Enhancing the Photocatalytic Activity of La/Y Co-Doped ZnWO4 under UV Irradiation

2020 ◽  
Vol 842 ◽  
pp. 214-222
Author(s):  
Chu Wen Rao ◽  
Wei Zhang ◽  
Zheng Fa Hu ◽  
Zu Yong Feng ◽  
Ying Jun Chen ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Uv Irradiation ◽  
Photoelectron Spectroscopy ◽  
Broad Band ◽  
Solid State Reaction Method ◽  
High Photocatalytic Activity ◽  
Photocatalytic Decomposition ◽  
X Ray ◽  
Co Doping ◽  
Broad Band Emission

In this paper, ZnWO4: La3+, Y3+ photocatalysts were synthesized by a high-temperature solid state reaction method. The effects of La3+ and Y3+ doping contents on the phase, morphologies and optical properties of the samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Diffuse reflectance spectra (DRS), photoluminescence spectra (PL), Raman and UV-visible spectroscopy, respectively. The as-prepared ZnWO4:La3+, Y3+ photocatalysts showed photoluminescence with a broad band emission, and high photocatalytic activity in degradation of rhodamine B (RhB) under simulated UV irradiation. The results showed that co-doping in ZnWO4 can enhance light harvesting capability to generate more electron-hole pairs, and acted as a trap center by decreasing the recombination of photogenerated electrons and holes. All the results obtained by the work suggest that ZnWO4: La3+, Y3+ photocatalysts are promising materials for the photocatalytic decomposition of pollutants.

scholarly journals Study of the Effect of TiO2 Layer on the Adsorption and Photocatalytic Activity of TiO2-MoS2 Heterostructures under Visible-Infrared Light

2020 ◽  
Vol 2020 ◽  
pp. 1-9 ◽  
Author(s):  
N. Cruz-González ◽  
O. Calzadilla ◽  
J. Roque ◽  
F. Chalé-Lara ◽  
J. K. Olarte ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Nitrogen Adsorption ◽  
High Photocatalytic Activity ◽  
Infrared Light ◽  
Polluted Water ◽  
Light Spectrum ◽  
X Ray

In the last decade, the urgent need to environmental protection has promoted the development of new materials with potential applications to remediate air and polluted water. In this work, the effect of the TiO2 thin layer over MoS2 material in photocatalytic activity is reported. We prepared different heterostructures, using a combination of electrospinning, solvothermal, and spin-coating techniques. The properties of the samples were analyzed by scanning electron microscopy (SEM), transmission electron microscopy (TEM), atomic force microscopy (AFM), X-ray diffraction (XRD), nitrogen adsorption-desorption isotherms, UV-Vis diffuse reflectance spectroscopy (UV-Vis-DRS), and X-ray photoelectron spectroscopy (XPS). The adsorption and photocatalytic activity were evaluated by discoloration of rhodamine B solution. The TiO2-MoS2/TiO2 heterostructure presented three optical absorption edges at 1.3 eV, 2.28 eV, and 3.23 eV. The high adsorption capacity of MoS2 was eliminated with the addition of TiO2 thin film. The samples show high photocatalytic activity in the visible-IR light spectrum.

scholarly journals Photocatalytic Degradation of Estriol Using Iron-Doped TiO2 under High and Low UV-Irradiation

2018 ◽  
Author(s):  
Irwing M. Ramírez-Sánchez ◽  
Erick R. Bandala
Keyword(s):  
Photocatalytic Activity ◽  
Electron Microscope ◽  
Uv Irradiation ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Bet Surface Area ◽  
Doped Tio2 ◽  
X Ray ◽  
Transmission Electron ◽  
Iron Doped

Iron Doped TiO2 nanoparticles (Fe-TiO2) were synthesized and photocatalitically investigated under high and low fluence values of UV-radiation. The Fe-TiO2 physical characterization was performed using X-ray Powder Diffraction (XRD), Brunauer-Emmett-Teller (BET) surface area analysis, Transmission Electron Microscope (TEM), Scanning Electron Microscope (SEM), Diffuse Reflectance Spectroscopy (DRS), and X-Ray Photoelectron Spectroscopy (XPS) technique. The XPS evidenced that ferric ion (Fe3+) was in the lattice of TiO2 and co-dopants no intentionally added were also present due to the precursors of the synthetic method. The Fe3+ concentration played a key role in the photocatalytic generation of hydroxyl radical (•OH) and estriol (E3) degradation. Fe-TiO2 materials accomplished E3 degradation, and it was found that the catalyst with 0.3 at. % content of Fe (0.3 Fe-TiO2) enhanced the photocatalytic activity under low UV-irradiation compared with no intentionally Fe-added TiO2 (zero-iron TiO2) and Aeroxide® TiO2 P25. Furthermore, the enhanced photocatalytic activity of 0.3 Fe-TiO2 under low UV-irradiation may have applications when radiation intensity must be controlled, as in medical applications, or when strong UV absorbing species are present in water.

scholarly journals Preparation and Characterization of Defective TiO2. The Effect of the Reaction Environment on Titanium Vacancies Formation

Materials ◽  
2020 ◽  
Vol 13 (12) ◽  
pp. 2763
Author(s):  
Zuzanna Bielan ◽  
Szymon Dudziak ◽  
Agnieszka Sulowska ◽  
Daniel Pelczarski ◽  
Jacek Ryl ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Hydrothermal Reaction ◽  
High Photocatalytic Activity ◽  
Paramagnetic Resonance ◽  
X Ray ◽  
Light Activity ◽  
Cheap Alternative

Among various methods of improving visible light activity of titanium(IV) oxide, the formation of defects and vacancies (both oxygen and titanium) in the crystal structure of TiO2 is an easy and relatively cheap alternative to improve the photocatalytic activity. In the presented work, visible light active defective TiO2 was obtained by the hydrothermal reaction in the presence of three different oxidizing agents: HIO3, H2O2, and HNO3. Further study on the effect of used oxidant and calcination temperature on the physicochemical and photocatalytic properties of defective TiO2 was performed. Obtained nanostructures were characterized by X-ray diffractometry (XRD), specific surface area (BET) measurements, UV-Vis diffuse reflectance spectroscopy (DR-UV/Vis), photoluminescence spectroscopy (PL), X-ray photoelectron spectroscopy (XPS), and electron paramagnetic resonance (EPR) spectroscopy. Degradation of phenol as a model pollutant was measured in the range of UV-Vis and Vis irradiation, demonstrating a significant increase of photocatalytic activity of defective TiO2 samples above 420 nm, comparing to non-defected TiO2. Correlation of EPR, UV-Vis, PL, and photodegradation results revealed that the optimum concentration of HIO3 to achieve high photocatalytic activity was in the range of 20–50 mol%. Above that dosage, titanium vacancies amount is too high, and the obtained materials’ photoactivity was significantly decreased. Studies on the photocatalytic mechanism using defective TiO2 have also shown that •O2− radical is mainly responsible for pollutant degradation.

scholarly journals Properties and Photocatalytic Activity ofβ-Ga2O3Nanorods under Simulated Solar Irradiation

2015 ◽  
Vol 2015 ◽  
pp. 1-5 ◽  
Author(s):  
Yinzhen Wang ◽  
Ning Li ◽  
Pingping Duan ◽  
Xuwei Sun ◽  
Benli Chu ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Photoelectron Spectroscopy ◽  
Light Emission ◽  
Methyl Orange Solution ◽  
High Photocatalytic Activity ◽  
Solar Irradiation ◽  
X Ray ◽  
Transmission Electron ◽  
Blue Solution ◽  
Simulated Solar Irradiation

β-Ga2O3nanorods are prepared by hydrothermal method and characterized by X-ray diffraction, high-resolution transmission electron microscopy, Raman spectroscopy, X-ray photoelectron spectroscopy, and photoluminescence spectra. The results reveal that high crystallinity, monoclinic phase ofβ-Ga2O3nanorods were prepared with a diameter of about 60 nm and length of 500 nm. Photoluminescence study indicates that theβ-Ga2O3nanorods exhibit a broad blue light emission at room temperature. Theβ-Ga2O3nanorods displayed high photocatalytic activity under simulated solar irradiation; after 2 h irradiation, over 95% of methylene blue solution and over 90% of methyl orange solution were decolorized. Since this process does not require additional hydrogen peroxide and uses solar light, it can be developed as an economically feasible and environmentally friendly method to treat dye effluent.

scholarly journals Synthesis of C-N-S-Tridoped TiO2 from Vietnam Ilmenite Ore and Its Visible Light-Driven-Photocatalytic Activity for Tetracyline Degradation

2020 ◽  
Vol 2020 ◽  
pp. 1-14 ◽  
Author(s):  
Nguyen Thi Lan ◽  
Vo Hoang Anh ◽  
Hoang Duc An ◽  
Nguyen Phi Hung ◽  
Dao Ngoc Nhiem ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Nitrogen Adsorption ◽  
Photocatalytic Decomposition ◽  
Raman Scattering Spectroscopy ◽  
X Ray ◽  
Visible Light Driven

In this study, C-N-S-tridoped TiO2 composite was fabricated from TiO2 prepared from ilmenite ore and thiourea by means of hydrothermal method. The obtained material was characterized by X-ray diffraction, Raman scattering spectroscopy, UV-Vis diffuse reflectance spectroscopy, nitrogen adsorption-desorption isotherms, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). It was found that C-N-S-tridoped TiO2 material has a large specific surface area, showing good photocatalytic activity on the degradation of antibiotic tetracycline in visible light region. The study on the mechanism of tetracycline photodegradation using the liquid chromatography with mass spectrometry was performed. It was found that tetracycline has been degraded over C-N-S-tridoped TiO2 catalyst into many different intermediates which can eventually be converted into CO2 and H2O. The kinetics of photocatalytic decomposition of tetracycline were investigated. In addition, the obtained material could catalyze well the degradation of other antibiotics (ciprofloxacin and chloramphenicol) and dyes (rhodamine-B, methylene blue, and organe red). The catalyst was stable after five recycles with slight loss of catalytic activity, which indicates great potential for practical application of C-N-S-tridoped TiO2 catalyst in treatment of wastewater containing tetracycline in particular or antibiotics in general.

Simplified Synthesis and Luminous Mechanism of Eu2+-Doped α-Si3N4 Nanowires with Strong Green Luminescent Properties

2017 ◽  
Vol 727 ◽  
pp. 635-641 ◽  
Author(s):  
Rui Su ◽  
Zhi Feng Huang ◽  
Fei Chen ◽  
Qiang Shen ◽  
Lian Meng Zhang
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Broad Band ◽  
Luminescent Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
Broad Band Emission ◽  
Band Emission ◽  
Nitridation Process ◽  
Transmission Electron

Ultra-long, single crystal, Eu-doped α-Si3N4 nanowires were prepared by a simple approach involving nitriding Eu-doped cryomilled nanocrystalline Si powder in NH3 flow at 1350 °C for 4 h. Phases, chemical composition and microcosmic feature of cryomilled powders and as-prepared nanowires were tested by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), respectively. The results suggested that Eu was successfully introduced into Si lattice after the cryomilling process and then entered into the lattice of α-Si3N4 during the nitridation process. The as-synthesized Eu-doped α-Si3N4 nanowires had highly uniform dimension with 20~30 nm in diameter and ~100 μm in length. The room temperature photoluminescence (PL) spectrum of as-synthesized nanowires showed a broad band emission center at 570 nm which was attributed to the transition from 4f65d to 4f7 in Eu2+. The transition from Eu3+ to Eu2+ during nitridation process was tested by X-ray photoelectron spectroscopy (XPS).

scholarly journals Гетероструктурные AgCl/BN-наноматериалы с высокой сорбционной способностью и фотокаталитической активностью

2021 ◽  
Vol 47 (19) ◽  
pp. 47
Author(s):  
А.С. Конопацкий ◽  
Д.В. Попова ◽  
В.В. Калинина ◽  
Д.В. Лейбо ◽  
А.Т. Матвеев ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Photoelectron Spectroscopy ◽  
High Photocatalytic Activity ◽  
Organic Dye ◽  
Surface Microstructure ◽  
X Ray ◽  
Sorption Ability ◽  
Heterogeneous Structures ◽  
Scanning Electron

In this work, the photocatalytic activity and sorption capacity of heterogeneous structures AgCl/h-BN obtained by the polyol method were studied in comparison with the initial micron-sized h-BN powder. The chemical and phase composition, as well as the surface microstructure, were analyzed by scanning electron microscopy, energy dispersive spectroscopy, X-ray phase analysis, and X-ray photoelectron spectroscopy. High photocatalytic activity and sorption ability of heterogeneous structures AgCl/BN in the reaction of the organic dye methylene blue decomposition under ultraviolet irradiation were demonstrated.

Structural, Morphological, Optical and Photocatalytic Properties of Os and N Co-Doped TiO2 Films

2020 ◽  
Vol 853 ◽  
pp. 235-242
Author(s):  
Zhi Li ◽  
Chun Yu Ma
Keyword(s):  
Photocatalytic Activity ◽  
Photoelectron Spectroscopy ◽  
Uv Light ◽  
Rf Magnetron Sputtering ◽  
Photocatalytic Properties ◽  
X Ray ◽  
Force Microscopy ◽  
Co Doping ◽  
Atomic Force ◽  
Co Doped

In the present work, Os and N co-doped TiO2 films were first prepared using a reactive RF magnetron sputtering of Ti–Os metallic target. The effect of Os concentration varying from 0 to 3.0at.% on structure as well as morphology and subsequent changes in optical and photocatalytic properties were studied by X-ray diffraction (XRD), scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS), optical absorption spectra and photoluminescence (PL) spectroscopy. XRD and SEM results show that the co-doping of Os and N favors the crystal growth of TiO2 and leads to a low anatase thermal stability relative to N monodoping. The band gap of the N/Os co-doped films is reduced from 3.42 eV to 3.22 eV compared with the N-TiO2 film. PL investigation further exhibits the effects of Os doping on the electronic structures and defects in N-TiO2.The photocatalytic activities of the films were evaluated by the degradation of methylene blue in aqueous solution under UV light. It was found that the photocatalytic activity increases with increasing Os content first, and then decreases after the optimal Os content. Therefore, the photocatalytic activity of Os/N co-modified TiO2 photocatalysts can be adjusted by the Os content.

scholarly journals A Facile Synthesis of Graphene-WO3Nanowire Clusters with High Photocatalytic Activity for O2Evolution

2014 ◽  
Vol 2014 ◽  
pp. 1-6
Author(s):  
M.-J. Zhou ◽  
N. Zhang ◽  
Z. H. Hou
Keyword(s):  
Photocatalytic Activity ◽  
Water Splitting ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
High Photocatalytic Activity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Charge Transfer Rate ◽  
Ft Ir

In the present work, graphene-WO3nanowire clusters were synthesizedviaa facile hydrothermal method. The obtained graphene-WO3nanowire clusters were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR), Raman spectroscopy, and ultraviolet-visible diffuse reflectance spectroscopy (DRS) techniques. The photocatalytic oxygen (O2) evolution properties of the as-synthesized samples were investigated by measuring the amount of evolved O2from water splitting. The graphene-WO3nanowire clusters exhibited enhanced performance compared to pure WO3nanowire clusters for O2evolution. The amount of evolved O2from water splitting after 8 h for the graphene-WO3nanowire clusters isca.0.345 mmol/L, which is more than 1.9 times as much as that of the pure WO3nanowire clusters (ca.0.175 mmol/L). The high photocatalytic activity of the graphene-WO3nanowire clusters was attributed to a high charge transfer rate in the presence of graphene.

scholarly journals Photocatalytic Degradation of Estriol Using Iron-Doped TiO2 under High and Low UV Irradiation

Catalysts ◽  
2018 ◽  
Vol 8 (12) ◽  
pp. 625 ◽  
Author(s):  
Irwing Ramírez-Sánchez ◽  
Erick Bandala
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Uv Irradiation ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Bet Surface Area ◽  
Doped Tio2 ◽  
X Ray ◽  
Tio2 Lattice ◽  
Iron Doped

Iron-doped TiO2 nanoparticles (Fe-TiO2) were synthesized and photocatalitically investigated under high and low fluence values of UV radiation. The Fe-TiO2 physical characterization was performed using X-ray Powder Diffraction (XRD), Brunauer–Emmett–Teller (BET) surface area analysis, Transmission Electron Microscopy (TEM), Scanning Electron Microscopy (SEM), Diffuse Reflectance Spectroscopy (DRS), and X-ray Photoelectron Spectroscopy (XPS). The XPS evidenced that the ferric ion (Fe3+) was in the TiO2 lattice and unintentionally added co-dopants were also present because of the precursors of the synthetic method. The Fe3+ concentration played a key role in the photocatalytic generation of hydroxyl radicals (•OH) and estriol (E3) degradation. Fe-TiO2 accomplished E3 degradation, and it was found that the catalyst with 0.3 at.% content of Fe (0.3 Fe-TiO2) enhanced the photocatalytic activity under low UV irradiation compared with TiO2 without intentionally added Fe (zero-iron TiO2) and Aeroxide® TiO2 P25. Furthermore, the enhanced photocatalytic activity of 0.3 Fe-TiO2 under low UV irradiation may have applications when radiation intensity must be controlled, as in medical applications, or when strong UV absorbing species are present in water.

Sign in / Sign up

Export Citation Format

Share Document