scholarly journals Preparation of Fluorine-DopedTiO2Photocatalysts with Controlled Crystalline Structure

2008 ◽  
Vol 2008 ◽  
pp. 1-9 ◽  
Author(s):  
N. Todorova ◽  
T. Giannakopoulou ◽  
G. Romanos ◽  
T. Vaimakis ◽  
Jiaguo Yu ◽  
...  

Nanocrystalline F-dopedTiO2powders were prepared by sol-gel route. The thermal behavior of the powders was recorded by DTA/TG technique. The crystalline phase of the fluorinatedTiO2powders was determined by X-ray diffraction technique. It was demonstrated that F-doping usingCF3COOH favors the formation of rutile along with anatase phase even at low temperature. Moreover, the rutile's phase content increases with the increase of the quantity of the fluorine precursor in the starting solution. The surface area of the powders and the pore size distribution were studied byN2adsorption-desorption using BET and BJH methods. X-ray photoelectron spectroscopy (XPS) revealed that the fluorine is presented in theTiO2powders mainly as metal fluoride in quantities∼16 at %. The F-dopedTiO2showed a red-shift absorption in UV-vis region which was attributed to the increased content of rutile phase in the powders. The powders exhibited enhanced photocatalytic activity in decomposition of acetone.

2021 ◽  
Vol 11 (5) ◽  
pp. 706-716
Author(s):  
Nada D. Al-Khthami ◽  
Tariq Altalhi ◽  
Mohammed Alsawat ◽  
Mohamed S. Amin ◽  
Yousef G. Alghamdi ◽  
...  

Different organic pollutants have been remediated photo catalytically by applying perovskite photocatalysts. Atrazine (ATR) is a pesticide commonly detected as a pollutant in drinking, surface and ground water. Herein, FeYO3@rGO heterojunction was synthesized and applied for photooxidation decomposition of ATR. First, FeYO 3nanoparticles (NPs) were prepared via routine sol-gel. After that, FeYO3 NPs were successfully incorporated with different percentages (5, 10, 15 and 20 wt.%) of reduced graphene oxide (rGO) in the synthesis of novel FeYO3@rGO photocatalyst. Morphological, structural, surface, optoelectrical and optical characteristics of constructed materials were identified via X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Transmission electron microscopy (TEM), adsorption/desorption isotherms, diffusive reflectance (DR) spectra, and photoluminescence response (PL). Furthermore, photocatalytic achievement of the constructed materials was evaluated via photooxidative degradation of ATR. Various investigations affirmed the usefulness of rGO incorporation on the advancement of formed photocatalysts. Actually, novel nanocomposite containing rGO (15 wt.%) possessed diminished bandgap energy, as well as magnified visible light absorption. Furthermore, such nanocomposite presented exceptional photocatalytic achievement when exposed to visible light as ATR was perfectly photooxidized over finite amount (1.6 g · L-1) from the optimized photocatalyst when illuminated for 30 min. The advanced photocatalytic performance of constructed heterojunctions could be accredited mainly to depressed recombination amid induced charges. The constructed FeYO3@rGO nanocomposite is labelled as efficient photocatalyst for remediation of herbicides from aquatic environments.


Materials ◽  
2019 ◽  
Vol 12 (11) ◽  
pp. 1771 ◽  
Author(s):  
Stefan Neatu ◽  
Mihaela M. Trandafir ◽  
Adelina Stănoiu ◽  
Ovidiu G. Florea ◽  
Cristian E. Simion ◽  
...  

This study presents the synthesis and characterization of lanthanum-modified alumina supported cerium–manganese mixed oxides, which were prepared by three different methods (coprecipitation, impregnation and citrate-based sol-gel method) followed by calcination at 500 °C. The physicochemical properties of the synthesized materials were investigated by various characterization techniques, namely: nitrogen adsorption-desorption isotherms, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and H2–temperature programmed reduction (TPR). This experimental study demonstrated that the role of the catalytic surface is much more important than the bulk one. Indeed, the incipient impregnation of CeO2–MnOx catalyst, supported on an optimized amount of 4 wt.% La2O3–Al2O3, provided the best results of the catalytic combustion of methane on our catalytic micro-convertors. This is mainly due to: (i) the highest pore size dimensions according to the Brunauer-Emmett-Teller (BET) investigations, (ii) the highest amount of Mn4+ or/and Ce4+ on the surface as revealed by XPS, (iii) the presence of a mixed phase (Ce2MnO6) as shown by X-ray diffraction; and (iv) a higher reducibility of Mn4+ or/and Ce4+ species as displayed by H2–TPR and therefore more reactive oxygen species.


2012 ◽  
Vol 2012 ◽  
pp. 1-8 ◽  
Author(s):  
Aidong Tang ◽  
Yuehua Deng ◽  
Jiao Jin ◽  
Huaming Yang

A novel nanocomposite ZnFe2O4-TiO2/MCM-41 (ZTM) was synthesized by a sol-gel method and characterized through X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), N2adsorption-desorption, Raman spectroscopy, and ultraviolet visible (UV-vis) spectrophotometry. The results confirmed the incorporation of ZnFe2O4-TiO2nanoparticles inside the pores of the mesoporous MCM-41 host without destroying its integrity. ZnFe2O4nanoparticles can inhibit the transformation of anatase into rutile phase of TiO2. Incorporation of ZnFe2O4-TiO2within MCM-41 avoided the agglomeration of nanoparticles and reduced the band gap energy of TiO2to enhance its visible light photocatalytic activity. UV-vis absorption edges of ZTM nanocomposites redshifted with the increase of Zn/Ti molar ratio. The nanocomposite approach could be a potential choice for enhancing the photoactivity of TiO2, indicating an interesting application in the photodegradation and photoelectric fields.


2013 ◽  
Vol 745-746 ◽  
pp. 685-689
Author(s):  
Jun Yan Wu ◽  
Fei Chen ◽  
Qiang Shen ◽  
Lian Meng Zhang

Antimony-doped tin oxide (ATO) nanoparticles with controlled doping level were prepared by a nonaqueous solution route, using alcohol as the solvent, citric acid as an agent, tin (IV) tetrachloride as tin source and antimony (III) chlorideas as antimony sources. As-synthesized samples were characterized by Thermogravimetric analysis (TGA), powder X-ray diffraction (XRD), transmission electron micrographs (TEM), N2 adsorption-desorption isotherms, and X-ray photoelectron spectroscopy (XPS). The results showed that the content of citric acid was the most important processing parameter which was largely governing the reaction course and the complete incorporation of Sb. When the citric acid to metal mol ratio was 2, the particles were the highly crystallized ATO nanoparticles of about 20nm and the Sb atoms were indeed incorporated into the SnO2 crystal structure (cassiterite SnO2).


2018 ◽  
Vol 930 ◽  
pp. 73-78
Author(s):  
Eduardo Felipe de Carli ◽  
Natali Amarante da Cruz ◽  
Hiana Muniz Garcia ◽  
Jusinei Meireles Stropa ◽  
Lis Regiane Vizolli Favarin ◽  
...  

Important changes in anatase crystal structure are responsible for the consequent anatase-to-rutile phase transition in titanium dioxide powders. In order to investigate several structural rearrangements occurring in anatase phase obtained by hydrolysis-based method such as Sol-Gel method the X-ray diffraction techniques followed by Rietveld method seems to better approach. Several alterations in anatase lattice parameters can occur by doping insertion and the investigation of isostructural zircon silicate can provide interesting ones. In the present paper, the monitoring of anatase structure reordering and the consequent anatase-to-rutile phase transition along the thermal treatment up to higher temperatures were monitored carrying out DSC and XRD characterizations. The insertion of 6 mol% of zircon silicate leads to the fully anatase stabilization up to 900 °C due the control of ordering process, even that a continuous increasing in anatase tetragonality is present during the entire process. We can conclude the reconstructive anatase-to-rutile phase transition is delayed to very higher temperatures can consequence of more stable cross-linked metal oxide bond in anatase phase.


2019 ◽  
Vol 56 ◽  
pp. 28-38 ◽  
Author(s):  
Uraiwan Werapun ◽  
Jaraslak Pechwang

TiO2 and iron-doped TiO2 were synthesized by sol-gel method. TiO2 and 0.5 %mol Fe:TiO2 were calcined at 500 and 800 °C for 3 h. The synthesized particles were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), UV-VIS diffuse reflectance spectrophotometry (UV/DRS), scanning electron microscopy (SEM) and scanning electron microscope-energy dispersive X-Ray analysis (SEM-EDX). The XRD patterns of all samples that were calcined at 500 °C showed only anatase phase. On increasing temperature from 500 to 800 °C, the anatase phase transformed to rutile phase. For 0.5 %mol Fe:TiO2, pseudobrookite (Fe2TiO5) phase was observed at 800 °C. The particles that contained rutile showed higher antibacterial activities against E.coli, B. subtilis, and S. aureus than anatase phase, under fluorescent irradiation.


1997 ◽  
Vol 12 (2) ◽  
pp. 439-443 ◽  
Author(s):  
R. Rodríguez-Talavera ◽  
S. Vargas ◽  
R. Arroyo-Murillo ◽  
R. Montiel-Campos ◽  
E. Haro-Poniatowski

Titania matrices prepared by a sol-gel technique were doped with several cations (La, Zn, Al, K, Na, Ca, Ba, and Co). The effect of the dopants on the thermal and structural properties of the materials is analyzed. The dopant concentration was 2% mol with respect to titanium, and in all cases the same anion (nitrate) was used. The transition temperatures from amorphous to anatase and from anatase to rutile were measured using x-ray diffraction. The amorphous-anatase transition is independent, for almost all samples, of the type of dopant used; however, the anatase-to-rutile phase transition depends strongly on the kind of cation. This means that the temperature range where the anatase phase exists can be controlled by choosing the appropriate dopant. We have found a correlation between the anatase-rutile phase transition temperature and the radius of the cations and their electric charge.


2014 ◽  
Vol 896 ◽  
pp. 481-484 ◽  
Author(s):  
Nafi'ah Ardhani ◽  
Agus Supriyanto ◽  
Akhmad Herman Yuwono ◽  
Risa Suryana

TiO2 nanoparticles have been successfully synthesized using the sol-gel method with main materials of titanium tetraisopropoxide (TTIP) and HClO4 solutions. Mass ratios (Rw) of aquadest and TTIP were 0.85, 2.00, and 3.50 which were going to be investigated in crystallization of TiO2 phases. Pre-heating was performed on TiO2 at 60°C for one day then it was annealed at 150°C for 3 hours. The DSSC structure was formed by using the synthesized-TiO2 as semiconductor material and beta-carotene as dye sensitizer. The x-ray diffraction (XRD) spectrum indicated that TiO2 peaks had anatase phases on crystal orientation of (101), (004), and (200) while TiO2 of rutile phase only appeared on orientation of (211). The highest intensity for all Rw was dominated by (101) anatase phase. From XRD spectrum data of (101) peak, the Scherrer’s method predicted that crystal size of TiO2 was 3.48 nm, 4.36 nm, and 4.47 nm for Rw of 0.85, 2.00, and 3.50, respectively. The Tauc’s method was applied on the UV-Vis data that predicted the bandgap energy (Eg) of TiO2 for Rw of 2.00 (Eg=3.14 eV) was higher than Rw of 0.85 (Eg=3.02 eV) and 3.50 (Eg=3.04 eV). The I-V characteristic calculation of DSSC structures were obtained that the efficiency optimum is 0.01% for Rw of 2.00. It is considered that bandgap energy value correlated to stability of Ti-OH bonds that caused the exited-electrons are easily injected to conduction band of TiO2. The performance of DSSC using the synthesized-TiO2 which consists of anatase and rutile can be improved about ten times compared to that using the pure-TiO2 rutile.


2014 ◽  
Vol 8 (4) ◽  
pp. 195-202 ◽  
Author(s):  
Marija Milanovic ◽  
Ljubica Nikolic

Pure and lanthanum doped titania nanopowders were synthesized through a room temperature sol-gel method using a template of polyethylene glycol (PEG). The progress of the synthesis in terms of phase formation and size of nanoparticles was monitored by X-ray diffraction, FTIR spectroscopy and SEM analysis. After calcination at 450?C in air, the results have shown the presence of small particles crystallized predominantly in the form of anatase phase, with significant agglomeration. Nitrogen adsorption-desorption measurements confirmed that all prepared powders are mesoporous with an average pore diameter in range 3.1-3.8 nm. The addition of lanthanum ions leads to the nanopowders with the highest specific surface (BET) area (203m2/g). The obtained powders were compared to TiO2 prepared without a template.


2013 ◽  
Vol 800 ◽  
pp. 464-470 ◽  
Author(s):  
Wei Chao Liu ◽  
Huan Yan Xu ◽  
Tian Nuo Shi ◽  
Li Cheng Wu ◽  
Ping Li

TiO2/tourmaline composite photocatalyst was prepared by sol-gel method using tetrabutyl orthotitanate (Ti (OC4H9)4) as a precursor. As a comparison, pure TiO2 was prepared at the same experimental conditons without the addition of tourmaline. The obtained composite photocatalyst was characterized by X-Ray diffraction (XRD) and scanning electron microscope (SEM) and its photocatalytic activity was also investigated through the photodiscoloration of methyl orange (MO) under UV irradiation. The XRD results indicated that, in the composite photocatalyst, TiO2 existed in the form of anatase and rutile, with the sintering temperature and tourmaline content increasing, the anatase phase trended to the transformation to rutile phase. The SEM results revealed that the nanosized particles of TiO2 were well dispersed and immobilized on the surface of tourmaline, especially for the sample with 2% tourmaline content. Compared with pure TiO2, the composite photocatalyst exhibited a higher photocatalytic activity. When the pure TiO2 was used as the photocatalyst, the MO discoloration ratio only reached 55%. However, the MO discoloration ratio could approach 100% in presence of TiO2/tourmaline composit photocatalyst under the same conditions. The effects of tourmaline content and sintering temperature on the photocatalytic activity of the composite were studied in this work and the results suggested that the sample with 2% tourmaline content and sintered at the temperature of 550°C exhibited the best photocatalytic activity. Finally, the possible mechanism for the photodiscoloration of MO was put forward.


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