scholarly journals Hierarchical Porous Batio3 Nano-Hexagons as A Visible Light Photocatalyst

2018 ◽  
Vol 7 (4.5) ◽  
pp. 105 ◽  
Author(s):  
Harsha Bantawal ◽  
D Krishna Bhat
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
X Rays ◽  
Hydrothermal Route ◽  
Visible Light Photocatalyst ◽  
X Ray ◽  
Hierarchical Porous ◽  
Bet Analysis

Hierarchical porous BaTiO3 nano-hexagons was synthesized via a simple hydrothermal route by using TiO2 and Ba(OH)2.8H2O as starting materials under alkaline environment and its photocatalytic activity was evaluated under visible light by taking methylene blue (MB) as a model pollutant. The prepared BaTiO3 was characterized by powder X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscopy (FESEM), energy dispersive X-rays analysis (EDX), high resolution transmission electron microscopy (HRTEM), Brunauer-Emmett-Teller (BET) analysis and diffused reflectance spectroscopy (DRS) techniques. It is noteworthy that the BaTiO3 nano-hexagons exhibited significant photocatalytic activity towards the degradation of MB under visible light irradiation. This significant photocatalytic activity of BaTiO3 under visible light is mainly attributed to the special morphology and formation of Ti3+ defects.  

scholarly journals Design and fabrication of Ag3VO4/g-C3N4 heterostructure photocatalyst for enhanced visible light degradation of various organic pollutants

2021 ◽  
Author(s):  
N Sujatha ◽  
M Meenachi ◽  
S Mohammed Harshulkhanb ◽  
H.H Hegazy
Keyword(s):  
Electron Microscopy ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Light Irradiation ◽  
X Rays ◽  
Hydrothermal Route ◽  
X Ray ◽  
Visible Light Degradation

Abstract In later years, numerous viable photocatalysts have been created in order to illuminate the issues of natural toxins. In this work, heterostructured photocatalysts Ag3VO4/g-C3N4 were prepared by effortless hydrothermal route in order to anchor Ag3VO4 on the surface of the g-C3N4 nanosheets. The prepared samples were fairly characterized using X-ray diffraction (XRD), Energy dispersive analysis of X-rays (EDAX), Scanning electron microscopy (SEM), Transmission electron microscopy (TEM), UV-vis diffuse reflectance spectroscopy (UV-DRS), photoluminescence, and X-ray photoelectron spectroscopy (XPS) techniques. The photocatalytic activity of the samples was evaluated by degrading malachite green (MG) and 2,4 dimethyl phenol (DMP) in aqueous solution under visible light irradiation. Compared with Ag3VO4 and g-C3N4, the heterojuncted photocatalyst 50 wt% Ag3VO4/g-C3N4 exhibits the best activity such as high degradation efficiency (99%), high apparent constant (0.0923 min− 1) and long term stability towards DMP under visible light irradiation. The development of a phase scheme heterojunction between Ag3VO4 and g-C3N4 improved the photocatalytic efficiency of Ag3VO4/g-C3N4 composites. Furthermore, the porous structure of g-C3N4 and the effect of Ag surface plasmon resonance (SPR) speed up the isolation and transfer of electron-hole pairs, reducing the likelihood of recombination.

Facile Synthesis and Characterization of Spinel NiFe2O4 Nanoparticles and Studies of Their Photocatalytic Activity for Oxidation of Alcohols

2020 ◽  
Vol 12 (3) ◽  
pp. 357-365 ◽  
Author(s):  
Xiangrong Ma ◽  
Rui Dang ◽  
Jieying Liu ◽  
Fang Yang ◽  
Huigui Li ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Photoelectron Spectroscopy ◽  
Average Particle Size ◽  
Average Particle ◽  
X Ray ◽  
Bet Analysis ◽  
Oxidation Of Alcohols ◽  
20 Nm ◽  
Adsorption Desorption

In this paper, we report a novel and facile approach for the synthesis of spinel NiFe2O4 nanoparticles and studies of its photocatalytic activity for oxidation of alcohols. The as-synthesized catalyst was thoroughly characterized by powder X-ray diffraction (XRD), scanning electron microscopy (SEM), elemental mapping, transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS), and N2 adsorption–desorption isotherm (BET) analysis. The TEM image reveals cubic shapes with an average particle size of 10–20 nm. The as-synthesized spinel NiFe2O4 has proved to be an excellent photocatalyst for oxidation of alcohol to the aldehyde with a conversion of 80% and selectivity of 99%. The catalyst has also proved to be noteworthy as it does not loss its catalytic activity even after five cycles of reuse.

scholarly journals Preparation of g-C3N4/MoS2 Composite Material and Its Visible Light Catalytic Performance

2021 ◽  
Author(s):  
Yu Fan ◽  
Yan-ning Yang ◽  
Chen Ding
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Photogenerated Electron ◽  
Catalytic Performance ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Calcination Method

Abstract The g-C3N4 nanosheet was prepared by calcination method, the MoS2 nanosheet was prepared by hydrothermal method. The g-C3N4/MoS2 composites were prepared by ultrasonic composite in anhydrous ethanol. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), ultraviolet-visible spectroscopy (UV-Vis), and photoluminescence (PL) techniques were used to characterize the materials. The photocatalytic degradation of Rhodamine B (Rh B) by g-C3N4/MoS2 composites with different mass ratios was investigated under visible light. The results show that a small amount of MoS2 combined with g-C3N4 can significantly improve photocatalytic activity. The g-C3N4/MoS2 composite with a mass ratio of 1:8 has the highest photocatalytic activity, and the degradation rate of Rh B increases from 50% to 99.6%. The main reason is that MoS2 and g-C3N4 have a matching band structure. The separation rate of photogenerated electron-hole pairs is enhanced. So the g-C3N4/MoS2 composite can improve the photocatalytic activity. The photocatalytic mechanism was proposed through the active matter capture experiment.

scholarly journals Growth Process and CQDs-modified Bi4Ti3O12 Square Plates with Enhanced Photocatalytic Performance

Micromachines ◽  
2019 ◽  
Vol 10 (1) ◽  
pp. 66 ◽  
Author(s):  
Xinxin Zhao ◽  
Hua Yang ◽  
Ziming Cui ◽  
Xiangxian Wang ◽  
Zao Yi
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Growth Process ◽  
Photocatalytic Performance ◽  
Simulated Sunlight ◽  
Hydrothermal Route ◽  
Electron Hole ◽  
X Ray ◽  
Photocurrent Spectroscopy

Bi4Ti3O12 square plates were synthesized via a hydrothermal route, and their growth process was systematically investigated. Carbon quantum dots (CQDs) were prepared using glucose as the carbon source, which were then assembled on the surface of Bi4Ti3O12 square plates via a hydrothermal route with the aim of enhancing the photocatalytic performance. XRD (X-ray powder diffraction), SEM (scanning electron microscopy), TEM (transmission electron microscopy), UV-vis DRS (diffuse reflectance spectroscopy), XPS (X-ray photoelectron spectroscopy), FTIR (Fourier transform infrared spectroscopy), PL (photoluminescence) spectroscopy, EIS (electrochemical impedance spectroscopy) and photocurrent spectroscopy were used to systematically characterize the as-prepared samples. It is demonstrated that the decoration of CQDs on Bi4Ti3O12 plates leads to an increased visible light absorption, slightly increased bandgap, increased photocurrent density, decreased charge-transfer resistance, and decreased PL intensity. Simulated sunlight and visible light were separately used as a light source to evaluate the photocatalytic activity of the samples toward the degradation of RhB in aqueous solution. Under both simulated sunlight and visible light irradiation, CQDs@Bi4Ti3O12 composites with an appropriate amount of CQDs exhibit obviously enhanced photocatalytic performance. However, the decoration of excessive CQDs gives rise to a decrease in the photocatalytic activity. The enhanced photocatalytic activity of CQDs-modified Bi4Ti3O12 can be attributed to the following reasons: (1) The electron transfer between Bi4Ti3O12 and CQDs promotes an efficient separation of photogenerated electron/hole pairs in Bi4Ti3O12; (2) the up-conversion photoluminescence emitted from CQDs could induce the generation of additional electron/hole pairs in Bi4Ti3O12; and (3) the photoexcited electrons in CQDs could participate in the photocatalytic reactions.

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.

Fabrication of Novel Z-Scheme Bi2WO6/NaBiO3 Nanocomposites with Enhanced Photocatalytic Activity in the Degradation of 2,3-Dichlorophenol

2020 ◽  
Vol 20 (5) ◽  
pp. 3105-3116 ◽  
Author(s):  
Xin-Yue Gu ◽  
Qiu Wang ◽  
Da-Peng Zhang ◽  
Xin-Xiang Geng ◽  
Zhen-Xing Zha ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Energy Dispersive Spectrometer ◽  
Energy Levels ◽  
Degradation Process ◽  
Photoelectrochemical Performance ◽  
X Ray ◽  
Oxidative Species

The Z-scheme Bi2WO6/NaBiO3 nanocomposites were first fabricated by a facile hydrothermal method, and were then characterized by X-ray diffraction, transmission electron microscopy, scanning electron microscopy, energy dispersive spectrometer, Fourier-transform-infrared spectroscopy, X-ray photoelectron spectroscopy and N2 adsorption–desorption. The as-prepared Bi2WO6/NaBiO3 nanocomposites exhibit outstanding photocatalytic activity and recyclability. A 98.4% photodegradation of 2,3-dichlorophenol (50 mg·L−1) was attained in the presence of Bi2WO6/NaBiO3 (1:10) under the visible-light irradiation in 30 min. In particular, the photocatalytic mechanism has been discussed in detail, based on four aspects: (1) oxidative species, (2) photoelectrochemical performance, (3) conduction band and valence band energy levels and (4) possible transition states and reactions. In conclusion, O−2 is the main active oxidative species in the Bi2WO6/NaBiO3 nanocomposite. The material has higher photocurrent and visible light adsorption but lower electron–hole pairs recombination, which contributes to distinguished photocatalytic efficiency. The Z-scheme photocatalytic path was proposed and the possible degradation process and routes have been summarized.

scholarly journals Fabrication of Bi-DopedTiO2Spheres with Ultrasonic Spray Pyrolysis and Investigation of Their Visible-Light Photocatalytic Properties

2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Jianhui Huang ◽  
Wahkit Cheuk ◽  
Yifan Wu ◽  
Frank S. C. Lee ◽  
Wingkei Ho
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Spray Pyrolysis ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Ultrasonic Spray Pyrolysis ◽  
X Ray ◽  
Ultrasonic Spray ◽  
Doped Titania

Bismuth-doped TiO2submicrospheres were synthesized by ultrasonic spray pyrolysis. The prepared bismuth-doped titania was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV-visible diffuse reflectance spectroscopy (UV-vis DRS), and X-ray photoelectron spectroscopy (XPS). Aqueous photocatalytic activity was evaluated by the decomposition of methyl orange under visible-light irradiation. The results indicate that doping of bismuth remarkably affects the phase composition, crystal structure, and the photocatalytic activity. The sample with 2% Bi exhibits the optimum photocatalytic activity.

Synthesis of MoS2/TiO2 Nanophotocatalyst and Its Enhanced Visible Light Driven Photocatalytic Performance

2019 ◽  
Vol 19 (6) ◽  
pp. 3519-3527 ◽  
Author(s):  
Wei Teng ◽  
Youmei Wang ◽  
Qin Lin ◽  
Hui Zhu ◽  
Yubin Tang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Irradiation Time ◽  
Metal Sulfide ◽  
Active Species ◽  
X Ray ◽  
Radical Trapping ◽  
Layered Transition Metal

Molybdenum disulfide (MoS2), as a typical layered transition metal sulfide, has been widely used in photocatalysis. Here, we report layered MoS2 nanosheet-coated TiO2 heterostructures that were prepared using a simple photo-assisted deposition method. The as-prepared samples were investigated in detail by using X-ray diffraction, Raman spectroscopy, scanning electron microscopy, transmission electron microscopy, and X-ray photoelectron spectroscopy. Results demonstrated that the MoS2 nanosheets uniformly covered the outer surface of TiO2. The visible light-sensitive photocatalytic activity was evaluated by the removal of methylene blue (MB) and 2-chlorophenol (2-CP) in aqueous solution. Thus, the MoS2/TiO2 heterostructures exhibited improved photocatalytic degradation activity under visible light compared with the pure TiO2. Under visible light irradiation for 90 min, the degradation efficiencies of MB and 2-CP over the MoS2/TiO2 sample (sunlight irradiation time: 30 min) are as high as 93.6% and 70.6%, respectively. Furthermore, the corresponding mechanism of enhanced photocatalytic activity is proposed on the basis of the comprehensively investigated results from the radical trapping experiments, photoluminescence spectroscopy, and electron spin resonance analysis. The hole oxidation, hydroxyl radicals, and superoxide anion radicals act as the active species simultaneously in the photodegradation of the dye molecules. However, of these species, hole oxidation played the most important roles in the photocatalytic reaction.

Improved visible-light photocatalytic activity of sodium tantalum oxide via biomass-derived silk fibroin doping

2018 ◽  
Vol 89 (7) ◽  
pp. 1332-1339
Author(s):  
Yehua Sun ◽  
Yuzhuo Luo ◽  
Yaofeng Zhu ◽  
Yaqin Fu
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Silk Fibroin ◽  
Photoelectron Spectroscopy ◽  
Structural Changes ◽  
Diffuse Reflectance Spectroscopy ◽  
Hydrothermal Process ◽  
X Ray ◽  
Transmission Electron

Biomass-derived silk fibroin (SF)-doped NaTaO3 catalysts were successfully synthesized by a simple hydrothermal process using SF as the dopant. The as-prepared samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and ultraviolet-visible diffuse reflectance spectroscopy (UV-vis DRS) analyses. The samples were tested as photocatalysts in the degradation of methylene blue under UV and visible light. XRD results showed the monoclinic structure of NaTaO3 lacking significant structural changes after anion doping. SEM and TEM images revealed the nanocubic morphology of the samples, the crystal particle sizes of which were about 100–300 nm. The XPS spectrum showed the peak of Ta4p3&N1s, indicating the combination of N and Ta. The UV-vis DRS results of the samples revealed a cut-off edge that red shifted from 315 nm of the pure NaTaO3 to 324 nm of the SF-doped counterpart. SF doping helped narrow the band gap and rendered the prepared sample sensitive to visible light. Under UV and visible-light irradiation, SF-doped NaTaO3 exhibited higher photocatalytic activity than that the undoped compound. SF-doped NaTaO3 samples also exhibited excellent stability during the recycling photocatalytic process.

scholarly journals Visible Light Driven Spherical CuBi2O4 with Surface Oxygen Vacancy Enhanced Photocatalytic Activity: Catalyst Fabrication, Performance, and Reaction Mechanism

Catalysts ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 945
Author(s):  
Xin Zhong ◽  
Yihong Cai ◽  
Heping Bai ◽  
Wei Huang ◽  
Binxue Zhou
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Oxygen Vacancy ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Interface Reaction ◽  
Surface Oxygen ◽  
X Ray ◽  
Valence States ◽  
Surface Oxygen Vacancy

Here, a spherical CuBi2O4 catalyst with surface oxygen vacancy was fabricated through a facile hydrothermal method, which exhibited remarkable enhanced photocatalytic activity of refractory chemicals in the heterogeneous sulfate radical-based Fenton-like reaction under visible light emitting diode (LED) light irradiation. The property of the catalysts was systematically characterized by scanning electron microscopy (SEM)/high resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and UV/vis methods. The effects of parameters of solution pH, potassium peroxymonosulfate (PMS) concentration, catalyst dosage, and catalyst reusability on Rhodamine B (RhB) degradation were investigated. In the interface reaction, the improved photodegradation efficiency could be attributed to the decomposition of PMS, which produced sulfate radicals and hydroxyl radicals owing to the transmission of photo-generated electron/hole pairs. Herein, the introduction of surface oxygen vacancy as well as the cycling of copper valence states (Cu(II)/Cu(I) pairs) can facilitate the production of free reactive radicals, leading to the high degradation efficiency. The catalyst showed high removal efficiency and presented good cycle stability in the reaction. Additionally, the free radical quencher experiment and electron spin resonance (EPR) experiments were conducted, and a proposed photocatalytic mechanism was also illustrated.

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