scholarly journals Enhanced Photocatalytic Activity of W-Doped and W-La-Codoped TiO2Nanomaterials under Simulated Sunlight

2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
Chenghe Hua ◽  
Xiaoli Dong ◽  
Xiuying Wang ◽  
Mang Xue ◽  
Xiufang Zhang ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Absorption Edge ◽  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
Methyl Orange Solution ◽  
High Photocatalytic Activity ◽  
Simulated Sunlight ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron

W-doped TiO2and W-La-codoped TiO2nanomaterials were successfully synthesized via the sol-gel method. The products were characterized by X-ray diffraction, UV-vis diffuse reflectance spectrophotometer, transmission electron microscopy, and X-ray photoelectron spectroscopy. The presence of W and La results in significant red shift of absorption edge for TiO2-based nanomaterials. The weight ratios of La and W in the composites play important roles in the absorption edge for TiO2-based nanomaterials. The photocatalytic activities of both W-doped TiO2and W-La-codoped TiO2photocatalysts for decolorization of methyl orange solution were evaluated under simulated sunlight irradiation. The results showed that both W-doped and W-La-codoped can effectively improve the photocatalytic behaviors of TiO2nanomaterials ascribed to the improved photoinduced charge carriers separation, enhanced light absorption, and large surface area. Furthermore, W-La-codoped TiO2exhibited higher photocatalytic activity than W-doped TiO2. Considering their high photocatalytic activity, the doped TiO2nanomaterials could be applied in wastewater treatment and environmental purification.

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 Improved Visible Light Photocatalytic Activity for TiO2Nanomaterials by Codoping with Zinc and Sulfur

2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Qianzhi Xu ◽  
Xiuying Wang ◽  
Xiaoli Dong ◽  
Chun Ma ◽  
Xiufang Zhang ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
Sunlight Irradiation ◽  
X Ray ◽  
Transmission Electron ◽  
Photoinduced Charge

S/Zn codoped TiO2nanomaterials were synthesized by a sol-gel method. X-ray diffraction, UV-vis diffuse reflectance spectroscopy, transmission electron microscopy, photoluminescence spectroscopy, and X-ray photoelectron spectroscopy were used to characterize the morphology, structure, and optical properties of the prepared samples. The introduction of Zn and S resulted in significant red shift of absorption edge for TiO2-based nanomaterials. The photocatalytic activity was evaluated by degrading reactive brilliant red X-3B solution under simulated sunlight irradiation. The results showed S/Zn codoped TiO2exhibited higher photocatalytic activity than pure TiO2and commercial P25, due to the photosynergistic effect of obvious visible light absorption, efficient separation of photoinduced charge carriers, and large surface area. Moreover, the content of Zn and S in the composites played important roles in photocatalytic activity of TiO2-based nanomaterials.

scholarly journals One-Step Synthesis of b-N-TiO2/C Nanocomposites with High Visible Light Photocatalytic Activity to Degrade Microcystis aeruginosa

Catalysts ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 579
Author(s):  
Xu Zhang ◽  
Min Cai ◽  
Naxin Cui ◽  
Guifa Chen ◽  
Guoyan Zou ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Chlorophyll A ◽  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
Paramagnetic Resonance ◽  
X Ray ◽  
Transmission Electron ◽  
One Step

Black TiO2 with doped nitrogen and modified carbon (b-N-TiO2/C) were successfully prepared by sol-gel method in the presence of urea as a source of nitrogen and carbon. The photocatalysts were characterized by field emission scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Raman, electron paramagnetic resonance (EPR), and UV-vis diffuse reflectance spectra (DRS). The doped nitrogen, introduced defects, and modified carbon played a synergistic role in enhancing photocatalytic activity of b-N-TiO2/C for the degradation of chlorophyll-a in algae cells. The sample, with a proper amount of phase composition and oxygen vacancies, showed the highest efficiency to degrade chlorophyll-a, and the addition of H2O2 promoted this photocatalysis degradation. Based on the trapping experiments and electron spin resonance (ESR) signals, a photocatalytic mechanism of b-N-TiO2/C was proposed. In the photocatalytic degradation of chlorophyll-a, the major reactive species were identified as OH and O2−. This research may provide new insights into the photocatalytic inactivation of algae cells by composite photocatalysts.

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.

Preparation and Photocatalytic Property of TiO2/NiFe2O4 Composite Photocatalysts

2012 ◽  
Vol 518-523 ◽  
pp. 775-779 ◽  
Author(s):  
Dong Dong Tan ◽  
De Fu Bi ◽  
Peng Hui Shi ◽  
Shi Hong Xu
Keyword(s):  
Photocatalytic Activity ◽  
Sol Gel ◽  
Photocatalytic Property ◽  
Methyl Orange Solution ◽  
X Ray Diffraction ◽  
Doping Amount ◽  
X Ray ◽  
Uv Illumination ◽  
Composite Photocatalysts ◽  
Orange Solution

The TiO2/NiFe2O4 (TN) composite nanoparticles with different mass ratios of NiFe2O4 to TiO2 were prepared via sol-gel method. X-ray diffraction was used to characterize the phase structure of TN. The results indicated that adulterating a smidgen of NiFe2O4 into the TiO2 (about 0.1%) can promote the phase transformation of TiO2, however, when the doping amount of NiFe2O4 surpasses 1%, the introduction of NiFe2O4 can inhibit the growth of TiO2 crystal grain and reduce the size of TiO2 crystal grain. The degradation experiment of methyl orange solution under UV illumination (253.7 nm) showed that the content of NiFe2O4 in the TN was higher, the photocatalytic activity of TN was worse, and the 0.1% TiO2/NiFe2O4 calcined at 400 °C presented the best photocatalytic activity.

FeYO3@rGO nanocomposites: Synthesis, characterization and application in photooxidative degradation of atrazine under visible light

2021 ◽  
Vol 11 (5) ◽  
pp. 706-716
Author(s):  
Nada D. Al-Khthami ◽  
Tariq Altalhi ◽  
Mohammed Alsawat ◽  
Mohamed S. Amin ◽  
Yousef G. Alghamdi ◽  
...  
Keyword(s):  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
Bandgap Energy ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Reduced Graphene ◽  
Structural Surface ◽  
Adsorption Desorption

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.

scholarly journals Hydrothermal Synthesis of Iodine-Doped Nanoplates with Enhanced Visible and Ultraviolet-Induced Photocatalytic Activities

2012 ◽  
Vol 2012 ◽  
pp. 1-12 ◽  
Author(s):  
Jiang Zhang ◽  
Zheng-Hong Huang ◽  
Yong Xu ◽  
Feiyu Kang
Keyword(s):  
Photocatalytic Activity ◽  
Photoelectron Spectroscopy ◽  
Oxygen Vacancies ◽  
Diffuse Reflectance Spectroscopy ◽  
Synergetic Effect ◽  
X Ray Diffraction ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Photocatalytic Activities

The iodine-doped Bi2WO6(I-BWO) photocatalyst was prepared via a hydrothermal method using potassium iodide as the source of iodine. The samples were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM) and selected area electron diffraction (SAED), X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance spectroscopy (DRS), and photoluminescence (PL) spectroscopy. The photocatalytic activity of I-BWO for the degradation of rhodamine B (RhB) was higher than that of pure BWO and I2-BWO regardless of visible light (>420 nm) or ultraviolet light (<400 nm) irradiation. The results of DRS analysis showed that the I-BWO and I2-BWO catalysts had narrower band gaps. XPS analysis proved that the multivalent iodine species including I0and were coadsorbed on the defect surface of Bi2WO6in I-BWO. The enhanced PL intensity revealed that a large number of defects of oxygen vacancies were formed by the doping of iodine. The enhanced photocatalytic activity of I-BWO for degradation of RhB was caused by the synergetic effect of a small crystalline size, a narrow band gap, and plenty of oxygen vacancies.

Influence of Ag Doping on the Crystal Structure and Photocatalytic Activity of FeVO4

2011 ◽  
Vol 197-198 ◽  
pp. 919-925 ◽  
Author(s):  
Min Wang ◽  
Qiong Liu
Keyword(s):  
Photocatalytic Activity ◽  
Methyl Orange ◽  
Photoelectron Spectroscopy ◽  
Methyl Orange Solution ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
Electron Hole ◽  
X Ray ◽  
Orange Solution ◽  
Decoloration Rate

Silver (Ag+) doped iron (III) vanadate (FeVO4) samples are prepared by the precipitation method and then characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), and X-ray photoelectron spectroscopy(XPS). The photocatalytic activity under visible light is evaluated by photocatalytic degradation of methyl orange (MO) in the solution. The results show that both FeVO4 and Ag+ doped FeVO4 samples are triclinic, the later have different surface morphology, and some needle-shaped materials appear in the later. From XPS, there are more Fe2+ ions in Ag+ doped FeVO4 sample than that in FeVO4 one without Ag+. It indicates that Ag+ doping can increase the density of the surface oxygen vacancies of catalysts, which can act as electron traps promoting the electron-hole separation and then increase the photo-activity. The decoloration rate after Ag+ doping against methyl orange solution can reach about 81%, and be more about 20％ than that of pure FeVO4.

scholarly journals Photocatalytic Performance of SiO2/CNOs/TiO2 to Accelerate the Degradation of Rhodamine B under Visible Light

Nanomaterials ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 1671 ◽  
Author(s):  
Weike Zhang ◽  
Yanrong Zhang ◽  
Kai Yang ◽  
Yanqing Yang ◽  
Jia Jia ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Visible Light ◽  
Rhodamine B ◽  
Photoelectron Spectroscopy ◽  
Degradation Rate ◽  
Photocatalytic Performance ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Electronic Microscope

A silicon dioxide/carbon nano onions/titanium dioxide (SiO2/CNOs/TiO2) composite was synthesized by a simple sol-gel method and characterized by the methods of X-ray diffraction (XRD), scanning electronic microscope (SEM), X-ray photoelectron spectroscopy (XPS), Brunauer–Emmett–Teller (BET), Fourier transform infrared (FTIR), thermogravimetric analysis (TG), differential scanning calorimeter (DSC) and UV-Vis diffuse reflectance spectra (UV-Vis DRS). In this work, the photocatalytic activity of the SiO2/CNOs/TiO2 photocatalyst was assessed by testing the degradation rate of Rhodamine B (RhB) under visible light. The results indicated that the samples exhibited the best photocatalytic activity when the composite consisted of 3% CNOs and the optimum dosage of SiO2/CNOs/TiO2(3%) was 1.5 g/L as evidenced by the highest RhB degradation rate (96%). The SiO2/CNOs/TiO2 composite greatly improved the quantum efficiency of TiO2. This work provides a new option for the modification of subsequent nanocomposite oxide nanoparticles.

scholarly journals Ultrasound enhanced heterogeneous activation of peroxymonosulfate by a Co-NiOx catalyst

2017 ◽  
Vol 76 (6) ◽  
pp. 1436-1446 ◽  
Author(s):  
Chenmo Wei ◽  
Jing Zhang ◽  
Yongli Zhang ◽  
Gucheng Zhang ◽  
Peng Zhou ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
Maximum Efficiency ◽  
Acid Orange 7 ◽  
X Ray Diffraction ◽  
X Ray ◽  
Surface Hydroxyl ◽  
Transmission Electron ◽  
Initial Ph ◽  
Reactive Oxidant

Sulfate radical-based advanced oxidation processes have had considerable attention due to the highly oxidizing function of sulfate radicals (SO4−·) resulting in acceleration of organic pollutants degradation in aqueous environments. A Co-Ni mixed oxide nanocatalyst, which was prepared by the sol-gel method, was employed to activate peroxymonosulfate (PMS, HSO5−) to produce SO4−· with Acid Orange 7 (AO7) selected as a radical probe. The catalyst was characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR) and transmission electron microscopy (TEM). The characterization results indicated that the ingredient of the catalyst had been changed and the amount of surface hydroxyl increased significantly with the addition of Ni. Therefore, it proved that Co-NiOx catalyst was more effective than CoOx to activate PMS. Moreover, ultrasound (US) can increase the degradation rate of AO7 and US/Co-NiOx/PMS system. This study also focused on some synthesis parameters and the system reached the maximum efficiency under the condition when [PMS] = 0.4 mM, [catalyst] = 0.28 g/L, Pus = 200 W. The AO7 removal in these systems follows first order kinetics. Last but not least, quenching studies was conducted which indicated that the amount of hydroxyl radicals (·OH) increases with the increase of initial pH and SO4−· was the primary reactive oxidant for AO7 degradation.

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