Ultrasound Assisted Synthesis of Visible Light Responsive Nitrogen Doped TiO2 Nano Photocatalyst

2013 ◽  
Vol 856 ◽  
pp. 22-24 ◽  
Author(s):  
Ramita Batra ◽  
Nidhi Sharotri ◽  
Dhiraj Sud

The present study is an attempt to synthesize N-doped TiO2 nanophotocatalyst using sonochemical method, having photocatalytic activity in the visible region. Non-metal doped nanocatalysts have been successfully synthesized and characterized structurally and physiochemically by using XRD, SEM, TEM, EDX, UV-VIS, FT-IR, Raman and PL. The photocatalytic activity of the synthesized photocatalyst was investigated for the degradation of 2-CP as model compound. The result confirms the successful synthesis of N-doped photocatalyst with particle size 34 nm having anatase phase and shows new peak in a visible region at 587 nm..

2012 ◽  
Vol 573-574 ◽  
pp. 110-114 ◽  
Author(s):  
Jin Xia ◽  
Ri Ya Jin ◽  
Kai Xuan Guo ◽  
Si Jing Yang

Titanium dioxide powders were synthesized by ultrasonic-assisted hydrolysis reaction of titanium tetra-isopropoxide at the low-temperature. The samples were characterized by Fourier transform infrared spectroscopy (FT-IR), powder X-ray diffraction (XRD). The photocatalytic activity of samples were investigated by the degradation of methyl orange under UV light radiation (6W, λ= 352nm) at room temperature. The results indicated that the products were mainly composed of high homogeneity anatase phases, and the methyl orange degradation rate can reach more than 90% under ultraviolet irradiation 180min. The photocatalytic activity of the samples prepared by ultrasonic method is higher than that of the samples prepared by conventional hydrolysis method.


2018 ◽  
Vol 10 (3) ◽  
pp. 337-345 ◽  
Author(s):  
Chengxiang Zheng ◽  
Hua Yang ◽  
Yang Yang ◽  
Haimin Zhang

A facile sonochemical method was used to synthesize Ag3PO4 particles and the effect of pH value, reaction temperature and reaction time on the products was investigated. It is found that the samples prepared at neutral (pH = 7) and alkaline (pH = 11) environments exhibit a similar particle morphology and size. The particles are shaped like spheres with a size distribution majorly focusing on a range of 200–450 nm, and the average particle size is about 300 nm. The sample prepared at acidic environment (pH = 3) is composed of polyhedral microparticles with size of 5–8 μm. At relatively low temperatures of 20–50 °C, the spherical nanoparticles do not undergo obvious morphology/size changes; however, when the temperature is increased up to 80 °C, the nanoparticles are aggregated to form large-sized polyhedral microparticles in the size range of 4–7 μm. Compared to the pH value and reaction temperature, the reaction time has a minor effect on the morphology of Ag3PO4 particles. RhB was chosen as the target pollutant to evaluate the photocatalytic activity of the as-prepared Ag3PO4 samples under simulated-sunlight irradiation. It is shown that the samples consisting of spherical nanoparticles exhibit an extremely high photocatalytic activity, and the degradation percentage of RhB after reaction for 50 min reaches over 90%. The samples of polyhedral microparticles have a relatively low photocatalytic activity, which is possibly due to their large particle size. Hydroxyl (.OH) radical was detected by spectrofluorimetry using terephthalic acid as a .OH scavenger and was not found to be produced over the simulated-sunlight-irradiated Ag3PO4 catalyst. The effect of ethanol, benzoquinone and ammonium oxalate on dye degradation was also investigated. Based on experimental results, the direct oxidation by h+ is suggested to the dominant mechanism toward the dye degradation.


2010 ◽  
Vol 113-116 ◽  
pp. 1945-1950 ◽  
Author(s):  
Jie Luo ◽  
Xin Yuan Yang ◽  
De Liang Li

Using cesium nitrate and strontium nitrate as doping metal ions source, Cs-doped TiO2 and Sr-doped TiO2 photocatalysts were successfully synthesized through the hydrolysis of tetrabutyl titanate by an acid-catalyzed sol-gel method. The photocatalytic activities of these catalysts prepared at 600 °C for 2 h were evaluated by the degradation of methyl orange in aqueous solution under solar light irradiation, and the as-prepared samples with higher photocatalytic efficiency were characterized by means of X-ray diffraction (XRD) and UV-Vis absorption spectroscopy. The XRD patterns indicate that the crystal structure still remains as anatase phase for the doped samples, and the average crystal size of TiO2, 0.1 at% Cs-doped TiO2 and 0.3 at% Sr-doped TiO2 is 21.3, 13.1 and 10.8 nm, respectively. The band gap absorption shows red shift to the visible region for the doped samples from the UV-Vis spectrogram. The results show that the photocatalytic activity of TiO2 nanoparticles doped with Cs+ and Sr2+ exhibits a significant improvement and their degradation efficiencies are more than 30% in comparison with those of TiO2 under the same condition, and the optimal doping concentration is determined to be 0.1 at% and 0.3 at% for Cs+ and Sr2+, respectively.


2022 ◽  
Author(s):  
Venkatesh D ◽  
Pavalamalar S ◽  
Silambarasan R ◽  
Anbalagan K

Abstract The photocatalytic activity of well-fabricated, economical SnO2/TiO2 nanocomposite synthesized via hydrothermal route was validated using the (NH3-trz)[Fe(dipic)2] complex under ultra-violet illumination. The structural features of (NH3-trz)[Fe(dipic)2] complex was explored in detail. The catalysts were systematically examined with XRD, SEM, FT-IR UV-vis, PL, micro-Raman, VSM, AFM, HRTEM. The photoreactivity of the model compound (NH3-trz)[Fe(dipic)2] in water/binary solvent systems was investigated. The rate of photoreaction (k) of nanocomposite (0.1432 sec-1) is higher than the SnO2 (0.0373 sec-1) and TiO2 (0.1422 sec-1) in H2O:PriOH (70:30%) than the rest of the solvents system. The pathways, mechanistic feature of accumulated reactive species on nanocomposite to induce adherent [Fe(dipic)2]- anion and photo-reductive products were studied. The generation of hydroxyl radical on the surface of each catalyst can be identified as 7-hydroxycoumarin and discussed.


2019 ◽  
Vol 22 (2) ◽  
pp. 47-51 ◽  
Author(s):  
Abdul Haris ◽  
Gunawan Gunawan ◽  
Didik Setiyo Widodo ◽  
Rahmad Nuryanto ◽  
Retno Ariadi Lusiana ◽  
...  

Copper and sulfur modified TiO2(Cu-S-TiO2) photocatalyst was successfully synthesized using TiCl4, Cu(NO3)2.3H2O and H2SO4 as precursors by the sol-gel method andcalcination at 450°C for 4 hours. The synthesized photocatalyst was characterized by X-Ray Diffraction (XRD), Scanning Electron Microscopy-Energy Dispersive Spectroscopy (SEM-EDS), Diffuse Reflectance Spectroscopy (DRS), Brunauer Emmett Teller (BET) method. The XRD results showed that the Cu-S-TiO2 photocatalyst had an anatase phase with a crystal grain size of 17.54 nm. However, the SEM image of the modified TiO2 showed inhomogeneous phase due to the crystal clustering of imperfect homogenization during the synthesis and sintering processes. The patterns of EDSof Cu-S-TiO2depicted the elements of Ti, O, Cu and S with doping of Cu and S c.a. 7 and 1%, respectively. Analysis using DRS UV-Vis showed Cu-S-TiO2 was able to shift the absorption of the TiO2 photocatalyst wavelength to the visible region with a band energy gap of 1.9 eV. The BET analysis results showed that the specific surface area (SBET), pore volume (Vp) and average pore volume radius (Dp) were measured from large Cu-S-TiO2, therefore Cu-S-TiO2 had good physicochemical and photocatalytic properties. The photocatalytic activity of 0.1 g Cu-S-TiO2 with 15 Watt tungsten light irradiation for 4 h was able to degrade 50 mL remazol black B 10 mg/L c.a. 92.60 %.


2011 ◽  
Vol 694 ◽  
pp. 824-830 ◽  
Author(s):  
Li Guo ◽  
Feng Fu ◽  
Dan Jun Wang ◽  
Xiao Dan Qiang ◽  
Qing Bo Wei ◽  
...  

Silver-doped nano-TiO2 photocatalyst were synthesized via a simple hydrothermal route. The samples were characterized by XRD, XPS, FE-SEM and UV-Vis absorption spectrum techniques. Rhodamine B was selected as the model-pollutant to evaluate the photocatalytic activity of the samples. The XRD results indicated that the Ag-doped TiO2 were pure anatase phase. The UV-Vis spectroscopy revealed that the Ag doping can increase the absorption intensity of TiO2 in the visible region, which results in the improving the photocatalytic activity of TiO2 photocatalyst. Photocatalytic experimental results revealed that Ag-doping TiO2 catalyst shows the enhancement photocatalytic activity.


2018 ◽  
Author(s):  
azadeh ebrahimian pirbazari ◽  
Pejman Monazzam ◽  
Behnam Fakhari Kisomi

In this work, TiO2 nanoparticles containing different amounts of cobalt were synthesized by sol-gel method using titanium (IV) isopropoxide and cobalt chloride as titanium and cobalt precursors, respectively. X-ray diffraction (XRD) results showed prepared samples include 100% anatase phase. The presence of cobalt in TiO2 nanoparticle network was established by XRD, scanning electron microscopy equipped with energy dispersive X-ray microanalysis (SEM-EDX), Fourier transform infrared (FT-IR) and N2 physisorption techniques. The increase of cobalt doping enhanced redshif in the diffuse reflectance spectra. The photocatalytic activity of the prepared samples was tested for degradation of methylene blue (MB) as a model of dye. Although the photocatalytic activity of pure TiO2 was found to be higher than that of Co/TiO2 samples under UV irradiation, the presence of 0.24% cobalt dopant in TiO2 nanoparticles resulted in a photocatalyst with the highest activity under visible light


Crystals ◽  
2021 ◽  
Vol 11 (10) ◽  
pp. 1254
Author(s):  
Wanichaya Mekprasart ◽  
Sorapong Pavasupree ◽  
C. K. Jayasankar ◽  
Balaji Rao Ravuri ◽  
Chakkaphan Wattanawikkam ◽  
...  

A novel one-step preparation of sonochemical method was applied to synthesize Co/Zn co-doped TiO2 nanoparticles using a sonicator of 750 W, 20 kHz for 30 min at room temperature. The formation of the anatase TiO2 phase for all as-prepared samples was observed from XRD results with a crystalline size in nanoscale. The use of ultrasound allowed for the successful doping of both Co and Zn into the TiO2 lattice, which was confirmed by Synchrotron light including X-ray near edge structure (XANES) and Extended X-ray absorption fine structure (EXAFS) spectroscopy. Ti K-edge, Co K-edge, and Zn K-edge XANES spectra exhibited the dominating +4, +2, and +2 valence state of Ti, Co, and Zn in as-prepared samples, respectively. A detailed XANES and EXAFS data analysis give strong evidence that the Co/Zn dopants partially replace the Ti atom of the TiO2 host. The Co/Zn co-doping extends the light absorption of the host to the visible region and restricts the e+/h+ recombination. The photocatalytic activity of samples was tested for degradation of Rhodamine B dye solution under visible light irradiation. The as-synthesized of the co-doped catalyst was presented as highly efficient, with 2.5 and 5 times dye degradation compared with single-doped and bare TiO2.


NANO ◽  
2015 ◽  
Vol 10 (05) ◽  
pp. 1550076 ◽  
Author(s):  
Tianjiao Bi ◽  
Jiafeng Wan ◽  
Shilin Yang ◽  
Xiujuan Yu ◽  
Fangwei Ma

Nitrogen-doped mesoporous carbon spheres (NMCSs) supporting anatase TiO 2 ( NMCSs – TiO 2) were prepared by a simple two-step solvothermal approach. The characterizations for the physicochemical properties of prepared samples under different solvothermal temperatures were carried out by X-ray diffraction (XRD) analyses, scanning electron microscopy (SEM), transmission electron microscopy (TEM), N 2 adsorption–desorption (Brunauer–Emmett–Teller (BET) measurements), Fourier transform infrared (FT-IR) spectroscopy, Raman scattering and UV-Vis diffuse reflectance spectra, were combined in order to determine the crystal phase and grain size, shape, degree of mesoporous carbon incorporation, and nature of the resultant oxycarbide chemical bonding on the surface and in the bulk. The high relative photocatalytic activity of NMCSs – TiO 2 nanoparticle was evaluated through a study of the decomposition of phenol under visible-light excitation.


2006 ◽  
Vol 2006 ◽  
pp. 1-4 ◽  
Author(s):  
Sesha S. Srinivasan ◽  
Jeremy Wade ◽  
Elias K. Stefanakos

A new coprecipitation/hydrolysis synthesis route is used to create aTiO2-ZnFe2O4nanocomposite that is directed towards extending the photoresponse ofTiO2from UV to visible wavelengths (>400 nm). The effect ofTiO2's accelerated anatase-rutile phase transformation due to the presence of the coupledZnFe2O4narrow-bandgap semiconductor is evaluated. The transformation's dependence on pH, calcinations temperature, particle size, andZnFe2O4concentration has been analyzed using XRD, SEM, and UV-visible spectrometry. The requirements for retaining the highly photoactive anatase phase present in aZnFe2O4nanocomposite are outlined. The visible-light-activated photocatalytic activity of theTiO2-ZnFe2O4nanocomposites has been compared to an AldrichTiO2reference catalyst, using a solar-simulated photoreactor for the degradation of phenol.


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