorporated TiO2 NPs shows absorbance at 460 nm. The energy conversion efficiency for Au doped TiO2 NPs when compared to pure and Pt doped TiO2 NPs. In addition to that, Au noble metal present TiO2 matrix and an improve open-circuit voltage (Voc) of DSSC. Synthesized NPs was evaluated into antibacterial and antifungal activities by disk diffusion method. It is observed that NPs have not shown any activities in all tested bacterial and fungal strains. In this eco-friendly synthesis method to provide non toxic and environmental friendly nanomaterials can be used for solar energy device application.

Fabrication and Characteristics of Macroporous TiO2 Photocatalyst

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Guiyun Yi

2014-01-01

Full Text Available Macroporous TiO2 photocatalyst was synthesized by a facile nanocasting method using polystyrene (PS spherical particles as the hard template. The synthesized photocatalyst was characterized by transmission electron microscope (TEM, scanning electron microscopy (SEM, thermogravimetry-differential thermogravimetry (TG-DTG, X-ray diffraction (XRD, and N2-sorption. TEM, SEM, and XRD characterizations confirmed that the macroporous TiO2 photocatalyst is composed of anatase phase. The high specific surface area of 87.85 m2/g can be achieved according to the N2-sorption analysis. Rhodamine B (RhB was chosen as probe molecule to evaluate the photocatalytic activity of the TiO2 catalysts. Compared with the TiO2 materials synthesized in the absence of PS spherical template, the macroporous TiO2 photocatalyst sintered at 500°C exhibits much higher activity on the degradation of RhB under the UV irradiation, which can be assigned to the well-structured macroporosity. The macroporous TiO2 material presents great potential in the fields of environmental remediation and energy conversion and storage.

Few layer graphene wrapped mixed phase TiO2 nanofiber as a potential electrode material for high performance supercapacitor applications

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Thirugnanam, Lavanya; Sundara, Ramaprabhu

2018-06-01

A combination of favorable composition and optimized anatase/rutile mixed-phase TiO2 (MPTNF)/Hydrogen exfoliated graphene (HEG) composite nanofibers (MPTNF/HEG) and anatase/rutile mixed-phase TiO2/reduced graphene oxide (rGO) composite nanofibers (MPTNF/rGO) have been reported to enhance the electrochemical properties for supercapacitor applications. These composite nanofibers have been synthesized by an efficient route of electrospinning together with the help of easy chemical methods. Both the composites exhibit good charge storage capability with enhanced pseudocapacitance and electric double-layer capacitance (EDLC) as confirmed by cyclic voltammetry studies. MPTNF/HEG composite showed maximum specific capacitance of 210.5 F/g at the current density of 1 A/g, which was mainly due to its availability of the more active sites for ions adsorption on a few layers of graphene wrapped TiO2 nanofiber surface. The synergistic effect of anatase/rutile mixed phase with one dimensional nanostructure and the electronic interaction between TiO2 and few layer graphene provided the subsequent improvement of ion adsorption capacity. Also exhibit excellent electrochemical performance to improve the capacitive properties of TiO2 electrode materials which is required for the development of flexible electrodes in energy storage devices and open up new opportunities for high performance supercapacitors.

DNA mediated wire-like clusters of self-assembled TiO2 nanomaterials: supercapacitor and dye sensitized solar cell applications

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Nithiyanantham, U.; Ramadoss, Ananthakumar; Ede, Sivasankara Rao; Kundu, Subrata

2014-06-01

A new route for the formation of wire-like clusters of TiO2 nanomaterials self-assembled in DNA scaffold within an hour of reaction time is reported. TiO2 nanomaterials are synthesized by the reaction of titanium-isopropoxide with ethanol and water in the presence of DNA under continuous stirring and heating at 60 °C. The individual size of the TiO2 NPs self-assembled in DNA and the diameter of the wires can be tuned by controlling the DNA to Ti-salt molar ratios and other reaction parameters. The eventual diameter of the individual particles varies between 15 +/- 5 nm ranges, whereas the length of the nanowires varies in the 2-3 μm range. The synthesized wire-like DNA-TiO2 nanomaterials are excellent materials for electrochemical supercapacitor and DSSC applications. From the electrochemical supercapacitor experiment, it was found that the TiO2 nanomaterials showed different specific capacitance (Cs) values for the various nanowires, and the order of Cs values are as follows: wire-like clusters (small size) > wire-like clusters (large size). The highest Cs of 2.69 F g-1 was observed for TiO2 having wire-like structure with small sizes. The study of the long term cycling stability of wire-like clusters (small size) electrode were shown to be stable, retaining ca. 80% of the initial specific capacitance, even after 5000 cycles. The potentiality of the DNA-TiO2 nanomaterials was also tested in photo-voltaic applications and the observed efficiency was found higher in the case of wire-like TiO2 nanostructures with larger sizes compared to smaller sizes. In future, the described method can be extended for the synthesis of other oxide based materials on DNA scaffold and can be further used in other applications like sensors, Li-ion battery materials or treatment for environmental waste water.A new route for the formation of wire-like clusters of TiO2 nanomaterials self-assembled in DNA scaffold within an hour of reaction time is reported. TiO2 nanomaterials are

Synthesis of titanate, TiO2 (B), and anatase TiO2 nanofibers from natural rutile sand

International Nuclear Information System (INIS)

Pavasupree, Sorapong; Suzuki, Yoshikazu; Yoshikawa, Susumu; Kawahata, Ryoji

2005-01-01

Titanate nanofibers were synthesized by hydrothermal method (150 deg. C for 72 h) using natural rutile sand as the starting materials. TiO 2 (B) and anatase TiO 2 (high crystallinity) nanofibers with the diameters of 20-100 nm and the lengths of 10-100 μm were obtained by calcined titanate nanofibers for 4 h at 400 and 700 deg. C (in air), respectively. The samples characterized by XRD, SEM, TEM, SAED, HRTEM, and BET surface area. This synthesis method provides a simple route to fabricate one-dimensional nanostructured TiO 2 from low cost material. -- Graphical abstract: Titanate nanofibers (b) were synthesized by hydrothermal method (150 deg. C for 72 h) using natural rutile sand (a) as the starting materials. TiO 2 (B) (c) and anatase TiO 2 (d) nanofibers with the diameters of 20-50 nm and the lengths of 10-100 μm were obtained by calcined titanate nanofibers for 4 h at 400 deg. C and 700 deg. C (in air), respectively

Enhanced photoelectrochemical and photocatalytic behaviors of MFe2O4 (M = Ni, Co, Zn and Sr) modified TiO2 nanorod arrays

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Gao, Xin; Liu, Xiangxuan; Zhu, Zuoming; Wang, Xuanjun; Xie, Zheng

2016-07-01

Modified TiO2 nanomaterials are considered to be promising in energy conversion and ferrites modification may be one of the most efficient modifications. In this research, various ferrites, incorporated with various cations (MFe2O4, M = Ni, Co, Zn, and Sr), are utilized to modify the well aligned TiO2 nanorod arrays (NRAs), which is synthesized by hydrothermal method. It is found that all MFe2O4/TiO2 NRAs show obvious red shift into the visible light region compared with the TiO2 NRAs. In particular, NiFe2O4 modification is demonstrated to be the best way to enhance the photoelectrochemical and photocatalytic activity of TiO2 NRAs. Furthermore, the separation and transfer of charge carriers after MFe2O4 modification are clarified by electrochemical impedance spectroscopy measurements. Finally, the underlying mechanism accounting for the enhanced photocatalytic activity of MFe2O4/TiO2 NRAs is proposed. Through comparison among different transition metals modified TiO2 with the same synthesis process and under the same evaluating condition, this work may provide new insight in designing modified TiO2 nanomaterials as visible light active photocatalysts.

Study of the highly ordered TiO2 nanotubes physical properties prepared with two-step anodization

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Pishkar, Negin; Ghoranneviss, Mahmood; Ghorannevis, Zohreh; Akbari, Hossein

2018-06-01

Highly ordered hexagonal closely packed titanium dioxide nanotubes (TiO2 NTs) were successfully grown by a two-step anodization process. The TiO2 NTs were synthesized by electrochemical anodization of titanium foils in an ethylene glycol based electrolyte solution containing 0.3 wt% NH4F and 2 vol% deionized (DI) water at constant potential (50 V) for 1 h at room temperature. Physical properties of the TiO2 NTs, which were prepared via one and two-step anodization, were investigated. Atomic Force Microscopy (AFM) analysis revealed that anodization and subsequently peeled off the TiO2 NTs caused to the periodic pattern on the Ti surface. In order To study the nanotubes morphology, Field Emission Scanning Electron Microscopy (FESEM) was used, which was revealed that the two-step anodization resulted highly ordered hexagonal TiO2 NTs. Crystal structures of the TiO2 NTs were mainly anatase, determined by X-ray diffraction analysis. Optical studies were performed by Diffuse Reflection Spectra (DRS) and Photoluminescence (PL) analysis showed that the band gap of TiO2 NTs prepared via two-step anodization was lower than the band gap of samples prepared by one-step anodization process.

Optical and morphological properties of ZnO- and TiO2-derived nanostructures synthesized via a microwave-assisted hydrothermal method

CSIR Research Space (South Africa)

Moloto, N

2012-01-01

Full Text Available Corporation International Journal of Photoenergy Volume 2012, Article ID 189069, 6 pages doi:10.1155/2012/189069 Research Article Optical and Morphological Properties of ZnO- and TiO2-Derived Nanostructures Synthesized via a Microwave... International Journal of Photoenergy the sol-gel, hydrothermal process, and pulse laser deposition [22?24]. Although the sol-gel method is widely accepted for the preparation of both ZnO and TiO2 nanostructures, the calcinations process is essential and can...

Genotoxic and cytotoxic activity of green synthesized TiO2 nanoparticles

Science.gov (United States)

Koca, Fatih Doğan; Duman, Fatih

2018-03-01

Nowadays, nanomaterials that are smaller than 100 nm in size are very attractive owing to their enhanced physicochemical properties. Although they have been used widely for industrial applications, their toxicity still remains a problem. This article is a new record of the synthesis of titanium dioxide nanoparticles (TiO2 NPs) by a Mentha aquatica leaf extract and determination of its toxicity to rat marrow mesenchymal stem cells. In this study, we aimed to determine the genotoxic and cytotoxic effects of biologically synthetized TiO2 NPs. The characteristic peak of the nanomaterial was observed at 354 nm. The mean size of the nanomaterial was measured to be 69 nm from SEM images. According to zeta analysis, the surface charge of the nanomaterial was - 37.6 mV. The crystalline structure of the nanomaterial was determined using XRD analysis. It was concluded that the obtained nanomaterial was TiO2 The results of the FT-IR analysis showed that the functional groups that were found in the plant extract could play an important role in the formation and stabilization of TiO2 NPs. The effective size of the TiO2 NPs was found to be 304 nm using DLS analysis. The TGA analysis results showed that the total mass loss was 4% at 900 °C. According to DNA cleavage analysis results, TiO2 NPs cause damage to the plasmid pBR322 DNA in a concentration-dependant matter. It has been noted that TiO2 NPs lead to decreased cell viability during increased time and concentration of applications on rat marrow mesenchymal stem cells. It has also been determined that bulk TiO2 causes a greater reduction in the stem cell viability compared to the biosynthesized NPs. The obtained results could be useful for further application and toxicity studies.

Hydrothermal synthesis of BiVO4/TiO2 composites and their application for degradation of gaseous benzene under visible light irradiation

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Hu, Yin; Chen, Wei; Fu, Jianping; Ba, Mingwei; Sun, Fuqian; Zhang, Peng; Zou, Jiyong

2018-04-01

Benzene is currently recognized as one of the most toxic contaminants. Our previously published study revealed that BiVO4/TiO2 is an excellent photocatalyst toward the degradation of benzene. Herein, BiVO4/TiO2 has been synthesized via a sol-gel method and a facile hydrothermal route by adjusting the precursor hydrolysis rate with the use of different acids (CH3COOH, HNO3 and H2SO4). The influence of these acids on the physicochemical characteristics and photocatalytic performance is discussed in detail. X-ray diffraction and N2 sorption analyses confirm that acid has an important effect on the crystalline composition and BET specific surface area. BiVO4/TiO2 synthesized in CH3COOH has better photocatalytic activity for the degradation of gaseous benzene than that in HNO3 and H2SO4 under visible light irradiation. Results of XPS measurement demonstrate that the hydroxyl group in BiVO4/TiO2-CH3COOH is more abundant than that in BiVO4/TiO2-HNO3 and BiVO4/TiO2-H2SO4. The photocurrent signal is investigated by electrochemical measurement, which indicates that more effective separation of photogenerated carriers occurs in the BiVO4/TiO2/CH3COOH system. It is hoped that our work can offer valuable information on the design of TiO2 composites with enhanced properties.

Amorphous TiO2 Shells: A Vital Elastic Buffering Layer on Silicon Nanoparticles for High-Performance and Safe Lithium Storage.

Science.gov (United States)

Yang, Jianping; Wang, Yunxiao; Li, Wei; Wang, Lianjun; Fan, Yuchi; Jiang, Wan; Luo, Wei; Wang, Yang; Kong, Biao; Selomulya, Cordelia; Liu, Hua Kun; Dou, Shi Xue; Zhao, Dongyuan

2017-12-01

Smart surface coatings of silicon (Si) nanoparticles are shown to be good examples for dramatically improving the cyclability of lithium-ion batteries. Most coating materials, however, face significant challenges, including a low initial Coulombic efficiency, tedious processing, and safety assessment. In this study, a facile sol-gel strategy is demonstrated to synthesize commercial Si nanoparticles encapsulated by amorphous titanium oxide (TiO 2 ), with core-shell structures, which show greatly superior electrochemical performance and high-safety lithium storage. The amorphous TiO 2 shell (≈3 nm) shows elastic behavior during lithium discharging and charging processes, maintaining high structural integrity. Interestingly, it is found that the amorphous TiO 2 shells offer superior buffering properties compared to crystalline TiO 2 layers for unprecedented cycling stability. Moreover, accelerating rate calorimetry testing reveals that the TiO 2 -encapsulated Si nanoparticles are safer than conventional carbon-coated Si-based anodes. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Eu"2"+ doped TiO_2 nano structures synthesized by HYSYCVD for thermoluminescence dosimetry

International Nuclear Information System (INIS)

Perez A, J. A.; Leal C, A. L.; Melendrez A, R.; Barboza F, M.

2016-10-01

Titania (TiO_2) has attracted interest owing his potential applications as dosimetry material given his excellent optical, electrical and thermal properties and the ability to shape his structure make TiO_2 suitable for research and dosimetry applications. In this work, a systematic study to know the magnitude of processing parameters influence on thermoluminescent properties of undoped (TiO_2) and doped (TiO_2:Eu"2"+) nano materials obtained by hybrid precursor systems chemical vapor deposition (HYSYCVD) technique is presented. Synthesis of one dimension nano structures of TiO_2:Eu"2"+ was carried out using K_2TiF_6 and EuCl_2 as dopant at 0.5, 1, 2.5 and 5 wt %. The nano structures samples were irradiated with β-ray in a doses range of 0.083-3000 Gy. All thermoluminescence (Tl) glow curves showed 3 broad Tl peaks around 373, 473 and 573 K, and a dosimetric linear behavior from 0.083 to 300 Gy. The Tl has a good reproducibility, with deviations of around 5%, making these TiO_2:Eu"2"+ nano materials suitable for dosimetric applications. (Author)

Studies on the Fe3+ Doping Effect on Structural, Optical and Catalytic Properties of Hydrothermally Synthesized TiO2 Photocatalyst

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Kamble, Ravi [Department of Physics, Jaysingpur College, Jaysingpur-416101, India; Sabale, Sandip [P.G. Department of Chemistry, Jaysingpur College, Jaysingpur-416101, Maharashtra, India; Chikode, Prashant [Department of Physics, Jaysingpur College, Jaysingpur-416101, India; Puri, Vijaya [Department of Physics, Shivaji University, Kolhapur-416004, India; Yu, Xiao-Ying [Earth and Biological Sciences Directorate, Pacific Northwest National Laboratory (PNNL), Richland, WA 99352, United States; Mahajan, Smita [Department of Physics, Jaysingpur College, Jaysingpur-416101, India

2017-08-01

Pure TiO2 and Fe3+-TiO2 nanoparticles have been prepared by simple hydrothermal method with different Fe3+ concentrations. The synthesized nanoparticles are analysed to determine its structural, optical, morphological and compositional properties using X-ray diffraction, Raman, UV-DRS, photoluminescence, Mossbauer, XPS, TEM and SEM/EDS. The EDS micrograph confirms the existence of Fe3+ atoms in the TiO2 matrix with 0.85, 1.52 and 1.87 weight percent. The crystallite size and band gap decrease with increase in Fe3+concentration. The average particle size obtained from TEM is 7-11 nm which is in good agreement with XRD results. Raman bands at 640 cm-1, 517 cm-1 and 398 cm-1 further confirm pure phase anatase in all samples. XPS shows the proper substitutions of few sites of Ti4+ ions by Fe3+ ions in the TiO2 host lattice. The intensity of PL spectra for Fe3+-TiO2 shows a gradual decrease in the peak intensity with increasing Fe3+ concentration in TiO2, and it indicates lower recombination rate as Fe3+ ions increases. These nanoparticles are further studied for its photocatalytic activities using malachite green dye under UV light, visible light and sunlight.

Crystal growth and design of a facile synthesized uniform single crystalline football-like anatase TiO2 microspheres with exposed {0 0 1} facets

International Nuclear Information System (INIS)

Liu, Bitao; Jin, Chunhua; Ju, Yue; Peng, Lingling; Tian, Liangliang; Wang, Jinbiao; Zhang, Tiejun

2014-01-01

Graphical abstract: - Highlights: • Football-like TiO 2 synthesized by a facile hydrothermal method. • The formation mechanism of football-like TiO 2 was investigated. • The DSSC efficiency assembled by football-like TiO 2 is 23.3% higher than P25. - Abstract: Uniform football-like anatase TiO 2 particles exposed by {0 0 1} facets were successfully synthesized by an environment-friendly, facile and low-temperature hydrothermal method in water solution without any additional capping agent. The crystallographic structure and the growth mechanism of anatase TiO 2 particles were investigated systematically by X-ray diffraction pattern (XRD), field emission scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectra (XPS), respectively. The formation mechanism of football-like anatase TiO 2 particles exposed by {0 0 1} facets is investigated. It was found that there existed a selective adsorption of F − ions on different facets by analyzed with the density functional theory (DFT) computer simulation results, and it would lead to a selective nucleation and crystal growth of anatase football-like TiO 2 particles. Additionally, this type of exposed {0 0 1} facets football-like TiO 2 microspheres were used as a scattering overlayer on a transparent P25 film for fabrication of photoanodes for dye-sensitized solar cells (DSSCs). The results showed that an overall light conversion efficiency of this film was 6.31%, which is higher than that of the overall efficiency (5.13%) obtained from the P25 photoanode owing to the superior light scattering effect of microspheres and excellent light reflecting ability of the mirror-like plane {0 0 1} facets

Fabrication, characterization and photocatalytic properties of Ag nanoparticles modified TiO2 NTs

International Nuclear Information System (INIS)

Wang Qingyao; Yang Xiuchun; Liu Dan; Zhao Jianfu

2012-01-01

Graphical abstract: The TiO 2 NTs were first treated with bi-functional mercaptoacetic acid linkers (HOOC–R–S). The –OH group on the surface of TiO 2 NT provides a strong affinity with the carboxylate group in the linker molecules. The thiol functional group in the linker molecules facilitates the binding with Ag from AgNO 3 solution. After Ag + ions were reduced by NaBH 4 , Ag nanoparticles formed by nucleation and growth. Highlights: ► Ag nanoparticles with an average diameter of 9.2 nm were filled in the TiO 2 nanotubes by a successive ionic layer adsorption and reaction (SILAR) technique. ► Bi-functional mercaptoacetic acid linkers were used to bind TiO 2 nanotubes with Ag nanoparticles. ► Ag nanoparticles modification of TiO 2 NTs largely enhanced the photocatalytic degradation of methyl orange under ultraviolet light irradiation. - Abstract: Ordered anatase TiO 2 nanotubes (TiO 2 NTs) on Ti substrate were synthesized by electrochemical anodization and subsequently vapor-thermal treatment. Ag nanoparticles were decorated on TiO 2 NTs by successive ionic layer adsorption and reaction (SILAR) technique. Raman spectroscopy, X-ray absorption near edge spectroscopy (XANES), X-ray diffraction (XRD), UV–vis diffuse reflectance spectroscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were used for the characterization of surface morphology, phase composition, and microstructure of the original TiO 2 NTs, the vapor-thermally treated TiO 2 NTs and the Ag nanoparticles decorated TiO 2 NTs. The results indicate that vapor-thermal treatment favors to the transformation of amorphous TiO 2 into anatase phase. Increasing the SILAR cycle times favors to increase the loaded amounts of Ag nanoparticles in TiO 2 NTs. Ag nanoparticles are uniformly distributed in the TiO 2 NTs, and the SILAR process does not damage the ordered tubular structure. A possible formation mechanism of Ag/TiO 2 NTs has also been proposed. The

Room temperature one-step synthesis of microarrays of N-doped flower-like anatase TiO2 composed of well-defined multilayer nanoflakes by Ti anodization

Science.gov (United States)

Wang, Chenglin; Wang, Mengye; Xie, Kunpeng; Wu, Qi; Sun, Lan; Lin, Zhiqun; Lin, Changjian

2011-07-01

Microarrays of N-doped flower-like TiO2 composed of well-defined multilayer nanoflakes were synthesized at room temperature by electrochemical anodization of Ti in NH4F aqueous solution. The TiO2 flowers were of good anatase crystallinity. The effects of anodizing time, applied voltage and NH4F concentration on the flower-like morphology were systematically examined. It was found that the morphologies of the anodized Ti were related to the anodizing time and NH4F concentration. The size and density of the TiO2 flowers could be tuned by changing the applied voltage. The obtained N-doped flower-like TiO2 microarrays exhibited intense absorption in wavelengths ranging from 320 to 800 nm. Under both UV and visible light irradiation, the photocatalytic activity of the N-doped flower-like TiO2 microarrays in the oxidation of methyl orange showed a significant increase compared with that of commercial P25 TiO2 film.

Corrosion protection of AISI 1018 steel using Co-doped TiO_2/polypyrrole nanocomposites in 3.5% NaCl solution

International Nuclear Information System (INIS)

Ladan, Magaji; Basirun, Wan Jeffrey; Kazi, Salim Newaz; Rahman, Fariza Abdul

2017-01-01

A polypyrrole nanocomposites (PPy NTCs) have been effectively synthesized in the presence of TiO_2 and Co-doped TiO_2 nanoparticles (NPs) by an in situ chemical oxidative polymerization. Field Emission Scanning Electron Microscopy and Transmission Electron Microscopy revealed a tube shape structure of the PPy. The TEM results confirmed that the nanocomposite size of Co-doped TiO_2/PPy NTCs was smaller than TiO_2/PPy NTCs thereby increasing the interaction between the PPy nanotube and the AISI steel surface. The corrosion performance of the coatings was evaluated by electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization measurements in 3.5% NaCl solution. The EIS results show that the log |Z| of AISI 1018 coated with Co-doped TiO_2/PPy NTCs and TiO_2/PPy NTCs reached about 8.2 and 6.0 respectively after 30 days of exposure in 3.5% NaCl solution. This is likely due to the increased surface area of the PPy synthesized in the presence of Co-doped TiO_2 NPs. The EIS results are confirmed by the potentiodynamic polarization and open circuit potential values of the Co-doped TiO_2/PPy which indicated little changes between 1 and 30 days of exposure which confirms the protection ability of this coating. . It is evident that the presence of Co-doped TiO_2 NPs can enhance the resistance against corrosion at the steel/electrolyte interface. - Highlights: • Polymerization of pyrrole monomer in the presence of Co-doped TiO_2 decreases the size of the polypyrrole nanotube (PPy NT). • The corrosion protection increases with the increase in PPy NT dispersion. • The corrosion resistance of steel coated with Co-doped TiO_2/PPy NTCs is considerably higher. • TiO_2/PPy with Co doping reduces the charge transfer across the electrolyte/AISI 1018 steel interface.

Non-aqueous hybrid supercapacitors fabricated with mesoporous TiO2 microspheres and activated carbon electrodes with superior performance

Science.gov (United States)

Cai, Yong; Zhao, Bote; Wang, Jie; Shao, Zongping

2014-05-01

Mesoporous TiO2 microspheres, synthesized by a facile template-free solvothermal method and subsequent heat treatment, are exploited as the electrode for hybrid supercapacitors. The effects of the calcination temperature on the phase composition, particulate microstructure and morphology are characterized by XRD, Raman, FE-SEM and N2 adsorption/desorption measurements. Hybrid supercapacitors utilizing the as-prepared TiO2 mesoporous microspheres as the negative electrode and activated carbon (AC) as the positive electrode in a non-aqueous electrolyte are fabricated. The electrochemical performance of these hybrid supercapacitors is studied by galvanostatic charge-discharge and cyclic voltammetry (CV). The hybrid supercapacitor built from TiO2 microspheres calcined at 400 °C shows the best performance, delivering an energy density of 79.3 Wh kg-1 at a power density of 178.1 W kg-1. Even at a power density of 9.45 kW kg-1, an energy density of 31.5 Wh kg-1 is reached. These values are much higher than the AC-AC symmetric supercapacitor. In addition, the hybrid supercapacitor exhibits excellent cycling performance, retaining 98% of the initial energy density after 1000 cycles. Such outstanding electrochemical performance of the hybrid supercapacitor is attributed to the matched reaction kinetics between the two electrodes with different energy storage mechanisms.

Electrochemical Behavior of TiO2 Nanoparticle Doped WO3 Thin Films

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Suvarna R. Bathe

2014-01-01

Full Text Available Nanoparticle TiO2 doped WO3 thin films by pulsed spray pyrolysis technique have been studied on fluorine tin doped (FTO and glass substrate. XRD shows amorphous nature for undoped and anatase phase of TiO2 having (101 plane for nanoparticle TiO2 doped WO3 thin film. SEM shows microfibrous reticulated porous network for WO3 with 600 nm fiber diameter and nanocrystalline having size 40 nm for TiO2 nanoparticle doped WO3 thin film. TiO2 nanoparticle doped WO3 thin film shows ~95% reversibility due to may be attributed to nanocrystalline nature of the film, which helpful for charge insertion and deinsertion process. The diffusion coefficient for TiO2 nanoparticle doped WO3 film is less than undoped WO3.

Defect-rich TiO2-δ nanocrystals confined in a mooncake-shaped porous carbon matrix as an advanced Na ion battery anode

Science.gov (United States)

He, Hanna; Zhang, Qi; Wang, Haiyan; Zhang, Hehe; Li, Jiadong; Peng, Zhiguang; Tang, Yougen; Shao, Minhua

2017-06-01

Inferior electronic conductivity and sluggish sodium ion diffusion are still two big challenges for TiO2 anode material for Na ion batteries (SIBs). Herein, we synthesize TiO2/C composites by the pyrolysis of MIL-125(Ti) precursor and successfully introduce defects to TiO2/C composite by a simple magnesium reduction. The as-prepared defect-rich TiO2-δ/C composite shows mooncake-shaped morphology consisting of TiO2-δ nanocrystals with an average particle size of 5 nm well dispersed in the carbon matrix. When used as a SIBs anode, the defect-rich TiO2-δ/C composite exhibits a high reversible capacity of 330.2 mAh g-1 at 50 mA g-1 at the voltage range of 0.001-3.0 V and long-term cycling stability with negligible decay after 5000 cycles. Compared with other four TiO2/C samples, the electrochemical performance of defect-rich TiO2-δ/C is highly improved, which may benefit from the enhanced electronic/ionic conductivities owing to the defect-rich features, high surface area rendering shortened electronic and ionic diffusion path, and the suppress of the TiO2 crystal aggregation during sodiation and desodiation process by the carbon matrix.

Effect of TiO_2 Loading on Pt-Ru Catalysts During Alcohol Electrooxidation

International Nuclear Information System (INIS)

Hasa, Bjorn; Kalamaras, Evangelos; Papaioannou, Evangelos I.; Vakros, John; Sygellou, Labrini; Katsaounis, Alexandros

2015-01-01

Highlights: • TiO_2 can be used to modify Pt-Ru based electrodes for alcohol oxidation. • TiO_2 modified electrodes with lower amount of metals had higher active surface area than pure Pt-Ru electrodes. • TiO_2 modified electrodes showed comparable performance with pure Pt-Ru electrode both in a single cell and in a PEM fuel cell under alcohol fuelling. - Abstract: In this study, Pt-Ru based electrodes modified by TiO_2 were prepared by means of thermal decomposition of chloride and isopropoxide precursors on Ti substrates, characterised by X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), X-ray Photoelectron Spectroscopy (XPS), electrochemical techniques and CO stripping and used as anodes for alcohol oxidation. The minimization of the metal loading without electrocatalytic activity losses was also explored. TiO_2 was chosen due to its chemical stability, low cost and excellent properties as substrate for metal dispersion. It was found that TiO_2 loading up to 50% results in a 3-fold increase of the Electrochemically Active Surface (EAS). This conclusion has been confirmed by CO stripping experiments. All samples have been evaluated during the electrochemical oxidation of methanol, ethanol and glycerol. In all cases, the Pt_2_5-Ru_2_5-(TiO_2)_5_0 electrode had better electrocatalytic activity than the pure Pt_5_0-Ru_5_0 anode. The best modified electrode, (Pt_2_5-Ru_2_5-(TiO_2)_5_0), was also evaluated as anode in a PEM fuel cell under methanol fuelling conditions. The observed higher performance of the TiO_2 modified electrodes was attributed to the enhanced Pt-Ru dispersion as well as the formation of smaller Pt and Ru particles.

Novel Ag@TiO2 nanocomposite synthesized by electrochemically active biofilm for nonenzymatic hydrogen peroxide sensor.

Science.gov (United States)

Khan, Mohammad Mansoob; Ansari, Sajid Ali; Lee, Jintae; Cho, Moo Hwan

2013-12-01

A novel nonenzymatic sensor for H2O2 was developed based on an Ag@TiO2 nanocomposite synthesized using a simple and cost effective approach with an electrochemically active biofilm. The optical, structural, morphological and electrochemical properties of the as-prepared Ag@TiO2 nanocomposite were examined by UV-vis spectroscopy, X-ray diffraction, transmission electron microscopy and cyclic voltammetry (CV). The Ag@TiO2 nanocomposite was fabricated on a glassy carbon electrode (GCE) and their electrochemical performance was analyzed by CV, differential pulse voltammetry and electrochemical impedance spectroscopy. The Ag@TiO2 nanocomposite modified GCE (Ag@TiO2/GCE) displayed excellent performance towards H2O2 sensing at -0.73 V in the linear response range from 0.83 μM to 43.3 μM, within a detection limit and sensitivity of 0.83 μM and ~65.2328±0.01 μA μM(-1) cm(-2), respectively. In addition, Ag@TiO2/GCE exhibited good operational reproducibility and long term stability. © 2013.

Visible-light photocatalytic activity of the metastable Bi20TiO32 synthesized by a high-temperature quenching method

International Nuclear Information System (INIS)

Cheng Hefeng; Huang Baibiao; Dai Ying; Qin Xiaoyan; Zhang Xiaoyang; Wang Zeyan; Jiang Minhua

2009-01-01

Metastable Bi 20 TiO 32 samples were synthesized by a high-temperature quenching method using α-Bi 2 O 3 and anatase TiO 2 as raw materials. The photocatalytic activity of the as-prepared samples was measured with the photodegradation of methyl orange at room temperature under visible light irradiation. The Bi 20 TiO 32 samples exhibited good absorption in the visible light region with a band gap of about 2.38 eV and the band structure of Bi 20 TiO 32 was studied. Photodegradation against methyl orange was much better than α-Bi 2 O 3 prepared by the same way. The photocatalytic activity of Bi 20 TiO 32 samples is supposed to be associated with the hybridized Bi 6s and O 2p orbitals. In addition, the dispersive characteristic of Bi 6s orbital in the hybridized valence band facilitates the mobility of the photogenerated carriers and hampers their recombination. - Graphical abstract: Metastable Bi 20 TiO 32 samples were successfully synthesized by a quenching process. Photodegradation against methyl orange showed high visible-light activity and it was supposed to be associated with its corresponding band structure.

Electrochemical and spectroelectrochemical characterization of different mesoporous TiO2 film electrodes for the immobilization of Cytochrome c

Science.gov (United States)

Katsiaounis, Stavros; Tiflidis, Christina; Tsekoura, Christina; Topoglidis, Emmanuel

2018-03-01

In this work three different mesoporous TiO2 film electrodes were prepared and used for the immobilization of Cytochrome c (Cyt-c). Films prepared via a standard sol-gel route (SG-films) were compared with commercially available benchmark nanotitania materials, namely P25 Degussa (P25-films) and Dyesol nanopaste (Dyesol films). Their properties, film deposition characteristics and their abilities to adsorb protein molecules in a stable and functional way were examined. We investigated whether it is possible, rather than preparing TiO2 films using multistep, lengthy and not always reproducible sol-gel procedures, to use commercially available nanotitania materials and produce reproducible films faster that exhibit all the properties that make TiO2 films ideal for protein immobilization. Although these materials are formulated primarily for dye-sensitized solar cell applications, in this study we found out that protein immobilization is facile and remarkably stable on all of them. We also investigated their electrochemical properties by using cyclic voltammetry and spectroelectrochemistry and found out that not only direct reduction of Fe(III)-heme to Fe(II)-heme of immobilized Cyt-c was possible on all films but that the adsorbed protein remained electroactive.

Effect of TiO2 on the Gas Sensing Features of TiO2/PANi Nanocomposites

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Duong Ngoc Huyen

2011-02-01

Full Text Available A nanocomposite of titanium dioxide (TiO2 and polyaniline (PANi was synthesized by in-situ chemical polymerization using aniline (ANi monomer and TiCl4 as precursors. SEM pictures show that the nanocomposite was created in the form of long PANi chains decorated with TiO2 nanoparticles. FTIR, Raman and UV-Vis spectra reveal that the PANi component undergoes an electronic structure modification as a result of the TiO2 and PANi interaction. The electrical resistor of the nanocomposite is highly sensitive to oxygen and NH3 gas, accounting for the physical adsorption of these gases. A nanocomposite with around 55% TiO2 shows an oxygen sensitivity of 600–700%, 20–25 times higher than that of neat PANi. The n-p contacts between TiO2 nanoparticles and PANi matrix give rise to variety of shallow donors and acceptor levels in the PANi band gap which enhance the physical adsorption of gas molecules.

Preparation of TiO2/boron-doped diamond/Ta multilayer films and use as electrode materials for supercapacitors

Science.gov (United States)

Shi, Chao; Li, Hongji; Li, Cuiping; Li, Mingji; Qu, Changqing; Yang, Baohe

2015-12-01

We report nanostructured TiO2/boron-doped diamond (BDD)/Ta multilayer films and their electrochemical performances as supercapacitor electrodes. The BDD films were grown on Ta substrates using electron-assisted hot filament chemical vapor deposition. Ti metal layers were deposited on the BDD surfaces by radio frequency magnetron sputtering, and nanostructured TiO2/BDD/Ta thin films were prepared by electrochemical etching and thermal annealing. The successful formation of TiO2 and Ta layered nanostructures was demonstrated using scanning electron and transmission electron microscopies. The electrochemical responses of these electrodes were evaluated by examining their use as electrical double-layer capacitors, using cyclic voltammetry, and galvanostatic charge/discharge and impedance measurements. When the TiO2/BDD/Ta film was used as the working electrode with 0.1 M Na2SO4 as the electrolyte, the capacitor had a specific capacitance of 5.23 mF cm-2 at a scan rate of 5 mV s-1 for a B/C ratio of 0.1% w/w. Furthermore, the TiO2/BDD/Ta film had improved electrochemical stability, with a retention of 89.3% after 500 cycles. This electrochemical behavior is attributed to the quality of the BDD, the surface roughness and electrocatalytic activities of the TiO2 layer and Ta nanoporous structures, and the synergies between them. These results show that TiO2/BDD/Ta films are promising as capacitor electrodes for special applications.

TiO2/PbS/ZnS heterostructure for panchromatic quantum dot sensitized solar cells synthesized by wet chemical route

Science.gov (United States)

Bhat, T. S.; Mali, S. S.; Sheikh, A. D.; Korade, S. D.; Pawar, K. K.; Hong, C. K.; Kim, J. H.; Patil, P. S.

2017-11-01

So far we developed the efficient photoelectrodes which can harness the UV as well as the visible regime of the solar spectrum effectively. In order to exploit a maximum portion of solar spectrum, it is necessary to study the synergistic effect of a photoelectrode comprising UV and visible radiations absorbing materials. Present research work highlights the efforts to study the synchronized effect of TiO2 and PbS on the power conversion efficiency of quantum dot sensitized solar cell (QDSSC). A cascade structure of TiO2/PbS/ZnS QDSSC is achieved to enhance the photoconversion efficiency of TiO2/PbS system by incorporating a surface passivation layer of ZnS which avoids the recombination of charge carriers. A QDSSC is fabricated using a simple and cost-effective technique such as hydrothermally grown TiO2 nanorod arrays decorated with PbS and ZnS using successive ionic layer adsorption and reaction (SILAR) method. Synthesized electrode materials are characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscopy (FE-SEM), High resolution-transmission electron microscopy (TEM), STEM-EDS mapping, optical and solar cell performances. Phase formation of TiO2, PbS and ZnS get confirmed from the XPS study. FE-SEM images of the photoelectrode show uniform coverage of PbS QDs onto the TiO2 nanorods which increases with increasing number of SILAR cycles. The ZnS layer not only improves the charge transport but also reduces the photocorrosion of lead chalcogenides in the presence of a liquid electrolyte. Finally, the photoelectrochemical (PEC) study is carried out using an optimized photoanode comprising TiO2/PbS/ZnS assembly. Under AM 1.5G illumination the TiO2/PbS/ZnS QDSSC photoelectrode shows 4.08 mA/cm2 short circuit current density in a polysulfide electrolyte which is higher than that of a bare TiO2 nanorod array.

Study of phase development and thermal stability in as synthesized TiO2 nanoparticles by laser pyrolysis: ethylene uptake and oxygen enrichment

Science.gov (United States)

Ilie, Alina Georgiana; Scarisoreanu, Monica; Dutu, Elena; Dumitrache, Florian; Banici, Ana-Maria; Fleaca, Claudiu Teodor; Vasile, Eugenia; Mihailescu, Ion

2018-01-01

Laser pyrolysis has proven a viable and trustworthy method of TiO2 nanoparticles fabrication, ensuring good quality and wide variety of nanoparticle morphologies and sizes. This work is aimed to phase control, experimentally studied, by parameter modulation, during one step laser pyrolysis synthesis or in combination with thermal annealing. High phase purity anatase and rutile TiO2 nanoparticles, oxygen abundant, are synthesized from TiCl4 and C2H4 gas mixtures, in the presence of air as oxygen donor, under CO2 laser radiation. The nano-titania samples are analyzed by X-ray Diffraction, EDAX, TEM and Raman spectroscopy and reveal good phase stability and distinct morphology. This study extends the method applicability onto rutile majoritarian TiO2 synthesis and generation of thermally stable anatase titania, a well-known catalyst.

TiO2 film decorated with highly dispersed polyoxometalate nanoparticles synthesized by micelle directed method for the efficiency enhancement of dye-sensitized solar cells

Science.gov (United States)

He, Lifei; Chen, Li; Zhao, Yue; Chen, Weilin; Shan, Chunhui; Su, Zhongmin; Wang, Enbo

2016-10-01

In this work, two kinds of polyoxometalate (POM) nanoparticles with controlled shapes and structures were synthesized by micelle directed method and then composited with TiO2 via calcination to remove the surfactants owing to the excellent electronic storage and transmission ability of POM, finally obtaining two kinds of TiO2 composites with highly dispersed and small-sized POM nanoparticles (∼1 nm). The TiO2 composites were then induced into the photoanodes of dye-sensitized (N719) solar cells (DSSCs). The separation of electron-holes becomes more favorable due to the nanostructure and high dispersion of POM which provide more active sites than pure POM tending to agglomeration. The TiO2 composite photoanodes finally yielded the power conversion efficiency (PCE) of 8.4% and 8.2%, respectively, which were 42% and 39% higher than the pristine TiO2 based anodes. In addition, the mechanisms of POM in DSSC are proposed.

Synthesis of Nd3+doped TiO2 nanoparticles and Its Optical Behaviour

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Ezhil Arasi S.

2017-04-01

Full Text Available Pure and Rare earth ion doped TiO2 nanoparticles were synthesized by Sol-gel method. The synthesized TiO2 nanoparticles were characterized by X-ray diffraction, Raman spectroscopy, UV–Vis spectroscopy and photoluminescence emission spectra. From the UV-visible measurement, the absorption edge of Nd3+-TiO2 was shifted to a higher wavelength side with decreasing band gap. Photoluminescence emission studies reveal the energy transfer mechanism of Nd3+ doped TiO2 nanoparticles explain.

Photocatalytic behaviors and structural characterization of nanocrystalline Fe-doped TiO2 synthesized by mechanical alloying

International Nuclear Information System (INIS)

Kim, Dong Hyun; Hong, Hyun Seon; Kim, Sun Jae; Song, Jae Sung; Lee, Kyung Sub

2004-01-01

Nanocrystalline Fe-doped TiO 2 powders were synthesized by mechanical alloying (MA) with varying Fe contents from 0 up to 4.8 wt.% to shift the absorption threshold into the visible light region. The photocatalytic feasibility of the Fe-doped TiO 2 powder was evaluated by quantifying the visible light absorption capacity using ultraviolet and visible (UV-Vis) spectroscopy and photoluminescence spectroscopy. Effects of Fe additions on the crystal structures and the morphologies of the Fe-doped powders were also investigated as a function of the doping content using transmission electron microscopy-electron diffraction pattern (TEM-EDP), X-ray diffraction (XRD) and energy dispersive X-ray (EDAX) and X-ray photoelectron spectroscopy (XPS). The UV-Vis study showed that the UV absorption for the Fe-doped powder moved to a longer wavelength (red shift) and the photoefficiency was enhanced. Based on the analysis of the photoluminescence spectra, the red shift was believed to be induced by localizing the dopant level near the valence band of TiO 2 . The UV-Vis absorption depended on the Fe concentration. TEM-EDP and XRD investigations showed that the Fe-doped powder had a rutile phase in which the added Fe atoms were dissolved. The rutile phase was composed of spherical particles and chestnut bur shaped particles, resulting in a larger surface area than the spherical P-25 powder

Novel Ag@TiO2 nanocomposite synthesized by electrochemically active biofilm for nonenzymatic hydrogen peroxide sensor

International Nuclear Information System (INIS)

Khan, Mohammad Mansoob; Ansari, Sajid Ali; Lee, Jintae; Cho, Moo Hwan

2013-01-01

A novel nonenzymatic sensor for H 2 O 2 was developed based on an Ag@TiO 2 nanocomposite synthesized using a simple and cost effective approach with an electrochemically active biofilm. The optical, structural, morphological and electrochemical properties of the as-prepared Ag@TiO 2 nanocomposite were examined by UV–vis spectroscopy, X-ray diffraction, transmission electron microscopy and cyclic voltammetry (CV). The Ag@TiO 2 nanocomposite was fabricated on a glassy carbon electrode (GCE) and their electrochemical performance was analyzed by CV, differential pulse voltammetry and electrochemical impedance spectroscopy. The Ag@TiO 2 nanocomposite modified GCE (Ag@TiO 2 /GCE) displayed excellent performance towards H 2 O 2 sensing at − 0.73 V in the linear response range from 0.83 μM to 43.3 μM, within a detection limit and sensitivity of 0.83 μM and ∼ 65.2328 ± 0.01 μAμM −1 cm −2 , respectively. In addition, Ag@TiO 2 /GCE exhibited good operational reproducibility and long term stability. - Graphical abstract: Synthesis of Ag@TiO 2 nanocomposite by electrochemically active biofilm for H 2 O 2 sensing. - Highlights: • Electrochemically active biofilm (EAB) • EAB mediated synthesis of Ag@TiO 2 nanocomposite • Ag@TiO 2 nanocomposite modified glassy carbon electrode • Ag@TiO 2 /GCE for H 2 O 2 sensing • Nonenzymatic sensor for H 2 O 2

Enhancement of Perovskite Solar Cells Efficiency using N-Doped TiO2 Nanorod Arrays as Electron Transfer Layer.

Science.gov (United States)

Zhang, Zhen-Long; Li, Jun-Feng; Wang, Xiao-Li; Qin, Jian-Qiang; Shi, Wen-Jia; Liu, Yue-Feng; Gao, Hui-Ping; Mao, Yan-Li

2017-12-01

In this paper, N-doped TiO 2 (N-TiO 2 ) nanorod arrays were synthesized with hydrothermal method, and perovskite solar cells were fabricated using them as electron transfer layer. The solar cell performance was optimized by changing the N doping contents. The power conversion efficiency of solar cells based on N-TiO 2 with the N doping content of 1% (N/Ti, atomic ratio) has been achieved 11.1%, which was 14.7% higher than that of solar cells based on un-doped TiO 2 . To get an insight into the improvement, some investigations were performed. The structure was examined with X-ray powder diffraction (XRD), and morphology was examined by scanning electron microscopy (SEM). Energy dispersive spectrometer (EDS) and Tauc plot spectra indicated the incorporation of N in TiO 2 nanorods. Absorption spectra showed higher absorption of visible light for N-TiO 2 than un-doped TiO 2 . The N doping reduced the energy band gap from 3.03 to 2.74 eV. The photoluminescence (PL) and time-resolved photoluminescence (TRPL) spectra displayed the faster electron transfer from perovskite layer to N-TiO 2 than to un-doped TiO 2 . Electrochemical impedance spectroscopy (EIS) showed the smaller resistance of device based on N-TiO 2 than that on un-doped TiO 2 .

A thick hierarchical rutile TiO2 nanomaterial with multilayered structure

International Nuclear Information System (INIS)

Zhu, Shengli; Xie, Guoqiang; Yang, Xianjin; Cui, Zhenduo

2013-01-01

Highlights: ► We synthesized a new rutile TiO 2 nanomaterial with a hierarchical nanostructure. ► The nano architecture structure consist of nanorods and nanoflower arrays. ► The rutile TiO 2 nanomaterial is thick in size (several 10 μm). ► The TiO 2 nanomaterials present a multilayer structure. - Abstract: In the present paper, we synthesized a new type of rutile TiO 2 nanomaterial with a hierarchical nanostructure using a novel method, which combined dealloying process with chemical synthesis. The structure characters were examined using X-ray diffraction, scanning electron microscopy and transmission electron microscopy. The rutile TiO 2 nanomaterial is thick in size (several 10 μm). The hierarchical structure of the rutile TiO 2 nanomaterial consists of large quantities nanorods and nanoflower arrays. The nanoflowers consist of serveral nanopetals with diameter of 100–200 nm. The cross section of TiO 2 nanomaterials presents a multilayer structure with the layer thickness of about 3–5 μm. The rutile TiO 2 nanomaterial has high specific surface area. The formation mechanism of the rutile TiO 2 nanomaterial was discussed according to the experimental results. The rutile TiO 2 nanomaterial has potential applications in catalysis, photocatalysis and solar cells

Enhanced electrochemical oxidation of synthetic dyeing wastewater using SnO2-Sb-doped TiO2-coated granular activated carbon electrodes with high hydroxyl radical yields

International Nuclear Information System (INIS)

Li, Xinyang; Wu, Yue; Zhu, Wei; Xue, Fangqing; Qian, Yi; Wang, Chengwen

2016-01-01

Highlights: • We study granular activated carbon (GAC) electrodes coated with catalysts. • GAC coated with ATOT demonstrates an impressive ·OH yield. • This electrode can be used in continuous-flow three-dimensional electrode reactors. • We use Rhodamine B as a model organic compound for removal. • The GAC/ATOT performs better than all other electrodes examined. - Abstract: In this study, granular activated carbon (GAC) coated with SnO 2 -Sb doped TiO 2 (GAC/ATOT) with a high hydroxyl radical (·OH) yield is prepared via the sol-gel method. This material is utilized as a granular electrode in a continuous-flow three-dimensional electrode reactor (CTDER) for the enhanced treatment of synthetic dyeing wastewater containing Rhodamine B (RhB). We then characterize the physical properties, electrochemical properties, and electrochemical oxidation performance of the granular electrode. The results show that using the GAC/ATOT electrode in a CTDER significantly enhances the chemical oxygen demand (COD) removal, decreases the energy consumption, and improves the current efficiency of the wastewater. This is primarily attributed to the higher catalytic activity of GAC/ATOT for ·OH production compared to that of other candidates, such as TiO 2 coated GAC (GAC/T), Sb doped SnO 2 coated GAC (GAC/ATO), and pure GAC. The mechanism of the enhanced electrochemical oxidation afforded by using GAC/ATOT indicates that the high ·OH yield in the reactor packed with GAC/ATOT electrodes contributes to the enhanced electrochemical oxidation performance with respect to organic compounds.

Morphology and electrical properties of electrochemically synthesized pyrrole–formyl pyrrole copolymer

Energy Technology Data Exchange (ETDEWEB)

Gholami, Mehrdad, E-mail: mehrdad897@um.edu.my [Department of Chemistry, University of Malaya, Kuala Lumpur 50603 (Malaysia); Department of Chemistry, Marvdasht Branch, Islamic Azad University, P.O. Box 465, Marvdasht (Iran, Islamic Republic of); Nia, Pooria Moozarm, E-mail: pooriamn@yahoo.com [Department of Chemistry, University of Malaya, Kuala Lumpur 50603 (Malaysia); Alias, Yatimah, E-mail: yatimah70@um.edu.my [Department of Chemistry, University of Malaya, Kuala Lumpur 50603 (Malaysia)

2015-12-01

Graphical abstract: - Highlights: • The (Py–co-FPy) copolymer was synthesized electrochemically. • This copolymer has 1.6 times higher surface coverage compared to polypyrrole. • This copolymer showed 2.5 times lower resistance compared to polypyrrole. • The conjugated structure between Py and FPy causes enhancement of conductivity. • This conducting copolymer has a strong potential to be used in various applications. - Abstract: A direct electrochemical copolymerization of pyrrole–formyl pyrrole (Py–co-FPy) was carried out by oxidative copolymerization of formyl pyrrole and pyrrole in LiClO{sub 4} aqueous solution through galvanostatic method. The (Py–co-FPy) copolymer was characterized using Fourier-transform infrared spectroscopy (FT-IR), field emission scanning electron microscope (FESEM), energy-filtering transmission electron microscope (EFTEM), thermal gravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS), cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The FESEM images showed that the synthesized copolymer had a hollow whelk-like helixes structure, which justifies the enhancement of charge transportation through the copolymer film. Cyclic voltammetry studies revealed that the electrocatalytic activity of synthesized copolymer has improved and the surface coverage in copolymer enhanced 1.6 times compared to polypyrrole alone. Besides, (Py–co-FPy) copolymer showed 2.5 times lower electrochemical charge transfer resistance (R{sub ct}) value in impedance spectroscopy. Therefore, this copolymer has a strong potential to be used in several applications such as sensor applications.

Analysis of X-ray diffraction of the titanium dioxide (TiO_2) synthesized by the Pechini Method for application in heterogeneous photocatalysis processes

International Nuclear Information System (INIS)

Oliveira, P.L.; Araujo, D.S.; Costa, A.C.F.M.; Oliveira, L.S.C.

2016-01-01

Titanium dioxide (TiO_2) is a polymorph commonly applied to heterogeneous photocatalysis processes for being relatively inexpensive and photo - stable. It is usually found in three different crystalline phases (anatase, rutile and brookite), which directly interfere in their photocatalytic efficiency. Therefore, this study aimed to investigate the obtainment of TiO_2 by Pechini method in different conditions for application in the heterogeneous photocatalysis process. For this purpose, it was evaluated by analysis of X-ray diffraction (XRD ) the behavior of TiO_2 materials synthesized in proportions of 2:1 and 3:1 (titanium isopropoxide/citric acid), pyrolyzed at 300°C/3h and 400°C /h and calcined at 400°C and 500°C/1h. The results revealed that the TiO_2 samples produced in the ratio of 2:1 and 3:1 isopropoxide/citric acid and calcined at 500°C/h presented the best results. (author)

Investigation of the temperature effect on electrochemical behaviors of TiO2 for gel type valve regulated lead-acid batteries

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Metin GENÇTEN

2016-12-01

Full Text Available In this study, the effect of temperature on the electrochemical behaviors of gel electrolyte systems was investigated for valve regulated lead-acid battery at 0≤ T ≤50 oC. Fumed silica and mixture of fumed silica and TiO2 were used as gel electrolytes. TiO2 has a good combination with fumed silica. They were characterized by cyclic voltammetry, electrochemical impedance spectroscopy and battery tests. The anodic peak currents and redox capacities of the gel electrolytes increased with increasing of temperature. The highest anodic peak current and redox capacity were observed at 30 oC in fumed silica and at 40 oC in fumed silica:TiO2 based gel systems. The solution and charge transfer resistance values decreased in fumed silica:TiO2 gel system by increasing temperature. In battery tests, discharge curves were obtained for each gel system at 0, 25 and 50 oC. The discharge time of mixture gel electrolyte system was higher than that of fumed silica based gel electrolyte at low (0 oC and high (50 oC temperatures. The best performance was obtained in fumed silica based gel electrolyte at 25 oC.

Electrochemically synthesized nanocrystalline spinel thin film for high performance supercapacitor

Energy Technology Data Exchange (ETDEWEB)

Gupta, Vinay [Carbon Technology Unit, Engineering Materials Division, National Physical Laboratory, New-Delhi, 110012 (India); Art, Science and Technology Center for Cooperative Research, Kyushu University, Kasuga-shi, Fukuoka, 816-8580 (Japan); Japan Science and Technology Agency, Kawaguchi-shi, Saitama, 332-0012 (Japan); Gupta, Shubhra; Miura, Norio [Art, Science and Technology Center for Cooperative Research, Kyushu University, Kasuga-shi, Fukuoka, 816-8580 (Japan)

2010-06-01

Spinels are not known for their supercapacitive nature. Here, we have explored electrochemically synthesized nanostructured NiCo{sub 2}O{sub 4} spinel thin-film electrode for electrochemical supercapacitors. The nanostructured NiCo{sub 2}O{sub 4} spinel thin film exhibited a high specific capacitance value of 580 F g{sup -1} and an energy density of 32 Wh kg{sup -1} at the power density of 4 kW kg{sup -1}, accompanying with good cyclic stability. (author)

Synthesis, structure and photocatalytic activity of nano TiO2 and ...

Indian Academy of Sciences (India)

salicylic acid over combustion-synthesized nano TiO2 under UV and solar exposure has been carried out. Under identical conditions of UV exposure, the initial degra- dation rate of phenol with combustion-synthesized TiO2 is two times higher than the initial degradation rate of phenol with Degussa P25, the commercial ...

Controlled synthesis of TiO2-B nanowires and nanoparticles for dye-sensitized solar cells

International Nuclear Information System (INIS)

Qi Lihong; Liu Yongjun; Li Chunyan

2010-01-01

Controllable synthesis of the TiO 2 -B nanowires (NWs) and nanoparticles (NPs) had been achieved via a facile hydrothermal route, respectively, only by tuning the solution volume. The dye-sensitized solar cells prototypes had been fabricated using TiO 2 -B NW and NP electrodes, respectively. The TiO 2 -B NP cells had higher photocurrent and photoelectrical conversion efficiency than the TiO 2 -B NW cells though the latter exhibited larger photovoltage compared to the former. The key factors such as the photogenerated electron injection drive force, surface defects and the interfacial charge transfer, which determined the photoelectrical properties, had been systematically researched with the surface photovoltage spectra (SPS) and the electrochemical impedance spectra (EIS). The SPS proved that there was larger photoelectron injection drive force in TiO 2 -B NP photoelectrode than that in NW photoelectrode. And the electrochemical impedance spectra (EIS) revealed that TiO 2 -B NP cells had faster interface charge transfer compared to TiO 2 -B NW cells. Both proved that NP cells had the higher photocurrents.

Selective Oxidation Using Flame Aerosol Synthesized Iron and Vanadium-Doped Nano-TiO2

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Zhong-Min Wang

2011-01-01

Full Text Available Selective photocatalytic oxidation of 1-phenyl ethanol to acetophenone using titanium dioxide (TiO2 raw and doped with Fe or V, prepared by flame aerosol deposition method, was investigated. The effects of metal doping on crystal phase and morphology of the synthesized nanostructured TiO2 were analyzed using XRD, TEM, Raman spectroscopy, and BET nitrogen adsorbed surface area measurement. The increase in the concentration of V and Fe reduced the crystalline structure and the anatase-to-rutile ratios of the synthesized TiO2. Synthesized TiO2 became fine amorphous powder as the Fe and V concentrations were increased to 3 and 5%, respectively. Doping V and Fe to TiO2 synthesized by the flame aerosol increased photocatalytic activity by 6 folds and 2.5 folds, respectively, compared to that of pure TiO2. It was found that an optimal doping concentration for Fe and V were 0.5% and 3%, respectively. The type and concentration of the metal dopants and the method used to add the dopant to the TiO2 are critical parameters for enhancing the activity of the resulting photocatalyst. The effects of solvents on the photocatalytic reaction were also investigated by using both water and acetonitrile as the reaction medium.

Pt Catalyst Supported within TiO2 Mesoporous Films for Oxygen Reduction Reaction

International Nuclear Information System (INIS)

Huang, Dekang; Zhang, Bingyan; Bai, Jie; Zhang, Yibo; Wittstock, Gunther; Wang, Mingkui; Shen, Yan

2014-01-01

In this study, dispersed Pt nanoparticles into mesoporous TiO 2 thin films are fabricated by a facile electrochemical deposition method as electro-catalysts for oxygen reduction reaction. The mesoporous TiO 2 thin films coated on the fluorine-doped tin oxide glass by screen printing allow a facile transport of reactants and products. The structural properties of the resulted Pt/TiO 2 electrode are evaluated by field emission scanning electron microscopy, energy dispersive X-ray spectrometry, X-ray diffraction, and X-ray photoelectron spectroscopy. Cyclic voltammetry measurements are performed to study the electrochemical properties of the Pt/TiO 2 electrode. Further study demonstrates the stability of the Pt catalyst supported within TiO 2 mesoporous films for the oxygen reduction reaction

Formation of hydroxyl radicals and kinetic study of 2-chlorophenol photocatalytic oxidation using C-doped TiO2, N-doped TiO2, and C,N Co-doped TiO2 under visible light.

Science.gov (United States)

Ananpattarachai, Jirapat; Seraphin, Supapan; Kajitvichyanukul, Puangrat

2016-02-01

This work reports on synthesis, characterization, adsorption ability, formation rate of hydroxyl radicals (OH(•)), photocatalytic oxidation kinetics, and mineralization ability of C-doped titanium dioxide (TiO2), N-doped TiO2, and C,N co-doped TiO2 prepared by the sol-gel method. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and UV-visible spectroscopy were used to analyze the titania. The rate of formation of OH(•) for each type of titania was determined, and the OH-index was calculated. The kinetics of as-synthesized TiO2 catalysts in photocatalytic oxidation of 2-chlorophenol (2-CP) under visible light irradiation were evaluated. Results revealed that nitrogen was incorporated into the lattice of titania with the structure of O-Ti-N linkages in N-doped TiO2 and C,N co-doped TiO2. Carbon was joined to the Ti-O-C bond in the C-doped TiO2 and C,N co-doped TiO2. The 2-CP adsorption ability of C,N co-doped TiO2 and C-doped TiO2 originated from a layer composed of a complex carbonaceous mixture at the surface of TiO2. C,N co-doped TiO2 had highest formation rate of OH(•) and photocatalytic activity due to a synergistic effect of carbon and nitrogen co-doping. The order of photocatalytic activity per unit surface area was the same as that of the formation rate of OH(•) unit surface area in the following order: C,N co-doped TiO2 > C-doped TiO2 > N-doped TiO2 > undoped TiO2.

Rapid charge-discharge property of Li4Ti5O12-TiO2 nanosheet and nanotube composites as anode material for power lithium-ion batteries.

Science.gov (United States)

Yi, Ting-Feng; Fang, Zi-Kui; Xie, Ying; Zhu, Yan-Rong; Yang, Shuang-Yuan

2014-11-26

Well-defined Li4Ti5O12-TiO2 nanosheet and nanotube composites have been synthesized by a solvothermal process. The combination of in situ generated rutile-TiO2 in Li4Ti5O12 nanosheets or nanotubes is favorable for reducing the electrode polarization, and Li4Ti5O12-TiO2 nanocomposites show faster lithium insertion/extraction kinetics than that of pristine Li4Ti5O12 during cycling. Li4Ti5O12-TiO2 electrodes also display lower charge-transfer resistance and higher lithium diffusion coefficients than pristine Li4Ti5O12. Therefore, Li4Ti5O12-TiO2 electrodes display lower charge-transfer resistance and higher lithium diffusion coefficients. This reveals that the in situ TiO2 modification improves the electronic conductivity and electrochemical activity of the electrode in the local environment, resulting in its relatively higher capacity at high charge-discharge rate. Li4Ti5O12-TiO2 nanocomposite with a Li/Ti ratio of 3.8:5 exhibits the lowest charge-transfer resistance and the highest lithium diffusion coefficient among all samples, and it shows a much improved rate capability and specific capacity in comparison with pristine Li4Ti5O12 when charging and discharging at a 10 C rate. The improved high-rate capability, cycling stability, and fast charge-discharge performance of Li4Ti5O12-TiO2 nanocomposites can be ascribed to the improvement of electrochemical reversibility, lithium ion diffusion, and conductivity by in situ TiO2 modification.

Structure and electrochemical hydrogen storage properties of Ti2Ni alloy synthesized by ball milling

International Nuclear Information System (INIS)

Hosni, B.; Li, X.; Khaldi, C.; ElKedim, O.; Lamloumi, J.

2014-01-01

Highlights: • The Ti 2 Ni alloy activation requires only one cycle of charge and discharge, regardless of the temperature. • By increasing the temperature the capacity loss, undergoes an increase and it is more pronounced for the 60 °C. • A good correlation is found between the evolutions of the different electrochemical parameters according to the temperature. - Abstract: The structure and the electrochemical hydrogen storage properties of amorphous Ti 2 Ni alloy synthesized by ball milling and used as an anode in nickel–metal hydride batteries were studied. Nominal Ti 2 Ni was synthesized under argon atmosphere at room temperature using a planetary high-energy ball mill. The structural and morphological characterization of the amorphous Ti 2 Ni alloy is carried out by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The electrochemical characterization of the Ti 2 Ni electrodes is carried out by the galvanostatic charging and discharging, the constant potential discharge, the open circuit potential and the potentiodynamic polarization techniques. The Ti 2 Ni alloy activation requires only one cycle of charge and discharge, regardless of the temperature. The electrochemical discharge capacity of the Ti 2 Ni alloy, during the first eight cycles, and at a temperature of 30 °C, remained practically unchanged and a good held cycling is observed. By increasing the temperature, the electrochemical discharge capacity loss after eight cycles undergoes an increase and it is more pronounced for the temperature 60 °C. At 30 °C, the anodic corrosion current density is 1 mA cm −2 and then it undergoes a rapid drop, remaining substantially constant (0.06 mA cm −2 ) in the range 40–60 °C, before undergoing a slight increase to 70 °C (0.3 mA cm −2 ). This variation is in good agreement with the maximum electrochemical discharge capacity values found for the different temperatures. By increasing the

Photogenerated cathode protection properties of nano-sized TiO2/WO3 coating

International Nuclear Information System (INIS)

Zhou Minjie; Zeng Zhenou; Zhong Li

2009-01-01

Nano-sized TiO 2 /WO 3 bilayer coatings were prepared on type 304 stainless steel substrate by sol-gel method. The performance of photo-electrochemical and photogenerated cathode protection of the coating was investigated by the electrochemical method. The results show that the bilayer coating with four TiO 2 layers and three WO 3 layers exhibits the highest photo-electrochemical efficiency and the best corrosion resistance property. Type 304 stainless steel with the coating can maintain cathode protection for 6 h in the dark after irradiation by UV illumination for 1 h. In addition, the mechanism of the photogenerated cathode protection for the bilayer coating was also explored.

TiO2 coated SnO2 nanosheet films for dye-sensitized solar cells

International Nuclear Information System (INIS)

Cai Fengshi; Yuan Zhihao; Duan Yueqing; Bie Lijian

2011-01-01

TiO 2 -coated SnO 2 nanosheet (TiO 2 -SnO 2 NS) films about 300 nm in thickness were fabricated on fluorine-doped tin oxide glass by a two-step process with facile solution-grown approach and subsequent hydrolysis of TiCl 4 aqueous solution. The as-prepared TiO 2 -SnO 2 NSs were characterized by scanning electron microscopy and X-ray diffraction. The performances of the dye-sensitized solar cells (DSCs) with TiO 2 -SnO 2 NSs were analyzed by current-voltage measurements and electrochemical impedance spectroscopy. Experimental results show that the introduction of TiO 2 -SnO 2 NSs can provide an efficient electron transition channel along the SnO 2 nanosheets, increase the short current density, and finally improve the conversion efficiency for the DSCs from 4.52 to 5.71%.

Computational Fluid Dynamics (CFD Analysis of Phthalic Anhydride’s Yield Using Lab Synthesized and Commercially Available (V2O5/TiO2 Catalyst

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A. Sarosh

2018-04-01

Full Text Available V2O5/TiO2 is an important catalyst used in many industrial reactions like selective oxidation of o-xylene to phthalic anhydride, selective catalytic reduction of NOx, selective oxidation of alkanes, etc. The partial oxidation of o-xylene to synthesize phthalic anhydride is an exothermic reaction and leaves hot spots on the catalyst’s surface. The yield of phthalic anhydride strongly depends on the activity and stability of the catalyst. In this work, a computational fluid dynamics (CFD analysis has been conducted to compare the yield of lab prepared catalyst with the commercially used catalyst. This work is first attempt to simulate V2O5/TiO2 catalyst for cracking heavy hydrocarbons in the petrochemical industry using k- ε turbulence and species transport models in CFD. The results obtained are in the form of scaled residuals, area-weighted average, and contours of pressure and temperature. Simulation results of lab synthesized and commercially used catalysts, applying finite volume method (FVM are compared, which emphasize the scope of CFD modeling in the catalytic cracking process of petrochemical industry.

Glycine assisted synthesis of flower-like TiO2 hierarchical spheres and its application in photocatalysis

International Nuclear Information System (INIS)

Tao, Yu-gui; Xu, Yan-qiu; Pan, Jun; Gu, Hao; Qin, Chang-yun; Zhou, Peng

2012-01-01

Graphical abstract: Flower-like anatase TiO 2 hierarchical spheres assembled by nanosheets were synthesized by glycine assistant via a simple hydrothermal approach and after-annealing process. The obtained TiO 2 sample showed good photocatalytic activity of decomposition of methyl orange under sunlight. Highlights: ► Flower-like TiO 2 hierarchical spheres were synthesized by glycine assistant. ► Reaction time, temperature, solution pH and glycine dosage were studied. ► The formation of the flower-like TiO 2 spheres is an Ostwald ripening process. ► Flower-like TiO 2 showed high photocatalytic activity under sunlight. - Abstract: Flower-like anatase TiO 2 hierarchical spheres assembled by nanosheets were synthesized by glycine assistant via a simple hydrothermal approach and after-annealing process. These flower-like spheres are about 2 μm in diameter with sheet thickness about 20 nm. Results showed reaction time, temperature, solution pH and glycine dosage all played an important role in control of shape and size of the as-synthesized TiO 2 nanocrystals. The photocatalytic activity of this nano-TiO 2 was evaluated by the photocatalytic oxidation decomposition of methyl orange under sunlight illumination in the presence of hydrogen peroxide (H 2 O 2 ). The photocatalytic activity of the obtained TiO 2 was higher than that of commercial TiO 2 .

Synthesis, Characterization and Properties of CeO2-doped TiO2 Composite Nanocrystals

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Oman ZUAS

2013-12-01

Full Text Available Pure TiO2 and CeO2-doped TiO2 (3 % CeO2-97 %TiO2 composite nanocrystals were synthesized via co-precipitation method and characterized using TGA, XRD, FTIR, DR-UV-vis and TEM. The XRD data revealed that the phase structure of the synthesized samples was mainly in pure anatase having crystallite size in the range of 7 nm – 11 nm. Spherical shapes with moderate aggregation of the crystal particles were observed under the TEM observation. The presence of the CeO2 at TiO2 site has not only affected morphologically but also induced the electronic property of the TiO2 by lowering the band gap energy from 3.29 eV (Eg-Ti to 3.15 eV (Eg-CeTi. Performance evaluation of the synthesized samples showed that both samples have a strong adsorption capacity toward Congo red (CR dye in aqueous solution at room temperature experiment, where  the capacity of the CeTi was higher than the Ti sample. Based on DR-UV data, the synthesized samples obtained in this study may also become promising catalysts for photo-assisted removal of synthetic dye in aqueous solution. DOI: http://dx.doi.org/10.5755/j01.ms.19.4.2732

Complex impedance study on nano-CeO2 coating TiO2

International Nuclear Information System (INIS)

Zhang Mei; Wang Honglian; Wang Xidong; Li Wenchao

2006-01-01

Titanium dioxide (TiO 2 ) nanoparticles and cerium dioxide (CeO 2 ) nanoparticles coated titanium dioxide (TiO 2 ) nanoparticles (CeO 2 -TiO 2 nanoparticles) have been successfully synthesized by sol-gel method. The complex impedance of the materials was investigated. The grain resistance, boundary resistance and activation energy of the nanoparticles were calculated according to Arrhenius equation. According to calculating results, the active capacity of pure TiO 2 nanoparticles has been improved because of nano-CeO 2 coating. An optimal CeO 2 content of 4.9 mol% was achieved. The high resolution electron microscopy images of CeO 2 -TiO 2 nanoparticles showed that TiO 2 nanoparticles, as a core, were covered by CeO 2 nanoparticles. The average size of CeO 2 coating TiO 2 nanoparticles was about 70 nm. Scanning electron microscopy observation indicted that CeO 2 nanoparticle coating improved the separation, insulation, and stability the CeO 2 -TiO 2 nanoparticles, which was benefit to the activity of materials

Synthesis of calcium-phosphorous doped TiO2 nanotubes by anodization and reverse polarization: A promising strategy for an efficient biofunctional implant surface

International Nuclear Information System (INIS)

Alves, Sofia A.; Patel, Sweetu B.; Sukotjo, Cortino; Mathew, Mathew T.; Filho, Paulo N.; Celis, Jean-Pierre

2017-01-01

Highlights: • A new surface modification methodology for bio-functionalization of TiO2 NTs is addressed • Bone-like structured TiO2 nanotubular surfaces containing Ca and P were synthesized. • Ca/P-doped TiO2 NTs enhanced adhesion and proliferation of osteoblastic-like cells. • The bio-functionalization granted improved bio-electrochemical stability to TiO2 NTs. - Abstract: The modification of surface features such as nano-morphology/topography and chemistry have been employed in the attempt to design titanium oxide surfaces able to overcome the current dental implants failures. The main goal of this study is the synthesis of bone-like structured titanium dioxide (TiO 2 ) nanotubes enriched with Calcium (Ca) and Phosphorous (P) able to enhance osteoblastic cell functions and, simultaneously, display an improved corrosion behavior. To achieve the main goal, TiO 2 nanotubes were synthetized and doped with Ca and P by means of a novel methodology which relied, firstly, on the synthesis of TiO 2 nanotubes by anodization of titanium in an organic electrolyte followed by reverse polarization and/or anodization, in an aqueous electrolyte. Results show that hydrophilic bone-like structured TiO 2 nanotubes were successfully synthesized presenting a highly ordered nano-morphology characterized by non-uniform diameters. The chemical analysis of such nanotubes confirmed the presence of CaCO 3 , Ca 3 (PO 4 ) 2 , CaHPO 4 and CaO compounds. The nanotube surfaces submitted to reverse polarization, presented an improved cell adhesion and proliferation compared to smooth titanium. Furthermore, these surfaces displayed a significantly lower passive current in artificial saliva, and so, potential to minimize their bio-degradation through corrosion processes. This study addresses a very simple and promising multidisciplinary approach bringing new insights for the development of novel methodologies to improve the outcome of osseointegrated implants.

Electrocatalytic glucose oxidation via hybrid nanomaterial catalyst of multi-wall TiO2 nanotubes supported Ni(OH)2 nanoparticles: Optimization of the loading level

International Nuclear Information System (INIS)

Gu, Yingying; Liu, Yicheng; Yang, Haihong; Li, Benqiang; An, Yarui

2015-01-01

Highlights: • Multi-wall TiO 2 nanotube supported Ni(OH) 2 nanoparticles, Ni(OH) 2 /TNTs, was prepared and investigated as anode electro-catalysts for glucose oxidation. • Ni(OH) 2 -24.2%/TNTs obtains the best catalytic activity. • Compared with Ni(OH) 2, the current density of Ni(OH) 2 -24.2%/TNTs increased 5.9 times in 0.1 M NaOH solution. - Abstract: The novel hybrid nanomaterial catalyst of multi-wall TiO 2 nanotube supported Ni(OH) 2 nanoparticles (Ni(OH) 2 /TNTs) was prepared through hydrothermal method and investigated as anode electro-catalysts for glucose oxidation. The nanostructure was characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM), thermogravimetry-differential thermal analysis (TGA) and nitrogen adsorption-desorption (BET-BJH). The electrochemical performance was measured by a range of electrochemical measurements. Compared with Ni(OH) 2 , the current density of Ni(OH) 2 /TNTs modified GC electrode increased 5.9 times in 0.1 M NaOH solution. The results indicated that the synthesized nanoparticles exhibited good electro-catalytic activity and stability for glucose oxidation. Meanwhile, the hybrid nanomaterial of Ni(OH) 2 /TNTs may be a potential candidate catalyst for direct glucose fuel cell

Synthesis and photocatalytic activity of Ce-doped TiO2 and TiO2 nanotubes

International Nuclear Information System (INIS)

Arruda, L.B.; Pereira, E.A.; Paula, F.R.; Lisboa Filho, P.N.

2016-01-01

Full text: One-dimensional nanostructures have been intensively studied, from the point of view of their synthesis and mechanisms of formation, as well as their applications in photonics, solar energy conversion, environmental and photocatalysis, since their properties due high surface area, electrical conductivity and light dispersion effects. Titanium dioxide (TiO2) nanoparticles have been demonstrated to be an effective multifunctional material especially when the particle size is less than 50 nm exhibit photoinduced activities that originate from the semiconductor band gap. TiO2 is semiconductor more used in photocatalysis, for this reason various properties have been thoroughly investigated in order to show that the photocatalytic activity and TiO2 reaction mechanism are influenced by structure, defects and impurities, surface morphology. and interfaces in addition to the concentration of dopants, such as rare-earth elements. Cerium ions, for example, vary between Ce4+ and Ce3 + oxidation state making the cerium oxide appear as CeO2 and Ce2O3 under oxidation and reduction conditions. These different electronic structures of Ce3+ (4f15d0) and Ce4+ (4f05d0) provide different catalytic and optical properties at the TiO2. In this work, samples of Ce-doped TiO2 and TiO2 were synthesized by alkali route, and its photocatalytic activity analyzed in order to create a relationship between the response obtained and the structure and morphology of each sample. Alkali route consists in submitting TiO2 (anatase) powder directly in medium of the NaOH (10M) and maintained at 120°C/20 hours by a glycerin bath with subsequent washed with water and HCl (0.1M) until reaching the desired pH. The synthesized samples were then studied by X-ray diffraction (XRD), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). The photocatalytic decomposition of rhodamine B (Rh.B) it was performed under UV irradiation and visible light in air. For the obtained

Synthesis and photocatalytic activity of Ce-doped TiO2 and TiO2 nanotubes

Energy Technology Data Exchange (ETDEWEB)

Arruda, L.B.; Pereira, E.A.; Paula, F.R.; Lisboa Filho, P.N. [Universidade Estadual Paulista Julio de Mesquita Filho (UNESP), SP (Brazil)

2016-07-01

Full text: One-dimensional nanostructures have been intensively studied, from the point of view of their synthesis and mechanisms of formation, as well as their applications in photonics, solar energy conversion, environmental and photocatalysis, since their properties due high surface area, electrical conductivity and light dispersion effects. Titanium dioxide (TiO2) nanoparticles have been demonstrated to be an effective multifunctional material especially when the particle size is less than 50 nm exhibit photoinduced activities that originate from the semiconductor band gap. TiO2 is semiconductor more used in photocatalysis, for this reason various properties have been thoroughly investigated in order to show that the photocatalytic activity and TiO2 reaction mechanism are influenced by structure, defects and impurities, surface morphology. and interfaces in addition to the concentration of dopants, such as rare-earth elements. Cerium ions, for example, vary between Ce4+ and Ce3 + oxidation state making the cerium oxide appear as CeO2 and Ce2O3 under oxidation and reduction conditions. These different electronic structures of Ce3+ (4f15d0) and Ce4+ (4f05d0) provide different catalytic and optical properties at the TiO2. In this work, samples of Ce-doped TiO2 and TiO2 were synthesized by alkali route, and its photocatalytic activity analyzed in order to create a relationship between the response obtained and the structure and morphology of each sample. Alkali route consists in submitting TiO2 (anatase) powder directly in medium of the NaOH (10M) and maintained at 120°C/20 hours by a glycerin bath with subsequent washed with water and HCl (0.1M) until reaching the desired pH. The synthesized samples were then studied by X-ray diffraction (XRD), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). The photocatalytic decomposition of rhodamine B (Rh.B) it was performed under UV irradiation and visible light in air. For the obtained

Nanostructured TiO2 Doped with Nb as a Novel Support for PEMFC

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Edgar Valenzuela

2013-01-01

Full Text Available Nowadays, one of the major issues of the PEMFC concerns the durability. Historically, carbon has been used as a catalyst support in PEMFC; nevertheless, under the environmental conditions of the cell, the carbon is oxidized, leaving the catalyst unsupported. In order to increase the stability and durability of the catalyst in the PEMFC, a novel nanostructured metallic oxide support is proposed. In this work, TiO2 was doped with Nb to obtain a material that combines chemical stability, high surface area, and an adequate electronic conductivity in order to be a successful catalyst support candidate for long-term PEMFC applications. The TiO2-Nb nanostructured catalyst support was physically and electrochemically characterized. According to the results, the TiO2-Nb offers high surface area and good particle dispersion; also, the electrochemical activity and stability of the support were evaluated under high potential conditions, where the TiO2-Nb proved to be much more stable than carbon.

Facile approach to synthesize Ni(OH)2 nanoflakes on MWCNTs for high performance electrochemical supercapacitors

International Nuclear Information System (INIS)

Shahid, Muhammad; Liu Jingling; Shakir, Imran; Warsi, Muhammad Farooq; Nadeem, Muhammad; Kwon, Young-Uk

2012-01-01

Highlights: ► Deposition of ultra-thin Ni(OH) 2 nanoflakes on MWCNTs. ► Full utilization of the Ni(OH) 2 nanoflakes which provide maximum pseudocapacitance while minimizing the high surface area. ► The ultra-thin layer of Ni(OH) 2 nanoflakes on highly conductive MWCNTs is favorable for fast ion and electron transfer. ► The ultra-thin layer of Ni(OH) 2 nanoflakes on MWCNTs exhibited good cycling stability and lifetime. - Abstract: Ultrathin nanoflakes of Ni(OH) 2 were synthesized onto multi-walled carbon nanotubes (MWCNTs) by simple low cost chemically precipitation method for high performance electrochemical supercapacitor applications. The synthesized ultrathin Ni(OH) 2 exhibit high specific capacitance of 1735 Fg −1 at a scan rate of 5 mV s −1 with excellent rate capability. This high performance of Ni(OH) 2 nanoflakes was attributed to its complete accessibility to the electrolyte and maximum utilization of metal hydroxides. Findings of this work suggest that synthesized electrodes offer low-cost and scalable solution for high-performance energy storage devices.

Preparation of anatase TiO2 nanoparticles using low hydrothermal temperature for dye-sensitized solar cell

Science.gov (United States)

Sofyan, N.; Ridhova, A.; Yuwono, A. H.; Udhiarto, A.

2018-03-01

One device being developed as an alternative source of renewable energy by utilizing solar energy source is dye-sensitized solar cells (DSSC). This device works using simple photosynthetic-electrochemical principle in the molecular level. In this device, the inorganic oxide semiconductor of titanium dioxide (TiO2) has a great potential for the absorption of the photon energy from the solar energy source, especially in the form of TiO2 nanoparticle structure. This nanoparticle structure is expected to improve the performance of DSSC because the surface area to weight ratio of this nanostructures is very large. In this study, the synthesis of TiO2 nanoparticle from its precursors has been performed along with the fabrication of the DSSC device. Effort to improve the size of nanocrystalline anatase TiO2 was accomplished by low hydrothermal treatment at various temperatures whereas the crystallinity of the anatase phase in the structure was performed by calcination process. Characterization of the materials was performed using X-ray Diffraction (XRD) and scanning electron microscope (SEM), while the DSSC performance was examined through a high precision current versus voltage (I-V) curve analyzer. The results showed that pure anatase TiO2 nanoparticles could be obtained at low hydrothermal of 100, 125, and 150 °C followed by calcination at 450 °C. The best performance of photocurrent-voltage characteristic was given by TiO2 hydrothermally synthesized at 150 °C with power conversion efficiency (PCE) of 4.40 %, whereas the standard TiO2 nanoparticles has PCE only 4.02 %. This result is very promising in terms low temperature and thus low cost of anatase TiO2 semiconductor preparation for DSSC application.

Photoelectrolysis of water using heterostructural composite of TiO2 nanotubes and nanoparticles

International Nuclear Information System (INIS)

Das, Prajna P; Mohapatra, Susanta K; Misra, Mano

2008-01-01

Efficient photoelectrolysis of water to generate hydrogen (H 2 ) can be carried out by designing photocatalysts with good absorption as well as charge transport properties. One dimensional (1D), self-organized titania (TiO 2 ) nanotubes are known to have excellent charge transport properties and TiO 2 nanoparticles (NPs) are good for better photon absorption. This paper describes the synthesis of a composite photocatalyst combining the above two properties of TiO 2 nanocomposites with different morphologies. TiO 2 NPs (5-9 nm nanocrystals form 500-700 nm clusters) have been synthesized from TiCl 4 precursor on TiO 2 nanotubular arrays (∼80 nm diameter and ∼550 nm length) synthesized by the sonoelectrochemical anodization method. This TiO 2 nanotube-nanoparticle composite photoanode has enabled obtaining of enhanced photocurrent density (2.2 mA cm -2 ) as compared with NTs (0.9 mA cm -2 ) and NPs (0.65 mA cm -2 ) alone.

Improvement of epoxy resin properties by incorporation of TiO2 nanoparticles surface modified with gallic acid esters

International Nuclear Information System (INIS)

Radoman, Tijana S.; Džunuzović, Jasna V.; Jeremić, Katarina B.; Grgur, Branimir N.; Miličević, Dejan S.; Popović, Ivanka G.; Džunuzović, Enis S.

2014-01-01

Highlights: • Nanocomposites of epoxy resin and TiO 2 nanoparticles surface modified with gallates. • The T g of epoxy resin was increased by incorporation of surface modified TiO 2 . • WVTR of epoxy resin decreased in the presence of surface modified TiO 2 nanoparticles. • WVTR of nanocomposites was reduced with increasing gallates hydrophobic chain length. • Modified TiO 2 nanoparticles react as oxygen scavengers, inhibiting steel corrosion. - Abstract: Epoxy resin/titanium dioxide (epoxy/TiO 2 ) nanocomposites were obtained by incorporation of TiO 2 nanoparticles surface modified with gallic acid esters in epoxy resin. TiO 2 nanoparticles were obtained by acid catalyzed hydrolysis of titanium isopropoxide and their structural characterization was performed by X-ray diffraction and transmission electron microscopy. Three gallic acid esters, having different hydrophobic part, were used for surface modification of the synthesized TiO 2 nanoparticles: propyl, hexyl and lauryl gallate. The gallate chemisorption onto surface of TiO 2 nanoparticles was confirmed by Fourier transform infrared and ultraviolet–visible spectroscopy, while the amount of surface-bonded gallates was determined using thermogravimetric analysis. The influence of the surface modified TiO 2 nanoparticles, as well as the length of hydrophobic part of the gallate used for surface modification of TiO 2 nanoparticles, on glass transition temperature, barrier, dielectric and anticorrosive properties of epoxy resin was investigated by differential scanning calorimetry, water vapor transmission test, dielectric spectroscopy, electrochemical impedance spectroscopy and polarization measurements. Incorporation of surface modified TiO 2 nanoparticles in epoxy resin caused increase of glass transition temperature and decrease of the water vapor permeability of epoxy resin. The water vapor transmission rate of epoxy/TiO 2 nanocomposites was reduced with increasing hydrophobic part chain length of

Coexistence of an anatase/TiO2(B) heterojunction and an exposed (001) facet in TiO2 nanoribbon photocatalysts synthesized via a fluorine-free route and topotactic transformation.

Science.gov (United States)

Wang, Changhua; Zhang, Xintong; Liu, Yichun

2014-05-21

In this work, we report a novel approach to fabricate hierarchical TiO2 microspheres (HTMS) assembled by ultrathin nanoribbons where an anatase/TiO2(B) heterojunction and high energy facet coexist. The as-adopted approach involves (1) nonaqueous solvothermal treatment of a mixture of tetrabutyl titanate and acetic acid and (2) topotactical transformation into HTMS via thermal annealing. By this approach, the TiO2(B) phase usually synthesized from an alkaline treatment route could be initially formed. Subsequently, phase transition from TiO2(B) to anatase TiO2 occurs upon thermal treatment. It is demonstrated that such phase transition is accompanied by crystallographic orientation along the c-axis of anatase and TiO2(B) crystals, resulting in not only a coherent interface between two phases but also oriented attachment of anatase mesocrystals along the [001] direction, and finally high-energy (001) facet exposure. Interestingly, this work provides an alternative fluorine-free route for the synthesis of TiO2 crystals with high-energy (001) facet exposure. The structural analysis reveals that lattice-match induced topotactic transformation from TiO2(B) to anatase is the sole reason for the (001) facet exposure of anatase TiO2. The photocatalytic test for acetaldehyde decomposition shows that HTMS with anatase/TiO2(B) heterojunction and high-energy (001) facet exhibits superior photocatalytic efficiency compared with the relevant commercial product P25, which can be ascribed to the synergistic effect of large surface area, anatase/TiO2(B) heterojunction as well as high-energy facet exposure.

Coexistence of an anatase/TiO2(B) heterojunction and an exposed (001) facet in TiO2 nanoribbon photocatalysts synthesized via a fluorine-free route and topotactic transformation

Science.gov (United States)

Wang, Changhua; Zhang, Xintong; Liu, Yichun

2014-04-01

In this work, we report a novel approach to fabricate hierarchical TiO2 microspheres (HTMS) assembled by ultrathin nanoribbons where an anatase/TiO2(B) heterojunction and high energy facet coexist. The as-adopted approach involves (1) nonaqueous solvothermal treatment of a mixture of tetrabutyl titanate and acetic acid and (2) topotactical transformation into HTMS via thermal annealing. By this approach, the TiO2(B) phase usually synthesized from an alkaline treatment route could be initially formed. Subsequently, phase transition from TiO2(B) to anatase TiO2 occurs upon thermal treatment. It is demonstrated that such phase transition is accompanied by crystallographic orientation along the c-axis of anatase and TiO2(B) crystals, resulting in not only a coherent interface between two phases but also oriented attachment of anatase mesocrystals along the [001] direction, and finally high-energy (001) facet exposure. Interestingly, this work provides an alternative fluorine-free route for the synthesis of TiO2 crystals with high-energy (001) facet exposure. The structural analysis reveals that lattice-match induced topotactic transformation from TiO2(B) to anatase is the sole reason for the (001) facet exposure of anatase TiO2. The photocatalytic test for acetaldehyde decomposition shows that HTMS with anatase/TiO2(B) heterojunction and high-energy (001) facet exhibits superior photocatalytic efficiency compared with the relevant commercial product P25, which can be ascribed to the synergistic effect of large surface area, anatase/TiO2(B) heterojunction as well as high-energy facet exposure.

Ecotoxicity of TiO2 to Daphnia similis under irradiation

International Nuclear Information System (INIS)

Marcone, Glauciene P.S.; Oliveira, Ádria C.; Almeida, Gilberto; Umbuzeiro, Gisela A.; Jardim, Wilson F.

2012-01-01

Graphical abstract: EC50 (mg L −1 ) values to TiO 2 samples obtained in toxicity tests with Daphnia similis under different conditions of illumination (UV A and visible radiation) and in the dark (as standard protocols). P25: commercial sample containing 30% rutile and 70% anatase; M-S: synthesized sample containing 30% rutile and 70% anatase; Anatase-S: synthesized sample containing 100% anatase; Rutile-S: synthesized sample containing 100% rutile and P25*: commercial sample containing 100% rutile. Highlights: ► Some key physicochemical parameters of nano TiO 2 explain the toxicity observed. ► Under UV A radiation, TiO 2 becomes more toxic to D. similis. ► Toxicity tests of photoactive nano materials require photons as control parameter. - Abstract: Currently, there are a large number of products (sunscreen, pigments, cosmetics, plastics, toothpastes and photocatalysts) that use TiO 2 nanoparticles. Due to this large production, these nanoparticles can be released into the aquatic, terrestrial and aerial environments at relative high concentration. TiO 2 in natural water has the capacity to harm aquatic organisms such as the Daphnia (Cladocera) species, mainly because the photocatalytic properties of this semiconductor. However, very few toxicity tests of TiO 2 nanoparticles have been conducted under irradiation. The aim of this study was to evaluate anatase and rutile TiO 2 toxicity to Daphnia similis exploring their photocatalytic properties by incorporating UV A and visible radiation as a parameter in the assays. Anatase and rutile TiO 2 samples at the highest concentration tested (100 mg L −1 ) were not toxic to D. similis, neither in the dark nor under visible light conditions. The anatase form and a mixture of anatase and rutile, when illuminated by a UV A black light with a peak emission wavelength of 360 nm, presented photo-dependent EC50 values of 56.9–7.8 mg L −1 , which indicates a toxicity mechanism caused by ROS (reactive oxygen species

Structure and electrochemical hydrogen storage properties of Ti{sub 2}Ni alloy synthesized by ball milling

Energy Technology Data Exchange (ETDEWEB)

Hosni, B. [Equipe des Hydrures Métalliques, Laboratoire de Mécanique, Matériaux et Procédés, Ecole Nationale Supérieure d’Ingénieurs de Tunis, ENSIT Ex ESSTT, Université de Tunis, 5 Avenue Taha Hussein, 1008 Tunis (Tunisia); Li, X. [FEMTO-ST, MN2S, Université de Technologie de Belfort-Montbéliard, Site de Sévenans, 90010 Belfort cedex (France); Khaldi, C., E-mail: chokri.khaldi@esstt.rnu.tn [Equipe des Hydrures Métalliques, Laboratoire de Mécanique, Matériaux et Procédés, Ecole Nationale Supérieure d’Ingénieurs de Tunis, ENSIT Ex ESSTT, Université de Tunis, 5 Avenue Taha Hussein, 1008 Tunis (Tunisia); ElKedim, O. [FEMTO-ST, MN2S, Université de Technologie de Belfort-Montbéliard, Site de Sévenans, 90010 Belfort cedex (France); Lamloumi, J. [Equipe des Hydrures Métalliques, Laboratoire de Mécanique, Matériaux et Procédés, Ecole Nationale Supérieure d’Ingénieurs de Tunis, ENSIT Ex ESSTT, Université de Tunis, 5 Avenue Taha Hussein, 1008 Tunis (Tunisia)

2014-12-05

Highlights: • The Ti{sub 2}Ni alloy activation requires only one cycle of charge and discharge, regardless of the temperature. • By increasing the temperature the capacity loss, undergoes an increase and it is more pronounced for the 60 °C. • A good correlation is found between the evolutions of the different electrochemical parameters according to the temperature. - Abstract: The structure and the electrochemical hydrogen storage properties of amorphous Ti{sub 2}Ni alloy synthesized by ball milling and used as an anode in nickel–metal hydride batteries were studied. Nominal Ti{sub 2}Ni was synthesized under argon atmosphere at room temperature using a planetary high-energy ball mill. The structural and morphological characterization of the amorphous Ti{sub 2}Ni alloy is carried out by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The electrochemical characterization of the Ti{sub 2}Ni electrodes is carried out by the galvanostatic charging and discharging, the constant potential discharge, the open circuit potential and the potentiodynamic polarization techniques. The Ti{sub 2}Ni alloy activation requires only one cycle of charge and discharge, regardless of the temperature. The electrochemical discharge capacity of the Ti{sub 2}Ni alloy, during the first eight cycles, and at a temperature of 30 °C, remained practically unchanged and a good held cycling is observed. By increasing the temperature, the electrochemical discharge capacity loss after eight cycles undergoes an increase and it is more pronounced for the temperature 60 °C. At 30 °C, the anodic corrosion current density is 1 mA cm{sup −2} and then it undergoes a rapid drop, remaining substantially constant (0.06 mA cm{sup −2}) in the range 40–60 °C, before undergoing a slight increase to 70 °C (0.3 mA cm{sup −2}). This variation is in good agreement with the maximum electrochemical discharge capacity values found for the

TiO2/Cu2O composite based on TiO2 NTPC photoanode for photoelectrochemical (PEC) water splitting under visible light

KAUST Repository

Shi, Le

2015-05-01

Water splitting through photoelectrochemical reaction is widely regarded as a major method to generate H2 , a promising source of renewable energy to deal with the energy crisis faced up to human being. Efficient exploitation of visible light in practice of water splitting with pure TiO2 material, one of the most popular semiconductor material used for photoelectrochemical water splitting, is still challenging. One dimensional TiO2 nanotubes is highly desired with its less recombination with the short distance for charge carrier diffusion and light-scattering properties. This work is based on TiO2 NTPC electrode by the optimized two-step anodization method from our group. A highly crystalized p-type Cu2O layer was deposited by optimized pulse potentiostatic electrochemical deposition onto TiO2 nanotubes to enhance the visible light absorption of a pure p-type TiO2 substrate and to build a p-n junction at the interface to improve the PEC performance. However, because of the real photocurrent of Cu2O is far away from its theoretical limit and also poor stability in the aqueous environment, a design of rGO medium layer was added between TiO2 nanotube and Cu2O layer to enhance the photogenerated electrons and holes separation, extend charge carrier diffusion length (in comparison with those of conventional pure TiO2 or Cu2O materials) which could significantly increase photocurrent to 0.65 mA/cm2 under visible light illumination (>420 nm) and also largely improve the stability of Cu2O layer, finally lead to an enhancement of water splitting performance.

Synergistic effects between TiO2 and carbon nanotubes (CNTs) in a TiO2/CNTs system under visible light irradiation.

Science.gov (United States)

Wu, Chung-Hsin; Kuo, Chao-Yin; Chen, Shih-Ting

2013-01-01

This study synthesized a TiO2/carbon nanotubes (CNTs) composite via the sol-gel method. The surface characteristics of the TiO2/CNTs composite were determined by X-ray diffraction, transmission electron microscopy, specific surface area analyser, ultraviolent (UV)-vis spectroscopy, X-ray photoelectron spectroscopy and Raman spectrometer. The photocatalytic activity ofthe TiO2/CNTs composite was evaluated by decolourizing C.I. Reactive Red 2 (RR2) under visible light irradiation. Furthermore, the effects of calcination temperature, pH, RR2 concentration, and the TiO2/CNTs composite dosage on RR2 decolourization were determined simultaneously. The optimal calcination temperature to generate TiO2 and the TiO2/CNTs composite was 673 K, as the percentage of anatase crystallization at this temperature was highest. The specific surface area of the TiO2/CNTs composite and TiO2 were 45 and 42 m2/g, respectively. The band gap of TiO2 and the TiO2/CNTs composite was 2.97 and 2.71 eV by UV-vis measurements, respectively. Experimental data indicate that the Ti-O-C bond formed in the TiO2/CNTs composite. The RR2 decolourization rates can be approximated by pseudo-first-order kinetics; moreover, only the TiO2/CNTs composite had photocatalytic activity under visible light irradiation. At pH 7, the RR2 decolourization rate constant of 0.5, 1 and 2 g/L TiO2/CNTs addition was 0.005, 0.0015, and 0.0047 min(-1), respectively. Decolourization rate increased as pH and the RR2 concentration decreased. The CNTs functioned as electron acceptors, promoting separation of photoinduced electron-hole pairs to retard their recombination; thus, photocatalytic activity of the TiO2/CNTs composite exceeded that of TiO2.

Spray pyrolysed Ru:TiO2 thin film electrodes prepared for electrochemical supercapacitor

Science.gov (United States)

Fugare, B. Y.; Thakur, A. V.; Kore, R. M.; Lokhande, B. J.

2018-04-01

Ru doped TiO2 thin films are prepared by using 0.06 M aqueous solution of potassium titanium oxalate (pto), and 0.005 M aqueous solution of ruthenium tri chloride (RuCl3) precursors. The deposition was carried on stainless steel (SS) by using well known ultrasonic spray pyrolysis technique (USPT) at 723° K by maintaining the spray rate 12 cc/min and compressed air flow rate 10 Lmin-1. Prepared Ru:TiO2 thin films were characterized by structurally, morphologically and electrochemically. Deposited RuO2 shows amorphous structure and TiO2 shows tetragonal crystal structure with rutile as prominent phase at very low decomposition temperature. SEM micrographs of RuO2 exhibits porous, interconnected, spherical grains type morphology and TiO2 shows porous, nanorods and nanoplates like morphology and also Ru doped TiO2 shows porous, spherical, granular and nanorods type morphology. The electrochemical cyclic voltammetery shows mixed capacitive behavior. The achieved highest value of specific capacitance 2692 F/g was Ru doped TiO2 electrode in 0.5 M H2SO4.

Gold nanoparticles-immobilized, hierarchically ordered, porous TiO2 nanotubes for biosensing of glutathione

Directory of Open Access Journals (Sweden)

Sheen Mers SV

2015-10-01

Full Text Available SV Sheen Mers,1,2 Elumalai Thambuswamy Deva Kumar,1 V Ganesh1,2 1Electrodics and Electrocatalysis (EEC Division, Council of Scientific and Industrial Research–Central Electrochemical Research Institute (CSIR–CECRI, Karaikudi, Tamil Nadu, India; 2Academy of Scientific and Innovative Research (AcSIR, New Delhi, India Abstract: Glutathione (GSH is vital for several functions of our human body such as neutralization of free radicals and reactive oxygen compounds, maintaining the active forms of vitamin C and E, regulation of nitric oxide cycle, iron metabolism, etc. It is also an endogenous antioxidant in most of the biological reactions. Given the importance of GSH, a simple strategy is proposed in this work to develop a biosensor for quantitative detection of GSH. This particular biosensor comprises of gold nanoparticles (Au NPs-immobilized, hierarchically ordered titanium dioxide (TiO2 porous nanotubes. Hexagonally arranged, honeycomb-like nanoporous tubular TiO2 electrodes are prepared by using a simple electrochemical anodization process by applying a constant potential of 30 V for 24 hours using ethylene glycol consisting of ammonium fluoride as an electrolytic medium. Structural morphology and crystalline nature of such TiO2 nanotubes are analyzed using field emission scanning electron microscope (FESEM and X-ray diffraction (XRD. Interestingly, nanocomposites of TiO2 with Au NPs is prepared in an effort to alter the intrinsic properties of TiO2, especially tuning of its band gap. Au NPs are prepared by a well-known Brust and Schiffrin method and are immobilized onto TiO2 electrodes which act as a perfect electrochemical sensing platform for GSH detection. Structural characterization and analysis of these modified electrodes are performed using FESEM, XRD, and UV-visible spectroscopic studies. GSH binding events on Au NPs-immobilized porous TiO2 electrodes are monitored by electrochemical techniques, namely, cyclic voltammetry (CV and

Enhanced photoelectrocatalytic performance for degradation of diclofenac and mechanism with TiO2 nano-particles decorated TiO2 nano-tubes arrays photoelectrode

International Nuclear Information System (INIS)

Cheng, Xiuwen; Liu, Huiling; Chen, Qinghua; Li, Junjing; Wang, Pu

2013-01-01

In this study, TiO 2 nano-particles decorated TiO 2 nano-tubes arrays (TiO 2 NPs/TiO 2 NTAs) photoelectrodes have been successfully prepared through anodization, combined with ultrasonic strategy, followed by annealing post-treatment. The morphology and structure of the as-prepared TiO 2 NPs/TiO 2 NTAs photoelectrodes were characterized by scanning electrons microscopy (SEM), N 2 adsorption/desorption isotherms, X-ray diffraction (XRD) and UV–visible light diffuse reflection spectroscopy (DRS). In addition, the generation of hydroxyl radicals (·OH) was detected by a photoluminescence (PL) spectra using terephthalic acid (TA) as a probe molecule. Furthermore, the photoelectrochemical (PECH) properties of TiO 2 NPs/TiO 2 NTAs photoanode were investigated through transient open circuit potential (OCP), photocurrent response (PCR) and electrochemical impedance spectroscopy (EIS). It was found that TiO 2 NPs/TiO 2 NTAs photoelectrode exhibited a distinct decrease of OCP of −0.219 mV cm −2 and PCR of 0.049 mA cm −2 , while a significantly enhanced photoelectrocatalytic (PEC) efficiency of 63.6% (0.4 V vs. SCE) for the degradation of diclofenac. Moreover, the enhanced PEC mechanism of TiO 2 NPs/TiO 2 NTAs photoanode was proposed. The high PEC performance could be attributed to the decoration of TiO 2 NPs, which could improve the mobility and separation efficiency of photoinduced charge carriers under external potential

Properties of Sn-doped TiO2 nanotubes fabricated by anodization of co-sputtered Ti–Sn thin films

International Nuclear Information System (INIS)

Kyeremateng, Nana Amponsah; Hornebecq, Virginie; Knauth, Philippe; Djenizian, Thierry

2012-01-01

Self-organized Sn-doped TiO 2 nanotubes (nts) were fabricated for the first time, by anodization of co-sputtered Ti and Sn thin films. This nanostructured material was characterized by scanning electron microscopy, energy dispersive X-ray spectroscopy, X-ray diffraction, UV–vis spectroscopy and transmission electron microscopy. Due to their remarkable properties, Sn-doped TiO 2 nts can find potential applications in Li-ion microbatteries, photovoltaics, and catalysis. Particularly, the electrochemical performance as an anode material for Li-ion microbatteries was evaluated in Li test cells. With current density of 70 μA cm −2 (1 C) and cut-off potential of 1 V, Sn-doped TiO 2 nts showed improved performance compared to simple TiO 2 nts, and differential capacity plots revealed that the material undergoes full electrochemical reaction as a Rutile-type TiO 2 .

Sensing and electrical properties of TiO2 nanoparticles

International Nuclear Information System (INIS)

Usman, M.

2011-01-01

The purpose of this work was to synthesize TiO 2 nanoparticles using Coprecipitation method. 2 different samples were synthesized, one with a modifier and other without using a modifier. After synthesis, newly formed nanoparticles were characterized b different techniques to find various properties of these nanoparticles. Scanning electron Microscopy (SEM) was used to study structure and morphology of Cu nanoparticles and for compositional analysis Energy dispersive spectroscopy (EDS) was used. X-Ray Diffraction (XRD) Studies were also carried out to find phase an average particle Size. To find the band gap of our nanoparticles, UV-Visible Spectroscopy was also done. Non-Modified nanoparticles were as small as 12nm reported by SEM images which were synthesized using a modifier were as small as 10nm. Modified TiO 2 nanoparticles were used in humidity sensing devices and it properties as a humidity sensor were examined by doing Impedance spectroscopy, D measurements and Dielectric measurements. Our TiO 2 humidity sensor showed sensitivity for humidity at low and mid-range frequencies while its response time was 4 seconds when we changed RH% to 90 from 40% and measured the impedance. (author)

Anti-fish bacterial pathogen effect of visible light responsive Fe3O4@TiO2 nanoparticles immobilized on glass using TiO2 sol–gel

International Nuclear Information System (INIS)

Yeh, N.; Lee, Y.C.; Chang, C.Y.; Cheng, T.C.

2013-01-01

This paper demonstrates a fish pathogen reduction procedure that uses TiO 2 sol–gel coating Fe 3 O 4 @TiO 2 powder on glass substrate. Such procedure can effectively relieve two constraints that haunt TiO 2 sterilization applications: 1) the need for UV for overcoming the wide band gap of pure TiO 2 and 2) the difficulty of its recovering from water for reuse. In the process, visible light responsive Fe 3 O 4 /TiO 2 nanoparticles are synthesized and immobilized on glass using TiO 2 sol–gel as the binder for fish bacterial pathogen disinfection test. After 3 h of visible light irradiation, the immobilized Fe 3 O 4 @TiO 2 's inhibition efficiencies for fish bacterial pathogen are, respectively, 50% for Edwardsiella tarda (BCRC 10670) and 23% for Aeromonas hydrophila (BCRC 13018)

VO2/TiO2 Nanosponges as Binder-Free Electrodes for High-Performance Supercapacitors

Science.gov (United States)

Hu, Chenchen; Xu, Henghui; Liu, Xiaoxiao; Zou, Feng; Qie, Long; Huang, Yunhui; Hu, Xianluo

2015-11-01

VO2/TiO2 nanosponges with easily tailored nanoarchitectures and composition were synthesized by electrostatic spray deposition as binder-free electrodes for supercapacitors. Benefiting from the unique interconnected pore network of the VO2/TiO2 electrodes and the synergistic effect of high-capacity VO2 and stable TiO2, the as-formed binder-free VO2/TiO2 electrode exhibits a high capacity of 86.2 mF cm-2 (~548 F g-1) and satisfactory cyclability with 84.3% retention after 1000 cycles. This work offers an effective and facile strategy for fabricating additive-free composites as high-performance electrodes for supercapacitors.

VO2/TiO2 Nanosponges as Binder-Free Electrodes for High-Performance Supercapacitors.

Science.gov (United States)

Hu, Chenchen; Xu, Henghui; Liu, Xiaoxiao; Zou, Feng; Qie, Long; Huang, Yunhui; Hu, Xianluo

2015-11-04

VO2/TiO2 nanosponges with easily tailored nanoarchitectures and composition were synthesized by electrostatic spray deposition as binder-free electrodes for supercapacitors. Benefiting from the unique interconnected pore network of the VO2/TiO2 electrodes and the synergistic effect of high-capacity VO2 and stable TiO2, the as-formed binder-free VO2/TiO2 electrode exhibits a high capacity of 86.2 mF cm(-2) (~548 F g(-1)) and satisfactory cyclability with 84.3% retention after 1000 cycles. This work offers an effective and facile strategy for fabricating additive-free composites as high-performance electrodes for supercapacitors.

Efficient photodecomposition of herbicide imazapyr over mesoporous Ga2O3-TiO2 nanocomposites.

Science.gov (United States)

Ismail, Adel A; Abdelfattah, Ibrahim; Faisal, M; Helal, Ahmed

2018-01-15

The unabated release of herbicide imazapyr into the soil and groundwater led to crop destruction and several pollution-related concerns. In this contribution, heterogeneous photocatalytic technique was employed utilizing mesoporous Ga 2 O 3 -TiO 2 nanocomposites for degrading imazapyr herbicide as a model pollutant molecule. Mesoporous Ga 2 O 3 -TiO 2 nanocomposites with varied Ga 2 O 3 contents (0-5wt%) were synthesized through sol-gel process. XRD and Raman spectra exhibited extremely crystalline anatase TiO 2 phase at low Ga 2 O 3 content which gradually reduced with the increase of Ga 2 O 3 content. TEM images display uniform TiO 2 particles (10±2nm) with mesoporous structure. The mesoporous TiO 2 exhibits large surface areas of 167m 2 g -1 , diminished to 108m 2 g -1 upon 5% Ga 2 O 3 incorporation, with tunable mesopore diameter in the range of 3-9nm. The photocatalytic efficiency of synthesized Ga 2 O 3 -TiO 2 nanocomposites was assessed by degrading imazapyr herbicide and comparing with commercial photocatalyst UV-100 and mesoporous Ga 2 O 3 under UV illumination. 0.1% Ga 2 O 3 -TiO 2 nanocomposite is considered the optimum photocatalyst, which degrades 98% of imazapyr herbicide within 180min. Also, the photodegradation rate of imazapyr using 0.1% Ga 2 O 3 -TiO 2 nanocomposite is nearly 10 and 3-fold higher than that of mesoporous Ga 2 O 3 and UV-100, respectively. The high photonic efficiency and long-term stability of the mesoporous Ga 2 O 3 -TiO 2 nanocomposites are ascribed to its stronger oxidative capability in comparison with either mesoporous TiO 2 , Ga 2 O 3 or commercial UV-100. Copyright © 2017 Elsevier B.V. All rights reserved.

Synthesis and photocatalytic activity of anatase TiO2 nanoparticles for degradation of methyl orange

Science.gov (United States)

Singh, Manmeet; Duklan, Neha; Singh, Pritpal; Sharma, Jeewan

2018-05-01

In present study, TiO2 nanoparticles, in anatase form, were successfully synthesized using TiCl4 as precursor. These nanoparticles were synthesized by sol-gel method at room temperature (298 K). As prepared samples were characterized for phase structure, optical absorption and surface properties using X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), Raman spectroscopy and UV-Visible spectroscopy. The synthesized TiO2 nanoparticles sample was compared with one of the most efficient commercial photocatalyst Degussa TiO2 also known as P(25). The effect of phase composition of anatase TiO2 nanoparticles, as compared to P(25), on photocatalytic decomposition of organic dye, methyl orange (MO) was studies under UV light illumination. An enhanced degradation of hazardous dye was observed in the presence of anatase TiO2 nanoparticles as compared to P(25) due to slow recombination rate. Other possible reasons for this enhancement have also been discussed.

Oriented epitaxial TiO2 nanowires for water splitting

Science.gov (United States)

Hou, Wenting; Cortez, Pablo; Wuhrer, Richard; Macartney, Sam; Bozhilov, Krassimir N.; Liu, Rong; Sheppard, Leigh R.; Kisailus, David

2017-06-01

Highly oriented epitaxial rutile titanium dioxide (TiO2) nanowire arrays have been hydrothermally grown on polycrystalline TiO2 templates with their orientation dependent on the underlying TiO2 grain. Both the diameter and areal density of the nanowires were tuned by controlling the precursor concentration, and the template surface energy and roughness. Nanowire tip sharpness was influenced by precursor solubility and diffusivity. A new secondary ion mass spectrometer technique has been developed to install additional nucleation sites in single crystal TiO2 templates and the effect on nanowire growth was probed. Using the acquired TiO2 nanowire synthesis knowhow, an assortment of nanowire arrays were installed upon the surface of undoped TiO2 photo-electrodes and assessed for their photo-electrochemical water splitting performance. The key result obtained was that the presence of short and dispersed nanowire arrays significantly improved the photocurrent when the illumination intensity was increased from 100 to 200 mW cm-2. This is attributed to the alignment of the homoepitaxially grown nanowires to the [001] direction, which provides the fastest charge transport in TiO2 and an improved pathway for photo-holes to find water molecules and undertake oxidation. This result lays a foundation for achieving efficient water splitting under conditions of concentrated solar illumination.

Solid-state synthesis of Li_4Ti_5O_1_2 whiskers from TiO_2-B

International Nuclear Information System (INIS)

Yao, Wenjun; Zhuang, Wei; Ji, Xiaoyan; Chen, Jingjing; Lu, Xiaohua; Wang, Changsong

2016-01-01

Highlights: • The Li_4Ti_5O_1_2 whiskers were synthesized from TiO_2-B whiskers via a solid state reaction. • The TiO_2-B crystal structure for lithium diffusion is easier than anatase. • The separated diffusion and reaction process is crucial for the solid-state syntheses of Li_4Ti_5O_1_2 whiskers. - Abstract: In this work, Li_4Ti_5O_1_2 (LTO) was synthesized from the precursors of TiO_2-B and anatase whiskers, respectively. The synthesized LTO whiskers from TiO_2-B whiskers via a solid state reaction at 650 °C have a high degree of crystallinity with an average diameter of 300 nm. However, when anatase whiskers were used as the precursor, only particle morphology LTO was produced at 750 °C. The further analysis of the precursors, the intermediate products and the final products reveal that the crystal structure of the anatase hinders the diffusion of lithium, leading to a typical reaction–diffusion process. Under this condition, only particle morphology LTO can be produced. However, the crystal structure of the TiO_2-B is easy for lithium diffusion and the process is performed in two separated steps (i.e., diffusion and reaction), which makes it possible to decrease the solid-state reaction temperature down to 650 °C and then maintain the morphologies of whiskers.

Structural and electrochemical studies of TiO2 complexes with (4,4'-((1E,1'E)-(2,5-bis(octyloxy)-1,4-phenylene)bis(ethene-2,1-diyl))bis-(E)-N-(2,5-bis(octyloxy)benzylidene)) imine derivative bases towards organic devices.

Science.gov (United States)

Rozycka, Anna; Iwan, Agnieszka; Bogdanowicz, Krzysztof Artur; Filapek, Michal; Górska, Natalia; Hreniak, Agnieszka; Marzec, Monika

2018-06-12

Three (4,4'-((1E,1'E)-(2,5-bis(octyloxy)-1,4-phenylene)bis(ethene-2,1-diyl))bis-(E)-N-(2,5-bis(octyloxy)benzylidene)) imine derivatives were synthesized via a condensation reaction with p-toluenesulfonic acid as a catalyst. The effects of the end groups and vinylene (-HC[double bond, length as m-dash]CH-) moieties on the structural, thermal, optical, electrochemical and photovoltaic properties of imines were investigated to check the influence of TiO2 on the imine properties. The thermal behavior of imines and their complexes with TiO2 was widely investigated using FT-IR, XRD, DSC and POM methods in order to determine the order type in the imine structure. All imines present the highest occupied molecular orbital (HOMO) levels of about -5.39 eV (SAI1 and SAI2) and -5.27 eV (SAI3) and the lowest unoccupied molecular orbital (LUMO) levels at about -3.17 eV. The difference of the end groups in the imines in each case did not affect redox properties. Generally, both oxidation and reduction are easier after TiO2 addition and it also changes the HOMO-LUMO levels of imines. Moreover, changes in the characteristic bands for imines in the region 1500-1700 cm-1 observed as a drastic decrease of intensity or even disappearance of bands in the imine : TiO2 mixture suggest the formation of a complex (C[double bond, length as m-dash]N)-TiO2. Organic devices with the configuration of ITO/TiO2/SAIx (or SAIx : TiO2)/Au were fabricated and investigated in the presence and absence of visible light irradiation with an intensity of 93 mW cm-2. In all imines and complexes with TiO2, the generation of the photocurrent indicates their use as photodiodes and the best result was observed for SAI3 : TiO2 complexes.

XRD analysis of undoped and Fe doped TiO2 nanoparticles by Williamson Hall method

International Nuclear Information System (INIS)

Bharti, Bandna; Barman, P. B.; Kumar, Rajesh

2015-01-01

Undoped and Fe doped titanium dioxide (TiO 2 ) nanoparticles were synthesized by sol-gel method at room temperature. The synthesized samples were annealed at 500°C. For structural analysis, the prepared samples were characterized by X-ray diffraction (XRD). The crystallite size of TiO 2 and Fe doped TiO 2 nanoparticles were calculated by Scherer’s formula, and was found to be 15 nm and 11 nm, respectively. Reduction in crystallite size of TiO 2 with Fe doping was observed. The anatase phase of Fe-doped TiO 2 nanoparticles was also confirmed by X-ray diffraction. By using Williamson-Hall method, lattice strain and crystallite size were also calculated. Williamson–Hall plot indicates the presence of compressive strain for TiO 2 and tensile strain for Fe-TiO 2 nanoparticles annealed at 500°C

Facile synthesis of porous TiO_2 photocatalysts using waste sludge as the template

International Nuclear Information System (INIS)

Wang, Xiaopeng; Huang, Shouqiang; Zhu, Nanwen; Lou, Ziyang; Yuan, Haiping

2015-01-01

Graphical abstract: Waste sludge is introduced to synthesize the waste sludge templated TiO_2 photocatalyst with porous structure, which possesses better photocatalytic activity compared to pure TiO_2. - Highlights: • Waste sludge is introduced to synthesize the TiO_2 photocatalyst. • Waste sludge templated TiO_2 sample possesses porous structure. • Waste sludge templated TiO_2 sample exhibits high photocatalytic activity. - Abstract: A resource utilization method of waste sludge is present by the synthesis of waste sludge templated TiO_2 photocatalysts. The organic materials in waste sludge are used as the pore-forming agents, and the transition metals included in the remaining waste sludge through calcination (WSC) can serve as the dopants for the WSC-TiO_2 (WSCT) photocatalyst. The visible and UV–visible light driven photocatalytic activities of WSCT are much better compared to those of pure TiO_2 and WSC, and it is originated from the higher light absorption property and the efficient electron–hole pair separation provided by waste sludge.

SiO2@TiO2 Coating: Synthesis, Physical Characterization and Photocatalytic Evaluation

Directory of Open Access Journals (Sweden)

A. Rosales

2018-03-01

Full Text Available Use of silicon dioxide (SiO2 and titanium dioxide (TiO2 have been widely investigated individually in coatings technology, but their combined properties promote compatibility for different innovative applications. For example, the photocatalytic properties of TiO2 coatings, when exposed to UV light, have interesting environmental applications, such as air purification, self-cleaning and antibacterial properties. However, as reported in different pilot projects, serious durability problems, associated with the adhesion between the substrate and TiO2, have been evidenced. Thus, the aim of this work is to synthesize SiO2 together with TiO2 to increase the durability of the photocatalytic coating without affecting its photocatalytic potential. Therefore, synthesis using sonochemistry, synthesis without sonochemistry, physical characterization, photocatalytic evaluation, and durability of the SiO2, SiO2@TiO2 and TiO2 coatings are presented. Results indicate that using SiO2 improved the durability of the TiO2 coating without affecting its photocatalytic properties. Thus, this novel SiO2@TiO2 coating shows potential for developing long-lasting, self-cleaning and air-purifying construction materials.

Synthesis, characterization and photocatalytic activity of Fe2O3-TiO2 nanoparticles and nanocomposites

Directory of Open Access Journals (Sweden)

M. Ahmadi Golsefidi

2016-01-01

Full Text Available In this pepper Fe2O3 nanoparticles were synthesized via a fast microwave method. Then Fe2O3-TiO2 nanocomposites were synthesized by a sonochemical-assisted method. The prepared products were characterized by X-ray diffraction pattern, scanning electron microscopy and Fourier transform infrared spectroscopy. The photocatalytic behaviour of Fe2O3-TiO2 nanocomposites was evaluated using the degradation of Rhodamine B under ultra violet irradiation. The results show that nanocomposites have applicable magnetic and photocatalytic performance.

Electrochemical degradation of triazole fungicides in aqueous solution using TiO2-NTs/SnO2-Sb/PbO2 anode: Experimental and DFT studies

International Nuclear Information System (INIS)

Han, Weiqing; Zhong, Congqiang; Liang, Linyue; Sun, Yunlong; Guan, Ying; Wang, Lianjun; Sun, Xiuyun; Li, Jiansheng

2014-01-01

Triazole fungicides (TFs) are toxic and bio-refractory contaminants widely spread in environment. This study investigated electrochemical degradation of TFs in aqueous solution at TiO 2 -NTs/SnO 2 -Sb/PbO 2 anode with particular attention to the effect of molecular structure. Three TFs with triazole ring in one biologically treated water including tricyclazole (TC), 1H-1,2,4-triazole (Tz) and propiconazole (PPC) were selected as the target compounds. Results of bulk electrolysis showed that degradation of all TFs was fit to a pseudo first-order equation. The three compounds were degraded with the following sequence: PPC > TC> Tz in terms of their rates of oxidation. Quantum chemical calculation using the density function theory (DFT) method was combined with experimental results to describe the degradation sequence of TFs. Atom charge was calculated by DFT method and active sites of TFs were identified respectively. Analysis of intermediates by GC-MS and LC-(ESI)-MS/MS showed agreement with calculation results. In addition, the acute toxicity of TC and PPC treated solution significantly decreased after treatment by electrochemical oxidation

Characterization and electrochemical performances of MoO2 modified LiFePO4/C cathode materials synthesized by in situ synthesis method

International Nuclear Information System (INIS)

He, Jichuan; Wang, Haibin; Gu, Chunlei; Liu, Shuxin

2014-01-01

Graphical abstract: The MoO 2 modified LiFePO 4 /C cathode materials were synthesized by in situ synthesis method. MoO 2 can sufficiently coat on the LiFePO 4 /C particles surface and does not alter LiFePO 4 crystal structure, and the adding of MoO 2 decreases the particles size and increases the tap density of cathode materials. The existence of MoO 2 improves electrochemical performance of LiFePO 4 cathode materials in specific capability and lithium ion diffusion and charge transfer resistance of cathode materials. - Highlights: • The MoO 2 modified LiFePO 4 /C cathode materials were synthesized by in situ synthesis method. • The existence of MoO 2 decreases the particles size and increases the tap density of cathode materials. • MoO 2 can sufficiently coat on the surface of LiFePO 4 /C cathode materials. • The existence of MoO 2 enhanced electrochemical performance of LiFePO 4 /C cathode materials. - Abstract: The MoO 2 modified LiFePO 4 /C cathode materials were synthesized by in situ synthesis method. Phase compositions and microstructures of the products were characterized by X-ray powder diffraction (XRD), SEM, TEM and EDS. Results indicate that MoO 2 can sufficiently coat on the LiFePO 4 surface and does not alter LiFePO 4 crystal structure, the existence of MoO 2 decreases the particles size and increases the tap density of cathode materials. The electrochemical behavior of cathode materials was analyzed using galvanostatic measurement, cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The results show that the existence of MoO 2 improves electrochemical performance of LiFePO 4 cathode materials in specific capability and lithium ion diffusion and charge transfer resistance. The initial charge–discharge specific capacity and apparent lithium ion diffusion coefficient increase, the charge transfer resistance decreases with MoO 2 content and maximizes around the MoO 2 content is 5 wt%. It has been had further proved that

Electrical conductivity characteristic of TiO2 nanowires from hydrothermal method

International Nuclear Information System (INIS)

Othman, Mohd Azlishah; Amat, Noor Faridah; Ahmad, Badrul Hisham; Rajan, Jose

2014-01-01

One dimensional nanostructures of titanium dioxide (TiO 2 ) were synthesized via hydrothermal method by mixing TiO 2 as precursor in aqueous solution of NaOH as solvent. Then, heat and washing treatment was applied. Thus obtained wires had diameter ∼15 nm. TiO 2 nanowires will be used as a network in solar cell such dye-sensitized solar cell in order to improve the performance of electron movement in the device. To improve the performance of electron movement, the characteristics of TiO 2 nanowires have been analyses using field emission scanning electron microscopy (FESEM) analysis, x-ray diffractometer (XRD) analysis and brunauer emmett teller (BET) analysis. Finally, electrical conductivity of TiO 2 nanowires was determined by measuring the resistance of the TiO 2 nanowires paste on microscope glass.

Biocorrosion studies of TiO2 nanoparticle-coated Ti-6Al-4V implant in simulated biofluids

International Nuclear Information System (INIS)

Zaveri, Nikita; McEwen, Gerald D.; Karpagavalli, Ramji; Zhou Anhong

2010-01-01

The corrosion behaviors of the TiO 2 nanoparticles coated bioimplant Ti-6Al-4V exposed to three different simulated biofluids (SBF), namely, (1) NaCl solution, (2) Hank's solution, and (3) Cigada solution, were studied by using micro-Raman spectroscopy, electrochemical techniques, and scanning electron microscopy (SEM) with energy dispersive X-ray spectroscopy (EDS). The different electrochemical impedance spectroscopy models were applied to fit the data obtained from the implants before and after the coating of TiO 2 nanoparticles (50-100 nm). It was found that the TiO 2 nanoparticle coatings increased the thickness of the pre-existing oxide layer on the Ti-6Al-4V surface, serving to improve the bioimplant corrosion resistance.

Biocorrosion studies of TiO2 nanoparticle-coated Ti-6Al-4V implant in simulated biofluids

Science.gov (United States)

Zaveri, Nikita; McEwen, Gerald D.; Karpagavalli, Ramji; Zhou, Anhong

2010-06-01

The corrosion behaviors of the TiO2 nanoparticles coated bioimplant Ti-6Al-4V exposed to three different simulated biofluids (SBF), namely, (1) NaCl solution, (2) Hank's solution, and (3) Cigada solution, were studied by using micro-Raman spectroscopy, electrochemical techniques, and scanning electron microscopy (SEM) with energy dispersive X-ray spectroscopy (EDS). The different electrochemical impedance spectroscopy models were applied to fit the data obtained from the implants before and after the coating of TiO2 nanoparticles (50-100 nm). It was found that the TiO2 nanoparticle coatings increased the thickness of the pre-existing oxide layer on the Ti-6Al-4V surface, serving to improve the bioimplant corrosion resistance.

Fullerene C70 decorated TiO2 nanowires for visible-light-responsive photocatalyst

International Nuclear Information System (INIS)

Cho, Er-Chieh; Ciou, Jing-Hao; Zheng, Jia-Huei; Pan, Job; Hsiao, Yu-Sheng; Lee, Kuen-Chan; Huang, Jen-Hsien

2015-01-01

Graphical abstract: - Highlights: • TiO 2 nanowire decorated with C 60 and C 70 derivatives has been synthesized. • The fullerenes impede the charge recombination due to its high electron affinity. • The fullerenes expand the utilization of solar light from UV to visible light. • The modified-TiO 2 has great biocompatibility. - Abstract: In this study, we have synthesized C 60 and C 70 -modified TiO 2 nanowire (NW) through interfacial chemical bonding. The results indicate that the fullerenes (C 60 and C 70 derivatives) can act as sinks for photogenerated electrons in TiO 2 , while the fullerene/TiO 2 is illuminated under ultraviolet (UV) light. Therefore, in comparison to the pure TiO 2 NWs, the modified TiO 2 NWs display a higher photocatalytic activity under UV irradiation. Moreover, the fullerenes also can function as a sensitizer to TiO 2 which expand the utilization of solar light from UV to visible light. The results reveal that the C 70 /TiO 2 NWs show a significant photocatalytic activity for degradation of methylene blue (MB) in visible light region. To better understand the mechanism responsible for the effect of fullerenes on the photocatalytic properties of TiO 2 , the electron only devices and photoelectrochemical cells based on fullerenes/TiO 2 are also fabricated and evaluated.

High cyclability of carbon-coated TiO2 nanoparticles as anode for sodium-ion batteries

International Nuclear Information System (INIS)

Ge, Yeqian; Jiang, Han; Zhu, Jiadeng; Lu, Yao; Chen, Chen; Hu, Yi; Qiu, Yiping; Zhang, Xiangwu

2015-01-01

Highlights: • Titanium oxide nanopaticles were modified by carbon coating from pyrolyzing of PVP. • Carbon coating gave rise to excellent cycling ability of TiO 2 for sodium-ion batteries. • The reversible capacity of carbon-coated TiO 2 reached 242.3 mAh g −1 at 30 mA g −1 . • Good rate performance of carbon-coated TiO 2 was presented up to 800 mA g −1 . - Abstract: Owing to the merits of good chemical stability, elemental abundance and nontoxicity, titanium dioxide (TiO 2 ) has drawn increasing attraction for use as anode material in sodium-ion batteries. Nanostructured TiO 2 was able to achieve high energy density. However, nanosized TiO 2 is typically electrochemical instable, which leads to poor cycling performance. In order to improve the cycling stability, carbon from thermolysis of poly(vinyl pyrrolidone) was coated onto TiO 2 nanoparticles. Electronic conductivity and electrochemical stability were enhanced by coating carbon onto TiO 2 nanoparticles. The resultant carbon-coated TiO 2 nanoparticles exhibited high reversible capacity (242.3 mAh g −1 ), high coulombic efficiency (97.8%), and good capacity retention (87.0%) at 30 mA g −1 over 100 cycles. By comparison, untreated TiO 2 nanoparticles showed comparable reversible capacity (237.3 mAh g −1 ) and coulombic efficiency (96.2%), but poor capacity retention (53.2%) under the same condition. The rate performance of carbon-coated TiO 2 nanoparticles was also displayed as high as 127.6 mAh g −1 at a current density of 800 mA g −1 . The improved cycling performance and rate capability were mostly attributed to protective carbon layer helping stablize solid electrolyte interface formation of TiO 2 nanoparticles and improving the electronic conductivity. Therefore, it is demonstrated that carbon-coated TiO 2 nanoparticles are promising anode candidate for sodium-ion batteries

Development of high efficient visible light-driven N, S-codoped TiO2 nanowires photocatalysts

International Nuclear Information System (INIS)

Zhang, Yanlin; Liu, Peihong; Wu, Honghai

2015-01-01

Highlights: • A facile hydrothermal route to synthesize N, S-codoped TiO 2 nanowires. • The codoped TiO 2 nanowires have TiO 2 (B) and anatase phase. • The significant shift of the optical absorption edge toward the visible region. • The photocatalyst showed high photocatalytic activity for atrazine. - Abstract: One-dimensional (1D) nanowire material (especially nonmetal doped 1D nanowires) synthesized by a facile way is of great significance and greatly desired as it has higher charge carrier mobility and lower carrier recombination rate. N, S-codoped TiO 2 nanowires were synthesized using titanium sulfate as a precursor and isopropanol as a protective capping agent by a hydrothermal route. The obtained doped nanowires were characterized by XRD, SEM, HRTEM, SAED, XPS, BET and UV–vis absorption spectrum. The incorporation of N and S into TiO 2 NWs can lead to the expansion of its lattice and remarkably lower its electron-transfer resistance. Photocatalytic activity measurement showed that the N, S-codoped TiO 2 nanowires with high quantum efficiency revealed the best photocatalytic performance for atrazine degradation under visible light irradiation compared to N, S-codoped TiO 2 nanoparticles and S-doped TiO 2 nanowires, which was attributed to (i) the synergistic effect of N and S doping in narrowing the band gap, separating electron–hole pairs and increasing the photoinduced electrons, and (ii) extending the anatase-to-rutile transformation temperature above 600 °C

Mo-doped Gray Anatase TiO2: Lattice Expansion for Enhanced Sodium Storage

International Nuclear Information System (INIS)

Liao, Hanxiao; Xie, Lingling; Zhang, Yan; Qiu, Xiaoqing; Li, Simin; Huang, Zhaodong; Hou, Hongshuai; Ji, Xiaobo

2016-01-01

Gray-colored Mo 6+ -doped anatase TiO 2 is prepared uniformly with particle size of 10–20 nm, and is firstly employed as anode material in sodium-ion batteries (SIBs), presenting excellent electrochemical performances. It delivered reversible specific capacities of 231.8 mAh g −1 at 0.1 C (33.5 mA g −1 ) after 100 cycles and 108.3 mAh g −1 at 5 C (1.68 A g −1 ), comparing to 170.5 mAh g −1 at 0.1 C and only 41.7 mAh g −1 at 5C for the bare TiO 2 . The improved electrochemical performances might be beneficial from the doping of Mo 6+ , which can effectively enhance the conductivity of TiO 2 resulting from induced conduction band electrons, interstitial oxygen defects and vacancies. In addition, the doping can also lead to the lattice expansion, which can facilitate the diffusion of Na + . In combination with natural abundance and environmental benignity, Mo 6+ -doped TiO 2 can be expected to be utilized as an anode material for enhanced sodium storage.

Characteristics and properties of a novel in situ method of synthesizing mesoporous TiO2 nanopowders by a simple coprecipitation process without adding surfactant

International Nuclear Information System (INIS)

Yeh, Shang-Wei; Ko, Horng-Huey; Chiang, Hsiu-Mei; Chen, Yen-Ling; Lee, Jian-Hong; Wen, Chiu-Ming; Wang, Moo-Chin

2014-01-01

Highlights: • The TiO 2 precursor powder contained anatase and 19.5% NH 4 Cl. • Mesoporous anatase TiO 2 nanopowders were successfully synthesized. • Uncalcined precursor powder contained the phases of type I NH 4 Cl and anatase TiO 2 . • Anatase size increases from 3.3 to 14.3 nm when calcined at 473–773 K for 2 h. • The average pore size between 3.80 and 14.0 nm when calcined between 473 and 773 K. - Abstract: In situ synthesis of mesoporous TiO 2 nanopowders using titanium tetrachloride (TiCl 4 ) and NH 4 OH as initial materials has been successfully fabricated by a coprecipitation process without the addition of surfactant. Characteristics and properties of the mesoporous TiO 2 nanopowders were investigated using differential scanning calorimetry/thermogravimetry (DSC/TG), X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET) and Barrent–Joyner–Halenda (BJH) analyses, transmission electron microscopy (TEM), selected area electron diffraction (SAED) and high resolution TEM (HRTEM). The results of TG and XRD showed that the NH 4 Cl decomposed between 513 and 673 K. XRD results showed that the anatase TiO 2 only contained a single phase when the calcination temperature of the precursor powder was less than 673 K. Whereas phases of anatase and rutile TiO 2 coexist after calcining at 773 K for 2 h. The crystalline size of the anatase and rutile TiO 2 was 14.3 and 26.6 nm, respectively, when the precursor powder was calcined at 773 K for 2 h. The BET and BJH results showed a significant increase in surface area and pore volumes when the NH 4 Cl was completely decomposed. The maximum values of BET specific surface area and volume were 172.8 m 2 /g and 0.392 cm 3 /g, respectively. The average pore sizes when calcination was at 473 and 773 K for 2 h were 3.8 and 14.0 nm, respectively

TiO2-coated Hollow Glass Microspheres with Superhydrophobic and High IR-reflective Properties Synthesized by a Soft-chemistry Method.

Science.gov (United States)

Wong, Yinting; Zhong, Dan; Song, Aotian; Hu, Yan

2017-04-26

This manuscript proposes a soft-chemistry method to develop superhydrophobic and highly IR-reflective hollow glass microspheres (HGM). The anatase TiO2 and a superhydrophobic agent were coated on the HGM surface in one step. TBT and PFOTES were selected as the Ti source and the superhydrophobic agent, respectively. They were both coated on the HGM, and after the hydrothermal process, the TBT turned to anatase TiO2. In this way, a PFOTES/TiO2-coated HGM (MCHGM) was prepared. For comparison, PFOTES single-coated HGM (F-SCHGM) and TiO2 single-coated HGM (Ti-SCHGM) were synthesized as well. The PFOTES and TiO2 coatings on the HGM surface were demonstrated through X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy-dispersive detector (EDS) characterizations. The MCHGM showed a higher contact angle (153°) but a lower sliding angle (16°) than F-SCHGM, with a contact angle of 141.2° and a sliding angle of 67°. In addition, both Ti-SCHGM and MCHGM displayed similar IR reflectivity values, which were about 5.8% higher than the original HGM and F-SCHGM. Also, the PFOTES coating barely changed the thermal conductivity. Therefore, F-SCHGM, with a thermal conductivity of 0.0479 W/(m·K), was quite like the original HGM, which was 0.0475 W/(m·K). MCHGM and Ti-SCHGM were also similar. Their thermal conductivity values were 0.0543 W/(m·K) and 0.0543 W/(m·K), respectively. The TiO2 coating slightly increased the thermal conductivity, but with the increase in reflectivity, the overall heat-insulation property was enhanced. Finally, since the IR-reflecting property is provided by the HGM coating, if the coating is fouled, the reflectivity decreases. Therefore, with the superhydrophobic coating, the surface is protected from fouling, and its lifetime is also prolonged.

Flow-Regulated Growth of Titanium Dioxide (TiO2 ) Nanotubes in Microfluidics.

Science.gov (United States)

Fan, Rong; Chen, Xinye; Wang, Zihao; Custer, David; Wan, Jiandi

2017-08-01

Electrochemical anodization of titanium (Ti) in a static, bulk condition is used widely to fabricate self-organized TiO 2 nanotube arrays. Such bulk approaches, however, require extended anodization times to obtain long TiO 2 nanotubes and produce only vertically aligned nanotubes. To date, it remains challenging to develop effective strategies to grow long TiO 2 nanotubes in a short period of time, and to control the nanotube orientation. Here, it is shown that the anodic growth of TiO 2 nanotubes is significantly enhanced (≈16-20 times faster) under flow conditions in microfluidics. Flow not only controls the diameter, length, and crystal orientations of TiO 2 nanotubes, but also regulates the spatial distribution of nanotubes inside microfluidic devices. Strikingly, when a Ti thin film is deposited on silicon substrates and anodized in microfluidics, both vertically and horizontally aligned (relative to the bottom substrate) TiO 2 nanotubes can be produced. The results demonstrate previously unidentified roles of flow in the regulation of growth of TiO 2 nanotubes, and provide powerful approaches to effectively grow long, oriented TiO 2 nanotubes, and construct hierarchical TiO 2 nanotube arrays on silicon-based materials. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

TiO2/Bi2(BDC)3/BiOCl nanoparticles decorated ultrathin nanosheets with excellent photocatalytic reaction activity and selectivity

International Nuclear Information System (INIS)

Zhou, Shu-Mei; Ma, De-Kun; Cai, Ping; Chen, Wei; Huang, Shao-Ming

2014-01-01

Graphical abstract: TiO 2 /Bi 2 (BDC) 3 /BiOCl nanoparticles decorated ultrathin nanosheets showed excellent photocatalytic reaction activity and selectivity. - Highlights: • TiO 2 /Bi 2 (BDC) 3 /BiOCl nanoparticles decorated ultrathin nanosheets were synthesized through a facile hydrothermal process. • The products showed excellent photocatalytic activities for the degradation of various dyes. • The photocatalytic activities of the composite materials could be easily adjusted through tuning the content of TiO 2 . • TiO 2 /Bi 2 (BDC) 3 /BiOCl displayed obvious photocatalytic selectivity in mixed dyes systems of rhodamine B and eosin Y. - Abstract: Photocatalysts with excellent photocatalytic reaction activity and ideal selectivity are highly desirable for pollutants clearance and purification of targeted organics from a mixture. Continued efforts toward the goal, we here present a facile hydrothermal route to synthesize TiO 2 /Bi-benzenedicarboxylate/BiOCl nanoparticles decorated ultrathin nanosheets with a thickness less than 5 nm on a large scale. The as-synthesized products showed excellent photocatalytic activities for the degradation of various dyes such as rhodamine B, eosin Y and methylene blue in aqueous solution under visible light irradiation. The photocatalytic activities of TiO 2 /Bi-benzenedicarboxylate/BiOCl nanocomposites for the degradation of rhodamine B and eosin Y could be adjusted through tuning the content of TiO 2 . With increasing the amount of TiO 2 , the composites showed declining photocatalytic activities in decomposing of rhodamine B while on the contrary they displayed enhanced photocatalytic activities in decomposing of eosin Y. Interestingly, TiO 2 /Bi-benzenedicarboxylate/BiOCl composite nanosheets showed obvious photocatalytic selectivity in a mixed dyes system. The photocatalytic reaction and selectivity mechanisms of the nanocomposites for the degradation of the dyes were discussed on the basis of experimental results. The

Synthesis and photocatalytic activity of mesoporous – (001) facets TiO_2 single crystals

International Nuclear Information System (INIS)

Dong, Yeshuo; Fei, Xuening; Zhou, Yongzhu

2017-01-01

Highlights: • The (001) facets of TiO_2 single crystals with mesoporous structure. • The (010) and (100) facets of TiO_2 single crystals were covered by the flower – shaped TiO_2 crystals. • This special structure could promote charge separation and provide more active sites, which will lead to a substantial increase in photocatalytic activity. - Abstract: In this work, the mesoporous – (001) facets TiO_2 single crystals have been successfully synthesized through a two-step solvothermal route without any template. Their structure and morphology were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), ultraviolet-visible (UV–vis) diffuse reflectance spectroscopy and energy dispersive X-ray spectrometer (EDX). Based on the different characteristics and atomic arrangements on each facet of anatase TiO_2 single crystals, we synthesized these mesoporous – (001) facets TiO_2 single crystals by controlling the interaction characteristics of hydrofluoric acid (HF) and isopropanol (i-PrOH) on the crystal facets. It can been seen that the (001) facets of these as-synthesized TiO_2 single crystals have a clear mesoporous structure through the SEM images and BET methods. Moreover, the other four facets were covered by the flower – shaped TiO_2 crystals with the generation of the mesoporous – (001) facets. This special and interesting morphology could promote charge separation and provide more active sites, which will lead to a substantial increase in photocatalytic activity. Moreover, it is more intuitive to reflect that the different crystal facets possess the different properties due to their atomic arrangement. Besides, according to the different synthetic routes, we proposed and discussed a plausible synthesis mechanism of these mesoporous – (001) facets TiO_2 single crystals.

Application of nitrogen-doped TiO2 nano-tubes in dye-sensitized solar cells

DEFF Research Database (Denmark)

Tran, Vy Anh; Thinh Troung, Trieu; Pham Phan, Thu Anh

2017-01-01

Our research aimed to improve the overall energy conversion efficiency of DSCs by applying nitrogen-doped TiO2 nano-tubes (N-TNT) for the preparation of DSCs photo-anodes. The none-doped TiO2 nano-tubes (TNTs) were synthesized by alkaline hydrothermal treatment of Degussa P25 TiO2 particles in 10...

Homogeneous growth of TiO2-based nanotubes on nitrogen-doped reduced graphene oxide and its enhanced performance as a Li-ion battery anode

Science.gov (United States)

Mehraeen, Shayan; Taşdemir, Adnan; Alkan Gürsel, Selmiye; Yürüm, Alp

2018-06-01

The pursuit of a promising replacement candidate for graphite as a Li-ion battery anode, which can satisfy both engineering criteria and market needs has been the target of researchers for more than two decades. In this work, we have investigated the synergistic effect of nitrogen-doped reduced graphene oxide (NrGO) and nanotubular TiO2 to achieve high rate capabilities with high discharge capacities through a simple, one-step and scalable method. First, nanotubes of hydrogen titanate were hydrothermally grown on the surface of NrGO sheets, and then converted to a mixed phase of TiO2-B and anatase (TB) by thermal annealing. Specific surface area, thermal gravimetric, structural and morphological characterizations were performed on the synthesized product. Electrochemical properties were investigated by cyclic voltammetry and cyclic charge/discharge tests. The prepared anode showed high discharge capacity of 150 mAh g‑1 at 1 C current rate after 50 cycles. The promising capacity of synthesized NrGO-TB was attributed to the unique and novel microstructure of NrGO-TB in which long nanotubes of TiO2 have been grown on the surface of NrGO sheets. Such architecture synergistically reduces the solid-state diffusion distance of Li+ and increases the electronic conductivity of the anode.

Homogeneous growth of TiO2-based nanotubes on nitrogen-doped reduced graphene oxide and its enhanced performance as a Li-ion battery anode.

Science.gov (United States)

Mehraeen, Shayan; Taşdemir, Adnan; Gürsel, Selmiye Alkan; Yürüm, Alp

2018-06-22

The pursuit of a promising replacement candidate for graphite as a Li-ion battery anode, which can satisfy both engineering criteria and market needs has been the target of researchers for more than two decades. In this work, we have investigated the synergistic effect of nitrogen-doped reduced graphene oxide (NrGO) and nanotubular TiO 2 to achieve high rate capabilities with high discharge capacities through a simple, one-step and scalable method. First, nanotubes of hydrogen titanate were hydrothermally grown on the surface of NrGO sheets, and then converted to a mixed phase of TiO 2 -B and anatase (TB) by thermal annealing. Specific surface area, thermal gravimetric, structural and morphological characterizations were performed on the synthesized product. Electrochemical properties were investigated by cyclic voltammetry and cyclic charge/discharge tests. The prepared anode showed high discharge capacity of 150 mAh g -1 at 1 C current rate after 50 cycles. The promising capacity of synthesized NrGO-TB was attributed to the unique and novel microstructure of NrGO-TB in which long nanotubes of TiO 2 have been grown on the surface of NrGO sheets. Such architecture synergistically reduces the solid-state diffusion distance of Li + and increases the electronic conductivity of the anode.

TiO2 beads and TiO2-chitosan beads for urease immobilization

International Nuclear Information System (INIS)

Ispirli Doğaç, Yasemin; Deveci, İlyas; Teke, Mustafa; Mercimek, Bedrettin

2014-01-01

The aim of the present study is to synthesize TiO 2 beads for urease immobilization. Two different strategies were used to immobilize the urease on TiO 2 beads. In the first method (A), urease enzyme was immobilized onto TiO 2 beads by adsorption and then crosslinking. In the second method (B), TiO 2 beads were coated with chitosan-urease mixture. To determine optimum conditions of immobilization, different parameters were investigated. The parameters of optimization were initial enzyme concentration (0.5; 1; 1.5; 2 mg/ml), alginate concentration (1; 2; 3%), glutaraldehyde concentration (1; 2; 3% v/v) and chitosan concentration (2; 3; 4 mg/ml). The optimum enzyme concentrations were determined as 1.5 mg/ml for A and 1.0 mg/ml for B. The other optimum conditions were found 2.0% (w/v) for alginate concentration (both A and B); 3.0 mg/ml for chitosan concentration (B) and 2.0% (v/v) for glutaraldehyde concentration (A). The optimum temperature (20-60 °C), optimum pH (3.0-10.0), kinetic parameters, thermal stability (4–70 °C), pH stability (4.0-9.0), operational stability (0-230 min) and reusability (20 times) were investigated for characterization. The optimum temperatures were 30 °C (A), 40 °C (B) and 35 °C (soluble). The temperature profiles of the immobilized ureases were spread over a large area. The optimum pH values for the soluble urease and immobilized urease prepared by using methods (A) and (B) were found to be 7.5, 7.0, 7.0, respectively. The thermal stabilities of immobilized enzyme sets were studied and they maintained 50% activity at 65 °C. However, at this temperature free urease protected only 15% activity. - Highlights: • TiO 2 and TiO 2 -chitosan beads for urease immobilization have been prepared and characterized. • The beads used in this work are good matrices for the immobilization of urease. • The immobilized urease was shown to have good properties and stabilities (pH and thermal stability, operational stability). • The 50

Effect of sonochemical synthesized TiO2 nanoparticles and coagulation bath temperature on morphology, thermal stability and pure water flux of asymmetric cellulose acetate membranes prepared via phase inversion method

Directory of Open Access Journals (Sweden)

Abedini Reza

2012-01-01

Full Text Available In this study, asymmetric pure CA and CA/ TiO2 composite membranes were prepared via phase inversion by dispersing TiO2 nanopaticles in the CA casting solutions induced by immersion precipitation in water coagulation bath. TiO2 nanoparticles, which were synthesized by the sonochemical method, were added into the casting solution with different concentrations. Effects of TiO2 nanoparticles concentration (0 wt. %, 5wt.%, 10wt.%, 15wt.%, 20wt.% and 25wt.% and coagulation bath temperature (CBT= 25°C, 50°C and 75°C on morphology, thermal stability and pure water flux (PWF of the prepared membranes were studied and discussed. Increasing TiO2 concentration in the casting solution film along with higher CBT resulted in increasing the membrane thickness, water content (WC, membrane porosity and pure water flux (PWF, also these changes facilitate macrovoids formation. Thermal gravimetric analysis (TGA shows that thermal stability of the composite membranes were improved by the addition of TiO2 nanopaticles. Also TGA results indicated that increasing CBT in each TiO2 concentration leads to the decreasing of decomposition temperature (Td of hybrid membranes.

Gel electrolytes based on poly(acrylonitrile)/sulpholane with hybrid TiO2/SiO2 filler for advanced lithium polymer batteries

International Nuclear Information System (INIS)

Kurc, Beata

2014-01-01

Highlights: • Paper describes properties of gel electrolyte based on PAN with TMS and TiO 2 -SiO 2 . • The TiO 2 -SiO 2 oxide composite was precipitated in the emulsion system and used as the fillers. • The capacity of the graphite anode depends on the current rate and the amount of TiO 2 -SiO 2 . • For PE3 electrolyte was obtained practical capacity more than 90% of the theoretical capacity. - Abstract: This paper describes the synthesis and properties of a new type of ceramic fillers for composite polymer gel electrolytes. Hybrid TiO 2 -SiO 2 ceramic powders have been obtained by co-precipitation from titanium(IV) sulfate solution using sodium silicate as the precipitating agent. The resulting submicron-size powders have been applied as fillers for composite polymer gel electrolytes for Li-ion batteries based on polyacrylonitrile (PAN) membranes. The powders and gel electrolytes have been examined structurally and electrochemically, showing favorable properties in terms of electrolyte uptake and electrochemical characteristics in Li-ion cells

Evaluation of micro-abrasion-corrosion on SiO2-TiO2-ZrO2 coatings synthesized by the sol-gel method

Science.gov (United States)

Bautista Ruiz, J.; Aperador, W.; Caballero Gómez, J.

2016-02-01

The medical science and the engineering, work to improve the materials used in the manufacture of joint implants, since they have a direct impact on the quality of people life. The surgical interventions are increasing worldwide with a high probability of a second or even a third intervention. Around these circumstances, it was evaluated the behaviour against microabrasion-corrosion phenomena on SiO2 TiO2 ZrO2 coatings, synthesized by the sol-gel method with concentration of the Si/Ti/Zr precursors: 10/70/20 and 10/20/70. The coatings were deposited on AISI 316 LVM stainless steel substrates. The morphological characterization of the wear was made by AFM techniques. It was observed that the coatings with higher levels of titanium have a good response to the phenomena of microabrasion-corrosion.

Nanoscale Optimization and Statistical Modeling of Photoelectrochemical Water Splitting Efficiency of N-Doped TiO2 Nanotubes

KAUST Repository

Isimjan, Tayirjan T.

2014-12-19

Highly ordered nitrogen-doped titanium dioxide (N-doped TiO2) nanotube array films with enhanced photo-electrochemical water splitting efficiency (PCE) for hydrogen generation were fabricated by electrochemical anodization, followed by annealing in a nitrogen atmosphere. Morphology, structure and composition of the N-doped TiO2 nanotube array films were investigated by FE-SEM, XPS, UV-Vis and XRD. The effect of annealing temperature, heating rate and annealing time on the morphology, structure, and photo-electrochemical property of the N-doped TiO2 nanotube array films were investigated. A design of experiments method was applied in order to minimize the number of experiments and obtain a statistical model for this system. From the modelling results, optimum values for the influential factors were obtained in order to achieve the maximum PCE. The optimized experiment resulted in 7.42 % PCE which was within 95 % confidence interval of the predicted value by the model. © 2014 Springer Science+Business Media.

Charge transfer in photorechargeable composite films of TiO2 and polyaniline

Science.gov (United States)

Nomiyama, Teruaki; Sasabe, Kenichi; Sakamoto, Kenta; Horie, Yuji

2015-07-01

A photorechargeable battery (PRB) is a photovoltaic device having an energy storage function in a single cell. The photoactive electrode of PRB is a bilayer film consisting of bare porous TiO2 and a TiO2-polyaniline (PANi) mixture that work as a photovoltaic current generator and an electrochemical energy storage by ion dedoping, respectively. To study the charge transfer between TiO2 and PANi, the photorechargeable quantum efficiency QE ([electron count on discharge]/[incident photon count on photocharge]) was measured by varying the thickness LS of the TiO2-PANi mixture. The quantum efficiency QEuv for UV photons had a maximum of ˜7% at LS ˜ 7 µm. The time constant τTP for the charge transfer was about 10-1 s, which was longer ten times or more than the lifetime of excited electrons within TiO2. These facts reveal that the main rate-limiting factor in the photocharging process is the charge transfer between TiO2 and PANi.

Electrochemical Performance of a Carbon Nanotube/La-Doped TiO2 Nanocomposite and its Use for Preparation of an Electrochemical Nicotinic Acid Sensor

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Hanxing Liu

2008-11-01

Full Text Available A carbon nanotube/La-doped TiO2 (La-TiO2 nanocomposite (CLTN was prepared by a procedure similar to a complex/adsorption process. Scanning electron microscopy (SEM images show that the La-TiO2 distributes on the carbon nanotube walls. The CLTN was mixed with paraffin to form a CLTN paste for the CLTN paste electrode (CLTNPE. The electrochemical characteristics of CLTNPE were compared with that of conventional carbon electrodes such as the carbon paste electrode (CPE and glass carbon electrode (GC. The CLTNPE exhibits electrochemical activity and was used to investigate the electrochemistry of nicotinic acid (NA. The modified electrode has a strong electrocatalytic effect on the redox of NA. The cyclic voltammetry (CV redox potential of NA at the CLTNPE is 320 mV. The oxidation process of NA on the CLTNPE is pH dependent. A sensitive chronoamperometric response for NA was obtained covering a linear range from 1.0×10-6 mol·L-1 to 1.2×10-4 mol·L-1, with a detection limit of 2.7×10-7 mol·L-1. The NA sensor displays a remarkable sensitivity and stability. The mean recovery of NA in the human urine is 101.8%, with a mean variation coefficient (RSD of 2.6%.

TiO2 synthesized by microwave assisted solvothermal method: Experimental and theoretical evaluation

International Nuclear Information System (INIS)

Moura, K.F.; Maul, J.; Albuquerque, A.R.; Casali, G.P.; Longo, E.; Keyson, D.; Souza, A.G.; Sambrano, J.R.; Santos, I.M.G.

2014-01-01

In this study, a microwave assisted solvothermal method was used to synthesize TiO 2 with anatase structure. The synthesis was done using Ti (IV) isopropoxide and ethanol without templates or alkalinizing agents. Changes in structural features were observed with increasing time of synthesis and evaluated using periodic quantum chemical calculations. The anatase phase was obtained after only 1 min of reaction besides a small amount of brookite phase. Experimental Raman spectra are in accordance with the theoretical one. Micrometric spheres constituted by nanometric particles were obtained for synthesis from 1 to 30 min, while spheres and sticks were observed after 60 min. - Graphical abstract: FE-SEM images of anatase obtained with different periods of synthesis associated with the order–disorder degree. Display Omitted - Highlights: • Anatase microspheres were obtained by the microwave assisted hydrothermal method. • Only ethanol and titanium isopropoxide were used as precursors during the synthesis. • Raman spectra and XRD patterns were compared with quantum chemical calculations. • Time of synthesis increased the short-range disorder in one direction and decreased in another

TiO2 Microflowers Assembled by 6-nm Single-Crystal Stranded Wires with Improved Photoelectrochemical Performances

International Nuclear Information System (INIS)

Liu, Chunlei; Zhou, Wei; Yu, Li; Zhang, Gong; Qu, Jiuhui; Liu, Huijuan

2017-01-01

Highlights: •The 6-nm single-crystal stranded wires of TiO 2 exhibited a photocurrent of 0.33 mA cm −2 compared to that of the P25/TF (0.06 mA cm −2 ), which greatly facilited the electron transfer rate. •A photoelectrochemical (PEC) system combining degradation of bisphenol A and H 2 production was constructed based on the TiO 2 -SWs/TF. •This PEC system exhibited a 94% bisphenol A degradation efficiency within 60 min at 1.2 V and H 2 production simultaneously. •A power consumption of only 0.02 kWh m −3 was consumed by the TiO 2 -SWs/TF in PEC system. •Two pathways for PEC degradation of bisphenol A were proposed based on the intermediates identified by UPLC-Q-TOF-MS. -- Abstract: As the diffusion length of charge carriers in TiO 2 is around 10 nm, it would be an efficient way to increase the photocatalytic properties by controlling the size within 10 nm. Herein, TiO 2 microflowers assembled by 6-nm single-crystal stranded wires grown on Ti foam (TiO 2 -SWs/TF) were synthesized which facilated electron transfer rate with a photocurrent of 0.33 mA cm −2 compared to that of the P25/TF (0.06 mA cm −2 ). A photoelectrochemical (PEC) system combining degradation of bisphenol A and H 2 production was constructed based on the as-obtained TiO 2 -SWs/TF as photoanode and Pt wire as cathode. This PEC system exhibited excellent ability for simultaneous bisphenol A degradation and H 2 production, giving a 94% bisphenol A degradation efficiency within 60 min at 1.2 vs (Ag/AgCl) V with power consumption of only 0.02 kWh m −3 . The excellent PEC degradation of bisphenol A by the TiO 2 -SWs/TF could mainly be ascribed to the fast electron transfer via the 6-nm ultrathin wires and synergetic effect of photocatalysis and electrochemical process. Two pathways for PEC degradation of bisphenol A were proposed based on the intermediates identified by Ultra Performance liquid chromatography-quadruple-time of flight-mass spectrometry (UPLC-Q-TOF-MS).

Improvement of light harvesting and device performance of dye-sensitized solar cells using rod-like nanocrystal TiO2 overlay coating on TiO2 nanoparticle working electrode

International Nuclear Information System (INIS)

Liu, Xueyang; Fang, Jian; Gao, Mei; Wang, Hongxia; Yang, Weidong; Lin, Tong

2015-01-01

Novel TiO 2 single crystalline nanorods were synthesized by electrospinning and hydrothermal treatment. The role of the TiO 2 nanorods on TiO 2 nanoparticle electrode in improvement of light harvesting and photovoltaic properties of dye-sensitized solar cells (DSSCs) was examined. Although the TiO 2 nanorods had lower dye loading than TiO 2 nanoparticle, they showed higher light utilization behaviour. Electron transfer in TiO 2 nanorods received less resistance than that in TiO 2 nanoparticle aggregation. By just applying a thin layer of TiO 2 nanorods on TiO 2 nanoparticle working electrode, the DSSC device light harvesting ability and energy conversion efficiency were improved significantly. The thickness of the nanorod layer in the working electrode played an important role in determining the photovoltaic property of DSSCs. An energy conversion efficiency as high as 6.6% was found on a DSSC device with the working electrode consisting of a 12 μm think TiO 2 nanoparticle layer covered with 3 μm thick TiO 2 nanorods. The results obtained from this study may benefit further design of highly efficient DSSCs. - Highlights: • Single crystalline TiO 2 nanorods were prepared for DSSC application. • TiO 2 nanorods show effective light scattering performance. • TiO 2 nanorods have higher electron transfer efficiency than TiO 2 nanoparticles. • TiO 2 nanorods on TiO 2 nanoparticle electrode improve DSSC efficiency

High pressure synthesis of amorphous TiO2 nanotubes

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Quanjun Li

2015-09-01

Full Text Available Amorphous TiO2 nanotubes with diameters of 8-10 nm and length of several nanometers were synthesized by high pressure treatment of anatase TiO2 nanotubes. The structural phase transitions of anatase TiO2 nanotubes were investigated by using in-situ high-pressure synchrotron X-ray diffraction (XRD method. The starting anatase structure is stable up to ∼20GPa, and transforms into a high-density amorphous (HDA form at higher pressure. Pressure-modified high- to low-density transition was observed in the amorphous form upon decompression. The pressure-induced amorphization and polyamorphism are in good agreement with the previous results in ultrafine TiO2 nanoparticles and nanoribbons. The relationship between the LDA form and α-PbO2 phase was revealed by high-resolution transmission electron microscopy (HRTEM study. In addition, the bulk modulus (B0 = 158 GPa of the anatase TiO2 nanotubes is smaller than those of the corresponding bulks and nanoparticles (180-240 GPa. We suggest that the unique open-ended nanotube morphology and nanosize play important roles in the high pressure phase transition of TiO2 nanotubes.

Photo catalytic reduction of benzophenone on TiO2: Effect of preparation method and reaction conditions

International Nuclear Information System (INIS)

Albiter E, E.; Valenzuela Z, M. A.; Alfaro H, S.; Flores V, S. O.; Rios B, O.; Gonzalez A, V. J.; Cordova R, I.

2010-01-01

The photo catalytic reduction of benzophenone was studied focussing on improving the yield to benzhydrol. TiO 2 was synthesized by means of a hydrothermal technique. TiO 2 (Degussa TiO 2 -P25) was used as a reference. Catalysts were characterized by X-ray diffraction and nitrogen physisorption. The photo catalytic reduction was carried out in a batch reactor at 25 C under nitrogen atmosphere, acetonitrile as solvent and isopropanol as electron donor. A 200 W Xe-Hg lamp (λ= 360 nm) was employed as irradiation source. The chemical composition of the reaction system was determined by HPLC. Structural and textural properties of the synthesized TiO 2 depended on the type of acid used during sol formation step. Using HCl, a higher specific surface area and narrower pore size distribution of TiO 2 was obtained in comparison with acetic acid. As expected, the photochemical reduction of benzophenone yielded benzopinacol as main product, whereas, benzhydrol is only produced in presence of TiO 2 (i.e. photo catalytic route). In general, the hydrothermally synthesized catalysts were less active and with a lower yield to benzhydrol. The optimal reaction conditions to highest values of benzhydrol yield (70-80%) were found at 2 g/L (catalyst loading) and 0.5 m M of initial concentration of benzophenone, using commercial TiO 2 -P25. (Author)

Preparation and solar-light photocatalytic activity of TiO2 composites: TiO2/kaolin, TiO2/diatomite, and TiO2/zeolite

Science.gov (United States)

Li, Y.; Li, S. G.; Wang, J.; Li, Y.; Ma, C. H.; Zhang, L.

2014-12-01

Three TiO2 loaded composites, TiO2/kaolin, TiO2/diatomite, and TiO2/zeolite, were prepared in order to improve the solar-light photocatalytic activity of TiO2. The results showed that the photocatalytic activity could obviously be enhanced by loading appropriate amount of inorganic mineral materials. Meanwhile, TiO2 content, heat-treatment temperature and heat-treatment time on the photocatalytic activity were reviewed. Otherwise, the effect of solar light irradiation time and dye concentration on the photocatalytic degradation of Acid Red B was investigated. Furthermore, the degradation mechanism and adsorption process were also discussed.

Nanoscale Optimization and Statistical Modeling of Photoelectrochemical Water Splitting Efficiency of N-Doped TiO2 Nanotubes

KAUST Repository

Isimjan, Tayirjan T.; Trifkovic, Milana; Abdullahi, Inusa; Rohani, Sohrab M F; Ray, Ajay

2014-01-01

Highly ordered nitrogen-doped titanium dioxide (N-doped TiO2) nanotube array films with enhanced photo-electrochemical water splitting efficiency (PCE) for hydrogen generation were fabricated by electrochemical anodization, followed by annealing

Photocatalytic decouloration of malachite green dye by application of TiO2 nanotubes

International Nuclear Information System (INIS)

Prado, Alexandre G.S.; Costa, Leonardo L.

2009-01-01

The nanotubes of titania were synthesized in a hydrothermal system and characterized by scanning electronic microscopy (SEM), FT-IR, FT-Raman, and surface charge density by surface area analyzer. These nanomaterials were applied to photocatalyse malachite green dye degradation. Photodegradation capacity of TiO 2 nanotubes was compared to TiO 2 anatase photoactivity. Malachite dye was completely degraded in 75 and 105 min of reaction photocatalysed by TiO 2 nanotubes and TiO 2 anatase, respectively. Catalysts displayed high photodegradation activity at pH 4. TiO 2 nanotubes were easily recycled whereas the reuse of TiO 2 anatase was not effective. Nanotubes maintained 80% of their activity after 10 catalytic cycles and TiO 2 anatase presented only 8% of its activity after 10 cycles.

Amorphous and crystalline TiO2 nanotube arrays for enhanced Li-ion intercalation properties.

Science.gov (United States)

Guan, Dongsheng; Cai, Chuan; Wang, Ying

2011-04-01

We have employed a simple process of anodizing Ti foils to prepare TiO2 nanotube arrays which show enhanced electrochemical properties for applications as Li-ion battery electrode materials. The lengths and pore diameters of TiO2 nanotubes can be finely tuned by varying voltage, electrolyte composition, or anodization time. The as-prepared nanotubes are amorphous and can be converted into anatase nanotubes with heat treatment at 480 degrees C. Rutile crystallites emerge in the anatase nanotube when the annealing temperature is increased to 580 degrees C, resulting in TiO2 nanotubes of mixed phases. The morphological features of nanotubes remain unchanged after annealing. Li-ion insertion performance has been studied for amorphous and crystalline TiO2 nanotube arrays. Amorphous nanotubes with a length of 3.0 microm and an outer diameter of 125 nm deliver a capacity of 91.2 microA h cm(-2) at a current density of 400 microA cm(-2), while those with a length of 25 microm and an outer diameter of 158 nm display a capacity of 533 microA h cm-2. When the 3-microm long nanotubes become crystalline, they deliver lower capacities: the anatase nanotubes and nanotubes of mixed phases show capacities of 53.8 microA h cm-2 and 63.1 microA h cm(-2), respectively at the same current density. The amorphous nanotubes show excellent capacity retention ability over 50 cycles. The cycled nanotubes show little change in morphology compared to the nanotubes before electrochemical cycling. All the TiO2 nanotubes demonstrate higher capacities than amorphous TiO2 compact layer reported in literature. The amorphous TiO2 nanotubes with a length of 1.9 microm exhibit a capacity five times higher than that of TiO2 compact layer even when the nanotube array is cycled at a current density 80 times higher than that for the compact layer. These results suggest that anodic TiO2 nanotube arrays are promising electrode materials for rechargeable Li-ion batteries.

CeO2-TiO2 Photocatalyst: Ionic Liquid-Mediated Synthesis, Characterization, and Performance for Diisopropanolamine Visible Light Degradation

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Jagath Retchahan Sivalingam

2018-01-01

Full Text Available CeO2-TiO2 photocatalyst with Ce:Ti molar ratio of 1:9 was synthesized via co-precipitation method in the presence of 1-ethyl-3-methyl imidazolium octylsulfate, [EMIM][OctSO4] (CeO2-TiO2-IL. The ionic liquid acts as a templating agent for particle growth. The CeO2-TiO2 and TiO2 photocatalysts were also synthesized without any ionic liquid for comparison. Calcination was conducted on the as-synthesized materials at 400˚C for 2 h. The photocatalysts were characterized using diffuse reflectance UV-Vis spectroscopy (DR-UV-Vis, field emission scanning electron microscopy (FESEM, X-ray powder diffraction (XRD, and surface area and pore size analyzer (SAP. The presence of CeO2 has changed the optical property of TiO2. It has extended the absorption edge of TiO2 from UV to visible region. The calculated band gap energy decreased from 2.82 eV (TiO2 to 2.30 eV (CeO2-TiO2-IL. The FESEM morphology showed that samples forms aggregates and the surface smoothens when ionic liquid was added. The average crystallite size of TiO2, CeO2-TiO2, and CeO2-TiO2-IL were 20.8 nm, 5.5 nm, and 4 nm. In terms of performance, photodegradation of 1000 ppm of diisopropanolamine (DIPA was conducted in the presence of hydrogen peroxide (H2O2 and visible light irradiation which was provided by a 500 W halogen lamp. The best performance was displayed by CeO2-TiO2-IL calcined at 400˚C. It was able to remove 82.0% DIPA and 54.8% COD after 6 h reaction.  Copyright © 2018 BCREC Group. All rights reserved Received: 26th July 2017; Revised: 22nd October 2017; Accepted: 29th October 2017; Available online: 22nd January 2018; Published regularly: 2nd April 2018 How to Cite: Sivalingam, J.R., Kait, C.F., Wilfred, C.D. (2018. CeO2-TiO2 Photocatalyst: Ionic Liquid-Mediated Synthesis, Characterization, and Performance for Diisopropanolamine Visible Light Degradation. Bulletin of Chemical Reaction Engineering & Catalysis, 13 (1: 170-178 (doi:10.9767/bcrec.13.1.1396.170-178

Synthesis of mesoporous TiO2 in aqueous alcoholic medium and evaluation of its photocatalytic activity

International Nuclear Information System (INIS)

Kumaresan, L.; Prabhu, A.; Palanichamy, M.; Murugesan, V.

2011-01-01

Research highlights: → Mesoporous TiO 2 synthesized using P123 as soft template in sol-gel method. → Nanoparticle aggregates are better for photocatalytic activity than free nanoparticles. → Particle to particle transport of electrons in the conduction band of aggregates are important factor. - Abstract: Mesoporous TiO 2 was synthesized using triblock copolymer as the structure directing template in ethanol/water, isopropanol/water or 1-butanol/water medium by sol-gel method. The presence of intense peak at low angle in the XRD patterns confirmed the orderly arrangement of mesopores in the material. Among the three different alcohols, ethanol had influenced better in controlling the particle size than others. The enhanced specific surface area also revealed the formation of mesopores. Aggregates of particles were clearly seen in the TEM images and the size of the particles was approximately 10 nm. The photocatalytic activity of mesoporous TiO 2 was evaluated using aqueous alachlor as a model pollutant. The activity of mesoporous TiO 2 synthesized in ethanol/water mole ratio of 50 was higher than other mesoporous TiO 2 and commercial TiO 2 (Degussa P-25). The transport of excited electrons from one particle to its neighboring nanoparticles of mesoporous TiO 2 is suggested to be the cause for enhanced photocatalytic activity.

Synthesis and electrochemical analysis of polyaniline/TiO2 composites prepared with various molar ratios between aniline monomer and para-toluenesulfonic acid

International Nuclear Information System (INIS)

Oh, Misoon; Kim, Seok

2012-01-01

Graphical abstract: Polyaniline (PANI)/TiO 2 composites were prepared by in situ polymerization using para-toluenesulfonic acid (p-TSA). The composites showed different morphology and specific capacitances as a function of aniline concentration, which are related to the morphology (shape or size) of particles. Scheme of the formation of composites consisting of PANI film and the micelle structures is shown. Highlights: ► PANI/TiO 2 composite were prepared with a different concentration of monomer and dopant. ► Aniline/acid ratio influenced the morphological and electrochemical properties. ► The composites showed different capacitances as a function of aniline concentrations. ► Aniline/acid ratio could influence on the dispersion and surface roughness of particles. - Abstract: Polyaniline (PANI)/titanium dioxide (TiO 2 ) composites were prepared with a chemical oxidation polymerization of aniline monomer (ANI) with various molar ratios between ANI and para toluenesulfonic acid (p-TSA). To find an effect of the [ANI]:[p-TSA] molar ratio on the electrochemical properties of the prepared PANI/TiO 2 composites, the composites were synthesized under same conditions except the p-TSA concentrations. The prepared composite films had more homogeneous TiO 2 dispersion with changing [ANI]:[p-TSA] molar ratios from 6:1 to 1:1. p-TSA surfactant-like doping acid helped the dispersion of TiO 2 particles in the PANI matrix. PANI covering the TiO 2 surfaces was confirmed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Prepared PANI films on the TiO 2 particles had the smoothest surface when the ANI and p-TSA had 1:1 molar ratio in the reaction solution. The composite prepared with molar ratio [ANI]:[p-TSA] of 3:1 had the highest capacitance (800 F g −1 ) among the prepared composites.

Engineering the TiO2 -graphene interface to enhance photocatalytic H2 production.

Science.gov (United States)

Liu, Lichen; Liu, Zhe; Liu, Annai; Gu, Xianrui; Ge, Chengyan; Gao, Fei; Dong, Lin

2014-02-01

In this work, TiO2 -graphene nanocomposites are synthesized with tunable TiO2 crystal facets ({100}, {101}, and {001} facets) through an anion-assisted method. These three TiO2 -graphene nanocomposites have similar particle sizes and surface areas; the only difference between them is the crystal facet exposed in TiO2 nanocrystals. UV/Vis spectra show that band structures of TiO2 nanocrystals and TiO2 -graphene nanocomposites are dependent on the crystal facets. Time-resolved photoluminescence spectra suggest that the charge-transfer rate between {100} facets and graphene is approximately 1.4 times of that between {001} facets and graphene. Photoelectrochemical measurements also confirm that the charge-separation efficiency between TiO2 and graphene is greatly dependent on the crystal facets. X-ray photoelectron spectroscopy reveals that Ti-C bonds are formed between {100} facets and graphene, while {101} facets and {001} facets are connected with graphene mainly through Ti-O-C bonds. With Ti-C bonds between TiO2 and graphene, TiO2 -100-G shows the fastest charge-transfer rate, leading to higher activity in photocatalytic H2 production from methanol solution. TiO2 -101-G with more reductive electrons and medium interfacial charge-transfer rate also shows good H2 evolution rate. As a result of its disadvantageous electronic structure and interfacial connections, TiO2 -001-G shows the lowest H2 evolution rate. These results suggest that engineering the structures of the TiO2 -graphene interface can be an effective strategy to achieve excellent photocatalytic performances. Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Glycine assisted synthesis of flower-like TiO 2 hierarchical spheres and its application in photocatalysis

KAUST Repository

Tao, Yugui; Xu, Yanqiu; Pan, Jun; Gu, Hao; Qin, Changyun; Zhou, Peng

2012-01-01

Flower-like anatase TiO 2 hierarchical spheres assembled by nanosheets were synthesized by glycine assistant via a simple hydrothermal approach and after-annealing process. These flower-like spheres are about 2 μm in diameter with sheet thickness about 20 nm. Results showed reaction time, temperature, solution pH and glycine dosage all played an important role in control of shape and size of the as-synthesized TiO 2 nanocrystals. The photocatalytic activity of this nano-TiO 2 was evaluated by the photocatalytic oxidation decomposition of methyl orange under sunlight illumination in the presence of hydrogen peroxide (H 2O 2). The photocatalytic activity of the obtained TiO 2 was higher than that of commercial TiO 2. © 2012 Elsevier B.V.

Glycine assisted synthesis of flower-like TiO 2 hierarchical spheres and its application in photocatalysis

KAUST Repository

Tao, Yugui

2012-11-01

Flower-like anatase TiO 2 hierarchical spheres assembled by nanosheets were synthesized by glycine assistant via a simple hydrothermal approach and after-annealing process. These flower-like spheres are about 2 μm in diameter with sheet thickness about 20 nm. Results showed reaction time, temperature, solution pH and glycine dosage all played an important role in control of shape and size of the as-synthesized TiO 2 nanocrystals. The photocatalytic activity of this nano-TiO 2 was evaluated by the photocatalytic oxidation decomposition of methyl orange under sunlight illumination in the presence of hydrogen peroxide (H 2O 2). The photocatalytic activity of the obtained TiO 2 was higher than that of commercial TiO 2. © 2012 Elsevier B.V.

Tuning metal support interactions enhances the activity and durability of TiO2-supported Pt nanocatalysts

International Nuclear Information System (INIS)

Hsieh, Bing-Jen; Tsai, Meng-Che; Pan, Chun-Jern; Su, Wei-Nien; Rick, John; Chou, Hung-Lung; Lee, Jyh-Fu; Hwang, Bing-Joe

2017-01-01

Highlights: • The coverage of TiO x on Pt can be modified by thermal and fluoric acid treatments. • Strong metal support interaction (SMSI) can be testified by electrochemical method. • For the first time, the SMSI effect is observed at 200 °C with supporting TEM images. • Increased activity and stability are attributed to stronger SMSI. • This tunable approach is valid for other oxide supported catalysts, e.g. Pt/Nb-TiO 2 . - Abstract: A facile approach to enhance catalytic activity and durability of TiO 2 -supported Pt nanocatalysts by tuning strong metal support interaction (SMSI) is investigated in this work. No need for a high temperature treatment, the strong metal-support interaction (SMSI) in TiO 2 -supported Pt can be induced at 200° C by H 2 reduction. Moreover, electrochemical methods (methanol oxidation reaction and cyclic voltammetry) are first reported ever to be effective characterization tools for the coverage state caused by SMSI. In addition, the SMSI has also been confirmed by X-ray photoelectron spectroscopy, X-ray absorption spectroscopy, and Transmission Electron Microscopy. It is found that the encapsulation of TiO 2-x species on the surface Pt clusters was induced and modified by thermal reduction and fluoric acid treatment. The catalytic activity and durability of the TiO 2 -supported Pt nanocatalysts are strongly dependent of the state of SMSI. The proposed SMSI-tunable approach to enhance the ORR activity and stability is also proved applicable to Pt/Ti 0.9 Nb 0.1 O 2 nanocatalysts. We believe that the reported approach paves the way for manipulating the activity and stability of other TiO 2 -supported metal nanocatalysts. Furthermore, the suggested electrochemical methods offer facile and effective ways to verify the presence of coverage state before combining with other physical analysis.

Synthesis and Characterization of Hierarchical Structured TiO2 Nanotubes and Their Photocatalytic Performance on Methyl Orange

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Kai Liu

2015-01-01

Full Text Available Hierarchical structured TiO2 nanotubes were prepared by mechanical ball milling of highly ordered TiO2 nanotube arrays grown by electrochemical anodization of titanium foil. Scanning electron microscopy, transmission electron microscopy, X-ray diffraction, specific surface area analysis, UV-visible absorption spectroscopy, photocurrent measurement, photoluminescence spectra, electrochemical impedance spectra, and photocatalytic degradation test were applied to characterize the nanocomposites. Surface area increased as the milling time extended. After 5 h ball milling, TiO2 hierarchical nanotubes exhibited a corn-like shape and exhibited enhanced photoelectrochemical activity in comparison to commercial P25. The superior photocatalytic activity is suggested to be due to the combined advantages of high surface area of nanoparticles and rapid electron transfer as well as collection of the nanotubes in the hierarchical structure. The hierarchical structured TiO2 nanotubes could be applied into flexible applications on solar cells, sensors, and other photoelectrochemical devices.

Hydrothermal synthesis, characterization, photocatalytic activity and dye-sensitized solar cell performance of mesoporous anatase TiO2 nanopowders

International Nuclear Information System (INIS)

Pavasupree, Sorapong; Jitputti, Jaturong; Ngamsinlapasathian, Supachai; Yoshikawa, Susumu

2008-01-01

Mesoporous anatase TiO 2 nanopowder was synthesized by hydrothermal method at 130 deg. C for 12 h. The samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), selected-area electron diffraction (SAED), HRTEM, and Brunauer-Emmett-Teller (BET) surface area. The as-synthesized sample with narrow pore size distribution had average pore diameter about 3-4 nm. The specific BET surface area of the as-synthesized sample was about 193 m 2 /g. Mesoporous anatase TiO 2 nanopowders (prepared by this study) showed higher photocatalytic activity than the nanorods TiO 2 , nanofibers TiO 2 mesoporous TiO 2 , and commercial TiO 2 nanoparticles (P-25, JRC-01, and JRC-03). The solar energy conversion efficiency (η) of the cell using the mesoporous anatase TiO 2 was about 6.30% with the short-circuit current density (Jsc) of 13.28 mA/cm 2 , the open-circuit voltage (Voc) of 0.702 V and the fill factor (ff) of 0.676; while η of the cell using P-25 reached 5.82% with Jsc of 12.74 mA/cm 2 , Voc of 0.704 V and ff of 0.649

Light-induced antifungal activity of TiO2 nanoparticles/ZnO nanowires

International Nuclear Information System (INIS)

Haghighi, N.; Abdi, Y.; Haghighi, F.

2011-01-01

Antifungal activity of TiO 2 /ZnO nanostructures under visible light irradiation was investigated. A simple chemical method was used to synthesize ZnO nanowires. Zinc acetate dihydrate, Polyvinyl Pyrrolidone and deionized water were used as precursor, capping and solvent, respectively. TiO 2 nanoparticles were deposited on ZnO nanowires using an atmospheric pressure chemical vapor deposition system. X-ray diffraction pattern of TiO 2 /ZnO nano-composite has represented the diffraction peaks relating to the crystal planes of the TiO 2 (anatase and rutile) and ZnO. TiO 2 /ZnO nanostructure antifungal effect on Candida albicans biofilms was studied and compared with the activity of TiO 2 nanoparticles and ZnO nanowires. The high efficiency photocatalytic activity of TiO 2 nanoparticles leads to increased antifungal activity of ZnO nanowires. Scanning electron microscope was utilized to study the morphology of the as prepared nanostructures and the degradation of the yeast.

A new approach of tailoring wetting properties of TiO2 nanotubular surfaces

KAUST Repository

Isimjan, Tayirjan T.; Yan, Zhu; Yang, D. Q.; Rohani, Sohrab M F; Ray, Ajay

2012-01-01

TiO2 nanotube layers were grown on a Ti surface by electrochemical anodization. As prepared, these layers showed a superhydrophilic wetting behavior. Modified with 1H, 1H, 2H, 2H-perfluorooctyltriethoxysilane (PTES), the layers showed a

The Influence of TiO2 Nanoparticles on LaFeO3/TiO2 Nanocomposites for Reduction of Aqueous Organic Dyes

International Nuclear Information System (INIS)

Afifah, N.; Saleh, R.

2016-01-01

A series of Lanthanum ferrite (LaFeO3) nanoparticles over titanium dioxide (TiO2) were synthesized using sol-gel method at room temperature by varying the loading of LaFeO3 on TiO2. The magnetic properties of samples were measured using vibrating sample magnetometer and photosonocatalytic activity towards the degradation of methylene blue under light (UV or visible) and ultrasound irradiation was also evaluated. The morphology and structure of the samples were characterized by field emission scanning electron microscope, energy dispersive analysis and X-ray diffraction. Furthermore the optical properties were also characterized by UV-visible diffuse reflectance. The experimental results showed that the prepared perovskites had sphere-like shape and strong visible light absorption. LaFeO3 demonstrated ferromagnetic properties and the magnetization decreased with the incorporation of TiO2 in the samples. However, the incorporation of TiO2 increased the photosonocatalytic activity and extended the photoresponding to UV light. (paper)

Photolithographically Patterned TiO2 Films for Electrolyte-Gated Transistors.

Science.gov (United States)

Valitova, Irina; Kumar, Prajwal; Meng, Xiang; Soavi, Francesca; Santato, Clara; Cicoira, Fabio

2016-06-15

Metal oxides constitute a class of materials whose properties cover the entire range from insulators to semiconductors to metals. Most metal oxides are abundant and accessible at moderate cost. Metal oxides are widely investigated as channel materials in transistors, including electrolyte-gated transistors, where the charge carrier density can be modulated by orders of magnitude upon application of relatively low electrical bias (2 V). Electrolyte gating offers the opportunity to envisage new applications in flexible and printed electronics as well as to improve our current understanding of fundamental processes in electronic materials, e.g. insulator/metal transitions. In this work, we employ photolithographically patterned TiO2 films as channels for electrolyte-gated transistors. TiO2 stands out for its biocompatibility and wide use in sensing, electrochromics, photovoltaics and photocatalysis. We fabricated TiO2 electrolyte-gated transistors using an original unconventional parylene-based patterning technique. By using a combination of electrochemical and charge carrier transport measurements we demonstrated that patterning improves the performance of electrolyte-gated TiO2 transistors with respect to their unpatterned counterparts. Patterned electrolyte-gated (EG) TiO2 transistors show threshold voltages of about 0.9 V, ON/OFF ratios as high as 1 × 10(5), and electron mobility above 1 cm(2)/(V s).

Dye-Sensitized Solar Cells with Anatase TiO2 Nanorods Prepared by Hydrothermal Method

Directory of Open Access Journals (Sweden)

Ming-Jer Jeng

2013-01-01

Full Text Available The hydrothermal method provides an effective reaction environment for the synthesis of nanocrystalline materials with high purity and well-controlled crystallinity. In this work, we started with various sizes of commercial TiO2 powders and used the hydrothermal method to prepare TiO2 thin films. We found that the synthesized TiO2 nanorods were thin and long when smaller TiO2 particles were used, while larger TiO2 particles produced thicker and shorter nanorods. We also found that TiO2 films prepared by TiO2 nanorods exhibited larger surface roughness than those prepared by the commercial TiO2 particles. It was found that a pure anatase phase of TiO2 nanorods can be obtained from the hydrothermal method. The dye-sensitized solar cells fabricated with TiO2 nanorods exhibited a higher solar efficiency than those fabricated with commercial TiO2 nanoparticles directly. Further, triple-layer structures of TiO2 thin films with different particle sizes were investigated to improve the solar efficiency.

TiO2/EVOH based reactive interlayer in Surlyn for organic device encapsulation

International Nuclear Information System (INIS)

Kopanati, Gayathri N; Madras, Giridhar; Ramamurthy, Praveen C

2016-01-01

Barrier materials are important for improving the stability and lifetimes of organic electronic devices. A simple technique for improving the barrier properties of polymer films was considered in this work by using TiO 2 nanoparticles in the interlayer to be incorporated in the polymer film. TiO 2 was synthesized by the solution combustion technique, was further functionalized using stearic acid or octadecylamine to induce hydrophobicity and enhance processing of the composite interlayer. The grafting of these compounds on to TiO 2 was investigated using Fourier transform infrared spectroscopy, Raman spectroscopy, elemental analysis and thermo-gravimetric analysis. The functionalized and neat TiO 2 were blended with poly (vinyl alcohol-ethylene) (EVOH) and were melt compressed between Surlyn films. The resulting nanocomposite films were tested for their transparency and barrier properties using UV–visible spectroscopy and calcium degradation test, respectively. Further, the effectiveness of these barrier films in encapsulating organic devices was determined from accelerated aging tests. Therefore, the synthesized barrier films with neat and functionalized TiO 2 in the interlayers proved to be effective as moisture barrier composite films. (paper)

Synthesis of ascorbic acid enhanced TiO2 photocatalyst: its characterization and catalytic activity in CO2 photoreduction

Directory of Open Access Journals (Sweden)

Mohd Farid Bin Mohd Na'aim

2018-04-01

Full Text Available To date, the development of solar environmental remediation has shifted more emphasis on the green and simple synthesis of catalyst for CO2 photocatalysis process. Herein, TiO2 photocatalyst was successfully synthesized via hydrothermal method. The effects of the different molar ratio of ascorbic acid C6H8O6, (AA added during the preparation of TiO2 nanoparticles were comprehensively studied. The characterization of TiO2 nanocrystals was performed via XRD, XPS, DRUV-vis, and FTIR. The results show the AA loading into TiO2 nanoparticles significantly intensified the XRD spectra of anatase structure. In fact, this feature had signified a reactivity of the photocatalyst in the visible region. In an instance, BET surface area was also enhanced with the highest recorded value of 135.14 m2/g for 0.8AA. Meanwhile, the CO2 photoreduction over synthesized TiO2 had produced the highest amount of HCOOH at 39.3 μmol/g cat for 0.8AA within 6 hours of reaction time. Furthermore, the DRUV-vis analysis had illustrated better light absorption ability of 0.8AA. This profound finding is attributed to the correlation between large surface area, pure anatase phase, and high adsorbed water molecules. Therefore, this study had significantly demonstrated the potential of modified TiO2 with AA in CO2 photocatalysis area while simultaneously presents a green and simple method for TiO2 synthesis.

TiO2-SnS2 nanocomposites: solar-active photocatalytic materials for water treatment.

Science.gov (United States)

Kovacic, Marin; Kusic, Hrvoje; Fanetti, Mattia; Stangar, Urska Lavrencic; Valant, Matjaz; Dionysiou, Dionysios D; Bozic, Ana Loncaric

2017-08-01

The study is aimed at evaluating TiO 2 -SnS 2 composites as effective solar-active photocatalysts for water treatment. Two strategies for the preparation of TiO 2 -SnS 2 composites were examined: (i) in-situ chemical synthesis followed by immobilization on glass plates and (ii) binding of two components (TiO 2 and SnS 2 ) within the immobilization step. The as-prepared TiO 2 -SnS 2 composites and their sole components (TiO 2 or SnS 2 ) were inspected for composition, crystallinity, and morphology using Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), X-ray diffraction (XRD), and scanning electron microscopy/energy-dispersive X-ray spectroscopy (SEM/EDX) analyses. Diffuse reflectance spectroscopy (DRS) was used to determine band gaps of immobilized TiO 2 -SnS 2 and to establish the changes in comparison to respective sole components. The activity of immobilized TiO 2 -SnS 2 composites was tested for the removal of diclofenac (DCF) in aqueous solution under simulated solar irradiation and compared with that of single component photocatalysts. In situ chemical synthesis yielded materials of high crystallinity, while their morphology and composition strongly depended on synthesis conditions applied. TiO 2 -SnS 2 composites exhibited higher activity toward DCF removal and conversion in comparison to their sole components at acidic pH, while only in situ synthesized TiO 2 -SnS 2 composites showed higher activity at neutral pH.

Decolorization of dyeing wastewater in continuous photoreactors using tio2 coated glass tube media

Directory of Open Access Journals (Sweden)

Jutaporn Chanathaworn

2014-02-01

Full Text Available The present study deals with a decolorization development of malachite green (MG dyeing wastewater using TiO2 thin films coated glass tube media in photoreactor. The TiO2 photocatalyst was synthesized by three methods: TTIP sol-gel, TiO2 powder-modified sol, and TiO2 powder suspension coating on raschig ring glass tube media and was investigated crystallinity phase by SEM, XRD, and AFM. Degradation kinetics of the dyeing wastewater by photocatalytic was carried out under UV light irradiation. The Langmuir first-order model provided the best fit to the experimental data. The catalyst prepared by powder suspension technique and coated on glass tube had given the highest of decolorization kinetics and efficiency. Continuous photoreactor packed with the TiO2 coating media was designed and proven to be the high effectiveness for MG dyeing degradation and stable throughout the recyclability test. The light intensity, dye solution flow rate, and TiO2 loading were the most important parameters that response to decolorization efficiency. The optimum condition of photo decolorization of MG dye solution can be obtained from RSM model. Effectiveness of the synthesized TiO2 thin films using suspension technique and the continuous photoreactor design were obtained with a great potential to be proven for wastewater treatment at industrial scale.

SYNTHESIS OF MAGNETIC NANOPARTICLES OF TiO2-NiFe2O4: CHARACTERIZATION AND PHOTOCATALYTIC ACTIVITY ON DEGRADATION OF RHODAMINE B

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Rahmayeni Rahmayeni

2012-12-01

Full Text Available Magnetic nanoparticles of TiO2-(xNiFe2O4 with x = 0.01, 0.1, and 0.3have been synthesized by mixture of titanium isopropoxide (TIP and nitric metal as precursors. The particles were characterized by XRD, SEM-EDX, and VSM. XRD pattern show the peaks at 2q = 25.3°, 38.4° and 47.9° which are referred as anatase phase of TiO2. Meanwhile NiFe2O4 phase was observed clearly for x = 0.3. The present of NiFe2O4 can prevent the transformation of TiO2 from anatase to rutile when the calcination temperature increased. Microstructure analyses by SEM show the homogeneous form and size of particles. The magnetic properties analysis by VSM indicates that TiO2-NiFe2O4 is paramagnetic behavior. TiO2 doped NiFe2O4 has higher photocatalytic activity than TiO2 synthesized for degradation of Rhodamine B in aqueous solution under solar light irradiation.

Direct access to highly crystalline mesoporous nano TiO2 using sterically bulky organic acid templates

Science.gov (United States)

Bakre, Pratibha V.; Tilve, S. G.

2018-05-01

Sterically bulky monocarboxylic acid templates pivalic acid and phenoxyacetic acid are reported for the first time as organic templates in the sol-gel synthesis of TiO2. Mesoporous nanoparticulates of pure anatase phase and of well defined size were synthesized. The characterization of the materials prepared was done by various methods such as XRD, SEM, TEM, FTIR, UV-DRS, BET, etc. The prepared TiO2 samples were evaluated for the day light photodegradation of methylene blue by comparing with Degussa P25 and templates free synthesized TiO2 and were found to be more efficient.

Structure and electrochemical properties of Mg2SnO4 nanoparticles synthesized by a facile co-precipitation method

International Nuclear Information System (INIS)

Tang, Hao; Cheng, Cuixia; Yu, Gaige; Liu, Haowen; Chen, Weiqing

2015-01-01

Nanosized Mg 2 SnO 4 has been synthesized by a facile co-precipitation method. The structure and morphology of the as-prepared samples are characterized by X-ray diffraction (XRD), X-ray photoelectron spectrometer (XPS), fourier Transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM) and scanning electron microscopy (SEM). It is found that Mg 2 SnO 4 sample is very sensitive to the aging time of the precursor. The single phase Mg 2 SnO 4 nanoparticles with ∼23 nm can be obtained at 900 °C using the aging 35 min percusor as source. The electrochemical properties of the powder obtained at 900 °C are investigated by galvanostatic discharge-charge tests and cyclic voltammograms (CVs). The initial specific discharge capacity reaches as high as 927.7 mAh g −1 at 0.2 mA cm −2 in 0.05–3.0 V, which indicates that Mg 2 SnO 4 nanoparticles could be a promising candidate of anode material for Li-ion batteries. - Highlights: • Nanosized Mg 2 SnO 4 has been synthesized by a facile co-precipitation method. • We find that Mg 2 SnO 4 sample is very sensitive to the ageing time of the precursor. • The single phase Mg 2 SnO 4 nanoparticles with about 23 nm can be obtained by calcining the ageing 35 min percusor at 900 °C. • The obtained powders show a better electrochemical performance

TiO2/PCL hybrid materials synthesized via sol–gel technique for biomedical applications

International Nuclear Information System (INIS)

Catauro, M.; Bollino, F.; Papale, F.; Marciano, S.; Pacifico, S.

2015-01-01

The aim of the present work has been the synthesis of organic/inorganic hybrid materials based on titanium dioxide and poly(ε-caprolactone) (PCL) to be used in the biomedical field. Several materials have been synthesized using sol–gel methods by adding different amounts of polymer to the inorganic sol. The obtained gels have been characterized using Fourier transform infrared (FT-IR) spectroscopy, scanning electron microscopy (SEM) and atomic force microscopy (AFM). The FT-IR data allowed us to hypothesize that the structure formed was that of an interpenetrating network, realized by hydrogen bonds between Ti-OH groups in the sol–gel intermediate species and carbonyl groups in the polymer repeating units. SEM and AFM analyses highlighted that the obtained materials were nanostructurated hybrids. To evaluate the biological properties of the hybrids, their bioactivity and cytotoxicity were investigated as a function of the PCL amount. The bioactivity of the synthesized systems was proven by the formation of a hydroxyapatite layer on the surface of samples soaked in a fluid simulating human blood plasma (SBF). MTT cytotoxicity tests and Trypan Blue dye exclusion tests were carried out exposing NIH-3T3 mouse embryonic fibroblasts for 24 and 48 h to extracts from the investigated hybrid materials. The results showed that all the hybrids had a non-cytotoxic effect on target cells. - Highlights: • TiO 2 /PCL hybrids were obtained by the sol–gel process for biomedical applications. • Synthesized materials were found to be first-class hybrid nanocomposites. • Hybrids appear to be bioactive, a fundamental characteristic for osseointegration. • MTT and Trypan Blue viability test show that the materials are biocompatible. • The organic phase is able to modulate the biocompatibility of the materials

Synthesis of hybrid cellulose nanocomposite bonded with dopamine SiO2/TiO2 and its antimicrobial activity

Science.gov (United States)

Ramesh, Sivalingam; Kim, Gwang-Hoon; Kim, Jaehwan; Kim, Joo-Hyung

2015-04-01

Organic-inorganic hybrid material based cellulose was synthesized by the sol-gel approach. The explosion of activity in this area in the past decade has made tremendous progress in industry or academic both fundamental understanding of sol-gel process and applications of new functionalized hybrid materials. In this present research work, we focused on cellulose-dopamine functionalized SiO2/TiO2 hybrid nanocomposite by sol-gel process. The cellulose-dopamine hybrid nanocomposite was synthesized via γ-aminopropyltriethoxysilane (γ-APTES) coupling agent by in-situ sol-gel process. The chemical structure of cellulose-amine functionalized dopamine bonding to cellulose structure with covalent cross linking hybrids was confirmed by FTIR spectral analysis. The morphological analysis of cellulose-dopamine nanoSiO2/TiO2 hybrid nanocomposite materials was characterized by XRD, SEM and TEM. From this different analysis results indicate that the optical transparency, thermal stability, control morphology of cellulose-dopamine-SiO2/TiO2 hybrid nanocomposite. Furthermore cellulose-dopamine-SiO2/TiO2 hybrid nanocomposite was tested against pathogenic bacteria for antimicrobial activity.

Ultra-fine structural characterization and bioactivity evaluation of TiO2 nanotube layers.

Science.gov (United States)

Jang, JaeMyung; Kwon, TaeYub; Kim, KyoHan

2008-10-01

For an application as biomedical materials of high performance with a good biocompatibility, the TiO2 nanotube-type oxide film on Ti substrate has been fabricated by electrochemical method, and the effects of surface characteristics of TiO2 naotube layer have been investigated. The surface morphology of TiO2 nanotube layer depends on factors such as anodizing time, current density, and electrolyte temperature. Moreover, the cell and pore size gradually were increased with the passage of anodizing time. X-ray diffraction (XRD) results indicated that the TiO2 nanotube layer formed in acidic electrolytes was mainly composed of anatase structure containing rutile. From the analysis of chemical states of TiO2 nanotube layer using X-ray photoelectron spectroscopy (XPS), Ti2p, P2p and O1s were observed in the nanotubes layer, which were penetrated from the electrolyte into the oxide layer during anodic process. The incorporated phosphate species were found mostly in the forms of HPO4-, PO4-, and PO3-. From the result of biological evaluation in simulated body fluid (SBF) the TiO2 nanotube layer was effective for bioactive property.

Photodegradation of Reactive Golden Yellow R Dye Catalyzed by Effective Titania (TiO2)

International Nuclear Information System (INIS)

Bedurus, E.A.; Marinah Mohd Ariffin; Mohd Hasmizam Razali

2015-01-01

In the present research, Microwave Assisted Synthesis (MAS) method was applied to synthesize titania (TiO 2 ) at 150 degree Celsius in a range of 2-6 hours heating time. Each prepared TiO 2 were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD) and nitrogen gas (N 2 ) sorption analysis (Brunaeur-Emmett-Teller (BET) and Barrett-Joyner-Halenda (BJH) calculation) techniques. The TiO 2 prepared by MAS 150 degree Celsius (4 hours) has emerged with the highest photo catalytic activity. Within 4 hours, the TiO 2 managed to catalyze the degradation of Reactive Golden Yellow R dye up to 98.51 %. This is because of the TiO 2 possessed high crystallinity of anatase phase, small crystallite size and high pore volume compared to other prepared TiO 2 . (author)

Probing Photocatalytic Characteristics of Sb-Doped TiO2 under Visible Light Irradiation

Directory of Open Access Journals (Sweden)

Lingjing Luo

2014-01-01

Full Text Available Sb-doped TiO2 nanoparticle with varied dopant concentrations was synthesized using titanium tetrachloride (TiCl4 and antimony chloride (SbCl3 as the precursors. The properties of Sb-doped TiO2 nanoparticles were characterized by X-ray diffraction (XRD, scanning electron microscope (SEM, fluorescence spectrophotometer, and Uv-vis spectrophotometer. The absorption edge of TiO2 nanoparticles could be extended to visible region after doping with antimony, in contrast to the UV absorption of pure TiO2. The results showed that the photocatalytic activity of Sb-doped TiO2 nanoparticles was much more active than pure TiO2. The 0.1% Sb-doped TiO2 nanoparticles demonstrated the best photocatalytic activity which was better than that of the Degussa P25 under visible light irradiation using terephthalic acid as fluorescent probe. The effects of Sb dopant on the photocatalytic activity and the involved mechanism were extensively investigated in this work as well.

Constructing superhydrophobic WO3@TiO2 nanoflake surface beyond amorphous alloy against electrochemical corrosion on iron steel

Science.gov (United States)

Yu, S. Q.; Ling, Y. H.; Wang, R. G.; Zhang, J.; Qin, F.; Zhang, Z. J.

2018-04-01

To eliminate harmful localized corrosion, a new approach by constructing superhydrophobic WO3@TiO2 hierarchical nanoflake surface beyond FeW amorphous alloy formed on stainless steel was proposed. Facile dealloying and liquid deposition was employed at low temperature to form a nanostructured layer composing inner WO3 nanoflakes coated with TiO2 nanoparticles (NPs) layer. After further deposition of PFDS on nanoflakes, the contact angle reached 162° while the corrosion potential showed a negative shift of 230 mV under illumination, resulting in high corrosion resistance in 3.5 wt% NaCl solution. The tradeoff between superhydrophobic surface and photo-electro response was investigated. It was found that this surface feature makes 316 SS be immune to localized corrosion and a pronounced photo-induced process of electron storage/release as well as the stability of the functional layer were detected with or without illumination, and the mechanism behind this may be related to the increase of surface potential due to water repellence and the delayed cathodic protection of semiconducting coating derived mainly from the valence state changes of WO3. This study demonstrates a simple and low-cost electrochemical approach for protection of steel and novel means to produce superhydrophobic surface and cathodic protection with controllable electron storage/release on engineering scale.

Synthesis of carbon-coated TiO 2 nanotubes for high-power lithium-ion batteries

Science.gov (United States)

Park, Sang-Jun; Kim, Young-Jun; Lee, Hyukjae

Carbon-coated TiO 2 nanotubes are prepared by a simple one-step hydrothermal method with an addition of glucose in the starting powder, and are characterized by morphological analysis and electrochemical measurement. A thin carbon coating on the nanotube surface effectively suppresses severe agglomeration of TiO 2 nanotubes during hydrothermal reaction and post calcination. This action results in better ionic and electronic kinetics when applied to lithium-ion batteries. Consequently, carbon-coated TiO 2 nanotubes deliver a remarkable lithium-ion intercalation/deintercalation performance, such as reversible capacities of 286 and 150 mAh g -1 at 250 and 7500 mA g -1, respectively.

Sonochemical synthesis and characterization of Pt/CNT, Pt/TiO2, and Pt/CNT/TiO2 electrocatalysts for methanol electro-oxidation

International Nuclear Information System (INIS)

Bedolla-Valdez, Z.I.; Verde-Gómez, Y.; Valenzuela-Muñiz, A.M.; Gochi-Ponce, Y.; Oropeza-Guzmán, M.T.; Berhault, Gilles; Alonso-Núñez, G.

2015-01-01

Highlights: • Pt/CNT/TiO 2 electrocatalyst was successfully prepared by the sonochemical method. • The electrocatalyst Pt/CNT/TiO 2 was synthesized without heat treatments, additives or surfactants. • The TiO 2 -Pt interaction improves the CO-tolerance of Pt/CNT/TiO 2 , as well as the electrocatalyst stability. • Low amount of multi-walled carbon nanotubes increases the current density of Pt/CNT/TiO 2 significantly compared to Pt/TiO 2 . - Abstract: Pt electrocatalyst supported on composite formed of multi-walled carbon nanotubes and titanium oxide (CNT/TiO 2 ) was successfully synthesized by a sonochemical method without heat treatments, surfactants or additives. This electrocatalyst could be used for direct methanol fuel cells (DMFC) applications. For comparison, Pt/CNT and Pt/TiO 2 electrocatalysts were prepared as reference samples. Structural properties and morphology of the synthesized materials were examined by X-ray diffraction, transmission electron microscopy, Raman spectroscopy, X-ray photoelectron spectroscopy and their specific surface areas were determined by the Brunauer-Emmett-Teller method. The Pt and acid-treated CNT contents were analyzed by inductively coupled plasma atomic emission spectroscopy and thermogravimetric analysis, respectively. The electrochemical properties of the synthesized electrocatalysts were evaluated by cyclic voltammetry (CV) and chronoamperometry in a three-electrode cell at room temperature. The evaluation performed using electrochemical techniques suggests that TiO 2 promotes the CO-tolerance due to TiO 2 -Pt interaction. The CV tests demonstrated that 6 wt.% of acid-treated CNT increases significantly the current density when Pt selectively interacts with TiO 2 .

Hierarchically multifunctional K-OMS-2/TiO2/Fe3O4 heterojunctions for the photocatalytic oxidation of humic acid under solar light irradiation.

Science.gov (United States)

Zhang, Tong; Yan, Xiaoli; Sun, Darren Delai

2012-12-01

A multifunctional heterojunctioned K-OMS-2/TiO(2)/Fe(3)O(4) (KTF) nanocomposite was successfully synthesized using a combination of hydrothermal and co-precipitation techniques. The resultant sample was characterized by XRD, FESEM, TEM, N(2) adsorption, XPS and VSM. Its photocatalytic activity was demonstrated in the photocatalytic degradation of humic acid (HA). Morphology characterization showed the hierarchical structure of the synthesized material, and XRD results revealed that both the rutile and anatase TiO(2) structures are present in the sample. The average pore diameters and BET surface area of the synthesized KTF heterojunctions were 40 nm and 134.42 m(2)/g, respectively. XPS spectra confirmed the presence of Fe(3)O(4) and TiO(2) in the synthesized material, and the valences of Mn were kept at +3 and +4 after the grafting of Fe(3)O(4) and TiO(2). The synthesized material showed good magnetic response and photocatalytic activity under simulated solar light irradiation, and 85.7% of HA was decomposed after 120 min in the presence of KTF nanocomposites. The reusability study suggested that the magnetic recovered material was stable enough for multiple recycling usages, verifying its potential application in water purification. Copyright © 2012 Elsevier B.V. All rights reserved.

Epitaxial TiO 2/SnO 2 core-shell heterostructure by atomic layer deposition

KAUST Repository

Nie, Anmin; Liu, Jiabin; Li, Qianqian; Cheng, Yingchun; Dong, Cezhou; Zhou, Wu; Wang, Pengfei; Wang, Qingxiao; Yang, Yang; Zhu, Yihan; Zeng, Yuewu; Wang, Hongtao

2012-01-01

Taking TiO 2/SnO 2 core-shell nanowires (NWs) as a model system, we systematically investigate the structure and the morphological evolution of this heterostructure synthesized by atomic layer deposition/epitaxy (ALD/ALE). All characterizations

Rutile TiO2 nanorod arrays directly grown on Ti foil substrates towards lithium-ion micro-batteries

International Nuclear Information System (INIS)

Dong Shanmu; Wang Haibo; Gu Lin; Zhou Xinhong; Liu Zhihong; Han Pengxian; Wang Ya; Chen Xiao; Cui Guanglei; Chen Liquan

2011-01-01

Nanosized rutile TiO 2 is one of the most promising candidates for anode material in lithium-ion micro-batteries owing to their smaller dimension in ab-plane resulting in an enhanced performance for area capacity. However, few reports have yet emerged up to date of rutile TiO 2 nanorod arrays growing along c-axis for Li-ion battery electrode application. In this study, single-crystalline rutile TiO 2 nanorod arrays growing directly on Ti foil substrates have been fabricated using a template-free method. These nanorods can significantly improve the electrochemical performance of rutile TiO 2 in Li-ion batteries. The capacity increase is about 10 times in comparison with rutile TiO 2 compact layer.

TiO2-B Nanoribbons Anchored with NiO Nanosheets as Hybrid Anode Materials for Rechargeable Lithium ion Batteries

DEFF Research Database (Denmark)

Zhang, J. Y.; Shen, J.X.; Wang, T.L.

2015-01-01

A new type of TiO2-B nanoribbon anchored with NiO nanosheets (TiO2@NiO) is synthesized via a hydrothermal process and a subsequent homogeneous precipitation method. XRD analysis indicates that TiO2-B and cubic NiO phases exist in the composites. According to SEM images, the morphology of the TiO2...

In situ glow discharge plasma electrolytic synthesis of reduced TiO2 for enhanced visible light photocatalysis

Science.gov (United States)

Feng, Guang; Wu, Botao; Qayyum Khan, Abdul; Zeng, Heping

2018-05-01

Reduced titanium dioxide (TiO2‑x) due to its extraordinary visible light absorption has been widely investigated in photodegradation and water splitting nowadays. However, conventional routes to synthesize reduced TiO2 usually demand multiple preparation steps, harsh controlled conditions or expensive facilities. Here we developed a single-step in situ approach to prepare the gray TiO2‑x nanoparticles (sub-10 nm) effectively by the glow discharge plasma electrolysis (GDPE) under atmospheric pressure. The co-existence of self-doped oxygen vacancies and Ti3+ in the generated TiO2‑x nanoparticles is demonstrated by electron paramagnetic resonance (EPR). The tunable ratio of bulk/surface defect can be realized by controlling the glow discharge power directly. It should be noticed that Ti3+ in the synthesized TiO2‑x are quite stable in ambient air. The UV–vis spectra of gray TiO2‑x show an enhanced visible light absorption, which leads to high visible-light photocatalytic activity. Moreover, the as-prepared TiO2‑x after 6 months storage still shows excellent stability during photocatalytic reactions. Owing to its simplicity and effectivity, this preparation method with GDPE should provide a large-scale production for TiO2‑x with high photoactivity.

Improved electrochemical performance of Li1.2Mn0.54Ni0.13Co0.13O2 cathode material synthesized by citric acid assisted sol-gel method for lithium ion batteries

Science.gov (United States)

Li, Shiyou; Liang, Youwei; Lei, Dan; Xie, Yingchun; Ai, Ling; Xie, Jing

2018-03-01

A citric acid assisted sol-gel method is employed for synthesizing Li1.2Mn0.54Ni0.13Co0.13O2 used as a cathode material in lithium-ion batteries. Powder X-ray diffraction (XRD) and scanning electron microscopy (SEM) characterizations prove that materials have a typical a-NaFeO2 structure with primary nano-sized particles. Electrochemical performances have been investigated by charge-discharge test and results show that the synthesized product exhibits excellent electrochemical performance with a high initial discharge capacity of 253.5 mAh g-1 at 0.1 C and a preferable capacity retention of 84.8% after 50 cycles.

Enhanced supercapacitor performance using hierarchical TiO2 nanorod/Co(OH)2 nanowall array electrodes

International Nuclear Information System (INIS)

Ramadoss, Ananthakumar; Kim, Sang Jae

2014-01-01

Graphical abstract: - Highlights: • TiO 2 /Co(OH) 2 hierarchical nanostructure was prepared by a combination of hydrothermal and cathodic electrodeposition method. • Hierarchical nanostructure electrode exhibited a maximum capacitance of 274.3 mF cm −2 at a scan rate of 5 mV s −1 . • Combination of Co(OH) 2 nanowall with TiO 2 NR into a single system enhanced the electrochemical behavior of supercapacitor electrode. - Abstract: We report novel hierarchical TiO 2 nanorod (NR)/porous Co(OH) 2 nanowall array electrodes for high-performance supercapacitors fabricated using a two-step process that involves hydrothermal and electrodeposition techniques. Field-emission scanning electron microscope images reveal a bilayer structure consisting of TiO 2 NR arrays with porous Co(OH) 2 nanowalls. Compared with the bare TiO 2 NRs, the hierarchical TiO 2 NRs/Co(OH) 2 electrodes showed improved pseudocapacitive performance in a 2-M KOH electrolyte solution, exhibiting an areal specific capacitance of 274.3 mF cm −2 at a scan rate of 5 mV s −1 . The electrodes exhibited good stability, retaining 82.5% of the initial capacitance after 4000 cycles. The good pseudocapacitive performance of the hierarchical nanostructures is mainly due to the porous structure, which provides fast ion and electron transfer, a large surface area, short ion diffusion paths, and a favourable volume change during the cycling process

Simply synthesized TiO2 nanorods as an effective scattering layer for quantum dot sensitized solar cells

International Nuclear Information System (INIS)

Samadpour, Mahmoud; Zad, Azam Iraji; Molaei, Mehdi

2014-01-01

TiO 2 nanorod layers are synthesized by simple chemical oxidation of Ti substrates. Diffuse reflectance spectroscopy measurements show effective light scattering properties originating from nanorods with length scales on the order of one micron. The films are sensitized with CdSe quantum dots (QDs) by successive ionic layer adsorption and reaction (SILAR) and integrated as a photoanode in quantum dot sensitized solar cells (QDSCs). Incorporating nanorods in photoanode structures provided 4- to 8-fold enhancement in light scattering, which leads to a high power conversion efficiency, 3.03% (V oc = 497 mV, J sc = 11.32 mA/cm 2 , FF = 0.54), in optimized structures. High efficiency can be obtained just by tuning the photoanode structure without further treatments, which will make this system a promising nanostructure for efficient quantum dot sensitized solar cells. (condensed matter: electronic structure, electrical, magnetic, and optical properties)

Electrochemically induced transformation of NiS nanoparticles into Ni(OH)2 in KOH aqueous solution toward electrochemical capacitors

International Nuclear Information System (INIS)

Hou Linrui; Yuan Changzhou; Li Diankai; Yang Long; Shen Laifa; Zhang Fang; Zhang Xiaogang

2011-01-01

Highlights: → NiS is synthesized by means of the H 2 O/CS 2 interface under hydrothermal treatment. → NiS itself owns poor electrochemical capacitance in 2 M KOH solution. → NiS is electrochemically induced and transformed into electroactive Ni(OH) 2 . → Ni(OH) 2 is responsible for good energy storage of the NiS in the KOH solution. → The new formed Ni(OH) 2 delivers large energy density at high rates. - Abstract: Nickel sulfide nanoparticles (NPs) are first synthesized by virtue of a unique H 2 O/CS 2 interface under mild hydrothermal treatment. Electrochemical data reveals that the as-synthesized NiS NPs themselves own poor supercapacitive behavior at initial cyclic voltammetry (CV) cycles in 2 M KOH solution, while a specific capacitance of 893 F g -1 can be surprisingly obtained at a current density of 5 A g -1 just after continuous 320 CV cycles. X-ray diffraction and Fourier transform infrared techniques demonstrate that what is really responsible for the good electrochemical capacitance in the KOH aqueous solution is the new electrochemically formed Ni(OH) 2 phase, rather than NiS NPs themselves. The Ni(OH) 2 is slowly formed during the continuous CV cycling process, in which the electrochemically induced phase transformation from NiS to Ni(OH) 2 phase takes place. Furthermore, the new Ni(OH) 2 phase demonstrates the great ability of delivering large specific capacitance at high rates.

Characterization and improved solar light activity of vanadium doped TiO2/diatomite hybrid catalysts

International Nuclear Information System (INIS)

Wang, Bin; Zhang, Guangxin; Leng, Xue; Sun, Zhiming; Zheng, Shuilin

2015-01-01

Highlights: • V-doped TiO 2 /diatomite composite photocatalyst was synthesized. • The physiochemical property and solar light photoactivity were characterized. • The presence and influence of V ions in TiO 2 matrix was systematically analyzed. • The photocatalysis for Rhodamine B were studied under solar light illumination. - Abstract: V-doped TiO 2 /diatomite composite photocatalysts with different vanadium concentrations were synthesized by a modified sol–gel method. The diatomite was responsible for the well dispersion of TiO 2 nanoparticles on the matrix and consequently inhibited the agglomeration. V-TiO 2 /diatomite hybrids showed red shift in TiO 2 absorption edge with enhanced absorption intensity. Most importantly, the dopant energy levels were formed in the TiO 2 bandgap due to V 4+ ions substituted to Ti 4+ sites. The 0.5% V-TiO 2 /diatomite photocatalyst displayed narrower bandgap (2.95 eV) compared to undoped sample (3.13 eV) and other doped samples (3.05 eV) with higher doping concentration. The photocatalytic activities of V doped TiO 2 /diatomite samples for the degradation of Rhodamine B under stimulated solar light illumination were significantly improved compared with the undoped sample. In our case, V 4+ ions incorporated in TiO 2 lattice were responsible for increased visible-light absorption and electron transfer to oxygen molecules adsorbed on the surface of TiO 2 to produce superoxide radicals ·O 2 – , while V 5+ species presented on the surface of TiO 2 particles in the form of V 2 O 5 contributed to e – –h + separation. In addition, due to the combination of diatomite as support, this hybrid photocatalyst could be separated from solution quickly by natural settlement and exhibited good reusability

Electrochemical Characteristics and Li+ Ion Intercalation Kinetics of Dual-phase Li4Ti5O12/Li2TiO3 Composite in Voltage Range of 0−3 V

KAUST Repository

Bhatti, Humaira S

2016-04-20

Li4Ti5O12, Li2TiO3 and dual-phase Li4Ti5O12/Li2TiO3 composite were prepared by sol-gel method with average particle size of 1 µm, 0.3 µm and 0.4 µm, respectively. Though Li2TiO3 is electrochemically inactive, the rate capability of Li4Ti5O12/Li2TiO3 is comparable to Li4Ti5O12 at different current rates. Li4Ti5O12/Li2TiO3 also shows good rate performance of 90 mA h g-1 at high rate of 10 C in voltage range of 1−3 V, attributable to increased interfaces in the composite. While Li4Ti5O12 delivers capacity retention of 88.6 % at 0.2 C over 50 cycles, Li4Ti5O12/Li2TiO3 exhibits no capacity fading at 0.2 C (40 cycles) and capacity retention of 98.45 % at 0.5 C (50 cycles). This highly stable cycling performance is attributed to the contribution of Li2TiO3 in preventing undesirable reaction of Li4Ti5O12 with the electrolyte during cycling. CV curves of Li4Ti5O12/Li2TiO3 in 0−3 V range exhibit two anodic peaks at 1.51 V and 0.7−0.0 V, indicating two modes of lithium intercalation into the lattice sites of active material. Owing to enhanced intercalation/de-intercalation kinetics in 0−3 V, composite electrode delivers superior rate performance of 203 mAh/g at 2.85 C and 140 mAh/g at 5.7 C with good reversible capacity retention over 100 cycles.

Electrochemical Characteristics and Li+ Ion Intercalation Kinetics of Dual-phase Li4Ti5O12/Li2TiO3 Composite in Voltage Range of 0−3 V

KAUST Repository

Bhatti, Humaira S; Anjum, Dalaver H.; Ullah, Shafiq; Ahmed, Bilal; Habib, Amir; Karim, Altaf; Hasanain, Syed Khurshid

2016-01-01

Li4Ti5O12, Li2TiO3 and dual-phase Li4Ti5O12/Li2TiO3 composite were prepared by sol-gel method with average particle size of 1 µm, 0.3 µm and 0.4 µm, respectively. Though Li2TiO3 is electrochemically inactive, the rate capability of Li4Ti5O12/Li2TiO3 is comparable to Li4Ti5O12 at different current rates. Li4Ti5O12/Li2TiO3 also shows good rate performance of 90 mA h g-1 at high rate of 10 C in voltage range of 1−3 V, attributable to increased interfaces in the composite. While Li4Ti5O12 delivers capacity retention of 88.6 % at 0.2 C over 50 cycles, Li4Ti5O12/Li2TiO3 exhibits no capacity fading at 0.2 C (40 cycles) and capacity retention of 98.45 % at 0.5 C (50 cycles). This highly stable cycling performance is attributed to the contribution of Li2TiO3 in preventing undesirable reaction of Li4Ti5O12 with the electrolyte during cycling. CV curves of Li4Ti5O12/Li2TiO3 in 0−3 V range exhibit two anodic peaks at 1.51 V and 0.7−0.0 V, indicating two modes of lithium intercalation into the lattice sites of active material. Owing to enhanced intercalation/de-intercalation kinetics in 0−3 V, composite electrode delivers superior rate performance of 203 mAh/g at 2.85 C and 140 mAh/g at 5.7 C with good reversible capacity retention over 100 cycles.

Modified gas diffusion layer for fuel cells synthesized by pulsed laser ablation

International Nuclear Information System (INIS)

Ebrasu, Daniela; Stefanescu, Ioan; Dorcioman, Gabriela; Serban, Nicolae; Axente, Emil; Sima, Felix; Ristoscu, Carmen; Mihailescu, Ioan N.; Enculescu, Ionut

2010-01-01

Full text; In this paper there are presented the first results regarding the development of a modified gas diffusion layer for fuel cells consisting of a simple or teflonized carbon cloth deposited by pulsed laser with metal oxide nanostructures. These are designed to operate both as co-catalyst, and oxidic support for other electrochemically active catalysts. We selected TiO 2 , ZnO and Al 2 O 3 doped (2 wt.%) ZnO which were uniformly distributed over the surface of gas diffusion layers in order to improve the catalytic activity, stability and lifetime, and reduce the production costs of proton exchange membrane fuel cells. We evidenced by scanning electron microscopy and energy dispersive spectroscopy that our depositions consisted of TiO 2 nanoparticles while in the case of ZnO and Al 2 O 3 doped (2 wt.%) ZnO transparent quasicontinuous films were synthesized. (authors)

High Efficiency Dye-sensitized Solar Cells Constructed with Composites of TiO2 and the Hot-bubbling Synthesized Ultra-Small SnO2 Nanocrystals.

Science.gov (United States)

Mao, Xiaoli; Zhou, Ru; Zhang, Shouwei; Ding, Liping; Wan, Lei; Qin, Shengxian; Chen, Zhesheng; Xu, Jinzhang; Miao, Shiding

2016-01-13

An efficient photo-anode for the dye-sensitized solar cells (DSSCs) should have features of high loading of dye molecules, favorable band alignments and good efficiency in electron transport. Herein, the 3.4 nm-sized SnO2 nanocrystals (NCs) of high crystallinity, synthesized via the hot-bubbling method, were incorporated with the commercial TiO2 (P25) particles to fabricate the photo-anodes. The optimal percentage of the doped SnO2 NCs was found at ~7.5% (SnO2/TiO2, w/w), and the fabricated DSSC delivers a power conversion efficiency up to 6.7%, which is 1.52 times of the P25 based DSSCs. The ultra-small SnO2 NCs offer three benefits, (1) the incorporation of SnO2 NCs enlarges surface areas of the photo-anode films, and higher dye-loading amounts were achieved; (2) the high charge mobility provided by SnO2 was confirmed to accelerate the electron transport, and the photo-electron recombination was suppressed by the highly-crystallized NCs; (3) the conduction band minimum (CBM) of the SnO2 NCs was uplifted due to the quantum size effects, and this was found to alleviate the decrement in the open-circuit voltage. This work highlights great contributions of the SnO2 NCs to the improvement of the photovoltaic performances in the DSSCs.

Photocatalytic properties of P25-doped TiO2 composite film synthesized via sol-gel method on cement substrate.

Science.gov (United States)

Guo, Xiang; Rao, Lei; Wang, Peifang; Wang, Chao; Ao, Yanhui; Jiang, Tao; Wang, Wanzhong

2018-04-01

TiO 2 films have received increasing attention for the removal of organic pollutants via photocatalysis. To develop a simple and effective method for improving the photodegradation efficiency of pollutants in surface water, we herein examined the preparation of a P25-TiO 2 composite film on a cement substrate via a sol-gel method. In this case, Rhodamine B (RhB) was employed as the target organic pollutant. The self-generated TiO 2 film and the P25-TiO 2 composite film were characterized by X-ray diffraction (XRD), N 2 adsorption/desorption measurements, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and diffuse reflectance spectroscopy (DRS). The photodegradation efficiencies of the two films were studied by RhB removal in water under UV (ultraviolet) irradiation. Over 4day exposure, the P25-TiO 2 composite film exhibited higher photocatalytic performance than the self-generated TiO 2 film. The photodegradation rate indicated that the efficiency of the P25-TiO 2 composite film was enhanced by the addition of the rutile phase Degussa P25 powder. As such, cooperation between the anatase TiO 2 and rutile P25 nanoparticles was beneficial for separation of the photo-induced electrons and holes. In addition, the influence of P25 doping on the P25-TiO 2 composite films was evaluated. We found that up to a certain saturation point, increased doping enhanced the photodegradation ability of the composite film. Thus, we herein demonstrated that the doping of P25 powders is a simple but effective strategy to prepare a P25-TiO 2 composite film on a cement substrate, and the resulting film exhibits excellent removal efficiency in the degradation of organic pollutants. Copyright © 2017. Published by Elsevier B.V.

Photocatalytic application of TiO2/SiO2-based magnetic nanocomposite (Fe3O4@SiO2/TiO2 for reusing of textile wastewater

Directory of Open Access Journals (Sweden)

Laleh Enayati Ahangar

2016-01-01

Full Text Available In this research we have developed a treatment method for textile wastewater by TiO2/SiO2-based magnetic nanocomposite. Textile wastewater includes a large variety of dyes and chemicals and needs treatments. This manuscript presents a facile method for removing dyes from the textile wastewater by using TiO2/SiO2-based nanocomposite (Fe3O4@SiO2/TiO2 under UV irradiation. This magnetic nanocomposite, as photocatalytically active composite, is synthesized via solution method in mild conditions. A large range of cationic, anionic and neutral dyes including: methyl orange, methylene blue, neutral red, bromocresol green and methyl red are used for treatment investigations. Neutral red and bromocresol green have good results in reusing treatment. The high surface area of nanocomposites improve the kinetic of wastewater treatment. In this method, by using the magnetic properties of Fe3O4 nanoparticles, TiO2-based photocatalyst could be separated and reused for 3 times. The efficiency of this method is respectively 100% and 65% for low concentration (10 ppm and high concentration (50 ppm of neutral red and bromocrosol green after 3 h treatment. The efficiency of treatment using the second used nanocomposite was 90% for 10 ppm of the same dyes.

TiO2/Pt/TiO2 Sandwich Nanostructures: Towards Alcohol Sensing and UV Irradiation-Assisted Recovery

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Rungroj Maolanon

2017-01-01

Full Text Available The TiO2/Pt/TiO2 sandwich nanostructures were synthesized by RF magnetron sputtering and demonstrated as an alcohol sensor at room-temperature operation with a fast recovery by UV irradiation. The TiO2/Pt/TiO2 layers on SiO2/Si substrate were confirmed by Auger electron spectroscopy with the interdiffusion of each layer. The TiO2/Pt/TiO2 layers on printed circuit board show the superior sensor response to alcohol in terms of the sensitivity and stability compared to the nonsandwich structure, that is, the only Pt layer or the TiO2/Pt structures. Moreover, the recovery time of the TiO2/Pt/TiO2 was improved by UV irradiation-assisted recovery. The optimum TiO2/Pt/TiO2 with thicknesses of the undermost TiO2 layer, a Pt layer, and the topmost TiO2 layer being 50 nm, 6 nm, and 5 nm, respectively, showed the highest response to ethanol down to 10 ppm. Additionally, TiO2/Pt/TiO2 shows an excellent sensing stability and exhibits different sensing selectivity among ethanol, methanol, and 2-propanol. The sensing mechanism could be attributed to the change of Pt work function during vapor adsorption. The TiO2 layer plays an important role in UV-assisted recovery by photocatalytic activity and the topmost TiO2 acts as protective layer for Pt.

Preparation of flexible TiO2 photoelectrodes for dye-sensitized solar cells

Science.gov (United States)

Li, Wen-Ren; Wang, Hsiu-Hsuan; Lin, Chia-Feng; Su, Chaochin

2014-09-01

Dye-sensitized solar cells (DSSCs) based on nanocrystalline TiO2 photoelectrodes on indium tin oxide (ITO) coated polymer substrates have drawn great attention due to its lightweight, flexibility and advantages in commercial applications. However, the thermal instability of polymer substrates limits the process temperature to below 150 °C. In order to assure high and firm interparticle connection between TiO2 nanocrystals (TiO2-NC) and polymer substrates, the post-treatment of flexible TiO2 photoelectrodes (F-TiO2-PE) by mechanical compression was employed. In this work, Degussa P25 TiO2-NC was mixed with tert-butyl alcohol and DI-water to form TiO2 paste. F-TiO2-PE was then prepared by coating the TiO2 paste onto ITO coated polyethylene terephthalate (PET) substrate using doctor blade followed by low temperature sintering at 120 °C for 2 hours. To study the effect of mechanical compression, we applied 50 and 100 kg/cm2 pressure on TiO2/PET to complete the fabrication of F-TiO2-PE. The surface morphology of F-TiO2-PE was characterized using scanning electron microscopy. The resultant F-TiO2-PE sample exhibited a smooth, crack-free structure indicating the great improvement in the interparticle connection of TiO2-NC. Increase of compression pressure could lead to the increase of DSSC photoconversion efficiency. The best photoconversion efficiency of 4.19 % (open circuit voltage (Voc) = 0.79 V, short-circuit photocurrent density (Jsc) = 7.75 mA/cm2, fill factor (FF) = 0.68) was obtained for the F-TiO2-PE device, which showed great enhancement compared with the F-TiO2-PE cell without compression treatment. The effect of compression in DSSC performance was vindicated by the electrochemical impedance spectroscopy measurement.

Studies on Nano-Engineered TiO2 Photo Catalyst for Effective Degradation of Dye

Science.gov (United States)

Sowmya, S. R.; Madhu, G. M.; Hashir, Mohammed

2018-02-01

All Heterogeneous photo catalysis employing efficient photo-catalyst is the advanced dye degradation technology for the purification of textile effluent. The present work focuses on Congo red dye degradation employing synthesized Ag doped TiO2 nanoparticles as photocatalyst which is characterized using SEM, XRD and FTIR. Studies are conducted to study the effect of various parameters such as initial dye concentration, catalyst loading and pH of solution. Ag Doped TiO2 photocatalyst improve the efficacy of TiO2 by reducing high band gap and electron hole recombination of TiO2. The reaction kinetics is analyzed and the process is found to follow pseudo first order kinetics.

CdS-sensitized TiO2 nanocorals: hydrothermal synthesis, characterization, application.

Science.gov (United States)

Mali, S S; Desai, S K; Dalavi, D S; Betty, C A; Bhosale, P N; Patil, P S

2011-10-01

Cadmium sulfide (CdS) nanoparticle-sensitized titanium oxide nanocorals (TNC) were synthesized using a two-step deposition process. The TiO(2) nanocorals were grown on the conducting glass substrates (FTO) using A hydrothermal process and CdS nanoparticles were loaded on TNC using successive ionic layer adsorption and reaction (SILAR) method. The TiO(2), CdS and TiO(2)-CdS samples were characterized by optical absorption, X-ray diffraction (XRD), FT-Raman, FT-IR, scanning electron microscopy (SEM) and contact angle. Further, their photoelectrochemical (PEC) performance was tested in NaOH, Na(2)S-NaOH-S and Na(2)S electrolytes, respectively. When CdS nanoparticles are coated on TNCs, the optical absorption is found to be enhanced and band edge is red-shifted towards visible region. The TiO(2)-CdS sample exhibits improved photoelectrochemical (PEC) performance with maximum short circuit current of (J(sc)) 1.04 mA cm(-2). After applying these TiO(2)-CdS electrodes in photovoltaic cells, the photocurrent was found to be enhanced by 2.7 and 32.5 times, as compared with those of bare CdS and TiO(2) nanocorals films electrodes respectively. Also, the power conversion efficiency of TiO(2)-CdS electrodes is 0.72%, which is enhanced by about 16 and 29 times for TiO(2), CdS samples. This journal is © The Royal Society of Chemistry and Owner Societies 2011

Development of high efficient visible light-driven N, S-codoped TiO2 nanowires photocatalysts

Science.gov (United States)

Zhang, Yanlin; Liu, Peihong; Wu, Honghai

2015-02-01

One-dimensional (1D) nanowire material (especially nonmetal doped 1D nanowires) synthesized by a facile way is of great significance and greatly desired as it has higher charge carrier mobility and lower carrier recombination rate. N, S-codoped TiO2 nanowires were synthesized using titanium sulfate as a precursor and isopropanol as a protective capping agent by a hydrothermal route. The obtained doped nanowires were characterized by XRD, SEM, HRTEM, SAED, XPS, BET and UV-vis absorption spectrum. The incorporation of N and S into TiO2 NWs can lead to the expansion of its lattice and remarkably lower its electron-transfer resistance. Photocatalytic activity measurement showed that the N, S-codoped TiO2 nanowires with high quantum efficiency revealed the best photocatalytic performance for atrazine degradation under visible light irradiation compared to N, S-codoped TiO2 nanoparticles and S-doped TiO2 nanowires, which was attributed to (i) the synergistic effect of N and S doping in narrowing the band gap, separating electron-hole pairs and increasing the photoinduced electrons, and (ii) extending the anatase-to-rutile transformation temperature above 600 °C.

Effects of Homogenization Scheme of TiO2 Screen-Printing Paste for Dye-Sensitized Solar Cells

Directory of Open Access Journals (Sweden)

Seigo Ito

2012-01-01

Full Text Available TiO2 porous electrodes have been fabricated for photoelectrodes in dye-sensitized solar cells (DSCs using TiO2 screen-printing paste from nanocrystalline TiO2 powder dried from the synthesized sol. We prepared the TiO2 screen-printing paste by two different methods to disperse the nanocrystalline TiO2 powder: a “ball-milling route” and a “mortal-grinding route.” The TiO2 ball-milling (TiO2-BM route gave monodisperse TiO2 nanoparticles, resulting in high photocurrent density (14.2 mA cm−2 and high photoconversion efficiency (8.27%. On the other hand, the TiO2 mortal-grinding (TiO2-MG route gave large aggregate of TiO2 nanoparticles, resulting in low photocurrent density (11.5 mA cm−2 and low photoconversion efficiency (6.43%. To analyze the photovoltaic characteristics, we measured the incident photon-to-current efficiency, light absorption spectroscopy, and electrical impedance spectroscopy of DSCs.

Highly stable colloidal TiO2 nanocrystals with strong violet-blue emission

International Nuclear Information System (INIS)

Ghamsari, Morteza Sasani; Gaeeni, Mohammad Reza; Han, Wooje; Park, Hyung-Ho

2016-01-01

Improved sol–gel method has been applied to prepare highly stable colloidal TiO 2 nanocrystals. The synthesized titania nanocrystals exhibit strong emission in the violet-blue wavelength region. Very long evolution time was obtained by preventing the sol to gel conversion with reflux process. FTIR, XRD, UV–vis absorption, photoluminescence and high resolution transmission electron microscope (HRTEM) were used to study the optical properties, crystalline phase, morphology, shape and size of prepared TiO 2 colloidal nanocrystals. HRTEM showed that the diameter of TiO 2 colloidal nanocrystals is about 5 nm. Although the PL spectra show similar spectral features upon excitation wavelengths at 280, 300 and 350 nm, but their emission intensities are significantly different from each other. Photoluminescence quantum yield for TiO 2 colloidal nanocrystals is estimated to be 49% with 280 nm excitation wavelength which is in agreement and better than reported before. Obtained results confirm that the prepared colloidal TiO 2 sample has enough potential for optoelectronics applications.

Bioactivity studies on TiO2-bearing Na2O–CaO–SiO2–B2O3 glasses

International Nuclear Information System (INIS)

Jagan Mohini, G.; Sahaya Baskaran, G.; Ravi Kumar, V.; Piasecki, M.; Veeraiah, N.

2015-01-01

Soda lime silica borate glasses mixed with different concentrations of TiO 2 are synthesized by the melt-quenching technique. As a part of study on bioactivity of these glasses, the samples were immersed in simulated body fluid (SBF) solution for prolonged times (~ 21 days) during which weight loss along with pH measurements is carried out at specific intervals of time. The XRD and SEM analyses of post-immersed samples confirm the formation of crystalline hydroxyapatite layer (HA) on the surface of the samples. To assess the role of TiO 2 on the formation of HA layer and degradability of the samples the spectroscopic studies viz. optical absorption and IR spectral studies on post- and pre-immersed samples have been carried out. The analysis of the results of degradability together with spectroscopic studies as a function of TiO 2 concentration indicated that about 6.0 mol% of TiO 2 is the optimal concentration for achieving better bioactivity of these glasses. The presence of the maximal concentration octahedral titanium ions in this glass that facilitates the formation of HA layer is found to be the reason for such a higher bioactivity. - Highlights: • Soda lime silica borate glasses mixed with TiO 2 are synthesized. • Bioactivity of the glasses is studied by immersing them in SBF solution. • XRD and SEM studies indicated the formation of hydroxyapatite layer on the surface. • Quantum of degradability is the highest in the glasses mixed with 6.0 mol% of TiO 2. • The results are analyzed using IR and optical absorption studies

Comparing the photocatalytic activity of TiO2 at macro- and microscopic scales

DEFF Research Database (Denmark)

Torras-Rosell, Antoni; Johannsen, Sabrina Rostgaard; Dirscherl, Kai

2016-01-01

. The photocatalytic properties of TiO2 at macro- and microscopic scales are investigated by comparing photocatalytic degradation of acetone and electrochemical experiments to Kelvin probe force microscopy. The good agreement between the macro- and microscopic experiments suggests that Kelvin probe force microscopy...

Titanium dioxide@polypyrrole core-shell nanowires for all solid-state flexible supercapacitors

Science.gov (United States)

Yu, Minghao; Zeng, Yinxiang; Zhang, Chong; Lu, Xihong; Zeng, Chenghui; Yao, Chenzhong; Yang, Yangyi; Tong, Yexiang

2013-10-01

Herein, we developed a facile two-step process to synthesize TiO2@PPy core-shell nanowires (NWs) on carbon cloth and reported their improved electrochemical performance for flexible supercapacitors (SCs). The fabricated solid-state SC device based on TiO2@PPy core-shell NWs not only has excellent flexibility, but also exhibits remarkable electrochemical performance.Herein, we developed a facile two-step process to synthesize TiO2@PPy core-shell nanowires (NWs) on carbon cloth and reported their improved electrochemical performance for flexible supercapacitors (SCs). The fabricated solid-state SC device based on TiO2@PPy core-shell NWs not only has excellent flexibility, but also exhibits remarkable electrochemical performance. Electronic supplementary information (ESI) available: Experimental details, XRD pattern, FT-IR absorption spectrum and CV curves of TiO2@PPy NWs, and SEM images of the PPy. See DOI: 10.1039/c3nr03578f

Electrochemical Performance of LixMn2-yFeyO4-zClz Synthesized Through In-Situ Glycine Nitrate Combustion

Science.gov (United States)

2016-06-13

Electrochemical Performance of LixMn2-yFeyO4-zClz Synthesized Through In-Situ Glycine Nitrate Combustion Ashley L. Ruth, Paula C. Latorre, and...sites as well as the formation of Mn3+ ions via the Jahn- Teller effect. The use of the glycine nitrate combustion synthesis produces small particles at...advantage of submicron ceramic synthesis, namely the glycine nitrate combustion process (GNP), we propose the capability for in-situ B-site doping

Structural phase analysis and photoluminescence properties of Mg-doped TiO2 nanoparticles

Science.gov (United States)

Ali, T.; Ashraf, M. Anas; Ali, S. Asad; Ahmed, Ateeq; Tripathi, P.

2018-05-01

In this paper, we report the synthesis, characterization and photoluminescence properties of Mg-doped TiO2 nanoparticles (NPs). The samples were synthesized by sol-gel method and characterized using the standard analytical techniques such as X-ray diffraction (XRD), Transmission electron microscope (TEM), Energy dispersive X-ray spectroscopy (EDX), UV-visible and photoluminescence spectroscopy. The powder XRD spectra revealed that the synthesized samples are pure and crystalline in nature and showing tetragonal anatase phase of TiO2 NPs. UV-visible spectrum illustrates that an absorption edge shifts toward the visible region. This study may provide a new insight for making the nanomaterials which can be used in photocatalytic applications.

Hierarchical carambola-like Li4Ti5O12-TiO2 composites as advanced anode materials for lithium-ion batteries

International Nuclear Information System (INIS)

Zhang, Yu; Zhang, Yun; Huang, Ling; Zhou, Zhongfu; Wang, Jingfeng; Liu, Heng; Wu, Hao

2016-01-01

Hierarchically structured Li 4 Ti 5 O 12 -TiO 2 (LTO-TiO 2 ) composites are synthesized using a facile hydrothermal approach upon reaction time control. With control over the time of hydrothermal reaction at 18 h, a hierarchical dual-phase LTO-TiO 2 composite with appropriate amount of anatase TiO 2 can be obtained, and it possesses a uniform carambola-like framework assembled by numerous ultrathin nanosheets, which enable a relatively large specific surface area, along with abundant interlayer channels to favor electrolyte penetration. When used as anode materials for lithium-ion batteries, such carambola-like LTO-TiO 2 composite exhibits remarkably improved capacity, high-rate capability, and cycling stability over other LTO-TiO 2 samples, which are synthesized at different time of hydrothermal reaction. Specifically, it deliveries a discharge capacity as high as 115.1 and 91.2 mAh g −1 at a very high current rate of 20 and 40C, respectively, while a stable reversible capacity of 171.7 mAh g −1 can be retained after 200 charge-discharge cycles at 1C, corresponding to 88.6% capacity retention. The excellent electrochemical performances benefit from the unique hierarchical carambola-like structure together with the mutually complementary intrinsic advantages between LTO and TiO 2 . The robust and porous nanosheets-assembled LTO-TiO 2 framework not only offers a shorter transport pathway for electron and Li-ion migration within this composite material, but also is able to alleviate the structure distortion during the fast Li-ion insertion/extraction process. The work described here shows that the hierarchical carambola-like LTO-TiO 2 composite is a promising anode material for high-power and long-life lithium-ion batteries.

The Influence of NiO Addition in TiO2 Structure and Its Photoactivity

Science.gov (United States)

Wahyuningsih, S.; Ramelan, A. H.; Purwanti, P. D.; Munawaroh, H.; Ichsan, S.; Kristiawan, Y. R.

2018-03-01

The synthesis of TiO2 together with the TiO2-NiO composite using various annealing temperatures has been studied. The synthesis of TiO2 was performed by sol gel method using Titanium Tetra Isopropoxide (TTIP) precursor, whereas the synthesis of TiO2-NiO composite was done by wet impregnation method using NiNO3.6H2O precursor. This study aims to determine the influence of NiO addition in its structure and photoactivity. The diffraction of synthesized TiO2 at 400 °C temperature shows anatase TiO2 peak at 2θ = 25.35 °. The addition of NiO dopant to the synthesis of TiO2 process is carried out by annealing at 300 °C, 400 °C, 500 °C, 600 °C, and 700 °C, respectively. The TiO2-NiO composite has been prepared and shows the diffraction peak of NiO at 2θ=43° about 33.08 to 36.68%. The optimum result of Rhodamine B photodegradation with TiO2 was 43.15%, while the optimum result of Rhodamine B degradation with TiO2-NiO composite was 92.85%.

Photocatalytic Decolorization Study of Methyl Orange by TiO2–Chitosan Nanocomposites

Directory of Open Access Journals (Sweden)

Imelda Fajriati

2014-10-01

Full Text Available The photocatalytic decolorization of methyl orange (MO by TiO2-chitosan nanocomposite has been studied. This study was started by synthesizing TiO2-chitosan nanocomposites using sol-gel method with various concentrations of Titanium(IV isopropoxide (TTIP as the TiO2 precursor. The structure, surface morphology, thermal and optical property of TiO2-chitosan nanocomposite were characterized by X-ray diffraction (XRD, fourier transform infra red (FTIR spectroscopy, scanning electron microscopy (SEM, thermogravimetric analysis (TGA, and diffuse reflectance ultra violet (DRUV spectroscopy. The photocatalytic activity of TiO2-chitosan nanocomposite was evaluated by photocatalytic decolorization of methyl orange as a model pollutant. The results indicate that the particle size of TiO2 increases with increasing ofthe concentration of TTIP, in which TiO2 with smallest particle size exhibit the highest photocatalytic activity. The highest photocatalytic decolorization was obtained at 5 h of contact time, initial concentration of MO at 20 ppm and at solution pH of 4. Using these conditions, over 90% of MO was able to be decolorized using 0.02 g of TiO2-chitosan nanocomposite under UV light irradiation. The TiO2-chitosan nanocomposite could be reused, which meant that the TiO2-chitosan nanocomposites can be developed as an effective and economical photocatalyst to decolorize or treat dye in wastewater.

The Effect of Calcination Temperature on the Performance of TiO2 Aggregates-based Dye Solar Cells (DSCs)

International Nuclear Information System (INIS)

Siti Nur Azella Zaine; Norani Muti Mohamed; Mohamad Azmi Bustam

2011-01-01

In this paper, the effect of calcination temperature on the physicochemical properties of synthesized TiO 2 aggregates and their influence on overall light conversion efficiency of dye solar cell (DSc) were investigated. Samples of TiO 2 aggregates (mean size of 0.45 μm) composing of nano crystallites (10-40 nm) were synthesized through hydrolysis of dilute titanium alkoxide in ethanol. Phase and microstructure of the TiO 2 obtained have been characterized using FESEM, XRD and UV-Vis spectroscopy. I-V characterization shows that TiO 2 aggregates based DSC demonstrated better performance compared to nanoparticles (P-25)-based DSC. The optimum calcination temperature was found to be about 500 degree Celsius with efficiency of 4.456 %, which is 30 % increment compared to P-25-based DSC under the same condition. (author)

Electrochemically Active Biofilms Assisted Nanomaterial Synthesis for Environmental Applications

KAUST Repository

Ahmed, Elaf

2017-12-01

Nanomaterials have a great potential for environmental applications due to their high surface areas and high reactivity. This dissertation investigated the use of electrochemically active biofilms (EABs) as a synthesis approach for the fabrication and environmental applications of different nanomaterials. Bacteria in EABs generate electrons upon consuming electron donor and have the ability to transport these electrons to solid or insoluble substrates through extracellular electron transport (EET) mechanism. The extracellularly transported electrons, once utilized, can lead to nanoparticle synthesis. In this dissertation, noble metal (i.e., Au, Pd, and Pt) ultra-small nanoparticles (USNPs) were first synthesized with the assistance by the EABs. The assynthesized USNPs had a size range between 2 and 7 nm and exhibited excellent catalytic performance in dye decomposition. Also in this research, a two-dimensional (2D) cobalt nanosheet was successfully synthesized in the presence of EABs. A simple biogenic route led to the transformation of cobalt acetate to produce a green, toxic free homogeneous 2D cobalt nanosheet structure. Further, TiO2 nanotubes were successfully combined with the noble metal USNPs to enhance their photocatalytic activity. In this work, for the first time, the noble metal USNPs were directly reduced and decorated on the internal surfaces of the TiO2 nanotubes structure assisted by the EABs. The USNPs modified TiO2 nanotubes generated significantly improved photoelectrocatatlyic performances. This dissertation shines lights on the use of EABs in ultra-small nanoparticle synthesis.

Facile preparation of a TiO2 quantum dot/graphitic carbon nitride heterojunction with highly efficient photocatalytic activity

Science.gov (United States)

Wang, Xing; Jiang, Subin; Huo, Xuejian; Xia, Rui; Muhire, Elisée; Gao, Meizhen

2018-05-01

In this article, mechanical grinding, an effortless and super-effective synthetic strategy, is used to successfully synthesize a TiO2 quantum dot (TiO2QD)/graphitic carbon nitride (g-C3N4) heterostructure. X-ray photoelectron spectroscopy results together with transmission electron microscopy reveal the formation of the TiO2QD/g-C3N4 heterostructure with strong interfacial interaction. Because of the advantages of this characteristic, the prepared heterostructure exhibits excellent properties for photocatalytic wastewater treatment. Notably, the optimum photocatalytic activity of the TiO2QD/g-C3N4 heterostructure is nearly 3.4 times higher than that of the g-C3N4 nanosheets used for the photodegradation of rhodamine B pollutant. In addition, the stability and possible degradation mechanism of the TiO2QD/g-C3N4 heterojunction are studied in detail. This method may stimulate an effective approach to synthesizing QD-sensitized semiconductor materials and facilitate their application in environmental protection.

Effect of zinc doping on the bandgap and photoluminescence of Zn2+-doped TiO2 nanowires

Science.gov (United States)

Loan, Trinh Thi; Huong, Vu Hoang; Tham, Vu Thi; Long, Nguyen Ngoc

2018-03-01

This study was focused on the effect of Zn2+ dopant concentration on the absorption edge and photoluminescence of anatase TiO2 nanowires synthesized by hydrothermal technique. For the undoped anatase TiO2 nanowires, the indirect band gap of 3.26 eV and the direct band gap of 3.58 eV are assigned to the indirect Γ3 → X1b and direct X2b → X1b transitions, respectively. The Zn2+-doping makes the absorption edge of TiO2:Zn2+ nanowires shift towards the lower energy side (red shift). On the other hand, the replacing Ti4+ ions with Zn2+ ions creates oxygen vacancies (VO) and shallow defects associated with VO. Just these defects are responsible for the enhanced luminescence of Zn2+-doped TiO2 nanowires.

Synthesis of TiO2 nanorod-decorated graphene sheets and their highly efficient photocatalytic activities under visible-light irradiation

International Nuclear Information System (INIS)

Lee, Eunwoo; Hong, Jin-Yong; Kang, Haeyoung; Jang, Jyongsik

2012-01-01

Highlights: ► TiO 2 nanorods were successfully decorated on the surface of graphene sheets. ► Population of TiO 2 nanorods can be controlled by changing experimental conditions. ► TiO 2 nanorod-decorated graphene sheets have an expanded light absorption range. ► TiO 2 nanorod-decorated graphene sheets showed unprecedented photocatalytic activity. - Abstract: The titanium dioxide (TiO 2 ) nanorod-decorated graphene sheets photocatalysts with different TiO 2 nanorods population have been synthesized by a simple non-hydrolytic sol–gel approach. Electron microscopy and X-ray diffraction analysis indicated that the TiO 2 nanorods are well-dispersed and successfully anchored on the graphene sheet surface through the formation of covalent bonds between Ti and C atoms. The photocatalytic activities are evaluated in terms of the efficiencies of photodecomposition and adsorption of methylene blue (MB) in aqueous solution under visible-light irradiation. The as-synthesized TiO 2 nanorod-decorated graphene sheets showed unprecedented photodecomposition efficiency compared to the pristine TiO 2 nanorods and the commercial TiO 2 (P-25, Degussa) under visible-light. It is believed that this predominant photocatalytic activity is due to the synergistic contribution of both a retarded charge recombination rate caused by a high electronic mobility of graphene and an increased surface area originated from nanometer-sized TiO 2 nanorods. Furthermore, photoelectrochemical study is performed to give deep insights into the primary roles of graphene that determines the photocatalytic activity.

Nanoporous MnO{sub x} thin-film electrodes synthesized by electrochemical lithiation/delithiation for supercapacitors

Energy Technology Data Exchange (ETDEWEB)

Xia, Hui; Lai, Man On; Lu, Li [Department of Mechanical Engineering, National University of Singapore, 9 Engineering Drive 1, Singapore 117576 (Singapore)

2011-02-15

Nanoporous MnO{sub x} thin-film electrodes are synthesized using a combination of pulsed laser deposition (PLD) and electrochemical lithiation/delithiation methods. A dense Mn{sub 3}O{sub 4} thin-film deposited by PLD can transform into a nanoporous MnO{sub x} thin-film after electrochemical lithiation/delithiation. A nanoporous MnO{sub x} thin-film electrode exhibits significantly improved supercapacitive performance compared with an as-deposited Mn{sub 3}O{sub 4} thin-film electrode. A MnO{sub x} thin-film finally transforms into a MnO{sub 2} thin-film through an electrochemical oxidation process during continuous cyclic voltammetry scanning. (author)

Fabrication and characterization of mesoporous TiO2/polypyrrole-based nanocomposite for electrorheological fluid

International Nuclear Information System (INIS)

Wei Chuan; Zhu Yihua; Jin Yi; Yang Xiaoling; Li Chunzhong

2008-01-01

Mesoporous TiO 2 /polypyrrole (PPy)-based nanocomposite for electrorheological fluid was synthesized through one-pot method. By exploiting the combination conductivity of PPy and high dielectric constant of TiO 2 , the ER fluid exhibited an enhanced effect. The shear stress was 3.3 times as high as that of mesoporous TiO 2 . Powder X-ray diffraction (XRD), TEM and Fourier transform infrared (FT-IR) spectroscopy were employed to characterize the as-made samples. Using a modified rotational viscometer, the electrorheological effect was measured. Dielectric spectra were also given to explain the mechanism

TiO2 Deposition on AZ31 Magnesium Alloy Using Plasma Electrolytic Oxidation

Directory of Open Access Journals (Sweden)

Leon White

2013-01-01

Full Text Available Plasma electrolytic oxidation (PEO has been used in the past as a useful surface treatment technique to improve the anticorrosion properties of Mg alloys by forming protective layer. Coatings were prepared on AZ31 magnesium alloy in phosphate electrolyte with the addition of TiO2 nanoparticles using plasma electrolytic oxidation (PEO. This present work focuses on developing a TiO2 functional coating to create a novel electrophotocatalyst while observing the surface morphology, structure, composition, and corrosion resistance of the PEO coating. Microstructural characterization of the coating was investigated by X-ray diffraction (XRD and scanning electron microscopy (SEM followed by image analysis and energy dispersive spectroscopy (EDX. The corrosion resistance of the PEO treated samples was evaluated with electrochemical impedance spectroscopy (EIS and DC polarization tests in 3.5 wt.% NaCl. The XRD pattern shows that the components of the oxide film include Mg from the substrate as well as MgO and Mg2TiO4 due to the TiO2 nanoparticle addition. The results show that the PEO coating with TiO2 nanoparticles did improve the corrosion resistance when compared to the AZ31 substrate alloy.

The Effects of Leaching Process to the TiO2 Synthesis from Bangka Ilmenite

Science.gov (United States)

Wahyuningsih, S.; Ramelan, A. H.; Pramono, E.; Argawan, P.; Djatisulistya, A.; Firdiyono, F.; Sulistiyono, E.; Sari, P. P.

2018-03-01

Ilmenite mineral is a naturally occurring iron titanate (FeTiO3) and is abundant in nature. The separation of components into TiO2 and Fe2O3 must be expand. The purpose of this research is to synthesis TiO2 nanoparticles from the filtrate of Bangka ilmenite leaching process. Leaching of ilmenite was done with H2SO4 and HCl at various concentrations. The formation of TiO2 crystal determined by hydrolysis conditions and condensation reaction. TiO2 synthesized from the filtrate of sulfuric acid leaching that produced from TiO2 anatase phase when hydrolyzed in an aquaregia solvent and low concentrations of HCl (0.1M). Hydrolysis conditions at higher concentrations of HCl (1M) was produced TiO2 anatase-rutile phase. The synthesis of TiO2 from the filtrate of hydrochloric acid leaching was produced anatase phase. While the condition under the alcoholic solvent (2-propanol: H2O (v/v) = 9: 1) anatase phase crystallites grow in the temperature range up to 550 °C, above this temperature, TiO2 transform into rutile phase.

Low-temperature preparation and microwave photocatalytic activity study of TiO2-mounted activated carbon

International Nuclear Information System (INIS)

Liu Yazi; Yang Shaogui; Hong Jun; Sun Cheng

2007-01-01

TiO 2 thin films were deposited on granular activated carbon by a dip-coating method at low temperature (373 K), using microwave radiation to enhance the crystallization of titania nanoparticles. Uniform and continuous anatase titania films were deposited on the surface of activated carbon. BET surface area of TiO 2 -mounted activated carbon (TiO 2 /AC) decreased a little in comparison with activated carbon. TiO 2 /AC possessed strong optical absorption capacity with a band gap absorption edge around 360 nm. The photocatalytic activity did not increase when the as-synthesized TiO 2 /AC was thermally treated, but was much higher than commercial P-25 in degradation of phenol by irradiation of electrodeless discharge lamps (EDLs)

Flexible all-solid-state high-performance supercapacitor based on electrochemically synthesized carbon quantum dots/polypyrrole composite electrode

International Nuclear Information System (INIS)

Jian, Xuan; Yang, Hui-min; Li, Jia-gang; Zhang, Er-hui; Cao, Le-le; Liang, Zhen-hai

2017-01-01

Highlights: • Porous nanostructure carbon quantum dots/polypyrrole composite film was successfully synthesized by direct electrochemical method. • A flexible all-solid-state supercapacitor device was fabricated using the carbon quantum dots/polypyrrole composite electrode. • The flexible supercapacitor exhibits high specific capacitance, excellent reliability and long cycling life. - Abstract: Recently, carbon quantum dots (CQDs) as a new zero-dimensional carbon nanomaterial have become a focus in electrochemical energy storage. In this paper, flexible all-solid-state supercapacitors (ASSSs) were electrochemically synthesized by on-step co-deposition of appropriate amounts of pyrrole monomer and CQDs in aqueous solution. The different electrodeposition time plays an important role in controlling morphologies of stainless steel wire meshes (SSWM)-supported CQDs/PPy composite film. The morphologies and compositions of the obtained CQDs/PPy composite electrodes were characterized by scanning electron microscope (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), Raman spectrum and X-ray photoelectron spectroscopy (XPS). Furthermore, a novel flexible ASSS device was fabricated using CQDs/PPy composite as the electrode and separated by polyvinyl alcohol/LiCl gel electrolyte. Benefiting from superior electrochemical properties of CQDs and PPy, the as-prepared CQDs/PPy composite ASSSs exhibit outstanding electrochemical performance with the areal capacitance 315 mF cm −2 (corresponding to specific capacitance of 308 F g −1 ) at a current density of 0.2 mA cm −2 and long cycle life with 85.7% capacitance retention after 2 000 cycles.

Self-Assembly of TiO2/CdS Mesoporous Microspheres with Enhanced Photocatalytic Activity via Hydrothermal Method

Directory of Open Access Journals (Sweden)

Sujing Yu

2014-01-01

Full Text Available Self assembly of TiO2/CdS mesoporous microspheres was synthesized via hydrothermal method. The samples were characterized by X-ray powder diffraction (XRD, ultraviolet-visible diffuse reflectance spectroscopy (DRS, transmission electron microscopy (TEM, energy-dispersive spectroscopy analysis (EDS, high-resolution transmission electron microscopy (HRTEM, Brunauer-Emmett-Teller (BET, X-ray photoelectron spectroscopy (XPS, and photoluminescence spectra (PL. The as-synthesized TiO2/CdS mesoporous microspheres showed superior photocatalytic activity for the degradation of RhB under either visible light or simulated sunlight irradiation; the 10 wt% TiO2/CdS sample showed the best performance. Moreover, this catalyst showed improved stability, and the activity did not decrease significantly after four recycles. The heterojunction between TiO2 and CdS may be favorable for the transport of photoinduced electrons from CdS to TiO2. In addition, the mesoporous structure could increase the utilization of light energy and facilitate the diffusion of reactants and products during the photocatalytic reaction.

Dependence of Photocatalytic Activity of TiO2-SiO2 Nanopowders

Directory of Open Access Journals (Sweden)

M. Riazian

2014-10-01

Full Text Available Structural properties and chemical composition change the photocatalytic activity in TiO2-SiO2 nanopowder composite. The SiO2-TiO2 nanostructure is synthesized based on sol–gel method. The nanoparticles are characterized by x-ray fluorescents (XRF, x- ray diffraction (XRD, tunneling electron microscopy (TEM, field emission scanning electron microscopy (FE-SEM, UV-vis. Spectrophotometer and furrier transmission create infrared absorption (FTIR techniques. The rate constant k for the degradation of methylen blue in its aqueous solution under UV irradiation is determined as a measure of photocatalytic activity. Dependence between photocatalytic activity and SiO2 content in the composite is determined. Rate constant k is found dependent on the content of SiO2 in the composite that calcined at 900 oC. The addition of low composition SiO2 to the TiO2 matrix (lower than 45% enhances the photocatalytic activity due to thermal stability and increasing in the surface area. The effects of chemical compositions on the surface topography and the crystallization of phases are studied.

Optimization of charge transfer and transport processes at the CdSe quantum dots/TiO2 nanorod interface by TiO2 interlayer passivation

International Nuclear Information System (INIS)

Jaramillo-Quintero, O A; Rincon, M E; Triana, M A

2017-01-01

Surface trap states hinder charge transfer and transport properties in TiO 2 nanorods (NRs), limiting its application on optoelectronic devices. Here, we study the interfacial processes between rutile TiO 2 NR and CdSe quantum dots (QDs) using TiO 2 interlayer passivation treatments. Anatase or rutile TiO 2 thin layers were deposited on an NR surface by two wet-chemical deposition treatments. Reduced interfacial charge recombination between NRs and CdSe QDs was observed by electrochemical impedance spectroscopy with the introduction of TiO 2 thin film interlayers compared to bare TiO 2 NRs. These results can be ascribed to in-gap trap state passivation of the TiO 2 NR surface, which led to an increase in open circuit voltage. Moreover, the rutile thin layer was more efficient than anatase to promote a higher photo-excited electron transfer from CdSe QDs to TiO 2 NRs due to a large driving force for charge injection, as confirmed by surface photovoltage spectroscopy. (paper)

Lithium ion conducting PVA:PVdF polymer electrolytes doped with nano SiO2 and TiO2 filler